Expanded cocirculation of stable subtypes, emerging lineages, and new sporadic reassortants of porcine influenza viruses in swine populations in Northwest Germany.
Identifieur interne : 000190 ( Main/Curation ); précédent : 000189; suivant : 000191Expanded cocirculation of stable subtypes, emerging lineages, and new sporadic reassortants of porcine influenza viruses in swine populations in Northwest Germany.
Auteurs : Timm C. Harder ; Elisabeth Grosse Beilage ; Elke Lange ; Carolin Meiners ; Stefanie Döhring ; Stefan Pesch ; Thomas Noé ; Christian Grund ; Martin Beer ; Elke StarickSource :
- Journal of virology [ 1098-5514 ] ; 2013.
Descripteurs français
- KwdFr :
- ARN viral (génétique), Allemagne (épidémiologie), Animaux, Infections à Orthomyxoviridae (immunologie), Infections à Orthomyxoviridae (médecine vétérinaire), Infections à Orthomyxoviridae (virologie), Lignage cellulaire, Maladies des porcs (génétique), Maladies des porcs (virologie), Maladies des porcs (épidémiologie), Phylogénie, Poumon (immunologie), Poumon (virologie), Sialidase (génétique), Sous-type H1N2 du virus de la grippe A (), Sous-type H1N2 du virus de la grippe A (isolement et purification), Sous-type H1N2 du virus de la grippe A (pathogénicité), Sous-type H3N2 du virus de la grippe A (), Sous-type H3N2 du virus de la grippe A (isolement et purification), Sous-type H3N2 du virus de la grippe A (pathogénicité), Suidae, Syndrome de détresse respiratoire de l'adulte (génétique), Syndrome de détresse respiratoire de l'adulte (virologie), Syndrome de détresse respiratoire de l'adulte (épidémiologie).
- MESH :
- génétique : ARN viral, Maladies des porcs, Sialidase, Syndrome de détresse respiratoire de l'adulte.
- immunologie : Infections à Orthomyxoviridae, Poumon.
- isolement et purification : Sous-type H1N2 du virus de la grippe A, Sous-type H3N2 du virus de la grippe A.
- médecine vétérinaire : Infections à Orthomyxoviridae.
- pathogénicité : Sous-type H1N2 du virus de la grippe A, Sous-type H3N2 du virus de la grippe A.
- virologie : Infections à Orthomyxoviridae, Maladies des porcs, Poumon, Syndrome de détresse respiratoire de l'adulte.
- épidémiologie : Allemagne, Maladies des porcs, Syndrome de détresse respiratoire de l'adulte.
- Animaux, Lignage cellulaire, Phylogénie, Sous-type H1N2 du virus de la grippe A, Sous-type H3N2 du virus de la grippe A, Suidae.
- Wicri :
- geographic : Allemagne.
English descriptors
- KwdEn :
- Animals, Cell Lineage, Germany (epidemiology), Influenza A Virus, H1N2 Subtype (classification), Influenza A Virus, H1N2 Subtype (isolation & purification), Influenza A Virus, H1N2 Subtype (pathogenicity), Influenza A Virus, H3N2 Subtype (classification), Influenza A Virus, H3N2 Subtype (isolation & purification), Influenza A Virus, H3N2 Subtype (pathogenicity), Lung (immunology), Lung (virology), Neuraminidase (genetics), Orthomyxoviridae Infections (immunology), Orthomyxoviridae Infections (veterinary), Orthomyxoviridae Infections (virology), Phylogeny, RNA, Viral (genetics), Respiratory Distress Syndrome, Adult (epidemiology), Respiratory Distress Syndrome, Adult (genetics), Respiratory Distress Syndrome, Adult (virology), Swine, Swine Diseases (epidemiology), Swine Diseases (genetics), Swine Diseases (virology).
- MESH :
- chemical , genetics : Neuraminidase, RNA, Viral.
- geographic , epidemiology : Germany.
- classification : Influenza A Virus, H1N2 Subtype, Influenza A Virus, H3N2 Subtype.
- epidemiology : Respiratory Distress Syndrome, Adult, Swine Diseases.
- genetics : Respiratory Distress Syndrome, Adult, Swine Diseases.
- immunology : Lung, Orthomyxoviridae Infections.
- isolation & purification : Influenza A Virus, H1N2 Subtype, Influenza A Virus, H3N2 Subtype.
- pathogenicity : Influenza A Virus, H1N2 Subtype, Influenza A Virus, H3N2 Subtype.
- veterinary : Orthomyxoviridae Infections.
- virology : Lung, Orthomyxoviridae Infections, Respiratory Distress Syndrome, Adult, Swine Diseases.
- Animals, Cell Lineage, Phylogeny, Swine.
Abstract
The emergence of the human 2009 pandemic H1N1 (H1N1pdm) virus from swine populations refocused public and scientific attention on swine as an important source of influenza A viruses bearing zoonotic potential. Widespread and year-round circulation of at least four stable lineages of porcine influenza viruses between 2009 and 2012 in a region of Germany with a high-density swine population is documented here. European avian influenza virus-derived H1N1 (H1N1av) viruses dominated the epidemiology, followed by human-derived subtypes H1N2 and H3N2. H1N1pdm viruses and, in particular, recently emerging reassortants between H1N1pdm and porcine HxN2 viruses (H1pdmN2) were detected in about 8% of cases. Further reassortants between these main lineages were diagnosed sporadically. Ongoing diversification both at the phylogenetic and at the antigenic level was evident for the H1N1av lineage and for some of its reassortants. The H1avN2 reassortant R1931/11 displayed conspicuously distinct genetic and antigenic features and was easily transmitted from pig to pig in an experimental infection. Continuing diverging evolution was also observed in the H1pdmN2 lineage. These viruses carry seven genome segments of the H1N1pdm virus, including a hemagglutinin gene that encodes a markedly antigenically altered protein. The zoonotic potential of this lineage remains to be determined. The results highlight the relevance of surveillance and control of porcine influenza virus infections. This is important for the health status of swine herds. In addition, a more exhaustive tracing of the formation, transmission, and spread of new reassortant influenza A viruses with unknown zoonotic potential is urgently required.
DOI: 10.1128/JVI.00381-13
PubMed: 23824819
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Timm C. Harder<affiliation><nlm:affiliation>Friedrich-Loeffler-Institut (FLI), Institute of Diagnostic Virology.</nlm:affiliation>
<wicri:noCountry code="subField">Institute of Diagnostic Virology</wicri:noCountry>
</affiliation>
Le document en format XML
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<front><div type="abstract" xml:lang="en">The emergence of the human 2009 pandemic H1N1 (H1N1pdm) virus from swine populations refocused public and scientific attention on swine as an important source of influenza A viruses bearing zoonotic potential. Widespread and year-round circulation of at least four stable lineages of porcine influenza viruses between 2009 and 2012 in a region of Germany with a high-density swine population is documented here. European avian influenza virus-derived H1N1 (H1N1av) viruses dominated the epidemiology, followed by human-derived subtypes H1N2 and H3N2. H1N1pdm viruses and, in particular, recently emerging reassortants between H1N1pdm and porcine HxN2 viruses (H1pdmN2) were detected in about 8% of cases. Further reassortants between these main lineages were diagnosed sporadically. Ongoing diversification both at the phylogenetic and at the antigenic level was evident for the H1N1av lineage and for some of its reassortants. The H1avN2 reassortant R1931/11 displayed conspicuously distinct genetic and antigenic features and was easily transmitted from pig to pig in an experimental infection. Continuing diverging evolution was also observed in the H1pdmN2 lineage. These viruses carry seven genome segments of the H1N1pdm virus, including a hemagglutinin gene that encodes a markedly antigenically altered protein. The zoonotic potential of this lineage remains to be determined. The results highlight the relevance of surveillance and control of porcine influenza virus infections. This is important for the health status of swine herds. In addition, a more exhaustive tracing of the formation, transmission, and spread of new reassortant influenza A viruses with unknown zoonotic potential is urgently required. </div>
</front>
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<DateCompleted><Year>2013</Year>
<Month>12</Month>
<Day>27</Day>
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<ArticleTitle>Expanded cocirculation of stable subtypes, emerging lineages, and new sporadic reassortants of porcine influenza viruses in swine populations in Northwest Germany.</ArticleTitle>
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<Abstract><AbstractText>The emergence of the human 2009 pandemic H1N1 (H1N1pdm) virus from swine populations refocused public and scientific attention on swine as an important source of influenza A viruses bearing zoonotic potential. Widespread and year-round circulation of at least four stable lineages of porcine influenza viruses between 2009 and 2012 in a region of Germany with a high-density swine population is documented here. European avian influenza virus-derived H1N1 (H1N1av) viruses dominated the epidemiology, followed by human-derived subtypes H1N2 and H3N2. H1N1pdm viruses and, in particular, recently emerging reassortants between H1N1pdm and porcine HxN2 viruses (H1pdmN2) were detected in about 8% of cases. Further reassortants between these main lineages were diagnosed sporadically. Ongoing diversification both at the phylogenetic and at the antigenic level was evident for the H1N1av lineage and for some of its reassortants. The H1avN2 reassortant R1931/11 displayed conspicuously distinct genetic and antigenic features and was easily transmitted from pig to pig in an experimental infection. Continuing diverging evolution was also observed in the H1pdmN2 lineage. These viruses carry seven genome segments of the H1N1pdm virus, including a hemagglutinin gene that encodes a markedly antigenically altered protein. The zoonotic potential of this lineage remains to be determined. The results highlight the relevance of surveillance and control of porcine influenza virus infections. This is important for the health status of swine herds. In addition, a more exhaustive tracing of the formation, transmission, and spread of new reassortant influenza A viruses with unknown zoonotic potential is urgently required. </AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Harder</LastName>
<ForeName>Timm C</ForeName>
<Initials>TC</Initials>
<AffiliationInfo><Affiliation>Friedrich-Loeffler-Institut (FLI), Institute of Diagnostic Virology.</Affiliation>
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<Author ValidYN="Y"><LastName>Grosse Beilage</LastName>
<ForeName>Elisabeth</ForeName>
<Initials>E</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lange</LastName>
<ForeName>Elke</ForeName>
<Initials>E</Initials>
</Author>
<Author ValidYN="Y"><LastName>Meiners</LastName>
<ForeName>Carolin</ForeName>
<Initials>C</Initials>
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<Author ValidYN="Y"><LastName>Döhring</LastName>
<ForeName>Stefanie</ForeName>
<Initials>S</Initials>
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<Author ValidYN="Y"><LastName>Pesch</LastName>
<ForeName>Stefan</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y"><LastName>Noé</LastName>
<ForeName>Thomas</ForeName>
<Initials>T</Initials>
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<Author ValidYN="Y"><LastName>Grund</LastName>
<ForeName>Christian</ForeName>
<Initials>C</Initials>
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<Author ValidYN="Y"><LastName>Beer</LastName>
<ForeName>Martin</ForeName>
<Initials>M</Initials>
</Author>
<Author ValidYN="Y"><LastName>Starick</LastName>
<ForeName>Elke</ForeName>
<Initials>E</Initials>
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<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000821" MajorTopicYN="Y">virology</QualifierName>
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<MeshHeading><DescriptorName UI="D009439" MajorTopicYN="N">Neuraminidase</DescriptorName>
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