Department of Pathology, School of Veterinary Medicine, University of São Paulo, São Paulo 05508-270, Brazil.
Department of Genetics, Physiology, and Microbiology, Faculty of Biology, Complutense University of Madrid, 28040 Madrid, Spain.
Viruses. 2024 Aug 30;16(9):1389. doi: 10.3390/v16091389.
Chicken Parvovirus (ChPV) belongs to the genus and is implicated in enteric diseases like runting-stunting syndrome (RSS) in poultry. In RSS, chicken health is affected by diarrhea, depression, and increased mortality, causing significant economic losses in the poultry industry. This study aimed to characterize the ChPV genomes detected in chickens with RSS through a metagenomic approach and compare the molecular and evolutionary characteristics within the species. The intestinal content of broiler flocks affected with RSS was submitted to viral metagenomics. The assembled prevalent genomes were identified as ChPV after sequence and phylogenetic analysis, which consistently clustered separately from Turkey Parvovirus (TuPV). The strain USP-574-A presented signs of genomic recombination. The selective pressure analysis indicated that most of the coding genes in are evolving under diversifying (negative) selection. Protein modeling of ChPV and TuPV viral capsids identified high conservancy over the VP2 region. The prediction of epitopes identified several co-localized antigenic peptides from ChPV and TuPV, especially for T-cell epitopes, highlighting the immunological significance of these sites. However, most of these peptides presented host-specific variability, obeying an adaptive scenario. The results of this study show the evolutionary path of ChPV and TuPV, which are influenced by diversifying events such as genomic recombination and selective pressure, as well as by adaptation processes, and their subsequent immunological impact.
鸡细小病毒(ChPV)属于细小病毒属,与家禽的肠道疾病有关,如矮小综合征(RSS)。在 RSS 中,鸡的健康受到腹泻、抑郁和死亡率增加的影响,给家禽业造成了重大的经济损失。本研究旨在通过宏基因组学方法对 RSS 鸡中检测到的 ChPV 基因组进行特征描述,并比较种内的分子和进化特征。从受 RSS 影响的肉鸡群的肠道内容物中提取病毒宏基因组。经过序列和系统发育分析,将组装的流行基因组鉴定为 ChPV,与火鸡细小病毒(TuPV)明显不同。USP-574-A 株显示出基因组重组的迹象。选择压力分析表明,大多数编码基因在 中都在经历多样化(负)选择。ChPV 和 TuPV 病毒衣壳的蛋白建模确定了 VP2 区域的高度保守性。抗原表位的预测鉴定了来自 ChPV 和 TuPV 的几个共定位抗原肽,特别是 T 细胞表位,突出了这些位点的免疫学意义。然而,这些肽中的大多数都具有宿主特异性变异性,遵循适应场景。本研究的结果显示了 ChPV 和 TuPV 的进化路径,它们受到基因组重组和选择压力等多样化事件以及适应过程的影响,以及它们随后的免疫影响。