The bacterial type VI secretion machine: Yet another player for protein transport across membranes

Alain Filloux*, Abderrahman Hachani, Sophie Bleves

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

299 Citations (Scopus)

Abstract

Several secretion systems have evolved that are widespread among Gram-negative bacteria. Recently, a new secretion system was recognized, which is named the type VI secretion system (T6SS). The T6SS components are encoded within clusters of genes initially identified as IAHP for lcmF-associated homologous proteins, since they were all found to contain a gene encoding an lcmF-like component. lcmF was previously reported as a component of the type IV secretion system (T4SS). However, with the exception of DotU, other T4SS components are not encoded within T6SS loci. Thus, the T6SS is probably a novel kind of complex multi-component secretion machine, which is often involved in interaction with eukaryotic hosts, be it a pathogenic or a symbiotic relationship. The expression of T6SS genes has been reported to be mostly induced in vivo. Interestingly, expression and assembly of T6SSs are tightly controlled at both the transcriptional and the post-translational level. This may allow a timely control of T6SS assembly and function. Two types of proteins, generically named Hcp and VgrG, are secreted via these systems, but it is not entirely clear whether they are truly secreted effector proteins or are actually components of the T6SS. The precise role and mode of action of the T6SS is still unknown. This review describes current knowledge about the T6SS and summarizes its hallmarks and its differences from other secretion systems.

Original languageEnglish
Pages (from-to)1570-1583
Number of pages14
JournalMicrobiology
Volume154
Issue number6
DOIs
Publication statusPublished - 2008
Externally publishedYes

ASJC Scopus Subject Areas

  • Microbiology

Fingerprint

Dive into the research topics of 'The bacterial type VI secretion machine: Yet another player for protein transport across membranes'. Together they form a unique fingerprint.

Cite this