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      Non-Toxin-Producing Bacillus cereus Strains Belonging to the B. anthracis Clade Isolated from the International Space Station

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          Abstract

          The International Space Station Microbial Observatory (Microbial Tracking-1) study is generating a microbial census of the space station’s surfaces and atmosphere by using advanced molecular microbial community analysis techniques supported by traditional culture-based methods and modern bioinformatic computational modeling. This approach will lead to long-term, multigenerational studies of microbial population dynamics in a closed environment and address key questions, including whether microgravity influences the evolution and genetic modification of microorganisms. The spore-forming Bacillus cereus sensu lato group consists of pathogenic ( B. anthracis), food poisoning ( B. cereus), and biotechnologically useful ( B. thuringiensis) microorganisms; their presence in a closed system such as the ISS might be a concern for the health of crew members. A detailed characterization of these potential pathogens would lead to the development of suitable countermeasures that are needed for long-term future missions and a better understanding of microorganisms associated with space missions.

          ABSTRACT

          In an ongoing Microbial Observatory investigation of the International Space Station (ISS), 11 Bacillus strains (2 from the Kibo Japanese experimental module, 4 from the U.S. segment, and 5 from the Russian module) were isolated and their whole genomes were sequenced. A comparative analysis of the 16S rRNA gene sequences of these isolates showed the highest similarity (>99%) to the Bacillus anthracis- B. cereus- B. thuringiensis group. The fatty acid composition, polar lipid profile, peptidoglycan type, and matrix-assisted laser desorption ionization–time of flight profiles were consistent with the B. cereus sensu lato group. The phenotypic traits such as motile rods, enterotoxin production, lack of capsule, and resistance to gamma phage/penicillin observed in ISS isolates were not characteristics of B. anthracis. Whole-genome sequence characterizations showed that ISS strains had the plcR non- B. anthracis ancestral “C” allele and lacked anthrax toxin-encoding plasmids pXO1 and pXO2, excluding their identification as B. anthracis. The genetic identities of all 11 ISS isolates characterized via gyrB analyses arbitrarily identified them as members of the B. cereus group, but traditional DNA-DNA hybridization (DDH) showed that the ISS isolates are similar to B. anthracis (88% to 90%) but distant from the B. cereus (42%) and B. thuringiensis (48%) type strains. The DDH results were supported by average nucleotide identity (>98.5%) and digital DDH (>86%) analyses. However, the collective phenotypic traits and genomic evidence were the reasons to exclude the ISS isolates from B. anthracis. Nevertheless, multilocus sequence typing and whole-genome single nucleotide polymorphism analyses placed these isolates in a clade that is distinct from previously described members of the B. cereus sensu lato group but closely related to B. anthracis.

          IMPORTANCE The International Space Station Microbial Observatory (Microbial Tracking-1) study is generating a microbial census of the space station’s surfaces and atmosphere by using advanced molecular microbial community analysis techniques supported by traditional culture-based methods and modern bioinformatic computational modeling. This approach will lead to long-term, multigenerational studies of microbial population dynamics in a closed environment and address key questions, including whether microgravity influences the evolution and genetic modification of microorganisms. The spore-forming Bacillus cereus sensu lato group consists of pathogenic ( B. anthracis), food poisoning ( B. cereus), and biotechnologically useful ( B. thuringiensis) microorganisms; their presence in a closed system such as the ISS might be a concern for the health of crew members. A detailed characterization of these potential pathogens would lead to the development of suitable countermeasures that are needed for long-term future missions and a better understanding of microorganisms associated with space missions.

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          Molecular Cloning : A Laboratory Manual

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            Introducing EzTaxon-e: a prokaryotic 16S rRNA gene sequence database with phylotypes that represent uncultured species.

            Despite recent advances in commercially optimized identification systems, bacterial identification remains a challenging task in many routine microbiological laboratories, especially in situations where taxonomically novel isolates are involved. The 16S rRNA gene has been used extensively for this task when coupled with a well-curated database, such as EzTaxon, containing sequences of type strains of prokaryotic species with validly published names. Although the EzTaxon database has been widely used for routine identification of prokaryotic isolates, sequences from uncultured prokaryotes have not been considered. Here, the next generation database, named EzTaxon-e, is formally introduced. This new database covers not only species within the formal nomenclatural system but also phylotypes that may represent species in nature. In addition to an identification function based on Basic Local Alignment Search Tool (blast) searches and pairwise global sequence alignments, a new objective method of assessing the degree of completeness in sequencing is proposed. All sequences that are held in the EzTaxon-e database have been subjected to phylogenetic analysis and this has resulted in a complete hierarchical classification system. It is concluded that the EzTaxon-e database provides a useful taxonomic backbone for the identification of cultured and uncultured prokaryotes and offers a valuable means of communication among microbiologists who routinely encounter taxonomically novel isolates. The database and its analytical functions can be found at http://eztaxon-e.ezbiocloud.net/.
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              Digital DNA-DNA hybridization for microbial species delineation by means of genome-to-genome sequence comparison

              The pragmatic species concept for Bacteria and Archaea is ultimately based on DNA-DNA hybridization (DDH). While enabling the taxonomist, in principle, to obtain an estimate of the overall similarity between the genomes of two strains, this technique is tedious and error-prone and cannot be used to incrementally build up a comparative database. Recent technological progress in the area of genome sequencing calls for bioinformatics methods to replace the wet-lab DDH by in-silico genome-to-genome comparison. Here we investigate state-of-the-art methods for inferring whole-genome distances in their ability to mimic DDH. Algorithms to efficiently determine high-scoring segment pairs or maximally unique matches perform well as a basis of inferring intergenomic distances. The examined distance functions, which are able to cope with heavily reduced genomes and repetitive sequence regions, outperform previously described ones regarding the correlation with and error ratios in emulating DDH. Simulation of incompletely sequenced genomes indicates that some distance formulas are very robust against missing fractions of genomic information. Digitally derived genome-to-genome distances show a better correlation with 16S rRNA gene sequence distances than DDH values. The future perspectives of genome-informed taxonomy are discussed, and the investigated methods are made available as a web service for genome-based species delineation.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                mSystems
                mSystems
                msys
                msys
                mSystems
                mSystems
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2379-5077
                27 June 2017
                May-Jun 2017
                : 2
                : 3
                : e00021-17
                Affiliations
                [a ]Biotechnology and Planetary Protection Group, Jet Propulsion Laboratory, California Institute of Technology, Pasadena, California, USA
                [b ]National Biodefense Analysis and Countermeasures Center, Ft. Detrick, Maryland, USA
                [c ]Department of Medical Microbiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
                [d ]Department of Microbiology and Plant Biology, University of Oklahoma, Norman, Oklahoma, USA
                [e ]National Research Institute of Fisheries Science, Japan Fisheries Research and Education Agency, Kanagawa, Japan
                [f ]The Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, USA
                [g ]Johnson Space Center, Houston, Texas, USA
                [h ]Marshall Space Flight Center, Huntsville, Alabama, USA
                University of California, Riverside
                Author notes
                Address correspondence to Kasthuri Venkateswaran, kjvenkat@ 123456jpl.nasa.gov .

                Citation Venkateswaran K, Singh NK, Checinska Sielaff A, Pope RK, Bergman NH, van Tongeren SP, Patel NB, Lawson PA, Satomi M, Williamson CHD, Sahl JW, Keim P, Pierson D, Perry J. 2017. Non-toxin-producing Bacillus cereus strains belonging to the B. anthracis clade isolated from the International Space Station. mSystems 2:e00021-17. https://doi.org/10.1128/mSystems.00021-17.

                Author information
                http://orcid.org/0000-0002-6742-0873
                http://orcid.org/0000-0003-0089-5820
                Article
                mSystems00021-17
                10.1128/mSystems.00021-17
                5487513
                28680972
                d55df64e-def7-4e70-8826-a103f0e963da
                Copyright © 2017 Venkateswaran et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 16 March 2017
                : 23 May 2017
                Page count
                supplementary-material: 4, Figures: 4, Tables: 5, Equations: 0, References: 84, Pages: 16, Words: 10873
                Funding
                Funded by: National Aeronautics and Space Administration (NASA) https://doi.org/10.13039/100000104
                Award ID: 19-12829-26
                Award Recipient : Kasthuri Venkateswaran
                Funded by: U.S. Department of Homeland Security (DHS) https://doi.org/10.13039/100000180
                Award ID: HSHQDC-07-C-00020
                Award Recipient : Robert K. Pope Award Recipient : Nicholas H. Bergman
                Funded by: European Space Agency (ESA) https://doi.org/10.13039/501100000844
                Award ID: AO-LS-99-MAP-LSS-018
                Award Recipient : Sandra P. van Tongeren
                Categories
                Research Article
                Applied and Environmental Science
                Custom metadata
                May/June 2017

                bacillus,bacillus anthracis,bacillus cereus,genomics,iss,spores
                bacillus, bacillus anthracis, bacillus cereus, genomics, iss, spores

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