An optimised protocol for detection of SARS-CoV-2 in stool
Abstract Background SARS-CoV-2 has been detected in stool samples of COVID-19 patients, with potential implications for faecal-oral transmission. Compared to nasopharyngeal swab samples, the complexity of the stool matrix poses a challenge in the detection of the virus that has not yet been solved....
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doaj-c68b9cb353b14be58a3ed5940cd45e4a2021-09-12T11:07:26ZengBMCBMC Microbiology1471-21802021-09-012111810.1186/s12866-021-02297-wAn optimised protocol for detection of SARS-CoV-2 in stoolTianqi Li0Enriqueta Garcia-Gutierrez1Daniel A. Yara2Jacob Scadden3Jade Davies4Chloe Hutchins5Alp Aydin6Justin O’Grady7Arjan Narbad8Stefano Romano9Lizbeth Sayavedra10Gut Health and Microbes, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceMicrobes in the Food Chain, Quadram Institute BioscienceMicrobes in the Food Chain, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceGut Health and Microbes, Quadram Institute BioscienceAbstract Background SARS-CoV-2 has been detected in stool samples of COVID-19 patients, with potential implications for faecal-oral transmission. Compared to nasopharyngeal swab samples, the complexity of the stool matrix poses a challenge in the detection of the virus that has not yet been solved. However, robust and reliable methods are needed to estimate the prevalence and persistence of SARS-CoV-2 in the gut and to ensure the safety of microbiome-based procedures such as faecal microbiota transplant (FMT). The aim of this study was to establish a sensitive and reliable method for detecting SARS-CoV-2 in stool samples. Results Stool samples from individuals free of SARS-CoV-2 were homogenised in saline buffer and spiked with a known titre of inactivated virus ranging from 50 to 750 viral particles per 100 mg stool. Viral particles were concentrated by ultrafiltration, RNA was extracted, and SARS-CoV-2 was detected via real-time reverse-transcription polymerase chain reaction (RT-qPCR) using the CDC primers and probes. The RNA extraction procedure we used allowed for the detection of SARS-CoV-2 via RT-qPCR in most of the stool samples tested. We could detect as few as 50 viral particles per 100 mg of stool. However, high variability was observed across samples at low viral titres. The primer set targeting the N1 region provided more reliable and precise results and for this primer set our method had a limit of detection of 1 viral particle per mg of stool. Conclusions Here we describe a sensitive method for detecting SARS-CoV-2 in stool samples. This method can be used to establish the persistence of SARS-CoV-2 in stool and ensure the safety of clinical practices such as FMT.https://doi.org/10.1186/s12866-021-02297-wFMTCOVID19RT-qPCRStoolClinical-test |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tianqi Li Enriqueta Garcia-Gutierrez Daniel A. Yara Jacob Scadden Jade Davies Chloe Hutchins Alp Aydin Justin O’Grady Arjan Narbad Stefano Romano Lizbeth Sayavedra |
spellingShingle |
Tianqi Li Enriqueta Garcia-Gutierrez Daniel A. Yara Jacob Scadden Jade Davies Chloe Hutchins Alp Aydin Justin O’Grady Arjan Narbad Stefano Romano Lizbeth Sayavedra An optimised protocol for detection of SARS-CoV-2 in stool BMC Microbiology FMT COVID19 RT-qPCR Stool Clinical-test |
author_facet |
Tianqi Li Enriqueta Garcia-Gutierrez Daniel A. Yara Jacob Scadden Jade Davies Chloe Hutchins Alp Aydin Justin O’Grady Arjan Narbad Stefano Romano Lizbeth Sayavedra |
author_sort |
Tianqi Li |
title |
An optimised protocol for detection of SARS-CoV-2 in stool |
title_short |
An optimised protocol for detection of SARS-CoV-2 in stool |
title_full |
An optimised protocol for detection of SARS-CoV-2 in stool |
title_fullStr |
An optimised protocol for detection of SARS-CoV-2 in stool |
title_full_unstemmed |
An optimised protocol for detection of SARS-CoV-2 in stool |
title_sort |
optimised protocol for detection of sars-cov-2 in stool |
publisher |
BMC |
series |
BMC Microbiology |
issn |
1471-2180 |
publishDate |
2021-09-01 |
description |
Abstract Background SARS-CoV-2 has been detected in stool samples of COVID-19 patients, with potential implications for faecal-oral transmission. Compared to nasopharyngeal swab samples, the complexity of the stool matrix poses a challenge in the detection of the virus that has not yet been solved. However, robust and reliable methods are needed to estimate the prevalence and persistence of SARS-CoV-2 in the gut and to ensure the safety of microbiome-based procedures such as faecal microbiota transplant (FMT). The aim of this study was to establish a sensitive and reliable method for detecting SARS-CoV-2 in stool samples. Results Stool samples from individuals free of SARS-CoV-2 were homogenised in saline buffer and spiked with a known titre of inactivated virus ranging from 50 to 750 viral particles per 100 mg stool. Viral particles were concentrated by ultrafiltration, RNA was extracted, and SARS-CoV-2 was detected via real-time reverse-transcription polymerase chain reaction (RT-qPCR) using the CDC primers and probes. The RNA extraction procedure we used allowed for the detection of SARS-CoV-2 via RT-qPCR in most of the stool samples tested. We could detect as few as 50 viral particles per 100 mg of stool. However, high variability was observed across samples at low viral titres. The primer set targeting the N1 region provided more reliable and precise results and for this primer set our method had a limit of detection of 1 viral particle per mg of stool. Conclusions Here we describe a sensitive method for detecting SARS-CoV-2 in stool samples. This method can be used to establish the persistence of SARS-CoV-2 in stool and ensure the safety of clinical practices such as FMT. |
topic |
FMT COVID19 RT-qPCR Stool Clinical-test |
url |
https://doi.org/10.1186/s12866-021-02297-w |
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