Dengue virus is a globally distributed flavivirus with 4 distinct serotypes (DENV1, 2, 3 and 4) and is primarily transmitted by the Aedes aegypti mosquito, which is found throughout the tropical and subtropical regions of over 100 countries. DENV poses a significant worldwide public health threat with approximately 2.5 to 3 billion people residing in DENV endemic areas, among whom 100 to 200 million individuals will be infected and approximately 30,000 patients will succumb to the disease, annually (Mayo Clinic Laboratories, 2019).
NS1 is produced during all four DENV infections and is released as a hexamer circulating in great quantities in acute-phase blood of infected humans. In diagnostics, DENV NS1 is used as an antigen test for rapid detection on the first day of fever, before antibodies appear some 5 or more days later. It has emerged as an alternative biomarker to both serologic and molecular based techniques for diagnosis of acute DENV infection. NS1 antigenemia is detectable within 24 hours and up to 9 days following symptoms onset. This overlaps with the DENV viraemic phase and NS1 is often detectable prior to IgM seroconversion. Vaccines have also been developed using NS1. Mice immunized with all four DENV NS1 proteins have been shown to be completely protected against homologous DENV challenges, whereas immunization with DENV1 NS1 only partially protected against heterologous DENV2 challenge (reviewed in Halstead, 2019). An NS1-based vaccine is currently under development (Espinosa et al., 2019). A live-attenuated tetravalent dengue vaccine (LATV), containing genes for three of the four DENV NS1 proteins, is also in phase 3 clinical testing, and appears to provide durable and solid protection against DENV in both seronegatives and seropositives (reviewed in Halstead, 2019).
Interestingly, mosquito insect cells also secrete NS1 efficiently (Alcalá, 2018) and recombinant DENV NS1 can be produced in the baculovirus Sf9 insect expression system and purified from cell culture supernatant (Akey et al., 2014; Muller et al., 2012). DENV NS1 secreted from insect cells is hexameric and presents the same open-barrel structure as that observed in secreted NS1 derived from vertebrate cells (Thiemmeca et al., 2016). Mammalian cell-derived NS1 shows both high mannose and complex type N-linked glycans, whereas soluble NS1 secreted from DENV-infected insect cells contains only high mannose glycans. Insect cell-derived secreted NS1 also has different physical properties including smaller and more heterogeneous sizes, and the formation of less stable NS1 hexamers. However, both mammalian and insect cell-derived NS1 bind to complement proteins C1s, C4 and C4 binding protein as well as to a novel partner, mannose-binding lectin (MBL) which protects DENV from MBL-mediated neutralization (Thiemmeca et al., 2016). Complement antagonism functions of soluble NS1 (both insect-cell and mammalian cell-derived) could protect DENV from complement-mediated neutralization, thereby facilitating viral spread either at the earliest stages of infection (during mosquito feeding) or during subsequent replication cycles of DENV in a human host (Thiemmeca et al., 2016).
Source:Recombinant protein corresponding to Dengue Virus Serotype 3 NS1, expressed in insect cells.
Applications:Suitable for use in Immunoassay Development. Other applications not tested.
Storage and Stability:May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 6 months after receipt at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
