A New Front in Microbial Warfare-Delivery of Antifungal Effectors by the Type VI Secretion System.

J Fungi (Basel)

Institute for Cell and Molecular Biosciences, Faculty of Medicine, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.

Published: June 2019

AI Article Synopsis

  • Microbes live in diverse communities and have complex interactions, including competition among themselves, often influenced by the Type VI secretion system (T6SS) found in Gram-negative bacteria.
  • The T6SS acts like a molecular weapon, enabling bacteria to inject antibacterial proteins into rival bacteria, but it has also been discovered to target fungi with newly identified effector proteins, Tfe1 and Tfe2.
  • Tfe1 and Tfe2 work through different mechanisms to kill fungal cells, suggesting that the use of T6SS for antifungal purposes is common and could significantly impact many microbial communities, including those in human health and infections.

Article Abstract

Microbes typically exist in mixed communities and display complex synergistic and antagonistic interactions. The Type VI secretion system (T6SS) is widespread in Gram-negative bacteria and represents a contractile nano-machine that can fire effector proteins directly into neighbouring cells. The primary role assigned to the T6SS is to function as a potent weapon during inter-bacterial competition, delivering antibacterial effectors into rival bacterial cells. However, it has recently emerged that the T6SS can also be used as a powerful weapon against fungal competitors, and the first fungal-specific T6SS effector proteins, Tfe1 and Tfe2, have been identified. These effectors act via distinct mechanisms against a variety of fungal species to cause cell death. Tfe1 intoxication triggers plasma membrane depolarisation, whilst Tfe2 disrupts nutrient uptake and induces autophagy. Based on the frequent coexistence of bacteria and fungi in microbial communities, we propose that T6SS-dependent antifungal activity is likely to be widespread and elicited by a suite of antifungal effectors. Supporting this hypothesis, homologues of Tfe1 and Tfe2 are found in other bacterial species, and a number of T6SS-elaborating species have been demonstrated to interact with fungi. Thus, we envisage that antifungal T6SS will shape many polymicrobial communities, including the human microbiota and disease-causing infections.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617251PMC
http://dx.doi.org/10.3390/jof5020050DOI Listing

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