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An orphan cbb-type cytochrome oxidase subunit supports Pseudomonas aeruginosa biofilm growth and virulence

eLife, ISSN: 2050-084X, Vol: 6
2017
  • 69
    Citations
  • 0
    Usage
  • 113
    Captures
  • 7
    Mentions
  • 135
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    69
  • Captures
    113
  • Mentions
    7
    • News Mentions
      6
      • News
        6
    • Blog Mentions
      1
      • Blog
        1
  • Social Media
    135
    • Shares, Likes & Comments
      135
      • Facebook
        135

Most Recent Blog

Researchers Identify How Bacterium Survives in Oxygen-poor Environments

NewsBiologists have revealed a mechanism by which bacterial cells in crowded, oxygen-deprived environments access oxygen for energy production, ensuring survival of the cell. The finding could explain how some bacteria are able to thrive in oxygen-poor environments.Contributed Author: Columbia UniversityTopics: Biology

Most Recent News

Researchers Identify How Bacterium Survives in Oxygen-poor Environments

biologists have revealed a mechanism by which bacterial cells in crowded, oxygen-deprived environments access oxygen for energy production, ensuring survival of the cell. The finding

Article Description

Hypoxia is a common challenge faced by bacteria during associations with hosts due in part to the formation of densely packed communities (biofilms). cbb-type cytochrome c oxidases, which catalyze the terminal step in respiration and have a high affinity for oxygen, have been linked to bacterial pathogenesis. The pseudomonads are unusual in that they often contain multiple full and partial (i.e. ‘orphan’) operons for cbb3-type oxidases and oxidase subunits. Here, we describe a unique role for the orphan catalytic subunit CcoN4 in colony biofilm development and respiration in the opportunistic pathogen Pseudomonas aeruginosa PA14. We also show that CcoN4 contributes to the reduction of phenazines, antibiotics that support redox balancing for cells in biofilms, and to virulence in a Caenorhabditis elegans model of infection. These results highlight the relevance of the colony biofilm model to pathogenicity and underscore the potential of cbb-type oxidases as therapeutic targets.

Bibliographic Details

http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85036529038&origin=inward; http://dx.doi.org/10.7554/elife.30205; http://www.ncbi.nlm.nih.gov/pubmed/29160206; https://elifesciences.org/articles/30205#decision-letter; http://dx.doi.org/10.7554/elife.30205.021; https://elifesciences.org/articles/30205#fig1; http://dx.doi.org/10.7554/elife.30205.003; https://elifesciences.org/articles/30205#table4; http://dx.doi.org/10.7554/elife.30205.019; https://elifesciences.org/articles/30205#table3; http://dx.doi.org/10.7554/elife.30205.018; https://elifesciences.org/articles/30205#fig5; http://dx.doi.org/10.7554/elife.30205.013; https://elifesciences.org/articles/30205; https://elifesciences.org/articles/30205#author-response; http://dx.doi.org/10.7554/elife.30205.022; https://elifesciences.org/articles/30205#abstract; http://dx.doi.org/10.7554/elife.30205.001; https://elifesciences.org/articles/30205#fig2; http://dx.doi.org/10.7554/elife.30205.004; https://elifesciences.org/articles/30205#fig4; http://dx.doi.org/10.7554/elife.30205.011; https://elifesciences.org/articles/30205#table1; http://dx.doi.org/10.7554/elife.30205.016; https://elifesciences.org/articles/30205#table2; http://dx.doi.org/10.7554/elife.30205.017; https://elifesciences.org/articles/30205#fig3; http://dx.doi.org/10.7554/elife.30205.009; https://elifesciences.org/articles/30205#fig6; http://dx.doi.org/10.7554/elife.30205.015; https://elifesciences.org/articles/30205#digest; http://dx.doi.org/10.7554/elife.30205.002; https://cdn.elifesciences.org/articles/30205/elife-30205-v1.pdf; https://cdn.elifesciences.org/articles/30205/elife-30205-v1.xml; https://dx.doi.org/10.7554/elife.30205

Jo, Jeanyoung; Cortez, Krista L; Cornell, William Cole; Price-Whelan, Alexa; Dietrich, Lars Ep

eLife Sciences Organisation, Ltd.

Neuroscience; Immunology and Microbiology; Biochemistry, Genetics and Molecular Biology

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