Professor Terence Ndonyi Bukong and his team of virologists, in partnership with Professor Patrick Labonté, discovered this potential therapeutic target. They unveiled that the cellular protein RTN3 was involved in mediating an important pathway essential in Hepatitis C virus disease development, and progression. This promising discovery could lead to better treatments for the disease, which kills approximately 500,000 people annually.

Master of disguise

Normally, the immune system needs to recognize a virus to attack it and prevent infection. The Hepatitis C virus, however, is a master of disguise. It moves around, undetected, in exosomes, which are cell-released microvesicles vesicles that normally function in cellular communication, transport, and cellular waste disposal. This novel research revealed that the Hepatitis C viruses interact with a key area of the RTN3 protein utilizing it to insert their viral RNA into exosomes.

"We are the first researchers to demonstrate the exosomal role that this protein plays in hepatitis C pathogenesis," said Dr. Bukong, who led the study published in the journal PLOS One. "By identifying the areas of the protein that lead to the formation of an infectious exosome, we can now look for distinctive molecules that block the interaction with the viral RNA." He went on to say, "This would prevent the viral RNA from being able to enter exosomes and hide from the body's immune system."

The discovery of this interaction between the virus and the RTN3 protein opens the door to more research on other viruses that use exosomes to evade detection. "For example, studies have shown that HIV, Zika, and Hepatitis B viruses also hide inside exosomes. This disguise creates a problem for the optimal function of vaccines because even if antibodies are developed, they are unable to block viral infection or transmission," Dr. Bukong explained. "If the RTN3 protein also plays an important role in these other illnesses, it could help us make more effective treatments, and, potentially, more effective vaccines."

Story Source:

Materials provided by Institut national de la recherche scientifique - INRS. Original written by Audrey-Maude Vezina. Note: Content may be edited for style and length.

Journal Reference:

1. Jingjing Li, Ebtisam Abosmaha, Carla S. Coffin, Patrick Labonté, Terence Ndonyi Bukong. Reticulon-3 modulates the incorporation of replication competent hepatitis C virus molecules for release inside infectious exosomes. PLOS ONE, 2020; 15 (9): e0239153 DOI: 10.1371/journal.pone.0239153