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  • Molecular epidemiology of Neisseria gonorrhoeae isolates from Saskatchewan, Canada: utility of NG-MAST in predicting antimicrobial susceptibility regionally.

Molecular epidemiology of Neisseria gonorrhoeae isolates from Saskatchewan, Canada: utility of NG-MAST in predicting antimicrobial susceptibility regionally.

Sexually transmitted infections (2014-02-08)
Sidharath D Thakur, Paul N Levett, Gregory B Horsman, Jo-Anne R Dillon
ABSTRACT

To investigate the molecular epidemiology of isolates of Neisseria gonorrhoeae from Saskatchewan, Canada, using Neisseria gonorrhoeae multi antigen sequence typing (NG-MAST), and to assess associations between antimicrobial susceptibility (AMS) and specific strain types (STs). 320 consecutive gonococcal isolates, collected between 2003 and 2008, were typed by NG-MAST. STs were grouped if one of their alleles was common and the other differed by ≤1% in DNA sequence. AMS was determined by agar dilution (CLSI) to seven antibiotics. N gonorrhoeae isolates were resolved into 82 individual NG-MAST STs and 18 NG-MAST ST groups with groups 25, 3655, 921, 3654, 3657 and 3656 comprising 53.4% (171/320) of the isolates. N gonorrhoeae isolates susceptible to all the tested antimicrobials were significantly (p<0.05) associated with ST 25 (87%). Other significant associations between ST and AMS included: ST 3654 and isolates with minimum inhibitory concentrations of ≥0.03 mg/L to third generation cephalosporins; ST 3711 (100%) and TRNG; and ST/group 3654 (43%) and chromosomal resistance to penicillin and tetracycline. Several NG-MAST STs/groups were significantly associated with isolates with chromosomal resistance to tetracycline. Isolates resistant to ciprofloxacin (n=5) and azithromycin (n=2) appeared as individual STs. Significant associations were observed among individual STs, sex and age of the patient, and regional and temporal distributions. Associations between N gonorrhoeae AMS and NG-MAST STs were identified and may be useful in predicting AMS regionally. Because STs in different countries vary considerably, the use of NG-MAST for the prediction of AMS globally requires further study.

MATERIALS
Product Number
Brand
Product Description

Supelco
Spectinomycin dihydrochloride pentahydrate, VETRANAL®, analytical standard
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Tetracycline, 98.0-102.0% (HPLC)
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Tetracycline, 98.0-102.0% (HPLC)
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Spectinomycin dihydrochloride pentahydrate, potency: ≥603 μg per mg
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Spectinomycin dihydrochloride pentahydrate, powder, BioReagent, suitable for cell culture
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Spectinomycin dihydrochloride pentahydrate, powder, γ-irradiated
Azithromycin, European Pharmacopoeia (EP) Reference Standard
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Azithromycin, United States Pharmacopeia (USP) Reference Standard
Azithromycin for system suitability, European Pharmacopoeia (EP) Reference Standard
USP
Azithromycin Identity, United States Pharmacopeia (USP) Reference Standard
Supelco
Ciprofloxacin HCl, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Azithromycin, Pharmaceutical Secondary Standard; Certified Reference Material
USP
Spectinomycin hydrochloride, United States Pharmacopeia (USP) Reference Standard
Azithromycin for peak identification, European Pharmacopoeia (EP) Reference Standard
Supelco
Tetracycline hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Ciprofloxacin, VETRANAL®, analytical standard
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Azithromycin dihydrate, ≥98% (HPLC)
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Ciprofloxacin, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Tetracycline hydrochloride, VETRANAL®, analytical standard
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Ciprofloxacin, ≥98% (HPLC)
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Azithromycin
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Tetracycline hydrochloride, powder, BioReagent, suitable for cell culture
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Tetracycline hydrochloride, ≥95% (European Pharmacopoeia HPLC assay)
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Ceftriaxone disodium salt hemi(heptahydrate), third-generation cephalosporin antibiotic
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Tetracycline hydrochloride, meets USP testing specifications
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Tetracycline hydrochloride, powder
USP
Ceftriaxone sodium, United States Pharmacopeia (USP) Reference Standard
Ceftriaxone sodium, European Pharmacopoeia (EP) Reference Standard
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Ciprofloxacin hydrochloride, European Pharmacopoeia (EP) Reference Standard