Reactive oxygen species production and Brugia pahangi survivorship in Aedes polynesiensis with artificial Wolbachia infection types.
Identifieur interne : 001E09 ( PubMed/Corpus ); précédent : 001E08; suivant : 001E10Reactive oxygen species production and Brugia pahangi survivorship in Aedes polynesiensis with artificial Wolbachia infection types.
Auteurs : Elizabeth S. Andrews ; Philip R. Crain ; Yuqing Fu ; Daniel K. Howe ; Stephen L. DobsonSource :
- PLoS pathogens [ 1553-7374 ] ; 2012.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Reactive Oxygen Species.
- metabolism : Brugia pahangi, Elephantiasis, Filarial, Wolbachia.
- microbiology : Aedes.
- parasitology : Aedes, Elephantiasis, Filarial.
- prevention & control : Elephantiasis, Filarial.
- Animals, Female, Oxidative Stress.
Abstract
Heterologous transinfection with the endosymbiotic bacterium Wolbachia has been shown previously to induce pathogen interference phenotypes in mosquito hosts. Here we examine an artificially infected strain of Aedes polynesiensis, the primary vector of Wuchereria bancrofti, which is the causative agent of Lymphatic filariasis (LF) throughout much of the South Pacific. Embryonic microinjection was used to transfer the wAlbB infection from Aedes albopictus into an aposymbiotic strain of Ae. polynesiensis. The resulting strain (designated "MTB") experiences a stable artificial infection with high maternal inheritance. Reciprocal crosses of MTB with naturally infected wild-type Ae. polynesiensis demonstrate strong bidirectional incompatibility. Levels of reactive oxygen species (ROS) in the MTB strain differ significantly relative to that of the wild-type, indicating an impaired ability to regulate oxidative stress. Following a challenge with Brugia pahangi, the number of filarial worms achieving the infective stage is significantly reduced in MTB as compared to the naturally infected and aposymbiotic strains. Survivorship of MTB differed significantly from that of the wild-type, with an interactive effect between survivorship and blood feeding. The results demonstrate a direct correlation between decreased ROS levels and decreased survival of adult female Aedes polynesiensis. The results are discussed in relation to the interaction of Wolbachia with ROS production and antioxidant expression, iron homeostasis and the insect immune system. We discuss the potential applied use of the MTB strain for impacting Ae. polynesiensis populations and strategies for reducing LF incidence in the South Pacific.
DOI: 10.1371/journal.ppat.1003075
PubMed: 23236284
Links to Exploration step
pubmed:23236284Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Reactive oxygen species production and Brugia pahangi survivorship in Aedes polynesiensis with artificial Wolbachia infection types.</title><author><name sortKey="Andrews, Elizabeth S" sort="Andrews, Elizabeth S" uniqKey="Andrews E" first="Elizabeth S" last="Andrews">Elizabeth S. Andrews</name><affiliation><nlm:affiliation>Department of Entomology, College of Agriculture, University of Kentucky, Lexington, Kentucky, United States of America.</nlm:affiliation></affiliation></author><author><name sortKey="Crain, Philip R" sort="Crain, Philip R" uniqKey="Crain P" first="Philip R" last="Crain">Philip R. Crain</name></author><author><name sortKey="Fu, Yuqing" sort="Fu, Yuqing" uniqKey="Fu Y" first="Yuqing" last="Fu">Yuqing Fu</name></author><author><name sortKey="Howe, Daniel K" sort="Howe, Daniel K" uniqKey="Howe D" first="Daniel K" last="Howe">Daniel K. Howe</name></author><author><name sortKey="Dobson, Stephen L" sort="Dobson, Stephen L" uniqKey="Dobson S" first="Stephen L" last="Dobson">Stephen L. Dobson</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2012">2012</date><idno type="RBID">pubmed:23236284</idno><idno type="pmid">23236284</idno><idno type="doi">10.1371/journal.ppat.1003075</idno><idno type="wicri:Area/PubMed/Corpus">001E09</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001E09</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Reactive oxygen species production and Brugia pahangi survivorship in Aedes polynesiensis with artificial Wolbachia infection types.</title><author><name sortKey="Andrews, Elizabeth S" sort="Andrews, Elizabeth S" uniqKey="Andrews E" first="Elizabeth S" last="Andrews">Elizabeth S. Andrews</name><affiliation><nlm:affiliation>Department of Entomology, College of Agriculture, University of Kentucky, Lexington, Kentucky, United States of America.</nlm:affiliation></affiliation></author><author><name sortKey="Crain, Philip R" sort="Crain, Philip R" uniqKey="Crain P" first="Philip R" last="Crain">Philip R. Crain</name></author><author><name sortKey="Fu, Yuqing" sort="Fu, Yuqing" uniqKey="Fu Y" first="Yuqing" last="Fu">Yuqing Fu</name></author><author><name sortKey="Howe, Daniel K" sort="Howe, Daniel K" uniqKey="Howe D" first="Daniel K" last="Howe">Daniel K. Howe</name></author><author><name sortKey="Dobson, Stephen L" sort="Dobson, Stephen L" uniqKey="Dobson S" first="Stephen L" last="Dobson">Stephen L. Dobson</name></author></analytic><series><title level="j">PLoS pathogens</title><idno type="eISSN">1553-7374</idno><imprint><date when="2012" type="published">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aedes (microbiology)</term><term>Aedes (parasitology)</term><term>Animals</term><term>Brugia pahangi (metabolism)</term><term>Elephantiasis, Filarial (metabolism)</term><term>Elephantiasis, Filarial (parasitology)</term><term>Elephantiasis, Filarial (prevention & control)</term><term>Female</term><term>Oxidative Stress</term><term>Reactive Oxygen Species (metabolism)</term><term>Wolbachia (metabolism)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Reactive Oxygen Species</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Brugia pahangi</term><term>Elephantiasis, Filarial</term><term>Wolbachia</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Aedes</term></keywords><keywords scheme="MESH" qualifier="parasitology" xml:lang="en"><term>Aedes</term><term>Elephantiasis, Filarial</term></keywords><keywords scheme="MESH" qualifier="prevention & control" xml:lang="en"><term>Elephantiasis, Filarial</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Female</term><term>Oxidative Stress</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Heterologous transinfection with the endosymbiotic bacterium Wolbachia has been shown previously to induce pathogen interference phenotypes in mosquito hosts. Here we examine an artificially infected strain of Aedes polynesiensis, the primary vector of Wuchereria bancrofti, which is the causative agent of Lymphatic filariasis (LF) throughout much of the South Pacific. Embryonic microinjection was used to transfer the wAlbB infection from Aedes albopictus into an aposymbiotic strain of Ae. polynesiensis. The resulting strain (designated "MTB") experiences a stable artificial infection with high maternal inheritance. Reciprocal crosses of MTB with naturally infected wild-type Ae. polynesiensis demonstrate strong bidirectional incompatibility. Levels of reactive oxygen species (ROS) in the MTB strain differ significantly relative to that of the wild-type, indicating an impaired ability to regulate oxidative stress. Following a challenge with Brugia pahangi, the number of filarial worms achieving the infective stage is significantly reduced in MTB as compared to the naturally infected and aposymbiotic strains. Survivorship of MTB differed significantly from that of the wild-type, with an interactive effect between survivorship and blood feeding. The results demonstrate a direct correlation between decreased ROS levels and decreased survival of adult female Aedes polynesiensis. The results are discussed in relation to the interaction of Wolbachia with ROS production and antioxidant expression, iron homeostasis and the insect immune system. We discuss the potential applied use of the MTB strain for impacting Ae. polynesiensis populations and strategies for reducing LF incidence in the South Pacific.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23236284</PMID><DateCreated><Year>2012</Year><Month>12</Month><Day>13</Day></DateCreated><DateCompleted><Year>2013</Year><Month>05</Month><Day>23</Day></DateCompleted><DateRevised><Year>2016</Year><Month>10</Month><Day>19</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1553-7374</ISSN><JournalIssue CitedMedium="Internet"><Volume>8</Volume><Issue>12</Issue><PubDate><Year>2012</Year></PubDate></JournalIssue><Title>PLoS pathogens</Title><ISOAbbreviation>PLoS Pathog.</ISOAbbreviation></Journal><ArticleTitle>Reactive oxygen species production and Brugia pahangi survivorship in Aedes polynesiensis with artificial Wolbachia infection types.</ArticleTitle><Pagination><MedlinePgn>e1003075</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1371/journal.ppat.1003075</ELocationID><Abstract><AbstractText>Heterologous transinfection with the endosymbiotic bacterium Wolbachia has been shown previously to induce pathogen interference phenotypes in mosquito hosts. Here we examine an artificially infected strain of Aedes polynesiensis, the primary vector of Wuchereria bancrofti, which is the causative agent of Lymphatic filariasis (LF) throughout much of the South Pacific. Embryonic microinjection was used to transfer the wAlbB infection from Aedes albopictus into an aposymbiotic strain of Ae. polynesiensis. The resulting strain (designated "MTB") experiences a stable artificial infection with high maternal inheritance. Reciprocal crosses of MTB with naturally infected wild-type Ae. polynesiensis demonstrate strong bidirectional incompatibility. Levels of reactive oxygen species (ROS) in the MTB strain differ significantly relative to that of the wild-type, indicating an impaired ability to regulate oxidative stress. Following a challenge with Brugia pahangi, the number of filarial worms achieving the infective stage is significantly reduced in MTB as compared to the naturally infected and aposymbiotic strains. Survivorship of MTB differed significantly from that of the wild-type, with an interactive effect between survivorship and blood feeding. The results demonstrate a direct correlation between decreased ROS levels and decreased survival of adult female Aedes polynesiensis. The results are discussed in relation to the interaction of Wolbachia with ROS production and antioxidant expression, iron homeostasis and the insect immune system. We discuss the potential applied use of the MTB strain for impacting Ae. polynesiensis populations and strategies for reducing LF incidence in the South Pacific.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Andrews</LastName><ForeName>Elizabeth S</ForeName><Initials>ES</Initials><AffiliationInfo><Affiliation>Department of Entomology, College of Agriculture, University of Kentucky, Lexington, Kentucky, United States of America.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Crain</LastName><ForeName>Philip R</ForeName><Initials>PR</Initials></Author><Author ValidYN="Y"><LastName>Fu</LastName><ForeName>Yuqing</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Howe</LastName><ForeName>Daniel K</ForeName><Initials>DK</Initials></Author><Author ValidYN="Y"><LastName>Dobson</LastName><ForeName>Stephen L</ForeName><Initials>SL</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>AI-067434</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>12</Month><Day>06</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>PLoS Pathog</MedlineTA><NlmUniqueID>101238921</NlmUniqueID><ISSNLinking>1553-7366</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D017382">Reactive Oxygen Species</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>PLoS Biol. 2005 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MajorTopicYN="N">Aedes</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName><QualifierName UI="Q000469" MajorTopicYN="Y">parasitology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017179" MajorTopicYN="N">Brugia pahangi</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004605" MajorTopicYN="N">Elephantiasis, Filarial</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000469" MajorTopicYN="N">parasitology</QualifierName><QualifierName UI="Q000517" MajorTopicYN="N">prevention & control</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018384" MajorTopicYN="N">Oxidative Stress</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017382" MajorTopicYN="N">Reactive Oxygen Species</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020577" MajorTopicYN="N">Wolbachia</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading></MeshHeadingList><OtherID Source="NLM">PMC3516568</OtherID></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2012</Year><Month>04</Month><Day>30</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2012</Year><Month>10</Month><Day>22</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>12</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>12</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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