4.5 Article

Conditional toxicity and synergy drive diversity among antibacterial effectors

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NATURE MICROBIOLOGY
卷 3, 期 4, 页码 440-446

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41564-018-0113-y

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资金

  1. NIH [R01-AI080609]
  2. Defense Threat Reduction Agency [HDTRA1-13-1-0014]
  3. UW Cellular and Molecular Biology Training Grant [T32GM007270]
  4. Investigator in the Pathogenesis of Infectious Disease Award from the Burroughs Wellcome Fund
  5. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI080609] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK089507] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007270] Funding Source: NIH RePORTER

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Bacteria in polymicrobial habitats contend with a persistent barrage of competitors, often under rapidly changing environmental conditions(1). The direct antagonism of competitor cells is thus an important bacterial survival strategy(2). Towards this end, many bacterial species employ an arsenal of antimicrobial effectors with multiple activities; however, the benefits conferred by the simultaneous deployment of diverse toxins are unknown. Here we show that the multiple effectors delivered to competitor bacteria by the type VI secretion system (T6SS) of Pseudomonas aeruginosa display conditional efficacy and act synergistically. One of these effectors, Tse4, is most active in high-salinity environments and synergizes with effectors that degrade the cell wall or inactivate intracellular electron carriers. We find Tse4 synergizes with these disparate mechanisms by forming pores that disrupt the Delta psi component of the proton motive force. Our results provide evidence that the concomitant delivery of a cocktail of effectors serves as a bet-hedging strategy to promote bacterial competitiveness in the face of unpredictable and variable environmental conditions.

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