Expectoration of flaviviruses during sugar feeding by mosquitoes (Diptera: Culicidae)

被引:0
作者
Van den Hurk, Andrew F. [1 ]
Johnson, Petrina H.
Hall-Mendelin, Sonja
Northill, Judy A.
Simmons, Russell J.
Jansen, Cassie C.
Frances, Stephen P.
Smitil, Greg A.
Ritchie, Scott A.
机构
[1] Queensland Hlth Sci Serv, Coopers Plains 4108, Australia
[2] Univ Queensland, Sch Mol & Microbial Sci, Dept Microbiol & Parasitol, St Lucia, Qld 4072, Australia
[3] Univ Queensland, Australian Biosecur Cooperat Res Ctr, St Lucia, Qld 4072, Australia
[4] Australian Army Malaria Inst, Enoggera, Qld 4052, Australia
[5] Queensland Hlth, Trop Populat Hlth Unit, Cairns 4870, Australia
[6] James Cook Univ N Queensland, Sch Publ Hlth & Trop Med, Cairns, Qld 4870, Australia
关键词
mosquito; Flavivirus; saliva; sucrose; expectoration;
D O I
10.1603/0022-2585(2007)44[845:EOFDSF]2.0.CO;2
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Biological transmission of arboviruses to a vertebrate host occurs when virions are expelled along with saliva during blood feeding by a hematophagous arthropod. We undertook experiments to determine whether mosquitoes expectorate flaviviruses in their saliva while sugar feeding. Batches of Culex annuhrostris Skuse and Culex gelidus Theobald (Diptera: Culicidae) were orally infected with Japanese encephalitis (family Flaviviridae, genus Flavivirus, JEV), Kunjin (family Flaviviridae, genus Flavivirus, KUNV; a subtype of West Nile virus), and Murray Valley encephalitis (family Flaviviridae, genus Flaviviris, MVEV) viruses. After a 7-d extrinsic incubation, these mosquitoes were offered sucrose meals via cotton pledgets, which were removed daily and processed for viral RNA by using real-time TaqMan reverse transcriptase-polymerase chain reaction (RT-PCR) assays. JEV, MVEV, and KUNV RNA was detected in all pledgets removed from batches of Cx, gelidus on days 7-14 postexposure. In contrast, detection rates were variable for Cx. annuhrostris, with KUNV detected in 0.3 M sucrose pledgets on all days postexposure, and JEV and MVEV detected on 57 and 50% of days postexposure, respectively. Higher concentrations of sucrose in the pledget did not increase virus detection rates. When individual JEV-infected Cx. gelidus were exposed to the sucrose pledget, 73% of mosquitoes expectorated virus with titers that were detectable by TaqMan RT-PCR. These results clearly show that flaviviruses are expectorated by infected mosquitoes during the process of sugar feeding on artificial pledgets. Potential applications of the method for arboviral bioassays and field surveillance are discussed.
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页码:845 / 850
页数:6
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