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. 2018 Aug 27;56(9):e00365-18. doi: 10.1128/JCM.00365-18

TABLE 5.

Performance of the real-time PCR in predicting antimicrobial resistance to four antibiotic classes directly from Neisseria gonorrhoeae-positive genital specimens with paired N. gonorrhoeae isolatesa

Reaction Associated antibiotic No. of isolates with the following result:
Sensitivity (95% CI)b Specificity (95% CI)b
TP FP FN TN Total
penA Asp345del ± penA Gly545Ser ESCs 1c 2d 0 37 40 1.00 (0.03, 1.00) 0.95 (0.83, 0.99)
23S rRNA C2611T and/or 23S rRNA A2059G AZM 1 0 0 39 40 1.00 (0.03, 1.00) 1.00 (0.91, 1.00)
gyrA Ser91Phe CIP 18 0 0 22 40 1.00 (0.81, 1.00) 1.00 (0.85, 1.00)
16S rRNA C1192T SPC 0 0 0 40 40 NA 1.00 (0.91, 1.00)
a

CI, confidence interval; TP, true positive; FP, false positive; FN, false negative; TN, true negative; ESCs, extended-spectrum cephalosporins; AZM, azithromycin; CIP, ciprofloxacin; SPC, spectinomycin; NA, not applicable.

b

Sensitivity and specificity were calculated on the basis of the susceptibility phenotype (MICs) of the paired culture isolates.

c

This isolate harbored a penA mosaic X allele and was correctly identified as ESC resistant by the penA Asp345del reaction.

d

One isolate was correctly predicted to harbor a mosaic penA allele on the basis of the molecular characterization but was susceptible to ESCs.