Ball-Goodrich L J, Leland S E, Johnson E A, Paturzo F X, Jacoby R O
Section of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut 06520-8016, USA.
J Virol. 1998 Apr;72(4):3289-99. doi: 10.1128/JVI.72.4.3289-3299.1998.
A newly recognized parvovirus of laboratory rats, designated rat parvovirus type 1a (RPV-1a), was found to be antigenically distinct. It was cloned, sequenced, and compared with the University of Massachusetts strain of rat virus (RV-UMass) and other autonomous parvoviruses. RPV-1a VP1 identity with these viruses never exceeded 69%, thus explaining its antigenic divergence. In addition, RPV-1a had reduced amino acid identity in NS coding regions (82%), reflecting phylogenetic divergence from other rodent parvoviruses. RPV-1a infection in rats had a predilection for endothelium and lymphoid tissues as previously reported for RV. Infectious RPV-1a was isolated 3 weeks after inoculation of infant rats, suggesting that it, like RV, may result in persistent infection. In contrast to RV, RPV-1a was enterotropic, a characteristic previously associated with parvovirus infections of mice rather than rats. RPV-1a also differed from RV in that infection was nonpathogenic for infant rats under conditions where RV infection causes high morbidity and mortality. Thus, RPV-1a is the prototype virus of an antigenically, genetically, and biologically distinct rodent parvovirus serogroup.
一种新发现的实验大鼠细小病毒,命名为大鼠细小病毒1a型(RPV-1a),被发现具有独特的抗原性。它被克隆、测序,并与马萨诸塞大学的大鼠病毒株(RV-UMass)及其他自主细小病毒进行了比较。RPV-1a与这些病毒的VP1同一性从未超过69%,这就解释了其抗原性差异。此外,RPV-1a在NS编码区的氨基酸同一性降低(82%),反映出与其他啮齿动物细小病毒的系统发育差异。正如之前对RV的报道,大鼠感染RPV-1a后对内皮和淋巴组织有偏好性。在接种幼鼠3周后分离出具有传染性的RPV-1a,这表明它可能像RV一样导致持续性感染。与RV不同的是,RPV-1a具有嗜肠性,这一特征之前与小鼠而非大鼠的细小病毒感染有关。RPV-1a与RV的另一个不同之处在于,在RV感染会导致幼鼠高发病率和死亡率的条件下,RPV-1a感染对幼鼠无致病性。因此,RPV-1a是一个在抗原性、遗传性和生物学特性上都不同的啮齿动物细小病毒血清群的原型病毒。