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Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease
Bartonella henselae, the pathogen that causes cat-scratch disease (CSD), is relatively rare in the clinic. CSD usually causes mild clinical manifestations, which self-heal in a matter of weeks. However, in immunocompromised patients, CSD may cause systemic disorders that can lead to critical illness...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524480/ https://www.ncbi.nlm.nih.gov/pubmed/36189365 http://dx.doi.org/10.3389/fcimb.2022.946849 |
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author | Li, Mingxia Yan, Kunli Jia, Peisheng Wei, Erhu Wang, Huaili |
author_facet | Li, Mingxia Yan, Kunli Jia, Peisheng Wei, Erhu Wang, Huaili |
author_sort | Li, Mingxia |
collection | PubMed |
description | Bartonella henselae, the pathogen that causes cat-scratch disease (CSD), is relatively rare in the clinic. CSD usually causes mild clinical manifestations, which self-heal in a matter of weeks. However, in immunocompromised patients, CSD may cause systemic disorders that can lead to critical illness. Due to the diversity of symptom signs and the lack of a golden standard for diagnosis, identifying atypical CSD in a timely manner presents a challenge. Metagenomic next-generation sequencing (mNGS), is a promising technology that has been widely used in the detection of pathogens in clinical infectious diseases in recent years. mNGS can detect multiple pathogens quickly and accurately from any given source. Here, we present a case of atypical CSD, which was diagnosed using mNGS. The patient manifested a fever of unknown infectious origin, and routine antibiotic treatment was ineffective. mNGS was employed to test the patient’s peripheral blood, which led to the detection of B. henselae. This was rarely seen in previous CSD reports. We surmised that the patient presented with atypical CSD and thus a targeted therapy was recommended. Crucially, the patient recovered rapidly. Based on this case study findings, we recommend that CSD should be included in the differential diagnosis for fever of unknown origin and that mNGS may be helpful in the diagnosis of CSD. |
format | Online Article Text |
id | pubmed-9524480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95244802022-10-01 Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease Li, Mingxia Yan, Kunli Jia, Peisheng Wei, Erhu Wang, Huaili Front Cell Infect Microbiol Cellular and Infection Microbiology Bartonella henselae, the pathogen that causes cat-scratch disease (CSD), is relatively rare in the clinic. CSD usually causes mild clinical manifestations, which self-heal in a matter of weeks. However, in immunocompromised patients, CSD may cause systemic disorders that can lead to critical illness. Due to the diversity of symptom signs and the lack of a golden standard for diagnosis, identifying atypical CSD in a timely manner presents a challenge. Metagenomic next-generation sequencing (mNGS), is a promising technology that has been widely used in the detection of pathogens in clinical infectious diseases in recent years. mNGS can detect multiple pathogens quickly and accurately from any given source. Here, we present a case of atypical CSD, which was diagnosed using mNGS. The patient manifested a fever of unknown infectious origin, and routine antibiotic treatment was ineffective. mNGS was employed to test the patient’s peripheral blood, which led to the detection of B. henselae. This was rarely seen in previous CSD reports. We surmised that the patient presented with atypical CSD and thus a targeted therapy was recommended. Crucially, the patient recovered rapidly. Based on this case study findings, we recommend that CSD should be included in the differential diagnosis for fever of unknown origin and that mNGS may be helpful in the diagnosis of CSD. Frontiers Media S.A. 2022-09-16 /pmc/articles/PMC9524480/ /pubmed/36189365 http://dx.doi.org/10.3389/fcimb.2022.946849 Text en Copyright © 2022 Li, Yan, Jia, Wei and Wang 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 Li, Mingxia Yan, Kunli Jia, Peisheng Wei, Erhu Wang, Huaili Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease |
title | Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease |
title_full | Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease |
title_fullStr | Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease |
title_full_unstemmed | Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease |
title_short | Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease |
title_sort | metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524480/ https://www.ncbi.nlm.nih.gov/pubmed/36189365 http://dx.doi.org/10.3389/fcimb.2022.946849 |
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