Characterization of ralstonia solanacearum (Smith) Yabuuchi et al. causing bacterial wilt in ginger using molecular marker
By: Sambasivam P K.
Contributor(s): Girija D (Guide).
Material type:
BookPublisher: Vellanikkara Department of Plant Pathology, College of Horticulture 2003DDC classification: 632.3 Online resources: Click here to access online Dissertation note: MSc Abstract: In Kerala, bacterial wilt caused by Ralstonia solanacearum is one of the major
constraints in ginger cultivation. Earlier, the pathogen was characterized based on
cultural, morphological and biochemical tests. Since these methods are time
consuming and involve repeated subculturing and tedious biochemical tests, an
attempt was made to characterize the pathogen at molecular level using plasmid
profile and RAPD technique.
Wilted plant samples were collected from ginger growing tracts of Palakkad,
Eranukulam and Wynad districts. The pathogen was isolated on TZC medium, it
produced creamy white pink centred fluidal colonies. Stock cultures prepared by
suspending single colonies in sterile water were maintained at 4 QC.
Pathogenicity of the isolates was established using pseudostem inoculation
method. Tomato and brinjal were found to be collateral hosts of the pathogen. Based
on hypersensitivity reaction on capsicum the isolates were identified as race 3. This
was further confirmed by RAPD assay.
The isolates were found to. be Gram negative and showed positive reaction for
solubility. in KOH, nitrate reduction, production of catalase and oxidase enzyme,
fermentation of glucose. All the isolates utilized lactose, maltose, cellobiose, manitol,
sorbitol but not dulcitol and hence, were grouped as biovar III A.
Plasmid profile developed for the isolates showed presence of two bands of
. .
approximately 21 kb size .. Plasmids when transformed to E. coli DH 5a cells,
conferred resistance to ampicillin and rifampicin, indicating that the genes encoding
resistance to these antibiotics were located on the plasmid.
RAPD analysis using 16 primers showed much diversity among the isolates.
Primers OPU .13, OPU 17 and OPX 9 showed 100 per cent polymorphism.
Dendrogram obtained through cluster analysis showed one major and one sub cluster.
All the Palakkad isolates were grouped under a single cluster.
The present study indicated possibility of using molecular marker as a tool to
detect even slight variability among R. solanacearum isolates infecting ginger.
| Item type | Current location | Call number | Status | Date due | Barcode |
|---|---|---|---|---|---|
Theses
|
KAU Central Library, Thrissur Theses | 632.3 SAM/CH (Browse shelf) | Available | 172207 |
MSc
In Kerala, bacterial wilt caused by Ralstonia solanacearum is one of the major
constraints in ginger cultivation. Earlier, the pathogen was characterized based on
cultural, morphological and biochemical tests. Since these methods are time
consuming and involve repeated subculturing and tedious biochemical tests, an
attempt was made to characterize the pathogen at molecular level using plasmid
profile and RAPD technique.
Wilted plant samples were collected from ginger growing tracts of Palakkad,
Eranukulam and Wynad districts. The pathogen was isolated on TZC medium, it
produced creamy white pink centred fluidal colonies. Stock cultures prepared by
suspending single colonies in sterile water were maintained at 4 QC.
Pathogenicity of the isolates was established using pseudostem inoculation
method. Tomato and brinjal were found to be collateral hosts of the pathogen. Based
on hypersensitivity reaction on capsicum the isolates were identified as race 3. This
was further confirmed by RAPD assay.
The isolates were found to. be Gram negative and showed positive reaction for
solubility. in KOH, nitrate reduction, production of catalase and oxidase enzyme,
fermentation of glucose. All the isolates utilized lactose, maltose, cellobiose, manitol,
sorbitol but not dulcitol and hence, were grouped as biovar III A.
Plasmid profile developed for the isolates showed presence of two bands of
. .
approximately 21 kb size .. Plasmids when transformed to E. coli DH 5a cells,
conferred resistance to ampicillin and rifampicin, indicating that the genes encoding
resistance to these antibiotics were located on the plasmid.
RAPD analysis using 16 primers showed much diversity among the isolates.
Primers OPU .13, OPU 17 and OPX 9 showed 100 per cent polymorphism.
Dendrogram obtained through cluster analysis showed one major and one sub cluster.
All the Palakkad isolates were grouped under a single cluster.
The present study indicated possibility of using molecular marker as a tool to
detect even slight variability among R. solanacearum isolates infecting ginger.
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