AT LEAST 12 GENOTYPES OF HEPATITIS-C VIRUS PREDICTED BY SEQUENCE-ANALYSIS OF THE PUTATIVE E1-GENE OF ISOLATES COLLECTED WORLDWIDE

被引:392
作者
BUKH, J
PURCELL, RH
MILLER, RH
机构
[1] Laboratory of Infectious Diseases, NIAID, National Institutes of Health, Bethesda
关键词
NON-A; NON-B HEPATITIS; GENETIC HETEROGENEITY; POLYMERASE CHAIN REACTION; DENDROGRAM; TAXONOMY;
D O I
10.1073/pnas.90.17.8234
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In a previous study we sequenced the 5' noncoding (NC) region of 44 isolates of hepatitis C virus (HCV) and identified heterogeneous domains that provided evidence for additional genetic groups of HCV not previously recognized. In this study we have determined the complete nucleotide sequence of the putative envelope 1 (E1) gene in 51 HCV isolates from around the world and found that they could be grouped into at least 12 distinct genotypes. The E1 gene sequence of 8 of these genotypes has not been reported previously. Although the genetic relatedness of HCV isolates determined by the previous analysis of the 5' NC region predicted the relationships observed in the E1 gene, analysis of the 5' NC sequence alone did not accurately predict all HCV genotypes. The nucleotide and amino acid sequence identities of the E1 gene among HCV isolates of the same genotype were in the range of 88.0-99.1% and 89.1-98.4%, respectively, whereas those of HCV isolates of different genotypes were in the range of 53.5-78.6% and 49.0-82.8%, respectively. The latter differences are similar to those found when comparing the envelope gene sequences of the various serotypes of the related flaviviruses as well as other RNA viruses. We found that some genotypes of HCV were widely distributed around the world, whereas others were identified only in discreet geographical regions. Four genotypes were identified exclusively in Aftica and comprised the majority of HCV isolates on that continent. The E1 gene was exactly 576 nucleotides in length in all 51 HCV isolates with no in-frame stop codons. Analysis of the predicted El protein identified several conserved domains that may be important for maintaining its biological function: (i) eight invariant cysteine residues, (ii) three potential N-linked glycosylation sites, (iii) a domain of nine amino adds (GHRMAWDMM), and (iv) an amino acid doublet (GV) near the putative cleavage site at the C terminus of the protein. In conclusion, the discovery of at least 12 genotypes of HCV has important implications for HCV diagnosis and vaccine development.
引用
收藏
页码:8234 / 8238
页数:5
相关论文
共 30 条
[1]   GENOMIC CHARACTERIZATION AND MUTATION-RATE OF HEPATITIS-C VIRUS ISOLATED FROM A PATIENT WHO CONTRACTED HEPATITIS DURING AN EPIDEMIC OF NON-A, NON-B HEPATITIS IN JAPAN [J].
ABE, K ;
INCHAUSPE, G ;
FUJISAWA, K .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :2725-2729
[2]   IMPROVEMENT OF PCR AMPLIFIED DNA SEQUENCING WITH THE AID OF DETERGENTS [J].
BACHMANN, B ;
LUKE, W ;
HUNSMANN, G .
NUCLEIC ACIDS RESEARCH, 1990, 18 (05) :1309-1309
[3]   IMPORTANCE OF PRIMER SELECTION FOR THE DETECTION OF HEPATITIS-C VIRUS-RNA WITH THE POLYMERASE CHAIN-REACTION ASSAY [J].
BUKH, J ;
PURCELL, RH ;
MILLER, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (01) :187-191
[4]   SEQUENCE-ANALYSIS OF THE 5' NONCODING REGION OF HEPATITIS-C VIRUS [J].
BUKH, J ;
PURCELL, RH ;
MILLER, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (11) :4942-4946
[5]   AT LEAST 5 RELATED, BUT DISTINCT, HEPATITIS-C VIRAL GENOTYPES EXIST [J].
CHA, TA ;
BEALL, E ;
IRVINE, B ;
KOLBERG, J ;
CHIEN, D ;
KUO, G ;
URDEA, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (15) :7144-7148
[6]   ANALYSIS OF A NEW HEPATITIS-C VIRUS TYPE AND ITS PHYLOGENETIC RELATIONSHIP TO EXISTING VARIANTS [J].
CHAN, SW ;
MCOMISH, F ;
HOLMES, EC ;
DOW, B ;
PEUTHERER, JF ;
FOLLETT, E ;
YAP, PL ;
SIMMONDS, P .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :1131-1141
[7]   THE TAIWANESE HEPATITIS-C VIRUS GENOME - SEQUENCE DETERMINATION AND MAPPING THE 5' TERMINI OF VIRAL GENOMIC AND ANTIGENOMIC RNA [J].
CHEN, PJ ;
LIN, MH ;
TAI, KF ;
LIU, PC ;
LIN, CJ ;
CHEN, DS .
VIROLOGY, 1992, 188 (01) :102-113
[8]   GENETIC ORGANIZATION AND DIVERSITY OF THE HEPATITIS-C VIRUS [J].
CHOO, QL ;
RICHMAN, KH ;
HAN, JH ;
BERGER, K ;
LEE, C ;
DONG, C ;
GALLEGOS, C ;
COIT, D ;
MEDINASELBY, A ;
BARR, PJ ;
WEINER, AJ ;
BRADLEY, DW ;
KUO, G ;
HOUGHTON, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2451-2455
[9]   NUCLEOTIDE-SEQUENCE OF DENGUE-2 RNA AND COMPARISON OF THE ENCODED PROTEINS WITH THOSE OF OTHER FLAVIVIRUSES [J].
HAHN, YS ;
GALLER, R ;
HUNKAPILLER, T ;
DALRYMPLE, JM ;
STRAUSS, JH ;
STRAUSS, EG .
VIROLOGY, 1988, 162 (01) :167-180
[10]   CLUSTAL - A PACKAGE FOR PERFORMING MULTIPLE SEQUENCE ALIGNMENT ON A MICROCOMPUTER [J].
HIGGINS, DG ;
SHARP, PM .
GENE, 1988, 73 (01) :237-244