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Gonococcal resistance to zoliflodacin could emerge via transformation from commensal Neisseria species. An in-vitro transformation study
by
Manoharan-Basil, Sheeba Santhini
, Abdellati, Saïd
, de Block, Tessa
, Van Den Bossche, Dorien
, Van Dijck, Christophe
, Laumen, Jolein Gyonne Elise
, De Baetselier, Irith
, Kenyon, Chris
in
631/1647/2234
/ 631/326/2521
/ 692/4017
/ Amino acids
/ Clinical trials
/ Deoxyribonucleic acid
/ DNA
/ Genetic transformation
/ Genomics
/ Gonorrhea
/ Humanities and Social Sciences
/ Minimum inhibitory concentration
/ multidisciplinary
/ Mutation
/ Neisseria
/ Quinolones
/ Science
/ Science (multidisciplinary)
2024
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Gonococcal resistance to zoliflodacin could emerge via transformation from commensal Neisseria species. An in-vitro transformation study
by
Manoharan-Basil, Sheeba Santhini
, Abdellati, Saïd
, de Block, Tessa
, Van Den Bossche, Dorien
, Van Dijck, Christophe
, Laumen, Jolein Gyonne Elise
, De Baetselier, Irith
, Kenyon, Chris
in
631/1647/2234
/ 631/326/2521
/ 692/4017
/ Amino acids
/ Clinical trials
/ Deoxyribonucleic acid
/ DNA
/ Genetic transformation
/ Genomics
/ Gonorrhea
/ Humanities and Social Sciences
/ Minimum inhibitory concentration
/ multidisciplinary
/ Mutation
/ Neisseria
/ Quinolones
/ Science
/ Science (multidisciplinary)
2024
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Gonococcal resistance to zoliflodacin could emerge via transformation from commensal Neisseria species. An in-vitro transformation study
by
Manoharan-Basil, Sheeba Santhini
, Abdellati, Saïd
, de Block, Tessa
, Van Den Bossche, Dorien
, Van Dijck, Christophe
, Laumen, Jolein Gyonne Elise
, De Baetselier, Irith
, Kenyon, Chris
in
631/1647/2234
/ 631/326/2521
/ 692/4017
/ Amino acids
/ Clinical trials
/ Deoxyribonucleic acid
/ DNA
/ Genetic transformation
/ Genomics
/ Gonorrhea
/ Humanities and Social Sciences
/ Minimum inhibitory concentration
/ multidisciplinary
/ Mutation
/ Neisseria
/ Quinolones
/ Science
/ Science (multidisciplinary)
2024
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Gonococcal resistance to zoliflodacin could emerge via transformation from commensal Neisseria species. An in-vitro transformation study
Journal Article
Gonococcal resistance to zoliflodacin could emerge via transformation from commensal Neisseria species. An in-vitro transformation study
2024
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Overview
One of the most promising new treatments for gonorrhoea currently in phase 3 clinical trials is zoliflodacin. Studies have found very little resistance to zoliflodacin in currently circulating
N. gonorrhoeae
strains, and in-vitro experiments demonstrated that it is difficult to induce resistance. However, zoliflodacin resistance may emerge in commensal
Neisseria
spp., which could then be transferred to
N. gonorrhoeae
via transformation. In this study, we investigated this commensal-resistance-pathway hypothesis for zoliflodacin. To induce zoliflodacin resistance, ten wild-type susceptible isolates belonging to 5
Neisseria
species were serially passaged for up to 48 h on gonococcal agar plates containing increasing zoliflodacin concentrations. Within 7 to 10 days, all strains except
N. lactamica
, exhibited MICs of ≥ 4 µg/mL, resulting in MIC increase ranging from 8- to 64-fold. The last passaged strains and their baseline were sequenced. We detected mutations previously reported to cause zoliflodacin resistance in GyrB (D429N and S467N), novel mutations in the quinolone resistance determining region (QRDR) (M464R and T472P) and mutations outside the QRDR at amino acid positions 28 and 29 associated with low level resistance (MIC 2 µg/mL). Genomic DNA from the laboratory evolved zoliflodacin-resistant strains was transformed into the respective baseline wild-type strain, resulting in MICs of ≥ 8 µg/mL in most cases. WGS of transformants with decreased zoliflodacin susceptibility revealed presence of the same zoliflodacin resistance determinants as observed in the donor strains. Two inter-species transformation experiments were conducted to investigate whether zoliflodacin resistance determinants of commensal
Neisseria
spp. could be acquired by
N. gonorrhoeae
.
N. gonorrhoeae
strain WHO P was exposed to (i) pooled genomic DNA from the two resistant
N. mucosa
strains and (ii) a
gyrB
amplicon of the resistant
N. subflava
strain 45/1_8. Transformants of both experiments exhibited an MIC of 2 µg/mL and whole genome analysis revealed uptake of the mutations detected in the donor strains. This is the first in-vitro study to report that zoliflodacin resistance can be induced in commensal
Neisseria
spp. and subsequently transformed into
N. gonorrhoeae.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
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