Sherry B, Blum M A
Department of Microbiology, Pathology, College of Veterinary Medicine, North Carolina State University, Raleigh 27606.
J Virol. 1994 Dec;68(12):8461-5. doi: 10.1128/JVI.68.12.8461-8465.1994.
Previously, we showed that the M1 gene (encoding a viral core protein, mu 2, whose function is unknown) was associated with the efficiently myocarditic phenotype of a reovirus variant, 8B. Here, we have extended our genetic analysis of 8B and conducted genetic analyses of two other reovirus strains (T1L [serotype 1 strain Lang] and Abney). Our results demonstrate that multiple viral core proteins are determinants of reovirus-induced myocarditis. In contrast to our previous association of mu 2 with induction of myocarditis, this provides strong evidence that a core function achieved through the interaction of multiple core proteins is responsible for induction of the disease.
此前,我们发现M1基因(编码一种病毒核心蛋白μ2,其功能未知)与呼肠孤病毒变体8B的高效致心肌炎表型相关。在此,我们扩展了对8B的基因分析,并对另外两种呼肠孤病毒株(T1L [1型朗株]和阿布尼株)进行了基因分析。我们的结果表明,多种病毒核心蛋白是呼肠孤病毒诱导心肌炎的决定因素。与我们之前将μ2与心肌炎诱导联系起来的研究不同,这有力地证明了通过多种核心蛋白相互作用实现的核心功能是导致该疾病的原因。