Instituto de Biotecnologia, Universidade de Caxias do Sul (UCS), Caxias do Sul, Rio Grande do Sul, Brazil.
Laboratório de Diagnóstico Molecular, Programa de Pós-Graduação em Biologia Celular e Molecular aplicada à Saúde, Universidade Luterana do Brasil (ULBRA), Canoas, Rio Grande do Sul, Brazil.
Infect Genet Evol. 2022 Mar;98:105225. doi: 10.1016/j.meegid.2022.105225. Epub 2022 Jan 29.
Canine parvovirus type 2 (CPV-2) is a relevant pathogen for dogs and causes a severe disease in carnivore species. CPV-2 reached pandemic proportions after the 1970s with the worldwide dissemination, generating antigenic and genetic variants (CPV-2a, CPV-2b, and CPV-2c) with different pathobiology in comparison with the original type CPV-2. The present study aimed to assess the current global CPV-2 molecular phylogeny and to analyze genetic diversity and temporal spreading of variants from Brazil. A total of 284 CPV-2 whole-genome sequences (WGS) and 684 VP2 complete genes (including 23 obtained in the present study) were compared to analyze phylogenetic relationships. Bayesian coalescent analysis estimated the time to the most recent common ancestor (tMRCA) and the population dynamics of the different CPV-2 lineages in the last decades. The WGS phylogenetic tree demonstrated two main clades disseminated worldwide today. The VP2 gene tree showed a total of four well-defined clades distributed in different geographic regions, including one with CPV-2 sequences exclusive from Brazil. These clades do not have a relationship with the previous classification into CPV-2a, CPV-2b, and CPV-2c, despite some having a predominance of one or more antigenic types. Temporal analysis demonstrated that the main CPV-2 clades evolved within a few years (from the 1980s to 1990s) in North America and they spread worldwide afterwards. Population dynamics analysis demonstrated that CPV-2 presented a major dissemination increase at the end of the 1980s / beginning of the 1990s followed by a period of stability and a second minor increase from 2000 to 2004.
犬细小病毒 2 型 (CPV-2) 是犬的相关病原体,可引起肉食动物物种的严重疾病。自 20 世纪 70 年代以来,CPV-2 在全球范围内传播,产生了具有不同病理生物学特性的抗原和遗传变异体 (CPV-2a、CPV-2b 和 CPV-2c)。本研究旨在评估当前全球 CPV-2 的分子系统发育,并分析巴西变异体的遗传多样性和时间传播。共比较了 284 个 CPV-2 全基因组序列 (WGS) 和 684 个 VP2 完整基因 (包括本研究中获得的 23 个),以分析系统发育关系。贝叶斯共祖分析估计了不同 CPV-2 谱系在过去几十年中的最近共同祖先 (tMRCA) 和种群动态。WGS 系统发育树显示,目前全球有两个主要的分支。VP2 基因树显示,共有四个明确界定的分支分布在不同的地理区域,包括一个分支含有来自巴西的 CPV-2 序列。这些分支与之前的 CPV-2a、CPV-2b 和 CPV-2c 分类没有关系,尽管其中一些分支以一种或多种抗原类型为主。时间分析表明,主要的 CPV-2 分支在北美几年内进化 (从 20 世纪 80 年代到 90 年代),随后在全球传播。种群动态分析表明,CPV-2 在 20 世纪 80 年代末/90 年代初出现了一次大规模传播增加,随后是一段稳定期,然后在 2000 年至 2004 年期间出现了第二次较小的增加。