GENETIC-STUDIES OF CEFOTAXIME RESISTANCE IN STREPTOCOCCUS-PNEUMONIAE - RELATIONSHIP TO TRANSFORMATION DEFICIENCY

被引:6
作者
SEROUDE, L [1 ]
HESPERT, S [1 ]
SELAKOVITCHCHENU, L [1 ]
GASC, AM [1 ]
LEFRANCOIS, J [1 ]
SICARD, M [1 ]
机构
[1] CNRS,MICROBIOL & GENET MOLEC LAB,118 ROUTE NARBONNE,F-31062 TOULOUSE,FRANCE
关键词
TRANSFORMATION; STREPTOCOCCUS PNEUMONIAE; CEFOTAXIME; BETA-LACTAM; RESISTANCE; PBP; COMPETENCE;
D O I
10.1016/0923-2508(93)90196-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A laboratory pneumococcal strain resistant to cefotaxime was studied by DNA-induced transformation in order to characterize its genetic structure. At least three independent genes were required to confer the highest level of resistance to this beta-lactam antibiotic. The accumulation of mutations in these three genes accounted for three levels of resistance. Mutation of the gene encoding penicillin-binding protein 2x was very likely responsible for the first step of resistance, which was a prerequisite for sequential increase in resistance. Additionally, strains highly resistant to cefotaxime were defective for natural transformation. Revertants of these strains were frequently observed. Such strains had recovered full transformability, suggesting a correlation between the inability to be transformed and a high level of resistance to cefotaxime. The possibility of electrotransforming these highly resistant strains suggests that natural transformation is probably blocked at the DNA-uptake level.
引用
收藏
页码:389 / 394
页数:6
相关论文
共 12 条
[1]  
CLAVERYS JP, 1986, MICROBIOL REV, V50, P133, DOI 10.1128/MMBR.50.2.133-165.1986
[2]   EXCISION AND REPAIR OF MISMATCHED BASE-PAIRS IN TRANSFORMATION OF STREPTOCOCCUS-PNEUMONIAE [J].
CLAVERYS, JP ;
ROGER, M ;
SICARD, AM .
MOLECULAR & GENERAL GENETICS, 1980, 178 (01) :191-201
[3]  
GASC AM, 1988, J GEN MICROBIOL, V134, P3019
[4]  
HAKENBECK R, 1987, J GEN MICROBIOL, V133, P755
[5]   MULTIPLE CHANGES OF PENICILLIN-BINDING PROTEINS IN PENICILLIN-RESISTANT CLINICAL ISOLATES OF STREPTOCOCCUS-PNEUMONIAE [J].
HAKENBECK, R ;
TARPAY, M ;
TOMASZ, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1980, 17 (03) :364-371
[6]   ANTIBODIES AGAINST THE BENZYLPENICILLOYL MOIETY AS A PROBE FOR PENICILLIN-BINDING PROTEINS [J].
HAKENBECK, R ;
BRIESE, T ;
ELLERBROK, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 157 (01) :101-106
[7]   NUCLEOTIDE-SEQUENCES OF THE PBPX GENES ENCODING THE PENICILLIN-BINDING PROTEINS 2X FROM STREPTOCOCCUS-PNEUMONIAE R6 AND A CEFOTAXIME-RESISTANT MUTANT, C506 [J].
LAIBLE, G ;
HAKENBECK, R ;
SICARD, MA ;
JORIS, B ;
GHUYSEN, JM .
MOLECULAR MICROBIOLOGY, 1989, 3 (10) :1337-1348
[8]  
LAIBLE G, 1987, MOL MICROBIOL, V1, P355
[9]   INHIBITION OF TRANSFORMATION IN STREPTOCOCCUS-PNEUMONIAE BY LYSOGENY [J].
MOYNET, DJ ;
TIRABY, GJ .
JOURNAL OF BACTERIOLOGY, 1980, 141 (03) :1298-1304
[10]   A PLASMID VECTOR ALLOWING POSITIVE SELECTION OF RECOMBINANT PLASMIDS IN STREPTOCOCCUS-PNEUMONIAE [J].
PRATS, H ;
MARTIN, B ;
POGNONEC, P ;
BURGER, AC ;
CLAVERYS, JP .
GENE, 1985, 39 (01) :41-48