Genomic sequencing had a huge impact on the global response to COVID-19, and the technology has improved as more researchers put it to use. To better respond to the next pandemic, scientists need to build on that knowledge while also recognizing the gaps in our capabilities that remain, according to an essay, “Towards a post-pandemic future for global pathogen genome sequencing” published in PLOS Biology.
“The COVID-19 pandemic in many ways represented the culmination of sequencing and analysis that had been building for years,” said Jason Sahl, PhD, associate professor in the department of biological sciences at Northern Arizona University. “We wanted to highlight that although interest in the pandemic has waned, other threats still exist, and maintaining our momentum while also building new infrastructure will be vital for improving public health responses to existing and emerging threats.”
Sahl and fellow associate professor Jason Ladner, PhD, along with colleagues at the Pathogen & Microbiome Institute, are working on applying and analyzing innovative genomic technology in the study of pathogens, and have studied various infectious agents, including Ebola, Zika, Yersinia pestis (which causes plague), anthrax, and Burkholderia pseudomallei (which causes melioidosis, an infectious bacterial disease).
In their essay, they focus on the history of pathogens and genomic sequencing to help readers understand that the patterns we see now aren’t new. In the 1960s, scientists thought they had infectious disease resolved with the development of vaccines, antibiotics, personal hygiene, sanitation norms, and more.
“What we did not fully appreciate at the time, however, was the incredible diversity of human pathogens, their capacity for rapid evolution, and the dynamic nature of interactions between pathogens and their hosts,” Ladner and Sahl write. “Combined, these factors have substantially complicated our attempts to mitigate the impacts of infectious disease.”
Sixty years later, pathogens remain complicated. The biologists provide a roadmap for various stakeholders in preparation for the next pandemic: highlighting deficits in research for scientists to address; pointing out the critical need for collaboration and investment for policymakers; and explaining the history of pathogen genomic sequencing to public health officials, media, philanthropists, and others so they can understand the full potential of pathogen sequencing for public health.
“We wrote this essay to contribute to the broader discussion of how pathogen genome sequencing should be used in the future to improve public health and what types of investments and innovations we need to facilitate this,” noted Ladner. “This is no longer a niche topic, but one with broad appeal for scientists in multiple different fields, officials setting health care policy, and media who are working to understand recent advances and communicate them to the general public.”
