Zika
Zika virus attracted world-wide attention due to a very large outbreak in Brazil in 2015/2016, which readily spread across South America, into the Caribbean and to the southern states of the USA.
The Native Antigen Company supply a range of products to support researchers working with Zika virus including recombinant proteins, native viral lysates, antibodies and immunoassays.
Zika virus background
Zika virus (ZIKV) is an emerging disease that is spread by Aedes mosquitoes. The virus was first isolated in Central Africa, and has since spread to South Asia and recently to South America. Outbreaks were reported in Micronesia in 2007 and in Brazil in 2015, confirming at least 13 autochthonous infections. The Zika virus outbreak in Brazil in 2016 has gained world-wide attention, and has been linked to an increasing number of microcephaly cases. In April 2016, the Centers for Disease Control and Prevention in the USA, confirmed the link between ZIKV infection of the foetus with microcephaly (CDC).
Zika virus can cause mild fever, rash, myalgia, arthralgia and headaches, with one in four infected individuals being asymptomatic. Due to similar symptoms, ZIKV infected individuals can easily be misdiagnosed as a dengue infection and vice-versa. Currently, there is no vaccine or specific treatment available for ZIKV infection.
Analysis of ZIKV sequences from infected patients have shown that the strain circulating in South America in 2015 differs to the strain originally isolated in 1947 in Uganda (the “Uganda” strain). The South American strain was first isolated and sequenced from a patient in Suriname, and hence is known as the Zika Suriname strain (Enfissi, A) .
References
- Centers for Disease Control and Prevention. CDC Concludes Zika Causes Microcephaly and Other Birth Defects.
- Enfissi A. et al (2016). Zika virus genome from the Americas. Lancet 387(10015):227-8
Zika Virus Antigens
We offer an extensive range of Zika virus antigens, both expressed as recombinant proteins in our mammalian expression system and as native viral prpearations.
NS1 proteins are available from both the prototypic Uganda strain, and from the Suriname strain, responsible for the major outbreak in 2016. These proteins are fully glycosylated and are in hexameric format.
We also offer Zika Virus-like particles (VLPs), which are intact particles comprising 180 copies of Envelope and prM/M proteins. These have been extensively analysed demonstrating that they are antigenically similar to native Dengue virus. Complementing both NS1 and VLP proteins, are soluble Zika virus Envelope protein.
Our products derived from native Zika virus are prepared from infected cell cultures, and include whole cell lysates alongside sucrose-density gradient purified virus.
Zika Virus Antibodies
At The Native Antigen Company we offer three mouse monoclonal antibodies that are highly specific for Zika virus NS1 protein. These do not cross-react with any other flavivirus NS1 proteins, allowing highly specific detection of Zika NS1 protein. In addition to purified versions of these antibodies, we also offer biotin-conjugated formats, facilitating the use of antibody pairs in immunoassay development.
We are also pleased to offer chimeric versions of one of the mouse monoclonal antibodies in human IgG and human IgM format. These reagents can be used as defined controls in serological assays for Zika virus infection.
Zika Virus Immunoassays
We are pleased to offer two ELISAs for Zika virus research, whose development has benefited from our expertise in Zika virus biology and reagent preparation.
A capture assay to measure levels of Zika virus NS1 protein in serum, plasma and urine is available, with the highest sensitivity of any assay commercially available, detecting NS1 to levels as low as 5pg/ml.
We also offer a serological assay for the detection of total antibody response (IgG IgA and IgM) to Zika infection. This assay is designed for immunosurveilance applications, and has extremely high specificity in areas of endemic Dengue infection, where cross-reactivity has been a significant problem with early commercial assays. The novel format of this assay provides results in only 100 minutes, and it is also suitable for use in all species.
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