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Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective
In the current COVID-19 crisis, many national healthcare systems are confronted with a huge demand for mass testing and an acute shortage of diagnostic resources. Considering group testing as a viable solution, this pilot study was carried out to find the maximum number of samples that can be pooled...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Indian Journal of Medical Microbiology. Published by Elsevier B.V.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709612/ https://www.ncbi.nlm.nih.gov/pubmed/33154262 http://dx.doi.org/10.4103/ijmm.IJMM_20_273 |
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author | Deka, Sangeeta Kalita, Deepjyoti Mangla, Amit Shankar, Ravi |
author_facet | Deka, Sangeeta Kalita, Deepjyoti Mangla, Amit Shankar, Ravi |
author_sort | Deka, Sangeeta |
collection | PubMed |
description | In the current COVID-19 crisis, many national healthcare systems are confronted with a huge demand for mass testing and an acute shortage of diagnostic resources. Considering group testing as a viable solution, this pilot study was carried out to find the maximum number of samples that can be pooled together to accurately detect one positive sample carrying the severe acute respiratory syndrome-coronavirus 2 viral RNA from different pools. We made different pool sizes ranging from 5 to 30 samples. Three positive samples, covering the common range of polymerase chain reaction (PCR) threshold cycle values (an indirect indicator of viral load) observed in our patients, were selected, and different pools were made with known negative samples. The pools underwent real-time qualitative PCR for the determination of effective maximum pool size. It was observed that up to 20-sample pools of all positive samples could accurately be detected in terms of both E gene and RdRp gene, leading to considerable conservation of resources, time and workforce. However, while deciding the optimal pool size, the infection level in that particular geographical area and sensitivity of the test assay used (limit of detection) have to be taken into account. |
format | Online Article Text |
id | pubmed-7709612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Indian Journal of Medical Microbiology. Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77096122020-12-03 Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective Deka, Sangeeta Kalita, Deepjyoti Mangla, Amit Shankar, Ravi Indian J Med Microbiol Brief Communication In the current COVID-19 crisis, many national healthcare systems are confronted with a huge demand for mass testing and an acute shortage of diagnostic resources. Considering group testing as a viable solution, this pilot study was carried out to find the maximum number of samples that can be pooled together to accurately detect one positive sample carrying the severe acute respiratory syndrome-coronavirus 2 viral RNA from different pools. We made different pool sizes ranging from 5 to 30 samples. Three positive samples, covering the common range of polymerase chain reaction (PCR) threshold cycle values (an indirect indicator of viral load) observed in our patients, were selected, and different pools were made with known negative samples. The pools underwent real-time qualitative PCR for the determination of effective maximum pool size. It was observed that up to 20-sample pools of all positive samples could accurately be detected in terms of both E gene and RdRp gene, leading to considerable conservation of resources, time and workforce. However, while deciding the optimal pool size, the infection level in that particular geographical area and sensitivity of the test assay used (limit of detection) have to be taken into account. Indian Journal of Medical Microbiology. Published by Elsevier B.V. 2020 2020-12-02 /pmc/articles/PMC7709612/ /pubmed/33154262 http://dx.doi.org/10.4103/ijmm.IJMM_20_273 Text en Copyright © 2020 Indian Journal of Medical Microbiology. Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Brief Communication Deka, Sangeeta Kalita, Deepjyoti Mangla, Amit Shankar, Ravi Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective |
title | Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective |
title_full | Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective |
title_fullStr | Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective |
title_full_unstemmed | Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective |
title_short | Analysis of Multi-Sample Pools in the Detection of SARS-CoV-2 RNA for Mass Screening: An Indian Perspective |
title_sort | analysis of multi-sample pools in the detection of sars-cov-2 rna for mass screening: an indian perspective |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709612/ https://www.ncbi.nlm.nih.gov/pubmed/33154262 http://dx.doi.org/10.4103/ijmm.IJMM_20_273 |
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