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      Comparative pathogenomics of Clostridium tetani

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          Abstract

          Clostridium tetani and Clostridium botulinum produce two of the most potent neurotoxins known, tetanus neurotoxin and botulinum neurotoxin, respectively. Extensive biochemical and genetic investigation has been devoted to identifying and characterizing various C. botulinum strains. Less effort has been focused on studying C. tetani likely because recently sequenced strains of C. tetani show much less genetic diversity than C. botulinum strains and because widespread vaccination efforts have reduced the public health threat from tetanus. Our aim was to acquire genomic data on the U.S. vaccine strain of C. tetani to better understand its genetic relationship to previously published genomic data from European vaccine strains. We performed high throughput genomic sequence analysis on two wild-type and two vaccine C. tetani strains. Comparative genomic analysis was performed using these and previously published genomic data for seven other C. tetani strains. Our analysis focused on single nucleotide polymorphisms (SNP) and four distinct constituents of the mobile genome (mobilome): a hypervariable flagellar glycosylation island region, five conserved bacteriophage insertion regions, variations in three CRISPR (clustered regularly interspaced short palindromic repeats)-Cas (CRISPR-associated) systems, and a single plasmid. Intact type IA and IB CRISPR/Cas systems were within 10 of 11 strains. A type IIIA CRISPR/Cas system was present in two strains. Phage infection histories derived from CRISPR-Cas sequences indicate C. tetani encounters phages common among commensal gut bacteria and soil-borne organisms consistent with C. tetani distribution in nature. All vaccine strains form a clade distinct from currently sequenced wild type strains when considering variations in these mobile elements. SNP, flagellar glycosylation island, prophage content and CRISPR/Cas phylogenic histories provide tentative evidence suggesting vaccine and wild type strains share a common ancestor.

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          Most cited references32

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          CRISPR--a widespread system that provides acquired resistance against phages in bacteria and archaea.

          Arrays of clustered, regularly interspaced short palindromic repeats (CRISPRs) are widespread in the genomes of many bacteria and almost all archaea. These arrays are composed of direct repeats that are separated by similarly sized non-repetitive spacers. CRISPR arrays, together with a group of associated proteins, confer resistance to phages, possibly by an RNA-interference-like mechanism. This Progress discusses the structure and function of this newly recognized antiviral mechanism.
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            Self-targeting by CRISPR: gene regulation or autoimmunity?

            The recently discovered prokaryotic immune system known as CRISPR (clustered regularly interspaced short palindromic repeats) is based on small RNAs ('spacers') that restrict phage and plasmid infection. It has been hypothesized that CRISPRs can also regulate self gene expression by utilizing spacers that target self genes. By analyzing CRISPRs from 330 organisms we found that one in every 250 spacers is self-targeting, and that such self-targeting occurs in 18% of all CRISPR-bearing organisms. However, complete lack of conservation across species, combined with abundance of degraded repeats near self-targeting spacers, suggests that self-targeting is a form of autoimmunity rather than a regulatory mechanism. We propose that accidental incorporation of self nucleic acids by CRISPR can incur an autoimmune fitness cost, and this could explain the abundance of degraded CRISPR systems across prokaryotes. Copyright 2010 Elsevier Ltd. All rights reserved.
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              CRISPRTarget

              The bacterial and archaeal CRISPR/Cas adaptive immune system targets specific protospacer nucleotide sequences in invading organisms. This requires base pairing between processed CRISPR RNA and the target protospacer. For type I and II CRISPR/Cas systems, protospacer adjacent motifs (PAM) are essential for target recognition, and for type III, mismatches in the flanking sequences are important in the antiviral response. In this study, we examine the properties of each class of CRISPR. We use this information to provide a tool (CRISPRTarget) that predicts the most likely targets of CRISPR RNAs (http://bioanalysis.otago.ac.nz/CRISPRTarget). This can be used to discover targets in newly sequenced genomic or metagenomic data. To test its utility, we discover features and targets of well-characterized Streptococcus thermophilus and Sulfolobus solfataricus type II and III CRISPR/Cas systems. Finally, in Pectobacterium species, we identify new CRISPR targets and propose a model of temperate phage exposure and subsequent inhibition by the type I CRISPR/Cas systems.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: InvestigationRole: Writing – original draftRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: Methodology
                Role: ConceptualizationRole: Data curationRole: MethodologyRole: ResourcesRole: Supervision
                Role: Data curationRole: Formal analysisRole: Methodology
                Role: ConceptualizationRole: InvestigationRole: MethodologyRole: Project administrationRole: ResourcesRole: SupervisionRole: Writing – original draftRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                11 August 2017
                2017
                : 12
                : 8
                : e0182909
                Affiliations
                [1 ] Laboratory of Respiratory and Special Pathogens, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, Maryland, United States of America
                [2 ] Facility for Biotechnology Resources, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, Maryland, United States of America
                Aarhus Universitet, DENMARK
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0002-1963-4033
                http://orcid.org/0000-0001-5432-8421
                Article
                PONE-D-17-01504
                10.1371/journal.pone.0182909
                5553647
                28800585
                e550d1f4-58da-4199-8f55-436482e0977d

                This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

                History
                : 12 January 2017
                : 26 July 2017
                Page count
                Figures: 9, Tables: 2, Pages: 24
                Funding
                Funded by: FDA/CBER intramural funding
                Award Recipient :
                FDA/CBER intramural funding supported this work.
                Categories
                Research Article
                Biology and Life Sciences
                Organisms
                Bacteria
                Gut Bacteria
                Clostridium Tetani
                Biology and Life Sciences
                Organisms
                Viruses
                Bacteriophages
                Medicine and Health Sciences
                Infectious Diseases
                Infectious Disease Control
                Vaccines
                Biology and Life Sciences
                Organisms
                Bacteria
                Gut Bacteria
                Clostridium Botulinum
                Research and Analysis Methods
                Database and Informatics Methods
                Bioinformatics
                Sequence Analysis
                Sequence Alignment
                Biology and Life Sciences
                Computational Biology
                Comparative Genomics
                Biology and Life Sciences
                Genetics
                Genomics
                Comparative Genomics
                Biology and Life Sciences
                Evolutionary Biology
                Evolutionary Systematics
                Phylogenetics
                Phylogenetic Analysis
                Biology and Life Sciences
                Taxonomy
                Evolutionary Systematics
                Phylogenetics
                Phylogenetic Analysis
                Computer and Information Sciences
                Data Management
                Taxonomy
                Evolutionary Systematics
                Phylogenetics
                Phylogenetic Analysis
                Biology and Life Sciences
                Biotechnology
                Bioengineering
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Engineering and Technology
                Bioengineering
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Biology and Life Sciences
                Synthetic Biology
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Engineering and Technology
                Synthetic Biology
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Biology and Life Sciences
                Synthetic Biology
                Synthetic Genomics
                Synthetic Genome Editing
                Crispr
                Engineering and Technology
                Synthetic Biology
                Synthetic Genomics
                Synthetic Genome Editing
                Crispr
                Custom metadata
                All relevant data are within the paper and its Supporting Information files. All whole genome shotgun (WGS) sequencing assemblies generated during this study have been deposited in NCBI under WGS projects JRGG01 for C2, JRGH01 for ATCC 9441, JRGJ01 for ATCC 19406, and JRGI01 for ATCC 453. The GenBank accession numbers for C. tetani phages are KM983333.1 for phiCTC2A, KM983334.1 for phiCTC2B, KM983329.1 for phiCT9441A, KM983330.1 for phiCT19406A, KM983331.1 for phiCT19406B, KM983332.1 for phiCT19406C, KM983327.1 for phiCT453A, KM983328.1 for phiCT453B.

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