Reduced infection in mosquitoes exposed to blood meals containing previously frozen flaviviruses

被引:28
作者
Richards, Stephanie L. [1 ]
Pesko, Kendra [1 ]
Alto, Barry W. [1 ]
Mores, Christopher N. [1 ]
机构
[1] Univ Florida, Inst Food & Agr Sci, Florida Med Entomol Lab, Vero Beach, FL 32962 USA
关键词
flavivirus; artificial feeding; mosquito; arthropod-borne virus;
D O I
10.1016/j.virusres.2007.06.019
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The increased difficulty and expense of using live animals for delivering infectious blood meals in arthropod-borne virus vector experiments has resulted in an increase in the use of artificial feeding systems. Compared to live hosts, artificial systems require higher viral titers to attain mosquito infection, thereby limiting the utility of such systems with low or moderate titer virus stocks. Based on the report that freshly propagated virus is more infectious than previously frozen virus. we determined whether such a preparation would enhance the ability to use artificial feeding systems. Culex quinquefasciatus and Aedes aegypti mosquitoes were offered blood in artificial membrane feeders containing freshly collected or previously frozen St. Louis encephalitis and dengue serotype-2 viruses (family Floviviridae), respectively. Infection rates and estimates of vector competence were significantly lower (P < 0.05) for mosquitoes feeding on blood meals containing frozen-thawed compared to freshly collected virus. We indicate that the use of freshly propagated virus in artificial feeding systems can be an effective blood delivery method for low-titer viruses and viruses that are otherwise inefficient at infecting vectors in such systems. Fresh viruses used in artificial feeding systems may be a viable alternative to the heavily regulated and expensive use of live animals. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:224 / 227
页数:4
相关论文
共 17 条
[1]  
Alto BW, 2003, J AM MOSQUITO CONTR, V19, P347
[2]   Efficiency of dengue serotype 2 virus strains to infect and disseminate in Aedes aegpti [J].
Armstrong, PM ;
Rico-Hesse, R .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2003, 68 (05) :539-544
[3]   Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays [J].
Bustin, SA .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2000, 25 (02) :169-193
[4]   Development and evaluation of serotype- and group-specific fluorogenic reverse transcriptase PCR (TaqMan) assays for dengue virus [J].
Callahan, JD ;
Wu, SJL ;
Dion-Schultz, A ;
Mangold, BE ;
Peruski, LF ;
Watts, DM ;
Porter, KR ;
Murphy, GR ;
Suharyono, W ;
King, CC ;
Hayes, CG ;
Temenak, JJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (11) :4119-4124
[5]   ST-LOUIS ENCEPHALITIS VIRUS IN MOSQUITOES [J].
CHAMBERLAIN, RW ;
SUDIA, WD ;
GILLETT, JD .
AMERICAN JOURNAL OF HYGIENE, 1959, 70 (03) :221-236
[6]   THE EFFECT OF LABORATORY COLONIZATION ON THE VECTOR-PATHOGEN INTERACTIONS OF EGYPTIAN CULEX-PIPIENS AND RIFT-VALLEY FEVER VIRUS [J].
GARGAN, TP ;
BAILEY, CL ;
HIGBEE, GA ;
GAD, A ;
ELSAID, S .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1983, 32 (05) :1154-1163
[7]   VARIATION IN SUSCEPTIBILITY TO ORAL INFECTION WITH DENGUE VIRUSES AMONG GEOGRAPHIC STRAINS OF AEDES-AEGYPTI [J].
GUBLER, DJ ;
NALIM, S ;
TAN, R ;
SAIPAN, H ;
SULIANTISAROSO, J .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1979, 28 (06) :1045-1052
[8]   Mechanisms of inactivation of HSV-2 during storage in frozen and lyophilized forms [J].
Hansen, RK ;
Zhai, SL ;
Skepper, JN ;
Johnston, MD ;
Alpar, HO ;
Slater, NKH .
BIOTECHNOLOGY PROGRESS, 2005, 21 (03) :911-917
[9]  
JUPP PG, 1976, MOSQ NEWS, V36, P166
[10]   Nucleic acid sequence-based amplification assays for rapid detection of West Nile and St. Louis encephalitis viruses [J].
Lanciotti, RS ;
Kerst, AJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (12) :4506-4513