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Media from triplicate cultures were collected daily for the metabolomics analysis.
To test this notion, the pH of the media from triplicate wells containing control and SmAQP siRNA-treated parasites was measured using an Oakton Acorn pH Meter (Vermon Hill, IL, USA).
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D. discoideum cell viability during L. pneumophila infection was assessed from triplicate samples by diluting cells from the infection media and allowing them to recover on SM agar plates inoculated with Klebsiella aerogenes bacteria as a food source.
Briefly, 100 µl of media from each sample was added (in triplicate) to a 96-well plate before adding 100 µl of reaction mixture (30 min, 20 °C) before dual absorbance measurements (490 and 600 nm).
Results are mean values from triplicate cultures.
Standard deviations are calculated from triplicate experiments.
Error bars indicate SEM from triplicate values.
Data are means ± SDs from triplicate experiments.
Error bars SEM from triplicate values.
A standard error of 5% was derived from triplicate measurement.
Error bars indicate standard deviation calculated from triplicate experiments.
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