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. Author manuscript; available in PMC: 2018 Sep 14.
Published in final edited form as: ACS Infect Dis. 2018 Jul 30;4(9):1377–1384. doi: 10.1021/acsinfecdis.8b00104

Figure 3.

Figure 3

Growth of ATCC 49226 as measured via direct-qPCR and OD. One-hundred-thousand N. gonorrhoeae cells were inoculated into 10 mL of GW medium with (black points) and without (red points) 0.06 μL/mL of ciprofloxacin. Samples (300 μL) were taken every hour to perform the tests. All Cq values measured were normalized by subtracting each measured value with Cq at 0 h. (A) Direct-qPCR method exhibits higher quantification range and it differentiates the growth of drug-treated and nontreated cells in 1 h cultivation. (B) OD method shows a comparatively limited quantification capability with a narrower dynamic range. It differentiates the growth of drug-treated and nontreated cells in 9 h cultivation. As a point of comparison, 24-h incubation is the typical time frame cited for plate-based cultivation.11