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10.1186/s12931-020-01340-0

http://scihub22266oqcxt.onion/10.1186/s12931-020-01340-0
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32228581!7104712!32228581
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suck abstract from ncbi

pmid32228581      Respir+Res 2020 ; 21 (1): 77
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  • Microbial burden and viral exacerbations in a longitudinal multicenter COPD cohort #MMPMID32228581
  • Bouquet J; Tabor DE; Silver JS; Nair V; Tovchigrechko A; Griffin MP; Esser MT; Sellman BR; Jin H
  • Respir Res 2020[Mar]; 21 (1): 77 PMID32228581show ga
  • BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a heterogeneous disease characterized by frequent exacerbation phenotypes independent of disease stage. Increasing evidence shows that the microbiota plays a role in disease progression and severity, but long-term and international multicenter assessment of the variations in viral and bacterial communities as drivers of exacerbations are lacking. METHODS: Two-hundred severe COPD patients from Europe and North America were followed longitudinally for 3 years. We performed nucleic acid detection for 20 respiratory viruses and 16S ribosomal RNA gene sequencing to evaluate the bacterial microbiota in 1179 sputum samples collected at stable, acute exacerbation and follow-up visits. RESULTS: Similar viral and bacterial taxa were found in patients from the USA compared to Bulgaria and Czech Republic but their microbiome diversity was significantly different (P < 0.001) and did not impact exacerbation rates. Virus infection was strongly associated with exacerbation events (P < 5E-20). Human rhinovirus (13.1%), coronavirus (5.1%) and influenza virus (3.6%) constitute the top viral pathogens in triggering exacerbation. Moraxella and Haemophilus were 5-fold and 1.6-fold more likely to be the dominating microbiota during an exacerbation event. Presence of Proteobacteria such as Pseudomonas or Staphylococcus amongst others, were associated with exacerbation events (OR > 0.17; P < 0.02) but more strongly associated with exacerbation frequency (OR > 0.39; P < 4E-10), as confirmed by longitudinal variations and biotyping of the bacterial microbiota, and suggesting a role of the microbiota in sensitizing the lung. CONCLUSIONS: This study highlights bacterial taxa in lung sensitization and viral triggers in COPD exacerbations. It provides a global overview of the diverse targets for drug development and explores new microbiome analysis methods to guide future patient management applications.
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Bacteria/genetics/*isolation & purification[MESH]
  • |Bacterial Load[MESH]
  • |Disease Progression[MESH]
  • |Europe/epidemiology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Incidence[MESH]
  • |Longitudinal Studies[MESH]
  • |Lung/*microbiology/*virology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pulmonary Disease, Chronic Obstructive/diagnosis/epidemiology/*microbiology/*virology[MESH]
  • |Retrospective Studies[MESH]
  • |Risk Factors[MESH]
  • |Sputum/microbiology/virology[MESH]
  • |Time Factors[MESH]
  • |United States/epidemiology[MESH]
  • |Viral Load[MESH]


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