Voevodin A F, Johnson B K, Samilchuk E I, Stone G A, Druilhet R, Greer W J, Gibbs C J
Department of Microbiology, Faculty of Medicine, Kuwait University, Safat, Kuwait.
Virology. 1997 Nov 24;238(2):212-20. doi: 10.1006/viro.1997.8826.
Serum and peripheral blood leukocytes from the chimpanzees (Pan troglodytes) of the colony of the Laboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, NIH, were tested for the presence of STLV-I-specific antibodies and proviral DNA. Antibodies were determined by gelatin particle agglutination and Western blot (WB) assays utilizing HTLV-I antigens. Proviral DNA was detected by four PCR assays targeting three different regions of STLV-I genome: the fragments of the env and pol genes and LTR. Twenty of twenty-two DNA samples from WB-positive animals were PCR positive. None of the DNA samples from WB-negative (n = 5) and WB-indeterminate (n = 4) animals was PCR positive. The results of the nested and double nested env PCR tests were fully concordant; the seminested LTR PCR test was much less sensitive. The DNA sequences from the env (483 bp) and the pol (200 bp) genes and LTR (705 bp) were determined for six, two, and two chimpanzee STLV-I isolates, respectively. Phylogenetic analysis revealed that chimpanzee STLV-I isolates can be attributed to three clades. The first of these clades (SS-PTR1/CSA) included STLV-I isolates from the chimpanzees and West African subspecies of African green monkeys (Cercopithecus a. sabaeus). The other clades (S-PTR2 and S-PTR3) included STLV-I isolates only from chimpanzees. However, both S-PTR2 and S-PTR3 clustered together with Central African HTLV-I comprising the human/simian clade (HS-HSA/PTR). This pattern of phylogenetic clustering suggests that interspecies transmission of STLV-I occurred between chimpanzees and African green monkey subspecies as well between chimpanzees and human populations in Central Africa.
美国国立卫生研究院国家神经疾病与中风研究所中枢神经系统研究实验室的黑猩猩(Pan troglodytes)群体的血清和外周血白细胞,被检测是否存在STLV-I特异性抗体和前病毒DNA。抗体通过使用HTLV-I抗原的明胶颗粒凝集试验和蛋白质印迹(WB)分析来测定。前病毒DNA通过针对STLV-I基因组三个不同区域的四种PCR分析来检测:env和pol基因片段以及长末端重复序列(LTR)。来自WB阳性动物的22个DNA样本中有20个PCR呈阳性。来自WB阴性(n = 5)和WB不确定(n = 4)动物的DNA样本均无PCR阳性。巢式和双重巢式env PCR试验的结果完全一致;半巢式LTR PCR试验的敏感性要低得多。分别对6株、2株和2株黑猩猩STLV-I分离株测定了env(483 bp)、pol(200 bp)基因和LTR(705 bp)的DNA序列。系统发育分析表明,黑猩猩STLV-I分离株可归为三个进化枝。其中第一个进化枝(SS-PTR1/CSA)包括来自黑猩猩和非洲绿猴(Cercopithecus a. sabaeus)西非亚种的STLV-I分离株。其他进化枝(S-PTR2和S-PTR3)仅包括来自黑猩猩的STLV-I分离株。然而,S-PTR2和S-PTR3都与包括人类/猿猴进化枝(HS-HSA/PTR)的中非HTLV-I聚集在一起。这种系统发育聚类模式表明,STLV-I在黑猩猩和非洲绿猴亚种之间以及黑猩猩和中非人群之间发生了种间传播。