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Adaptation to the cervical environment is associated with increased antibiotic susceptibility in Neisseria gonorrhoeae
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Centre for Genomic Pathogen Surveillance, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
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2020 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 11, no 1, article id 4126Article in journal (Refereed) Published
Abstract [en]

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.

Place, publisher, year, edition, pages
Nature Publishing Group, 2020. Vol. 11, no 1, article id 4126
National Category
Infectious Medicine
Identifiers
URN: urn:nbn:se:oru:diva-85129DOI: 10.1038/s41467-020-17980-1ISI: 000563565300017PubMedID: 32807804Scopus ID: 2-s2.0-85089466060OAI: oai:DiVA.org:oru-85129DiVA, id: diva2:1464933
Note

Funding Agencies:

United States Department of Health & Human Services

National Institutes of Health (NIH) - USA

NIH National Institute of Allergy & Infectious Diseases (NIAID) F32AI1451571R01AI132606-01

Smith Family Foundation  

National Science Foundation (NSF) NSF - Office of the Director (OD)

United States Department of Health & Human Services

National Institutes of Health (NIH) - USA

NIH National Institute of General Medical Sciences (NIGMS) T32GM007753

National Health and Medical Research Council of Australia GNT1123854

Research Computing Group at Harvard Medical School  

Meningitis Research Foundation (MRF)

Available from: 2020-09-08 Created: 2020-09-08 Last updated: 2023-03-28Bibliographically approved

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Golparian, DanielUnemo, Magnus

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