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Production of an engineered killer peptide in Nicotiana benthamiana by using a Potato virus X expression system

TitoloProduction of an engineered killer peptide in Nicotiana benthamiana by using a Potato virus X expression system
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2005
AutoriDonini, Marcello, Lico Chiara, Baschieri Selene, Conti S., Magliani W., Polonelli L., and Benvenuto Eugenio
RivistaApplied and Environmental Microbiology
Volume71
Paginazione6360-6367
Parole chiaveAmino acids, Anti-Bacterial Agents, antibiotic resistance, Antibodies, Antifungal Agents, antimicrobial activity, article, Bacteria (microorganisms), Bioengineering, Biotechnology, Botryotinia fuckeliana, Botrytis cinerea, Broad spectrum yeast killer toxin, Candida albicans, Capsid Proteins, Chimeric virus particles (CVP), coat protein, Fungi, Fusarium oxysporum, Genetically Modified, Human pathogens, idiotypic antibody, in vitro study, in vivo study, killer peptide, Microbial Sensitivity Tests, molecular dynamics, Molecular farming, Mycotoxin, Nicotiana benthamiana, nonhuman, Pathology, Pectobacterium carotovorum, Peptides, plant disease, Plant Diseases, Plant leaves, plant pathogen interaction, Plants, Plants (botany), polypeptide, Potato virus X, Potexvirus, Potyvirus, product recovery, protein engineering, protein expression, Proteins, Pseudomonas syringae, Pseudomonas syringae pv. tabaci, Recombinant Fusion Proteins, Sequence Analysis, Staphylococcus aureus, Tobacco, Toxic materials, unclassified drug, Virion, virus protein, virus vector, Yeast
Abstract

The decapeptide killer peptide (KP) derived from the sequence of a single-chain, anti-idiotypic antibody acting as a functional internal image of a microbicidal, broad-spectrum yeast killer toxin (KT) was shown to exert a strong microbicidal activity against human pathogens. With the aim to exploit this peptide to confer resistance to plant pathogens, we assayed its antimicrobial activity against a broad spectrum of phytopathogenic bacteria and fungi. Synthetic KP exhibited antimicrobial activity in vitro towards Pseudomonas syringae, Erwinia carotovora, Botrytis cinerea, and Fusarium oxysporum. KP was also expressed in plants by using a Potato virus X (PVX)-derived vector as a fusion to the viral coat protein, yielding chimeric virus particles (CVPs) displaying the heterologous peptide. Purified CVPs showed enhanced antimicrobial activity against the above-mentioned plant pathogens and human pathogens such as Staphylococcus aureus and Candida albicans. Moreover, in vivo assays designed to challenge KP-expressing plants (as CVPs) with Pseudomonas syringae pv. tabaci showed enhanced resistance to bacterial attack. The results indicate that the PVX-based display system is a high-yield, rapid, and efficient method to produce and evaluate antimicrobial peptides in plants, representing a milestone for the large-scale production of high-added-value peptides through molecular farming. Moreover, KP is a promising molecule to be stably engineered in plants to confer broad-spectrum resistance to phytopathogens. Copyright © 2005, American Society for Microbiology. All Rights Reserved.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-26844580747&doi=10.1128%2fAEM.71.10.6360-6367.2005&partnerID=40&md5=c7b88518ab8914fbdb7732258de5a1f4
DOI10.1128/AEM.71.10.6360-6367.2005
Citation KeyDonini20056360