AUTHOR=Jeon Min-Young , Han Jee Eun , Lee Dong Gwang , Cho Young-Lai , Jang Ju-Hong , Lee Jangwook , Park Jong-Gil , Kwon Do Hyung , Park Seon Young , Kim Wantae , Lee Kyunglee , Kim Ji Hyung , Lee Nam-Kyung 

TITLE=Novel sandwich immunoassay detects a shrimp AHPND-causing binary PirABVp toxin produced by Vibrio parahaemolyticus

JOURNAL=Frontiers in Cellular and Infection Microbiology

VOLUME=Volume 13 - 2023

YEAR=2023

URL=https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2023.1294801

DOI=10.3389/fcimb.2023.1294801

ISSN=2235-2988

ABSTRACT=The binary PirA/PirB toxin expressed by Vibrio parahaemolyticus (PirAB Vp ) is a virulent complex that causes acute hepatopancreatic necrosis disease (AHPND) in shrimps, affecting 2 This is a provisional file, not the final typeset article the global shrimp farming industry. AHPND is currently diagnosed by detecting pirA and pirB genes by PCR; however, several V. parahaemolyticus strains do not produce the two toxins as proteins. Thus, an immunoassay using antibodies may be the most effective tool for detecting toxin molecules. In this study, we report a sandwich ELISA-based immunoassay for the detection of PirAB Vp . Methods: We utilized a single-chain variable fragment (scFv) antibody library to select scFvs against the PirA or PirB subunits. Phage display panning rounds were conducted to screen and identify scFv antibodies directed against each recombinant toxin subunit. Selected scFvs were converted into IgGs to develop a sandwich immunoassay to detect recombinant and bacterial PirAB Vp . Results: Antibodies produced as IgG forms showed sub-nanomolar to nanomolar affinities (KD), and; a pair of anti-PirA antibody as a capture and anti-PirB antibody as a detector showed a limit of detection of 201.7 ng/mL for recombinant PirAB Vp . The developed immunoassay detected PirAB Vp in the protein lysates of AHPND-causing V. parahaemolyticus (Vp AHPND ) and showed a significant detectability in moribund or dead shrimp infected with a Vp AHPND virulent strain compared to that in non-infected shrimp. Discussion: These results indicate that the developed immunoassay is a reliable method for diagnosing AHPND by detecting PirAB Vp at the protein level, and could be further utilized to accurately determine the virulence of already presentextant or newly identified Vp AHPND in the global shrimp culture industry.