Rt-pcr检测犬瘟热病毒在无症状和未接种疫苗的幼犬

F. Alves, H. L. D. Puerto, G. F. Braz, J. C. M. Cruz, J. Reis, M. Heinemann, R. Leite, A. Vasconcelos, A. S. Martins
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摘要

本研究的目的是利用逆转录聚合酶链反应(RT-PCR)对无症状犬瘟热犬进行犬瘟热病毒筛查。采集12只10-45日龄未接种疫苗的无症状幼犬的血液样本;混合品种、年龄和性别的。以感染犬瘟热病毒Lederle株的Vero细胞为阳性对照。采用酸硫氰酸胍-苯酚-氯仿萃取法,分离RNA并用DNA-free™试剂盒(Ambion Inc., Foster, California, USA)处理。设计了犬瘟热病毒核衣壳蛋白编码区基因特异性引物,扩增片段长度为319 bp。利用犬S26的另一个目标片段(75 bp)作为内源对照。共分析12只动物,阳性8只(67%),阴性4只(33%)。总之,利用RT- PCR技术在感染早期准确诊断犬瘟热病毒,可以提高对感染幼犬的识别和隔离,防止疾病传播。DOI: http://dx.doi.org/10.17525/vrrjournal.v14i2.30
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RT-PCR DETECTS CANINE DISTEMPER VIRUS IN ASYMPTOMATIC AND NON-VACCINATED PUPPIES
The objective of the present study was to use reverse transcription-polymerase chain reaction (RT-PCR) for canine distemper virus screening in puppies with asymptomatic canine distemper. Blood samples were taken from 12 non-vaccinated asymptomatic puppies, 10-45 days of age; of mixed breeds, ages, and sexes. Vero cells infected with canine distemper virus strain Lederle were used as the positive control. Using acid guanidinium thiocyanate-phenol-chloroform extraction, RNA was isolated and treated with a DNA-free™ kit (Ambion Inc., Foster, California, USA). Primers specific to the nucleocapsid protein coding region gene of canine distemper virus were designed and were able to amplify a fragment of 319 bp. Another target fragment of canine S26 (75 bp) was utilized as the endogenous control. Eight animals (67%) were positive and 4 (33%) were negative in a total of 12 animals analyzed. In conclusion, accurate diagnosis for canine distemper virus in early stages of infection using RT- PCR enhances identification of any infected puppies to be quarantined and prevents spread of disease. DOI: http://dx.doi.org/10.17525/vrrjournal.v14i2.30
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