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Goodridge, L.

Publications and source records attributed to Goodridge, L..

2 recordsLinked to original sources

TSPDB: A curated resource of tailspike proteins with potential applications in phage research

Phages are ubiquitous viruses that drive bacterial evolution through infection and replication within host bacteria. Phage tailspike proteins (TSPs) are key components of phage tail structures, exhibiting polysaccharide depolymerase activity and host specificity. Despite their potential as novel antimicrobials, few TSPs have been fully characterized due to laborious detection techniques. To address this, we present TSPDB, a curated resource for rapid detection of TSPs in genomics and metagenomics sequence data. We mined public databases, obtaining 17,211 TSP sequences, which were filtered to exclude duplicates and partial sequences, resulting in 8,099 unique TSP sequences. TSPDB contains TSPs from over 400 bacterial genera, with significant diversity among them as revealed by the phylogenetic analysis. The top 13 genera represented were Gram-positive, with Bacillus, Streptococcus, and Clostridium being the most common. Of note, Phage TSPs in Gram-positive bacteria were on average 1 Kbp larger than those in Gram-negative bacteria. TSPDB has been applied in a recent study to screen phage genomes, demonstrating its potential for functional annotation. TSPDB serves as a comprehensive repository and a resource for researchers in phage biology, particularly in phage associated therapy and antimicrobial or biocontrol applications. TSPDB is compatible with bioinformatics tools for in silico detection of TSPs in genomics and metagenomic data, and is freely accessible on GitHub and Figshare, providing a valuable resource for the scientific community.

genomics↗

Phylogenomics of novel clones of Aeromonas veronii recovered from a freshwater lake reveals unique biosynthetic gene clusters

Aquatic ecosystems are important reservoirs for clinically relevant pathogens and antimicrobial resistance genes, thus present a significant risk to global health. Here, we assessed the phylogenomics of Aeromonas veronii (A. veronii) recovered from Lake Wilcox in Ontario using a combination of morphological, biochemical, and whole-genome sequencing (WGS) techniques. Eleven distinct bacterial colonies were isolated and identified as A. veronii (n=9), and two other Aeromonas species (A. caviae and A. allosaccharophila), with significant discrepancies noted between biochemical and WGS identification methods. Of note, 67% (n=6/9) of A. veronii isolates were human pathogens (Pathogenicity score [≥] 0.50). The genomic analysis revealed high genetic diversity among the A. veronii isolates, including the discovery of 41 novel alleles and seven new sequence types (ST) suggesting the lake as a reservoir for multiple human pathogenic clones of this bacterium. The comparison of the newly isolated and sequenced A. veronii with 214 A. veronii genomes revealed significant genetic diversity and suggests potential broad geographical dissemination of strains. Chromosomal genes (OXA-912 and cphA [cphA3, cphA4, cphA7]) genes encoding resistance to {beta}-lactamases were detected in all isolates. Human and non-human pathogenic strains of A. veronii differed in their virulence gene content, with type III secretion systems being associated with human pathogenic isolates. Mobilome analysis revealed the absence of plasmids in A. veronii isolates and the presence of 13 intact the great majority of which were P22-like (Peduoviridae) phages, and nine different insertion sequence families. Novel biosynthetic gene clusters were identified and characterized, indicating the potential for unique secondary metabolite production in A. veronii with different pathogenic potential. Overall, this study underscores the importance of continuous surveillance of aquatic ecosystems for the presence of pathogens, contributing to our understanding of their evolution, potential for human pathogenicity, and the ecological roles of their genetic elements.

microbiology↗