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A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri

In this study, we measured the drug resistance conferred by mdfA mutations in two Shigella flexneri strains. A mutant in mdfA genes was constructed by polymerase chain reaction–based, one-step inactivation of chromosomal genes. The antimicrobial susceptibility of parent and mutant strains to fluoroq...

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Detalles Bibliográficos
Autores principales: Kim, Jun-Young, Jeon, Se-Mi, Kim, Hyungjun, Park, Mi-Sun, Kim, Seong-Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Centers for Disease Control and Prevention 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767090/
https://www.ncbi.nlm.nih.gov/pubmed/24159476
http://dx.doi.org/10.1016/j.phrp.2011.11.049
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author Kim, Jun-Young
Jeon, Se-Mi
Kim, Hyungjun
Park, Mi-Sun
Kim, Seong-Han
author_facet Kim, Jun-Young
Jeon, Se-Mi
Kim, Hyungjun
Park, Mi-Sun
Kim, Seong-Han
author_sort Kim, Jun-Young
collection PubMed
description In this study, we measured the drug resistance conferred by mdfA mutations in two Shigella flexneri strains. A mutant in mdfA genes was constructed by polymerase chain reaction–based, one-step inactivation of chromosomal genes. The antimicrobial susceptibility of parent and mutant strains to fluoroquinolones was determined by minimal inhibitory concentration (MICs). The △mdfA mutants were somewhat more susceptible to fluoroquinolones than the parent strains. The low level changes in MICs of the △mdfA mutants suggest that mdfA contributed the fluoroquinolone resistance in S flexneri. This finding found that the increased expression level of an MdfA efflux pump mediated fluoroquinolone resistance, but it is not likely a major effecter of higher resistance levels.
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spelling pubmed-37670902013-10-24 A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri Kim, Jun-Young Jeon, Se-Mi Kim, Hyungjun Park, Mi-Sun Kim, Seong-Han Osong Public Health Res Perspect Articles In this study, we measured the drug resistance conferred by mdfA mutations in two Shigella flexneri strains. A mutant in mdfA genes was constructed by polymerase chain reaction–based, one-step inactivation of chromosomal genes. The antimicrobial susceptibility of parent and mutant strains to fluoroquinolones was determined by minimal inhibitory concentration (MICs). The △mdfA mutants were somewhat more susceptible to fluoroquinolones than the parent strains. The low level changes in MICs of the △mdfA mutants suggest that mdfA contributed the fluoroquinolone resistance in S flexneri. This finding found that the increased expression level of an MdfA efflux pump mediated fluoroquinolone resistance, but it is not likely a major effecter of higher resistance levels. Korea Centers for Disease Control and Prevention 2011-12 /pmc/articles/PMC3767090/ /pubmed/24159476 http://dx.doi.org/10.1016/j.phrp.2011.11.049 Text en Copyright ©2011, Korea Centers for Disease Control and Prevention http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( (http://creativecommons.org/licenses/by-nc/3.0) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Kim, Jun-Young
Jeon, Se-Mi
Kim, Hyungjun
Park, Mi-Sun
Kim, Seong-Han
A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri
title A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri
title_full A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri
title_fullStr A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri
title_full_unstemmed A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri
title_short A Contribution of MdfA to Resistance to Fluoroquinolones in Shigella flexneri
title_sort contribution of mdfa to resistance to fluoroquinolones in shigella flexneri
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767090/
https://www.ncbi.nlm.nih.gov/pubmed/24159476
http://dx.doi.org/10.1016/j.phrp.2011.11.049
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