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1.
Int J Mol Sci ; 19(5)2018 May 19.
Article in English | MEDLINE | ID: mdl-29783743

ABSTRACT

In this study, we report how the cholera toxin (CT) A subunit (CTA), the enzyme moiety responsible for signaling alteration in host cells, enters the exosomal pathway, secretes extracellularly, transmits itself to a cell population. The first evidence for long-term transmission of CT's toxic effect via extracellular vesicles was obtained in Chinese hamster ovary (CHO) cells. To follow the CT intracellular route towards exosome secretion, we used a novel strategy for generating metabolically-labeled fluorescent exosomes that can be counted by flow cytometry assay (FACS) and characterized. Our results clearly show the association of CT with exosomes, together with the heat shock protein 90 (HSP90) and Protein Disulfide Isomerase (PDI) molecules, proteins required for translocation of CTA across the ER membrane into the cytoplasm. Confocal microscopy showed direct internalization of CT containing fluorescent exo into CHO cells coupled with morphological changes in the recipient cells that are characteristic of CT action. Moreover, Me665 cells treated with CT-containing exosomes showed an increase in Adenosine 3',5'-Cyclic Monophosphate (cAMP) level, reaching levels comparable to those seen in cells exposed directly to CT. Our results prompt the idea that CT can exploit an exosome-mediated cell communication pathway to extend its pathophysiological action beyond an initial host cell, into a multitude of cells. This finding could have implications for cholera disease pathogenesis and epidemiology.


Subject(s)
ADP-Ribosylation Factors/metabolism , Cholera Toxin/metabolism , Exosomes/metabolism , Animals , CHO Cells , Cell Line, Tumor , Cell Membrane/metabolism , Cholera/etiology , Cholera Toxin/chemistry , Cholera Toxin/toxicity , Cricetinae , Cricetulus , Cyclic AMP/metabolism , HSP90 Heat-Shock Proteins/metabolism , Humans , Protein Disulfide-Isomerases/metabolism , Protein Subunits/metabolism , Protein Transport
2.
Rev Synth ; 133(3): 319-44, 2012.
Article in French | MEDLINE | ID: mdl-22851415

ABSTRACT

Judicial reasoning has often been seen as mere rhetoric. Yet, as I argue here, this reasoning actually stems from the exigencies of truth. This in turn requires questioning the relationship between logic and rhetoric in the legal field. The logic referred to is probability, which is most appropriate to pragmatic rationality. Hence, to shed light on judicial reasoning, this essay puts the relationship between judicial logic and probabilistic logic in historical perspective whilst taking into account the existing literature on the topic.

3.
Infect Immun ; 76(9): 4046-54, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18559424

ABSTRACT

A Listeria monocytogenes bacteriophage was used to identify a phage-resistant Tn917 insertion mutant of the mouse-virulent listerial strain F6214-1. The mutant was attenuated when it was inoculated orally into female A/J mice and failed to replicate efficiently in cultured mouse enterocytes. Phage binding studies indicated that the mutant had a cell surface alteration that precluded phage attachment. All phenotypes associated with the mutation could be complemented in trans by a single open reading frame (ORF) that corresponded to the ORF interrupted by the Tn917 insertion. The complementation effected was, in all cases, at a level indistinguishable from that of the parent. The Tn917 insertion interrupted a gene that is predicted to encode a group 2 glycosyl transferase (provisionally designated glcV). A similar glcV gene is present in Listeria welshimeri and Listeria innocua and in some serotypes of L. monocytogenes. We speculate that the loss of the glcV product results in a defective phage receptor and that this alteration coincidentally influences a feature of the normal host-pathogen interaction required for virulence. Interestingly, the glcV lesion, while preventing phage attachment, did not alter the mutant's ability to bind to cultured mouse enterocyte monolayers. Rather, the mutation appeared to alter a subsequent step in intracellular replication measured by a reduction in plaque-forming efficiency and plaque size. In vivo, the mutant was undetectable in the liver and spleen 48 h after oral inoculation. The mutation is significant in part because it is one of the few that produce attenuation when the mutant is delivered orally.


Subject(s)
Bacteriophages/physiology , Enterocytes/microbiology , Listeria monocytogenes/pathogenicity , Listeria monocytogenes/virology , Virulence Factors/genetics , Virus Attachment , Animals , Bacterial Adhesion , DNA Transposable Elements , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Female , Genetic Complementation Test , Glycosyltransferases/genetics , Listeriosis/microbiology , Liver/microbiology , Mice , Mice, Inbred A , Molecular Sequence Data , Mutagenesis, Insertional , Receptors, Virus/genetics , Sequence Analysis, DNA , Spleen/microbiology , Survival Analysis , Viral Plaque Assay , Virulence
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