Tropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease

Tropheryma whipplei is a bacterium associated with Whipple’s disease, which commonly manifests as weight loss, arthralgia, and diarrhea. The most frequently involved organs comprise the heart and eyes, in addition to the central nervous system. Few studies have explored the relationship between T. w...

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Autores principales: Yifan Guo, Lijuan Li, Zhenzhong Li, Lingxiao Sun, Hui Wang
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:3db59ea3069347f79abbd0a60efaebb52021-12-01T13:44:46ZTropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease1664-302X10.3389/fmicb.2021.760696https://doaj.org/article/3db59ea3069347f79abbd0a60efaebb52021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fmicb.2021.760696/fullhttps://doaj.org/toc/1664-302XTropheryma whipplei is a bacterium associated with Whipple’s disease, which commonly manifests as weight loss, arthralgia, and diarrhea. The most frequently involved organs comprise the heart and eyes, in addition to the central nervous system. Few studies have explored the relationship between T. whipplei and pneumonia. Herein, we report three patients with interstitial lung disease (ILD) of unknown cause, whose bronchoalveolar lavage fluid (BALF) were evaluated via Nanopore sequencing. In our in-house BALF Nanopore platform, human DNA was removed with saponin, to improve the reads ratio of microorganisms/host. T. whipplei was the sole or most abundant pathogen in all the patients, comprising 1,385, 826, and 285 reads. The positive result was confirmed via quantitative polymerase chain reaction (PCR) with two pairs of primers (cycle threshold value: 33.26/36.29; 31.68/32.01; 28.82/28.80) and Sanger sequencing. To our knowledge, this is the first report of T. whipplei detection using Nanopore-based sequencing. The turnaround time was approximately 6–8 h in clinical laboratories, including less than 1 h for analysis. In conclusion, the results of this study confirm that Nanopore sequencing can rapidly detect rare pathogens, to improve clinical diagnosis. In addition, diagnosis of Whipple’s disease should be combined other laboratory findings, such as periodic acid-Schiff (PAS) staining, and considered a possibility in middle-aged men presenting with ILD and a clinical history of unexplained arthralgia and/or fever.Yifan GuoYifan GuoLijuan LiLijuan LiZhenzhong LiZhenzhong LiLingxiao SunHui WangHui WangFrontiers Media S.A.articleTropheryma whippleiNanoporemetagenomic next-generation sequencingpneumoniainfectionMicrobiologyQR1-502ENFrontiers in Microbiology, Vol 12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Tropheryma whipplei
Nanopore
metagenomic next-generation sequencing
pneumonia
infection
Microbiology
QR1-502
spellingShingle Tropheryma whipplei
Nanopore
metagenomic next-generation sequencing
pneumonia
infection
Microbiology
QR1-502
Yifan Guo
Yifan Guo
Lijuan Li
Lijuan Li
Zhenzhong Li
Zhenzhong Li
Lingxiao Sun
Hui Wang
Hui Wang
Tropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease
description Tropheryma whipplei is a bacterium associated with Whipple’s disease, which commonly manifests as weight loss, arthralgia, and diarrhea. The most frequently involved organs comprise the heart and eyes, in addition to the central nervous system. Few studies have explored the relationship between T. whipplei and pneumonia. Herein, we report three patients with interstitial lung disease (ILD) of unknown cause, whose bronchoalveolar lavage fluid (BALF) were evaluated via Nanopore sequencing. In our in-house BALF Nanopore platform, human DNA was removed with saponin, to improve the reads ratio of microorganisms/host. T. whipplei was the sole or most abundant pathogen in all the patients, comprising 1,385, 826, and 285 reads. The positive result was confirmed via quantitative polymerase chain reaction (PCR) with two pairs of primers (cycle threshold value: 33.26/36.29; 31.68/32.01; 28.82/28.80) and Sanger sequencing. To our knowledge, this is the first report of T. whipplei detection using Nanopore-based sequencing. The turnaround time was approximately 6–8 h in clinical laboratories, including less than 1 h for analysis. In conclusion, the results of this study confirm that Nanopore sequencing can rapidly detect rare pathogens, to improve clinical diagnosis. In addition, diagnosis of Whipple’s disease should be combined other laboratory findings, such as periodic acid-Schiff (PAS) staining, and considered a possibility in middle-aged men presenting with ILD and a clinical history of unexplained arthralgia and/or fever.
format article
author Yifan Guo
Yifan Guo
Lijuan Li
Lijuan Li
Zhenzhong Li
Zhenzhong Li
Lingxiao Sun
Hui Wang
Hui Wang
author_facet Yifan Guo
Yifan Guo
Lijuan Li
Lijuan Li
Zhenzhong Li
Zhenzhong Li
Lingxiao Sun
Hui Wang
Hui Wang
author_sort Yifan Guo
title Tropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease
title_short Tropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease
title_full Tropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease
title_fullStr Tropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease
title_full_unstemmed Tropheryma whipplei Detection by Nanopore Sequencing in Patients With Interstitial Lung Disease
title_sort tropheryma whipplei detection by nanopore sequencing in patients with interstitial lung disease
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/3db59ea3069347f79abbd0a60efaebb5
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