Subtyping analysis reveals new variants and accelerated evolution of Clostridioides difficile toxin B
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Title
Subtyping analysis reveals new variants and accelerated evolution of Clostridioides difficile toxin B
Authors
Keywords
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Journal
Communications Biology
Volume 3, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-07-03
DOI
10.1038/s42003-020-1078-y
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Related references
Note: Only part of the references are listed.- Evolview v3: a webserver for visualization, annotation, and management of phylogenetic trees
- (2019) Balakrishnan Subramanian et al. NUCLEIC ACIDS RESEARCH
- Selection and characterization of ultrahigh potency designed ankyrin repeat protein inhibitors of C. difficile toxin B
- (2019) Rudo Simeon et al. PLOS BIOLOGY
- Toxin B Variants from Clostridium difficile Strains VPI 10463 and NAP1/027 Share Similar Substrate Profile and Cellular Intoxication Kinetics but Use Different Host Cell Entry Factors
- (2019) Diana López-Ureña et al. Toxins
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- (2019) Nitin Kumar et al. NATURE GENETICS
- Designed Ankyrin Repeat Protein (DARPin) Neutralizers of TcdB from Clostridium difficile Ribotype 027
- (2019) Zeyu Peng et al. mSphere
- MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms
- (2018) Sudhir Kumar et al. MOLECULAR BIOLOGY AND EVOLUTION
- Structural basis for recognition of frizzled proteins byClostridium difficiletoxin B
- (2018) Peng Chen et al. SCIENCE
- Novel Clade C-I Clostridium difficile strains escape diagnostic tests, differ in pathogenicity potential and carry toxins on extrachromosomal elements
- (2018) Gabriel Ramírez-Vargas et al. Scientific Reports
- The Conserved Cys-2232 in Clostridioides difficile Toxin B Modulates Receptor Binding
- (2018) Soo-Young Chung et al. Frontiers in Microbiology
- Difference in Mono-O-Glucosylation of Ras Subtype GTPases Between Toxin A and Toxin B From Clostridioides difficile Strain 10463 and Lethal Toxin From Clostridium sordellii Strain 6018
- (2018) Harald Genth et al. Frontiers in Microbiology
- DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets
- (2017) Julio Rozas et al. MOLECULAR BIOLOGY AND EVOLUTION
- Bezlotoxumab for Prevention of Recurrent Clostridium difficile Infection
- (2017) Mark H. Wilcox et al. NEW ENGLAND JOURNAL OF MEDICINE
- Intrinsic Toxin-Derived Peptides Destabilize and Inactivate Clostridium difficile TcdB
- (2017) Jason L. Larabee et al. mBio
- Historical Perspectives and Guidelines for Botulinum Neurotoxin Subtype Nomenclature
- (2017) Michael Peck et al. Toxins
- Analysis of TcdB Proteins within the Hypervirulent Clade 2 Reveals an Impact of RhoA Glucosylation on Clostridium difficile Proinflammatory Activities
- (2016) Carlos Quesada-Gómez et al. INFECTION AND IMMUNITY
- Frizzled proteins are colonic epithelial receptors for C. difficile toxin B
- (2016) Liang Tao et al. NATURE
- Clostridium difficile infection
- (2016) Wiep Klaas Smits et al. Nature Reviews Disease Primers
- kSNP3.0: SNP detection and phylogenetic analysis of genomes without genome alignment or reference genome: Table 1
- (2015) Shea N Gardner et al. BIOINFORMATICS
- Diversity and Evolution in the Genome of Clostridium difficile
- (2015) Daniel R. Knight et al. CLINICAL MICROBIOLOGY REVIEWS
- Emergence of toxin A-negative, toxin B-positive Clostridium difficile strains: epidemiological and clinical considerations
- (2015) Amy M King et al. Future Microbiology
- Exposure of Neutralizing Epitopes in the Carboxyl-terminal Domain of TcdB Is Altered by a Proximal Hypervariable Region
- (2015) Jason L. Larabee et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Identification of an epithelial cell receptor responsible forClostridium difficileTcdB-induced cytotoxicity
- (2015) Michelle E. LaFrance et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Defining the Roles of TcdA and TcdB in Localized Gastrointestinal Disease, Systemic Organ Damage, and the Host Response during Clostridium difficile Infections
- (2015) Glen P. Carter et al. mBio
- Clostridium difficile: New Insights into the Evolution of the Pathogenicity Locus
- (2015) Marc Monot et al. Scientific Reports
- RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
- (2014) Alexandros Stamatakis BIOINFORMATICS
- Chondroitin sulfate proteoglycan 4 functions as the cellular receptor for Clostridium difficile toxin B
- (2014) Pengfei Yuan et al. CELL RESEARCH
- Haemorrhagic toxin and lethal toxin fromClostridium sordelliistrain vpi9048: molecular characterization and comparative analysis of substrate specificity of the large clostridial glucosylating toxins
- (2014) Harald Genth et al. CELLULAR MICROBIOLOGY
- The Complexity and Diversity of the Pathogenicity Locus in Clostridium difficile Clade 5
- (2014) Briony Elliott et al. Genome Biology and Evolution
- Evolutionary History of the Clostridium difficile Pathogenicity Locus
- (2013) Kate E. Dingle et al. Genome Biology and Evolution
- Substrate Specificity of Clostridial Glucosylating Toxins and Their Function on Colonocytes Analyzed by Proteomics Techniques
- (2013) Johannes Zeiser et al. JOURNAL OF PROTEOME RESEARCH
- aLeaves facilitates on-demand exploration of metazoan gene family trees on MAFFT sequence alignment server with enhanced interactivity
- (2013) Shigehiro Kuraku et al. NUCLEIC ACIDS RESEARCH
- Clostridium difficile 027/BI/NAP1 Encodes a Hypertoxic and Antigenically Variable Form of TcdB
- (2013) Jordi M. Lanis et al. PLoS Pathogens
- Multilocus Sequence Typing of Total-Genome-Sequenced Bacteria
- (2012) M. V. Larsen et al. JOURNAL OF CLINICAL MICROBIOLOGY
- Multicenter Evaluation of a Sequence-Based Protocol for Subtyping Shiga Toxins and Standardizing Stx Nomenclature
- (2012) F. Scheutz et al. JOURNAL OF CLINICAL MICROBIOLOGY
- SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing
- (2012) Anton Bankevich et al. JOURNAL OF COMPUTATIONAL BIOLOGY
- TcdB from hypervirulent Clostridium difficile exhibits increased efficiency of autoprocessing
- (2012) Jordi M. Lanis et al. MOLECULAR MICROBIOLOGY
- Evidence of non-random mutation rates suggests an evolutionary risk management strategy
- (2012) Iñigo Martincorena et al. NATURE
- Macro and Micro Diversity of Clostridium difficile Isolates from Diverse Sources and Geographical Locations
- (2012) Richard A. Stabler et al. PLoS One
- Toward a structural understanding of Clostridium difficile toxins A and B
- (2012) Rory N. Pruitt et al. Frontiers in Cellular and Infection Microbiology
- The role of toxin A and toxin B in Clostridium difficile infection
- (2010) Sarah A. Kuehne et al. NATURE
- Variations in TcdB Activity and the Hypervirulence of Emerging Strains of Clostridium difficile
- (2010) Jordi M. Lanis et al. PLoS Pathogens
- BLAST+: architecture and applications
- (2009) Christiam Camacho et al. BMC BIOINFORMATICS
- Multilocus Sequence Typing ofClostridium difficile
- (2009) David Griffiths et al. JOURNAL OF CLINICAL MICROBIOLOGY
- Toxin B is essential for virulence of Clostridium difficile
- (2009) Dena Lyras et al. NATURE
- Clostridium difficile infection: new developments in epidemiology and pathogenesis
- (2009) Maja Rupnik et al. NATURE REVIEWS MICROBIOLOGY
- Genetic Relatedness of Clostridium difficile Isolates from Various Origins Determined by Triple-Locus Sequence Analysis Based on Toxin Regulatory Genes tcdC, tcdR, and cdtR
- (2008) P. J. M. Bouvet et al. JOURNAL OF CLINICAL MICROBIOLOGY
- Comparative analysis of BI/NAP1/027 hypervirulent strains reveals novel toxin B-encoding gene (tcdB) sequences
- (2008) R. A. Stabler et al. JOURNAL OF MEDICAL MICROBIOLOGY
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