Literature DB >> 16842578

Development of extended-spectrum activity in TEM beta-lactamases in hyper-mutable, mutS Escherichia coli.

M J Ellington1, D M Livermore, T L Pitt, L M C Hall, N Woodford.   

Abstract

TEM-1 and TEM(pUC19)beta-lactamases can gain activity against ceftazidime and other expanded-spectrum cephalosporins via point mutation. The frequency of emergent resistance to ceftazidime at 4 x MIC was elevated >or= 250-fold in hyper-mutable, MutS-deficient Escherichia coli harbouring these beta-lactamase genes on high- or low-copy plasmids. Moreover, although ceftazidime-resistant mutants, or those with reduced susceptibility, were selected in both the wild-type and mutS hosts, many more mutants in the mutS host showed ceftazidimase-type extended-spectrum beta-lactamase (ESBL) activity. This correlated with a G-A point mutation at position 484 in the bla(TEM-1) and bla(TEM-pUC19) genes, conferring the Arg164His amino-acid substitution found in the TEM-29 ESBL. Non-ESBL mutants lacked changes in bla(TEM).

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Year:  2006        PMID: 16842578     DOI: 10.1111/j.1469-0691.2006.01424.x

Source DB:  PubMed          Journal:  Clin Microbiol Infect        ISSN: 1198-743X            Impact factor:   8.067


  2 in total

1.  Mutational events in cefotaximase extended-spectrum beta-lactamases of the CTX-M-1 cluster involved in ceftazidime resistance.

Authors:  Angela Novais; Rafael Cantón; Teresa M Coque; Andrés Moya; Fernando Baquero; Juan Carlos Galán
Journal:  Antimicrob Agents Chemother       Date:  2008-04-28       Impact factor: 5.191

2.  Convergent in vivo and in vitro selection of ceftazidime resistance mutations at position 167 of CTX-M-3 beta-lactamase in hypermutable Escherichia coli strains.

Authors:  Marina N Stepanova; Maxim Pimkin; Anatoly A Nikulin; Varvara K Kozyreva; Elena D Agapova; Mikhail V Edelstein
Journal:  Antimicrob Agents Chemother       Date:  2008-01-22       Impact factor: 5.191

  2 in total

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