ULTRASTRUCTURE OF INTERACTIONS BETWEEN XANTHOMONAS-CAMPESTRIS PV VESICATORIA AND PEPPER, INCLUDING IMMUNOCYTOCHEMICAL LOCALIZATION OF EXTRACELLULAR POLYSACCHARIDES AND THE AVRBS3 PROTEIN
被引:50
作者:
BROWN, I
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机构:UNIV LONDON WYE COLL, DEPT BIOCHEM & BIOL SCI, ASHFORD TN25 5AH, KENT, ENGLAND
BROWN, I
MANSFIELD, J
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机构:UNIV LONDON WYE COLL, DEPT BIOCHEM & BIOL SCI, ASHFORD TN25 5AH, KENT, ENGLAND
MANSFIELD, J
IRLAM, I
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机构:UNIV LONDON WYE COLL, DEPT BIOCHEM & BIOL SCI, ASHFORD TN25 5AH, KENT, ENGLAND
IRLAM, I
CONRADSSTRAUCH, J
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机构:UNIV LONDON WYE COLL, DEPT BIOCHEM & BIOL SCI, ASHFORD TN25 5AH, KENT, ENGLAND
CONRADSSTRAUCH, J
BONAS, U
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机构:UNIV LONDON WYE COLL, DEPT BIOCHEM & BIOL SCI, ASHFORD TN25 5AH, KENT, ENGLAND
BONAS, U
机构:
[1] UNIV LONDON WYE COLL, DEPT BIOCHEM & BIOL SCI, ASHFORD TN25 5AH, KENT, ENGLAND
[2] INST GENBIOL FORSCH BERLIN GMBH, W-1000 BERLIN 33, GERMANY
BACTERIAL PATHOGENICITY;
DISEASE RESISTANCE;
ELECTRON MICROSCOPY;
D O I:
10.1094/MPMI-6-376
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The ultrastructure of interactions between the bacterial spot pathogen Xanthomonas campestris pv. vesicatoria and its host, pepper, was investigated. Development of colonies of the race 2 strain 85-10 and transconjugants expressing the cloned avirulence gene avrBs3 on plasmids pL3XV1-6 and pD36 was examined in pepper cultivars Early Cal Wonder (ECW) and ECW-30R; these cultivars are isogenic apart from the absence or presence, respectively, of the Bs3 allele for resistance to X. c. pv. vesicatoria. Resistance is expressed by the hypersensitive reaction (HR). Immunocytochemical staining allowed examination of the contribution of extracellular polysaccharide (EPS) to colony development and differentiation between material of bacterial and plant origin in the intercellular space. Early growth of colonies was identical in resistant and susceptible leaves. Bacteria were not specifically attached to mesophyll cells in resistant leaves but during compatible and incompatible interactions rapidly became coated by a thick layer of EPS within 4 hr after inoculation. Labeling with monoclonal antibodies (MAbs) A6 and D1 with specificity for the xanthan side chain was most dense around the bacterial cell wall; more extracellular label was found with A6. By contrast, with MAb B3, which has specificity for the pyruvylated terminal mannose of the xanthan side chain, label was primarily intracellular at the poles of bacterial cells. Labeling with B3 was greatly reduced in bacteria within tissue which had undergone the HR. The AvrBs3 protein was located by immunocytochemistry within the cytoplasm of cells of X. c. pv. vesicatoria overexpressing the avrBs3 gene in vitro and in the plant. Exchange of signals between bacteria and plant during both the compatible and incompatible interactions was indicated by the localized deposition of paramural papillae in mesophyll cells. The collapse of pepper cells during the HR followed plasma membrane damage and vesiculation of the cytoplasm initially close to the bacterial colony. The histological studies have defined the structural and temporal framework within which recognition and response occur in pepper and indicate the changing conditions to which cells of X. c. pv. vesicatoria are exposed during colonization of the intercellular space.