A Rapid, Accurate, Single Molecule Counting Method Detects Clostridium difficile Toxin B in Stool Samples
We describe a new rapid and accurate immunoassay-based technology capable of counting single target molecules using digital imaging without magnification. Using the technology, we developed a rapid test for Clostridium difficile toxin B, which is responsible for the pathology underlying potentially...
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creator | Gite, Sadanand Archambault, Destiny Cappillino, Michael P. Cunha, David Dorich, Victoria Shatova, Tatyana Tempesta, Andrew Walsh, Bruce Walsh, Jessica A. Williams, Adam Kirby, James E. Bowers, Jayson Straus, Don |
description | We describe a new rapid and accurate immunoassay-based technology capable of counting single target molecules using digital imaging without magnification. Using the technology, we developed a rapid test for
Clostridium difficile
toxin B, which is responsible for the pathology underlying potentially fatal
C. difficile
infections (CDI). There are currently no tests for CDI that are rapid, sensitive, and specific. The MultiPath
C. difficile
toxin B test images and counts complexes of target-specific magnetic and fluorescent particles that have been tethered together by toxin B molecules in minimally processed stool samples. The performance characteristics of the 30 minute test include a limit of detection of 45 pg/mL, dynamic range covering 4–5 orders of magnitude, and coefficient of variation of less than 10%. The MultiPath test detected all toxinotypes and ribotypes tested, including the one most commonly occurring in the US and EU; shows no cross reactivity with relevant bacterial species; and is robust to potential interferants commonly present in stool samples. On a training set of 320 clinical stool samples, the MultiPath
C. difficile
toxin B test showed 97.0% sensitivity (95% CI, 91.4–99.4%); 98.3% specificity (95% CI, 96.8–99.2%); and 98.2% accuracy (95% CI, 96.7–99.0%) compared to the cellular cytotoxicity neutralization assay (CCNA) reference method. Based on these compelling performance characteristics, we believe the MultiPath technology can address the lack of rapid, sensitive, specific, and easy-to-use diagnostic tests for
C. difficile
. |
doi_str_mv | 10.1038/s41598-018-26353-0 |
format | Article |
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Clostridium difficile
toxin B, which is responsible for the pathology underlying potentially fatal
C. difficile
infections (CDI). There are currently no tests for CDI that are rapid, sensitive, and specific. The MultiPath
C. difficile
toxin B test images and counts complexes of target-specific magnetic and fluorescent particles that have been tethered together by toxin B molecules in minimally processed stool samples. The performance characteristics of the 30 minute test include a limit of detection of 45 pg/mL, dynamic range covering 4–5 orders of magnitude, and coefficient of variation of less than 10%. The MultiPath test detected all toxinotypes and ribotypes tested, including the one most commonly occurring in the US and EU; shows no cross reactivity with relevant bacterial species; and is robust to potential interferants commonly present in stool samples. On a training set of 320 clinical stool samples, the MultiPath
C. difficile
toxin B test showed 97.0% sensitivity (95% CI, 91.4–99.4%); 98.3% specificity (95% CI, 96.8–99.2%); and 98.2% accuracy (95% CI, 96.7–99.0%) compared to the cellular cytotoxicity neutralization assay (CCNA) reference method. Based on these compelling performance characteristics, we believe the MultiPath technology can address the lack of rapid, sensitive, specific, and easy-to-use diagnostic tests for
C. difficile
.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-26353-0</identifier><identifier>PMID: 29849171</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/2521 ; 692/699/255/1911 ; 82 ; 82/1 ; Algorithms ; Antigens ; Clinical medicine ; Clostridium difficile ; Coefficient of variation ; Cytotoxicity ; Digital imaging ; Enzymes ; Humanities and Social Sciences ; Immunoassay ; Inflammatory bowel disease ; Influenza ; Laboratories ; multidisciplinary ; Neutralization ; Science ; Science (multidisciplinary) ; Toxin B ; Toxins</subject><ispartof>Scientific reports, 2018-05, Vol.8 (1), p.8364-8, Article 8364</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-da2daa8344ea5e7d308d7b8bf9370d8045223f234eb6102f93e3b6705330d3683</citedby><cites>FETCH-LOGICAL-c513t-da2daa8344ea5e7d308d7b8bf9370d8045223f234eb6102f93e3b6705330d3683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976643/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976643/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29849171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gite, Sadanand</creatorcontrib><creatorcontrib>Archambault, Destiny</creatorcontrib><creatorcontrib>Cappillino, Michael P.</creatorcontrib><creatorcontrib>Cunha, David</creatorcontrib><creatorcontrib>Dorich, Victoria</creatorcontrib><creatorcontrib>Shatova, Tatyana</creatorcontrib><creatorcontrib>Tempesta, Andrew</creatorcontrib><creatorcontrib>Walsh, Bruce</creatorcontrib><creatorcontrib>Walsh, Jessica A.</creatorcontrib><creatorcontrib>Williams, Adam</creatorcontrib><creatorcontrib>Kirby, James E.</creatorcontrib><creatorcontrib>Bowers, Jayson</creatorcontrib><creatorcontrib>Straus, Don</creatorcontrib><title>A Rapid, Accurate, Single Molecule Counting Method Detects Clostridium difficile Toxin B in Stool Samples</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>We describe a new rapid and accurate immunoassay-based technology capable of counting single target molecules using digital imaging without magnification. Using the technology, we developed a rapid test for
Clostridium difficile
toxin B, which is responsible for the pathology underlying potentially fatal
C. difficile
infections (CDI). There are currently no tests for CDI that are rapid, sensitive, and specific. The MultiPath
C. difficile
toxin B test images and counts complexes of target-specific magnetic and fluorescent particles that have been tethered together by toxin B molecules in minimally processed stool samples. The performance characteristics of the 30 minute test include a limit of detection of 45 pg/mL, dynamic range covering 4–5 orders of magnitude, and coefficient of variation of less than 10%. The MultiPath test detected all toxinotypes and ribotypes tested, including the one most commonly occurring in the US and EU; shows no cross reactivity with relevant bacterial species; and is robust to potential interferants commonly present in stool samples. On a training set of 320 clinical stool samples, the MultiPath
C. difficile
toxin B test showed 97.0% sensitivity (95% CI, 91.4–99.4%); 98.3% specificity (95% CI, 96.8–99.2%); and 98.2% accuracy (95% CI, 96.7–99.0%) compared to the cellular cytotoxicity neutralization assay (CCNA) reference method. Based on these compelling performance characteristics, we believe the MultiPath technology can address the lack of rapid, sensitive, specific, and easy-to-use diagnostic tests for
C. difficile
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Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gite, Sadanand</au><au>Archambault, Destiny</au><au>Cappillino, Michael P.</au><au>Cunha, David</au><au>Dorich, Victoria</au><au>Shatova, Tatyana</au><au>Tempesta, Andrew</au><au>Walsh, Bruce</au><au>Walsh, Jessica A.</au><au>Williams, Adam</au><au>Kirby, James E.</au><au>Bowers, Jayson</au><au>Straus, Don</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Rapid, Accurate, Single Molecule Counting Method Detects Clostridium difficile Toxin B in Stool Samples</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-05-30</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>8364</spage><epage>8</epage><pages>8364-8</pages><artnum>8364</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>We describe a new rapid and accurate immunoassay-based technology capable of counting single target molecules using digital imaging without magnification. Using the technology, we developed a rapid test for
Clostridium difficile
toxin B, which is responsible for the pathology underlying potentially fatal
C. difficile
infections (CDI). There are currently no tests for CDI that are rapid, sensitive, and specific. The MultiPath
C. difficile
toxin B test images and counts complexes of target-specific magnetic and fluorescent particles that have been tethered together by toxin B molecules in minimally processed stool samples. The performance characteristics of the 30 minute test include a limit of detection of 45 pg/mL, dynamic range covering 4–5 orders of magnitude, and coefficient of variation of less than 10%. The MultiPath test detected all toxinotypes and ribotypes tested, including the one most commonly occurring in the US and EU; shows no cross reactivity with relevant bacterial species; and is robust to potential interferants commonly present in stool samples. On a training set of 320 clinical stool samples, the MultiPath
C. difficile
toxin B test showed 97.0% sensitivity (95% CI, 91.4–99.4%); 98.3% specificity (95% CI, 96.8–99.2%); and 98.2% accuracy (95% CI, 96.7–99.0%) compared to the cellular cytotoxicity neutralization assay (CCNA) reference method. Based on these compelling performance characteristics, we believe the MultiPath technology can address the lack of rapid, sensitive, specific, and easy-to-use diagnostic tests for
C. difficile
.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29849171</pmid><doi>10.1038/s41598-018-26353-0</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/326/2521 692/699/255/1911 82 82/1 Algorithms Antigens Clinical medicine Clostridium difficile Coefficient of variation Cytotoxicity Digital imaging Enzymes Humanities and Social Sciences Immunoassay Inflammatory bowel disease Influenza Laboratories multidisciplinary Neutralization Science Science (multidisciplinary) Toxin B Toxins |
title | A Rapid, Accurate, Single Molecule Counting Method Detects Clostridium difficile Toxin B in Stool Samples |
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