7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Next-generation sequencing for hypothesis-free genomic detection of invasive tropical infections in poly-microbially contaminated, formalin-fixed, paraffin-embedded tissue samples – a proof-of-principle assessment

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          The potential of next-generation sequencing (NGS) for hypothesis-free pathogen diagnosis from (poly-)microbially contaminated, formalin-fixed, paraffin embedded tissue samples from patients with invasive fungal infections and amebiasis was investigated. Samples from patients with chromoblastomycosis ( n = 3), coccidioidomycosis ( n = 2), histoplasmosis ( n = 4), histoplasmosis or cryptococcosis with poor histological discriminability ( n = 1), mucormycosis ( n = 2), mycetoma ( n = 3), rhinosporidiosis ( n = 2), and invasive Entamoeba histolytica infections ( n = 6) were analyzed by NGS (each one Illumina v3 run per sample). To discriminate contamination from putative infections in NGS analysis, mean and standard deviation of the number of specific sequence fragments (paired reads) were determined and compared in all samples examined for the pathogens in question.

          Results

          For matches between NGS results and histological diagnoses, a percentage of species-specific reads greater than the 4th standard deviation above the mean value of all 23 assessed sample materials was required. Potentially etiologically relevant pathogens could be identified by NGS in 5 out of 17 samples of patients with invasive mycoses and in 1 out of 6 samples of patients with amebiasis.

          Conclusions

          The use of NGS for hypothesis-free pathogen diagnosis from contamination-prone formalin-fixed, paraffin-embedded tissue requires further standardization.

          Related collections

          Most cited references50

          • Record: found
          • Abstract: found
          • Article: not found

          The potential and challenges of nanopore sequencing.

          A nanopore-based device provides single-molecule detection and analytical capabilities that are achieved by electrophoretically driving molecules in solution through a nano-scale pore. The nanopore provides a highly confined space within which single nucleic acid polymers can be analyzed at high throughput by one of a variety of means, and the perfect processivity that can be enforced in a narrow pore ensures that the native order of the nucleobases in a polynucleotide is reflected in the sequence of signals that is detected. Kilobase length polymers (single-stranded genomic DNA or RNA) or small molecules (e.g., nucleosides) can be identified and characterized without amplification or labeling, a unique analytical capability that makes inexpensive, rapid DNA sequencing a possibility. Further research and development to overcome current challenges to nanopore identification of each successive nucleotide in a DNA strand offers the prospect of 'third generation' instruments that will sequence a diploid mammalian genome for approximately $1,000 in approximately 24 h.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Performance comparison of benchtop high-throughput sequencing platforms.

            Three benchtop high-throughput sequencing instruments are now available. The 454 GS Junior (Roche), MiSeq (Illumina) and Ion Torrent PGM (Life Technologies) are laser-printer sized and offer modest set-up and running costs. Each instrument can generate data required for a draft bacterial genome sequence in days, making them attractive for identifying and characterizing pathogens in the clinical setting. We compared the performance of these instruments by sequencing an isolate of Escherichia coli O104:H4, which caused an outbreak of food poisoning in Germany in 2011. The MiSeq had the highest throughput per run (1.6 Gb/run, 60 Mb/h) and lowest error rates. The 454 GS Junior generated the longest reads (up to 600 bases) and most contiguous assemblies but had the lowest throughput (70 Mb/run, 9 Mb/h). Run in 100-bp mode, the Ion Torrent PGM had the highest throughput (80–100 Mb/h). Unlike the MiSeq, the Ion Torrent PGM and 454 GS Junior both produced homopolymer-associated indel errors (1.5 and 0.38 errors per 100 bases, respectively).
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Accurate multiplex polony sequencing of an evolved bacterial genome.

              We describe a DNA sequencing technology in which a commonly available, inexpensive epifluorescence microscope is converted to rapid nonelectrophoretic DNA sequencing automation. We apply this technology to resequence an evolved strain of Escherichia coli at less than one error per million consensus bases. A cell-free, mate-paired library provided single DNA molecules that were amplified in parallel to 1-micrometer beads by emulsion polymerase chain reaction. Millions of beads were immobilized in a polyacrylamide gel and subjected to automated cycles of sequencing by ligation and four-color imaging. Cost per base was roughly one-ninth as much as that of conventional sequencing. Our protocols were implemented with off-the-shelf instrumentation and reagents.
                Bookmark

                Author and article information

                Contributors
                Frickmann@bnitm.de
                Carsten.Kuenne@mpi-bn.mpg.de
                Hagen@bnitm.de
                andreas.podbielski@med.uni-rostock.de
                jana.normann@med.uni-rostock.de
                sven@poppert.eu
                Mario.Looso@mpi-bn.mpg.de
                bernd.kreikemeyer@med.uni-rostock.de
                Journal
                BMC Microbiol
                BMC Microbiol
                BMC Microbiology
                BioMed Central (London )
                1471-2180
                8 April 2019
                8 April 2019
                2019
                : 19
                : 75
                Affiliations
                [1 ]ISNI 0000 0000 8715 7852, GRID grid.452235.7, Department of Microbiology and Hospital Hygiene, , Bundeswehr Hospital Hamburg, ; Bernhard-Nocht Str. 74, 20359 Hamburg, Germany
                [2 ]ISNI 0000000121858338, GRID grid.10493.3f, Institute for Microbiology, Virology and Hygiene, , University Medicine Rostock, ; Schillingallee 70, 18057 Rostock, Germany
                [3 ]ISNI 0000 0004 0491 220X, GRID grid.418032.c, Department of Bioinformatics, , Max-Planck Institute for Heart and Lung Research Bad Nauheim, ; Parkstraße 1, 61231 Bad Nauheim, Germany
                [4 ]Department of Preventive Medicine, Bundeswehr Medical Academy, Neuherbergstraße 11, 80937 Munich, Germany
                [5 ]ISNI 0000 0004 0587 0574, GRID grid.416786.a, Swiss Tropical and Public Health Institute, ; Socinstrasse 57, 4051 Basel, Switzerland
                [6 ]ISNI 0000 0004 1937 0642, GRID grid.6612.3, Faculty of Medicine, University Basel, ; Socinstrasse 57, 4051 Basel, Switzerland
                Author information
                http://orcid.org/0000-0002-8967-9528
                Article
                1448
                10.1186/s12866-019-1448-0
                6454699
                30961537
                65192388-a924-4d7c-a48e-cff5d169523c
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 3 January 2018
                : 28 March 2019
                Funding
                Funded by: German Ministry of Defense (MoD)
                Award ID: 12K2-S-451315
                Award Recipient :
                Funded by: European Funds for Regional Development
                Award ID: EU-EFRE
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Microbiology & Virology
                ngs,next-generation sequencing,hypothesis-free diagnosis of infection,invasive fungal infections,invasive amebiasis,ffpe, formalin-fixed, paraffin-embedded samples,molecular diagnostics,tropical infectious diseases,metagenome

                Comments

                Comment on this article