Evidence of recombination in natural populations of hepatitis A virus

被引:40
作者
Costa-Mattioli, M
Ferré, V
Casane, D
Perez-Bercoff, R
Coste-Burel, M
Imbert-Marcille, BM
Andre, ECM
Bressollette-Bodin, C
Billaudel, S
Cristina, J
机构
[1] Univ Republica, Fac Ciencias, Ctr Invest Nucl, Mol Virol Lab, Montevideo 11400, Uruguay
[2] Univ Paris 06, UMR7622, Paris, France
[3] CNRS, Lab Genet Virus, F-91198 Gif Sur Yvette, France
关键词
D O I
10.1016/S0042-6822(03)00109-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Genetic analysis of selected genome regions of hepatitis A virus (HAV) suggested that distinct genotypes of HAV could be found in different geographical regions. At least seven HAV genotypes have been identified all over the world, including four human genotypes (I, II, III, and VII) and three simian strains (IV, V, and VI). Phylogenetic analysis using full-length VP1 sequences revealed that human strain 9F94 has a close genetic relation with strain SLF-88 (sub-genotype VII). Nevertheless, the same analysis using full-length VP2 or VP3 sequences revealed that strain 9F94 has a close genetic relation with strain MBB (sub-genotype IB). To test the possibility of genetic recombination, phylogenetic studies were carried out, revealing that a crossing over had taken place in the VP1 capsid protein. These findings indicate that capsid-recombination can play a significant role in shaping the genetic diversity of HAV and, as such, can have important implications for its evolution, biology, and control. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:51 / 59
页数:9
相关论文
共 48 条
[1]  
Alvarez-Valin F, 2000, GENETICS, V155, P1683
[2]   Characterization of recombinant hepatitis A virus genomes containing exogenous sequences at the 2A/2B junction [J].
Beard, MR ;
Cohen, L ;
Lemon, SM ;
Martin, A .
JOURNAL OF VIROLOGY, 2001, 75 (03) :1414-1426
[3]  
Comeron JM, 1995, J MOL EVOL, V41, P1152, DOI 10.1007/BF00173196
[4]   Molecular evolution of Hepatitis A virus:: a new classification based on the complete VP1 protein [J].
Costa-Mattioli, M ;
Cristina, J ;
Romero, H ;
Perez-Bercof, R ;
Casane, D ;
Colina, R ;
Garcia, L ;
Vega, I ;
Glikman, G ;
Romanowsky, V ;
Castello, A ;
Nicand, E ;
Gassin, M ;
Billaudel, S ;
Ferré, V .
JOURNAL OF VIROLOGY, 2002, 76 (18) :9516-9525
[5]   Genetic variability of hepatitis A virus in South America reveals heterogeneity and co-circulation during epidemic outbreaks [J].
Costa-Mattioli, M ;
Ferre, V ;
Monpoeho, S ;
Garcia, L ;
Colina, R ;
Billaudel, S ;
Vega, I ;
Perez-Bercoff, R ;
Cristina, J .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :2647-2652
[6]   Genetic analysis of hepatitis A virus outbreak in France confirms the co-circulation of subgenotypes Ia, Ib and reveals a new genetic lineage [J].
Costa-Mattioli, M ;
Monpoeho, S ;
Schvoerer, C ;
Besse, B ;
Aleman, MH ;
Billaudel, S ;
Cristina, J ;
Ferré, V .
JOURNAL OF MEDICAL VIROLOGY, 2001, 65 (02) :233-240
[7]   Genomic features of intertypic recombinant Sabin poliovirus strains excreted by primary vaccinees [J].
Cuervo, NS ;
Guillot, S ;
Romanenkova, N ;
Combiescu, M ;
Aubert-Combiescu, A ;
Seghier, M ;
Caro, V ;
Crainic, R ;
Delpeyroux, F .
JOURNAL OF VIROLOGY, 2001, 75 (13) :5740-5751
[8]   Hepatitis A: Old and new [J].
Cuthbert, JA .
CLINICAL MICROBIOLOGY REVIEWS, 2001, 14 (01) :38-+
[9]   RNA virus mutations and fitness for survival [J].
Domingo, E ;
Holland, JJ .
ANNUAL REVIEW OF MICROBIOLOGY, 1997, 51 :151-178
[10]  
Felsenstein J., 1993, PHYLIP PHYLOGENY INF