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68<br />

ANA LUISA ANAYA<br />

effects on microbial composition of the soybean rhizosphere were also determined by<br />

identifying microorganisms. Bacteria strains were identified rising fatty acid analysis,<br />

and fungus identification was done rising standard morphological measurements and<br />

appropriate taxonomic keys. Results showed that most amendments alone or in<br />

combination with benzaldehyde reduced damage from plant parasitic nematodes.<br />

Benzaldehyde applied alone or in combination with the amendments exerted a selective<br />

action on the activity and composition of microbial populations in the soybean<br />

rhizosphere. In control soils the bacterial flora was predominantly Gram-negative,<br />

while in soils amended with velvetbean or kudzu alone or with benzaldehyde. Grampositive<br />

bacteria were dominant. Mycoflora promoted by the different amendments or<br />

combinations with benzaldehyde included species of Aspergillus, Myrothecium,<br />

Penicillium, and Trichoderma.<br />

Calvet et al. (2001) evaluated the survival of two species of plant parasitic<br />

nematodes: the root-lesion nematode Pratylenchus brachyurus, and the root-knot<br />

nematode Meloidogyne javanica, in saturated atmospheres of 12 natural chemical<br />

compounds. The infectivity of two isolates of arbuscular mycorrhizal fungi: Glomus<br />

mosseae and Glomus intraradices, under identical experimental conditions, was also<br />

determined. All the compounds tested exerted a highly significant control against M.<br />

javanica and among them, benzaldehyde, salicilaldehyde, borneol, p-anisaldehyde<br />

and cinnamaldehyde caused a mortality rate above 50% over P. brachyurus. The<br />

infectivity of G. intraradices was inhibited by cinnamaldehyde, salicilaldehyde, thymol,<br />

carvacrol, p-anisaldehyde, and benzaldehyde, while only cinnamaldehyde and thymol<br />

significantly inhibited mycorrhizal colonization by G. mosseae.<br />

When soybean plant responses to Meloidogyne incognita infestation were<br />

compared to resistant (Bryan) and susceptible (Brim) cultivars at 0, 1, 3, 10, 20, and<br />

34 days after infestation, Qiu and collaborators (1997) observed that the resistant<br />

cultivar had higher chitinase activity than the susceptible cultivar at every sample<br />

time beginning at the third day. Results from isoelectric focusing gel electrophoresis<br />

analyses indicated that three acidic chitinase isozymes with isoelectric points (pIs) of<br />

4.8, 4.4, and 4.2 accumulated to a greater extent in the resistant compared to the<br />

susceptible cultivar following challenge. SDS-PAGE analysis of root proteins revealed<br />

that two proteins with molecular weights of approximately 31 and 46 kD accumulated<br />

more rapidly and to a higher level in the resistant than in the susceptible cultivar.<br />

Additionally, three major protein bands (33, 22, and 20 kD) with chitinase activity<br />

were detected with a modified SDS-PAGE analysis in which glycolchitin was added<br />

into the gel matrix. These results indicate that higher chitinase activity and early<br />

induction of specific chitinase isozymes may be associated with resistance to rootknot<br />

nematode in soybean.<br />

Antagonists, most likely favored by selected cover crops, include mainly fungal<br />

egg parasites, trapping fungi, endoparasitic fungi, fungal parasites of females,<br />

endomycorrhizal fungi, planthealth promoting rhizobacteria, and obligate bacterial<br />

parasites. There are several hypotheses on how cover crops can enhance nematodeantagonistic<br />

activities. A series of ecological events may be involved. The decomposing

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