Type VI Secretion System Dynamics Reveals a Novel Secretion Mechanism in Pseudomonas aeruginosa

The type VI secretion system (T6SS) inhibits the growth of neighboring bacterial cells through a contact-mediated mechanism. Here, we describe a detailed characterization of the protein localization dynamics in the T6SS. It has been proposed that the type VI secretion process is driven by a conforma...

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Veröffentlicht in:Journal of bacteriology 2018-06, Vol.200 (11)
Hauptverfasser: Corbitt, Jacqueline, Yeo, Jun Seok, Davis, C Ian, LeRoux, Michele, Wiggins, Paul A
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Sprache:eng
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Zusammenfassung:The type VI secretion system (T6SS) inhibits the growth of neighboring bacterial cells through a contact-mediated mechanism. Here, we describe a detailed characterization of the protein localization dynamics in the T6SS. It has been proposed that the type VI secretion process is driven by a conformational-change-induced contraction of the T6SS sheath. However, although the contraction of an optically resolvable TssBC sheath and the subsequent localization of ClpV are observed in , coordinated assembly and disassembly of TssB and ClpV are observed without TssB contraction in These dynamics are inconsistent with the proposed contraction sheath model. Motivated by the phenomenon of dynamic instability, we propose a new model in which ATP hydrolysis, rather than conformational change, generates the force for secretion. The type VI secretion system (T6SS) is widely conserved among Gram-negative bacteria and is a central determinant of bacterial fitness in polymicrobial communities. The secretion system targets bacteria and secretes effectors that inhibit the growth of neighboring cells, using a contact-mediated-delivery system. Despite significant homology to the previously characterized T6SS, our analysis reveals that effector secretion is driven by a distinct force generation mechanism in The presence of two distinct force generation mechanisms in T6SS represents an example of the evolutionary diversification of force generation mechanisms.
ISSN:0021-9193
1098-5530
DOI:10.1128/JB.00744-17