New Delhi, March 16 A team of researchers has developed a new gene-based technology that offers rapid, highly sensitive detection of multi-drug-resistant bacteria and other pathogens at low concentrations.
This research was featured in an article in the Proceedings of the National Academy of Sciences of the United States of America (PNAS).
Researchers designed a CRISPR-based test that rapidly detects low levels of pathogen genetic material in blood. This is done without the need for nucleic acid amplification.
Bioengineering professor Rashid Bashir from University of Illinois Grainger College of Engineering, led a team of researchers for the project.
In CRISPR/Cas-based diagnostic tests, guide RNAs bind pathogen DNA or RNA, triggering Cas enzymes to become active and cleave the reporter nucleic acids that fluoresce when cleaved. However, the single CRISPR-based technique does not detect pathogens at low levels without a pre-amplification step.
Bashir’s team created a CRISPR-based diagnostic test that bypasses that amplification step by combining two CRISPR/Cas units in a complex called CRISPR-Cascade.
One unit contains a guide RNA specific for a pathogen nucleic acid of choice and a Cas protein. When the Cas cleaves specially engineered nucleic acids that are added to the system, parts of the nucleic acids are free to bind and activate a second CRISPR/Cas, triggering a positive feedback loop that results in a high signal-to-noise ratio.
The test demonstrated unprecedented sensitivity. It also detected multi-drug-resistant Staphylococcus aureus DNA without prior amplification at concentrations that were orders of magnitude lower than the limit of a test using a single Cas.
The test provided a simple “yes/no” result for the presence of any one pathogen in samples spiked with four common bloodstream pathogens.
The researchers said these results could be used toward developing highly sensitive CRISPR-based diagnostic tests that can detect pathogens in minutes without nucleic acid amplification.
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