Abstract

Proline-rich antimicrobial peptides (PR-AMPs) are a group of cationic host defense peptides that are characterized by a high content of proline residues. Up to now, they have been reported in some insects, vertebrate and invertebrate animals, but are not found in plants. In this study, we performed an in silico screening of antimicrobial peptides, which led to discovery of a Brassica napus gene encoding a novel PR-AMP. This gene encodes a 35-amino acid peptide with 13 proline residues, designated BnPRP1. BnPRP1 has 40.5% identity with a known proline-rich antimicrobial peptide SP-B from the pig. BnPRP1 was artificially synthetized and cloned into the prokaryotic expression vector pET30a/His-EDDIE-GFP. Recombinant BnPRP1 was produced in Escherichia coli and has a predicted molecular mass of 3.8 kDa. Analysis of its activity demonstrated that BnPRP1 exhibited strong antimicrobial activity against Gram-positive bacterium, Gram-negative bacterium, yeast and also had strong antifungal activity against several pathogenic fungi, such as Sclerotinia sclerotiorum, Mucor sp., Magnaporthe oryzae and Botrytis cinerea. Circular dichroism (CD) revealed the main secondary structure of BnPRP1 was the random coil. BnPRP1 gene expression detected by qRT-PCR is responsive to pathogen inoculation. At 48 hours after S. sclerotiorum inoculation, the expression of BnPRP1 increased significantly in the susceptible lines while slight decrease occurred in resistant lines. These suggested that BnPRP1 might play a role in the plant defense response against S. sclerotiorum. BnPRP1 isolated from B. napus was the first PR-AMP member that was characterized in plants, and its homology sequences were found in some other Brassicaceae plants by the genome sequences analysis. Compared with the known PR-AMPs, BnPRP1 has the different primary sequences and antimicrobial activity. Above all, this study gives a chance to cast a new light on further understanding about the AMPs’ mechanism and application.

Highlights

  • Antimicrobial peptides (AMPs) are a group of diverse endogenous antibiotics and innate immune components that protect hosts against microbial infection and are produced ubiquitously in the natural environment

  • To identify potential antimicrobial peptides, first batch of sequences (i.e. B. napus ESTs generated in our lab and downloaded from GenBank) were aligned with known AMP sequences

  • BnPRP1 only shared similarity with four known Proline-rich antimicrobial peptides (PR-AMPs), in which SP-B isolated from the porcine salivary gland granules [17], BacFL31 identified from Enterococcus faecium [29], Abaecins isolated from bumblebee and honeybee [30,31]

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Summary

Introduction

Antimicrobial peptides (AMPs) are a group of diverse endogenous antibiotics and innate immune components that protect hosts against microbial infection and are produced ubiquitously in the natural environment. Unlike other types of AMPs, Proline-rich antimicrobial peptides (PR-AMPs) act via distinctive ‘non-lytic’ mechanisms [6,7,8]. PR-AMPs penetrate into microbial membranes without disrupting membranes integrity, and bind to and interact with the specific intracellular target(s). These features make them attractive for both basic and applied research efforts, and provide novel insights into the mechanism of action of anti-infection chemical agents in both bacterial and eukaryotic cells

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