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Mucoid Pseudomonas aeruginosa in cystic fibrosis: characterization of muc mutations in clinical isolates and analysis of clearance in a mouse model of respiratory infection.

A distinguishing feature of Pseudomonas aeruginosa isolates from cystic fibrosis (CF) patients is their mucoid, exopolysaccharide alginate-overproducing phenotype. One mechanism of conversion to mucoidy is based on mutations in the algU mucABCD cluster, encoding the stress sigma factor AlgU and its...

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Detalles Bibliográficos
Publicado en:Infect Immun
Principais autores: Boucher, J C, Yu, H, Mudd, M H, Deretic, V
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Microbiology (ASM) 1997
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Acceso en liña:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC175548/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9284161/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/iai.65.9.3838-3846.1997
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