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Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing
Leishmaniasis is a vector-borne disease caused by Leishmania. Although the incidence of leishmaniasis in China is currently low, it has not been completely eradicated. In 2019, visceral leishmaniasis was diagnosed in three patients using bone marrow microscopic examination and metagenomic next-gener...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538539/ https://www.ncbi.nlm.nih.gov/pubmed/33072623 http://dx.doi.org/10.3389/fcimb.2020.528884 |
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author | Chen, Hongbin Fan, Chunhong Gao, Hua Yin, Yuyao Wang, Xiaojuan Zhang, Yawei Wang, Hui |
author_facet | Chen, Hongbin Fan, Chunhong Gao, Hua Yin, Yuyao Wang, Xiaojuan Zhang, Yawei Wang, Hui |
author_sort | Chen, Hongbin |
collection | PubMed |
description | Leishmaniasis is a vector-borne disease caused by Leishmania. Although the incidence of leishmaniasis in China is currently low, it has not been completely eradicated. In 2019, visceral leishmaniasis was diagnosed in three patients using bone marrow microscopic examination and metagenomic next-generation sequencing (mNGS). The bone marrow mNGS results from the three patients indicated that 99.9, 99.6, and 30.3% of non-human reads matched the Leishmania genome, and plasma mNGS results from one of the patients revealed that 46.2% of non-human reads matched the Leishmania genome. In the second patient's plasma, no Leishmania sequences were detected by plasma mNGS, and the third patient's plasma was unavailable. The pathogen in all three patients was identified as Leishmania infantum. Leishmania amastigotes were observed by microscopic examination of bone marrow smears in all three patients, but were not found in peripheral blood smears. This indicates that the sensitivity of mNGS is higher than that of smear microscopy and that mNGS can be used to identify Leishmania at the species level. All three patients were elderly male farmers, two from Shanxi and one from Beijing. All three patients had splenomegaly and pancytopenia. Originally, these patients were misdiagnosed and treated for extended periods in other hospitals. Diagnoses of visceral leishmaniasis took place 6, 2, and 2 months after the onset of symptoms in the three patients. In conclusion, this study confirms that bone marrow mNGS can be used to quickly and accurately confirm a diagnosis in patients with suspected leishmaniasis. |
format | Online Article Text |
id | pubmed-7538539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75385392020-10-17 Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing Chen, Hongbin Fan, Chunhong Gao, Hua Yin, Yuyao Wang, Xiaojuan Zhang, Yawei Wang, Hui Front Cell Infect Microbiol Cellular and Infection Microbiology Leishmaniasis is a vector-borne disease caused by Leishmania. Although the incidence of leishmaniasis in China is currently low, it has not been completely eradicated. In 2019, visceral leishmaniasis was diagnosed in three patients using bone marrow microscopic examination and metagenomic next-generation sequencing (mNGS). The bone marrow mNGS results from the three patients indicated that 99.9, 99.6, and 30.3% of non-human reads matched the Leishmania genome, and plasma mNGS results from one of the patients revealed that 46.2% of non-human reads matched the Leishmania genome. In the second patient's plasma, no Leishmania sequences were detected by plasma mNGS, and the third patient's plasma was unavailable. The pathogen in all three patients was identified as Leishmania infantum. Leishmania amastigotes were observed by microscopic examination of bone marrow smears in all three patients, but were not found in peripheral blood smears. This indicates that the sensitivity of mNGS is higher than that of smear microscopy and that mNGS can be used to identify Leishmania at the species level. All three patients were elderly male farmers, two from Shanxi and one from Beijing. All three patients had splenomegaly and pancytopenia. Originally, these patients were misdiagnosed and treated for extended periods in other hospitals. Diagnoses of visceral leishmaniasis took place 6, 2, and 2 months after the onset of symptoms in the three patients. In conclusion, this study confirms that bone marrow mNGS can be used to quickly and accurately confirm a diagnosis in patients with suspected leishmaniasis. Frontiers Media S.A. 2020-09-23 /pmc/articles/PMC7538539/ /pubmed/33072623 http://dx.doi.org/10.3389/fcimb.2020.528884 Text en Copyright © 2020 Chen, Fan, Gao, Yin, Wang, Zhang and Wang. http://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 Chen, Hongbin Fan, Chunhong Gao, Hua Yin, Yuyao Wang, Xiaojuan Zhang, Yawei Wang, Hui Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing |
title | Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing |
title_full | Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing |
title_fullStr | Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing |
title_full_unstemmed | Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing |
title_short | Leishmaniasis Diagnosis via Metagenomic Next-Generation Sequencing |
title_sort | leishmaniasis diagnosis via metagenomic next-generation sequencing |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538539/ https://www.ncbi.nlm.nih.gov/pubmed/33072623 http://dx.doi.org/10.3389/fcimb.2020.528884 |
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