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Excessive salt accumulation in soils is a major ecological and agronomical problem, in particular in arid and semi-arid areas. Excessive soil salinity affects the establishment, development, and growth of plants, resulting in important losses in productivity. Plants have evolved biochemical and molecular mechanisms that may act in a concerted manner and constitute the integrated physiological response to soil salinity. These include the synthesis and accumulation of compatible solutes to avoid cell dehydration and maintain root water uptake, the regulation of ion homeostasis to control ion uptake by roots, compartmentation and transport into shoots, the fine regulation of water uptake and distribution to plant tissues by the action of aquaporins, the reduction of oxidative damage through improved antioxidant capacity and the maintenance of photosynthesis at values adequate for plant growth. Arbuscular mycorrhizal (AM) symbiosis can help the host plants to cope with the detrimental effects of high soil salinity. There is evidence that AM symbiosis affects and regulates several of the above mentioned mechanisms, but the molecular bases of such effects are almost completely unknown. This review summarizes current knowledge about the effects of AM symbiosis on these physiological mechanisms, emphasizing new perspectives and challenges in physiological and molecular studies on salt-stress alleviation by AM symbiosis.

A common effect of several abiotic stresses is to cause tissue dehydration. Such dehydration is caused by the imbalance between root water uptake and leaf transpiration. Under some specific stress conditions, regulation of root water uptake is more crucial to overcome stress injury than regulation of leaf transpiration. This review first describes present knowledge about how water is taken up by roots and then discusses how specific stress situations such as drought, salinity, low temperature, and flooding modify root water uptake. The rate of root water uptake of a given plant is the result of its root hydraulic characteristics, which are ultimately regulated by aquaporin activity and, to some extent, by suberin deposition. Present knowledge about the effects of different stresses on these features is also summarized. Finally, current findings regarding how molecular signals such as the plant hormones abscisic acid, ethylene, and salicylic acid, and how reactive oxygen species may modulate the final response of root water uptake under stress conditions are discussed.

The arbuscular mycorrhizal (AM) symbiosis enhances plant tolerance to water deficit through the alteration of plant physiology and the expression of plant genes. These changes have been postulated to be caused (among others) by different contents of abscisic acid (ABA) between AM and non-AM plants. However, there are no studies dealing with the effects of exogenous ABA on the expression of stress-related genes and on the physiology of AM plants. The aim of the present study was to evaluate the influence of AM symbiosis and exogenous ABA application on plant development, physiology, and expression of several stress-related genes after both drought and a recovery period. Results show that the application of exogenous ABA had contrasting effects on AM and non-AM plants. Only AM plants fed with exogenous ABA maintained shoot biomass production unaltered by drought stress. The addition of exogenous ABA enhanced considerably the ABA content in shoots of non-AM plants, concomitantly with the expression of the stress marker genes Lsp5cs and Lslea and the gene Lsnced. By contrast, the addition of exogenous ABA decreased the content of ABA in shoots of AM plants and did not produce any further enhancement of the expression of these three genes. AM plants always exhibited higher values of root hydraulic conductivity and reduced transpiration rate under drought stress. From plants subjected to drought, only the AM plants recovered their root hydraulic conductivity completely after the 3 d recovery period. As a whole, the results indicate that AM plants regulate their ABA levels better and faster than non-AM plants, allowing a more adequate balance between leaf transpiration and root water movement during drought and recovery.

In this study, it has been determined whether the arbuscular mycorrhizal (AM) symbiosis is able to alter the pattern of dehydrin (LEA D-11 group) transcript accumulation under drought stress, and whether such a possible alteration functions in the protection of the host plants against drought. Two dehydrin-encoding genes have been cloned from Glycine max (gmlea 8 and gmlea 10) and one from Lactuca sativa (lslea 1) and they have been analysed for their contribution to the response against drought in mycorrhizal soybean and lettuce plants. Results with soybean plants showed that most of the treatments did not show LEA gene expression under well-watered conditions. The higher gene expression was found in non-inoculated plants subjected to drought. Only plants singly inoculated with Bradyrhizobium japonicum showed an important level of LEA gene expression under well-watered conditions and a reduced level under drought-stress conditions. The same results were confirmed in subsequent experiments and at the latest stage of a time-course experiment. In lettuce, the lslea 1 gene was also induced by drought stress in all treatments. However, the level of induction was clearly higher in roots from non-inoculated plants than in roots from the two AM treatments assayed. The overall results demonstrated that the levels of lea transcript accumulation in mycorrhizal treatments subjected to drought were considerably lower than in the corresponding non-mycorrhizal plants, indicating that the accumulation of LEA proteins is not a mechanism by which the AM symbiosis protects their host plant.

This study investigated several aspects related to drought tolerance in arbuscular mycorrhizal (AM) soybean plants. The investigation included both shoot and root tissues in order to reveal the preferred target tissue for AM effects against drought stress. Non-AM and AM soybean plants were grown under well-watered or drought-stressed conditions, and leaf water status, solute accumulation, oxidative damage to lipids, and other parameters were determined. Results showed that AM plants were protected against drought, as shown by their significantly higher shoot-biomass production. The leaf water potential was also higher in stressed AM plants (-1.9 MPa) than in non-AM plants (-2.5 MPa). The AM roots had accumulated more proline than non-AM roots, while the opposite was observed in shoots. Lipid peroxides were 55% lower in shoots of droughted AM plants than in droughted non-AM plants. Since there was no correlation between the lower oxidative damage to lipids in AM plants and the activity of antioxidant enzymes, it seems that first the AM symbiosis enhanced osmotic adjustment in roots, which could contribute to maintaining a water potential gradient favourable to the water entrance from soil into the roots. This enabled higher leaf water potential in AM plants during drought and kept the plants protected against oxidative stress, and these cumulative effects increased the plant tolerance to drought.

In the present study three cDNA fragments were cloned using degenerate primers for Mn-sod genes and PCR: two showed a high degree of identity with Mn-sods from plants and the third with Fe-sod. Arbuscular mycorrhizal (AM) symbiosis down-regulated their expression pattern under well-watered conditions. In contrast, AM symbiosis in combination with drought stress considerably increased the expression of the Mn-sod II gene and this correlated well with plant tolerance to drought. These results would suggest that mycorrhizal protection against oxidative stress caused by drought may be an important mechanism by which AM fungi protect the host plant against drought.