Cargando…
Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience
PURPOSE: There is a critical shortage of the commercial SARS-CoV2 detection kits and a major problem for testing capacity in Bangladesh since December, 2019 to combat the Covid19 pandemic. So this study was aimed to assess SARS-CoV2 detection with a commercial RNA detection kit by the qualitative re...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884839/ http://dx.doi.org/10.1016/j.ijid.2021.12.100 |
_version_ | 1784660256084721664 |
---|---|
author | Farhana, N. Choudhury, R. Khanam, F. |
author_facet | Farhana, N. Choudhury, R. Khanam, F. |
author_sort | Farhana, N. |
collection | PubMed |
description | PURPOSE: There is a critical shortage of the commercial SARS-CoV2 detection kits and a major problem for testing capacity in Bangladesh since December, 2019 to combat the Covid19 pandemic. So this study was aimed to assess SARS-CoV2 detection with a commercial RNA detection kit by the qualitative real time PCR from respiratory specimens (nasal or throat swab) of Covid19 suspected cases. METHODS & MATERIALS: This cross sectional study was done by convenience sampling from Munshiganj district and four different hospitals in Dhaka city from 28 November 2020 to 4 December 2020. Nasal or throat swab samples were collected from Covid19 suspected cases and sent to NIPSOM RT-PCR lab, National Institute of Preventive and Social Medicine (a public health laboratory), NIPSOM, Mohakhali, Dhaka, Bangladesh. A commercial kit [Adaltis MOLGen SARS-CoV-2 (3Genes) RealTime PCR, Italy] containing the primer and probe set in fluorimeter channel was used to detect three genes of SARS-CoV-2: RNA-dependent RNA polymerase (RdRp), envelope (E) and nucleocapsid (N) with endogenous internal control (IC). Threshold cycle (Ct) value was selected at ≤40 for each positive gene and detection of at least two different genes (RdRp and E gene or N gene) was interpreted as SARS-CoV2 positive. RESULTS: A total of 1061 samples of Covid19 suspected cases within 4 to 98 years of age were included in this study and male female ratio was 1.33:1. Among 1061 samples, 299 (28.18%) were tested positive for SARS-CoV2 with mean age of 43.33 years and male was found predominantly. Of them, 94.98% were positive for RdRp, E and N genes whereas all (100%) were found positive for only RdRp and E gene. Here, the Ct value of IC ranged within <20 to 40 and 44.48% was found at Ct 30–35 followed by 36.79% at Ct 25–30 and 10.37% at Ct 35–40. For individual RdRp gene, E gene and N gene, highest Ct values were at 30–35 with 26.42%, 30.43% and 28.87% respectively. CONCLUSION: To address accurate and safely diagnosis of SARS CoV-2, this commercial RNA detection kit will help during the COVID-19 pandemic. |
format | Online Article Text |
id | pubmed-8884839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88848392022-03-01 Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience Farhana, N. Choudhury, R. Khanam, F. Int J Infect Dis Ps05.08 (830) PURPOSE: There is a critical shortage of the commercial SARS-CoV2 detection kits and a major problem for testing capacity in Bangladesh since December, 2019 to combat the Covid19 pandemic. So this study was aimed to assess SARS-CoV2 detection with a commercial RNA detection kit by the qualitative real time PCR from respiratory specimens (nasal or throat swab) of Covid19 suspected cases. METHODS & MATERIALS: This cross sectional study was done by convenience sampling from Munshiganj district and four different hospitals in Dhaka city from 28 November 2020 to 4 December 2020. Nasal or throat swab samples were collected from Covid19 suspected cases and sent to NIPSOM RT-PCR lab, National Institute of Preventive and Social Medicine (a public health laboratory), NIPSOM, Mohakhali, Dhaka, Bangladesh. A commercial kit [Adaltis MOLGen SARS-CoV-2 (3Genes) RealTime PCR, Italy] containing the primer and probe set in fluorimeter channel was used to detect three genes of SARS-CoV-2: RNA-dependent RNA polymerase (RdRp), envelope (E) and nucleocapsid (N) with endogenous internal control (IC). Threshold cycle (Ct) value was selected at ≤40 for each positive gene and detection of at least two different genes (RdRp and E gene or N gene) was interpreted as SARS-CoV2 positive. RESULTS: A total of 1061 samples of Covid19 suspected cases within 4 to 98 years of age were included in this study and male female ratio was 1.33:1. Among 1061 samples, 299 (28.18%) were tested positive for SARS-CoV2 with mean age of 43.33 years and male was found predominantly. Of them, 94.98% were positive for RdRp, E and N genes whereas all (100%) were found positive for only RdRp and E gene. Here, the Ct value of IC ranged within <20 to 40 and 44.48% was found at Ct 30–35 followed by 36.79% at Ct 25–30 and 10.37% at Ct 35–40. For individual RdRp gene, E gene and N gene, highest Ct values were at 30–35 with 26.42%, 30.43% and 28.87% respectively. CONCLUSION: To address accurate and safely diagnosis of SARS CoV-2, this commercial RNA detection kit will help during the COVID-19 pandemic. Published by Elsevier Ltd. 2022-03 2022-02-28 /pmc/articles/PMC8884839/ http://dx.doi.org/10.1016/j.ijid.2021.12.100 Text en Copyright © 2021 Published by Elsevier Ltd. 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 | Ps05.08 (830) Farhana, N. Choudhury, R. Khanam, F. Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience |
title | Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience |
title_full | Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience |
title_fullStr | Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience |
title_full_unstemmed | Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience |
title_short | Detection of SARS-CoV2 by a Commercial RNA Detection Kit: a Public Health Laboratory Experience |
title_sort | detection of sars-cov2 by a commercial rna detection kit: a public health laboratory experience |
topic | Ps05.08 (830) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884839/ http://dx.doi.org/10.1016/j.ijid.2021.12.100 |
work_keys_str_mv | AT farhanan detectionofsarscov2byacommercialrnadetectionkitapublichealthlaboratoryexperience AT choudhuryr detectionofsarscov2byacommercialrnadetectionkitapublichealthlaboratoryexperience AT khanamf detectionofsarscov2byacommercialrnadetectionkitapublichealthlaboratoryexperience |