High susceptibility to the novel antimicrobial zoliflodacin among Neisseria gonorrhoeae isolates in eight WHO Enhanced Gonococcal Antimicrobial Surveillance Programme countries in three WHO regions, 2021-2024UNC Project Malawi, Lilongwe, Malawi.
Research Institute for Tropical Medicine, Department of Health, Manila, Philippines.
Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.
Division of AIDS and STIs, Department of Disease Control and Prevention, Bangrak STIs Center, Thailand Ministry of Public Health, Bangkok, Thailand.
Sexually Transmitted Infections Program, Ministry of Health, Kampala, Uganda.
National Hospital of Dermatology and Venereology and Hanoi Medical University, Hanoi, Vietnam.
Centre for HIV and STIs, National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg, South Africa.
UNC Project Malawi, Lilongwe, Malawi.
Centre for HIV and STIs, National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg, South Africa.
Ho Chi Minh City Hospital of Dermatology and Venereology, Ho Chi Minh City, Vietnam.
Laboratory of the National Institute of Public Health, Phnom Penh, Cambodia.
Department of Laboratory Medicine, Faculty of Medicine and Health, WHO Collaborating Centre for Gonorrhoea and other Sexually Transmitted Infections, National Reference Laboratory for Sexually Transmitted Infections, Örebro University, Örebro, Sweden.
Sulianti Saroso Infectious Disease Hospital, Jakarta, Indonesia.
Research Institute for Tropical Medicine, Department of Health, Manila, Philippines.
Sulianti Saroso Infectious Disease Hospital, Jakarta, Indonesia.
National Center for HIV/AIDS, Dermatology and Sexually Transmitted Diseases, Phnom Penh, Cambodia.
WHO Country Office, Hanoi, Vietnam.
Global HIV, Hepatitis and STI Programmes, WHO, Geneva, Switzerland.
Global HIV, Hepatitis and STI Programmes, WHO, Geneva, Switzerland.
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2025 (English)In: IJID Regions, E-ISSN 2772-7076, Vol. 15, article id 100624Article in journal (Refereed) Published
Abstract [en]
OBJECTIVES: Zoliflodacin, a novel spiropyrimidinetrione, showed non-inferiority compared with recommended ceftriaxone plus azithromycin treatment in a recent global phase III randomized controlled trial for gonorrhea treatment. We evaluated the susceptibility of zoliflodacin among 2993 contemporary gonococcal isolates collected in 2021-2024 in eight World Health Organization (WHO) Enhanced Gonococcal Antimicrobial Surveillance Programme countries in the WHO Southeast Asian Region (Indonesia, Thailand), WHO Western Pacific Region (Cambodia, the Philippines, Viet Nam), and WHO African Region (Malawi, South Africa, Uganda).
METHODS: Minimum inhibitory concentrations (MICs) of zoliflodacin were determined using the agar dilution technique, and the zoliflodacin target gene (gyrB) was examined with Illumina sequencing.
RESULTS: Zoliflodacin exhibited high activity: MICs ranging from 0.001 to 1 mg/l and a modal MIC of 0.032 mg/l. The zoliflodacin MIC distribution showed mostly a wild-type profile; however, two isolates from Cambodia had MICs of 0.5 mg/l and 1 mg/l. These isolates also harbored the GyrB D429N mutation, associated with increased zoliflodacin MICs.
CONCLUSIONS: We show a high susceptibility to zoliflodacin internationally, including against ceftriaxone- and azithromycin-resistant gonococcal strains. Our findings support the continued clinical development of zoliflodacin as a treatment for gonorrhea, although cautious and monitored introduction and continuous international resistance surveillance are imperative.
Place, publisher, year, edition, pages
Elsevier, 2025. Vol. 15, article id 100624
Keywords [en]
Gonorrhea, In vitro susceptibility, Neisseria gonorrhoeae, Treatment, WHO EGASP, Zoliflodacin
National Category
Infectious Medicine
Identifiers
URN: urn:nbn:se:oru:diva-120774DOI: 10.1016/j.ijregi.2025.100624ISI: 001468900900001PubMedID: 40256400Scopus ID: 2-s2.0-105002221120OAI: oai:DiVA.org:oru-120774DiVA, id: diva2:1954884
Funder
Region Örebro County2025-04-282025-04-282025-08-28Bibliographically approved