One‐Pot <scp>RAA</scp> ‐ <scp>CRISPR</scp> /Cas12a Assay for Rapid Detection of Infectious Hypodermal and Haematopoietic Necrosis Virus ( <scp>IHHNV</scp> ) in Shrimp Aquaculture

The infectious hypodermal and haematopoietic necrosis virus (IHHNV) represents a significant viral threat to global shrimp aquaculture, leading to considerable economic losses. In this study, we have developed a one-step, one-pot isothermal assay for the detection of IHHNV, employing recombinase-aided amplification in conjunction with clustered regularly interspaced short palindromic repeats-Cas12a (RAA-CRISPR/Cas12a). The assay is performed at a constant temperature of 37°C, achieving a detection limit of 10 copies per reaction for the fluorescence assay and 1 copy per reaction for the lateral flow dipstick (LFD) assay within a 60-min timeframe. Additionally, we evaluated the assay against four other prevalent shrimp pathogens (WSSV, DIV1, EHP, VpAHPND) and observed no cross-reactivity. This straightforward detection method exhibits high sensitivity and specificity for IHHNV, offering a promising approach for early and rapid field diagnosis.

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Publication Details

Journal
Journal of Fish Diseases
Published
2026-04-30
DOI
https://doi.org/10.1111/jfd.70196
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
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article

One‐Pot RAA ‐ CRISPR /Cas12a Assay for Rapid Detection of Infectious Hypodermal and Haematopoietic Necrosis Virus ( IHHNV ) in Shrimp Aquaculture

Zheng Sun, Yichen Zhao, Ying Zhan, Zewei Hou et al.
Journal of Fish Diseases
CRISPR and Genetic Engineering
article

One‐Pot RAA ‐ CRISPR /Cas12a Assay for Rapid Detection of Infectious Hypodermal and Haematopoietic Necrosis Virus ( IHHNV ) in Shrimp Aquaculture

Zheng Sun, Yichen Zhao, Ying Zhan, Zewei Hou, Hao Wang, Xilin Dai
article en

Abstract

The infectious hypodermal and haematopoietic necrosis virus (IHHNV) represents a significant viral threat to global shrimp aquaculture, leading to considerable economic losses. In this study, we have developed a one-step, one-pot isothermal assay for the detection of IHHNV, employing recombinase-aided amplification in conjunction with clustered regularly interspaced short palindromic repeats-Cas12a (RAA-CRISPR/Cas12a). The assay is performed at a constant temperature of 37°C, achieving a detection limit of 10 copies per reaction for the fluorescence assay and 1 copy per reaction for the lateral flow dipstick (LFD) assay within a 60-min timeframe. Additionally, we evaluated the assay against four other prevalent shrimp pathogens (WSSV, DIV1, EHP, VpAHPND) and observed no cross-reactivity. This straightforward detection method exhibits high sensitivity and specificity for IHHNV, offering a promising approach for early and rapid field diagnosis.

Journal of Fish Diseases
Shanghai Ocean University (CN)
Openalex Percentile: Top 12%
CRISPR and Genetic Engineering
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