Heterogeneous nature of the genome of the ARILVAX yellow fever 17D vaccine revealed by consensus sequencing

被引:28
作者
Pugachev, KV
Ocran, SW
Guirakhoo, F
Furby, D
Monath, TP
机构
[1] Acambis Inc, Cambridge, MA 02139 USA
[2] Evans Vaccines, Liverpool L24 9GR, Merseyside, England
关键词
yellow fever vaccine; 17D strain; nucleotide sequence;
D O I
10.1016/S0264-410X(01)00439-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Consensus sequencing of the genome of the ARILVAX live attenuated yellow fever (YF) 17D vaccine was performed directly on reconstituted virus from a vial of the vaccine secondary seed (without plaque-purification or cloning of cDNA). The genome of ARILVAX was identical in organization and size (10,862 nucleotides (nt)) to other published YF 17D sequences. A total of 12 nt heterogeneities were detected indicating that the vaccine is a heterogeneous population. Some of these indicated the presence of quasispecies with residues not reported previously for other sequenced YF 17D strains. A number of nts clearly differed from some YF vaccine strain sequences but coincided with the others, which could be due to the use of consensus sequencing approach in this study. Most (but not all) of the heterogeneities and nt differences were silent (i.e. did not result in an amino acid change). The differences are inconsequential to safety and effectiveness of ARILVAX. Other YF 17D vaccines are undoubtedly also heterogeneous and need to be re-examined using the consensus approach. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:996 / 999
页数:4
相关论文
共 16 条
[1]  
[Anonymous], VACCINES
[2]   GROWTH-RESTRICTED DENGUE VIRUS MUTANTS CONTAINING DELETIONS IN THE 5' NONCODING REGION OF THE RNA GENOME [J].
CAHOUR, A ;
PLETNEV, A ;
VAZEILLEFALCOZ, M ;
ROSEN, L ;
LAI, CJ .
VIROLOGY, 1995, 207 (01) :68-76
[3]   CORRELATION BETWEEN AMOUNT OF VIRUS WITH ALTERED NUCLEOTIDE-SEQUENCE AND THE MONKEY TEST FOR ACCEPTABILITY OF ORAL POLIOVIRUS VACCINE [J].
CHUMAKOV, KM ;
POWERS, LB ;
NOONAN, KE ;
RONINSON, IB ;
LEVENBOOK, IS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (01) :199-203
[4]  
DOSSANTOS CND, 1995, VIRUS RES, V35, P35
[5]   NUCLEOTIDE-SEQUENCE COMPARISON OF THE GENOME OF 2 17D-204 YELLOW-FEVER VACCINES [J].
DUPUY, A ;
DESPRES, P ;
CAHOUR, A ;
GIRARD, M ;
BOULOY, M .
NUCLEIC ACIDS RESEARCH, 1989, 17 (10) :3989-3989
[6]  
GALLER R, 2001, IN PRESS VIROLOGY, V290
[7]   COMPARISON OF THE VIRULENT ASIBI STRAIN OF YELLOW-FEVER VIRUS WITH THE 17D VACCINE STRAIN DERIVED FROM IT [J].
HAHN, CS ;
DALRYMPLE, JM ;
STRAUSS, JH ;
RICE, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (07) :2019-2023
[8]   The serine protease and RNA-stimulated nucleoside triphosphatase and RNA helicase functional domains of dengue virus type 2 NS3 converge within a region of 20 amino acids [J].
Li, HT ;
Clum, S ;
You, SH ;
Ebner, KE ;
Padmanabhan, R .
JOURNAL OF VIROLOGY, 1999, 73 (04) :3108-3116
[9]   THE ENVELOPE GLYCOPROTEIN FROM TICK-BORNE ENCEPHALITIS-VIRUS AT 2 ANGSTROM RESOLUTION [J].
REY, FA ;
HEINZ, FX ;
MANDL, C ;
KUNZ, C ;
HARRISON, SC .
NATURE, 1995, 375 (6529) :291-298
[10]   NUCLEOTIDE-SEQUENCE OF YELLOW-FEVER VIRUS - IMPLICATIONS FOR FLAVIVIRUS GENE-EXPRESSION AND EVOLUTION [J].
RICE, CM ;
LENCHES, EM ;
EDDY, SR ;
SHIN, SJ ;
SHEETS, RL ;
STRAUSS, JH .
SCIENCE, 1985, 229 (4715) :726-733