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Updated: Oct 13, 2026

Fluorescence in situ Hybridizations (FISH) for the Localization of Viruses and Endosymbiotic Bacteria in Plant and Insect Tissues
Published on: February 24, 2014
Partial characterization of fimbriae of Xanthomonas campestris pv. hyacinthi
J van Doorn1, P M Boonekamp, B Oudega
1Bulb Research Centre, Department of Plant Quality, 2160 AB Lisse, Netherlands
Abstract:
Xanthomonas campestris pv. hyacinthi is a plant-pathogenic bacterium that causes yellow disease in Hyacinthus. X. c. pv.hyacinthi produces monopolarly attached fimbriae with a diameter of approximately 5 nm and a length of at least 6 micron. Fimbriae were purified by acid precipitation and preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis. No hemagglutinating activity of purified fimbriae was found when the fimbriae were tested with several types of erythrocytes. The fimbrial protein subunit had a relative molecular mass of 17 kDa; an isoelectric point was found at pH 4.1. Analysis of the N-terminal amino acid sequence of the fimbrial subunit indicated that X. c. pv. hyacinthi expresses type 4 fimbriae. A polyclonal rabbit antiserum was raised against the purified fimbriae. This antiserum recognized fimbriae of X. c. pv. hyacinthi in immunogold electron microscopy and immunoblotting experiments. Immunofluorescence studies showed that X. c. pv. hyacinthi cells as well as purified native fimbriae were attached to stomata of hyacinth leaves, suggesting a role for these surface antigens in the first stages of yellow disease.
Insights
Xanthomonas campestris pv. hyacinthi bacteria use type 4 fimbriae to attach to hyacinth stomata, initiating yellow disease. These fimbriae play a key role in the early infection stages of this plant pathogen.
Area of Science:
- Plant Pathology
- Bacteriology
- Microbiology
Background:
- Xanthomonas campestris pv. hyacinthi causes yellow disease in hyacinths.
- The bacterium possesses monopolarly attached fimbriae, approximately 5 nm in diameter and at least 6 µm long.
Purpose of the Study:
- To characterize the fimbriae of X. c. pv. hyacinthi.
- To investigate the role of fimbriae in the pathogenesis of hyacinth yellow disease.
Main Methods:
- Fimbrial purification using acid precipitation and SDS-PAGE.
- Analysis of fimbrial protein subunit properties (molecular mass, isoelectric point, N-terminal sequence).
- Serological characterization using polyclonal antiserum and immunofluorescence microscopy.
Main Results:
- Purified fimbriae showed no hemagglutinating activity.
- The fimbrial subunit has a molecular mass of 17 kDa and an isoelectric point of pH 4.1.
- N-terminal sequencing identified the fimbriae as type 4, and antiserum confirmed their presence and location on bacterial cells and hyacinth stomata.
Conclusions:
- Xanthomonas campestris pv. hyacinthi expresses type 4 fimbriae.
- These fimbriae are involved in the attachment of bacterial cells to hyacinth stomata.
- Fimbriae likely play a crucial role in the initial stages of yellow disease development.
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