Smartphone Screen Testing, a novel pre-diagnostic method to identify SARS-CoV-2 infectious individuals
Abstract
The COVID-19 pandemic will likely take years to control globally, and constant epidemic surveillance will be required to limit the spread of SARS-CoV-2, especially considering the emergence of new variants that could hamper the effect of vaccination efforts. We developed a simple and robust - Phone Screen Testing (PoST) - method to detect positive SARS-CoV-2 individuals by RT-PCR testing of smartphone screen swab samples. We show that 81.3-100% of individuals with high-viral load SARS-CoV-2 nasopharyngeal positive samples also test positive for PoST, suggesting this method is effective in identifying COVID-19 contagious individuals. Furthermore, we successfully identified polymorphisms associated with SARS-CoV-2 Alpha, Beta and Gamma variants, in SARS-CoV-2 positive PoST samples. Overall, we report that PoST is a new non-invasive, cost-effective, and easy to implement smartphone-based smart alternative for SARS-CoV-2 testing, which could help to contain COVID-19 outbreaks and identification of variants of concern in the years to come.
Data availability
All the data used generated by this study was provided in the uploaded manuscript and source files.
Article and author information
Author details
Funding
Moorfields Eye Charity (Career Development Award 001155)
- Rodrigo M Young
Moorfields Eye Charity (Springboard Award GR001210)
- Rodrigo M Young
Agencia Nacional de Investigacion y Desarrollo Chile (ANID-Covid0789)
- Luis A Quiñones
Agencia Nacional de Investigacion y Desarrollo Chile (ANID-Covid1038)
- Ana M Sandino
Agencia Nacional de Investigacion y Desarrollo Chile (ANID-Covid1038)
- Ana M Sandino
Fondecyt (1211841)
- Felipe Reyes-Lopez
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Ethics
Human subjects: Informed consent and consent to publish was obtained from all the individuals that participated in this study before performing the sampling process. This has been made explicit in the materials and methods section of the article. Ethical approval was obtained by the Ethics and Scientific Committee of Clinica Davila (Santiago, Chile) under the approval titled: "Identificación de marcadores de riesgo asociados a la severidad del Covid-19 en el microbioma respiratorio".
Copyright
© 2021, Young et al.
This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.
Download links
Downloads (link to download the article as PDF)
Open citations (links to open the citations from this article in various online reference manager services)
Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)
Further reading
-
Mobile phones could be used to test for COVID-19
-
- Microbiology and Infectious Disease
Chlamydia trachomatis serovar L2 (Ct), an obligate intracellular bacterium that does not encode FtsZ, divides by a polarized budding process. In the absence of FtsZ, we show that FtsK, a chromosomal translocase, is critical for divisome assembly in Ct. Chlamydial FtsK forms discrete foci at the septum and at the base of the progenitor mother cell, and our data indicate that FtsK foci at the base of the mother cell mark the location of nascent divisome complexes that form at the site where a daughter cell will emerge in the next round of division. The divisome in Ct has a hybrid composition, containing elements of the divisome and elongasome from other bacteria, and FtsK is recruited to nascent divisomes prior to the other chlamydial divisome proteins assayed, including the PBP2 and PBP3 transpeptidases, and MreB and MreC. Knocking down FtsK prevents divisome assembly in Ct and inhibits cell division and septal peptidoglycan synthesis. We further show that MreB does not function like FtsZ and serve as a scaffold for the assembly of the Ct divisome. Rather, MreB is one of the last proteins recruited to the chlamydial divisome, and it is necessary for the formation of septal peptidoglycan rings. Our studies illustrate the critical role of chlamydial FtsK in coordinating divisome assembly and peptidoglycan synthesis in this obligate intracellular bacterial pathogen.