Type IV secretion systems: Advances in structure, function, and activation.
Tiago R D CostaLaith HarbPratick KharaLanying ZengBo HuPeter J ChristiePublished in: Molecular microbiology (2021)
Bacterial type IV secretion systems (T4SSs) are a functionally diverse translocation superfamily. They consist mainly of two large subfamilies: (i) conjugation systems that mediate interbacterial DNA transfer and (ii) effector translocators that deliver effector macromolecules into prokaryotic or eukaryotic cells. A few other T4SSs export DNA or proteins to the milieu, or import exogenous DNA. The T4SSs are defined by 6 or 12 conserved "core" subunits that respectively elaborate "minimized" systems in Gram-positive or -negative bacteria. However, many "expanded" T4SSs are built from "core" subunits plus numerous others that are system-specific, which presumptively broadens functional capabilities. Recently, there has been exciting progress in defining T4SS assembly pathways and architectures using a combination of fluorescence and cryoelectron microscopy. This review will highlight advances in our knowledge of structure-function relationships for model Gram-negative bacterial T4SSs, including "minimized" systems resembling the Agrobacterium tumefaciens VirB/VirD4 T4SS and "expanded" systems represented by the Helicobacter pylori Cag, Legionella pneumophila Dot/Icm, and F plasmid-encoded Tra T4SSs. Detailed studies of these model systems are generating new insights, some at atomic resolution, to long-standing questions concerning mechanisms of substrate recruitment, T4SS channel architecture, conjugative pilus assembly, and machine adaptations contributing to T4SS functional versatility.
Keyphrases
- helicobacter pylori
- single molecule
- gram negative
- multidrug resistant
- circulating tumor
- healthcare
- escherichia coli
- dendritic cells
- cell free
- machine learning
- signaling pathway
- mass spectrometry
- oxidative stress
- helicobacter pylori infection
- regulatory t cells
- cell proliferation
- high resolution
- endoplasmic reticulum stress
- transcription factor
- nucleic acid
- energy transfer
- pi k akt