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Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients

Mucormycoses are invasive infections by Rhizopus species and other Mucorales. Over 10 months, four solid organ transplant (SOT) recipients at our centre developed mucormycosis due to Rhizopus microsporus (n=2), R. arrhizus (n=1) or Lichtheimia corymbifera (n=1), at a median 31.5 days (range: 13–34)...

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Autores principales: Nguyen, M. Hong, Kaul, Drishti, Muto, Carlene, Cheng, Shaoji J., Richter, R. Alex, Bruno, Vincent M., Liu, Guojun, Beyhan, Sinem, Sundermann, Alexander J., Mounaud, Stephanie, Pasculle, A. William, Nierman, William C., Driscoll, Eileen, Cumbie, Richard, Clancy, Cornelius J., Dupont, Christopher L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116672/
https://www.ncbi.nlm.nih.gov/pubmed/33245689
http://dx.doi.org/10.1099/mgen.0.000473
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author Nguyen, M. Hong
Kaul, Drishti
Muto, Carlene
Cheng, Shaoji J.
Richter, R. Alex
Bruno, Vincent M.
Liu, Guojun
Beyhan, Sinem
Sundermann, Alexander J.
Mounaud, Stephanie
Pasculle, A. William
Nierman, William C.
Driscoll, Eileen
Cumbie, Richard
Clancy, Cornelius J.
Dupont, Christopher L.
author_facet Nguyen, M. Hong
Kaul, Drishti
Muto, Carlene
Cheng, Shaoji J.
Richter, R. Alex
Bruno, Vincent M.
Liu, Guojun
Beyhan, Sinem
Sundermann, Alexander J.
Mounaud, Stephanie
Pasculle, A. William
Nierman, William C.
Driscoll, Eileen
Cumbie, Richard
Clancy, Cornelius J.
Dupont, Christopher L.
author_sort Nguyen, M. Hong
collection PubMed
description Mucormycoses are invasive infections by Rhizopus species and other Mucorales. Over 10 months, four solid organ transplant (SOT) recipients at our centre developed mucormycosis due to Rhizopus microsporus (n=2), R. arrhizus (n=1) or Lichtheimia corymbifera (n=1), at a median 31.5 days (range: 13–34) post-admission. We performed whole genome sequencing (WGS) on 72 Mucorales isolates (45 R. arrhizus, 19 R. delemar, six R. microsporus, two Lichtheimia species) from these patients, from five patients with community-acquired mucormycosis, and from hospital and regional environments. Isolates were compared by core protein phylogeny and global genomic features, including genome size, guanine–cytosine percentages, shared protein families and paralogue expansions. Patient isolates fell into six core phylogenetic lineages (clades). Phylogenetic and genomic similarities of R. microsporus isolates recovered 7 months apart from two SOT recipients in adjoining hospitals suggested a potential common source exposure. However, isolates from other patients and environmental sites had unique genomes. Many isolates that were indistinguishable by core phylogeny were distinct by one or more global genomic comparisons. Certain clades were recovered throughout the study period, whereas others were found at particular time points. In conclusion, mucormycosis cases could not be genetically linked to a definitive environmental source. Comprehensive genomic analyses eliminated false associations between Mucorales isolates that would have been assigned using core phylogenetic or less extensive genomic comparisons. The genomic diversity of Mucorales mandates that multiple isolates from individual patients and environmental sites undergo WGS during epidemiological investigations. However, exhaustive surveillance of fungal populations in a hospital and surrounding community is probably infeasible.
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spelling pubmed-81166722021-05-13 Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients Nguyen, M. Hong Kaul, Drishti Muto, Carlene Cheng, Shaoji J. Richter, R. Alex Bruno, Vincent M. Liu, Guojun Beyhan, Sinem Sundermann, Alexander J. Mounaud, Stephanie Pasculle, A. William Nierman, William C. Driscoll, Eileen Cumbie, Richard Clancy, Cornelius J. Dupont, Christopher L. Microb Genom Research Article Mucormycoses are invasive infections by Rhizopus species and other Mucorales. Over 10 months, four solid organ transplant (SOT) recipients at our centre developed mucormycosis due to Rhizopus microsporus (n=2), R. arrhizus (n=1) or Lichtheimia corymbifera (n=1), at a median 31.5 days (range: 13–34) post-admission. We performed whole genome sequencing (WGS) on 72 Mucorales isolates (45 R. arrhizus, 19 R. delemar, six R. microsporus, two Lichtheimia species) from these patients, from five patients with community-acquired mucormycosis, and from hospital and regional environments. Isolates were compared by core protein phylogeny and global genomic features, including genome size, guanine–cytosine percentages, shared protein families and paralogue expansions. Patient isolates fell into six core phylogenetic lineages (clades). Phylogenetic and genomic similarities of R. microsporus isolates recovered 7 months apart from two SOT recipients in adjoining hospitals suggested a potential common source exposure. However, isolates from other patients and environmental sites had unique genomes. Many isolates that were indistinguishable by core phylogeny were distinct by one or more global genomic comparisons. Certain clades were recovered throughout the study period, whereas others were found at particular time points. In conclusion, mucormycosis cases could not be genetically linked to a definitive environmental source. Comprehensive genomic analyses eliminated false associations between Mucorales isolates that would have been assigned using core phylogenetic or less extensive genomic comparisons. The genomic diversity of Mucorales mandates that multiple isolates from individual patients and environmental sites undergo WGS during epidemiological investigations. However, exhaustive surveillance of fungal populations in a hospital and surrounding community is probably infeasible. Microbiology Society 2020-11-27 /pmc/articles/PMC8116672/ /pubmed/33245689 http://dx.doi.org/10.1099/mgen.0.000473 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Article
Nguyen, M. Hong
Kaul, Drishti
Muto, Carlene
Cheng, Shaoji J.
Richter, R. Alex
Bruno, Vincent M.
Liu, Guojun
Beyhan, Sinem
Sundermann, Alexander J.
Mounaud, Stephanie
Pasculle, A. William
Nierman, William C.
Driscoll, Eileen
Cumbie, Richard
Clancy, Cornelius J.
Dupont, Christopher L.
Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients
title Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients
title_full Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients
title_fullStr Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients
title_full_unstemmed Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients
title_short Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients
title_sort genetic diversity of clinical and environmental mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116672/
https://www.ncbi.nlm.nih.gov/pubmed/33245689
http://dx.doi.org/10.1099/mgen.0.000473
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