Abstract:One of the most adverse effects of phosphorus (P) deficiency on N-2-fixing legumes is the generation of harmful active oxygen species which cause oxidative stress. And although oxidative stress has been widely studied in roots and shoots of various plant species, it has not yet sufficiently been documented in bean nodules so far. In this study, two recombinant inbred lines RIL115 (P-deficiency tolerant) and RIL147 (P-deficiency sensitive) of common bean and Concesa (local variety) were inoculated separately wi… Show more
“…Nodules have the potential to generate high levels of ROS due to high rates of bacteroid respiration, the oxidation of several proteins (nitrogenase, ferredoxin and hydrogenase) with strong reducing potentials, and autoxidation of the oxygenated form of leghemoglobin (Becana et al ., ). Oxidative stress is known to be a critical factor associated with Pi deficiency, and is caused by the overproduction of harmful ROS in the nodules of N 2 ‐fixing legumes when nodule metabolism is disturbed by either a biotic or abiotic stressor (Bargaz et al ., ). In a previous study, it was suggested that Pi deficiency‐induced oxidative stress may be implicated in down‐regulating the SNF capacity in Mm SWRI9‐inoculated plants (Nasr Esfahani et al ., ).…”
Phosphate (Pi) deficiency is known to be a major limitation for symbiotic nitrogen fixation (SNF), and hence legume crop productivity globally. However, very little information is available on the adaptive mechanisms, particularly in the important legume crop chickpea (Cicer arietinum L.), which enable nodules to respond to low-Pi availability. Thus, to elucidate these mechanisms in chickpea nodules at molecular level, we used an RNA sequencing approach to investigate transcriptomes of the nodules in Mesorhizobium mediterraneum SWRI9-(MmSWRI9)-chickpea and M. ciceri CP-31-(McCP-31)-chickpea associations under Pi-sufficient and Pi-deficient conditions, of which the McCP-31-chickpea association has a better SNF capacity than the MmSWRI9-chickpea association during Pi starvation. Our investigation revealed that more genes showed altered expression patterns in MmSWRI9-induced nodules than in McCP-31-induced nodules (540 vs. 225) under Pi deficiency, suggesting that the Pi-starvation-more-sensitive MmSWRI9-induced nodules required expression change in a larger number of genes to cope with low-Pi stress than the Pi-starvation-less-sensitive McCP-31-induced nodules. The functional classification of differentially expressed genes (DEGs) was examined to gain an understanding of how chickpea nodules respond to Pi starvation, caused by soil Pi deficiency. As a result, more DEGs involved in nodulation, detoxification, nutrient/ion transport, transcriptional factors, key metabolic pathways, Pi remobilization and signalling were found in Pi-starved MmSWRI9-induced nodules than in Pi-starved McCP-31-induced nodules. Our findings have enabled the identification of molecular processes that play important roles in the acclimation of nodules to Pi deficiency, ultimately leading to the development of Pi-efficient chickpea symbiotic associations suitable for Pi-deficient soils.
“…Nodules have the potential to generate high levels of ROS due to high rates of bacteroid respiration, the oxidation of several proteins (nitrogenase, ferredoxin and hydrogenase) with strong reducing potentials, and autoxidation of the oxygenated form of leghemoglobin (Becana et al ., ). Oxidative stress is known to be a critical factor associated with Pi deficiency, and is caused by the overproduction of harmful ROS in the nodules of N 2 ‐fixing legumes when nodule metabolism is disturbed by either a biotic or abiotic stressor (Bargaz et al ., ). In a previous study, it was suggested that Pi deficiency‐induced oxidative stress may be implicated in down‐regulating the SNF capacity in Mm SWRI9‐inoculated plants (Nasr Esfahani et al ., ).…”
Phosphate (Pi) deficiency is known to be a major limitation for symbiotic nitrogen fixation (SNF), and hence legume crop productivity globally. However, very little information is available on the adaptive mechanisms, particularly in the important legume crop chickpea (Cicer arietinum L.), which enable nodules to respond to low-Pi availability. Thus, to elucidate these mechanisms in chickpea nodules at molecular level, we used an RNA sequencing approach to investigate transcriptomes of the nodules in Mesorhizobium mediterraneum SWRI9-(MmSWRI9)-chickpea and M. ciceri CP-31-(McCP-31)-chickpea associations under Pi-sufficient and Pi-deficient conditions, of which the McCP-31-chickpea association has a better SNF capacity than the MmSWRI9-chickpea association during Pi starvation. Our investigation revealed that more genes showed altered expression patterns in MmSWRI9-induced nodules than in McCP-31-induced nodules (540 vs. 225) under Pi deficiency, suggesting that the Pi-starvation-more-sensitive MmSWRI9-induced nodules required expression change in a larger number of genes to cope with low-Pi stress than the Pi-starvation-less-sensitive McCP-31-induced nodules. The functional classification of differentially expressed genes (DEGs) was examined to gain an understanding of how chickpea nodules respond to Pi starvation, caused by soil Pi deficiency. As a result, more DEGs involved in nodulation, detoxification, nutrient/ion transport, transcriptional factors, key metabolic pathways, Pi remobilization and signalling were found in Pi-starved MmSWRI9-induced nodules than in Pi-starved McCP-31-induced nodules. Our findings have enabled the identification of molecular processes that play important roles in the acclimation of nodules to Pi deficiency, ultimately leading to the development of Pi-efficient chickpea symbiotic associations suitable for Pi-deficient soils.
“…Seven days after, the seedlings were inoculated with 10 mL of each strain of rhizobia Containing approximately 10 8 CFU/mL (CFU = Colony-forming unit). Plants were watered three times a week with the distillated water and the nitrogen free nutrient solution during the trial period (Bargaz et al 2013). After one week, plants randomly selected were subjected to maximal irrigation (100%), optimal irrigation (FC 1 : 80% of field capacity) and under water deficit (FC 2 : 40% of field capacity).…”
The effects of drought on growth, several physiological and biochemical processes in six winter varieties (Zhour, Rizki, Douyet, V46, V34 and P37) of chickpea (Cicer arietinum L.) and two rhizobial strains (MC07 and MC10) were studied. The experiment was conducted under greenhouse conditions. Seedlings were grown under three regimes moistening and inoculated separately: 100 % of field capacity (control), 80% of field capacity (optimal irrigation) and 40% of field capacity (water deficit). The results showed that the hydric deficit had significantly perturbed the dry biomass, proline activity, total chlorophyll and nitrogen contents. Moreover, this constraint negatively affected the water deficit saturation (WDS), the membrane permeability and the stomatal conductance of leaves. Under drought, the varieties Zhour and Rizki showed a better water efficiency that was translated by high level in proline accumulation, membrane stability, total chlorophyll and nitrogen contents. These parameters were maintained at the adequate levels with the rhizobial strain MC07 which showed a tolerance in the drought condition. On the contrary, the symbiotic combination least powerful according to the studied parameters is formed by the variety P37-MC10.
“…5 The latter, with carbon supply regulation and N feedback, contribute to regulating SNF. 43 Moreover, oxidative stress is not induced only under P-deficiency, 34,44 but also in response to high P concentration in nodules where respiration is expected to be not associated to SNF. [5][6][7][8][9][10][11][12][13][14][15][16] This is evidenced by the absence of correlation between the efficiency in use of rhizobial symbiosis and SNF.…”
Section: Relation With Oxidative Stress In N 2 -Fixing Nodulesmentioning
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