Literature DB >> 19604278

The importance of strain variation in virulence of Candida dubliniensis and Candida albicans: results of a blinded histopathological study of invasive candidiasis.

L R Asmundsdóttir1, H Erlendsdóttir, B A Agnarsson, M Gottfredsson.   

Abstract

The pathogenic yeast Candida dubliniensis is increasingly reported as a cause of systemic fungal infections. We compared the virulence of 9 clinical bloodstream isolates of C. dubliniensis with 3 C. albicans isolates in a murine model of invasive candidiasis. Quantification of organisms and inflammatory changes in kidneys of infected animals were evaluated in a blinded, systematic manner. Average 7-day mortality among animals infected with C. dubliniensis was 21.0% (33/157 animals; range for strains: 0-57.1%); and with C. albicans 23.2%, (23/99 animals; range for strains: 6.7-85.0%) (p 0.65). Greater strain variation was noted within species than between the two species. Both species comprised strains of either high or low virulence, and six of the nine C. dubliniensis strains showed negligible virulence. Colony counts determined on samples from liver and kidneys did not differ between species. According to histopathological analysis, C. dubliniensis produced significantly lower levels of hyphae than C. albicans (p <0.001). Candida albicans caused a greater inflammatory response in kidneys (p <0.001) and was more commonly associated with granulomatous inflammation (p 0.003) and greater mononuclear infiltrate (p <0.001). According to multivariate analysis, increasing tissue burden of both hyphal forms (p 0.032) and yeasts (p 0.016) was independently associated with death, whereas higher levels of mononuclear cells were protective (p <0.001). The results suggest a great overlap between the virulence properties of C. dubliniensis and C. albicans. Both yeast and hyphal forms are independently associated with mortality, suggesting similar virulence for both. The source of the fungal isolates may be a neglected confounding factor in virulence studies in animal models.

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Year:  2009        PMID: 19604278     DOI: 10.1111/j.1469-0691.2009.02840.x

Source DB:  PubMed          Journal:  Clin Microbiol Infect        ISSN: 1198-743X            Impact factor:   8.067


  14 in total

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Authors:  Gary P Moran; David C Coleman; Derek J Sullivan
Journal:  Eukaryot Cell       Date:  2010-11-12

2.  Usefulness of the Non-conventional Caenorhabditis elegans Model to Assess Candida Virulence.

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Journal:  Mycopathologia       Date:  2017-05-18       Impact factor: 2.574

Review 3.  Candidiasis: predisposing factors, prevention, diagnosis and alternative treatment.

Authors:  Natália Martins; Isabel C F R Ferreira; Lillian Barros; Sónia Silva; Mariana Henriques
Journal:  Mycopathologia       Date:  2014-05-01       Impact factor: 2.574

4.  Differential filamentation of Candida albicans and Candida dubliniensis Is governed by nutrient regulation of UME6 expression.

Authors:  Leanne O'Connor; Nicole Caplice; David C Coleman; Derek J Sullivan; Gary P Moran
Journal:  Eukaryot Cell       Date:  2010-07-16

5.  Different tumor necrosis factor α antagonists have different effects on host susceptibility to disseminated and oropharyngeal candidiasis in mice.

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Journal:  Virulence       Date:  2014-07-09       Impact factor: 5.882

6.  Antimicrobial photodynamic inactivation inhibits Candida albicans virulence factors and reduces in vivo pathogenicity.

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Journal:  Antimicrob Agents Chemother       Date:  2012-11-05       Impact factor: 5.191

7.  Nationwide study of candidemia, antifungal use, and antifungal drug resistance in Iceland, 2000 to 2011.

Authors:  Lena Ros Asmundsdottir; Helga Erlendsdottir; Magnus Gottfredsson
Journal:  J Clin Microbiol       Date:  2012-12-26       Impact factor: 5.948

8.  Comparative Analysis of the Capacity of the Candida Species To Elicit Vaginal Immunopathology.

Authors:  Hubertine M E Willems; David J Lowes; Katherine S Barker; Glen E Palmer; Brian M Peters
Journal:  Infect Immun       Date:  2018-11-20       Impact factor: 3.441

9.  Candida albicans versus Candida dubliniensis: Why Is C. albicans More Pathogenic?

Authors:  Gary P Moran; David C Coleman; Derek J Sullivan
Journal:  Int J Microbiol       Date:  2011-09-04

10.  Th1-Th17 cells mediate protective adaptive immunity against Staphylococcus aureus and Candida albicans infection in mice.

Authors:  Lin Lin; Ashraf S Ibrahim; Xin Xu; Joshua M Farber; Valentina Avanesian; Beverlie Baquir; Yue Fu; Samuel W French; John E Edwards; Brad Spellberg
Journal:  PLoS Pathog       Date:  2009-12-24       Impact factor: 6.823

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