Virulence differences between monkeypox virus isolates from West Africa and the Congo basin

被引:349
作者
Chen, NH
Li, GY
Liszewski, MK
Atkinson, JP
Jahrling, PB
Feng, ZH
Schriewer, J
Buck, C
Wang, CL
Lefkowitz, EJ
Esposito, JJ
Harms, T
Damon, IK
Roper, RL
Upton, C
Buller, RML
机构
[1] St Louis Univ, Hlth Sci Ctr, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
[2] Univ Victoria, Dept Biochem & Microbiol, Victoria, BC V8W 2Y2, Canada
[3] Washington Univ, Sch Med, Dept Internal Med, Div Rheumatol, St Louis, MO 63110 USA
[4] USA, Res Inst Infect Dis, Headquarters, Ft Detrick, MD 21702 USA
[5] ATCC, Virol Collect, Manassas, VA 20108 USA
[6] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[7] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, Atlanta, GA 30333 USA
[8] E Carolina Univ, Brody Sch Med, Dept Microbiol & Immunol, Greenville, NC 27834 USA
关键词
monkeypox; genomic sequences; genetic diversity; virulence genes; non-human primates;
D O I
10.1016/j.virol.2005.05.030
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Studies indicate that West African and Congo basin isolates of monkeypox virus (MPXV) are genetically distinct. Here, we show Congo basin MPXV-ZAI-V79 is more virulent for cynomolgus monkeys as compared to presumed West African MPXV-COP-58. This finding may explain the lack of case-fatalities in the U.S. 2003 monkeypox outbreak, which was caused by a West African virus. Virulence differences between West African and Congo basin MPXV are further supported by epidemiological analyses that observed a similar prevalence of antibodies in non-vaccinated humans in both regions, while > 90% of reported cases occurred in the Congo basin, and no fatal cases were observed outside of this region. To determine the basis for this difference in virulence, we sequenced the genomes of one human West African isolate, and two presumed West African isolates and compared the sequences to Congo basin MPXV-ZAI-96-I-16. The analysis identified DIOL, D14L, B10R, B14R, and B19R as possible virulence genes, with D14L (ortholog of vaccinia complement protein) as a leading candidate. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:46 / 63
页数:18
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