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National genomic surveillance integrating standardized quantitative susceptibility testing clarifies antimicrobial resistance in Enterobacterales

Author

Listed:
  • Shizuo Kayama

    (National Institute of Infectious Diseases)

  • Koji Yahara

    (National Institute of Infectious Diseases)

  • Yo Sugawara

    (National Institute of Infectious Diseases)

  • Sayoko Kawakami

    (National Institute of Infectious Diseases)

  • Kohei Kondo

    (National Institute of Infectious Diseases)

  • Hui Zuo

    (National Institute of Infectious Diseases)

  • Shoko Kutsuno

    (National Institute of Infectious Diseases)

  • Norikazu Kitamura

    (National Institute of Infectious Diseases)

  • Aki Hirabayashi

    (National Institute of Infectious Diseases)

  • Toshiki Kajihara

    (National Institute of Infectious Diseases)

  • Hitomi Kurosu

    (National Institute of Infectious Diseases)

  • Liansheng Yu

    (National Institute of Infectious Diseases)

  • Masato Suzuki

    (National Institute of Infectious Diseases)

  • Junzo Hisatsune

    (National Institute of Infectious Diseases)

  • Motoyuki Sugai

    (National Institute of Infectious Diseases)

Abstract

Antimicrobial resistance is a global health concern; Enterobacterales resistant to third-generation cephalosporins (3GCs) and carbapenems are of the highest priority. Here, we conducted genome sequencing and standardized quantitative antimicrobial susceptibility testing of 4,195 isolates of Escherichia coli and Klebsiella pneumoniae resistant to 3GCs and Enterobacterales with reduced meropenem susceptibility collected across Japan. Our analyses provided a complete classification of 3GC resistance mechanisms. Analyses with complete reference plasmids revealed that among the blaCTX-M extended-spectrum β-lactamase genes, blaCTX-M-8 was typically encoded in highly similar plasmids. The two major AmpC β-lactamase genes were blaCMY-2 and blaDHA-1. Long-read sequencing of representative plasmids revealed that approximately 60% and 40% of blaCMY-2 and blaDHA-1 were encoded by such plasmids, respectively. Our analyses identified strains positive for carbapenemase genes but phenotypically susceptible to carbapenems and undetectable by standard antimicrobial susceptibility testing. Systematic long-read sequencing enabled reconstruction of 183 complete plasmid sequences encoding three major carbapenemase genes and elucidation of their geographical distribution stratified by replicon types and species carrying the plasmids and potential plasmid transfer events. Overall, we provide a blueprint for a national genomic surveillance study that integrates standardized quantitative antimicrobial susceptibility testing and characterizes resistance determinants.

Suggested Citation

  • Shizuo Kayama & Koji Yahara & Yo Sugawara & Sayoko Kawakami & Kohei Kondo & Hui Zuo & Shoko Kutsuno & Norikazu Kitamura & Aki Hirabayashi & Toshiki Kajihara & Hitomi Kurosu & Liansheng Yu & Masato Suz, 2023. "National genomic surveillance integrating standardized quantitative susceptibility testing clarifies antimicrobial resistance in Enterobacterales," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43516-4
    DOI: 10.1038/s41467-023-43516-4
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    References listed on IDEAS

    as
    1. Allison L Hicks & Nicole Wheeler & Leonor Sánchez-Busó & Jennifer L Rakeman & Simon R Harris & Yonatan H Grad, 2019. "Evaluation of parameters affecting performance and reliability of machine learning-based antibiotic susceptibility testing from whole genome sequencing data," PLOS Computational Biology, Public Library of Science, vol. 15(9), pages 1-21, September.
    2. Silvia Argimón & Melissa A. L. Masim & June M. Gayeta & Marietta L. Lagrada & Polle K. V. Macaranas & Victoria Cohen & Marilyn T. Limas & Holly O. Espiritu & Janziel C. Palarca & Jeremiah Chilam & Man, 2020. "Integrating whole-genome sequencing within the National Antimicrobial Resistance Surveillance Program in the Philippines," Nature Communications, Nature, vol. 11(1), pages 1-15, December.
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