Reisen William K, Fang Ying, Lothrop Hugh D, Martinez Vincent M, Wilson Jennifer, Oconnor Paul, Carney Ryan, Cahoon-Young Barbara, Shafii Marzieh, Brault Aaron C
Department of Pathology, Microbiology and Immunology, Center for Vectorborne Diseases, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
J Med Entomol. 2006 Mar;43(2):344-55. doi: 10.1603/0022-2585(2006)043[0344:oownvi]2.0.co;2.
West Nile virus (family Flaviviridae, genus Flavivirus, WNV) invaded southern California during 2003, successfully overwintered, amplified to epidemic levels, and then dispersed to every county in the state. Although surveillance programs successfully tracked and measured these events, mechanisms that allowed the efficient overwintering and subsequent amplification of WNV have not been elucidated. Our current research provided evidence for three mechanisms whereby WNV may have persisted in southern California during the winters of 2003-2004 and 2004-2005: 1) continued enzootic transmission, 2) vertical transmission by Culex mosquitoes, and 3) chronic infection in birds. WNV was detected in 140 dead birds comprising 32 species, including 60 dead American crows, thereby verifying transmission during the November-March winter period. Dead American crows provide evidence of recent transmission because this species always succumbs rapidly after infection. However, WNV RNA was not detected concurrently in 43,043 reproductively active female mosquitoes comprising 11 species and tested in 1,258 pools or antibody in sera from 190 sentinel chickens maintained in 19 flocks. Although efficient vertical transmission by WNV was demonstrated experimentally for Culex tarsalis Coquillett infected per os, 369 females collected diapausing in Kern County and tested in 32 pools were negative for WNV. Vertical transmission was detected in Culex pipiens quinquefasciatus Say adults reared from field-collected immatures collected from Kern County and Los Angeles during the summer transmission period. Chronic infection was detected by finding WNV RNA in 34 of 82 birds that were inoculated with WNV experimentally, held for >6 wk after infection, and then necropsied. Frequent detection of WNV RNA in kidney tissue in experimentally infected birds >6 wk postinfection may explain, in part, the repeated detection of WNV RNA in dead birds recovered during winter, especially in species such as mourning doves that typically do not die after experimental infection. In summary, our study provides limited evidence to support multiple modes of WNV persistence i n southern California. Continued transmission andvertical transmission by Culex p. quinquefasciatus Say seem likely candidates for further study.
西尼罗河病毒(黄病毒科黄病毒属,WNV)于2003年侵入南加利福尼亚,成功越冬,数量扩增至流行水平,随后扩散至该州的每个县。尽管监测计划成功追踪并衡量了这些事件,但西尼罗河病毒高效越冬及随后数量扩增的机制仍未阐明。我们目前的研究为西尼罗河病毒在2003 - 2004年及2004 - 2005年冬季于南加利福尼亚持续存在的三种机制提供了证据:1)持续的动物间传播;2)库蚊的垂直传播;3)鸟类的慢性感染。在140只死亡鸟类中检测到西尼罗河病毒,这些鸟类分属32个物种,其中包括60只死亡的美洲乌鸦,从而证实了在11月至次年3月的冬季期间存在病毒传播。死亡的美洲乌鸦为近期传播提供了证据,因为该物种在感染后总是很快死亡。然而,在43043只处于繁殖期的雌蚊(分属11个物种,共1258池)以及19群中190只哨兵鸡的血清中均未同时检测到西尼罗河病毒RNA或抗体。尽管通过实验证明,经口感染的塔尔西斯库蚊(Culex tarsalis Coquillett)存在高效垂直传播,但在克恩县采集的369只滞育雌蚊(共32池)中未检测到西尼罗河病毒。在夏季传播期从克恩县和洛杉矶采集的野外未成熟幼虫饲养的致倦库蚊(Culex pipiens quinquefasciatus Say)成虫中检测到垂直传播。在82只经实验接种西尼罗河病毒、感染后饲养超过6周然后进行尸检的鸟类中,有34只检测到慢性感染。感染后6周以上的实验感染鸟类肾脏组织中频繁检测到西尼罗河病毒RNA,这可能部分解释了在冬季回收的死亡鸟类中反复检测到西尼罗河病毒RNA的现象,尤其是在诸如哀鸽等通常在实验感染后不会死亡的物种中。总之,我们的研究提供了有限的证据来支持西尼罗河病毒在南加利福尼亚持续存在的多种模式。致倦库蚊的持续传播和垂直传播似乎是值得进一步研究的可能因素。