POINT MUTATION IN MENINGOCOCCAL POR-A GENE ASSOCIATED WITH INCREASED ENDEMIC DISEASE

被引:168
作者
MCGUINNESS, BT
CLARKE, IN
LAMBDEN, PR
BARLOW, AK
POOLMAN, JT
JONES, DM
HECKELS, JE
机构
[1] UNIV SOUTHAMPTON,SCH MED,DEPT MICROBIOL,SOUTHAMPTON SO9 4XY,HANTS,ENGLAND
[2] RIJKSINST VOLKSGEZONDHEID MILIEUHYG,3720 BA BILTHOVEN,NETHERLANDS
[3] WITHINGTON HOSP,PUBL HLTH LAB SERV,MENINGOCOCCAL REFERENCE LAB,MANCHESTER M20 8LR,LANCS,ENGLAND
基金
英国医学研究理事会;
关键词
D O I
10.1016/0140-6736(91)91297-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The por A gene, which encodes expression of meningococcal class 1 outer membrane protein, responsible for antigenic subtype specificity, has been cloned and sequenced in an isolate of Neisseria meningitidis (B:15:P1.7,16) from a patient in the Gloucester area with meningococcal meningitis. Comparison of the sequence with that of the equivalent gene from the P1.7,16 reference strain reveals a point mutation which generates a single amino acid change in the epitope responsible for P1.16 specificity. Monoclonal antibodies with P1.16 specificity do not react with synthetic peptides that correspond to the altered epitope, and do not promote complement-mediated bactericidal killing of the isolate. Analysis of other strains shows widespread distribution of infections due to B:15:P1.7,16 meningococci with the altered epitope (P1.16b) in England and Wales.
引用
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页码:514 / 517
页数:4
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