In vivo activity of Nisin A and Nisin V against Listeria monocytogenes in mice
dc.contributor.author | Campion, Alicia M. | |
dc.contributor.author | Casey, Pat G. | |
dc.contributor.author | Field, Des | |
dc.contributor.author | Cotter, Paul D. | |
dc.contributor.author | Hill, Colin | |
dc.contributor.author | Ross, R. Paul | |
dc.contributor.funder | Enterprise Ireland | en |
dc.contributor.funder | Higher Education Authority | en |
dc.contributor.funder | Irish Research Council for Science Engineering and Technology | en |
dc.contributor.funder | Science Foundation Ireland | en |
dc.contributor.funder | Irish Government | |
dc.date.accessioned | 2016-02-25T17:15:42Z | |
dc.date.available | 2016-02-25T17:15:42Z | |
dc.date.issued | 2013-02-01 | |
dc.description.abstract | Background: 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.sponsorship | Higher 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.status | Peer reviewed | en |
dc.description.version | Published Version | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.articleid | 23 | |
dc.identifier.citation | CAMPION, 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/10.1186/1471-2180-13-23 | en |
dc.identifier.doi | 10.1186/1471-2180-13-23 | |
dc.identifier.endpage | 8 | en |
dc.identifier.issn | 1471-2180 | |
dc.identifier.journaltitle | BMC Microbiology | en |
dc.identifier.startpage | 1 | en |
dc.identifier.uri | https://hdl.handle.net/10468/2401 | |
dc.identifier.volume | 13 | en |
dc.language.iso | en | en |
dc.publisher | BioMed 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.uri | http://creativecommons.org/licenses/by/2.0 | en |
dc.subject | Antimicrobial | en |
dc.subject | Lantibiotic | en |
dc.subject | Bacteriocin | en |
dc.subject | Peptide engineering | en |
dc.subject | Mutagenesis | en |
dc.subject | Nisin | en |
dc.title | In vivo activity of Nisin A and Nisin V against Listeria monocytogenes in mice | en |
dc.type | Article (peer-reviewed) | en |