Integrating host response and unbiased microbe detection for lower respiratory tract infection diagnosis in critically ill adults

Author:

Langelier Charles,Kalantar Katrina L.,Moazed Farzad,Wilson Michael R.ORCID,Crawford Emily D.,Deiss Thomas,Belzer Annika,Bolourchi Samaneh,Caldera Saharai,Fung Monica,Jauregui Alejandra,Malcolm Katherine,Lyden Amy,Khan Lillian,Vessel Kathryn,Quan Jenai,Zinter Matt,Chiu Charles Y.,Chow Eric D.,Wilson Jenny,Miller Steve,Matthay Michael A.,Pollard Katherine S.,Christenson Stephanie,Calfee Carolyn S.,DeRisi Joseph L.

Abstract

Lower respiratory tract infections (LRTIs) lead to more deaths each year than any other infectious disease category. Despite this, etiologic LRTI pathogens are infrequently identified due to limitations of existing microbiologic tests. In critically ill patients, noninfectious inflammatory syndromes resembling LRTIs further complicate diagnosis. To address the need for improved LRTI diagnostics, we performed metagenomic next-generation sequencing (mNGS) on tracheal aspirates from 92 adults with acute respiratory failure and simultaneously assessed pathogens, the airway microbiome, and the host transcriptome. To differentiate pathogens from respiratory commensals, we developed a rules-based model (RBM) and logistic regression model (LRM) in a derivation cohort of 20 patients with LRTIs or noninfectious acute respiratory illnesses. When tested in an independent validation cohort of 24 patients, both models achieved accuracies of 95.5%. We next developed pathogen, microbiome diversity, and host gene expression metrics to identify LRTI-positive patients and differentiate them from critically ill controls with noninfectious acute respiratory illnesses. When tested in the validation cohort, the pathogen metric performed with an area under the receiver-operating curve (AUC) of 0.96 (95% CI, 0.86–1.00), the diversity metric with an AUC of 0.80 (95% CI, 0.63–0.98), and the host transcriptional classifier with an AUC of 0.88 (95% CI, 0.75–1.00). Combining these achieved a negative predictive value of 100%. This study suggests that a single streamlined protocol offering an integrated genomic portrait of pathogen, microbiome, and host transcriptome may hold promise as a tool for LRTI diagnosis.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

Chan Zuckerberg Biohub

Gladstone Institutes

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference65 articles.

1. World Health Organization (2017) The top 10 causes of death. Available at www.who.int/en/news-room/fact-sheets/detail/the-top-10-causes-of-death. Accessed October, 1, 2018.

2. US Centers for Disease Control and Prevention (2018) Deaths: Leading Causes for 2016. Available at https://www.cdc.gov/nchs/fastats/leading-causes-of-death.htm. Accessed October 1, 2018.

3. Trends and patterns of differences in infectious disease mortality among US counties, 1980–2014;El Bcheraoui;JAMA,2018

4. Community-Acquired Pneumonia Requiring Hospitalization among U.S. Adults

5. The current epidemiology and clinical decisions surrounding acute respiratory infections

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3