namely, pathways related to bacterial chemotaxis and flagellar assembly, as well as genes encoding efflux-mediated antibiotic resistance mechanisms and virulence-related genes. The results indicated that the microbiome of CF patients with low pulmonary function is enriched in virulence-related genes and in genes encoding efflux-mediated antibiotic resistance mechanisms. Overall, the microbiome of severely affected adults with CF seems to encode different mechanisms for the facilitation of microbial colonization and persistence in the lung, consistent with the characteristics of multidrug-resistant microbial communities that are commonly observed in patients with severe lung disease. © 2017 by the authors. Licensee MDPI, Basel, Switzerland.
|Titolo:||A different microbiome gene repertoire in the airways of cystic fibrosis patients with severe lung disease|
|Data di pubblicazione:||2017|
|Appare nelle tipologie:||1.1 Articolo in rivista|