Genomic Epidemiology of Gonococcal Resistance to Extended-Spectrum Cephalosporins, Macrolides, and Fluoroquinolones in the United States, 2000–2013

December 22, 2016 at 8:18 am

Journal of Infectious Diseases November 15, 2016 V.214 N.10 P.1579-1587

Yonatan H. Grad, Simon R. Harris, Robert D. Kirkcaldy, Anna G. Green, Debora S. Marks, Stephen D. Bentley, David Trees, and Marc Lipsitch

1Department of Immunology and Infectious Diseases

2Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T. H. Chan School of Public Health

3Division of Infectious Diseases, Brigham and Women’s Hospital and Harvard Medical School

4Department of Systems Biology, Harvard Medical School, Boston, Massachusetts

5Centers for Disease Control and Prevention, Atlanta, Georgia

6Wellcome Trust Sanger Institute, Hinxton

7Department of Medicine, University of Cambridge and Addenbrookes Hospital, Cambridge, United Kingdom

Background

Treatment of Neisseria gonorrhoeae infection is empirical and based on population-wide susceptibilities. Increasing antimicrobial resistance underscores the potential importance of rapid diagnostic tests, including sequence-based tests, to guide therapy. However, the usefulness of sequence-based diagnostic tests depends on the prevalence and dynamics of the resistance mechanisms.

Methods

We define the prevalence and dynamics of resistance markers to extended-spectrum cephalosporins, macrolides, and fluoroquinolones in 1102 resistant and susceptible clinical N. gonorrhoeae isolates collected from 2000 to 2013 via the Centers for Disease Control and Prevention’s Gonococcal Isolate Surveillance Project.

Results

Reduced extended-spectrum cephalosporin susceptibility is predominantly clonal and associated with the mosaic penA XXXIV allele and derivatives (sensitivity 98% for cefixime and 91% for ceftriaxone), but alternative resistance mechanisms have sporadically emerged. Reduced azithromycin susceptibility has arisen through multiple mechanisms and shows limited clonal spread; the basis for resistance in 36% of isolates with reduced azithromycin susceptibility is unclear. Quinolone-resistant N. gonorrhoeae has arisen multiple times, with extensive clonal spread.

Conclusions

Quinolone-resistant N. gonorrhoeae and reduced cefixime susceptibility appear amenable to development of sequence-based diagnostic tests, whereas the undefined mechanisms of resistance to ceftriaxone and azithromycin underscore the importance of phenotypic surveillance. The identification of multidrug-resistant isolates highlights the need for additional measures to respond to the threat of untreatable gonorrhea.

PDF

http://jid.oxfordjournals.org/content/214/10/1579.full.pdf+html

Entry filed under: Antimicrobianos, Bacterias, Epidemiología, Infecciones de transmision sexual, Metodos diagnosticos, Resistencia bacteriana, Sepsis, Update. Tags: .

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