How the dengue virus replicates in infected cells

Dengue virus is one of the most prevalent mosquito-transmitted human pathogens. Despite the serious socio-economic impact of dengue-associated diseases, the only licensed vaccine has limited efficacy and an antiviral therapy is not available. NS1 is secreted from infected cells, counteracts antiviral immune responses, and contributes to the severe clinical manifestations of dengue. In addition, NS1 is essential for the viral replication cycle, but the underlying molecular mechanism is unknown. To address this gap in knowledge, Bartenschlager and colleagues used a combination of genetic, biochemical and imaging approaches to determine the role of NS1 in the viral replication cycle.

The researchers identified a cluster of amino acid residues in NS1 that is important for efficient secretion of this protein. Moreover, they identified a novel interaction between NS1 and the precursor of a viral protein called NS4A-2K-4B; this interaction is required for viral RNA replication. The researchers also demonstrated that NS1 is required for the generation of the membranous dengue virus replication organelle in infected cells. This function does not require RNA replication and is independent from NS1's interaction with NS4A-2K-4B. Taken together, the results provide new insights into the role of NS1 in viral RNA replication and establish a genetic map of residues in NS1 required for the diverse functions of this protein.

The authors add, "A detailed study of nonstructural protein 1 of Dengue virus identified determinants required for secretion of this protein, viral RNA replication and formation of the membranous replication organelle of this virus. A novel interaction of NS1 with a previously unrecognized NS4A-2K-NS4B precursor of the virus was found to be required for Dengue virus replication."