Development and implementation of a scalable and versatile test for COVID-19 diagnostics in rural communities
| dc.contributor.author | Ceci, A. | |
| dc.contributor.author | Muñoz-Ballester, Carmen | |
| dc.contributor.author | Tegge, A. N. | |
| dc.contributor.author | Brown, K. L. | |
| dc.contributor.author | Umans, R. A. | |
| dc.contributor.author | Michel, F. M. | |
| dc.contributor.author | Patel, D. | |
| dc.contributor.author | Tewari, B. | |
| dc.contributor.author | Martin, J. | |
| dc.contributor.author | Alcoreza, O. | |
| dc.contributor.author | Maynard, T. | |
| dc.contributor.author | Martinez-Martinez, D. | |
| dc.contributor.author | Bordwine, P. | |
| dc.contributor.author | Bissell, N. | |
| dc.contributor.author | Friedlander, M. J. | |
| dc.contributor.author | Sontheimer, H. | |
| dc.contributor.author | Finkielstein, C. V. | |
| dc.date.accessioned | 2026-02-03T18:14:37Z | |
| dc.date.issued | 2021-07-20 | |
| dc.description.abstract | Rapid and widespread testing of severe acute respiratory coronavirus 2 (SARS-CoV-2) is essential for an effective public health response aimed at containing and mitigating the coronavirus disease 2019 (COVID-19) pandemic. Successful health policy implementation relies on early identification of infected individuals and extensive contact tracing. However, rural communities, where resources for testing are sparse or simply absent, face distinctive challenges to achieving this success. Accordingly, we report the development of an academic, public land grant University laboratory-based detection assay for the identification of SARS-CoV-2 in samples from various clinical specimens that can be readily deployed in areas where access to testing is limited. The test, which is a quantitative reverse transcription polymerase chain reaction (RT-qPCR)-based procedure, was validated on samples provided by the state laboratory and submitted for FDA Emergency Use Authorization. Our test exhibits comparable sensitivity and exceeds specificity and inclusivity values compared to other molecular assays. Additionally, this test can be re-configured to meet supply chain shortages, modified for scale up demands, and is amenable to several clinical specimens. Test development also involved 3D engineering critical supplies and formulating a stable collection media that allowed samples to be transported for hours over a dispersed rural region without the need for a cold-chain. These two elements that were critical when shortages impacted testing and when personnel needed to reach areas that were geographically isolated from the testing center. Overall, using a robust, easy-to-adapt methodology, we show that an academic laboratory can supplement COVID-19 testing needs and help local health departments assess and manage outbreaks. This additional testing capacity is particularly germane for smaller cities and rural regions that would otherwise be unable to meet the testing demand. | |
| dc.description.sponsorship | We gratefully acknowledge the originating and submitting laboratories of the SARS-CoV-2 sequences from GISAID’s database on which our predicted inclusivity analysis is based. Implementation of this program included important contributions from not only the researchers listed in this article, but also from the leadership at our University (Virginia Tech). Establishment of the testing laboratory was through a highly collaborative approach under the auspices of the university’s student health center, local health districts and state health department epidemiologists and information technology teams. This project was supported by a Go Virginia Economic Resilience and Recovery Grant (20-GOVA-ERR-02A and 20-GOVA-ERR-02D), the Department of General Services of the Commonwealth of Virginia (DGS-201020-UVT), and funds from Virginia Tech, the Fralin Biomedical Research Institute at VTC, and the Fralin Life Sciences Institute. F.M.M. acknowledges support from NSF through CAREER-1652237 and the Virginia Tech Center for Earth and Environmental Nanotechnology “NanoEarth” (NNCI-1542100). | |
| dc.description.uri | https://www.nature.com/articles/s41467-021-24552-4 | |
| dc.format.extent | 14 pages | |
| dc.genre | journal articles | |
| dc.identifier | doi:10.13016/m2udsd-vlag | |
| dc.identifier.citation | Ceci, A., C. Muñoz-Ballester, A. N. Tegge, et al. “Development and Implementation of a Scalable and Versatile Test for COVID-19 Diagnostics in Rural Communities.” Nature Communications 12, no. 1 (2021): 4400. https://doi.org/10.1038/s41467-021-24552-4. | |
| dc.identifier.uri | https://doi.org/10.1038/s41467-021-24552-4 | |
| dc.identifier.uri | http://hdl.handle.net/11603/41642 | |
| dc.language.iso | en | |
| dc.publisher | Springer Nature | |
| dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
| dc.relation.ispartof | UMBC Biological Sciences Department | |
| dc.rights | Attribution 4.0 International | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Gene expression profiling | |
| dc.subject | Genomic analysis | |
| dc.title | Development and implementation of a scalable and versatile test for COVID-19 diagnostics in rural communities | |
| dc.type | Text | |
| dcterms.creator | https://orcid.org/0000-0002-2298-7753 |
