Microbial signatures in the lower airways of mechanically ventilated COVID-19 patients associated with poor clinical outcome.
Imran SulaimanMatthew ChungLuis F AngelJun-Chieh J TsayBenjamin G WuStephen T YeungKelsey KrolikowskiYonghua LiRalf DuerrRosemary SchlugerSara A ThannickalAkiko KoideSamaan RafeqClea BarnettRadu PostelnicuChang WangStephanie BanakisLizzette Pérez-PérezGuomiao ShenGeorge JourPeter MeynJoseph CarpenitoXiuxiu LiuKun JiDestiny CollazoAnthony LabarbieraNancy AmorosoShari B BrosnahanVikramjit MukherjeeDavid KaufmanElisa EstenssoroAnthony LubinskyDeepak PradhanDaniel H StermanMichael WeidenAdriana HeguyLaura EvansTimothy M UyekiJose C ClementeEmmie de WitAnn Marie SchmidtBo ShopsinLudovic DesvignesChan WangHuilin LiBin ZhangChristian V ForstShohei KoideKenneth A StaplefordKamal M KhannaElodie GhedinLeopoldo N SegalPublished in: Nature microbiology (2021)
Respiratory failure is associated with increased mortality in COVID-19 patients. There are no validated lower airway biomarkers to predict clinical outcome. We investigated whether bacterial respiratory infections were associated with poor clinical outcome of COVID-19 in a prospective, observational cohort of 589 critically ill adults, all of whom required mechanical ventilation. For a subset of 142 patients who underwent bronchoscopy, we quantified SARS-CoV-2 viral load, analysed the lower respiratory tract microbiome using metagenomics and metatranscriptomics and profiled the host immune response. Acquisition of a hospital-acquired respiratory pathogen was not associated with fatal outcome. Poor clinical outcome was associated with lower airway enrichment with an oral commensal (Mycoplasma salivarium). Increased SARS-CoV-2 abundance, low anti-SARS-CoV-2 antibody response and a distinct host transcriptome profile of the lower airways were most predictive of mortality. Our data provide evidence that secondary respiratory infections do not drive mortality in COVID-19 and clinical management strategies should prioritize reducing viral replication and maximizing host responses to SARS-CoV-2.
Keyphrases
- sars cov
- respiratory tract
- mechanical ventilation
- respiratory failure
- respiratory syndrome coronavirus
- acute respiratory distress syndrome
- immune response
- intensive care unit
- cardiovascular events
- newly diagnosed
- extracorporeal membrane oxygenation
- cystic fibrosis
- healthcare
- risk factors
- ejection fraction
- coronavirus disease
- gene expression
- type diabetes
- microbial community
- single cell
- patient reported outcomes
- toll like receptor
- cross sectional
- dna methylation
- rna seq
- single molecule
- acute care