How Zika virus remodels its host cell to boost viral production

How Zika virus remodels its host cell to boost viral production


Researchers have discovered how a Zika virus protein reshapes its host cell to aid viral replication. The study, which will be published in the Journal of Cell Biology, reveals that the viral protein NS1 converts an interior cellular compartment called the endoplasmic reticulum (ER) into a protective region where the virus can survive and replicate. Blocking this process could be a novel therapeutic strategy to treat patients infected with Zika or similar viral pathogens, such as the yellow fever and dengue viruses.

The Zika virus causes relatively mild symptoms in most cases but can result in severe birth defects when pregnant women are infected. Once the virus enters a host cell, it reshapes the cell's ER, causing this membrane-bound compartment to fold inward and form small pockets where the virus can replicate its genetic material, without being attacked by the host cell's immune defenses.

"The architecture of this viral replication compartment is well known, but how the Zika virus remodels the ER is obscure," says a researcher in the study.

In the new study, the authors find that this remodeling process is carried out by a viral protein called NS1 that accumulates in the ER of infected cells. The researchers discovered that NS1 inserts itself into the ER membrane, causing it to fold inward and form viral replication compartments. NS1 expressed in the ER lumen induced ER perinuclear aggregation with an ultrastructure resembling that of the replication compartment. Data from model membrane system indicated that the membrane-binding and membrane-remodeling properties of NS1 depend on its hydrophobic insertion into the membrane.

When the researchers mutated NS1 to prevent it from inserting into the ER membrane, the protein was unable to remodel the ER and viral replication was inhibited.

"We conclude that NS1-induced ER remodeling is the basis of replication compartment biogenesis and that viral replication and production are abolished in the absence of this process," says said the co-lead of the study.

The Zika virus is closely related to a number of other viruses, including the yellow fever virus, dengue virus, and West Nile virus, that also convert the ER of their host cells into specialized viral replication compartments. The authors found that the dengue virus's NS1 protein also induces ER remodeling, suggesting that all of these pathogenic viruses use similar mechanisms to generate their replication compartments and that blocking this process could be a new therapeutic strategy to treat Zika and other viral infections.

https://rupress.org/jcb/article/doi/10.1083/jcb.201903062/133534/Zika-NS1induced-ER-remodeling-is-essential-for

http://sciencemission.com/site/index.php?page=news&type=view&id=publications%2Fzika-ns1-induced-er&filter=22

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