An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers

Detalhes bibliográficos
Autor(a) principal: Negri, M.
Data de Publicação: 2011
Outros Autores: Botelho, C. M., Silva, Sónia Carina, Lopes, Luís Miguel Reis Henriques, Henriques, Mariana, Azeredo, Joana, Oliveira, Rosário
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/22465
Resumo: The aim of the present study was to investigate the interaction ofCandida tropicalis with three different human cell lines: TCC-SUP (epithelial cells from urinary bladder); HeLa (epithelial cells from cervical carcinoma); Caco-2 (epithelial cells from colorectal adenocarcinoma). In particular to assess the degree of cell damage and activity reduction induced by C. tropicalis adhesion and the role of SAPT gene expression in this process. Two C. tropicalis strains were used in this study, the reference strain ATCC 750 and a clinical isolate from urine (U69). The ability of C. tropicalis to adhere to a confluent layer of human cells was determined using an adaptation of the crystal violet staining method; cell damage and cell activity inhibition induced by the adhesion of C. tropicalis were assessed by LDH and MTS reduction, respectively. Candida tropicalis aspartyl proteinase (SAPT) gene expression was determined by real-time PCR. Candida tropicalis strains were able to adhere to the different human cells, although, in a strain and cell dependent manner. Concerning cellular response to C. tropicalis, the highest cell activity inhibition was obtained for Caco-2, followed by TCC-SUP and HeLa cells. The highest percentage of cell damage (around 14%) was observed for TCC-SUP in contact with the U69 isolate and for Caco-2 in contact with the reference strain. Real time PCR analysis revealed a wide range of expression profiles of SAP genes for both C. tropicalis strains in contact with the different types of epithelial cells. SAPT3 was the gene expressed at the highest level for both C. tropicalis strains in contact with the three human epithelial cell lines. It is important to highlight that human cells response to C. tropicalis adhesion, as well as SAPs production, is strain and epithelial cell line dependent.
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spelling An in vitro evaluation of Candida tropicalis infectivity using human cell monolayersScience & TechnologyThe aim of the present study was to investigate the interaction ofCandida tropicalis with three different human cell lines: TCC-SUP (epithelial cells from urinary bladder); HeLa (epithelial cells from cervical carcinoma); Caco-2 (epithelial cells from colorectal adenocarcinoma). In particular to assess the degree of cell damage and activity reduction induced by C. tropicalis adhesion and the role of SAPT gene expression in this process. Two C. tropicalis strains were used in this study, the reference strain ATCC 750 and a clinical isolate from urine (U69). The ability of C. tropicalis to adhere to a confluent layer of human cells was determined using an adaptation of the crystal violet staining method; cell damage and cell activity inhibition induced by the adhesion of C. tropicalis were assessed by LDH and MTS reduction, respectively. Candida tropicalis aspartyl proteinase (SAPT) gene expression was determined by real-time PCR. Candida tropicalis strains were able to adhere to the different human cells, although, in a strain and cell dependent manner. Concerning cellular response to C. tropicalis, the highest cell activity inhibition was obtained for Caco-2, followed by TCC-SUP and HeLa cells. The highest percentage of cell damage (around 14%) was observed for TCC-SUP in contact with the U69 isolate and for Caco-2 in contact with the reference strain. Real time PCR analysis revealed a wide range of expression profiles of SAP genes for both C. tropicalis strains in contact with the different types of epithelial cells. SAPT3 was the gene expressed at the highest level for both C. tropicalis strains in contact with the three human epithelial cell lines. It is important to highlight that human cells response to C. tropicalis adhesion, as well as SAPs production, is strain and epithelial cell line dependent.The authors acknowledge Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil, for supporting M. N.'s work through the grant BEX 4642/06-6 and FCT, Portugal, for supporting C. B. (SFRH/BPD/20987/2004) and S. S. (SFRH/BD/28341/2006). The authors would like to acknowledge Ana Rita Costa for the revision of the written English.Society for General MicrobiologyUniversidade do MinhoNegri, M.Botelho, C. M.Silva, Sónia CarinaLopes, Luís Miguel Reis HenriquesHenriques, MarianaAzeredo, JoanaOliveira, Rosário20112011-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/22465eng0022-261510.1099/jmm.0.031195-021566089http://jmm.sgmjournals.org/content/60/9/1270.full.pdf+html?sid=47fab603-3751-43e6-8479-4fd3574640d9info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:53:53Zoai:repositorium.sdum.uminho.pt:1822/22465Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:53:22.426735Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
title An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
spellingShingle An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
Negri, M.
Science & Technology
title_short An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
title_full An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
title_fullStr An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
title_full_unstemmed An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
title_sort An in vitro evaluation of Candida tropicalis infectivity using human cell monolayers
author Negri, M.
author_facet Negri, M.
Botelho, C. M.
Silva, Sónia Carina
Lopes, Luís Miguel Reis Henriques
Henriques, Mariana
Azeredo, Joana
Oliveira, Rosário
author_role author
author2 Botelho, C. M.
Silva, Sónia Carina
Lopes, Luís Miguel Reis Henriques
Henriques, Mariana
Azeredo, Joana
Oliveira, Rosário
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Negri, M.
Botelho, C. M.
Silva, Sónia Carina
Lopes, Luís Miguel Reis Henriques
Henriques, Mariana
Azeredo, Joana
Oliveira, Rosário
dc.subject.por.fl_str_mv Science & Technology
topic Science & Technology
description The aim of the present study was to investigate the interaction ofCandida tropicalis with three different human cell lines: TCC-SUP (epithelial cells from urinary bladder); HeLa (epithelial cells from cervical carcinoma); Caco-2 (epithelial cells from colorectal adenocarcinoma). In particular to assess the degree of cell damage and activity reduction induced by C. tropicalis adhesion and the role of SAPT gene expression in this process. Two C. tropicalis strains were used in this study, the reference strain ATCC 750 and a clinical isolate from urine (U69). The ability of C. tropicalis to adhere to a confluent layer of human cells was determined using an adaptation of the crystal violet staining method; cell damage and cell activity inhibition induced by the adhesion of C. tropicalis were assessed by LDH and MTS reduction, respectively. Candida tropicalis aspartyl proteinase (SAPT) gene expression was determined by real-time PCR. Candida tropicalis strains were able to adhere to the different human cells, although, in a strain and cell dependent manner. Concerning cellular response to C. tropicalis, the highest cell activity inhibition was obtained for Caco-2, followed by TCC-SUP and HeLa cells. The highest percentage of cell damage (around 14%) was observed for TCC-SUP in contact with the U69 isolate and for Caco-2 in contact with the reference strain. Real time PCR analysis revealed a wide range of expression profiles of SAP genes for both C. tropicalis strains in contact with the different types of epithelial cells. SAPT3 was the gene expressed at the highest level for both C. tropicalis strains in contact with the three human epithelial cell lines. It is important to highlight that human cells response to C. tropicalis adhesion, as well as SAPs production, is strain and epithelial cell line dependent.
publishDate 2011
dc.date.none.fl_str_mv 2011
2011-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/22465
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dc.language.iso.fl_str_mv eng
language eng
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10.1099/jmm.0.031195-0
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http://jmm.sgmjournals.org/content/60/9/1270.full.pdf+html?sid=47fab603-3751-43e6-8479-4fd3574640d9
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dc.publisher.none.fl_str_mv Society for General Microbiology
publisher.none.fl_str_mv Society for General Microbiology
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