pR_(ST98) is a large and conjugative resistant plasmid(R plasmid)of 98.6 mega-dalton from multi-drug resistant Salmonella typhi(S.typhi),which was classified to incompatibility group C(Inc C).It has been found that pR...pR_(ST98) is a large and conjugative resistant plasmid(R plasmid)of 98.6 mega-dalton from multi-drug resistant Salmonella typhi(S.typhi),which was classified to incompatibility group C(Inc C).It has been found that pR_(ST98) made its host bacteria not only antibiotic resistant but also more virulent.In this study we explored the possibility of plasmid pR_(ST98) in S.typhi carrying the Salmonella plasmid virulence gene-spv.The plasmid pR_(ST98) was isolated, purified and then digested by nine restriction endonucleases to make the plasmid enzyme profile.Spv-specific PCR and Southern blot were applied to identify the virulence gene on pR_(ST98).The amplified spv fragments spvR and spvB were cloned into pGEM-T EASY and then the DNA sequences were analysed.The fragments of pR_(ST98) digested by endonucleases Bgl Ⅱ,Pst Ⅰ and Sac Ⅱ were identified,which may be useful for molecular analysis and further epidemiological surveillance of pR_(ST98).The results of PCR and Southern blot showed that spv homologous genetic sequence which had been found in all pathogenesis Salmonella spp.except S.typhi was also presented on pR_(ST98).The ORF of spvR and spvB of pR_(ST98) were 894 bp and 1,776 bp,respectively.They have more than 99% homology with that of spvR and spvB on virulence plasmid in S.typhmurium.The genotype research on pR_(ST98) revealed that there is a plasmid carrying genes responsible for drug resistance and virulence in S.typhi.This is the first report for such kind chimerical plasmid in S.typhi.Cellular & Molecular Immunology.2005;2(2):136-140.展开更多
The R plasmid curing experiment was performed in vitro with E. coli strain E. 102 bearing Rplasmid with multiple drug resistance as target bacteria and Rhizoma Coptidis as elimination agent, and theinfluence at differ...The R plasmid curing experiment was performed in vitro with E. coli strain E. 102 bearing Rplasmid with multiple drug resistance as target bacteria and Rhizoma Coptidis as elimination agent, and theinfluence at different acting time of it on R plasmid elimination was also observed. Results showed that whenthe acting time was 24 hours, the cure rate of R plasmid was 2 . 42 % and when the action time increased to 48hours, the cure rate was elevated to 22. 57% . The missing pattern s of R plasmid might occur in diap-pearence of either multiple or single resistance.展开更多
文摘pR_(ST98) is a large and conjugative resistant plasmid(R plasmid)of 98.6 mega-dalton from multi-drug resistant Salmonella typhi(S.typhi),which was classified to incompatibility group C(Inc C).It has been found that pR_(ST98) made its host bacteria not only antibiotic resistant but also more virulent.In this study we explored the possibility of plasmid pR_(ST98) in S.typhi carrying the Salmonella plasmid virulence gene-spv.The plasmid pR_(ST98) was isolated, purified and then digested by nine restriction endonucleases to make the plasmid enzyme profile.Spv-specific PCR and Southern blot were applied to identify the virulence gene on pR_(ST98).The amplified spv fragments spvR and spvB were cloned into pGEM-T EASY and then the DNA sequences were analysed.The fragments of pR_(ST98) digested by endonucleases Bgl Ⅱ,Pst Ⅰ and Sac Ⅱ were identified,which may be useful for molecular analysis and further epidemiological surveillance of pR_(ST98).The results of PCR and Southern blot showed that spv homologous genetic sequence which had been found in all pathogenesis Salmonella spp.except S.typhi was also presented on pR_(ST98).The ORF of spvR and spvB of pR_(ST98) were 894 bp and 1,776 bp,respectively.They have more than 99% homology with that of spvR and spvB on virulence plasmid in S.typhmurium.The genotype research on pR_(ST98) revealed that there is a plasmid carrying genes responsible for drug resistance and virulence in S.typhi.This is the first report for such kind chimerical plasmid in S.typhi.Cellular & Molecular Immunology.2005;2(2):136-140.
文摘The R plasmid curing experiment was performed in vitro with E. coli strain E. 102 bearing Rplasmid with multiple drug resistance as target bacteria and Rhizoma Coptidis as elimination agent, and theinfluence at different acting time of it on R plasmid elimination was also observed. Results showed that whenthe acting time was 24 hours, the cure rate of R plasmid was 2 . 42 % and when the action time increased to 48hours, the cure rate was elevated to 22. 57% . The missing pattern s of R plasmid might occur in diap-pearence of either multiple or single resistance.
