Register      Login
Sexual Health Sexual Health Society
Publishing on sexual health from the widest perspective
RESEARCH ARTICLE (Open Access)

Genotypic determinants of fluoroquinolone and macrolide resistance in Neisseria gonorrhoeae

Catherine L. Hall A , Mark A. Harrison A , Marcus J. Pond A , Christine Chow A , Emma M. Harding-Esch A B and S. Tariq Sadiq A B C D
+ Author Affiliations
- Author Affiliations

A Applied Diagnostic Research and Evaluation Unit, St George’s University of London, Institute for Infection & Immunity, Cranmer Terrace, Tooting, London SW17 0RE, UK.

B National Infection Service, Public Health England, 61 Colindale Avenue, London NW9 5EQ, UK.

C St George’s University Hospitals NHS Foundation Trust, Blackshaw Road, Tooting, London SW17 0QT, UK.

D Corresponding author. Email: ssadiq@sgul.ac.uk

Sexual Health 16(5) 479-487 https://doi.org/10.1071/SH18225
Submitted: 29 November 2018  Accepted: 1 April 2019   Published: 1 August 2019

Journal Compilation © CSIRO 2019 Open Access CC BY-NC-ND

Abstract

Background: High rates of antimicrobial resistance (AMR) in Neisseria gonorrhoeae hinder effective treatment, but molecular AMR diagnostics may help address the challenge. This study aimed to appraise the literature for resistance-associated genotypic markers linked to fluoroquinolones and macrolides, to identify and review their use in diagnostics. Methods: Medline and EMBASE databases were searched and data pooled to evaluate associations between genotype and phenotypic resistance. The minimum inhibitory concentration (MIC) cut-offs were ≤ 0.06 mg L−1 for non-resistance to ciprofloxacin and ≤ 0.5 mg L−1 for non-resistance to azithromycin. Results: Diagnostic accuracy estimates were limited by data availability and reporting. It was found that: 1) S91 and D95 mutations in the GyrA protein independently predicted ciprofloxacin resistance and, used together, gave 98.6% (95% confidence interval (CI) 98.0–99.0%) sensitivity and 91.4% (95%CI 88.6–93.7%) specificity; 2) the number of 23S rRNA gene alleles with C2611T or A2059G mutations was highly correlated with azithromycin resistance, with mutation in any allele giving a sensitivity and specificity of 66.1% (95%CI 62.1–70.0%) and 98.9% (95%CI 97.5–99.5%) respectively. Estimated negative (NPV) and positive predictive values (PPV) for a 23S rRNA diagnostic were 98.6% (95%CI 96.8–99.4%) and 71.5% (95%CI 68.0–74.8%) respectively; 3) mutation at amino acid position G45 in the MtrR protein independently predicted azithromycin resistance; however, when combined with 23S rRNA, did not improve the PPV or NPV. Conclusions: Viable candidates for markers of resistance detection for incorporation into diagnostics were demonstrated. Such tests may enhance antibiotic stewardship and treatment options.

Additional keywords: 23S rRNA, azithromycin, ciprofloxacin, gyrA, sexually transmissible infections.


References

[1]  The Review on Antimicrobial Resistance. Tackling drug-resistant infections globally: final report and recommendations. London: Review on Antimicrobial Resistance; 2016. Available online at: http://amr-review.org/sites/default/files/160518_Final%20paper_with%20cover.pdf [verified 3 November 2015].http://amr-review.org/sites/default/files/160518_Final%20paper_with%20cover.pdf

[2]  Chisholm SA, Wilson J, Alexander S, Tripodo F, Al-Shahib A, Schaefer U, Lythgow K, Fifer H. An outbreak of high-level azithromycin resistant Neisseria gonorrhoeae in England. Sex Transm Infect 2016; 92 365–7.
An outbreak of high-level azithromycin resistant Neisseria gonorrhoeae in England.Crossref | GoogleScholarGoogle Scholar | 26601852PubMed |

[3]  Eyre DW, Sanderson ND, Lord E, Regisford-Reimmer N, Chau K, Barker L, Morgan M, Newnham R, Golparian D, Unemo M, Crook DW, Peto TE, Hughes G, Cole MJ, Fifer H, Edwards A, Andersson MI. Gonorrhoea treatment failure caused by a Neisseria gonorrhoeae strain with combined ceftriaxone and high-level azithromycin resistance, England, February 2018. Euro Surveill 2018; 23 1800323
Gonorrhoea treatment failure caused by a Neisseria gonorrhoeae strain with combined ceftriaxone and high-level azithromycin resistance, England, February 2018.Crossref | GoogleScholarGoogle Scholar | 29991383PubMed |

[4]  Low N, Unemo M. Molecular tests for the detection of antimicrobial resistant Neisseria gonorrhoeae: when, where, and how to use? Curr Opin Infect Dis 2016; 29 45–51.
Molecular tests for the detection of antimicrobial resistant Neisseria gonorrhoeae: when, where, and how to use?Crossref | GoogleScholarGoogle Scholar | 26658656PubMed |

[5]  Mohammed H, Ison CA, Obi C, Chisholm S, Cole M, Quaye N, Hughes G;, GRASP Collective Group. Frequency and correlates of culture-positive infection with Neisseria gonorrhoeae in England: a review of sentinel surveillance data. Sex Transm Infect 2015; 91 287–93.
Frequency and correlates of culture-positive infection with Neisseria gonorrhoeae in England: a review of sentinel surveillance data.Crossref | GoogleScholarGoogle Scholar | 25352692PubMed |

[6]  Manhart LE, Gillespie CW, Lowens MS, Khosropour CM, Colombara DV, Golden MR, Hakhu NR, Thomas KK, Hughes JP, Jensen NL, Totten PA. Standard treatment regimens for nongonococcal urethritis have similar but declining cure rates: a randomized controlled trial. Clin Infect Dis 2013; 56 934–42.
Standard treatment regimens for nongonococcal urethritis have similar but declining cure rates: a randomized controlled trial.Crossref | GoogleScholarGoogle Scholar | 23223595PubMed |

[7]  Sadiq ST, Dave J, Butcher PD. Point-of-care antibiotic susceptibility testing for gonorrhoea: improving therapeutic options and sparing the use of cephalosporins. Sex Transm Infect 2010; 86 445–6.
Point-of-care antibiotic susceptibility testing for gonorrhoea: improving therapeutic options and sparing the use of cephalosporins.Crossref | GoogleScholarGoogle Scholar | 20940156PubMed |

[8]  Gaydos C, Hardick J. Point of care diagnostics for sexually transmitted infections: perspectives and advances. Expert Rev Anti Infect Ther 2014; 12 657–72.
Point of care diagnostics for sexually transmitted infections: perspectives and advances.Crossref | GoogleScholarGoogle Scholar | 24484215PubMed |

[9]  Unemo M.. Challenges with antimicrobial susceptibility testing for Neisseria gonorrhoeae in the era of extensively drug-resistant gonorrhoea — molecular antimicrobial resistance testing crucial. Pathog Glob Health 2014; 108 214–5.
Challenges with antimicrobial susceptibility testing for Neisseria gonorrhoeae in the era of extensively drug-resistant gonorrhoea — molecular antimicrobial resistance testing crucial.Crossref | GoogleScholarGoogle Scholar | 25175873PubMed |

[10]  Ohnishi M, Golparian D, Shimuta K, Saika T, Hoshina S, Iwasaku K, Nakayama S, Kitawaki J, Unemo M. Is Neisseria gonorrhoeae initiating a future era of untreatable gonorrhea?: detailed characterization of the first strain with high-level resistance to ceftriaxone. Antimicrob Agents Chemother 2011; 55 3538–45.
Is Neisseria gonorrhoeae initiating a future era of untreatable gonorrhea?: detailed characterization of the first strain with high-level resistance to ceftriaxone.Crossref | GoogleScholarGoogle Scholar | 21576437PubMed |

[11]  Public Health England. GRASP 2016 Report. Surveillance of antimicrobial resistance in Neisseria gonorrhoeae. London: Public Health England; 2016.

[12]  Leclercq R. Mechanisms of resistance to macrolides and lincosamides: nature of the resistance elements and their clinical implications. Clin Infect Dis 2002; 34 482–92.
| 11797175PubMed |

[13]  Unemo M, Shafer WM. Antimicrobial resistance in Neisseria gonorrhoeae in the 21st century: past, evolution, and future. Clin Microbiol Rev 2014; 27 587–613.
Antimicrobial resistance in Neisseria gonorrhoeae in the 21st century: past, evolution, and future.Crossref | GoogleScholarGoogle Scholar | 24982323PubMed |

[14]  Chisholm SA, Dave J, Ison CA. High-level azithromycin resistance occurs in Neisseria gonorrhoeae as a result of a single point mutation in the 23S rRNA genes. Antimicrob Agents Chemother 2010; 54 3812–6.
High-level azithromycin resistance occurs in Neisseria gonorrhoeae as a result of a single point mutation in the 23S rRNA genes.Crossref | GoogleScholarGoogle Scholar | 20585125PubMed |

[15]  Belland RJ, Morrison SG, Ison C, Huang WM. Neisseria gonorrhoeae acquires mutations in analogous regions of gyrA and parC in fluoroquinolone-resistant isolates. Mol Microbiol 1994; 14 371–80.
Neisseria gonorrhoeae acquires mutations in analogous regions of gyrA and parC in fluoroquinolone-resistant isolates.Crossref | GoogleScholarGoogle Scholar | 7830580PubMed |

[16]  Redgrave LS, Sutton SB, Webber MA, Piddock LJ. Fluoroquinolone resistance: mechanisms, impact on bacteria, and role in evolutionary success. Trends Microbiol 2014; 22 438–45.
Fluoroquinolone resistance: mechanisms, impact on bacteria, and role in evolutionary success.Crossref | GoogleScholarGoogle Scholar | 24842194PubMed |

[17]  Chitsaz M, Brown MH. The role played by drug efflux pumps in bacterial multidrug resistance. Essays Biochem 2017; 61 127–39.
The role played by drug efflux pumps in bacterial multidrug resistance.Crossref | GoogleScholarGoogle Scholar | 28258236PubMed |

[18]  The European Committee on Antimicrobial Susceptibility Testing. Breakpoint tables for interpretation of MICs and zone diameters. Version 7.1. Basel: European Society of Clinical Microbiology and Infectious Diseases; 2017. Available online at: http://www.eucast.org [verified 3 November 2015].http://www.eucast.org

[19]  Public Health England. Sexually transmitted infections and chlamydia screening in England 2016. London: Public Health England; 2017.

[20]  Zaman S, Fitzpatrick M, Lindahl L, Zengel J. Novel mutations in ribosomal proteins L4 and L22 that confer erythromycin resistance in Escherichia coli. Mol Microbiol 2007; 66 1039–50.
Novel mutations in ribosomal proteins L4 and L22 that confer erythromycin resistance in Escherichia coli.Crossref | GoogleScholarGoogle Scholar | 17956547PubMed |

[21]  Bissonnette L, Bergeron MG. Infectious disease management through point-of-care personalized medicine molecular diagnostic technologies. J Pers Med 2012; 2 50–70.
Infectious disease management through point-of-care personalized medicine molecular diagnostic technologies.Crossref | GoogleScholarGoogle Scholar | 25562799PubMed |

[22]  Tanaka M, Sakuma S, Takahashi K, Nagahuzi T, Saika T, Kobayashi I, Kumazawa J. Analysis of quinolone resistance mechanisms in Neisseria gonorrhoeae isolates in vitro. Sex Transm Infect 1998; 74 59–62.
Analysis of quinolone resistance mechanisms in Neisseria gonorrhoeae isolates in vitro.Crossref | GoogleScholarGoogle Scholar | 9634306PubMed |

[23]  Heisig P. Genetic evidence for a role of parC mutations in development of high-level fluoroquinolone resistance in Escherichia coli. Antimicrob Agents Chemother 1996; 40 879–85.
Genetic evidence for a role of parC mutations in development of high-level fluoroquinolone resistance in Escherichia coli.Crossref | GoogleScholarGoogle Scholar | 8849244PubMed |

[24]  Tait-Kamradt A, Davies T, Cronan M, Jacobs MR, Appelbaum PC, Sutcliffe J. Mutations in 23S rRNA and ribosomal protein L4 account for resistance in pneumococcal strains selected in vitro by macrolide passage. Antimicrob Agents Chemother 2000; 44 2118–25.
Mutations in 23S rRNA and ribosomal protein L4 account for resistance in pneumococcal strains selected in vitro by macrolide passage.Crossref | GoogleScholarGoogle Scholar | 10898684PubMed |

[25]  Ilina EN, Vereshchagin VA, Borovskaya AD, Malakhova MV, Sidorenko SV, Al-Khafaji NC, Kubanova AA, Govarun VM. Relation between genetic markers of drug resistance and susceptibility profile of clinical Neisseria gonorrhoeae strains. Antimicrob Agents Chemother 2008; 52 2175–82.
Relation between genetic markers of drug resistance and susceptibility profile of clinical Neisseria gonorrhoeae strains.Crossref | GoogleScholarGoogle Scholar | 18378705PubMed |

[26]  Balashov S, Mordechai E, Adelson ME, Gygax SE. Multiplex bead suspension array for screening Neisseria gonorrhoeae antibiotic resistance genetic determinants in noncultured clinical samples. J Mol Diagn 2013; 15 116–29.
| 23159594PubMed |

[27]  Gaydos CA. Review of use of a new rapid real-time PCR, the Cepheid GeneXpert(R) (Xpert) CT/NG assay, for Chlamydia trachomatis and Neisseria gonorrhoeae: results for patients while in a clinical setting. Expert Rev Mol Diagn 2014; 14 135–7.
Review of use of a new rapid real-time PCR, the Cepheid GeneXpert(R) (Xpert) CT/NG assay, for Chlamydia trachomatis and Neisseria gonorrhoeae: results for patients while in a clinical setting.Crossref | GoogleScholarGoogle Scholar | 24450867PubMed |

[28]  Allan-Blitz LT, Humphries RM, Hemarajata P, Bhatti A, Pandori MW, Siedner MJ, Klausner JD. Implementation of a rapid genotypic assay to promote targeted ciprofloxacin therapy of Neisseria gonorrhoeae in a large health system. Clin Infect Dis 2017; 64 1268–70.
| 28034887PubMed |