Quino Quispe Raquel, Luna Espinoza Luis, Rímac Beltrán Rocío, Rosadio Alcántara Raúl, Maturrano Hernández Lenin
Biology and Molecular Genetics Laboratory, Department of Veterinary Medicine, Universidad Nacional Mayor de San Marcos, Av. Circunvalación s/n cuadra 28 San Borja, Lima, Peru.
Virusdisease. 2018 Mar;29(1):109-112. doi: 10.1007/s13337-018-0425-9. Epub 2018 Jan 30.
Canine parvovirus type 2 (CPV-2) has been reported worldwide as the main agent related to acute hemorrhagic enteritis of high morbidity and variable mortality in puppies. The detection and characterization of this virus is essential to understand the etiology of the disease and to develop control measures. To characterize the virus circulating in Peruvian dogs and to provide new insights into the local diversity of CPV-2, rectal swabs from 39 puppies with clinical symptoms and with no history of previous vaccinations were analyzed. Total DNA was extracted by fast boiling method, and PCR and sequencing were performed using specific primers that amplify a 1316 bp fragment corresponding to the VP2 gene of CPV-2. CPV-2 was detected in 62% of the analyzed samples. The sequencing of PCR product was possible in 9 samples, which were identified as type 2a (4 samples) and type 2c (5 samples). A phylogenetic analysis of both variants circulating in Peruvian dogs showed similarities to Equatorian and Uruguayan strains. This work constitutes the first report about genetic characterization of CPV-2 in Peru.
犬细小病毒2型(CPV-2)作为导致幼犬急性出血性肠炎的主要病原体,在全球范围内均有报道,该病发病率高,死亡率不一。对该病毒进行检测和特征分析,对于了解疾病病因及制定防控措施至关重要。为了鉴定在秘鲁犬中传播的病毒,并为CPV-2的局部多样性提供新见解,我们分析了39只出现临床症状且无既往疫苗接种史的幼犬的直肠拭子。采用快速煮沸法提取总DNA,并使用特异性引物进行PCR和测序,该引物可扩增出对应CPV-2 VP2基因的1316 bp片段。在62%的分析样本中检测到CPV-2。9个样本的PCR产物能够进行测序,其中4个样本被鉴定为2a型,5个样本为2c型。对秘鲁犬中传播的两种变体进行的系统发育分析表明,它们与厄瓜多尔和乌拉圭毒株具有相似性。这项工作是关于秘鲁CPV-2基因特征的首次报道。