Humoral immunity and protection of mice challenged with homotypic or heterotypic parvovirus.

Laboratory animal science Pub Date : 1999-08-01
G M Hansen, F X Paturzo, A L Smith
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Abstract

Background and objectives: Two serotypes of autonomously replicating parvoviruses infect laboratory mice. Genome regions coding for the nonstructural proteins of minute virus of mice [MVM] and mouse parvovirus [MPV] are almost identical, whereas capsid-coding sequences are divergent. We addressed these questions: Does humoral immunity confer protection from acute infection after challenge with homotypic or heterotypic parvovirus, and if it confers protection against acute MPV infection, does it also protect against persistent MPV infection?

Methods: Infant mice without maternal antibody or antibody to MVM or MPV and young adult mice given normal mouse serum or antibody to MVM or MPV were challenged with homotypic or heterotypic virus. In situ hybridization with target tissues was the indicator of infection.

Results: Humoral immunity failed to confer protection against acute heterotypic parvovirus infection. In passive transfer studies, MPV DNA was observed occasionally in lymph nodes, intestine, or the spleen of MPV-challenged mice given homotypic antibody and kept for 6 or 28 days. Variable proportions of mice given MPV antibody and homotypic challenge had viral DNA in lymphoid tissues 56 days after virus inoculation.

Conclusion: A mouse or colony that has sustained infection with MVM or MPV is probably fully susceptible to infection with the heterotypic virus.

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同型或异型细小病毒攻毒小鼠的体液免疫和保护作用。
背景和目的:两种血清型的自主复制细小病毒感染实验室小鼠。小鼠微小病毒(MVM)和小鼠细小病毒(MPV)的非结构蛋白基因组编码区域几乎相同,而衣壳编码序列则不同。我们解决了这些问题:体液免疫在同型或异型细小病毒攻击后是否赋予对急性感染的保护,如果它赋予对急性MPV感染的保护,它是否也保护对持续性MPV感染的保护?方法:不含母源抗体或MVM或MPV抗体的幼鼠和给予正常小鼠血清或MVM或MPV抗体的幼鼠分别用同种或异型病毒攻毒。与靶组织的原位杂交是感染的指标。结果:体液免疫不能对急性异型细小病毒感染提供保护。在被动转移研究中,偶有MPV DNA在给予同型抗体的MPV攻击小鼠的淋巴结、肠或脾脏中被观察到,并保存6或28天。接种病毒56天后,不同比例的MPV抗体和同型攻毒小鼠淋巴组织中均有病毒DNA。结论:持续感染MVM或MPV的小鼠或群体可能完全容易感染异型病毒。
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