The device quickly detects Zika
Engineers have developed a rapid, low-cost genetic test for Zika. The $2 device, about the size of a soda can, doesn’t require electricity or technical expertise and only needs a bit of saliva.
Color-changing paper in the lid turns blue if the genetic assay chip inside detects the virus.
Rapid, accurate diagnosis is especially important for pregnant women who may be infected, researchers say. However, the only approved tests for the virus currently require highly sensitive laboratory equipment. Diagnostic tools that can be used in the field while the patient waits would be a critical tool for fighting the Zika epidemic.
Assays that detect genetic material from the Zika virus itself are considered the gold standard in diagnostics. Alternatives, such as tests that look for antibodies the body creates in response to the virus, are insufficient as they may produce false negatives from people who are infected but haven’t yet produced enough antibodies, or false positives from people who have antibodies for a different disease that is similar enough to trigger the test.
Tests that look for RNA sequences from the virus itself, known as a reverse transcriptase-polymerase chain reaction, or RT-PCR, avoid both problems. However, RT-PCR requires delicate laboratory work. Viral gene sequences in a patient’s sample must be amplified or repeatedly copied, to levels where they can be detected, a process that normally involves multiple precise temperature changes.
“The CDC has approved, on an emergency basis, only these kinds of laboratory-based molecular tests for the Zika virus,” says Changchun Liu, research assistant professor of mechanical engineering and applied mechanics at the University of Pennsylvania.
“Generally, lateral flow tests, which directly change the color of a test strip based on the presence of Zika antibodies, suffer from low sensitivity. And since antibodies to the Zika virus cross-react with other similar viruses prevalent in Zika-endemic areas, lateral flow tests for Zika also suffer from low specificity.”
With the amplification step as the main hurdle to a portable genetic test, researchers investigated the possibility of using an alternative technique known as LAMP, or loop-mediated isothermal amplification, which only requires the sample to be kept at a specific temperature, not cycled through multiple precise temperature changes as in RT-PCR.
As a trade-off for this simplified amplification process, LAMP requires even more specialized “primers,” short gene sequences that are designed to match the regions of the virus’ DNA targeted by the test.
“Although Zika primers for RT-PCR have been published in the literature, LAMP primers have not,” says Haim Bau, professor of mechanical engineering and applied mechanics. “So, using data mining, we identified highly conserved regions of the Zika virus genome that are divergent from other known pathogens. We then designed appropriate primers to recognize this sequence.
“In parallel, we engineered a low-cost, point-of-care system that consists of a diagnostic cassette and a processor. The cassette isolates, concentrates, and purifies nucleic acids and carries out enzymatic amplification. The test results are indicated by the change in the color of a dye, which can be inspected visually.”