Antimicrobial Susceptibility and Characterization of Resistance Mechanisms of Corynebacteriumurealyticum Clinical Isolates.

dc.contributor.authorChapartegui-González, Itziar
dc.contributor.authorFernández-Martínez, Marta
dc.contributor.authorRodríguez-Fernández, Ana
dc.contributor.authorRocha, Danilo J P
dc.contributor.authorAguiar, Eric R G R
dc.contributor.authorPacheco, Luis G C
dc.contributor.authorRamos-Vivas, José
dc.contributor.authorCalvo, Jorge
dc.contributor.authorMartínez-Martínez, Luis
dc.contributor.authorNavas, Jesús
dc.date.accessioned2025-01-07T16:51:13Z
dc.date.available2025-01-07T16:51:13Z
dc.date.issued2020-07-13
dc.description.abstractCorynebacterium urealyticum is a non-diphtherial urease-producing clinically relevant corynebacterial, most frequently involved in urinary tract infections. Most of the C. urealyticum clinical isolates are frequently resistant to several antibiotics. We investigated the susceptibility of 40 C. urealyticum isolated in our institution during the period 2005-2017 to eight compounds representative of the main clinically relevant classes of antimicrobial agents. Antimicrobial susceptibility was determined by the Epsilometer test. Resistance genes were searched by PCR. All strains were susceptible to vancomycin whereas linezolid and rifampicin also showed good activity (MICs90 = 1 and 0.4 mg/L, respectively). Almost all isolates (39/40, 97.5%) were multidrug resistant. The highest resistance rate was observed for ampicillin (100%), followed by erythromycin (95%) and levofloxacin (95%). Ampicillin resistance was associated with the presence of the blaA gene, encoding a class A β-lactamase. The two rifampicin-resistant strains showed point mutations driving amino acid replacements in conserved residues of RNA polymerase subunit β (RpoB). Tetracycline resistance was due to an efflux-mediated mechanism. Thirty-nine PFGE patterns were identified among the 40 C. urealyticum, indicating that they were not clonally related, but producing sporadic infections. These findings raise the need of maintaining surveillance strategies among this multidrug resistant pathogen.
dc.identifier.doi10.3390/antibiotics9070404
dc.identifier.issn2079-6382
dc.identifier.pmcPMC7400432
dc.identifier.pmid32668585
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC7400432/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2079-6382/9/7/404/pdf?version=1594627779
dc.identifier.urihttps://hdl.handle.net/10668/28030
dc.issue.number7
dc.journal.titleAntibiotics (Basel, Switzerland)
dc.journal.titleabbreviationAntibiotics (Basel)
dc.language.isoen
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCorynebacterium urealyticum
dc.subjectantimicrobials
dc.subjectcoryneform
dc.subjectmultidrug resistance
dc.subjectwhole genome sequencing
dc.titleAntimicrobial Susceptibility and Characterization of Resistance Mechanisms of Corynebacteriumurealyticum Clinical Isolates.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number9

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