Wong Gary, Qiu Xiangguo, de La Vega Marc-Antoine, Fernando Lisa, Wei Haiyan, Bello Alexander, Fausther-Bovendo Hugues, Audet Jonathan, Kroeker Andrea, Kozak Robert, Tran Kaylie, He Shihua, Tierney Kevin, Soule Geoff, Moffat Estella, Günther Stephan, Gao George F, Strong Jim, Embury-Hyatt Carissa, Kobinger Gary
Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada Department of Medical Microbiology CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing.
Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada Department of Medical Microbiology.
J Infect Dis. 2016 Oct 15;214(suppl 3):S281-S289. doi: 10.1093/infdis/jiw267. Epub 2016 Sep 19.
Enhanced virulence and/or transmission of West African Ebola virus (EBOV) variants, which are divergent from their Central African counterparts, are suspected to have contributed to the sizable toll of the recent Ebola virus disease (EVD) outbreak. This study evaluated the pathogenicity and shedding in rhesus macaques infected with 1 of 2 West African isolates (EBOV-C05 or EBOV-C07) or a Central African isolate (EBOV-K). All animals infected with EBOV-C05 or EBOV-C07 died of EVD, whereas 2 of 3 EBOV-K-infected animals died. The viremia level was elevated 10-fold in EBOV-C05-infected animals, compared with EBOV-C07- or EBOV-K-infected animals. More-severe lung pathology was observed in 2 of 6 EBOV-C05/C07-infected macaques. This is the first detailed analysis of the recently circulating EBOV-C05/C07 in direct comparison to EBOV-K with 6 animals per group, and it showed that EBOV-C05 but not EBOV-C07 can replicate at higher levels and cause more tissue damage in some animals. Increased virus shedding from individuals who are especially susceptible to EBOV replication is possibly one of the many challenges facing the community of healthcare and policy-making responders since the beginning of the outbreak.
与中非埃博拉病毒(EBOV)毒株不同的西非EBOV变种的毒力和/或传播能力增强,被怀疑是导致近期埃博拉病毒病(EVD)疫情造成重大伤亡的原因。本研究评估了恒河猴感染2种西非分离株(EBOV-C05或EBOV-C07)之一或1种中非分离株(EBOV-K)后的致病性和病毒脱落情况。所有感染EBOV-C05或EBOV-C07的动物均死于EVD,而3只感染EBOV-K的动物中有2只死亡。与感染EBOV-C07或EBOV-K的动物相比,感染EBOV-C05的动物病毒血症水平升高了10倍。在6只感染EBOV-C05/C07的猕猴中,有2只出现了更严重的肺部病理变化。这是首次对最近流行的EBOV-C05/C07与EBOV-K进行直接比较的详细分析,每组6只动物,结果显示EBOV-C05而非EBOV-C07能够在某些动物体内更高水平地复制并造成更多组织损伤。自疫情爆发以来,特别易受EBOV复制影响的个体病毒脱落增加,可能是医疗保健和政策应对群体面临的众多挑战之一。