Otsyula M, Yee J, Jennings M, Suleman M, Gettie A, Tarara R, Isahakia M, Marx P, Lerche N
Institute of Primate Research, Nairobi, Kenya.
Ann Trop Med Parasitol. 1996 Feb;90(1):65-70. doi: 10.1080/00034983.1996.11813027.
Sera (165 samples in 1988 and 66, follow-up samples in 1989) were collected from olive baboons, African green monkeys, Syke's monkeys and grey mangabeys kept in a semi-free, breeding colony at the Institute of Primate Research (IPR) in Nairobi, Kenya. The levels of antibodies to simian T-lymphotropic virus (STLV) or simian immunodeficiency virus (SIV), and the reactivity patterns of positive sera to various lentivirus subgroup antigens, were then determined. The results of tests using enzyme-immunoassay kits were confirmed by western blots. The prevalence of antibodies which reacted with the Kenyan SIVagm(KEN) isolate was 28% in the African green monkeys tested and 34% in the Syke's monkeys. STLV seroprevalence was 25% in the African greens and 20% in the Syke's. No antibodies to either SIV or STLV were detected in the olive baboons or grey mangabeys. More SIV-positive samples were detected in western blots when SIVagm(KEN) was used as antigen than when SIVagm(CAR014), a geographically distinct isolate from the Central African Republic, was used. However, SIVagm(KEN)-positive sera were more reactive against SIVagm(CAR014) than SIVsmm and SIVmac subgroup antigens, indicating that the two isolates from the African green monkey, CAR014 and KEN, remain antigenetically close even though they were recovered in two geographically distinct regions. To date, no clinical disease has been linked with SIV and STLV infection in the African green or Syke's monkeys in the colony. However, the relatively high prevalence of anti-SIV and anti-STLV antibodies in these monkeys offers an opportunity for prospective studies on the transmission and natural history of both viruses in a single colony.
血清样本(1988年采集165份,1989年采集66份随访样本)取自肯尼亚内罗毕灵长类动物研究所(IPR)半自由繁殖群体中的东非狒狒、非洲绿猴、西克氏猴和灰颊白眉猴。随后测定了针对猴嗜T淋巴细胞病毒(STLV)或猴免疫缺陷病毒(SIV)的抗体水平,以及阳性血清对各种慢病毒亚组抗原的反应模式。使用酶免疫分析试剂盒进行检测的结果通过蛋白质印迹法得到了证实。在接受检测的非洲绿猴中,与肯尼亚SIVagm(KEN)分离株发生反应的抗体流行率为28%,在西克氏猴中为34%。STLV血清阳性率在非洲绿猴中为25%,在西克氏猴中为20%。在东非狒狒或灰颊白眉猴中未检测到针对SIV或STLV的抗体。当使用SIVagm(KEN)作为抗原时,蛋白质印迹法检测到的SIV阳性样本比使用来自中非共和国地理上不同的分离株SIVagm(CAR014)时更多。然而,SIVagm(KEN)阳性血清对SIVagm(CAR014)的反应性比对SIVsmm和SIVmac亚组抗原更强,这表明来自非洲绿猴的两个分离株CAR014和KEN,尽管是在两个地理上不同的地区分离得到的,但在抗原性上仍然相近。迄今为止,在该群体中的非洲绿猴或西克氏猴中,尚未发现临床疾病与SIV和STLV感染有关。然而,这些猴子中抗SIV和抗STLV抗体的相对高流行率为对这两种病毒在单个群体中的传播和自然史进行前瞻性研究提供了机会。