The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication
The intracellular pathogen Brucella abortus survives and replicates inside host cells within an endoplasmic reticulum (ER)-derived replicative organelle named the "Brucella-containing vacuole" (BCV). Here, we developed a subcellular fractionation method to isolate BCVs and characterize for...
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description | The intracellular pathogen Brucella abortus survives and replicates inside host cells within an endoplasmic reticulum (ER)-derived replicative organelle named the "Brucella-containing vacuole" (BCV). Here, we developed a subcellular fractionation method to isolate BCVs and characterize for the first time the protein composition of its replicative niche. After identification of BCV membrane proteins by 2 dimensional (2D) gel electrophoresis and mass spectrometry, we focused on two eukaryotic proteins: the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the small GTPase Rab 2 recruited to the vacuolar membrane of Brucella. These proteins were previously described to localize on vesicular and tubular clusters (VTC) and to regulate the VTC membrane traffic between the endoplasmic reticulum (ER) and the Golgi. Inhibition of either GAPDH or Rab 2 expression by small interfering RNA strongly inhibited B. abortus replication. Consistent with this result, inhibition of other partners of GAPDH and Rab 2, such as COPI and PKC iota, reduced B. abortus replication. Furthermore, blockage of Rab 2 GTPase in a GDP-locked form also inhibited B. abortus replication. Bacteria did not fuse with the ER and instead remained in lysosomal-associated membrane vacuoles. These results reveal an essential role for GAPDH and the small GTPase Rab 2 in B. abortus virulence within host cells. |
doi_str_mv | 10.1371/journal.ppat.1000487 |
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Here, we developed a subcellular fractionation method to isolate BCVs and characterize for the first time the protein composition of its replicative niche. After identification of BCV membrane proteins by 2 dimensional (2D) gel electrophoresis and mass spectrometry, we focused on two eukaryotic proteins: the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the small GTPase Rab 2 recruited to the vacuolar membrane of Brucella. These proteins were previously described to localize on vesicular and tubular clusters (VTC) and to regulate the VTC membrane traffic between the endoplasmic reticulum (ER) and the Golgi. Inhibition of either GAPDH or Rab 2 expression by small interfering RNA strongly inhibited B. abortus replication. Consistent with this result, inhibition of other partners of GAPDH and Rab 2, such as COPI and PKC iota, reduced B. abortus replication. Furthermore, blockage of Rab 2 GTPase in a GDP-locked form also inhibited B. abortus replication. Bacteria did not fuse with the ER and instead remained in lysosomal-associated membrane vacuoles. These results reveal an essential role for GAPDH and the small GTPase Rab 2 in B. abortus virulence within host cells.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1000487</identifier><identifier>PMID: 19557163</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Bacteria ; Bacteriology ; Biochemistry ; Brucella abortus ; Brucella abortus - cytology ; Brucella abortus - growth & development ; Cell Biology/Membranes and Sorting ; Cell division ; Cell Line ; Cell Membrane ; Cell Membrane - chemistry ; Cell Membrane - microbiology ; Cell Survival ; Endoplasmic Reticulum ; Endoplasmic Reticulum - microbiology ; Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) ; Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - chemistry ; Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - metabolism ; Guanosine triphosphatase ; Host-Pathogen Interactions ; Host-Pathogen Interactions - physiology ; Immunohistochemistry ; Immunology ; Infections ; Life Sciences ; Mass spectrometry ; Membrane Proteins ; Membrane Proteins - chemistry ; Membrane Proteins - metabolism ; Microbiology and Parasitology ; Microbiology/Cellular Microbiology and Pathogenesis ; Oxidoreductases ; Physiological aspects ; Proteins ; rab2 GTP-Binding Protein ; rab2 GTP-Binding Protein - chemistry ; rab2 GTP-Binding Protein - metabolism ; Secretory Pathway ; Secretory Pathway - physiology ; Vacuoles ; Vacuoles - chemistry ; Vacuoles - enzymology ; Vacuoles - microbiology</subject><ispartof>PLoS pathogens, 2009-06, Vol.5 (6), p.e1000487-e1000487</ispartof><rights>COPYRIGHT 2009 Public Library of Science</rights><rights>Attribution</rights><rights>Fugier et al. 2009</rights><rights>2009 Fugier et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Fugier E, Salcedo SP, de Chastellier C, Pophillat M, Muller A, et al. (2009) The Glyceraldehyde-3-Phosphate Dehydrogenase and the Small GTPase Rab 2 Are Crucial for Brucella Replication. PLoS Pathog 5(6): e1000487. doi:10.1371/journal.ppat.1000487</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c665t-535bc2dcc990b60f990a3999a5d65ebf4eb93ca4b319c9368e168108b7fa87703</citedby><cites>FETCH-LOGICAL-c665t-535bc2dcc990b60f990a3999a5d65ebf4eb93ca4b319c9368e168108b7fa87703</cites><orcidid>0000-0002-5547-0240 ; 0000-0002-2829-9804</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695806/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695806/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19557163$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00431863$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Fugier, Emilie</creatorcontrib><creatorcontrib>Salcedo, Suzana P</creatorcontrib><creatorcontrib>de Chastellier, Chantal</creatorcontrib><creatorcontrib>Pophillat, Matthieu</creatorcontrib><creatorcontrib>Muller, Alexandre</creatorcontrib><creatorcontrib>Arce-Gorvel, Vilma</creatorcontrib><creatorcontrib>Fourquet, Patrick</creatorcontrib><creatorcontrib>Gorvel, Jean-Pierre</creatorcontrib><title>The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication</title><title>PLoS pathogens</title><addtitle>PLoS Pathog</addtitle><description>The intracellular pathogen Brucella abortus survives and replicates inside host cells within an endoplasmic reticulum (ER)-derived replicative organelle named the "Brucella-containing vacuole" (BCV). Here, we developed a subcellular fractionation method to isolate BCVs and characterize for the first time the protein composition of its replicative niche. After identification of BCV membrane proteins by 2 dimensional (2D) gel electrophoresis and mass spectrometry, we focused on two eukaryotic proteins: the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the small GTPase Rab 2 recruited to the vacuolar membrane of Brucella. These proteins were previously described to localize on vesicular and tubular clusters (VTC) and to regulate the VTC membrane traffic between the endoplasmic reticulum (ER) and the Golgi. Inhibition of either GAPDH or Rab 2 expression by small interfering RNA strongly inhibited B. abortus replication. Consistent with this result, inhibition of other partners of GAPDH and Rab 2, such as COPI and PKC iota, reduced B. abortus replication. Furthermore, blockage of Rab 2 GTPase in a GDP-locked form also inhibited B. abortus replication. Bacteria did not fuse with the ER and instead remained in lysosomal-associated membrane vacuoles. These results reveal an essential role for GAPDH and the small GTPase Rab 2 in B. abortus virulence within host cells.</description><subject>Animals</subject><subject>Bacteria</subject><subject>Bacteriology</subject><subject>Biochemistry</subject><subject>Brucella abortus</subject><subject>Brucella abortus - cytology</subject><subject>Brucella abortus - growth & development</subject><subject>Cell Biology/Membranes and Sorting</subject><subject>Cell division</subject><subject>Cell Line</subject><subject>Cell Membrane</subject><subject>Cell Membrane - chemistry</subject><subject>Cell Membrane - microbiology</subject><subject>Cell Survival</subject><subject>Endoplasmic Reticulum</subject><subject>Endoplasmic Reticulum - microbiology</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - chemistry</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - metabolism</subject><subject>Guanosine triphosphatase</subject><subject>Host-Pathogen Interactions</subject><subject>Host-Pathogen Interactions - physiology</subject><subject>Immunohistochemistry</subject><subject>Immunology</subject><subject>Infections</subject><subject>Life Sciences</subject><subject>Mass spectrometry</subject><subject>Membrane Proteins</subject><subject>Membrane Proteins - chemistry</subject><subject>Membrane Proteins - metabolism</subject><subject>Microbiology and Parasitology</subject><subject>Microbiology/Cellular Microbiology and Pathogenesis</subject><subject>Oxidoreductases</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>rab2 GTP-Binding Protein</subject><subject>rab2 GTP-Binding Protein - chemistry</subject><subject>rab2 GTP-Binding Protein - metabolism</subject><subject>Secretory Pathway</subject><subject>Secretory Pathway - physiology</subject><subject>Vacuoles</subject><subject>Vacuoles - chemistry</subject><subject>Vacuoles - enzymology</subject><subject>Vacuoles - microbiology</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVkl-L1DAUxYso7rr6DUQLgrAPHZOmSZoXYVx0d2BQWcfnkKa3f4ZM003axfn2pjNVd8QX6UMup79zLzm5UfQSowUmHL_b2tF1yiz6Xg0LjBDKcv4oOseUkoQTnj1-UJ9Fz7zfBgQTzJ5GZ1hQyjEj55HZNBDXZq_BKVNCsy8hIUnfWN83aoD4IDlbQ6c8xKor4yEY_E4ZE19vvk7irSriNFYOYu1G3SoTV9bFH0INxqjYQW9arYbWds-jJ5UyHl7M50X0_dPHzdVNsv5yvbparhPNGB0SSmih01JrIVDBUBUORYQQipaMQlFlUAiiVVYQLLQgLAfMcozyglcq5xyRi-j1sW9vrJdzUF7iNBeIUpSlgVgdidKqrexdu1NuL61q5UGwrpbKDa02INMizVFFC5oJyECHglMgWKOMp1gJEXq9n6eNxQ5KDd0QsjxpevqnaxtZ23uZMkFzxEKDy2OD5i_bzXItJy08HME5I_c4sG_nYc7ejeAHuWv9IegO7Ogl41lKWUYD-OYI1ipcou0qG2brCZbLFJGU41RM1OIfVPhK2LXadlC1QT8xXJ4YAjPAj6FWo_dy9e32P9jPp2x2ZLWz3juofgeBkZz2_dczymnf5bzvwfbqYfZ_TPOCk5_bR_qJ</recordid><startdate>20090601</startdate><enddate>20090601</enddate><creator>Fugier, Emilie</creator><creator>Salcedo, Suzana P</creator><creator>de Chastellier, Chantal</creator><creator>Pophillat, Matthieu</creator><creator>Muller, Alexandre</creator><creator>Arce-Gorvel, Vilma</creator><creator>Fourquet, Patrick</creator><creator>Gorvel, Jean-Pierre</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5547-0240</orcidid><orcidid>https://orcid.org/0000-0002-2829-9804</orcidid></search><sort><creationdate>20090601</creationdate><title>The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication</title><author>Fugier, Emilie ; Salcedo, Suzana P ; de Chastellier, Chantal ; Pophillat, Matthieu ; Muller, Alexandre ; Arce-Gorvel, Vilma ; Fourquet, Patrick ; Gorvel, Jean-Pierre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c665t-535bc2dcc990b60f990a3999a5d65ebf4eb93ca4b319c9368e168108b7fa87703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Bacteria</topic><topic>Bacteriology</topic><topic>Biochemistry</topic><topic>Brucella abortus</topic><topic>Brucella abortus - cytology</topic><topic>Brucella abortus - growth & development</topic><topic>Cell Biology/Membranes and Sorting</topic><topic>Cell division</topic><topic>Cell Line</topic><topic>Cell Membrane</topic><topic>Cell Membrane - chemistry</topic><topic>Cell Membrane - microbiology</topic><topic>Cell Survival</topic><topic>Endoplasmic Reticulum</topic><topic>Endoplasmic Reticulum - microbiology</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - chemistry</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - metabolism</topic><topic>Guanosine triphosphatase</topic><topic>Host-Pathogen Interactions</topic><topic>Host-Pathogen Interactions - physiology</topic><topic>Immunohistochemistry</topic><topic>Immunology</topic><topic>Infections</topic><topic>Life Sciences</topic><topic>Mass spectrometry</topic><topic>Membrane Proteins</topic><topic>Membrane Proteins - chemistry</topic><topic>Membrane Proteins - metabolism</topic><topic>Microbiology and Parasitology</topic><topic>Microbiology/Cellular Microbiology and Pathogenesis</topic><topic>Oxidoreductases</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>rab2 GTP-Binding Protein</topic><topic>rab2 GTP-Binding Protein - chemistry</topic><topic>rab2 GTP-Binding Protein - metabolism</topic><topic>Secretory Pathway</topic><topic>Secretory Pathway - physiology</topic><topic>Vacuoles</topic><topic>Vacuoles - chemistry</topic><topic>Vacuoles - enzymology</topic><topic>Vacuoles - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fugier, Emilie</creatorcontrib><creatorcontrib>Salcedo, Suzana P</creatorcontrib><creatorcontrib>de Chastellier, Chantal</creatorcontrib><creatorcontrib>Pophillat, Matthieu</creatorcontrib><creatorcontrib>Muller, Alexandre</creatorcontrib><creatorcontrib>Arce-Gorvel, Vilma</creatorcontrib><creatorcontrib>Fourquet, Patrick</creatorcontrib><creatorcontrib>Gorvel, Jean-Pierre</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fugier, Emilie</au><au>Salcedo, Suzana P</au><au>de Chastellier, Chantal</au><au>Pophillat, Matthieu</au><au>Muller, Alexandre</au><au>Arce-Gorvel, Vilma</au><au>Fourquet, Patrick</au><au>Gorvel, Jean-Pierre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2009-06-01</date><risdate>2009</risdate><volume>5</volume><issue>6</issue><spage>e1000487</spage><epage>e1000487</epage><pages>e1000487-e1000487</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>The intracellular pathogen Brucella abortus survives and replicates inside host cells within an endoplasmic reticulum (ER)-derived replicative organelle named the "Brucella-containing vacuole" (BCV). Here, we developed a subcellular fractionation method to isolate BCVs and characterize for the first time the protein composition of its replicative niche. After identification of BCV membrane proteins by 2 dimensional (2D) gel electrophoresis and mass spectrometry, we focused on two eukaryotic proteins: the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the small GTPase Rab 2 recruited to the vacuolar membrane of Brucella. These proteins were previously described to localize on vesicular and tubular clusters (VTC) and to regulate the VTC membrane traffic between the endoplasmic reticulum (ER) and the Golgi. Inhibition of either GAPDH or Rab 2 expression by small interfering RNA strongly inhibited B. abortus replication. Consistent with this result, inhibition of other partners of GAPDH and Rab 2, such as COPI and PKC iota, reduced B. abortus replication. Furthermore, blockage of Rab 2 GTPase in a GDP-locked form also inhibited B. abortus replication. Bacteria did not fuse with the ER and instead remained in lysosomal-associated membrane vacuoles. These results reveal an essential role for GAPDH and the small GTPase Rab 2 in B. abortus virulence within host cells.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>19557163</pmid><doi>10.1371/journal.ppat.1000487</doi><orcidid>https://orcid.org/0000-0002-5547-0240</orcidid><orcidid>https://orcid.org/0000-0002-2829-9804</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bacteria Bacteriology Biochemistry Brucella abortus Brucella abortus - cytology Brucella abortus - growth & development Cell Biology/Membranes and Sorting Cell division Cell Line Cell Membrane Cell Membrane - chemistry Cell Membrane - microbiology Cell Survival Endoplasmic Reticulum Endoplasmic Reticulum - microbiology Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - chemistry Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - metabolism Guanosine triphosphatase Host-Pathogen Interactions Host-Pathogen Interactions - physiology Immunohistochemistry Immunology Infections Life Sciences Mass spectrometry Membrane Proteins Membrane Proteins - chemistry Membrane Proteins - metabolism Microbiology and Parasitology Microbiology/Cellular Microbiology and Pathogenesis Oxidoreductases Physiological aspects Proteins rab2 GTP-Binding Protein rab2 GTP-Binding Protein - chemistry rab2 GTP-Binding Protein - metabolism Secretory Pathway Secretory Pathway - physiology Vacuoles Vacuoles - chemistry Vacuoles - enzymology Vacuoles - microbiology |
title | The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication |
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