Rapid visual nucleic acid detection of Vibrio alginolyticus by RPA combined with CRISPR/Cas13a

preprint OA: closed
View at publisher

Abstract

Vibrio alginolyticus ( V. alginolyticus) is a common pathogen that infects humans and animals. In addition to causing serious economic losses in aquaculture, it can also infect humans. The rapid detection of nucleic acids of V. alginolyticus with high sensitivity and specificity in the field is very important for the diagnosis and treatment of infection caused by V. alginolyticus. Here, we established a simple, fast and effective molecular method for the identification of V. alginolyticus that does not rely on expensive instruments and professionals. The method integrates RPA technology with CRISPR technology in a single PCR tube. Using this method, the results can be visualized by lateral flow dipstick in less than 50 minutes. The method was confirmed to achieve high specificity for the detection of V. alginolyticus with no cross-reactivity with similar Vibrio and common clinical pathogens. This diagnostic method shows high sensitivity; the detection limit of the RPA-CRISPR/Cas13a-LFD is 10 copies μL -1. The results for 55 wild strains were consistent with TaqMan-qPCR, and it can be concluded that the methods have 100% sensitivity and 100% specificity. In conclusion, RPA-CRISPR/Cas13a offers great potential as a useful tool for reliable and rapid diagnosis of V. alginolyticus infection, especially in limited conditions.

My notes (saved in your browser only)

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

europepmc
last seen: 2026-05-19T01:45:01.086888+00:00