Viruses rely on host for energy production. The viral protein NS1 binds to an enzyme GAPDH to improve the energy supply required to support viral replication.
Brazilian scientists have discovered the mechanism that dengue virus uses to bind with human enzyme to replicate and spread faster in the body. NS1 is one of the seven proteins composing the dengue virus and more specifically its replication machinery.
It is an abundant protein detected in the serum of infected patients and used as a target for early detection.Without NS1, the virus cannot replicate whereas NS1 mutation decreases virus yield.
Using a unique technique, the team found that the viral protein that NS1 binds to is well-known to any cell biologist is called "GAPDH".
GAPDH is an enzyme involved in process where the glucose is broken down to generate energy in humans.
The enzyme is ubiquitous and very abundant in animal cells and is also involved in non-metabolic processes such as control of gene expression.
Because GAPD is so abundant in the cell, the group also performed other complementing tests to confirm that the binding between NS1 and GAPDH is specific and not a spurious finding.
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Indeed, energy production modulation is a remarkable feature that improves the energy supply required for supporting active viral replication, he added.
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Dengue is a mosquito-borne tropical disease currently endemic in more than 10 countries, including India.
According to the World Health Organization (WHO), 390 million people are infected by dengue every year.
The disease can be caused by one of the four types of dengue virus transmitted by the Aedes aegypty mosquito, the main vector for dengue.
In humans, symptoms of dengue infection include fever, headache, muscle and joint pain and a characteristic skin rash.
In some cases, dengue infection can take a dangerous turn and develop into a life-threatening hemorrhagic fever and dengue shock syndrome.
The paper has been published in the Journal of Virology.
Source-IANS