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墨西哥西部流行的犬细小病毒 2c 型基因组序列。

Genome Sequences of Canine Parvovirus Type 2c Prevalent in Western Mexico.

机构信息

Unidad de Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C. Av. Normalistas No. 800. Col. Colinas de la Normal, CP. 44270, Guadalajara, Jalisco, México.

Departmento de Medicina Veterinaria, Centro Universitario de Ciencias Biológicas Y Agropecuarias, Cam. Ramón Padilla Sánchez 2100, Las Agujas, 44600 Zapopan, Jal. Universidad de Guadalajara, Zapopan, Jalisco, México.

出版信息

Arch Razi Inst. 2024 Apr 30;79(2):387-394. doi: 10.32592/ARI.2024.79.2.387. eCollection 2024 Apr.

DOI:10.32592/ARI.2024.79.2.387
PMID:39463712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11512174/
Abstract

Canine parvovirus type 2 (CPV-2) is one of the main etiologies of viral gastroenteritis in dogs across the globe. This disease is mainly characterized by the presence of diarrhea, abdominal pain, vomiting, anorexia, and dehydration. This virus is responsible for high mortality and morbidity rates in unvaccinated dogs and those younger than three months. The monitoring of viral variants in our region has demonstrated that in the last seven years, variant CPV-2c has been circulating exclusively, which is unusual if we consider that in the rest of the world, at least two variants co-circulate among dog populations. To the best of our knowledge, no studies in Mexico have reported genomic sequences of CPV-2, which are relevant for population comparisons at the genetic level. Therefore, the present study aimed to sequence genomes associated with CPV-2c. To meet this objective, rectal swab samples were collected from dogs with suspected CPV-2 infection. Five positive cases diagnosed by lateral flow testing and polymerase chain reaction were selected for viral genome sequencing. Comparative analyses illustrated that the obtained genome sequences were > 99% homologous to those reported for CPV-2 in the GenBank. On the other hand, 52 nucleotide mutations were identified in the  gene, out of which three impacted amino acid transition (T226S, F267Y, and A440T). Phylogenetic analysis of the  gene demonstrated that the five sequences clustered in a clade called "III", pertaining to sequences from USA and Uruguay. To our knowledge, this was the first report of genomic sequences associated with CPV-2 in Mexico, which is of great relevance for the epidemiological-molecular understanding and evolution of the virus.

摘要

犬细小病毒 2 型(CPV-2)是全球犬类病毒性胃肠炎的主要病因之一。这种疾病的主要特征是腹泻、腹痛、呕吐、食欲不振和脱水。该病毒可导致未接种疫苗的犬和 3 个月以下的犬死亡率和发病率居高不下。对本地区病毒变异的监测表明,在过去的 7 年中,变异型 CPV-2c 一直在单独传播,这与我们所知的世界其他地区的情况不同,在其他地区,至少有两种变异型在犬群中同时传播。据我们所知,墨西哥尚无关于 CPV-2 的基因组序列的研究报告,这些序列对于在遗传水平上进行种群比较非常重要。因此,本研究旨在对 CPV-2c 相关的基因组进行测序。为了实现这一目标,从疑似 CPV-2 感染的犬只中采集直肠拭子样本。选择了 5 个经侧向流动检测和聚合酶链反应(PCR)确诊为阳性的病例进行病毒基因组测序。比较分析表明,获得的基因组序列与 GenBank 中报告的 CPV-2 序列高度同源。另一方面,在基因中发现了 52 个核苷酸突变,其中 3 个影响氨基酸转换(T226S、F267Y 和 A440T)。基因的系统发育分析表明,这 5 个序列聚类在一个称为“III”的分支中,属于来自美国和乌拉圭的序列。据我们所知,这是墨西哥首次报告与 CPV-2 相关的基因组序列,这对于了解病毒的流行病学-分子特征和进化具有重要意义。

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本文引用的文献

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Arch Virol. 2022 Nov;167(11):2109-2121. doi: 10.1007/s00705-022-05522-7. Epub 2022 Jul 6.
2
Molecular characterization of canine parvovirus from domestic dogs in Nigeria: Introduction and spread of a CPV-2c mutant and replacement of older CPV-2a by the "new CPV-2a" strain.尼日利亚家犬中犬细小病毒的分子特征:CPV-2c突变体的引入与传播以及“新型CPV-2a”毒株对旧有CPV-2a的取代
Virusdisease. 2021 Jun;32(2):361-368. doi: 10.1007/s13337-021-00689-0. Epub 2021 May 12.
3
Origin and genetic diversity of canine parvovirus 2c circulating in Mexico.在墨西哥传播的犬细小病毒2c的起源和遗传多样性
Arch Virol. 2019 Feb;164(2):371-379. doi: 10.1007/s00705-018-4072-7. Epub 2018 Oct 30.
4
Molecular characterization of canine parvovirus variants (CPV-2a, CPV-2b, and CPV-2c) based on the gene in affected domestic dogs in Ecuador.基于厄瓜多尔受感染家犬基因的犬细小病毒变体(CPV - 2a、CPV - 2b和CPV - 2c)的分子特征分析
Vet World. 2018 Apr;11(4):480-487. doi: 10.14202/vetworld.2018.480-487. Epub 2018 Apr 16.
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