Molecular typing of Salmonella typhi strains from Dhaka (Bangladesh) and development of DNA probes identifying plasmid-encoded multidrug-resistant isolates

被引:34
作者
Hermans, PWM
Saha, SK
vanLeeuwen, WJ
Verbrugh, HA
vanBelkum, A
Goessens, WHF
机构
[1] ERASMUS UNIV ROTTERDAM,UNIV ROTTERDAM HOSP,DEPT CLIN MICROBIOL,3000 DR ROTTERDAM,NETHERLANDS
[2] NATL INST PUBL HLTH & ENVIRONM PROTECT,LAB BACTERIOL & ANTIMICROBIAL AGENTS,3720 BA BILTHOVEN,NETHERLANDS
[3] DHAKA SHISHU CHILDRENS HOSP,DHAKA 1207,BANGLADESH
关键词
D O I
10.1128/JCM.34.6.1373-1379.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Seventy-eight Salmonella typhi strains isolated in 1993 and 1995 from patients living in Dhaka, Bangladesh, were subjected to phage typing, ribotyping, IS200 fingerprinting, and PCR fingerprinting. The collection displayed a high degree of genetic homogeneity, because restricted numbers of phage types and DNA fingerprints were observed. A significant number of the S. typhi strains (67%) were demonstrated to be multiple drug resistant (MDR). The vast majority of the MDR strains were resistant to chloramphenicol, ampicillin, trimethoprim, streptomycin, sulfamethoxazole, and tetracycline (R type CATmSSuT) a resistance phenotype that has also frequently been observed in India, Only two strains displayed a distinct MDR phenotype, R type AT-mSSuT. Pulsed-field gel electrophoresis demonstrated the presence of large plasmids exclusively in the MDR strains of both R types. The plasmids present in the S. typhi strains of R type CATmSSuT could be conjugated to Escherichia coli and resulted in the complete transfer of the MDR phenotype. PCR fingerprinting allowed discrimination of MDR and susceptible strains. The DNA fragments enabling discrimination of MDR and susceptible S. typhi strains by PCR were useful genetic markers for identifying MDR encoded by large plasmids of the H1 incompatibility group.
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收藏
页码:1373 / 1379
页数:7
相关论文
共 32 条
[1]   MULTIRESISTANT SALMONELLA-TYPHI IN BANGLADESH [J].
ALBERT, MJ ;
HAIDER, K ;
NAHAR, S ;
KIBRIYA, AKMG ;
HOSSAIN, MA .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1991, 27 (04) :554-555
[2]   RIBOSOMAL-RNA GENE RESTRICTION PATTERNS PROVIDE INCREASED SENSITIVITY FOR TYPING SALMONELLA-TYPHI STRAINS [J].
ALTWEGG, M ;
HICKMANBRENNER, FW ;
FARMER, JJ .
JOURNAL OF INFECTIOUS DISEASES, 1989, 160 (01) :145-149
[3]  
EDELMAN R, 1986, REV INFECT DIS, V8, P329
[4]   DISTRIBUTION OF INSERTION-SEQUENCE IS200 IN SALMONELLA AND SHIGELLA [J].
GIBERT, I ;
BARBE, J ;
CASADESUS, J .
JOURNAL OF GENERAL MICROBIOLOGY, 1990, 136 :2555-2560
[5]   DEVELOPMENT OF SPECIES-SPECIFIC DNA PROBES FOR CAMPYLOBACTER-JEJUNI, CAMPYLOBACTER-COLI, AND CAMPYLOBACTER-LARIDIS BY POLYMERASE CHAIN-REACTION FINGERPRINTING [J].
GIESENDORF, BAJ ;
VANBELKUM, A ;
KOEKEN, A ;
STEGEMAN, H ;
HENKENS, MHC ;
VANDERPLAS, J ;
GOOSSENS, H ;
NIESTERS, HGM ;
QUINT, WGV .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (06) :1541-1546
[6]   RIBOSOMAL RIBONUCLEIC-ACID GENE RESTRICTION PATTERNS AS POTENTIAL TAXONOMIC TOOLS [J].
GRIMONT, F ;
GRIMONT, PAD .
ANNALES DE L INSTITUT PASTEUR-MICROBIOLOGIE, 1986, 137B (02) :165-175
[7]  
GUINEE PAM, 1978, METHOD MICROBIOL, V11, P157
[8]   COMPARATIVE-STUDY OF 5 DIFFERENT DNA FINGERPRINT TECHNIQUES FOR MOLECULAR TYPING OF STREPTOCOCCUS-PNEUMONIAE STRAINS [J].
HERMANS, PWM ;
SLUIJTER, M ;
HOOGENBOEZEM, T ;
HEERSMA, H ;
VANBELKUM, A ;
DEGROOT, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (06) :1606-1612
[9]  
HORNICK RB, 1985, REV INFECT DIS, V7, P536
[10]   IS200 - A SALMONELLA-SPECIFIC INSERTION-SEQUENCE [J].
LAM, S ;
ROTH, JR .
CELL, 1983, 34 (03) :951-960