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Bacterial type IV secretion systems in human disease
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 156003
Author(s) Llosa, Matxalen; Roy, Craig; Dehio, Christoph
Author(s) at UniBasel Dehio, Christoph
Year 2009
Title Bacterial type IV secretion systems in human disease
Journal Molecular microbiology
Volume 73
Number 2
Pages / Article-Number 141-51
Keywords Bacterial Proteins/*metabolism; Biological Transport; DNA; Bacterial/metabolism; Gram-Negative Bacteria/*metabolism/pathogenicity; Gram-Negative Bacterial Infections/immunology; Humans; Models; Molecular; Protein Structure; Quaternary; Structure-Activity Relationship; Virulence
Abstract Type IV secretion (T4S) systems are versatile machines involved in many processes relevant to bacterial virulence, such as horizontal DNA transfer and effector translocation into human cells. A recent workshop organized by the International University of Andalousia in Baeza, Spain, covered most aspects of bacterial T4S relevant to human disease, ranging from the structural and mechanistic analysis of the T4S systems to the physiological roles of the translocated effector proteins in subverting cellular functions in infected humans. This review reports the highlights from this workshop, which include the first visualization of a T4S system core complex spanning both membranes of Gram-negative bacteria, the identification of the first host receptors for T4S systems, the identification and characterization of novel T4S effector proteins, the analysis of the molecular function of effector proteins in subverting human cellular functions and an analysis of the role of T4S systems in the evolution of pathogenic bacteria. Our increasing knowledge of the biology of T4S systems improves our ability to exploit them as biotechnological tools or to use them as novel targets for a new generation of antimicrobials.
Publisher Blackwell
ISSN/ISBN 0950-382X
edoc-URL http://edoc.unibas.ch/dok/A5258995
Full Text on edoc No
Digital Object Identifier DOI 10.1111/j.1365-2958.2009.06751.x
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/19508287
ISI-Number WOS:000267883900002
Document type (ISI) Journal Article, Review
 
   

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19/04/2024