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. 2017 Jan 19;140:76–82. doi: 10.1016/j.antiviral.2017.01.012

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© 2017 Elsevier B.V. All rights reserved.

Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

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Fig. 4 — rpIFN-L1 displayed more efficiency to inhibit PEDV in IPEC-J2 cells than IFN-α. IPEC-J2 were treated with rpIFN-L1 or porcine IFN-a at indicated concentrations for 24 h in 24-well plates and then were infected with PEDV (CV777). PEDV infection was quantified by measuring RNA with RT-qPCR. The results are presented as the mean ± SEM (N = 3–4).