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Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia

This report shows the contribution of next-generation metagenomic sequencing (mNGS) as an alternative to challenging diagnostic infection in immunosuppressed individuals. Herein, we report three acute leukemia patients who developed severe invasive infections due to different etiologies: fungi, viru...

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Autores principales: Garnica, Marcia, Pierrotti, Ligia Camera, Oliveira, Paula Vanessa de, Mazzi, Mariana, Chebabo, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392121/
https://www.ncbi.nlm.nih.gov/pubmed/33639095
http://dx.doi.org/10.1016/j.bjid.2021.101548
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author Garnica, Marcia
Pierrotti, Ligia Camera
Oliveira, Paula Vanessa de
Mazzi, Mariana
Chebabo, Alberto
author_facet Garnica, Marcia
Pierrotti, Ligia Camera
Oliveira, Paula Vanessa de
Mazzi, Mariana
Chebabo, Alberto
author_sort Garnica, Marcia
collection PubMed
description This report shows the contribution of next-generation metagenomic sequencing (mNGS) as an alternative to challenging diagnostic infection in immunosuppressed individuals. Herein, we report three acute leukemia patients who developed severe invasive infections due to different etiologies: fungi, viruses, and protozoa. mNGS improved the diagnosis of the infections and provided the opportunity for adequate therapy. The mNGS is a hypothesis-free diagnostic platform, increasing potential in challenging diseases in hematological patients due to the extended diagnostic panel and the expedite access to the result.
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spelling pubmed-93921212022-08-23 Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia Garnica, Marcia Pierrotti, Ligia Camera Oliveira, Paula Vanessa de Mazzi, Mariana Chebabo, Alberto Braz J Infect Dis Case Report This report shows the contribution of next-generation metagenomic sequencing (mNGS) as an alternative to challenging diagnostic infection in immunosuppressed individuals. Herein, we report three acute leukemia patients who developed severe invasive infections due to different etiologies: fungi, viruses, and protozoa. mNGS improved the diagnosis of the infections and provided the opportunity for adequate therapy. The mNGS is a hypothesis-free diagnostic platform, increasing potential in challenging diseases in hematological patients due to the extended diagnostic panel and the expedite access to the result. Elsevier 2021-02-25 /pmc/articles/PMC9392121/ /pubmed/33639095 http://dx.doi.org/10.1016/j.bjid.2021.101548 Text en © 2021 Sociedade Brasileira de Infectologia. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Garnica, Marcia
Pierrotti, Ligia Camera
Oliveira, Paula Vanessa de
Mazzi, Mariana
Chebabo, Alberto
Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia
title Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia
title_full Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia
title_fullStr Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia
title_full_unstemmed Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia
title_short Metagenomic next-generation sequencing (mNGS) for diagnostically challenging infectious diseases in patients with acute leukemia
title_sort metagenomic next-generation sequencing (mngs) for diagnostically challenging infectious diseases in patients with acute leukemia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392121/
https://www.ncbi.nlm.nih.gov/pubmed/33639095
http://dx.doi.org/10.1016/j.bjid.2021.101548
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