Author
SU, C - Taiwan Agricultural Chemicals And Toxic Substances Research Institute | |
DENG, W - National Chung-Hsing University | |
JAN, F - National Chung-Hsing University | |
CHANG, C - University Of Georgia | |
HUANG, H - University Of South Florida | |
Chen, Jianchi |
Submitted to: American Phytopathological Society Abstracts
Publication Type: Abstract Only Publication Acceptance Date: 5/9/2014 Publication Date: 11/1/2014 Citation: Su, C.C., Deng, W.L., Jan, F.L., Chang, C.J., Huang, H., Chen, J. 2014. Characterization of Xylella fastidiosa pear leaf scorch strain in Taiwan through whole genome sequence analyses. American Phytopathological Society Abstracts. 104(S3):115. Interpretive Summary: Technical Abstract: Xylella fastidiosa is a Gram-negative bacterium causing diseases in many economically important crops mostly in the Americas but also in Asia and Europe. A strain of X. fastidiosa was found to cause pear leaf scorch (PLS) disease in Taiwan in 1992. Because of nutritional fastidiousness, characterization of X. fastidiosa through traditional cultivation-based methodologies yielded limited information. Whole genome sequencing is a powerful tool to generate biological information for fastidious prokaryotes. In this whole genome sequencing project, a PLS strain (PLS229) was isolated from a symptomatic pear tree of cultivar Hengshan (Pyrus pyrifolia) at Houli (24°20’14”N, 120°44’11”E), Taiwan. PLS229 was triple-cloned and cultured in PD2 medium at 28°C for 5-6 days. Total genomic DNA was extracted and sequenced using the 454 GS-FLX system. The PLS229 bacterium has a genome size of 2,733,013 bp with a G+C content of 53.1%. The PLS229 genome was annotated to have 3,259 open reading frames and 50 RNA genes. The whole genome sequence of PLS229 shared 99% similarity to X. fastidiosa subsp. fastidiosa (Temecula1 and M23), subsp. multiplex (M12) and subsp. pauca (9a5c) at the rrs (16S ribosomal RNA gene) locus. In contrast, strain PLS229 was more distantly related (88-89% nucleotide sequence similarity) to all three subspecies at loci gyrB, dnaK, and rpoD, suggesting a possible new subspecies. |