Abstract
We have demonstrated by using an in vitro approach that interruption of the OmpK36 porin gene by insertion sequences (ISs) is a common type of mutation that causes loss of porin expression and increased resistance to cefoxitin in Klebsiella pneumoniae. This mechanism also operates in vivo: of 13 porin-deficient cefoxitin-resistant clinical isolates of K. pneumoniae, 4 presented ISs in their ompK36 gene.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Bacterial Proteins*
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Cefoxitin / pharmacology
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Cephamycins / pharmacology
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DNA Transposable Elements / genetics
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Drug Resistance, Microbial / genetics
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Humans
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Klebsiella pneumoniae / drug effects
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Klebsiella pneumoniae / genetics*
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Klebsiella pneumoniae / metabolism
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Mutagenesis, Insertional
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Porins / biosynthesis
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Porins / genetics*
Substances
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Bacterial Proteins
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Cephamycins
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DNA Transposable Elements
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OmpK36 protein, Klebsiella pneumoniae
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Porins
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Cefoxitin