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      Evolution of the U.S. Biological Select Agent Rathayibacter toxicus

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          Abstract

          Rathayibacter toxicus is a toxin-producing species found in Australia and is often fatal to grazing animals. The threat of introduction of the species into the United States led to its inclusion in the Federal Select Agent Program, which makes R. toxicus a highly regulated species. This work provides novel insights into the evolution of R. toxicus. R. toxicus is the only species in the genus to have acquired a CRISPR adaptive immune system to protect against bacteriophages. Results suggest that coexistence with the bacteriophage NCPPB3778 led to the massive shrinkage of the R. toxicus genome, species divergence, and the maintenance of low genetic diversity in extant bacterial groups. This work contributes to an understanding of the evolution and ecology of an agriculturally important species of bacteria.

          ABSTRACT

          Rathayibacter toxicus is a species of Gram-positive, corynetoxin-producing bacteria that causes annual ryegrass toxicity, a disease often fatal to grazing animals. A phylogenomic approach was employed to model the evolution of R. toxicus to explain the low genetic diversity observed among isolates collected during a 30-year period of sampling in three regions of Australia, gain insight into the taxonomy of Rathayibacter, and provide a framework for studying these bacteria. Analyses of a data set of more than 100 sequenced Rathayibacter genomes indicated that Rathayibacter forms nine species-level groups. R. toxicus is the most genetically distant, and evidence suggested that this species experienced a dramatic event in its evolution. Its genome is significantly reduced in size but is colinear to those of sister species. Moreover, R. toxicus has low intergroup genomic diversity and almost no intragroup genomic diversity between ecologically separated isolates. R. toxicus is the only species of the genus that encodes a clustered regularly interspaced short palindromic repeat (CRISPR) locus and that is known to host a bacteriophage parasite. The spacers, which represent a chronological history of infections, were characterized for information on past events. We propose a three-stage process that emphasizes the importance of the bacteriophage and CRISPR in the genome reduction and low genetic diversity of the R. toxicus species.

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          Most cited references56

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          CRISPR interference limits horizontal gene transfer in staphylococci by targeting DNA.

          Horizontal gene transfer (HGT) in bacteria and archaea occurs through phage transduction, transformation, or conjugation, and the latter is particularly important for the spread of antibiotic resistance. Clustered, regularly interspaced, short palindromic repeat (CRISPR) loci confer sequence-directed immunity against phages. A clinical isolate of Staphylococcus epidermidis harbors a CRISPR spacer that matches the nickase gene present in nearly all staphylococcal conjugative plasmids. Here we show that CRISPR interference prevents conjugation and plasmid transformation in S. epidermidis. Insertion of a self-splicing intron into nickase blocks interference despite the reconstitution of the target sequence in the spliced mRNA, which indicates that the interference machinery targets DNA directly. We conclude that CRISPR loci counteract multiple routes of HGT and can limit the spread of antibiotic resistance in pathogenic bacteria.
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            Extreme genome reduction in symbiotic bacteria.

            Since 2006, numerous cases of bacterial symbionts with extraordinarily small genomes have been reported. These organisms represent independent lineages from diverse bacterial groups. They have diminutive gene sets that rival some mitochondria and chloroplasts in terms of gene numbers and lack genes that are considered to be essential in other bacteria. These symbionts have numerous features in common, such as extraordinarily fast protein evolution and a high abundance of chaperones. Together, these features point to highly degenerate genomes that retain only the most essential functions, often including a considerable fraction of genes that serve the hosts. These discoveries have implications for the concept of minimal genomes, the origins of cellular organelles, and studies of symbiosis and host-associated microbiota.
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              The Ka/Ks ratio: diagnosing the form of sequence evolution

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                Author and article information

                Contributors
                Role: Editor
                Journal
                mBio
                MBio
                mbio
                mbio
                mBio
                mBio
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2150-7511
                28 August 2018
                Jul-Aug 2018
                : 9
                : 4
                : e01280-18
                Affiliations
                [a ]Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, USA
                [b ]Molecular and Cellular Biology Program, Oregon State University, Corvallis, Oregon, USA
                [c ]Department of Soil Science, “Luiz de Queiroz” College of Agriculture, University of São Paulo, Piracicaba, SP, Brazil
                [d ]Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel
                [e ]Foreign Disease-Weed Science Research Unit, USDA-ARS, Frederick, Maryland, USA
                [f ]Plant, Soil and Entomological Sciences, University of Idaho, Moscow, Idaho, USA
                [g ]Department of Plant Pathology, Washington State University, Pullman, Washington, USA
                [h ]Horticultural Crops Research Laboratory, USDA-ARS, Corvallis, Oregon, USA
                [i ]Center for Genome Research and Biocomputing, Oregon State University, Corvallis, Oregon, USA
                University of Nebraska—Lincoln
                Author notes
                Address correspondence to Jeff H. Chang, changj@ 123456science.oregonstate.edu .
                Author information
                https://orcid.org/0000-0003-1229-4272
                https://orcid.org/0000-0002-3603-2691
                https://orcid.org/0000-0002-0045-1368
                https://orcid.org/0000-0003-1656-7602
                https://orcid.org/0000-0002-1833-0695
                Article
                mBio01280-18
                10.1128/mBio.01280-18
                6113626
                30154261
                9e513b21-afcb-403b-a641-611d32e74599
                Copyright © 2018 Davis et al.

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

                History
                : 12 June 2018
                : 24 July 2018
                Page count
                supplementary-material: 4, Figures: 5, Tables: 0, Equations: 0, References: 86, Pages: 16, Words: 11713
                Funding
                Funded by: National Science Foundation (NSF), https://doi.org/10.13039/100000001;
                Award ID: DGE-1314109
                Award Recipient :
                Funded by: USDA | National Institute of Food and Agriculture (NIFA), https://doi.org/10.13039/100005825;
                Award ID: 2017-67012-26126
                Award Recipient :
                Funded by: USDA | Animal and Plant Health Inspection Service (APHIS), https://doi.org/10.13039/100009168;
                Award ID: 3.0532.01
                Award Recipient :
                Funded by: USDA | Animal and Plant Health Inspection Service (APHIS), https://doi.org/10.13039/100009168;
                Award ID: 3.0532.02
                Award Recipient :
                Funded by: USDA | Animal and Plant Health Inspection Service (APHIS), https://doi.org/10.13039/100009168;
                Award ID: 13-8130-0247-CA
                Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Funded by: USDA | Animal and Plant Health Inspection Service (APHIS), https://doi.org/10.13039/100009168;
                Award ID: 14-8130-0367-CA
                Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Categories
                Research Article
                Custom metadata
                July/August 2018

                Life sciences
                crispr,evolution,speciation,bacteriophages,plant pathogens
                Life sciences
                crispr, evolution, speciation, bacteriophages, plant pathogens

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