Ehlers Bernhard, Küchler Judit, Yasmum Nezlisah, Dural Güzin, Voigt Sebastian, Schmidt-Chanasit Jonas, Jäkel Thomas, Matuschka Franz-Rainer, Richter Dania, Essbauer Sandra, Hughes David J, Summers Candice, Bennett Malcolm, Stewart James P, Ulrich Rainer G
P14 Molekulare Genetik und Epidemiologie von Herpesviren, Robert Koch-Institut, Nordufer 20, D-13353 Berlin, Germany.
J Virol. 2007 Aug;81(15):8091-100. doi: 10.1128/JVI.00255-07. Epub 2007 May 16.
Rodent herpesviruses such as murine cytomegalovirus (host, Mus musculus), rat cytomegalovirus (host, Rattus norvegicus), and murine gammaherpesvirus 68 (hosts, Apodemus species) are important tools for the experimental study of human herpesvirus diseases. However, alphaherpesviruses, roseoloviruses, and lymphocryptoviruses, as well as rhadinoviruses, that naturally infect Mus musculus (house mouse) and other Old World mice are unknown. To identify hitherto-unknown rodent-associated herpesviruses, we captured M. musculus, R. norvegicus, and 14 other rodent species in several locations in Germany, the United Kingdom, and Thailand. Samples of trigeminal ganglia, dorsal root ganglia, brains, spleens, and other organs, as well as blood, were analyzed with a degenerate panherpesvirus PCR targeting the DNA polymerase (DPOL) gene. Herpesvirus-positive samples were subjected to a second degenerate PCR targeting the glycoprotein B (gB) gene. The sequences located between the partial DPOL and gB sequences were amplified by long-distance PCR and sequenced, resulting in a contiguous sequence of approximately 3.5 kbp. By DPOL PCR, we detected 17 novel betaherpesviruses and 21 novel gammaherpesviruses but no alphaherpesvirus. Of these 38 novel herpesviruses, 14 were successfully analyzed by the complete bigenic approach. Most importantly, the first gammaherpesvirus of Mus musculus was discovered (Mus musculus rhadinovirus 1 [MmusRHV1]). This virus is a member of a novel group of rodent gammaherpesviruses, which is clearly distinct from murine herpesvirus 68-like rodent gammaherpesviruses. Multigenic phylogenetic analysis, using an 8-kbp locus, revealed that MmusRHV1 diverged from the other gammaherpesviruses soon after the evolutionary separation of Epstein-Barr virus-like lymphocryptoviruses from human herpesvirus 8-like rhadinoviruses and alcelaphine herpesvirus 1-like macaviruses.
啮齿动物疱疹病毒,如鼠巨细胞病毒(宿主为小家鼠)、大鼠巨细胞病毒(宿主为褐家鼠)和鼠γ疱疹病毒68(宿主为姬鼠属物种),是人类疱疹病毒疾病实验研究的重要工具。然而,自然感染小家鼠(家鼠)和其他旧大陆小鼠的α疱疹病毒、玫瑰疹病毒、淋巴细胞隐病毒以及嗜皮瘤病毒尚不清楚。为了鉴定迄今未知的与啮齿动物相关的疱疹病毒,我们在德国、英国和泰国的多个地点捕获了小家鼠、褐家鼠以及其他14种啮齿动物。使用针对DNA聚合酶(DPOL)基因的简并全疱疹病毒PCR对三叉神经节、背根神经节、大脑、脾脏和其他器官以及血液样本进行分析。对疱疹病毒阳性样本进行第二轮针对糖蛋白B(gB)基因的简并PCR。通过长距离PCR扩增并测序位于部分DPOL和gB序列之间的序列,得到了一个约3.5 kbp的连续序列。通过DPOL PCR,我们检测到17种新型β疱疹病毒和21种新型γ疱疹病毒,但未检测到α疱疹病毒。在这38种新型疱疹病毒中,有14种通过完整的双基因方法成功分析。最重要的是,发现了小家鼠的第一种γ疱疹病毒(小家鼠嗜皮瘤病毒1 [MmusRHV1])。这种病毒是一组新型啮齿动物γ疱疹病毒的成员,与鼠疱疹病毒68样啮齿动物γ疱疹病毒明显不同。使用一个8-kbp位点进行的多基因系统发育分析表明,在爱泼斯坦-巴尔病毒样淋巴细胞隐病毒与人类疱疹病毒8样嗜皮瘤病毒和非洲猪瘟病毒1样马卡病毒进化分离后不久,MmusRHV1就与其他γ疱疹病毒分道扬镳。