PLoS ONE · 2013 · 39 citations · 27 references
Veterinary MedicineInfectious DiseasesPoultry SciencePoultry BiosecurityPoultry MedicinePoultry MicrobiologyPoultry DiagnosticsPoultry EpidemiologyPoultry Infectious DiseasesPoultry Respiratory DiseasesPoultry VirologyViral Diseases Of PoultryAnimal SeroprevalenceAvian Influenza InfectionAvian Influenza VirusAvian Influenza VirusesImmunodiagnostic AssaysInfection Risk FactorsMolecular Detection AssaysPoultry-associated Pathogens
OBJECTIVE: Estimate the seroprevalence of influenza A virus in various commercial poultry farms and evaluate specific risk factors as well as analyze their genetic nature using molecular assays. MATERIALS AND METHODS: This report summarizes the findings of a national survey realized from October 2010 to May 2011 on 800 flocks in 20 governorates. Serum samples were screened for the presence of specific influenza virus antibodies using cELISA test. Additionally, swab samples were tested by real time and conventional RT-PCR and compared with results obtained by others assays. Phylogenetic and genetic analyses of the glycoproteins were established for some strains. RESULTS: Out of the 800 chicken and turkey flocks tested by cELISA, 223 showed positive anti-NP antibodies (28.7%, 95% CI: 25.6-32.1). Significantly higher seroprevalence was found among the coastal areas compared to inland and during the autumn and winter. Broiler flocks showed significantly lower seroprevalence than layers and broiler breeders. The influenza virus infection prevalence increased after the laying phase among layer flocks. In addition, AIV seropositivity was significantly associated with low biosecurity measures. The Ag EIA and rRT-PCR tests revealed significantly higher numbers of AI positive samples as compared to cell cultures or egg inoculation. All new strains were subtyped as H9N2 by real time and conventional RT-PCR. Drift mutations, addition or deletion of glycosylation sites were likely to have occurred in the HA and NA glycoproteins of Tunisian strains resulting in multiple new amino acid substitutions. This fact may reflect different evolutionary pressures affecting these glycoproteins. The role of these newly detected substitutions should be tested. CONCLUSION: Our findings highlight the potential risk of AIV to avian health. Strict enforcement of biosecurity measures and possible vaccination of all poultry flocks with continuous monitoring of poultry stations may ensure reduction of AIV prevalence and avoid emergence of more pathogenic strains.
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Erica Spackman, Dennis A. Senne, Thomas J. Myers et al. · Journal of Clinical Microbiology · 2002 · 1.7K citations · Full text
Veterinary Medicine, Infectious Diseases, Poultry Science +17
Receptor Specificity in Human, Avian, and Equine H2 and H3 Influenza Virus Isolates
Robert Connor, Yoshihiro Kawaoka, Robert G. Webster et al. · Virology · 1994 · 796 citations
Characterization of Avian H5N1 Influenza Viruses from Poultry in Hong Kong
K. F. Shortridge, Nan Zhou, Yi Guan et al. · Virology · 1998 · 591 citations