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Cell-to-cell propagation of the bacterial toxin CNF1 via extracellular vesicles: potential impact on the therapeutic use of the toxin.
Fabbri, Alessia; Cori, Sara; Zanetti, Cristiana; Guidotti, Marco; Sargiacomo, Massimo; Loizzo, Stefano; Fiorentini, Carla.
Affiliation
  • Fabbri A; Department of Therapeutic Research and Medicines Evaluation, Istituto Superiore di Sanità, Rome 00161, Italy. alessia.fabbri@iss.it.
  • Cori S; Department of Therapeutic Research and Medicines Evaluation, Istituto Superiore di Sanità, Rome 00161, Italy. sara_cori@hotmail.it.
  • Zanetti C; Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome 00161, Italy. cristiana.zanetti@iss.it.
  • Guidotti M; Department of Veterinary Public Health and Food Safety, Istituto Superiore di Sanità, Rome 00161, Italy. marco.guidotti@iss.it.
  • Sargiacomo M; Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome 00161, Italy. massimo.sargiacomo@iss.it.
  • Loizzo S; Department of Therapeutic Research and Medicines Evaluation, Istituto Superiore di Sanità, Rome 00161, Italy. stefano.loizzo@iss.it.
  • Fiorentini C; Department of Therapeutic Research and Medicines Evaluation, Istituto Superiore di Sanità, Rome 00161, Italy. carla.fiorentini@iss.it.
Toxins (Basel) ; 7(11): 4610-21, 2015 Nov 05.
Article in En | MEDLINE | ID: mdl-26556375
ABSTRACT
Eukaryotic cells secrete extracellular vesicles (EVs), either constitutively or in a regulated manner, which represent an important mode of intercellular communication. EVs serve as vehicles for transfer between cells of membrane and cytosolic proteins, lipids and RNA. Furthermore, certain bacterial protein toxins, or possibly their derived messages, can be transferred cell to cell via EVs. We have herein demonstrated that eukaryotic EVs represent an additional route of cell-to-cell propagation for the Escherichia coli protein toxin cytotoxic necrotizing factor 1 (CNF1). Our results prove that EVs from CNF1 pre-infected epithelial cells can induce cytoskeleton changes, Rac1 and NF-κB activation comparable to that triggered by CNF1. The observation that the toxin is detectable inside EVs derived from CNF1-intoxicated cells strongly supports the hypothesis that extracellular vesicles can offer to the toxin a novel route to travel from cell to cell. Since anthrax and tetanus toxins have also been reported to engage in the same process, we can hypothesize that EVs represent a common mechanism exploited by bacterial toxins to enhance their pathogenicity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Toxins / Escherichia coli Proteins / Extracellular Vesicles Limits: Humans Language: En Journal: Toxins (Basel) Year: 2015 Document type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Toxins / Escherichia coli Proteins / Extracellular Vesicles Limits: Humans Language: En Journal: Toxins (Basel) Year: 2015 Document type: Article Affiliation country: Italy