Bird Brian H, Githinji Jane W K, Macharia Joseph M, Kasiiti Jacqueline L, Muriithi Rees M, Gacheru Stephen G, Musaa Joseph O, Towner Jonathan S, Reeder Serena A, Oliver Jennifer B, Stevens Thomas L, Erickson Bobbie R, Morgan Laura T, Khristova Marina L, Hartman Amy L, Comer James A, Rollin Pierre E, Ksiazek Thomas G, Nichol Stuart T
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, Coordinating Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, MS G-14, Atlanta, GA 30329, USA.
J Virol. 2008 Nov;82(22):11152-66. doi: 10.1128/JVI.01519-08. Epub 2008 Sep 10.
Rift Valley fever (RVF) virus historically has caused widespread and extensive outbreaks of severe human and livestock disease throughout Africa, Madagascar, and the Arabian Peninsula. Following unusually heavy rainfall during the late autumn of 2006, reports of human and animal illness consistent with RVF virus infection emerged across semiarid regions of the Garissa District of northeastern Kenya and southern Somalia. Following initial RVF virus laboratory confirmation, a high-throughput RVF diagnostic facility was established at the Kenyan Central Veterinary Laboratories in Kabete, Kenya, to support the real-time identification of infected livestock and to facilitate outbreak response and control activities. A total of 3,250 specimens from a variety of animal species, including domesticated livestock (cattle, sheep, goats, and camels) and wildlife collected from a total of 55 of 71 Kenyan administrative districts, were tested by molecular and serologic assays. Evidence of RVF infection was found in 9.2% of animals tested and across 23 districts of Kenya, reflecting the large number of affected livestock and the geographic extent of the outbreak. The complete S, M, and/or L genome segment sequence was obtained from a total of 31 RVF virus specimens spanning the entire known outbreak period (December-May) and geographic areas affected by RVF virus activity. Extensive genomic analyses demonstrated the concurrent circulation of multiple virus lineages, gene segment reassortment, and the common ancestry of the 2006/2007 outbreak viruses with those from the 1997-1998 east African RVF outbreak. Evidence of recent increases in genomic diversity and effective population size 2 to 4 years prior to the 2006-2007 outbreak also was found, indicating ongoing RVF virus activity and evolution during the interepizootic/epidemic period. These findings have implications for further studies of basic RVF virus ecology and the design of future surveillance/diagnostic activities, and they highlight the critical need for safe and effective vaccines and antiviral compounds to combat this significant veterinary and public health threat.
裂谷热(RVF)病毒在历史上曾在非洲、马达加斯加和阿拉伯半岛引发广泛而严重的人畜疾病疫情。2006年秋末降雨异常充沛后,肯尼亚东北部加里萨区和索马里南部的半干旱地区出现了与裂谷热病毒感染相符的人畜患病报告。在裂谷热病毒得到实验室初步确认后,肯尼亚中央兽医实验室在卡贝特设立了一个高通量裂谷热诊断设施,以支持对感染牲畜的实时识别,并促进疫情应对和控制活动。对从肯尼亚71个行政区中的55个行政区采集的包括家畜(牛、绵羊、山羊和骆驼)和野生动物在内的各种动物物种的3250份样本进行了分子和血清学检测。在9.2%的检测动物中以及肯尼亚的23个行政区发现了裂谷热感染证据,这反映出受影响牲畜数量众多以及疫情的地理范围。从跨越整个已知疫情期(12月至5月)以及受裂谷热病毒活动影响的地理区域的总共31份裂谷热病毒样本中获得了完整的S、M和/或L基因组片段序列。广泛的基因组分析表明多种病毒谱系同时传播、基因片段重配,以及2006/2007年疫情病毒与1997 - 1998年东非裂谷热疫情病毒有着共同的祖先。还发现了在2006 - 2007年疫情前2至4年基因组多样性和有效种群大小近期增加的证据,这表明在动物间流行期/流行期期间裂谷热病毒持续活动和进化。这些发现对进一步研究裂谷热病毒基础生态学以及未来监测/诊断活动的设计具有启示意义,并且凸显了对抗这种重大兽医和公共卫生威胁的安全有效疫苗和抗病毒化合物的迫切需求。