Abstract

Yersinia ruckeri is the aetiological agent of enteric redmouth (ERM) disease and is responsible for significant economic losses in farmed salmonids. Enteric redmouth disease is associated primarily with rainbow trout (Oncorhynchus mykiss, Walbaum) but its incidence in Atlantic salmon (Salmo salar) is increasing. Outer membrane proteins (OMPs) of Gram-negative bacteria are located at the host-pathogen interface and play important roles in virulence. The outer membrane of Y. ruckeri is poorly characterised and little is known about its composition and the roles of individual OMPs in virulence. Here, we employed a bioinformatic pipeline to first predict the OMP composition of Y. ruckeri. Comparative proteomic approaches were subsequently used to identify those proteins expressed in vitro in eight representative isolates recovered from Atlantic salmon and rainbow trout. One hundred and forty-one OMPs were predicted from four Y. ruckeri genomes and 77 of these were identified in three or more genomes and were considered as “core” proteins. Gel-free and gel-based proteomic approaches together identified 65 OMPs in a single reference isolate and subsequent gel-free analysis identified 64 OMPs in the eight Atlantic salmon and rainbow trout isolates. Together, our gel-free and gel-based proteomic analyses identified 84 unique OMPs in Y. ruckeri. SignificanceYersinia ruckeri is an important pathogen of Atlantic salmon and rainbow trout and is of major economic significance to the aquaculture industry worldwide. Disease outbreaks are becoming more problematic in Atlantic salmon and there is an urgent need to investigate in further detail the cell-surface (outer membrane) composition of strains infecting each of these host species. Currently, the outer membrane of Y. ruckeri is poorly characterised and very little is known about the OMP composition of strains infecting each of these salmonid species. This study represents the most comprehensive comparative outer membrane proteomic analysis of Y. ruckeri to date, encompassing isolates of different biotypes, serotypes, OMP-types and hosts of origin and provides insights into the potential roles of these diverse proteins in host-pathogen interactions. The study has identified key OMPs likely to be involved in disease pathogenesis and makes a significant contribution to furthering our understanding of the cell-surface composition of this important fish pathogen that will be relevant to the development of improved vaccines and therapeutics.

Highlights

  • The Gram-negative enterobacterium Yersinia ruckeri is the aetiological agent of enteric redmouth disease (ERM) of fish and has been recovered worldwide [1,2,3,4,5] from many different species [5,6,7,8,9,10]

  • Gel-free proteomics was subsequently used to identify and compare the expression of Outer membrane proteins (OMPs) in the eight Y. ruckeri isolates from Atlantic salmon and rainbow trout

  • We aimed to identify OMPs of Y. ruckeri that were uniquely associated with a single host species and putatively involved in host adaptation to Atlantic salmon or rainbow trout

Read more

Summary

Introduction

The Gram-negative enterobacterium Yersinia ruckeri is the aetiological agent of enteric redmouth disease (ERM) of fish and has been recovered worldwide [1,2,3,4,5] from many different species [5,6,7,8,9,10]. Farmed salmonid fish, rainbow trout (Oncorhynchus mykiss, Walbaum) and Atlantic salmon (Salmo salar), are most commonly affected and the disease can lead to significant economic losses [11]. ERM is characterised by a haemorrhagic septicaemia and haemorrhages in and around the oral cavity, leading to the name ‘redmouth’ disease [1,5,12]. Vaccination plays an important role in protecting rainbow trout and Atlantic salmon against Y. ruckeri. In recent years, there has been an increasing incidence of vaccine breakdown in Atlantic salmon, largely because current vaccines are aimed at rainbow trout and based on serotypes specific to this species [15,16,17,18].

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call