Fonseca Antônio Augusto, Magalhães Cristina Gonçalves, Sales Erica Bravo, D'Ambros Régia Maria, Ciacci-Zanella Janice, Heinemann Marcos Bryan, Leite Rômulo Cerqueira, Dos Reis Jenner Karlisson Pimenta
LANAGRO/MG, Avenida Rômulo Joviano, Caixa Postal 50, Centro, 33600-000 Pedro Leopoldo, Minas Gerais, CEP, Brazil.
ISRN Microbiol. 2011 Nov 24;2011:458294. doi: 10.5402/2011/458294. Print 2011.
Suid herpesvirus 1 (SuHV-1) is the causative agent of Aujeszky's disease. The infectious agent has only one serotype, but it was classified by restriction enzyme analysis of the whole genome into four genotypes, named I to IV. The aim of this study was to standardize a rapid method for genotyping SuHV-1 without virus isolation, using a multiplex-PCR followed by enzymatic restriction analysis. The complete genome of the virus was analyzed in silico to determine the restriction sites for the enzyme BamHI. Primers were designed to flank sites with emphasis on certain points of differentiation of genotypes. The standard PCRs were able to detect the SuHV-1 and also to differentiate genotypes from brain tissue of infected pigs. The BamHI-PCR is a rapid, practical, and sensitive way to genotype SuHV-1.
猪疱疹病毒1型(SuHV-1)是奥耶斯基氏病的病原体。该传染源只有一个血清型,但通过对全基因组的限制性酶切分析被分为四个基因型,命名为I至IV型。本研究的目的是建立一种无需病毒分离的快速SuHV-1基因分型方法,采用多重PCR随后进行酶切分析。对病毒的全基因组进行了电子分析以确定BamHI酶的限制性位点。设计引物以侧翼位点为重点,着重于基因型的某些差异点。标准PCR能够检测SuHV-1,并从感染猪的脑组织中区分基因型。BamHI-PCR是一种快速、实用且灵敏的SuHV-1基因分型方法。