Cargando…

Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans

Dispersion is an essential step in the lifecycle of biofilms, since it enables the dissemination of microbial cells and, consequently, the potential colonization of new sites. Filamentous fungi belonging to the Scedosporium/Lomentospora genera are opportunistic human pathogens able to form multidrug...

Descripción completa

Detalles Bibliográficos
Autores principales: Mello, Thaís P., Barcellos, Iuri C., Branquinha, Marta H., Santos, André L.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203734/
https://www.ncbi.nlm.nih.gov/pubmed/37229517
http://dx.doi.org/10.1016/j.crmicr.2023.100191
_version_ 1785045694246027264
author Mello, Thaís P.
Barcellos, Iuri C.
Branquinha, Marta H.
Santos, André L.S.
author_facet Mello, Thaís P.
Barcellos, Iuri C.
Branquinha, Marta H.
Santos, André L.S.
author_sort Mello, Thaís P.
collection PubMed
description Dispersion is an essential step in the lifecycle of biofilms, since it enables the dissemination of microbial cells and, consequently, the potential colonization of new sites. Filamentous fungi belonging to the Scedosporium/Lomentospora genera are opportunistic human pathogens able to form multidrug-resistant biofilms on surfaces of different chemical compositions, environments and nutritional conditions. Despite the rising understanding of how biofilms are formed by Scedosporium/Lomentospora species, the cell dispersal step has not yet been explored. In the present study, the cell dispersion was investigated during biofilm formation by S. apiospermum, S. minutisporum, S. aurantiacum and L. prolificans cells. The results revealed that conidia were the major type of dispersed cells, which were detected throughout biofilm development (from 24 to 72 h). Dispersion was not influenced by increased glucose concentration (the main source for energetic metabolism) neither the presence of voriconazole (the most common antifungal used to treat scedosporiosis); however, the presence of mucin (a component of mucous, present in the lungs of cystic fibrosis patients, who are usually affected by these filamentous fungi) triggered cell dispersion. Contrarily, a poor nutritional environment (e.g., phosphate-buffered saline) inhibited this step. Overall, our study reveals new insights into the biofilm development of Scedosporium/Lomentospora species.
format Online
Article
Text
id pubmed-10203734
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-102037342023-05-24 Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans Mello, Thaís P. Barcellos, Iuri C. Branquinha, Marta H. Santos, André L.S. Curr Res Microb Sci Research Paper Dispersion is an essential step in the lifecycle of biofilms, since it enables the dissemination of microbial cells and, consequently, the potential colonization of new sites. Filamentous fungi belonging to the Scedosporium/Lomentospora genera are opportunistic human pathogens able to form multidrug-resistant biofilms on surfaces of different chemical compositions, environments and nutritional conditions. Despite the rising understanding of how biofilms are formed by Scedosporium/Lomentospora species, the cell dispersal step has not yet been explored. In the present study, the cell dispersion was investigated during biofilm formation by S. apiospermum, S. minutisporum, S. aurantiacum and L. prolificans cells. The results revealed that conidia were the major type of dispersed cells, which were detected throughout biofilm development (from 24 to 72 h). Dispersion was not influenced by increased glucose concentration (the main source for energetic metabolism) neither the presence of voriconazole (the most common antifungal used to treat scedosporiosis); however, the presence of mucin (a component of mucous, present in the lungs of cystic fibrosis patients, who are usually affected by these filamentous fungi) triggered cell dispersion. Contrarily, a poor nutritional environment (e.g., phosphate-buffered saline) inhibited this step. Overall, our study reveals new insights into the biofilm development of Scedosporium/Lomentospora species. Elsevier 2023-05-10 /pmc/articles/PMC10203734/ /pubmed/37229517 http://dx.doi.org/10.1016/j.crmicr.2023.100191 Text en © 2023 The Authors. Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Mello, Thaís P.
Barcellos, Iuri C.
Branquinha, Marta H.
Santos, André L.S.
Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans
title Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans
title_full Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans
title_fullStr Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans
title_full_unstemmed Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans
title_short Cell dispersion during biofilm formation by Scedosporium apiospermum, Scedosporium aurantiacum, Scedosporium minutisporum and Lomentospora prolificans
title_sort cell dispersion during biofilm formation by scedosporium apiospermum, scedosporium aurantiacum, scedosporium minutisporum and lomentospora prolificans
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203734/
https://www.ncbi.nlm.nih.gov/pubmed/37229517
http://dx.doi.org/10.1016/j.crmicr.2023.100191
work_keys_str_mv AT mellothaisp celldispersionduringbiofilmformationbyscedosporiumapiospermumscedosporiumaurantiacumscedosporiumminutisporumandlomentosporaprolificans
AT barcellosiuric celldispersionduringbiofilmformationbyscedosporiumapiospermumscedosporiumaurantiacumscedosporiumminutisporumandlomentosporaprolificans
AT branquinhamartah celldispersionduringbiofilmformationbyscedosporiumapiospermumscedosporiumaurantiacumscedosporiumminutisporumandlomentosporaprolificans
AT santosandrels celldispersionduringbiofilmformationbyscedosporiumapiospermumscedosporiumaurantiacumscedosporiumminutisporumandlomentosporaprolificans