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February 27, 2026Frontiers in Cellular and Infection Microbiology4 citationsOpen Access

CRISPR-based diagnostics for infectious diseases: mechanisms, advancements and clinical transformation prospects

ZPZhenzhen PanLXLing XuZFZihao Fan

Key Points

  • The aim is to explore advancements in CRISPR-based diagnostic tools for detecting infectious diseases.
  • Review of CRISPR technologies
  • Analysis of specific applications like SHERLOCK and DETECTR
  • Evaluation of sensitivity, specificity, and operational simplicity
  • Assessment of barriers to implementation
  • CRISPR diagnostics offer ultra-sensitive detection of pathogens
  • Methods are rapid and field-deployable
  • Higher specificity compared to traditional methods
  • Potential challenges include cost and accessibility

Abstract

Infectious diseases continue to pose significant global public health challenges, necessitating the development of rapid, sensitive, specific, and field-deployable diagnostic platforms. The discovery of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) and CRISPR-associated proteins (Cas) has revolutionized genome editing and concurrently enabled a new generation of molecular diagnostic tools. Leveraging the inherent trans-cleavage activities of Cas enzymes, platforms such as SHERLOCK (Specific High-sensitivity Enzymatic Reporter unLOCKing) and DETECTR (DNA Endonuclease-Targeted CRISPR Trans Reporter) have emerged, combining target recognition precision with reporter systems to achieve ultra-sensitive detection of pathogen-specific nucleic acids. This review systematically examines the mechanistic foundations of CRISPR diagnostics, synthesizes recent advancements in infectious disease applications, evaluates their advantages in sensitivity, specificity, operational simplicity, and multiplexing capacity, and critically analyzes current implementation barriers and future translational pathways.

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Cite This Study

Pan et al. (2026) studied this question.

synapsesocial.com/papers/69a134b8ed1d949a99abe2cfhttps://doi.org/10.3389/fcimb.2026.1769226
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