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Mycoplasma pneumoniae, an Underutilized Model for Bacterial Cell Biology
In recent decades, bacterial cell biology has seen great advances, and numerous model systems have been developed to study a wide variety of cellular processes, including cell division, motility, assembly of macromolecular structures, and biogenesis of cell polarity. Considerable attention has been...
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Published in: | Journal of bacteriology 2014-11, Vol.196 (21), p.3675-3682 |
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description | In recent decades, bacterial cell biology has seen great advances, and numerous model systems have been developed to study a wide variety of cellular processes, including cell division, motility, assembly of macromolecular structures, and biogenesis of cell polarity. Considerable attention has been given to these model organisms, which include Escherichia coli, Bacillus subtilis, Caulobacter crescentus, and Myxococcus xanthus. Studies of these processes in the pathogenic bacterium Mycoplasma pneumoniae and its close relatives have also been carried out on a smaller scale, but this work is often overlooked, in part due to this organism's reputation as minimalistic and simple. In this minireview, I discuss recent work on the role of the M. pneumoniae attachment organelle (AO), a structure required for adherence to host cells, in these processes. The AO is constructed from proteins that generally lack homology to those found in other organisms, and this construction occurs in coordination with cell cycle events. The proteins of the M. pneumoniae AO share compositional features with proteins with related roles in model organisms. Once constructed, the AO becomes activated for its role in a form of gliding motility whose underlying mechanism appears to be distinct from that of other gliding bacteria, including Mycoplasma mobile. Together with the FtsZ cytoskeletal protein, motility participates in the cell division process. My intention is to bring this deceptively complex organism into alignment with the better-known model systems. |
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Considerable attention has been given to these model organisms, which include Escherichia coli, Bacillus subtilis, Caulobacter crescentus, and Myxococcus xanthus. Studies of these processes in the pathogenic bacterium Mycoplasma pneumoniae and its close relatives have also been carried out on a smaller scale, but this work is often overlooked, in part due to this organism's reputation as minimalistic and simple. In this minireview, I discuss recent work on the role of the M. pneumoniae attachment organelle (AO), a structure required for adherence to host cells, in these processes. The AO is constructed from proteins that generally lack homology to those found in other organisms, and this construction occurs in coordination with cell cycle events. The proteins of the M. pneumoniae AO share compositional features with proteins with related roles in model organisms. Once constructed, the AO becomes activated for its role in a form of gliding motility whose underlying mechanism appears to be distinct from that of other gliding bacteria, including Mycoplasma mobile. Together with the FtsZ cytoskeletal protein, motility participates in the cell division process. My intention is to bring this deceptively complex organism into alignment with the better-known model systems.</description><identifier>ISSN: 0021-9193</identifier><identifier>EISSN: 1098-5530</identifier><identifier>DOI: 10.1128/jb.01865-14</identifier><identifier>PMID: 25157081</identifier><identifier>CODEN: JOBAAY</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacillus subtilis ; Bacteria ; Bacterial Adhesion - physiology ; Bacterial Proteins - chemistry ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacteriology ; biogenesis ; Biosynthesis ; Caulobacter crescentus ; Cell division ; cell polarity ; Cellular biology ; cytoskeleton ; Escherichia coli ; Gene Expression Regulation, Bacterial - physiology ; Minireview ; Mycoplasma mobile ; Mycoplasma pneumoniae ; Mycoplasma pneumoniae - cytology ; Mycoplasma pneumoniae - physiology ; Mycoplasma pneumoniae - ultrastructure ; Myxococcus xanthus ; Proteins</subject><ispartof>Journal of bacteriology, 2014-11, Vol.196 (21), p.3675-3682</ispartof><rights>Copyright © 2014, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright American Society for Microbiology Nov 2014</rights><rights>Copyright © 2014, American Society for Microbiology. All Rights Reserved. 2014 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-21f5850cbf110e5bfef6bbf1665b7890fd029290d781c4b5c9519d18faaf64bb3</citedby><cites>FETCH-LOGICAL-c532t-21f5850cbf110e5bfef6bbf1665b7890fd029290d781c4b5c9519d18faaf64bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248795/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248795/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25157081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Balish, Mitchell F</creatorcontrib><title>Mycoplasma pneumoniae, an Underutilized Model for Bacterial Cell Biology</title><title>Journal of bacteriology</title><addtitle>J Bacteriol</addtitle><description>In recent decades, bacterial cell biology has seen great advances, and numerous model systems have been developed to study a wide variety of cellular processes, including cell division, motility, assembly of macromolecular structures, and biogenesis of cell polarity. Considerable attention has been given to these model organisms, which include Escherichia coli, Bacillus subtilis, Caulobacter crescentus, and Myxococcus xanthus. Studies of these processes in the pathogenic bacterium Mycoplasma pneumoniae and its close relatives have also been carried out on a smaller scale, but this work is often overlooked, in part due to this organism's reputation as minimalistic and simple. In this minireview, I discuss recent work on the role of the M. pneumoniae attachment organelle (AO), a structure required for adherence to host cells, in these processes. The AO is constructed from proteins that generally lack homology to those found in other organisms, and this construction occurs in coordination with cell cycle events. The proteins of the M. pneumoniae AO share compositional features with proteins with related roles in model organisms. Once constructed, the AO becomes activated for its role in a form of gliding motility whose underlying mechanism appears to be distinct from that of other gliding bacteria, including Mycoplasma mobile. Together with the FtsZ cytoskeletal protein, motility participates in the cell division process. My intention is to bring this deceptively complex organism into alignment with the better-known model systems.</description><subject>Bacillus subtilis</subject><subject>Bacteria</subject><subject>Bacterial Adhesion - physiology</subject><subject>Bacterial Proteins - chemistry</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>biogenesis</subject><subject>Biosynthesis</subject><subject>Caulobacter crescentus</subject><subject>Cell division</subject><subject>cell polarity</subject><subject>Cellular biology</subject><subject>cytoskeleton</subject><subject>Escherichia coli</subject><subject>Gene Expression Regulation, Bacterial - physiology</subject><subject>Minireview</subject><subject>Mycoplasma mobile</subject><subject>Mycoplasma pneumoniae</subject><subject>Mycoplasma pneumoniae - cytology</subject><subject>Mycoplasma pneumoniae - physiology</subject><subject>Mycoplasma pneumoniae - ultrastructure</subject><subject>Myxococcus xanthus</subject><subject>Proteins</subject><issn>0021-9193</issn><issn>1098-5530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqN0cFvFCEUBnBibOxaPXnXSbyY2Kk8BmbgYuJu1GraeNA9E2BgZcMMK8yYrH-9rFub2pMnQvjlC-99CD0DfAFA-JutvsDAW1YDfYAWgAWvGWvwQ7TAmEAtQDSn6HHOW4yBUkYeoVPCgHWYwwJdXu9N3AWVB1XtRjsPcfTKnldqrNZjb9M8-eB_2b66jr0NlYupWioz2eRVqFY2hGrpY4ib_RN04lTI9unNeYbWH95_W13WV18-flq9u6oNa8hUE3CMM2y0A8CWaWddq8ulbZnuuMCux0QQgfuOg6GaGcFA9MCdUq6lWjdn6O0xdzfrwfbGjlNSQe6SH1Tay6i8_Pdl9N_lJv6UlFDeCVYCXt0EpPhjtnmSg8-mTKJGG-csoW0YJhxE-x-UtIVzeqAv79FtnNNYNlEU0A5KKBT1-qhMijkn627_DVgeypSfl_JPmRJo0c_vjnpr_7ZXwIsjcCpKtUk-y_VXgoEdmu5wI5rfW4KidQ</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>Balish, Mitchell F</creator><general>American Society for Microbiology</general><scope>FBQ</scope><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></search><sort><creationdate>20141101</creationdate><title>Mycoplasma pneumoniae, an Underutilized Model for Bacterial Cell Biology</title><author>Balish, Mitchell F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c532t-21f5850cbf110e5bfef6bbf1665b7890fd029290d781c4b5c9519d18faaf64bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Bacillus subtilis</topic><topic>Bacteria</topic><topic>Bacterial Adhesion - physiology</topic><topic>Bacterial Proteins - chemistry</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacteriology</topic><topic>biogenesis</topic><topic>Biosynthesis</topic><topic>Caulobacter crescentus</topic><topic>Cell division</topic><topic>cell polarity</topic><topic>Cellular biology</topic><topic>cytoskeleton</topic><topic>Escherichia coli</topic><topic>Gene Expression Regulation, Bacterial - physiology</topic><topic>Minireview</topic><topic>Mycoplasma mobile</topic><topic>Mycoplasma pneumoniae</topic><topic>Mycoplasma pneumoniae - cytology</topic><topic>Mycoplasma pneumoniae - physiology</topic><topic>Mycoplasma pneumoniae - ultrastructure</topic><topic>Myxococcus xanthus</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balish, Mitchell F</creatorcontrib><collection>AGRIS</collection><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 - 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Once constructed, the AO becomes activated for its role in a form of gliding motility whose underlying mechanism appears to be distinct from that of other gliding bacteria, including Mycoplasma mobile. Together with the FtsZ cytoskeletal protein, motility participates in the cell division process. My intention is to bring this deceptively complex organism into alignment with the better-known model systems.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>25157081</pmid><doi>10.1128/jb.01865-14</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacillus subtilis Bacteria Bacterial Adhesion - physiology Bacterial Proteins - chemistry Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacteriology biogenesis Biosynthesis Caulobacter crescentus Cell division cell polarity Cellular biology cytoskeleton Escherichia coli Gene Expression Regulation, Bacterial - physiology Minireview Mycoplasma mobile Mycoplasma pneumoniae Mycoplasma pneumoniae - cytology Mycoplasma pneumoniae - physiology Mycoplasma pneumoniae - ultrastructure Myxococcus xanthus Proteins |
title | Mycoplasma pneumoniae, an Underutilized Model for Bacterial Cell Biology |
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