Genomic Characterization of Extensively Drug-Resistant NDM-Producing Acinetobacter baumannii Clinical Isolates With the Emergence of Novel blaADC-257

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorZafer, Mai M
dc.contributor.authorHussein, Amira F. A
dc.contributor.authorAl-Agamy, Mohamed H
dc.contributor.authorRadwan, Hesham H
dc.contributor.authorHamed, Samira M
dc.date.accessioned2021-12-13T08:00:31Z
dc.date.available2021-12-13T08:00:31Z
dc.date.issued22/11/2021
dc.descriptionScopusen_US
dc.description.abstractAcinetobacter baumannii has become a major challenge to clinicians worldwide due to its high epidemic potential and acquisition of antimicrobial resistance. This work aimed at investigating antimicrobial resistance determinants and their context in four extensively drug-resistant (XDR) NDM-producing A. baumannii clinical isolates collected between July and October 2020 from Kasr Al-Ainy Hospital, Cairo, Egypt. A total of 20 A. baumannii were collected and screened for acquired carbapenemases (blaNDM, blaVIM and blaIMP) using PCR. Four NDM producer A. baumannii isolates were identified and selected for whole-genome sequencing, in silico multilocus sequence typing, and resistome analysis. Antimicrobial susceptibility profiles were determined using disk diffusion and broth microdilution tests. All blaNDM-positive A. baumannii isolates were XDR. Three isolates belonged to high-risk international clones (IC), namely, IC2 corresponding to ST570Pas/1701Oxf (M20) and IC9 corresponding to ST85Pas/ST1089Oxf (M02 and M11). For the first time, we report blaNDM-1 gene on the chromosome of an A. baumannii strain that belongs to sequence type ST164Pas/ST1418Oxf. Together with AphA6, blaNDM-1 was bracketed by two copies of ISAba14 in ST85Pas isolates possibly facilitating co-transfer of amikacin and carbapenem resistance. A novel blaADC allele (blaADC-257) with an upstream ISAba1 element was identified in M19 (ST/CC164Pas and ST1418Oxf/CC234Oxf). blaADC genes harbored by M02 and M11 were uniquely interrupted by IS1008. Tn2006-associated blaOXA-23 was carried by M20. blaOXA-94 genes were preceded by ISAba1 element in M02 and M11. AbGRI3 was carried by M20 hosting the resistance genes aph(3`)-Ia, aac(6`)-Ib`, catB8, ant(3``)-Ia, sul1, armA, msr(E), and mph(E). Nonsynonymous mutations were identified in the quinolone resistance determining regions (gyrA and parC) of all isolates. Resistance to colistin in M19 was accompanied by missense mutations in lpxACD and pmrABC genes. The current study provided an insight into the genomic background of XDR phenotype in A. baumannii recovered from patients in Egypt. WGS revealed strong association between resistance genes and diverse mobile genetic elements with novel insertion sites and genetic organizations. Copyright © 2021 Zafer, Hussein, Al-Agamy, Radwan and Hamed.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=21100226442&tip=sid&clean=0
dc.identifier.citationZafer MM, Hussein AFA, Al-Agamy MH, Radwan HH and Hamed SM (2021) Genomic Characterization of Extensively Drug- Resistant NDM-Producing Acinetobacter baumannii Clinical Isolates With the Emergence of Novel blaADC-257. Front. Microbiol. 12:736982. doi: 10.3389/fmicb.2021.736982en_US
dc.identifier.doihttps://doi.org/10.3389/fmicb.2021.736982
dc.identifier.otherhttps://doi.org/10.3389/fmicb.2021.736982
dc.identifier.urihttp://repository.msa.edu.eg/xmlui/handle/123456789/4795
dc.language.isoen_USen_US
dc.publisherFrontiers Media S.A.en_US
dc.relation.ispartofseriesFrontiers in Microbiology.;Volume 1222 November 2021 Article number 736982
dc.subjectAcinetobacter baumanniien_US
dc.subjectAcinetobacter baumanniien_US
dc.subjectblaNDMen_US
dc.subjectextensive drug resistanceen_US
dc.subjecthealthcare-associated infectionsen_US
dc.subjectmultilocus sequence typingen_US
dc.subjectwhole-genome sequencing associated infectionsen_US
dc.subjectmultilocus sequence typingen_US
dc.subjectwhole-genome sequencingen_US
dc.titleGenomic Characterization of Extensively Drug-Resistant NDM-Producing Acinetobacter baumannii Clinical Isolates With the Emergence of Novel blaADC-257en_US
dc.typeArticleen_US

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