Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species Complex

The opportunistic fungal pathogens belonging to the <i>Candida haemulonii</i> complex and the phylogenetically related species <i>Candida auris</i> are well-known for causing infections that are difficult to treat due to their multidrug-resistance profiles. <i>Candida a...

Full description

Bibliographic Details
Main Authors: Lívia S. Ramos, Claudia M. Parra-Giraldo, Marta H. Branquinha, André L. S. Santos
Format: Article
Language:English
Published: MDPI AG 2023-07-01
Series:Tropical Medicine and Infectious Disease
Subjects:
Online Access:https://www.mdpi.com/2414-6366/8/8/382
_version_ 1797583108194697216
author Lívia S. Ramos
Claudia M. Parra-Giraldo
Marta H. Branquinha
André L. S. Santos
author_facet Lívia S. Ramos
Claudia M. Parra-Giraldo
Marta H. Branquinha
André L. S. Santos
author_sort Lívia S. Ramos
collection DOAJ
description The opportunistic fungal pathogens belonging to the <i>Candida haemulonii</i> complex and the phylogenetically related species <i>Candida auris</i> are well-known for causing infections that are difficult to treat due to their multidrug-resistance profiles. <i>Candida auris</i> is even more worrisome due to its ability to cause outbreaks in healthcare settings. These emerging yeasts produce a wide range of virulence factors that facilitate the development of the infectious process. In recent years, the aggregative phenotype has been receiving attention, as it is mainly associated with defects in cellular division and its possible involvement in helping the fungus to escape from the host immune responses. In the present study, we initially investigated the aggregation ability of 18 clinical isolates belonging to the <i>C. haemulonii</i> species complex (<i>C. haemulonii sensu stricto</i>, <i>C. duobushaemulonii</i>, and <i>C. haemulonii</i> var. <i>vulnera</i>) and <i>C. auris</i>. Subsequently, we evaluated the effects of physicochemical factors on fungal aggregation competence. The results demonstrated that cell-to-cell aggregation was a typically time-dependent event, in which almost all studied fungal isolates of both the <i>C. haemulonii</i> species complex and <i>C. auris</i> exhibited high aggregation after 2 h of incubation at 37 °C. Interestingly, the fungal cells forming the aggregates remained viable. The aggregation of all isolates was not impacted by pH, temperature, β-mercaptoethanol (a protein-denaturing agent), or EDTA (a chelator agent). Conversely, proteinase K, trypsin, and sodium dodecyl sulfate (SDS) significantly diminished the fungal aggregation. Collectively, our results demonstrated that the aggregation ability of these opportunistic yeast pathogens is time-dependent, and surface proteins and hydrophobic interactions seem to mediate cell aggregation since the presence of proteases and anionic detergents affected the aggregation capability. However, further studies are necessary to better elucidate the molecular aspects of this intriguing phenomenon.
first_indexed 2024-03-10T23:32:10Z
format Article
id doaj.art-f48e0b190db2480590fdc309a37f7b12
institution Directory Open Access Journal
issn 2414-6366
language English
last_indexed 2024-03-10T23:32:10Z
publishDate 2023-07-01
publisher MDPI AG
record_format Article
series Tropical Medicine and Infectious Disease
spelling doaj.art-f48e0b190db2480590fdc309a37f7b122023-11-19T03:15:44ZengMDPI AGTropical Medicine and Infectious Disease2414-63662023-07-018838210.3390/tropicalmed8080382Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species ComplexLívia S. Ramos0Claudia M. Parra-Giraldo1Marta H. Branquinha2André L. S. Santos3Laboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes (LEAMER), Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro 21941-902, BrazilUnidad de Proteómica y Micosis Humanas, Grupo de Enfermedades Infecciosas, Departamento de Microbiología, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, ColombiaLaboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes (LEAMER), Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro 21941-902, BrazilLaboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes (LEAMER), Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro 21941-902, BrazilThe opportunistic fungal pathogens belonging to the <i>Candida haemulonii</i> complex and the phylogenetically related species <i>Candida auris</i> are well-known for causing infections that are difficult to treat due to their multidrug-resistance profiles. <i>Candida auris</i> is even more worrisome due to its ability to cause outbreaks in healthcare settings. These emerging yeasts produce a wide range of virulence factors that facilitate the development of the infectious process. In recent years, the aggregative phenotype has been receiving attention, as it is mainly associated with defects in cellular division and its possible involvement in helping the fungus to escape from the host immune responses. In the present study, we initially investigated the aggregation ability of 18 clinical isolates belonging to the <i>C. haemulonii</i> species complex (<i>C. haemulonii sensu stricto</i>, <i>C. duobushaemulonii</i>, and <i>C. haemulonii</i> var. <i>vulnera</i>) and <i>C. auris</i>. Subsequently, we evaluated the effects of physicochemical factors on fungal aggregation competence. The results demonstrated that cell-to-cell aggregation was a typically time-dependent event, in which almost all studied fungal isolates of both the <i>C. haemulonii</i> species complex and <i>C. auris</i> exhibited high aggregation after 2 h of incubation at 37 °C. Interestingly, the fungal cells forming the aggregates remained viable. The aggregation of all isolates was not impacted by pH, temperature, β-mercaptoethanol (a protein-denaturing agent), or EDTA (a chelator agent). Conversely, proteinase K, trypsin, and sodium dodecyl sulfate (SDS) significantly diminished the fungal aggregation. Collectively, our results demonstrated that the aggregation ability of these opportunistic yeast pathogens is time-dependent, and surface proteins and hydrophobic interactions seem to mediate cell aggregation since the presence of proteases and anionic detergents affected the aggregation capability. However, further studies are necessary to better elucidate the molecular aspects of this intriguing phenomenon.https://www.mdpi.com/2414-6366/8/8/382<i>Candida haemulonii</i> cladecell-cell interactionemerging yeastsdrug resistancevirulencephysicochemical conditions
spellingShingle Lívia S. Ramos
Claudia M. Parra-Giraldo
Marta H. Branquinha
André L. S. Santos
Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species Complex
Tropical Medicine and Infectious Disease
<i>Candida haemulonii</i> clade
cell-cell interaction
emerging yeasts
drug resistance
virulence
physicochemical conditions
title Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species Complex
title_full Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species Complex
title_fullStr Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species Complex
title_full_unstemmed Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species Complex
title_short Cell Aggregation Capability of Clinical Isolates from <i>Candida auris</i> and <i>Candida haemulonii</i> Species Complex
title_sort cell aggregation capability of clinical isolates from i candida auris i and i candida haemulonii i species complex
topic <i>Candida haemulonii</i> clade
cell-cell interaction
emerging yeasts
drug resistance
virulence
physicochemical conditions
url https://www.mdpi.com/2414-6366/8/8/382
work_keys_str_mv AT liviasramos cellaggregationcapabilityofclinicalisolatesfromicandidaaurisiandicandidahaemuloniiispeciescomplex
AT claudiamparragiraldo cellaggregationcapabilityofclinicalisolatesfromicandidaaurisiandicandidahaemuloniiispeciescomplex
AT martahbranquinha cellaggregationcapabilityofclinicalisolatesfromicandidaaurisiandicandidahaemuloniiispeciescomplex
AT andrelssantos cellaggregationcapabilityofclinicalisolatesfromicandidaaurisiandicandidahaemuloniiispeciescomplex