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Airway microbiota across age and disease spectrum in cystic fibrosis.
Zemanick, Edith T; Wagner, Brandie D; Robertson, Charles E; Ahrens, Richard C; Chmiel, James F; Clancy, John P; Gibson, Ronald L; Harris, William T; Kurland, Geoffrey; Laguna, Theresa A; McColley, Susanna A; McCoy, Karen; Retsch-Bogart, George; Sobush, Kurtis T; Zeitlin, Pamela L; Stevens, Mark J; Accurso, Frank J; Sagel, Scott D; Harris, J Kirk.
Afiliação
  • Zemanick ET; University of Colorado School of Medicine, Aurora, CO, USA edith.zemanick@childrenscolorado.org.
  • Wagner BD; University of Colorado School of Medicine, Aurora, CO, USA.
  • Robertson CE; Colorado School of Public Health, University of Colorado Denver, Aurora, CO, USA.
  • Ahrens RC; University of Colorado School of Medicine, Aurora, CO, USA.
  • Chmiel JF; University of Iowa, Iowa City, IA, USA.
  • Clancy JP; Case Western Reserve University School of Medicine, Rainbow Babies and Children's Hospital, Cleveland, OH, USA.
  • Gibson RL; Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Harris WT; University of Washington, Seattle Children's Hospital, Seattle, WA, USA.
  • Kurland G; University of Alabama, Birmingham, AL, USA.
  • Laguna TA; Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • McColley SA; University of Minnesota, Minneapolis, MN, USA.
  • McCoy K; Ann and Robert H. Lurie Children's Hospital of Chicago and Northwestern University, Chicago, IL, USA.
  • Retsch-Bogart G; Nationwide Children's Hospital, Columbus, OH, USA.
  • Sobush KT; University of North Carolina, Chapel Hill, NC, USA.
  • Zeitlin PL; St Louis University School of Medicine, St Louis, MO, USA.
  • Stevens MJ; Johns Hopkins University, Baltimore, MD, USA.
  • Accurso FJ; University of Colorado School of Medicine, Aurora, CO, USA.
  • Sagel SD; University of Colorado School of Medicine, Aurora, CO, USA.
  • Harris JK; University of Colorado School of Medicine, Aurora, CO, USA.
Eur Respir J ; 50(5)2017 11.
Article em En | MEDLINE | ID: mdl-29146601
ABSTRACT
Our objectives were to characterise the microbiota in cystic fibrosis (CF) bronchoalveolar lavage fluid (BALF), and determine its relationship to inflammation and disease status.BALF from paediatric and adult CF patients and paediatric disease controls undergoing clinically indicated bronchoscopy was analysed for total bacterial load and for microbiota by 16S rDNA sequencing.We examined 191 BALF samples (146 CF and 45 disease controls) from 13 CF centres. In CF patients aged <2 years, nontraditional taxa (e.gStreptococcus, Prevotella and Veillonella) constituted ∼50% of the microbiota, whereas in CF patients aged ≥6 years, traditional CF taxa (e.gPseudomonas, Staphylococcus and Stenotrophomonas) predominated. Sequencing detected a dominant taxon not traditionally associated with CF (e.gStreptococcus or Prevotella) in 20% of CF BALF and identified bacteria in 24% of culture-negative BALF. Microbial diversity and relative abundance of Streptococcus, Prevotella and Veillonella were inversely associated with airway inflammation. Microbiota communities were distinct in CF compared with disease controls, but did not differ based on pulmonary exacerbation status in CF.The CF microbiota detected in BALF differs with age. In CF patients aged <2 years, Streptococcus predominates, whereas classic CF pathogens predominate in most older children and adults.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores Etários / Fibrose Cística / Microbiota / Inflamação / Pulmão Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores Etários / Fibrose Cística / Microbiota / Inflamação / Pulmão Idioma: En Ano de publicação: 2017 Tipo de documento: Article