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dc.contributor.authorRekadwad, Bhagwan Narayan
dc.contributor.authorPramod, Nanditha
dc.contributor.authorRao, Manik Prabhu Narsing
dc.contributor.authorHashem, Abeer
dc.contributor.authorAvila-Quezada, Graciela Dolores
dc.contributor.authorAbd_Allah, Elsayed Fathi
dc.date.accessioned2024-04-10T01:58:32Z
dc.date.available2024-04-10T01:58:32Z
dc.date.issued2023
dc.identifier10.1016/j.sjbs.2023.103869
dc.identifier.issn1319562X
dc.identifier.urihttps://hdl.handle.net/20.500.12728/10733
dc.description.abstractThe detection of developing antimicrobial resistance (AMR) has become a global issue. The detection of developing antimicrobial resistance has become a global issue. The growing number of AMR bacteria poses a new threat to public health. Therefore, a less laborious and quick confirmatory test becomes important for further investigations into developing AMR in the environment and in clinical settings. This study aims to present a comprehensive analysis and validation of unique and antimicrobial-resistant strains from the WHO priority list of antimicrobial-resistant bacteria and previously reported AMR strains such as Acinetobacter baumannii, Aeromonas spp., Anaeromonas frigoriresistens, Anaeromonas gelatinfytica, Bacillus spp., Campylobacter jejuni subsp. jejuni, Enterococcus faecalis, Escherichia coli, Haemophilus influenzae, Helicobacter pylori, Klebsiella pneumonia subsp. pneumoniae, Pseudomonas aeruginosa, Salmonella enterica subsp. enterica serovar Typhimurium, Thermanaeromonas toyohensis, and Vibrio proteolyticus. Using in-house designed gene-specific primers, 18 different antibiotic resistance genes (algJ, alpB, AQU-1, CEPH-A3, ciaB, CMY-1-MOX-7, CMY-1-MOX-9, CMY-1/MOX, cphA2, cphA5, cphA7, ebpA, ECP_4655, fliC, OXA-51, RfbU, ThiU2, and tolB) from 46 strains were selected and validated. Hence, this study provides insight into the identification of strain-specific, unique antimicrobial resistance genes. Targeted amplification and verification using selected unique marker genes have been reported. Thus, the present detection and validation use a robust method for the entire experiment. Results also highlight the presence of another set of 18 antibiotic-resistant and unique genes (Aqu1, cphA2, cphA3, cphA5, cphA7, cmy1/mox7, cmy1/mox9, asaI, ascV, asoB, oxa-12, acr-2, pepA, uo65, pliI, dr0274, tapY2, and cpeT). Of these sets of genes, 15 were found to be suitable for the detection of pathogenic strains belonging to the genera Aeromonas, Pseudomonas, Helicobacter, Campylobacter, Enterococcus, Klebsiella, Acinetobacter, Salmonella, Haemophilus, and Bacillus. Thus, we have detected and verified sets of unique and antimicrobial resistance genes in bacteria on the WHO Priority List and from published reports on AMR bacteria. This study offers advantages for confirming antimicrobial resistance in all suspected AMR bacteria and monitoring the development of AMR in non-AMR bacteria, in the environment, and in clinical settings. © 2023 The Author(s)es_ES
dc.description.sponsorshipDeemed to be University; King Saud University, KSUes_ES
dc.language.isoenes_ES
dc.publisherElsevier B.V.es_ES
dc.subjectAntimicrobial resistancees_ES
dc.subjectGenome-based detection methodes_ES
dc.subjectMolecular detection of pathogenic bacteriaes_ES
dc.subjectMultiplex PCRes_ES
dc.subjectPathogenic bacterial strainses_ES
dc.subjectStrain-specific geneses_ES
dc.titleIdentification and specificity validation of unique and antimicrobial resistance genes to trace suspected pathogenic AMR bacteria and to monitor the development of AMR in non-AMR strains in the environment and clinical settingses_ES
dc.typeArticlees_ES


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