A multisite implementation of a real-time polymerase chain reaction assay to predict ciprofloxacin susceptibility in Neisseria gonorrhoeae.


Journal

Diagnostic microbiology and infectious disease
ISSN: 1879-0070
Titre abrégé: Diagn Microbiol Infect Dis
Pays: United States
ID NLM: 8305899

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 08 06 2018
revised: 26 12 2018
accepted: 27 12 2018
pubmed: 7 2 2019
medline: 8 11 2019
entrez: 7 2 2019
Statut: ppublish

Résumé

There are no commercially available Food and Drug Administration-cleared rapid tests for Neisseria gonorrhoeae antimicrobial susceptibility testing. This study evaluated the performance of a laboratory-developed real-time polymerase chain reaction assay for genotyping the gyrA gene to determine antimicrobial susceptibility to ciprofloxacin. Validation and clinical performance of the gyrA assay were evaluated across 3 geographic locations (Los Angeles, San Francisco, Philadelphia). Following validation, clinical specimens were collected in Aptima Combo2® CT/NG transport medium from asymptomatic persons who tested positive for Neisseria gonorrhoeae and evaluated for assay percent reportable (i.e., proportion of N. gonorrhoeae-positive specimens that yielded a gyrA genotype). The percentage of gyrA genotyping results differed by laboratory and specimen type. The proportion of specimens that were reportable was best for urine/genital specimens (genotyped = 76.4% (95% confidence interval, 69.9-82%)) followed by rectal (genotyped = 67.2% (95% confidence interval, 63.4-70.6%)) and then pharyngeal specimens (genotyped = 36.1%, (95% confidence interval, 31.9-40.5%)). Overall, asymptomatic patients with N. gonorrhoeae yielded an interpretable genotype 57.2% (784/1370) of the time, of which 480 were wild-type gyrA, resulting in 61% (480/784) being potentially treatable with ciprofloxacin.

Identifiants

pubmed: 30723007
pii: S0732-8893(19)30028-8
doi: 10.1016/j.diagmicrobio.2018.12.018
pmc: PMC7427424
mid: NIHMS1615794
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Ciprofloxacin 5E8K9I0O4U
DNA Gyrase EC 5.99.1.3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

213-217

Subventions

Organisme : NIAID NIH HHS
ID : HHSN272201300014I
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI139265
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI117256
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

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Auteurs

Olivia Ellis (O)

UCLA Jonathan and Karin Fielding School of Public Health, Department of Environmental Health Sciences, University of California, USA.

Peera Hemarajata (P)

Los Angeles Department of Public Health, Public Health Laboratories, Los Angeles, CA, USA.

Akbar Shahkolahi (A)

Social and Scientific Systems, Inc., Clinical Research and Biosciences Group, Silver Spring, MD, USA.

Godfred Masinde (G)

San Francisco Department of Public Health, San Francisco Public Health Laboratory, San Francisco, CA, USA.

Kerry Buchs (K)

Philadelphia Department of Public Health, Philadelphia Public Health Laboratory, Philadelphia, PA, USA.

Romney M Humphries (RM)

Accelerate Diagnostics, Tucson, AZ, USA. Electronic address: rhumphries@axdx.com.

Jeffrey D Klausner (JD)

UCLA Division of Infectious Diseases, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.

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Classifications MeSH