Hannah C. Howson-Wells
Enterovirus D68 epidemic, UK, 2018, was caused by subclades B3 and D1, predominantly in children and adults, respectively, with both subclades exhibiting extensive genetic diversity
Howson-Wells, Hannah C.; Tsoleridis, Theocharis; Zainuddin, Izzah; Tarr, Alexander W.; Irving, William L.; Ball, Jonathan K.; Berry, Louise; Clark, Gemma; McClure, C. Patrick
Authors
Theocharis Tsoleridis
Izzah Zainuddin
Dr ALEXANDER TARR alex.tarr@nottingham.ac.uk
ASSOCIATE PROFESSOR
William L. Irving
Jonathan K. Ball
Louise Berry
Gemma Clark
Dr PATRICK MCCLURE PATRICK.MCCLURE@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR
Abstract
Enterovirus D68 (EV-D68) has recently been identified in biennial epidemics coinciding with diagnoses of non-polio acute flaccid paralysis/myelitis (AFP/AFM). We investigated the prevalence, genetic relatedness and associated clinical features of EV-D68 in 193 EV-positive samples from 193 patients in late 2018, UK. EV-D68 was detected in 83 (58%) of 143 confirmed EV-positive samples. Sequencing and phylogenetic analysis revealed extensive genetic diversity, split between subclades B3 (n=50) and D1 (n=33), suggesting epidemiologically unrelated infections. B3 predominated in children and younger adults, and D1 in older adults and the elderly (P=0.0009). Clinical presentation indicated causation or exacerbation of respiratory distress in 91.4% of EV-D68-positive individuals, principally cough (75.3%), shortness of breath (56.8%), coryza (48.1%), wheeze (46.9%), supplemental oxygen required (46.9%) and fever (38.9%). Two cases of AFM were observed, one with EV-D68 detectable in the cerebrospinal fluid, but otherwise neurological symptoms were rarely reported (n=4). Both AFM cases and all additional instances of intensive care unit (ICU) admission (n=5) were seen in patients infected with EV-D68 subclade B3. However, due to the infrequency of severe infection in our cohort, statistical significance could not be assessed.
Citation
Howson-Wells, H. C., Tsoleridis, T., Zainuddin, I., Tarr, A. W., Irving, W. L., Ball, J. K., Berry, L., Clark, G., & McClure, C. P. (2022). Enterovirus D68 epidemic, UK, 2018, was caused by subclades B3 and D1, predominantly in children and adults, respectively, with both subclades exhibiting extensive genetic diversity. Microbial Genomics, 8(5), https://doi.org/10.1099/mgen.0.000825
Journal Article Type | Article |
---|---|
Acceptance Date | Apr 13, 2022 |
Online Publication Date | May 9, 2022 |
Publication Date | May 9, 2022 |
Deposit Date | Nov 9, 2022 |
Publicly Available Date | Nov 9, 2022 |
Journal | Microbial Genomics |
Electronic ISSN | 2057-5858 |
Publisher | Microbiology Society |
Peer Reviewed | Peer Reviewed |
Volume | 8 |
Issue | 5 |
DOI | https://doi.org/10.1099/mgen.0.000825 |
Keywords | General Medicine |
Public URL | https://nottingham-repository.worktribe.com/output/8049344 |
Publisher URL | https://www.microbiologyresearch.org/content/journal/mgen/10.1099/mgen.0.000825 |
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Enterovirus D68 epidemic, UK, 2018, was caused by subclades B3 and D1, predominantly in children and adults, respectively, with both subclades exhibiting extensive genetic diversity
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