TY - JOUR
T1 - Species identification and antibiotic resistance prediction by analysis of whole-genome sequence data by use of ARESdb
T2 - An analysis of isolates from the unyvero lower respiratory tract infection trial
AU - Ferreira, Ines
AU - Beisken, Stephan
AU - Lueftinger, Lukas
AU - Weinmaier, Thomas
AU - Klein, Matthias
AU - Bacher, Johannes
AU - Patel, Robin
AU - von Haeseler, Arndt
AU - Posch, Andreas E.
N1 - Funding Information:
Isolates were provided by Northwestern Medicine, Chicago, IL; Beaumont Health, Royal Oak, MI; University of California, Los Angeles, CA; Summa Health, Akron, OH; Johns Hopkins Hospital, Baltimore, MD; Columbia University, New York, NY; University of Rochester, Rochester, NY; and University of Washington, Seattle, WA. This work was supported by the Austrian Research Promotion Agency (FFG) (grants 863729, 866389, and 874595) as well as the Vienna Business Agency (grant 2447823). I.F., S.B., L.L., and T.W. are employees of Ares Genetics GmbH. A.E.P. is Chief Executive Officer of Ares Genetics GmbH. M.K. and J.B. are employees of Curetis GmbH, and J.B. is Chief Operating Officer of Curetis N.V. R.P. reports grants from CD Diagnostics, Merck, Hutchison Biofilm Medical Solutions, Accelerate Diagnostics, ContraFect, TenNor Therapeutics Limited, and Shionogi and is a consultant to Curetis, Specific Technologies, Next Gen Diagnostics, PathoQuest, Selux Diagnostics, 1928 Diagnostics, and Qvella; monies are paid to Mayo Clinic. In addition, R.P. has a patent on Bordetella pertussis-Bordetella parapertussis PCR issued, a patent on a device/method for sonication with royalties paid by Samsung to Mayo Clinic, and a patent on an anti-biofilm substance issued. R.P. receives travel reimbursement from ASM and IDSA, an editor’s stipend from IDSA, and honoraria from the National Board of Medical Examiners, Up-to-Date, and the Infectious Diseases Board Review Course. I.F. and S.B. wrote the manuscript. I.F., L.L., and M.K. performed the computational analysis, and T.W. and S.B. carried out bioinformatics data processing. R.P., J.B., A.V.H. and A.E.P. designed the study. All of the authors reviewed the manuscript, provided comments, and approved the final manuscript.
Publisher Copyright:
Copyright © 2020 Ferreira et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
PY - 2020/7
Y1 - 2020/7
N2 - Whole-genome sequencing (WGS) is now routinely performed in clinical microbiology laboratories to assess isolate relatedness. With appropriately developed analytics, the same data can be used for prediction of antimicrobial susceptibility. We assessed WGS data for identification using open-source tools and antibiotic susceptibility testing (AST) prediction using ARESdb compared to matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) identification and broth microdilution phenotypic susceptibility testing on clinical isolates from a multicenter clinical trial of the FDA-cleared Unyvero lower respiratory tract infection (LRTI) application (Curetis). For the trial, more than 2,000 patient samples were collected from intensive care units across nine hospitals and tested for LRTI. The isolate subset used in this study included 620 clinical isolates originating from 455 LRTI culture-positive patient samples. Isolates were sequenced using the Illumina Nextera XT protocol and FASTQ files with raw reads uploaded to the ARESdb cloud platform (ares-genetics.cloud; released for research use in 2020). The platform combines Ares Genetics’ proprietary database ARESdb with state-of-the-art bioinformatics tools and curated public data. For identification, WGS showed 99 and 93% concordance with MALDI-TOF MS at the genus and species levels, respectively. WGS-predicted susceptibility showed 89% categorical agreement with phenotypic susceptibility across a total of 129 species-compound pairs analyzed, with categorical agreement exceeding 90% in 78 species-compound pairs and reaching 100% in 32. Results of this study add to the growing body of literature showing that, with improvement of analytics, WGS data could be used to predict antimicrobial susceptibility.
AB - Whole-genome sequencing (WGS) is now routinely performed in clinical microbiology laboratories to assess isolate relatedness. With appropriately developed analytics, the same data can be used for prediction of antimicrobial susceptibility. We assessed WGS data for identification using open-source tools and antibiotic susceptibility testing (AST) prediction using ARESdb compared to matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) identification and broth microdilution phenotypic susceptibility testing on clinical isolates from a multicenter clinical trial of the FDA-cleared Unyvero lower respiratory tract infection (LRTI) application (Curetis). For the trial, more than 2,000 patient samples were collected from intensive care units across nine hospitals and tested for LRTI. The isolate subset used in this study included 620 clinical isolates originating from 455 LRTI culture-positive patient samples. Isolates were sequenced using the Illumina Nextera XT protocol and FASTQ files with raw reads uploaded to the ARESdb cloud platform (ares-genetics.cloud; released for research use in 2020). The platform combines Ares Genetics’ proprietary database ARESdb with state-of-the-art bioinformatics tools and curated public data. For identification, WGS showed 99 and 93% concordance with MALDI-TOF MS at the genus and species levels, respectively. WGS-predicted susceptibility showed 89% categorical agreement with phenotypic susceptibility across a total of 129 species-compound pairs analyzed, with categorical agreement exceeding 90% in 78 species-compound pairs and reaching 100% in 32. Results of this study add to the growing body of literature showing that, with improvement of analytics, WGS data could be used to predict antimicrobial susceptibility.
KW - Antimicrobial resistance
KW - Antimicrobial susceptibility testing
KW - Infectious disease diagnostics
KW - Lower respiratory tract infection
KW - Whole-genome sequencing
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U2 - 10.1128/JCM.00273-20
DO - 10.1128/JCM.00273-20
M3 - Article
C2 - 32295890
AN - SCOPUS:85086946260
SN - 0095-1137
VL - 58
JO - Journal of Clinical Microbiology
JF - Journal of Clinical Microbiology
IS - 7
M1 - e00273-20
ER -