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Mucormycosis in 2023: an update on pathogenesis and management

Mucormycosis (MCR) is an emerging and frequently lethal fungal infection caused by the Mucorales family, with Rhizopus, Mucor, and Lichtheimia, accounting for > 90% of all cases. MCR is seen in patients with severe immunosuppression such as those with hematologic malignancy or transplantation, Di...

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Autores principales: Alqarihi, Abdullah, Kontoyiannis, Dimitrios P., Ibrahim, Ashraf S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552646/
https://www.ncbi.nlm.nih.gov/pubmed/37808914
http://dx.doi.org/10.3389/fcimb.2023.1254919
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author Alqarihi, Abdullah
Kontoyiannis, Dimitrios P.
Ibrahim, Ashraf S.
author_facet Alqarihi, Abdullah
Kontoyiannis, Dimitrios P.
Ibrahim, Ashraf S.
author_sort Alqarihi, Abdullah
collection PubMed
description Mucormycosis (MCR) is an emerging and frequently lethal fungal infection caused by the Mucorales family, with Rhizopus, Mucor, and Lichtheimia, accounting for > 90% of all cases. MCR is seen in patients with severe immunosuppression such as those with hematologic malignancy or transplantation, Diabetes Mellitus (DM) and diabetic ketoacidosis (DKA) and immunocompetent patients with severe wounds. The recent SARS COV2 epidemy in India has resulted in a tremendous increase in MCR cases, typically seen in the setting of uncontrolled DM and corticosteroid use. In addition to the diversity of affected hosts, MCR has pleiotropic clinical presentations, with rhino-orbital/rhino-cerebral, sino-pulmonary and necrotizing cutaneous forms being the predominant manifestations. Major insights in MCR pathogenesis have brought into focus the host receptors (GRP78) and signaling pathways (EGFR activation cascade) as well as the adhesins used by Mucorales for invasion. Furthermore, studies have expanded on the importance of iron availability and the complex regulation of iron homeostasis, as well as the pivotal role of mycotoxins as key factors for tissue invasion. The molecular toolbox to study Mucorales pathogenesis remains underdeveloped, but promise is brought by RNAi and CRISPR/Cas9 approaches. Important recent advancements have been made in early, culture-independent molecular diagnosis of MCR. However, development of new potent antifungals against Mucorales remains an unmet need. Therapy of MCR is multidisciplinary and requires a high index of suspicion for initiation of early Mucorales-active antifungals. Reversal of underlying immunosuppression, if feasible, rapid DKA correction and in selected patients, surgical debulking are crucial for improved outcomes.
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spelling pubmed-105526462023-10-06 Mucormycosis in 2023: an update on pathogenesis and management Alqarihi, Abdullah Kontoyiannis, Dimitrios P. Ibrahim, Ashraf S. Front Cell Infect Microbiol Cellular and Infection Microbiology Mucormycosis (MCR) is an emerging and frequently lethal fungal infection caused by the Mucorales family, with Rhizopus, Mucor, and Lichtheimia, accounting for > 90% of all cases. MCR is seen in patients with severe immunosuppression such as those with hematologic malignancy or transplantation, Diabetes Mellitus (DM) and diabetic ketoacidosis (DKA) and immunocompetent patients with severe wounds. The recent SARS COV2 epidemy in India has resulted in a tremendous increase in MCR cases, typically seen in the setting of uncontrolled DM and corticosteroid use. In addition to the diversity of affected hosts, MCR has pleiotropic clinical presentations, with rhino-orbital/rhino-cerebral, sino-pulmonary and necrotizing cutaneous forms being the predominant manifestations. Major insights in MCR pathogenesis have brought into focus the host receptors (GRP78) and signaling pathways (EGFR activation cascade) as well as the adhesins used by Mucorales for invasion. Furthermore, studies have expanded on the importance of iron availability and the complex regulation of iron homeostasis, as well as the pivotal role of mycotoxins as key factors for tissue invasion. The molecular toolbox to study Mucorales pathogenesis remains underdeveloped, but promise is brought by RNAi and CRISPR/Cas9 approaches. Important recent advancements have been made in early, culture-independent molecular diagnosis of MCR. However, development of new potent antifungals against Mucorales remains an unmet need. Therapy of MCR is multidisciplinary and requires a high index of suspicion for initiation of early Mucorales-active antifungals. Reversal of underlying immunosuppression, if feasible, rapid DKA correction and in selected patients, surgical debulking are crucial for improved outcomes. Frontiers Media S.A. 2023-09-21 /pmc/articles/PMC10552646/ /pubmed/37808914 http://dx.doi.org/10.3389/fcimb.2023.1254919 Text en Copyright © 2023 Alqarihi, Kontoyiannis and Ibrahim https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Alqarihi, Abdullah
Kontoyiannis, Dimitrios P.
Ibrahim, Ashraf S.
Mucormycosis in 2023: an update on pathogenesis and management
title Mucormycosis in 2023: an update on pathogenesis and management
title_full Mucormycosis in 2023: an update on pathogenesis and management
title_fullStr Mucormycosis in 2023: an update on pathogenesis and management
title_full_unstemmed Mucormycosis in 2023: an update on pathogenesis and management
title_short Mucormycosis in 2023: an update on pathogenesis and management
title_sort mucormycosis in 2023: an update on pathogenesis and management
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552646/
https://www.ncbi.nlm.nih.gov/pubmed/37808914
http://dx.doi.org/10.3389/fcimb.2023.1254919
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