Literature DB >> 24863401

Pseudomonas aeruginosa phenotypes associated with eradication failure in children with cystic fibrosis.

Nicole Mayer-Hamblett1, Bonnie W Ramsey2, Hemantha D Kulasekara3, Daniel J Wolter4, Laura S Houston4, Christopher E Pope4, Bridget R Kulasekara3, Catherine R Armbruster3, Jane L Burns2, George Retsch-Bogart5, Margaret Rosenfeld2, Ronald L Gibson2, Samuel I Miller6, Umer Khan7, Lucas R Hoffman8.   

Abstract

BACKGROUND: Pseudomonas aeruginosa is a key respiratory pathogen in people with cystic fibrosis (CF). Due to its association with lung disease progression, initial detection of P. aeruginosa in CF respiratory cultures usually results in antibiotic treatment with the goal of eradication. Pseudomonas aeruginosa exhibits many different phenotypes in vitro that could serve as useful prognostic markers, but the relative relationships between these phenotypes and failure to eradicate P. aeruginosa have not been well characterized.
METHODS: We measured 22 easily assayed in vitro phenotypes among the baseline P. aeruginosa isolates collected from 194 participants in the 18-month EPIC clinical trial, which assessed outcomes after antibiotic eradication therapy for newly identified P. aeruginosa. We then evaluated the associations between these baseline isolate phenotypes and subsequent outcomes during the trial, including failure to eradicate after antipseudomonal therapy, emergence of mucoidy, and occurrence of an exacerbation.
RESULTS: Baseline P. aeruginosa isolates frequently exhibited phenotypes thought to represent chronic adaptation, including mucoidy. Wrinkly colony surface and irregular colony edges were both associated with increased risk of eradication failure (hazard ratios [95% confidence intervals], 1.99 [1.03-3.83] and 2.14 [1.32-3.47], respectively). Phenotypes reflecting defective quorum sensing were significantly associated with subsequent mucoidy, but no phenotype was significantly associated with subsequent exacerbations during the trial.
CONCLUSIONS: Pseudomonas aeruginosa phenotypes commonly considered to reflect chronic adaptation were observed frequently among isolates at early detection. We found that 2 easily assayed colony phenotypes were associated with failure to eradicate after antipseudomonal therapy, both of which have been previously associated with altered biofilm formation and defective quorum sensing.
© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Pseudomonas aeruginosa; antibiotic treatment; cystic fibrosis; eradication; phenotypic characterization

Mesh:

Substances:

Year:  2014        PMID: 24863401      PMCID: PMC4148602          DOI: 10.1093/cid/ciu385

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  39 in total

1.  Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis.

Authors:  M Rosenfeld; J Emerson; F Accurso; D Armstrong; R Castile; K Grimwood; P Hiatt; K McCoy; S McNamara; B Ramsey; J Wagener
Journal:  Pediatr Pulmonol       Date:  1999-11

2.  Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial.

Authors:  Felix Ratjen; Anne Munck; Pearl Kho; Gerhild Angyalosi
Journal:  Thorax       Date:  2009-12-08       Impact factor: 9.139

Review 3.  Differential adaptation of microbial pathogens to airways of patients with cystic fibrosis and chronic obstructive pulmonary disease.

Authors:  Gerd Döring; Iyer G Parameswaran; Timothy F Murphy
Journal:  FEMS Microbiol Rev       Date:  2011-01       Impact factor: 16.408

Review 4.  Clonal epidemiology of Pseudomonas aeruginosa in cystic fibrosis.

Authors:  Nina Cramer; Lutz Wiehlmann; Burkhard Tümmler
Journal:  Int J Med Microbiol       Date:  2010-10-14       Impact factor: 3.473

Review 5.  Adaptation of Pseudomonas aeruginosa during persistence in the cystic fibrosis lung.

Authors:  Michael Hogardt; Jürgen Heesemann
Journal:  Int J Med Microbiol       Date:  2010-10-12       Impact factor: 3.473

6.  Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients.

Authors:  David A D'Argenio; Manhong Wu; Lucas R Hoffman; Hemantha D Kulasekara; Eric Déziel; Eric E Smith; Hai Nguyen; Robert K Ernst; Theodore J Larson Freeman; David H Spencer; Mitchell Brittnacher; Hillary S Hayden; Sara Selgrade; Mikkel Klausen; David R Goodlett; Jane L Burns; Bonnie W Ramsey; Samuel I Miller
Journal:  Mol Microbiol       Date:  2007-04       Impact factor: 3.501

Review 7.  Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis.

Authors:  Simon C Langton Hewer; Alan R Smyth
Journal:  Cochrane Database Syst Rev       Date:  2009-10-07

8.  Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression.

Authors:  Lucas R Hoffman; Hemantha D Kulasekara; Julia Emerson; Laura S Houston; Jane L Burns; Bonnie W Ramsey; Samuel I Miller
Journal:  J Cyst Fibros       Date:  2008-10-29       Impact factor: 5.482

9.  Instantaneous within-patient diversity of Pseudomonas aeruginosa quorum-sensing populations from cystic fibrosis lung infections.

Authors:  Cara N Wilder; Gopal Allada; Martin Schuster
Journal:  Infect Immun       Date:  2009-10-05       Impact factor: 3.441

10.  Nutrient availability as a mechanism for selection of antibiotic tolerant Pseudomonas aeruginosa within the CF airway.

Authors:  Lucas R Hoffman; Anthony R Richardson; Laura S Houston; Hemantha D Kulasekara; Willm Martens-Habbena; Mikkel Klausen; Jane L Burns; David A Stahl; Daniel J Hassett; Ferric C Fang; Samuel I Miller
Journal:  PLoS Pathog       Date:  2010-01-08       Impact factor: 6.823

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  29 in total

1.  Pel Polysaccharide Biosynthesis Requires an Inner Membrane Complex Comprised of PelD, PelE, PelF, and PelG.

Authors:  Gregory B Whitfield; Lindsey S Marmont; Alex Ostaszewski; Jacquelyn D Rich; John C Whitney; Matthew R Parsek; Joe J Harrison; P Lynne Howell
Journal:  J Bacteriol       Date:  2020-03-26       Impact factor: 3.490

2.  Use of a Multiplex Transcript Method for Analysis of Pseudomonas aeruginosa Gene Expression Profiles in the Cystic Fibrosis Lung.

Authors:  Alex H Gifford; Sven D Willger; Emily L Dolben; Lisa A Moulton; Dana B Dorman; Heather Bean; Jane E Hill; Thomas H Hampton; Alix Ashare; Deborah A Hogan
Journal:  Infect Immun       Date:  2016-09-19       Impact factor: 3.441

3.  Social cheating in a Pseudomonas aeruginosa quorum-sensing variant.

Authors:  Ruiyi Chen; Eric Déziel; Marie-Christine Groleau; Amy L Schaefer; E Peter Greenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2019-03-07       Impact factor: 11.205

4.  Small Colony Variants of Pseudomonas aeruginosa Display Heterogeneity in Inhibiting Aspergillus fumigatus Biofilm.

Authors:  Rajesh Anand; Richard B Moss; Gabriele Sass; Niaz Banaei; Karl V Clemons; Marife Martinez; David A Stevens
Journal:  Mycopathologia       Date:  2017-08-07       Impact factor: 2.574

5.  The Cyclic AMP-Vfr Signaling Pathway in Pseudomonas aeruginosa Is Inhibited by Cyclic Di-GMP.

Authors:  Henrik Almblad; Joe J Harrison; Morten Rybtke; Julie Groizeleau; Michael Givskov; Matthew R Parsek; Tim Tolker-Nielsen
Journal:  J Bacteriol       Date:  2015-04-20       Impact factor: 3.490

6.  Importance of the Exopolysaccharide Matrix in Antimicrobial Tolerance of Pseudomonas aeruginosa Aggregates.

Authors:  Lise Goltermann; Tim Tolker-Nielsen
Journal:  Antimicrob Agents Chemother       Date:  2017-03-24       Impact factor: 5.191

7.  Divergent, coexisting Pseudomonas aeruginosa lineages in chronic cystic fibrosis lung infections.

Authors:  David Williams; Benjamin Evans; Sam Haldenby; Martin J Walshaw; Michael A Brockhurst; Craig Winstanley; Steve Paterson
Journal:  Am J Respir Crit Care Med       Date:  2015-04-01       Impact factor: 21.405

8.  Repeated isolation of an antibiotic-dependent and temperature-sensitive mutant of Pseudomonas aeruginosa from a cystic fibrosis patient.

Authors:  Daniel J Wolter; Alison Scott; Catherine R Armbruster; Dale Whittington; John S Edgar; Xuan Qin; Anne Marie Buccat; Sharon McNamara; Marcella Blackledge; Adam Waalkes; Stephen J Salipante; Robert K Ernst; Lucas R Hoffman
Journal:  J Antimicrob Chemother       Date:  2021-02-11       Impact factor: 5.790

9.  Pseudomonas aeruginosa in vitro phenotypes distinguish cystic fibrosis infection stages and outcomes.

Authors:  Nicole Mayer-Hamblett; Margaret Rosenfeld; Ronald L Gibson; Bonnie W Ramsey; Hemantha D Kulasekara; George Z Retsch-Bogart; Wayne Morgan; Daniel J Wolter; Christopher E Pope; Laura S Houston; Bridget R Kulasekara; Umer Khan; Jane L Burns; Samuel I Miller; Lucas R Hoffman
Journal:  Am J Respir Crit Care Med       Date:  2014-08-01       Impact factor: 21.405

Review 10.  [Chronic Pseudomonas aeruginosa airway colonization in cystic fibrosis patients : Prevention concepts].

Authors:  A-M Dittrich
Journal:  Internist (Berl)       Date:  2017-11       Impact factor: 0.743

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