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1.
Microbiologyopen ; 8(6): e00765, 2019 06.
Artigo em Inglês | MEDLINE | ID: mdl-30427123

RESUMO

Plasmodiophora brassicae, a parasitic protist, induces club-shaped tumor-like growth of host Brassicas roots and hypocotyls after infection. Due to its soil-borne nature and intracellular, biotrophic parasitism the infection biology and early pathogenesis remains in doubt. In this study, we have established a new protocol, based on a two-step axenic culture of P. brassicae with its host tissues, for easy and in planta observation of cellular interactions between P. brassicae and host plants: first, coculture of P. brassicae with infected canola root tissues, on growth-medium plates, enables the propagation of P. brassicae that serves as pure inoculum for pathogenicity assays, and second, the pure inoculum is subsequently used for pathogenicity tests on both canola and Arabidopsis seedlings grown on medium plates in Petri dishes. During the first axenic culture, we established a staining protocol by which the pathogen was fluorescently labeled with Nile red and calcofluor white, thus allowing in planta observation of pathogen development. In the pathogenicity assays, our results showed that axenic cultures of P. brassicae, in calli, remains fully virulent and completes its life cycle in both canola and Arabidopsis roots grown in Petri dishes. Combining visualization of fluorescent probe-labeled P. brassicae structures with fluorescent protein tagging of Arabidopsis cellular components, further revealed dynamic responses of host cells at the early stages of P. brassicae infection. Thus, established protocols for in planta detection of P. brassicae structures and the live cell imaging of P. brassicae-Arabidopsis interactions provide a novel strategy for improving our detailed knowledge of P. brassicae infection in host tissues.


Assuntos
Arabidopsis/microbiologia , Doenças das Plantas/microbiologia , Plasmodioforídeos/fisiologia , Arabidopsis/crescimento & desenvolvimento , Cultura Axênica , Brassica napus/crescimento & desenvolvimento , Brassica napus/microbiologia , Interações Hospedeiro-Patógeno , Plasmodioforídeos/química , Plasmodioforídeos/patogenicidade , Plântula/crescimento & desenvolvimento , Plântula/microbiologia , Coloração e Rotulagem , Virulência
2.
Protist ; 162(3): 423-34, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21497131

RESUMO

Plasmodiophora brassicae is a soil-borne obligate intracellular parasite in the phylum Cercozoa of the Rhizaria that causes clubroot disease of crucifer crops. To control the disease, understanding the distribution and infection routes of the pathogen is essential, and thus development of reliable molecular markers to discriminate geographic populations is required. In this study, the nuclear ribosomal RNA gene (rDNA) repeat unit of P. brassicae was determined, with particular emphasis on the structure of large subunit (LSU) rDNA, in which polymorphic regions were expected to be present. The complete rDNA complex was 9513bp long, which included the small subunit, 5.8S and LSU rDNAs as well as the internal transcribed spacer and intergenic spacer regions. Among eight field populations collected from throughout Honshu Island, Japan, a 1.1 kbp region of the LSU rDNA, including the divergent 8 domain, exhibited intraspecific polymorphisms that reflected geographic isolation of the populations. Two new group I introns were found in this region in six out of the eight populations, and the sequences also reflected their geographic isolation. The polymorphic region found in this study may have potential for the development of molecular markers for discrimination of field populations/isolates of this organism.


Assuntos
DNA Ribossômico/genética , Plasmodioforídeos/genética , Polimorfismo Genético/genética , Sequência de Bases , Brassica/parasitologia , Brassica rapa/parasitologia , DNA de Protozoário/química , DNA de Protozoário/genética , DNA Ribossômico/química , Éxons/genética , Marcadores Genéticos , Geografia , Íntrons/genética , Japão , Dados de Sequência Molecular , Filogenia , Plasmodioforídeos/química , Análise de Sequência de DNA
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