Chakraborty P, Behera S K, Lalhriatchhungi M H, Roychoudhury P, Maibam L, Behera P, Chaudhary J K, Prasad H, Rajesh J B, Lalhmangaihzuali M, Mary H C J, Lalrosanga L H, Dawngliana M S, Chander V, Kumar M
Ph.D. Student in Veterinary Medicine, Department of Veterinary Medicine, West Bengal University of Animal and Fishery Sciences, West Bengal, Kolkata-700037, India.
Department of Veterinary Medicine, College of Veterinary Sciences and Animal Husbandry, Central Agricultural University, Selesih-796 015, Aizawl, Mizoram, India.
Iran J Vet Res. 2024;25(3):261-272. doi: 10.22099/ijvr.2024.49573.7295.
Canine parvovirus type-2 (CPV-2) is a highly contagious enteric pathogen of puppies with worldwide distribution.
Molecular epidemiology, genetic characterization, phylogenetic analysis, and isolation of the CPV-2 virus from clinically affected dogs in Mizoram, India over eight years.
A total of 202 samples (199 fecal samples, 2 vomita, and 1 tissue sample) were screened by PCR assay.
103 out of 202 samples (50.99%) tested positive. Of the 103 positive samples, 83 samples were cloned and sequenced. Sequence analysis showed CPV-2c as the predominant variant (63.85%) followed by the 2a variant (26.5%), 2b (8.43%), and FPV (1.2%). Phylogenetic analyses of the CPV-2c sequences formed separate clusters and were ancestrally related to Japanese, Chinese, and Italian 2c sequences. Similarly, 2a isolates formed separate clusters under different clades and were ancestrally related to Indian, Singaporean, Japanese, Uruguayan, and Chinese 2a isolates. 2b isolates formed a single cluster with the Chinese 2b isolate. FPV isolate clustered with North American FPV. Both synonymous and non-synonymous mutations (unique to this study) were evident in all the types of CPV-2s indicative of active evolution with regional variation. In the cell culture medium, CPV-2 showed cytopathogenic effects at the third passage level.
The study, the first in-depth report on CPV-2, showed a shift towards CPV-2c as the predominant variant in Mizoram. This variant clustered separately from current vaccine strains, highlighting the need for extensive epidemiological surveillance to better understand viral phylogenomics and evaluate current vaccine efficacy.
犬细小病毒2型(CPV-2)是一种具有高度传染性的幼犬肠道病原体,在全球范围内均有分布。
对印度米佐拉姆邦临床感染犬只进行为期八年的CPV-2病毒分子流行病学、基因特征、系统发育分析及分离。
通过聚合酶链反应(PCR)检测法对总共202份样本(199份粪便样本、2份呕吐物样本和1份组织样本)进行筛查。
202份样本中有103份(50.99%)检测呈阳性。在这103份阳性样本中,83份样本进行了克隆和测序。序列分析显示CPV-2c为主要变体(63.85%),其次是2a变体(26.5%)、2b变体(8.43%)和猫泛白细胞减少症病毒(FPV,1.2%)。对CPV-2c序列的系统发育分析形成了单独的聚类,并且在谱系上与日本、中国和意大利的2c序列相关。同样,2a分离株在不同分支下形成单独的聚类,并且在谱系上与印度、新加坡、日本、乌拉圭和中国的2a分离株相关。2b分离株与中国的2b分离株形成单一聚类。FPV分离株与北美FPV聚类。在所有类型的CPV-2中,同义突变和非同义突变(本研究特有)均很明显,这表明其在区域变异的情况下正在积极进化。在细胞培养基中,CPV-2在第三代传代水平显示出细胞病变效应。
该研究是关于CPV-2的首份深入报告,显示米佐拉姆邦的主要变体已向CPV-2c转变。该变体与当前疫苗株聚类不同,这突出表明需要进行广泛的流行病学监测,以更好地了解病毒系统发育基因组学并评估当前疫苗的效力。