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Related Concept Videos

Flow Cytometry01:23

Flow Cytometry

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The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
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Molecular Probe Optimization to Determine Cell Mortality in a Photosynthetic Organism Microcystis aeruginosa Using Flow Cytometry
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Optimizing FlowCam Imaging Flow Cytometry Operation for Classification and Quantification of Microcystis

Dmitry Malashenkov1, Veronika Dashkova2, Ivan A Vorobjev1,3

  • 1Department of Biology, School of Sciences and Humanities, Nazarbayev University, Astana, Kazakhstan.

Methods in Molecular Biology (Clifton, N.J.)
|April 19, 2023
PubMed
Summary

Quantifying Microcystis blooms is challenging. Imaging flow cytometry (IFC) with FlowCam offers an objective method to identify and count different Microcystis species in environmental samples.

Keywords:
CyanoHABsCyanobacteriaFlowCamImaging flow cytometryMicrocystisPhytoplankton

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Area of Science:

  • Environmental microbiology
  • Aquatic ecology
  • Phycology

Background:

  • Microcystis cyanobacteria cause toxic blooms globally.
  • Distinguishing Microcystis morphospecies is crucial but difficult with light microscopy.
  • Current methods for Microcystis quantification are often time-consuming and imprecise.

Purpose of the Study:

  • To present a FlowCam methodology for Microcystis morphospecies identification and quantification.
  • To analyze five common European Microcystis morphospecies using imaging flow cytometry.
  • To provide objective data for Microcystis bloom analysis.

Main Methods:

  • Utilized a benchtop imaging flow cytometer (FlowCam).
  • Developed sample processing and analysis protocols for environmental samples.
  • Focused on five European Microcystis morphospecies found in temperate zones.

Main Results:

  • The FlowCam technique successfully detected and differentiated Microcystis morphospecies.
  • Objective qualitative and quantitative data were generated.
  • The method facilitates statistical analysis of Microcystis populations.

Conclusions:

  • Imaging flow cytometry provides an efficient and objective approach for Microcystis analysis.
  • FlowCam methodology enables accurate quantification of co-occurring Microcystis morphospecies.
  • This technique supports better understanding and management of Microcystis blooms.