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Assessing novel partner antimicrobials to protect ceftriaxone against gonococcal resistance: An in vitro evaluation.
Abdellati, Saïd; Gestels, Zina; Baranchyk, Yuliia; de Block, Tessa; Van Den Bossche, Dorien; De Baetselier, Irith; Manoharan-Basil, Sheeba Santhini; Kenyon, Chris.
Afiliación
  • Abdellati S; STI Unit, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • Gestels Z; Clinical Reference Laboratory, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • Baranchyk Y; STI Unit, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • de Block T; STI Unit, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • Van Den Bossche D; Clinical Reference Laboratory, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • De Baetselier I; Clinical Reference Laboratory, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • Manoharan-Basil SS; Clinical Reference Laboratory, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • Kenyon C; STI Unit, Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Int J STD AIDS ; : 9564624241280082, 2024 Sep 03.
Article en En | MEDLINE | ID: mdl-39226039
ABSTRACT

BACKGROUND:

The emergence of ceftriaxone-resistant Neisseria gonorrhoeae poses a significant threat to existing treatment regimens. Our study aimed to assess the efficacy of antimicrobials that could be combined with ceftriaxone to reduce the probability of ceftriaxone resistance emerging and spreading in N. gonorrhoeae. METHODS AND

RESULTS:

Broth microdilution was used to determine the minimal inhibitory concentrations (MICs) for a panel of ceftriaxone-resistant (WHO X, Y, Z) and ceftriaxone-susceptible (WHO L, N, P) N. gonorrhoeae WHO reference strains for the following antimicrobials ceftriaxone, doxycycline, azithromycin, zoliflodacin, fosfomycin, pristinamycin, ramoplanin, gentamicin and NAI-107. The MICs for zoliflodacin and pristinamycin for all strains were lower than or equal to the available breakpoints. A checkerboard assay was used to determine the drug-drug combination effect, which showed either an indifferent or an additive effect for all the combinations tested with ceftriaxone.

CONCLUSIONS:

The low MICs of zoliflodacin and pristinamycin for the three ceftriaxone-resistant strains suggest that these antimicrobials could be used as partner drugs with ceftriaxone to reduce the probability of ceftriaxone resistance spreading in areas with a high prevalence of ceftriaxone resistance.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Int J STD AIDS Asunto de la revista: SINDROME DA IMUNODEFICIENCIA ADQUIRIDA (AIDS) Año: 2024 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Int J STD AIDS Asunto de la revista: SINDROME DA IMUNODEFICIENCIA ADQUIRIDA (AIDS) Año: 2024 Tipo del documento: Article País de afiliación: Bélgica