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Division without Binary Fission: Cell Division in the FtsZ-Less Chlamydia
is an obligate intracellular bacterial pathogen that has significantly reduced its genome size in adapting to its intracellular niche. Among the genes that has eliminated is , encoding the central organizer of cell division that directs cell wall synthesis in the division septum. These Gram-negative...
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Published in: | Journal of bacteriology 2020-08, Vol.202 (17) |
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container_title | Journal of bacteriology |
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creator | Ouellette, Scot P Lee, Junghoon Cox, John V |
description | is an obligate intracellular bacterial pathogen that has significantly reduced its genome size in adapting to its intracellular niche. Among the genes that
has eliminated is
, encoding the central organizer of cell division that directs cell wall synthesis in the division septum. These Gram-negative pathogens have cell envelopes that lack peptidoglycan (PG), yet they use PG for cell division purposes. Recent research into chlamydial PG synthesis, components of the chlamydial divisome, and the mechanism of chlamydial division have significantly advanced our understanding of these processes in a unique and important pathogen. For example, it has been definitively confirmed that chlamydiae synthesize a canonical PG structure during cell division. Various studies have suggested and provided evidence that
uses MreB to substitute for FtsZ in organizing and coordinating the divisome during division, components of which have been identified and characterized. Finally, as opposed to using an FtsZ-dependent binary fission process,
employs an MreB-dependent polarized budding process to divide. A brief historical context for these key advances is presented along with a discussion of the current state of knowledge of chlamydial cell division. |
doi_str_mv | 10.1128/JB.00252-20 |
format | article |
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has eliminated is
, encoding the central organizer of cell division that directs cell wall synthesis in the division septum. These Gram-negative pathogens have cell envelopes that lack peptidoglycan (PG), yet they use PG for cell division purposes. Recent research into chlamydial PG synthesis, components of the chlamydial divisome, and the mechanism of chlamydial division have significantly advanced our understanding of these processes in a unique and important pathogen. For example, it has been definitively confirmed that chlamydiae synthesize a canonical PG structure during cell division. Various studies have suggested and provided evidence that
uses MreB to substitute for FtsZ in organizing and coordinating the divisome during division, components of which have been identified and characterized. Finally, as opposed to using an FtsZ-dependent binary fission process,
employs an MreB-dependent polarized budding process to divide. A brief historical context for these key advances is presented along with a discussion of the current state of knowledge of chlamydial cell division.</description><identifier>ISSN: 0021-9193</identifier><identifier>EISSN: 1098-5530</identifier><identifier>DOI: 10.1128/JB.00252-20</identifier><identifier>PMID: 32540934</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacteriology ; Cell division ; Cell Division - physiology ; Cell envelopes ; Cell walls ; Chlamydia ; Cytoskeletal Proteins - genetics ; Cytoskeletal Proteins - metabolism ; Fission ; Gene Expression Regulation, Bacterial - physiology ; Genomes ; Humans ; Intracellular ; Minireview ; Pathogens ; Peptidoglycans ; Septum ; Synthesis</subject><ispartof>Journal of bacteriology, 2020-08, Vol.202 (17)</ispartof><rights>Copyright © 2020 American Society for Microbiology.</rights><rights>Copyright American Society for Microbiology Sep 2020</rights><rights>Copyright © 2020 American Society for Microbiology. 2020 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-652fc9e6918957c719f52703df5c01c9fe72f55132d987d530feb09919561db93</citedby><cites>FETCH-LOGICAL-c409t-652fc9e6918957c719f52703df5c01c9fe72f55132d987d530feb09919561db93</cites><orcidid>0000-0002-3721-6839</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/PMC7417837/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417837/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3174,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32540934$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Margolin, William</contributor><creatorcontrib>Ouellette, Scot P</creatorcontrib><creatorcontrib>Lee, Junghoon</creatorcontrib><creatorcontrib>Cox, John V</creatorcontrib><title>Division without Binary Fission: Cell Division in the FtsZ-Less Chlamydia</title><title>Journal of bacteriology</title><addtitle>J Bacteriol</addtitle><description>is an obligate intracellular bacterial pathogen that has significantly reduced its genome size in adapting to its intracellular niche. Among the genes that
has eliminated is
, encoding the central organizer of cell division that directs cell wall synthesis in the division septum. These Gram-negative pathogens have cell envelopes that lack peptidoglycan (PG), yet they use PG for cell division purposes. Recent research into chlamydial PG synthesis, components of the chlamydial divisome, and the mechanism of chlamydial division have significantly advanced our understanding of these processes in a unique and important pathogen. For example, it has been definitively confirmed that chlamydiae synthesize a canonical PG structure during cell division. Various studies have suggested and provided evidence that
uses MreB to substitute for FtsZ in organizing and coordinating the divisome during division, components of which have been identified and characterized. Finally, as opposed to using an FtsZ-dependent binary fission process,
employs an MreB-dependent polarized budding process to divide. A brief historical context for these key advances is presented along with a discussion of the current state of knowledge of chlamydial cell division.</description><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>Cell division</subject><subject>Cell Division - physiology</subject><subject>Cell envelopes</subject><subject>Cell walls</subject><subject>Chlamydia</subject><subject>Cytoskeletal Proteins - genetics</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Fission</subject><subject>Gene Expression Regulation, Bacterial - physiology</subject><subject>Genomes</subject><subject>Humans</subject><subject>Intracellular</subject><subject>Minireview</subject><subject>Pathogens</subject><subject>Peptidoglycans</subject><subject>Septum</subject><subject>Synthesis</subject><issn>0021-9193</issn><issn>1098-5530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpdkc9LwzAcxYMobk5P3iXgRZDO_FwbD4KrTh0DL3rxEro0sRldM5t2sv_ezM2hXhL4fj-873s8AE4x6mNMkqvxsI8Q4SQiaA90MRJJxDlF-6AbxjgSWNAOOPJ-hhBmjJND0KGEMyQo64KnO7u03roKftqmcG0Dh7bK6hUcWb8eX8NUlyXcUbaCTaHhqPFv0UR7D9OizOar3GbH4MBkpdcn278HXkf3L-ljNHl-eEpvJ5EKJ5towIlRQg8ETgSPVYyF4SRGNDdcIayE0TExnGNKcpHEeQhi9BSJkIIPcD4VtAduNrqLdjrXudJVU2elXNR2HnxLl1n5d1PZQr67pYwZjhMaB4GLrUDtPlrtGzm3XoWUWaVd6yVhmCGUJGx96_wfOnNtXYV4gaKcMxyeQF1uKFU772ttdmYwkuuK5HgovyuSBAX67Lf_HfvTCf0CnjmKJA</recordid><startdate>20200810</startdate><enddate>20200810</enddate><creator>Ouellette, Scot P</creator><creator>Lee, Junghoon</creator><creator>Cox, John V</creator><general>American Society for Microbiology</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>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3721-6839</orcidid></search><sort><creationdate>20200810</creationdate><title>Division without Binary Fission: Cell Division in the FtsZ-Less Chlamydia</title><author>Ouellette, Scot P ; Lee, Junghoon ; Cox, John V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-652fc9e6918957c719f52703df5c01c9fe72f55132d987d530feb09919561db93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacteriology</topic><topic>Cell division</topic><topic>Cell Division - physiology</topic><topic>Cell envelopes</topic><topic>Cell walls</topic><topic>Chlamydia</topic><topic>Cytoskeletal Proteins - genetics</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Fission</topic><topic>Gene Expression Regulation, Bacterial - physiology</topic><topic>Genomes</topic><topic>Humans</topic><topic>Intracellular</topic><topic>Minireview</topic><topic>Pathogens</topic><topic>Peptidoglycans</topic><topic>Septum</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ouellette, Scot P</creatorcontrib><creatorcontrib>Lee, Junghoon</creatorcontrib><creatorcontrib>Cox, John V</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>Nucleic Acids Abstracts</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bacteriology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ouellette, Scot P</au><au>Lee, Junghoon</au><au>Cox, John V</au><au>Margolin, William</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Division without Binary Fission: Cell Division in the FtsZ-Less Chlamydia</atitle><jtitle>Journal of bacteriology</jtitle><addtitle>J Bacteriol</addtitle><date>2020-08-10</date><risdate>2020</risdate><volume>202</volume><issue>17</issue><issn>0021-9193</issn><eissn>1098-5530</eissn><abstract>is an obligate intracellular bacterial pathogen that has significantly reduced its genome size in adapting to its intracellular niche. Among the genes that
has eliminated is
, encoding the central organizer of cell division that directs cell wall synthesis in the division septum. These Gram-negative pathogens have cell envelopes that lack peptidoglycan (PG), yet they use PG for cell division purposes. Recent research into chlamydial PG synthesis, components of the chlamydial divisome, and the mechanism of chlamydial division have significantly advanced our understanding of these processes in a unique and important pathogen. For example, it has been definitively confirmed that chlamydiae synthesize a canonical PG structure during cell division. Various studies have suggested and provided evidence that
uses MreB to substitute for FtsZ in organizing and coordinating the divisome during division, components of which have been identified and characterized. Finally, as opposed to using an FtsZ-dependent binary fission process,
employs an MreB-dependent polarized budding process to divide. A brief historical context for these key advances is presented along with a discussion of the current state of knowledge of chlamydial cell division.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>32540934</pmid><doi>10.1128/JB.00252-20</doi><orcidid>https://orcid.org/0000-0002-3721-6839</orcidid><oa>free_for_read</oa></addata></record> |
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source | American Society for Microbiology Journals; PubMed Central |
subjects | Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacteriology Cell division Cell Division - physiology Cell envelopes Cell walls Chlamydia Cytoskeletal Proteins - genetics Cytoskeletal Proteins - metabolism Fission Gene Expression Regulation, Bacterial - physiology Genomes Humans Intracellular Minireview Pathogens Peptidoglycans Septum Synthesis |
title | Division without Binary Fission: Cell Division in the FtsZ-Less Chlamydia |
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