In Vitro Evaluation of Combination Antifungal Activity against Fusarium Species Isolated from Ocular Tissues of Keratomycosis Patients

Purpose To determine the minimum inhibitory concentrations (MICs) of five antifungal agents against Fusarium species isolated from ocular tissues and to evaluate anti-Fusarium species activities of eight combination treatments in vitro. Design Experimental research. Methods Thirty-eight isolates of...

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Veröffentlicht in:American journal of ophthalmology 2008-11, Vol.146 (5), p.724-728.e1
Hauptverfasser: Li, Li, Wang, Zhiqun, Li, Ran, Luo, Shiyun, Sun, Xuguang
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container_issue 5
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container_title American journal of ophthalmology
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creator Li, Li
Wang, Zhiqun
Li, Ran
Luo, Shiyun
Sun, Xuguang
description Purpose To determine the minimum inhibitory concentrations (MICs) of five antifungal agents against Fusarium species isolated from ocular tissues and to evaluate anti-Fusarium species activities of eight combination treatments in vitro. Design Experimental research. Methods Thirty-eight isolates of Fusarium species were collected from patients' ocular tissues and were cultured in vitro. The MICs of natamycin, terbinafine, itraconazole fluconazole, and amphotericin B, either used alone or combined with other compounds, were evaluated by checkerboard microdilution technique based on the Clinical Laboratory Standards Institute proposed standard. The interactions were assessed using the Fractional Inhibitory Concentration Index model. Results In the MIC study, the MIC90 of each drug used alone were: natamycin, 16 μg/ml; terbinafine, 8 μg/ml; itraconazole, >16 μg/ml; fluconazole, >64 μg/ml; and amphotericin B, 4 μg/ml. Synergism was obtained in the amphotericin B plus terbinafine (81.6%) group and in the amphotericin B plus itraconazole (84.2%) group, with an obviously decreased MIC value of amphotericin B. Antagonism was shown in the natamycin plus azoles and in the natamycin plus terbinafine groups in 52.6% to 60.5% of Fusarium species strains. Conclusions Amphotericin B plus terbinafine or itraconazole demonstrated more effective anti-Fusarium species activity than single-use in vitro treatment, which implies that these combinations may be helpful in treating fungal keratitis. The combinations of natamycin plus azoles or natamycin plus terbinafine were not satisfactory and can be avoided. Further in vivo studies are needed to elucidate the potential usefulness of these combination therapies.
doi_str_mv 10.1016/j.ajo.2008.06.008
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Design Experimental research. Methods Thirty-eight isolates of Fusarium species were collected from patients' ocular tissues and were cultured in vitro. The MICs of natamycin, terbinafine, itraconazole fluconazole, and amphotericin B, either used alone or combined with other compounds, were evaluated by checkerboard microdilution technique based on the Clinical Laboratory Standards Institute proposed standard. The interactions were assessed using the Fractional Inhibitory Concentration Index model. Results In the MIC study, the MIC90 of each drug used alone were: natamycin, 16 μg/ml; terbinafine, 8 μg/ml; itraconazole, &gt;16 μg/ml; fluconazole, &gt;64 μg/ml; and amphotericin B, 4 μg/ml. Synergism was obtained in the amphotericin B plus terbinafine (81.6%) group and in the amphotericin B plus itraconazole (84.2%) group, with an obviously decreased MIC value of amphotericin B. Antagonism was shown in the natamycin plus azoles and in the natamycin plus terbinafine groups in 52.6% to 60.5% of Fusarium species strains. Conclusions Amphotericin B plus terbinafine or itraconazole demonstrated more effective anti-Fusarium species activity than single-use in vitro treatment, which implies that these combinations may be helpful in treating fungal keratitis. The combinations of natamycin plus azoles or natamycin plus terbinafine were not satisfactory and can be avoided. Further in vivo studies are needed to elucidate the potential usefulness of these combination therapies.</description><identifier>ISSN: 0002-9394</identifier><identifier>EISSN: 1879-1891</identifier><identifier>DOI: 10.1016/j.ajo.2008.06.008</identifier><identifier>PMID: 18707669</identifier><identifier>CODEN: AJOPAA</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Amphotericin B - pharmacology ; Antifungal Agents - pharmacology ; Biological and medical sciences ; Corneal Diseases - microbiology ; Crop diseases ; Drug Evaluation ; Drug Synergism ; Drugs ; Eye - microbiology ; Eye Infections, Fungal - microbiology ; Fluconazole - pharmacology ; Fungal infections ; Fungi ; Fusarium - drug effects ; Fusarium - isolation &amp; purification ; Humans ; In Vitro Techniques ; Itraconazole - pharmacology ; Laboratories ; Medical sciences ; Medical treatment ; Methods ; Microbial Sensitivity Tests ; Miscellaneous ; Naphthalenes - pharmacology ; Natamycin - pharmacology ; Ophthalmology ; Statistical analysis ; Studies</subject><ispartof>American journal of ophthalmology, 2008-11, Vol.146 (5), p.724-728.e1</ispartof><rights>Elsevier Inc.</rights><rights>2008 Elsevier Inc.</rights><rights>2009 INIST-CNRS</rights><rights>Copyright Elsevier Limited Nov 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c530t-385be3edf533ec7150fe144045dd24a8be9906405a1d7e03486a062beff8d7323</citedby><cites>FETCH-LOGICAL-c530t-385be3edf533ec7150fe144045dd24a8be9906405a1d7e03486a062beff8d7323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ajo.2008.06.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20828924$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18707669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Li</creatorcontrib><creatorcontrib>Wang, Zhiqun</creatorcontrib><creatorcontrib>Li, Ran</creatorcontrib><creatorcontrib>Luo, Shiyun</creatorcontrib><creatorcontrib>Sun, Xuguang</creatorcontrib><title>In Vitro Evaluation of Combination Antifungal Activity against Fusarium Species Isolated from Ocular Tissues of Keratomycosis Patients</title><title>American journal of ophthalmology</title><addtitle>Am J Ophthalmol</addtitle><description>Purpose To determine the minimum inhibitory concentrations (MICs) of five antifungal agents against Fusarium species isolated from ocular tissues and to evaluate anti-Fusarium species activities of eight combination treatments in vitro. Design Experimental research. Methods Thirty-eight isolates of Fusarium species were collected from patients' ocular tissues and were cultured in vitro. The MICs of natamycin, terbinafine, itraconazole fluconazole, and amphotericin B, either used alone or combined with other compounds, were evaluated by checkerboard microdilution technique based on the Clinical Laboratory Standards Institute proposed standard. The interactions were assessed using the Fractional Inhibitory Concentration Index model. Results In the MIC study, the MIC90 of each drug used alone were: natamycin, 16 μg/ml; terbinafine, 8 μg/ml; itraconazole, &gt;16 μg/ml; fluconazole, &gt;64 μg/ml; and amphotericin B, 4 μg/ml. Synergism was obtained in the amphotericin B plus terbinafine (81.6%) group and in the amphotericin B plus itraconazole (84.2%) group, with an obviously decreased MIC value of amphotericin B. Antagonism was shown in the natamycin plus azoles and in the natamycin plus terbinafine groups in 52.6% to 60.5% of Fusarium species strains. Conclusions Amphotericin B plus terbinafine or itraconazole demonstrated more effective anti-Fusarium species activity than single-use in vitro treatment, which implies that these combinations may be helpful in treating fungal keratitis. The combinations of natamycin plus azoles or natamycin plus terbinafine were not satisfactory and can be avoided. 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Wang, Zhiqun ; Li, Ran ; Luo, Shiyun ; Sun, Xuguang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c530t-385be3edf533ec7150fe144045dd24a8be9906405a1d7e03486a062beff8d7323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amphotericin B - pharmacology</topic><topic>Antifungal Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Corneal Diseases - microbiology</topic><topic>Crop diseases</topic><topic>Drug Evaluation</topic><topic>Drug Synergism</topic><topic>Drugs</topic><topic>Eye - microbiology</topic><topic>Eye Infections, Fungal - microbiology</topic><topic>Fluconazole - pharmacology</topic><topic>Fungal infections</topic><topic>Fungi</topic><topic>Fusarium - drug effects</topic><topic>Fusarium - isolation &amp; purification</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Itraconazole - pharmacology</topic><topic>Laboratories</topic><topic>Medical sciences</topic><topic>Medical treatment</topic><topic>Methods</topic><topic>Microbial Sensitivity Tests</topic><topic>Miscellaneous</topic><topic>Naphthalenes - pharmacology</topic><topic>Natamycin - pharmacology</topic><topic>Ophthalmology</topic><topic>Statistical analysis</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Li</creatorcontrib><creatorcontrib>Wang, Zhiqun</creatorcontrib><creatorcontrib>Li, Ran</creatorcontrib><creatorcontrib>Luo, Shiyun</creatorcontrib><creatorcontrib>Sun, Xuguang</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><jtitle>American journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Li</au><au>Wang, Zhiqun</au><au>Li, Ran</au><au>Luo, Shiyun</au><au>Sun, Xuguang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vitro Evaluation of Combination Antifungal Activity against Fusarium Species Isolated from Ocular Tissues of Keratomycosis Patients</atitle><jtitle>American journal of ophthalmology</jtitle><addtitle>Am J Ophthalmol</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>146</volume><issue>5</issue><spage>724</spage><epage>728.e1</epage><pages>724-728.e1</pages><issn>0002-9394</issn><eissn>1879-1891</eissn><coden>AJOPAA</coden><abstract>Purpose To determine the minimum inhibitory concentrations (MICs) of five antifungal agents against Fusarium species isolated from ocular tissues and to evaluate anti-Fusarium species activities of eight combination treatments in vitro. Design Experimental research. Methods Thirty-eight isolates of Fusarium species were collected from patients' ocular tissues and were cultured in vitro. The MICs of natamycin, terbinafine, itraconazole fluconazole, and amphotericin B, either used alone or combined with other compounds, were evaluated by checkerboard microdilution technique based on the Clinical Laboratory Standards Institute proposed standard. The interactions were assessed using the Fractional Inhibitory Concentration Index model. Results In the MIC study, the MIC90 of each drug used alone were: natamycin, 16 μg/ml; terbinafine, 8 μg/ml; itraconazole, &gt;16 μg/ml; fluconazole, &gt;64 μg/ml; and amphotericin B, 4 μg/ml. Synergism was obtained in the amphotericin B plus terbinafine (81.6%) group and in the amphotericin B plus itraconazole (84.2%) group, with an obviously decreased MIC value of amphotericin B. Antagonism was shown in the natamycin plus azoles and in the natamycin plus terbinafine groups in 52.6% to 60.5% of Fusarium species strains. Conclusions Amphotericin B plus terbinafine or itraconazole demonstrated more effective anti-Fusarium species activity than single-use in vitro treatment, which implies that these combinations may be helpful in treating fungal keratitis. The combinations of natamycin plus azoles or natamycin plus terbinafine were not satisfactory and can be avoided. Further in vivo studies are needed to elucidate the potential usefulness of these combination therapies.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>18707669</pmid><doi>10.1016/j.ajo.2008.06.008</doi><tpages>5</tpages></addata></record>
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subjects Amphotericin B - pharmacology
Antifungal Agents - pharmacology
Biological and medical sciences
Corneal Diseases - microbiology
Crop diseases
Drug Evaluation
Drug Synergism
Drugs
Eye - microbiology
Eye Infections, Fungal - microbiology
Fluconazole - pharmacology
Fungal infections
Fungi
Fusarium - drug effects
Fusarium - isolation & purification
Humans
In Vitro Techniques
Itraconazole - pharmacology
Laboratories
Medical sciences
Medical treatment
Methods
Microbial Sensitivity Tests
Miscellaneous
Naphthalenes - pharmacology
Natamycin - pharmacology
Ophthalmology
Statistical analysis
Studies
title In Vitro Evaluation of Combination Antifungal Activity against Fusarium Species Isolated from Ocular Tissues of Keratomycosis Patients
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