Inexpensive optical device proves able to detect and distinguish H1N1 from other flu viruses
MAY 6, 2009--Together with the CDC, InDevR (Boulder, CO) has confirmed that its FluChip product can detect swine-origin H1N1 influenza A viruses, and distinguish them from seasonal flu and avian viruses. Less susceptible to failure than qRT-PCR assays, it will hold up as the virus evolves. InDevR will now manufacture FluChip Kits for State Public Health labs, and will combine FluChip with another technology to make the assay inexpensive and easy to use in any lab with basic PCR capabilities.
MAY 6, 2009--Together with the Influenza Division of the Centers for Disease Control and Prevention (CDC) in Atlanta, the biotech startup InDevR (Boulder, CO) has confirmed that the M gene version of InDevR's FluChip product can detect swine-origin H1N1 influenza A viruses, and clearly distinguish them from seasonal influenza viruses (A/H1N1 and A/H3N2) as well as the deadly avian A/H5N1 virus.
The CDC provided InDevR scientists with non-infectious genetic material from swine-origin influenza viruses earlier this week. The FluChip performance was evaluated with several of these samples in a side-by-side comparison with seasonal human influenza viruses. "The FluChip assay detected all of the 6 swine-origin H1N1 viruses tested, and the resulting pattern, or signature, on the microarray was dramatically different than the signature for seasonal A/H1N1 and A/H3N2 viruses. Interestingly, the signature of the swine H1N1 virus indicated an avian component within the M-gene, which is consistent with its reported Eurasian lineage, said Dr. Erica Dawson, the Lead Scientist on the project at InDevR and co-inventor of the FluChip technology.
The FluChip is expected to be a powerful addition to the influenza surveillance toolkit since it will be less susceptible to failure than qRT-PCR assays as the virus continues to evolve. According to Rowlen, who is now CEO at InDevR, the reason that the M-gene version of the FluChip is more robust has to do with the fact that the diagnostic target is a stable, internal gene which codes for the virus' matrix proteins. Current qRT-PCR subtyping assays target a more highly mutable gene that codes for a protein, hemagglutinin (HA), which is subject to antigenic drift. "As has happened in the past, if the HA gene changes in a critical region, qRT-PCR will fail and the researcher won't know why until the gene is re-sequenced," said Rowlen.
Based on these early FluChip results and with support from the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH), InDevR will immediately begin manufacturing FluChip Kits for placement in a limited number of State Public Health labs. The Colorado Department of Public Health and Environment (CDPHE) will be the first site to receive FluChip assays for use as a complement to the newly released swine qRT-PCR assay. "We are excited about helping to evaluate the FluChip technology. The ability to rapidly and reliably determine whether or not an influenza virus is seasonal or extraordinary would be tremendous," said Dr. Hugh Maguire, Program Manager of Microbiology and Molecular Science at the CDPHE.
InDevR will combine the FluChip technology with an innovative detection technology (NESA), which InDevR also licensed from the University of Colorado and further developed with NIAID support, to make the FluChip assay inexpensive and easy to use in any lab that has basic PCR capabilities.
Representative results results from the study proving FluChip's H1N1 capabilities are available on InDevR's website.