Literature DB >> 27643682

Alternative fluorescent labeling strategies for characterizing gram-positive pathogenic bacteria: Flow cytometry supported counting, sorting, and proteome analysis of Staphylococcus aureus retrieved from infected host cells.

Petra Hildebrandt1,2, Kristin Surmann1,2, Manuela Gesell Salazar1, Nicole Normann1,2, Uwe Völker1,2, Frank Schmidt3,4.   

Abstract

Staphylococcus aureus is a Gram-positive opportunistic pathogen that is able to cause a broad range of infectious diseases in humans. Furthermore, S. aureus is able to survive inside nonprofessional phagocytic host cell which serve as a niche for the pathogen to hide from the immune system and antibiotics therapies. Modern OMICs technologies provide valuable tools to investigate host-pathogen interactions upon internalization. However, these experiments are often hampered by limited capabilities to retrieve bacteria from such an experimental setting. Thus, the aim of this study was to develop a labeling strategy allowing fast detection and quantitation of S. aureus in cell lysates or infected cell lines by flow cytometry for subsequent proteome analyses. Therefore, S. aureus cells were labeled with the DNA stain SYTO® 9, or Vancomycin BODIPY® FL (VMB), a glycopeptide antibiotic binding to most Gram-positive bacteria which was conjugated to a fluorescent dye. Staining of S. aureus HG001 with SYTO 9 allowed counting of bacteria from pure cultures but not in cell lysates from infection experiments. In contrast, with VMB it was feasible to stain bacteria from pure cultures as well as from samples of infection experiments. VMB can also be applied for histocytochemistry analysis of formaldehyde fixed cell layers grown on coverslips. Proteome analyses of S. aureus labeled with VMB revealed that the labeling procedure provoked only minor changes on proteome level and allowed cell sorting and analysis of S. aureus from infection settings with sensitivity similar to continuous gfp expression. Furthermore, VMB labeling allowed precise counting of internalized bacteria and can be employed for downstream analyses, e.g., proteomics, of strains not easily amendable to genetic manipulation such as clinical isolates.
© 2016 International Society for Advancement of Cytometry. © 2016 International Society for Advancement of Cytometry.

Entities:  

Keywords:  S. aureus; cell counting and sorting; flow cytometry; fluorescence labeling of S. aureus; fluorescence microscopy; fluorescent vancomycin conjugate; gram-positive bacteria; internalization; proteomics

Mesh:

Substances:

Year:  2016        PMID: 27643682     DOI: 10.1002/cyto.a.22981

Source DB:  PubMed          Journal:  Cytometry A        ISSN: 1552-4922            Impact factor:   4.355


  3 in total

1.  Signatures of cytoplasmic proteins in the exoproteome distinguish community- and hospital-associated methicillin-resistant Staphylococcus aureus USA300 lineages.

Authors:  Solomon A Mekonnen; Laura M Palma Medina; Corinna Glasner; Eleni Tsompanidou; Anne de Jong; Stefano Grasso; Marc Schaffer; Ulrike Mäder; Anders R Larsen; Heidi Gumpert; Henrik Westh; Uwe Völker; Andreas Otto; Dörte Becher; Jan Maarten van Dijl
Journal:  Virulence       Date:  2017-05-05       Impact factor: 5.882

2.  Detection and Discrimination of Bacterial Colonies with Mueller Matrix Imaging.

Authors:  Saeedesadat Badieyan; Arezou Dilmaghani-Marand; Mohammad Javad Hajipour; Ali Ameri; Mohammad Reza Razzaghi; Hashem Rafii-Tabar; Morteza Mahmoudi; Pezhman Sasanpour
Journal:  Sci Rep       Date:  2018-07-17       Impact factor: 4.379

3.  Identification of surface proteins in a clinical Staphylococcus haemolyticus isolate by bacterial surface shaving.

Authors:  Runa Wolden; Maria Pain; Roger Karlsson; Anders Karlsson; Elizabeth G Aarag Fredheim; Jorunn Pauline Cavanagh
Journal:  BMC Microbiol       Date:  2020-04-07       Impact factor: 3.605

  3 in total

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