• Title/Summary/Keyword: Pseudomonas syringae pv. theae

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Occurrence of Brown Blight of Tea Plant Caused by Pseudomonas syringae pv. theae in Korea (Pseudomonas syringae pv. theae에 의한 차나무 갈색마름병 발생)

  • Choi, Jae-Eul;Cha, Sun-Kyung;Ryuk, Jin-Ah;Choi, Chun-Hwan;Nou, Ill-Sup
    • Research in Plant Disease
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    • v.9 no.4
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    • pp.213-216
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    • 2003
  • A bacterial disease of tea plants(Camellia sinensis L.) was found in the graftage nursery grown under vinyl house conditions in Suncheon city, Korea, in spring of 2002. The primary symptoms of the disease include small, water-soaked and dark brown spot development on the young leaves. This spot gradually increases in size, especially taking on elongate shape along the midrib or vein of the leaf, and then turns black. The diseased leaves were defoliated easily. Ten strains were isolated from the infected leaf. Inoculation on tea leaf with these isolates produced the same symptoms of naturally infected plants. On the basis of stain reactions, morphological characterization, colony pattern, physiological and biochemical reactions, the bacterium was identified as Pseudomonas syringae pv. theae. This is the first report of brown blight of tea plant in Korea.

Molecular Characteristics of Pseudomonas syringae pv. actinidiae Strains Isolated in Korea and a Multiplex PCR Assay for Haplotype Differentiation

  • Koh, Hyun Seok;Kim, Gyoung Hee;Lee, Young Sun;Koh, Young Jin;Jung, Jae Sung
    • The Plant Pathology Journal
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    • v.30 no.1
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    • pp.96-101
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    • 2014
  • The molecular features of Pseudomonas syringae pv. actinidiae strains isolated in Korea were compared with strains isolated in Japan and Italy. Sequencing of eight P. syringae pv. actinidiae and three P. syringae pv. theae strains revealed a total of 44 single nucleotide polymorphisms across 4,818 bp of the concatenated alignment of nine genes. A multiplex PCR assay was developed for the detection of P. syringae pv. actinidiae and for the specific detection of recent haplotype strains other than strains isolated since the 1980s in Korea. The primer pair, designated as TacF and TacR, specifically amplified a 545-bp fragment with the genomic DNA of new haplotype of P. syringae pv. actinidiae strains. A multiplex PCR conducted with the TacF/TacR primer pair and the universal primer pair for all P. syringae pv. actinidiae strains can be simultaneously applied for the detection of P. syringae pv. actinidiae and for the differentiation of new haplotype strains.