GENETIC-DIFFERENCES ACCOUNTING FOR EVOLUTION AND PATHOGENICITY OF SIMIAN IMMUNODEFICIENCY VIRUS FROM A SOOTY MANGABEY MONKEY AFTER CROSS-SPECIES TRANSMISSION TO A PIG-TAILED MACAQUE

被引:40
作者
COURGNAUD, V
LAURE, F
FULTZ, PN
MONTAGNIER, L
BRECHOT, C
SONIGO, P
机构
[1] INST COCHIN GENET MOLEC,CNRS,UPR GENET VIRUS 0415,22 RUE MECHAIN,F-75014 PARIS,FRANCE
[2] CHU NECKER,INSERM,U75,F-75015 PARIS,FRANCE
[3] INST PASTEUR,UNITE ONCOL VIRALE,F-75724 PARIS 15,FRANCE
[4] INST PASTEUR,HYBRIDOTEST LAB,F-75724 PARIS 15,FRANCE
[5] UNIV ALABAMA,BIRMINGHAM,AL 35294
关键词
D O I
10.1128/JVI.66.1.414-419.1992
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We determined the nucleotide sequences of two related isolates of simian immunodeficiency virus from the sooty mangabey monkey (SIVsmm) that exhibit dramatic differences in virulence. These isolates are separated by one experimental cross-species transmission, from sooty mangabey to pig-tailed macaque. The parental virus (SIVsmm9), nonpathogenic in the original host (sooty mangabeys), causes a chronic AIDS-like disease in macaques. In contrast, the variant virus (SIVsmmPBj14) induces an acute lethal disease in various macaque species and is also pathogenic for sooty mangabeys. The combination of necessary and sufficient mutations that determined the acutely lethal phenotype on the SIVsmm9 genetic background is included within a maximal set of 57 point mutations, plus two insertions located in the long terminal repeat (22 bp spanning an NF-kappa-B-like enhancer element) and in the surface envelope glycoprotein (5 amino acids). Comparisons of synonymous and nonsynonymous nucleotide substitutions in the genome of SIVsmm indicated that selective pressures, probably due to the host immune response, favored amino acid changes in the envelope. This immunoevolutionary mechanism could explain the increase in diversity and the apparition of new virulent phenotypes after cross-species transmission.
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收藏
页码:414 / 419
页数:6
相关论文
共 30 条
  • [1] LONG TERMINAL REPEAT (LTR) SEQUENCES, ENV, AND A REGION NEAR THE 5' LTR INFLUENCE THE PATHOGENIC POTENTIAL OF RECOMBINANTS BETWEEN ROUS-ASSOCIATED VIRUS TYPE-0 AND TYPE-1
    BROWN, DW
    BLAIS, BP
    ROBINSON, HL
    [J]. JOURNAL OF VIROLOGY, 1988, 62 (09) : 3431 - 3437
  • [2] SELECTION OF GENETIC-VARIANTS OF SIMIAN IMMUNODEFICIENCY VIRUS IN PERSISTENTLY INFECTED RHESUS-MONKEYS
    BURNS, DPW
    DESROSIERS, RC
    [J]. JOURNAL OF VIROLOGY, 1991, 65 (04) : 1843 - 1854
  • [3] SEQUENCE OF SIMIAN IMMUNODEFICIENCY VIRUS FROM MACAQUE AND ITS RELATIONSHIP TO OTHER HUMAN AND SIMIAN RETROVIRUSES
    CHAKRABARTI, L
    GUYADER, M
    ALIZON, M
    DANIEL, MD
    DESROSIERS, RC
    TIOLLAIS, P
    SONIGO, P
    [J]. NATURE, 1987, 328 (6130) : 543 - 547
  • [4] THE CYTOPLASMIC DOMAIN OF SIMIAN IMMUNODEFICIENCY VIRUS TRANSMEMBRANE PROTEIN MODULATES INFECTIVITY
    CHAKRABARTI, L
    EMERMAN, M
    TIOLLAIS, P
    SONIGO, P
    [J]. JOURNAL OF VIROLOGY, 1989, 63 (10) : 4395 - 4403
  • [5] SINGLE AMINO-ACID CHANGES IN HIV ENVELOPE AFFECT VIRAL TROPISM AND RECEPTOR-BINDING
    CORDONNIER, A
    MONTAGNIER, L
    EMERMAN, M
    [J]. NATURE, 1989, 340 (6234) : 571 - 574
  • [6] THE SIMIAN IMMUNODEFICIENCY VIRUSES
    DESROSIERS, RC
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 : 557 - 578
  • [7] SEQUENCE-ANALYSIS AND ACUTE PATHOGENICITY OF MOLECULARLY CLONED SIVSMM-PBJ14
    DEWHURST, S
    EMBRETSON, JE
    ANDERSON, DC
    MULLINS, JI
    FULTZ, PN
    [J]. NATURE, 1990, 345 (6276) : 636 - 640
  • [8] RECENT ADVANCES IN THE POLYMERASE CHAIN-REACTION
    ERLICH, HA
    GELFAND, D
    SNINSKY, JJ
    [J]. SCIENCE, 1991, 252 (5013) : 1643 - 1651
  • [9] FENYO EM, 1988, J VIROL, V62, P4414
  • [10] ISOLATION OF A T-LYMPHOTROPIC RETROVIRUS FROM NATURALLY INFECTED SOOTY MANGABEY MONKEYS (CERCOCEBUS-ATYS)
    FULTZ, PN
    MCCLURE, HM
    ANDERSON, DC
    SWENSON, RB
    ANAND, R
    SRINIVASAN, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (14) : 5286 - 5290