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The Yin and Yang of Pneumolysin During Pneumococcal Infection
Pneumolysin (PLY) is a pore-forming toxin produced by the human pathobiont , the major cause of pneumonia worldwide. PLY, a key pneumococcal virulence factor, can form transmembrane pores in host cells, disrupting plasma membrane integrity and deregulating cellular homeostasis. At lytic concentratio...
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Published in: | Frontiers in immunology 2022-04, Vol.13, p.878244-878244 |
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description | Pneumolysin (PLY) is a pore-forming toxin produced by the human pathobiont
, the major cause of pneumonia worldwide. PLY, a key pneumococcal virulence factor, can form transmembrane pores in host cells, disrupting plasma membrane integrity and deregulating cellular homeostasis. At lytic concentrations, PLY causes cell death. At sub-lytic concentrations, PLY triggers host cell survival pathways that cooperate to reseal the damaged plasma membrane and restore cell homeostasis. While PLY is generally considered a pivotal factor promoting
colonization and survival, it is also a powerful trigger of the innate and adaptive host immune response against bacterial infection. The dichotomy of PLY as both a key bacterial virulence factor and a trigger for host immune modulation allows the toxin to display both "Yin" and "Yang" properties during infection, promoting disease by membrane perforation and activating inflammatory pathways, while also mitigating damage by triggering host cell repair and initiating anti-inflammatory responses. Due to its cytolytic activity and diverse immunomodulatory properties, PLY is integral to every stage of
pathogenesis and may tip the balance towards either the pathogen or the host depending on the context of infection. |
doi_str_mv | 10.3389/fimmu.2022.878244 |
format | article |
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, the major cause of pneumonia worldwide. PLY, a key pneumococcal virulence factor, can form transmembrane pores in host cells, disrupting plasma membrane integrity and deregulating cellular homeostasis. At lytic concentrations, PLY causes cell death. At sub-lytic concentrations, PLY triggers host cell survival pathways that cooperate to reseal the damaged plasma membrane and restore cell homeostasis. While PLY is generally considered a pivotal factor promoting
colonization and survival, it is also a powerful trigger of the innate and adaptive host immune response against bacterial infection. The dichotomy of PLY as both a key bacterial virulence factor and a trigger for host immune modulation allows the toxin to display both "Yin" and "Yang" properties during infection, promoting disease by membrane perforation and activating inflammatory pathways, while also mitigating damage by triggering host cell repair and initiating anti-inflammatory responses. Due to its cytolytic activity and diverse immunomodulatory properties, PLY is integral to every stage of
pathogenesis and may tip the balance towards either the pathogen or the host depending on the context of infection.</description><identifier>ISSN: 1664-3224</identifier><identifier>EISSN: 1664-3224</identifier><identifier>DOI: 10.3389/fimmu.2022.878244</identifier><identifier>PMID: 35529870</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>cholesterol-dependent cytolysin ; Immunology ; plasma membrane ; pneumonia ; pore-forming toxin ; pro- and anti-inflammatory immune responses ; Streptococcus pneumoniae</subject><ispartof>Frontiers in immunology, 2022-04, Vol.13, p.878244-878244</ispartof><rights>Copyright © 2022 Pereira, Xu, Leong and Sousa.</rights><rights>Copyright © 2022 Pereira, Xu, Leong and Sousa 2022 Pereira, Xu, Leong and Sousa</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-fac1d8ec90d9b7963f0214a8f8a20687c8e53dafc5a5150c839040c31d3752933</citedby><cites>FETCH-LOGICAL-c465t-fac1d8ec90d9b7963f0214a8f8a20687c8e53dafc5a5150c839040c31d3752933</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/PMC9074694/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074694/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35529870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pereira, Joana M</creatorcontrib><creatorcontrib>Xu, Shuying</creatorcontrib><creatorcontrib>Leong, John M</creatorcontrib><creatorcontrib>Sousa, Sandra</creatorcontrib><title>The Yin and Yang of Pneumolysin During Pneumococcal Infection</title><title>Frontiers in immunology</title><addtitle>Front Immunol</addtitle><description>Pneumolysin (PLY) is a pore-forming toxin produced by the human pathobiont
, the major cause of pneumonia worldwide. PLY, a key pneumococcal virulence factor, can form transmembrane pores in host cells, disrupting plasma membrane integrity and deregulating cellular homeostasis. At lytic concentrations, PLY causes cell death. At sub-lytic concentrations, PLY triggers host cell survival pathways that cooperate to reseal the damaged plasma membrane and restore cell homeostasis. While PLY is generally considered a pivotal factor promoting
colonization and survival, it is also a powerful trigger of the innate and adaptive host immune response against bacterial infection. The dichotomy of PLY as both a key bacterial virulence factor and a trigger for host immune modulation allows the toxin to display both "Yin" and "Yang" properties during infection, promoting disease by membrane perforation and activating inflammatory pathways, while also mitigating damage by triggering host cell repair and initiating anti-inflammatory responses. Due to its cytolytic activity and diverse immunomodulatory properties, PLY is integral to every stage of
pathogenesis and may tip the balance towards either the pathogen or the host depending on the context of infection.</description><subject>cholesterol-dependent cytolysin</subject><subject>Immunology</subject><subject>plasma membrane</subject><subject>pneumonia</subject><subject>pore-forming toxin</subject><subject>pro- and anti-inflammatory immune responses</subject><subject>Streptococcus pneumoniae</subject><issn>1664-3224</issn><issn>1664-3224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkU1PHSEUhiemphr1B3RjZtnNvQIHGFi0SWO_bmLSLuzCFeEe4IqZAQszTfz3neuoUTaQl3Oec5KnaT5QsgZQ-iLEYZjWjDC2Vp1inB80x1RKvgLG-LtX76PmrNY7Mh-uAUC8b45ACKZVR46bT9e3vr2JqbXJtTc27doc2t_JT0PuH-qcf51KnNMlwoxo-3aTgscx5nTaHAbbV3_2dJ80f75_u778ubr69WNz-eVqhVyKcRUsUqc8auL0ttMSAmGUWxWUZUSqDpUX4GxAYQUVBBVowgkCddDNiwKcNJuF67K9M_clDrY8mGyjeQxy2Rlbxoi9N2i1cAQpuK3ixHdKqXmi1wgd1TTwmfV5Yd1P28E79Gkstn8DffuT4q3Z5X9Gk45LvQd8fAKU_HfydTRDrOj73iafp2qYlJQryUHNpXQpxZJrLT68jKHE7C2aR4tmb9EsFuee89f7vXQ8O4P_MXmYZw</recordid><startdate>20220422</startdate><enddate>20220422</enddate><creator>Pereira, Joana M</creator><creator>Xu, Shuying</creator><creator>Leong, John M</creator><creator>Sousa, Sandra</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220422</creationdate><title>The Yin and Yang of Pneumolysin During Pneumococcal Infection</title><author>Pereira, Joana M ; Xu, Shuying ; Leong, John M ; Sousa, Sandra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-fac1d8ec90d9b7963f0214a8f8a20687c8e53dafc5a5150c839040c31d3752933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>cholesterol-dependent cytolysin</topic><topic>Immunology</topic><topic>plasma membrane</topic><topic>pneumonia</topic><topic>pore-forming toxin</topic><topic>pro- and anti-inflammatory immune responses</topic><topic>Streptococcus pneumoniae</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pereira, Joana M</creatorcontrib><creatorcontrib>Xu, Shuying</creatorcontrib><creatorcontrib>Leong, John M</creatorcontrib><creatorcontrib>Sousa, Sandra</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pereira, Joana M</au><au>Xu, Shuying</au><au>Leong, John M</au><au>Sousa, Sandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Yin and Yang of Pneumolysin During Pneumococcal Infection</atitle><jtitle>Frontiers in immunology</jtitle><addtitle>Front Immunol</addtitle><date>2022-04-22</date><risdate>2022</risdate><volume>13</volume><spage>878244</spage><epage>878244</epage><pages>878244-878244</pages><issn>1664-3224</issn><eissn>1664-3224</eissn><abstract>Pneumolysin (PLY) is a pore-forming toxin produced by the human pathobiont
, the major cause of pneumonia worldwide. PLY, a key pneumococcal virulence factor, can form transmembrane pores in host cells, disrupting plasma membrane integrity and deregulating cellular homeostasis. At lytic concentrations, PLY causes cell death. At sub-lytic concentrations, PLY triggers host cell survival pathways that cooperate to reseal the damaged plasma membrane and restore cell homeostasis. While PLY is generally considered a pivotal factor promoting
colonization and survival, it is also a powerful trigger of the innate and adaptive host immune response against bacterial infection. The dichotomy of PLY as both a key bacterial virulence factor and a trigger for host immune modulation allows the toxin to display both "Yin" and "Yang" properties during infection, promoting disease by membrane perforation and activating inflammatory pathways, while also mitigating damage by triggering host cell repair and initiating anti-inflammatory responses. Due to its cytolytic activity and diverse immunomodulatory properties, PLY is integral to every stage of
pathogenesis and may tip the balance towards either the pathogen or the host depending on the context of infection.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>35529870</pmid><doi>10.3389/fimmu.2022.878244</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | cholesterol-dependent cytolysin Immunology plasma membrane pneumonia pore-forming toxin pro- and anti-inflammatory immune responses Streptococcus pneumoniae |
title | The Yin and Yang of Pneumolysin During Pneumococcal Infection |
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