Blomqvist Gunilla A M, Martin Krister, Morein Bror
The National Veterinary Institute, Department of Virology, Uppsala, Sweden.
Contemp Top Lab Anim Sci. 2002 Jul;41(4):53-7.
In searching for the cause of experimental variations in respiratory research data, serology revealed the prevalence of antibodies against parainfluenza virus type 3 (PIV 3) in guinea pigs. The aim of the present study was to explore the transmission rate, course, and kinetics of enzootic PIV 3 infection in guinea pig breeding units. In the first part of the study, blood samples to be analyzed for PIV 3 antibodies were collected from guinea pigs of a PIV 3-positive breeding colony at different times after birth. In the same breeding unit, 6 of 12 2-week-old guinea pigs were relocated and separately housed. The PIV 3 serum antibody titers of the two groups were compared at various times from birth to 13 weeks after birth. In the second part of the study, the spread of infectious virus and virus persistence were explored by housing seronegative sentinel animals together with 2- to 3-week-old guinea pigs from three different PIV 3-positive breeding units. The guinea pigs remaining in the breeding colony as well as those removed and housed separately showed declining serum antibody titers for about 1 month after birth, thereafter the titers were stable until about 8 weeks after birth. Five weeks later, the mean antibody titer of the guinea pigs remaining in the breeding colony had increased to a markedly higher level than that of the relocated, separately housed guinea pigs. Seroconversion was demonstrated in 7 of the 14 sentinels housed with the 2- to 3-week-old guinea pigs from PIV 3-positive breeding units. Sentinels housed together with PIV 3-positive guinea pigs 24 weeks after the start of the experiment did not seroconvert. We conclude that young guinea pigs born to PIV 3-positive mothers were protected by maternal immunity against infection with PIV 3 during their first 14 days of life. The guinea pig offspring became infected during the period from about 2 weeks until 8 weeks after birth, as demonstrated by seroconversion of sentinel animals and an increasing mean antibody titer seen beyond 8 weeks of age. The study did not reveal any indication of virus persistence or prolonged carrier status.
在探寻呼吸研究数据实验性变异的原因时,血清学检测发现豚鼠中存在抗3型副流感病毒(PIV 3)抗体。本研究的目的是探究豚鼠繁殖单元中PIV 3地方流行性感染的传播率、病程及动力学。在研究的第一部分,从一个PIV 3阳性繁殖群体的豚鼠出生后的不同时间采集血液样本,用于分析PIV 3抗体。在同一个繁殖单元中,将12只2周龄豚鼠中的6只重新安置并单独饲养。比较两组豚鼠从出生到出生后13周不同时间的PIV 3血清抗体滴度。在研究的第二部分,通过将血清学阴性的哨兵动物与来自三个不同PIV 3阳性繁殖单元的2至3周龄豚鼠饲养在一起,探究传染性病毒的传播及病毒持续性。留在繁殖群体中的豚鼠以及被移出并单独饲养的豚鼠出生后约1个月血清抗体滴度下降,此后滴度稳定直至出生后约8周。5周后,留在繁殖群体中的豚鼠平均抗体滴度升至明显高于重新安置并单独饲养的豚鼠的水平。与来自PIV 3阳性繁殖单元的2至3周龄豚鼠饲养在一起的14只哨兵动物中有7只出现血清转化。实验开始24周后与PIV 3阳性豚鼠饲养在一起的哨兵动物未出现血清转化。我们得出结论,PIV 3阳性母亲所生的幼龄豚鼠在出生后的前14天受到母源免疫保护,免受PIV 3感染。如哨兵动物的血清转化及8周龄后平均抗体滴度增加所示,豚鼠后代在出生后约2周直至8周期间受到感染。该研究未发现任何病毒持续性或长期携带状态的迹象。