Griffith B P, McCormick S R, Booss J, Hsiung G D
Am J Pathol. 1986 Jan;122(1):112-9.
Outbred guinea pigs have previously been utilized in an experimental model for the study of congenital infection with cytomegalovirus (CMV). Development of an inbred model of intrauterine CMV infection would allow analysis of the cells involved in CMV immunity, studies of transplacental CMV transfer, and investigation of the cellular immune factors that participate in intrauterine CMV infections. This study was therefore designed to assess the inbred guinea pig as a model for the study of congenital CMV infection. Intrauterine fetal and placental infection with CMV was demonstrated in inbred Strain 2 guinea pigs, and the maternal factors influencing transplacental transmission of CMV were evaluated. Infectious virus was recovered from placentas and offspring of mothers that experienced primary CMV infection during pregnancy, but not from placentas and offspring of mothers that were inoculated with CMV prior to pregnancy. However, histologic lesions consisting of focal necrosis and inflammation were seen in tissues of offspring from both groups of mothers. Inoculation of seronegative pregnant Strain 2 animals with low doses of virus (2.5 to 3.5 log10 TCID50) resulted in both placental and fetal CMV infection without significant maternal death. Infection of placentas and offspring occurred in utero regardless of the stage of pregnancy. In addition, infectious virus was detectable in fetal tissues at the time of maternal viremia but also later during the course of maternal infection, ie, 4 weeks after inoculation. These findings indicate that the inbred guinea pig model can be used to investigate the pathogenesis of intrauterine CMV infections.
远交系豚鼠先前已被用于巨细胞病毒(CMV)先天性感染的实验模型研究。建立宫内CMV感染的近交系模型将有助于分析参与CMV免疫的细胞、研究经胎盘的CMV传播,以及调查参与宫内CMV感染的细胞免疫因子。因此,本研究旨在评估近交系豚鼠作为先天性CMV感染研究模型的可行性。在近交系2豚鼠中证实了宫内胎儿和胎盘感染CMV,并评估了影响CMV经胎盘传播的母体因素。从孕期发生原发性CMV感染的母亲的胎盘和后代中分离出了感染性病毒,但从孕前接种CMV的母亲的胎盘和后代中未分离出。然而,两组母亲后代的组织中均可见局灶性坏死和炎症组成的组织学病变。给血清阴性的怀孕近交系2动物接种低剂量病毒(2.5至3.5 log10 TCID50)导致胎盘和胎儿CMV感染,且母体无明显死亡。无论怀孕阶段如何,胎盘和后代的感染均发生在子宫内。此外,在母体病毒血症时胎儿组织中可检测到感染性病毒,在母体感染过程后期(即接种后4周)也可检测到。这些发现表明近交系豚鼠模型可用于研究宫内CMV感染的发病机制。