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Characterization of a Pathogenic Escherichia coli Strain Derived from Oreochromis spp. Farms Using Whole-Genome Sequencing
Published on: December 23, 2022
Single-nucleotide polymorphism phylotyping of Escherichia coli
Florence Hommais1, Sabrina Pereira, Cécile Acquaviva
1UMR 5122, Université Claude Bernard Lyon 1, 10 rue Dubois, 69622 Villeurbanne cedex, France. hommais@univ-lyon1.fr
This study introduces a fast, automated bacterial phylogenetic grouping method using single-nucleotide polymorphisms (SNPs). This technique accurately identifies Escherichia coli groups, offering a more meaningful alternative to traditional methods.
Area of Science:
- Microbiology
- Genetics
- Bioinformatics
Background:
- Phylogenetic grouping is crucial for understanding bacterial diversity and evolution.
- Existing methods like MLST, multilocus enzyme electrophoresis, ribotyping, and PCR phylotyping have limitations in speed, automation, or phylogenetic rigor.
- Escherichia coli exhibits significant genetic diversity, necessitating accurate phylogenetic classification.
Purpose of the Study:
- To develop and validate a rapid, automated phylogenetic grouping technique for bacteria using single-nucleotide polymorphisms (SNPs).
- To establish a robust SNP-based method for classifying Escherichia coli into its main phylogenetic groups (A, B1, E, D, B2) and subgroups.
- To compare the efficacy and meaningfulness of the SNP phylotyping method against established bacterial typing techniques.
Main Methods:
- Selection of 13 informative single-nucleotide polymorphisms (SNPs) from five key genes (trpA, trpB, putP, icdA, polB) previously used in multilocus sequence typing (MLST).
- In silico validation of the SNP approach using existing sequence data from 65 pathogenic Escherichia coli strains.
- Experimental determination of SNPs via dideoxy single-base extension in 183 commensal and clinical Escherichia coli isolates, followed by comparison with established typing methods.
Main Results:
- The SNP phylotyping method demonstrated high consistency with established methods in assigning phylogenetic groups to Escherichia coli strains.
- The method successfully recovered the main phylogenetic groups (A, B1, E, D, B2) and subgroups within the species.
- SNP phylotyping proved to be more meaningful and phylogenetically grounded compared to multilocus enzyme electrophoresis, ribotyping, and PCR phylotyping.
Conclusions:
- The described SNP-based method offers a rapid, automatable, and phylogenetically robust approach for bacterial grouping.
- This SNP phylotyping technique provides more meaningful results than traditional methods for Escherichia coli.
- The SNP approach holds potential for application across a wide range of bacterial species for phylogenetic analysis.
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