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非人类灵长类动物在结膜暴露于埃博拉病毒后的自然史。

Natural history of nonhuman primates after conjunctival exposure to Ebola virus.

机构信息

Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, 77550, USA.

Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77550, USA.

出版信息

Sci Rep. 2023 Mar 13;13(1):4175. doi: 10.1038/s41598-023-31027-7.

Abstract

Transmission of Ebola virus (EBOV) primarily occurs via contact exposure of mucosal surfaces with infected body fluids. Historically, nonhuman primate (NHP) challenge studies have employed intramuscular (i.m.) or small particle aerosol exposure, which are largely lethal routes of infection, but mimic worst-case scenarios such as a needlestick or intentional release, respectively. When exposed by more likely routes of natural infection, limited NHP studies have shown delayed onset of disease and reduced mortality. Here, we performed a series of systematic natural history studies in cynomolgus macaques with a range of conjunctival exposure doses. Challenge with 10,000 plaque forming units (PFU) of EBOV was uniformly lethal, whereas 5/6 subjects survived lower dose challenges (100 or 500 PFU). Conjunctival challenge resulted in a protracted time-to death compared to i.m. Asymptomatic infection was observed in survivors with limited detection of EBOV replication. Inconsistent seropositivity in survivors may suggest physical or natural immunological barriers are sufficient to prevent widespread viral dissemination.

摘要

埃博拉病毒(EBOV)的主要传播途径是接触感染体液的粘膜表面。从历史上看,非人类灵长类动物(NHP)的挑战研究采用了肌肉内(i.m.)或小颗粒气溶胶暴露,这两种途径都是高度致命的感染途径,但分别模拟了最坏情况,例如针刺或故意释放。当通过更可能的自然感染途径暴露时,有限的 NHP 研究表明疾病的发病时间延迟和死亡率降低。在这里,我们用一系列不同剂量的结膜暴露对食蟹猴进行了一系列系统的自然史研究。用 10000 个蚀斑形成单位(PFU)的 EBOV 进行攻毒均导致动物全部死亡,而用 100 或 500 PFU 进行攻毒则有 5/6 的动物存活下来。与肌肉内攻毒相比,结膜攻毒导致动物死亡的时间延长。在幸存者中观察到无症状感染,并且仅检测到有限的 EBOV 复制。幸存者中不一致的血清阳性可能表明物理或自然免疫屏障足以阻止病毒的广泛传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0874/10011569/60e94065769f/41598_2023_31027_Fig1_HTML.jpg

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