Takara Bio USA, Inc. and bioSyntagma, Inc. Develop Method for Large-Scale Automated COVID-19 Testing

MOUNTAIN VIEW, Calif.–(BUSINESS WIRE)–#COVID19–Takara Bio USA, Inc. (TBUSA), a pioneering life science instrument and reagent company and wholly owned subsidiary of Takara Bio Inc., collaborated with bioSyntagma, Inc. and their partners to develop and validate a new high-throughput method for detecting SARS-CoV-2. The method employs automation technology and reagents from TBUSA to detect viral RNA via real-time PCR and will enable rapid, large-scale testing of thousands of patient samples per day.

The method uses TBUSA’s SmartChip™ real-time PCR instrument, chips, and reagents to run 5,184 reactions per chip in less than 30 minutes of direct hands-on time. Each reaction is at nanoliter scale, which reduces variability via elimination of the standard preamplification step and reduces costs via decreased reagent volume. The trusted SmartChip Real-Time PCR System is already widely used for detection of antibiotic and antimicrobial resistance around the world, and is ideally suited to address the major need for rapid and accurate SARS-CoV-2 detection.

President of TBUSA Carol Lou states, “As shelter-in-place orders are lifted, controlling the COVID-19 pandemic will depend on our ability to detect SARS-CoV-2 from a large number of samples with precision, reproducibility, and speed. To support this effort, we optimized our existing chemistries and developed SmartChip protocols that maximize the number of samples processed while minimizing costs. The work we have accomplished with bioSyntagma, plus their partners’ further development of diagnostic tests based on our work, will contribute to comprehensive and faster detection of COVID-19.”

Scottsdale-based bioSyntagma is a biotech spinoff of Arizona State University and serves as the development and validation partner of P2 Diagnostics, LLC. The new SmartChip testing method will be adopted by this and other molecular testing labs that are certified by CLIA (Clinical Laboratory Improvement Amendments) and therefore eligible to develop and perform COVID-19 diagnostic tests. “The rapid development of this novel COVID-19 detection method was made possible through a highly productive collaboration between bioSyntagma and TBUSA, and the results of this effort will soon have an impact on the ability to detect SARS-CoV-2 in nasal and saliva samples from many patients,” said David Richardson, CEO of bioSyntagma.

bioSyntagma and partners are seeking an Emergency Use Authorization (EUA) from the FDA for COVID-19 detection using the TBUSA SmartChip method. Ipsum Diagnostics, LLC and Hackensack University Medical Center—two of TBUSA’s customers in the US—have already obtained EUAs for their COVID-19 tests using Takara Bio’s one-step RT-PCR reagents.

About Takara Bio

Takara Bio USA, Inc. is a wholly owned subsidiary of Takara Bio Inc. that manufactures and distributes kits, reagents, and instruments for the life sciences, including NGS, PCR, gene delivery, genome editing, stem cell research, nucleic acid and protein purification, and automated sample preparation.

Takara Bio Inc., a world leader in biotechnology research and development, offers a host of life science research solutions, from enzymes and GMP reagents to contracted cell and gene therapy manufacturing services, and is the developer of RetroNectin® reagent, a world standard in gene therapy protocols. Takara Bio is committed to preventing disease and improving the quality of life for all people through the use of biotechnology.

About bioSyntagma

bioSyntagma, Inc. is a precision medicine company that enables advanced biomarker discovery and patient screening. Its suite of AI-enabled technologies powers comprehensive spatial, multi-omic mapping of cancer patient biopsies, so patients can be matched with relevant therapies and provided recommendations to avoid acquired drug resistance. In keeping with its mission of extending lives and giving patients more time with family, bioSyntagma responded to the global pandemic by developing high-throughput COVID-19 tests with strategic partners.

About P2 Diagnostics

P2 Diagnostics, LLC offers high-throughput testing with rapid turnaround times to meet growing needs as COVID-19 spreads around the world. Having created an EUA/FDA-validated RT-qPCR test, P2 Diagnostics provides services to local communities, municipalities, and businesses with the vision of enabling the workforce to return with confidence and reuniting distanced families.

Contacts

Lorna Neilson, PhD

VP, Corporate Development

[email protected]
650.919.7372