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Published on: November 23, 2012
Streptococcus agalactiae and Streptococcus difficile 16S-23S intergenic rDNA: genetic homogeneity and
B R Berridge1, H Bercovier, P F Frelier
1Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843, USA. bberridge@cvm.tamu.edu
Abstract:
Streptococcus difficile is a non-hemolytic Gram-positive bacterial coccus that causes septicemia and meningoencephalitis in farmed tilapia (Oreochromis sp.) and rainbow trout (Oncorhynchus mykiss). Recent studies have demonstrated S. difficile to be a group B, type Ib streptococcus with a whole cell protein electrophoretic profile indistinguishable from S. agalactiae and a biochemical profile similar to that observed for other group B, type Ib streptococci isolated from fish and frogs. The aim of this study was to expand on these findings by comparative nucleic acid sequence analysis of the 16S-23S ribosomal DNA (rDNA) intergenic spacers of S. difficile and S. agalactiae. The 97.7% sequence homology identified in these studies supports the taxonomic relationship of these two organisms. The sequence data generated were also used to construct a pair of species-specific PCR primers for use in molecular detection and identification schemes.
Insights
Streptococcus difficile, a fish pathogen, is taxonomically related to Streptococcus agalactiae, sharing 97.7% DNA sequence homology. This finding aids in developing new PCR detection methods for fish bacterial infections.
Area of Science:
- Veterinary Microbiology
- Aquatic Animal Health
- Bacterial Taxonomy
Background:
- Streptococcus difficile causes septicemia and meningoencephalitis in farmed tilapia and rainbow trout.
- Previous research indicated S. difficile is a group B, type Ib streptococcus, similar to S. agalactiae.
Purpose of the Study:
- To confirm the taxonomic relationship between S. difficile and S. agalactiae.
- To develop species-specific PCR primers for detecting S. difficile in fish.
Main Methods:
- Comparative nucleic acid sequence analysis of the 16S-23S ribosomal DNA (rDNA) intergenic spacers.
- Construction of species-specific PCR primers.
Main Results:
- Identified 97.7% sequence homology between the 16S-23S rDNA intergenic spacers of S. difficile and S. agalactiae.
- Successfully generated species-specific PCR primers.
Conclusions:
- The high sequence homology supports the close taxonomic relationship between S. difficile and S. agalactiae.
- The developed PCR primers are suitable for molecular detection and identification of S. difficile.
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