Department of Animal Medicine, Production and Health (MAPS), University of Padua, Viale dell'Università 16, 35020, Legnaro, PD, Italy.
"San Marco" Private Veterinary Clinic, Via dell'Industria 3, 35030, Veggiano, PD, Italy.
Sci Rep. 2019 Aug 2;9(1):11266. doi: 10.1038/s41598-019-47773-6.
After its first identification in 1978, canine parvovirus (CPV) has been recognized all around the world as a major threat for canine population health. This ssDNA virus is characterized by a high substitution rate and several genetic and phenotypic variants emerged over time. Overall, the definition of 3 main antigenic variants was established based on specific amino acid markers located in a precise capsid position. However, the detection of several minor variants and incongruence observed between the antigenic classification and phylogeny have posed doubts on the reliability of this scheme. At the same time, CPV heterogeneity has favored the hypothesis of a differential virulence among variants, although no robust and consistent demonstration has been provided yet. The present study rejects the antigenic variant concept and attempts to evaluate the association between CPV strain phylogeny, reconstructed using the whole information contained in the VP2 coding gene, and several clinical and hemato-biochemical parameters, assessed from 34 CPV infected dogs at admission. By using different statistical approaches, the results of the present study show an association between viral phylogeny and host parameters ascribable to immune system, coagulation profile, acute phase response and, more generally, to the overall picture of the animal response. Particularly, a strong and significant phylogenetic signal was proven for neutrophil count and WBC. Therefore, despite the limited sample size, a relation between viral phylogeny and disease severity has been observed for the first time, suggesting that CPV virulence is an inherited trait. The likely existence of clades with different virulence highlights once more the relevance of intensive epidemiological monitoring and research on CPV evolution to better understand the virulence determinants, their epidemiology and develop adequate countermeasures.
自 1978 年首次发现以来,犬细小病毒(CPV)已被全球公认为犬群健康的主要威胁。这种单链 DNA 病毒的特点是替换率高,随着时间的推移出现了几种遗传和表型变体。总体而言,根据位于特定衣壳位置的特定氨基酸标记,确定了 3 种主要抗原变体的定义。然而,检测到的几种次要变体以及在抗原分类和系统发育之间观察到的不一致性,使人们对该方案的可靠性产生了怀疑。同时,CPV 的异质性使得人们假设变体之间存在差异毒力,尽管尚未提供可靠且一致的证据。本研究否定了抗原变体的概念,并试图评估使用 VP2 编码基因中包含的全部信息重建的 CPV 株系统发育与从入院时的 34 只 CPV 感染犬评估的几个临床和血液生化参数之间的相关性。通过使用不同的统计方法,本研究的结果表明,病毒系统发育与可归因于免疫系统、凝血谱、急性期反应以及更普遍地与动物反应全貌的宿主参数之间存在相关性。特别是,中性粒细胞计数和白细胞计数表现出强烈且显著的系统发育信号。因此,尽管样本量有限,但首次观察到病毒系统发育与疾病严重程度之间存在关系,表明 CPV 的毒力是一种遗传特征。不同毒力的进化枝的存在再次突出了加强对 CPV 进化的流行病学监测和研究的重要性,以更好地了解毒力决定因素、它们的流行病学并制定适当的对策。