Defining the Range of Pathogens Susceptible to Ifitm3 Restriction Using a Knockout Mouse Model: e80723
The interferon-inducible transmembrane (IFITM) family of proteins has been shown to restrict a broad range of viruses in vitro and in vivo by halting progress through the late endosomal pathway. Further, single nucleotide polymorphisms (SNPs) in its sequence have been linked with risk of developing...
Gespeichert in:
Veröffentlicht in: | PloS one 2013-11, Vol.8 (11) |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 11 |
container_start_page | |
container_title | PloS one |
container_volume | 8 |
creator | Everitt, Aaron R Clare, Simon McDonald, Jacqueline U Kane, Leanne Harcourt, Katherine Ahras, Malika Lall, Amar Hale, Christine Rodgers, Angela Young, Douglas B |
description | The interferon-inducible transmembrane (IFITM) family of proteins has been shown to restrict a broad range of viruses in vitro and in vivo by halting progress through the late endosomal pathway. Further, single nucleotide polymorphisms (SNPs) in its sequence have been linked with risk of developing severe influenza virus infections in humans. The number of viruses restricted by this host protein has continued to grow since it was first demonstrated as playing an antiviral role; all of which enter cells via the endosomal pathway. We therefore sought to test the limits of antimicrobial restriction by Ifitm3 using a knockout mouse model. We showed that Ifitm3 does not impact on the restriction or pathogenesis of bacterial (Salmonella typhimurium, Citrobacter rodentium, Mycobacterium tuberculosis) or protozoan (Plasmodium berghei) pathogens, despite in vitro evidence. However, Ifitm3 is capable of restricting respiratory syncytial virus (RSV) in vivo either through directly restricting RSV cell infection, or by exerting a previously uncharacterised function controlling disease pathogenesis. This represents the first demonstration of a virus that enters directly through the plasma membrane, without the need for the endosomal pathway, being restricted by the IFITM family; therefore further defining the role of these antiviral proteins. |
doi_str_mv | 10.1371/journal.pone.0080723 |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1496890400</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1496890400</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_14968904003</originalsourceid><addsrcrecordid>eNqVjs1OwzAQhK1KSJSfN-CwRy4N67hNE678iAohoQLnyg3r1K27G2L7_QmIF-Ayc5lvZpS60lhos9Q3e8kD21D0wlQg1rgszURNdWPKWVWiOVVnMe4RF6auqqly9-Q8e-4g7QjWljsCcfBq00464ghvObbUJ78NBElg5Xw6GlhTTINvkxeGj_iDW3hmaQ-SE7xIjjTqJ4VboN8HF-rE2RDp8s_P1fXjw_vd06wf5CuPZZujH3dCsEwjvdHzpqobnCOaf0S_AR8WUNw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1496890400</pqid></control><display><type>article</type><title>Defining the Range of Pathogens Susceptible to Ifitm3 Restriction Using a Knockout Mouse Model: e80723</title><source>Public Library of Science (PLoS) Journals Open Access</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Everitt, Aaron R ; Clare, Simon ; McDonald, Jacqueline U ; Kane, Leanne ; Harcourt, Katherine ; Ahras, Malika ; Lall, Amar ; Hale, Christine ; Rodgers, Angela ; Young, Douglas B</creator><creatorcontrib>Everitt, Aaron R ; Clare, Simon ; McDonald, Jacqueline U ; Kane, Leanne ; Harcourt, Katherine ; Ahras, Malika ; Lall, Amar ; Hale, Christine ; Rodgers, Angela ; Young, Douglas B</creatorcontrib><description>The interferon-inducible transmembrane (IFITM) family of proteins has been shown to restrict a broad range of viruses in vitro and in vivo by halting progress through the late endosomal pathway. Further, single nucleotide polymorphisms (SNPs) in its sequence have been linked with risk of developing severe influenza virus infections in humans. The number of viruses restricted by this host protein has continued to grow since it was first demonstrated as playing an antiviral role; all of which enter cells via the endosomal pathway. We therefore sought to test the limits of antimicrobial restriction by Ifitm3 using a knockout mouse model. We showed that Ifitm3 does not impact on the restriction or pathogenesis of bacterial (Salmonella typhimurium, Citrobacter rodentium, Mycobacterium tuberculosis) or protozoan (Plasmodium berghei) pathogens, despite in vitro evidence. However, Ifitm3 is capable of restricting respiratory syncytial virus (RSV) in vivo either through directly restricting RSV cell infection, or by exerting a previously uncharacterised function controlling disease pathogenesis. This represents the first demonstration of a virus that enters directly through the plasma membrane, without the need for the endosomal pathway, being restricted by the IFITM family; therefore further defining the role of these antiviral proteins.</description><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0080723</identifier><language>eng</language><subject>Citrobacter rodentium ; Influenza virus ; Mycobacterium tuberculosis ; Plasmodium berghei ; Respiratory syncytial virus ; Salmonella typhimurium</subject><ispartof>PloS one, 2013-11, Vol.8 (11)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Everitt, Aaron R</creatorcontrib><creatorcontrib>Clare, Simon</creatorcontrib><creatorcontrib>McDonald, Jacqueline U</creatorcontrib><creatorcontrib>Kane, Leanne</creatorcontrib><creatorcontrib>Harcourt, Katherine</creatorcontrib><creatorcontrib>Ahras, Malika</creatorcontrib><creatorcontrib>Lall, Amar</creatorcontrib><creatorcontrib>Hale, Christine</creatorcontrib><creatorcontrib>Rodgers, Angela</creatorcontrib><creatorcontrib>Young, Douglas B</creatorcontrib><title>Defining the Range of Pathogens Susceptible to Ifitm3 Restriction Using a Knockout Mouse Model: e80723</title><title>PloS one</title><description>The interferon-inducible transmembrane (IFITM) family of proteins has been shown to restrict a broad range of viruses in vitro and in vivo by halting progress through the late endosomal pathway. Further, single nucleotide polymorphisms (SNPs) in its sequence have been linked with risk of developing severe influenza virus infections in humans. The number of viruses restricted by this host protein has continued to grow since it was first demonstrated as playing an antiviral role; all of which enter cells via the endosomal pathway. We therefore sought to test the limits of antimicrobial restriction by Ifitm3 using a knockout mouse model. We showed that Ifitm3 does not impact on the restriction or pathogenesis of bacterial (Salmonella typhimurium, Citrobacter rodentium, Mycobacterium tuberculosis) or protozoan (Plasmodium berghei) pathogens, despite in vitro evidence. However, Ifitm3 is capable of restricting respiratory syncytial virus (RSV) in vivo either through directly restricting RSV cell infection, or by exerting a previously uncharacterised function controlling disease pathogenesis. This represents the first demonstration of a virus that enters directly through the plasma membrane, without the need for the endosomal pathway, being restricted by the IFITM family; therefore further defining the role of these antiviral proteins.</description><subject>Citrobacter rodentium</subject><subject>Influenza virus</subject><subject>Mycobacterium tuberculosis</subject><subject>Plasmodium berghei</subject><subject>Respiratory syncytial virus</subject><subject>Salmonella typhimurium</subject><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqVjs1OwzAQhK1KSJSfN-CwRy4N67hNE678iAohoQLnyg3r1K27G2L7_QmIF-Ayc5lvZpS60lhos9Q3e8kD21D0wlQg1rgszURNdWPKWVWiOVVnMe4RF6auqqly9-Q8e-4g7QjWljsCcfBq00464ghvObbUJ78NBElg5Xw6GlhTTINvkxeGj_iDW3hmaQ-SE7xIjjTqJ4VboN8HF-rE2RDp8s_P1fXjw_vd06wf5CuPZZujH3dCsEwjvdHzpqobnCOaf0S_AR8WUNw</recordid><startdate>20131101</startdate><enddate>20131101</enddate><creator>Everitt, Aaron R</creator><creator>Clare, Simon</creator><creator>McDonald, Jacqueline U</creator><creator>Kane, Leanne</creator><creator>Harcourt, Katherine</creator><creator>Ahras, Malika</creator><creator>Lall, Amar</creator><creator>Hale, Christine</creator><creator>Rodgers, Angela</creator><creator>Young, Douglas B</creator><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope></search><sort><creationdate>20131101</creationdate><title>Defining the Range of Pathogens Susceptible to Ifitm3 Restriction Using a Knockout Mouse Model: e80723</title><author>Everitt, Aaron R ; Clare, Simon ; McDonald, Jacqueline U ; Kane, Leanne ; Harcourt, Katherine ; Ahras, Malika ; Lall, Amar ; Hale, Christine ; Rodgers, Angela ; Young, Douglas B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_14968904003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Citrobacter rodentium</topic><topic>Influenza virus</topic><topic>Mycobacterium tuberculosis</topic><topic>Plasmodium berghei</topic><topic>Respiratory syncytial virus</topic><topic>Salmonella typhimurium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Everitt, Aaron R</creatorcontrib><creatorcontrib>Clare, Simon</creatorcontrib><creatorcontrib>McDonald, Jacqueline U</creatorcontrib><creatorcontrib>Kane, Leanne</creatorcontrib><creatorcontrib>Harcourt, Katherine</creatorcontrib><creatorcontrib>Ahras, Malika</creatorcontrib><creatorcontrib>Lall, Amar</creatorcontrib><creatorcontrib>Hale, Christine</creatorcontrib><creatorcontrib>Rodgers, Angela</creatorcontrib><creatorcontrib>Young, Douglas B</creatorcontrib><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Everitt, Aaron R</au><au>Clare, Simon</au><au>McDonald, Jacqueline U</au><au>Kane, Leanne</au><au>Harcourt, Katherine</au><au>Ahras, Malika</au><au>Lall, Amar</au><au>Hale, Christine</au><au>Rodgers, Angela</au><au>Young, Douglas B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Defining the Range of Pathogens Susceptible to Ifitm3 Restriction Using a Knockout Mouse Model: e80723</atitle><jtitle>PloS one</jtitle><date>2013-11-01</date><risdate>2013</risdate><volume>8</volume><issue>11</issue><eissn>1932-6203</eissn><abstract>The interferon-inducible transmembrane (IFITM) family of proteins has been shown to restrict a broad range of viruses in vitro and in vivo by halting progress through the late endosomal pathway. Further, single nucleotide polymorphisms (SNPs) in its sequence have been linked with risk of developing severe influenza virus infections in humans. The number of viruses restricted by this host protein has continued to grow since it was first demonstrated as playing an antiviral role; all of which enter cells via the endosomal pathway. We therefore sought to test the limits of antimicrobial restriction by Ifitm3 using a knockout mouse model. We showed that Ifitm3 does not impact on the restriction or pathogenesis of bacterial (Salmonella typhimurium, Citrobacter rodentium, Mycobacterium tuberculosis) or protozoan (Plasmodium berghei) pathogens, despite in vitro evidence. However, Ifitm3 is capable of restricting respiratory syncytial virus (RSV) in vivo either through directly restricting RSV cell infection, or by exerting a previously uncharacterised function controlling disease pathogenesis. This represents the first demonstration of a virus that enters directly through the plasma membrane, without the need for the endosomal pathway, being restricted by the IFITM family; therefore further defining the role of these antiviral proteins.</abstract><doi>10.1371/journal.pone.0080723</doi></addata></record> |
fulltext | fulltext |
identifier | EISSN: 1932-6203 |
ispartof | PloS one, 2013-11, Vol.8 (11) |
issn | 1932-6203 |
language | eng |
recordid | cdi_proquest_miscellaneous_1496890400 |
source | Public Library of Science (PLoS) Journals Open Access; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Citrobacter rodentium Influenza virus Mycobacterium tuberculosis Plasmodium berghei Respiratory syncytial virus Salmonella typhimurium |
title | Defining the Range of Pathogens Susceptible to Ifitm3 Restriction Using a Knockout Mouse Model: e80723 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T20%3A05%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Defining%20the%20Range%20of%20Pathogens%20Susceptible%20to%20Ifitm3%20Restriction%20Using%20a%20Knockout%20Mouse%20Model:%20e80723&rft.jtitle=PloS%20one&rft.au=Everitt,%20Aaron%20R&rft.date=2013-11-01&rft.volume=8&rft.issue=11&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0080723&rft_dat=%3Cproquest%3E1496890400%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1496890400&rft_id=info:pmid/&rfr_iscdi=true |