Abstract

COVID-19 has exposed stark inequalities between resource-rich and resource-poor countries. International UN- and WHO-led efforts, such as COVAX, have provided SARS-CoV-2 vaccines but half of African countries have less than 2% vaccinated in their population, and only 15 have reached 10% by October 2021, further disadvantaging local economic recovery. Key for this implementation and preventing further mutation and spread is the frequency of voluntary [asymptomatic] testing. It is limited by expensive PCR and LAMP tests, uncomfortable probes deep in the throat or nose, and the availability of hardware to administer in remote locations. There is an urgent need for an inexpensive “end-to-end” system to deliver sensitive and reliable, non-invasive tests in resource-poor and field-test conditions. We introduce a non-invasive saliva-based LAMP colorimetric test kit and a $51 lab-in-a-backpack system that detects as few as 4 viral RNA copies per μL. It consists of eight chemicals, a thermometer, a thermos bottle, two micropipettes and a 1000–4000 rcf electronically operated centrifuge made from recycled computer hard drives (CentriDrive). The centrifuge includes a 3D-printed rotor and a 12 V rechargeable Li-ion battery, and its 12 V standard also allows wiring directly to automobile batteries, to enable field-use of this and other tests in low infrastructure settings. The test takes 90 minutes to process 6 samples and has reagent costs of $3.5 per sample. The non-invasive nature of saliva testing would allow higher penetration of testing and wider adoption of the test across cultures and settings (including refugee camps and disaster zones). The attached graphical procedure would make the test suitable for self-testing at home, performing it in the field, or in mobile testing centers by minimally trained staff.

Highlights

  • The coronavirus disease 2019 (COVID-19) pandemic has over 240 million confirmed cases worldwide, increasing at over half a million new cases per day during the second wave of the pandemic, and resulting in over 5 million deaths by the end of Oct 2021 [1]

  • SARS-CoV-2 RNA was mixed with saliva at varying concentrations and tested with the CentriDrive system to determine the sensitivity of virus detection

  • The results showed that the reverse transcription loop-mediated isothermal amplification (RT-LAMP) reaction, after the centrifugation, could detect SARS-CoV-2 at 4 viral genome copies/μL

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Summary

Ethics statement

For solutions where saliva was used in mixture with buffers, only authors’ own self-collected saliva was used.

Results
Detection procedure
Conclusions
Full Text
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