ArticleCurrent microbiology2025
Genomic Constellation of Foodborne Proteus Mirabilis Isolates Harboring AMR, Virulence Genes and Comparative WGS Analysis.
Article in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Comparative genomic analysis of clinical Pseudomonas aeruginosa isolates from Iraq: insights into genome diversity, antimicrobial resistance, and phylogenetic relatedness.Molecular biology reports · 2026Article
- A One Health Perspective onMicroorganisms · 2026Review
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Authors and funding
12 authors.
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Abstract
Proteus mirabilis is a foodborne and environmental pathogen causing catheter-associated urinary tract infections (CAUTIs) with antimicrobial resistance (AMR) and virulence. As the potential of Indian strains remains underexplored, whole-genome sequence (WGS) data of 18 strains were analyzed for AMR, virulence, and genetic relatedness. The disc diffusion method assessed phenotypic AMR. Genomic DNA sequencing was performed on Illumina MiSeq platform, followed by quality control, read assembly, gap closure, and annotation using software tools. Various tools were used to predict antimicrobial resistance genes (ARGs), resistome, virulence, mobile genetic elements (MGEs), pathogenicity, single nucleotide polymorphisms (SNPs), and plasmids. Phylogenetic analysis based on SNPs was performed using maximum likelihood (ML) and neighbor-joining (NJ) methods. All isolates showed resistance to tetracycline but were sensitive to gentamicin, amoxicillin/clavulanic acid, and streptomycin. Genome sizes ranged from 3,824 to 4,296 kb (average 3691.6 ± 164.3) and 5-26 ARGs per isolate. Common intrinsic resistance genes, including tetJ, tet(D), K. pneumoniae KpnF, and amphenicol resistance genes (cat and catA4) were present in all but one isolate. Predominant ARGs were linked to tetracycline, quinolone, cephalosporin, cephamycin, penam, quaternary ammonium compounds, and glycopeptide groups present in MGEs. Isolates contained numerous virulence genes (n = 4785) across 10 categories. The average SNP count was 4114.27 ± 3216.91, with four isolates showing no SNPs. Phylogenetic analysis revealed diversity (D= -1.6910, P = 0.0047) among 86 reference strains. Ongoing monitoring through WGS analysis is essential for understanding and managing infections caused by this pathogen.
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