Smith A L
Lab Anim Sci. 1983 Feb;33(1):37-9.
Several methods (hemagglutination inhibition, immunofluorescence, enzyme-linked immunosorbent assay, and serum neutralization) for detection of serum antibody to minute virus of mice were compared using sera from random-bred, weanling mice experimentally inoculated by either the intraperitoneal or oral route. Antibody was detected by all methods in sera from intraperitoneally inoculated mice by 4 days post-inoculation, while sera from orally infected mice contained detectable antibody on day 7 by all methods except neutralization. Serum neutralizing antibody was detected much later and at lower levels in sera of orally infected mice than in sera of intraperitoneally inoculated mice. Virus was recovered from the intestines of both inoculation groups and from the kidneys of intraperitoneally inoculated mice. Among the latter animals, virus was still detectable 10 days post-inoculation, several days after serum neutralizing antibody had developed. Sentinel dams with litters placed in cages with intraperitoneally inoculated mice 10 days after the inoculation were seropositive by immunofluorescence and enzyme-linked immunosorbent assay when tested 3 weeks after contact.
使用随机繁殖的断奶小鼠经腹腔或口服途径进行实验接种后获得的血清,比较了几种检测小鼠微小病毒血清抗体的方法(血凝抑制、免疫荧光、酶联免疫吸附测定和血清中和)。接种后4天,通过所有方法在经腹腔接种小鼠的血清中检测到抗体,而经口服感染小鼠的血清在第7天通过除中和以外的所有方法检测到可检测到的抗体。与经腹腔接种小鼠的血清相比,经口服感染小鼠血清中的血清中和抗体检测到的时间要晚得多,且水平较低。在两个接种组的肠道以及经腹腔接种小鼠的肾脏中均回收了病毒。在后者的动物中,接种后10天仍可检测到病毒,此时血清中和抗体已经产生了几天。接种后10天将带有幼崽的哨兵母鼠放置在与经腹腔接种小鼠的笼子中,接触3周后通过免疫荧光和酶联免疫吸附测定检测呈血清阳性。