* authors contributed equally
E-Cigarette Use, Cigarette Smoking, and Sex are Associated with Nasal Microbiome Dysbiosis.
Authors:
Reference: Nicotine Tob Res. 2024 Jul 17; .
Mucus polymer concentration and in vivo adaptation converge to define the antibiotic response of Pseudomonas aeruginosa during chronic lung infection.
Authors:
Reference: mBio. 2024 Apr 23; e0345123.
Saliva sampling method influences oral microbiome composition and taxa distribution associated with oral diseases.
Authors:
Reference: PLoS One. 2024 Mar 28; 19(3):e0301016.
Longitudinal changes in the cystic fibrosis airway microbiota with time and treatment.
Authors:
Reference: J Cyst Fibros. 2024 May 17; 23(2):252-261.
Viral afterlife: SARS-CoV-2 as a reservoir of immunomimetic peptides that reassemble into proinflammatory supramolecular complexes.
Authors:
Reference: Proc Natl Acad Sci. 2024 Feb 06; 121(6):e2300644120.
Hyperglycemia potentiates increased Staphylococcus aureus virulence and resistance to growth inhibition by Pseudomonas aeruginosa.
Authors:
Reference: Microbiol Spectrum. 2023 Dec 12; 11(6):e0229923.
A Novel Co-Culture Model Reveals Enhanced CFTR Rescue in Primary Cystic Fibrosis Airway Epithelial Cultures with Persistent Pseudomonas aeruginosa Infection.
Authors:
Reference: Cells. 2023 Nov 13; 12(22):2618.
Revisiting Host-Pathogen Interactions in Cystic Fibrosis Lungs in the Era of CFTR Modulators.
Authors:
Reference: Int J Mol Sci. 2023 Mar 5; 24(5):5010.
The changing landscape of the cystic fibrosis lung environment: From the perspective of Pseudomonas aeruginosa.
Authors:
Reference: Curr Opin Pharmacol. 2022 Aug 1; 65:102262.
Cystic Fibrosis Airway Mucus Hyperconcentration Produces a Vicious Cycle of Mucin, Pathogen, and Inflammatory Interactions that Promote Disease Persistence.
Authors:
Reference: Am J Respir Cel Mol Biol. 2022 Apr 29; 67(2):253-265.
Protease-Anti-Protease Compartmentalization in SARS-CoV-2 ARDS: Therapeutic Implications.
Authors:
Reference: eBioMedicine. 2022 Feb 22; 77:103894.
Global Regulatory Pathways Converge To Control Expression of Pseudomonas aeruginosa Type IV Pili.
Authors:
Reference: mBio. 2022 Feb 22; 13(1):e0369621.
Role of miR-2392 in driving SARS-CoV-2 infection.
Authors:
Reference: Cell Rep. 2021 Sep 30; 37(3):109839.
Cautionary notes on the use of arabinose- and rhamnose-inducible expression vectors in Pseudomonas aeruginosa.
Authors:
Reference: J Bacteriol. 2021 Jul 22; 203(16):JB0022421.
SARS-CoV-2 infection of the oral cavity and saliva.
Authors:
Reference: Nat Med. 2021 May; 27(5):892-903.
Host Adaptation Predisposes Pseudomonas aeruginosa to Type VI Secretion System-Mediated Predation by the Burkholderia cepacia Complex.
Authors:
Reference: Cell Host Microbe. 2020 Oct 7; 28(4):534-547.e3.
One-hit wonder: Late after burn injury, granulocytes can clear one bacterial infection but cannot control a subsequent infection.
Authors:
Reference: Burns. 2019 May; 45(3):627-640.
Mucus accumulation in the lungs precedes structural changes and infection in children with cystic fibrosis.
Authors:
Reference: Sci Transl Med. 2019 Apr 3; 11(486).
RsmV, a Small Noncoding Regulatory RNA in Pseudomonas aeruginosa That Sequesters RsmA and RsmF from Target mRNAs.
Authors:
Reference: J Bacteriol. 2018 Aug 15; 200(16).
Anaerobic bacteria cultured from cystic fibrosis airways correlate to milder disease: a multisite study.
Authors:
Reference: Eur Respir J. 2018 Jul; 52(1).
Functional Analyses of the RsmY and RsmZ Small Noncoding Regulatory RNAs in Pseudomonas aeruginosa.
Authors:
Reference: J Bacteriol. 2018 Jun 1; 200(11).
Evaluation of e-liquid toxicity using an open-source high-throughput screening assay.
Authors:
Reference: PLoS Biol. 2018 Mar; 16(3):e2003904.
Initial acquisition and succession of the cystic fibrosis lung microbiome is associated with disease progression in infants and preschool children.
Authors:
Reference: PLoS Pathog. 2018 Jan; 14(1):e1006798.
Pseudomonas aeruginosa exoproducts determine antibiotic efficacy against Staphylococcus aureus.
Authors:
Reference: PLoS Biol. 2017 Nov; 15(11):e2003981.
Primary and Secondary Sequence Structure Requirements for Recognition and Discrimination of Target RNAs by Pseudomonas aeruginosa RsmA and RsmF.
Authors:
Reference: J Bacteriol. 2016 Sep 15; 198(18):2458-69.
Phosphoryl Group Flow within the Pseudomonas aeruginosa Pil-Chp Chemosensory System: DIFFERENTIAL FUNCTION OF THE EIGHT PHOSPHOTRANSFERASE AND THREE RECEIVER DOMAINS.
Authors:
Reference: J Biol Chem. 2016 Aug 19; 291(34):17677-91.
Vfr Directly Activates exsA Transcription To Regulate Expression of the Pseudomonas aeruginosa Type III Secretion System.
Authors:
Reference: J Bacteriol. 2016 May; 198(9):1442-50.
Production of extended-spectrum β-lactamases and the potential indirect pathogenic role of Prevotella isolates from the cystic fibrosis respiratory microbiota.
Authors:
Reference: Int J Antimicrob Agents. 2016 Feb; 47(2):140-5.
The Role of Short-Chain Fatty Acids, Produced by Anaerobic Bacteria, in the Cystic Fibrosis Airway.
Authors:
Reference: Am J Respir Crit Care Med. 2015 Dec 1;192(11):1314-24.
The RNA Helicase DeaD Stimulates ExsA Translation To Promote Expression of the Pseudomonas aeruginosa Type III Secretion System.
Authors:
Reference: J Bacteriol.2015 Aug;197(16):2664-74.
A hierarchical cascade of second messengers regulates Pseudomonas aeruginosa surface behaviors.
Authors:
Reference: mBio. 2015 Jan 27;6(1).
Mechanisms of reduced susceptibility and genotypic prediction of antibiotic resistance in Prevotella isolated from cystic fibrosis (CF) and non-CF patients.
Authors:
Reference: J Antimicrob Chemother. 2014 Oct;69(10):2690-8.
Flagellin treatment prevents increased susceptibility to systemic bacterial infection after injury by inhibiting anti-inflammatory IL-10+ IL-12- neutrophil polarization.
Authors:
Reference: PLoS One. 2014;9(1):e85623.
The AlgZR two-component system recalibrates the RsmAYZ posttranscriptional regulatory system to inhibit expression of the Pseudomonas aeruginosa type III secretion system.
Authors:
Reference: J Bacteriol. 2014 Jan;196(2):357-66.
Antibiotic resistance in Prevotella species isolated from patients with cystic fibrosis.
Authors:
Reference: J Antimicrob Chemother. 2013 Oct;68(10):2369-74.
An unusual CsrA family member operates in series with RsmA to amplify posttranscriptional responses in Pseudomonas aeruginosa.
Authors:
Reference: Proc Natl Acad Sci USA. 2013 Sep 10;110(37):15055-60.
Lung microbiota and bacterial abundance in patients with bronchiectasis when clinically stable and during exacerbation.
Authors:
Reference: Am J Respir Crit Care Med. 2013 May 15;187(10):1118-26.
Mucus clearance, MyD88-dependent and MyD88-independent immunity modulate lung susceptibility to spontaneous bacterial infection and inflammation.
Authors:
Reference: Mucosal Immunol. 2012 Jul;5(4):397-408.
Significance of the microbiome in obstructive lung disease.
Authors:
Reference: Thorax. 2012 May;67(5):456-63.
Global regulatory pathways and cross-talk control Pseudomonas aeruginosa environmental lifestyle and virulence phenotype.
Authors:
Reference: Curr Issues Mol Biol. 2012;14(2):47-70.
Crystal structure and regulation mechanisms of the CyaB adenylyl cyclase from the human pathogen Pseudomonas aeruginosa.
Authors:
Reference: J Mol Biol. 2012 Feb 17;416(2):271-86.
Pseudomonas aeruginosa PilY1 binds integrin in an RGD- and calcium-dependent manner.
Authors:
Reference: PLoS One. 2011;6(12):e29629.
Use of culture and molecular analysis to determine the effect of antibiotic treatment on microbial community diversity and abundance during exacerbation in patients with cystic fibrosis.
Authors:
Reference: Thorax. 2011 Jul;66(7):579-84.
Analysis of the bacterial communities present in lungs of patients with cystic fibrosis from American and British centers.
Authors:
Reference: J Clin Microbiol. 2011 Jan;49(1):281-91.
The development of ciprofloxacin resistance in Pseudomonas aeruginosa involves multiple response stages and multiple proteins.
Authors:
Reference: Antimicrob Agents Chemother. 2010 Nov;54(11):4626-35.
Activation of the Pseudomonas aeruginosa AlgU regulon through mucA mutation inhibits cyclic AMP/Vfr signaling.
Authors:
Reference: J Bacteriol. 2010 Nov;192(21):5709-17.
Infection of human mucosal tissue by Pseudomonas aeruginosa requires sequential and mutually dependent virulence factors and a novel pilus-associated adhesin.
Authors:
Reference: Cell Microbiol. 2010 Aug;12(8):1158-73.
The Pseudomonas aeruginosa Vfr regulator controls global virulence factor expression through cyclic AMP-dependent and -independent mechanisms.
Authors:
Reference: J Bacteriol. 2010 Jul;192(14):3553-64.
In vitro and in vivo characterization of the Pseudomonas aeruginosa cyclic AMP (cAMP) phosphodiesterase CpdA, required for cAMP homeostasis and virulence factor regulation.
Authors:
Reference: J Bacteriol. 2010 Jun;192(11):2779-90.
The Pseudomonas aeruginosa Chp chemosensory system regulates intracellular cAMP levels by modulating adenylate cyclase activity.
Authors:
Reference: Mol Microbiol. 2010 May;76(4):889-904.
Crystal structure analysis reveals Pseudomonas PilY1 as an essential calcium-dependent regulator of bacterial surface motility.
Authors:
Reference: Proc Natl Acad Sci USA. 2010 Jan 19;107(3):1065-70.
Airway epithelial inflammation-induced endoplasmic reticulum Ca2+ store expansion is mediated by X-box binding protein-1.
Authors:
Reference: J Biol Chem. 2009 May 29;284(22):14904-13.
Pseudomonas aeruginosa AlgR controls cyanide production in an AlgZ-dependent manner.
Authors:
Reference: J Bacteriol. 2009 May;191(9):2993-3002.
Detection of anaerobic bacteria in high numbers in sputum from patients with cystic fibrosis.
Authors:
Reference: Am J Respir Crit Care Med. 2008 May 1;177(9):995-1001.
Genetic and functional analyses of PptA, a phospho-form transferase targeting type IV pili in Neisseria gonorrhoeae.
Authors:
Reference: J Bacteriol. 2008 Jan;190(1):387-400.
Pseudomonas aeruginosa Type IV pilus expression in Neisseria gonorrhoeae: effects of pilin subunit composition on function and organelle dynamics.
Authors:
Reference: J Bacteriol. 2007 Sep;189(18):6676-85.
Substitutions in the N-terminal alpha helical spine of Neisseria gonorrhoeae pilin affect Type IV pilus assembly, dynamics and associated functions.
Authors:
Reference: Mol Microbiol. 2007 Jan;63(1):69-85.
Transcriptional regulation of the Pseudomonas aeruginosa type III secretion system.
Authors:
Reference: Mol Microbiol. 2006 Nov;62(3):631-40.
Bacterial neuraminidase facilitates mucosal infection by participating in biofilm production.
Authors:
Reference: J Clin Invest. 2006 Aug;116(8):2297-2305.
Acquisition and evolution of the exoU locus in Pseudomonas aeruginosa.
Authors:
Reference: J Bacteriol. 2006 Jun;188(11):4037-50.
The alternative sigma factor AlgT represses Pseudomonas aeruginosa flagellum biosynthesis by inhibiting expression of fleQ.
Authors:
Reference: J Bacteriol. 2005 Dec;187(23):7955-62.
Genome-wide analysis of host responses to the Pseudomonas aeruginosa type III secretion system yields synergistic effects.
Authors:
Reference: Cell Microbiol. 2005 Nov;7(11):1635-46.
A conserved set of pilin-like molecules controls type IV pilus dynamics and organelle-associated functions in Neisseria gonorrhoeae.
Authors:
Reference: Mol Microbiol. 2005 May;56(4):903-17.
A novel anti-anti-activator mechanism regulates expression of the Pseudomonas aeruginosa type III secretion system.
Authors:
Reference: Mol Microbiol. 2004 Jul;53(1):297-308.
Type IV pilus retraction in pathogenic Neisseria is regulated by the PilC proteins.
Authors:
Reference: EMBO J. 2004 May 5;23(9):2009-17.
Pseudomonas aeruginosa regulates flagellin expression as part of a global response to airway fluid from cystic fibrosis patients.
Authors:
Reference: Proc Natl Acad Sci USA. 2004 Apr 27;101(17):6664-8.
Sequence polymorphism in the glycosylation island and flagellins of Pseudomonas aeruginosa.
Authors:
Reference: J Bacteriol. 2004 Apr;186(7):2115-22.
The multi-talented bacterial adenylate cyclases.
Authors:
Reference: Int J Med Microbiol. 2004 Apr;293(7-8):479-82.
Effect of metabolic imbalance on expression of type III secretion genes in Pseudomonas aeruginosa.
Authors:
Reference: Infect Immun. 2004 Mar;72(3):1383-90.
An adenylate cyclase-controlled signaling network regulates Pseudomonas aeruginosa virulence in a mouse model of acute pneumonia.
Authors:
Reference: Infect Immun. 2004 Mar;72(3):1677-84.
A four-tiered transcriptional regulatory circuit controls flagellar biogenesis in Pseudomonas aeruginosa.
Authors:
Reference: Mol Microbiol. 2003 Nov;50(3):809-24.
Conservation of genome content and virulence determinants among clinical and environmental isolates of Pseudomonas aeruginosa.
Authors:
Reference: Proc Natl Acad Sci USA. 2003 Jul 8;100(14):8484-9.
Coordinate regulation of bacterial virulence genes by a novel adenylate cyclase-dependent signaling pathway.
Authors:
Reference: Dev Cell. 2003 Feb;4(2):253-63.
Type IV pili are not specifically required for contact dependent translocation of exoenzymes by Pseudomonas aeruginosa.
Authors:
Reference: Microb Pathog. 2002 Dec;33(6):265-77.
Competence for natural transformation in Neisseria gonorrhoeae: components of DNA binding and uptake linked to type IV pilus expression.
Authors:
Reference: Mol Microbiol. 2002 Nov;46(3):749-60.
Modification of type IV pilus-associated epithelial cell adherence and multicellular behavior by the PilU protein of Neisseria gonorrhoeae.
Authors:
Reference: Infect Immun. 2002 Jul;70(7):3891-903.
Neisseria gonorrhoeae PilV, a type IV pilus-associated protein essential to human epithelial cell adherence.
Authors:
Reference: Proc Natl Acad Sci USA. 2001 Dec 18;98(26):15276-81.
Structural alterations in a type IV pilus subunit protein result in concurrent defects in multicellular behaviour and adherence to host tissue.
Authors:
Reference: Mol Microbiol. 2001 Oct;42(2):293-307.
Components and dynamics of fiber formation define a ubiquitous biogenesis pathway for bacterial pili.
Authors:
Reference: EMBO J. 2000 Dec 1;19(23):6408-18.
Charged tmRNA but not tmRNA-mediated proteolysis is essential for Neisseria gonorrhoeae viability.
Authors:
Reference: EMBO J. 2000 Mar 1;19(5):1098-107.
The comP locus of Neisseria gonorrhoeae encodes a type IV prepilin that is dispensable for pilus biogenesis but essential for natural transformation.
Authors:
Reference: Mol Microbiol. 1999 Mar;31(5):1345-57.
Suppression of an absolute defect in type IV pilus biogenesis by loss-of-function mutations in pilT, a twitching motility gene in Neisseria gonorrhoeae.
Authors:
Reference: Proc Natl Acad Sci USA. 1998 Dec 8;95(25):14973-8.
PilT mutations lead to simultaneous defects in competence for natural transformation and twitching motility in piliated Neisseria gonorrhoeae.
Authors:
Reference: Mol Microbiol. 1998 Jul;29(1):321-30.