Synthetic biomarker technology differentiates between prior Zika and dengue infections

A newly discovered Zika virus-specific synthetic molecule is capable of differentiating Zika-immune patient samples from samples of patients previously infected with the related dengue virus. The technology may lead to the development of better diagnostics and vaccine candidates.

The study, published in Proceedings of the National Academy of Sciences, has been led by researchers at the University of Pittsburgh School of Public Health and The Herbert Wertheim UF Scripps Institute for Biomedical Innovation & Technology, is the first to apply an innovative ‘epitope surrogate’ technology to Zika. Until now, researchers and clinicians have lacked diagnostic tools to easily differentiate between prior infections with different flaviviruses, a family of mostly mosquito- and tick-borne viruses that include Zika and dengue. This has posed challenges for clinical-epidemiologic studies, viral diagnostics and vaccine development.

“If you go to places like Brazil, nearly everybody is going to have some immunity to dengue, and also to Zika,” says first author Priscila Castanha PhD (pictured above), an Assistant Professor in the Department of Infectious Disease and Microbiology at Pitt Public Health. “This makes it very difficult to test new treatments or determine how widespread an emerging disease may be in areas endemic for flaviviruses, which cause a high burden of illness globally.”

Antibodies for Zika virus, a mosquito-borne virus that spread to the Americas in 2015 and still causes sporadic disease, can be confused in many diagnostic tests with antibodies for dengue virus, making it difficult to tell if someone who tests positive previously had dengue, Zika or both. It is especially important for reproductive-age women to know if they already had Zika – and likely have immunity – because infection during pregnancy can cause birth defects. Knowing if they have immunity or not could guide the extent of people’s efforts to avoid mosquitoes in endemic areas during pregnancy.

The research team used an approach pioneered by co-senior author Thomas Kodadek PhD, a chemist with The Wertheim UF Scripps Institute to screen half a million ‘peptide-inspired conformationally constrained oligomers’, or PICCOs, against blood samples from people infected with dengue or Zika virus. The PICCOs are nonorganic molecular shapes hooked onto microscopic plastic beads. They mimic epitopes, which are the parts of a pathogen that an antibody would connect to in order to neutralise the threat.

If any of the PICCOs match the corresponding shape of an antibody in the blood sample, the antibody will hook onto them and researchers can ‘fish’ it out. The presence of an antibody against a virus in someone’s blood means that they were previously infected with or vaccinated against that virus, prompting their immune system to produce antibodies.

“The technology is amazing. You don’t need to know the sequence, or the structure, or even the pathogen,” said co-senior author Donald Burke, M.D., Pitt Public Health dean emeritus. “As long as you have chosen the right sets of patient blood samples to compare, you can tease out the important antibodies that differ between the patient sets, along with the corresponding synthetic molecule biomarkers.”

The researchers identified 40 PICCOs that engaged Zika virus antibodies. After screening against dengue-positive blood, one PICCO, dubbed CZV1-1, was particularly good at hooking Zika antibodies, but not dengue. This single CZV1-1 PICCO synthetic molecule correctly identified people previously infected with Zika virus 85.3% of the time and only generated false positives in 1.6% of tests, rates comparable to COVID-19 antibody tests.

This research was funded by a grant from the National Institute of Allergy and Infectious Diseases (R01AI127677).


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