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Toxin B is essential for virulence of Clostridium difficileDisruption of the Gut Microbiome: Clostridium difficile Infection and the Threat of Antibiotic ResistanceThe conjugation protein TcpC from Clostridium perfringens is structurally related to the type IV secretion system protein VirB8 from Gram-negative bacteriaPore-forming activity of alpha-toxin is essential for clostridium septicum-mediated myonecrosis.Options for improving effectiveness of rotavirus vaccines in developing countries.The binary toxin CDT enhances Clostridium difficile virulence by suppressing protective colonic eosinophilia.Utility of the clostridial site-specific recombinase TnpX to clone toxic-product-encoding genes and selectively remove genomic DNA fragments.The cysteine protease α-clostripain is not essential for the pathogenesis of Clostridium perfringens-mediated myonecrosis.Characterization of the ends and target sites of the novel conjugative transposon Tn5397 from Clostridium difficile: excision and circularization is mediated by the large resolvase, TndX.The role of toxin A and toxin B in Clostridium difficile-associated disease: Past and present perspectives.The anti-sigma factor TcdC modulates hypervirulence in an epidemic BI/NAP1/027 clinical isolate of Clostridium difficile.Identification of essential residues in the Erm(B) rRNA methyltransferase of Clostridium perfringens.Environmental response and autoregulation of Clostridium difficile TxeR, a sigma factor for toxin gene expression.TcsL is an essential virulence factor in Clostridium sordellii ATCC 9714Spo0A differentially regulates toxin production in evolutionarily diverse strains of Clostridium difficileThe pore-forming α-toxin from clostridium septicum activates the MAPK pathway in a Ras-c-Raf-dependent and independent mannerBinaphthyl-1,2,3-triazole peptidomimetics with activity against Clostridium difficile and other pathogenic bacteria.Clostridium sordellii genome analysis reveals plasmid localized toxin genes encoded within pathogenicity lociAberrant actin depolymerization triggers the pyrin inflammasome and autoinflammatory disease that is dependent on IL-18, not IL-1β.Defining the Roles of TcdA and TcdB in Localized Gastrointestinal Disease, Systemic Organ Damage, and the Host Response during Clostridium difficile InfectionsClostridium difficile drug pipeline: challenges in discovery and development of new agentsCdtR Regulates TcdA and TcdB Production in Clostridium difficileInfluence of gastric acid on susceptibility to infection with ingested bacterial pathogensNovel molecular type of Clostridium difficile in neonatal pigs, Western AustraliaThe Sialidase NanS Enhances Non-TcsL Mediated Cytotoxicity of Clostridium sordelliiThe NanI and NanJ sialidases of Clostridium perfringens are not essential for virulence.tISCpe8, an IS1595-family lincomycin resistance element located on a conjugative plasmid in Clostridium perfringens.CYP101J2, CYP101J3, and CYP101J4, 1,8-Cineole-Hydroxylating Cytochrome P450 Monooxygenases from Sphingobium yanoikuyae Strain B2.Small animal models for the study of Clostridium difficile disease pathogenesis.Regulation of toxin production in the pathogenic clostridia.Antibiotic resistance, virulence factors and genetics of Clostridium sordellii.Solution structure and DNA binding of the catalytic domain of the large serine resolvase TnpX.Construction and analysis of chromosomal Clostridium difficile mutants.Extrachromosomal and integrated genetic elements in Clostridium difficile.Involvement of Bacteria Other Than Clostridium difficile in Antibiotic-Associated Diarrhoea.Genomic diversity of necrotic enteritis-associated strains of Clostridium perfringens: a review.Transcriptional analysis of the tet(P) operon from Clostridium perfringens.Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation.Bovine antibodies targeting primary and recurrent Clostridium difficile disease are a potent antibiotic alternative.Evidence that compatibility of closely related replicons in Clostridium perfringens depends on linkage to parMRC-like partitioning systems of different subfamilies.
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