Monteiro Francielle Liz, Cargnelutti Juliana F, Martins Bruno, Noll Jessica G, Weiblen Rudi, Flores Eduardo F
Setor de Virologia, Departamento de Medicina Veterinária Preventiva (Monteiro, Cargnelutti, Martins, Noll, Weiblen, Flores), Universidade Federal de Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.
Programa de Pós-Graduação em Medicina Veterinária (Monteiro, Martins, Noll, Weiblen, Flores), Universidade Federal de Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.
J Vet Diagn Invest. 2019 Mar;31(2):255-258. doi: 10.1177/1040638719826299. Epub 2019 Jan 30.
The pestiviruses bovine viral diarrhea virus 1 and 2 (BVDV-1 and -2, respectively) and HoBi-like pestivirus (HoBiPeV) are important pathogens of cattle, and a number of reverse-transcription PCR (RT-PCR)-based assays have been developed for their detection in clinical specimens. We evaluated a newly designed set of pan-bovine pestivirus primers (BP189-389) in a gel-based RT-PCR screening test for pestiviruses in the sera of beef calves destined for export from southern Brazil. Serum samples positive for BVDV antigens by an antigen ELISA ( n = 135) were submitted to RT-PCR assays using different sets of primers, followed by nucleotide sequencing of the amplicons. RT-PCR with pestivirus primers 324-326 detected 110 positive samples: BVDV-1 ( n = 62), BVDV-2 ( n = 38), and HoBiPeV ( n = 10). A PCR using primers HCV90-368 detected 97 positive samples (64 BVDV-1; 33 BVDV-2). An additional RT-PCR round using BVDV-2-specific primers (2F-2R) detected 45 positive samples (including 38 detected by primers 324-326 and 33 by HCV90-368); whereas a RT-PCR using HoBiPeV-specific primers (N2-R5) detected 26 positive samples (including 10 detected by primers 324-326).The assay using the primers BP189-389 detected all 135 ELISA-positive samples, including the 26 HoBiPeV detected by primers N2-R5. Our results demonstrated that primers BP189-389 compare favorably against other primer sets in the detection of bovine pestiviruses, especially HoBiPeV. This conventional PCR may be useful for efficient detection of pestiviruses in bovine sera and other specimens as well, especially in laboratories without real-time PCR equipment.
瘟病毒属的牛病毒性腹泻病毒1型和2型(分别为BVDV-1和BVDV-2)以及类霍比瘟病毒(HoBiPeV)是牛的重要病原体,已经开发了许多基于逆转录聚合酶链反应(RT-PCR)的检测方法用于在临床标本中检测它们。我们在基于凝胶的RT-PCR筛选试验中评估了一组新设计的泛牛瘟病毒引物(BP189-389),用于检测从巴西南部出口的肉牛犊血清中的瘟病毒。通过抗原酶联免疫吸附测定(ELISA)呈BVDV抗原阳性的血清样本(n = 135)使用不同的引物组进行RT-PCR测定,随后对扩增子进行核苷酸测序。使用瘟病毒引物324-326的RT-PCR检测到110个阳性样本:BVDV-1(n = 62)、BVDV-2(n = 38)和HoBiPeV(n = 10)。使用引物HCV90-368的PCR检测到97个阳性样本(64个BVDV-1;33个BVDV-2)。使用BVDV-2特异性引物(2F-2R)进行的另一轮RT-PCR检测到45个阳性样本(包括38个由引物324-326检测到的和33个由HCV90-368检测到的);而使用HoBiPeV特异性引物(N2-R5)的RT-PCR检测到26个阳性样本(包括10个由引物324-326检测到的)。使用引物BP189-389的检测方法检测到了所有135个ELISA阳性样本,包括由引物N2-R5检测到的26个HoBiPeV样本。我们的结果表明,在检测牛瘟病毒尤其是HoBiPeV方面,引物BP189-389比其他引物组更具优势。这种传统PCR对于有效检测牛血清和其他标本中的瘟病毒可能也很有用,特别是在没有实时PCR设备的实验室中。