Acquisition and loss of CTX-M plasmids in Shigella species associated with MSM transmission in the UK

Publication date

2021-08-24

Authors

Locke, Rebecca K
Greig, David R
Jenkins, Claire
Dallman, Timothy J.ISNI 000000042668536X
Cowley, Lauren A

Editors

Advisors

Supervisors

Document Type

Article
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cc_by

Abstract

Shigellosis in men who have sex with men (MSM) is caused by multidrug resistant Shigellae, exhibiting resistance to antimicrobials including azithromycin, ciprofloxacin and more recently the third-generation cephalosporins. We sequenced four blaCTX-M-27-positive MSM Shigella isolates (2018–20) using Oxford Nanopore Technologies; three S. sonnei (identified as two MSM clade 2, one MSM clade 5) and one S. flexneri 3a, to explore AMR context. All S. sonnei isolates harboured Tn7/Int2 chromosomal integrons, whereas S. flexneri 3a contained the Shigella Resistance Locus. All strains harboured IncFII pKSR100-like plasmids (67-83kbp); where present blaCTX-M-27 was located on these plasmids flanked by IS26 and IS903B, however blaCTX-M-27 was lost in S. flexneri 3a during storage between Illumina and Nanopore sequencing. IncFII AMR regions were mosaic and likely reorganised by IS26; three of the four plasmids contained azithromycin-resistance genes erm(B) and mph(A) and one harboured the pKSR100 integron. Additionally, all S. sonnei isolates possessed a large IncB/O/K/Z plasmid, two of which carried aph(3’)-Ib/aph(6)-Id/sul2 and tet(A). Monitoring the transmission of mobile genetic elements with co-located AMR determinants is necessary to inform empirical treatment guidance and clinical management of MSM-associated shigellosis.

Keywords

Antimicrobial resistance, CTX-M, ESBL, MSM, Public health, Shigella, Epidemiology, Microbiology, Molecular Biology, Genetics, SDG 3 - Good Health and Well-being

Citation

Locke, R K, Greig, D R, Jenkins, C, Dallman, T J & Cowley, L A 2021, 'Acquisition and loss of CTX-M plasmids in Shigella species associated with MSM transmission in the UK', Microbial genomics, vol. 7, no. 8, 000644, pp. 1-16. https://doi.org/10.1099/mgen.0.000644