2017
DOI: 10.1016/j.tim.2016.12.003
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Rules of Engagement: The Type VI Secretion System in Vibrio cholerae

Abstract: Microbial species often exist in complex communities where they must avoid predation and compete for favorable niches. The type VI secretion system (T6SS) is a contact-dependent bacterial weapon that allows for direct killing of competitors through the translocation of proteinaceous toxins. Vibrio cholerae is a Gram-negative pathogen that can use its T6SS during antagonistic interactions with neighboring prokaryotic and eukaryotic competitors. The T6SS not only promotes V. cholerae's survival during its aquati… Show more

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Cited by 101 publications
(98 citation statements)
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References 96 publications
(166 reference statements)
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“…The cavity around VgrG/PAAR spike is~1,110 × 10 3 Å 3 large and may accommodate up to~450-kDa large proteins, or three copies of up to~150-kDa protein. This is consistent with sizes of known effectors: 129-kDa VgrG-1, 113-kDa VgrG-3, or 155-kDa pair VasX-VasW (Dong et al, 2013;Joshi et al, 2017). Since 77-kDa VgrG-2 with no extension domain is required for T6SS assembly (Appendix Fig S3; Pukatzki et al, 2007), there is also enough space for effectors interacting with VgrGs, such as 72-kDa TseL (Dong et al, 2013), in agreement with the model that many effectors bind to the VgrG/PAAR spike ( Fig EV6; Shneider et al, 2013).…”
Section: Discussionsupporting
confidence: 86%
“…The cavity around VgrG/PAAR spike is~1,110 × 10 3 Å 3 large and may accommodate up to~450-kDa large proteins, or three copies of up to~150-kDa protein. This is consistent with sizes of known effectors: 129-kDa VgrG-1, 113-kDa VgrG-3, or 155-kDa pair VasX-VasW (Dong et al, 2013;Joshi et al, 2017). Since 77-kDa VgrG-2 with no extension domain is required for T6SS assembly (Appendix Fig S3; Pukatzki et al, 2007), there is also enough space for effectors interacting with VgrGs, such as 72-kDa TseL (Dong et al, 2013), in agreement with the model that many effectors bind to the VgrG/PAAR spike ( Fig EV6; Shneider et al, 2013).…”
Section: Discussionsupporting
confidence: 86%
“…T6SS effectors are toxic to eukaryotic and prokaryotic cells (Joshi et al, 2017). For example, interactions between the V. cholerae T6SS and eukaryotic cells have been implicated in intestinal inflammation, and recent studies have linked interactions between the T6SS and the endogenous microbiome to the virulence of V. cholerae (Fast et al, 2018a;Ma and Mekalanos, 2010;Zhao et al, 2018).…”
Section: Ipc Suppression Of Growth In Response To the T6ss Requires Imentioning
confidence: 99%
“…To explain the differences in T6SS activity and to provide insight into the T6SS's biological functions, it is, therefore, important to understand the underlying regulatory pathways in pandemic V. cholerae strains. Accordingly, several minor and major T6SS regulators have been identified in V. cholerae (Joshi et al ., ) by changing their abundance through deletion or forced expression of the respective genes, which resulted in changes in T6SS gene expression or T6SS activity. Two of these major regulators, TfoX and TfoY (Borgeaud et al ., ; Metzger et al ., ), contain TfoX‐like N‐ and C‐terminal domains and proteins containing such domains are usually annotated as regulators of natural competence for transformation due to the presence of these domains in the competence regulator Sxy of Haemophilus influenzae (Redfield, ) and TfoX in V. cholerae (Meibom et al ., ).…”
Section: Introductionmentioning
confidence: 99%