New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model

<p>Abstract</p> <p>Background</p> <p>Antimicrobial peptides (AMPs) are an ancient group of defense molecules. AMPs are widely distributed in nature (being present in mammals, birds, amphibians, insects, plants, and microorganisms). They display bactericidal as well as i...

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Main Authors: Capparelli Rosanna, De Chiara Francesco, Nocerino Nunzia, Montella Rosa, Iannaccone Marco, Fulgione Andrea, Romanelli Alessandra, Avitabile Concetta, Blaiotta Giuseppe, Capuano Federico
Format: Article
Language:English
Published: BMC 2012-11-01
Series:BMC Immunology
Online Access:http://www.biomedcentral.com/1471-2172/13/61
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spelling doaj-d7290216a3a242ec8b7aefe95f0b61752020-11-25T03:57:41ZengBMCBMC Immunology1471-21722012-11-011316110.1186/1471-2172-13-61New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine modelCapparelli RosannaDe Chiara FrancescoNocerino NunziaMontella RosaIannaccone MarcoFulgione AndreaRomanelli AlessandraAvitabile ConcettaBlaiotta GiuseppeCapuano Federico<p>Abstract</p> <p>Background</p> <p>Antimicrobial peptides (AMPs) are an ancient group of defense molecules. AMPs are widely distributed in nature (being present in mammals, birds, amphibians, insects, plants, and microorganisms). They display bactericidal as well as immunomodulatory properties. The aim of this study was to investigate the antimicrobial and anti-inflammatory activities of a combination of two AMPs (temporin B and the royal jellein I) against <it>Staphylococcus epidermidis</it>.</p> <p>Results</p> <p>The temporin B (TB-KK) and the royal jelleins I, II, III chemically modified at the C terminal (RJI-C, RJII-C, RJIII-C), were tested for their activity against 10 different <it>Staphylococcus epidermidis</it> strains, alone and in combination. Of the three royal jelleins, RJI-C showed the highest activity. Moreover, the combination of RJI-C and TB-KK (MIX) displayed synergistic activity. In vitro, the MIX displayed low hemolytic activity, no NO<sub>2</sub><sup>-</sup> production and the ability to curb the synthesis of the pro-inflammatory cytokines TNF-α and IFN-γ to the same extent as acetylsalicylic acid. In vivo, the MIX sterilized mice infected with <it>Staphylococcus epidermidis</it> in eleven days and inhibited the expression of genes encoding the prostaglandin-endoperoxide synthase 2 (COX-2) and CD64, two important parameters of inflammation.</p> <p>Conclusion</p> <p>The study shows that the MIX – a combination of two naturally occurring peptides - displays both antimicrobial and anti-inflammatory activities.</p> http://www.biomedcentral.com/1471-2172/13/61
collection DOAJ
language English
format Article
sources DOAJ
author Capparelli Rosanna
De Chiara Francesco
Nocerino Nunzia
Montella Rosa
Iannaccone Marco
Fulgione Andrea
Romanelli Alessandra
Avitabile Concetta
Blaiotta Giuseppe
Capuano Federico
spellingShingle Capparelli Rosanna
De Chiara Francesco
Nocerino Nunzia
Montella Rosa
Iannaccone Marco
Fulgione Andrea
Romanelli Alessandra
Avitabile Concetta
Blaiotta Giuseppe
Capuano Federico
New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model
BMC Immunology
author_facet Capparelli Rosanna
De Chiara Francesco
Nocerino Nunzia
Montella Rosa
Iannaccone Marco
Fulgione Andrea
Romanelli Alessandra
Avitabile Concetta
Blaiotta Giuseppe
Capuano Federico
author_sort Capparelli Rosanna
title New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model
title_short New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model
title_full New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model
title_fullStr New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model
title_full_unstemmed New perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model
title_sort new perspectives for natural antimicrobial peptides: application as antinflammatory drugs in a murine model
publisher BMC
series BMC Immunology
issn 1471-2172
publishDate 2012-11-01
description <p>Abstract</p> <p>Background</p> <p>Antimicrobial peptides (AMPs) are an ancient group of defense molecules. AMPs are widely distributed in nature (being present in mammals, birds, amphibians, insects, plants, and microorganisms). They display bactericidal as well as immunomodulatory properties. The aim of this study was to investigate the antimicrobial and anti-inflammatory activities of a combination of two AMPs (temporin B and the royal jellein I) against <it>Staphylococcus epidermidis</it>.</p> <p>Results</p> <p>The temporin B (TB-KK) and the royal jelleins I, II, III chemically modified at the C terminal (RJI-C, RJII-C, RJIII-C), were tested for their activity against 10 different <it>Staphylococcus epidermidis</it> strains, alone and in combination. Of the three royal jelleins, RJI-C showed the highest activity. Moreover, the combination of RJI-C and TB-KK (MIX) displayed synergistic activity. In vitro, the MIX displayed low hemolytic activity, no NO<sub>2</sub><sup>-</sup> production and the ability to curb the synthesis of the pro-inflammatory cytokines TNF-α and IFN-γ to the same extent as acetylsalicylic acid. In vivo, the MIX sterilized mice infected with <it>Staphylococcus epidermidis</it> in eleven days and inhibited the expression of genes encoding the prostaglandin-endoperoxide synthase 2 (COX-2) and CD64, two important parameters of inflammation.</p> <p>Conclusion</p> <p>The study shows that the MIX – a combination of two naturally occurring peptides - displays both antimicrobial and anti-inflammatory activities.</p>
url http://www.biomedcentral.com/1471-2172/13/61
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