Paper Type |
Contributed Paper |
Title |
Biological Control of Rigidoporus microporus the Cause of White Root Disease in Rubber Using PGPRs In vivo |
Author |
Mathurot Chaiharn*, Nikhom Sujada, Wasu Pathom-aree and Saisamorn Lumyong |
Email |
mathurot@mju.ac.th |
Abstract: White root disease caused by Rigidoporus microporus is abundant in Hevea brasiliensis
plantations in Thailand. Disease control by systemic fungicides is expensive, pollutes the
environment and causes health hazards. Plant growth-promoting rhizobacteria (PGPRs) obtained
from rubber growing areas were screened for antagonistic activity against R. microporus. In the
present study, 120 strains of Actinomycetes and 98 strains of fluorescent pseudomonad were
screened for antagonistic traits as siderophore, β-1,3-glucanase, chitinase, cellulase, catalase and
antifungal activity, in vitro. On the basis of dual culture assays, Lac 19, Lac 17 and LBR 14 strains
were selected based on their bioactive compound-producing activities which included catalase,
chitinase and cellulase. According to cell wall composition analysis and 16S rRNA homology,
these strains were identified as Streptomyces seoulensis Lac 19, Streptomyces malaysiensis Lac 17, and
Streptomyces ahygroscopicus LBR 14, respectively. Application of biocontrol agents, S. malaysiensis
Lac 17 and S. ahygroscopicus LBR 14, in nursery stage of H. brasiliensis showed greater suppression
of the disease in the same level as hexaconazole. The application of selected Streptomyces would
be an alternative for the control of R. microporus in the long-term rubber plantation.
|
|
Start & End Page |
850 - 866 |
Received Date |
2018-10-31 |
Revised Date |
|
Accepted Date |
2019-05-16 |
Full Text |
Download |
Keyword |
Hevea brasiliensis, white root disease, Rigidoporus microporus, biocontrol, PGPRs |
Volume |
Vol.46 No.5 (September 2019) |
DOI |
|
Citation |
Chaiharn M., Sujada N., Pathom-aree W. and Lumyong S., Biological Control of Rigidoporus microporus the Cause of White Root Disease in Rubber Using PGPRs In vivo, Chiang Mai J. Sci., 2019; 46(5): 850-866. |
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