{"title":"犬瘟热病毒CD1901和Lederle株多重RT-PCR鉴别方法的建立","authors":"Dong-Kun Yang, Yu-Ri Park, Yesel Park, B. Hyun","doi":"10.4167/jbv.2022.52.1.011","DOIUrl":null,"url":null,"abstract":"license/by-nc/3.0/). Canine distemper virus (CDV) is a life-threatening pathogen in dogs. Clinical, pathological and molecular methods are required to diagnose CDV infection, and it is important to differentiate between the Korean CDV strain CD1901 and Lederle CDV vaccine strain. Therefore, in this study, we used multiplex reverse-transcription polymerase chain reaction (RT-PCR) to differentiate between the CD1901 and Lederle strains. A primer set was designed based on the CDV nucleoprotein gene and nucleotide sequence variation in the fusion (F) gene. First, 224-bp DNA bands were amplified from viral RNA of the CD1901 and Lederle strains. Then, 428- and 326-bp DNA bands were amplified in the CD1901 and Lederle strain, respectively. The multiplex RT-PCR detection limits were 2.53 and 0.8 median tissue culture infectious dose/reaction for the CD1901 and Lederle strains, respectively. No cross-reactions were detected in non-CDV reference viruses, including rabies virus, parvovirus, canine adenovirus types 1 and 2, and parainfluenza virus. The results indicate that our one-step multiplex RT-PCR is useful for differentiating between wildtype and vaccine CDV distemper. The CD1901 and Lederle strains were propagated in Vero/dSLAM cells expressing the dog SLAM gene in Dulbecco’s modified Eagle’s medium containing two antibiotics, an antifungal agent, and 10% heat-inactivated fetal bovine serum (Gibco BRL, Grand Island, NY, USA). The CD1901 and Lederle strains were used as positive controls for multiplex RT-PCR, and the analytical sensitivity and analytical specificity of the primers were determined. Four commercial distemper/adeno/parvo/parainfluenza (DAPP) vaccines containing CDV, canine adenovirus type 1 (CAV-1) or canine adenovirus type 2 (CAV-2), canine parvovirus (CPV), and canine parainfluenza virus (CPIV) manufactured by Korean biological companies were used for multiplex showed high sensitivity and specificity for differentiating between","PeriodicalId":39739,"journal":{"name":"Journal of Bacteriology and Virology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Establishment of Multiplex RT-PCR for Differentiating between the CD1901 and Lederle Strains of Canine Distemper Virus\",\"authors\":\"Dong-Kun Yang, Yu-Ri Park, Yesel Park, B. Hyun\",\"doi\":\"10.4167/jbv.2022.52.1.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"license/by-nc/3.0/). Canine distemper virus (CDV) is a life-threatening pathogen in dogs. Clinical, pathological and molecular methods are required to diagnose CDV infection, and it is important to differentiate between the Korean CDV strain CD1901 and Lederle CDV vaccine strain. Therefore, in this study, we used multiplex reverse-transcription polymerase chain reaction (RT-PCR) to differentiate between the CD1901 and Lederle strains. A primer set was designed based on the CDV nucleoprotein gene and nucleotide sequence variation in the fusion (F) gene. First, 224-bp DNA bands were amplified from viral RNA of the CD1901 and Lederle strains. Then, 428- and 326-bp DNA bands were amplified in the CD1901 and Lederle strain, respectively. The multiplex RT-PCR detection limits were 2.53 and 0.8 median tissue culture infectious dose/reaction for the CD1901 and Lederle strains, respectively. No cross-reactions were detected in non-CDV reference viruses, including rabies virus, parvovirus, canine adenovirus types 1 and 2, and parainfluenza virus. The results indicate that our one-step multiplex RT-PCR is useful for differentiating between wildtype and vaccine CDV distemper. The CD1901 and Lederle strains were propagated in Vero/dSLAM cells expressing the dog SLAM gene in Dulbecco’s modified Eagle’s medium containing two antibiotics, an antifungal agent, and 10% heat-inactivated fetal bovine serum (Gibco BRL, Grand Island, NY, USA). The CD1901 and Lederle strains were used as positive controls for multiplex RT-PCR, and the analytical sensitivity and analytical specificity of the primers were determined. 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引用次数: 0
摘要
许可/通过数控/ 3.0 /)。犬瘟热病毒(CDV)是一种威胁狗生命的病原体。诊断CDV感染需要临床、病理和分子方法,区分韩国CD1901株和Lederle CDV疫苗株是很重要的。因此,在本研究中,我们采用多重反转录聚合酶链反应(RT-PCR)来区分CD1901和Lederle菌株。根据CDV核蛋白基因和融合基因(F)的核苷酸序列变异设计引物。首先,从CD1901和Lederle株的病毒RNA中扩增出224 bp的DNA条带。然后在CD1901和Lederle菌株中分别扩增出428和326 bp的DNA条带。CD1901和Lederle菌株的多重RT-PCR检测限分别为2.53和0.8中位组织培养感染剂量/反应。狂犬病病毒、细小病毒、犬腺病毒1型和2型、副流感病毒等非cdv参比病毒未见交叉反应。结果表明,我们的一步多重RT-PCR可用于区分野生型和疫苗型CDV犬瘟热。CD1901和Lederle菌株在含有两种抗生素、一种抗真菌剂和10%热灭活胎牛血清的Dulbecco改良Eagle培养基(Gibco BRL, Grand Island, NY, USA)中表达狗SLAM基因的Vero/dSLAM细胞中繁殖。以CD1901和Lederle菌株为阳性对照进行多重RT-PCR,测定引物的分析敏感性和分析特异性。利用国内生物企业生产的含有CDV、犬腺病毒1型(CAV-1)、犬腺病毒2型(CAV-2)、犬细小病毒(CPV)、犬副流感病毒(CPIV)的4种市产犬瘟热/腺病毒/细小病毒/副流感(DAPP)疫苗进行多重检测,具有较高的敏感性和特异性
Establishment of Multiplex RT-PCR for Differentiating between the CD1901 and Lederle Strains of Canine Distemper Virus
license/by-nc/3.0/). Canine distemper virus (CDV) is a life-threatening pathogen in dogs. Clinical, pathological and molecular methods are required to diagnose CDV infection, and it is important to differentiate between the Korean CDV strain CD1901 and Lederle CDV vaccine strain. Therefore, in this study, we used multiplex reverse-transcription polymerase chain reaction (RT-PCR) to differentiate between the CD1901 and Lederle strains. A primer set was designed based on the CDV nucleoprotein gene and nucleotide sequence variation in the fusion (F) gene. First, 224-bp DNA bands were amplified from viral RNA of the CD1901 and Lederle strains. Then, 428- and 326-bp DNA bands were amplified in the CD1901 and Lederle strain, respectively. The multiplex RT-PCR detection limits were 2.53 and 0.8 median tissue culture infectious dose/reaction for the CD1901 and Lederle strains, respectively. No cross-reactions were detected in non-CDV reference viruses, including rabies virus, parvovirus, canine adenovirus types 1 and 2, and parainfluenza virus. The results indicate that our one-step multiplex RT-PCR is useful for differentiating between wildtype and vaccine CDV distemper. The CD1901 and Lederle strains were propagated in Vero/dSLAM cells expressing the dog SLAM gene in Dulbecco’s modified Eagle’s medium containing two antibiotics, an antifungal agent, and 10% heat-inactivated fetal bovine serum (Gibco BRL, Grand Island, NY, USA). The CD1901 and Lederle strains were used as positive controls for multiplex RT-PCR, and the analytical sensitivity and analytical specificity of the primers were determined. Four commercial distemper/adeno/parvo/parainfluenza (DAPP) vaccines containing CDV, canine adenovirus type 1 (CAV-1) or canine adenovirus type 2 (CAV-2), canine parvovirus (CPV), and canine parainfluenza virus (CPIV) manufactured by Korean biological companies were used for multiplex showed high sensitivity and specificity for differentiating between