Besselsen David G, Romero Melissa J, Wagner April M, Henderson Kenneth S, Livingston Robert S
University Animal Care, University of Arizona, Tucson, AZ, USA.
Charles River Laboratories, Wilmington, MA, USA.
J Gen Virol. 2006 Jun;87(Pt 6):1543-1556. doi: 10.1099/vir.0.81547-0.
Random-source DNA samples obtained from naturally infected laboratory mice (n=381) were evaluated by PCR and RFLP analysis to determine the prevalence of murine parvovirus strains circulating in contemporary laboratory mouse colonies. Mouse parvovirus (MPV) was detected in 77% of samples, Minute virus of mice (MVM) was detected in 16% of samples and both MVM and MPV were detected in 7% of samples. MVMm, a strain recently isolated from clinically ill NOD-mu chain knockout mice, was detected in 91% of MVM-positive samples, with the Cutter strain of MVM (MVMc) detected in the remaining samples. The prototypic and immunosuppressive strains of MVM were not detected in any of the samples. MPV-1 was detected in 78% of the MPV-positive samples and two newly identified murine parvoviruses, tentatively named MPV-2 and MPV-3, were detected in 21 and 1% of the samples, respectively. The DNA sequence encompassing coding regions of the viral genome and the predicted protein sequences for MVMm, MPV-2 and MPV-3 were determined and compared with those of other rodent parvovirus strains and LuIII parvovirus. The genomic organization for the newly identified viral strains was similar to that of other rodent parvoviruses, and nucleotide sequence identities indicated that MVMm was most similar to MVMc (96.1%), MPV-3 was most similar to hamster parvovirus (HaPV) (98.1%) and MPV-2 was most similar to MPV-1 (95.3%). The genetic similarity of MPV-3 and HaPV suggests that HaPV epizootics in hamsters may result from cross-species transmission, with mice as the natural rodent host for this virus.
从自然感染的实验小鼠(n = 381)中获取随机来源的DNA样本,通过聚合酶链反应(PCR)和限制性片段长度多态性分析(RFLP)进行评估,以确定当代实验小鼠群体中流行的小鼠细小病毒株的患病率。77%的样本中检测到小鼠细小病毒(MPV),16%的样本中检测到小鼠微小病毒(MVM),7%的样本中同时检测到MVM和MPV。在91%的MVM阳性样本中检测到最近从临床患病的NOD-μ链敲除小鼠中分离出的MVMm株,其余样本中检测到MVM的Cutter株(MVMc)。在任何样本中均未检测到MVM的原型株和免疫抑制株。78%的MPV阳性样本中检测到MPV-1,在21%和1%的样本中分别检测到两种新鉴定的小鼠细小病毒,暂命名为MPV-2和MPV-3。确定了包含病毒基因组编码区的DNA序列以及MVMm、MPV-2和MPV-3的预测蛋白质序列,并与其他啮齿动物细小病毒株和LuIII细小病毒进行了比较。新鉴定的病毒株的基因组结构与其他啮齿动物细小病毒相似,核苷酸序列同一性表明MVMm与MVMc最相似(96.1%),MPV-3与仓鼠细小病毒(HaPV)最相似(98.1%),MPV-2与MPV-1最相似(95.3%)。MPV-3与HaPV的遗传相似性表明,仓鼠中的HaPV流行病可能是由跨物种传播引起的,小鼠是该病毒的天然啮齿动物宿主。