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Fluorescence Microscopy Methods for Determining the Viability of Bacteria in Association with Mammalian Cells
Published on: September 5, 2013
Neutrophils with toxic granulation show high fluorescence with bis(Zn2+-dipicolylamine) complex
Yeong Sic Kim1, Hun Hee Park, Hyun-Woo Rhee
1Department of Laboratory Medicine, Catholic University Medical College, Seoul, Korea.
Abstract:
Although blood neutrophils with toxic granulation provide an excellent means of evaluating acute bacterial infections, the methods are labor-intensive and their reproducibilities depend on the staining technique and the observer's judgment. We measured the flavin adenine dinucleotide (FAD) content of normal neutrophils and neutrophils with toxic granulation by flow cytometry after incubating them with bis(Zn(2+)-dipicolylamine) complex. A total of 122 blood samples (78 with neutrophils with toxic granulation, 44 with normal neutrophils without toxic granulation) were analyzed. The mean autofluorescence levels of neutrophils in the toxic granulation (+) group and toxic granulation (-) group were both 1.9 x 10(3) MESF (mean equivalent soluble fluorochrome) values. However, after incubating neutrophils with bis(Zn(2+)-dipicolylamine) complex for 15 min, the mean fluorescence intensities of neutrophils in the toxic granulation (+) and toxic granulation (-) groups were significantly enhanced by 71- and 19-fold to 138+/-78 x 10(3) MESF and 37+/-37 x 10(3) MESF, respectively (p <0.001). An MESF cutoff value of 79 x 10(3) showed a sensitivity of 93.2% and a specificity of 81.8% for neutrophils with toxic granulation. Similarly, the MESF level ratio, defined as the ratio of the MESF value after incubation with bis(Zn(2+)-dipicolylamine) complex to the autofluorescence MESF value, at a cutoff value of 41, showed a sensitivity of 92.3% and a specificity of 81.8% for the detection of neutrophils with toxic granulation. The MESF values of neutrophils after incubation with bis(Zn(2+)-dipicolylamine) complex did not correlate with the leukocyte (p >0.05) or neutrophil counts (p >0.05). In conclusion, measurement of FAD fluorescence intensity in neutrophils by flow cytometry after incubation with bis(Zn(2+)-dipicolylamine) complex is an easy, objective, and reliable method of detecting neutrophils with toxic granulation.
Insights
This study introduces a new, objective flow cytometry method using flavin adenine dinucleotide (FAD) fluorescence to detect neutrophils with toxic granulation, improving bacterial infection evaluation. The method offers high sensitivity and specificity, making it a reliable diagnostic tool.
Area of Science:
- Hematology
- Clinical Chemistry
- Immunology
Background:
- Blood neutrophils with toxic granulation are indicators of acute bacterial infections.
- Current detection methods are labor-intensive and subjective, relying on staining and observer judgment.
- Objective and reproducible methods are needed for accurate assessment of neutrophils with toxic granulation.
Purpose of the Study:
- To develop and validate an objective flow cytometry method for detecting neutrophils with toxic granulation.
- To measure flavin adenine dinucleotide (FAD) content in neutrophils using a novel bis(Zn(2+)-dipicolylamine) complex.
Main Methods:
- Analyzed 122 blood samples using flow cytometry.
- Incubated neutrophils with bis(Zn(2+)-dipicolylamine) complex to measure FAD fluorescence intensity.
- Calculated mean equivalent soluble fluorochrome (MESF) values and MESF level ratios.
Main Results:
- Neutrophils with toxic granulation showed significantly enhanced FAD fluorescence (71-fold increase) compared to normal neutrophils (19-fold increase) after incubation.
- An MESF cutoff value of 79 x 10(3) achieved 93.2% sensitivity and 81.8% specificity.
- The MESF level ratio cutoff of 41 demonstrated 92.3% sensitivity and 81.8% specificity for detecting neutrophils with toxic granulation.
Conclusions:
- Measurement of FAD fluorescence intensity via flow cytometry is an easy, objective, and reliable method for detecting neutrophils with toxic granulation.
- This technique offers improved diagnostic capabilities for acute bacterial infections compared to traditional methods.

