Antimicrobial Resistance and Molecular Typing of Neisseria gonorrhoeae Isolates From the Eastern Cape Province in South Africa

Author:

Peters Remco P.H.,Jung Hyunsul1,Mitchev Nireshni2,Mdingi Mandisa M.3,Gigi Ranjana,Shroufi Amir4,Martinez Fernando P.5,Bamford Colleen

Affiliation:

1. Department of Medical Microbiology, University of Pretoria, Pretoria

2. School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa

3. Research Unit, Foundation for Professional Development, East London

4. Drugs for Neglected Diseases Initiative (DNDi) & Global Antibiotic Research & Development Partnership (GARDP) Southern Africa, Cape Town, South Africa

5. Global Antibiotic Research & Development Partnership (GARDP), Geneva, Switzerland

Abstract

Background There is a paucity of Neisseria gonorrhoeae antimicrobial resistance data from resource-constrained settings because of the lack of diagnostic testing and limited scale of surveillance programs. This study aimed to determine the antimicrobial resistance profile of N. gonorrhoeae in the rural Eastern Cape province of South Africa. Methods Specimens for N. gonorrhoeae culture were obtained from men with urethral discharge and women with vaginal discharge attending primary health care facilities. Direct inoculation of the agar plates was performed followed by culture and drug susceptibility testing using the Etest at the laboratory. Whole-genome sequencing of the isolates was performed to identify resistance-determining variants. Results One hundred N. gonorrhoeae isolates were obtained. Most strains were nonsusceptible to ciprofloxacin (76%), tetracycline (75%), and penicillin G (72%). The gyrA S91F mutation was present in 68 of 72 ciprofloxacin-resistant isolates (94%), with concurrent parC mutations in 47 of 68 (69%); gyrA I250M was the only mutation in 4 other resistant strains. One azithromycin-resistant isolate was identified with a minimal inhibitory concentration (MIC) of 8.0 mg/L and the 23S rDNA gene mutation C2597T. The median MIC of cefixime was 0.016 mg/L (range, 0.016–0.064 mg/L), and that of ceftriaxone was 0.016 mg/L (range, 0.016 mg/L). Whole-genome sequencing showed 58 sequence types as revealed in N. gonorrhoeae sequence typing for antimicrobial resistance and 70 sequence types in N. gonorrhoeae multiantigen sequence typing. Conclusions This study confirmed high rates of N. gonorrhoeae antimicrobial resistance to ciprofloxacin, penicillin G, and tetracycline in our setting. The MICs of cephalosporins are reassuring for ceftriaxone use in syndromic treatment regimens, but the identification of azithromycin resistance warrants further attention.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Microbiology (medical),Public Health, Environmental and Occupational Health,Dermatology

Reference21 articles.

1. Adult gonorrhoea, chlamydia and syphilis prevalence, incidence, treatment, and syndromic case reporting in South Africa: Estimates using the Spectrum-STI model, 1990–2017;PLoS One,2018

2. Diagnosing sexually transmitted infections in resource-constrained settings: Challenges and way forward;J Int AIDS Soc,2019

3. Antimicrobial resistance in Neisseria gonorrhoeae in the 21st century: Past, evolution, and future;Clin Microbiol Rev,2014

4. Phenotypic and genetic characterization of the first two cases of extended-spectrum-cephalosporin-resistant Neisseria gonorrhoeae infection in South Africa and association with cefixime treatment failure;J Antimicrob Chemother,2013

5. Antimicrobial resistance of Neisseria gonorrhoeae isolates from high-risk men in Johannesburg, South Africa;Antimicrob Agents Chemother,2020

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