|
|
 |
|
Gloria Sánchez-Moragas, PhD
Institute of Agrochemistry and Food Technology - CSIC, Valencia, Spain
|
|
"Although the amount of data to analyze is huge it is exciting to try to see, even if it's not a 100 percent consensus, if we can get a consensus for which one is the best (indicator) and can it be applied by the industry."
The project focuses on irrigation water and human fecal matter, which are the main produce transmission routes for human enteric viruses.
Testing for these pathogens frequently relies on the presence of bacterial indicators. Yet they may not accurately reflect a viral presence, Sánchez-Moragas said.
"Several studies show that fecal coliforms are not good indicators for viruses because fecal coliforms are bacteria, and bacteria are less resistant than viruses," she said. "We've had situations where fecal coliforms weren't present but viruses were present and caused an outbreak."
Even within the scientific community, she says, there is not a strong consensus about whether specific bacteriophages -- viruses that infect bacteria -- are reliable indicators of human pathogenic viruses.
Standard genomic sequencing of a virus involves a complex multi-step procedure to isolate and then amplify genetic material from one organism before tests akin to molecular fingerprinting can be run. Specific equipment and trained personnel are required to perform the analysis, and these types of tests are mainly used for research.
Where Sánchez-Moragas' project differs is it uses metagenomics to try to analyze and separate all of the genetic material found in an entire irrigation water, human fecal or produce sample.
The key to metagenomics is in sample preparation, and these researchers already have developed a protocol.
"You don't culture your pathogen," she said. "You produce the sequences of all of the genomes."
From there, the researchers will try to correlate the presence of indicators or bacteriophages to the presence of human pathogenic viruses.
They will also validate the metagenomic testing method by comparing the results to those produced from real-time PCR, a type of individual genetic fingerprinting considered an industry standard.
With much of the laboratory work already completed, Sánchez-Moragas said the laborious job of analyzing the genetic sequences begins, and that's where Pérez-Cataluña will be involved.
"This is the most difficult task of the project, because once we have set the method, now what we're doing is analyzing the millions of sequences," Sánchez-Moragas said. "We need to see if we find differences between the positives and negatives and apply standard analysis to verify all of these results."
