Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/112399
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dc.contributor.authorEijkelkamp, B.en
dc.contributor.authorBegg, S.en
dc.contributor.authorPederick, V.en
dc.contributor.authorTrapetti, C.en
dc.contributor.authorGregory, M.en
dc.contributor.authorWhittall, J.en
dc.contributor.authorPaton, J.en
dc.contributor.authorMcDevitt, C.en
dc.date.issued2018en
dc.identifier.citationFrontiers in Microbiology, 2018; 9(MAY):813-1-813-12en
dc.identifier.issn1664-302Xen
dc.identifier.issn1664-302Xen
dc.identifier.urihttp://hdl.handle.net/2440/112399-
dc.descriptionPublished: 11 May 2018en
dc.description.abstractFree fatty acids hold dual roles during infection, serving to modulate the host immune response while also functioning directly as antimicrobials. Of particular importance are the long chain polyunsaturated fatty acids, which are not commonly found in bacterial organisms, that have been proposed to have antibacterial roles. Arachidonic acid (AA) is a highly abundant long chain polyunsaturated fatty acid and we examined its effect upon Streptococcus pneumoniae. Here, we observed that in a murine model of S. pneumoniae infection the concentration of AA significantly increases in the blood. The impact of AA stress upon the pathogen was then assessed by a combination of biochemical, biophysical and microbiological assays. In vitro bacterial growth and intra-macrophage survival assays revealed that AA has detrimental effects on pneumococcal fitness. Subsequent analyses demonstrated that AA exerts antimicrobial activity via insertion into the pneumococcal membrane, although this did not increase the susceptibility of the bacterium to antibiotic, oxidative or metal ion stress. Transcriptomic profiling showed that AA treatment also resulted in a dramatic down-regulation of the genes involved in fatty acid biosynthesis, in addition to impacts on other metabolic processes, such as carbon-source utilization. Hence, these data reveal that AA has two distinct mechanisms of perturbing the pneumococcal membrane composition. Collectively, this work provides a molecular basis for the antimicrobial contribution of AA to combat pneumococcal infections.en
dc.description.statementofresponsibilityBart A. Eijkelkamp, Stephanie L. Begg, Victoria G. Pederick, Claudia Trapetti, Melissa K. Gregory, Jonathan J. Whittall, James C. Paton and Christopher A. McDevitten
dc.language.isoenen
dc.publisherFrontiers Mediaen
dc.rightsCopyright © 2018 Eijkelkamp, Begg, Pederick, Trapetti, Gregory,Whittall, Paton and McDevitt. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en
dc.subjectHost lipids; free fatty acids; membrane fluidity; macrophages; antibacterial fatty acids; FASIIen
dc.titleArachidonic acid stress impacts pneumococcal fatty acid homeostasisen
dc.typeJournal articleen
dc.identifier.rmid0030088726en
dc.identifier.doi10.3389/fmicb.2018.00813en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1080784en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1122582en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1071659en
dc.relation.granthttp://purl.org/au-research/grants/arc/DP150104515en
dc.relation.granthttp://purl.org/au-research/grants/arc/DP170102102en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1142695en
dc.relation.granthttp://purl.org/au-research/grants/arc/FT170100006en
dc.identifier.pubid421523-
pubs.library.collectionMolecular and Biomedical Science publicationsen
pubs.library.teamDS03en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidEijkelkamp, B. [0000-0003-0179-8977]en
dc.identifier.orcidBegg, S. [0000-0002-7298-9335]en
dc.identifier.orcidGregory, M. [0000-0002-6538-6720]en
dc.identifier.orcidPaton, J. [0000-0001-9807-5278]en
dc.identifier.orcidMcDevitt, C. [0000-0003-1596-4841]en
Appears in Collections:Molecular and Biomedical Science publications

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