Ward R L, McNeal M M, Sheridan J F
James N. Gamble Institute of Medical Research, Cincinnati, Ohio 45219.
J Virol. 1990 Oct;64(10):5070-5. doi: 10.1128/JVI.64.10.5070-5075.1990.
Although mice have been used as an animal model for studies on rotavirus disease, these studies have been limited by the short time period after birth during which mice are susceptible to rotavirus illness (i.e., approximately 15 days). To overcome this limitation, an adult mouse model was developed in which the endpoint was infection rather than illness. The model developed utilized a strain of mouse rotavirus (EDIM) adapted to grow in culture by multiple passages in MA104 cells. The second cell culture passage of EDIM caused severe diarrhea in neonatal BALB/c mice, and little or no amelioration of disease was observed after nine cell culture passages, even when this preparation was plaque purified. Oral administration of 2 x 10(3) PFU of passage 9 also consistently caused infection of mice 4, 10, 15, 30, 60, 120, and 180 days of age as determined by viral shedding and seroconversion. Reinoculation of these mice with the same virus preparation at 2, 3, or 4 months after the first inoculation produced no evidence of reinfection. In contrast, infection of neonatal mice with the heterotypic WC3 bovine rotavirus did not prevent reinfection with culture-adapted EDIM. Thus, this strain of EDIM caused consistent infection of previously uninoculated neonatal and adult BALB/c mice and produced homotypic but not heterotypic protection against reinfection.
尽管小鼠已被用作轮状病毒疾病研究的动物模型,但这些研究受到出生后小鼠对轮状病毒疾病易感的时间段较短(即约15天)的限制。为克服这一限制,开发了一种成年小鼠模型,其终点是感染而非疾病。所开发的模型利用了一种通过在MA104细胞中多次传代而适应在培养物中生长的小鼠轮状病毒(EDIM)毒株。EDIM的第二次细胞培养传代在新生BALB/c小鼠中引起严重腹泻,并且在九次细胞培养传代后未观察到疾病有任何减轻,即使该制剂经过空斑纯化也是如此。口服接种第9代的2×10³PFU也始终能导致4、10、15、30、60、120和180日龄小鼠感染,这可通过病毒排出和血清转化来确定。在首次接种后2、3或4个月用相同病毒制剂对这些小鼠进行再次接种,未发现再次感染的迹象。相比之下,用异型WC3牛轮状病毒感染新生小鼠并不能预防用适应培养的EDIM再次感染。因此,这种EDIM毒株能使先前未接种的新生和成年BALB/c小鼠持续感染,并产生同型而非异型的抗再感染保护作用。