In vivo activity of Nisin A and Nisin V against Listeria monocytogenes in mice

dc.contributor.authorCampion, Alicia M.
dc.contributor.authorCasey, Pat G.
dc.contributor.authorField, Des
dc.contributor.authorCotter, Paul D.
dc.contributor.authorHill, Colin
dc.contributor.authorRoss, R. Paul
dc.contributor.funderEnterprise Irelanden
dc.contributor.funderHigher Education Authorityen
dc.contributor.funderIrish Research Council for Science Engineering and Technologyen
dc.contributor.funderScience Foundation Irelanden
dc.contributor.funderIrish Government
dc.date.accessioned2016-02-25T17:15:42Z
dc.date.available2016-02-25T17:15:42Z
dc.date.issued2013-02-01
dc.description.abstractBackground: Lantibiotics are post-translationally modified antimicrobial peptides, of which nisin A is the most extensively studied example. Bioengineering of nisin A has resulted in the generation of derivatives with increased in vitro potency against Gram-positive bacteria. Of these, nisin V (containing a Met21Val change) is noteworthy by virtue of exhibiting enhanced antimicrobial efficacy against a wide range of clinical and food-borne pathogens, including Listeria monocytogenes. However, this increased potency has not been tested in vivo. Results: Here we address this issue by assessing the ability of nisin A and nisin V to control a bioluminescent strain of Listeria monocytogenes EGDe in a murine infection model. More specifically, Balb/c mice were infected via the intraperitoneal route at a dose of 1 × 105 cfu/animal and subsequently treated intraperitoneally with either nisin V, nisin A or a PBS control. Bioimaging of the mice was carried out on day 3 of the trial. Animals were then sacrificed and levels of infection were quantified in the liver and spleen. Conclusion: This analysis revealed that nisin V was more effective than Nisin A with respect to controlling infection and therefore merits further investigation with a view to potential chemotherapeutic applications.en
dc.description.sponsorshipHigher Education Authority (Programme for Research in Third-Level Institutions (PRTLI) PhD Programme in Molecular Cell Biology awarded to Alicia Campion); Irish Government (National Development Plan); Science Foundation Ireland (Centre for Science, Engineering and Technology (SFI-CSET) Principal Investigator funding to Paul D. Cotter, Colin Hill and R. Paul Ross)en
dc.description.statusPeer revieweden
dc.description.versionPublished Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.articleid23
dc.identifier.citationCAMPION, A., CASEY, P. G., FIELD, D., COTTER, P. D., HILL, C. & ROSS, R. P. 2013. In vivo activity of Nisin A and Nisin V against Listeria monocytogenes in mice. BMC Microbiology, 13:23, 1-8. http://dx.doi.org/10.1186/1471-2180-13-23en
dc.identifier.doi10.1186/1471-2180-13-23
dc.identifier.endpage8en
dc.identifier.issn1471-2180
dc.identifier.journaltitleBMC Microbiologyen
dc.identifier.startpage1en
dc.identifier.urihttps://hdl.handle.net/10468/2401
dc.identifier.volume13en
dc.language.isoenen
dc.publisherBioMed Central Ltd.en
dc.rights© Campion et al.; licensee BioMed Central Ltd. 2013. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.rights.urihttp://​creativecommons.​org/​licenses/​by/​2.​0en
dc.subjectAntimicrobialen
dc.subjectLantibioticen
dc.subjectBacteriocinen
dc.subjectPeptide engineeringen
dc.subjectMutagenesisen
dc.subjectNisinen
dc.titleIn vivo activity of Nisin A and Nisin V against Listeria monocytogenes in miceen
dc.typeArticle (peer-reviewed)en
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