Secretory aspartyl proteinases (Saps) of Candida albicans are key virulence traits which cause inflammasome-dependent, aseptic inflammation in a mouse model of vaginitis. In this paper, neutrophil migration in response to Sap2, Sap6 and chemo-attractive products released from Sap-treated vaginal epithelium was measured in vitro, ex vivo and in vivo. Our results show that Sap2 and Sap6 induce neutrophil migration and production of potent chemoattractive chemokines such as IL-8 and MIP-2 by vaginal epithelial cells. Our data suggest that at least part of MIP-2 production depends upon IL-1β activity. The vaginal fluid of Candida-infected mice contained a heat-labile inhibitor of neutrophil candidacidal activity that was absent from the vaginal fluid of Sap-treated mice. Overall, our data provide additional information on the capacity of C. albicans Saps to cause aseptic vaginal inflammation and highlight the potential role of some chemokines released from vaginal epithelial cells in this phenomenon.

In vivo induction of neutrophils chemotaxis by secretory aspartyl proteinases of Candida albicans / Gabrielli, E.; Sabbatini, S.; Roselletti, E.; Kasper, L.; Perito, S.; Hube, B.; Cassone, A.; Vecchiarelli, A.; Pericolini, Eva. - In: VIRULENCE. - ISSN 2150-5594. - 7:7(2016), pp. 819-825. (Intervento presentato al convegno 13th ASM Conference on Candida and Candidiasis tenutosi a Seattle, WA nel 13-17 April 2016) [10.1080/21505594.2016.1184385].

In vivo induction of neutrophils chemotaxis by secretory aspartyl proteinases of Candida albicans

PERICOLINI, Eva
2016

Abstract

Secretory aspartyl proteinases (Saps) of Candida albicans are key virulence traits which cause inflammasome-dependent, aseptic inflammation in a mouse model of vaginitis. In this paper, neutrophil migration in response to Sap2, Sap6 and chemo-attractive products released from Sap-treated vaginal epithelium was measured in vitro, ex vivo and in vivo. Our results show that Sap2 and Sap6 induce neutrophil migration and production of potent chemoattractive chemokines such as IL-8 and MIP-2 by vaginal epithelial cells. Our data suggest that at least part of MIP-2 production depends upon IL-1β activity. The vaginal fluid of Candida-infected mice contained a heat-labile inhibitor of neutrophil candidacidal activity that was absent from the vaginal fluid of Sap-treated mice. Overall, our data provide additional information on the capacity of C. albicans Saps to cause aseptic vaginal inflammation and highlight the potential role of some chemokines released from vaginal epithelial cells in this phenomenon.
2016
29-apr-2016
7
7
819
825
In vivo induction of neutrophils chemotaxis by secretory aspartyl proteinases of Candida albicans / Gabrielli, E.; Sabbatini, S.; Roselletti, E.; Kasper, L.; Perito, S.; Hube, B.; Cassone, A.; Vecchiarelli, A.; Pericolini, Eva. - In: VIRULENCE. - ISSN 2150-5594. - 7:7(2016), pp. 819-825. (Intervento presentato al convegno 13th ASM Conference on Candida and Candidiasis tenutosi a Seattle, WA nel 13-17 April 2016) [10.1080/21505594.2016.1184385].
Gabrielli, E.; Sabbatini, S.; Roselletti, E.; Kasper, L.; Perito, S.; Hube, B.; Cassone, A.; Vecchiarelli, A.; Pericolini, Eva
File in questo prodotto:
File Dimensione Formato  
Gabrielli E. et al. Virulence 2016 PMN chemiotassi.pdf

Open access

Descrizione: Gabrielli E. et al, Virulence, 2016
Tipologia: Versione pubblicata dall'editore
Dimensione 1.06 MB
Formato Adobe PDF
1.06 MB Adobe PDF Visualizza/Apri
VOR_In vivo induction of neutrophil.pdf

Open access

Tipologia: Versione pubblicata dall'editore
Dimensione 1.43 MB
Formato Adobe PDF
1.43 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1120015
Citazioni
  • ???jsp.display-item.citation.pmc??? 33
  • Scopus 49
  • ???jsp.display-item.citation.isi??? 43
social impact