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Updated: Aug 9, 2026

A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues
Published on: February 19, 2019
Both msa genes in Renibacterium salmoninarum are needed for full virulence in bacterial kidney disease
Alison M Coady1, Anthony L Murray, Diane G Elliott
1Northwest Fisheries Science Center, 2725 Montlake Boulevard East, Seattle, WA 98112, USA.
Abstract:
Renibacterium salmoninarum, a gram-positive diplococcobacillus that causes bacterial kidney disease among salmon and trout, has two chromosomal loci encoding the major soluble antigen (msa) gene. Because the MSA protein is widely suspected to be an important virulence factor, we used insertion-duplication mutagenesis to generate disruptions of either the msa1 or msa2 gene. Surprisingly, expression of MSA protein in broth cultures appeared unaffected. However, the virulence of either mutant in juvenile chinook salmon (Oncorhynchus tshawytscha) by intraperitoneal challenge was severely attenuated, suggesting that disruption of the msa1 or msa2 gene affected in vivo expression.
Insights
Disrupting the major soluble antigen (msa) gene in Renibacterium salmoninarum did not affect protein levels in vitro but severely reduced virulence in salmonids, indicating its importance in disease.
Area of Science:
- Bacteriology
- Fish Pathology
- Molecular Biology
Background:
- Renibacterium salmoninarum causes bacterial kidney disease in salmonids.
- The major soluble antigen (MSA) protein is a suspected virulence factor.
- Two chromosomal loci, msa1 and msa2, encode the MSA gene.
Purpose of the Study:
- To investigate the role of msa1 and msa2 genes in R. salmoninarum virulence.
- To determine the effect of gene disruption on MSA protein expression and fish disease.
Main Methods:
- Insertion-duplication mutagenesis was used to disrupt msa1 and msa2 genes.
- MSA protein expression was analyzed in broth cultures.
- Virulence of mutant strains was assessed in juvenile chinook salmon (Oncorhynchus tshawytscha) via intraperitoneal challenge.
Main Results:
- Disruption of msa1 or msa2 did not alter MSA protein expression in vitro.
- Mutant strains exhibited severely attenuated virulence in chinook salmon.
- In vivo expression or function of MSA appears critical for disease development.
Conclusions:
- The msa1 and msa2 genes are essential for R. salmoninarum virulence in salmonids.
- MSA protein plays a crucial role in bacterial kidney disease pathogenesis.
- Gene disruption impacts in vivo virulence, not necessarily in vitro protein production.
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