Phage-specific diverse effects of bacterial viruses on the immune system
[...]it cannot be excluded that in the future, after phage discovery, research may shift towards phage-immune system interactions, whereas, to date, work on phage interactions with their natural target (bacteria) has prevailed. Diversity of phage action on the immune system was also confirmed by rec...
Gespeichert in:
Veröffentlicht in: | Future microbiology 2019-09, Vol.14 (14), p.1171-1174 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1174 |
---|---|
container_issue | 14 |
container_start_page | 1171 |
container_title | Future microbiology |
container_volume | 14 |
creator | Górski, Andrzej Międzybrodzki, Ryszard Jończyk-Matysiak, Ewa Żaczek, Maciej Borysowski, Jan |
description | [...]it cannot be excluded that in the future, after phage discovery, research may shift towards phage-immune system interactions, whereas, to date, work on phage interactions with their natural target (bacteria) has prevailed. Diversity of phage action on the immune system was also confirmed by recent data showing that a filamentous Pseudomonas Pf phage inhibits TNF production and phagocytosis while Escherichia coli filamentous Fol phage does not have such effects (8). [...]our data indicate that both T4 coliphage and A5/80 Staphylococcus aureus phage significantly reduce the expression of human adenovirus genes, but synthesis of viral DNA is inhibited only by T4 coliphage (14). [...]prophages are the major contributor to bacterial inter-strain immune heterogeneity manifested as variation of adaptive T- and B-cell immune responses of human lymphocytes, in vitro, to S. aureus and Streptococcus pyogenes (15). If indeed polysialic acid is a ligand for receptors of some phages it could enable those phages to bind to immune cells as the presence of polysialic acid has also been demonstrated on human DCs, NK cells and a subpopulation of T cells (27,28). [...]it is likely that various phages may use different cellular ligands to attach to and transcytose target cells including those of the immune system. |
doi_str_mv | 10.2217/fmb-2019-0222 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6802706</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2293970713</sourcerecordid><originalsourceid>FETCH-LOGICAL-c465t-60b73c79dbec9162127028d95b080e29e086066397f543f1660b202d7884469c3</originalsourceid><addsrcrecordid>eNp1kctLxDAQh4Mo7vo4epWCFy_VZNImzUUQUVdY0IOeQ5tO3Egfa9Iu-N-bZXVRwVNe3_wmw0fICaMXAExe2rZKgTKVUgDYIVMmM5FSBWx3u2d8Qg5CeKM0L5hi-2TCWc7zyEzJ7GlRvmIalmicdSap3Qp9wAStRTOEpLdJVZoBvSubZOX8GDBedsmwwMS17dhhEj7CgO0R2bNlE_D4az0kL3e3zzezdP54_3BzPU9NJvIhFbSS3EhVV2gUE8BAUihqlVe0oAgKaSGoEFxJm2fcMhELgEItiyLLhDL8kFxtcpdj1WJtsBt82eild23pP3RfOv37pXML_dqvtCho7CViwPlXgO_fRwyDbl0w2DRlh_0YNICK3alkPKJnf9C3fvRdHE8DZ5DJjEsZqXRDGd-H4NFuP8OoXjvS0ZFeO9JrR5E__TnBlv6WEgG1Aew4jB6DcdgZ1JtTrHDGdfhP-CdKLZ8f</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2312474377</pqid></control><display><type>article</type><title>Phage-specific diverse effects of bacterial viruses on the immune system</title><source>Open Access: PubMed Central</source><source>MEDLINE</source><creator>Górski, Andrzej ; Międzybrodzki, Ryszard ; Jończyk-Matysiak, Ewa ; Żaczek, Maciej ; Borysowski, Jan</creator><creatorcontrib>Górski, Andrzej ; Międzybrodzki, Ryszard ; Jończyk-Matysiak, Ewa ; Żaczek, Maciej ; Borysowski, Jan</creatorcontrib><description>[...]it cannot be excluded that in the future, after phage discovery, research may shift towards phage-immune system interactions, whereas, to date, work on phage interactions with their natural target (bacteria) has prevailed. Diversity of phage action on the immune system was also confirmed by recent data showing that a filamentous Pseudomonas Pf phage inhibits TNF production and phagocytosis while Escherichia coli filamentous Fol phage does not have such effects (8). [...]our data indicate that both T4 coliphage and A5/80 Staphylococcus aureus phage significantly reduce the expression of human adenovirus genes, but synthesis of viral DNA is inhibited only by T4 coliphage (14). [...]prophages are the major contributor to bacterial inter-strain immune heterogeneity manifested as variation of adaptive T- and B-cell immune responses of human lymphocytes, in vitro, to S. aureus and Streptococcus pyogenes (15). If indeed polysialic acid is a ligand for receptors of some phages it could enable those phages to bind to immune cells as the presence of polysialic acid has also been demonstrated on human DCs, NK cells and a subpopulation of T cells (27,28). [...]it is likely that various phages may use different cellular ligands to attach to and transcytose target cells including those of the immune system.</description><identifier>ISSN: 1746-0913</identifier><identifier>EISSN: 1746-0921</identifier><identifier>DOI: 10.2217/fmb-2019-0222</identifier><identifier>PMID: 31535921</identifier><language>eng</language><publisher>England: Future Medicine Ltd</publisher><subject>Animals ; Antibiotics ; Arthritis ; Bacteria ; Bacteria - immunology ; Bacteria - virology ; Bacterial infections ; Bacteriophages - immunology ; Cytokines ; Cytokines - immunology ; Dendritic cells ; DNA biosynthesis ; Drug resistance ; E coli ; Gene expression ; Heterogeneity ; Humans ; Immune response (cell-mediated) ; Immune system ; immunity ; immunomodulation ; inflammation ; Lymphocytes ; Lymphocytes B ; Lymphocytes T ; phage ; Phage Therapy ; Phages ; Phagocytosis ; Pneumonia ; Polysialic acid ; Prophages ; Proteins ; Studies ; transcytosis ; Tumor necrosis factor ; Viruses</subject><ispartof>Future microbiology, 2019-09, Vol.14 (14), p.1171-1174</ispartof><rights>2019 Andrzej Gorski</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Andrzej Gorski 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-60b73c79dbec9162127028d95b080e29e086066397f543f1660b202d7884469c3</citedby><cites>FETCH-LOGICAL-c465t-60b73c79dbec9162127028d95b080e29e086066397f543f1660b202d7884469c3</cites><orcidid>0000-0001-9556-2820</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/PMC6802706/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802706/$$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/31535921$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Górski, Andrzej</creatorcontrib><creatorcontrib>Międzybrodzki, Ryszard</creatorcontrib><creatorcontrib>Jończyk-Matysiak, Ewa</creatorcontrib><creatorcontrib>Żaczek, Maciej</creatorcontrib><creatorcontrib>Borysowski, Jan</creatorcontrib><title>Phage-specific diverse effects of bacterial viruses on the immune system</title><title>Future microbiology</title><addtitle>Future Microbiol</addtitle><description>[...]it cannot be excluded that in the future, after phage discovery, research may shift towards phage-immune system interactions, whereas, to date, work on phage interactions with their natural target (bacteria) has prevailed. Diversity of phage action on the immune system was also confirmed by recent data showing that a filamentous Pseudomonas Pf phage inhibits TNF production and phagocytosis while Escherichia coli filamentous Fol phage does not have such effects (8). [...]our data indicate that both T4 coliphage and A5/80 Staphylococcus aureus phage significantly reduce the expression of human adenovirus genes, but synthesis of viral DNA is inhibited only by T4 coliphage (14). [...]prophages are the major contributor to bacterial inter-strain immune heterogeneity manifested as variation of adaptive T- and B-cell immune responses of human lymphocytes, in vitro, to S. aureus and Streptococcus pyogenes (15). If indeed polysialic acid is a ligand for receptors of some phages it could enable those phages to bind to immune cells as the presence of polysialic acid has also been demonstrated on human DCs, NK cells and a subpopulation of T cells (27,28). [...]it is likely that various phages may use different cellular ligands to attach to and transcytose target cells including those of the immune system.</description><subject>Animals</subject><subject>Antibiotics</subject><subject>Arthritis</subject><subject>Bacteria</subject><subject>Bacteria - immunology</subject><subject>Bacteria - virology</subject><subject>Bacterial infections</subject><subject>Bacteriophages - immunology</subject><subject>Cytokines</subject><subject>Cytokines - immunology</subject><subject>Dendritic cells</subject><subject>DNA biosynthesis</subject><subject>Drug resistance</subject><subject>E coli</subject><subject>Gene expression</subject><subject>Heterogeneity</subject><subject>Humans</subject><subject>Immune response (cell-mediated)</subject><subject>Immune system</subject><subject>immunity</subject><subject>immunomodulation</subject><subject>inflammation</subject><subject>Lymphocytes</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>phage</subject><subject>Phage Therapy</subject><subject>Phages</subject><subject>Phagocytosis</subject><subject>Pneumonia</subject><subject>Polysialic acid</subject><subject>Prophages</subject><subject>Proteins</subject><subject>Studies</subject><subject>transcytosis</subject><subject>Tumor necrosis factor</subject><subject>Viruses</subject><issn>1746-0913</issn><issn>1746-0921</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kctLxDAQh4Mo7vo4epWCFy_VZNImzUUQUVdY0IOeQ5tO3Egfa9Iu-N-bZXVRwVNe3_wmw0fICaMXAExe2rZKgTKVUgDYIVMmM5FSBWx3u2d8Qg5CeKM0L5hi-2TCWc7zyEzJ7GlRvmIalmicdSap3Qp9wAStRTOEpLdJVZoBvSubZOX8GDBedsmwwMS17dhhEj7CgO0R2bNlE_D4az0kL3e3zzezdP54_3BzPU9NJvIhFbSS3EhVV2gUE8BAUihqlVe0oAgKaSGoEFxJm2fcMhELgEItiyLLhDL8kFxtcpdj1WJtsBt82eild23pP3RfOv37pXML_dqvtCho7CViwPlXgO_fRwyDbl0w2DRlh_0YNICK3alkPKJnf9C3fvRdHE8DZ5DJjEsZqXRDGd-H4NFuP8OoXjvS0ZFeO9JrR5E__TnBlv6WEgG1Aew4jB6DcdgZ1JtTrHDGdfhP-CdKLZ8f</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Górski, Andrzej</creator><creator>Międzybrodzki, Ryszard</creator><creator>Jończyk-Matysiak, Ewa</creator><creator>Żaczek, Maciej</creator><creator>Borysowski, Jan</creator><general>Future Medicine Ltd</general><scope>FUMOA</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>EHMNL</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9556-2820</orcidid></search><sort><creationdate>20190901</creationdate><title>Phage-specific diverse effects of bacterial viruses on the immune system</title><author>Górski, Andrzej ; Międzybrodzki, Ryszard ; Jończyk-Matysiak, Ewa ; Żaczek, Maciej ; Borysowski, Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-60b73c79dbec9162127028d95b080e29e086066397f543f1660b202d7884469c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Antibiotics</topic><topic>Arthritis</topic><topic>Bacteria</topic><topic>Bacteria - immunology</topic><topic>Bacteria - virology</topic><topic>Bacterial infections</topic><topic>Bacteriophages - immunology</topic><topic>Cytokines</topic><topic>Cytokines - immunology</topic><topic>Dendritic cells</topic><topic>DNA biosynthesis</topic><topic>Drug resistance</topic><topic>E coli</topic><topic>Gene expression</topic><topic>Heterogeneity</topic><topic>Humans</topic><topic>Immune response (cell-mediated)</topic><topic>Immune system</topic><topic>immunity</topic><topic>immunomodulation</topic><topic>inflammation</topic><topic>Lymphocytes</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>phage</topic><topic>Phage Therapy</topic><topic>Phages</topic><topic>Phagocytosis</topic><topic>Pneumonia</topic><topic>Polysialic acid</topic><topic>Prophages</topic><topic>Proteins</topic><topic>Studies</topic><topic>transcytosis</topic><topic>Tumor necrosis factor</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Górski, Andrzej</creatorcontrib><creatorcontrib>Międzybrodzki, Ryszard</creatorcontrib><creatorcontrib>Jończyk-Matysiak, Ewa</creatorcontrib><creatorcontrib>Żaczek, Maciej</creatorcontrib><creatorcontrib>Borysowski, Jan</creatorcontrib><collection>Future Medicine (Open Access)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>UK & Ireland Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Future microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Górski, Andrzej</au><au>Międzybrodzki, Ryszard</au><au>Jończyk-Matysiak, Ewa</au><au>Żaczek, Maciej</au><au>Borysowski, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phage-specific diverse effects of bacterial viruses on the immune system</atitle><jtitle>Future microbiology</jtitle><addtitle>Future Microbiol</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>14</volume><issue>14</issue><spage>1171</spage><epage>1174</epage><pages>1171-1174</pages><issn>1746-0913</issn><eissn>1746-0921</eissn><abstract>[...]it cannot be excluded that in the future, after phage discovery, research may shift towards phage-immune system interactions, whereas, to date, work on phage interactions with their natural target (bacteria) has prevailed. Diversity of phage action on the immune system was also confirmed by recent data showing that a filamentous Pseudomonas Pf phage inhibits TNF production and phagocytosis while Escherichia coli filamentous Fol phage does not have such effects (8). [...]our data indicate that both T4 coliphage and A5/80 Staphylococcus aureus phage significantly reduce the expression of human adenovirus genes, but synthesis of viral DNA is inhibited only by T4 coliphage (14). [...]prophages are the major contributor to bacterial inter-strain immune heterogeneity manifested as variation of adaptive T- and B-cell immune responses of human lymphocytes, in vitro, to S. aureus and Streptococcus pyogenes (15). If indeed polysialic acid is a ligand for receptors of some phages it could enable those phages to bind to immune cells as the presence of polysialic acid has also been demonstrated on human DCs, NK cells and a subpopulation of T cells (27,28). [...]it is likely that various phages may use different cellular ligands to attach to and transcytose target cells including those of the immune system.</abstract><cop>England</cop><pub>Future Medicine Ltd</pub><pmid>31535921</pmid><doi>10.2217/fmb-2019-0222</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0001-9556-2820</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1746-0913 |
ispartof | Future microbiology, 2019-09, Vol.14 (14), p.1171-1174 |
issn | 1746-0913 1746-0921 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6802706 |
source | Open Access: PubMed Central; MEDLINE |
subjects | Animals Antibiotics Arthritis Bacteria Bacteria - immunology Bacteria - virology Bacterial infections Bacteriophages - immunology Cytokines Cytokines - immunology Dendritic cells DNA biosynthesis Drug resistance E coli Gene expression Heterogeneity Humans Immune response (cell-mediated) Immune system immunity immunomodulation inflammation Lymphocytes Lymphocytes B Lymphocytes T phage Phage Therapy Phages Phagocytosis Pneumonia Polysialic acid Prophages Proteins Studies transcytosis Tumor necrosis factor Viruses |
title | Phage-specific diverse effects of bacterial viruses on the immune system |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T19%3A18%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Phage-specific%20diverse%20effects%20of%20bacterial%20viruses%20on%20the%20immune%20system&rft.jtitle=Future%20microbiology&rft.au=G%C3%B3rski,%20Andrzej&rft.date=2019-09-01&rft.volume=14&rft.issue=14&rft.spage=1171&rft.epage=1174&rft.pages=1171-1174&rft.issn=1746-0913&rft.eissn=1746-0921&rft_id=info:doi/10.2217/fmb-2019-0222&rft_dat=%3Cproquest_pubme%3E2293970713%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2312474377&rft_id=info:pmid/31535921&rfr_iscdi=true |