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Conversion of Pseudomonas aeruginosa to mucoidy in cystic fibrosis: environmental stress and regulation of bacterial virulence by alternative sigma factors.

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TLDR
The conversion of Pseudomonas aeruginosa into the mucoid, exopolysaccharide alginate-overproducing form is considered to be a major pathogenic determinant expressed by this organism during chronic respiratory infections in cystic fibrosis.
Abstract
The conversion of Pseudomonas aeruginosa into the mucoid, exopolysaccharide alginate-overproducing form is considered to be a major pathogenic determinant expressed by this organism during chronic respiratory infections in cystic fibrosis (CF) (5, 28, 32). Despite the fact that CF has a relatively recent history as a medically recognized syndrome (since 1938), the problem of conversion to mucoidy in P. aeruginosa has become an instant classic of microbial pathogenesis (for recent reviews, see references 28, 54, and 61). Most P. aeruginosa strains have the genetic capacity to synthesize alginate, but mucoid mutants that overproduce this exopolysaccharide are rarely noticed among environmental isolates. In contrast, P. aeruginosa strains from CF are frequently mucoid (28, 32). Several mutations causing conversion to mucoidy (see Fig. 1) and genes that participate in these processes have been recently defined (see Table 1); the mutations are superimposed on a system consisting of a putative alternative sigma factor, which most likely plays a more general role in bacterial stress response, and its accessory negative regulators (23, 30, 51-53, 61).

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Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia.

TL;DR: This review summarizes the latest advances in understanding host-pathogen interactions in CF with an emphasis on the role and control of conversion to mucoidy in P. aeruginosa and B. cepacia.
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High Frequency of Hypermutable Pseudomonas aeruginosa in Cystic Fibrosis Lung Infection

TL;DR: Determination of spontaneous mutation rates in 128 P. aeruginosa isolates from 30 CF patients revealed that 36% of the patients were colonized by a hypermutable (mutator) strain that persisted for years in most patients, revealing a link between high mutations rates in vivo and the evolution of antibiotic resistance.
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The Metabolic Basis Of Inherited Disease.

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Role of Antibiotic Penetration Limitation in Klebsiella pneumoniae Biofilm Resistance to Ampicillin and Ciprofloxacin

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Combination of fluorescent in situ hybridization and microautoradiography-a new tool for structure-function analyses in microbial ecology

TL;DR: A new microscopic method for simultaneously determining in situ the identities, activities, and specific substrate uptake profiles of individual bacterial cells within complex microbial communities was developed by combining fluorescent in situ hybridization performed with rRNA-targeted oligonucleotide probes and microautoradiography.
References
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Journal ArticleDOI

Mutants of Salmonella typhimurium that cannot survive within the macrophage are avirulent

TL;DR: In this article, the authors identify the genes important for intracellular survival of Salmonella typhimurium and identify the mutants that have a diminished capacity for survival within macrophages.
Journal ArticleDOI

The Metabolic Basis Of Inherited Disease.

TL;DR: This volume, more than most, explains the contributions of the laboratory to clinical medicine, and shedding light on fundamental metabolic sequences and biologic mechanisms.
Journal ArticleDOI

The sigma 70 family: sequence conservation and evolutionary relationships.

TL;DR: The cr subunit confers promoter-specific transcription initiation on RNA polymerase, and recently, sequence information has become available for many more members of the u70 family.
Journal ArticleDOI

Cystic fibrosis: molecular biology and therapeutic implications.

TL;DR: Several new approaches to drug therapy for cystic fibrosis are now emerging, and the possibility of successful gene therapy by transfer of the normal gene to airway epithelial cells is being vigorously pursued.
Journal ArticleDOI

Production of mucoid microcolonies by Pseudomonas aeruginosa within infected lungs in cystic fibrosis.

TL;DR: It is concluded that the cells of P. aeruginosa that infect cystic fibrosis patients form microcolony that are enveloped in a fibrous anionic matrix and that these microcolonies can be duplicated in in vitro cultures and in animal model systems.
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