Identification of the cell targets important for propolis-induced cell death in Candida albicans
•Propolis is a mixture of resinous substances which are collected from plants by bees.•We showed the antifungal activity of propolis against all C. albicans morphotypes.•Propolis is able to control C. albicans infections in a mouse model of vulvovaginal candidiasis.•Our results indicate that propoli...
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Veröffentlicht in: | Fungal genetics and biology 2013-11, Vol.60, p.74-86 |
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creator | de Castro, Patrícia Alves Bom, Vinícius Leite Pedro Brown, Neil Andrew Almeida, Ricardo Sérgio Couto de Ramalho, Leandra Naira Zambelli Savoldi, Marcela Goldman, Maria Helena S. Berretta, Andresa A. Goldman, Gustavo Henrique |
description | •Propolis is a mixture of resinous substances which are collected from plants by bees.•We showed the antifungal activity of propolis against all C. albicans morphotypes.•Propolis is able to control C. albicans infections in a mouse model of vulvovaginal candidiasis.•Our results indicate that propolis could be a used for controlling candidiasis.
Candida albicans is the most common fungal pathogen of humans, forming both commensal and opportunistic pathogenic interactions, causing a variety of skin and soft tissue infections in healthy people. In immunocompromised patients C. albicans can result in invasive, systemic infections that are associated with a high incidence of mortality. Propolis is a complex mixture of several resinous substances which are collected from plants by bees. Here, we demonstrated the fungicidal activity of propolis against all three morphogenetic types of C. albicans and that propolis-induced cell death was mediated via metacaspase and Ras signaling. To identify genes that were involved in propolis tolerance, we screened ∼800 C. albicans homozygous deletion mutants for decreased tolerance to propolis. Fifty-one mutant strains were identified as being hypersensitive to propolis including seventeen genes involved in cell adhesion, biofilm formation, filamentous growth, phenotypic switching and pathogenesis (HST7, GIN4, VPS34, HOG1, ISW2, SUV3, MDS3, HDA2, KAR3, YHB1, NUP85, CDC10, MNN9, ACE2, FKH2, and SNF5). We validated these results by showing that propolis inhibited the transition from yeast-like to hyphal growth. Propolis was shown to contain compounds that conferred fluorescent properties to C. albicans cells. Moreover, we have shown that a topical pharmaceutical preparation, based upon propolis, was able to control C. albicans infections in a mouse model for vulvovaginal candidiasis. Our results strongly indicate that propolis could be used as a strategy for controlling candidiasis. |
doi_str_mv | 10.1016/j.fgb.2013.07.001 |
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Candida albicans is the most common fungal pathogen of humans, forming both commensal and opportunistic pathogenic interactions, causing a variety of skin and soft tissue infections in healthy people. In immunocompromised patients C. albicans can result in invasive, systemic infections that are associated with a high incidence of mortality. Propolis is a complex mixture of several resinous substances which are collected from plants by bees. Here, we demonstrated the fungicidal activity of propolis against all three morphogenetic types of C. albicans and that propolis-induced cell death was mediated via metacaspase and Ras signaling. To identify genes that were involved in propolis tolerance, we screened ∼800 C. albicans homozygous deletion mutants for decreased tolerance to propolis. Fifty-one mutant strains were identified as being hypersensitive to propolis including seventeen genes involved in cell adhesion, biofilm formation, filamentous growth, phenotypic switching and pathogenesis (HST7, GIN4, VPS34, HOG1, ISW2, SUV3, MDS3, HDA2, KAR3, YHB1, NUP85, CDC10, MNN9, ACE2, FKH2, and SNF5). We validated these results by showing that propolis inhibited the transition from yeast-like to hyphal growth. Propolis was shown to contain compounds that conferred fluorescent properties to C. albicans cells. Moreover, we have shown that a topical pharmaceutical preparation, based upon propolis, was able to control C. albicans infections in a mouse model for vulvovaginal candidiasis. Our results strongly indicate that propolis could be used as a strategy for controlling candidiasis.</description><identifier>ISSN: 1087-1845</identifier><identifier>EISSN: 1096-0937</identifier><identifier>DOI: 10.1016/j.fgb.2013.07.001</identifier><identifier>PMID: 23856128</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>animal models ; Animals ; Anti-Infective Agents - pharmacology ; Antifungal Agents - pharmacology ; antifungal properties ; Apoidea ; biofilm ; Candida albicans ; Candida albicans - drug effects ; Candida albicans - genetics ; candidiasis ; Candidiasis, Vulvovaginal - drug therapy ; Candidiasis, Vulvovaginal - microbiology ; Caspases - metabolism ; cell adhesion ; cell death ; Deletion mutants ; Female ; fungi ; genes ; homozygosity ; hyphae ; Mice ; Mice, Inbred BALB C ; mortality ; mutants ; pathogenesis ; pathogens ; Propolis ; Propolis - pharmacology ; Proto-Oncogene Proteins p21(ras) - metabolism ; Vulvovaginal candidiasis</subject><ispartof>Fungal genetics and biology, 2013-11, Vol.60, p.74-86</ispartof><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-3d39d21022b6ce0a1fcc3be4bc19db379b78e485747735f493303c83a399cf4d3</citedby><cites>FETCH-LOGICAL-c420t-3d39d21022b6ce0a1fcc3be4bc19db379b78e485747735f493303c83a399cf4d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fgb.2013.07.001$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23856128$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Castro, Patrícia Alves</creatorcontrib><creatorcontrib>Bom, Vinícius Leite Pedro</creatorcontrib><creatorcontrib>Brown, Neil Andrew</creatorcontrib><creatorcontrib>Almeida, Ricardo Sérgio Couto de</creatorcontrib><creatorcontrib>Ramalho, Leandra Naira Zambelli</creatorcontrib><creatorcontrib>Savoldi, Marcela</creatorcontrib><creatorcontrib>Goldman, Maria Helena S.</creatorcontrib><creatorcontrib>Berretta, Andresa A.</creatorcontrib><creatorcontrib>Goldman, Gustavo Henrique</creatorcontrib><title>Identification of the cell targets important for propolis-induced cell death in Candida albicans</title><title>Fungal genetics and biology</title><addtitle>Fungal Genet Biol</addtitle><description>•Propolis is a mixture of resinous substances which are collected from plants by bees.•We showed the antifungal activity of propolis against all C. albicans morphotypes.•Propolis is able to control C. albicans infections in a mouse model of vulvovaginal candidiasis.•Our results indicate that propolis could be a used for controlling candidiasis.
Candida albicans is the most common fungal pathogen of humans, forming both commensal and opportunistic pathogenic interactions, causing a variety of skin and soft tissue infections in healthy people. In immunocompromised patients C. albicans can result in invasive, systemic infections that are associated with a high incidence of mortality. Propolis is a complex mixture of several resinous substances which are collected from plants by bees. Here, we demonstrated the fungicidal activity of propolis against all three morphogenetic types of C. albicans and that propolis-induced cell death was mediated via metacaspase and Ras signaling. To identify genes that were involved in propolis tolerance, we screened ∼800 C. albicans homozygous deletion mutants for decreased tolerance to propolis. Fifty-one mutant strains were identified as being hypersensitive to propolis including seventeen genes involved in cell adhesion, biofilm formation, filamentous growth, phenotypic switching and pathogenesis (HST7, GIN4, VPS34, HOG1, ISW2, SUV3, MDS3, HDA2, KAR3, YHB1, NUP85, CDC10, MNN9, ACE2, FKH2, and SNF5). We validated these results by showing that propolis inhibited the transition from yeast-like to hyphal growth. Propolis was shown to contain compounds that conferred fluorescent properties to C. albicans cells. Moreover, we have shown that a topical pharmaceutical preparation, based upon propolis, was able to control C. albicans infections in a mouse model for vulvovaginal candidiasis. Our results strongly indicate that propolis could be used as a strategy for controlling candidiasis.</description><subject>animal models</subject><subject>Animals</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Antifungal Agents - pharmacology</subject><subject>antifungal properties</subject><subject>Apoidea</subject><subject>biofilm</subject><subject>Candida albicans</subject><subject>Candida albicans - drug effects</subject><subject>Candida albicans - genetics</subject><subject>candidiasis</subject><subject>Candidiasis, Vulvovaginal - drug therapy</subject><subject>Candidiasis, Vulvovaginal - microbiology</subject><subject>Caspases - metabolism</subject><subject>cell adhesion</subject><subject>cell death</subject><subject>Deletion mutants</subject><subject>Female</subject><subject>fungi</subject><subject>genes</subject><subject>homozygosity</subject><subject>hyphae</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>mortality</subject><subject>mutants</subject><subject>pathogenesis</subject><subject>pathogens</subject><subject>Propolis</subject><subject>Propolis - pharmacology</subject><subject>Proto-Oncogene Proteins p21(ras) - metabolism</subject><subject>Vulvovaginal candidiasis</subject><issn>1087-1845</issn><issn>1096-0937</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2PFCEURYnRzJfzA9woSzdVQgFFEVemo84kk7hwZo0UPHroVEML9CT--6FTo0tX7y3Ovbk5CL2jpKeEjp92vd_O_UAo64nsCaGv0AUlauyIYvL16Z9kRycuztFlKbsGUMHpGTof2CRGOkwX6Netg1iDD9bUkCJOHtdHwBaWBVeTt1ALDvtDytXEin3K-JDTIS2hdCG6owW3sg5MfcQh4o2JLjiDzTK3zljeojfeLAWuX-4Vevj29X5z0939-H67-XLXWT6Q2jHHlBsoGYZ5tEAM9dayGfhsqXIzk2qWE_BJSC4lE54rxgizEzNMKeu5Y1fo49rb9v0-Qql6H8ppmomQjkVTLpQYSTsNpStqcyolg9eHHPYm_9GU6JNYvdNNrD6J1UTq5q1l3r_UH-c9uH-JvyYb8GEFvEnabHMo-uFnaxAtTQYueCM-rwQ0DU8Bsi42QGwKQwZbtUvhPwOeAZjUkeo</recordid><startdate>20131101</startdate><enddate>20131101</enddate><creator>de Castro, Patrícia Alves</creator><creator>Bom, Vinícius Leite Pedro</creator><creator>Brown, Neil Andrew</creator><creator>Almeida, Ricardo Sérgio Couto de</creator><creator>Ramalho, Leandra Naira Zambelli</creator><creator>Savoldi, Marcela</creator><creator>Goldman, Maria Helena S.</creator><creator>Berretta, Andresa A.</creator><creator>Goldman, Gustavo Henrique</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20131101</creationdate><title>Identification of the cell targets important for propolis-induced cell death in Candida albicans</title><author>de Castro, Patrícia Alves ; Bom, Vinícius Leite Pedro ; Brown, Neil Andrew ; Almeida, Ricardo Sérgio Couto de ; Ramalho, Leandra Naira Zambelli ; Savoldi, Marcela ; Goldman, Maria Helena S. ; Berretta, Andresa A. ; Goldman, Gustavo Henrique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-3d39d21022b6ce0a1fcc3be4bc19db379b78e485747735f493303c83a399cf4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>animal models</topic><topic>Animals</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Antifungal Agents - pharmacology</topic><topic>antifungal properties</topic><topic>Apoidea</topic><topic>biofilm</topic><topic>Candida albicans</topic><topic>Candida albicans - drug effects</topic><topic>Candida albicans - genetics</topic><topic>candidiasis</topic><topic>Candidiasis, Vulvovaginal - drug therapy</topic><topic>Candidiasis, Vulvovaginal - microbiology</topic><topic>Caspases - metabolism</topic><topic>cell adhesion</topic><topic>cell death</topic><topic>Deletion mutants</topic><topic>Female</topic><topic>fungi</topic><topic>genes</topic><topic>homozygosity</topic><topic>hyphae</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>mortality</topic><topic>mutants</topic><topic>pathogenesis</topic><topic>pathogens</topic><topic>Propolis</topic><topic>Propolis - pharmacology</topic><topic>Proto-Oncogene Proteins p21(ras) - metabolism</topic><topic>Vulvovaginal candidiasis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Castro, Patrícia Alves</creatorcontrib><creatorcontrib>Bom, Vinícius Leite Pedro</creatorcontrib><creatorcontrib>Brown, Neil Andrew</creatorcontrib><creatorcontrib>Almeida, Ricardo Sérgio Couto de</creatorcontrib><creatorcontrib>Ramalho, Leandra Naira Zambelli</creatorcontrib><creatorcontrib>Savoldi, Marcela</creatorcontrib><creatorcontrib>Goldman, Maria Helena S.</creatorcontrib><creatorcontrib>Berretta, Andresa A.</creatorcontrib><creatorcontrib>Goldman, Gustavo Henrique</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Fungal genetics and biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Castro, Patrícia Alves</au><au>Bom, Vinícius Leite Pedro</au><au>Brown, Neil Andrew</au><au>Almeida, Ricardo Sérgio Couto de</au><au>Ramalho, Leandra Naira Zambelli</au><au>Savoldi, Marcela</au><au>Goldman, Maria Helena S.</au><au>Berretta, Andresa A.</au><au>Goldman, Gustavo Henrique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of the cell targets important for propolis-induced cell death in Candida albicans</atitle><jtitle>Fungal genetics and biology</jtitle><addtitle>Fungal Genet Biol</addtitle><date>2013-11-01</date><risdate>2013</risdate><volume>60</volume><spage>74</spage><epage>86</epage><pages>74-86</pages><issn>1087-1845</issn><eissn>1096-0937</eissn><abstract>•Propolis is a mixture of resinous substances which are collected from plants by bees.•We showed the antifungal activity of propolis against all C. albicans morphotypes.•Propolis is able to control C. albicans infections in a mouse model of vulvovaginal candidiasis.•Our results indicate that propolis could be a used for controlling candidiasis.
Candida albicans is the most common fungal pathogen of humans, forming both commensal and opportunistic pathogenic interactions, causing a variety of skin and soft tissue infections in healthy people. In immunocompromised patients C. albicans can result in invasive, systemic infections that are associated with a high incidence of mortality. Propolis is a complex mixture of several resinous substances which are collected from plants by bees. Here, we demonstrated the fungicidal activity of propolis against all three morphogenetic types of C. albicans and that propolis-induced cell death was mediated via metacaspase and Ras signaling. To identify genes that were involved in propolis tolerance, we screened ∼800 C. albicans homozygous deletion mutants for decreased tolerance to propolis. Fifty-one mutant strains were identified as being hypersensitive to propolis including seventeen genes involved in cell adhesion, biofilm formation, filamentous growth, phenotypic switching and pathogenesis (HST7, GIN4, VPS34, HOG1, ISW2, SUV3, MDS3, HDA2, KAR3, YHB1, NUP85, CDC10, MNN9, ACE2, FKH2, and SNF5). We validated these results by showing that propolis inhibited the transition from yeast-like to hyphal growth. Propolis was shown to contain compounds that conferred fluorescent properties to C. albicans cells. Moreover, we have shown that a topical pharmaceutical preparation, based upon propolis, was able to control C. albicans infections in a mouse model for vulvovaginal candidiasis. Our results strongly indicate that propolis could be used as a strategy for controlling candidiasis.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23856128</pmid><doi>10.1016/j.fgb.2013.07.001</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | animal models Animals Anti-Infective Agents - pharmacology Antifungal Agents - pharmacology antifungal properties Apoidea biofilm Candida albicans Candida albicans - drug effects Candida albicans - genetics candidiasis Candidiasis, Vulvovaginal - drug therapy Candidiasis, Vulvovaginal - microbiology Caspases - metabolism cell adhesion cell death Deletion mutants Female fungi genes homozygosity hyphae Mice Mice, Inbred BALB C mortality mutants pathogenesis pathogens Propolis Propolis - pharmacology Proto-Oncogene Proteins p21(ras) - metabolism Vulvovaginal candidiasis |
title | Identification of the cell targets important for propolis-induced cell death in Candida albicans |
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