College of Animal and Veterinary Sciences, Southwest Minzu University, and Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Chengdu, China.
J Vet Diagn Invest. 2021 Nov;33(6):1193-1196. doi: 10.1177/10406387211029691. Epub 2021 Jul 8.
Bovine parvovirus 1 (BPV1) is a causative agent of respiratory, gastrointestinal, and reproductive cattle diseases. We collected 149 yak diarrhea fecal samples from 9 farms in the Qinghai-Tibet Plateau. The samples were screened for BPV1 by PCR, and 2 samples were positive for BPV1. The complete genomes of these BPV1 isolates were sequenced successfully. The sequences of these 2 variants were both 5,515 bp in length and shared 96.5-96.8% identity with 2 previously reported BPV1 genomes (GenBank DQ335247, NC_001540). Twenty-six identical amino acid mutations were found in the 2 yak variants, including 7 amino acid substitutions in receptor-binding regions of the VP2 protein, and 5 amino acid substitutions in the NS1 protein C-terminal region that functions to activate transcription. The new genome sequences contribute to better understanding of the evolution and molecular characteristics of BPV1.
牛细小病毒 1 型(BPV1)是一种引起呼吸道、胃肠道和生殖系统疾病的病原体。我们从青藏高原的 9 个农场采集了 149 份牦牛腹泻粪便样本,通过 PCR 对 BPV1 进行了筛查,发现有 2 份样本呈 BPV1 阳性。这两种 BPV1 分离株的完整基因组都成功地被测序。这两种变体的序列长度均为 5515bp,与之前报道的 2 个 BPV1 基因组(GenBank DQ335247,NC_001540)的同源性为 96.5-96.8%。在这两种牦牛变体中发现了 26 个相同的氨基酸突变,包括 VP2 蛋白受体结合区的 7 个氨基酸取代,以及 NS1 蛋白 C 末端区域的 5 个氨基酸取代,该区域的功能是激活转录。新的基因组序列有助于更好地了解 BPV1 的进化和分子特征。