Aminoglycoside Resistance: Updates with a Focus on Acquired 16S Ribosomal RNA Methyltransferases

Jun Ichi Wachino; Yohei Doi; Yoshichika Arakawa

doi:10.1016/j.idc.2020.06.002

Aminoglycoside Resistance: Updates with a Focus on Acquired 16S Ribosomal RNA Methyltransferases

Research output: Contribution to journal › Review article › peer-review

Abstract

The clinical usefulness of aminoglycosides has been revisited as an effective choice against β-lactam–resistant and fluoroquinolone-resistant gram-negative bacterial infections. Plazomicin, a next-generation aminoglycoside, was introduced for the treatment of complicated urinary tract infections and acute pyelonephritis. In contrast, bacteria have resisted aminoglycosides, including plazomicin, by producing 16S ribosomal RNA (rRNA) methyltransferases (MTases) that confer high-level and broad-range aminoglycoside resistance. Aminoglycoside-resistant 16S rRNA MTase-producing gram-negative pathogens are widespread in various settings and are becoming a grave concern. This article provides up-to-date information with a focus on aminoglycoside-resistant 16S rRNA MTases.

Original language	English
Pages (from-to)	887-902
Number of pages	16
Journal	Infectious Disease Clinics of North America
Volume	34
Issue number	4
DOIs	https://doi.org/10.1016/j.idc.2020.06.002
Publication status	Published - 12-2020
Externally published	Yes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

Microbiology (medical)
Infectious Diseases

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10.1016/j.idc.2020.06.002

Cite this

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title = "Aminoglycoside Resistance: Updates with a Focus on Acquired 16S Ribosomal RNA Methyltransferases",

abstract = "The clinical usefulness of aminoglycosides has been revisited as an effective choice against β-lactam–resistant and fluoroquinolone-resistant gram-negative bacterial infections. Plazomicin, a next-generation aminoglycoside, was introduced for the treatment of complicated urinary tract infections and acute pyelonephritis. In contrast, bacteria have resisted aminoglycosides, including plazomicin, by producing 16S ribosomal RNA (rRNA) methyltransferases (MTases) that confer high-level and broad-range aminoglycoside resistance. Aminoglycoside-resistant 16S rRNA MTase-producing gram-negative pathogens are widespread in various settings and are becoming a grave concern. This article provides up-to-date information with a focus on aminoglycoside-resistant 16S rRNA MTases.",

author = "Wachino, \{Jun Ichi\} and Yohei Doi and Yoshichika Arakawa",

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doi = "10.1016/j.idc.2020.06.002",

language = "English",

volume = "34",

pages = "887--902",

journal = "Infectious Disease Clinics of North America",

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T1 - Aminoglycoside Resistance

T2 - Updates with a Focus on Acquired 16S Ribosomal RNA Methyltransferases

AU - Wachino, Jun Ichi

AU - Doi, Yohei

AU - Arakawa, Yoshichika

PY - 2020/12

Y1 - 2020/12

N2 - The clinical usefulness of aminoglycosides has been revisited as an effective choice against β-lactam–resistant and fluoroquinolone-resistant gram-negative bacterial infections. Plazomicin, a next-generation aminoglycoside, was introduced for the treatment of complicated urinary tract infections and acute pyelonephritis. In contrast, bacteria have resisted aminoglycosides, including plazomicin, by producing 16S ribosomal RNA (rRNA) methyltransferases (MTases) that confer high-level and broad-range aminoglycoside resistance. Aminoglycoside-resistant 16S rRNA MTase-producing gram-negative pathogens are widespread in various settings and are becoming a grave concern. This article provides up-to-date information with a focus on aminoglycoside-resistant 16S rRNA MTases.

AB - The clinical usefulness of aminoglycosides has been revisited as an effective choice against β-lactam–resistant and fluoroquinolone-resistant gram-negative bacterial infections. Plazomicin, a next-generation aminoglycoside, was introduced for the treatment of complicated urinary tract infections and acute pyelonephritis. In contrast, bacteria have resisted aminoglycosides, including plazomicin, by producing 16S ribosomal RNA (rRNA) methyltransferases (MTases) that confer high-level and broad-range aminoglycoside resistance. Aminoglycoside-resistant 16S rRNA MTase-producing gram-negative pathogens are widespread in various settings and are becoming a grave concern. This article provides up-to-date information with a focus on aminoglycoside-resistant 16S rRNA MTases.

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U2 - 10.1016/j.idc.2020.06.002

DO - 10.1016/j.idc.2020.06.002

M3 - Review article

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VL - 34

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JO - Infectious Disease Clinics of North America

JF - Infectious Disease Clinics of North America

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ER -

Aminoglycoside Resistance: Updates with a Focus on Acquired 16S Ribosomal RNA Methyltransferases

Abstract

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All Science Journal Classification (ASJC) codes

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