Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children
Identifieur interne : 000690 ( Pmc/Corpus ); précédent : 000689; suivant : 000691Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children
Auteurs : Leah Cuthbertson ; Stephen W. C. Oo ; Michael J. Cox ; Siew-Kim Khoo ; Des W. Cox ; Glenys Chidlow ; Kimberley Franks ; Franciska Prastanti ; Meredith L. Borland ; James E. Gern ; David W. Smith ; Joelene A. Bizzintino ; Ingrid A. Laing ; Peter N. Le Souëf ; Miriam F. Moffatt ; William O. C. CooksonSource :
- PLoS ONE [ 1932-6203 ] ; 2019.
Abstract
Acute viral wheeze in children is a major cause of hospitalisation and a major risk factor for the development of asthma. However, the role of the respiratory tract microbiome in the development of acute wheeze is unclear. To investigate whether severe wheezing episodes in children are associated with bacterial dysbiosis in the respiratory tract, oropharyngeal swabs were collected from 109 children with acute wheezing attending the only tertiary paediatric hospital in Perth, Australia. The bacterial community from these samples was explored using next generation sequencing and compared to samples from 75 non-wheezing controls. No significant difference in bacterial diversity was observed between samples from those with wheeze and healthy controls. Within the wheezing group, attendance at kindergarten or preschool was however, associated with increased bacterial diversity. Rhinovirus (RV) infection did not have a significant effect on bacterial community composition. A significant difference in bacterial richness was observed between children with RV-A and RV-C infection, however this is likely due to the differences in age group between the patient cohorts. The bacterial community within the oropharynx was found to be diverse and heterogeneous. Age and attendance at day care or kindergarten were important factors in driving bacterial diversity. However, wheeze and viral infection were not found to significantly relate to the bacterial community. Bacterial airway microbiome is highly variable in early life and its role in wheeze remains less clear than viral influences.
Url:
DOI: 10.1371/journal.pone.0223990
PubMed: 31622414
PubMed Central: 6797130
Links to Exploration step
PMC:6797130Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children</title><author><name sortKey="Cuthbertson, Leah" sort="Cuthbertson, Leah" uniqKey="Cuthbertson L" first="Leah" last="Cuthbertson">Leah Cuthbertson</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author><author><name sortKey="Oo, Stephen W C" sort="Oo, Stephen W C" uniqKey="Oo S" first="Stephen W. C." last="Oo">Stephen W. C. Oo</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff003"><addr-line>Respiratory Department, Perth Children’s Hospital, Perth, Western Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cox, Michael J" sort="Cox, Michael J" uniqKey="Cox M" first="Michael J." last="Cox">Michael J. Cox</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author><author><name sortKey="Khoo, Siew Kim" sort="Khoo, Siew Kim" uniqKey="Khoo S" first="Siew-Kim" last="Khoo">Siew-Kim Khoo</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cox, Des W" sort="Cox, Des W" uniqKey="Cox D" first="Des W." last="Cox">Des W. Cox</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Chidlow, Glenys" sort="Chidlow, Glenys" uniqKey="Chidlow G" first="Glenys" last="Chidlow">Glenys Chidlow</name><affiliation><nlm:aff id="aff005"><addr-line>Department of Microbiology, PathWest Laboratory Medicine WA, QEII Medical Centre, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Franks, Kimberley" sort="Franks, Kimberley" uniqKey="Franks K" first="Kimberley" last="Franks">Kimberley Franks</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Prastanti, Franciska" sort="Prastanti, Franciska" uniqKey="Prastanti F" first="Franciska" last="Prastanti">Franciska Prastanti</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Borland, Meredith L" sort="Borland, Meredith L" uniqKey="Borland M" first="Meredith L." last="Borland">Meredith L. Borland</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff006"><addr-line>Emergency Department, Perth Children’s Hospital, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff007"><addr-line>Division of Emergency Medicine, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Gern, James E" sort="Gern, James E" uniqKey="Gern J" first="James E." last="Gern">James E. Gern</name><affiliation><nlm:aff id="aff008"><addr-line>Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Smith, David W" sort="Smith, David W" uniqKey="Smith D" first="David W." last="Smith">David W. Smith</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff005"><addr-line>Department of Microbiology, PathWest Laboratory Medicine WA, QEII Medical Centre, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff009"><addr-line>Medical School, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Bizzintino, Joelene A" sort="Bizzintino, Joelene A" uniqKey="Bizzintino J" first="Joelene A." last="Bizzintino">Joelene A. Bizzintino</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Laing, Ingrid A" sort="Laing, Ingrid A" uniqKey="Laing I" first="Ingrid A." last="Laing">Ingrid A. Laing</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Le Souef, Peter N" sort="Le Souef, Peter N" uniqKey="Le Souef P" first="Peter N." last="Le Souëf">Peter N. Le Souëf</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Moffatt, Miriam F" sort="Moffatt, Miriam F" uniqKey="Moffatt M" first="Miriam F." last="Moffatt">Miriam F. Moffatt</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cookson, William O C" sort="Cookson, William O C" uniqKey="Cookson W" first="William O. C." last="Cookson">William O. C. Cookson</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff010"><addr-line>Royal Brompton and Harefield NHS Foundation Trust, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">31622414</idno><idno type="pmc">6797130</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797130</idno><idno type="RBID">PMC:6797130</idno><idno type="doi">10.1371/journal.pone.0223990</idno><date when="2019">2019</date><idno type="wicri:Area/Pmc/Corpus">000690</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000690</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children</title><author><name sortKey="Cuthbertson, Leah" sort="Cuthbertson, Leah" uniqKey="Cuthbertson L" first="Leah" last="Cuthbertson">Leah Cuthbertson</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author><author><name sortKey="Oo, Stephen W C" sort="Oo, Stephen W C" uniqKey="Oo S" first="Stephen W. C." last="Oo">Stephen W. C. Oo</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff003"><addr-line>Respiratory Department, Perth Children’s Hospital, Perth, Western Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cox, Michael J" sort="Cox, Michael J" uniqKey="Cox M" first="Michael J." last="Cox">Michael J. Cox</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author><author><name sortKey="Khoo, Siew Kim" sort="Khoo, Siew Kim" uniqKey="Khoo S" first="Siew-Kim" last="Khoo">Siew-Kim Khoo</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cox, Des W" sort="Cox, Des W" uniqKey="Cox D" first="Des W." last="Cox">Des W. Cox</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Chidlow, Glenys" sort="Chidlow, Glenys" uniqKey="Chidlow G" first="Glenys" last="Chidlow">Glenys Chidlow</name><affiliation><nlm:aff id="aff005"><addr-line>Department of Microbiology, PathWest Laboratory Medicine WA, QEII Medical Centre, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Franks, Kimberley" sort="Franks, Kimberley" uniqKey="Franks K" first="Kimberley" last="Franks">Kimberley Franks</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Prastanti, Franciska" sort="Prastanti, Franciska" uniqKey="Prastanti F" first="Franciska" last="Prastanti">Franciska Prastanti</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Borland, Meredith L" sort="Borland, Meredith L" uniqKey="Borland M" first="Meredith L." last="Borland">Meredith L. Borland</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff006"><addr-line>Emergency Department, Perth Children’s Hospital, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff007"><addr-line>Division of Emergency Medicine, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Gern, James E" sort="Gern, James E" uniqKey="Gern J" first="James E." last="Gern">James E. Gern</name><affiliation><nlm:aff id="aff008"><addr-line>Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Smith, David W" sort="Smith, David W" uniqKey="Smith D" first="David W." last="Smith">David W. Smith</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff005"><addr-line>Department of Microbiology, PathWest Laboratory Medicine WA, QEII Medical Centre, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff009"><addr-line>Medical School, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Bizzintino, Joelene A" sort="Bizzintino, Joelene A" uniqKey="Bizzintino J" first="Joelene A." last="Bizzintino">Joelene A. Bizzintino</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Laing, Ingrid A" sort="Laing, Ingrid A" uniqKey="Laing I" first="Ingrid A." last="Laing">Ingrid A. Laing</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Le Souef, Peter N" sort="Le Souef, Peter N" uniqKey="Le Souef P" first="Peter N." last="Le Souëf">Peter N. Le Souëf</name><affiliation><nlm:aff id="aff002"><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff004"><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></nlm:aff></affiliation></author><author><name sortKey="Moffatt, Miriam F" sort="Moffatt, Miriam F" uniqKey="Moffatt M" first="Miriam F." last="Moffatt">Miriam F. Moffatt</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cookson, William O C" sort="Cookson, William O C" uniqKey="Cookson W" first="William O. C." last="Cookson">William O. C. Cookson</name><affiliation><nlm:aff id="aff001"><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="aff010"><addr-line>Royal Brompton and Harefield NHS Foundation Trust, London, England, United Kingdom</addr-line></nlm:aff></affiliation></author></analytic><series><title level="j">PLoS ONE</title><idno type="eISSN">1932-6203</idno><imprint><date when="2019">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Acute viral wheeze in children is a major cause of hospitalisation and a major risk factor for the development of asthma. However, the role of the respiratory tract microbiome in the development of acute wheeze is unclear. To investigate whether severe wheezing episodes in children are associated with bacterial dysbiosis in the respiratory tract, oropharyngeal swabs were collected from 109 children with acute wheezing attending the only tertiary paediatric hospital in Perth, Australia. The bacterial community from these samples was explored using next generation sequencing and compared to samples from 75 non-wheezing controls. No significant difference in bacterial diversity was observed between samples from those with wheeze and healthy controls. Within the wheezing group, attendance at kindergarten or preschool was however, associated with increased bacterial diversity. Rhinovirus (RV) infection did not have a significant effect on bacterial community composition. A significant difference in bacterial richness was observed between children with RV-A and RV-C infection, however this is likely due to the differences in age group between the patient cohorts. The bacterial community within the oropharynx was found to be diverse and heterogeneous. Age and attendance at day care or kindergarten were important factors in driving bacterial diversity. However, wheeze and viral infection were not found to significantly relate to the bacterial community. Bacterial airway microbiome is highly variable in early life and its role in wheeze remains less clear than viral influences.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Goto, T" uniqKey="Goto T">T Goto</name></author><author><name sortKey="Tsugawa, Y" uniqKey="Tsugawa Y">Y Tsugawa</name></author><author><name sortKey="Mansbach, Jm" uniqKey="Mansbach J">JM Mansbach</name></author><author><name sortKey="Camargo, Ca" uniqKey="Camargo C">CA Camargo</name></author><author><name sortKey="Hasegawa, K" uniqKey="Hasegawa K">K Hasegawa</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Bisgaard, H" uniqKey="Bisgaard H">H Bisgaard</name></author><author><name sortKey="Hermansen, Mn" uniqKey="Hermansen M">MN Hermansen</name></author><author><name sortKey="Buchvald, F" uniqKey="Buchvald F">F Buchvald</name></author><author><name sortKey="Loland, L" uniqKey="Loland L">L Loland</name></author><author><name 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<front><journal-meta><journal-id journal-id-type="nlm-ta">PLoS One</journal-id><journal-id journal-id-type="iso-abbrev">PLoS ONE</journal-id><journal-id journal-id-type="publisher-id">plos</journal-id><journal-id journal-id-type="pmc">plosone</journal-id><journal-title-group><journal-title>PLoS ONE</journal-title></journal-title-group><issn pub-type="epub">1932-6203</issn><publisher><publisher-name>Public Library of Science</publisher-name><publisher-loc>San Francisco, CA USA</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">31622414</article-id><article-id pub-id-type="pmc">6797130</article-id><article-id pub-id-type="doi">10.1371/journal.pone.0223990</article-id><article-id pub-id-type="publisher-id">PONE-D-19-20152</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Biology and Life Sciences</subject><subj-group><subject>Microbiology</subject><subj-group><subject>Medical Microbiology</subject><subj-group><subject>Microbiome</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Biology and Life Sciences</subject><subj-group><subject>Genetics</subject><subj-group><subject>Genomics</subject><subj-group><subject>Microbial Genomics</subject><subj-group><subject>Microbiome</subject></subj-group></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Biology and Life Sciences</subject><subj-group><subject>Microbiology</subject><subj-group><subject>Microbial Genomics</subject><subj-group><subject>Microbiome</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Medicine and Health Sciences</subject><subj-group><subject>Pulmonology</subject><subj-group><subject>Bronchiolitis</subject></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Research and Analysis Methods</subject><subj-group><subject>Database and Informatics Methods</subject><subj-group><subject>Biological Databases</subject><subj-group><subject>Sequence Databases</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Research and Analysis Methods</subject><subj-group><subject>Database and Informatics Methods</subject><subj-group><subject>Bioinformatics</subject><subj-group><subject>Sequence Analysis</subject><subj-group><subject>Sequence Databases</subject></subj-group></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Medicine and Health Sciences</subject><subj-group><subject>Pulmonology</subject><subj-group><subject>Respiratory Infections</subject></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>People and Places</subject><subj-group><subject>Population Groupings</subject><subj-group><subject>Age Groups</subject><subj-group><subject>Children</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>People and Places</subject><subj-group><subject>Population Groupings</subject><subj-group><subject>Families</subject><subj-group><subject>Children</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Medicine and Health Sciences</subject><subj-group><subject>Infectious Diseases</subject><subj-group><subject>Viral Diseases</subject><subj-group><subject>Rhinovirus Infection</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Biology and Life Sciences</subject><subj-group><subject>Microbiology</subject><subj-group><subject>Virology</subject><subj-group><subject>Viral Transmission and Infection</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Biology and life sciences</subject><subj-group><subject>Biochemistry</subject><subj-group><subject>Nucleic acids</subject><subj-group><subject>RNA</subject><subj-group><subject>Non-coding RNA</subject><subj-group><subject>Ribosomal RNA</subject></subj-group></subj-group></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Biology and life sciences</subject><subj-group><subject>Biochemistry</subject><subj-group><subject>Ribosomes</subject><subj-group><subject>Ribosomal RNA</subject></subj-group></subj-group></subj-group></subj-group><subj-group subj-group-type="Discipline-v3"><subject>Biology and life sciences</subject><subj-group><subject>Cell biology</subject><subj-group><subject>Cellular structures and organelles</subject><subj-group><subject>Ribosomes</subject><subj-group><subject>Ribosomal RNA</subject></subj-group></subj-group></subj-group></subj-group></subj-group></article-categories><title-group><article-title>Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children</article-title><alt-title alt-title-type="running-head">Viral respiratory infections and the bacterial microbiota in wheezing children</alt-title></title-group><contrib-group><contrib contrib-type="author" equal-contrib="yes"><contrib-id authenticated="true" contrib-id-type="orcid">http://orcid.org/0000-0002-9604-2269</contrib-id><name><surname>Cuthbertson</surname><given-names>Leah</given-names></name><role content-type="http://credit.casrai.org/">Formal analysis</role><role content-type="http://credit.casrai.org/">Methodology</role><role content-type="http://credit.casrai.org/">Writing – original draft</role><role content-type="http://credit.casrai.org/">Writing – review & editing</role><xref ref-type="aff" rid="aff001"><sup>1</sup></xref><xref ref-type="corresp" rid="cor001">*</xref></contrib><contrib contrib-type="author" equal-contrib="yes"><name><surname>Oo</surname><given-names>Stephen W. C.</given-names></name><role content-type="http://credit.casrai.org/">Data curation</role><role content-type="http://credit.casrai.org/">Investigation</role><role content-type="http://credit.casrai.org/">Methodology</role><role content-type="http://credit.casrai.org/">Writing – review & editing</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff003"><sup>3</sup></xref></contrib><contrib contrib-type="author"><name><surname>Cox</surname><given-names>Michael J.</given-names></name><role content-type="http://credit.casrai.org/">Methodology</role><role content-type="http://credit.casrai.org/">Writing – review & editing</role><xref ref-type="aff" rid="aff001"><sup>1</sup></xref></contrib><contrib contrib-type="author"><name><surname>Khoo</surname><given-names>Siew-Kim</given-names></name><role content-type="http://credit.casrai.org/">Data curation</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff004"><sup>4</sup></xref></contrib><contrib contrib-type="author"><name><surname>Cox</surname><given-names>Des W.</given-names></name><role content-type="http://credit.casrai.org/">Data curation</role><role content-type="http://credit.casrai.org/">Investigation</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref></contrib><contrib contrib-type="author"><name><surname>Chidlow</surname><given-names>Glenys</given-names></name><role content-type="http://credit.casrai.org/">Investigation</role><xref ref-type="aff" rid="aff005"><sup>5</sup></xref></contrib><contrib contrib-type="author"><name><surname>Franks</surname><given-names>Kimberley</given-names></name><role content-type="http://credit.casrai.org/">Data curation</role><role content-type="http://credit.casrai.org/">Investigation</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff004"><sup>4</sup></xref></contrib><contrib contrib-type="author"><name><surname>Prastanti</surname><given-names>Franciska</given-names></name><role content-type="http://credit.casrai.org/">Data curation</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff004"><sup>4</sup></xref></contrib><contrib contrib-type="author"><name><surname>Borland</surname><given-names>Meredith L.</given-names></name><role content-type="http://credit.casrai.org/">Data curation</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff006"><sup>6</sup></xref><xref ref-type="aff" rid="aff007"><sup>7</sup></xref></contrib><contrib contrib-type="author"><name><surname>Gern</surname><given-names>James E.</given-names></name><role content-type="http://credit.casrai.org/">Investigation</role><role content-type="http://credit.casrai.org/">Methodology</role><xref ref-type="aff" rid="aff008"><sup>8</sup></xref></contrib><contrib contrib-type="author"><name><surname>Smith</surname><given-names>David W.</given-names></name><role content-type="http://credit.casrai.org/">Investigation</role><role content-type="http://credit.casrai.org/">Methodology</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff005"><sup>5</sup></xref><xref ref-type="aff" rid="aff009"><sup>9</sup></xref></contrib><contrib contrib-type="author"><name><surname>Bizzintino</surname><given-names>Joelene A.</given-names></name><role content-type="http://credit.casrai.org/">Conceptualization</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff004"><sup>4</sup></xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">http://orcid.org/0000-0002-1641-9899</contrib-id><name><surname>Laing</surname><given-names>Ingrid A.</given-names></name><role content-type="http://credit.casrai.org/">Conceptualization</role><role content-type="http://credit.casrai.org/">Data curation</role><role content-type="http://credit.casrai.org/">Project administration</role><xref ref-type="aff" rid="aff002"><sup><italic>2</italic></sup></xref><xref ref-type="aff" rid="aff004"><sup>4</sup></xref></contrib><contrib contrib-type="author"><name><surname>Le Souëf</surname><given-names>Peter N.</given-names></name><role content-type="http://credit.casrai.org/">Conceptualization</role><role content-type="http://credit.casrai.org/">Supervision</role><role content-type="http://credit.casrai.org/">Writing – review & editing</role><xref ref-type="aff" rid="aff002"><sup>2</sup></xref><xref ref-type="aff" rid="aff004"><sup>4</sup></xref><xref ref-type="author-notes" rid="econtrib001"><sup>‡</sup></xref></contrib><contrib contrib-type="author"><name><surname>Moffatt</surname><given-names>Miriam F.</given-names></name><role content-type="http://credit.casrai.org/">Conceptualization</role><role content-type="http://credit.casrai.org/">Supervision</role><xref ref-type="aff" rid="aff001"><sup>1</sup></xref><xref ref-type="author-notes" rid="econtrib001"><sup>‡</sup></xref></contrib><contrib contrib-type="author"><name><surname>Cookson</surname><given-names>William O. C.</given-names></name><role content-type="http://credit.casrai.org/">Conceptualization</role><role content-type="http://credit.casrai.org/">Supervision</role><role content-type="http://credit.casrai.org/">Writing – review & editing</role><xref ref-type="aff" rid="aff001"><sup>1</sup></xref><xref ref-type="aff" rid="aff010"><sup>10</sup></xref><xref ref-type="author-notes" rid="econtrib001"><sup>‡</sup></xref></contrib></contrib-group><aff id="aff001"><label>1</label><addr-line>National Heart and Lung Institute, Imperial College, London, England, United Kingdom</addr-line></aff><aff id="aff002"><label>2</label><addr-line>Division of Paediatrics, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></aff><aff id="aff003"><label>3</label><addr-line>Respiratory Department, Perth Children’s Hospital, Perth, Western Australia</addr-line></aff><aff id="aff004"><label>4</label><addr-line>Telethon Kids Institute, Perth, Australia</addr-line></aff><aff id="aff005"><label>5</label><addr-line>Department of Microbiology, PathWest Laboratory Medicine WA, QEII Medical Centre, Perth, Australia</addr-line></aff><aff id="aff006"><label>6</label><addr-line>Emergency Department, Perth Children’s Hospital, Perth, Australia</addr-line></aff><aff id="aff007"><label>7</label><addr-line>Division of Emergency Medicine, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></aff><aff id="aff008"><label>8</label><addr-line>Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America</addr-line></aff><aff id="aff009"><label>9</label><addr-line>Medical School, Faculty of Health and Medical Sciences, University of Western Australia, Perth, Australia</addr-line></aff><aff id="aff010"><label>10</label><addr-line>Royal Brompton and Harefield NHS Foundation Trust, London, England, United Kingdom</addr-line></aff><contrib-group><contrib contrib-type="editor"><name><surname>Jin</surname><given-names>Dong-Yan</given-names></name><role>Editor</role><xref ref-type="aff" rid="edit1"></xref></contrib></contrib-group><aff id="edit1"><addr-line>University of Hong Kong, HONG KONG</addr-line></aff><author-notes><fn fn-type="COI-statement" id="coi001"><p><bold>Competing Interests: </bold>The authors have declared that no competing interests exist.</p></fn><fn fn-type="other" id="econtrib001"><p>‡ These authors also contributed equally to this work.</p></fn><corresp id="cor001">* E-mail: <email>l.cuthbertson@imperial.ac.uk</email></corresp></author-notes><pub-date pub-type="epub"><day>17</day><month>10</month><year>2019</year></pub-date><pub-date pub-type="collection"><year>2019</year></pub-date><volume>14</volume><issue>10</issue><elocation-id>e0223990</elocation-id><history><date date-type="received"><day>17</day><month>7</month><year>2019</year></date><date date-type="accepted"><day>2</day><month>10</month><year>2019</year></date></history><permissions><copyright-statement>© 2019 Cuthbertson et al</copyright-statement><copyright-year>2019</copyright-year><copyright-holder>Cuthbertson et al</copyright-holder><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p></license></permissions><self-uri content-type="pdf" xlink:href="pone.0223990.pdf"></self-uri><abstract><p>Acute viral wheeze in children is a major cause of hospitalisation and a major risk factor for the development of asthma. However, the role of the respiratory tract microbiome in the development of acute wheeze is unclear. To investigate whether severe wheezing episodes in children are associated with bacterial dysbiosis in the respiratory tract, oropharyngeal swabs were collected from 109 children with acute wheezing attending the only tertiary paediatric hospital in Perth, Australia. The bacterial community from these samples was explored using next generation sequencing and compared to samples from 75 non-wheezing controls. No significant difference in bacterial diversity was observed between samples from those with wheeze and healthy controls. Within the wheezing group, attendance at kindergarten or preschool was however, associated with increased bacterial diversity. Rhinovirus (RV) infection did not have a significant effect on bacterial community composition. A significant difference in bacterial richness was observed between children with RV-A and RV-C infection, however this is likely due to the differences in age group between the patient cohorts. The bacterial community within the oropharynx was found to be diverse and heterogeneous. Age and attendance at day care or kindergarten were important factors in driving bacterial diversity. However, wheeze and viral infection were not found to significantly relate to the bacterial community. Bacterial airway microbiome is highly variable in early life and its role in wheeze remains less clear than viral influences.</p></abstract><funding-group><award-group id="award001"><funding-source><institution-wrap><institution-id institution-id-type="funder-id">http://dx.doi.org/10.13039/501100000925</institution-id><institution>National Health and Medical Research Council</institution></institution-wrap></funding-source><award-id>#458513</award-id><principal-award-recipient><name><surname>Moffatt</surname><given-names>Miriam F.</given-names></name></principal-award-recipient></award-group><award-group id="award002"><funding-source><institution-wrap><institution-id institution-id-type="funder-id">http://dx.doi.org/10.13039/501100000925</institution-id><institution>National Health and Medical Research Council</institution></institution-wrap></funding-source><award-id>#1045760</award-id><principal-award-recipient><name><surname>Cookson</surname><given-names>William O. C.</given-names></name></principal-award-recipient></award-group><award-group id="award003"><funding-source><institution-wrap><institution-id institution-id-type="funder-id">http://dx.doi.org/10.13039/501100000952</institution-id><institution>Asthma Foundation ACT</institution></institution-wrap></funding-source><principal-award-recipient><name><surname>Le Souëf</surname><given-names>Peter N.</given-names></name></principal-award-recipient></award-group><award-group id="award004"><funding-source><institution-wrap><institution-id institution-id-type="funder-id">http://dx.doi.org/10.13039/100004440</institution-id><institution>Wellcome Trust</institution></institution-wrap></funding-source><award-id>P40069</award-id><principal-award-recipient><name><surname>Moffatt</surname><given-names>Miriam F.</given-names></name></principal-award-recipient></award-group><award-group id="award005"><funding-source><institution>Asmarley trust</institution></funding-source><principal-award-recipient><name><surname>Cookson</surname><given-names>William O. C.</given-names></name></principal-award-recipient></award-group><award-group id="award006"><funding-source><institution>Telethon research fellowship (AU)</institution></funding-source><principal-award-recipient><name><surname>Oo</surname><given-names>Stephen W. C.</given-names></name></principal-award-recipient></award-group><award-group id="award007"><funding-source><institution-wrap><institution-id institution-id-type="funder-id">http://dx.doi.org/10.13039/100010289</institution-id><institution>Princess Margaret Hospital Foundation</institution></institution-wrap></funding-source><principal-award-recipient><name><surname>Oo</surname><given-names>Stephen W. C.</given-names></name></principal-award-recipient></award-group><funding-statement>This study was funded by an NHMRC program grant (#458513), NHMRC project grant (#1045760), the West Australian Institute of Medical Research and the Asthma Foundation of Western Australia (AFWA), the Wellcome Trust (P40069) and the Asmarley Trust. Fellowship support was also provided for SWCO (Telethon Research Fellowship and Princess Margaret Hospital Foundation Clinical Fellowship).</funding-statement></funding-group><counts><fig-count count="2"></fig-count><table-count count="1"></table-count><page-count count="15"></page-count></counts><custom-meta-group><custom-meta id="data-availability"><meta-name>Data Availability</meta-name><meta-value>Sequences were submitted to the European nucleotide database, project number PRJEB32061.</meta-value></custom-meta></custom-meta-group></article-meta><notes><title>Data Availability</title><p>Sequences were submitted to the European nucleotide database, project number PRJEB32061.</p></notes></front><body><sec sec-type="intro" id="sec001"><title>Introduction</title><p>Respiratory infections are a significant cause of morbidity in young children, with over half of hospitalisations in children under 5 years of age being related to respiratory disease [<xref rid="pone.0223990.ref001" ref-type="bibr">1</xref>]. Evidence suggests that environmental and infectious exposures in early life are a major risk factor for the development of disease [<xref rid="pone.0223990.ref002" ref-type="bibr">2</xref>, <xref rid="pone.0223990.ref003" ref-type="bibr">3</xref>], including asthma [<xref rid="pone.0223990.ref004" ref-type="bibr">4</xref>–<xref rid="pone.0223990.ref006" ref-type="bibr">6</xref>].</p><p>Acute wheeze is the most common reason for children to present to hospital with between 80–90% of these cases being attributed to viral infection [<xref rid="pone.0223990.ref007" ref-type="bibr">7</xref>, <xref rid="pone.0223990.ref008" ref-type="bibr">8</xref>]. While a number of respiratory viruses have been implicated in wheeze the most common are respiratory syncytial virus (RSV) and rhinovirus (RV)[<xref rid="pone.0223990.ref009" ref-type="bibr">9</xref>]. In infants aged less than one year RSV infections predominate, but after this RV is also viewed as an important risk factor for acute wheeze [<xref rid="pone.0223990.ref010" ref-type="bibr">10</xref>].</p><p>The influence of the respiratory tract bacterial community in the context of wheeze is still being established. Recent studies in this area have implicated organisms such as <italic>Moraxella catarrhalis</italic>, <italic>Haemophilus influenzae</italic> and <italic>Staphylococcus aureus</italic> in increased rates of wheeze [<xref rid="pone.0223990.ref011" ref-type="bibr">11</xref>, <xref rid="pone.0223990.ref012" ref-type="bibr">12</xref>]. It has been suggested this may be due to immune modulation by these organisms, in infants resulting in increased risk of asthma development in later life [<xref rid="pone.0223990.ref013" ref-type="bibr">13</xref>].</p><p>Using 16s rRNA gene sequencing of respiratory samples from children presenting to hospital with acute wheezing, this study aimed to examine whether the bacterial community in the airways of children with acute respiratory wheeze was altered compared with that of non-wheezing children. Changes in the bacterial community were also explored to determine if acute RV infection or species had a significant effect on the airway microbiota.</p></sec><sec sec-type="materials|methods" id="sec002"><title>Methods</title><p>Children between 0–16 years were recruited as part of the MAVRIC (Mechanisms of Acute Viral Respiratory Infection in Children) study on presentation to Princess Margaret Hospital (PMH) for Children, Perth, Western Australia between January 2004 and January 2014. Cases and controls were recruited through all seasons, and a questionnaire was administered to all subjects to determine symptoms of any current illness, including coryzal symptoms, and risk factors, including birth history, postnatal and in utero cigarette smoke exposure, daycare attendance, atopy and allergy history, diagnoses of acute illness (children were excluded if they had any chronic illness other than asthma), recent antibiotic use, systemic steroids.</p><p>Recurrence data was collected on cases included in the study from birth. Hospital presentation records were used to determine frequency of respiratory presentations both prior to and following presentation. Five patterns were determined described as “few”, “persistent”, “multiple A”, “multiple B”, and “atypical”. (See supplemental methods for further definitions).</p><p>Cases recruited had acute wheezing illness with no other co-morbid conditions besides asthma, eczema, or atopy. Controls with no pre-existing chronic disease including chronic respiratory illness were recruited from four sources: siblings and relatives of cases, PMH patients (presenting with minor injury/fractured limbs), volunteers from the local community or day care facilities. A proportion of controls had symptoms of mild acute respiratory infection but no wheeze. Blood, oropharyngeal (OP) swabs and nasal samples (wash or blow) were collected from each participant.</p><p>Several cases were followed up within 9 months of recruitment and viral, OP swab and blood samples were repeated at this time.</p><p>This study was approved by the PMH for Children, Perth, Western Australia Human ethics committee (Reference: 1761EP). At least one parent or guardian provided informed written consent for children, prior to participation in the study.</p><sec id="sec003"><title>Atopy</title><p>Skin prick tests were performed to 11 allergens (cow’s milk, whole egg, cat pelt, dog dander, rye grass, mixed grasses, <italic>D</italic>. <italic>pteronyssinus</italic>, <italic>D</italic>. <italic>farinae</italic>, cockroach and <italic>Aspergillus fumigatus</italic>, <italic>Alternaria tenuis</italic>), a wheal size ≥3mm or self-reported allergic reaction to an allergen was used determined atopy.</p></sec><sec id="sec004"><title>Bloods cell counts and cathelicidin measurements</title><p>Blood cell counts were determined by PathWest Laboratory Medicine WA (PathWest) at PMH hospital pathology lab.</p><p>Cathelicidin (LL-37) was measured in plasma using a commercially available ELISA kit (Hycult Biotech).</p></sec><sec id="sec005"><title>Viral detection</title><p>A nasal blow or wash was collected at recruitment and placed immediately on ice prior to storage at -80°C. Nasal specimens were typed for RV species using methods previously described [<xref rid="pone.0223990.ref014" ref-type="bibr">14</xref>] using modified primers [<xref rid="pone.0223990.ref015" ref-type="bibr">15</xref>]. Briefly, a semi-nested RT-PCR with primers that amplify the 260-bp variable region of the 5’ untranslated region of the RV genome was completed. RV-positive samples were sequenced and assigned an RV strain type and species following sequence alignment with sequences of the 101 classic serotypes and the 53 newly assigned genotypes, using ClustalX software (University College Dublin, Dublin, Ireland) [<xref rid="pone.0223990.ref016" ref-type="bibr">16</xref>].</p><p>A second aliquot from each nasal specimen was tested for RSV, influenza A and B, parainfluenza 1–4, RSV, and human metapneumovirus (hMPV) at PathWest using routine diagnostic methods including PCR [<xref rid="pone.0223990.ref017" ref-type="bibr">17</xref>], direct or indirect fluorescent antibody testing, or immunofluorescence after cell culture as previously described [<xref rid="pone.0223990.ref018" ref-type="bibr">18</xref>]. Whenever possible, samples were also tested for enterovirus, coronavirus, and bocavirus.</p></sec><sec id="sec006"><title>Bacterial detection</title><p>Sterile dry rayon swabs (Copan) were used to sample the soft palate of the oropharynx. Specific care was made not to contaminate samples with any other part of the mouth. Any swab that made contact with the tongue or cheek were disposed of and a new swab was performed, for full details see supplementary materials. Samples were immediately put on ice and stored at -80°C.</p><p>DNA was extracted from samples utilizing an MPbio FastDNA SPIN Kit for soil as per manufacturers’ instructions and frozen at -80°C. Samples were transported on dry ice to Imperial College London, for bacterial analysis.</p></sec><sec id="sec007"><title>Quantitative PCR</title><p>Total bacterial burden was measured using a SYBR green quantitative PCR assay using the primers 520F, <monospace>5’- AYTGGGYDTAAAGNG</monospace> and 820R, <monospace>5’-TACNVGGGTATCTAATCC</monospace>, targeting the V4 region of the 16S rRNA gene as described in Cuthbertson <italic>et al</italic> 2017[<xref rid="pone.0223990.ref019" ref-type="bibr">19</xref>]. All reactions were performed in triplicate and included standards and non-template controls on the ViiA 7 Real-time PCR system (Life Technologies, Paisley, UK) using SYBR Fast qPCR Master mix (KAPA Biosystems, Wilmington, MA, USA). Standards were generated from near full length cloned 16S rRNA gene of <italic>Vibrio natregens</italic>. Plasmids quantified using Quantit picogreen dsDNA Assay kit (Promega, Madison, USA), samples were then serially diluted 10 fold to form standards ranging from 1 x 10<sup>8</sup>–1 x 10<sup>4</sup>.</p></sec><sec id="sec008"><title>16S rRNA sequencing</title><p>Community analysis was carried out using 16S rRNA gene sequencing. Custom dual barcoded fusion primers were used to target the previously quantified region of the 16S rRNA gene as previously described [<xref rid="pone.0223990.ref019" ref-type="bibr">19</xref>]. Each sequencing run contained a PCR negative control and a Mock community, consisting of 34 16S rRNA gene clones of known bacterial species in equal proportions. Sequencing was carried out using the Illumina MiSeq platform using the Illumina V2 2x250bp cycle kit. Sequences were submitted to the European nucleotide database, project number PRJEB32061.</p></sec><sec id="sec009"><title>Sequencing analysis</title><p>Downstream sequencing analysis was carried out using Quantitative Insights in Microbial Ecology (QIIME) Version 1.9.0 due to the dual barcoded indexs used in this study. All sequences were trimmed to 200bp and joined with a minimum of 150bp overlap, a maximum of 10% mismatch was stipulated. Sequences were then demultiplexed and any phiX reads were removed, prior to OTU picking using open reference UCLUST OTU picking [<xref rid="pone.0223990.ref020" ref-type="bibr">20</xref>], clustering at 97% similarity using the Silva reference database (<ext-link ext-link-type="uri" xlink:href="http://www.arb-silva.de/">www.arb-silva.de</ext-link>), reads with less that 60% id were discarded and 10% of sequences that failed to id were included for de novo clustering. Representative sequences were picked from the most abundant read in the cluster. PYNAST [<xref rid="pone.0223990.ref021" ref-type="bibr">21</xref>] was used to align representative sequences before running the nearest alignment space termination (NAST) algorithm [<xref rid="pone.0223990.ref022" ref-type="bibr">22</xref>]. ChimeraSlayer (<ext-link ext-link-type="uri" xlink:href="http://microbiomeutil.sourceforge.net/">http://microbiomeutil.sourceforge.net/</ext-link>) was used to identify and remove any chimeric sequences. The Ribosomal Database Project (RDP) naive Bayesian classifier was used to apply taxonomic identification using Silva 115 NR database. Finally, an OTU biom table was created for further downstream analysis.</p><p>Exact sequence variants (ESVs) may in some circumstances improve identification of microbial taxa, but genomic sequencing of the airway microbiota is at an early stage. In order to avoid over-splitting of taxa and false inflation of diversity, we have taken the conservative approach of using OTUs in our analyses rather than amplicon sequence variants.</p></sec><sec id="sec010"><title>Statistical analysis</title><p>All further analysis was carried out using R version 3.3.2 [<xref rid="pone.0223990.ref023" ref-type="bibr">23</xref>]. Pre-processing and primary analysis was carried out in Phyloseq [<xref rid="pone.0223990.ref024" ref-type="bibr">24</xref>]. Contamination was removed using Decontam [<xref rid="pone.0223990.ref025" ref-type="bibr">25</xref>]. A minimum threshold of 2,000 reads was applied to all, samples with less than 2,000 reads were removed from further analysis. All remaining samples were then rarefied to the minimum number of reads present in the data subset.</p><p>Non-parametric Wilcoxon sign ranked tests were used to test significant differences between means. Pearson correlations were used to test the relationship between continuous clinical variables and diversity measures. Adonis permutational ANOVA was used to investigate changes in community composition while Random forest analysis was used to identify OTU’s associated with disease.</p></sec></sec><sec sec-type="results" id="sec011"><title>Results</title><p>After removal of sequencing controls and those with less than 2000 reads, a total of 201 samples were taken forward for analysis, see <xref rid="pone.0223990.t001" ref-type="table">Table 1</xref> (further information in <xref ref-type="supplementary-material" rid="pone.0223990.s001">S1 Table</xref>). This included 109 samples from children with acute wheeze (<xref ref-type="fig" rid="pone.0223990.g001">Fig 1</xref>) and paired stable follow-up samples from 17 of these children. Control samples from 75 children without symptoms of wheeze were collected, this cohort included children from day-care and siblings of those with acute wheeze (<xref ref-type="fig" rid="pone.0223990.g001">Fig 1</xref>).</p><fig id="pone.0223990.g001" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0223990.g001</object-id><label>Fig 1</label><caption><title>Stacked bar plots of cases (acute wheeze) and controls ordered by age.</title><p>Bacterial biomass and patient demographics are indicated in the plots below. Dark green indicates yes while pale green indicates no, white boxes indicate NA or missing information.</p></caption><graphic xlink:href="pone.0223990.g001"></graphic></fig><table-wrap id="pone.0223990.t001" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0223990.t001</object-id><label>Table 1</label><caption><title>Demographic table of acute cases and healthy controls.</title><p>Data indicates counts for cases (acute wheeze diagnosis) and healthy controls. N indicates the total number of subjects that information was obtained for each group. Count data is indicted as a count (% positive of N). Continuous data is recorded at median of N (mix–max). Differences in clinical variables were calculated using Wilcoxon sign rank test, differences in ethnic groups, sampling season an RV type were calculated using Chi-squared.</p></caption><alternatives><graphic id="pone.0223990.t001g" xlink:href="pone.0223990.t001"></graphic><table frame="hsides" rules="groups"><colgroup span="1"><col align="left" valign="middle" span="1"></col><col align="left" valign="middle" span="1"></col><col align="left" valign="middle" span="1"></col><col align="left" valign="middle" span="1"></col><col align="left" valign="middle" span="1"></col><col align="left" valign="middle" span="1"></col></colgroup><thead><tr><th align="left" rowspan="1" colspan="1"></th><th align="center" colspan="2" rowspan="1">Acute</th><th align="center" colspan="2" rowspan="1">Controls</th><th align="center" rowspan="1" colspan="1">Statistical comparison</th></tr><tr><th align="left" rowspan="1" colspan="1"></th><th align="center" rowspan="1" colspan="1">N</th><th align="center" rowspan="1" colspan="1">All</th><th align="center" rowspan="1" colspan="1">N</th><th align="center" rowspan="1" colspan="1">All</th><th align="center" rowspan="1" colspan="1">p</th></tr></thead><tbody><tr><td align="right" rowspan="1" colspan="1">Female (male)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">51 (58)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">38 (36)</td><td align="center" rowspan="1" colspan="1">0.546</td></tr><tr><td align="right" rowspan="1" colspan="1">Age (median (Min-Max))</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">3.83 (0.08–13.93)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">3.155 (0.8–18.5)</td><td align="center" rowspan="1" colspan="1">0.344</td></tr><tr><td align="right" rowspan="1" colspan="1">Gestation period (Min-Max)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">40 (38–43)</td><td align="center" rowspan="1" colspan="1">65</td><td align="center" rowspan="1" colspan="1">39 (35–42.5)</td><td align="center" rowspan="1" colspan="1">0.095</td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Ethnic group</bold></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"><bold>0.057</bold></td></tr><tr><td align="right" rowspan="1" colspan="1">Aboriginal (%)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">5 (5%)</td><td align="center" rowspan="1" colspan="1">70</td><td align="center" rowspan="1" colspan="1">2 (3%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">African/African American (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">12 (11%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">1 (1%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Asian/Indian (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">23 (21%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">16 (21%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Caucasian (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">54 (50%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">51 (68%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Maori (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">3 (3%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Pacific Islanders/Samoan (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">2 (2%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">PNG (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">2 (2%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Undetermined (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">8 (7%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">5 (7%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Season</bold></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"><bold>0.803</bold></td></tr><tr><td align="right" rowspan="1" colspan="1">Autum (%)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">20 (18%)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">4 (5%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Spring (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">18 (16%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">17 (23%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Summer (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">3 (3%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">3 (4%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Winter (%)</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">68 (62%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">51 (68%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Diagnosis</bold></td><td align="center" rowspan="1" colspan="1">xs</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Asthma exacerbation (%)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">37 (34%)</td><td align="center" rowspan="1" colspan="1">27</td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Viral wheeze (%)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">49 (45%)</td><td align="center" rowspan="1" colspan="1">27</td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Bronchiolitis (%)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">14 (13%)</td><td align="center" rowspan="1" colspan="1">27</td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1">0.05</td></tr><tr><td align="right" rowspan="1" colspan="1">Pneumonia (%)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">1 (0.9%)</td><td align="center" rowspan="1" colspan="1">27</td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1">0.632</td></tr><tr><td align="right" rowspan="1" colspan="1">URTI (%)</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">94 (86%)</td><td align="center" rowspan="1" colspan="1">64</td><td align="center" rowspan="1" colspan="1">29 (45%)</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Atopy (%)</td><td align="center" rowspan="1" colspan="1">89</td><td align="center" rowspan="1" colspan="1">54 (61%)</td><td align="center" rowspan="1" colspan="1">63</td><td align="center" rowspan="1" colspan="1">21 (33%)</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Severity Zscore (min-max)</td><td align="center" rowspan="1" colspan="1">85</td><td align="center" rowspan="1" colspan="1">0.3191 (-2.2306–2.0151)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">NA</td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Medication</bold></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Systemic steroids (%)</td><td align="center" rowspan="1" colspan="1">105</td><td align="center" rowspan="1" colspan="1">76 (72%)</td><td align="center" rowspan="1" colspan="1">67</td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Oxygen (%)</td><td align="center" rowspan="1" colspan="1">99</td><td align="center" rowspan="1" colspan="1">45 (45%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">NA</td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Blood counts</bold></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Platelets (min-max)</td><td align="center" rowspan="1" colspan="1">82</td><td align="center" rowspan="1" colspan="1">295 (105–611)</td><td align="center" rowspan="1" colspan="1">41</td><td align="center" rowspan="1" colspan="1">292 (35–655)</td><td align="center" rowspan="1" colspan="1">0.996</td></tr><tr><td align="right" rowspan="1" colspan="1">T-cells (min-max)</td><td align="center" rowspan="1" colspan="1">83</td><td align="center" rowspan="1" colspan="1">10.5 (3.5–27.9)</td><td align="center" rowspan="1" colspan="1">41</td><td align="center" rowspan="1" colspan="1">8.3 (4–13.4)</td><td align="center" rowspan="1" colspan="1">0.006</td></tr><tr><td align="right" rowspan="1" colspan="1">Neutrophils (min-max)</td><td align="center" rowspan="1" colspan="1">83</td><td align="center" rowspan="1" colspan="1">6.87 (0.47–20.41)</td><td align="center" rowspan="1" colspan="1">40</td><td align="center" rowspan="1" colspan="1">3.325 (0.71–8.19)</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Lymphocytes (min-max)</td><td align="center" rowspan="1" colspan="1">83</td><td align="center" rowspan="1" colspan="1">1.67 (0.27–8.61)</td><td align="center" rowspan="1" colspan="1">40</td><td align="center" rowspan="1" colspan="1">3.74 (1.17–7.94)</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Monocytes (min-max)</td><td align="center" rowspan="1" colspan="1">83</td><td align="center" rowspan="1" colspan="1">0.54 (0.275–3.39)</td><td align="center" rowspan="1" colspan="1">40</td><td align="center" rowspan="1" colspan="1">0.685 (0.3–2.18)</td><td align="center" rowspan="1" colspan="1">0.019</td></tr><tr><td align="right" rowspan="1" colspan="1">Eosinophils (min-max)</td><td align="center" rowspan="1" colspan="1">83</td><td align="center" rowspan="1" colspan="1">0.06 (0.015–2.67)</td><td align="center" rowspan="1" colspan="1">40</td><td align="center" rowspan="1" colspan="1">0.28 (0–1.42)</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Basophils (min-max)</td><td align="center" rowspan="1" colspan="1">83</td><td align="center" rowspan="1" colspan="1">0.01 (0–0.38)</td><td align="center" rowspan="1" colspan="1">40</td><td align="center" rowspan="1" colspan="1">0.05 (0–0.18)</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">tven1</td><td align="center" rowspan="1" colspan="1">81</td><td align="center" rowspan="1" colspan="1">2 (0.8–100.4)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">NA</td></tr><tr><td align="right" rowspan="1" colspan="1">O2 Saturation</td><td align="center" rowspan="1" colspan="1">89</td><td align="center" rowspan="1" colspan="1">95 (69–99)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">NA</td></tr><tr><td align="right" rowspan="1" colspan="1">ll37</td><td align="center" rowspan="1" colspan="1">60</td><td align="center" rowspan="1" colspan="1">2.0986 (0.2404–6.7606)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">NA</td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Viral infection</bold></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">RV</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">71 (65%)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">33 (43.99%)</td><td align="center" rowspan="1" colspan="1">0.004</td></tr><tr><td align="right" rowspan="1" colspan="1">RV group</td><td align="center" rowspan="1" colspan="1">71</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"><bold>0.009</bold></td></tr><tr><td align="right" rowspan="1" colspan="1">A</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">26 (37%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">17 (51.51%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">B</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">3 (4%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">6 (18.18%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">C</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">40 (56%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">10 (30.3%)</td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Unknown</td><td align="right" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1">2 (3%)</td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">RSV</td><td align="center" rowspan="1" colspan="1">76</td><td align="center" rowspan="1" colspan="1">16 (215)</td><td align="center" rowspan="1" colspan="1">63</td><td align="center" rowspan="1" colspan="1">2 (3%)</td><td align="center" rowspan="1" colspan="1">0.002</td></tr><tr><td align="right" rowspan="1" colspan="1">Adenovirus</td><td align="center" rowspan="1" colspan="1">76</td><td align="center" rowspan="1" colspan="1">3 (4%)</td><td align="center" rowspan="1" colspan="1">63</td><td align="center" rowspan="1" colspan="1">6 (10%)</td><td align="center" rowspan="1" colspan="1">0.187</td></tr><tr><td align="right" rowspan="1" colspan="1">Influenza virus</td><td align="center" rowspan="1" colspan="1">76</td><td align="center" rowspan="1" colspan="1">0 (0%)</td><td align="center" rowspan="1" colspan="1">63</td><td align="center" rowspan="1" colspan="1">1 (2%)</td><td align="center" rowspan="1" colspan="1">0.278</td></tr><tr><td align="right" rowspan="1" colspan="1">Parainfluenza virus</td><td align="center" rowspan="1" colspan="1">76</td><td align="center" rowspan="1" colspan="1">1 (1%)</td><td align="center" rowspan="1" colspan="1">63</td><td align="center" rowspan="1" colspan="1">2 (3%)</td><td align="center" rowspan="1" colspan="1">0.459</td></tr><tr><td align="right" rowspan="1" colspan="1">Corona virus</td><td align="center" rowspan="1" colspan="1">39</td><td align="center" rowspan="1" colspan="1">20 (51%)</td><td align="center" rowspan="1" colspan="1">63</td><td align="center" rowspan="1" colspan="1">1 (2%)</td><td align="center" rowspan="1" colspan="1">0.312</td></tr><tr><td align="right" rowspan="1" colspan="1">Human metapneumovirus</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">4 (5%)</td><td align="center" rowspan="1" colspan="1">63</td><td align="center" rowspan="1" colspan="1">0</td><td align="center" rowspan="1" colspan="1">0.065</td></tr><tr><td align="right" rowspan="1" colspan="1">Enterovirus</td><td align="center" rowspan="1" colspan="1">34</td><td align="center" rowspan="1" colspan="1">3 (9%)</td><td align="center" rowspan="1" colspan="1">9</td><td align="center" rowspan="1" colspan="1">3 (33%)</td><td align="center" rowspan="1" colspan="1">0.066</td></tr><tr><td align="right" rowspan="1" colspan="1">Bocavirus</td><td align="center" rowspan="1" colspan="1">5</td><td align="center" rowspan="1" colspan="1">2 (40%)</td><td align="center" rowspan="1" colspan="1">51</td><td align="center" rowspan="1" colspan="1">6 (12%)</td><td align="center" rowspan="1" colspan="1">0.092</td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Smoking</bold></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">Mother smoked ever</td><td align="center" rowspan="1" colspan="1">108</td><td align="center" rowspan="1" colspan="1">38 (35%)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">15 (20%)</td><td align="center" rowspan="1" colspan="1">0.023</td></tr><tr><td align="right" rowspan="1" colspan="1">Smoking now</td><td align="center" rowspan="1" colspan="1">108</td><td align="center" rowspan="1" colspan="1">18 (17%)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">2 (3%)</td><td align="center" rowspan="1" colspan="1">0.003</td></tr><tr><td align="right" rowspan="1" colspan="1">Smoked when pregnant</td><td align="center" rowspan="1" colspan="1">106</td><td align="center" rowspan="1" colspan="1">18 (16%)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">3 (4%)</td><td align="center" rowspan="1" colspan="1">0.007</td></tr><tr><td align="right" rowspan="1" colspan="1">smoked regularly during pregnancy</td><td align="center" rowspan="1" colspan="1">106</td><td align="center" rowspan="1" colspan="1">15(14%)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">1 (1%)</td><td align="center" rowspan="1" colspan="1">0.003</td></tr><tr><td align="right" rowspan="1" colspan="1">Anyone smoke in the house?</td><td align="center" rowspan="1" colspan="1">109</td><td align="center" rowspan="1" colspan="1">33 (30%)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">10 (13%)</td><td align="center" rowspan="1" colspan="1">0.008</td></tr><tr><td align="left" rowspan="1" colspan="1"><bold>Siblings and school</bold></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td><td align="center" rowspan="1" colspan="1"></td></tr><tr><td align="right" rowspan="1" colspan="1">No of Children</td><td align="center" rowspan="1" colspan="1">107</td><td align="center" rowspan="1" colspan="1">2 (0–5)</td><td align="center" rowspan="1" colspan="1">75</td><td align="center" rowspan="1" colspan="1">2 (0–5)</td><td align="center" rowspan="1" colspan="1">0.028</td></tr><tr><td align="right" rowspan="1" colspan="1">No of siblings</td><td align="center" rowspan="1" colspan="1">108</td><td align="center" rowspan="1" colspan="1">1 (0–8)</td><td align="center" rowspan="1" colspan="1">72</td><td align="center" rowspan="1" colspan="1">0 (0–3)</td><td align="center" rowspan="1" colspan="1">0.015</td></tr><tr><td align="right" rowspan="1" colspan="1">Kindergarten</td><td align="center" rowspan="1" colspan="1">107</td><td align="center" rowspan="1" colspan="1">52 (49%)</td><td align="center" rowspan="1" colspan="1">74</td><td align="center" rowspan="1" colspan="1">18 (24%)</td><td align="center" rowspan="1" colspan="1">0.001</td></tr><tr><td align="right" rowspan="1" colspan="1">Pre-school</td><td align="center" rowspan="1" colspan="1">107</td><td align="center" rowspan="1" colspan="1">42 (39%)</td><td align="center" rowspan="1" colspan="1">74</td><td align="center" rowspan="1" colspan="1">9 (12%)</td><td align="center" rowspan="1" colspan="1"><0.001</td></tr></tbody></table></alternatives></table-wrap><sec id="sec012"><title>Comparison of acute wheeze and controls</title><p>Samples from 109 children with acute wheeze and 75 control children were compared (<xref rid="pone.0223990.t001" ref-type="table">Table 1</xref> and <xref ref-type="fig" rid="pone.0223990.g001">Fig 1</xref>). No significant difference in alpha diversity was observed between the 2 groups (Richness, P = 0.363; Shannon-Weiner, P = 0.98; Inverse Simpsons, P = 0.654). Adonis permutational ANOVA revealed a significant difference in Bray-Curtis dissimilarity (R<sup>2</sup> = 0.016, P = 0.003), <xref ref-type="fig" rid="pone.0223990.g002">Fig 2A</xref>. However, the variation explained was only 1%, suggesting a relationship driven by a small number of samples (see <xref ref-type="supplementary-material" rid="pone.0223990.s008">S1 Fig</xref>).</p><fig id="pone.0223990.g002" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0223990.g002</object-id><label>Fig 2</label><caption><p><bold>NMDS plots based on Bray-Curtis dissimilarity comparing.</bold> A) non-wheezing controls (blue) to acute wheezing children (red), R<sup>2</sup> = 0.016. B) Wheezing children (red) and paired follow-up samples (blue). Numbers indicate paired samples from individual patients and are linked by arrows. Ellipses were added assuming a multivariate normal distribution.</p></caption><graphic xlink:href="pone.0223990.g002"></graphic></fig><p>A random forest model was used to predict wheeze based on OTUs in the bacterial community. The predictive power of the model for cases and controls was found to be poor (out of box (OOB) error rate = 34.24%, p = 0.37), therefore the model results were considered unreliable and was not used in further investigation. However, indicator species analysis revealed a significant association of a single <italic>Veillonella</italic> OTU with the acute group. DeSeq2 analysis indicated the same <italic>Veillonella</italic> OTU associated with cases while several <italic>Haemophilus</italic> OTUs were found to be associated with controls (<xref ref-type="supplementary-material" rid="pone.0223990.s009">S2 Fig</xref>)</p><p>Clinical variables were investigated to see if they were able to better explain bacterial community variation within this population. Wilcoxon rank sum test was used to investigate 33 binary variables across all samples (<xref ref-type="supplementary-material" rid="pone.0223990.s002">S2 Table</xref>). After Bonferroni correction for multiple testing, only the diagnosis of bronchiolitis was found to show a significant difference in bacterial richness (p = 0.006), Shannon-Weiner (p = 0.017) and inverse Simpsons (p = 0.062). Significant differences in Shannon-Weiner and inverse Simpsons were observed in those that required oxygen and those that had ever attended kindergarten. It was noted, however, that none of the controls were positive for bronchiolitis or required oxygen. Therefore, this relationship was further tested in the acute wheeze population. Kruskal-Wallis with Dunns test was used to investigate categorical variables, however no significant results were observed. We did not find any differences in the microbiota that were attributable to recorded breastfeeding. No data was available to explore the effect of delivery method in this study.</p><p>Pearson’s correlations were used to investigate relationships between 20 continuous variables and alpha diversity measures (<xref ref-type="supplementary-material" rid="pone.0223990.s003">S3 Table</xref>). Only bacterial biomass was found to have a weak significant correlation with bacterial richness. Significant changes in blood counts were not found to hold up to multiple testing and expected differences in the antimicrobial peptide cathlecidin were not found.</p><p>Adonis permutational ANOVA with 99,999 iterations was used to investigate changes in community composition with 58 variables. Only bacterial biomass, bronchiolitis diagnosis and regular attendance at day care were found to be significant (<xref ref-type="supplementary-material" rid="pone.0223990.s004">S4 Table</xref>).</p><p>Bronchiolitis diagnosis was found to show significant reduction in alpha diversity. Due to the control samples coming from a slightly older population true age matched case controls were unable to be compared (wheeze, median = 0.195 (min = 0.08 –max = 1.87), control, 1.38 (0.6–1.91)). However, when the microbiota in children with bronchiolitis were compared to those closest in age there was a significant reduction in alpha diversity (richness; p = 0.01, Shannon-Weiner, p = 0.003, inverse Simpsons, p = 0.005) that was not associated with change in bacterial biomass (p = 0.874). Changes in community composition using Bray-Curtis dissimilarity were found to explain 9.8% of the variation (p = 0.012), <xref ref-type="supplementary-material" rid="pone.0223990.s010">S3 Fig</xref>.</p></sec><sec id="sec013"><title>Acute wheeze</title><p>To explore variation within the group suffering from acute wheeze, this group was examined as a subset from the whole data set and clinical variables were explored (<xref ref-type="fig" rid="pone.0223990.g001">Fig 1</xref>). In the acute wheeze group, significant decrease in all alpha diversity measures (differences in bacterial diversity between subjects) were seen with bronchiolitis. Fourteen patients with doctor diagnosed bronchiolitis were included in the study, all of these patients were under the age of 2 years. Of those diagnosed, all patients also had wheeze. Nine of the patients were positive for RSV at the time of sampling, 5 of these were also positive for RV (<xref ref-type="fig" rid="pone.0223990.g001">Fig 1</xref>).</p><p>A significant increase was observed with attendance at kindergarten (<xref ref-type="supplementary-material" rid="pone.0223990.s005">S5 Table</xref>). Attendance at preschool showed a significant increase in bacterial richness (number of OTUs) only. Only patient age was found to show significant positive correlation with bacterial richness (<xref ref-type="supplementary-material" rid="pone.0223990.s006">S6 Table</xref>).</p><p>In the children with acute wheeze, bacterial biomass was found to explain 8.9% of the variation in beta diversity (p < 0.001). Bronchiolitis (r<sup>2</sup> = 0.042, p < 0.001) and attendance at kindergarten (r<sup>2</sup> = 0.052, p < 0.001) were also found to be significant in the acute wheeze dataset (<xref ref-type="supplementary-material" rid="pone.0223990.s007">S7 Table</xref>).</p><p>Within the 109 children with acute wheeze, 71 were below the age of 5. In the acute wheeze group, the under 5s bacterial biomass remained a significant driver of bacterial community composition (r<sup>2</sup> = 0.06, p < 0.001). However, no other variables were significant in the younger cohort.</p><p>Kruskal-Wallis was used to investigate wheeze recurrence patterns for the five patterns of wheeze observed in wheeze cases (<xref ref-type="supplementary-material" rid="pone.0223990.s011">S4 Fig</xref>). No significant difference in alpha bacterial diversity was observed within or between any of the above recurrence groups.</p></sec><sec id="sec014"><title>Rhinovirus (RV)</title><p>Within the participants suffering from acute wheeze, 71 patients had RV infection. RV strains from two patients were unable to be typed. Twenty-six patients were infected with RV-A, 3 with RV-B and 40 with RV-C. The sample numbers only allowed comparison of the bacterial community from patients with RV-A with those with RV-C. No significant difference in alpha diversity was observed. In the under 5s group, 15 patients had RV-A, 1 had RV-B and 27 had RV-C. A significant difference in richness (W = 123.5, p-value = 0.039) was observed between those with RV-A and RV-C, however no differences in diversity were observed. No significant difference in community composition was observed using adonis (R<sup>2</sup> = 0.039, p = 0.328).</p><p>Random forest modelling was unable to identify OTUs associated with viral species (p = 0.504).</p></sec><sec id="sec015"><title>Follow-up samples</title><p>Stable follow-up samples were collected from 17 individuals after an acute wheezing episode. No significant difference in bacterial biomass (V = 44, p-value = 0.132) or alpha diversity (richness, p = 0.289, Shannon, p = 0.145, Simpson, p = 0.109) was found when comparing paired samples with Wilcoxon signed rank test.</p><p>Between and within sample beta diversity was compared (<xref ref-type="fig" rid="pone.0223990.g002">Fig 2B</xref>). Significant differences between paired samples were observed with 5.8% of the variation explained by time of sampling (p = 0.013), however 57.6% of the variation was explained by individual (p = 0.013).</p></sec></sec><sec sec-type="conclusions" id="sec016"><title>Discussion</title><p>In this cohort of children, we found substantial diversity and heterogeneity in OP microbiota composition regardless of wheeze status. There were no significant microbiome differences between acute wheeze cases and non-wheezing controls on alpha diversity measures. Beta diversity was examined using a Bray-Curtis dissimilarity adonis model and while significant difference (p = 0.003) was found, only 1.6% of the variance is explained by differences between cases and controls. Further interrogation with Bray-Curtis dissimilarity hierarchical clustering (<xref ref-type="supplementary-material" rid="pone.0223990.s008">S1 Fig</xref>) reveals that the correlation is likely driven by a small number of samples and no pattern was observed between those that had wheeze and those that did not (<xref ref-type="fig" rid="pone.0223990.g002">Fig 2</xref>). Overall, despite cases having an acute wheezing illness serious enough to cause presentation to a children’s hospital emergency department, there were no clear differences in the bacterial community between cases and controls.</p><p>In the small number of cases with matched acute and convalescent samples taken up to 9 months later, we were similarly unable to find differences in alpha diversity between the cases and follow-up samples. Significant differences in beta diversity were observed between cases and follow-up samples, however the variation explained was 5.8% compared to within subject changes which explained 57.6% of the variation. The heterogeneous nature of the microbial community between patients makes investigation into microbial changes a challenge and supports the need for large-scale longitudinal investigation into community composition in health and disease.</p><p>Random forest analysis has been used in a number of recent studies to investigate predictive OTUs in microbiome analysis [<xref rid="pone.0223990.ref026" ref-type="bibr">26</xref>, <xref rid="pone.0223990.ref027" ref-type="bibr">27</xref>]. In this study, random forest was used to attempt to identify OTU predictors for wheeze. We found that the variation in the microbial community observed between these groups was high and this led to low confidence in the predictive power of the model. Random forest analysis of the bacterial community found bacterial OTUs to be poor predictors of wheeze. This analysis was also performed to determine if any OTUs were significantly associated with RV infection or between RV species. Neither model was found to have strong predictive power and estimated accuracy was low.</p><p>Diagnosis with bronchiolitis showed a significant difference in bacterial richness compared with the entire cohort, however this comprised only a small subset of patients (n = 13). When those with a diagnosis of bronchiolitis were compared to other cases that wheezed or age matched control subjects, significant differences in alpha and beta diversity were observed however this may have been driven by subjects with bronchiolitis being significantly younger than other groups of subjects. Bacterial diversity was found to be significantly reduced in these subjects with many patients dominated with <italic>Streptococcus sp</italic>. Further investigation into the streptococcal species, which is unable to be elucidated from 16S rRNA sequencing, would be important in further investigations. Longitudinal studies in young children to determine if low bacterial diversity in the respiratory tract is a risk factor for or the result of bronchiolitis would be important for future investigations.</p><p>In contrast to our findings, there are a number of studies that show significant differences in microbiome in relation to viral infections compared to healthy subjects [<xref rid="pone.0223990.ref011" ref-type="bibr">11</xref>, <xref rid="pone.0223990.ref028" ref-type="bibr">28</xref>–<xref rid="pone.0223990.ref030" ref-type="bibr">30</xref>]. These studies show haemophilus, streptococcus, moraxella associated with acute respiratory tract infections and staphylococcus, alloiococcus and corynebacterium in healthy samples. A number of factors account for the differences we find; firstly, they analyse nasopharyngeal (NP) samples compared to the OP samples analysed in our study. A number of studies have shown that these areas show significantly different bacterial communities, and that OP swabs are a better proxy for the lower respiratory tract microbiome. There are also age differences between other cohorts and ours.</p><p>Lastly analytical methods to look at the microbiome differ between studies. Analytical methods for microbiota are slowly being standardised, and much of the analytic techniques are borrowed from ecological analysis to try and accurately portray biodiversity and differences. In order to find differences, earlier studies have defaulted to simplistic groupings based on dominant organisms. However, we have observed that many samples are diverse and without a singular dominant organism. For example, Man <italic>et al</italic>, comparing those with lower respiratory tract infection and healthy controls, found no difference in alpha diversity, and using beta diversity measures found, similar to us, very small but significant differences between the groups (r<sup>2</sup> = 0.0031, p = <0.0001) [<xref rid="pone.0223990.ref028" ref-type="bibr">28</xref>]. To find significant differences in species, previous studies grouped samples based on perceived dominance and not necessarily by a dominance measure or beta diversity based on hierarchical clustering.</p><p>The greater variation in age within our population compared to other studies may have influenced our ability to find significant differences. Bacterial biomass was found to explain much of the variation in beta diversity within the acute population. Bacterial biomass was also found to show a weak positive correlation with age. Age was found to be a key variable in the analysis of this dataset and this relationship has been demonstrated in previous studies [<xref rid="pone.0223990.ref031" ref-type="bibr">31</xref>]. Age is interrelated with developmental changes in blood cell counts and immune function [<xref rid="pone.0223990.ref032" ref-type="bibr">32</xref>]. With these considerations, we considered changes in the microbiome while controlling for age.</p><p>A strength of our study is that we extracted blood from patients to examine differences in blood counts and antimicrobial peptides. However, variation in age in the study resulted in small and non-significant trends in blood cell counts. Cathelicidin was also examined as a candidate innate immunity marker as it has both anti-viral and anti-bacterial activity and lower levels have been shown to be associated with worsened severity in bronchiolitis [<xref rid="pone.0223990.ref033" ref-type="bibr">33</xref>]. However, we were unable to find a significant change in the bacterial community with changes in cathelicidin.</p><p>Seasonal influences in the same study location (Perth, Australia) have shown to have limited effects on microbiome in comprehensive longitudinal studies at least in infants [<xref rid="pone.0223990.ref029" ref-type="bibr">29</xref>]. Risk factors that are associated with hospitalisation as a result of respiratory infections in early life include maternal smoking during pregnancy, season of birth, delivery mode and gestational age[<xref rid="pone.0223990.ref034" ref-type="bibr">34</xref>]. When considered in this cohort of mostly hospitalised wheezing children (96%), these factors were not found to be significantly associated with bacterial or viral infection suggesting more work is required to fully understand any potential relationship.</p><p>At least one other study exists comparing OP microbiome samples between healthy adult patients and severe asthmatics showing no significant diversity differences [<xref rid="pone.0223990.ref035" ref-type="bibr">35</xref>]. An abundance of moraxella is found in prior studies in NP. Hilty <italic>et al</italic> demonstrate that Moraxella (proteobacteria) exists in oropharynx and may account for differences [<xref rid="pone.0223990.ref036" ref-type="bibr">36</xref>]. OP samples were specifically chosen as they showed greater representation to lower airway samples at least in stable patients [<xref rid="pone.0223990.ref036" ref-type="bibr">36</xref>, <xref rid="pone.0223990.ref037" ref-type="bibr">37</xref>]. Whether acute OP swabs reflect lower airway samples in acute wheeze or acute viral episodes is still unclear but, interestingly, Man <italic>et al</italic> did show that intensive care patients had reasonable similarity between NP samples and lower respiratory tracheal samples (Bray Curtis similarity p = 0.61), but did find key differences, specifically that staphylococcus, Corynebacterium, and Dolosigranulum sp. were almost exclusively present in NP samples and absent from endotracheal aspirates [<xref rid="pone.0223990.ref028" ref-type="bibr">28</xref>].</p><p>The bacterial community in the paediatric population is diverse and heterogeneous. The wide range of clinical factors tested did not fully explain the wide variation in the bacterial community in these subjects. Age had a significant influence on both the bacterial community and blood cell counts in this study and the wide age range within the study population helped explain some of the variation observed.</p><p>The simplest interpretation of our results is that acute wheezing illnesses are driven by viral infections and that these infections have little influence on the bacterial community during the acute phase of the illness. However, the heterogeneous nature of the subjects made it difficult to test for significant associations between clinical variables and the oropharyngeal bacterial community. Prospective longitudinal investigation of children pre, during and post viral infection may help identify if the bacterial community is either protective or a risk factor for viral infection and respiratory wheeze.</p></sec><sec sec-type="supplementary-material" id="sec017"><title>Supporting information</title><supplementary-material content-type="local-data" id="pone.0223990.s001"><label>S1 Table</label><caption><title>Participant demographics continued.</title><p>Data is recorded as n (%) or median (min-max). Data is recorded as a percentage of all data collected.</p><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s001.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s002"><label>S2 Table</label><caption><title>Comparison of categorical clinical variables with Wilcoxon rank sum test in the complete cohort to alpha diversity measures, richness, Shannon-Weiner and inverse Simpsons.</title><p>P values adjusted using Bonferonni correction for multiple testing.</p><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s002.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s003"><label>S3 Table</label><caption><title>Pearson’s correlations of continuous clinical variables and alpha diversity measures, richness, Shannon-Weiner and inverse Simpsons, in the complete cohort.</title><p>P values adjusted using Bonferonni correction for multiple testing.</p><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s003.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s004"><label>S4 Table</label><caption><title>Results of Bray-Curtis adonis permutational ANOVA examining clinical variables with 99,999 iterations.</title><p>P values adjusted using Bonferonni correction for multiple testing.</p><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s004.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s005"><label>S5 Table</label><caption><title>Comparison of categorical clinical variables in those with acute wheeze to alpha diversity measures, richness, Shannon-Weiner and inverse Simpsons.</title><p>P values adjusted using Bonferonni correction for multiple testing.</p><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s005.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s006"><label>S6 Table</label><caption><title>Pearson’s correlations of continuous clinical variables in those with acute wheeze and alpha diversity measures.</title><p>richness, Shannon-Weiner and inverse Simpsons. P values adjusted using Bonferonni correction for multiple testing.</p><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s006.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s007"><label>S7 Table</label><caption><title>Results of Bray-Curtis adonis permutational ANOVA examining clinical variables from individuals with acute wheeze with 99,999 iterations.</title><p>P values adjusted using Bonferonni correction for multiple testing.</p><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s007.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s008"><label>S1 Fig</label><caption><title>Stacked bar plot comparing OP samples from children with acute wheeze to healthy controls.</title><p>Hierarchical clustering based on Bray-Curtis dissimilarity was used to order stacked bar plots for individuals. Adonis permutational ANOVA explained 1.6% of the variation.</p><p>(TIFF)</p></caption><media xlink:href="pone.0223990.s008.tiff"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s009"><label>S2 Fig</label><caption><title>Volcano plot showing differential abundance of OTUs based on results from DeSeq2 analysis.</title><p>OTUs considered statistically significant (p-value < 0.001) were coloured based on genus level identification.</p><p>(PDF)</p></caption><media xlink:href="pone.0223990.s009.pdf"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s010"><label>S3 Fig</label><caption><title>Stacked bar plot comparing OP samples from children with bronchiolitis and acute wheeze to healthy controls.</title><p>Hierarchical clustering based on Bray-Curtis dissimilarity was used to order stacked bar plots for individuals. Adonis permutational ANOVA revealed bronchiolitis explained 9.8% of the variation.</p><p>(TIFF)</p></caption><media xlink:href="pone.0223990.s010.tiff"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s011"><label>S4 Fig</label><caption><title>Boxplots showing diversity measures associated with recurrence data from acute wheeze cases.</title><p>(TIFF)</p></caption><media xlink:href="pone.0223990.s011.tiff"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="pone.0223990.s012"><label>S1 File</label><caption><title>Supplementary methods.</title><p>(DOCX)</p></caption><media xlink:href="pone.0223990.s012.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material></sec></body><back><ref-list><title>References</title><ref id="pone.0223990.ref001"><label>1</label><mixed-citation publication-type="journal"><name><surname>Goto</surname><given-names>T</given-names></name>, <name><surname>Tsugawa</surname><given-names>Y</given-names></name>, <name><surname>Mansbach</surname><given-names>JM</given-names></name>, <name><surname>Camargo</surname><given-names>CA</given-names><suffix>Jr</suffix></name>, <name><surname>Hasegawa</surname><given-names>K</given-names></name>. <article-title>Trends in Infectious Disease Hospitalizations in US Children, 2000 to 2012</article-title>. <source>Pediatr Infect Dis J</source>. <year>2016</year>;<volume>35</volume>(<issue>6</issue>):<fpage>e158</fpage>–<lpage>63</lpage>. 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Epub 2011/06/18. <pub-id pub-id-type="doi">10.1164/rccm.201104-0655OC</pub-id><pub-id pub-id-type="pmid">21680950</pub-id></mixed-citation></ref></ref-list></back><sub-article id="pone.0223990.r001" article-type="aggregated-review-documents"><front-stub><article-id pub-id-type="doi">10.1371/journal.pone.0223990.r001</article-id><title-group><article-title>Decision Letter 0</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Jin</surname><given-names>Dong-Yan</given-names></name><role>Academic Editor</role></contrib></contrib-group><permissions><copyright-statement>© 2019 Dong-Yan Jin</copyright-statement><copyright-year>2019</copyright-year><copyright-holder>Dong-Yan Jin</copyright-holder><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p></license></permissions><related-article id="rel-obj001" ext-link-type="doi" xlink:href="10.1371/journal.pone.0223990" related-article-type="reviewed-article"></related-article><custom-meta-group><custom-meta><meta-name>Submission Version</meta-name><meta-value>0</meta-value></custom-meta></custom-meta-group></front-stub><body><p><named-content content-type="letter-date">30 Aug 2019</named-content></p><p>[EXSCINDED]</p><p>PONE-D-19-20152</p><p>Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children</p><p>PLOS ONE</p><p>Dear Dr Cuthbertson,</p><p>Thank you for submitting your manuscript to PLOS ONE.</p><p>Your paper was reviewed by two experts in the field and their comments follow. You need to optimize the analysis and clarify whether the subjects are infected by RSV or another virus as suggested by the two reviewers. We invite you to submit a revised version of the manuscript that addresses these points raised during the review process.</p><p>We would appreciate receiving your revised manuscript by Oct 14 2019 11:59PM. When you are ready to submit your revision, log on to <ext-link ext-link-type="uri" xlink:href="https://www.editorialmanager.com/pone/">https://www.editorialmanager.com/pone/</ext-link> and select the 'Submissions Needing Revision' folder to locate your manuscript file.</p><p>If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter.</p><p>To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: <ext-link ext-link-type="uri" xlink:href="http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols">http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols</ext-link></p><p>Please include the following items when submitting your revised manuscript:</p><p><list list-type="bullet"><list-item><p>A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). This letter should be uploaded as separate file and labeled 'Response to Reviewers'.</p></list-item><list-item><p>A marked-up copy of your manuscript that highlights changes made to the original version. This file should be uploaded as separate file and labeled 'Revised Manuscript with Track Changes'.</p></list-item><list-item><p>An unmarked version of your revised paper without tracked changes. This file should be uploaded as separate file and labeled 'Manuscript'.</p></list-item></list></p><p>Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.</p><p>We look forward to receiving your revised manuscript.</p><p>Kind regards,</p><p>Dong-Yan Jin</p><p>Academic Editor</p><p>PLOS ONE</p><p>Journal Requirements:</p><p>When submitting your revision, we need you to address these additional requirements.</p><p>1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at</p><p><ext-link ext-link-type="uri" xlink:href="http://www.journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf">http://www.journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf</ext-link> and <ext-link ext-link-type="uri" xlink:href="http://www.journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf">http://www.journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf</ext-link></p><p>Additional Editor Comments:</p><p>Revised paper will be re-reviewed by the original reviewers if they are available.</p><p>[Note: HTML markup is below. Please do not edit.]</p><p>Reviewers' comments:</p><p>Reviewer's Responses to Questions</p><p><bold>Comments to the Author</bold></p><p>1. Is the manuscript technically sound, and do the data support the conclusions?</p><p>The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. </p><p>Reviewer #1: Partly</p><p>Reviewer #2: Yes</p><p>**********</p><p>2. Has the statistical analysis been performed appropriately and rigorously? </p><p>Reviewer #1: No</p><p>Reviewer #2: Yes</p><p>**********</p><p>3. Have the authors made all data underlying the findings in their manuscript fully available?</p><p>The <ext-link ext-link-type="uri" xlink:href="http://www.plosone.org/static/policies.action#sharing">PLOS Data policy</ext-link> requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.</p><p>Reviewer #1: Yes</p><p>Reviewer #2: Yes</p><p>**********</p><p>4. Is the manuscript presented in an intelligible fashion and written in standard English?</p><p>PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.</p><p>Reviewer #1: Yes</p><p>Reviewer #2: Yes</p><p>**********</p><p>5. Review Comments to the Author</p><p>Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)</p><p>Reviewer #1: Re. Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children</p><p>It is an interesting research study to investigate the association between oral microbiota and acute wheeze in young children, in which the role of oral microbiota in influencing the viral infection, or acute wheeze in changing oral microbial community remains to be estimated. 109 case samples from children with acute wheeze (also paired follow-ups from 17 of these children) and 75 control samples from children without symptoms of wheeze were collected and compared for oral microbiota community and viral infection. Relevant clinical information, such as gender, age, atopy, blood cell counts, and cathelicidin measurements, were analyzed in combination of oral bacterial and viral data.</p><p>However, this work could be significantly improved with optimized bioinformatics and biostatistical analyses. The following comments may have the authors attentions:</p><p>1. QIIME 1 has been succeeded by QIIME 2 because of outdated workflow of QC control and OTU clustering in QIIME 1. The authors should update their analyses by using QIIME 2 or other pipelines that is more advanced than QIIME 1.9.0. This would ideally use amplicon sequence variants instead of 97% OTUs (see this paper for a discussion of this topic: <ext-link ext-link-type="uri" xlink:href="https://www.ncbi.nlm.nih.gov/pubmed/28731476">https://www.ncbi.nlm.nih.gov/pubmed/28731476</ext-link>). Meantime, key parameters of workflow for OTU clustering and taxa assignment would be clearly indicated.</p><p>2. The authors used 16S V4 region primers and quantitative PCR to measure oral bacterial biomass. If so, was there baseline control for normalization?</p><p>3. The authors used three key measures, including Richness, Shannon-Weiner and Inverse Simpsons, to compare the differences of oral microbiota communities between samples from children with and without acute wheeze. However, more detailed comparison of specific bacteria taxa should be performed to show the differential bacterial composition and abundance between cases and controls. For example, as shown in Figure 1, which bacteria(s) was/were the mostly changed in relative abundance; it could be estimated with LEfSe, Wilcoxon signed rank test or Turkey HSD etc.</p><p>4. The age should be one of important factors influencing oral microbial community. Given the wide range of years of children age (0.08-18.5 yeas), the authors should consider to divide the samples into different ago groups and compare the difference of bacterial composition and abundance.</p><p>5. Table 1 lacks statistical comparison of demographic information between cases and controls.</p><p>6. Figure 1 lacks the basic unit of Biomass. The percentage proportion of abundance should be indicated in the y-axis.</p><p>7. Figure 2 - is it possible that the authors try other PCoA method to cluster samples, for example, weighted or unweighted UniFrac methods?</p><p>8. The authors mentioned that "Specific care was made not to contaminate samples with any other part of the mouth". Was there more detailed information?</p><p>Reviewer #2: The article is very relevant and evaluated viral respiratory infections and the oropharyngeal bacterial microbiota in acutely</p><p>wheezing children. Although they concluded that the microbiota is not associated with viral infection and wheeze in children the article discuss important points that deserve to be published.</p><p>However, it not clear if the children with bronchiolitis are infected with RSV or other virus. This must be explored in the results and in the conclusion. Other important point is to performed and analysis of family and order of the microbiota comparing children with bronchiolitis and the controls.</p><p>Another point that should be explored in the manuscript is breastfeeding and cesarean delivery, that might be influencing the microbiota.</p><p>**********</p><p>6. PLOS authors have the option to publish the peer review history of their article (<ext-link ext-link-type="uri" xlink:href="https://journals.plos.org/plosone/s/editorial-and-peer-review-process#loc-peer-review-history">what does this mean?</ext-link>). If published, this will include your full peer review and any attached files.</p><p>If you choose “no”, your identity will remain anonymous but your review may still be made public.</p><p><bold>Do you want your identity to be public for this peer review?</bold> For information about this choice, including consent withdrawal, please see our <ext-link ext-link-type="uri" xlink:href="https://www.plos.org/privacy-policy">Privacy Policy</ext-link>.</p><p>Reviewer #1: No</p><p>Reviewer #2: No</p><p>[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files to be viewed.]</p><p>While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, <ext-link ext-link-type="uri" xlink:href="https://pacev2.apexcovantage.com/">https://pacev2.apexcovantage.com/</ext-link>. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at <email>figures@plos.org</email>. Please note that Supporting Information files do not need this step.</p></body></sub-article><sub-article id="pone.0223990.r002" article-type="author-comment"><front-stub><article-id pub-id-type="doi">10.1371/journal.pone.0223990.r002</article-id><title-group><article-title>Author response to Decision Letter 0</article-title></title-group><related-article id="rel-obj002" ext-link-type="doi" xlink:href="10.1371/journal.pone.0223990" related-article-type="editor-report"></related-article><custom-meta-group><custom-meta><meta-name>Submission Version</meta-name><meta-value>1</meta-value></custom-meta></custom-meta-group></front-stub><body><p><named-content content-type="author-response-date">17 Sep 2019</named-content></p><p>Dear Dr Jin, </p><p>Thank you for your response to our manuscript. We greatly appreciate the reviewers taking the time to consider this paper for publication in PlosOne, and their very helpful suggestions. We have taken all of their remarks into consideration as follows.</p><p>Reviewer #1</p><p>We note that the Reviewer considers this to be an interesting research study that would be improved by additions to the bioinformatic and biostatistical analyses. Our responses to specific points are: </p><p>1. QIIME 1 has been succeeded by QIIME 2 because of outdated workflow of QC control and OTU clustering in QIIME 1. The authors should update their analyses by using QIIME 2 or other pipelines that is more advanced than QIIME 1.9.0. This would ideally use amplicon sequence variants instead of 97% OTUs (see this paper for a discussion of this topic: <ext-link ext-link-type="uri" xlink:href="https://www.ncbi.nlm.nih.gov/pubmed/28731476">https://www.ncbi.nlm.nih.gov/pubmed/28731476</ext-link>). Meantime, key parameters of workflow for OTU clustering and taxa assignment would be clearly indicated.</p><p>We are aware of the update of QIIME 1.9.0 to QIIME 2, however QIIME 2 does yet not support dual barcoded data. A work around for this is to use internal illumina demultiplexing, but this process involves the removal of reads pre-analysis and is not optimal. We therefore clarified this reason on line 163 in the methods. </p><p>The Reviewer is quite right to draw attention to the potential use of amplicon sequence variants (ASVs). However, ASVs have not been universally accepted, and despite arguments for the use of exact sequence variants (ESVs), OTUs remain an appropriate method of analysis for 16S data. The most important reasons for using OTUs over ASVs or ESVs is that they may lead to the over splitting of OTUs and false inflation of diversity. Considering intragenomic heterogeneity it is possible that multiple ESVs may not be coming from distinct taxa. </p><p>We therefore acknowledge this debate in line 177 in the discussion by stating “Exact sequence variants (ESVs) may in some circumstances improve identification of microbial taxa, but genomic sequencing of the airway microbiota is at an early stage. In order to avoid over-splitting of taxa and false inflation of diversity, we have taken the conservative approach of using OTUs in our analyses rather than amplicon sequence variants”. </p><p>2. The authors used 16S V4 region primers and quantitative PCR to measure oral bacterial biomass. If so, was there baseline control for normalization?</p><p>The protocols for performing quantitative PCR (2) have been updated with edits to both the methods and supplementary methods. These updates clarify the procedure used performing oropharyngeal swabs and explain the internal controls implemented during qPCR analysis. Full details of the parameters used for sequencing analysis have been updated in the methods section of the paper on page7, line 148, referencing all parameters used in the analysis.</p><p>3. The authors used three key measures, including Richness, Shannon-Weiner and Inverse Simpsons, to compare the differences of oral microbiota communities between samples from children with and without acute wheeze. However, more detailed comparison of specific bacteria taxa should be performed to show the differential bacterial composition and abundance between cases and controls. For example, as shown in Figure 1, which bacteria(s) was/were the mostly changed in relative abundance; it could be estimated with LEfSe, Wilcoxon signed rank test or Turkey HSD etc.</p><p>We reported the use of Random Forest modelling in the paper to predict OTUs significantly associated with disease states. These models had low predictive power and the model results were not considered reliable (i.e. there is no great difference between the sample groups). Results of indicator species analysis (line 237) and DeSeq2 differential abundance analysis (line 238) have now been presented alongside these results in in line with the Reviewer’s comments. </p><p>Discriminant analysis has many assumptions and restrictions, including equal sample sizes and homogeneity of variance/covariance that do not apply here.</p><p>4. The age should be one of important factors influencing oral microbial community. Given the wide range of years of children age (0.08-18.5 yeas), the authors should consider to divide the samples into different ago groups and compare the difference of bacterial composition and abundance.</p><p>We agree with reviewer 1, age is an important factor influencing the microbial community in this study. Several analyses were carried out to investigate the effect of age on the microbial community including controlling for age in the investigation of all clinical characteristics. The cohort of children below the age of 5 were investigated, only bacterial biomass was found to be significantly associated with age in this group. Further groups could not be analysed meaningfully due to the uneven distribution of the age data across the study.</p><p>5. Table 1 lacks statistical comparison of demographic information between cases and controls.</p><p>Statistical comparisons in the form of p-values have been added to Table 1 .</p><p>6. Figure 1 lacks the basic unit of Biomass. The percentage proportion of abundance should be indicated in the y-axis.</p><p>The units on Figure 1 have been updated to express the units of bacterial biomass.</p><p>7. Figure 2 - is it possible that the authors try other PCoA method to cluster samples, for example, weighted or unweighted UniFrac methods?</p><p>We thank reviewer one for suggesting alternative methods of clustering samples based on figure 2. Unweighted UniFrac relies on presences /absence data and does not take into account community composition which can be biased toward rare OTUs. On the other hand, weighted UniFrac uses phylogenetic information to infer genetic relationships based on evolutionary assumptions and this may lead to the introduction of errors. </p><p>We have created alternative plots using these measures, but our conclusion is that Bray-Curtis dissimilarity is very commonly used for good reasons, and it remains the most easily understood measure for this plot.</p><p>8. The authors mentioned that "Specific care was made not to contaminate samples with any other part of the mouth". Was there more detailed information?</p><p>The protocols for performing oropharyngeal swabs have been updated with edits to both the methods and supplementary methods (page 7, line 135). </p><p>Reviewer #2: </p><p>The article is very relevant and evaluated viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children. Although they concluded that the microbiota is not associated with viral infection and wheeze in children the article discuss important points that deserve to be published. </p><p>We note with gratitude that the Reviewer considers this to be an interesting research study that would be improved by additions to the bioinformatic and biostatistical analyses. Our responses to specific points are:</p><p>1. It not clear if the children with bronchiolitis are infected with RSV or other virus. This must be explored in the results and in the conclusion. Other important point is to performed and analysis of family and order of the microbiota comparing children with bronchiolitis and the controls.</p><p>We have clarified the viral results associated with bronchiolitis diagnosis at the time of sampling in the results (line 274) and with reference to figure 1 in the manuscript.</p><p>2. Another point that should be explored in the manuscript is breastfeeding and Caesarean delivery, that might be influencing the microbiota.</p><p>We now state on page paragraph that “We did not find any differences in the microbiota that were attributable to recorded breastfeeding. No data was available to explore the effect of delivery method in this study.” Page 13, line 251.</p><p>Overall, we feel that the paper has been greatly improved by the Reviewers’ suggestions, and we trust these changes meet with your approval. </p><p>Regards, </p><p>Dr Leah Cuthbertson</p><supplementary-material content-type="local-data" id="pone.0223990.s013"><label>Attachment</label><caption><p>Submitted filename: <named-content content-type="submitted-filename">Response_to_reviewers.docx</named-content></p></caption><media xlink:href="pone.0223990.s013.docx"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material></body></sub-article><sub-article id="pone.0223990.r003" article-type="aggregated-review-documents"><front-stub><article-id pub-id-type="doi">10.1371/journal.pone.0223990.r003</article-id><title-group><article-title>Decision Letter 1</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Jin</surname><given-names>Dong-Yan</given-names></name><role>Academic Editor</role></contrib></contrib-group><permissions><copyright-statement>© 2019 Dong-Yan Jin</copyright-statement><copyright-year>2019</copyright-year><copyright-holder>Dong-Yan Jin</copyright-holder><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p></license></permissions><related-article id="rel-obj003" ext-link-type="doi" xlink:href="10.1371/journal.pone.0223990" related-article-type="reviewed-article"></related-article><custom-meta-group><custom-meta><meta-name>Submission Version</meta-name><meta-value>1</meta-value></custom-meta></custom-meta-group></front-stub><body><p><named-content content-type="letter-date">3 Oct 2019</named-content></p><p>Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children</p><p>PONE-D-19-20152R1</p><p>Dear Dr. Cuthbertson,</p><p>We are pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it complies with all outstanding technical requirements.</p><p>Within one week, you will receive an e-mail containing information on the amendments required prior to publication. When all required modifications have been addressed, you will receive a formal acceptance letter and your manuscript will proceed to our production department and be scheduled for publication.</p><p>Shortly after the formal acceptance letter is sent, an invoice for payment will follow. To ensure an efficient production and billing process, please log into Editorial Manager at <ext-link ext-link-type="uri" xlink:href="https://www.editorialmanager.com/pone/">https://www.editorialmanager.com/pone/</ext-link>, click the "Update My Information" link at the top of the page, and update your user information. If you have any billing related questions, please contact our Author Billing department directly at <email>authorbilling@plos.org</email>.</p><p>If your institution or institutions have a press office, please notify them about your upcoming paper to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, you must inform our press team as soon as possible and no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact <email>onepress@plos.org</email>.</p><p>With kind regards,</p><p>Dong-Yan Jin</p><p>Academic Editor</p><p>PLOS ONE</p><p>Additional Editor Comments (optional):</p><p>Reviewers' comments:</p><p>Reviewer's Responses to Questions</p><p><bold>Comments to the Author</bold></p><p>1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.</p><p>Reviewer #1: All comments have been addressed</p><p>Reviewer #2: (No Response)</p><p>**********</p><p>2. Is the manuscript technically sound, and do the data support the conclusions?</p><p>The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. </p><p>Reviewer #1: Yes</p><p>Reviewer #2: Yes</p><p>**********</p><p>3. Has the statistical analysis been performed appropriately and rigorously? </p><p>Reviewer #1: Yes</p><p>Reviewer #2: Yes</p><p>**********</p><p>4. Have the authors made all data underlying the findings in their manuscript fully available?</p><p>The <ext-link ext-link-type="uri" xlink:href="http://www.plosone.org/static/policies.action#sharing">PLOS Data policy</ext-link> requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.</p><p>Reviewer #1: Yes</p><p>Reviewer #2: Yes</p><p>**********</p><p>5. Is the manuscript presented in an intelligible fashion and written in standard English?</p><p>PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.</p><p>Reviewer #1: Yes</p><p>Reviewer #2: Yes</p><p>**********</p><p>6. Review Comments to the Author</p><p>Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)</p><p>Reviewer #1: (No Response)</p><p>Reviewer #2: The authors improved the manuscript accepting the suggestions of the Reviewers. All my concerns had been addressed.</p><p>**********</p><p>7. PLOS authors have the option to publish the peer review history of their article (<ext-link ext-link-type="uri" xlink:href="https://journals.plos.org/plosone/s/editorial-and-peer-review-process#loc-peer-review-history">what does this mean?</ext-link>). If published, this will include your full peer review and any attached files.</p><p>If you choose “no”, your identity will remain anonymous but your review may still be made public.</p><p><bold>Do you want your identity to be public for this peer review?</bold> For information about this choice, including consent withdrawal, please see our <ext-link ext-link-type="uri" xlink:href="https://www.plos.org/privacy-policy">Privacy Policy</ext-link>.</p><p>Reviewer #1: No</p><p>Reviewer #2: No</p></body></sub-article><sub-article id="pone.0223990.r004" article-type="editor-report"><front-stub><article-id pub-id-type="doi">10.1371/journal.pone.0223990.r004</article-id><title-group><article-title>Acceptance letter</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Jin</surname><given-names>Dong-Yan</given-names></name><role>Academic Editor</role></contrib></contrib-group><permissions><copyright-statement>© 2019 Dong-Yan Jin</copyright-statement><copyright-year>2019</copyright-year><copyright-holder>Dong-Yan Jin</copyright-holder><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p></license></permissions><related-article id="rel-obj004" ext-link-type="doi" xlink:href="10.1371/journal.pone.0223990" related-article-type="reviewed-article"></related-article></front-stub><body><p><named-content content-type="letter-date">7 Oct 2019</named-content></p><p>PONE-D-19-20152R1 </p><p>Viral respiratory infections and the oropharyngeal bacterial microbiota in acutely wheezing children </p><p>Dear Dr. Cuthbertson:</p><p>I am pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. </p><p>If your institution or institutions have a press office, please notify them about your upcoming paper at this point, to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact <email>onepress@plos.org</email>.</p><p>For any other questions or concerns, please email <email>plosone@plos.org</email>. </p><p>Thank you for submitting your work to PLOS ONE.</p><p>With kind regards,</p><p>PLOS ONE Editorial Office Staff</p><p>on behalf of</p><p>Prof. Dong-Yan Jin </p><p>Academic Editor</p><p>PLOS ONE</p></body></sub-article></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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