vet-lirn-amr-database-2017-2022.xlsx.zip

<b>Abstract</b><b>Background</b><br>Antimicrobial Resistance (AMR) is a major global health challenge, particularly in Africa, where antibiotic misuse worsens resistance. This study aims to identify potential drug targets in imipenem-resistant <i>E. coli</i> isolates from the Vet-LIRN database through a four-phase approach integrating interactive GIS analysis, genomic data analysis, subtractive genomics, and druggability assessments.<b>Methods</b><br>Phase I involved a literature review and the creation of interactive Geographical Information System (GIS) dashboards to examine resistance patterns for Ampicillin, Minocycline, and Imipenem across North America and Africa, using data from the ATLAS and Vet-LIRN databases. Phase II focused on genomic analysis of resistant and susceptible <i>E. coli</i> isolates to identify non-synonymous mutations linked to imipenem resistance. Phase III applied subtractive genomics to identify essential bacterial proteins unique to <i>E. coli</i> and absent in humans and dogs. Phase IV assessed the druggability of these proteins by matching with proteins in DrugBank, and interactions of the matched proteins with drugs in the DrugBank database.<b>Results</b><br>GIS analysis revealed significant geographical variations in resistance, with Africa showing higher resistance to Ampicillin (80%) compared to North America (55%). Genomic analysis identified 337 proteins in the imipenem-resistant <i>E. coli</i> isolates, with 68 considered potential drug targets. Of these, 29 proteins were homologous to DrugBank proteins that interacted with over 1,000 drugs. The cell wall/membrane protein group matched with over 80 drugs, metabolic enzymes group with 166 drugs, transport-related proteins group with more than 700 drugs, regulatory proteins with 1 drug, and DNA methylation/epigenetic proteins group with several drugs.<b>Conclusions</b><br>This study demonstrates that integrating GIS, genomics, substractive genomics, and druggability assessments enhances AMR research and provides a framework for identifying novel drug targets. The matched proteins in DrugBank interacting with over 1,000 drugs offer potential for drug repurposing, particularly against imipenem-resistant <i>E. coli</i> and other multidrug-resistant pathogens.