serological survey of avian influenza (h9n2) among different occupational groups in tehran and qazvin provinces in ir iran

Authors

elaheh anvar department of microbiology, faculty of biological science, shahid beheshti university, g.c., tehran, ir iran; influenza research lab, pasteur institute of iran, tehran, ir iran

seyed masoud hosseini department of microbiology, faculty of biological science, shahid beheshti university, g.c., tehran, ir iran; department of microbiology, faculty of biological sciences, shahid beheshti university, tehran, ir iran. tel: +98-21 29902721, mobil: +98-9123028767, fax: +98-2122431664

masoumeh tavasoti kheiri influenza research lab, pasteur institute of iran, tehran, ir iran

vahideh mazaheri influenza research lab, pasteur institute of iran, tehran, ir iran

abstract

objectives the aim of this was to indentify the presence of a/h9n2 virus among different high risk occupational groups, in tehran and qazvin provinces in seasonal outbreak in iran. background in the last decade h9n2 avian influenza viruses had caused outbreaks in poultry in many parts of the world. this subtype could infect other animals such as human and pig. avian h9n2 virus has acquired receptor binding characteristics typical of human’s strains, increasing the potential for reassortment in both human and pig respiratory tracts. this indicates that the a/h9n2 would be a potential threat to human population. conclusions the findings of this study show that h9n2 avian influenza virus can infect human. repeated interspecies transmission h9n2 viruses from poultry to human raises concerns about adapting of this subtype with new host. results only 3 (1.64%) in hi that showed titer ≥ 20 and 21 (11.53%) sera in elisa showed od > 0.7 were assumed positive for h9 virus infection. material and methods 182 sera were collected from the poultry farms and slaughterhouse workers, and animal vaccinators and also veterinarians in seasonal outbreak (december 2010, january 2011 and july 2011). hemagglutination inhibition (hi) and elisa assays were performed to detect anti-h9 antibody. sera adsorption was performed to eliminate cross-reactivity between anti-h3 and anti-h9. in hi test the titer ≥ 20 was considered to be positive.

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Journal title:
jundishapur journal of microbiology

جلد ۶، شماره ۴، صفحات ۰-۰

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