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Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America
Although continental populations of avian influenza viruses are genetically distinct, transcontinental reassortment in low pathogenic avian influenza (LPAI) viruses has been detected in migratory birds. Thus, genomic analyses of LPAI viruses could serve as an approach to prioritize species and regio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352445/ https://www.ncbi.nlm.nih.gov/pubmed/25567891 http://dx.doi.org/10.1111/j.1752-4571.2009.00071.x |
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author | Pearce, John M Ramey, Andrew M Flint, Paul L Koehler, Anson V Fleskes, Joseph P Franson, J Christian Hall, Jeffrey S Derksen, Dirk V Ip, Hon S |
author_facet | Pearce, John M Ramey, Andrew M Flint, Paul L Koehler, Anson V Fleskes, Joseph P Franson, J Christian Hall, Jeffrey S Derksen, Dirk V Ip, Hon S |
author_sort | Pearce, John M |
collection | PubMed |
description | Although continental populations of avian influenza viruses are genetically distinct, transcontinental reassortment in low pathogenic avian influenza (LPAI) viruses has been detected in migratory birds. Thus, genomic analyses of LPAI viruses could serve as an approach to prioritize species and regions targeted by North American surveillance activities for foreign origin highly pathogenic avian influenza (HPAI). To assess the applicability of this approach, we conducted a phylogenetic and population genetic analysis of 68 viral genomes isolated from the northern pintail (Anas acuta) at opposite ends of the Pacific migratory flyway in North America. We found limited evidence for Asian LPAI lineages on wintering areas used by northern pintails in California in contrast to a higher frequency on breeding locales of Alaska. Our results indicate that the number of Asian LPAI lineages observed in Alaskan northern pintails, and the nucleotide composition of LPAI lineages, is not maintained through fall migration. Accordingly, our data indicate that surveillance of Pacific Flyway northern pintails to detect foreign avian influenza viruses would be most effective in Alaska. North American surveillance plans could be optimized through an analysis of LPAI genomics from species that demonstrate evolutionary linkages with European or Asian lineages and in regions that have overlapping migratory flyways with areas of HPAI outbreaks. |
format | Online Article Text |
id | pubmed-3352445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33524452012-05-24 Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America Pearce, John M Ramey, Andrew M Flint, Paul L Koehler, Anson V Fleskes, Joseph P Franson, J Christian Hall, Jeffrey S Derksen, Dirk V Ip, Hon S Evol Appl Original Articles Although continental populations of avian influenza viruses are genetically distinct, transcontinental reassortment in low pathogenic avian influenza (LPAI) viruses has been detected in migratory birds. Thus, genomic analyses of LPAI viruses could serve as an approach to prioritize species and regions targeted by North American surveillance activities for foreign origin highly pathogenic avian influenza (HPAI). To assess the applicability of this approach, we conducted a phylogenetic and population genetic analysis of 68 viral genomes isolated from the northern pintail (Anas acuta) at opposite ends of the Pacific migratory flyway in North America. We found limited evidence for Asian LPAI lineages on wintering areas used by northern pintails in California in contrast to a higher frequency on breeding locales of Alaska. Our results indicate that the number of Asian LPAI lineages observed in Alaskan northern pintails, and the nucleotide composition of LPAI lineages, is not maintained through fall migration. Accordingly, our data indicate that surveillance of Pacific Flyway northern pintails to detect foreign avian influenza viruses would be most effective in Alaska. North American surveillance plans could be optimized through an analysis of LPAI genomics from species that demonstrate evolutionary linkages with European or Asian lineages and in regions that have overlapping migratory flyways with areas of HPAI outbreaks. Blackwell Publishing Ltd 2009-11 2009-04-15 /pmc/articles/PMC3352445/ /pubmed/25567891 http://dx.doi.org/10.1111/j.1752-4571.2009.00071.x Text en © 2009 The Authors. Journal compilation © 2009 Blackwell Publishing Ltd |
spellingShingle | Original Articles Pearce, John M Ramey, Andrew M Flint, Paul L Koehler, Anson V Fleskes, Joseph P Franson, J Christian Hall, Jeffrey S Derksen, Dirk V Ip, Hon S Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America |
title | Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America |
title_full | Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America |
title_fullStr | Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America |
title_full_unstemmed | Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America |
title_short | Avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for North America |
title_sort | avian influenza at both ends of a migratory flyway: characterizing viral genomic diversity to optimize surveillance plans for north america |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352445/ https://www.ncbi.nlm.nih.gov/pubmed/25567891 http://dx.doi.org/10.1111/j.1752-4571.2009.00071.x |
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