Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da Universidade Federal do Ceará (UFC) |
dARK ID: | ark:/83112/001300001gs9q |
Texto Completo: | http://www.repositorio.ufc.br/handle/riufc/5120 |
Resumo: | The Cryptococcus neoformans species complex contains the most important agents of fungal meningoencephalitis. Therapeutic choices are limited and issues related to toxicity and resistance to antifungals have been described. The present study evaluated the inhibitory effect of the antifolate combinations sulfamethoxazole–trimethoprim (SMX/TMP) and sulfadiazine–pyrimethamine (SDZ/PYR) against planktonic cells and biofilms of C. neoformans and C. gattii. The influence of the antifolate combinations on the amphotericin minimum inhibitory concentration (MIC) of planktonic cells was also investigated. In addition, the effect of these combinations on the cellular ergosterol content of planktonic cells was studied. Strains of C. neoformans (n015) and C. gattii (n015) obtained from environmental or clinical sources were evaluated by the broth microdilution method. SMX/TMP and SDZ/PYR showed antifungal activity against free living cells and sessile cells of Cryptococcus spp. Moreover, planktonic cells showed increased susceptibility to amphotericin B after pre-incubation with sub-inhibitory concentrations of SMX/ TMP or SDZ/PYR. The drug combinations SMX/TMP and SDZ/PYR were able to prevent the biofilm formation and showed inhibitory effect against mature biofilms of both species. Additionally, the study showed that antifolate drugs reduced the ergosterol content in C. neoformans and C. gattii planktonic cells. Our results highlight the antifungal potential of antifolate drugs. |
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Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin BBiofilmesCryptococcusAnfotericina BThe Cryptococcus neoformans species complex contains the most important agents of fungal meningoencephalitis. Therapeutic choices are limited and issues related to toxicity and resistance to antifungals have been described. The present study evaluated the inhibitory effect of the antifolate combinations sulfamethoxazole–trimethoprim (SMX/TMP) and sulfadiazine–pyrimethamine (SDZ/PYR) against planktonic cells and biofilms of C. neoformans and C. gattii. The influence of the antifolate combinations on the amphotericin minimum inhibitory concentration (MIC) of planktonic cells was also investigated. In addition, the effect of these combinations on the cellular ergosterol content of planktonic cells was studied. Strains of C. neoformans (n015) and C. gattii (n015) obtained from environmental or clinical sources were evaluated by the broth microdilution method. SMX/TMP and SDZ/PYR showed antifungal activity against free living cells and sessile cells of Cryptococcus spp. Moreover, planktonic cells showed increased susceptibility to amphotericin B after pre-incubation with sub-inhibitory concentrations of SMX/ TMP or SDZ/PYR. The drug combinations SMX/TMP and SDZ/PYR were able to prevent the biofilm formation and showed inhibitory effect against mature biofilms of both species. Additionally, the study showed that antifolate drugs reduced the ergosterol content in C. neoformans and C. gattii planktonic cells. Our results highlight the antifungal potential of antifolate drugs.European Journal of Clinical Microbiology & Infectious Diseases2013-06-24T12:43:26Z2013-06-24T12:43:26Z2013-04info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfCORDEIRO, R. A. et al. Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin. Eur. J. Clin. Microbiol. Infect. Dis., Berlin, v.32, n. 4, p.557-64, abr. 2013.0934-9723 Impresso1435-4373 On linehttp://www.repositorio.ufc.br/handle/riufc/5120ark:/83112/001300001gs9qCordeiro, R. de AguiarMourão, C. I.Rocha, M. F. G. RochaMarques, F. J. de FariasTeixeira, Carlos Eduardo CordeiroMiranda, D. F. de OliveiraPerdigão Neto, Lauro VieiraBrilhante, R. S. N.Bandeira, T. de Jesus Pinheiro GomesSidrim, J. J. C.engreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2022-07-19T13:59:13Zoai:repositorio.ufc.br:riufc/5120Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:46:12.059539Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false |
dc.title.none.fl_str_mv |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B |
title |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B |
spellingShingle |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B Cordeiro, R. de Aguiar Biofilmes Cryptococcus Anfotericina B |
title_short |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B |
title_full |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B |
title_fullStr |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B |
title_full_unstemmed |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B |
title_sort |
Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin B |
author |
Cordeiro, R. de Aguiar |
author_facet |
Cordeiro, R. de Aguiar Mourão, C. I. Rocha, M. F. G. Rocha Marques, F. J. de Farias Teixeira, Carlos Eduardo Cordeiro Miranda, D. F. de Oliveira Perdigão Neto, Lauro Vieira Brilhante, R. S. N. Bandeira, T. de Jesus Pinheiro Gomes Sidrim, J. J. C. |
author_role |
author |
author2 |
Mourão, C. I. Rocha, M. F. G. Rocha Marques, F. J. de Farias Teixeira, Carlos Eduardo Cordeiro Miranda, D. F. de Oliveira Perdigão Neto, Lauro Vieira Brilhante, R. S. N. Bandeira, T. de Jesus Pinheiro Gomes Sidrim, J. J. C. |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Cordeiro, R. de Aguiar Mourão, C. I. Rocha, M. F. G. Rocha Marques, F. J. de Farias Teixeira, Carlos Eduardo Cordeiro Miranda, D. F. de Oliveira Perdigão Neto, Lauro Vieira Brilhante, R. S. N. Bandeira, T. de Jesus Pinheiro Gomes Sidrim, J. J. C. |
dc.subject.por.fl_str_mv |
Biofilmes Cryptococcus Anfotericina B |
topic |
Biofilmes Cryptococcus Anfotericina B |
description |
The Cryptococcus neoformans species complex contains the most important agents of fungal meningoencephalitis. Therapeutic choices are limited and issues related to toxicity and resistance to antifungals have been described. The present study evaluated the inhibitory effect of the antifolate combinations sulfamethoxazole–trimethoprim (SMX/TMP) and sulfadiazine–pyrimethamine (SDZ/PYR) against planktonic cells and biofilms of C. neoformans and C. gattii. The influence of the antifolate combinations on the amphotericin minimum inhibitory concentration (MIC) of planktonic cells was also investigated. In addition, the effect of these combinations on the cellular ergosterol content of planktonic cells was studied. Strains of C. neoformans (n015) and C. gattii (n015) obtained from environmental or clinical sources were evaluated by the broth microdilution method. SMX/TMP and SDZ/PYR showed antifungal activity against free living cells and sessile cells of Cryptococcus spp. Moreover, planktonic cells showed increased susceptibility to amphotericin B after pre-incubation with sub-inhibitory concentrations of SMX/ TMP or SDZ/PYR. The drug combinations SMX/TMP and SDZ/PYR were able to prevent the biofilm formation and showed inhibitory effect against mature biofilms of both species. Additionally, the study showed that antifolate drugs reduced the ergosterol content in C. neoformans and C. gattii planktonic cells. Our results highlight the antifungal potential of antifolate drugs. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-06-24T12:43:26Z 2013-06-24T12:43:26Z 2013-04 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
CORDEIRO, R. A. et al. Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin. Eur. J. Clin. Microbiol. Infect. Dis., Berlin, v.32, n. 4, p.557-64, abr. 2013. 0934-9723 Impresso 1435-4373 On line http://www.repositorio.ufc.br/handle/riufc/5120 |
dc.identifier.dark.fl_str_mv |
ark:/83112/001300001gs9q |
identifier_str_mv |
CORDEIRO, R. A. et al. Antifolates inhibit Cryptococcus biofilms and enhance susceptibility of planktonic cells to amphotericin. Eur. J. Clin. Microbiol. Infect. Dis., Berlin, v.32, n. 4, p.557-64, abr. 2013. 0934-9723 Impresso 1435-4373 On line ark:/83112/001300001gs9q |
url |
http://www.repositorio.ufc.br/handle/riufc/5120 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
European Journal of Clinical Microbiology & Infectious Diseases |
publisher.none.fl_str_mv |
European Journal of Clinical Microbiology & Infectious Diseases |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da Universidade Federal do Ceará (UFC) instname:Universidade Federal do Ceará (UFC) instacron:UFC |
instname_str |
Universidade Federal do Ceará (UFC) |
instacron_str |
UFC |
institution |
UFC |
reponame_str |
Repositório Institucional da Universidade Federal do Ceará (UFC) |
collection |
Repositório Institucional da Universidade Federal do Ceará (UFC) |
repository.name.fl_str_mv |
Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC) |
repository.mail.fl_str_mv |
bu@ufc.br || repositorio@ufc.br |
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1818373961928409088 |