• 제목/요약/키워드: Pseudomonas syringae pv. syringae

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CaWRKY2, a Chili Pepper Transcription Factor, Is Rapidly Induced by Incompatible Plant Pathogens

  • Oh, Sang-Keun;Yi, So Young;Yu, Seung Hun;Moon, Jae Sun;Park, Jeong Mee;Choi, Doil
    • Molecules and Cells
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    • 제22권1호
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    • pp.58-64
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    • 2006
  • WRKY family proteins are a class of plant-specific transcription factors involved in stress response signaling pathways. In this study a gene encoding a putative WRKY protein was isolated from a pepper EST database (http://genepool.kribb.re.kr). The cDNA, named Capsicum annuum WRKY2 (CaWRKY2), encodes a putative polypeptide of 548 amino acids, containing two WRKY domains with zinc finger motifs and two potential nuclear localization signals. Northern blot analyses showed that CaWRKY2 mRNA was preferentially induced during incompatible interactions of pepper plants with PMMoV, Pseudomonas syringae pv. syringae 61, and Xanthomonas axonopodis pv. vesicatoria race 3. Furthermore, CaWRKY2 transcripts were strongly induced by wounding and ethephon treatment, whereas only moderate expression was detected following treatment with salicylic acid and jasmonic acid. CaWRKY2 was translocated to the nucleus when a CaWRKY2-smGFP fusion construct was expressed in onion epidermal cells. CaWRKY2 also had transcriptional activation activity in yeast. Taken together our data suggest that CaWRKY2 is a pathogen-inducible transcription factor that may have a role in early defense responses to biotic and abiotic stresses.

Isolation and Identification of Endophytic Bacteria with Plant Growth Promoting Activity and Biocontrol Potential from Wild Pistachio Trees

  • Etminani, Faegheh;Harighi, Behrouz
    • The Plant Pathology Journal
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    • 제34권3호
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    • pp.208-217
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    • 2018
  • In this study, samples were collected from the leaves and stems of healthy wild Pistachio trees (Pistacia atlantica L.) from various locations of Baneh and Marivan regions, Iran. In total, 61 endophytic bacteria were isolated and grouped according to phenotypic properties. Ten selected isolates from each group were further identified by partial sequencing of the 16S rRNA gene. Based on the results, isolates were identified as bacteria belonging to Pseudomonas, Stenotrophomonas, Bacillus, Pantoea and Serratia genus. The ability of these isolates was evaluated to phytohormone production such as auxin and gibberellin, siderophore production, phosphate solubilization, atmospheric nitrogen fixation, protease and hydrogen cyanide production. All strains were able to produce the plant growth hormone auxin and gibberellin in different amounts. The majority of strains were able to solubilize phosphate. The results of atmospheric nitrogen fixation ability, protease and siderophore production were varied among strains. Only Ba66 could produce a low amount of hydrogen cyanide. The results of biocontrol assay showed that Pb78 and Sp15 strains had the highest and lowest inhibition effects on bacterial plant pathogens, Pseudomonas syringae pv. syringae Pss20 and Pseudomonas tolaasii Pt18 under in vitro condition. Pb3, Pb24 and Pb71 strains significantly promote root formation on carrot slices. To our knowledge this is the first report of the isolation of endophytic bacterial strains belonging to Pantoea, Bacillus, Pseudomonas, Serratia and Stenotrophomonas genus from wild pistachio trees with plant growth promoting potential and biocontrol activity.

A Gene-Tagging System for Monitoring of Xanthomonas Species

  • Song, Wan-Yeon;Steven W. Hutcheson;Efs;Norman W. Schaad
    • The Plant Pathology Journal
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    • 제15권3호
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    • pp.137-143
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    • 1999
  • A novel chromosomal gene tagging technique using a specific fragment of the fatty acid desaturase-like open reading frame (des-like ORF) from the tox-argK gene cluster of Pseudomonas syringae pv. phaseolicola was developed to identify Xanthomonas spp.released into the environment as biocontrol agents. X. campestris pv. convolvuli FB-635, a pathogen of Convolvulus arvensis L., (bindweed), was chosen as the organism in which to develop and test the system. A 0.52 kb DES fragment amplified from P. syringae pv. phaseolicola C-199 was inserted into pGX15, a cosmid clone containing a 10.3 kb Eco RI-HindIII fragment derived from the xanthomonadin biosynthetic gene cluster contained in plasmid pIG102, to create a pigG::DES insertion. The 10.8 kb EcoRI-BamHI fragment carrying the pigG:: DES insertion was cloned into pLAFR3 to generate pLXP22. pLXP22 was then conjugated into X. campestris pv. convolvuli FB-635 and the pigG::DES insertion integrated into the bacterial chromosome by marker exchange. Rifampicin resistant, tetracycline sensitive, starch hydrolyzing, white colonies were used to differentiate the marked strain from yellow pigmented wild-type ones. PCR primers specific for the unique DES fragment were used for direct detection of the marked strain. Result showed the marked strain could be detected at very low levels even in the presence of high levels of other closely related or competitive bacteria. This PCR-based DES-tagging system provides a rapid and specific tool for directly monitoring the dispersal and persistence of Xanthomonas spp.released into the environment.

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천연물로부터 Quorum Sensing 저해제의 탐색 (Detection of a Quorum-Sensing Inhibitor from the Natural Products)

  • 김태우;차지영;이준승;민복기;백형석
    • 생명과학회지
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    • 제18권2호
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    • pp.206-212
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    • 2008
  • 인간이 서로 간의 의사소통을 위해 언어를 사용하듯이, 세균의 경우도 외부 환경 변화를 신속히 감지하여 서로 효과적으로 대응하기 위해서 주변 세포들과 소통할 수 있는 세균만의 독특한 화학적 언어를 사용하는 것으로 알려져 있다. 특히, 일정 세포 농도에 도달했을 때 자체적으로 생산된 화학적 신호를 통해 개체 수를 인지하고 그에 따라 특정 유전자의 발현을 동시에 조절하는 quorum sensing (QS) 기작은 다양한 세균 종들에서 광범위하게 존재한다. 본 연구는 다양한 천연물 추출물들을 대상으로 QS 저해 활성을 확인하였는데 QS 지시균주인 Agrobacterium tumefaciens NT1과 화학적으로 합성한 QS autoinducers을 사용한 bioassay를 수행하였다. 그 결과 양배추, 파, 양파의 추출물들에서 QS 저해 활성을 확인하였고, recycling preparative HPLC (prep-HPLC)를 통한 정제 과정을 통해, 83분 지점의 peak에 해당하는 성분들이 공통으로 QS 저해 활성을 가지고 있음을 확인하였다. 따라서 그 QS 저해 성분을 QSI-83으로 지정하고 thin layer chromatography (TLC)를 통해 P. syringae pv. tabaci의 autoinducers 합성을 저해하는 활성을 가지고 있음을 확인하였다. 또한 열에 대한 안정성과 세균 생장에서의 영향을 조사하였는데, 그 결과 QSI-83은 열에 안정하며 세균의 생장에는 영향을 끼치지 않는 물질임을 확인하였다. 따라서 우리는 천연물로부터 분리된 새로운 성분이 QS 저해제로서 이용될 수 있음을 제안한다.

클러스터 조사에 의한 마늘 세균점무늬병의 축차표본조사법 개발 (Development of Sequential Sampling Plan for Bacterial Leaf Blight of Garlic by Cluster Sampling)

  • 송정흡;양철준;양영택;심홍식;좌창숙
    • 식물병연구
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    • 제21권4호
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    • pp.268-272
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    • 2015
  • 마늘 세균점무늬병은 국내에서 제주지역 난지형 마늘에서 Pseudomonas syringae pv. morri에 의해 발생하는 세균병해로 주요 병해 중 하나이다. 본 연구는 자연로그를 취한 이항분산에 대한 관측분산의 회귀모델인 binary power law를 이용하여 포장 내 병 발생의 공간분포 특성을 분석하였다. 회귀식의 기울기(b) 값이 1.361로 기준치인 1보다 커 세균점무늬병은 공간적으로 집중분포하고 있었다. 축차표본조사법은 평균이병주율($p_m$)의 추정과 요방제수준($p_t$) 이상 또는 이하 여부를 판단할 수 있도록 개발하였다. 본 연구결과는 기존의 조사지점수 고정 조사 방법에 비해 조사비용 면에서 더 효율적인 동시에 조사결과의 정확도를 더 높일 수 있을 것으로 판단된다.

Role of Two Sets of RND-Type Multidrug Efflux Pump Transporter Genes, mexAB-oprM and mexEF-oprN, in Virulence of Pseudomonas syringae pv. tabaci 6605

  • Ichinose, Yuki;Nishimura, Takafumi;Harada, Minori;Kashiwagi, Ryota;Yamamoto, Mikihiro;Noutoshi, Yoshiteru;Toyoda, Kazuhiro;Taguchi, Fumiko;Takemoto, Daigo;Matsui, Hidenori
    • The Plant Pathology Journal
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    • 제36권2호
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    • pp.148-156
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    • 2020
  • Pseudomonas syringae pv. tabaci 6605 has two multidrug resistance (MDR) efflux pump transporters, MexAB-OprM and MexEF-OprN. To understand the role of these MDR efflux pumps in virulence, we generated deletion mutants, ΔmexB, ΔmexF, and ΔmexBΔmexF, and investigated their sensitivity to plant-derived antimicrobial compounds, antibiotics, and virulence. Growth inhibition assays with KB soft agar plate showed that growth of the wild-type (WT) was inhibited by 5 μl of 1 M catechol and 1 M coumarin but not by other plant-derived potential antimicrobial compounds tested including phytoalexins. The sensitivity to these compounds tended to increase in ΔmexB and ΔmexBΔmexF mutants. The ΔmexBΔmexF mutant was also sensitive to 2 M acetovanillone. The mexAB-oprM was constitutively expressed, and activated in the ΔmexF and ΔmexBΔmexF mutant strains. The swarming and swimming motilities were impaired in ΔmexF and ΔmexBΔmexF mutants. The flood inoculation test indicated that bacterial populations in all mutant strains were significantly lower than that of WT, although all mutants and WT caused similar disease symptoms. These results indicate that MexAB-OprM extrudes plant-derived catechol, acetovanillone, or coumarin, and contributes to bacterial virulence. Furthermore, MexAB-OprM and MexEF-OprN complemented each other's functions to some extent.

Isolation and Identification of Ice Nucleation Active Fusarium Strains from Rapid Apple Declined Trees in Korea

  • Avalos-Ruiz, Diane;Ten, Leonid N.;Kim, Chang-Kil;Lee, Seung-Yeol;Jung, Hee-Young
    • The Plant Pathology Journal
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    • 제38권4호
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    • pp.403-409
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    • 2022
  • In biological particles such as Fusarium species, ice nucleation activity (INA) has been observed. Fusarium strains isolated from apple declined trees in Korea were identified with a multilocus sequence analysis using the tef1 and rpb1 genes. Droplet-freezing and tube-freezing assays were used to determine the INA of the strains, using Pseudomonas syringae pv. syringae KACC 21200 as a positive control and resulting in seven INA+ fungal strains that were identified as F. tricinctum (KNUF-21-F17, KNUF-21-F18, KNUF-21-F29, KNUF-21-F32, KNUF-21-F38, KNUF-21-F43, and KNUF-21-F44). The effect of Fusarium INA+ KNUF-21-F29 was compared to that of INA- strains on Chrysanthemum morifolium cv. Shinma explants. A higher callus formation and no-shoot formation were observed, suggesting that fungal INA could play a role in cold injuries and be a factor to consider in rapid apple decline. To the best of our knowledge, this is the first report of INA fungal strains isolated in Korea.