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PMID: 2694951 Published · ppublish English Journal Article

Molecular characterization of the gene encoding SHV-3 beta-lactamase responsible for transferable cefotaxime resistance in clinical isolates of Klebsiella pneumoniae.

Antimicrobial agents and chemotherapy ·Vol. 33 ·No. 12 ·1989-12-00 ·Pages 2096-100

Nicolas MH, Jarlier V, Honore N, Philippon A, Cole ST

Abstract

In Klebsiella pneumoniae 86-4, cefotaxime resistance was due to a transferable broad-spectrum beta-lactamase, SHV-3. The plasmid-borne gene encoding SHV-3 has been cloned, and the primary structure of the enzyme was deduced from its nucleotide sequence. SHV-3 differs from SHV-1 in two positions. The extended substrate profile of SHV-3 probably results from the substitution of Ser-213 for Gly, as in SHV-2, whereas replacement of Arg-180 by Leu resulted in a decrease in the pI from 7.6 to 7.0. The blashv-3 gene is highly homologous (92% DNA sequence identity) with the chromosomal gene coding for LEN-1 beta-lactamase of K. pneumoniae, suggesting that the origin of the SHV-encoding genes now present on many plasmids may be chromosomal.

MeSH Terms
Base Sequence Cefotaxime/pharmacology Cloning, Molecular Cross Infection/microbiology Culture Media Drug Resistance, Microbial/genetics Electrophoresis, Agar Gel Escherichia coli/drug effects,genetics Klebsiella Infections/microbiology Klebsiella pneumoniae/drug effects,genetics Molecular Sequence Data Plasmids Restriction Mapping beta-Lactamases/genetics
Chemicals
Culture Media beta-lactamase SHV-3 beta-Lactamases Cefotaxime
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Nicolas M H
Laboratoire de Génétique Moléculaire Bactérienne, Institut Pasteur, Paris, France.
Jarlier V
Honore N
Philippon A
Cole S T
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1989-12-00
Pages
2096-100
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC172828
Subset
IM
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