Cargando…

A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool

Here we describe a method for the detection of Clostridium difficile from stool using a novel low-complexity and rapid extraction process called Heat Elution (HE). The HE method is two-step and takes just 10 minutes, no specialist instruments are required and there is minimal hands-on time. A test m...

Descripción completa

Detalles Bibliográficos
Autores principales: McElgunn, Cathal J., Pereira, Clint R., Parham, Nicholas J., Smythe, James E., Wigglesworth, Michael J., Smielewska, Anna, Parmar, Surendra A., Gandelman, Olga A., Brown, Nicholas M., Tisi, Laurence C., Curran, Martin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885522/
https://www.ncbi.nlm.nih.gov/pubmed/24416173
http://dx.doi.org/10.1371/journal.pone.0083808
_version_ 1782298757161811968
author McElgunn, Cathal J.
Pereira, Clint R.
Parham, Nicholas J.
Smythe, James E.
Wigglesworth, Michael J.
Smielewska, Anna
Parmar, Surendra A.
Gandelman, Olga A.
Brown, Nicholas M.
Tisi, Laurence C.
Curran, Martin D.
author_facet McElgunn, Cathal J.
Pereira, Clint R.
Parham, Nicholas J.
Smythe, James E.
Wigglesworth, Michael J.
Smielewska, Anna
Parmar, Surendra A.
Gandelman, Olga A.
Brown, Nicholas M.
Tisi, Laurence C.
Curran, Martin D.
author_sort McElgunn, Cathal J.
collection PubMed
description Here we describe a method for the detection of Clostridium difficile from stool using a novel low-complexity and rapid extraction process called Heat Elution (HE). The HE method is two-step and takes just 10 minutes, no specialist instruments are required and there is minimal hands-on time. A test method using HE was developed in conjunction with Loop-mediated Isothermal Amplification (LAMP) combined with the real-time bioluminescent reporter system known as BART targeting the toxin B gene (tcdB). The HE-LAMP-BART method was evaluated in a pilot study on clinical fecal samples (tcdB (+), n =  111; tcdB (−), n  = 107). The HE-LAMP-BART method showed 95.5% sensitivity and 100% specificity against a gold standard reference method using cytotoxigenic culture and also a silica-based robotic extraction followed by tcdB PCR to control for storage. From sample to result, the HE-LAMP-BART method typically took 50 minutes, whereas the PCR method took >2.5 hours. In a further study (tcdB (+), n =  47; tcdB (−), n  = 28) HE-LAMP-BART was compared to an alternative commercially available LAMP-based method, Illumigene (Meridian Bioscience, OH), and yielded 87.2% sensitivity and 100% specificity for the HE-LAMP-BART method compared to 76.6% and 100%, respectively, for Illumigene against the reference method. A subset of 27 samples (tcdB (+), n =  25; tcdB (−), n  = 2) were further compared between HE-LAMP-BART, Illumigene, GeneXpert (Cepheid, Sunnyvale, CA) and RIDA®QUICK C. difficile Toxin A/B lateral flow rapid test (R-Biopharm, Darmstadt, Germany) resulting in sensitivities of HE-LAMP-BART 92%, Illumigene 72% GeneXpert 96% and RIDAQuick 76% against the reference method. The HE-LAMP-BART method offers the advantages of molecular based approaches without the cost and complexity usually associated with molecular tests. Further, the rapid time-to-result and simple protocol means the method can be applied away from the centralized laboratory settings.
format Online
Article
Text
id pubmed-3885522
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-38855222014-01-10 A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool McElgunn, Cathal J. Pereira, Clint R. Parham, Nicholas J. Smythe, James E. Wigglesworth, Michael J. Smielewska, Anna Parmar, Surendra A. Gandelman, Olga A. Brown, Nicholas M. Tisi, Laurence C. Curran, Martin D. PLoS One Research Article Here we describe a method for the detection of Clostridium difficile from stool using a novel low-complexity and rapid extraction process called Heat Elution (HE). The HE method is two-step and takes just 10 minutes, no specialist instruments are required and there is minimal hands-on time. A test method using HE was developed in conjunction with Loop-mediated Isothermal Amplification (LAMP) combined with the real-time bioluminescent reporter system known as BART targeting the toxin B gene (tcdB). The HE-LAMP-BART method was evaluated in a pilot study on clinical fecal samples (tcdB (+), n =  111; tcdB (−), n  = 107). The HE-LAMP-BART method showed 95.5% sensitivity and 100% specificity against a gold standard reference method using cytotoxigenic culture and also a silica-based robotic extraction followed by tcdB PCR to control for storage. From sample to result, the HE-LAMP-BART method typically took 50 minutes, whereas the PCR method took >2.5 hours. In a further study (tcdB (+), n =  47; tcdB (−), n  = 28) HE-LAMP-BART was compared to an alternative commercially available LAMP-based method, Illumigene (Meridian Bioscience, OH), and yielded 87.2% sensitivity and 100% specificity for the HE-LAMP-BART method compared to 76.6% and 100%, respectively, for Illumigene against the reference method. A subset of 27 samples (tcdB (+), n =  25; tcdB (−), n  = 2) were further compared between HE-LAMP-BART, Illumigene, GeneXpert (Cepheid, Sunnyvale, CA) and RIDA®QUICK C. difficile Toxin A/B lateral flow rapid test (R-Biopharm, Darmstadt, Germany) resulting in sensitivities of HE-LAMP-BART 92%, Illumigene 72% GeneXpert 96% and RIDAQuick 76% against the reference method. The HE-LAMP-BART method offers the advantages of molecular based approaches without the cost and complexity usually associated with molecular tests. Further, the rapid time-to-result and simple protocol means the method can be applied away from the centralized laboratory settings. Public Library of Science 2014-01-08 /pmc/articles/PMC3885522/ /pubmed/24416173 http://dx.doi.org/10.1371/journal.pone.0083808 Text en © 2014 McElgunn et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
McElgunn, Cathal J.
Pereira, Clint R.
Parham, Nicholas J.
Smythe, James E.
Wigglesworth, Michael J.
Smielewska, Anna
Parmar, Surendra A.
Gandelman, Olga A.
Brown, Nicholas M.
Tisi, Laurence C.
Curran, Martin D.
A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool
title A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool
title_full A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool
title_fullStr A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool
title_full_unstemmed A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool
title_short A Low Complexity Rapid Molecular Method for Detection of Clostridium difficile in Stool
title_sort low complexity rapid molecular method for detection of clostridium difficile in stool
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885522/
https://www.ncbi.nlm.nih.gov/pubmed/24416173
http://dx.doi.org/10.1371/journal.pone.0083808
work_keys_str_mv AT mcelgunncathalj alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT pereiraclintr alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT parhamnicholasj alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT smythejamese alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT wigglesworthmichaelj alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT smielewskaanna alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT parmarsurendraa alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT gandelmanolgaa alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT brownnicholasm alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT tisilaurencec alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT curranmartind alowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT mcelgunncathalj lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT pereiraclintr lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT parhamnicholasj lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT smythejamese lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT wigglesworthmichaelj lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT smielewskaanna lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT parmarsurendraa lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT gandelmanolgaa lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT brownnicholasm lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT tisilaurencec lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool
AT curranmartind lowcomplexityrapidmolecularmethodfordetectionofclostridiumdifficileinstool