Salicylic acid restrains arsenic induced oxidative burst in two varieties of Artemisia annua L. by modulating antioxidant defence system and artemisinin production

2020 ◽  
Vol 202 ◽  
pp. 110851 ◽  
Author(s):  
M. Naeem ◽  
Yawar Sadiq ◽  
Ajmat Jahan ◽  
Aarifa Nabi ◽  
Tariq Aftab ◽  
...  
2015 ◽  
Vol 66 (2) ◽  
pp. 145 ◽  
Author(s):  
Nimir Eltyb Ahmed Nimir ◽  
Shiyuan Lu ◽  
Guisheng Zhou ◽  
Wenshan Guo ◽  
Baoluo Ma ◽  
...  

Salinity and high temperature are major abiotic stresses limiting sustainable crop production. Seed priming is a useful tool to enhance seedling growth and the antioxidant defence system of crops under salinity and temperature stress. This experiment was designed to determine the effects of gibberellic acid (GA3, 288.7 µm), kinetin (232.2 µm) and salicylic acid (362 µm) on some morphological and physiological parameters of sweet sorghum (Sorghum bicolor L. Moench) hybrid Yajin 13 under salinity (0, 100 and 200 mm NaCl) and temperature (25°C and 37°C) stress. Salinity and high temperature significantly reduced emergence percentage, shoot and root lengths, number of leaves, shoot fresh and dry weight, and chlorophyll a and b content. The activity of superoxide dismutase (SOD) and malondialdehyde (MDA) content were increased with an increase in both salinity and temperature stress. Hormone treatments positively affected all parameters except root fresh and dry weight, number of leaves, SOD activity and chlorophyll a. Under salinity stress at 200 mm NaCl, treatment with salicylic acid increased emergence percentage, emergence rate, chlorophyll b and protein content by 82.0%, 130%, 7.9% and 1.9%, respectively, relative to the control (no treatment). At 37°C, salicylic acid increased emergence percentage, emergence rate and number of roots by 72.5%, 108.5% and 63.8%, respectively, and decreased MDA content by 17.6% relative to the control. Our study indicated that seed priming with an appropriate concentration of exogenous hormones (salicylic acid, kinetin, GA3) is a useful, easy method for improving germination, seedling growth and the antioxidant defence system of sweet sorghum under conditions of high temperature and salinity.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Ana Maria Murta Santi ◽  
Paula Alves Silva ◽  
Isabella Fernandes Martins Santos ◽  
Silvane Maria Fonseca Murta

Abstract Background Superoxide dismutase (SOD), a central component of the antioxidant defence system of most organisms, removes excess superoxide anions by converting them to oxygen and hydrogen peroxide. As iron (Fe) SOD is absent in the human host, this enzyme is a promising molecular target for drug development against trypanosomatids. Results We obtained Leishmania infantum mutant clones with lower FeSOD-A expression and investigated their phenotypes. Our attempts to delete this enzyme-coding gene using three different methodologies (conventional allelic replacement or two different CRISPR/methods) failed, as FeSOD-A gene copies were probably retained by aneuploidy or gene amplification. Promastigote forms of WT and mutant parasites were used in quantitative reverse-transcription polymerase chain reaction (RT-qPCR) and western blot analyses, and these parasite forms were also used to assess drug susceptibility. RT-qPCR and western blot analyses revealed that FeSOD-A transcript and protein levels were lower in FeSOD-A−/−/+L. infantum mutant clones than in the wild-type (WT) parasite. The decrease in FeSOD-A expression in L. infantum did not interfere with the parasite growth or susceptibility to amphotericin B. Surprisingly, FeSOD-A−/−/+L. infantum mutant clones were 1.5- to 2.0-fold more resistant to trivalent antimony and 2.4- to 2.7-fold more resistant to miltefosine. To investigate whether the decrease in FeSOD-A expression was compensated by other enzymes, the transcript levels of five FeSODs and six enzymes from the antioxidant defence system were assessed by RT-qPCR. The transcript level of the enzyme ascorbate peroxidase increased in both the FeSOD-A−/−/+ mutants tested. The FeSOD-A−/−/+ mutant parasites were 1.4- to 1.75-fold less tolerant to oxidative stress generated by menadione. Infection analysis using THP-1 macrophages showed that 72 h post-infection, the number of infected macrophages and their intracellular multiplication rate were lower in the FeSOD-A−/−/+ mutant clones than in the WT parasite. Conclusions The unsuccessful attempts to delete FeSOD-A suggest that this gene is essential in L. infantum. This enzyme plays an important role in the defence against oxidative stress and infectivity in THP-1 macrophages. FeSOD-A-deficient L. infantum parasites deregulate their metabolic pathways related to antimony and miltefosine resistance. Graphic Abstract


2014 ◽  
Vol 20 (2) ◽  
pp. 161-169 ◽  
Author(s):  
Lin Li ◽  
Haihui Zhang ◽  
Li Zhang ◽  
Yonghong Zhou ◽  
Ruiwu Yang ◽  
...  

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