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      Imaging flow cytometry analysis of intracellular pathogens

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          Abstract

          Imaging flow cytometry has been applied to address questions in infection biology, in particular, infections induced by intracellular pathogens. This methodology, which utilizes specialized analytic software makes it possible to analyze hundreds of quantified features for hundreds of thousands of individual cellular or subcellular events in a single experiment. Imaging flow cytometry analysis of host cell-pathogen interaction can thus quantitatively addresses a variety of biological questions related to intracellular infection, including cell counting, internalization score, and subcellular patterns of co-localization. Here, we provide an overview of recent achievements in the use of fluorescently labeled prokaryotic or eukaryotic pathogens in human cellular infections in analysis of host-pathogen interactions. Specifically, we give examples of Imagestream-based analysis of cell lines infected with Toxoplasma gondii or Mycobacterium tuberculosis. Furthermore, we illustrate the capabilities of imaging flow cytometry using a combination of standard IDEAS™ software and the more recently developed Feature Finder algorithm, which is capable of identifying statistically significant differences between researcher-defined image galleries. We argue that the combination of imaging flow cytometry with these software platforms provides a powerful new approach to understanding host control of intracellular pathogens.

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          Author and article information

          Journal
          9426302
          20385
          Methods
          Methods
          Methods (San Diego, Calif.)
          1046-2023
          1095-9130
          9 March 2018
          15 September 2016
          01 January 2017
          19 March 2018
          : 112
          : 91-104
          Affiliations
          [1 ]Program in Cellular and Molecular Medicine, Boston Children’s Hospital
          [2 ]Department of pediatrics, Harvard Medical School
          [3 ]School of Science and Technology, Nazarbayev University
          [4 ]A.N. Belozersky Institute of Physico-Chemical Biology
          [5 ]Department of Cell Biology and Histology, M.V. Lomonosov Moscow State University
          Author notes
          [* ]Co-Corresponding Authors: Dr. Natasha S. Barteneva, Harvard Medical School, D-239, Armenise Building, 200 Longwood Ave, Boston, 02115, USA, Phone/fax: 1-617-713-8930, natasha.barteneva@ 123456childrens.harvard.edu , Dr. Anne E. Goldfeld, Program in Cellular and Molecular Medicine, BCH-Harvard Medical School, Warren-Alpert Building, 200 Longwood Ave, Boston, 02115, USA, Phone: 617-738778, Anne.Goldfeld@ 123456childrens.harvard.edu
          Article
          PMC5857943 PMC5857943 5857943 nihpa818797
          10.1016/j.ymeth.2016.09.007
          5857943
          27642004
          71931ba0-e7e9-4555-834b-d775491247b0
          History
          Categories
          Article

          intracellular pathogen,Rab7,Rab5,phagosome maturation,colocalization,cellular heterogeneity,Feature Finder, Toxoplasma gondii , Mycobacteria tuberculosis ,fluorescent protein,imaging flow cytometry

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