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Complete genome sequence of a distinct calla lily chlorotic spot virus isolated in mainland China

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Abstract

The first complete genome sequence of calla lily chlorotic spot virus (CCSV) from Lijiang in northwestern Yunnan Province was obtained using RT-PCR with designed primers. The genome of CCSV isolate LJ-1-Yunnan is tripartite. The small (S) RNA is 3182 nucleotides (nt) in length and encodes a nonstructural protein (NSs, 1383 nt) and a nuclear nucleocapsid (N, 834 nt), separated by an 836-nt intergenic region (IGR). The medium (M) RNA is 4749 nt in length and encodes a nonstructural movement protein (NSm, 930 nt) and a glycoprotein (GnGc, 3,372 nt), also separated by a 349-nt IGR. The large (L) RNA is 8912 nt in length and encodes a predicted RNA-dependent RNA polymerase (RdRp, 8652 nt). The nucleotide sequences of the three viral RNA segments are 92-94 % identical to the published CCSV genome sequence, and the amino acid sequences of the encoded proteins are 96-98 % identical. However, the IGRs of the S and M RNAs are less similar, with 86 and 72 % identity, respectively. Genome sequence comparisons and phylogenetic analysis indicate that the Lijiang CCSV isolate is a unique tospovirus isolate that differs from CCSV isolates in other geographic regions.

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Acknowledgments

This work was supported in part by grants from the National Science Foundation of China (Grant No. 31260451, 31471828, 30960224), Key New Product Development Projects in Yunnan Province (2014BB005), Reserve Personnel Fund for Young and Middle-Aged Academic Technical Leaders of Yunnan Province (2013HB071), and Academic Award for Up-and-Coming Doctoral Candidate of Yunnan Province.

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Correspondence to Ya-ting Liu.

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Y. Xu and S. Wang contributed equally to this work.

The nucleotide sequence data reported in this manuscript have been deposited at the NCBI under accession numbers (KT004452, KT004453, and KT004454).

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Xu, Y., Wang, Sb., Li, Yz. et al. Complete genome sequence of a distinct calla lily chlorotic spot virus isolated in mainland China. Arch Virol 161, 219–222 (2016). https://doi.org/10.1007/s00705-015-2630-9

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  • DOI: https://doi.org/10.1007/s00705-015-2630-9

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