Journal of Bacteriology · 2019 · 23 citations · 47 references
Life SciencesMicrobiologyMolecular BiologyBacteriologyMicrobial PathogenesisMicrobial PhysiologyBacterial BiofilmsBacterial PathogenesisBacterial SurvivalBiofilm FormationBiofilm-associated PathogenesisMicrobial BiofilmsAmyloid FibrillogenesisAmyloid FibrilsBiofilm DevelopmentBiofilm DynamicsBiofilm MorphogenesisInhibition Of Amyloid FormationOligomeric IntermediatesPathogenesis Of Enteric Infections
Amyloid proteins are the major proteinaceous components of biofilms, which are associated with up to 65% of human bacterial infections. Amyloids produced by human cells are also associated with diseases such as Alzheimer’s. The amyloid monomeric subunits self-associate to form oligomers, protofibrils, and finally mature fibrils. Amyloid β oligomers are more cytotoxic to cells than the mature amyloid fibrils. Here we detected oligomeric intermediates of curli for the first time. Like the oligomers of amyloid β, intermediate curli fibrils were more cytotoxic than the mature curli fibrillar aggregates when incubated with bone marrow-derived macrophages. The discovery of cytotoxic curli intermediates will enable research into the roles of amyloid intermediates in the pathogenesis of Salmonella and other bacteria that cause enteric infections.
47
NLRP3 is activated in Alzheimer’s disease and contributes to pathology in APP/PS1 mice
Michael T. Heneka, Markus P. Kummer, Andrea Stutz et al. · Nature · 2012 · 2.9K citations · Full text
Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases
Monica Bucciantini, Elisa Giannoni, Fabrizio Chiti et al. · Nature · 2002 · 2.4K citations
The NALP3 inflammasome is involved in the innate immune response to amyloid-β
Annett Halle, Veit Hornung, Gabor C. Petzold et al. · Nature Immunology · 2008 · 2.4K citations · Full text
Role of <i>Escherichia coli</i> Curli Operons in Directing Amyloid Fiber Formation
Matthew R. Chapman, Lloyd S. Robinson, Jerome S. Pinkner et al. · Science · 2002 · 1.3K citations · Full text