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Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients

BACKGROUND: Infections by several DNA viruses can severely impact outcomes in paediatric immunocompromised patients. Current testing, which is generally limited to singleplex qPCR assays, can miss both common and rarer viruses if they are not targeted. OBJECTIVES: To evaluate the performance of the...

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Autores principales: Shah, Divya, Brown, Julianne R., Lee, Jack C.D., Carpenter, Meredith L., Wall, Gavin, Breuer, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200058/
https://www.ncbi.nlm.nih.gov/pubmed/35755957
http://dx.doi.org/10.1016/j.jcvp.2022.100073
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author Shah, Divya
Brown, Julianne R.
Lee, Jack C.D.
Carpenter, Meredith L.
Wall, Gavin
Breuer, Judith
author_facet Shah, Divya
Brown, Julianne R.
Lee, Jack C.D.
Carpenter, Meredith L.
Wall, Gavin
Breuer, Judith
author_sort Shah, Divya
collection PubMed
description BACKGROUND: Infections by several DNA viruses can severely impact outcomes in paediatric immunocompromised patients. Current testing, which is generally limited to singleplex qPCR assays, can miss both common and rarer viruses if they are not targeted. OBJECTIVES: To evaluate the performance of the Galileo Viral Panel (Galileo), a sample-to-result shotgun metagenomics platform for the detection and quantification of 12 DNA viruses, compared to standard of care qPCR assays. STUDY DESIGN: A clinical performance evaluation was carried out using 43 prospectively collected EDTA plasma samples positive for one or more DNA viruses. Agreement between assays was assessed by overall, positive, and negative percent agreement, as well as quantitative agreement by linear regression and Bland-Altman analysis. RESULTS: Overall positive percent agreement was 84% (95% CI: 76%-90%), and negative percent agreement was 95% (95% CI: 92%-97%). There was a high correlation between Galileo and qPCR for ADV, CMV, EBV, and VZV (R(2) = 0.91) and a mean difference by Bland Altman of -0.43 log(10) IU or cp/ml (95% limits of agreement, -1.37 to 0.51). In addition, there was a high correlation between Galileo Signal Score and qPCR for TTV (R(2) = 0.85). CONCLUSION: We observed high qualitative and quantitative agreement between qPCR and Galileo. Galileo identified additional viruses that were not tested with routine qPCR and could impact clinical outcomes.
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spelling pubmed-92000582022-06-23 Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients Shah, Divya Brown, Julianne R. Lee, Jack C.D. Carpenter, Meredith L. Wall, Gavin Breuer, Judith J Clin Virol Plus Article BACKGROUND: Infections by several DNA viruses can severely impact outcomes in paediatric immunocompromised patients. Current testing, which is generally limited to singleplex qPCR assays, can miss both common and rarer viruses if they are not targeted. OBJECTIVES: To evaluate the performance of the Galileo Viral Panel (Galileo), a sample-to-result shotgun metagenomics platform for the detection and quantification of 12 DNA viruses, compared to standard of care qPCR assays. STUDY DESIGN: A clinical performance evaluation was carried out using 43 prospectively collected EDTA plasma samples positive for one or more DNA viruses. Agreement between assays was assessed by overall, positive, and negative percent agreement, as well as quantitative agreement by linear regression and Bland-Altman analysis. RESULTS: Overall positive percent agreement was 84% (95% CI: 76%-90%), and negative percent agreement was 95% (95% CI: 92%-97%). There was a high correlation between Galileo and qPCR for ADV, CMV, EBV, and VZV (R(2) = 0.91) and a mean difference by Bland Altman of -0.43 log(10) IU or cp/ml (95% limits of agreement, -1.37 to 0.51). In addition, there was a high correlation between Galileo Signal Score and qPCR for TTV (R(2) = 0.85). CONCLUSION: We observed high qualitative and quantitative agreement between qPCR and Galileo. Galileo identified additional viruses that were not tested with routine qPCR and could impact clinical outcomes. Elsevier Ltd 2022-06 /pmc/articles/PMC9200058/ /pubmed/35755957 http://dx.doi.org/10.1016/j.jcvp.2022.100073 Text en © 2022 The Authors. Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Shah, Divya
Brown, Julianne R.
Lee, Jack C.D.
Carpenter, Meredith L.
Wall, Gavin
Breuer, Judith
Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients
title Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients
title_full Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients
title_fullStr Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients
title_full_unstemmed Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients
title_short Use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients
title_sort use of a sample-to-result shotgun metagenomics platform for the detection and quantification of viral pathogens in paediatric immunocompromised patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200058/
https://www.ncbi.nlm.nih.gov/pubmed/35755957
http://dx.doi.org/10.1016/j.jcvp.2022.100073
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