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Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures

The longstanding paradigm is that most bloodstream infections (BSIs) are caused by a single organism. We performed whole genome sequencing of five-to-ten strains from blood culture (BC) bottles in each of ten patients with Candida glabrata BSI. We demonstrated that BCs contained mixed populations of...

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Autores principales: Badrane, Hassan, Cheng, Shaoji, Dupont, Christopher L, Hao, Binghua, Driscoll, Eileen, Morder, Kristin, Liu, Guojun, Newbrough, Anthony, Fleres, Giuseppe, Kaul, Drishti, Espinoza, Josh L, Clancy, Cornelius J, Nguyen, M. Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104189/
https://www.ncbi.nlm.nih.gov/pubmed/37066226
http://dx.doi.org/10.21203/rs.3.rs-2706400/v1
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author Badrane, Hassan
Cheng, Shaoji
Dupont, Christopher L
Hao, Binghua
Driscoll, Eileen
Morder, Kristin
Liu, Guojun
Newbrough, Anthony
Fleres, Giuseppe
Kaul, Drishti
Espinoza, Josh L
Clancy, Cornelius J
Nguyen, M. Hong
author_facet Badrane, Hassan
Cheng, Shaoji
Dupont, Christopher L
Hao, Binghua
Driscoll, Eileen
Morder, Kristin
Liu, Guojun
Newbrough, Anthony
Fleres, Giuseppe
Kaul, Drishti
Espinoza, Josh L
Clancy, Cornelius J
Nguyen, M. Hong
author_sort Badrane, Hassan
collection PubMed
description The longstanding paradigm is that most bloodstream infections (BSIs) are caused by a single organism. We performed whole genome sequencing of five-to-ten strains from blood culture (BC) bottles in each of ten patients with Candida glabrata BSI. We demonstrated that BCs contained mixed populations of clonal but genetically diverse strains. Genetically distinct strains from two patients exhibited phenotypes that were potentially important during BSIs, including differences in susceptibility to antifungal agents and phagocytosis. In both patients, the clinical microbiology lab recovered a fluconazole-susceptible index strain, but we identified mixed fluconazole-susceptible and –resistant populations. Diversity in drug susceptibility was likely clinically relevant, as fluconazole-resistant strains were subsequently recovered by the clinical laboratory during persistent or relapsing infections. In one patient, unrecognized respiration-deficient small colony variants were fluconazole-resistant and significantly attenuated for virulence during murine candidiasis. Our data suggest a new population-based paradigm of C. glabrata genotypic and phenotypic diversity during BSIs.
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spelling pubmed-101041892023-04-15 Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures Badrane, Hassan Cheng, Shaoji Dupont, Christopher L Hao, Binghua Driscoll, Eileen Morder, Kristin Liu, Guojun Newbrough, Anthony Fleres, Giuseppe Kaul, Drishti Espinoza, Josh L Clancy, Cornelius J Nguyen, M. Hong Res Sq Article The longstanding paradigm is that most bloodstream infections (BSIs) are caused by a single organism. We performed whole genome sequencing of five-to-ten strains from blood culture (BC) bottles in each of ten patients with Candida glabrata BSI. We demonstrated that BCs contained mixed populations of clonal but genetically diverse strains. Genetically distinct strains from two patients exhibited phenotypes that were potentially important during BSIs, including differences in susceptibility to antifungal agents and phagocytosis. In both patients, the clinical microbiology lab recovered a fluconazole-susceptible index strain, but we identified mixed fluconazole-susceptible and –resistant populations. Diversity in drug susceptibility was likely clinically relevant, as fluconazole-resistant strains were subsequently recovered by the clinical laboratory during persistent or relapsing infections. In one patient, unrecognized respiration-deficient small colony variants were fluconazole-resistant and significantly attenuated for virulence during murine candidiasis. Our data suggest a new population-based paradigm of C. glabrata genotypic and phenotypic diversity during BSIs. American Journal Experts 2023-04-03 /pmc/articles/PMC10104189/ /pubmed/37066226 http://dx.doi.org/10.21203/rs.3.rs-2706400/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. https://creativecommons.org/licenses/by/4.0/License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Badrane, Hassan
Cheng, Shaoji
Dupont, Christopher L
Hao, Binghua
Driscoll, Eileen
Morder, Kristin
Liu, Guojun
Newbrough, Anthony
Fleres, Giuseppe
Kaul, Drishti
Espinoza, Josh L
Clancy, Cornelius J
Nguyen, M. Hong
Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures
title Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures
title_full Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures
title_fullStr Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures
title_full_unstemmed Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures
title_short Genotypic diversity and unrecognized antifungal resistance among populations of Candida glabrata from positive blood cultures
title_sort genotypic diversity and unrecognized antifungal resistance among populations of candida glabrata from positive blood cultures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104189/
https://www.ncbi.nlm.nih.gov/pubmed/37066226
http://dx.doi.org/10.21203/rs.3.rs-2706400/v1
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