Comparative Study of the Effects of Fluconazole and Voriconazole on Candida glabrata, Candida parapsilosis and Candida rugosa Biofilms
Infections by non- albicans Candida species are a life-threatening condition, and formation of biofilms can lead to treatment failure in a clinical setting. This study was aimed to demonstrate the in vitro antibiofilm activity of fluconazole (FLU) and voriconazole (VOR) against C. glabrata , C. para...
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creator | Madhavan, Priya Jamal, Farida Pei, Chong Pei Othman, Fauziah Karunanidhi, Arunkumar Ng, Kee Peng |
description | Infections by non-
albicans Candida
species are a life-threatening condition, and formation of biofilms can lead to treatment failure in a clinical setting. This study was aimed to demonstrate the in vitro antibiofilm activity of fluconazole (FLU) and voriconazole (VOR) against
C. glabrata
,
C. parapsilosis
and
C. rugosa
with diverse antifungal susceptibilities to FLU and VOR. The antibiofilm activities of FLU and VOR in the form of suspension as well as pre-coatings were assessed by XTT [2,3-
bis
-(2-methoxy-4-nitro-5-sulfophenyl)-
2H
-tetrazolium-5-carboxanilide] reduction assay. Morphological and intracellular changes exerted by the antifungal drugs on
Candida
cells were examined by scanning electron microscope (SEM) and transmission electron microscope (TEM). The results of the antibiofilm activities showed that FLU drug suspension was capable of killing
C. parapsilosis
and
C. rugosa
at minimum inhibitory concentrations (MICs) of 4× MIC FLU and 256× MIC FLU, respectively. While VOR MICs ranging from 2× to 32× were capable of killing the biofilms of all
Candida
spp tested. The antibiofilm activities of pre-coated FLU were able to kill the biofilms at ¼× MIC FLU and ½× MIC FLU for
C. parapsilosis
and
C. rugosa
strains, respectively. While pre-coated VOR was able to kill the biofilms, all three
Candida
sp at ½× MIC VOR. SEM and TEM examinations showed that FLU and VOR treatments exerted significant impact on
Candida
cell with various degrees of morphological changes. In conclusion, a fourfold reduction in MIC
50
of FLU and VOR towards ATCC strains of
C. glabrata
,
C. rugosa
and
C. rugosa
clinical strain was observed in this study. |
doi_str_mv | 10.1007/s11046-018-0243-z |
format | Article |
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albicans Candida
species are a life-threatening condition, and formation of biofilms can lead to treatment failure in a clinical setting. This study was aimed to demonstrate the in vitro antibiofilm activity of fluconazole (FLU) and voriconazole (VOR) against
C. glabrata
,
C. parapsilosis
and
C. rugosa
with diverse antifungal susceptibilities to FLU and VOR. The antibiofilm activities of FLU and VOR in the form of suspension as well as pre-coatings were assessed by XTT [2,3-
bis
-(2-methoxy-4-nitro-5-sulfophenyl)-
2H
-tetrazolium-5-carboxanilide] reduction assay. Morphological and intracellular changes exerted by the antifungal drugs on
Candida
cells were examined by scanning electron microscope (SEM) and transmission electron microscope (TEM). The results of the antibiofilm activities showed that FLU drug suspension was capable of killing
C. parapsilosis
and
C. rugosa
at minimum inhibitory concentrations (MICs) of 4× MIC FLU and 256× MIC FLU, respectively. While VOR MICs ranging from 2× to 32× were capable of killing the biofilms of all
Candida
spp tested. The antibiofilm activities of pre-coated FLU were able to kill the biofilms at ¼× MIC FLU and ½× MIC FLU for
C. parapsilosis
and
C. rugosa
strains, respectively. While pre-coated VOR was able to kill the biofilms, all three
Candida
sp at ½× MIC VOR. SEM and TEM examinations showed that FLU and VOR treatments exerted significant impact on
Candida
cell with various degrees of morphological changes. In conclusion, a fourfold reduction in MIC
50
of FLU and VOR towards ATCC strains of
C. glabrata
,
C. rugosa
and
C. rugosa
clinical strain was observed in this study.</description><identifier>ISSN: 0301-486X</identifier><identifier>EISSN: 1573-0832</identifier><identifier>DOI: 10.1007/s11046-018-0243-z</identifier><identifier>PMID: 29380188</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Antifungal agents ; Biofilms ; Biomedical and Life Sciences ; Candida ; Candida parapsilosis ; Coatings ; Comparative analysis ; Electron microscopes ; Eukaryotic Microbiology ; Fluconazole ; Fungicides ; Health aspects ; Influenza ; Life Sciences ; Medical Microbiology ; Microbial Ecology ; Microbiology ; Minimum inhibitory concentration ; Morphology ; Original Paper ; Plant Sciences ; Scanning electron microscopy ; Transmission electron microscopes ; Transmission electron microscopy ; Voriconazole</subject><ispartof>Mycopathologia (1975), 2018-06, Vol.183 (3), p.499-511</ispartof><rights>Springer Science+Business Media B.V., part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Mycopathologia is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-3ce510808acceedaeca047378ea44c287654fb140a54a22e29cb13ceb98fb3cc3</citedby><cites>FETCH-LOGICAL-c539t-3ce510808acceedaeca047378ea44c287654fb140a54a22e29cb13ceb98fb3cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11046-018-0243-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11046-018-0243-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29380188$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Madhavan, Priya</creatorcontrib><creatorcontrib>Jamal, Farida</creatorcontrib><creatorcontrib>Pei, Chong Pei</creatorcontrib><creatorcontrib>Othman, Fauziah</creatorcontrib><creatorcontrib>Karunanidhi, Arunkumar</creatorcontrib><creatorcontrib>Ng, Kee Peng</creatorcontrib><title>Comparative Study of the Effects of Fluconazole and Voriconazole on Candida glabrata, Candida parapsilosis and Candida rugosa Biofilms</title><title>Mycopathologia (1975)</title><addtitle>Mycopathologia</addtitle><addtitle>Mycopathologia</addtitle><description>Infections by non-
albicans Candida
species are a life-threatening condition, and formation of biofilms can lead to treatment failure in a clinical setting. This study was aimed to demonstrate the in vitro antibiofilm activity of fluconazole (FLU) and voriconazole (VOR) against
C. glabrata
,
C. parapsilosis
and
C. rugosa
with diverse antifungal susceptibilities to FLU and VOR. The antibiofilm activities of FLU and VOR in the form of suspension as well as pre-coatings were assessed by XTT [2,3-
bis
-(2-methoxy-4-nitro-5-sulfophenyl)-
2H
-tetrazolium-5-carboxanilide] reduction assay. Morphological and intracellular changes exerted by the antifungal drugs on
Candida
cells were examined by scanning electron microscope (SEM) and transmission electron microscope (TEM). The results of the antibiofilm activities showed that FLU drug suspension was capable of killing
C. parapsilosis
and
C. rugosa
at minimum inhibitory concentrations (MICs) of 4× MIC FLU and 256× MIC FLU, respectively. While VOR MICs ranging from 2× to 32× were capable of killing the biofilms of all
Candida
spp tested. The antibiofilm activities of pre-coated FLU were able to kill the biofilms at ¼× MIC FLU and ½× MIC FLU for
C. parapsilosis
and
C. rugosa
strains, respectively. While pre-coated VOR was able to kill the biofilms, all three
Candida
sp at ½× MIC VOR. SEM and TEM examinations showed that FLU and VOR treatments exerted significant impact on
Candida
cell with various degrees of morphological changes. In conclusion, a fourfold reduction in MIC
50
of FLU and VOR towards ATCC strains of
C. glabrata
,
C. rugosa
and
C. rugosa
clinical strain was observed in this study.</description><subject>Antifungal agents</subject><subject>Biofilms</subject><subject>Biomedical and Life Sciences</subject><subject>Candida</subject><subject>Candida parapsilosis</subject><subject>Coatings</subject><subject>Comparative analysis</subject><subject>Electron microscopes</subject><subject>Eukaryotic Microbiology</subject><subject>Fluconazole</subject><subject>Fungicides</subject><subject>Health aspects</subject><subject>Influenza</subject><subject>Life Sciences</subject><subject>Medical Microbiology</subject><subject>Microbial Ecology</subject><subject>Microbiology</subject><subject>Minimum inhibitory concentration</subject><subject>Morphology</subject><subject>Original Paper</subject><subject>Plant Sciences</subject><subject>Scanning electron microscopy</subject><subject>Transmission electron microscopes</subject><subject>Transmission electron microscopy</subject><subject>Voriconazole</subject><issn>0301-486X</issn><issn>1573-0832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp1ks9u1DAQxi0EokvhAbigSFxaqSn-l8Q5llVLK1VCooC4WRNnElwl8WInVbsPwHPjdNtVF4F8sDzz-z7NjIeQt4weM0qLD4ExKvOUMpVSLkW6fkYWLCtESpXgz8mCCspSqfIfe-RVCNeURhUrXpI9XgoVVWpBfi9dvwIPo73B5Gqc6rvENcn4E5PTpkEzhvl51k3GDbB2HSYw1Ml35-024IZkGYO2hqTtoIpWcLSNzNarYDsXbLiXPib81LoAyUfrGtv14TV50UAX8M3DvU--nZ1-XZ6nl58_XSxPLlOTiXJMhcGMUUUVGINYAxqgshCFQpDScFXkmWwqJilkEjhHXpqKRVFVqqYSxoh9crDxXXn3a8Iw6t4Gg10HA7opaFaWgtK8FDyi7_9Cr93kh1jdPZVxyvInVAsdajs0bvRgZlN9EkvmikuuInX8DyqeGvt5khiHgLuCwx1BZEa8HVuYQtAXV192WbZhjXcheGz0ytse_J1mVM97ojd7ouOP63lP9Dpq3j00N1U91lvF42JEgG-AEFNDi_5J9_91_QPjX8fO</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Madhavan, Priya</creator><creator>Jamal, Farida</creator><creator>Pei, Chong Pei</creator><creator>Othman, Fauziah</creator><creator>Karunanidhi, Arunkumar</creator><creator>Ng, Kee Peng</creator><general>Springer Netherlands</general><general>Springer</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20180601</creationdate><title>Comparative Study of the Effects of Fluconazole and Voriconazole on Candida glabrata, Candida parapsilosis and Candida rugosa Biofilms</title><author>Madhavan, Priya ; 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albicans Candida
species are a life-threatening condition, and formation of biofilms can lead to treatment failure in a clinical setting. This study was aimed to demonstrate the in vitro antibiofilm activity of fluconazole (FLU) and voriconazole (VOR) against
C. glabrata
,
C. parapsilosis
and
C. rugosa
with diverse antifungal susceptibilities to FLU and VOR. The antibiofilm activities of FLU and VOR in the form of suspension as well as pre-coatings were assessed by XTT [2,3-
bis
-(2-methoxy-4-nitro-5-sulfophenyl)-
2H
-tetrazolium-5-carboxanilide] reduction assay. Morphological and intracellular changes exerted by the antifungal drugs on
Candida
cells were examined by scanning electron microscope (SEM) and transmission electron microscope (TEM). The results of the antibiofilm activities showed that FLU drug suspension was capable of killing
C. parapsilosis
and
C. rugosa
at minimum inhibitory concentrations (MICs) of 4× MIC FLU and 256× MIC FLU, respectively. While VOR MICs ranging from 2× to 32× were capable of killing the biofilms of all
Candida
spp tested. The antibiofilm activities of pre-coated FLU were able to kill the biofilms at ¼× MIC FLU and ½× MIC FLU for
C. parapsilosis
and
C. rugosa
strains, respectively. While pre-coated VOR was able to kill the biofilms, all three
Candida
sp at ½× MIC VOR. SEM and TEM examinations showed that FLU and VOR treatments exerted significant impact on
Candida
cell with various degrees of morphological changes. In conclusion, a fourfold reduction in MIC
50
of FLU and VOR towards ATCC strains of
C. glabrata
,
C. rugosa
and
C. rugosa
clinical strain was observed in this study.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>29380188</pmid><doi>10.1007/s11046-018-0243-z</doi><tpages>13</tpages></addata></record> |
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issn | 0301-486X 1573-0832 |
language | eng |
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source | SpringerLink Journals (MCLS) |
subjects | Antifungal agents Biofilms Biomedical and Life Sciences Candida Candida parapsilosis Coatings Comparative analysis Electron microscopes Eukaryotic Microbiology Fluconazole Fungicides Health aspects Influenza Life Sciences Medical Microbiology Microbial Ecology Microbiology Minimum inhibitory concentration Morphology Original Paper Plant Sciences Scanning electron microscopy Transmission electron microscopes Transmission electron microscopy Voriconazole |
title | Comparative Study of the Effects of Fluconazole and Voriconazole on Candida glabrata, Candida parapsilosis and Candida rugosa Biofilms |
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