MOLECULAR TYPING OF SALMONELLA-TYPHI STRAINS FROM DHAKA (BANGLADESH) AND DEVELOPMENT OF DNA PROBES IDENTIFYING PLASMID-ENCODED MULTIDRUG-RESISTANT ISOLATES

Citation
Pwm. Hermans et al., MOLECULAR TYPING OF SALMONELLA-TYPHI STRAINS FROM DHAKA (BANGLADESH) AND DEVELOPMENT OF DNA PROBES IDENTIFYING PLASMID-ENCODED MULTIDRUG-RESISTANT ISOLATES, Journal of clinical microbiology, 34(6), 1996, pp. 1373-1379
Citations number
32
Categorie Soggetti
Microbiology
ISSN journal
00951137
Volume
34
Issue
6
Year of publication
1996
Pages
1373 - 1379
Database
ISI
SICI code
0095-1137(1996)34:6<1373:MTOSSF>2.0.ZU;2-C
Abstract
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 collecti on displayed a high degree of genetic homogeneity, because restricted numbers of phage types and DNA fingerprints were observed. A significa nt number of the S. typhi strains (67%) were demonstrated to be multip le drug resistant (MDR). The vast majority of the MDR strains were res istant to chloramphenicol, ampicillin, trimethoprim, streptomycin, sul famethoxazole, and tetracycline (R type CATmSSuT) a resistance phenoty pe that has also frequently been observed in India, Only two strains d isplayed a distinct MDR phenotype, R type AT-mSSuT. Pulsed-field gel e lectrophoresis demonstrated the presence of large plasmids exclusively in the MDR strains of both R types. The plasmids present in the S. ty phi strains of R type CATmSSuT could be conjugated to Escherichia coli and resulted in the complete transfer of the MDR phenotype. PCR finge rprinting allowed discrimination of MDR and susceptible strains. The D NA fragments enabling discrimination of MDR and susceptible S. typhi s trains by PCR were useful genetic markers for identifying MDR encoded by large plasmids of the H1 incompatibility group.