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在对恒河猴进行阴道接种后,寨卡病毒优先在雌性生殖道中复制。

Zika virus preferentially replicates in the female reproductive tract after vaginal inoculation of rhesus macaques.

作者信息

Carroll Timothy, Lo Ming, Lanteri Marion, Dutra Joseph, Zarbock Katie, Silveira Paola, Rourke Tracy, Ma Zhong-Min, Fritts Linda, O'Connor Shelby, Busch Michael, Miller Christopher J

机构信息

Center for Comparative Medicine University of California, Davis, Davis, California, United States of America.

California National Primate Research Center, University of California, Davis, Davis, California, United States of America.

出版信息

PLoS Pathog. 2017 Jul 26;13(7):e1006537. doi: 10.1371/journal.ppat.1006537. eCollection 2017 Jul.

Abstract

Zika virus (ZIKV) is a mosquito-transmitted virus that can cause severe defects in an infected fetus. ZIKV is also transmitted by sexual contact, although the relative importance of sexual transmission is unclear. To better understand the role of sexual transmission in ZIKV pathogenesis, a nonhuman primate (NHP) model of vaginal transmission was developed. ZIKV was readily transmitted to mature cycling female rhesus macaque (RM) by vaginal inoculation with 104-106 plaque-forming units (PFU). However, there was variability in susceptibility between the individual RM with 1->8 vaginal inoculations required to establish infection. After treatment with Depoprovera, a widely used contraceptive progestin, two RM that initially resisted 8 vaginal ZIKV inoculations became infected after one ZIKV inoculation. Thus, Depoprovera seemed to enhance susceptibility to vaginal ZIKV transmission. Unexpectedly, the kinetics of virus replication and dissemination after intravaginal ZIKV inoculation were markedly different from RM infected with ZIKV by subcutaneous (SQ) virus inoculation. Several groups have reported that after SQ ZIKV inoculation vRNA is rapidly detected in blood plasma with vRNA less common in urine and saliva and only rarely detected in female reproductive tract (FRT) secretions. In contrast, in vaginally inoculated RM, plasma vRNA is delayed for several days and ZIKV replication in, and vRNA shedding from, the FRT was found in all 6 animals. Further, after intravaginal transmission ZIKV RNA shedding from FRT secretions was detected before or simultaneously with plasma vRNA, and persisted for at least as long. Thus, ZIKV replication in the FRT was independent of, and often preceded virus replication in the tissues contributing to plasma vRNA. These results support the conclusion that ZIKV preferentially replicates in the FRT after vaginal transmission, but not after SQ transmission, and raise the possibility that there is enhanced fetal infection and pathology after vaginal ZIKV transmission compared to a mosquito transmitted ZIKV.

摘要

寨卡病毒(ZIKV)是一种通过蚊子传播的病毒,可导致受感染胎儿出现严重缺陷。寨卡病毒也可通过性接触传播,尽管性传播的相对重要性尚不清楚。为了更好地了解性传播在寨卡病毒发病机制中的作用,建立了一种阴道传播的非人灵长类动物(NHP)模型。通过阴道接种104 - 106个空斑形成单位(PFU),寨卡病毒很容易传播给成熟的处于发情周期的雌性恒河猴(RM)。然而,个体恒河猴之间的易感性存在差异,需要1至8次阴道接种才能建立感染。在用广泛使用的避孕孕激素醋酸甲羟孕酮治疗后,最初抵抗8次阴道寨卡病毒接种的两只恒河猴在一次寨卡病毒接种后被感染。因此,醋酸甲羟孕酮似乎增强了对阴道寨卡病毒传播的易感性。出乎意料的是,阴道接种寨卡病毒后病毒复制和传播的动力学与通过皮下(SQ)接种病毒感染寨卡病毒的恒河猴明显不同。几个研究小组报告说,皮下接种寨卡病毒后,血浆中很快就能检测到病毒RNA(vRNA),尿液和唾液中较少见,在女性生殖道(FRT)分泌物中则很少检测到。相比之下,在阴道接种的恒河猴中,血浆vRNA的出现延迟了几天,并且在所有6只动物中都发现了寨卡病毒在FRT中的复制以及FRT中vRNA的脱落。此外,阴道传播后,在血浆vRNA之前或同时检测到FRT分泌物中寨卡病毒RNA的脱落,并且持续时间至少相同。因此,寨卡病毒在FRT中的复制独立于并常常先于对血浆vRNA有贡献的组织中的病毒复制。这些结果支持了这样的结论,即寨卡病毒在阴道传播后优先在FRT中复制,但在皮下传播后则不然,并且提出了与蚊子传播的寨卡病毒相比,阴道传播寨卡病毒后胎儿感染和病理情况可能增加的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fdf/5546709/827d2a110568/ppat.1006537.g001.jpg

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