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Adaptation to the cervical environment is associated with increased antibiotic susceptibility in Neisseria gonorrhoeae

Author

Listed:
  • Kevin C. Ma

    (Harvard T.H. Chan School of Public Health)

  • Tatum D. Mortimer

    (Harvard T.H. Chan School of Public Health)

  • Allison L. Hicks

    (Harvard T.H. Chan School of Public Health)

  • Nicole E. Wheeler

    (Wellcome Genome Campus)

  • Leonor Sánchez-Busó

    (Wellcome Genome Campus)

  • Daniel Golparian

    (Örebro University)

  • George Taiaroa

    (The University of Melbourne at The Peter Doherty Institute for Infection and Immunity)

  • Daniel H. F. Rubin

    (Harvard T.H. Chan School of Public Health)

  • Yi Wang

    (Harvard T.H. Chan School of Public Health)

  • Deborah A. Williamson

    (The University of Melbourne at The Peter Doherty Institute for Infection and Immunity)

  • Magnus Unemo

    (Örebro University)

  • Simon R. Harris

    (Wellcome Genome Campus)

  • Yonatan H. Grad

    (Harvard T.H. Chan School of Public Health
    Brigham and Women’s Hospital and Harvard Medical School)

Abstract

Neisseria gonorrhoeae is an urgent public health threat due to rapidly increasing incidence and antibiotic resistance. In contrast with the trend of increasing resistance, clinical isolates that have reverted to susceptibility regularly appear, prompting questions about which pressures compete with antibiotics to shape gonococcal evolution. Here, we used genome-wide association to identify loss-of-function (LOF) mutations in the efflux pump mtrCDE operon as a mechanism of increased antibiotic susceptibility and demonstrate that these mutations are overrepresented in cervical relative to urethral isolates. This enrichment holds true for LOF mutations in another efflux pump, farAB, and in urogenitally-adapted versus typical N. meningitidis, providing evidence for a model in which expression of these pumps in the female urogenital tract incurs a fitness cost for pathogenic Neisseria. Overall, our findings highlight the impact of integrating microbial population genomics with host metadata and demonstrate how host environmental pressures can lead to increased antibiotic susceptibility.

Suggested Citation

  • Kevin C. Ma & Tatum D. Mortimer & Allison L. Hicks & Nicole E. Wheeler & Leonor Sánchez-Busó & Daniel Golparian & George Taiaroa & Daniel H. F. Rubin & Yi Wang & Deborah A. Williamson & Magnus Unemo &, 2020. "Adaptation to the cervical environment is associated with increased antibiotic susceptibility in Neisseria gonorrhoeae," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17980-1
    DOI: 10.1038/s41467-020-17980-1
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    Cited by:

    1. Mona L. Taouk & George Taiaroa & Sebastian Duchene & Soo Jen Low & Charlie K. Higgs & Darren Y. J. Lee & Shivani Pasricha & Nasra Higgins & Danielle J. Ingle & Benjamin P. Howden & Marcus Y. Chen & Ch, 2024. "Longitudinal genomic analysis of Neisseria gonorrhoeae transmission dynamics in Australia," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    2. Chrispin Chaguza & Dorota Jamrozy & Merijn W. Bijlsma & Taco W. Kuijpers & Diederik Beek & Arie Ende & Stephen D. Bentley, 2022. "Population genomics of Group B Streptococcus reveals the genetics of neonatal disease onset and meningeal invasion," Nature Communications, Nature, vol. 13(1), pages 1-13, December.

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