Assembly of the bacterial type III secretion machinery
Abstract Many bacteria that live in contact with eukaryotic hosts, whether as symbionts or as pathogens, have evolved mechanisms that manipulate host cell behaviour to their benefit. One such mechanism, the type III secretion system, is employed by Gram-negative bacterial species to inject effector...
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Many bacteria that live in contact with eukaryotic hosts, whether as symbionts or as pathogens, have evolved mechanisms that manipulate host cell behaviour to their benefit. One such mechanism, the type III secretion system, is employed by Gram-negative bacterial species to inject effector proteins into host cells. This function is reflected by the overall shape of the machinery, which resembles a molecular syringe. Despite the simplicity of the concept, the type III secretion system is one of the most complex known bacterial nanomachines, incorporating one to more than hundred copies of up to twenty different proteins into a multi-MDa transmembrane complex. The structural core of the system is the so-called needle complex that spans the bacterial cell envelope as a tripartite ring system and culminates in a needle protruding from the bacterial cell surface. Substrate targeting and translocation are accomplished by an export machinery consisting of various inner membrane embedded and cytoplasmic components. The formation of such a multimembrane-spanning machinery is an intricate task that requires precise orchestration. This review gives an overview of recent findings on the assembly of type III secretion machines, discusses quality control and recycling of the system and proposes an integrated assembly model.
This review discusses the assembly of the type III secretion injectisome, a cell envelope spanning macromolecular machine used by Gram-negative bacteria to translocate bacterial effector proteins into host cells. |
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Many bacteria that live in contact with eukaryotic hosts, whether as symbionts or as pathogens, have evolved mechanisms that manipulate host cell behaviour to their benefit. One such mechanism, the type III secretion system, is employed by Gram-negative bacterial species to inject effector proteins into host cells. This function is reflected by the overall shape of the machinery, which resembles a molecular syringe. Despite the simplicity of the concept, the type III secretion system is one of the most complex known bacterial nanomachines, incorporating one to more than hundred copies of up to twenty different proteins into a multi-MDa transmembrane complex. The structural core of the system is the so-called needle complex that spans the bacterial cell envelope as a tripartite ring system and culminates in a needle protruding from the bacterial cell surface. Substrate targeting and translocation are accomplished by an export machinery consisting of various inner membrane embedded and cytoplasmic components. The formation of such a multimembrane-spanning machinery is an intricate task that requires precise orchestration. This review gives an overview of recent findings on the assembly of type III secretion machines, discusses quality control and recycling of the system and proposes an integrated assembly model.
This review discusses the assembly of the type III secretion injectisome, a cell envelope spanning macromolecular machine used by Gram-negative bacteria to translocate bacterial effector proteins into host cells.</description><identifier>ISSN: 0168-6445</identifier><identifier>ISSN: 1574-6976</identifier><identifier>EISSN: 1574-6976</identifier><identifier>DOI: 10.1111/1574-6976.12061</identifier><identifier>PMID: 24484471</identifier><identifier>CODEN: FMREE4</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Bacteria ; Bacterial Physiological Phenomena ; Bacterial Proteins - metabolism ; Bacterial Proteins - secretion ; Bacterial Secretion Systems - physiology ; Bacteriology ; Cytosol - metabolism ; injectisome ; Machinery ; macromolecular machines ; membrane proteins ; Pathogens ; protein complexes ; protein secretion ; Quality control ; Translocation ; virulence factors</subject><ispartof>FEMS microbiology reviews, 2014-07, Vol.38 (4), p.802-822</ispartof><rights>2014 Federation of European Microbiological Societies. 2014</rights><rights>2014 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd. All rights reserved</rights><rights>2014 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd. All rights reserved.</rights><rights>Copyright © 2014 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd. All rights reserved</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6161-e0ccdc3f36201843ad3bde3b62b13bd483f3bef592860f93df8bdf1901e349c73</citedby><cites>FETCH-LOGICAL-c6161-e0ccdc3f36201843ad3bde3b62b13bd483f3bef592860f93df8bdf1901e349c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1574-6976.12061$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1574-6976.12061$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45552,45553</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24484471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Diepold, Andreas</creatorcontrib><creatorcontrib>Wagner, Samuel</creatorcontrib><title>Assembly of the bacterial type III secretion machinery</title><title>FEMS microbiology reviews</title><addtitle>FEMS Microbiol Rev</addtitle><description>Abstract
Many bacteria that live in contact with eukaryotic hosts, whether as symbionts or as pathogens, have evolved mechanisms that manipulate host cell behaviour to their benefit. One such mechanism, the type III secretion system, is employed by Gram-negative bacterial species to inject effector proteins into host cells. This function is reflected by the overall shape of the machinery, which resembles a molecular syringe. Despite the simplicity of the concept, the type III secretion system is one of the most complex known bacterial nanomachines, incorporating one to more than hundred copies of up to twenty different proteins into a multi-MDa transmembrane complex. The structural core of the system is the so-called needle complex that spans the bacterial cell envelope as a tripartite ring system and culminates in a needle protruding from the bacterial cell surface. Substrate targeting and translocation are accomplished by an export machinery consisting of various inner membrane embedded and cytoplasmic components. The formation of such a multimembrane-spanning machinery is an intricate task that requires precise orchestration. This review gives an overview of recent findings on the assembly of type III secretion machines, discusses quality control and recycling of the system and proposes an integrated assembly model.
This review discusses the assembly of the type III secretion injectisome, a cell envelope spanning macromolecular machine used by Gram-negative bacteria to translocate bacterial effector proteins into host cells.</description><subject>Bacteria</subject><subject>Bacterial Physiological Phenomena</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacterial Proteins - secretion</subject><subject>Bacterial Secretion Systems - physiology</subject><subject>Bacteriology</subject><subject>Cytosol - metabolism</subject><subject>injectisome</subject><subject>Machinery</subject><subject>macromolecular machines</subject><subject>membrane proteins</subject><subject>Pathogens</subject><subject>protein complexes</subject><subject>protein secretion</subject><subject>Quality control</subject><subject>Translocation</subject><subject>virulence factors</subject><issn>0168-6445</issn><issn>1574-6976</issn><issn>1574-6976</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM9LwzAYhoMobk7P3qTgRYS6pPnR5DiG08FEED2HNv3KOtp1Ji3S_97MbkNE0FwSkud9-fIgdEnwHfFrTHjMQqFicUciLMgRGh5ujtEQEyFDwRgfoDPnVhhjrjg_RYOIMclYTIZITJyDKi27oM6DZglBmpgGbJGUQdNtIJjP54EDY6Ep6nVQJWZZrMF25-gkT0oHF7t9hN5m96_Tx3Dx_DCfThahEUSQELAxmaE5FREmktEko2kGNBVRSvyJSf-UQs5VJAXOFc1ymWY5UZgAZcrEdIRu-t6Nrd9bcI2uCmegLJM11K3ThHMZS8Ej_h-UCEqVwh69_oGu6tau_Uc8xahiUinqqXFPGVs7ZyHXG1tUie00wXprX29d661r_WXfJ652vW1aQXbg97o9wHvgoyih-6tPz55e9sW3fa5uN7-mwm9TfAKkBphF</recordid><startdate>201407</startdate><enddate>201407</enddate><creator>Diepold, Andreas</creator><creator>Wagner, Samuel</creator><general>Blackwell Publishing Ltd</general><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201407</creationdate><title>Assembly of the bacterial type III secretion machinery</title><author>Diepold, Andreas ; Wagner, Samuel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6161-e0ccdc3f36201843ad3bde3b62b13bd483f3bef592860f93df8bdf1901e349c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Bacteria</topic><topic>Bacterial Physiological Phenomena</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacterial Proteins - secretion</topic><topic>Bacterial Secretion Systems - physiology</topic><topic>Bacteriology</topic><topic>Cytosol - metabolism</topic><topic>injectisome</topic><topic>Machinery</topic><topic>macromolecular machines</topic><topic>membrane proteins</topic><topic>Pathogens</topic><topic>protein complexes</topic><topic>protein secretion</topic><topic>Quality control</topic><topic>Translocation</topic><topic>virulence factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Diepold, Andreas</creatorcontrib><creatorcontrib>Wagner, Samuel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS microbiology reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Diepold, Andreas</au><au>Wagner, Samuel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assembly of the bacterial type III secretion machinery</atitle><jtitle>FEMS microbiology reviews</jtitle><addtitle>FEMS Microbiol Rev</addtitle><date>2014-07</date><risdate>2014</risdate><volume>38</volume><issue>4</issue><spage>802</spage><epage>822</epage><pages>802-822</pages><issn>0168-6445</issn><issn>1574-6976</issn><eissn>1574-6976</eissn><coden>FMREE4</coden><abstract>Abstract
Many bacteria that live in contact with eukaryotic hosts, whether as symbionts or as pathogens, have evolved mechanisms that manipulate host cell behaviour to their benefit. One such mechanism, the type III secretion system, is employed by Gram-negative bacterial species to inject effector proteins into host cells. This function is reflected by the overall shape of the machinery, which resembles a molecular syringe. Despite the simplicity of the concept, the type III secretion system is one of the most complex known bacterial nanomachines, incorporating one to more than hundred copies of up to twenty different proteins into a multi-MDa transmembrane complex. The structural core of the system is the so-called needle complex that spans the bacterial cell envelope as a tripartite ring system and culminates in a needle protruding from the bacterial cell surface. Substrate targeting and translocation are accomplished by an export machinery consisting of various inner membrane embedded and cytoplasmic components. The formation of such a multimembrane-spanning machinery is an intricate task that requires precise orchestration. This review gives an overview of recent findings on the assembly of type III secretion machines, discusses quality control and recycling of the system and proposes an integrated assembly model.
This review discusses the assembly of the type III secretion injectisome, a cell envelope spanning macromolecular machine used by Gram-negative bacteria to translocate bacterial effector proteins into host cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>24484471</pmid><doi>10.1111/1574-6976.12061</doi><tpages>21</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Bacterial Physiological Phenomena Bacterial Proteins - metabolism Bacterial Proteins - secretion Bacterial Secretion Systems - physiology Bacteriology Cytosol - metabolism injectisome Machinery macromolecular machines membrane proteins Pathogens protein complexes protein secretion Quality control Translocation virulence factors |
title | Assembly of the bacterial type III secretion machinery |
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