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. 2018 Apr 17;10(4):201. doi: 10.3390/v10040201

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© 2018 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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PGG inhibits RABV adsorption and entry. For viral adsorption or entry assay, BHK-21 cells were treated with PGG for 1 h. (a) The vira1 P gene mRNA expression level was detected by qRT-PCR; (b) The virus titers of culture supernatants were determined by TCID₅₀ assay and plotted; (c) The expression level of viral P protein was analyzed by Western blotting; (d) The relative expression levels of viral P, normalizing to that of α-tubulin. (** p < 0.01).

PGG inhibits RABV adsorption and entry. For viral adsorption or entry assay, BHK-21 cells were treated with PGG for 1 h. (a) The vira1 P gene mRNA expression level was detected by qRT-PCR; (b) The virus titers of culture supernatants were determined by TCID₅₀ assay and plotted; (c) The expression level of viral P protein was analyzed by Western blotting; (d) The relative expression levels of viral P, normalizing to that of α-tubulin. (** p < 0.01).