Pathways Regulating the pbgP Operon and Colistin Resistance in Klebsiella pneumoniae Strains
In this study, we investigated colistin resistance mechanisms associated with the regulation of the pbgP operon in Klebsiella pneumoniae, using four isogenic pairs of colistin-susceptible strains and their colistin-resistant derivatives and two colistin-resistant clinical isolates. Amino acid sequen...
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Published in | Journal of microbiology and biotechnology Vol. 26; no. 9; pp. 1620 - 1628 |
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Main Authors | , , |
Format | Journal Article |
Language | Korean |
Published |
한국미생물생명공학회
30.09.2016
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Subjects | |
Online Access | Get full text |
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Summary: | In this study, we investigated colistin resistance mechanisms associated with the regulation of the pbgP operon in Klebsiella pneumoniae, using four isogenic pairs of colistin-susceptible strains and their colistin-resistant derivatives and two colistin-resistant clinical isolates. Amino acid sequence alterations of PhoPQ, PmrAB, and MgrB were investigated, and mRNA expression levels of phoQ, pmrB, pmrD, and pbgP were measured using quantitative real-time PCR. The phoQ and pmrB genes were deleted from two colistin-resistant derivatives, 134R and 063R. We found that phoQ, pmrD, and pbgP were significantly upregulated in all colistinresistant derivatives. However, pmrB was significantly upregulated in only two colistinresistant derivatives and one clinical strain. pmrB was not overexpressed in the other strains. The minimum inhibitory concentration of colistin was drastically lower in both phoQ- and pmrB-deleted mutants from a colistin-resistant derivative (134R) that was overexpressing phoQ and pmrB. However, colistin susceptibility was restored only in a phoQ-deleted mutant from a colistin-resistant derivative (063R) without overexpression of pmrB. In conclusion, two different regulations of the pbgP operon may associate with the development of colistinresisant K. pneumoniae. |
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Bibliography: | The Korean Society for Applied Microbiology KISTI1.1003/JNL.JAKO201629149592246 |
ISSN: | 1017-7825 1738-8872 |