Abstract

An efficient regeneration protocol was applied to regenerate shoots on salt stress-tolerant calli lines of aubergine (Solanum melongena). These NaCl-tolerant cell lines were obtained by two different methods. On the one hand, the developed callus tissue was transferred to a medium with a continuous salt content of 40, 80, 120, or 160 mM NaCl. On the other hand, the callus tissue was subjected to a stepwise increasing salinity to 160 mM NaCl every 30 days. With the second method, calli which could be selected were characterized by compact growth, a greenish color, and absence of necrotic zones. When grown on salt-free medium again, NaCl-tolerant calli showed a decline in relative growth rate and water content in comparison to the control line. This was more obvious in the 120 mM NaCl-tolerant callus. Lipid peroxidase activity increased in 40 and 80 mM NaCl-tolerant calli; yet did not increase further in 120 mM-tolerant callus. An increase in ascorbic acid content was observed in 80 and 120 mM NaCl-tolerant calli compared to the 40 mM NaCl-tolerant lines, in which ascorbic acid content was twice that of the control. All NaCl-tolerant lines showed significantly higher superoxide dismutase (SOD) (208–305–370 µmol min−1 mg−1 FW) and catalase (CAT) (136–211–238 µmol min−1 mg−1 FW) activities compared to control plants (231 and 126 µmol min−1 mg−1 FW). Plants were regenerated on the calli lines that could tolerate up to 120 mM NaCl. From the 32 plants tested in vitro, ten plants with a higher number of leaves and root length could be selected for further evaluation in the field. Their high salt tolerance was evident by their more elevated fresh and dry weight, their more increased relative water content, and a higher number and weight of fruits compared to the wild-type parental control. The presented work shows that somaclonal variation can be efficiently used to develop salt-tolerant mutants.

Highlights

  • High salinity affects more than 1000 million hectares of land around the world, and it is one of the biggest challenges for agriculture today [1,2,3]

  • Callus tissue grown in 80 mM NaCl MS medium showed less cell expansion, with some brownish parts reflecting cell necrosis (Figure 1c)

  • We established an in vitro protocol to regenerate plantlets from induced calli in order to set up screening tests

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Summary

Introduction

High salinity affects more than 1000 million hectares of land around the world, and it is one of the biggest challenges for agriculture today [1,2,3]. Excess of salt interferes with various plant physiological and biochemical processes, resulting in problems such as ion imbalance, mineral deficiency, osmotic stress, ion toxicity, and oxidative stress [4], reducing yield [5]. Salt stress induces oxidative stress by increasing the formation of reactive oxygen species (ROS) [6]. Plants with high levels of antioxidants have been reported to have greater resistance to the salt-induced oxidative damage [6]. Earlier investigations on tolerance or susceptibility behavior, under salinity conditions, and overall plant scale were unable to discriminate the systemic from cellular salinity tolerance process [7]. Tissue culture approach has occurred as an effective method to underline the cellular mechanisms contributing to salt tolerance response through the use of in vitro obtained NaCl-tolerant lines [8]

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