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. 2019 Jan 2;19(1):1. doi: 10.1093/jisesa/iey124

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Published by Oxford University Press on behalf of Entomological Society of America 2019. This work is written by (a) US Government employee(s) and is in the public domain in the US.

This Open Access article contains public sector information licensed under the Open Government Licence v2.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/2/).

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Fig. 1. — Single-nucleotide polymorphisms (SNPs) in selected segments of genes encoding 16S rRNA (A) and SecY (B). Sequences derived from sucrose sample TM1216 were compared with sequences of NAGY phytoplasma sequevars NAGYIIIα and NAGYIIIβ, ‘Candidatus Phytoplasma pruni’ strain PX11CT1 and NAGY-infected plant samples (Riesling and Chardonnay in A and B, respectively). Nucleotides that differ from those of samples TM1216 are shaded black, whereas unchanged nucleotides are shaded gray. (A) Alignment of the 16S rDNA genomic region. Numbers on top indicate base positions of SNPs with reference to ‘Ca. Phytoplasma pruni’ strain PX11CT1, GenBank JQ044393 (16S rRNA; bases 242, 790, 1,003, and 1,093). MseI recognition site is underlined. (B) Alignment of the secY gene genomic region. Numbers on top indicate base positions of SNPs with reference to ‘Ca. Phytoplasma pruni’ strain PX11CT1, GenBank JQ268254 (secY bases 308, 316, and 318). Start codon is underlined.