MOLECULAR RELATIONSHIPS BETWEEN 21 HUMAN RHINOVIRUS SEROTYPES

被引:37
作者
HORSNELL, C [1 ]
GAMA, RE [1 ]
HUGHES, PJ [1 ]
STANWAY, G [1 ]
机构
[1] UNIV ESSEX,DEPT BIOL,COLCHESTER CO4 3SQ,ESSEX,ENGLAND
关键词
D O I
10.1099/0022-1317-76-10-2549
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have analysed, by PCR using consensus primers followed by sequencing, 12 human rhinoviruses (HRVs) in a genomic region including that corresponding to the immunogenic site NIm-II. Together with published information, 21 sequences are available for comparison. In the region analysed, which encodes 112 amino acids, the majority (18) of the serotypes exhibited at least 70% amino acid identity to one another and some serotypes are very closely related. These include HRV-36, -58 and -89, known to exhibit antigenic cross-reactivity, which were shown to differ at only three amino acid positions. Three serotypes, HRV-3, -14 and -72, share at least 84% identity with one another but are less than 66% identical to the majority group. Interestingly, membership of these two molecular clusters correlates with the groupings determined by sensitivity to antivirus drugs, suggesting that they reflect a fundamental division of HRVs. In contrast, there is no correlation with receptor grouping, since the majority group contains members belonging to both HRV receptor groups.
引用
收藏
页码:2549 / 2555
页数:7
相关论文
共 36 条
[1]   MANY RHINOVIRUS SEROTYPES SHARE THE SAME CELLULAR RECEPTOR [J].
ABRAHAM, G ;
COLONNO, RJ .
JOURNAL OF VIROLOGY, 1984, 51 (02) :340-345
[2]   2 GROUPS OF RHINOVIRUSES REVEALED BY A PANEL OF ANTIVIRAL COMPOUNDS PRESENT SEQUENCE DIVERGENCE AND DIFFERENTIAL PATHOGENICITY [J].
ANDRIES, K ;
DEWINDT, B ;
SNOEKS, J ;
WOUTERS, L ;
MOEREELS, H ;
LEWI, PJ ;
JANSSEN, PAJ .
JOURNAL OF VIROLOGY, 1990, 64 (03) :1117-1123
[3]   EVIDENCE FOR THE DIRECT INVOLVEMENT OF THE RHINOVIRUS CANYON IN RECEPTOR-BINDING [J].
COLONNO, RJ ;
CONDRA, JH ;
MIZUTANI, S ;
CALLAHAN, PL ;
DAVIES, ME ;
MURCKO, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (15) :5449-5453
[4]   ANTIGENIC GROUPINGS OF 90 RHINOVIRUS SEROTYPES [J].
COONEY, MK ;
FOX, JP ;
KENNY, GE .
INFECTION AND IMMUNITY, 1982, 37 (02) :642-647
[5]  
DEUCHLER M, 1987, P NATIONAL ACADEMY S, V84, P2605
[6]   RHINOVIRAL RECEPTOR DISCRIMINATION - MUTATIONAL CHANGES IN THE CANYON REGIONS OF HUMAN RHINOVIRUS TYPE-2 AND TYPE-14 INDICATE A DIFFERENT SITE OF INTERACTION [J].
DUECHLER, M ;
KETTER, S ;
SKERN, T ;
KUECHLER, E ;
BLAAS, D .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :2287-2291
[7]  
Felsenstein J., 1989, PHYLIP 3 2 MANUAL
[8]   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
[9]   IS A RHINOVIRUS VACCINE POSSIBLE [J].
FOX, JP .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1976, 103 (04) :345-354
[10]   A SYNTHETIC PEPTIDE WHICH ELICITS NEUTRALIZING ANTIBODY AGAINST HUMAN RHINOVIRUS TYPE-2 [J].
FRANCIS, MJ ;
HASTINGS, GZ ;
SANGAR, DV ;
CLARK, RP ;
SYRED, A ;
CLARKE, BE ;
ROWLANDS, DJ ;
BROWN, F .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :2687-2691