Adaptation of two flaviviruses results in differences in genetic heterogeneity and virus adaptability

被引:36
作者
Ciota, Alexander T.
Lovelace, Amy O.
Jones, Susan A.
Payne, Anne
Kramer, Laura D.
机构
[1] New York State Dept Hlth, Wadsworth Ctr, Arbovirus Labs, Slingerlands, NY 12159 USA
[2] SUNY Albany, Sch Publ Hlth, Albany, NY USA
关键词
D O I
10.1099/vir.0.83061-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
West Nile virus (WNV) is a mosquito-borne flavivirus that was first introduced into the USA in the New York City area in 1999. Since its introduction, WNV has steadily increased both its host and geographical ranges. Outbreaks of the closely related flavivirus, St. Louis encephalitis virus (SLEV), occur in the USA periodically, but levels of activity and host range are more restricted than those of WNV. Understanding the selective pressures that drive arbovinus adaptation and evolution in their disparate mosquito and avian hosts is crucial to predicting their ability to persist and re-emerge. Here, we evaluated the in vivo phenotypes of mosquito cell-adapted WNV and SLEV. Results indicated that in vitro adaptations did not translate to in vivo adaptations for either virus, yet SLEV displayed attenuated growth in both mosquitoes and chickens, while WNV generally did not. In vitro growth analyses also indicated that WNV adaptations could be generalized to cell cultures derived from other mosquito species, while SLEV could not. Analysis of genetic diversity for passaged SLEV revealed a highly homogeneous population that differed significantly from previous results of high levels of diversity in WNV. We hypothesize that this difference in genetic diversity is directly related to the viruses' success in new and changing environments in the laboratory and that differences in a viruses' ability to produce and maintain heterogeneous populations in nature may in some instances explain the variable levels of success seen among arboviruses.
引用
收藏
页码:2398 / 2406
页数:9
相关论文
共 52 条
[1]   Fitness increase of memory genomes in a viral quasispecies [J].
Arias, A ;
Ruiz-Jarabo, CM ;
Escarmís, C ;
Domingo, E .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 339 (02) :405-412
[2]  
Austin RJ, 2004, CAN VET J, V45, P117
[3]   ATTENUATION OF WILD-TYPE YELLOW-FEVER VIRUS BY PASSAGE IN HELA-CELLS [J].
BARRETT, ADT ;
MONATH, TP ;
CROPP, CB ;
ADKINS, JA ;
LEDGER, TN ;
GOULD, EA ;
SCHLESINGER, JJ ;
KINNEY, RM ;
TRENT, DW .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :2301-2306
[4]  
Bosio CF, 2000, GENETICS, V156, P687
[5]   Minority memory genomes can influence the evolution of HIV-1 quasispecies in vivo [J].
Briones, Carlos ;
de Vicente, Aranzazu ;
Molina-Paris, Carmen ;
Domingo, Esteban .
GENE, 2006, 384 :129-138
[6]  
Chandler Laura J., 2001, American Journal of Tropical Medicine and Hygiene, V64, P12
[7]   E/NS1 modifications of dengue 2 virus after serial passages in mammalian and/or mosquito cells [J].
Chen, WJ ;
Wu, HR ;
Chiou, SS .
INTERVIROLOGY, 2003, 46 (05) :289-295
[8]   Role of the mutant spectrum in adaptation and replication of West Nile virus [J].
Ciota, Alexander T. ;
Ngo, Kiet A. ;
Lovelace, Amy O. ;
Payne, Anne F. ;
Zhou, Yangsheng ;
Shi, Pei-Yong ;
Kramer, Laura D. .
JOURNAL OF GENERAL VIROLOGY, 2007, 88 :865-874
[9]   Cell-specific adaptation of two flaviviruses following serial passage in mosquito cell culture [J].
Ciota, Alexander T. ;
Lovelace, Amy O. ;
Ngo, Kiet A. ;
Le, An N. ;
Maffei, Joseph G. ;
Franke, Mary A. ;
Payne, Anne F. ;
Jones, Susan A. ;
Kauffman, Elizabeth B. ;
Kramer, Laura D. .
VIROLOGY, 2007, 357 (02) :165-174
[10]  
Cooper LA, 2001, GENETICS, V157, P1403