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Background Dengue fever is the most important vector-borne viral disease. Four serotypes of dengue virus, DENV1 to DENV4, coexist. Infection by one serotype elicits long-lasting immunity to that serotype but not the other three.
Subsequent infection by a different serotype is a risk factor for severe dengue. Domain III (ED3) of the viral envelope protein interacts with cell receptors and contains epitopes recognized by neutralizing antibodies. We determined the serotype specificity and cross-reactivity of human IgMs directed against ED3 by using a well-characterized collection of 90 DENV-infected and 89 DENV-uninfected human serums. Results The DENV-infected serums contained IgMs that reacted with one or several ED3 serotypes. Touch sensor technologies. The discrimination by ED3 between serums infected by the homotypic DENV and uninfected serums varied with the serotype in the decreasing order DENV1 > DENV2 > DENV3 > DENV4. The ED3 domain of DENV1 gave the highest discrimination between DENV-infected and DENV-uninfected serums, whatever the infecting serotype, and thus behaved like a universal ED3 domain for the detection of IgMs against DENV. Some ED3 serotypes discriminated between IgMs directed against the homotypic and heterotypic DENVs.
The patterns of cross-reactivities and discriminations varied with the serotype. Background Dengue is a mosquito-borne infection of the tropics and subtropics. Cisco webex meeting app for mac.
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Some 2.5 billion people are at risk, and 50–100 millions are infected annually. Most infections are either asymptomatic or result in dengue fever, a relatively mild illness. However, a life threatening form, severe dengue, develops in 1–5% of infections [].