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Genomic Characterization and Pathogenicity Island Analysis of 17 Mexican Isolates of Corynebacterium
Mabel Gethsemani Jaimes-Gonzalez1, Roberto Montes-de-Oca-Jimenez1,2, Martha Elba Ruiz-Riva-Palacio2
1Research and Advanced Studies in Animal Health Center, Faculty of Veterinary Medicine and Zootechnics, Autonomy University of the State of Mexico, Km 15.5 Toluca Pan-American Highway Atlacomulco, Toluca C.P. 50200, State of Mexico, Mexico.
Abstract:
Pathogenicity islands (PAIs) are regions of bacterial genomes that harbor genes encoding virulence factors. Identifying molecules that enhance pathogenicity is crucial for understanding the mechanisms pathogens employ to cause disease and their evolution. Corynebacterium pseudotuberculosis (C. pseudotuberculosis) is a pathogenic microorganism that causes caseous lymphadenitis (CLA) in sheep and goats. Despite its prevalence in Mexico, its genetic material has not been analyzed for virulence factors acquired through horizontal gene transfer. Therefore, the aim of this study was to characterize the complete genomes of Mexican C. pseudotuberculosis strains and identify virulence-related genes harbored with PAIs. Seventeen strains of C.pseudotuberculosis biovar ovis isolated from Mexico were whole-genome sequenced using illumina technology, assembled de novo with SPAdes, and annotated using Prokka. PAIs were predicted with GIPSy based on genomic signatures associated with horizontal gene transfer, including G + C deviation, codon usage, virulence factors, transposases, and tRNA-flanking regions. Positive selection was assessed using POTION v1.2 by identifying orthologous groups enriched in non-synonymous substitutions. This represents the first comprehensive PAI analysis of Mexican C. pseudotuberculosis strains, identifying 14 putative pathogenicity islands harboring 51 virulence-associated genes. Additionally, positive selection analysis identified five coding sequences, including radA and rpiB, that are undergoing adaptive evolutionary changes. These findings elucidate the pathogenic mechanisms and genomic plasticity of Mexican C. pseudotuberculosis strains. They also highlight novel genetic targets for vaccine and therapeutic development against CLA.
Insights
This study identified 14 pathogenicity islands (PAIs) and 51 virulence genes in Mexican *Corynebacterium pseudotuberculosis* strains, revealing insights into caseous lymphadenitis (CLA) pathogenesis. These findings offer potential targets for new CLA vaccines and therapies.
Area of Science:
- Bacteriology
- Genomics
- Evolutionary Biology
Background:
- Pathogenicity islands (PAIs) are key genomic regions encoding bacterial virulence factors.
- Understanding these factors is vital for deciphering pathogen evolution and disease mechanisms.
- *Corynebacterium pseudotuberculosis* causes caseous lymphadenitis (CLA) in livestock, prevalent in Mexico, yet its genome lacks comprehensive PAI analysis.
Purpose of the Study:
- To characterize the complete genomes of Mexican *C. pseudotuberculosis* strains.
- To identify virulence-associated genes located within PAIs.
- To investigate genomic plasticity and evolutionary adaptations in these pathogens.
Main Methods:
- Whole-genome sequencing of 17 Mexican *C. pseudotuberculosis* biovar *ovis* strains.
- De novo genome assembly using SPAdes and annotation with Prokka.
- PAI prediction using GIPSy, analyzing genomic signatures of horizontal gene transfer.
- Positive selection analysis using POTION v1.2 to detect adaptive evolution.
Main Results:
- Identification of 14 putative pathogenicity islands (PAIs) in Mexican *C. pseudotuberculosis*.
- Discovery of 51 virulence-associated genes harbored within these PAIs.
- Detection of five coding sequences, including *radA* and *rpiB*, under positive selection, indicating adaptive evolution.
Conclusions:
- This study provides the first comprehensive PAI analysis of Mexican *C. pseudotuberculosis*.
- The identified PAIs and virulence genes offer insights into CLA pathogenesis and bacterial evolution.
- Novel genetic targets for developing vaccines and therapeutics against CLA have been highlighted.
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