Genome-wide analyses of translation can provide major contributions in our understanding of the complex interplay between virulent factors and host cells. So far, the activation of host translational control mechanisms by bacterial toxins, owing to specific recruitment of mRNAs, RNA-binding proteins (RBPs) and ncRNAs (non-coding RNAs), are far from being understood. In the present study, we characterize for the first time the changes experienced by the translational control system of host cells in response to the well-known Staphylococcus aureus ?-haemolysin (AHL) under both sublytic and lytic conditions. By comparing variations occurring in the cellular transcriptome and translatome, we give evidence that global gene expression is primarily rewired at the translational level, with the contribution of the RBP ELAVL1 (HuR) in the sublytic response. These results reveal the importance of translational control during host-pathogen interaction, opening new approaches for AHL-induced diseases.

Global translation variations in host cells upon attack of lytic and sublytic Staphylococcus aureus ?-haemolysin1

Mauro Dalla Serra;
2015

Abstract

Genome-wide analyses of translation can provide major contributions in our understanding of the complex interplay between virulent factors and host cells. So far, the activation of host translational control mechanisms by bacterial toxins, owing to specific recruitment of mRNAs, RNA-binding proteins (RBPs) and ncRNAs (non-coding RNAs), are far from being understood. In the present study, we characterize for the first time the changes experienced by the translational control system of host cells in response to the well-known Staphylococcus aureus ?-haemolysin (AHL) under both sublytic and lytic conditions. By comparing variations occurring in the cellular transcriptome and translatome, we give evidence that global gene expression is primarily rewired at the translational level, with the contribution of the RBP ELAVL1 (HuR) in the sublytic response. These results reveal the importance of translational control during host-pathogen interaction, opening new approaches for AHL-induced diseases.
2015
Istituto di Biofisica - IBF
alpha hemolysin
messenger RNA
RNA binding protein
transcriptome
untranslated RNA
bacterial toxin
ELAV like protein 1
ELAVL1 protein
human
hemolysin
staphylococcal alpha-toxin
transcriptome
Article
bioinformatics
control system
controlled study
gene expression
host cell
host pathogen interaction
human
human cell
immune response
nonhuman
priority journal
Staphylococcus au
DNA microarray
dose response
drug effects
gene expression profiling
genetic variation
genetics
immunoblotting
metabolism
mutation
procedures
protein synthesis
reverse transcription polymerase chain reaction
tumor cell line
Bacterial Toxins
Cell Line
Tumor
Dose-Response Relationship
Drug
ELAV-Like Protein 1
Gene Expression Profiling
Genetic Variation
Hemolysin Proteins
Humans
Immunoblotting
Mutation
Oligonucleotide Array Sequence Analysis
Protein Biosynthesis
Reverse Transcriptase Polymerase Chain Reaction
Transcriptome
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/425870
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