AJTMH ASTMH Job Mart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 65(6), 2001, pp. 738-746
Copyright © 2001 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 Google Scholar
Google Scholar
Right arrow Articles by Moncayo, A.
Right arrow Articles by Weaver, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Moncayo, A.
Right arrow Articles by Weaver, S.
Related Collections
Right arrow Viral Encephalitis
Right arrow Genomics
American Journal of Tropical Medicine and Hygiene, Vol 65, Issue 6, 738-746
Copyright © 2001 by American Society of Tropical Medicine and Hygiene

Research Articles


Genetic diversity and relationships among Venezuelan equine encephalitis virus field isolates from Colombia and Venezuela

AC Moncayo, GM Medina, Z Kalvatchev, AC Brault, R Barrera, J Boshell, C Ferro, JE Freier, JC Navarro, R Salas, J De Siger, C Vasquez, R Walder, and SC Weaver

During field studies of enzootic Venezuelan equine encephalitis (VEE) viruses associated with epizootic emergence, a large number of virus isolates were made in sylvatic foci of Venezuela and Colombia. To rapidly characterize these isolates, antigenic subtypes were determined by means of immunofluorescence and by single-strand conformational polymorphism (SSCP) analysis by use of an 856-bp fragment from the P62 gene, which we used to distinguish genetic variants. Representative isolates were sequenced to assess the sensitivity of SSCP to detect genetic differences. The SSCP analysis distinguished isolates differing by as little as 1 nucleotide; overall, differences of > or = 1 nucleotide were recognized 89% of the time, and the sensitivity to distinguish strains that differed by only 1 or 4 nucleotides was 17 and 57%, respectively. Phylogenetic analyses of representative sequences showed that all recent isolates from the Catatumbo region of western Venezuela and the middle Magdalena Valley of Colombia were closely related to epizootic subtype IAB and IC strains; strains from Yaracuy and Miranda States were more distantly related. Cocirculation of the same virus genotype in both Colombian and Venezuelan foci indicated that these viruses are readily transported between enzootic regions separated by > 300 km. The SSCP analysis appears to be a simple, fast, and relatively efficient method of screening VEE virus isolates to identify meaningful genetic variants.


This article has been cited by other articles:


Home page
J. Virol.Home page
M. Anishchenko, S. Paessler, I. P. Greene, P. V. Aguilar, A.-S. Carrara, and S. C. Weaver
Generation and Characterization of Closely Related Epizootic and Enzootic Infectious cDNA Clones for Studying Interferon Sensitivity and Emergence Mechanisms of Venezuelan Equine Encephalitis Virus
J. Virol., January 1, 2004; 78(1): 1 - 8.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
E. Wang, A. C. Brault, A. M. Powers, W. Kang, and S. C. Weaver
Glycosaminoglycan Binding Properties of Natural Venezuelan Equine Encephalitis Virus Isolates
J. Virol., December 20, 2002; 77(2): 1204 - 1210.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the American Society of Tropical Medicine and Hygiene.