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Azithromycin and Doxycycline Resistance Profiles of U.S. Mycoplasma genitalium Strains and Their Association with Treatment Outcomes.
Wood, Gwendolyn E; Jensen, Nicole L; Astete, Sabina; Jensen, Jørgen S; Kenny, George E; Khosropour, Christine M; Gillespie, Catherine W; Manhart, Lisa E; Totten, Patricia A.
Afiliação
  • Wood GE; Department of Medicine, University of Washingtongrid.34477.33, Seattle, Washington, USA.
  • Jensen NL; Department of Medicine, University of Washingtongrid.34477.33, Seattle, Washington, USA.
  • Astete S; Department of Medicine, University of Washingtongrid.34477.33, Seattle, Washington, USA.
  • Jensen JS; Statens Serum Institutgrid.6203.7, Copenhagen, Denmark.
  • Kenny GE; Department of Medicine, University of Washingtongrid.34477.33, Seattle, Washington, USA.
  • Khosropour CM; Department of Epidemiology, University of Washingtongrid.34477.33, Seattle, Washington, USA.
  • Gillespie CW; Department of Epidemiology, University of Washingtongrid.34477.33, Seattle, Washington, USA.
  • Manhart LE; Department of Epidemiology, University of Washingtongrid.34477.33, Seattle, Washington, USA.
  • Totten PA; Center for AIDS and STD, University of Washingtongrid.34477.33, Seattle, Washington, USA.
J Clin Microbiol ; 59(11): e0081921, 2021 10 19.
Article em En | MEDLINE | ID: mdl-34406799
Mycoplasma genitalium is a sexually transmitted bacterium associated with nongonococcal urethritis (NGU) in men and cervicitis, endometritis, and pelvic inflammatory disease in women. Effective treatment is challenging due to the inherent, and increasingly acquired, antibiotic resistance in this pathogen. In our treatment trial conducted from 2007 to 2011 in Seattle, WA, we demonstrated poor efficacy of azithromycin (AZM) and doxycycline (DOX) against M. genitalium among men with NGU. In the present study, we cultured M. genitalium from 74 of 80 (92.5%) PCR-positive men at enrollment (V-1) and defined the MICs of AZM (N = 56 isolates) of DOX (N = 62 isolates). Susceptibility to AZM was bimodal; MICs were >8 µg/ml (44.6%) and <0.004 µg/ml (55.4%) for these isolates. The association of MIC with treatment efficacy was determined for men initially treated with either AZM (N = 30) or DOX (N = 24). Men treated with AZM were more likely to experience microbiologic treatment failure (P < 0.001) if infected with isolates that had AZM MICs of >8 µg/ml (18/18 men) than those with isolates that had AZM MICs of <0.004 µg/ml (1/12 men). Clinical treatment failure also was more likely to occur (P = 0.002) with AZM MICs of >8 µg/ml (12/18 men) than with AZM MICs of <0.004 µg/ml (1/12 men). In contrast, DOX MICs ranged from <0.125 to 2 µg/ml and were not correlated with microbiologic (P = 0.71) or clinical treatment (P = 0.41) failure, demonstrating no relationship between DOX MICs and treatment efficacy. Given the rapid spread of AZM resistance and the emergence of quinolone resistance, the current second-line therapy, monitoring MICs and evaluating other potential treatments for M. genitalium will be critical.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Uretrite / Mycoplasma genitalium / Infecções por Mycoplasma Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Uretrite / Mycoplasma genitalium / Infecções por Mycoplasma Idioma: En Ano de publicação: 2021 Tipo de documento: Article