Henderson Kenneth S, Pritchett-Corning Kathleen R, Perkins Cheryl L, Banu Laila A, Jennings Steven M, Francis Brian C, Shek William R
Research Animal Diagnostic Services, Charles River, Wilmington, Massachusetts, USA
Office of Animal Resources, Harvard University, Cambridge, Massachusetts.
Comp Med. 2015 Feb;65(1):5-14.
This study characterized the effects of challenge with a field isolate of mouse parvovirus 1 (MPV1e) in C57BL/6NCrl (B6) and BALB/cAnNCrl (C) mice. We found that C mice were more susceptible to MPV1e infection than were B6 mice; ID50 were 50 to 100 times higher after gavage and 10-fold higher after intraperitoneal injection in B6 as compared with C mice. To evaluate the host strain effect on the pathogenesis of MPV1e, B6 and C mice were inoculated by gavage. Feces and tissues, including mesenteric lymph nodes (MLN), ileum, spleen and blood, were collected for analysis by quantitative PCR (qPCR) to assess infection and fecal shedding and by RT-qPCR to evaluate replication. Peak levels of MPV1e shedding, infection, and replication were on average 3.4, 4.3, and 6.2 times higher, respectively, in C than in B6 mice. Peaks occurred between 3 and 10 d after inoculation in C mice but between 5 and 14 d in B6 mice. Multiplexed fluorometric immunoassays detected seroconversion in 2 of 3 C mice at 7 d after inoculation and in all 3 B6 mice at 10 d. By 56 d after inoculation, viral replication was no longer detectable, and fecal shedding was very low; infection persisted in ileum, spleen, and MLN, with levels higher in C than B6 mice and highest in MLN. Therefore, the lower susceptibility of B6 mice, as compared with C mice, to MPV1e infection was associated with lower levels of infection, replication, and shedding and delayed seroconversion.
本研究描述了用小鼠细小病毒1(MPV1e)的一株野外分离株感染C57BL/6NCrl(B6)和BALB/cAnNCrl(C)小鼠的效果。我们发现,C小鼠比B6小鼠对MPV1e感染更易感;经口灌胃后,B6小鼠的半数感染剂量(ID50)比C小鼠高50至100倍,腹腔注射后高10倍。为评估宿主品系对MPV1e发病机制的影响,对B6和C小鼠进行经口灌胃接种。收集粪便和包括肠系膜淋巴结(MLN)、回肠、脾脏和血液在内的组织,通过定量PCR(qPCR)分析以评估感染和粪便排毒情况,并通过逆转录定量PCR(RT-qPCR)评估病毒复制情况。C小鼠的MPV1e排毒、感染和复制的峰值水平分别平均比B6小鼠高3.4倍、4.3倍和6.2倍。C小鼠在接种后3至10天出现峰值,而B6小鼠在5至14天出现峰值。多重荧光免疫测定法检测到,3只C小鼠中有2只在接种后7天发生血清转化,3只B6小鼠均在10天发生血清转化。接种后56天,不再能检测到病毒复制,粪便排毒量很低;感染在回肠、脾脏和MLN中持续存在,C小鼠中的水平高于B6小鼠,在MLN中最高。因此,与C小鼠相比,B6小鼠对MPV1e感染的易感性较低与感染、复制和排毒水平较低以及血清转化延迟有关。