Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin

Ciprofloxacin, a quinolone with good intracellular penetration may possibly be used for treatment of melioidosis caused by Burkholderia pseudomallei, but problems with resistance may be encountered. Amino acid substitutions in gyrA/gyrB have given rise to fluoroquinolone resistance in various microo...

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Main Authors: Liew, F.Y., Tay, S.T., Puthucheary, S.D.
Format: Article
Published: Malaysian Society of Parasitology and Tropical Medicine 2012
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Online Access:http://eprints.um.edu.my/3402/
http://www.ncbi.nlm.nih.gov/pubmed/22433895
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spelling my.um.eprints.34022019-02-13T09:07:21Z http://eprints.um.edu.my/3402/ Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin Liew, F.Y. Tay, S.T. Puthucheary, S.D. R Medicine Ciprofloxacin, a quinolone with good intracellular penetration may possibly be used for treatment of melioidosis caused by Burkholderia pseudomallei, but problems with resistance may be encountered. Amino acid substitutions in gyrA/gyrB have given rise to fluoroquinolone resistance in various microorganisms. Using published primers for gyrA and gyrB, PCR was performed on 11 isolates of B. pseudomallei with varying degrees of sensitivity to ciprofloxacin, followed by DNA sequencing to detect possible mutations. Results showed an absence of any point mutation in either gene. Local isolates have yet to develop full resistance to ciprofloxacin and probably other mechanisms of resistance may have been involved in the decreased sensitivity to ciprofloxacin. Malaysian Society of Parasitology and Tropical Medicine 2012 Article PeerReviewed Liew, F.Y. and Tay, S.T. and Puthucheary, S.D. (2012) Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin. Tropical Biomedicine, 28 (3). ISSN 0127-5720 http://www.ncbi.nlm.nih.gov/pubmed/22433895 PMID: 22433895
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine
spellingShingle R Medicine
Liew, F.Y.
Tay, S.T.
Puthucheary, S.D.
Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin
description Ciprofloxacin, a quinolone with good intracellular penetration may possibly be used for treatment of melioidosis caused by Burkholderia pseudomallei, but problems with resistance may be encountered. Amino acid substitutions in gyrA/gyrB have given rise to fluoroquinolone resistance in various microorganisms. Using published primers for gyrA and gyrB, PCR was performed on 11 isolates of B. pseudomallei with varying degrees of sensitivity to ciprofloxacin, followed by DNA sequencing to detect possible mutations. Results showed an absence of any point mutation in either gene. Local isolates have yet to develop full resistance to ciprofloxacin and probably other mechanisms of resistance may have been involved in the decreased sensitivity to ciprofloxacin.
format Article
author Liew, F.Y.
Tay, S.T.
Puthucheary, S.D.
author_facet Liew, F.Y.
Tay, S.T.
Puthucheary, S.D.
author_sort Liew, F.Y.
title Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin
title_short Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin
title_full Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin
title_fullStr Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin
title_full_unstemmed Reduced susceptibility of Malaysian clinical isolates of Burkholderia pseudomallei to ciprofloxacin
title_sort reduced susceptibility of malaysian clinical isolates of burkholderia pseudomallei to ciprofloxacin
publisher Malaysian Society of Parasitology and Tropical Medicine
publishDate 2012
url http://eprints.um.edu.my/3402/
http://www.ncbi.nlm.nih.gov/pubmed/22433895
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