Asset Details
Do you wish to reserve the book?
Characterization of aminoglycoside resistance in multidrug-resistant Klebsiella pneumoniae isolates
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Characterization of aminoglycoside resistance in multidrug-resistant Klebsiella pneumoniae isolates
Do you wish to request the book?
Characterization of aminoglycoside resistance in multidrug-resistant Klebsiella pneumoniae isolates
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Journal Article
Characterization of aminoglycoside resistance in multidrug-resistant Klebsiella pneumoniae isolates
2025
Overview
ABSTRACT Multidrug-resistant (MDR) Klebsiella pneumoniae, particularly the lineages resistant to carbapenems and aminoglycosides, is an escalating global public health threat across human, animal, and environmental reservoirs. We examined phenotypic and genetic features of MDR K. pneumoniae isolates. A total of 70 K. pneumoniae strains were collected from clinical (n=55), environmental (n=7), and animal (n=8) sources. To better understand the evolutionary relationship between these isolates, a phylogenetic analysis was performed alongside 35 publicly available K. pneumoniae genomes from NCBI and Pathogenwatch. Whole-genome sequencing (WGS) revealed that 43 isolates carried the blaKPC gene, including blaKPC-2 and blaKPC-3 variants, with different susceptibility profiles to aminoglycosides. Among all isolates, 84% (n = 59/70) were resistant to amikacin and 53% (n = 37/70) were resistant to gentamicin. Aminoglycoside resistance was primarily associated with aminoglycoside-modifying enzymes, including aph(3’)-Ia (52%), aac(3)-IIa/aadA2 (49%), and aac(6’)-Ib-cr (37%). Additionally, 16S rRNA methyltransferases rmtB and rmtG were detected in 14% of isolates and were associated with high-level amikacin MICs. Overall, 81% of strains were non-susceptible to at least one aminoglycoside, underscoring the clinical importance of these determinants. Phylogenetic analysis based on WGS data showed two main clusters (A and B), and the multilocus sequence type ST11 predominated among Brazilian isolates. Our findings showed a heterogeneous distribution of sequence type profiles across the two clusters and a close relationship between K. pneumoniae strains from human, animal, and environmental sources, highlighting the need for integrated One Health surveillance.
Publisher
Instituto De Medicina Tropical De Sao Paulo,Instituto de Medicina Tropical de São Paulo
Subject
/ Aminoglycosides - pharmacology
/ Animals
/ Anti-Bacterial Agents - pharmacology
/ Bacterial Proteins - genetics
/ Brazil
/ Drug Resistance, Multiple, Bacterial - genetics
/ Humans
/ Klebsiella pneumoniae - drug effects
/ Klebsiella pneumoniae - genetics
/ Klebsiella pneumoniae - isolation & purification
