High Prevalence of Arma-16s Rrna Methyltransferase Among Aminoglycoside-Resistant <i>klebsiella Pneumoniae</I> Bloodstream Isolates
| dc.contributor.author | Isler, Burcu | |
| dc.contributor.author | Falconer, Caitlin | |
| dc.contributor.author | Vatansever, Cansel | |
| dc.contributor.author | Ozer, Berna | |
| dc.contributor.author | Cinar, Gule | |
| dc.contributor.author | Aslan, Abdullah Tarik | |
| dc.contributor.author | Paterson, David L. | |
| dc.date.accessioned | 2024-07-05T15:16:30Z | |
| dc.date.available | 2024-07-05T15:16:30Z | |
| dc.date.issued | 2022-12-19 | |
| dc.description | Tukenmez Tigen, Elif/0000-0003-2027-4116; DOGAN, OZLEM/0000-0002-6505-4582; Azap, Alpay/0000-0001-5035-055X; Keske, Şiran/0000-0003-3823-4454; Vatansever, Cansel/0000-0003-3703-1882; Kapmaz, Mahir/0000-0002-4115-3914; Harris, Patrick/0000-0002-2895-0345; Isler, Burcu/0000-0003-1362-2434; Ergonul, Onder/0000-0003-1935-9235 | en_US |
| dc.description.abstract | Introduction. Aminoglycosides are used for the treatment of carbapenemase-producing Klebsiella pneumoniae (CPK) infections. 16S rRNA methyltransferases (RMTs) confer resistance to all aminoglycosides and are often cocarried with NDM. Hypothesis/Gap Statement. There is a dart of studies looking at the aminoglycoside resistance mechanisms for invasive CPK isolates, particularly in OXA-48 endemic settings. Aim. We aimed to determine the prevalence of RMTs and their association with beta lactamases and MLSTs amongst aminoglycoside-resistant CPK bloodstream isolates in an OXA-48 endemic setting. Methodology. CPK isolates (n=181), collected as part of a multicentre cohort study, were tested for amikacin, gentamicin and tobramycin susceptibility using custom-made sensititre plates (GN2XF, Thermo Fisher Scientific). All isolates were previously subjected to whole-genome sequencing. Carbapenemases, RMTs, MLSTs and plasmid incompatibility groups were detected on the assembled genomes. Results. Of the 181 isolates, 109(60 %) were resistant to all three aminoglycosides, and 96 of 109(88 %) aminoglycoside-resistant isolates carried an RMT (85 ArmA, 10 RmtC, 4 RmtF1; three isolates cocarried ArmA and RmtC). Main clonal types associated with ArmA were ST2096 (49/85, 58%) and ST14 (24/85, 28 %), harbouring mainly OXA-232 and OXA-48 +NDM, respectively. RmtC was cocarried with NDM (5/10) on ST395, and NDM +OXA-48 or NDM +KPC (4/10) on ST14, ST15 and ST16. All RMT producers also carried CTX-M- 15, and the majority cocarried SHV-106, TEM-150 and multiple other antibiotic resistance genes. The majority of the isolates harboured a combination of IncFIB, IncH and IncL/M type plasmids. Non-NDM producing isolates remained susceptible to ceftazidime-avibactam. Conclusion. Aminoglycoside resistance amongst CPK bloodstream isolates is extremely common and mainly driven by clonal spread of ArmA carried on ST2096 and ST14, associated with OXA-232 and OXA48 +NDM carriage, respectively. | en_US |
| dc.description.sponsorship | Pfizer Global Medical Grants [56644459]; Advance Queensland Industry Research Fellowship from the Queensland Government | en_US |
| dc.description.sponsorship | This work was supported by Pfizer Global Medical Grants (grant number 56644459). Dr Brian Forde's research is supported by Advance Queensland Industry Research Fellowship from the Queensland Government. | en_US |
| dc.description.sponsorship | Pfizer, (56644459); Pfizer; Queensland Government | |
| dc.identifier.doi | 10.1099/jmm.0.001629 | |
| dc.identifier.issn | 0022-2615 | |
| dc.identifier.issn | 1473-5644 | |
| dc.identifier.scopus | 2-s2.0-85147460921 | |
| dc.identifier.uri | https://doi.org/10.1099/jmm.0.001629 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14411/1645 | |
| dc.language.iso | en | en_US |
| dc.publisher | Microbiology Soc | en_US |
| dc.relation.ispartof | Journal of Medical Microbiology | |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | 16S rRNA methyltransferase | en_US |
| dc.subject | ArmA | en_US |
| dc.subject | aminoglycoside resistance | en_US |
| dc.subject | bloodstream | en_US |
| dc.subject | carbapenem-resistant | en_US |
| dc.subject | Klebsiella pneumoniae | en_US |
| dc.subject | NDM | en_US |
| dc.subject | OXA-48 | en_US |
| dc.subject | OXA-232 | en_US |
| dc.title | High Prevalence of Arma-16s Rrna Methyltransferase Among Aminoglycoside-Resistant <i>klebsiella Pneumoniae</I> Bloodstream Isolates | en_US |
| dc.type | Article | en_US |
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| gdc.author.id | Azap, Alpay/0000-0001-5035-055X | |
| gdc.author.id | Keske, Şiran/0000-0003-3823-4454 | |
| gdc.author.id | Vatansever, Cansel/0000-0003-3703-1882 | |
| gdc.author.id | Kapmaz, Mahir/0000-0002-4115-3914 | |
| gdc.author.id | Ergonul, Onder/0000-0003-1935-9235 | |
| gdc.author.id | Harris, Patrick/0000-0002-2895-0345 | |
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| gdc.author.wosid | Tukenmez Tigen, Elif/AAN-5897-2021 | |
| gdc.author.wosid | DOGAN, OZLEM/M-4757-2017 | |
| gdc.author.wosid | Azap, Alpay/KMA-1874-2024 | |
| gdc.author.wosid | Keske, Şiran/AAG-3483-2019 | |
| gdc.author.wosid | Vatansever, Cansel/KAM-1768-2024 | |
| gdc.author.wosid | Harris, Patrick/P-3813-2014 | |
| gdc.author.wosid | Keske, Şiran/Q-1451-2019 | |
| gdc.author.wosid | Gönen, Mehmet/O-7322-2015 | |
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| gdc.description.department | Atılım University | en_US |
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| gdc.description.issue | 12 | en_US |
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| gdc.oaire.keywords | Methyltransferases | |
| gdc.oaire.keywords | Microbial Sensitivity Tests | |
| gdc.oaire.keywords | beta-Lactamases | |
| gdc.oaire.keywords | Anti-Bacterial Agents | |
| gdc.oaire.keywords | Klebsiella Infections | |
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