Chen Ning, Li Dejiang, Yuan Xuemei, Li Xiaoliang, Hu Hongxia, Zhu Binglin, Wan Xiaoyuan, Fang Weihuan
Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Institute of Preventive Veterinary Medicine, Zhejiang University, 268 Kaixuan Road, 310029 Hangzhou, Zhejiang, People's Republic of China.
Virus Genes. 2010 Jun;40(3):389-96. doi: 10.1007/s11262-010-0465-8. Epub 2010 Mar 9.
An RT-nested PCR (RT-nPCR)-based restriction fragment length polymorphism (RFLP) analyses of the E2 gene were developed for genetic subtyping and differentiation of vaccinated and infected classical swine fever virus (CSFV) strains. RT-nPCR identified 96 CSFV-positive samples from 321 clinical specimens from southeastern China during 2003-2008. The PCR products of positive samples were further differentiated using MspI digestion, 23 were identified as the C-strain, 62 as field strains, and 11 as mixture of the vaccine strain and field ones. RFLP with BglI, DdeI, DraI, and PstI were then used for subtyping of the field CSFV isolates. Thirty-eight field isolates phylogenetically classified as subgroup 2.1 based on E2 were divided into 11 subtypes by this RFLP scheme. Both RFLP profiling and sequence-based phylogenetic analysis revealed genetic diversity of CSFV in the field. Three novel substitutions at amino acid positions 17, 93, and 286 were identified in the predominant subtype VI strains isolated in 2008 as compared to other strains including historical subtype VI strains. These results suggest that CSFV in China experienced gradual variations and evolutionary accumulation progress. Thus, the RFLP methods targeting on the CSFV E2 gene are suitable for epidemiological survey in endemic area where the C-strain is applied for vaccination. Combination of the RFLP schemes with sequence-based phylogenetic analysis could provide more detailed information on transmission of CSFV in the region or even its evolution.
基于逆转录巢式聚合酶链反应(RT-nested PCR)的猪瘟病毒(CSFV)E2基因限制性片段长度多态性(RFLP)分析被用于接种疫苗和感染的猪瘟病毒毒株的基因分型及鉴别。RT-nPCR从2003年至2008年中国东南部的321份临床样本中鉴定出96份CSFV阳性样本。阳性样本的PCR产物通过MspI酶切进一步鉴别,其中23份被鉴定为C株,62份为野毒株,11份为疫苗株与野毒株的混合株。随后,使用BglI、DdeI、DraI和PstI进行RFLP分析,对野毒株CSFV分离株进行亚型分析。根据E2基因,38株在系统发育上归类为2.1亚组的野毒株通过该RFLP方案被分为11个亚型。RFLP分析图谱和基于序列的系统发育分析均揭示了该地区CSFV的遗传多样性。与包括历史亚型VI株在内的其他毒株相比,2008年分离的优势亚型VI株在氨基酸位置17、93和286处发现了三个新的替换。这些结果表明,中国的CSFV经历了逐渐变异和进化积累过程。因此,针对CSFV E2基因的RFLP方法适用于使用C株进行疫苗接种的流行地区的流行病学调查。将RFLP方案与基于序列的系统发育分析相结合,可以提供有关该地区CSFV传播甚至其进化的更详细信息。