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. 2015 Oct 6;12:160. doi: 10.1186/s12985-015-0387-0

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© Kim et al. 2015

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — γ-PGA protects mice after a lethal dose of influenza A virus. C57BL/6 mice (n = 10 per group) were intranasally inoculated with 1 MLD₅₀ of either (a) PR8 or (b) CA04 viruses. Mice were given either intranasal CpG-ODN 24 h prior to virus infection or intranasal γ-PGA 24 h post- inoculation (hpi). Body weight and survival were monitored daily for 14 days