Literature DB >> 29653838

A Multicolor Split-Fluorescent Protein Approach to Visualize Listeria Protein Secretion in Infection.

Dilara Batan1, Esther Braselmann2, Michael Minson2, Dieu My Thanh Nguyen3, Pascale Cossart4, Amy E Palmer5.   

Abstract

Listeria monocytogenes is an intracellular food-borne pathogen that has evolved to enter mammalian host cells, survive within them, spread from cell to cell, and disseminate throughout the body. A series of secreted virulence proteins from Listeria are responsible for manipulation of host-cell defense mechanisms and adaptation to the intracellular lifestyle. Identifying when and where these virulence proteins are located in live cells over the course of Listeria infection can provide valuable information on the roles these proteins play in defining the host-pathogen interface. These dynamics and protein levels may vary from cell to cell, as bacterial infection is a heterogeneous process both temporally and spatially. No assay to visualize virulence proteins over time in infection with Listeria or other Gram-positive bacteria has been developed. Therefore, we adapted a live, long-term tagging system to visualize a model Listeria protein by fluorescence microscopy on a single-cell level in infection. This system leverages split-fluorescent proteins, in which the last strand of a fluorescent protein (a 16-amino-acid peptide) is genetically fused to the virulence protein of interest. The remainder of the fluorescent protein is produced in the mammalian host cell. Both individual components are nonfluorescent and will bind together and reconstitute fluorescence upon virulence-protein secretion into the host cell. We demonstrate accumulation and distribution within the host cell of the model virulence protein InlC in infection over time. A modular expression platform for InlC visualization was developed. We visualized InlC by tagging it with red and green split-fluorescent proteins and compared usage of a strong constitutive promoter versus the endogenous promoter for InlC production. This split-fluorescent protein approach is versatile and may be used to investigate other Listeria virulence proteins for unique mechanistic insights in infection progression.
Copyright © 2018 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 29653838      PMCID: PMC6050711          DOI: 10.1016/j.bpj.2018.03.016

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  60 in total

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Review 2.  A Critical and Comparative Review of Fluorescent Tools for Live-Cell Imaging.

Authors:  Elizabeth A Specht; Esther Braselmann; Amy E Palmer
Journal:  Annu Rev Physiol       Date:  2016-11-16       Impact factor: 19.318

3.  Listeriolysin O is essential for virulence of Listeria monocytogenes: direct evidence obtained by gene complementation.

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Authors:  Schuyler B Van Engelenburg; Theresa Nahreini; Amy E Palmer
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5.  Identification of a second Listeria secA gene associated with protein secretion and the rough phenotype.

Authors:  Laurel L Lenz; Daniel A Portnoy
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6.  Listeria monocytogenes dampens the DNA damage response.

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7.  Versatile protein tagging in cells with split fluorescent protein.

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Journal:  Nat Commun       Date:  2016-03-18       Impact factor: 14.919

8.  Visualizing the Translocation and Localization of Bacterial Type III Effector Proteins by Using a Genetically Encoded Reporter System.

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Review 9.  Animal models for oral transmission of Listeria monocytogenes.

Authors:  Sarah E F D'Orazio
Journal:  Front Cell Infect Microbiol       Date:  2014-02-11       Impact factor: 5.293

10.  Improved split fluorescent proteins for endogenous protein labeling.

Authors:  Siyu Feng; Sayaka Sekine; Veronica Pessino; Han Li; Manuel D Leonetti; Bo Huang
Journal:  Nat Commun       Date:  2017-08-29       Impact factor: 14.919

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4.  Fluorescent secreted bacterial effectors reveal active intravacuolar proliferation of Listeria monocytogenes in epithelial cells.

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