39
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Real-Time Culture-Independent Microbial Profiling Onboard the International Space Station Using Nanopore Sequencing

      research-article

      Read this article at

      ScienceOpenPublisherPMC
          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

          For the past two decades, microbial monitoring of the International Space Station (ISS) has relied on culture-dependent methods that require return to Earth for analysis. This has a number of limitations, with the most significant being bias towards the detection of culturable organisms and the inherent delay between sample collection and ground-based analysis. In recent years, portable and easy-to-use molecular-based tools, such as Oxford Nanopore Technologies’ MinION™ sequencer and miniPCR bio’s miniPCR™ thermal cycler, have been validated onboard the ISS. Here, we report on the development, validation, and implementation of a swab-to-sequencer method that provides a culture-independent solution to real-time microbial profiling onboard the ISS. Method development focused on analysis of swabs collected in a low-biomass environment with limited facility resources and stringent controls on allowed processes and reagents. ISS-optimized procedures included enzymatic DNA extraction from a swab tip, bead-based purifications, altered buffers, and the use of miniPCR and the MinION. Validation was conducted through extensive ground-based assessments comparing current standard culture-dependent and newly developed culture-independent methods. Similar microbial distributions were observed between the two methods; however, as expected, the culture-independent data revealed microbial profiles with greater diversity. Protocol optimization and verification was established during NASA Extreme Environment Mission Operations (NEEMO) analog missions 21 and 22, respectively. Unique microbial profiles obtained from analog testing validated the swab-to-sequencer method in an extreme environment. Finally, four independent swab-to-sequencer experiments were conducted onboard the ISS by two crewmembers. Microorganisms identified from ISS swabs were consistent with historical culture-based data, and primarily consisted of commonly observed human-associated microbes. This simplified method has been streamlined for high ease-of-use for a non-trained crew to complete in an extreme environment, thereby enabling environmental and human health diagnostics in real-time as future missions take us beyond low-Earth orbit.

          Related collections

          Most cited references69

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          The Sequence Alignment/Map format and SAMtools

          Summary: The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference sequences, supporting short and long reads (up to 128 Mbp) produced by different sequencing platforms. It is flexible in style, compact in size, efficient in random access and is the format in which alignments from the 1000 Genomes Project are released. SAMtools implements various utilities for post-processing alignments in the SAM format, such as indexing, variant caller and alignment viewer, and thus provides universal tools for processing read alignments. Availability: http://samtools.sourceforge.net Contact: rd@sanger.ac.uk
            • Record: found
            • Abstract: found
            • Article: not found

            Minimap2: pairwise alignment for nucleotide sequences

            Heng Li (2018)
            Recent advances in sequencing technologies promise ultra-long reads of ∼100 kb in average, full-length mRNA or cDNA reads in high throughput and genomic contigs over 100 Mb in length. Existing alignment programs are unable or inefficient to process such data at scale, which presses for the development of new alignment algorithms.
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Structure, Function and Diversity of the Healthy Human Microbiome

              Studies of the human microbiome have revealed that even healthy individuals differ remarkably in the microbes that occupy habitats such as the gut, skin, and vagina. Much of this diversity remains unexplained, although diet, environment, host genetics, and early microbial exposure have all been implicated. Accordingly, to characterize the ecology of human-associated microbial communities, the Human Microbiome Project has analyzed the largest cohort and set of distinct, clinically relevant body habitats to date. We found the diversity and abundance of each habitat’s signature microbes to vary widely even among healthy subjects, with strong niche specialization both within and among individuals. The project encountered an estimated 81–99% of the genera, enzyme families, and community configurations occupied by the healthy Western microbiome. Metagenomic carriage of metabolic pathways was stable among individuals despite variation in community structure, and ethnic/racial background proved to be one of the strongest associations of both pathways and microbes with clinical metadata. These results thus delineate the range of structural and functional configurations normal in the microbial communities of a healthy population, enabling future characterization of the epidemiology, ecology, and translational applications of the human microbiome.

                Author and article information

                Journal
                Genes (Basel)
                Genes (Basel)
                genes
                Genes
                MDPI
                2073-4425
                16 January 2021
                January 2021
                : 12
                : 1
                : 106
                Affiliations
                [1 ]JES Tech, Houston, TX 77058, USA; sarah.e.stahl@ 123456nasa.gov (S.S.-R.); hang.n.nguyen@ 123456nasa.gov (H.N.N.); christian.l.castro@ 123456nasa.gov (C.L.C.)
                [2 ]UCSC Genomics Institute, University of California, Santa Cruz, CA 95064, USA; miten@ 123456soe.ucsc.edu (M.J.); benedict@ 123456soe.ucsc.edu (B.P.); makeson@ 123456soe.ucsc.edu (M.A.)
                [3 ]Astronaut Office, NASA Johnson Space Center, Houston, TX 77058, USA; richard.r.arnold@ 123456nasa.gov (R.R.A.); serena.m.aunon@ 123456nasa.gov (S.M.A.-C.)
                [4 ]KBR, Houston, TX 77058, USA; gretta.m.sharp@ 123456nasa.gov
                [5 ]Project Management and Systems Engineering Division, NASA Johnson Space Center, Houston, TX 77058, USA; kristen.k.john@ 123456nasa.gov
                [6 ]Oxford Nanopore Technologies, New York, NY 10013, USA; Sissel.Juul@ 123456nanoporetech.com
                [7 ]Oxford Nanopore Technologies, Oxford Science Park, Oxford OX4 4DQ, UK; daniel.turner@ 123456nanoporetech.com (D.J.T.); david.stoddart@ 123456nanoporetech.com (D.S.)
                [8 ]Astromaterials Research and Exploration Science Division, NASA Johnson Space Center, Houston, TX 77058, USA; aaron.burton@ 123456nasa.gov
                [9 ]Biomedical Research and Environmental Sciences Division, NASA Johnson Space Center, Houston, TX 77058, USA
                Author notes
                [* ]Correspondence: sarah.wallace@ 123456nasa.gov ; Tel.: +1-281-483-7254
                Author information
                https://orcid.org/0000-0002-4571-3982
                https://orcid.org/0000-0002-1368-4531
                https://orcid.org/0000-0002-0315-4449
                https://orcid.org/0000-0001-9392-8075
                https://orcid.org/0000-0002-1194-4336
                Article
                genes-12-00106
                10.3390/genes12010106
                7830261
                33467183
                7501fe8c-fbe8-4aa5-ae20-c88dba1fce90
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 December 2020
                : 14 January 2021
                Categories
                Article

                nanopore sequencing,in-situ analysis,field-deployable methods,bacterial identification,spaceflight

                Comments

                Comment on this article

                Related Documents Log