Inthong N, Kaewmongkol S, Meekhanon N, Sirinarumitr K, Sirinarumitr T
Center for Agricultural Biotechnology, Kasetsart University, Kamphaeng Sean Campus, Nakhon Pathom 73140, Thailand.
Center of Excellence on Agricultural Biotechnology: (AG-BIO/PERDO-CHE), Bangkok 10900, Thailand.
Vet World. 2020 Feb;13(2):245-255. doi: 10.14202/vetworld.2020.245-255. Epub 2020 Feb 10.
According to the previous study, the circulating canine parvovirus (CPV) in Thailand is 2a and 2b. Nowadays, CPV mutants, including CPV-2c, have been identified in many parts of the world. This study aimed to investigate the genetic diversity of the circulating CPV in Thailand.
Eighty-five CPV-positive fecal samples were obtained from dogs with either acute hemorrhagic diarrhea or diarrhea. The complete gene of these samples was amplified using specific primers and polymerase chain reaction (PCR). The obtained full-length sequences were analyzed and a phylogenetic tree was constructed.
Sixty and 25 CPV-positive fecal samples were collected in 2010 and 2018, respectively. Thirty-four samples were new CPV-2a and 31 samples were new CPV-2b due to amino acids substitution at position 297 (Ser-Ala). In 2018, 5 new CPV-2a, 19 CPV-2c, and 1 feline panleukopenia virus (FPV) were found, but no new CPV-2b was detected. Moreover, most of the CPV in this study had amino acids mutations at positions 324 and 440. The phylogenetic construction demonstrated the close relationship between the current new CPV-2a with the previous CPV-2a reported from Thailand, China, Uruguay, Vietnam, Singapore, and India. Interestingly, the current new CPV-2b in this study was not closely related to the previous CPV-2b reported in Thailand. The CPV-2c in this study was closer to Asian CPV-2c and further from either European or South America CPV-2c. Interestingly, FPV was identified in a diarrhea dog.
The evolution of CPV in Thailand is very dynamic. Thus, it is important to monitor for CPV mutants and especially the clinical signs relating to these mutants to conduct surveillance for the emergence of new highly pathogenic CPV in the future.
根据之前的研究,泰国流行的犬细小病毒(CPV)为2a型和2b型。如今,包括CPV-2c在内的CPV突变株已在世界许多地区被发现。本研究旨在调查泰国流行的CPV的遗传多样性。
从患有急性出血性腹泻或腹泻的犬只中获取85份CPV阳性粪便样本。使用特异性引物和聚合酶链反应(PCR)扩增这些样本的完整基因。对获得的全长序列进行分析并构建系统发育树。
分别于2010年和2018年收集到60份和25份CPV阳性粪便样本。34份样本为新的CPV-2a型,31份样本为新的CPV-2b型,原因是297位氨基酸发生替换(丝氨酸-丙氨酸)。2018年,发现5份新的CPV-2a型、19份CPV-2c型和1份猫泛白细胞减少症病毒(FPV),但未检测到新的CPV-2b型。此外,本研究中的大多数CPV在324位和440位氨基酸发生了突变。系统发育构建表明,当前新的CPV-2a型与之前泰国、中国、乌拉圭、越南、新加坡和印度报道的CPV-2a型关系密切。有趣的是,本研究中当前新的CPV-2b型与泰国之前报道的CPV-2b型关系不密切。本研究中的CPV-2c型更接近亚洲的CPV-2c型,与欧洲或南美洲的CPV-2c型距离更远。有趣的是,在一只腹泻犬中鉴定出了FPV。
泰国CPV的进化非常活跃。因此,监测CPV突变株,尤其是与这些突变株相关的临床症状,对于未来监测新的高致病性CPV的出现非常重要。