LAUSR

Techniques currently used for assessment of bacterial count or growth are time‐consuming, offer low throughput, or they are complicated or expensive. The aim of the present work was to elaborate a new method that is able to detect the antibacterial effect of cells, subcellular particles, and soluble compounds in a fast, cost, and labor effective way. Our proposed technique is based on flow cytometry (FC) optimized for detection of small particles and on fluorescently labeled bacteria. It allows direct determination of the bacterial count in 3 hours. The effect of various human phagocytes and extracellular vesicles on gram‐positive and gram‐negative bacteria is investigated in parallel with the new, FC‐based method, with colony counting and with our previous, OD‐based method. Comparing the killing effect of wild type and NADPH oxidase‐deficient murine neutrophils presents an example of detection of a clinically important deficiency. Strong correlation was obtained between the results of the different techniques, but the reproducibility of the FC‐based test was superior to the OD‐based test. The major advantages of the new technique are: rapidity, low cost, high throughput, and simplicity.