Serine protease inhibitor 3 (Serpin3) from Penaeus vannamei selectively interacts with Vibrio parahaemolyticus PirA vp .

Autor: Le TN; Laboratory of Biosensors, Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Laboratory of Molecular Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Vietnam National University, Ho Chi Minh, Vietnam., Dinh TT; Laboratory of Biosensors, Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Laboratory of Molecular Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Vietnam National University, Ho Chi Minh, Vietnam., Mai-Hoang TD; Laboratory of Biosensors, Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Laboratory of Molecular Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Vietnam National University, Ho Chi Minh, Vietnam., Razzazi-Fazeli E; VetCore Facility for Research, Proteomics Facility, Veterinary Medicine University, Vienna, Austria., Tran-Van H; Laboratory of Biosensors, Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Laboratory of Molecular Biotechnology, University of Science, Ho Chi Minh, Vietnam.; Vietnam National University, Ho Chi Minh, Vietnam.
Jazyk: angličtina
Zdroj: Journal of fish diseases [J Fish Dis] 2025 Jan; Vol. 48 (1), pp. e13935. Date of Electronic Publication: 2024 Feb 25.
DOI: 10.1111/jfd.13935
Abstrakt: Acute Hepatopancreatic Necrosis Disease (AHPND) represents a significant challenge in the field of shrimp aquaculture. This disease is primarily caused by Vibrio parahaemolyticus strains harbouring the pVA1 plasmid encoding the PirA vp and PirB vp toxins. To combat this epidemic and mitigate its devastating consequences, it is crucial to identify and characterize the receptors responsible for the binding of these pathogenic toxins. Our studied discovered that Penaeus vannamei's Serine protease inhibitor 3 (PvSerpin3) derived from shrimp hepatopancreatic tissues could bind to recombinant PirA vp , confirming its role as a novel PirA vp -binding protein (P A BP). Through comprehensive computational methods, we revealed two truncated PirA vp -binding proteins derived from PvSerpin3 called Serpin3(13) and Serpin3(22), which had higher affinity to PirA vp than the full-length PvSerpin3. The P A BP genes were amplified from a cDNA library that was reversed from total RNA extracted from shrimp, cloned and expressed in Escherichia coli. Three P A BP inclusion bodies were refolded to obtain the soluble form, and the recovery efficacy was found to be 100% for Serpin3 and Serpin3(13), while Serpin3(22) had a recovery efficacy of roundly 50%. Co-Immunoprecipitation (co-IP) and dot blot assays substantiated the interaction of these recombinant P A BPs with both recombinant PirA vp and VP AHPND (XN89)-producing natural toxins.
(© 2024 John Wiley & Sons Ltd.)
Databáze: MEDLINE
Externí odkaz: