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安哥拉马尔堡病毒的毒力与在猕猴中的姆特-Elgon(Musoke)病毒相比:一项汇总生存分析。

Virulence of Marburg Virus Angola Compared to Mt. Elgon (Musoke) in Macaques: A Pooled Survival Analysis.

机构信息

Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.

出版信息

Viruses. 2018 Nov 21;10(11):658. doi: 10.3390/v10110658.

DOI:10.3390/v10110658
PMID:30469360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6267608/
Abstract

Angola variant (MARV/Ang) has replaced Mt. Elgon variant Musoke isolate (MARV/MtE-Mus) as the consensus standard variant for Marburg virus research and is regarded as causing a more aggressive phenotype of disease in animal models; however, there is a dearth of published evidence supporting the higher virulence of MARV/Ang. In this retrospective study, we used data pooled from eight separate studies in nonhuman primates experimentally exposed with either 1000 pfu intramuscular (IM) MARV/Ang or MARV/MtE-Mus between 2012 and 2017 at the United States Army Medical Research Institute of Infectious Diseases (USAMRIID). Multivariable Cox proportional hazards regression was used to evaluate the association of variant type with time to death, the development of anorexia, rash, viremia, and 10 select clinical laboratory values. A total of 47 cynomolgus monkeys were included, of which 18 were exposed to MARV/Ang in three separate studies and 29 to MARV/MtE-Mus in five studies. Following universally fatal Marburg virus exposure, compared to MARV/MtE-Mus, MARV/Ang was associated with an increased risk of death (HR = 22.10; 95% CI: 7.08, 68.93), rash (HR = 5.87; 95% CI: 2.76, 12.51) and loss of appetite (HR = 35.10; 95% CI: 7.60, 162.18). Our data demonstrate an increased virulence of MARV/Ang compared to MARV/MtE-Mus variant in the 1000 pfu IM cynomolgus macaque model.

摘要

安哥拉变体 (MARV/Ang) 已取代埃尔贡山变体 Musoke 分离株 (MARV/MtE-Mus),成为马尔堡病毒研究的共识标准变体,并且被认为在动物模型中引起更具侵袭性的疾病表型;然而,支持 MARV/Ang 更高毒力的已发表证据很少。在这项回顾性研究中,我们使用了 2012 年至 2017 年间在美国陆军传染病医学研究所 (USAMRIID) 进行的八项非人类灵长类动物实验中,分别用 1000 感染性剂量 (ID) 肌内 (IM) MARV/Ang 或 MARV/MtE-Mus 暴露的 8 项单独研究的数据。多变量 Cox 比例风险回归用于评估变体类型与死亡时间、厌食、皮疹、病毒血症和 10 种选择的临床实验室值之间的关联。共纳入 47 只食蟹猴,其中 18 只在三项单独研究中暴露于 MARV/Ang,29 只在五项研究中暴露于 MARV/MtE-Mus。与普遍致命的马尔堡病毒暴露后相比,MARV/Ang 与死亡风险增加相关(HR = 22.10;95%CI:7.08,68.93)、皮疹(HR = 5.87;95%CI:2.76,12.51)和食欲不振(HR = 35.10;95%CI:7.60,162.18)。我们的数据表明,在 1000 ID IM 食蟹猕猴模型中,MARV/Ang 的毒力比 MARV/MtE-Mus 变体增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/124e41965b06/viruses-10-00658-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/024649d480f3/viruses-10-00658-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/a04677f1206f/viruses-10-00658-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/6c17d7ffcb8f/viruses-10-00658-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/124e41965b06/viruses-10-00658-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/024649d480f3/viruses-10-00658-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/a04677f1206f/viruses-10-00658-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/6c17d7ffcb8f/viruses-10-00658-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6267608/124e41965b06/viruses-10-00658-g004.jpg

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