Chen Nanhai, Li Guiyun, Liszewski M Kathryn, Atkinson John P, Jahrling Peter B, Feng Zehua, Schriewer Jill, Buck Charles, Wang Chunlin, Lefkowitz Elliot J, Esposito Joseph J, Harms Tiara, Damon Inger K, Roper Rachel L, Upton Chris, Buller R Mark L
Department of Molecular Microbiology and Immunology, Saint Louis University Health Sciences Center, M432, St. Louis, MO 63104, USA.
Virology. 2005 Sep 15;340(1):46-63. doi: 10.1016/j.virol.2005.05.030.
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 D10L, D14L, B10R, B14R, and B19R as possible virulence genes, with D14L (ortholog of vaccinia complement protein) as a leading candidate.
研究表明,猴痘病毒(MPXV)的西非分离株和刚果盆地分离株在基因上是不同的。在这里,我们表明,与假定的西非MPXV-COP-58相比,刚果盆地的MPXV-ZAI-V79对食蟹猴的毒性更强。这一发现可能解释了2003年美国猴痘疫情中为何没有病例死亡,那次疫情是由一种西非病毒引起的。西非和刚果盆地MPXV之间的毒力差异进一步得到了流行病学分析的支持,该分析观察到两个地区未接种疫苗的人群中抗体流行率相似,而报告病例的90%以上发生在刚果盆地,该地区以外未观察到死亡病例。为了确定这种毒力差异的基础,我们对一株人类西非分离株、两株假定的西非分离株的基因组进行了测序,并将这些序列与刚果盆地的MPXV-ZAI-96-I-16进行了比较。分析确定D10L、D14L、B10R、B14R和B19R为可能的毒力基因,其中D14L(痘苗补体蛋白的直系同源物)是主要候选基因。