Lab Matters Fall 2019 | Page 26

FROM THE BENCH A Small Lab Makes a Big Push Towards Whole- Genome Sequencing for Foodborne Pathogens By Jill Sakai, writer As the US Centers for Disease Control and Prevention (CDC) and PulseNet move to establish whole-genome sequencing (WGS) rather than pulsed- field gel electrophoresis (PFGE) as the gold standard for foodborne disease surveillance and identification efforts, public health laboratories must adapt to changing technology, workflows, analysis and reporting methods. WGS offers superior precision and specificity for bacterial identification and molecular characterization, as well as the opportunity to consolidate workflows for serotyping, antibiotic resistance, virulence factors and more, said Kristy Kubota, MPH, PulseNet manager for APHL. The change also reflects advances in the diagnostics industry. “We’re seeing a shift in how clinical laboratories are testing patients for foodborne diseases such as E. coli and Salmonella, and they’re using molecular methods that do not yield isolates,” Kubota said. “As the clinical diagnostics industry moves away from isolates toward genomics, we need to change our surveillance so that we can be prepared for an era when there are no more isolates. One way to do that is to develop genomics-based testing on the public health side.” Technological and scientific advances are driving sequencing costs down, making WGS more feasible to implement on a public health level. However, the shift can still be a challenge, especially for labs with constrained resources or limited expertise in advanced sequencing methods and analysis. Even in the face of such barriers, the Maine State Health and Environmental Testing Laboratory has shown in the past three years how a smaller public health lab can successfully adopt WGS for surveillance and outbreak detection. 24 LAB MATTERS Fall 2019 E. coli Charting a New Course CDC’s push to eliminate PFGE started the conversation in Maine about moving to WGS. “We were kind of reluctant at the beginning to bring it on,” said Nicholas Matluk, MS, MB, (ASCP)CM the lab’s Clinical Laboratory Improvement Amendments (CLIA) microbiology supervisor and technical supervisor. “It is a very expensive technique compared to PFGE, and Maine is a low-incidence state for everything, including all the foodborne diseases.” Then he attended the 2016 American Society for Microbiology meeting in Boston, MA, where several WGS seminars and trainings showed him the platform’s potential to streamline multiple tests and workflows. “I saw that if we could use this for more than just foodborne pathogens, we would get bigger bang for our buck and make it cheaper down the line,” Matluk said. That approach can be especially important to lower the barrier for laboratories with fewer resources to draw on, said Joel Sevinsky, PhD, a consultant in public health bioinformatics. “The real promise of WGS is in the expansion of these technologies into other organisms and other programs. That’s where we’re really going to see cost and turnaround times going down. But it’s been difficult,” he said. “One of the real challenges is getting labs to adopt these technologies for more than just what’s required.” That’s one reason Maine’s efforts stand out. “Maine has transitioned a lot of their traditional testing to WGS testing. They validated it, they’re reporting results, they’re even thinking about moving in the direction of metagenomics,” said Sevinsky. “They ended up accomplishing this transition out of necessity. They were a small lab, trying to reduce costs and trying to get more for less. And they saw WGS as a way of doing that.” PublicHealthLabs @APHL APHL.org