Molecular Virology Division, St Luke's-Roosevelt Hospital Center, Columbia University Medical Center, New York, NY 10019, USA.
Dis Model Mech. 2013 Sep;6(5):1292-8. doi: 10.1242/dmm.012617. Epub 2013 Jul 25.
Heterosexual transmission accounts for the majority of new human immunodeficiency virus (HIV) cases worldwide. The current approach to investigate HIV heterosexual transmission in animals involves application of virus stock to the vaginal surface, a method that does not reproduce the physiological conditions of vaginal intercourse that influence the rate of transmission. We have previously described efficient infection of conventional mice using EcoHIV/NL4-3 and EcoHIV/NDK, chimeric HIV molecular clones constructed to express all HIV structural and regulatory genes except envelope, which is replaced by a rodent-tropic envelope gene. Here we investigated whether EcoHIV/NDK-infected male mice transmit virus to females during coitus, and the sensitivity of this transmission to HIV pre-exposure prophylaxis and the estrus state. Our general approach was to allow mating between EcoHIV/NDK-infected male mice and uninfected females for 1-7 nights. At 1-6 weeks after mating, mice were euthanized and virus burdens were measured by quantitative PCR (qPCR) amplification of HIV RNA or DNA in peritoneal macrophages, inguinal lymph node cells, spleen cells or vas deferens, or by ELISA for antibodies to HIV Gag. We found that 70-100% of female mice mated to EcoHIV/NDK-infected males acquired infection. Pericoital treatment of females with either 2',3'-dideoxcytidine (ddC) or tenofovir largely prevented their EcoHIV/NDK infection by mating (P<0.05 and P<0.003, respectively). In males, T cells were dispensable for virus transmission. The rate of EcoHIV/NDK sexual transmission to females in estrus declined sharply (P=0.003) but their infection by injection was unaffected, indicating that the local environment in the female reproductive tract influences susceptibility to HIV. We conclude that this system of EcoHIV/NDK transmission during mouse mating reproduces key features of heterosexual transmission of HIV in humans and can be used to investigate its biology and control.
异性传播占全球新发生人类免疫缺陷病毒 (HIV) 感染病例的大多数。目前,研究动物中 HIV 异性传播的方法是将病毒株应用于阴道表面,这种方法不能复制影响传播率的阴道性交生理条件。我们之前曾描述过使用 EcoHIV/NL4-3 和 EcoHIV/NDK 有效感染常规小鼠,这两种嵌合 HIV 分子克隆构建用于表达所有 HIV 结构和调节基因,除了被啮齿动物嗜性包膜基因取代的包膜基因。在这里,我们研究了 EcoHIV/NDK 感染的雄性小鼠在交配期间是否将病毒传播给雌性,以及这种传播对 HIV 暴露前预防和发情状态的敏感性。我们的一般方法是允许 EcoHIV/NDK 感染的雄性小鼠与未感染的雌性小鼠交配 1-7 晚。在交配后 1-6 周,处死小鼠并通过定量 PCR (qPCR) 扩增腹腔巨噬细胞、腹股沟淋巴结细胞、脾细胞或输精管中的 HIV RNA 或 DNA 或通过 ELISA 检测针对 HIV Gag 的抗体来测量病毒载量。我们发现,与感染 EcoHIV/NDK 的雄性小鼠交配的 70-100%雌性小鼠获得了感染。在发情期,对雌性进行 pericoital 治疗,用 2',3'-双脱氧胞苷 (ddC) 或替诺福韦治疗,在很大程度上防止了她们通过交配感染 EcoHIV/NDK (P<0.05 和 P<0.003,分别)。在雄性中,T 细胞对病毒传播不是必需的。EcoHIV/NDK 对发情期雌性的性传播率急剧下降(P=0.003),但它们通过注射感染不受影响,表明雌性生殖道的局部环境会影响对 HIV 的易感性。我们得出结论,这种在小鼠交配期间 EcoHIV/NDK 传播的系统复制了人类中 HIV 异性传播的关键特征,可以用于研究其生物学和控制。