Management of foot rot of black pepper (Piper nigrum L.) with mycoinoculant enriched vermicompost

Abstract

The study, "Management of foot rot of black pepper (Piper nigrum L.) with mycoinoculant enriched vermicompost" was done at the Department of Plant Pathology, College of Agriculture, Veliayani to explore the possibility of using vermicornpost as a carrier material for mass production of biocontrol agents and to test its efficacy in controlling the disease. The talc based inoculum of Trichoderma harzianum and soil based granular inoculum of Glomus Jasciculatum were mass produced in vermicompost either alone or in combination with farmyard manure or neem cake in the ratio 1 : 1 and 5 : 1 respectively and the efficacy was compared with the standard carrier material of FYM + neem cake (10 : 1). The population of T. harzianum 15 DAI was maximum in the treatment combination of VC + NC (5 : 1). However, the influence of these carrier materials on percentage of mycorrhizal infection 50 DAI was not statistically significant. Vermicompost as a carrier material for biocontrol agents was further tested in pepper var. Karimunda inoculated with P. capsici. Carrier materials as such had no significant influence on disease control. Reduction in foliar infection, disease index, stem infection and percentage mortality was observed in treatments with biocontrol agents. Disease control was maximum with the treatments involving T. harzianum while plant growth promotion was maximum with G. Jasciculatum. The physiological changes in pepper plants after inoculation with P. capsici and biocontrol agents were studied. The phenol and OD phenol content was more in pathogen inoculated plants. The defence related enzymes peroxidase, polyphenol oxidase and phenylalanine ammonia lyase were enhanced with pathogen inoculation as well as with the application of biocontrol agents. SDS-PAGE analysis of proteins with samples extracted from plants one day after inoculation of pathogen showed the presence of two novel proteins with molecular . weights of 78 kDa and 28 kDa in diseased samples which were absent in treatments without pathogen and also in plants treated with COC.