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Experimental antibacterial therapy with puroindolines,lactoferrin and lysozyme in Listeria monocytogenes-infected mice
Authors:Daniela Palumbo  Marco Iannaccone  Amalia Porta  Rosanna Capparelli
Affiliation:1. Groupe d''Etude sur l''Inflammation Chronique et l''Obésité (GEICO), Structure fédérative Environnement Biodiversité Santé-FED4126, Université de La Réunion, Plateforme CYROI, Saint Denis de La Réunion, France;2. Unité fonctionnelle de recherche biochimie, Centre Hospitalier Universitaire Félix Guyon, Saint Denis de La Réunion, France;3. Laboratoire de chimie des substances naturelles et sciences des aliments, Université de La Réunion, Saint Denis de La Réunion, France
Abstract:Puroindoline A and puroindoline B from plant seeds, bovine lactoferrin and chicken eggs lysozyme are antimicrobial proteins of innate immune system that lyse invading organisms. We investigate their potential antibacterial activity against Listeria monocytogenes in a mouse model. Bacteria were isolated from various organs for 7 days after challenge. Livers displayed consistently higher bacterial count (up to 107 cfu/g) than spleens, kidneys and brains. The efficacy of the AMPs was therefore established by measuring the infection level (cfu number) of these organs. Puroindoline A and puroindoline B (5 mg/mouse), lactoferrin and lysozyme (1.25 mg/mouse), intravenously injected individually, inhibited bacterial growth completely. Puroindoline A, puroindoline B and lactoferrin were effective when administered 24 h before infection; lysozyme was effective at the time of infection or 5 days after. Their combined use resulted in the enhancement of individual antibacterial activities. Complete inhibition of bacterial growth was observed using concurrently 0.059 mg/mouse of puroindoline A and 0.019 mg/mouse of puroindoline B, lactoferrin and lysozyme. Individual antimicrobial proteins reduced significantly the expression level of pro-inflammatory cytokines (IL-6, IL-8, INF-γ and TNF-α), acute phase proteins (C-reactive protein and fibrinogen) and the T lymphocyte antigens CD4, CD8a, CD8b and CD25. These results suggest their potential use for the control of L. monocytogenes infections.
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