• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

半番鸭源鸭1型甲肝病毒亚型的分离鉴定及其VP1基因分析

Identification and Sequencing of Duck Hepatitis A Virus 1 Subtype a Isolated from Mule Ducklings

  • 摘要: 自胰腺泛黄的雏半番鸭中分离获得1株病毒(命名为FJ1605株),经RT-PCR检测为鸭1型甲肝病毒,通过鸭胚中和试验发现该株病毒可被鸭1型甲肝病毒亚型(DHAV-1a)高免血清特异性中和,确定该株病毒为鸭1型甲肝病毒亚型。对该株病毒VP1基因进行分子特征分析,发现其核苷酸大小为714 bp,与GenBank登录的DHAV-1a同源性为98.1%~99.7%,与DHAV-1 FJ1220毒株同源性最高达99.7%;而与鸭2型甲肝病毒(DHAV-2)、鸭3型甲肝病毒(DHAV-3)VP1基因的核苷酸同源性仅分别为65.7%和68.3%左右。基于VP1基因的遗传进化分析表明,FJ1605分离株属鸭1型甲肝病毒亚型谱系。以该株病毒对7日龄雏半番鸭进行人工感染试验,可完全复制出同于临床病例的病变。以上结果显示,雏半番鸭也可感染DHAV-1a,且表现为胰腺泛黄。

     

    Abstract: A strain of duck hepatitis A virus 1 subtype a (DHAV-1a), coded as FJ1605, was isolated from the mule ducklings with pancreatitis. It was identified by RT-PCR analysis and a neutralization test in duck embryos that showed the strain specifically being neutralized by the anti-DHAV-1a hyperimmune serum. Molecular characteristics of VP1 gene of the virus was analyzed to indicate the nucleotide to be 714 bp in length with a homology with those of other DHAV-1a isolates ranging from 98.1% to 99.7% and sharing the greatest similarity to strain FJ1220.On the other hand, the homology between FJ1605 and DHAV-2 was merely 65.7%; and, that between FJ1605 and DHAV-3, approximately 68.3%. Phylogenetic analysis on the VP1 gene also showed FJ1605 to be in the viral lineage of DHAV-1a. Furthermore, an animal infection test clearly displayed the same clinical symptoms as those shown inclinical cases. Thus, it was concluded that the pancreatitis in the mule ducklings was caused by DHAV-1a.

     

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