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Review
. 2019 Feb;5(2):e000239.
doi: 10.1099/mgen.0.000239. Epub 2019 Jan 30.

Using genomics to understand antimicrobial resistance and transmission in Neisseria gonorrhoeae

Affiliations
Review

Using genomics to understand antimicrobial resistance and transmission in Neisseria gonorrhoeae

Leonor Sánchez-Busó et al. Microb Genom. 2019 Feb.

Abstract

Gonorrhoea infections are on the increase and strains that are resistant to all antimicrobials used to treat the disease have been found worldwide. These observations encouraged the World Health Organization to include Neisseria gonorrhoeae on their list of high-priority organisms in need of new treatments. Fortunately, concurrent resistance to both antimicrobials used in dual therapy is still rare. The fight against antimicrobial resistance (AMR) must begin from an understanding of how it evolves and spreads in sexual networks. Genome-based analyses have allowed the study of the gonococcal population dynamics and transmission, giving a novel perspective on AMR gonorrhoea. Here, we will review past, present and future treatment options for gonorrhoea and explain how genomics is helping to increase our understanding of the changing AMR and transmission landscape. This article contains data hosted by Microreact.

Keywords: antimicrobial resistance; genomics; gonorrhoea; sexual networks; transmission.

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Conflict of interest statement

The authors declare that that there are no conflicts of interest.

Figures

Fig. 1.
Fig. 1.
Distribution of AMR determinants on N. gonorrhoeae isolates from genome-based published papers. The most relevant known mutations [3] were tested from raw WGS data using ARIBA [53]. Those reported to produce the highest increase in MIC [29, 34] are coloured in red, while other associated mutations reported to cause a reduced susceptibility phenotype are coloured in orange and no known mutation in blue. Some mutations have not been proven to cause an MIC increase above the breakpoints. Note that some publications used a biased sampling to fulfil their particular work aims, so the maps are not fully representative of the incidence of the resistance mutations in particular locations. Maps were obtained using Microreact [54], and a dynamic version that includes the individual tested determinants can be found at https://microreact.org/project/rJQ6FGj8G. Grey represents isolates with missing metadata.

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