The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection Model

The objective of this study was to investigate the in vivo activity of the lantibiotic lacticin 3147 against the luminescent Staphylococcus aureus strain Xen 29 using a murine model. Female BALB/c mice (7 weeks old, 17 g) were divided into groups (n=5) and infected with the Xen 29 strain via the int...

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Main Authors: Clare Piper, Pat G. Casey, Colin Hill, Paul D. Cotter, R. Paul Ross
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:International Journal of Microbiology
Online Access:http://dx.doi.org/10.1155/2012/806230
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spelling doaj-ab7d5fea6692492bb4fb5008f8adeb9f2021-07-02T01:36:31ZengHindawi LimitedInternational Journal of Microbiology1687-918X1687-91982012-01-01201210.1155/2012/806230806230The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection ModelClare Piper0Pat G. Casey1Colin Hill2Paul D. Cotter3R. Paul Ross4Department of Microbiology, University College Cork, College Road, Cork, IrelandDepartment of Microbiology, University College Cork, College Road, Cork, IrelandDepartment of Microbiology, University College Cork, College Road, Cork, IrelandAlimentary Pharmabiotic Centre, Cork, IrelandAlimentary Pharmabiotic Centre, Cork, IrelandThe objective of this study was to investigate the in vivo activity of the lantibiotic lacticin 3147 against the luminescent Staphylococcus aureus strain Xen 29 using a murine model. Female BALB/c mice (7 weeks old, 17 g) were divided into groups (n=5) and infected with the Xen 29 strain via the intraperitoneal route at a dose of 1×106 cfu/animal. After 1.5 hr, the animals were treated subcutaneously with doses of phosphate-buffered saline (PBS; negative control) or lacticin 3147. Luminescent imaging was carried 3 and 5 hours postinfection. Mice were then sacrificed, and the levels of S. aureus Xen 29 in the liver, spleen, and kidneys were quantified. Notably, photoluminescence and culture-based analysis both revealed that lacticin 3147 successfully controlled the systemic spread of S. aureus in mice thus indicating that lacticin 3147 has potential as a chemotherapeutic agent for in vivo applications.http://dx.doi.org/10.1155/2012/806230
collection DOAJ
language English
format Article
sources DOAJ
author Clare Piper
Pat G. Casey
Colin Hill
Paul D. Cotter
R. Paul Ross
spellingShingle Clare Piper
Pat G. Casey
Colin Hill
Paul D. Cotter
R. Paul Ross
The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection Model
International Journal of Microbiology
author_facet Clare Piper
Pat G. Casey
Colin Hill
Paul D. Cotter
R. Paul Ross
author_sort Clare Piper
title The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection Model
title_short The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection Model
title_full The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection Model
title_fullStr The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection Model
title_full_unstemmed The Lantibiotic Lacticin 3147 Prevents Systemic Spread of Staphylococcus aureus in a Murine Infection Model
title_sort lantibiotic lacticin 3147 prevents systemic spread of staphylococcus aureus in a murine infection model
publisher Hindawi Limited
series International Journal of Microbiology
issn 1687-918X
1687-9198
publishDate 2012-01-01
description The objective of this study was to investigate the in vivo activity of the lantibiotic lacticin 3147 against the luminescent Staphylococcus aureus strain Xen 29 using a murine model. Female BALB/c mice (7 weeks old, 17 g) were divided into groups (n=5) and infected with the Xen 29 strain via the intraperitoneal route at a dose of 1×106 cfu/animal. After 1.5 hr, the animals were treated subcutaneously with doses of phosphate-buffered saline (PBS; negative control) or lacticin 3147. Luminescent imaging was carried 3 and 5 hours postinfection. Mice were then sacrificed, and the levels of S. aureus Xen 29 in the liver, spleen, and kidneys were quantified. Notably, photoluminescence and culture-based analysis both revealed that lacticin 3147 successfully controlled the systemic spread of S. aureus in mice thus indicating that lacticin 3147 has potential as a chemotherapeutic agent for in vivo applications.
url http://dx.doi.org/10.1155/2012/806230
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