Cargando…

Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study

BACKGROUND: Metagenomic next-generation sequencing (mNGS) of bronchoalveolar lavage fluid (BALF) has the potential to improve the pathogen identification in severe community-acquired pneumonia (SCAP). METHODS: In this 1.5-year, multicenter, prospective study, we investigated the usefulness of mNGS o...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Xiaodong, Li, Yuanyuan, Zhang, Ming, Li, Miaomiao, Zhang, Rong, Lu, Xin, Gao, Wei, Li, Qin, Xia, Yang, Pan, Pinhua, Li, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652912/
https://www.ncbi.nlm.nih.gov/pubmed/33170499
http://dx.doi.org/10.1007/s40121-020-00353-y
_version_ 1783607794150146048
author Wu, Xiaodong
Li, Yuanyuan
Zhang, Ming
Li, Miaomiao
Zhang, Rong
Lu, Xin
Gao, Wei
Li, Qin
Xia, Yang
Pan, Pinhua
Li, Qiang
author_facet Wu, Xiaodong
Li, Yuanyuan
Zhang, Ming
Li, Miaomiao
Zhang, Rong
Lu, Xin
Gao, Wei
Li, Qin
Xia, Yang
Pan, Pinhua
Li, Qiang
author_sort Wu, Xiaodong
collection PubMed
description BACKGROUND: Metagenomic next-generation sequencing (mNGS) of bronchoalveolar lavage fluid (BALF) has the potential to improve the pathogen identification in severe community-acquired pneumonia (SCAP). METHODS: In this 1.5-year, multicenter, prospective study, we investigated the usefulness of mNGS of BALF for identifying pathogens of SCAP in hospitalized adults, comparing it with other laboratory methods. RESULTS: Of 329 SCAP adults, a microbial etiology was established in 304 cases (92.4%). The overall microbial yield was 90.3% for mNGS versus 39.5% for other methods (P < 0.05). The most frequently detected pathogens in immunocompetent patients were Streptococcus pneumoniae (14.8%), rhinovirus (9.8%), Haemophilus influenzae (9.1%), Staphylococcus aureus (8.7%), and Chlamydia psittaci (8.0%), while in immunocompromised patients they were Pneumocystis jirovecii (44.6%), Klebsiella pneumoniae (18.5%), Streptococcus pneumoniae (15.4%), Haemophilus influenzae (13.8%), and Pseudomonas aeruginosa (13.8%). Notably, novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was identified from two patients solely by mNGS in January 2020; uncommon pathogens including Orientia tsutsugamushi and Nocardia otitidiscaviarum were identified from one patient, respectively. Furthermore, mixed infections were detected in 56.8% of the patients. CONCLUSIONS: A high microbial detection rate was achieved in SCAP adults using mNGS testing of BALF. The most frequently detected pathogens of SCAP differed between immunocompetent and immunocompromised patients. mNGS testing may be an powerful tool for early identification of potential pathogens for SCAP to initiate a precise antimicrobial therapy.
format Online
Article
Text
id pubmed-7652912
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Springer Healthcare
record_format MEDLINE/PubMed
spelling pubmed-76529122020-11-10 Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study Wu, Xiaodong Li, Yuanyuan Zhang, Ming Li, Miaomiao Zhang, Rong Lu, Xin Gao, Wei Li, Qin Xia, Yang Pan, Pinhua Li, Qiang Infect Dis Ther Original Research BACKGROUND: Metagenomic next-generation sequencing (mNGS) of bronchoalveolar lavage fluid (BALF) has the potential to improve the pathogen identification in severe community-acquired pneumonia (SCAP). METHODS: In this 1.5-year, multicenter, prospective study, we investigated the usefulness of mNGS of BALF for identifying pathogens of SCAP in hospitalized adults, comparing it with other laboratory methods. RESULTS: Of 329 SCAP adults, a microbial etiology was established in 304 cases (92.4%). The overall microbial yield was 90.3% for mNGS versus 39.5% for other methods (P < 0.05). The most frequently detected pathogens in immunocompetent patients were Streptococcus pneumoniae (14.8%), rhinovirus (9.8%), Haemophilus influenzae (9.1%), Staphylococcus aureus (8.7%), and Chlamydia psittaci (8.0%), while in immunocompromised patients they were Pneumocystis jirovecii (44.6%), Klebsiella pneumoniae (18.5%), Streptococcus pneumoniae (15.4%), Haemophilus influenzae (13.8%), and Pseudomonas aeruginosa (13.8%). Notably, novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was identified from two patients solely by mNGS in January 2020; uncommon pathogens including Orientia tsutsugamushi and Nocardia otitidiscaviarum were identified from one patient, respectively. Furthermore, mixed infections were detected in 56.8% of the patients. CONCLUSIONS: A high microbial detection rate was achieved in SCAP adults using mNGS testing of BALF. The most frequently detected pathogens of SCAP differed between immunocompetent and immunocompromised patients. mNGS testing may be an powerful tool for early identification of potential pathogens for SCAP to initiate a precise antimicrobial therapy. Springer Healthcare 2020-11-10 2020-12 /pmc/articles/PMC7652912/ /pubmed/33170499 http://dx.doi.org/10.1007/s40121-020-00353-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Original Research
Wu, Xiaodong
Li, Yuanyuan
Zhang, Ming
Li, Miaomiao
Zhang, Rong
Lu, Xin
Gao, Wei
Li, Qin
Xia, Yang
Pan, Pinhua
Li, Qiang
Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study
title Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study
title_full Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study
title_fullStr Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study
title_full_unstemmed Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study
title_short Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A Prospective Multicenter Study
title_sort etiology of severe community-acquired pneumonia in adults based on metagenomic next-generation sequencing: a prospective multicenter study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652912/
https://www.ncbi.nlm.nih.gov/pubmed/33170499
http://dx.doi.org/10.1007/s40121-020-00353-y
work_keys_str_mv AT wuxiaodong etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT liyuanyuan etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT zhangming etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT limiaomiao etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT zhangrong etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT luxin etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT gaowei etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT liqin etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT xiayang etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT panpinhua etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy
AT liqiang etiologyofseverecommunityacquiredpneumoniainadultsbasedonmetagenomicnextgenerationsequencingaprospectivemulticenterstudy