
Assembly and function of type III secretory systems
- Author
- Guy R Cornelis and Frédérique Van Gijsegem
- Organization
- Abstract
- Type III secretion systems allow Yersinia spp., Salmonella spp.. Shigella spp., Bordetella spp., and Pseudomonas aeruginosa and enteropathogenic Escherichia coli adhering at the surface of a eukaryotic cell to inject bacterial proteins across the two bacterial membranes and the eukaryotic cell membrane to destroy or subvert the target cell. These systems consist of a secretion apparatus, made of similar to 25 proteins, and an array of proteins released by this apparatus. Some of these released proteins are "effectors," which are delivered into the cytosol of the target cell, whereas the others are "translocators," which help the effecters to cross the membrane of the eukaryotic cell. Most of the effecters act on the cytoskeleton or on intracellular-signaling cascades. A protein injected by the enteropathogenic E. coli serves as a membrane receptor for the docking of the bacterium itself at the surface of the cell. Type III secretion systems also occur in plant pathogens where they are involved both in causing disease in susceptible hosts and in eliciting the so-called hypersensitive response in resistant or nonhost plants. They consist of 15-20 Hrp proteins building a secretion apparatus and two groups of effecters: harpins and avirulence proteins. Harpins are presumably secreted in the extracellular compartment, whereas avirulence proteins are thought to be targeted into plant cells. Although a coherent picture is clearly emerging, basic questions remain to be answered. In particular, little is known about how the type III apparatus fits together to deliver proteins in animal cells. It is even more mysterious for plant cells where a thick wall has to be crossed. In spite of these haunting questions, type TIT secretion appears as a fascinating trans-kingdom communication device.
- Keywords
- plant pathogens, microbial pathogenesis, secretion, translocation, effector, hypersensitive response, ENTEROPATHOGENIC ESCHERICHIA-COLI, PLANT-DISEASE RESISTANCE, YERSINIA YOP VIRULON, PROTEIN-TYROSINE-PHOSPHATASE, TARGET-CELL CONTACT, FLAGELLAR EXPORT APPARATUS, CHAPERONE-LIKE PROTEIN, MESSENGER-RNA SIGNAL, NF-KAPPA-B, PSEUDOMONAS-SYRINGAE
Downloads
-
(...).pdf
- full text
- |
- UGent only
- |
- |
- 537.47 KB
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-124883
- MLA
- Cornelis, Guy R., and Frédérique Van Gijsegem. “Assembly and Function of Type III Secretory Systems.” ANNUAL REVIEW OF MICROBIOLOGY, vol. 54, 2000, pp. 735–74, doi:10.1146/annurev.micro.54.1.735.
- APA
- Cornelis, G. R., & Van Gijsegem, F. (2000). Assembly and function of type III secretory systems. ANNUAL REVIEW OF MICROBIOLOGY, 54, 735–774. https://doi.org/10.1146/annurev.micro.54.1.735
- Chicago author-date
- Cornelis, Guy R, and Frédérique Van Gijsegem. 2000. “Assembly and Function of Type III Secretory Systems.” ANNUAL REVIEW OF MICROBIOLOGY 54: 735–74. https://doi.org/10.1146/annurev.micro.54.1.735.
- Chicago author-date (all authors)
- Cornelis, Guy R, and Frédérique Van Gijsegem. 2000. “Assembly and Function of Type III Secretory Systems.” ANNUAL REVIEW OF MICROBIOLOGY 54: 735–774. doi:10.1146/annurev.micro.54.1.735.
- Vancouver
- 1.Cornelis GR, Van Gijsegem F. Assembly and function of type III secretory systems. ANNUAL REVIEW OF MICROBIOLOGY. 2000;54:735–74.
- IEEE
- [1]G. R. Cornelis and F. Van Gijsegem, “Assembly and function of type III secretory systems,” ANNUAL REVIEW OF MICROBIOLOGY, vol. 54, pp. 735–774, 2000.
@article{124883, abstract = {{Type III secretion systems allow Yersinia spp., Salmonella spp.. Shigella spp., Bordetella spp., and Pseudomonas aeruginosa and enteropathogenic Escherichia coli adhering at the surface of a eukaryotic cell to inject bacterial proteins across the two bacterial membranes and the eukaryotic cell membrane to destroy or subvert the target cell. These systems consist of a secretion apparatus, made of similar to 25 proteins, and an array of proteins released by this apparatus. Some of these released proteins are "effectors," which are delivered into the cytosol of the target cell, whereas the others are "translocators," which help the effecters to cross the membrane of the eukaryotic cell. Most of the effecters act on the cytoskeleton or on intracellular-signaling cascades. A protein injected by the enteropathogenic E. coli serves as a membrane receptor for the docking of the bacterium itself at the surface of the cell. Type III secretion systems also occur in plant pathogens where they are involved both in causing disease in susceptible hosts and in eliciting the so-called hypersensitive response in resistant or nonhost plants. They consist of 15-20 Hrp proteins building a secretion apparatus and two groups of effecters: harpins and avirulence proteins. Harpins are presumably secreted in the extracellular compartment, whereas avirulence proteins are thought to be targeted into plant cells. Although a coherent picture is clearly emerging, basic questions remain to be answered. In particular, little is known about how the type III apparatus fits together to deliver proteins in animal cells. It is even more mysterious for plant cells where a thick wall has to be crossed. In spite of these haunting questions, type TIT secretion appears as a fascinating trans-kingdom communication device.}}, author = {{Cornelis, Guy R and Van Gijsegem, Frédérique}}, issn = {{0066-4227}}, journal = {{ANNUAL REVIEW OF MICROBIOLOGY}}, keywords = {{plant pathogens,microbial pathogenesis,secretion,translocation,effector,hypersensitive response,ENTEROPATHOGENIC ESCHERICHIA-COLI,PLANT-DISEASE RESISTANCE,YERSINIA YOP VIRULON,PROTEIN-TYROSINE-PHOSPHATASE,TARGET-CELL CONTACT,FLAGELLAR EXPORT APPARATUS,CHAPERONE-LIKE PROTEIN,MESSENGER-RNA SIGNAL,NF-KAPPA-B,PSEUDOMONAS-SYRINGAE}}, language = {{eng}}, pages = {{735--774}}, title = {{Assembly and function of type III secretory systems}}, url = {{http://dx.doi.org/10.1146/annurev.micro.54.1.735}}, volume = {{54}}, year = {{2000}}, }
- Altmetric
- View in Altmetric
- Web of Science
- Times cited: