Combined in silico approach and whole genome sequencing: Acinetobacter baumannii ST218 isolate harboring ADC-73 β-lactamase which has a similar C-loop with ADC-56 and ADC-68 β-lactamase

dc.authorid0000-0002-7757-6812en_US
dc.contributor.authorGülbüz, Melike
dc.contributor.authorSaral Sarıyer, Ayşegül
dc.date.accessioned2022-05-18T06:34:40Z
dc.date.available2022-05-18T06:34:40Z
dc.date.issued2022
dc.departmentAÇÜ, Sağlık Bilimleri Fakültesi, Beslenme ve Diyetetik Bölümüen_US
dc.description.abstractPurpose: Multidrug-resistant Acinetobacter baumannii is a noteworthy nosocomial-pathogen and these pathogen-borne infections are difficult to treat. It is significant to make strain typing with WGS and to add new genome data to the literature. Therefore, in our study, we aimed to strain typing of the A. baumannii (A24) isolated from Turkey and reveal informations about ADC-73 ?-lactamase. Methods: VITEK 2 system was used for the determination of antibiotic susceptibility. WGS was done on the Illumina NovaSeq 6000 platform. WGS results were analyzed with VFDB, ResFinder, PubMLST, IS Finder. Web-based bioinformatics software, homology modelling, molecular docking and dynamics simulations were used to determine all structural information about ADC-73 ?-lactamase. Results: A24 was found to be multidrug-resistant. Various virulence factors were found in A24. The sequence type of the isolate was determined as ST218. Genes encoding ?-lactamase and aminoglycoside modifying enzymes, and IS elements were present in the genome of A24. Besides, secondary and 3D structures of ADC-73 were analyzed. Following, cefepime and imipenem were docked to ADC-56, ADC-68, and ADC-73 and interactions and stability of substrates were simulated. The binding-energies of imipenem to ADC-68 and ADC-73 were calculated ?9.44 and ?5.98 kcal/mol, respectively. Likewise, binding-energies of cefepime to ADC-56 and ADC-73 were calculated as ?19.84 and ?36.54 kcal/mol. Conclusion: A. baumannii ST218 isolate containing ADC-73 was reported for the first time in Turkey by WGS, and the effect of G225S mutation in this ?-lactamase on conformational change and possible interactions with cefepime and impinem were investigated in silico.
dc.identifier.citationGülbüz, M., & Sariyer, A. S. (2022). Combined in silico approach and whole genome sequencing: Acinetobacter baumannii ST218 isolate harboring ADC-73 β-lactamase which has a similar C-loop with ADC-56 and ADC-68 β-lactamase. Journal of Molecular Graphics and Modelling, 108195.en_US
dc.identifier.doi10.1016/j.jmgm.2022.108195
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://hdl.handle.net/11494/3832
dc.identifier.volume114en_US
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorSaral Sarıyer, Ayşegül
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.relation.ispartofJournal of Molecular Graphics and Modelling
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectADC-73 β-lactamaseen_US
dc.subjectWhole genome analysisen_US
dc.subjectA. baumanniien_US
dc.subjectHomology modellingen_US
dc.subjectBioinformatics analysisen_US
dc.subjectMolecular dynamics simulationsen_US
dc.titleCombined in silico approach and whole genome sequencing: Acinetobacter baumannii ST218 isolate harboring ADC-73 β-lactamase which has a similar C-loop with ADC-56 and ADC-68 β-lactamaseen_US
dc.typeArticle

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