Optical Biosensor Rapidly Detects Monkeypox Virus | CPT PPP Coverage

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The researchers used samples collected from the lesions of a patient at UC San Diego Health with laboratory-confirmed mpox. They briefly incubated the samples with monoclonal monkeypox antibodies provided by Ray’s lab that bind to proteins on the surface of the virus. The virus-antibody complex was then transferred into tiny chambers on the surface of silicon chips on the sensor that were treated to fix these nanoparticles. 

Shining precise wavelengths of red and blue light simultaneously on the chips caused interference, which resulted in slightly different responses when the virus-antibody nanoparticles were present. A color camera was used to detect this small signal and count individual particles with high sensitivity. 

“You’re not trying to see the scattered light from the virus particle itself, but you’re looking at the interferometric signature of the field of scattered light mixed with the field that is reflected from the surface of the chip,” said Ünlü. He likens the process to FM radio, which mixes a weak signal containing information with a more powerful carrier signal at the same frequency, which, in turn, amplifies the weak signal.

The scientists also analyzed herpes simplex virus and cowpox virus samples, which have similar clinical presentations to mpox. The biosensor assay easily discriminated mpox samples from these other viruses, demonstrating that the specificity of the assay is essential for distinguishing mpox from these common viral diseases.

“Within two minutes, we can tell whether someone has monkeypox or not,” said Ray. “From collecting the virus samples to getting the real-time data takes around 20 minutes.”

In the clinic, the rapidity of the test would allow healthcare providers to diagnose mpox cases much more quickly than sending samples out to a lab. This is especially important for slowing community spread in countries where healthcare resources are sparse. Clinicians could also start treatment, if available, more quickly.

Ray envisions the tests being mass-produced as kits and sold to clinics, further reducing costs. A single boxed kit could be used to test for a variety of viruses, such as syphilis or HIV.

“The chip would be the same,” said Ray. “The only thing that would be different here is the binding antibody that would be specific for a particular virus.”

Ray and Ünlü are working together toward the goal of commercialization, not only to address the urgent need for rapid mpox tests in the Democratic Republic of the Congo but also to keep outbreaks from turning into pandemics. However, the researchers say this effort will require government support because there is little market for diagnostics addressing future threats.

“If we don’t take care of this particular epidemic right now, it is not going to be limited within Africa,” said Ray.

Additional co-authors on the study include: Howard Brickner, Alex E. Clark, Aaron F. Carlin, UC San Diego; Elif Seymour, iRiS Kinetics, Boston University Business Incubation Center; Michael B. Townsend, Panayampalli S. Satheshkumar, Centers for Disease Control and Prevention; Iris Celebi, Boston University; Megan Riley, axiVEND.

The study was funded, in part, by the National Institute of Allergy and Infectious Diseases at the National Institutes of Health (P30 AI036214), and the National Science Foundation (NSF-TT PFI 2329817).

Read the full study.

Disclosures: All authors completed and submitted the International Committee of Medical Journal Editors form to disclose potential conflicts of interest. No other potential conflicts of interest were disclosed.