Analysis of the Zonula occludens Toxin Found in the Genome of the Chilean Non-toxigenic Vibrio parahaemolyticus Strain PMC53.7

non-toxigenic strains are responsible for about 10% of acute gastroenteritis associated with this species, suggesting they harbor unique virulence factors. toxin (Zot), firstly described in , is a secreted toxin that increases intestinal permeability. Recently, we identified Zot-encoding genes in th...

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Veröffentlicht in:Frontiers in cellular and infection microbiology 2020-09, Vol.10, p.482
Hauptverfasser: Pérez-Reytor, Diliana, Pavón, Alequis, Lopez-Joven, Carmen, Ramírez-Araya, Sebastián, Peña-Varas, Carlos, Plaza, Nicolás, Alegría-Arcos, Melissa, Corsini, Gino, Jaña, Víctor, Pavez, Leonardo, Del Pozo, Talia, Bastías, Roberto, Blondel, Carlos J, Ramírez, David, García, Katherine
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Sprache:eng
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Zusammenfassung:non-toxigenic strains are responsible for about 10% of acute gastroenteritis associated with this species, suggesting they harbor unique virulence factors. toxin (Zot), firstly described in , is a secreted toxin that increases intestinal permeability. Recently, we identified Zot-encoding genes in the genomes of highly cytotoxic Chilean strains, including the non-toxigenic clinical strain PMC53.7. To gain insights into a possible role of Zot in , we analyzed whether it could be responsible for cytotoxicity. However, we observed a barely positive correlation between Caco-2 cell membrane damage and Zot mRNA expression during PMC53.7 infection and non-cytotoxicity induction in response to purified PMC53.7-Zot. Unusually, we observed a particular actin disturbance on cells infected with PMC53.7. Based on this observation, we decided to compare the sequence of PMC53.7-Zot with Zot of human pathogenic species such as , and other strains, using computational tools. The PMC53.7-Zot was compared with other toxins and identified as an endotoxin with conserved motifs in the N-terminus and a variable C-terminal region and without FCIGRL peptide. Notably, the C-terminal diversity among Zots meant that not all of them could be identified as toxins. Structurally, PMC53.7-Zot was modeled as a transmembrane protein. Our results suggested that it has partial 3D structure similarity with -Zot. Probably, the PMC53.7-Zot would affect the actin cytoskeletal, but, in the absence of FCIGRL, the mechanisms of actions must be elucidated.
ISSN:2235-2988
2235-2988
DOI:10.3389/fcimb.2020.00482