We observed significant Selleckchem Alvocidib aggregation of proline in P. formosus associated plants growing under salinity stress, suggesting a decline in ionic influx inside the cellular masses and rescuing cucumber plants to maintain its osmotic balance. Similarly, higher nitrogen uptake by endophyte-inoculated plants under salinity suggested the regulation of sodium ion toxicity to indirectly maintain chlorophyll and osmotic
balance [47]. Sodium and chloride ion toxicity can trigger the formation of ROS which can damage cellular functioning [45–48]. Resultantly, accumulation of antioxidants inside plant can extend greater resistance to oxidative damage [48]. Higher DPPH radical scavenging activity in P. formosus inoculated plants suggest greater oxidative selleck inhibitor stress regulation than non-inoculated
plants [4]. Several studies have suggested that fungal symbiosis helps plants to mitigate stress by increasing Baf-A1 datasheet antioxidant activities [29, 46, 48]. Under salinity stress, phytohormones like ABA can protect plants by stomatal closure to minimize water loss and then mediates stress damage [49]. It is widely described that ABA contents in plants increase under salt stress [1, 50]. However, our finding shows significantly lower ABA level in endophyte-associated plants as compared to endophyte-free plants. Previously, Jahromi et al. [51] observed the same findings after association of Glomus intraradices with lettuce plants. Similarly, when soybean were given salinity stress in the presence of phytohormones producing endophytic fungi (Penicillium funiculosum and Aspergillus fumigatus), ABA levels were declined [15, 16], whilst the plants experienced lesser amount of stress. Since ABA is involved in the regulation of stress signalling during plant growth therefore, its biosynthesis can be affected by acetylcholine the presence of fungal interaction in abiotic stress. Although other studies suggests that fungal inoculation have increased the ABA content in leaves
and roots compared with non-inoculation control plants [52]. However, the effect may fluctuate among difference class of microorganisms and plant species as some earlier reports have elaborated this [44, 53]. There are several studied which narrates the same findings of low ABA levels under stress and fungal association [44]. Exogenous application of GA3 improved soybean salinity stress tolerance by increasing plant biomass while accumulating lesser ABA [54]. Iqbal and Ashraf [55] observed that GA3 application can results in altered level of ABA under salinity stress in Triticum aestivum L. Although, higher ABA in salinity is correlated with inhibition of leaf expansion and shoots development in different species [56] however, P.