van Doorn L J, Quint W, Tsiquaye K, Voermans J, Paelinck D, Kos T, Maertens G, Schellekens H, Murray K
Diagnostic Center SSDZ, Delft, Netherlands.
J Infect Dis. 1994 Jun;169(6):1226-35. doi: 10.1093/infdis/169.6.1226.
Hepatitis C virus (HCV) infections in a cohort of chimpanzees were studied retrospectively. All animals had been inoculated intravenously with materials derived from a single-source chimpanzee plasma implicated in non-A, non-B hepatitis, prepared by extensive ultracentrifugation. Anti-HCV and HCV RNA were monitored by the confirmatory line immunoassay and by an RNA-capture polymerase chain reaction method, respectively. In a chronically infected chimpanzee, HCV RNA was detectable after 32 days and throughout the acute phase, dropped transiently below detection level, and became detectable again. In 3 other chimpanzees with acute resolving infections, HCV RNA was detected 7-11 days after inoculation and became permanently undetectable after alanine aminotransferase normalization. Various anti-HCV profiles were detected among the chimpanzees. Analysis of the hypervariable region in E2/NS1 in 7 chimpanzees suggested genome stability on transmission, revealed different mutation frequencies during chronic infection, and suggested the importance of immune selection during chronic HCV infection.
对一组黑猩猩的丙型肝炎病毒(HCV)感染情况进行了回顾性研究。所有动物均通过静脉注射由大量超速离心制备的、来自一只涉及非甲非乙型肝炎的单一来源黑猩猩血浆的材料。分别采用确证线免疫分析法和RNA捕获聚合酶链反应法监测抗HCV和HCV RNA。在一只慢性感染的黑猩猩中,接种32天后及整个急性期均检测到HCV RNA,其短暂降至检测水平以下,随后又再次可检测到。在另外3只急性感染消退的黑猩猩中,接种后7 - 11天检测到HCV RNA,在丙氨酸转氨酶恢复正常后永久无法检测到。在黑猩猩中检测到了各种抗HCV谱。对7只黑猩猩E2/NS1高变区的分析表明,病毒在传播过程中基因组稳定,揭示了慢性感染期间不同的突变频率,并提示了慢性HCV感染期间免疫选择的重要性。