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Gut microbiota signatures in cystic fibrosis: Loss of host CFTR function drives the microbiota enterophenotype.

Pamela VernocchiFederica Del ChiericoAlessandra RussoFabio MajoMartina RossittoMariacristina ValerioLuca CasadeiAntonietta La StoriaFrancesca De FilippisCristiano RizzoCesare ManettiPaola PaciDanilo ErcoliniFederico MariniErsilia Vita FiscarelliBruno DallapiccolaVincenzina LucidiAlfredo MiccheliLorenza Putignani
Published in: PloS one (2018)
All together, the results obtained suggest that the gut microbiota enterophenotypes of CF, together with endogenous and bacterial CF biomarkers, are direct expression of functional alterations at the intestinal level. Hence, it's possible to infer that CFTR impairment causes the gut ecosystem imbalance.This new understanding of CF host-gut microbiota interactions may be helpful to rationalize novel clinical interventions to improve the affected children's nutritional status and intestinal function.
Keyphrases
  • cystic fibrosis
  • pseudomonas aeruginosa
  • lung function
  • poor prognosis
  • climate change
  • young adults
  • risk assessment
  • genome wide
  • human health
  • chronic obstructive pulmonary disease