J Gen Virol Faster Access
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 89 (2008), 3073-3079; DOI 10.1099/vir.0.2008/003210-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wu, X.
Right arrow Articles by Xiao, S.-Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wu, X.
Right arrow Articles by Xiao, S.-Y.
Agricola
Right arrow Articles by Wu, X.
Right arrow Articles by Xiao, S.-Y.

Persistent infection and associated nucleotide changes of West Nile virus serially passaged in hamsters

Xiaoyan Wu1,2, Liang Lu1, Hilda Guzman1, Robert B. Tesh1 and Shu-Yuan Xiao1

1 Department of Pathology, and Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, Texas, USA
2 Department of Medicine, Zhong-nan Hospital, Wuhan University, Wuhan, Hubei Province, PR China

Correspondence
Shu-Yuan Xiao
syxiao{at}utmb.edu

Hamsters experimentally infected with the neuroinvasive West Nile virus (WNV) strain NY385-99 frequently develop persistent renal infection and viruria. Viruses recovered from the urine of such animals no longer cause neurological disease when inoculated into naïve hamsters. To examine if this phenotypic change is stable, and if additional nucleotide changes occur during further passages, a urine isolate from a persistently infected hamster (WNV 9317B) was serially passaged in hamsters, and representative isolates from each passage were analysed for pathogenesis in hamsters and by nucleotide sequencing. The progeny viruses tested all resulted in asymptomatic infection when inoculated into hamsters and caused no mortality. Most of the original nucleotide changes were retained in these serial WNV isolates. Changes were distributed throughout the genome at 116 sites, ranging from 0.082 to 0.262 %, compared with the parent strain NY385-99, and they were mostly in coding regions. Our findings indicate that WNV underwent additional genetic changes during serial passage in hamsters, but there was no reversion to neurotropism and virulence.




This article has been cited by other articles:


Home page
J. Virol.Home page
G. R. Medigeshi, A. J. Hirsch, J. D. Brien, J. L. Uhrlaub, P. W. Mason, C. Wiley, J. Nikolich-Zugich, and J. A. Nelson
West Nile Virus Capsid Degradation of Claudin Proteins Disrupts Epithelial Barrier Function
J. Virol., June 15, 2009; 83(12): 6125 - 6134.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
V. Siddharthan, H. Wang, N. E. Motter, J. O. Hall, R. D. Skinner, R. T. Skirpstunas, and J. D. Morrey
Persistent West Nile Virus Associated with a Neurological Sequela in Hamsters Identified by Motor Unit Number Estimation
J. Virol., May 1, 2009; 83(9): 4251 - 4261.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2008 by the Society for General Microbiology.