Genetic evidence for the origins of Venezuelan equine encephalitis virus subtype IAB outbreaks

被引:47
作者
Weaver, SC
Pfeffer, M
Marriott, K
Kang, WL
Kinney, RM
机构
[1] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Ctr Trop Dis, Galveston, TX 77555 USA
[3] Ctr Dis Control & Prevent, Div Vector Borne Infect Dis, Ft Collins, CO 80522 USA
关键词
D O I
10.4269/ajtmh.1999.60.441
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Epizootics of Venezuelan equine encephalitis (VEE) involving subtype IAB viruses occurred sporadically in South, Central and North America from 1938 to 1973, Incompletely inactivated vaccines have long been suspected as a source of the later epizootics. We tested this hypothesis by sequencing the PE2 glycoprotein precursor (1,677 nucleotides) or 26S/nonstructural protein 4 (nsP4) genome regions (4,490 nucleotides) for isolates representing most major outbreaks. Two distinct IAB genotypes were identified: 1) 1940s Peruvian strains and 2) 1938-1973 isolates from South, Central, and North America. Nucleotide sequences of these two genotypes differed by 1.1%, while the latter group showed only 0.6% sequence diversity. Early VEE virus IAB strains that were used for inactivated vaccine preparation had sequences identical to those predicted by phylogenetic analyses to be ancestors of the 1960s-1970s outbreaks. These data support the hypothesis of a vaccine origin for many VEE outbreaks. However, continuous, cryptic circulation of IAB viruses cannot be ruled out as a source of epizootic emergence.
引用
收藏
页码:441 / 448
页数:8
相关论文
共 41 条
[1]   LOCALIZATION OF 4 ANTIGENIC SITES INVOLVED IN VENEZUELAN EQUINE ENCEPHALOMYELITIS VIRUS PROTECTION [J].
AGAPOV, EV ;
RAZUMOV, IA ;
FROLOV, IV ;
KOLYKHALOV, AA ;
NETESOV, SV ;
LOKTEV, VB .
ARCHIVES OF VIROLOGY, 1994, 139 (1-2) :173-181
[2]   Venezuelan equine encephalomyelitis [J].
Beck, CE ;
Wyckoff, RWG .
SCIENCE, 1938, 88 :530-530
[3]   ATTENUATION OF VENEZUELAN EQUINE ENCEPHALOMYELITIS VIRUS BY IN VITRO CULTIVATION IN GUINEA-PIG HEART CELLS [J].
BERGE, TO ;
TIGERTT, WD ;
BANKS, IS .
AMERICAN JOURNAL OF HYGIENE, 1961, 73 (02) :209-&
[4]   VIBRATIONAL-RELAXATION IN MOLECULAR-CRYSTALS [J].
CALIFANO, S ;
SCHETTINO, V .
INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 1988, 7 (01) :19-57
[5]   Genetic conservation of highlands J viruses [J].
Cilnis, MJ ;
Kang, VL ;
Weaver, SC .
VIROLOGY, 1996, 218 (02) :343-351
[6]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[7]  
FELSENSTEIN J, 1985, EVOLUTION, V39, P783, DOI 10.1111/j.1558-5646.1985.tb00420.x
[8]  
Felsenstein J., 1990, PHYLIP MANUAL VERSIO
[9]   BIOCHEMICAL AND ANTIGENIC COMPARISONS OF THE ENVELOPE GLYCOPROTEINS OF VENEZUELAN EQUINE ENCEPHALOMYELITIS VIRUS-STRAINS [J].
FRANCE, JK ;
WYRICK, BC ;
TRENT, DW .
JOURNAL OF GENERAL VIROLOGY, 1979, 44 (SEP) :725-740
[10]   VARIANTS OF VENEZUELAN EQUINE ENCEPHALITIS-VIRUS THAT RESIST NEUTRALIZATION DEFINE A DOMAIN OF THE E2 GLYCOPROTEIN [J].
JOHNSON, BJB ;
BRUBAKER, JR ;
ROEHRIG, JT ;
TRENT, DW .
VIROLOGY, 1990, 177 (02) :676-683