Repository logo
 

The impact of microbials on gonococcal evolution

Accepted version
Peer-reviewed

Change log

Authors

Leonor Sánchez-Busó 1, Daniel Golparian2, Jukka Corander1,3,4, Yonatan H. Grad 5,6, Makoto Ohnishi7,8, Rebecca Flemming9, Julian Parkhill 1, Stephen D. Bentley1, Magnus Unemo2 and Simon R. Harris 1* 

Abstract

The sexually transmitted pathogen Neisseria gonorrhoeae is regarded as being on the way to becoming an untreatable superbug. Despite its clinical importance, little is known about its emergence and evolution, and how this corresponds with the introduction of antimicrobials. We present a genome-based phylogeographical analysis of 419 gonococcal isolates from across the globe. Results indicate that modern gonococci originated in Europe or Africa, possibly as late as the sixteenth century and subsequently disseminated globally. We provide evidence that the modern gonococcal population has been shaped by antimicrobial treatment of sexually transmitted infections as well as other infections, leading to the emergence of two major lineages with different evolutionary strategies. The well-described multidrug-resistant lineage is associated with high rates of homologous recombination and infection in high-risk sexual networks. A second, multisusceptible lineage is more associated with heterosexual networks, with potential implications for infection control.

Description

Keywords

Africa, Anti-Bacterial Agents, DNA, Bacterial, Drug Resistance, Multiple, Bacterial, Europe, Evolution, Molecular, Gonorrhea, Homologous Recombination, Humans, Neisseria gonorrhoeae, Phylogeny, Phylogeography, Sequence Analysis, DNA

Journal Title

Nature Microbiology

Conference Name

Journal ISSN

2058-5276
2058-5276

Volume Title

Publisher

Springer Nature

Rights

All rights reserved
Sponsorship
This work was funded by the Wellcome grant number 098051 and the Foundation for Medical Research at Örebro University Hospital, Örebro, Sweden. J.C. was funded by the ERC grant number 745258. Y.H.G. is supported by The Smith Family Foundation and the NIH/NIAID grant 1R01AI132606-01.