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Multicenter study evaluating novel multi-specimen pooling assay for the detection of SARS-CoV-2: High sensitivity and high throughput testing
Mass screening for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is important to prevent the spread of coronavirus disease 2019 (COVID-19). Pooling samples can increase the number of tests processed. LabTurbo AIO 48 is an automated platform that allows ribonucleic acid extraction and...
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Published in: | Journal of microbiology, immunology and infection immunology and infection, 2022-12, Vol.55 (6), p.1069-1075 |
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container_title | Journal of microbiology, immunology and infection |
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creator | Chung, Hsing-Yi Jian, Ming-Jr Chang, Chih-Kai Lin, Jung-Chung Yeh, Kuo-Ming Chen, Chien-Wen Yang, Ya-Sung Hsieh, Shan-Shan Chen, En-Sung Yang, Mei-Hsiu Tang, Sheng-Hui Perng, Cherng-Lih Yang, Ji-Rong Liu, Ming-Tsan Chang, Feng-Yee Shang, Hung-Sheng |
description | Mass screening for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is important to prevent the spread of coronavirus disease 2019 (COVID-19). Pooling samples can increase the number of tests processed. LabTurbo AIO 48 is an automated platform that allows ribonucleic acid extraction and sample analysis on the same instrument. We created a novel pooling assay on this platform for SARS-CoV-2 detection and demonstrated that the pooling strategy increases testing capacity without affecting accuracy and sensitivity.
Comparative limit of detection (LoD) assessment was performed on the LabTurbo AIO 48 platform and the current standard detection system based on real-time reverse transcription polymerase chain reaction (rRT-PCR) using 55 clinically positive samples. An additional 330 primary clinical samples were assessed.
Six samples pooled into one reaction tube were detected in approximately 2.5 h using the World Health Organization rRT-PCR protocol. LabTurbo AIO 48 also demonstrated a higher throughput than our reference rRT-PCR assay, with an LoD of 1000 copies/mL. The overall percentage agreement between the methods for the 330 samples was 100%.
We created a novel multi-specimen pooling assay using LabTurbo AIO 48 for the robust detection of SARS-CoV-2, allowing high-throughput results; this assay will aid in better control and prevention of COVID-19. The diagnostic assay was cost-effective and time-efficient; thus, the pooling strategy is a practical and effective method for diagnosing large quantities of specimens without compromising precision. |
doi_str_mv | 10.1016/j.jmii.2021.08.003 |
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Comparative limit of detection (LoD) assessment was performed on the LabTurbo AIO 48 platform and the current standard detection system based on real-time reverse transcription polymerase chain reaction (rRT-PCR) using 55 clinically positive samples. An additional 330 primary clinical samples were assessed.
Six samples pooled into one reaction tube were detected in approximately 2.5 h using the World Health Organization rRT-PCR protocol. LabTurbo AIO 48 also demonstrated a higher throughput than our reference rRT-PCR assay, with an LoD of 1000 copies/mL. The overall percentage agreement between the methods for the 330 samples was 100%.
We created a novel multi-specimen pooling assay using LabTurbo AIO 48 for the robust detection of SARS-CoV-2, allowing high-throughput results; this assay will aid in better control and prevention of COVID-19. The diagnostic assay was cost-effective and time-efficient; thus, the pooling strategy is a practical and effective method for diagnosing large quantities of specimens without compromising precision.</description><identifier>ISSN: 1684-1182</identifier><identifier>EISSN: 1995-9133</identifier><identifier>DOI: 10.1016/j.jmii.2021.08.003</identifier><identifier>PMID: 34538568</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Coronavirus disease 2019 ; COVID-19 - diagnosis ; COVID-19 Testing ; High throughput ; Humans ; Original ; Pooled specimen ; Real-Time Polymerase Chain Reaction - methods ; RNA, Viral - genetics ; SARS-CoV-2 ; Sensitivity and Specificity ; Severe acute respiratory coronavirus 2 ; Specimen Handling - methods</subject><ispartof>Journal of microbiology, immunology and infection, 2022-12, Vol.55 (6), p.1069-1075</ispartof><rights>2021</rights><rights>Copyright © 2021. Published by Elsevier B.V.</rights><rights>2021 Taiwan Society of Microbiology. Published by Elsevier Taiwan LLC. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-afcff232703a1d151e6995968cc36c37f6e236b8bb5ef3a1abcc7a91639ca12e3</citedby><cites>FETCH-LOGICAL-c521t-afcff232703a1d151e6995968cc36c37f6e236b8bb5ef3a1abcc7a91639ca12e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34538568$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chung, Hsing-Yi</creatorcontrib><creatorcontrib>Jian, Ming-Jr</creatorcontrib><creatorcontrib>Chang, Chih-Kai</creatorcontrib><creatorcontrib>Lin, Jung-Chung</creatorcontrib><creatorcontrib>Yeh, Kuo-Ming</creatorcontrib><creatorcontrib>Chen, Chien-Wen</creatorcontrib><creatorcontrib>Yang, Ya-Sung</creatorcontrib><creatorcontrib>Hsieh, Shan-Shan</creatorcontrib><creatorcontrib>Chen, En-Sung</creatorcontrib><creatorcontrib>Yang, Mei-Hsiu</creatorcontrib><creatorcontrib>Tang, Sheng-Hui</creatorcontrib><creatorcontrib>Perng, Cherng-Lih</creatorcontrib><creatorcontrib>Yang, Ji-Rong</creatorcontrib><creatorcontrib>Liu, Ming-Tsan</creatorcontrib><creatorcontrib>Chang, Feng-Yee</creatorcontrib><creatorcontrib>Shang, Hung-Sheng</creatorcontrib><title>Multicenter study evaluating novel multi-specimen pooling assay for the detection of SARS-CoV-2: High sensitivity and high throughput testing</title><title>Journal of microbiology, immunology and infection</title><addtitle>J Microbiol Immunol Infect</addtitle><description>Mass screening for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is important to prevent the spread of coronavirus disease 2019 (COVID-19). Pooling samples can increase the number of tests processed. LabTurbo AIO 48 is an automated platform that allows ribonucleic acid extraction and sample analysis on the same instrument. We created a novel pooling assay on this platform for SARS-CoV-2 detection and demonstrated that the pooling strategy increases testing capacity without affecting accuracy and sensitivity.
Comparative limit of detection (LoD) assessment was performed on the LabTurbo AIO 48 platform and the current standard detection system based on real-time reverse transcription polymerase chain reaction (rRT-PCR) using 55 clinically positive samples. An additional 330 primary clinical samples were assessed.
Six samples pooled into one reaction tube were detected in approximately 2.5 h using the World Health Organization rRT-PCR protocol. LabTurbo AIO 48 also demonstrated a higher throughput than our reference rRT-PCR assay, with an LoD of 1000 copies/mL. The overall percentage agreement between the methods for the 330 samples was 100%.
We created a novel multi-specimen pooling assay using LabTurbo AIO 48 for the robust detection of SARS-CoV-2, allowing high-throughput results; this assay will aid in better control and prevention of COVID-19. The diagnostic assay was cost-effective and time-efficient; thus, the pooling strategy is a practical and effective method for diagnosing large quantities of specimens without compromising precision.</description><subject>Coronavirus disease 2019</subject><subject>COVID-19 - diagnosis</subject><subject>COVID-19 Testing</subject><subject>High throughput</subject><subject>Humans</subject><subject>Original</subject><subject>Pooled specimen</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>RNA, Viral - genetics</subject><subject>SARS-CoV-2</subject><subject>Sensitivity and Specificity</subject><subject>Severe acute respiratory coronavirus 2</subject><subject>Specimen Handling - methods</subject><issn>1684-1182</issn><issn>1995-9133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9ks1u1DAUhSMEoqXwAiyQl2wS_BM7DkJI1QhopSIkCmwtx7lJPEriwXYizUPwzjhMqeiGlS3fc79rH58se0lwQTARb_bFfrK2oJiSAssCY_YoOyd1zfOaMPY47YUsc0IkPcuehbDHuGSUi6fZGSs5k1zI8-zX52WM1sAcwaMQl_aIYNXjoqOdezS7FUY0bZI8HMDYCWZ0cG7cijoEfUSd8ygOgFqIYKJ1M3Idur38epvv3I-cvkVXth9QgDnYaFcbj0jPLRq2wzh4t_TDYYkoQtgGPs-edHoM8OJuvci-f_zwbXeV33z5dL27vMkNpyTmujNdRxmtMNOkJZyASK-uhTSGCcOqTgBlopFNw6FLEt0YU-maCFYbTSiwi-z6xG2d3quDt5P2R-W0VX8OnO-V9smWEZTQTIoKMEhtygZIAy1hpgKhgXDBmsR6f2IdlmaCdrPS6_EB9GFltoPq3apkSQiXPAFe3wG8-7kkI9Rkg4Fx1DO4JSjKq7JioiablJ6kxrsQPHT3YwhWWybUXm2ZUFsmFJYqZSI1vfr3gvctf0OQBO9OAkiWrxa8CsbCbKC1Pv1p8sT-j_8br2TMvA</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Chung, Hsing-Yi</creator><creator>Jian, Ming-Jr</creator><creator>Chang, Chih-Kai</creator><creator>Lin, Jung-Chung</creator><creator>Yeh, Kuo-Ming</creator><creator>Chen, Chien-Wen</creator><creator>Yang, Ya-Sung</creator><creator>Hsieh, Shan-Shan</creator><creator>Chen, En-Sung</creator><creator>Yang, Mei-Hsiu</creator><creator>Tang, Sheng-Hui</creator><creator>Perng, Cherng-Lih</creator><creator>Yang, Ji-Rong</creator><creator>Liu, Ming-Tsan</creator><creator>Chang, Feng-Yee</creator><creator>Shang, Hung-Sheng</creator><general>Elsevier B.V</general><general>Taiwan Society of Microbiology. Published by Elsevier Taiwan LLC</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20221201</creationdate><title>Multicenter study evaluating novel multi-specimen pooling assay for the detection of SARS-CoV-2: High sensitivity and high throughput testing</title><author>Chung, Hsing-Yi ; Jian, Ming-Jr ; Chang, Chih-Kai ; Lin, Jung-Chung ; Yeh, Kuo-Ming ; Chen, Chien-Wen ; Yang, Ya-Sung ; Hsieh, Shan-Shan ; Chen, En-Sung ; Yang, Mei-Hsiu ; Tang, Sheng-Hui ; Perng, Cherng-Lih ; Yang, Ji-Rong ; Liu, Ming-Tsan ; Chang, Feng-Yee ; Shang, Hung-Sheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-afcff232703a1d151e6995968cc36c37f6e236b8bb5ef3a1abcc7a91639ca12e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Coronavirus disease 2019</topic><topic>COVID-19 - diagnosis</topic><topic>COVID-19 Testing</topic><topic>High throughput</topic><topic>Humans</topic><topic>Original</topic><topic>Pooled specimen</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>RNA, Viral - genetics</topic><topic>SARS-CoV-2</topic><topic>Sensitivity and Specificity</topic><topic>Severe acute respiratory coronavirus 2</topic><topic>Specimen Handling - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chung, Hsing-Yi</creatorcontrib><creatorcontrib>Jian, Ming-Jr</creatorcontrib><creatorcontrib>Chang, Chih-Kai</creatorcontrib><creatorcontrib>Lin, Jung-Chung</creatorcontrib><creatorcontrib>Yeh, Kuo-Ming</creatorcontrib><creatorcontrib>Chen, Chien-Wen</creatorcontrib><creatorcontrib>Yang, Ya-Sung</creatorcontrib><creatorcontrib>Hsieh, Shan-Shan</creatorcontrib><creatorcontrib>Chen, En-Sung</creatorcontrib><creatorcontrib>Yang, Mei-Hsiu</creatorcontrib><creatorcontrib>Tang, Sheng-Hui</creatorcontrib><creatorcontrib>Perng, Cherng-Lih</creatorcontrib><creatorcontrib>Yang, Ji-Rong</creatorcontrib><creatorcontrib>Liu, Ming-Tsan</creatorcontrib><creatorcontrib>Chang, Feng-Yee</creatorcontrib><creatorcontrib>Shang, Hung-Sheng</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of microbiology, immunology and infection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chung, Hsing-Yi</au><au>Jian, Ming-Jr</au><au>Chang, Chih-Kai</au><au>Lin, Jung-Chung</au><au>Yeh, Kuo-Ming</au><au>Chen, Chien-Wen</au><au>Yang, Ya-Sung</au><au>Hsieh, Shan-Shan</au><au>Chen, En-Sung</au><au>Yang, Mei-Hsiu</au><au>Tang, Sheng-Hui</au><au>Perng, Cherng-Lih</au><au>Yang, Ji-Rong</au><au>Liu, Ming-Tsan</au><au>Chang, Feng-Yee</au><au>Shang, Hung-Sheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multicenter study evaluating novel multi-specimen pooling assay for the detection of SARS-CoV-2: High sensitivity and high throughput testing</atitle><jtitle>Journal of microbiology, immunology and infection</jtitle><addtitle>J Microbiol Immunol Infect</addtitle><date>2022-12-01</date><risdate>2022</risdate><volume>55</volume><issue>6</issue><spage>1069</spage><epage>1075</epage><pages>1069-1075</pages><issn>1684-1182</issn><eissn>1995-9133</eissn><abstract>Mass screening for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is important to prevent the spread of coronavirus disease 2019 (COVID-19). Pooling samples can increase the number of tests processed. LabTurbo AIO 48 is an automated platform that allows ribonucleic acid extraction and sample analysis on the same instrument. We created a novel pooling assay on this platform for SARS-CoV-2 detection and demonstrated that the pooling strategy increases testing capacity without affecting accuracy and sensitivity.
Comparative limit of detection (LoD) assessment was performed on the LabTurbo AIO 48 platform and the current standard detection system based on real-time reverse transcription polymerase chain reaction (rRT-PCR) using 55 clinically positive samples. An additional 330 primary clinical samples were assessed.
Six samples pooled into one reaction tube were detected in approximately 2.5 h using the World Health Organization rRT-PCR protocol. LabTurbo AIO 48 also demonstrated a higher throughput than our reference rRT-PCR assay, with an LoD of 1000 copies/mL. The overall percentage agreement between the methods for the 330 samples was 100%.
We created a novel multi-specimen pooling assay using LabTurbo AIO 48 for the robust detection of SARS-CoV-2, allowing high-throughput results; this assay will aid in better control and prevention of COVID-19. The diagnostic assay was cost-effective and time-efficient; thus, the pooling strategy is a practical and effective method for diagnosing large quantities of specimens without compromising precision.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>34538568</pmid><doi>10.1016/j.jmii.2021.08.003</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Coronavirus disease 2019 COVID-19 - diagnosis COVID-19 Testing High throughput Humans Original Pooled specimen Real-Time Polymerase Chain Reaction - methods RNA, Viral - genetics SARS-CoV-2 Sensitivity and Specificity Severe acute respiratory coronavirus 2 Specimen Handling - methods |
title | Multicenter study evaluating novel multi-specimen pooling assay for the detection of SARS-CoV-2: High sensitivity and high throughput testing |
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