First infection by all four non-severe acute respiratory syndrome human coronaviruses takes place during childhood.
Identifieur interne : 001127 ( PubMed/Corpus ); précédent : 001126; suivant : 001128First infection by all four non-severe acute respiratory syndrome human coronaviruses takes place during childhood.
Auteurs : Weimin Zhou ; Wen Wang ; Huijuan Wang ; Roujian Lu ; Wenjie TanSource :
- BMC infectious diseases [ 1471-2334 ] ; 2013.
English descriptors
- KwdEn :
- Adolescent, Adult, Aged, Antibodies, Viral (immunology), Child, Child, Preschool, Coronavirus (genetics), Coronavirus (immunology), Coronavirus (isolation & purification), Coronavirus (physiology), Coronavirus Infections (diagnosis), Coronavirus Infections (immunology), Coronavirus Infections (virology), Female, Humans, Infant, Male, Middle Aged, Young Adult.
- MESH :
- chemical , immunology : Antibodies, Viral.
- diagnosis : Coronavirus Infections.
- genetics : Coronavirus.
- immunology : Coronavirus, Coronavirus Infections.
- isolation & purification : Coronavirus.
- physiology : Coronavirus.
- virology : Coronavirus Infections.
- Adolescent, Adult, Aged, Child, Child, Preschool, Female, Humans, Infant, Male, Middle Aged, Young Adult.
Abstract
Non-severe acute respiratory syndrome (non-SARS)-related human coronaviruses (HCoVs), including HCoV-229E, -HKU1, -NL63, and -OC43, have been detected in respiratory tract samples from children and adults. However, the natural prevalence of antibodies against these viruses in serum among population is unknown.
DOI: 10.1186/1471-2334-13-433
PubMed: 24040960
Links to Exploration step
pubmed:24040960Le document en format XML
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<affiliation><nlm:affiliation>Key Laboratory of Medical Virology, Ministry of Health; National Institute for Viral Disease Control and Prevention, China Centers for Disease Control and Prevention, Beijing 102206, China. tanwj28@yahoo.cn.</nlm:affiliation>
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<author><name sortKey="Wang, Wen" sort="Wang, Wen" uniqKey="Wang W" first="Wen" last="Wang">Wen Wang</name>
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<author><name sortKey="Wang, Huijuan" sort="Wang, Huijuan" uniqKey="Wang H" first="Huijuan" last="Wang">Huijuan Wang</name>
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<author><name sortKey="Lu, Roujian" sort="Lu, Roujian" uniqKey="Lu R" first="Roujian" last="Lu">Roujian Lu</name>
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<author><name sortKey="Tan, Wenjie" sort="Tan, Wenjie" uniqKey="Tan W" first="Wenjie" last="Tan">Wenjie Tan</name>
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<affiliation><nlm:affiliation>Key Laboratory of Medical Virology, Ministry of Health; National Institute for Viral Disease Control and Prevention, China Centers for Disease Control and Prevention, Beijing 102206, China. tanwj28@yahoo.cn.</nlm:affiliation>
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<author><name sortKey="Wang, Wen" sort="Wang, Wen" uniqKey="Wang W" first="Wen" last="Wang">Wen Wang</name>
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<author><name sortKey="Wang, Huijuan" sort="Wang, Huijuan" uniqKey="Wang H" first="Huijuan" last="Wang">Huijuan Wang</name>
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<author><name sortKey="Lu, Roujian" sort="Lu, Roujian" uniqKey="Lu R" first="Roujian" last="Lu">Roujian Lu</name>
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<author><name sortKey="Tan, Wenjie" sort="Tan, Wenjie" uniqKey="Tan W" first="Wenjie" last="Tan">Wenjie Tan</name>
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<series><title level="j">BMC infectious diseases</title>
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<term>Child</term>
<term>Child, Preschool</term>
<term>Coronavirus (genetics)</term>
<term>Coronavirus (immunology)</term>
<term>Coronavirus (isolation & purification)</term>
<term>Coronavirus (physiology)</term>
<term>Coronavirus Infections (diagnosis)</term>
<term>Coronavirus Infections (immunology)</term>
<term>Coronavirus Infections (virology)</term>
<term>Female</term>
<term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Antibodies, Viral</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Coronavirus Infections</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Coronavirus</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Coronavirus</term>
<term>Coronavirus Infections</term>
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<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Coronavirus</term>
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<term>Adult</term>
<term>Aged</term>
<term>Child</term>
<term>Child, Preschool</term>
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<front><div type="abstract" xml:lang="en">Non-severe acute respiratory syndrome (non-SARS)-related human coronaviruses (HCoVs), including HCoV-229E, -HKU1, -NL63, and -OC43, have been detected in respiratory tract samples from children and adults. However, the natural prevalence of antibodies against these viruses in serum among population is unknown.</div>
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<DateCompleted><Year>2014</Year>
<Month>06</Month>
<Day>23</Day>
</DateCompleted>
<DateRevised><Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
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<Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1471-2334</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>13</Volume>
<PubDate><Year>2013</Year>
<Month>Sep</Month>
<Day>16</Day>
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<Title>BMC infectious diseases</Title>
<ISOAbbreviation>BMC Infect. Dis.</ISOAbbreviation>
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<ArticleTitle>First infection by all four non-severe acute respiratory syndrome human coronaviruses takes place during childhood.</ArticleTitle>
<Pagination><MedlinePgn>433</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1186/1471-2334-13-433</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Non-severe acute respiratory syndrome (non-SARS)-related human coronaviruses (HCoVs), including HCoV-229E, -HKU1, -NL63, and -OC43, have been detected in respiratory tract samples from children and adults. However, the natural prevalence of antibodies against these viruses in serum among population is unknown.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">To measure antibodies to the spike (S) protein of the four common non-SARS HCoVs, recombinant S proteins of the four HCoVs were expressed and characterised in 293 T cell. An S-protein-based indirect immunofluorescence assay (IFA) was then developed to detect anti-S IgG and IgM for the four individual HCoVs and applied to serum samples from a general asymptomatic population (218 children and 576 adults) in Beijing.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Of 794 blood samples tested, only 29 (3.65%) were negative for anti-S IgG. The seropositivity of the four anti-S IgG antibodies was >70% within the general population. The majority of seroconversions to four-HCoV positivity first occurred in children. Both S-IgG and S-IgM antibodies were detectable among children and increased with age, reaching a plateau at 6 years of age. However, no anti-S IgM was detected in healthy adults.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Large proportions of children and adults in Beijing have evidence of anti-S IgG against four the HCoVs, and first infections by all four non-SARS HCoVs takes place during childhood.</AbstractText>
</Abstract>
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<ForeName>Weimin</ForeName>
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<AffiliationInfo><Affiliation>Key Laboratory of Medical Virology, Ministry of Health; National Institute for Viral Disease Control and Prevention, China Centers for Disease Control and Prevention, Beijing 102206, China. tanwj28@yahoo.cn.</Affiliation>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName>
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