A single strain of mumps virus has dominated the US since 2006, and is responsible for many of the large numbers of cases seen across the country in the widespread 2016-17 outbreaks. In a paper publishing February 11 in the open-access journal PLOS Biology, Pardis Sabeti from the Broad Institute of MIT and Harvard and colleagues analyze over 200 whole mumps virus genomes from patient swab samples, providing insights not obtained in standard public health surveillance efforts.
An unusually high number of mumps cases were reported in the US in 2016 and 2017, despite high rates of vaccination. The recent resurgence is partly explained by reduced vaccine-induced immunity but it was unclear how much genetic changes in the circulating viruses might be contributing to this.
The researchers sequenced whole mumps virus genomes from 203 patients, mostly from Massachusetts during 2016/17, but including 43 from other states collected between 2014 and 2017. Combining the whole genome sequences with epidemiological data, their analysis demonstrates the extent to which the disease is circulating in the United States, connects outbreaks previously thought to be unrelated, and traces transmission between communities.
The research indicates the value of high-quality genomic data in public health surveillance of mumps and suggests future efforts should incorporate whole genome sequencing. Pardis Sabeti says: "Understanding sequence data for pathogens like mumps virus can help understanding of the spread of infectious diseases more quickly and allow researchers to detect changes in the genome that could affect disease severity or the effectiveness of vaccines and diagnosis."
Peer-reviewed; Experimental study; Cells
In your coverage please use this URL to provide access to the freely available article in PLOS Biology: https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3000611
Citation: Wohl S, Metsky HC, Schaffner SF, Piantadosi A, Burns M, Lewnard JA, et al. (2020) Combining genomics and epidemiology to track mumps virus transmission in the United States. PLoS Biol 18(2): e3000611. https://doi.org/10.1371/journal.pbio.3000611
Funding: Funding was provided by: NIH NIAID U19AI110818 (Broad Institute); NIH NIAID U54GM088558 (J.A.L.); Howard Hughes Medical Institute (P.C.S.); Harvard University Burke Global Health Fellowship (P.C.S.); Amazon Web Services Cloud Credits for Research (P.C.S.). The project described was supported by award number T32GM007753 from the National Institute of General Medical Sciences (E.H.B.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing Interests: The authors have declared that no competing interests exist.