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Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay

Q fever is a zoonotic infectious disease caused by Coxiella burnetii. The clinical symptoms of acute Q fever are usually atypical, and routine serological tests of C. burnetii are not readily available, making the diagnosis of Q fever a challenge. In this case, we report a male patient who had repea...

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Autores principales: Yang, Yide, Shi, Qingmiao, Jin, Qian, Yang, Zhangnv, Li, Wangfang, Han, Jianfeng, Mao, Juanjuan, Zheng, Beiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204269/
https://www.ncbi.nlm.nih.gov/pubmed/35721056
http://dx.doi.org/10.3389/fmed.2022.846526
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author Yang, Yide
Shi, Qingmiao
Jin, Qian
Yang, Zhangnv
Li, Wangfang
Han, Jianfeng
Mao, Juanjuan
Zheng, Beiwen
author_facet Yang, Yide
Shi, Qingmiao
Jin, Qian
Yang, Zhangnv
Li, Wangfang
Han, Jianfeng
Mao, Juanjuan
Zheng, Beiwen
author_sort Yang, Yide
collection PubMed
description Q fever is a zoonotic infectious disease caused by Coxiella burnetii. The clinical symptoms of acute Q fever are usually atypical, and routine serological tests of C. burnetii are not readily available, making the diagnosis of Q fever a challenge. In this case, we report a male patient who had repeated fevers and was administered empirical anti-infective treatment, but the effect was poor. After conducting relevant laboratory and imagological examinations, the etiology has not yet been confirmed. Subsequently, metagenomic next-generation sequencing (mNGS) identified the sequence reads of C. burnetii from the patient's peripheral blood within 48 h, and then the diagnosis of acute Q fever was established. Moreover, the serological test of indirect immunofluorescence assay (IFA) of the C. burnetii antibody was further performed in the Centers for Disease Control, certifying the result of mNGS. The patient was ultimately treated with doxycycline and recovered well. mNGS is an unbiased and comprehensive method in infrequent or culture-negative pathogen identification. To our knowledge, this is the first case of acute Q fever identified by mNGS and confirmed by IFA in Taizhou, China. A further large-scale prospective clinical cohort study is worth carrying out to compare the diagnostic efficiency of mNGS with traditional serological methods and PCR in acute Q fever.
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spelling pubmed-92042692022-06-18 Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay Yang, Yide Shi, Qingmiao Jin, Qian Yang, Zhangnv Li, Wangfang Han, Jianfeng Mao, Juanjuan Zheng, Beiwen Front Med (Lausanne) Medicine Q fever is a zoonotic infectious disease caused by Coxiella burnetii. The clinical symptoms of acute Q fever are usually atypical, and routine serological tests of C. burnetii are not readily available, making the diagnosis of Q fever a challenge. In this case, we report a male patient who had repeated fevers and was administered empirical anti-infective treatment, but the effect was poor. After conducting relevant laboratory and imagological examinations, the etiology has not yet been confirmed. Subsequently, metagenomic next-generation sequencing (mNGS) identified the sequence reads of C. burnetii from the patient's peripheral blood within 48 h, and then the diagnosis of acute Q fever was established. Moreover, the serological test of indirect immunofluorescence assay (IFA) of the C. burnetii antibody was further performed in the Centers for Disease Control, certifying the result of mNGS. The patient was ultimately treated with doxycycline and recovered well. mNGS is an unbiased and comprehensive method in infrequent or culture-negative pathogen identification. To our knowledge, this is the first case of acute Q fever identified by mNGS and confirmed by IFA in Taizhou, China. A further large-scale prospective clinical cohort study is worth carrying out to compare the diagnostic efficiency of mNGS with traditional serological methods and PCR in acute Q fever. Frontiers Media S.A. 2022-05-26 /pmc/articles/PMC9204269/ /pubmed/35721056 http://dx.doi.org/10.3389/fmed.2022.846526 Text en Copyright © 2022 Yang, Shi, Jin, Yang, Li, Han, Mao and Zheng. 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 Medicine
Yang, Yide
Shi, Qingmiao
Jin, Qian
Yang, Zhangnv
Li, Wangfang
Han, Jianfeng
Mao, Juanjuan
Zheng, Beiwen
Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay
title Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay
title_full Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay
title_fullStr Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay
title_full_unstemmed Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay
title_short Case Report: Metagenomic Next-Generation Sequencing Clinches the Diagnosis of Acute Q Fever and Verified by Indirect Immunofluorescence Assay
title_sort case report: metagenomic next-generation sequencing clinches the diagnosis of acute q fever and verified by indirect immunofluorescence assay
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204269/
https://www.ncbi.nlm.nih.gov/pubmed/35721056
http://dx.doi.org/10.3389/fmed.2022.846526
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