Key result
Contemporary EV-D68 isolates exhibited decreased sensitivity to acid and temperature compared with an earlier isolate, and induced a robust type III interferon response in respiratory but not intestinal epithelium.
Why the study?
EV-D68 is linked to severe respiratory illness and acute flaccid myelitis and is detected in respiratory and stool samples, suggesting both respiratory and enteric transmission routes.
Contemporary EV-D68 isolates demonstrate altered environmental sensitivities and elicit tissue-specific innate immune responses, suggesting potential for both respiratory and enteric transmission.
Respiratory epithelium restricts contemporary EV-D68 via type III IFN while intestinal does not; leaves open isolate-specific transmission and AFM links for further study.
Enterovirus D68 (EV-D68) has been implicated in outbreaks of severe respiratory illness and acute flaccid myelitis (AFM) and is detected in patient respiratory samples and from stool and wastewater, suggesting both respiratory and enteric routes of transmission. Here, we used a panel of EV-D68 isolates, including a historical isolate and multiple contemporary isolates from AFM outbreak years, to define the dynamics of viral replication and the host response to infection in primary human airway cells and stem cell-derived enteroids. We show that some recent EV-D68 isolates have decreased sensitivity to acid and temperature compared with an earlier isolate and that the respiratory, but not intestinal, epithelium induces a robust type III interferon (IFN) response that restricts infection. Our findings define the differential responses of the respiratory and intestinal epithelium to contemporary EV-D68 isolates and suggest that some isolates have the potential to target both the human airway and gastrointestinal tracts.
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Freeman et al. (2021) studied Enterovirus D68 (EV-D68) infection. Contemporary EV-D68 isolates vs. Historical EV-D68 isolate was evaluated on Viral replication and host response (type III interferon response, sensitivity to acid and temperature). Contemporary EV-D68 isolates exhibited decreased sensitivity to acid and temperature compared with an earlier isolate, and induced a robust type III interferon response in respiratory but not intestinal epithelium.
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