Nagarajan S, Rajukumar K, Tosh C, Ramaswamy V, Purohit K, Saxena G, Behera P, Pattnaik B, Pradhan H K, Dubey S C
High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal 462021, Madhya Pradesh, India.
Vet Microbiol. 2009 Jan 1;133(1-2):154-63. doi: 10.1016/j.vetmic.2008.06.013. Epub 2008 Jun 22.
A total of 1246 faecal and tissue samples collected/received from 119 farms located in various states of India were processed for isolation of avian influenza viruses (AIV) during 2003-2004 as part of a program to monitor AIV infection in Indian poultry population. Avian influenza virus was isolated for the first time in India from poultry farms with history of drop in egg production, respiratory illness and increased mortality in Haryana state. A total of 29 H9N2 AIV isolates were obtained from the states of Punjab, Haryana, Uttar Pradesh, Gujarat, and Orissa and Union Territory Delhi. Subtyping was done by HI, RT-PCR and neuraminidase inhibition assay. Pathotyping of six representative isolates by intravenous pathogenicity index (0.0/3.0) in 6-8 weeks old chicken, trypsin dependency in cell culture and HA cleavage site analysis (335RSSR*GLF341) confirmed that these isolates are low pathogenic. Nucleotide sequence analysis of the HA gene showed that the Indian isolates are very closely related (95.0-99.6%) and shared a homology of 92-96% with H9N2 isolates from Germany and Asian regions other than that of mainland China. Deduced amino acid sequences showed the presence of L226 (234 in H9 numbering) which indicates a preference to binding of alpha (2-6) sialic acid receptors. Two of the six isolates had 7 glycosylation sites in the HA1 cleaved protein and the remaining four had 5 sites. Phylogenetic analysis showed that they share a common ancestor Qa/HK/G1/97 isolate which had contributed internal genes of H5N1 virus circulating in Vietnam. Further characterization of Indian H9N2 isolates is required to understand their nature and evolution.
作为监测印度家禽群体中禽流感病毒(AIV)感染情况项目的一部分,2003年至2004年期间,对从印度不同邦119个养殖场收集/接收的总共1246份粪便和组织样本进行了处理,以分离禽流感病毒。印度首次从哈里亚纳邦有产蛋量下降、呼吸道疾病和死亡率增加病史的家禽养殖场分离出禽流感病毒。从旁遮普邦、哈里亚纳邦、北方邦、古吉拉特邦、奥里萨邦以及德里联邦属地共获得了29株H9N2禽流感病毒分离株。通过血凝抑制试验(HI)、逆转录聚合酶链反应(RT-PCR)和神经氨酸酶抑制试验进行亚型鉴定。通过对6至8周龄鸡的静脉致病性指数(0.0/3.0)、细胞培养中的胰蛋白酶依赖性以及血凝素裂解位点分析(335RSSR*GLF341)对6株代表性分离株进行致病型鉴定,证实这些分离株为低致病性。血凝素(HA)基因的核苷酸序列分析表明,印度分离株之间亲缘关系非常密切(95.0 - 99.6%),并且与来自德国以及中国大陆以外亚洲地区的H9N2分离株具有92 - 96%的同源性。推导的氨基酸序列显示存在L226(H9编号为234),这表明其倾向于结合α(2 - 6)唾液酸受体。6株分离株中有2株在HA1裂解蛋白中有7个糖基化位点,其余4株有5个位点。系统发育分析表明,它们有一个共同的祖先Qa/HK/G1/97分离株,该分离株为越南流行的H5N1病毒贡献了内部基因。需要对印度H9N2分离株进行进一步鉴定,以了解它们的特性和进化情况。