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首页> 外文期刊>Disease models & mechanisms: DMM >Transmission of chimeric HIV by mating in conventional mice: prevention by pre-exposure antiretroviral therapy and reduced susceptibility during estrus
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Transmission of chimeric HIV by mating in conventional mice: prevention by pre-exposure antiretroviral therapy and reduced susceptibility during estrus

机译:通过在传统小鼠中交配来嵌合HIV的传播:通过暴露前抗逆转录病毒疗法的预防和发情期易感性的降低

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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.
机译:异性传播占全世界新的人类免疫缺陷病毒(HIV)病例的大部分。目前调查动物中HIV异性传播的方法涉及将病毒储备液施加到阴道表面,这种方法不会复制影响传播速率的阴道性交生理状况。我们先前已经描述了使用EcoHIV / NL4-3和EcoHIV / NDK对传统小鼠的有效感染,这是一种嵌合HIV分子克隆,被构建为表达除包膜外的所有HIV结构和调节基因,而被包被啮齿类动物的包膜基因所取代。在这里,我们调查了受EcoHIV / NDK感染的雄性小鼠在性交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。我们的一般方法是让感染EcoHIV / NDK的雄性小鼠和未感染的雌性小鼠交配1至7个晚上。交配后1至6周,对小鼠实施安乐死,并通过定量PCR(qPCR)扩增腹膜巨噬细胞,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HIV抗体来测定病毒负担插科打诨。我们发现与EcoHIV / NDK感染的雄性交配的雌性小鼠有70-100%获得了感染。用2',3'-二脱氧胞苷(ddC)或替诺福韦对女性进行的腹膜癌治疗可通过交配很大程度上预防其EcoHIV / NDK感染(分别为P <0.05和P <0.003)。在男性中,T细胞可用于病毒传播。 EcoHIV / NDK对女性发情期性传播的比率急剧下降(P = 0.003),但注射后她们的感染并未受到影响,这表明女性生殖道中的局部环境会影响对HIV的易感性。我们得出的结论是,这种在小鼠交配过程中传播EcoHIV / NDK的系统重现了HIV在人类中的异性传播的关键特征,可用于研究其生物学和控制。

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