دورية أكاديمية

In vitro activity of apramycin against 16S-RMTase-producing Gram-negative isolates

التفاصيل البيبلوغرافية
العنوان: In vitro activity of apramycin against 16S-RMTase-producing Gram-negative isolates
المؤلفون: Caméléna, François, Liberge, Mathilde, Rezzoug, Inès, Merimèche, Manel, Naas, Thierry, Berçot, Béatrice
المساهمون: Infection, Anti-microbiens, Modélisation, Evolution (IAME (UMR_S_1137 / U1137)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)-Université Sorbonne Paris Nord
المصدر: ISSN: 2213-7165.
بيانات النشر: HAL CCSD
Elsevier
سنة النشر: 2023
المجموعة: Université Paris 13: HAL
مصطلحات موضوعية: Aminoglycosides, 16S rRNA methyltransferases, ArmA, RmtB, AAC(3)-IV, Gram-negative bacilli, [SDV]Life Sciences [q-bio]
الوصف: International audience ; Objectives: Apramycin is an aminoglycoside (AG) with a unique structure that is little affected by plasmid-mediated mechanisms of AG resistance, including most AG-modifying enzymes and 16S rRNA methyltransferases (16S-RMTases). We evaluate the activity of apramycin against a collection of 16S-RMTase-producing isolates, including Enterobacterales, non-fermenting bacteria, and carbapenemase producers. Methods: In total, 164 non-duplicate 16S-RMTase-producing isolates, including 84 Enterobacterales, 53 Acinetobacter baumannii and 27 Pseudomonas aeruginosa isolates, were included in the study. Wholegenome sequencing (WGS) was performed on all isolates with Illumina technology. The minimum inhibitory concentration (MIC) of apramycin was determined by broth microdilution with customized Sensititre plates (Thermo Fisher Scientific, Dardilly, France). Results: We found that 95% (156/164) of the 16S-RMTase-producing isolates were susceptible to apramycin, with a MIC 50 of 4 mg/L and a MIC 90 of 16 mg/L, respectively. Resistance rates were higher in P. aeruginosa (11%) than in A. baumannii (4%) or Enterobacterales (4%) (P < 0.0 0 01 for each comparison). Eight isolates were resistant to apramycin, including one isolate with an MIC > 64 mg/L due to the acquisition of the aac(3)-IV gene. The genetic environment of the aac(3)-IV gene was similar to that in the pAH01-4 plasmid of an Escherichia coli isolate from chicken in China. Conclusion: Resistance to apramycin remains rare in 16S-RMTase-producing isolates. Apramycin may, therefore, be an interesting alternative treatment for infections caused by 16S-RMTase and carbapenemase producers.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: hal-04088355; https://u-paris.hal.science/hal-04088355Test; https://u-paris.hal.science/hal-04088355/documentTest; https://u-paris.hal.science/hal-04088355/file/apramycin.pdfTest
DOI: 10.1016/j.jgar.2023.02.005
الإتاحة: https://doi.org/10.1016/j.jgar.2023.02.005Test
https://u-paris.hal.science/hal-04088355Test
https://u-paris.hal.science/hal-04088355/documentTest
https://u-paris.hal.science/hal-04088355/file/apramycin.pdfTest
حقوق: http://creativecommons.org/licenses/by-nc-ndTest/ ; info:eu-repo/semantics/OpenAccess
رقم الانضمام: edsbas.35944FFC
قاعدة البيانات: BASE