Guangxi Key Laboratory of Veterinary Biotechnology, Guangxi Veterinary Research Institute, Nanning, 530000, Guangxi, China.
Key Laboratory of China (Guangxi)-ASEAN Cross-Border Animal Disease Prevention and Control, Ministry of Agriculture and Rural Affairs of China, Nanning, 530000, Guangxi, China.
Sci Rep. 2023 Aug 11;13(1):13083. doi: 10.1038/s41598-023-40349-5.
Avian parvoviruses cause several enteric poultry diseases that have been increasingly diagnosed in Guangxi, China, since 2014. In this study, the whole-genome sequences of 32 strains of chicken parvovirus (ChPV) and 3 strains of turkey parvovirus (TuPV) were obtained by traditional PCR techniques. Phylogenetic analyses of 3 genes and full genome sequences were carried out, and 35 of the Guangxi ChPV/TuPV field strains were genetically different from 17 classic ChPV/TuPV reference strains. The nucleotide sequence alignment between ChPVs/TuPVs from Guangxi and other countries revealed 85.2-99.9% similarity, and the amino acid sequences showed 87.8-100% identity. The phylogenetic tree of these sequences could be divided into 6 distinct ChPV/TuPV groups. More importantly, 3 novel ChPV/TuPV groups were identified for the first time. Recombination analysis with RDP 5.0 revealed 15 recombinants in 35 ChPV/TuPV isolates. These recombination events were further confirmed by Simplot 3.5.1 analysis. Phylogenetic analysis based on full genomes showed that Guangxi ChPV/TuPV strains did not cluster according to their geographic origin, and the identified Guangxi ChPV/TuPV strains differed from the reference strains. Overall, whole-genome characterizations of emerging Guangxi ChPV and TuPV field strains will provide more detailed insights into ChPV/TuPV mutations and recombination and their relationships with molecular epidemiological features.
自 2014 年以来,禽细小病毒在中国广西引起了几种肠型家禽疾病,这些疾病的诊断率逐渐上升。在本研究中,通过传统 PCR 技术获得了 32 株鸡细小病毒(ChPV)和 3 株火鸡细小病毒(TuPV)的全基因组序列。对 3 个基因和全基因组序列进行了系统进化分析,结果表明 35 株广西 ChPV/TuPV 田间分离株与 17 株经典 ChPV/TuPV 参考株在遗传上存在差异。广西 ChPV/TuPV 与其他国家的核苷酸序列比对显示相似度为 85.2-99.9%,氨基酸序列显示同源性为 87.8-100%。这些序列的系统进化树可分为 6 个不同的 ChPV/TuPV 组。更重要的是,首次鉴定出 3 个新的 ChPV/TuPV 组。RDP 5.0 的重组分析显示,在 35 株 ChPV/TuPV 分离株中有 15 个重组。Simplot 3.5.1 分析进一步证实了这些重组事件。基于全基因组的系统进化分析表明,广西 ChPV/TuPV 株群并未根据其地理来源聚类,而且鉴定出的广西 ChPV/TuPV 株群与参考株群存在差异。总的来说,对新兴的广西 ChPV 和 TuPV 田间分离株进行全基因组特征分析,将为 ChPV/TuPV 突变和重组及其与分子流行病学特征的关系提供更详细的见解。