Hypoxia inducible factor signaling modulates susceptibility to mycobacterial infection via a nitric oxide dependent mechanism
Tuberculosis is a current major world-health problem, exacerbated by the causative pathogen, Mycobacterium tuberculosis (Mtb), becoming increasingly resistant to conventional antibiotic treatment. Mtb is able to counteract the bactericidal mechanisms of leukocytes to survive intracellularly and deve...
Gespeichert in:
Veröffentlicht in: | PLoS pathogens 2013-12, Vol.9 (12), p.e1003789-e1003789 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e1003789 |
---|---|
container_issue | 12 |
container_start_page | e1003789 |
container_title | PLoS pathogens |
container_volume | 9 |
creator | Elks, Philip M Brizee, Sabrina van der Vaart, Michiel Walmsley, Sarah R van Eeden, Fredericus J Renshaw, Stephen A Meijer, Annemarie H |
description | Tuberculosis is a current major world-health problem, exacerbated by the causative pathogen, Mycobacterium tuberculosis (Mtb), becoming increasingly resistant to conventional antibiotic treatment. Mtb is able to counteract the bactericidal mechanisms of leukocytes to survive intracellularly and develop a niche permissive for proliferation and dissemination. Understanding of the pathogenesis of mycobacterial infections such as tuberculosis (TB) remains limited, especially for early infection and for reactivation of latent infection. Signaling via hypoxia inducible factor α (HIF-α) transcription factors has previously been implicated in leukocyte activation and host defence. We have previously shown that hypoxic signaling via stabilization of Hif-1α prolongs the functionality of leukocytes in the innate immune response to injury. We sought to manipulate Hif-α signaling in a well-established Mycobacterium marinum (Mm) zebrafish model of TB to investigate effects on the host's ability to combat mycobacterial infection. Stabilization of host Hif-1α, both pharmacologically and genetically, at early stages of Mm infection was able to reduce the bacterial burden of infected larvae. Increasing Hif-1α signaling enhanced levels of reactive nitrogen species (RNS) in neutrophils prior to infection and was able to reduce larval mycobacterial burden. Conversely, decreasing Hif-2α signaling enhanced RNS levels and reduced bacterial burden, demonstrating that Hif-1α and Hif-2α have opposing effects on host susceptibility to mycobacterial infection. The antimicrobial effect of Hif-1α stabilization, and Hif-2α reduction, were demonstrated to be dependent on inducible nitric oxide synthase (iNOS) signaling at early stages of infection. Our findings indicate that induction of leukocyte iNOS by stabilizing Hif-1α, or reducing Hif-2α, aids the host during early stages of Mm infection. Stabilization of Hif-1α therefore represents a potential target for therapeutic intervention against tuberculosis. |
doi_str_mv | 10.1371/journal.ppat.1003789 |
format | Article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1477947294</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A357592466</galeid><doaj_id>oai_doaj_org_article_9206a399214f4684810273aa9e20b3b8</doaj_id><sourcerecordid>A357592466</sourcerecordid><originalsourceid>FETCH-LOGICAL-c633t-16398b7bd547fdea71dd9fe9ecf91602713aff729100abae5875d33700a2099c3</originalsourceid><addsrcrecordid>eNqVkktv1DAUhSMEoqXwDxBEYgOLGfxKHG-QqgroSBVIPNbWjX0z9SiJg-1UnQX_HQ8zrToSG-SFH_nO8fXJLYqXlCwpl_T9xs9hhH45TZCWlBAuG_WoOKVVxReSS_H4wfqkeBbjhhBBOa2fFidM8Fqyqj4tfl9uJ3_roHSjnY1reyw7MMmHMrp1tnfjuhy8nXtIGMs4R4NTcq3rXdqWyZfD1vg2CzA46LNJhyY5P5Y32RLK0aXgTJkvsFhanHC0OKZyQHMNo4vD8-JJB33EF4f5rPj56eOPi8vF1dfPq4vzq4WpOU8LWnPVtLK1lZCdRZDUWtWhQtMpWhMmKYeuk0zlGKAFrBpZWc5l3jGilOFnxeu979T7qA_JRU2FlEpkncjEak9YDxs9BTdA2GoPTv898GGtISRnetSKkRq4UoyKTtSNaGiugAMoZKTlbZO9Phxum9sBrclPDtAfmR5_Gd21XvsbzZu6qRjJBm8PBsH_mjEmPbgcfN_DiH7e1a2IZJKJKqNv9ugacmk5f58dzQ7X57ySlWKirjO1_AeVh8XBGT9i5_L5keDdkSAzCW_TGuYY9er7t_9gvxyzYs-a4GMM2N2nQonetfXdz9G7ttaHts6yVw8TvRfd9TH_AwT_9fA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1490727245</pqid></control><display><type>article</type><title>Hypoxia inducible factor signaling modulates susceptibility to mycobacterial infection via a nitric oxide dependent mechanism</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>PubMed Central Open Access</source><source>Public Library of Science (PLoS)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Elks, Philip M ; Brizee, Sabrina ; van der Vaart, Michiel ; Walmsley, Sarah R ; van Eeden, Fredericus J ; Renshaw, Stephen A ; Meijer, Annemarie H</creator><contributor>Schneider, David S.</contributor><creatorcontrib>Elks, Philip M ; Brizee, Sabrina ; van der Vaart, Michiel ; Walmsley, Sarah R ; van Eeden, Fredericus J ; Renshaw, Stephen A ; Meijer, Annemarie H ; Schneider, David S.</creatorcontrib><description>Tuberculosis is a current major world-health problem, exacerbated by the causative pathogen, Mycobacterium tuberculosis (Mtb), becoming increasingly resistant to conventional antibiotic treatment. Mtb is able to counteract the bactericidal mechanisms of leukocytes to survive intracellularly and develop a niche permissive for proliferation and dissemination. Understanding of the pathogenesis of mycobacterial infections such as tuberculosis (TB) remains limited, especially for early infection and for reactivation of latent infection. Signaling via hypoxia inducible factor α (HIF-α) transcription factors has previously been implicated in leukocyte activation and host defence. We have previously shown that hypoxic signaling via stabilization of Hif-1α prolongs the functionality of leukocytes in the innate immune response to injury. We sought to manipulate Hif-α signaling in a well-established Mycobacterium marinum (Mm) zebrafish model of TB to investigate effects on the host's ability to combat mycobacterial infection. Stabilization of host Hif-1α, both pharmacologically and genetically, at early stages of Mm infection was able to reduce the bacterial burden of infected larvae. Increasing Hif-1α signaling enhanced levels of reactive nitrogen species (RNS) in neutrophils prior to infection and was able to reduce larval mycobacterial burden. Conversely, decreasing Hif-2α signaling enhanced RNS levels and reduced bacterial burden, demonstrating that Hif-1α and Hif-2α have opposing effects on host susceptibility to mycobacterial infection. The antimicrobial effect of Hif-1α stabilization, and Hif-2α reduction, were demonstrated to be dependent on inducible nitric oxide synthase (iNOS) signaling at early stages of infection. Our findings indicate that induction of leukocyte iNOS by stabilizing Hif-1α, or reducing Hif-2α, aids the host during early stages of Mm infection. Stabilization of Hif-1α therefore represents a potential target for therapeutic intervention against tuberculosis.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1003789</identifier><identifier>PMID: 24367256</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Animals, Genetically Modified ; Bacterial infections ; Basic Helix-Loop-Helix Transcription Factors - physiology ; Cells, Cultured ; Colleges & universities ; Disease Models, Animal ; Drug resistance ; Genetic Predisposition to Disease ; Health aspects ; Host-parasite relationships ; Hypoxia ; Hypoxia-Inducible Factor 1, alpha Subunit - physiology ; Microbiological research ; Mutagenesis ; Mycobacteria ; Mycobacterium ; Mycobacterium Infections, Nontuberculous - genetics ; Mycobacterium Infections, Nontuberculous - immunology ; Mycobacterium Infections, Nontuberculous - microbiology ; Mycobacterium marinum ; Neutrophils - metabolism ; Nitric oxide ; Nitric Oxide - metabolism ; Nitric Oxide Synthase Type II - physiology ; Nitrosation ; Pathogenesis ; Phenols ; Physiological aspects ; Rodents ; Signal Transduction - genetics ; Tuberculosis ; Zebrafish</subject><ispartof>PLoS pathogens, 2013-12, Vol.9 (12), p.e1003789-e1003789</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Elks et al 2013 Elks et al</rights><rights>2013 Elks et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Elks PM, Brizee S, van der Vaart M, Walmsley SR, van Eeden FJ, et al. (2013) Hypoxia Inducible Factor Signaling Modulates Susceptibility to Mycobacterial Infection via a Nitric Oxide Dependent Mechanism. PLoS Pathog 9(12): e1003789. doi:10.1371/journal.ppat.1003789</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c633t-16398b7bd547fdea71dd9fe9ecf91602713aff729100abae5875d33700a2099c3</citedby><cites>FETCH-LOGICAL-c633t-16398b7bd547fdea71dd9fe9ecf91602713aff729100abae5875d33700a2099c3</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/PMC3868520/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868520/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24367256$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Schneider, David S.</contributor><creatorcontrib>Elks, Philip M</creatorcontrib><creatorcontrib>Brizee, Sabrina</creatorcontrib><creatorcontrib>van der Vaart, Michiel</creatorcontrib><creatorcontrib>Walmsley, Sarah R</creatorcontrib><creatorcontrib>van Eeden, Fredericus J</creatorcontrib><creatorcontrib>Renshaw, Stephen A</creatorcontrib><creatorcontrib>Meijer, Annemarie H</creatorcontrib><title>Hypoxia inducible factor signaling modulates susceptibility to mycobacterial infection via a nitric oxide dependent mechanism</title><title>PLoS pathogens</title><addtitle>PLoS Pathog</addtitle><description>Tuberculosis is a current major world-health problem, exacerbated by the causative pathogen, Mycobacterium tuberculosis (Mtb), becoming increasingly resistant to conventional antibiotic treatment. Mtb is able to counteract the bactericidal mechanisms of leukocytes to survive intracellularly and develop a niche permissive for proliferation and dissemination. Understanding of the pathogenesis of mycobacterial infections such as tuberculosis (TB) remains limited, especially for early infection and for reactivation of latent infection. Signaling via hypoxia inducible factor α (HIF-α) transcription factors has previously been implicated in leukocyte activation and host defence. We have previously shown that hypoxic signaling via stabilization of Hif-1α prolongs the functionality of leukocytes in the innate immune response to injury. We sought to manipulate Hif-α signaling in a well-established Mycobacterium marinum (Mm) zebrafish model of TB to investigate effects on the host's ability to combat mycobacterial infection. Stabilization of host Hif-1α, both pharmacologically and genetically, at early stages of Mm infection was able to reduce the bacterial burden of infected larvae. Increasing Hif-1α signaling enhanced levels of reactive nitrogen species (RNS) in neutrophils prior to infection and was able to reduce larval mycobacterial burden. Conversely, decreasing Hif-2α signaling enhanced RNS levels and reduced bacterial burden, demonstrating that Hif-1α and Hif-2α have opposing effects on host susceptibility to mycobacterial infection. The antimicrobial effect of Hif-1α stabilization, and Hif-2α reduction, were demonstrated to be dependent on inducible nitric oxide synthase (iNOS) signaling at early stages of infection. Our findings indicate that induction of leukocyte iNOS by stabilizing Hif-1α, or reducing Hif-2α, aids the host during early stages of Mm infection. Stabilization of Hif-1α therefore represents a potential target for therapeutic intervention against tuberculosis.</description><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Bacterial infections</subject><subject>Basic Helix-Loop-Helix Transcription Factors - physiology</subject><subject>Cells, Cultured</subject><subject>Colleges & universities</subject><subject>Disease Models, Animal</subject><subject>Drug resistance</subject><subject>Genetic Predisposition to Disease</subject><subject>Health aspects</subject><subject>Host-parasite relationships</subject><subject>Hypoxia</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit - physiology</subject><subject>Microbiological research</subject><subject>Mutagenesis</subject><subject>Mycobacteria</subject><subject>Mycobacterium</subject><subject>Mycobacterium Infections, Nontuberculous - genetics</subject><subject>Mycobacterium Infections, Nontuberculous - immunology</subject><subject>Mycobacterium Infections, Nontuberculous - microbiology</subject><subject>Mycobacterium marinum</subject><subject>Neutrophils - metabolism</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase Type II - physiology</subject><subject>Nitrosation</subject><subject>Pathogenesis</subject><subject>Phenols</subject><subject>Physiological aspects</subject><subject>Rodents</subject><subject>Signal Transduction - genetics</subject><subject>Tuberculosis</subject><subject>Zebrafish</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVkktv1DAUhSMEoqXwDxBEYgOLGfxKHG-QqgroSBVIPNbWjX0z9SiJg-1UnQX_HQ8zrToSG-SFH_nO8fXJLYqXlCwpl_T9xs9hhH45TZCWlBAuG_WoOKVVxReSS_H4wfqkeBbjhhBBOa2fFidM8Fqyqj4tfl9uJ3_roHSjnY1reyw7MMmHMrp1tnfjuhy8nXtIGMs4R4NTcq3rXdqWyZfD1vg2CzA46LNJhyY5P5Y32RLK0aXgTJkvsFhanHC0OKZyQHMNo4vD8-JJB33EF4f5rPj56eOPi8vF1dfPq4vzq4WpOU8LWnPVtLK1lZCdRZDUWtWhQtMpWhMmKYeuk0zlGKAFrBpZWc5l3jGilOFnxeu979T7qA_JRU2FlEpkncjEak9YDxs9BTdA2GoPTv898GGtISRnetSKkRq4UoyKTtSNaGiugAMoZKTlbZO9Phxum9sBrclPDtAfmR5_Gd21XvsbzZu6qRjJBm8PBsH_mjEmPbgcfN_DiH7e1a2IZJKJKqNv9ugacmk5f58dzQ7X57ySlWKirjO1_AeVh8XBGT9i5_L5keDdkSAzCW_TGuYY9er7t_9gvxyzYs-a4GMM2N2nQonetfXdz9G7ttaHts6yVw8TvRfd9TH_AwT_9fA</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Elks, Philip M</creator><creator>Brizee, Sabrina</creator><creator>van der Vaart, Michiel</creator><creator>Walmsley, Sarah R</creator><creator>van Eeden, Fredericus J</creator><creator>Renshaw, Stephen A</creator><creator>Meijer, Annemarie H</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20131201</creationdate><title>Hypoxia inducible factor signaling modulates susceptibility to mycobacterial infection via a nitric oxide dependent mechanism</title><author>Elks, Philip M ; Brizee, Sabrina ; van der Vaart, Michiel ; Walmsley, Sarah R ; van Eeden, Fredericus J ; Renshaw, Stephen A ; Meijer, Annemarie H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c633t-16398b7bd547fdea71dd9fe9ecf91602713aff729100abae5875d33700a2099c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Bacterial infections</topic><topic>Basic Helix-Loop-Helix Transcription Factors - physiology</topic><topic>Cells, Cultured</topic><topic>Colleges & universities</topic><topic>Disease Models, Animal</topic><topic>Drug resistance</topic><topic>Genetic Predisposition to Disease</topic><topic>Health aspects</topic><topic>Host-parasite relationships</topic><topic>Hypoxia</topic><topic>Hypoxia-Inducible Factor 1, alpha Subunit - physiology</topic><topic>Microbiological research</topic><topic>Mutagenesis</topic><topic>Mycobacteria</topic><topic>Mycobacterium</topic><topic>Mycobacterium Infections, Nontuberculous - genetics</topic><topic>Mycobacterium Infections, Nontuberculous - immunology</topic><topic>Mycobacterium Infections, Nontuberculous - microbiology</topic><topic>Mycobacterium marinum</topic><topic>Neutrophils - metabolism</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide Synthase Type II - physiology</topic><topic>Nitrosation</topic><topic>Pathogenesis</topic><topic>Phenols</topic><topic>Physiological aspects</topic><topic>Rodents</topic><topic>Signal Transduction - genetics</topic><topic>Tuberculosis</topic><topic>Zebrafish</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elks, Philip M</creatorcontrib><creatorcontrib>Brizee, Sabrina</creatorcontrib><creatorcontrib>van der Vaart, Michiel</creatorcontrib><creatorcontrib>Walmsley, Sarah R</creatorcontrib><creatorcontrib>van Eeden, Fredericus J</creatorcontrib><creatorcontrib>Renshaw, Stephen A</creatorcontrib><creatorcontrib>Meijer, Annemarie H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elks, Philip M</au><au>Brizee, Sabrina</au><au>van der Vaart, Michiel</au><au>Walmsley, Sarah R</au><au>van Eeden, Fredericus J</au><au>Renshaw, Stephen A</au><au>Meijer, Annemarie H</au><au>Schneider, David S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypoxia inducible factor signaling modulates susceptibility to mycobacterial infection via a nitric oxide dependent mechanism</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2013-12-01</date><risdate>2013</risdate><volume>9</volume><issue>12</issue><spage>e1003789</spage><epage>e1003789</epage><pages>e1003789-e1003789</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>Tuberculosis is a current major world-health problem, exacerbated by the causative pathogen, Mycobacterium tuberculosis (Mtb), becoming increasingly resistant to conventional antibiotic treatment. Mtb is able to counteract the bactericidal mechanisms of leukocytes to survive intracellularly and develop a niche permissive for proliferation and dissemination. Understanding of the pathogenesis of mycobacterial infections such as tuberculosis (TB) remains limited, especially for early infection and for reactivation of latent infection. Signaling via hypoxia inducible factor α (HIF-α) transcription factors has previously been implicated in leukocyte activation and host defence. We have previously shown that hypoxic signaling via stabilization of Hif-1α prolongs the functionality of leukocytes in the innate immune response to injury. We sought to manipulate Hif-α signaling in a well-established Mycobacterium marinum (Mm) zebrafish model of TB to investigate effects on the host's ability to combat mycobacterial infection. Stabilization of host Hif-1α, both pharmacologically and genetically, at early stages of Mm infection was able to reduce the bacterial burden of infected larvae. Increasing Hif-1α signaling enhanced levels of reactive nitrogen species (RNS) in neutrophils prior to infection and was able to reduce larval mycobacterial burden. Conversely, decreasing Hif-2α signaling enhanced RNS levels and reduced bacterial burden, demonstrating that Hif-1α and Hif-2α have opposing effects on host susceptibility to mycobacterial infection. The antimicrobial effect of Hif-1α stabilization, and Hif-2α reduction, were demonstrated to be dependent on inducible nitric oxide synthase (iNOS) signaling at early stages of infection. Our findings indicate that induction of leukocyte iNOS by stabilizing Hif-1α, or reducing Hif-2α, aids the host during early stages of Mm infection. Stabilization of Hif-1α therefore represents a potential target for therapeutic intervention against tuberculosis.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24367256</pmid><doi>10.1371/journal.ppat.1003789</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1553-7374 |
ispartof | PLoS pathogens, 2013-12, Vol.9 (12), p.e1003789-e1003789 |
issn | 1553-7374 1553-7366 1553-7374 |
language | eng |
recordid | cdi_plos_journals_1477947294 |
source | MEDLINE; DOAJ Directory of Open Access Journals; PubMed Central Open Access; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Animals Animals, Genetically Modified Bacterial infections Basic Helix-Loop-Helix Transcription Factors - physiology Cells, Cultured Colleges & universities Disease Models, Animal Drug resistance Genetic Predisposition to Disease Health aspects Host-parasite relationships Hypoxia Hypoxia-Inducible Factor 1, alpha Subunit - physiology Microbiological research Mutagenesis Mycobacteria Mycobacterium Mycobacterium Infections, Nontuberculous - genetics Mycobacterium Infections, Nontuberculous - immunology Mycobacterium Infections, Nontuberculous - microbiology Mycobacterium marinum Neutrophils - metabolism Nitric oxide Nitric Oxide - metabolism Nitric Oxide Synthase Type II - physiology Nitrosation Pathogenesis Phenols Physiological aspects Rodents Signal Transduction - genetics Tuberculosis Zebrafish |
title | Hypoxia inducible factor signaling modulates susceptibility to mycobacterial infection via a nitric oxide dependent mechanism |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T11%3A42%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hypoxia%20inducible%20factor%20signaling%20modulates%20susceptibility%20to%20mycobacterial%20infection%20via%20a%20nitric%20oxide%20dependent%20mechanism&rft.jtitle=PLoS%20pathogens&rft.au=Elks,%20Philip%20M&rft.date=2013-12-01&rft.volume=9&rft.issue=12&rft.spage=e1003789&rft.epage=e1003789&rft.pages=e1003789-e1003789&rft.issn=1553-7374&rft.eissn=1553-7374&rft_id=info:doi/10.1371/journal.ppat.1003789&rft_dat=%3Cgale_plos_%3EA357592466%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1490727245&rft_id=info:pmid/24367256&rft_galeid=A357592466&rft_doaj_id=oai_doaj_org_article_9206a399214f4684810273aa9e20b3b8&rfr_iscdi=true |