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Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms
It is well known that prolonged antibiotic therapy alters the mucosal microbiota composition, increasing the risk of invasive fungal infection (IFI) in immunocompromised patients. The present study investigated the direct effect of β-lactam antibiotics cefepime (CEF) and amoxicillin (AMOX) on biofil...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609871/ https://www.ncbi.nlm.nih.gov/pubmed/31316472 http://dx.doi.org/10.3389/fmicb.2019.01337 |
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author | Cordeiro, Rossana de Aguiar Evangelista, Antonio Jose de Jesus Serpa, Rosana de Andrade, Ana Raquel Colares Mendes, Patrícia Bruna Leite de Oliveira, Jonathas Sales de Alencar, Lucas Pereira Pereira, Vandbergue Santos Lima-Neto, Reginaldo Gonçalves Brilhante, Raimunda Nogueira Sidrim, José Júlio Costa Maia, Débora Castelo Brancode Souza Collares Rocha, Marcos Fábio Gadelha |
author_facet | Cordeiro, Rossana de Aguiar Evangelista, Antonio Jose de Jesus Serpa, Rosana de Andrade, Ana Raquel Colares Mendes, Patrícia Bruna Leite de Oliveira, Jonathas Sales de Alencar, Lucas Pereira Pereira, Vandbergue Santos Lima-Neto, Reginaldo Gonçalves Brilhante, Raimunda Nogueira Sidrim, José Júlio Costa Maia, Débora Castelo Brancode Souza Collares Rocha, Marcos Fábio Gadelha |
author_sort | Cordeiro, Rossana de Aguiar |
collection | PubMed |
description | It is well known that prolonged antibiotic therapy alters the mucosal microbiota composition, increasing the risk of invasive fungal infection (IFI) in immunocompromised patients. The present study investigated the direct effect of β-lactam antibiotics cefepime (CEF) and amoxicillin (AMOX) on biofilm production by Candida albicans ATCC 10231. Antibacterials at the peak plasmatic concentration of each drug were tested against biofilms grown on polystyrene surfaces. Biofilms were evaluated for biomass production, metabolic activity, carbohydrate and protein contents, proteolytic activity, ultrastructure, and tolerance to antifungals. CEF and AMOX enhanced biofilm production by C. albicans ATCC 10231, stimulating biomass production, metabolic activity, viable cell counts, and proteolytic activity, as well as increased biovolume and thickness of these structures. Nevertheless, AMOX induced more significant changes in C. albicans biofilms than CEF. In addition, it was shown that AMOX increased the amount of chitin in these biofilms, making them more tolerant to caspofungin. Finally, it was seen that, in response to AMOX, C. albicans biofilms produce Hsp70 – a protein with chaperone function related to stressful conditions. These results may have a direct impact on the pathophysiology of opportunistic IFIs in patients at risk. |
format | Online Article Text |
id | pubmed-6609871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66098712019-07-17 Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms Cordeiro, Rossana de Aguiar Evangelista, Antonio Jose de Jesus Serpa, Rosana de Andrade, Ana Raquel Colares Mendes, Patrícia Bruna Leite de Oliveira, Jonathas Sales de Alencar, Lucas Pereira Pereira, Vandbergue Santos Lima-Neto, Reginaldo Gonçalves Brilhante, Raimunda Nogueira Sidrim, José Júlio Costa Maia, Débora Castelo Brancode Souza Collares Rocha, Marcos Fábio Gadelha Front Microbiol Microbiology It is well known that prolonged antibiotic therapy alters the mucosal microbiota composition, increasing the risk of invasive fungal infection (IFI) in immunocompromised patients. The present study investigated the direct effect of β-lactam antibiotics cefepime (CEF) and amoxicillin (AMOX) on biofilm production by Candida albicans ATCC 10231. Antibacterials at the peak plasmatic concentration of each drug were tested against biofilms grown on polystyrene surfaces. Biofilms were evaluated for biomass production, metabolic activity, carbohydrate and protein contents, proteolytic activity, ultrastructure, and tolerance to antifungals. CEF and AMOX enhanced biofilm production by C. albicans ATCC 10231, stimulating biomass production, metabolic activity, viable cell counts, and proteolytic activity, as well as increased biovolume and thickness of these structures. Nevertheless, AMOX induced more significant changes in C. albicans biofilms than CEF. In addition, it was shown that AMOX increased the amount of chitin in these biofilms, making them more tolerant to caspofungin. Finally, it was seen that, in response to AMOX, C. albicans biofilms produce Hsp70 – a protein with chaperone function related to stressful conditions. These results may have a direct impact on the pathophysiology of opportunistic IFIs in patients at risk. Frontiers Media S.A. 2019-06-28 /pmc/articles/PMC6609871/ /pubmed/31316472 http://dx.doi.org/10.3389/fmicb.2019.01337 Text en Copyright © 2019 Cordeiro, Evangelista, Serpa, Andrade, Mendes, Oliveira, Alencar, Pereira, Lima-Neto, Brilhante, Sidrim, Maia and Rocha. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Cordeiro, Rossana de Aguiar Evangelista, Antonio Jose de Jesus Serpa, Rosana de Andrade, Ana Raquel Colares Mendes, Patrícia Bruna Leite de Oliveira, Jonathas Sales de Alencar, Lucas Pereira Pereira, Vandbergue Santos Lima-Neto, Reginaldo Gonçalves Brilhante, Raimunda Nogueira Sidrim, José Júlio Costa Maia, Débora Castelo Brancode Souza Collares Rocha, Marcos Fábio Gadelha Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms |
title | Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms |
title_full | Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms |
title_fullStr | Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms |
title_full_unstemmed | Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms |
title_short | Cefepime and Amoxicillin Increase Metabolism and Enhance Caspofungin Tolerance of Candida albicans Biofilms |
title_sort | cefepime and amoxicillin increase metabolism and enhance caspofungin tolerance of candida albicans biofilms |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609871/ https://www.ncbi.nlm.nih.gov/pubmed/31316472 http://dx.doi.org/10.3389/fmicb.2019.01337 |
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