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Comparative meta-omics for identifying pathogens associated with prosthetic joint infection
Prosthetic joint infections (PJI) are economically and personally costly, and their incidence has been increasing in the United States. Herein, we compared 16S rRNA amplicon sequencing (16S), shotgun metagenomics (MG) and metatranscriptomics (MT) in identifying pathogens causing PJI. Samples were co...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8660779/ https://www.ncbi.nlm.nih.gov/pubmed/34887434 http://dx.doi.org/10.1038/s41598-021-02505-7 |
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author | Goswami, Karan Shope, Alexander J. Tokarev, Vasily Wright, Justin R. Unverdorben, Lavinia V. Ly, Truc Chen See, Jeremy McLimans, Christopher J. Wong, Hoi Tong Lock, Lauren Clarkson, Samuel Parvizi, Javad Lamendella, Regina |
author_facet | Goswami, Karan Shope, Alexander J. Tokarev, Vasily Wright, Justin R. Unverdorben, Lavinia V. Ly, Truc Chen See, Jeremy McLimans, Christopher J. Wong, Hoi Tong Lock, Lauren Clarkson, Samuel Parvizi, Javad Lamendella, Regina |
author_sort | Goswami, Karan |
collection | PubMed |
description | Prosthetic joint infections (PJI) are economically and personally costly, and their incidence has been increasing in the United States. Herein, we compared 16S rRNA amplicon sequencing (16S), shotgun metagenomics (MG) and metatranscriptomics (MT) in identifying pathogens causing PJI. Samples were collected from 30 patients, including 10 patients undergoing revision arthroplasty for infection, 10 patients receiving revision for aseptic failure, and 10 patients undergoing primary total joint arthroplasty. Synovial fluid and peripheral blood samples from the patients were obtained at time of surgery. Analysis revealed distinct microbial communities between primary, aseptic, and infected samples using MG, MT, (PERMANOVA p = 0.001), and 16S sequencing (PERMANOVA p < 0.01). MG and MT had higher concordance with culture (83%) compared to 0% concordance of 16S results. Supervised learning methods revealed MT datasets most clearly differentiated infected, primary, and aseptic sample groups. MT data also revealed more antibiotic resistance genes, with improved concordance results compared to MG. These data suggest that a differential and underlying microbial ecology exists within uninfected and infected joints. This study represents the first application of RNA-based sequencing (MT). Further work on larger cohorts will provide opportunities to employ deep learning approaches to improve accuracy, predictive power, and clinical utility. |
format | Online Article Text |
id | pubmed-8660779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86607792021-12-13 Comparative meta-omics for identifying pathogens associated with prosthetic joint infection Goswami, Karan Shope, Alexander J. Tokarev, Vasily Wright, Justin R. Unverdorben, Lavinia V. Ly, Truc Chen See, Jeremy McLimans, Christopher J. Wong, Hoi Tong Lock, Lauren Clarkson, Samuel Parvizi, Javad Lamendella, Regina Sci Rep Article Prosthetic joint infections (PJI) are economically and personally costly, and their incidence has been increasing in the United States. Herein, we compared 16S rRNA amplicon sequencing (16S), shotgun metagenomics (MG) and metatranscriptomics (MT) in identifying pathogens causing PJI. Samples were collected from 30 patients, including 10 patients undergoing revision arthroplasty for infection, 10 patients receiving revision for aseptic failure, and 10 patients undergoing primary total joint arthroplasty. Synovial fluid and peripheral blood samples from the patients were obtained at time of surgery. Analysis revealed distinct microbial communities between primary, aseptic, and infected samples using MG, MT, (PERMANOVA p = 0.001), and 16S sequencing (PERMANOVA p < 0.01). MG and MT had higher concordance with culture (83%) compared to 0% concordance of 16S results. Supervised learning methods revealed MT datasets most clearly differentiated infected, primary, and aseptic sample groups. MT data also revealed more antibiotic resistance genes, with improved concordance results compared to MG. These data suggest that a differential and underlying microbial ecology exists within uninfected and infected joints. This study represents the first application of RNA-based sequencing (MT). Further work on larger cohorts will provide opportunities to employ deep learning approaches to improve accuracy, predictive power, and clinical utility. Nature Publishing Group UK 2021-12-09 /pmc/articles/PMC8660779/ /pubmed/34887434 http://dx.doi.org/10.1038/s41598-021-02505-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Goswami, Karan Shope, Alexander J. Tokarev, Vasily Wright, Justin R. Unverdorben, Lavinia V. Ly, Truc Chen See, Jeremy McLimans, Christopher J. Wong, Hoi Tong Lock, Lauren Clarkson, Samuel Parvizi, Javad Lamendella, Regina Comparative meta-omics for identifying pathogens associated with prosthetic joint infection |
title | Comparative meta-omics for identifying pathogens associated with prosthetic joint infection |
title_full | Comparative meta-omics for identifying pathogens associated with prosthetic joint infection |
title_fullStr | Comparative meta-omics for identifying pathogens associated with prosthetic joint infection |
title_full_unstemmed | Comparative meta-omics for identifying pathogens associated with prosthetic joint infection |
title_short | Comparative meta-omics for identifying pathogens associated with prosthetic joint infection |
title_sort | comparative meta-omics for identifying pathogens associated with prosthetic joint infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8660779/ https://www.ncbi.nlm.nih.gov/pubmed/34887434 http://dx.doi.org/10.1038/s41598-021-02505-7 |
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