Researchers at Case Western Reserve University (CWRU) genetically sequenced the viral infections in 360 COVID patients. They found wide genetic variation in SARS-CoV-2 viruses, showing that all individual infections include multiple variants of the virus. Reporting about the virus usually highlights a single dominant strain, the researchers noted. This leads to under-reporting virus genetic variation and can have serious consequences in public health planning and response. “Our work brings attention to the complexity of infectious diseases that is often over-simplified when considering only the most abundant virus in an infection, and we demonstrate the importance of examining the variations that are historically considered noise,” said Ernest (Ricky) Chan. He is the director of the bioinformatics core with the Cleveland Institute for Computational Biology at the Case Western Reserve School of Medicine. “We see that genetic variants observed in low frequency in SARS-CoV-2 infections can be early indicators of new strains responsible for later transmission surges.” The paper, “COVID-19 Infection and Transmission Includes Complex Sequence Diversity,” was published on September 8, 2022, in the journal PLOS Genetics. The CWRU research team performed full genome sequencing of SARS-CoV-2 viruses from 250 patients in Northeast Ohio. They also used similar data from another 110 patients with full genetic sequences of infecting viruses provided through international research collaborators. These data were developed in the early days of the COVID-19 pandemic, at the time when the Alpha variant and then the Delta variant were of major concern. This work revealed that mutations found in Omicron BA.1 and BA.2 were already present as relatively minor variations at least a year before Omicron and its many iterations became “variants of concern.” A major COVID-19 resurgence last winter was mostly attributed to Omicron and its own variations. “Concentration on a majority consensus of virus variants within the global research community diverts attention from genetic variation that may contribute significantly to the continuing evolution of the COVID-19 pandemic,” said Peter Zimmerman. He is a professor in the Department of Pathology at the School of Medicine. “Focus on majority variants is a critical first step in development of diagnostics, therapeutics, and vaccines, however, the research community needs to quantify and report out variation, so that the public health community and the general public are better prepared and nimble in response to the ever-evolving virus.” Much effort continues to be made to define and track the emergence of virus lineages across the ongoing evolution of SARS-CoV-2 around the world. In the interest of time, global researchers have been depending on tracking and reporting on relatively dominant variations. However, given the multiple variations within single infections,the CWRU team noted that it is important to report a more complete representation of the viral genetic sequences to understand how these genetic changes can spread and potentially interact with different categories of patient conditions, including evasion from eradication efforts. Reference, “COVID-19 Infection and Transmission Includes Complex Sequence Diversity” by Ernest R. Chan, Lucas D. Jones, Marlin Linger, Jeffrey D. Kovach, Maria M. Torres-Teran, Audric Wertz, Curtis J. Donskey and Peter A. Zimmerman, 8 September 2022, in PLOS Genetics.DOI: 10.1371/journal.pgen.1010200
