DYNAMIC ANALYSIS OF HETEROGENEOUS HEPATITIS-C VIRUS POPULATIONS BY DIRECT SOLID-PHASE SEQUENCING

被引:24
作者
ODEBERG, J
YUN, ZB
SONNERBORG, A
UHLEN, M
LUNDEBERG, J
机构
[1] ROYAL INST TECHNOL,DEPT BIOCHEM,S-10044 STOCKHOLM,SWEDEN
[2] HUDDINGE UNIV HOSP,KAROLINSKA INST,DIV CLIN VIROL,STOCKHOLM,SWEDEN
关键词
D O I
10.1128/JCM.33.7.1870-1874.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In the present study, we used a semiautomated solid-phase direct sequencing method to analyze sequence diversity and variation of the hypervariable E2/NS1 region in the hepatitis C virus (HCTV) genome in isolates from patients seropositive for HCV, A total of 24 isolates of various origins were sequenced, Six of the patients, not subject to any antiviral therapy, were monitored longitudinally, and rapid sequence variations were observed over a period of 14 months. The nucleotide change rate was found to be 0.1 to 0.2 nucleotide substitution per genome site per year, Furthermore, isolates from five of the patients were used for a comparative study of the direct solid-phase sequencing approach versus the frequently used approach of sequencing individual reverse transcriptase PCR clones. The advantage of direct solid-phase sequencing for studying dynamic changes in heterogeneous populations of HCV is discussed.
引用
收藏
页码:1870 / 1874
页数:5
相关论文
共 17 条
[1]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[2]   ISOLATION OF A CDNA CLONE DERIVED FROM A BLOOD-BORNE NON-A, NON-B VIRAL-HEPATITIS GENOME [J].
CHOO, QL ;
KUO, G ;
WEINER, AJ ;
OVERBY, LR ;
BRADLEY, DW ;
HOUGHTON, M .
SCIENCE, 1989, 244 (4902) :359-362
[3]   HEPATITIS-C VIRUS AFTER INTERFERON TREATMENT HAS THE VARIATION IN THE HYPERVARIABLE REGION OF ENVELOPE 2 GENE [J].
ENOMOTO, N ;
SATO, C ;
KUROSAKI, M ;
MARUMO, F .
JOURNAL OF HEPATOLOGY, 1994, 20 (02) :252-261
[4]   DYNAMICS OF GENOME CHANGE IN THE E2/NS1 REGION OF HEPATITIS-C VIRUS IN-VIVO [J].
HIGASHI, Y ;
KAKUMU, S ;
YOSHIOKA, K ;
WAKITA, T ;
MIZOKAMI, M ;
OHBA, K ;
ITO, Y ;
ISHIKAWA, T ;
TAKAYANAGI, M ;
NAGAI, Y .
VIROLOGY, 1993, 197 (02) :659-668
[5]  
HULTMAN T, 1991, BIOTECHNIQUES, V10, P84
[6]   MARKED SEQUENCE DIVERSITY IN THE PUTATIVE ENVELOPE PROTEINS OF HEPATITIS-C VIRUSES [J].
KATO, N ;
OOTSUYAMA, Y ;
TANAKA, T ;
NAKAGAWA, M ;
NAKAZAWA, T ;
MURAISO, K ;
OHKOSHI, S ;
HIJIKATA, M ;
SHIMOTOHNO, K .
VIRUS RESEARCH, 1992, 22 (02) :107-123
[7]   RAPID-SEQUENCE VARIATION OF THE HYPERVARIABLE REGION OF HEPATITIS-C VIRUS DURING THE COURSE OF CHRONIC INFECTION [J].
KUROSAKI, M ;
ENOMOTO, N ;
MARUMO, F ;
SATO, C .
HEPATOLOGY, 1993, 18 (06) :1293-1299
[8]  
LEITNER T, 1993, BIOTECHNIQUES, V15, P120
[9]   THE MOLECULAR-BIOLOGY OF HEPATITIS-C VIRUS [J].
MATSUURA, Y ;
MIYAMURA, T .
SEMINARS IN VIROLOGY, 1993, 4 (05) :297-304
[10]   CHARACTERIZATION OF THE GENOMIC SEQUENCE OF TYPE-V (OR 3A) HEPATITIS-C VIRUS ISOLATES AND PCR PRIMERS FOR SPECIFIC DETECTION [J].
OKAMOTO, H ;
TOKITA, H ;
SAKAMOTO, M ;
HORIKITA, M ;
KOJIMA, M ;
IIZUKA, H ;
MISHIRO, S .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :2385-2390