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猪流行性腹泻病毒LJB/03 M基因的克隆与序列分析

Cloning and sequence analysis of the M gene of porcine epidemic diarrhea virus LJB/03.

作者信息

Jinghui Fan, Yijing Li

机构信息

Veterinary Department, Northeast Agriculture University, Harbin, 150030, P. R. China.

出版信息

Virus Genes. 2005 Jan;30(1):69-73. doi: 10.1007/s11262-004-4583-z.

Abstract

Porcine epidemic diarrhea virus (PEDV) LJB/03 was isolated from the fece of piglets infected with PEDV on a pig farm, Heilongjiang province, China. The M gene of LJB/03 was amplified from the RNA extracted directly from the fece samples by RT-PCR and cloned into pMD18-T vector. The M gene cDNA was sequenced and encompasses an open reading frame of 681 nucleotides, encoding a 226-amino acid protein. The LJB/03 M gene has a base composition of 152 adenines (22%), 153 cytosines (23%), 161 guanines (24%), and 214 thymines (31%). Sequence comparison with other PEDV strains selected from GenBank revealed that the LJB/03 M gene has a high sequence homology to those of other PEDV isolates, 97.80% with JMe2, 96.92% with KPEDV-9 (Korean field isolate), 97.36% with KPEDV-9 (Korean), 97.80% with Br1/87, and 97.94% with CV777. The encoded protein shared 97.79% amino acid identities compared with CV777, 97.35% with Br1/87, 97.79% with JMe2, 96.90% with KPEDV-9 (Korean field isolate), 96.46% with KPEDV-9 (Korean). Sequence analysis of the M gene, including genetic distance measurement, phylogenetic tree analysis, and residue substitution analysis, showed that all other PED viruses analyzed fell into three groups, and the LJB/03 itself branched in an independent group. These data revealed that the M gene nucleotide sequence of LJB/03 has some mutations in comparison with the other PED viruses.

摘要

猪流行性腹泻病毒(PEDV)LJB/03是从中国黑龙江省一个养猪场感染PEDV的仔猪粪便中分离得到的。通过RT-PCR从直接从粪便样本中提取的RNA中扩增出LJB/03的M基因,并将其克隆到pMD18-T载体中。对M基因cDNA进行测序,其包含一个681个核苷酸的开放阅读框,编码一个226个氨基酸的蛋白质。LJB/03 M基因的碱基组成为152个腺嘌呤(22%)、153个胞嘧啶(23%)、161个鸟嘌呤(24%)和214个胸腺嘧啶(31%)。与从GenBank中选择的其他PEDV毒株进行序列比较发现,LJB/03 M基因与其他PEDV分离株具有较高的序列同源性,与JMe2的同源性为97.80%,与KPEDV-9(韩国田间分离株)的同源性为96.92%,与KPEDV-9(韩国)的同源性为97.36%,与Br1/87的同源性为97.80%,与CV777的同源性为97.94%。与CV777相比,编码的蛋白质具有97.79%的氨基酸同一性,与Br1/87的同一性为97.35%,与JMe2的同一性为97.79%,与KPEDV-9(韩国田间分离株)的同一性为96.90%,与KPEDV-9(韩国)的同一性为96.46%。对M基因的序列分析,包括遗传距离测量、系统发育树分析和残基替代分析,表明所有分析的其他PED病毒分为三组,而LJB/03本身在一个独立的组中分支。这些数据表明,LJB/03的M基因核苷酸序列与其他PED病毒相比有一些突变。

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