JHU scientists have produced an innovative PCR-based assay system that rapidly provides broad bacterial detection, gram status, and species identification in a 2-4 hour time frame. This clinical assay is a vast improvement over currently used methods for diagnosis of a bacterial infection that often require days for bacterial culturing and identification. This system is based on a patented combination of probes to both common and unique regions of bacterial DNA. Sample processing and amplification methods have been optimized for efficiency and accuracy. The system has proven effective for pathogen detection in whole blood, synovial fluid and cerebrospinal fluid.
Technical Details:
An innovative technique that establishes a unique and highly specific assay, which eliminates ubiquitous background DNA in all PCR reagents (Taq polymerase, primers, dNTP's, PCR buffer, MgC12) by employing the use of a carefully selected restrivtion enzyme digest. This protocol thus allows for contamination-free universal amplification of bacterial DNA ans subsequent identification of clinically significant bacterial infections.
Looking for Partners:
There are numerous clinical scenarios where application of this invention would aid in expediting reliable and accurate diagnosis of local and systemic infections. In addition, the assay can be implemented in routine PCR applications in a basic laboratory setting The commercial applications of this technology are most obvious in the field of diagnostics and screening. This particular assay can be used towards the identification of a variety of both local and systemic infectious diseases: pneumonia, wound infections, neonatal sepsis, infective endocarditis, and many other serious infections.
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basic laboratory setting
contamination-free universal amplification
numerous clinical scenarios
systemic infectious diseases
routine pcr applications
