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The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood
Bloodstream infection (BSI) and sepsis are rising in incidence throughout the developed world. The spread of multi-drug resistant organisms presents increasing challenges to treatment. Surviving BSI is dependent on rapid and accurate identification of causal organisms, and timely application of appr...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934770/ https://www.ncbi.nlm.nih.gov/pubmed/27384540 http://dx.doi.org/10.1371/journal.pone.0158186 |
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author | Metzgar, David Frinder, Mark W. Rothman, Richard E. Peterson, Stephen Carroll, Karen C. Zhang, Sean X. Avornu, Gideon D. Rounds, Megan A. Carolan, Heather E. Toleno, Donna M. Moore, David Hall, Thomas A. Massire, Christian Richmond, Gregory S. Gutierrez, Jose R. Sampath, Rangarajan Ecker, David J. Blyn, Lawrence B. |
author_facet | Metzgar, David Frinder, Mark W. Rothman, Richard E. Peterson, Stephen Carroll, Karen C. Zhang, Sean X. Avornu, Gideon D. Rounds, Megan A. Carolan, Heather E. Toleno, Donna M. Moore, David Hall, Thomas A. Massire, Christian Richmond, Gregory S. Gutierrez, Jose R. Sampath, Rangarajan Ecker, David J. Blyn, Lawrence B. |
author_sort | Metzgar, David |
collection | PubMed |
description | Bloodstream infection (BSI) and sepsis are rising in incidence throughout the developed world. The spread of multi-drug resistant organisms presents increasing challenges to treatment. Surviving BSI is dependent on rapid and accurate identification of causal organisms, and timely application of appropriate antibiotics. Current culture-based methods used to detect and identify agents of BSI are often too slow to impact early therapy and may fail to detect relevant organisms in many positive cases. Existing methods for direct molecular detection of microbial DNA in blood are limited in either sensitivity (likely the result of small sample volumes) or in breadth of coverage, often because the PCR primers and probes used target only a few specific pathogens. There is a clear unmet need for a sensitive molecular assay capable of identifying the diverse bacteria and yeast associated with BSI directly from uncultured whole blood samples. We have developed a method of extracting DNA from larger volumes of whole blood (5 ml per sample), amplifying multiple widely conserved bacterial and fungal genes using a mismatch- and background-tolerant PCR chemistry, and identifying hundreds of diverse organisms from the amplified fragments on the basis of species-specific genetic signatures using electrospray ionization mass spectrometry (PCR/ESI-MS). We describe the analytical characteristics of the IRIDICA BAC BSI Assay and compare its pre-clinical performance to current standard-of-care methods in a collection of prospectively collected blood specimens from patients with symptoms of sepsis. The assay generated matching results in 80% of culture-positive cases (86% when common contaminants were excluded from the analysis), and twice the total number of positive detections. The described method is capable of providing organism identifications directly from uncultured blood in less than 8 hours. Disclaimer: The IRIDICA BAC BSI Assay is not available in the United States. |
format | Online Article Text |
id | pubmed-4934770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49347702016-07-18 The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood Metzgar, David Frinder, Mark W. Rothman, Richard E. Peterson, Stephen Carroll, Karen C. Zhang, Sean X. Avornu, Gideon D. Rounds, Megan A. Carolan, Heather E. Toleno, Donna M. Moore, David Hall, Thomas A. Massire, Christian Richmond, Gregory S. Gutierrez, Jose R. Sampath, Rangarajan Ecker, David J. Blyn, Lawrence B. PLoS One Research Article Bloodstream infection (BSI) and sepsis are rising in incidence throughout the developed world. The spread of multi-drug resistant organisms presents increasing challenges to treatment. Surviving BSI is dependent on rapid and accurate identification of causal organisms, and timely application of appropriate antibiotics. Current culture-based methods used to detect and identify agents of BSI are often too slow to impact early therapy and may fail to detect relevant organisms in many positive cases. Existing methods for direct molecular detection of microbial DNA in blood are limited in either sensitivity (likely the result of small sample volumes) or in breadth of coverage, often because the PCR primers and probes used target only a few specific pathogens. There is a clear unmet need for a sensitive molecular assay capable of identifying the diverse bacteria and yeast associated with BSI directly from uncultured whole blood samples. We have developed a method of extracting DNA from larger volumes of whole blood (5 ml per sample), amplifying multiple widely conserved bacterial and fungal genes using a mismatch- and background-tolerant PCR chemistry, and identifying hundreds of diverse organisms from the amplified fragments on the basis of species-specific genetic signatures using electrospray ionization mass spectrometry (PCR/ESI-MS). We describe the analytical characteristics of the IRIDICA BAC BSI Assay and compare its pre-clinical performance to current standard-of-care methods in a collection of prospectively collected blood specimens from patients with symptoms of sepsis. The assay generated matching results in 80% of culture-positive cases (86% when common contaminants were excluded from the analysis), and twice the total number of positive detections. The described method is capable of providing organism identifications directly from uncultured blood in less than 8 hours. Disclaimer: The IRIDICA BAC BSI Assay is not available in the United States. Public Library of Science 2016-07-06 /pmc/articles/PMC4934770/ /pubmed/27384540 http://dx.doi.org/10.1371/journal.pone.0158186 Text en © 2016 Metzgar 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Metzgar, David Frinder, Mark W. Rothman, Richard E. Peterson, Stephen Carroll, Karen C. Zhang, Sean X. Avornu, Gideon D. Rounds, Megan A. Carolan, Heather E. Toleno, Donna M. Moore, David Hall, Thomas A. Massire, Christian Richmond, Gregory S. Gutierrez, Jose R. Sampath, Rangarajan Ecker, David J. Blyn, Lawrence B. The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood |
title | The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood |
title_full | The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood |
title_fullStr | The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood |
title_full_unstemmed | The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood |
title_short | The IRIDICA BAC BSI Assay: Rapid, Sensitive and Culture-Independent Identification of Bacteria and Candida in Blood |
title_sort | iridica bac bsi assay: rapid, sensitive and culture-independent identification of bacteria and candida in blood |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934770/ https://www.ncbi.nlm.nih.gov/pubmed/27384540 http://dx.doi.org/10.1371/journal.pone.0158186 |
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