Xu J, Guo H-C, Wei Y-Q, Shu L, Wang J, Li J-S, Cao S-Z, Sun S-Q
State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China; College of Veterinary medicine, Sichuan Agricultural University, ya'an, China.
Transbound Emerg Dis. 2015 Feb;62(1):91-5. doi: 10.1111/tbed.12078. Epub 2013 Mar 18.
Canine parvovirus causes serious disease in dogs. Study of the genetic variation in emerging CPV strains is important for disease control strategy. The antigenic property of CPV is connected with specific amino acid changes, mainly in the capsid protein VP2. This study was carried out to characterize VP2 gene of CPV viruses from two provinces of China in 2011. The complete VP2 genes of the CPV-positive samples were amplified and sequenced. Genetic analysis based on the VP2 genes of CPV was conducted. All of the isolates screened and sequenced in this study were typed as CPV-2a except GS-K11 strain, which was typed as CPV-2b. Sequence comparison showed nucleotide identities of 98.8-100% among CPV strains, whereas the Aa similarities were 99.6-100%. Compared with the reference strains, there are three distinctive amino acid changes at VP2 gene residue 267, 324 and 440 of the strains isolated in this study. Of the 27 strains, fourteen (51.85%) had the 267 (Phe-Tyr) and 440 (Thr-Ala) substitution, all the 27 (100%) had 324 (Tyr-Ile) substitution. Phylogenetically, all of the strains isolated in this study formed a major monophyletic cluster together with one South Korean isolate, two Thailand isolates and four Chinese former isolates.
犬细小病毒会引发犬类的严重疾病。研究新兴犬细小病毒株的基因变异对于疾病控制策略至关重要。犬细小病毒的抗原特性与特定氨基酸变化相关,主要存在于衣壳蛋白VP2中。本研究旨在对2011年来自中国两个省份的犬细小病毒的VP2基因进行特征分析。对犬细小病毒阳性样本的完整VP2基因进行了扩增和测序。基于犬细小病毒的VP2基因进行了遗传分析。本研究中筛选和测序的所有分离株,除GS-K11株被鉴定为犬细小病毒-2b型外,其余均被鉴定为犬细小病毒-2a型。序列比较显示,犬细小病毒株之间的核苷酸同一性为98.8 - 100%,而氨基酸相似性为99.6 - 100%。与参考毒株相比;本研究分离的毒株在VP2基因第267、324和440位氨基酸残基处有三个明显的氨基酸变化。在27株毒株中,14株(51.85%)有267位(苯丙氨酸-酪氨酸)和440位(苏氨酸-丙氨酸)替换,所有27株(100%)有324位(酪氨酸-异亮氨酸)替换。在系统发育上,本研究分离的所有毒株与一株韩国分离株、两株泰国分离株和四株中国既往分离株共同形成一个主要的单系簇。