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Mitchell, Robert J.
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Heteroresistance to amikacin in Klebsiella aerogenes isolates from patients in an intensive care unit in Brazil

Author(s)
Crispim, Natalia RibeiroNunes, Gustavo DantasSoares, Gabriela GuerreraShilling, Rebecca ElizabethFerreira, Roumayne LopesCampos, Leslie CameloAlcobaca, Olinda Soares Athaideda Silva, Joao Pedro Maia de OliveiraRodrigues, Saulo HenriquePitondo-Silva, AndreFuentes, Andrea Soares da Costada Cunha, Anderson FerreiraMitchell, Robert J.Pranchevicius, Maria-Cristina da Silva
Issued Date
2026-04
DOI
10.1128/spectrum.02833-25
URI
https://scholarworks.unist.ac.kr/handle/201301/91648
Fulltext
https://journals.asm.org/doi/10.1128/spectrum.02833-25
Citation
MICROBIOLOGY SPECTRUM, v.14, no.4, pp.e0283325
Abstract
Heteroresistance is defined by the presence of subpopulations within a bacterial isolate that exhibit greater antibiotic resistance than the dominant population. In this study, we investigated amikacin heteroresistance in the opportunistic, nosocomial pathogen Klebsiella aerogenes (AHR-KA). Eight carbapenemase-resistant, but amikacin-susceptible, isolates from intensive care units of a Brazilian hospital were analyzed. Population analysis profiling identified five amikacin heteroresistant isolates (AHR-KA-1 to 5), with subpopulation frequencies ranging from 1.83 & times; 10-7 to 6.01 & times; 10-6. Among these, only AHR-KA-1 exhibited stable heteroresistance following serial passaging in antibiotic-free media. AHR-KA-1 demonstrated only slightly reduced growth rates when compared with those of the unstable AHR-KAs, parental, and control strains, suggesting no significant fitness cost associated with drug resistance. Time-kill assays for AHR-KA-1 showed an initial decline in cell viability, followed by regrowth at both 4 & times; and 8 & times; MIC. The draft genome of the stable isolate had a total length and G+C content similar to most of the sequenced genomes from K. aerogenes. Notably, AHR-KA-1 ' s aac(6 ')-Ib-cr variant contained D179Y and R102W mutations, conferring amikacin resistance. Moreover, quantitative reverse transcription PCR revealed significantly elevated expression of the aac(6 ')-Ib-cr gene in AHR-KA-1 before amikacin-free passage, compared to both the parental strain and the AHR-KA-1 strain after drug-free passage. Therefore, this study identified amikacin heteroresistance in carbapenemase-producing K. aerogenes, including a stable, mutation-driven phenotype with low fitness cost and rapid regrowth under high amikacin concentrations, underscoring its clinical relevance. These findings reinforce the importance of detecting heteroresistant subpopulations and strengthening surveillance to prevent treatment failure and the spread of undetected resistance.IMPORTANCEKlebsiella aerogenes, an opportunistic human pathogen, is frequently implicated in severe and invasive infections, particularly in immunocompromised individuals. The growing prevalence of antibiotic resistance among these strains poses a significant therapeutic challenge. The phenomenon of heteroresistance further complicates management, potentially leading to diagnostic difficulties due to the lack of standardized detection methods and subsequent treatment failures. Our studies identified and characterized K. aerogenes strains heteroresistant to amikacin, isolated from patients in an intensive care unit. Such data can serve as a foundational reference for understanding the clinical relevance, genomic variability, and pathogenic potential of K. aerogenes heteroresistance to antibiotics used in clinical settings.
Publisher
AMER SOC MICROBIOLOGY
ISSN
2165-0497
Keyword (Author)
whole-genome sequencingheteroresistanceintensive care unitresistance genesKlebsiella aerogenesamikacin
Keyword
COLISTIN HETERORESISTANCEAAC(6')-IB-CRGENESMUTATIONSEMRERESISTANCE

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