L. Mugisha, C. Kücherer, H. Ellerbrok, S. Junglen, J. Opuda-Asibo, O. Joseph, G. Pauli, F. Leendertz
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引用次数: 10
摘要
关于类人猿中逆转录病毒感染的信息很少,特别是非洲各地保护区的类人猿。为了调查逆转录病毒的流行情况以及来自不同国家(乌干达、刚果和卢旺达)的黑猩猩的不同逆转录病毒的可能传播情况,对居住在恩甘巴岛一个保护区的38只野生圈养孤儿黑猩猩进行了逆转录病毒感染分析。使用酶联免疫测定和聚合酶链反应(PCR)对保护区黑猩猩的样本进行了分析。通过系统发育分析对病毒进行了表征。所有黑猩猩的猴免疫缺陷病毒(SIV)和猴t细胞白血病病毒(STLV)抗体均为阴性。然而,28/38(73%)黑猩猩对SFV病毒(Simian foam Virus, SFV)呈阳性,这是利用聚合酶基因高度保守部分同源的通用整合酶引物通过PCR获得的425 bp DNA片段进行分析得到的结果。本研究获得的SFV序列的系统发育分析在特定的SFV p.t . schweinfurthii分支中形成了四个亚群,并且在新的SFV菌株之间存在显著的差异。我们提供的证据表明,在保护区内的黑猩猩中,SFV的交叉传播很可能是通过水平途径进行的。我们建议对所有被引入保护区的黑猩猩进行抗逆转录病毒和其他感染的测试。这也将有助于避免致病性病毒在圈养种群中传播。
Retroviruses in Wild-Born Semi-Captive East African Sanctuary Chimpanzees (Pan troglodytes schweinfurthii)
Information on retroviruses infections in great apes is scarce, especially for apes kept in sanctuaries throughout Africa. To investigate the prevalence of retroviruses and possible transmission of different retroviruses originating from chimpanzees of different origin (Uganda, Congo and Rwanda), 38 wild-born captive orphan chimpanzees residing in a sanctuary on Ngamba Island were analyzed for retroviral infections. Samples from sanctuary chimpanzees were analyzed using enzyme-linked immunoassays and polymerase chain reactions (PCR). Viruses were characterized by phylogenetic analysis. All chimpanzees were negative for antibodies against Simian Immunodeficiency Virus (SIV) and Simian T-cell Leukemia Virus (STLV). However, 28/38 (73%) chimpanzees were positive to Simian Foamy Virus (SFV) by analysis of a 425-bp DNA segment obtained by PCR using generic integrase primers homologous to highly conserved portions of the polymerase gene. Phylogenetic analysis of SFV sequences obtained in this study formed four sub clusters within the specific SFV P. t. schweinfurthii clade with significant variability among the new SFVs strains. We provide evidence of on-going cross-transmission of SFV among chimpanzees within the sanctuary mostly likely through horizontal routes. We propose to test all chimpanzees introduced into sanctuaries for retroviral and other infections. This will help avoid the spread also of pathogenic viruses in captive populations.