GENETIC-VARIATION OF HIV TYPE-1 IN 4 WORLD-HEALTH-ORGANIZATION-SPONSORED VACCINE EVALUATION SITES - GENERATION OF FUNCTIONAL ENVELOPE (GLYCOPROTEIN-160) CLONES REPRESENTATIVE OF SEQUENCE SUBTYPE-A, SUBTYPE-B, SUBTYPE-C, AND SUBTYPE-E

被引:109
作者
GAO, F
YUE, L
CRAIG, S
THORNTON, CL
ROBERTSON, DL
MCCUTCHAN, FE
BRADAC, JA
SHARP, PM
HAHN, BH
OSMANOV, S
BELSEY, EM
HEYWARD, W
ESPARZA, J
GALVAOCASTRO, B
VANDEPERRE, P
KARITA, E
WASI, C
SEMPALA, S
TUGUME, B
BIRYAHWAHO, B
RUBSAMENWAIGMANN, H
VONBRIESEN, H
ESSER, R
GREZ, M
HOLMES, H
NEWBERRY, A
RANJBAR, S
TOMLINSON, P
BRADAC, J
MCCUTCHAN, F
LOUWAGIE, J
HEGERICH, P
LOPEZGALINDEZ, C
OLIVARES, I
DOPAZO, J
MULLINS, JI
DELWART, EL
BACHMANN, HM
GOUDSMIT, J
DEWOLF, F
SARAGOSTI, S
SCHOCHETMAN, G
KALISH, M
LUO, CC
GEORGE, R
PAU, CP
WEBER, J
CHEINGSONGPOPOV, R
KALEEBU, P
NARA, P
机构
[1] UNIV ALABAMA, DEPT MED, BIRMINGHAM, AL 35294 USA
[2] UNIV ALABAMA, DEPT MICROBIOL, BIRMINGHAM, AL 35294 USA
[3] UNIV NOTTINGHAM, QUEENS MED CTR, DEPT GENET, NOTTINGHAM NG7 2UH, ENGLAND
[4] WALTER REED ARMY INST RES, HENRY M JACKSON FDN RES LAB, ROCKVILLE, MD 20850 USA
[5] NIAID, VACCINE RES & DEV BRANCH, BETHESDA, MD 20892 USA
[6] WHO, WHO NETWORK HIV ISOLAT & CHARACT, GLOBAL PROGRAMME AIDS, CH-1211 GENEVA, SWITZERLAND
[7] GEORG SPEYER HAUS CHEMOTHERAPEUT FORSCHUNGSINST, FRANKFURT, GERMANY
[8] NATL INST BIOL STAND & CONTROLS, LONDON NW3 6RB, ENGLAND
[9] NIAID, DIV AIDS, BETHESDA, MD 20892 USA
[10] WALTER REED ARMY INST RES, HENRY M JACKSON FDN RES LAB, ROCKVILLE, MD USA
[11] INST SALUD CARLOS 3, CTR NACL BIOL CELULAR & RETROVIRUS, MADRID, SPAIN
[12] STANFORD UNIV, SCH MED, DEPT MICROBIOL & IMMUNOL, STANFORD, CA 94305 USA
[13] UNIV AMSTERDAM, HUMAN RETROVIRUS LAB, AMSTERDAM, NETHERLANDS
[14] UNIV ALABAMA, DEPT MED, BIRMINGHAM, AL 35294 USA
[15] INST COCHIN GENET MOLEC, F-75014 PARIS, FRANCE
[16] CTR DIS CONTROL & PREVENT, ATLANTA, GA 30341 USA
[17] ST MARYS HOSP, SCH MED, LONDON, ENGLAND
[18] NCI, VIRUS BIOL UNIT, FREDERICK, MD 21701 USA
[19] KAROLINSKA INST, STOCKHOLM, SWEDEN
[20] SWEDISH INST INFECT DIS CONTROL, STOCKHOLM, SWEDEN
[21] LOS ALAMOS NATL LAB, LOS ALAMOS, NM USA
关键词
D O I
10.1089/aid.1994.10.1359
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As part of the WHO Network for HIV Isolation and Characterization, we PCR amplified, cloned, and sequenced gp120 and gp160 genes from 12 HIV-1 isolates collected in four WHO-sponsored vaccine evaluation sites (Brazil, Rwanda, Thailand, Uganda). Envelope clones were derived from PBMC-grown isolates obtained from asymptomatic individuals within 2 years of seroconversion. Analysis of their deduced amino acid sequences identified all but one to contain an uninterrupted open reading frame. Transient expression and biological characterization of selected gp160 constructs identified six clones to encode full length and functional envelope glycoproteins. Phylogenetic analysis of their nucleotide sequences revealed that they represent HIV-1 subtypes A, B, C, and E. Since current knowledge of HIV-1 envelope immunobiology is almost exclusively derived from subtype B viruses, these reagents should facilitate future envelope structure, function and antigenicity studies on a broader spectrum of viruses. This should assist in the design and evaluation of effective vaccines against HIV-1.
引用
收藏
页码:1359 / 1368
页数:10
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