Efficacy of Doxycycline-Sitafloxacin Sequential Therapy for Urogenital Mycoplasma genitalium Infection in Nanjing, China

Sex Transm Dis. 2025 Apr 1;52(4):259-265. doi: 10.1097/OLQ.0000000000002105. Epub 2024 Nov 21.

Abstract

Background: The aim of this study was to evaluate the efficacy of doxycycline-sitafloxacin sequential therapy in the treatment of Mycoplasma genitalium (Mg) urogenital infections in Nanjing, China.

Methods: Potential subjects were tested initially for Mg infection by nucleic acid amplification testing and again at least 21 days after completion of doxycycline (100 mg twice daily for 7 days)-sitafloxacin (100 mg twice daily for 7 days) sequential therapy. The presence of macrolide and quinolone resistance-associated mutations in 23S rRNA, parC, gyrA, and gyrB genes in Mg was examined at baseline and upon retesting of specimens from subjects that did not clear Mg.

Results: A total of 218 patients were screened for Mg, of whom 65 were positive for Mg; 63 Mg-infected patients were enrolled. Twenty-two (35%) Mg-infected subjects (16 heterosexual men, 5 women, and 1 man who had sex with men [MSM]) were successfully evaluated with a test of cure; 20 (91%) cleared Mg infection. In pretreatment specimens, mutations in 23S rRNA, parC (G248T [S83I]), gyrA (G277T [G93C]), and gyrB genes were present in 100% (19 of 19), 61.1% (11 of 18), 6.7% (1 of 15), and 7.1% (1 of 14), respectively. Mg clearance rates were 4 of 4 in infected subjects that possessed both wild-type parC and gyrA genes, and 9 of 10 when a parC G248T mutation and an otherwise wild-type gyrA gene were identified. Two subjects (9%) reported mild adverse events.

Conclusions: Doxycycline-sitafloxacin sequential therapy was well tolerated and effective against most urogenital Mg infections in Nanjing and may provide an option for treatment.

MeSH terms

  • Adult
  • Anti-Bacterial Agents* / administration & dosage
  • Anti-Bacterial Agents* / therapeutic use
  • China / epidemiology
  • Doxycycline* / administration & dosage
  • Doxycycline* / therapeutic use
  • Drug Resistance, Bacterial / genetics
  • Drug Therapy, Combination
  • Female
  • Fluoroquinolones* / administration & dosage
  • Fluoroquinolones* / therapeutic use
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Mycoplasma Infections* / drug therapy
  • Mycoplasma Infections* / epidemiology
  • Mycoplasma Infections* / microbiology
  • Mycoplasma genitalium* / drug effects
  • Mycoplasma genitalium* / genetics
  • Mycoplasma genitalium* / isolation & purification
  • RNA, Ribosomal, 23S / genetics
  • Treatment Outcome
  • Young Adult

Substances

  • Doxycycline
  • Fluoroquinolones
  • Anti-Bacterial Agents
  • sitafloxacin
  • RNA, Ribosomal, 23S