Please use this identifier to cite or link to this item: https://hdl.handle.net/1822/58893

TitleInflammatory cell recruitment in Candida glabrata biofilm cell-infected mice receiving antifungal chemotherapy
Author(s)Rodrigues, Célia F.
Correia, Alexandra
Vilanova, Manuel
Henriques, Mariana
KeywordsCandida glabrata
candidemia
echinocandins
resistance
biofilms
infection
micafungin
caspofungin
in vivo
Issue date26-Jan-2019
PublisherMultidisciplinary Digital Publishing Institute (MDPI)
JournalJournal of Clinical Medicine
CitationRodrigues, Célia F.; Correia, Alexandra; Vilanova, Manuel; Henriques, Mariana, Inflammatory Cell Recruitment in Candida glabrata Biofilm Cell-Infected Mice Receiving Antifungal Chemotherapy. Journal of Clinical Medicine, 8(2), 2019
Abstract(s)(1) Background: Due to a high rate of antifungal resistance, Candida glabrata is one of the most prevalent Candida spp. linked to systemic candidiasis, which is particularly critical in catheterized patients. The goal of this work was to simulate a systemic infection exclusively derived from C. glabrata biofilm cells and to evaluate the effectiveness of the treatment of two echinocandinscaspofungin (Csf) and micafungin (Mcf). (2) Methods: CD1 mice were infected with 48 h-biofilm cells of C. glabrata and then treated with Csf or Mcf. After 72 h, the efficacy of each drug was evaluated to assess the organ fungal burden through colony forming units (CFU) counting. The immune cell recruitment into target organs was evaluated by flow cytometry or histopathology analysis. (3) Results: Fungal burden was found to be higher in the liver than in the kidneys. However, none of the drugs was effective in completely eradicating C. glabrata biofilm cells. At the evaluated time point, flow cytometry analysis showed a predominant mononuclear response in the spleen, which was also evident in the liver and kidneys of the infected mice, as observed by histopathology analysis. (4) Conclusions: Echinocandins do not have a significant impact on liver and kidney fungal burden, or recruited inflammatory infiltrate, when mice are intravenously (i.v.) infected with C. glabrata biofilm-grown cells.
TypeArticle
URIhttps://hdl.handle.net/1822/58893
DOI10.3390/jcm8020142
ISSN2077-0383
e-ISSN2077-0383
Publisher versionhttps://www.mdpi.com/journal/jcm
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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