Revealing the Salmo salar NLRP3 Inflammasome: Insights from Structural Modeling and Transcriptome Analysis

Author:

Acevedo Waldo1ORCID,Morán-Figueroa Rodrigo234,Vargas-Chacoff Luis5678ORCID,Morera Francisco J.2348,Pontigo Juan Pablo9

Affiliation:

1. Biological Chemistry Laboratory, Institute of Chemistry, Faculty of Science, Pontificia Universidad Católica de Valparaíso, Valparaiso 2373223, Chile

2. Escuela de Medicina Veterinaria, Facultad de Agronomía y Sistemas Naturales, Pontificia Universidad Católica de Chile, Santiago 7810000, Chile

3. Escuela de Medicina Veterinaria, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago 7810000, Chile

4. Escuela de Medicina Veterinaria, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago 7810000, Chile

5. Institute of Marine Sciences and Limnology, Faculty of Sciences, Universidad Austral de Chile, Valdivia 5110566, Chile

6. IDEAL Research Center for Dynamics of High Latitude Marine Ecosystems, Universidad Austral de Chile, Valdivia 5110566, Chile

7. Millennium Institute Biodiversity of Antarctic and Subantarctic Ecosystems, BASE, University Austral of Chile, Valdivia 5090000, Chile

8. Integrative Biology Group, Valdivia 5110566, Chile

9. Laboratorio Institucional de Investigación, Facultad Ciencias de la Naturaleza, Medicina Veterinaria, Universidad San Sebastián, Lago Panguipulli 1390, Puerto Montt 5090000, Chile

Abstract

The NLRP3, one of the most heavily studied inflammasome-related proteins in mammals, remains inadequately characterized in Atlantic salmon (Salmo salar), despite the significant commercial importance of this salmonid. The NLRP3 inflammasome is composed of the NLRP3 protein, which is associated with procaspase-1 via an adapter molecule known as ASC. This work aims to characterize the Salmo salar NLRP3 inflammasome through in silico structural modeling, functional transcript expression determination in the SHK-1 cell line in vitro, and a transcriptome analysis on Atlantic salmon. The molecular docking results suggested a similar arrangement of the ternary complex between NLRP3, ASC, and caspase-1 in both the Atlantic salmon and the mammalian NLRP3 inflammasomes. Moreover, the expression results confirmed the functionality of the SsNLRP3 inflammasome in the SHK-1 cells, as evidenced by the lipopolysaccharide-induced increase in the transcription of genes involved in inflammasome activation, including ASC and NLRP3. Additionally, the transcriptome results revealed that most of the inflammasome-related genes, including ASC, NLRP3, and caspase-1, were down-regulated in the Atlantic salmon following its adaptation to seawater (also known as parr–smolt transformation). This is correlated with a temporary detrimental effected on the immune system. Collectively, these findings offer novel insights into the evolutionarily conserved role of NLRP3.

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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