Demonstrates rapid detection of tilapia lake virus using novel DNA aptamers, suggesting new diagnostic tools for aquatic diseases.
cells/mL within 5 min at temperatures ranging from 4°C to 28°C. The detection capability of LH-2 for TiLV infection was consistent with that of RT-qPCR, as validated in vivo. These results demonstrate that LH-2 possesses significant potential to be developed as a core recognition component for on-site rapid detection kits. This study provides critical molecular tools and a theoretical foundation for the rapid diagnosis of TiLV and the development of novel targeted prevention and control strategies. It strongly advances the practical application of aptamer technology in the precise prevention and control of aquatic diseases.
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Liu et al. (2026) studied this question.
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