CARIOGENICITY OF STREPTOCOCCUS-MUTANS V403 GLUCOSYLTRANSFERASE AND FRUCTOSYLTRANSFERASE MUTANTS CONSTRUCTED BY ALLELIC EXCHANGE

被引:126
作者
MUNRO, C
MICHALEK, SM
MACRINA, FL
机构
[1] VIRGINIA COMMONWEALTH UNIV,DEPT MICROBIOL & IMMUNOL,RICHMOND,VA 23298
[2] UNIV ALABAMA,DEPT MICROBIOL,BIRMINGHAM,AL 35294
关键词
D O I
10.1128/IAI.59.7.2316-2323.1991
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Streptococcus mutans produces several enzymes which metabolize sucrose. Three glucosyltransferase genes (gtfB, gtfC, and gtfD) and a single fructosyltransferase gene (ftf) encode enzymes which are important in formation of exopolysaccharides. Mutants of S. mutans V403 carrying single and multiple mutations of the gtfB, gtfC, gtfD, and ftf genes recently have been constructed by allelic exchange in our laboratory. Using selected strains from this panel of mutants, we examined the importance of water-insoluble glucan, water-soluble glucan, and fructan production in cariogenicity while controlling for the effects of strain and species variability. Genetic and biochemical characterization of mutants and assays of glucosyltransferase and fructosyltransferase activities were performed to ensure that the phenotypes of strains coincided with deficiencies predicted by genotype. The young gnotobiotic rat model of cariogenicity was used to assess virulence of the wild-type strain and isogenic mutants. Mutant strains were less virulent than the wild type in almost every location examined for caries on tooth surfaces and level of involvement of lesions (depth and severity). Inactivation of either gtfB and gtfC or ftf dramatically reduced virulence; the subsequent inactivation of gtfD did not enhance the effect of reduced virulence.
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页码:2316 / 2323
页数:8
相关论文
共 27 条
[11]   BROAD GEOGRAPHICAL-DISTRIBUTION OF HOMOLOGOUS ERYTHROMYCIN, KANAMYCIN, AND STREPTOMYCIN RESISTANCE DETERMINANTS AMONG GROUP-D STREPTOCOCCI OF HUMAN AND ANIMAL ORIGIN [J].
LEBLANC, DJ ;
INAMINE, JM ;
LEE, LN .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (04) :549-555
[12]   CHARACTERIZATION OF GENETIC-TRANSFORMATION IN STREPTOCOCCUS-MUTANS BY USING A NOVEL HIGH-EFFICIENCY PLASMID MARKER RESCUE SYSTEM [J].
LINDLER, LE ;
MACRINA, FL .
JOURNAL OF BACTERIOLOGY, 1986, 166 (02) :658-665
[13]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[14]  
MACRINA F L, 1990, Critical Reviews in Oral Biology and Medicine, V1, P207
[15]   PROCEDURE FOR ISOLATION OF DEOXYRIBONUCLEIC ACID FROM MICRO-ORGANISMS [J].
MARMUR, J .
JOURNAL OF MOLECULAR BIOLOGY, 1961, 3 (02) :208-&
[16]   SODIUM DODECYL-SULFATE ELECTROPHORESIS IN THE 1ST-DIMENSION AND ISOELECTRIC-FOCUSING IN THE 2ND-DIMENSION IN A SINGLE THIN-LAYER GEL, FOLLOWED BY ACTIVITY STAIN FOR GLYCOSYLTRANSFERASES [J].
MUKASA, H ;
TSUMORI, H ;
SHIMAMURA, A .
ELECTROPHORESIS, 1987, 8 (01) :29-34
[17]  
Nelson N, 1944, J BIOL CHEM, V153, P375
[18]   LINKAGE OF SUCROSE-METABOLIZING GENES IN STREPTOCOCCUS-MUTANS [J].
PERRY, D ;
KURAMITSU, HK .
INFECTION AND IMMUNITY, 1990, 58 (10) :3462-3464
[19]   MOLECULAR-ORGANIZATION AND EXPRESSION OF THE GTFA GENE OF STREPTOCOCCUS-MUTANS LM7 [J].
PUCCI, MJ ;
MACRINA, FL .
INFECTION AND IMMUNITY, 1986, 54 (01) :77-84
[20]   MOLECULAR-CLONING AND CHARACTERIZATION OF THE GLUCOSYLTRANSFERASE C GENE (GTFC) FROM STREPTOCOCCUS-MUTANS LM7 [J].
PUCCI, MJ ;
JONES, KR ;
KURAMITSU, HK ;
MACRINA, FL .
INFECTION AND IMMUNITY, 1987, 55 (09) :2176-2182