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PMID: 11309113 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Type IV secretion: intercellular transfer of macromolecules by systems ancestrally related to conjugation machines.

Molecular microbiology ·Vol. 40 ·No. 2 ·2001-04-00 ·Pages 294-305

Christie PJ

Abstract

Bacterial conjugation systems are highly promiscuous macromolecular transfer systems that impact human health significantly. In clinical settings, conjugation is exceptionally problematic, leading to the rapid dissemination of antibiotic resistance genes and other virulence traits among bacterial populations. Recent work has shown that several pathogens of plants and mammals - Agrobacterium tumefaciens, Bordetella pertussis, Helicobacter pylori and Legionella pneumophila - have evolved secretion pathways ancestrally related to conjugation systems for the purpose of delivering effector molecules to eukaryotic target cells. Each of these systems exports distinct DNA or protein substrates to effect a myriad of changes in host cell physiology during infection. Collectively, secretion pathways ancestrally related to bacterial conjugation systems are now referred to as the type IV secretion family. The list of putative type IV family members is increasing rapidly, suggesting that macromolecular transfer by these systems is a widespread phenomenon in nature.

MeSH Terms
Bacterial Proteins/genetics,metabolism Biological Transport Conjugation, Genetic DNA, Bacterial/genetics,metabolism Eukaryotic Cells/microbiology Evolution, Molecular Gram-Negative Bacteria/metabolism,pathogenicity Gram-Negative Bacterial Infections/microbiology Humans Protein Transport Virulence
Chemicals
Bacterial Proteins DNA, Bacterial
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Christie P J
Department of Microbiology and Molecular Genetics, The University of Texas-Houston Medical School, 6431 Fannin, Houston, TX 77030, USA. Peter.J.Christie@uth.tmc.edu
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Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
2001-04-00
Pages
294-305
Language
English
Region
England
NLM ID
8712028
PMCID
PMC3922410
Subset
IM
Grants
NIGMS NIH HHS · R01 GM048746 · United States
NIGMS NIH HHS · GM48746 · United States
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