Dittmer D, Stoddart C, Renne R, Linquist-Stepps V, Moreno M E, Bare C, McCune J M, Ganem D
Department of Microbiology, University of California, San Francisco, California 94143, USA.
J Exp Med. 1999 Dec 20;190(12):1857-68. doi: 10.1084/jem.190.12.1857.
Kaposi's sarcoma-associated herpesvirus (KSHV/HHV-8) is a novel human lymphotropic herpesvirus linked to several human neoplasms. To date, no animal model for infection by this virus has been described. We have examined the susceptibility of C.B-17 scid/scid mice implanted with human fetal thymus and liver grafts (SCID-hu Thy/Liv mice) to KSHV infection. KSHV virions were inoculated directly into the implants, and viral DNA and mRNA production was assayed using real-time quantitative polymerase chain reaction. This revealed a biphasic infection, with an early phase of lytic replication accompanied and followed by sustained latency. Ultraviolet irradiation of the inoculum abolished all DNA- and mRNA-derived signals, and infection was inhibited by ganciclovir. Viral gene expression was most abundant in CD19(+) B lymphocytes, suggesting that this model faithfully mimics the natural tropism of this virus. Short-term coinfection with HIV-1 did not alter the course of KSHV replication, nor did KSHV alter levels of HIV-1 p24 during the acute phase of the infection. Although no disease was evident in infected animals, SCID-hu Thy/Liv mice should allow the detailed study of KSHV tropism, latency, and drug susceptibility.
卡波西肉瘤相关疱疹病毒(KSHV/HHV - 8)是一种新型的嗜人淋巴细胞疱疹病毒,与多种人类肿瘤相关。迄今为止,尚未有关于该病毒感染的动物模型的描述。我们检测了植入人胎儿胸腺和肝脏移植物的C.B - 17 scid/scid小鼠(SCID - hu Thy/Liv小鼠)对KSHV感染的易感性。将KSHV病毒粒子直接接种到移植物中,并使用实时定量聚合酶链反应检测病毒DNA和mRNA的产生。这显示出一种双相感染,早期为裂解复制阶段,随后是持续的潜伏期。对接种物进行紫外线照射消除了所有DNA和mRNA衍生的信号,并且感染被更昔洛韦抑制。病毒基因表达在CD19(+) B淋巴细胞中最为丰富,这表明该模型忠实地模拟了这种病毒的天然嗜性。与HIV - 1的短期共感染并未改变KSHV复制的进程,在感染急性期KSHV也未改变HIV - 1 p24的水平。尽管在感染动物中未观察到明显疾病,但SCID - hu Thy/Liv小鼠应能用于详细研究KSHV的嗜性、潜伏期和药物敏感性。