SCIENTISTS DEVELOP PROTOTYPE TO DETECT AND DIFFERENTIATE MULTIPLE VECTOR-BORNE FLAVIVIRUSESAPRIL 25, 2019 @ 1.22 PM
The image depicts targeted identification (the beam) of secreted dengue NS1 protein in human blood upon infection. This proteomic assay tracks NS1, which is unique to different flaviviruses.
Photo credit: Max KOSOK, ASTAR’s Institute of Molecular and Cell Biology.
Scientists from Singapore's Agency for Science, Technology and Research (A*STAR), in collaboration with the Environmental Health Institute (EHI) of the National Environment Agency (NEA), and the National Centre for Infectious Diseases (NCID), have developed a new mass spectrometry-based method that can concurrently detect and differentiate multiple vector-borne flaviviruses, including dengue and Zika.
It has the potential to be developed into a diagnostic test that can screen for multiple diseases, using a small volume of biological samples in a single test. These findings were published in leading scientific journal Proceedings of the National Academy of Sciences of the United States of America (PNAS) on 18 March. The prototype protein-based test works by tracking a particular secreted flaviviral protein, known as nonstructural protein 1 (NS1), which is unique for each virus and type. This allows the test to detect multiple flaviviruses, as well as viral co-infections, in a single tube. Currently, each flavivirus diagnosis requires a specific test. Even if the samples can be combined in a single tube (such as with PCR), such combinations tend to compromise the detection sensitivity. NS1 is commonly used as a diagnostic target for dengue. Existing commercially available dengue NS1 tests do not distinguish between the four serotypes of dengue virus. This new diagnostic test produced gave 100 percent accuracy in distinguishing between different flaviviruses and their types. It can also be extended to test for newly emerging flaviviruses and their types, in a short timeframe. This diagnostic test was validated by well characterised dengue patient samples obtained from EHI and NCID. With prompt and more accurate flavivirus diagnosis, a more efficient response towards flavivirus infection is possible, thus improving disease management and control. “The proteomic test we have developed offers many advantages, including the ability to diagnose and determine multiple flaviviruses and their types over a longer diagnostic window in a single test. This makes it unique compared to existing diagnostic methods, and could be a boon for efforts to tackle such diseases,” explained Dr Jayantha Gunaratne, Principal Investigator at A STAR’s Institute of Molecular and Cell Biology, and lead researcher of the study. The research team plans to further develop the prototype test as an in vitro diagnostic device, and eventually commercialise it in accordance with local health regulatory requirements. 
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