AN INFECTIOUS CDNA COPY OF THE GENOME OF A NON-CARDIOVIRULENT COXSACKIEVIRUS B3 STRAIN - ITS COMPLETE SEQUENCE-ANALYSIS AND COMPARISON TO THE GENOMES OF CARDIOVIRULENT COXSACKIEVIRUSES

被引:98
作者
CHAPMAN, NM
TU, Z
TRACY, S
GAUNTT, CJ
机构
[1] UNIV NEBRASKA, MED CTR, DEPT PATHOL & MICROBIOL, OMAHA, NE 68198 USA
[2] UNIV TEXAS, HLTH SCI CTR, DEPT MICROBIOL, SAN ANTONIO, TX 78284 USA
关键词
D O I
10.1007/BF01309769
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genome of the non-cardiovirulent coxsackievirus B3 (CVB3) strain CVB3/0 was cloned and sequenced to aid in the elucidation of the viral genetic basis for the CVB3 cardiovirulent phenotype. Reverse-transcribed sub-genomic complementary DNA (cDNA) fragments were enzymatically amplified using generic oligonucleotide primers and were assembled as a complete infectious genomic copy (pCVB3-0) downstream of the T7 RNA polymerase promoter. Positive-strand viral RNA transcribed from pCVB3-0 using T7 RNA polymerase and transfected into HeLa cells produced infectious virus (CVB3/0c). No differences in phenotype were observed comparing growth of CVB3/0c to the parental CVB3/0 in HeLa single-step growth curves, virus yields, or plaque size. When inoculated into C3H/HeJ mice, CVB3/0c achieved cardiac titers equivalent to the parental CVB3/0 and like the parental virus, demonstrated a non-cardiovirulent phenotype. The nucleotide sequence of the cloned CVB3/0 genome was determined and compared to the genomes of infectious cDNA clones of cardiovirulent CVB3 strains. Two consistent differences among nucleotides in non-translated regions and 8 amino acid differences relative to two well-characterized infectious cDNA copies of genomes from cardiovirulent CVB3 strains were identified.
引用
收藏
页码:115 / 130
页数:16
相关论文
共 56 条
[1]  
AGOL VI, 1991, ADV VIRUS RES, V40, P103
[2]  
ALMOND JW, 1987, ANNU REV MICROBIOL, V41, P153
[3]   MURINE CELL-MEDIATED IMMUNE-RESPONSE RECOGNIZES AN ENTEROVIRUS GROUP-SPECIFIC ANTIGEN(S) [J].
BECK, MA ;
TRACY, SM .
JOURNAL OF VIROLOGY, 1989, 63 (10) :4148-4156
[4]   STRUCTURAL AND FUNCTIONAL-CHARACTERIZATION OF THE POLIOVIRUS REPLICATION COMPLEX [J].
BIENZ, K ;
EGGER, D ;
PFISTER, T ;
TROXLER, M .
JOURNAL OF VIROLOGY, 1992, 66 (05) :2740-2747
[5]  
BURCH GE, 1968, JAMA-J AM MED ASSOC, V203, P55
[6]  
Cherry JD., 1987, TXB PEDIAT INFECT DI, P1729
[7]  
DELANGEL RM, 1989, P NATL ACAD SCI USA, V86, P8299
[8]   ATTENUATION OF MENGO-VIRUS THROUGH GENETIC-ENGINEERING OF THE 5' NONCODING POLY(C) TRACT [J].
DUKE, GM ;
OSORIO, JE ;
PALMENBERG, AC .
NATURE, 1990, 343 (6257) :474-476
[9]  
ETCHISON D, 1982, J BIOL CHEM, V257, P4806
[10]   STRUCTURAL FACTORS THAT CONTROL CONFORMATIONAL TRANSITIONS AND SEROTYPE SPECIFICITY IN TYPE-3 POLIOVIRUS [J].
FILMAN, DJ ;
SYED, R ;
CHOW, M ;
MACADAM, AJ ;
MINOR, PD ;
HOGLE, JM .
EMBO JOURNAL, 1989, 8 (05) :1567-1579