F. Alves, H. L. D. Puerto, G. F. Braz, J. C. M. Cruz, J. Reis, M. Heinemann, R. Leite, A. Vasconcelos, A. S. Martins
{"title":"RT-PCR DETECTS CANINE DISTEMPER VIRUS IN ASYMPTOMATIC AND NON-VACCINATED PUPPIES","authors":"F. Alves, H. L. D. Puerto, G. F. Braz, J. C. M. Cruz, J. Reis, M. Heinemann, R. Leite, A. Vasconcelos, A. S. Martins","doi":"10.17525/VRRJOURNAL.V14I2.30","DOIUrl":null,"url":null,"abstract":"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","PeriodicalId":30621,"journal":{"name":"Virus Reviews Research","volume":"14 1","pages":"3"},"PeriodicalIF":0.0000,"publicationDate":"2009-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virus Reviews Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17525/VRRJOURNAL.V14I2.30","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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