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Mitochondrial Import of Dengue Virus NS3 Protease and Cleavage of GrpEL1, a Cochaperone of Mitochondrial Hsp70

Chaitanya Gandikota, Fareed Mohammed, Lekha Gandhi, Deepti Maisnam, Ushodaya Mattam, Deepika Rathore, Arpan Chatterjee, Katyayani Mallick, Arcy Billoria, V. S. Prasad, Naresh Babu V. Sepuri, Musturi Venkataramana

2020Journal of Virology27 citationsDOIOpen Access PDF

Abstract

Approximately 40% of the world’s population is at risk of dengue virus infection. There is currently no specific drug or potential vaccine for these infections. Lack of complete understanding of the pathogenesis of the virus is one of the hurdles that must be overcome in developing antivirals for this virus infection. In the present study, we observed that the dengue virus-coded protease imports to the mitochondrial matrix, and our report is the first ever of a virus-coded protein, either animal or human, importing to the mitochondrial matrix. Our analysis indicates that the observed mitochondrial import is due to an inherited mitochondrial transport signal. We also show that matrix-localized GrpE protein homolog 1 (GrpEL1), a cochaperone of mitochondrial Hsp70 (mtHsp70), is also the substrate of dengue virus protease, as observed in vitro and ex vivo in virus-infected cells and dengue virus-infected clinical samples. Hence, our studies reveal an essential aspect of the pathogenesis of dengue virus infections, which may aid in developing antidengue therapeutics.

Topics & Concepts

Dengue virusBiologyVirologyVirusDengue feverNS3FlaviviridaeProteaseViral diseaseHepatitis C virusEnzymeBiochemistryMosquito-borne diseases and controlMalaria Research and ControlViral Infections and Outbreaks Research
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