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作 者:王传彬[1] 田克恭[1] 王宏伟[1] 孙明[1] 遇秀玲[1] 金萍[1] 陈西钊[1]
机构地区:[1]全国畜牧兽医总站农业部兽医诊断中心,北京100094
出 处:《中国病毒学》2005年第6期632-636,共5页Virologica Sinica
摘 要:从鸡组织中获得了一株分离物,能凝集鸡红细胞,经负染后电镜观察可见球形、外被囊膜的病毒颗粒,直径约 90~100nm;经血凝抑制和神经氨酸酶抑制试验鉴定为H7N2亚型禽流感病毒(Avian influenza virus,AIV),命名 为A/Chicken/Hebei/1/2002(H7N2)(简称CK/HB/1/02)。将该病毒接种SPF鸡,测得静脉接种致病指数(IVPI) 为0.00,剖检可见实验鸡多种组织器官有出血性变化,判为低致病力AIV;接种后7d从实验鸡泄殖腔棉拭中回收 到病毒,并在血清中检测到H7亚型AIV抗体。经RT-PCR扩增了病毒HA1基因片段(约1.1kb),测定其核苷酸 序列并与GenBank中的序列比较。结果表明,该病毒的HA1基因序列与AIV标准株A/Afri.Star./Eng-Q/79 (H7N1)的HA1基因同源性最高,为99.4%;与以色列和意大利H7N2 AIV的同源性较高,为96.8%~98.2%;与 美国H7N2病毒的同源性很低,约为81.0%;其HA裂解位点的氨基酸序列为-KGR-GLF-,符合低致病力AIV的 特征。A virus isolate from domestic chicken agglutinated chicken erythrocytes and was found as globular enveloped virion of 90nm~100nm diameters under TEM. The isolate was identified as HTN2 Avian influenza virus(AIV) by HI and NI assays and designated as A/Chicken/Hebei/1/ 2002(H7N2,or briefly as CK/HB/1/02. After inoculating to SPF chicken, the virus was recovered from cloacal swabs and the antibody to H7 was detected at 7 days post-infection (DPI). The IVPI was 0.00 and postmortem examination showed hemorrhages in several tissues and organs indicating that the virus was LPAIV. HA gene of the isolate exhibited 99.4% nucleotide sequence identity to A/Afri. Star./Eng-Q/79(HTN1) virus, 96.8%~98.2% to H7N2 virus isolated from Italy and Israel, and only about 81.0% to American H7N2 Strain. The amino acid at the cleavage site of HA is -KGR-GLF-, which implies the isolate should be of low pathogenicity.
分 类 号:S852.65[农业科学—基础兽医学]
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