Publication

Antimicrobial Resistance in Neisseria gonorrhoeae: Proceedings of the STAR Sexually Transmitted InfectionClinical Trial Group Programmatic Meeting

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Last modified
  • 05/21/2025
Type of Material
Authors
    Anthony D. Cristillo, Social & Scientific Systems, IncClaire C. Bristow, University of California San DiegoElizabeth Torrone, Centers for Disease Control and PreventionJo-Anne Dillon, University of SaskatchewanRobert D. Kirkcaldy, Centers for Disease Control and PreventionHuan Dong, Charles R. Drew University of Medicine & ScienceYonatan H. Grad, Harvard UniversityRobert A. Nicholas, University of North CarolinaPeter A. Rice, University of MassachusettsKenneth Lawrence, Entasis TherapeuticsDavid Oldach, Cempra PharmaceuticalsWilliam M Shafer, Emory UniversityPei Zhou, Duke UniversityTeodora E. Wi, World Health OrganizationSheldon R. Morris, University of California San DiegoJeffrey D. Klausner, University of California Los Angeles
Language
  • English
Date
  • 2019-03-01
Publisher
  • Lippincott, Williams & Wilkins
Publication Version
Copyright Statement
  • © 2018 American Sexually Transmitted Diseases Association.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0148-5717
Volume
  • 46
Issue
  • 3
Start Page
  • E18
End Page
  • E25
Grant/Funding Information
  • None declared.
Abstract
  • The goal of the Sexually Transmitted Infection Clinical Trial Group's Antimicrobial Resistance (AMR) in Neisseria gonorrhoeae (NG) meeting was to assemble experts from academia, government, nonprofit and industry to discuss the current state of research, gaps and challenges in research and technology and priorities and new directions to address the continued emergence of multidrug-resistant NG infections. Topics discussed at the meeting, which will be the focus of this article, include AMR NG global surveillance initiatives, the use of whole genome sequencing and bioinformatics to understand mutations associated with AMR, mechanisms of AMR, and novel antibiotics, vaccines and other methods to treat AMR NG. Key points highlighted during the meeting include: (i) US and International surveillance programs to understand AMR in NG; (ii) the US National Strategy for combating antimicrobial-resistant bacteria; (iii) surveillance needs, challenges, and novel technologies; (iv) plasmid-mediated and chromosomally mediated mechanisms of AMR in NG; (v) novel therapeutic (eg, sialic acid analogs, factor H [FH]/Fc fusion molecule, monoclonal antibodies, topoisomerase inhibitors, fluoroketolides, LpxC inhibitors) and preventative (eg, peptide mimic) strategies to combat infection. The way forward will require renewed political will, new funding initiatives, and collaborations across academic and commercial research and public health programs.
Author Notes
  • Correspondence: Anthony D. Cristillo, PhD, MS, Social and Scientific Systems, Inc, 8757 Georgia Ave, 12th Floor, Silver Spring, MD. E-mail: acristillo@s-3.com
Keywords
Research Categories
  • Health Sciences, Immunology
  • Chemistry, Pharmaceutical
  • Chemistry, Biochemistry

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