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Index >> Rhizosphere and Phyllosphere >> Fungistasis

Fungistasis

Fungistasis
Root exudates influence the proliferation and survival of root infecting pathogens in soil either through soil fungistasis or inhibition of pathogens in the rhizosphere. The term soil fungistasis is used to explain the inability of non-dormant spores, sclerotia or propagules to germinate even under most favourable conditions of pH, temperature and moisture in soil. The fungi stasis could be released or undone by the rhizosphere effect of plants which creates a congenial environment for spore germination.

Sclerotia are perennating structures of certain plant pathogens and are different from spores in structure and behaviour.

Sclerotia may be a mass of loosely interwoven hyphae (e.g., Rhizoctonia solani) or they may have an organized structure- (Macrophomina phaseoli and Verticillium dahliae). Spores or sclerotia of many pathogenic fungi such as Rhizoctonia, Fusarium, Sclerotium, Aphanomyces, Pythium, Colletotrichum, Verticillium, Phytophthora and Plasmodiophora have been shown to germinate by the stimulus provided by the root exudates of susceptible cultivars of the host plants.

The stimulus for germination has been attributed to compounds exuded by plant roots which help to overcome, in some manner, the static nature of dormant reproductive structures in soil. The fungistasis of the sclerotia of Scelerotium cepivorum is released by certain volatile stimulators as­sociated with the roots of Allium. The volatile compounds have been iden­tified as alkyl sulphides which are produced when alkyl cysteine sulphoxides coming from roots of Allium are broken down by soil bacteria.

Once germination of spores takes place, the germ tube is less susceptible to soil fungistasis although its further development may be modified. For instance, macroconidia of Fusarium may germinate in soil and form germ­tubes but may then form chlamydospores instead of hyphae.

Chlamydospore formation is less frequent or postponed in sterile soils in­dicating the associative effects of other soil microorganisms normally present in unsterilized soil in such a morphogenesis. Indeed, it has been observed that chlamydospore production by F. solani is accelerated in the presence of Bacillus licheniformis.

Root exudates may provide a food base for the growth of antagonists which could suppress the growth of pathogenic microorganisms in soil. Many instances have been reported where the rhizosphere of resistant varieties harboured more numbers of Streptomyces and Trichoderma than that of the susceptible varieties. Such observations have been recorded with reference of Fusarium wilts of plants.

On examination of rhizosphere soil of pigeon-pea (Cajanus cajan) planted in seven different soils, it was observed that 13-33% of the rhizosphere isolates of Streptomyces from resis­tant varieties inhibited the growth of Fusarium udum the causal organism of pigeon-pea wilt whereas only 6% of the isolates from the rhizosphere of susceptible variety were found to be inhibitory to the wilt causing pathogen.

High incidence of Trichoderma viride in the rhizosphere of varieties of tomato resistant to Verticillium wilt has been noted with its ability to minimize the severity of wilt on susceptible plants in the presence of the pathogen. Substances in plant root exudates may influence the formation of in­fection structures such as appressoria as in the case of Pellicularia filamen­tosa and Rhizoctonia fragariae, although contrary evidences have also been obtained with regard to many other fungi.

Root exudates containing toxic substances such as glycosides and hydrocyanic acid may inhibit the growth of pathogens. A case in point is the exudation of hydrocyanic acid by the flax variety Bison resistant to Fusarium. Although several attempts have been made to correlate hydrocyanic acid content of root exudates with disease resistance, the results remain inconclusive. Thus, no unequivocal evidence has yet been brought forth to indicate the existence of specific compounds inhibitory to the growth and activity of pathogens in different cases of disease resis­tance.

Virus infections of plants result in stunting and foliar abnormalities which naturally reduce the area of the plant surface for photosynthetic activities. At different stages of disease development in Dolichos lablab in­fected with Dolichos enation mosaic virus, gross changes in the total num­bers of microorganisms in the rhizosphere take place accompanied by alterations in the incidence of amino acid and vitamin requiring bacteria. The changes induced in the rhizosphere due to virus infection could be restored to normalcy by spraying the leaves with thiouracil or gibberellins which are known to overcome foliar abnormalities and stunting symptoms associated with virus-infected plants.

One of the attributes of root exudates is the possible role they play in neutralizing the soil pH and altering the microclimate of the rhizosphere through liberation of water and carbon dioxide. Such changes may in­fluence infections of roots by pathogenic fungi.

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