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Integrating host response and unbiased microbe detection for lower respiratory tract infection diagnosis in critically ill adults.
Langelier, Charles; Kalantar, Katrina L; Moazed, Farzad; Wilson, Michael R; 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.
Afiliação
  • Langelier C; Division of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA 94143.
  • Kalantar KL; Chan Zuckerberg Biohub, San Francisco, CA 94158.
  • Moazed F; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158.
  • Wilson MR; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco, CA 94143.
  • Crawford ED; Weill Institute for Neurosciences, University of California, San Francisco, CA 94143.
  • Deiss T; Department of Neurology, University of California, San Francisco, CA 94143.
  • Belzer A; Chan Zuckerberg Biohub, San Francisco, CA 94158.
  • Bolourchi S; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158.
  • Caldera S; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco, CA 94143.
  • Fung M; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco, CA 94143.
  • Jauregui A; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco, CA 94143.
  • Malcolm K; Division of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA 94143.
  • Lyden A; Chan Zuckerberg Biohub, San Francisco, CA 94158.
  • Khan L; Division of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA 94143.
  • Vessel K; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco, CA 94143.
  • Quan J; Department of Medicine, University of California, San Francisco, CA 94143.
  • Zinter M; Chan Zuckerberg Biohub, San Francisco, CA 94158.
  • Chiu CY; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158.
  • Chow ED; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco, CA 94143.
  • Wilson J; Chan Zuckerberg Biohub, San Francisco, CA 94158.
  • Miller S; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158.
  • Matthay MA; Division of Critical Care Medicine, Department of Pediatrics, School of Medicine, University of California, San Francisco, CA 94143.
  • Pollard KS; Division of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA 94143.
  • Christenson S; Department of Laboratory Medicine, School of Medicine, University of California, San Francisco, CA 94143.
  • Calfee CS; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158.
  • DeRisi JL; Department of Emergency Medicine, Stanford University, Stanford, CA 94305.
Proc Natl Acad Sci U S A ; 115(52): E12353-E12362, 2018 12 26.
Article em En | MEDLINE | ID: mdl-30482864
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Respiratórias / Análise de Sequência de DNA Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Respiratórias / Análise de Sequência de DNA Idioma: En Ano de publicação: 2018 Tipo de documento: Article