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Host-Bacteria Interactions

Overview of attention for book
Cover of 'Host-Bacteria Interactions'

Table of Contents

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    Book Overview
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    Chapter 1 Galleria mellonella as an Infection Model for Select Agents.
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    Chapter 2 Drosophila as a model for intestinal infections.
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    Chapter 3 Zebrafish embryos as a model to study bacterial virulence.
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    Chapter 4 Studying host-pathogen interaction events in living mice visualized in real time using biophotonic imaging.
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    Chapter 5 Intravital two-photon imaging to understand bacterial infections of the Mammalian host.
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    Chapter 6 Cre Reporter Assay for Translocation (CRAfT): A Tool for the Study of Protein Translocation into Host Cells.
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    Chapter 7 Detection of the interaction between host and bacterial proteins: eukaryotic nucleolin interacts with francisella elongation factor tu.
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    Chapter 8 Hijacking the host proteasome for the temporal degradation of bacterial effectors.
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    Chapter 9 Live cell imaging of phosphoinositide dynamics during legionella infection.
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    Chapter 10 Investigating interference with apoptosis induction by bacterial proteins.
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    Chapter 11 Bimolecular fluorescence complementation for imaging protein interactions in plant hosts of microbial pathogens.
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    Chapter 12 Investigating TLR Signaling Responses in Murine Dendritic Cells Upon Bacterial Infection.
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    Chapter 13 siRNA Screens Using Drosophila Cells to Identify Host Factors Required for Infection.
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    Chapter 14 Purification of Intracellular Bacteria: Isolation of Viable Brucella abortus from Host Cells.
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    Chapter 15 RNA Sequencing of FACS-Sorted Immune Cell Populations from Zebrafish Infection Models to Identify Cell Specific Responses to Intracellular Pathogens.
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    Chapter 16 Taking the shortcut for high-throughput shotgun proteomic analysis of bacteria.
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    Chapter 17 Comparative Genomic Analysis at the PATRIC, A Bioinformatic Resource Center.
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    Chapter 18 A Markerless Deletion Method for Genetic Manipulation of Burkholderia cenocepacia and Other Multidrug-Resistant Gram-Negative Bacteria.
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    Chapter 19 Gene Inactivation in Coxiella burnetii.
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    Chapter 20 A Chemical Mutagenesis Approach to Identify Virulence Determinants in the Obligate Intracellular Pathogen Chlamydia trachomatis.
Attention for Chapter 6: Cre Reporter Assay for Translocation (CRAfT): A Tool for the Study of Protein Translocation into Host Cells.
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Chapter title
Cre Reporter Assay for Translocation (CRAfT): A Tool for the Study of Protein Translocation into Host Cells.
Chapter number 6
Book title
Host-Bacteria Interactions
Published in
Methods in molecular biology, July 2014
DOI 10.1007/978-1-4939-1261-2_6
Pubmed ID
Book ISBNs
978-1-4939-1260-5, 978-1-4939-1261-2
Authors

Amke den Dulk-Ras, Annette C Vergunst, Paul J J Hooykaas, Annette C. Vergunst, Paul J. J. Hooykaas

Editors

Annette C. Vergunst, David O'Callaghan

Abstract

Many pathogenic bacteria introduce virulence proteins, also called effector proteins, into host cells to accomplish infection. Such effector proteins are often translocated into host cells by bacterial type III (T3SS) or type IV secretion systems (T4SS). To better understand the molecular mechanisms underlying virulence, it is essential to identify the effector proteins and determine their functions. Several reporter assays have been established to identify translocated effector proteins and verify T3SS- or T4SS-dependent transport into host cells. Here we describe a protocol to monitor the translocation of candidate effector proteins using Cre recombinase as a reporter, and more specifically how this Cre Reporter Assay for Translocation (CRAfT) can be used to detect translocation of Vir proteins from Agrobacterium tumefaciens into yeast and plant cells. The assay can be adapted for the study of the T3SS or T4SS of human pathogens.

X Demographics

X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 31%
Student > Bachelor 4 31%
Other 1 8%
Lecturer 1 8%
Professor 1 8%
Other 1 8%
Unknown 1 8%
Readers by discipline Count As %
Agricultural and Biological Sciences 8 62%
Biochemistry, Genetics and Molecular Biology 3 23%
Medicine and Dentistry 1 8%
Unknown 1 8%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 31 August 2014.
All research outputs
#15,618,818
of 23,223,705 outputs
Outputs from Methods in molecular biology
#5,455
of 13,309 outputs
Outputs of similar age
#133,608
of 229,721 outputs
Outputs of similar age from Methods in molecular biology
#16
of 93 outputs
Altmetric has tracked 23,223,705 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,309 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 44th percentile – i.e., 44% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 229,721 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 32nd percentile – i.e., 32% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 93 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 76% of its contemporaries.