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A systematic view on influenza induced host shutoff

Authors :
Idit Anna Gelbart
Shalev Itzkovitz
Michal Mandelboim
Alina Shitrit
Yaron Drori
Noam Stern-Ginossar
Julie Tai
Adi Bercovich-Kinori
Shani Ben-Moshe
Source :
eLife, Vol 5 (2016), eLife
Publication Year :
2016
Publisher :
eLife Sciences Publications Ltd, 2016.

Abstract

Proteins carry out diverse activities in our cells. These proteins are constantly being built according to accurate instructions, which are encoded on molecules named messenger RNAs (mRNAs for short). The process of converting the instructions into proteins is called translation. Viruses infect host cells and take over the cellular machinery that is responsible for translation. This causes the cell to produce viral proteins at the expense of host proteins – a process called host shutoff. As a result, viral proteins take over the cell and the infection accelerates. There are two main strategies used by viruses to co-opt the cell’s translation machinery: either host mRNAs are destroyed, or the machines that read mRNA molecules are manipulated to read only the viral instructions. Most viruses appear to dedicate themselves to using just one of these strategies. However, evidence suggests that the Influenza A virus uses both strategies to induce host shutoff. To investigate the extent to which each of the shutoff strategies is used by the Influenza A virus, Bercovich-Kinori, Tai et al. have studied infected human lung cells. This revealed that the virus primarily reduces the amount of host mRNA in the cells to take over the mRNA pool. The host mRNAs were affected by the infection to different extents. For example, the mRNAs that coded for proteins that perform important roles for the virus, such as produce energy, were not affected by the virus. A future challenge is to find out exactly how the Influenza A virus distinguishes between different cellular mRNAs. This knowledge may help to develop new treatments for flu.

Details

Language :
English
Volume :
5
Database :
OpenAIRE
Journal :
eLife
Accession number :
edsair.doi.dedup.....dd067fcb125a588acf6fbbec84f3b6dc