Serogrouping and seroepidemiology of North European hantaviruses using a novel broadly targeted synthetic nucleoprotein antigen array.
Identifieur interne : 000B96 ( PubMed/Curation ); précédent : 000B95; suivant : 000B97Serogrouping and seroepidemiology of North European hantaviruses using a novel broadly targeted synthetic nucleoprotein antigen array.
Auteurs : Bengt Rönnberg [Suède] ; Olli Vapalahti [Finlande] ; Marco Goeijenbier [Pays-Bas] ; Chantal Reusken [Pays-Bas] ; Ke Gustafsson [Suède] ; Jonas Blomberg [Suède] ; Ke Lundkvist [Suède]Source :
- Infection ecology & epidemiology [ 2000-8686 ] ; 2017.
Abstract
Introduction: Hantaviruses are globally distributed zoonotic pathogens. Great diversity and high antigenic cross-reactivity makes diagnosis by traditional methods cumbersome. Materials and methods: 'Megapeptides', 119-120-mers from the amino terminus of the nucleoprotein of 16 hantaviruses, representing the four major branches of the hantavirus phylogenetic tree, were utilized in a novel IgG-based hantavirus suspension multiplex immunoassay (HSMIA) for detection of past hantavirus infections in 155 North European human samples. We compared HSMIA with established EIAs and focus reduction neutralization test (FRNT). Results and discussion: The Puumala hantavirus (PUUV) component in the HSMIA gave concordant results with a PUUV IgG EIA in 142 sera from Northern Sweden (of which 31 were EIA positive, 7 borderline and 104 EIA negative, sensitivity 30/31 = 97%, specificity 104/ 104 = 100%, 134/135 = 99% concordance), with another immunoassay in 40 PUUV IgG positive sera from Finland (36/40 = 90% sensitivity), and was concordant in 8 of 11 cases with PUUV and DOBV neutralization titers, respectively. Two major IgG reactivity patterns were found: (i) a PUUV-specific pattern covering phylogroup IV and its serogroups B and C; and (ii) a Dobrava virus (DOBV)-specific pattern, covering the serogroup A portion of phylogroup III. In addition, we found several minor patterns with reactivity to only one or two megapeptides indicating additional hantaviruses infecting humans in the Swedish and Finnish populations. Conclusion: The broadly reactive and rational HSMIA yielded results highly correlated with the established PUUV EIAs and the NT results. It is a sensitive and specific assay, which will be suited for efficient serosurveillance of hantaviruses in humans. Its use in animals should be further investigated.
DOI: 10.1080/20008686.2017.1350086
PubMed: 28815001
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<front><div type="abstract" xml:lang="en"><b>Introduction</b>
: Hantaviruses are globally distributed zoonotic pathogens. Great diversity and high antigenic cross-reactivity makes diagnosis by traditional methods cumbersome. <b>Materials and methods</b>
: 'Megapeptides', 119-120-mers from the amino terminus of the nucleoprotein of 16 hantaviruses, representing the four major branches of the hantavirus phylogenetic tree, were utilized in a novel IgG-based hantavirus suspension multiplex immunoassay (HSMIA) for detection of past hantavirus infections in 155 North European human samples. We compared HSMIA with established EIAs and focus reduction neutralization test (FRNT). <b>Results and discussion</b>
: The Puumala hantavirus (PUUV) component in the HSMIA gave concordant results with a PUUV IgG EIA in 142 sera from Northern Sweden (of which 31 were EIA positive, 7 borderline and 104 EIA negative, sensitivity 30/31 = 97%, specificity 104/ 104 = 100%, 134/135 = 99% concordance), with another immunoassay in 40 PUUV IgG positive sera from Finland (36/40 = 90% sensitivity), and was concordant in 8 of 11 cases with PUUV and DOBV neutralization titers, respectively. Two major IgG reactivity patterns were found: (i) a PUUV-specific pattern covering phylogroup IV and its serogroups B and C; and (ii) a Dobrava virus (DOBV)-specific pattern, covering the serogroup A portion of phylogroup III. In addition, we found several minor patterns with reactivity to only one or two megapeptides indicating additional hantaviruses infecting humans in the Swedish and Finnish populations. <b>Conclusion</b>
: The broadly reactive and rational HSMIA yielded results highly correlated with the established PUUV EIAs and the NT results. It is a sensitive and specific assay, which will be suited for efficient serosurveillance of hantaviruses in humans. Its use in animals should be further investigated.</div>
</front>
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<Month>11</Month>
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<Title>Infection ecology & epidemiology</Title>
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<ArticleTitle>Serogrouping and seroepidemiology of North European hantaviruses using a novel broadly targeted synthetic nucleoprotein antigen array.</ArticleTitle>
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<Abstract><AbstractText><b>Introduction</b>
: Hantaviruses are globally distributed zoonotic pathogens. Great diversity and high antigenic cross-reactivity makes diagnosis by traditional methods cumbersome. <b>Materials and methods</b>
: 'Megapeptides', 119-120-mers from the amino terminus of the nucleoprotein of 16 hantaviruses, representing the four major branches of the hantavirus phylogenetic tree, were utilized in a novel IgG-based hantavirus suspension multiplex immunoassay (HSMIA) for detection of past hantavirus infections in 155 North European human samples. We compared HSMIA with established EIAs and focus reduction neutralization test (FRNT). <b>Results and discussion</b>
: The Puumala hantavirus (PUUV) component in the HSMIA gave concordant results with a PUUV IgG EIA in 142 sera from Northern Sweden (of which 31 were EIA positive, 7 borderline and 104 EIA negative, sensitivity 30/31 = 97%, specificity 104/ 104 = 100%, 134/135 = 99% concordance), with another immunoassay in 40 PUUV IgG positive sera from Finland (36/40 = 90% sensitivity), and was concordant in 8 of 11 cases with PUUV and DOBV neutralization titers, respectively. Two major IgG reactivity patterns were found: (i) a PUUV-specific pattern covering phylogroup IV and its serogroups B and C; and (ii) a Dobrava virus (DOBV)-specific pattern, covering the serogroup A portion of phylogroup III. In addition, we found several minor patterns with reactivity to only one or two megapeptides indicating additional hantaviruses infecting humans in the Swedish and Finnish populations. <b>Conclusion</b>
: The broadly reactive and rational HSMIA yielded results highly correlated with the established PUUV EIAs and the NT results. It is a sensitive and specific assay, which will be suited for efficient serosurveillance of hantaviruses in humans. Its use in animals should be further investigated.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Rönnberg</LastName>
<ForeName>Bengt</ForeName>
<Initials>B</Initials>
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<AffiliationInfo><Affiliation>Section of Clinical Microbiology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Zoonosis Science Center, Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Laboratory of Clinical Microbiology, Uppsala University Hospital, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Vapalahti</LastName>
<ForeName>Olli</ForeName>
<Initials>O</Initials>
<AffiliationInfo><Affiliation>Department of Veterinary Biosciences and Virology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.</Affiliation>
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<Author ValidYN="Y"><LastName>Goeijenbier</LastName>
<ForeName>Marco</ForeName>
<Initials>M</Initials>
<Identifier Source="ORCID">0000-0002-3165-8193</Identifier>
<AffiliationInfo><Affiliation>Department of Viroscience, Erasmus MC, Rotterdam, The Netherlands.</Affiliation>
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<Author ValidYN="Y"><LastName>Reusken</LastName>
<ForeName>Chantal</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Department of Viroscience, Erasmus MC, Rotterdam, The Netherlands.</Affiliation>
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<Author ValidYN="Y"><LastName>Gustafsson</LastName>
<ForeName>Åke</ForeName>
<Initials>Å</Initials>
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<AffiliationInfo><Affiliation>Laboratory of Clinical Microbiology, Uppsala University Hospital, Uppsala, Sweden.</Affiliation>
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<Author ValidYN="Y"><LastName>Blomberg</LastName>
<ForeName>Jonas</ForeName>
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<Identifier Source="ORCID">0000-0001-6492-2491</Identifier>
<AffiliationInfo><Affiliation>Section of Clinical Microbiology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Zoonosis Science Center, Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Lundkvist</LastName>
<ForeName>Åke</ForeName>
<Initials>Å</Initials>
<Identifier Source="ORCID">0000-0002-1472-1373</Identifier>
<AffiliationInfo><Affiliation>Section of Clinical Microbiology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Zoonosis Science Center, Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Laboratory of Clinical Microbiology, Uppsala University Hospital, Uppsala, Sweden.</Affiliation>
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<Language>eng</Language>
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</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2017</Year>
<Month>07</Month>
<Day>26</Day>
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<MedlineTA>Infect Ecol Epidemiol</MedlineTA>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Hantavirus</Keyword>
<Keyword MajorTopicYN="N">emerging or re-emerging diseases</Keyword>
<Keyword MajorTopicYN="N">laboratory surveillance</Keyword>
<Keyword MajorTopicYN="N">megapeptide</Keyword>
<Keyword MajorTopicYN="N">pathogen surveillance</Keyword>
<Keyword MajorTopicYN="N">suspension multiplex immunoassay</Keyword>
<Keyword MajorTopicYN="N">synthetic antigen</Keyword>
<Keyword MajorTopicYN="N">viral haemorrhagic fever</Keyword>
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