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Diseases and Management of Crops under Protected Cultivation

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(<strong>Diseases</strong> <strong>and</strong> <strong>Management</strong> <strong>of</strong> <strong>Crops</strong> <strong>under</strong> <strong>Protected</strong> <strong>Cultivation</strong>)<br />

Once biocontrol bacteria are established in the rhizosphere, a wide variety <strong>of</strong> mechanisms can<br />

result in suppression <strong>of</strong> plant pathogens. Accordingly, except in the case <strong>of</strong> induced resistance, a<br />

biocontrol agent must occupy an ecological niche similar to that <strong>of</strong> the plant pathogen <strong>and</strong> its<br />

mode <strong>of</strong> action (competition, parasitism, antibiosis, induction <strong>of</strong> SAR) must interfere both spatially<br />

<strong>and</strong> temporally with precise steps in the development <strong>of</strong> the pathogen.<br />

Interactions between plants <strong>and</strong> rhizobacteria: The rhizosphere is a narrow zone <strong>of</strong> soil that is<br />

influenced by root secretions. The structure <strong>of</strong> rhizobacterial communities is determined by the<br />

plant species, <strong>and</strong> differences in the composition <strong>and</strong> amounts <strong>of</strong> root exudates probably account<br />

for the differences in microbial populations. Root exudates <strong>of</strong>fer a carbon-rich diet to the<br />

rhizosphere microorganisms which includes organic acids such as citrate, malate, succinate,<br />

pyruvate, fumarate, oxalate <strong>and</strong> acetate <strong>and</strong> sugars such as glucose, xylose, fructose, maltose,<br />

sucrose, galactose <strong>and</strong> ribose, constitute the ‘main course’, whereas variable amounts <strong>of</strong> amino<br />

acids, nucleobases <strong>and</strong> vitamins (such as thiamin <strong>and</strong> biotin) provide the ‘entrée’ or ‘dessert’. The<br />

ability <strong>of</strong> rhizobacteria to use organic acids as carbon sources correlates with rhizosphere<br />

competence. The rhizosphere, which is the narrow zone <strong>of</strong> soil that is influenced by root<br />

secretions, can contain up to 10 11 microbial cells per gram root <strong>and</strong> more than 30,000 prokaryotic<br />

species. The collective genome <strong>of</strong> this microbial community is much larger than that <strong>of</strong> the plant<br />

<strong>and</strong> is also referred to as the plant’s second genome. Chemotaxis, flagellar mobility,<br />

lipopolysaccharide (LPS) structure, the outer membrane protein OprF <strong>and</strong>, to a lesser extent, pili<br />

are all important for competitive root colonization. A root glycoprotein complex, agglutinin involved<br />

in the short-term adherence <strong>of</strong> Pseudomonads to the plant roots. Once biocontrol Pseudomonads<br />

have moved <strong>and</strong> attached to a root zone, microcolonies form in a few days. Other bacteria can<br />

reach the same site at a later time <strong>and</strong> intermingle with pre-existing microcolonies. The root collar,<br />

where the root joins the main stem, is a site <strong>of</strong> intense exudation <strong>and</strong> is more strongly colonized by<br />

bacteria than is the root tip.<br />

The rhizosphere microbiome: The micr<strong>of</strong>lora <strong>of</strong> most soils is carbon starved. Because plants<br />

secrete up to 40% <strong>of</strong> their photosynthates into the rhizosphere, the microbial population densities<br />

in the rhizosphere are much higher than in the surrounding bulk soil. This phenomenon is known<br />

as the ‘rhizosphere effect’. In general, rhizosphere microbial communities are less diverse than<br />

those <strong>of</strong> the bulk soil. It appears that, from the reservoir <strong>of</strong> microbial diversity that the bulk soil<br />

comprises, plant roots select for specific microorganisms to prosper in the rhizosphere. Together<br />

with the plant genotype, soil type is an important driver <strong>of</strong> the microbial community composition in<br />

the rhizosphere. Plants can determine the composition <strong>of</strong> the root microbiome by active secretion<br />

<strong>of</strong> compounds that specifically stimulate or repress members <strong>of</strong> the microbial community. Recent<br />

evidences suggest that plant genotype also determines microbiome composition. Differences in a<br />

single gene between plant genotypes can have a significant impact on the rhizosphere<br />

microbiome. The production <strong>of</strong> a single exogenous glucosinolate significantly altered the microbial<br />

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