Cargando…

153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia

BACKGROUND: Blood stream infections (BSI) are among the leading cause of morbidity and mortality, yet gold standard culture-based diagnostics have limited ability to guide therapeutic intervention due to multi-day turnaround time and low sensitivity. Day Zero Diagnostics has developed Blood2Bac(™),...

Descripción completa

Detalles Bibliográficos
Autores principales: Asundi, Archana, Billings, Nicole, Rogers, Zoe H, Roche, Samantha, Bombard, Jennifer, Kumcu, Michael E, Cunden, Lisa S, Nanayakkara, Imaly A, Tsui, Chiahao, Knysh, Paul, Maddux, Cabell, Munro, Zachary, Herriott, Ian, Huntley, Miriam, Lin, Nina H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776705/
http://dx.doi.org/10.1093/ofid/ofaa439.463
_version_ 1783630744363466752
author Asundi, Archana
Billings, Nicole
Rogers, Zoe H
Roche, Samantha
Bombard, Jennifer
Kumcu, Michael E
Cunden, Lisa S
Nanayakkara, Imaly A
Tsui, Chiahao
Knysh, Paul
Maddux, Cabell
Munro, Zachary
Herriott, Ian
Huntley, Miriam
Lin, Nina H
author_facet Asundi, Archana
Billings, Nicole
Rogers, Zoe H
Roche, Samantha
Bombard, Jennifer
Kumcu, Michael E
Cunden, Lisa S
Nanayakkara, Imaly A
Tsui, Chiahao
Knysh, Paul
Maddux, Cabell
Munro, Zachary
Herriott, Ian
Huntley, Miriam
Lin, Nina H
author_sort Asundi, Archana
collection PubMed
description BACKGROUND: Blood stream infections (BSI) are among the leading cause of morbidity and mortality, yet gold standard culture-based diagnostics have limited ability to guide therapeutic intervention due to multi-day turnaround time and low sensitivity. Day Zero Diagnostics has developed Blood2Bac(™), a culture-free, species agnostic process to enrich bacteria direct from whole blood. Coupled with whole genome sequencing (WGS) and Day Zero Diagnostics’ Keynome(®) algorithmic tools for species ID and antimicrobial resistance (AMR), we conducted the first proof-of-concept feasibility study in an inpatient clinical setting. METHODS: Study participants were enrolled and specimens collected from Boston Medical Center. Eligibility criteria included hospitalized adults with suspected and/or documented BSI, irrespective of empiric antibiotic therapy duration. Whole blood samples were processed with Blood2Bac, sequenced on a nanopore platform, and bacterial ID determined with Keynome ID. Keynome ID results were compared with blood culture results to measure concordance. RESULTS: Specimens from 21 participants were processed with Blood2Bac and nanopore sequencing. For 20/21 samples, Keynome ID calls were concordant with clinical blood culture, where 6 concordant positive and 14 were concordant negative. In 3 concordant samples, Keynome ID called positive while concurrent blood cultures were negative. However, all IDs corresponded with positive blood culture results from the day prior, suggesting potentially higher sensitivity for the Blood2Bac compared to blood culture. Two concordant positive IDs, resulted in >95% of the genome recovered and Keynome concomitantly resulted in AMR predictions with 100% accuracy compared to pathogen phenotype. In 1 discordant specimen, the Keynome ID result was negative while blood cultures 8 hours before were positive. In this case, the patient was on empiric therapy for 8 days prior to samples collection and cultures were negative 19-hours post specimen collection. CONCLUSION: These results highlight the sensitivity of a real-time blood WGS approach to identify BSI and its utility as a diagnostic to minimize unnecessary antibiotic exposure contributing to the antibiotic resistance crisis. DISCLOSURES: Archana Asundi, MD, Gilead (Scientific Research Study Investigator)Merck (Scientific Research Study Investigator)ViiV (Scientific Research Study Investigator) Nicole Billings, PhD, Day Zero Diagnostics (Employee) Zoe H. Rogers, MPH, Day Zero Diagnostics (Employee, Shareholder) Lisa S. Cunden, PhD, Day Zero Diagnostics (Shareholder) Imaly A. Nanayakkara, PhD, Day Zero Diagnostics (Employee, Shareholder) Chiahao Tsui, n/a, Day Zero Diagnostics (Employee, Shareholder) Paul Knysh, PhD, Day Zero Diagnostics (Employee) Cabell Maddux, n/a, Day Zero Diagnostics (Employee, Shareholder) Zachary Munro, n/a, Day Zero Diagnostics Inc. (Employee, Shareholder) Ian Herriott, BS, Day Zero Diagnostics (Employee, Shareholder) Miriam Huntley, PhD, Day Zero Diagnostics (Employee, Shareholder) Nina H. Lin, MD, Gilead Sciences (Scientific Research Study Investigator)ViiV (Scientific Research Study Investigator)
format Online
Article
Text
id pubmed-7776705
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77767052021-01-07 153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia Asundi, Archana Billings, Nicole Rogers, Zoe H Roche, Samantha Bombard, Jennifer Kumcu, Michael E Cunden, Lisa S Nanayakkara, Imaly A Tsui, Chiahao Knysh, Paul Maddux, Cabell Munro, Zachary Herriott, Ian Huntley, Miriam Lin, Nina H Open Forum Infect Dis Poster Abstracts BACKGROUND: Blood stream infections (BSI) are among the leading cause of morbidity and mortality, yet gold standard culture-based diagnostics have limited ability to guide therapeutic intervention due to multi-day turnaround time and low sensitivity. Day Zero Diagnostics has developed Blood2Bac(™), a culture-free, species agnostic process to enrich bacteria direct from whole blood. Coupled with whole genome sequencing (WGS) and Day Zero Diagnostics’ Keynome(®) algorithmic tools for species ID and antimicrobial resistance (AMR), we conducted the first proof-of-concept feasibility study in an inpatient clinical setting. METHODS: Study participants were enrolled and specimens collected from Boston Medical Center. Eligibility criteria included hospitalized adults with suspected and/or documented BSI, irrespective of empiric antibiotic therapy duration. Whole blood samples were processed with Blood2Bac, sequenced on a nanopore platform, and bacterial ID determined with Keynome ID. Keynome ID results were compared with blood culture results to measure concordance. RESULTS: Specimens from 21 participants were processed with Blood2Bac and nanopore sequencing. For 20/21 samples, Keynome ID calls were concordant with clinical blood culture, where 6 concordant positive and 14 were concordant negative. In 3 concordant samples, Keynome ID called positive while concurrent blood cultures were negative. However, all IDs corresponded with positive blood culture results from the day prior, suggesting potentially higher sensitivity for the Blood2Bac compared to blood culture. Two concordant positive IDs, resulted in >95% of the genome recovered and Keynome concomitantly resulted in AMR predictions with 100% accuracy compared to pathogen phenotype. In 1 discordant specimen, the Keynome ID result was negative while blood cultures 8 hours before were positive. In this case, the patient was on empiric therapy for 8 days prior to samples collection and cultures were negative 19-hours post specimen collection. CONCLUSION: These results highlight the sensitivity of a real-time blood WGS approach to identify BSI and its utility as a diagnostic to minimize unnecessary antibiotic exposure contributing to the antibiotic resistance crisis. DISCLOSURES: Archana Asundi, MD, Gilead (Scientific Research Study Investigator)Merck (Scientific Research Study Investigator)ViiV (Scientific Research Study Investigator) Nicole Billings, PhD, Day Zero Diagnostics (Employee) Zoe H. Rogers, MPH, Day Zero Diagnostics (Employee, Shareholder) Lisa S. Cunden, PhD, Day Zero Diagnostics (Shareholder) Imaly A. Nanayakkara, PhD, Day Zero Diagnostics (Employee, Shareholder) Chiahao Tsui, n/a, Day Zero Diagnostics (Employee, Shareholder) Paul Knysh, PhD, Day Zero Diagnostics (Employee) Cabell Maddux, n/a, Day Zero Diagnostics (Employee, Shareholder) Zachary Munro, n/a, Day Zero Diagnostics Inc. (Employee, Shareholder) Ian Herriott, BS, Day Zero Diagnostics (Employee, Shareholder) Miriam Huntley, PhD, Day Zero Diagnostics (Employee, Shareholder) Nina H. Lin, MD, Gilead Sciences (Scientific Research Study Investigator)ViiV (Scientific Research Study Investigator) Oxford University Press 2020-12-31 /pmc/articles/PMC7776705/ http://dx.doi.org/10.1093/ofid/ofaa439.463 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
Asundi, Archana
Billings, Nicole
Rogers, Zoe H
Roche, Samantha
Bombard, Jennifer
Kumcu, Michael E
Cunden, Lisa S
Nanayakkara, Imaly A
Tsui, Chiahao
Knysh, Paul
Maddux, Cabell
Munro, Zachary
Herriott, Ian
Huntley, Miriam
Lin, Nina H
153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia
title 153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia
title_full 153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia
title_fullStr 153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia
title_full_unstemmed 153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia
title_short 153. pilot Study of a Novel Whole-genome Sequencing Based Rapid Bacterial Identification Assay in Patients with Bacteremia
title_sort 153. pilot study of a novel whole-genome sequencing based rapid bacterial identification assay in patients with bacteremia
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776705/
http://dx.doi.org/10.1093/ofid/ofaa439.463
work_keys_str_mv AT asundiarchana 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT billingsnicole 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT rogerszoeh 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT rochesamantha 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT bombardjennifer 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT kumcumichaele 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT cundenlisas 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT nanayakkaraimalya 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT tsuichiahao 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT knyshpaul 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT madduxcabell 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT munrozachary 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT herriottian 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT huntleymiriam 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia
AT linninah 153pilotstudyofanovelwholegenomesequencingbasedrapidbacterialidentificationassayinpatientswithbacteremia