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. 2015 Jan 7;60(6):881–888. doi: 10.1093/cid/ciu940

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© The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.

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Figure 1. — Phylogenetic relationship of human astrovirus (HAstV)–VA1/HMO-C-UK1(a) () and -UK1(b) () to other astroviruses (AstVs) based on RNA-dependent RNA polymerase nucleotide sequences. indicates other AstV species that have been reported in patients with neurological disease. indicates sequences of animal origin, not human. Scale bar represents the number of base substitutions per site. Abbreviations: BAstV, bat astrovirus; MAstV, mink astrovirus; OAstV, ovine astrovirus; TAstV, turkey astrovirus.

Inline graphic — Phylogenetic relationship of human astrovirus (HAstV)–VA1/HMO-C-UK1(a) () and -UK1(b) () to other astroviruses (AstVs) based on RNA-dependent RNA polymerase nucleotide sequences. indicates other AstV species that have been reported in patients with neurological disease. indicates sequences of animal origin, not human. Scale bar represents the number of base substitutions per site. Abbreviations: BAstV, bat astrovirus; MAstV, mink astrovirus; OAstV, ovine astrovirus; TAstV, turkey astrovirus.

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