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Bacillus subtilis improves maize tolerance to salinity

Bacillus subtilis melhora a tolerância do milho a salinidade

ABSTRACT:

The aim of this study was to evaluate the biochemical responses of maize, under saline stress, inoculated with Bacillus subtilis. Four levels of salinity were assessed: 0mM, 50mM, 100mM, and 200mM of sodium chloride (NaCl). Saline conditions influenced negatively maize growth. However, the inoculation of B. subtilis improved the plant growth at highest level of NaCl. Chlorophyll content decreased while proline increased in inoculated plants submitted to highest salt levels. Also, B. subtilis increased the relative water content in leaves. B. subtilis improves the plant growth under salinity and ameliorates the biochemical damages in maize.

Key words:
Zea mays; PGPB; biochemical responses; enzymes

RESUMO:

O objetivo do estudo foi avaliar a resposta bioquímica do milho, sob stresse salino, inoculado com Bacillus subtilis. Quatro níveis de salinidade foram avaliados: 0mM, 50mM, 100mM e 200mM de cloreto de sódio (NaCl). Condições salinas influenciaram negativamente o crescimento do milho. Entretanto, a inoculação com B. subtilis melhorou o crescimento das plantas no maior nível de NaCl. O teor de clorofila decresceu enquanto que a prolina aumentou em plantas submetidas aos níveis salinos e inoculadas com B. subtilis. B. subtilis também aumentou o conteúdo de agua foliar. A inoculação com B. subtilis promove melhor crescimento das plantas sob salinidade e atenua os danos bioquímicos no milho.

Palavras-chave:
Zea mays; BPCP; resposta bioquímica; enzimas

Salinity of agricultural soils is nowadays one the most important problem worldwide since this process causes losses of crop productivity every year. Although, this process influences the plant growth and affects its physiological responses, plant growth-promoting bacteria (PGPB) can ameliorate some negative effects of salinity on plant growth (SHRISVASTAVA & KUMAR, 2015). The PGPBs contribute to plant growth through of direct and indirect mechanisms, such as nitrogen fixation and plant hormones, also promoting tolerance to plants on abiotic stress (GLICK, 2012GLICK, B.R. Plant Growth-Promoting Bacteria: Mechanisms and Applications. Scientifica, v.18, e963401, 2012. <https://www.hindawi.com/journals/scientifica/2012/963401/>. Accessed: Aug. 13, 2017. doi: 10.6064/2012/963401.
https://www.hindawi.com/journals/scienti...
). Considering abiotic stress promoted by salinity, studies have shown that some specific bacteria can help plants to survive under high salinity conditions, such as Pseudomonas fluorescens (SARAVANAKUMAR & SAMIYAPPAN, 2007SARAVANAKUMAR, D.; SAMIYAPPAN, R. ACC deaminase from Pseudomonas fluorescens mediated saline resistance in groundnut (Arachis hypogea) plants. Journal of Applied Microbiology, v.102, p.1283-1292, 2007. <https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-2672.2006.03179.x>. Accessed: Aug. 13, 2017. doi: 10.1111/j.1365-2672.2006.03179.x.
https://onlinelibrary.wiley.com/doi/pdf/...
), and P. putida (GAMALERO et al., 2010GAMALERO, E. et al Interactions between Pseudomonas putida UW4 and Gigaspora rosea BEG9 and their consequences for the growth of cucumber under salt stress conditions. Journal Applied Microbiology, v.108, p.236-245, 2010. <http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2672.2009.04414.x/abstract>. Accessed: Aug. 12, 2017.
http://onlinelibrary.wiley.com/doi/10.11...
). Although, these previous studies have stated, basically, Pseudomonas as the most important species for helping plants against the salt stress, B. subtilis can also produce substances, such as enzymes and volatile organic compounds (VOCs), for stress tolerance (MEDEIROS et al., 2011MEDEIROS, F.H. et al. Transcriptional profiling in cotton associated with B. subtilis (UFLA285) induced biotic-stress tolerance. Plant & Soil, v.347, p.327-337, 2011. <https://link.springer.com/article/10.1007/s11104-011-0852-5>. Accessed: Aug. 12, 2017.
https://link.springer.com/article/10.100...
). FARAG et al. (2006FARAG, M.A. et al. GC-MS SPME profiling of rhizobacterial volatiles reveals prospective inducers of growth promotion and induced systemic resistance in plants. Phytochemistry v.67, p.2262-2268, 2006. <http://www.sciencedirect.com/science/article/pii/S0031942206004250>. Accessed: Aug. 12, 2017. doi: 10.1016/j.phytochem.2006.07.021.
http://www.sciencedirect.com/science/art...
) reported that B. subtilis releases some VOCs that promoted plant growth and abiotic stress tolerance in Arabidopsis. However, it is unclear how is the influence of B. subtilis on the responses of maize under salt stress. Therefore, we investigated the effect of salinity on biochemical activity and growth of maize inoculated with B. subtilis under controlled conditions.

Seeds of Zea mays (SYN 7205) were sterilized and sowed into plastic pots containing 15kg of Paleudult soil (pH in water - 6.6; organic matter -10g dm-3; P-68.8mg dm-3; H+Al, K, Ca and Mg-17.6, 3, 25.9 and 7.2mmolc dm-3, respectively). The strain of B. subtilis used in this was PRBS-1. This strain was isolated and characterized by ARAUJO et al. (2005aARAUJO, F.F. et al. Phytohormones and antibiotics produced by B. subtilis and their effects on seed pathogenic fungi and on soybean root development. World Journal of Microbiology & Biotechnology, v.21, p.1639-1645, 2005a. <https://link.springer.com/content/pdf/10.1007%2Fs11274-005-3621-x.pdf>. Accessed: Mar. 25, 2018.
https://link.springer.com/content/pdf/10...
). The experiment was carried out under greenhouse condition in a completely randomized design with four replicates. Treatments consisted of four NaCl concentrations (0mM, 50mM, 100mM and 200mM diluted with water) with and without inoculation of B. subtilis. The rhizobacteria in the concentration of 109 cells per mL was inoculated by using 0.1mL of suspension per seed. At 10 days after plant emergence, saline solutions were applied by irrigation three times a week during a period of 30 days. The volume of solution added in each irrigation was calculated according to gravimetric method based on evapotranspiration. The measurement of Chlorophyll (SPAD unit) was assessed 37 days after plant sowing through of a portable chlorophyll meter. Plants were collected 45 days after plant sowing for evaluation of plant biomass. Samples of fresh leaves were collected for evaluation of proline, peroxidase, and relative water content. Proline concentration was evaluated according to BATES et al. (1973BATES, L.S. et al. Rapid determination of free proline for water-stress studies. Plant & Soil, v.39, p.205-207, 1973. <https://link.springer.com/article/10.1007/BF00018060>. Accessed: Aug. 12, 2017.
https://link.springer.com/article/10.100...
). The evaluation of relative water content (RWC) was proceeded using the values of fresh mass weight (MF), turgid (MT) and dry matter (DM) from leaf discs, using the formula (BARRS & WEATHERLEY, 1962BARRS, H.D.; WEATHERLEY, P.E. A re-examination of the relative turgidity technique for estimating water deficit in leaves. Australian Journal of Biological Science, v.15, p.413-428, 1962.): RWC=(MF-MS)/(MT-MS)×100%. Guaiacol Peroxidase (GPX) was measured with guaiacol according to ARAUJO et al. (2005b)ARAUJO, A.S.F.; MONTEIRO, R.T.R.; CARDOSO, P.F. Composted textile sludge on soybean and wheat seedlings. Pesquisa Agropecuaria Brasileira, v.40, p.549-554, 2005b. <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100204X2005000600004&lng=en&nrm=iso&tlng=pt>. Accessed: Dec. 12, 2017.
http://www.scielo.br/scielo.php?script=s...
. Data were compared through analysis of variance (ANOVA). The means were compared by using least significant difference values calculated at the 5% level.

Saline conditions affected negatively the plant dry weight in both non-inoculated and inoculated plants, with average reductions of 85% and 95% for shoot and root, respectively, in the highest level of salinity (Table 1). However, at the treatments without salinity (control) and with the highest salt concentration, the inoculation of B. subtilis promoted higher shoot and root dry weight than treatments without B. subtilis. Similarly, the chlorophyll indices were higher in plants inoculated with B. subtilis in the treatments without salts and with the highest salt concentration (Figure 1A). At the highest NaCl concentration (200mM), proline concentration increased while RWC decreased in non-inoculated plants. Inoculation of B. subtilis promoted a reduction in proline concentration as compared with plant without B. subtilis (Figure 1B). In contrast, RWC decreased about 80% from control to the highest salts concentration in non-inoculated plants (Figure 1C). However, at the highest salts concentration, the presence of B. subtilis promoted an increase on RWC as compared with plant without B. subtilis. There was not negative or positive effect of the presence of B. subtilis on peroxidase concentration in maize (Figure 1D).

Table 1
Influence of inoculation with B. subtilis on the growth of maize in at four different levels of salinity.

Figure 1
Influence of inoculation with B. subtilis on chlorophyll (A), proline content (B), RWC (C), and peroxidase (D) in maize submitted to four different levels of salinity. White bars - without B. subtilis; black bars - with B. subtilis.

These results showed that B. subtilis promotes positive influence on plant growth under normal conditions (without salinity). However, it is important to report that, under salts stress condition, B. subtilis showed ability for inducing plants tolerance to high salt concentration. Usually, under high salinity condition, plants increase the biosynthesis of ethylene, as a signal of stress, by production of 1-aminocyclopropane-1-carboxylic acid (ACC) decreasing their growth (GLICK, 2012GLICK, B.R. Plant Growth-Promoting Bacteria: Mechanisms and Applications. Scientifica, v.18, e963401, 2012. <https://www.hindawi.com/journals/scientifica/2012/963401/>. Accessed: Aug. 13, 2017. doi: 10.6064/2012/963401.
https://www.hindawi.com/journals/scienti...
). However, ACC can also be metabolized by bacteria through ACC-deaminase, favoring the plant growth and ameliorating the stress (VAN DE POEL; VAN DER STRAETEN, 2014VAN DE POEL, B.; VAN DER STRAETEN, D. 1-aminocyclopropane-1-carboxylicacid (ACC) in plants: more than just the precursor of ethylene. Frontiers in Plant Science, v.5, p.1-11, 2014. doi: 10.3389/fpls.2014.00640. Accessed: Mar. 26, 2018.
https://doi.org/10.3389/fpls.2014.00640....
). Specifically, the isolate of B. subtilis used in this study was already characterized as an ACC deaminase producer (MOREIRA & ARAUJO, 2013MOREIRA, A.L.L.; Araújo, F.F. Bioprospection of Bacillus spp. as potential growth promoters in Eucalyptus urograndis. Revista Árvore, v.37, p.933-943, 2013. <http://www.scielo.br/pdf/rarv/v37n5/16.pdf>. Accessed: Aug. 15, 2017. doi: 10.1590/S0100-67622013000500016.
http://www.scielo.br/pdf/rarv/v37n5/16.p...
) and it may have contributed for better growth of maize plants under high salinity. Results showed a decrease of about 50% in the chlorophyll content in plants grown under the highest salt concentration, and it suggests that high salinity decreases the chlorophyll content in plants of maize. However, plant inoculated with B. subtilis presented better tolerance to salts and showed higher chlorophyll content than non-inoculated plants. Similarly, MAHMOUD et al. (2017MAHMOUD, O.M.B. et al. Response to salt stress is modulated by growth-promoting rhizobacteria inoculation in two contrasting barley cultivars Acta Physiologiae Plantarum, v.39, p.120-129, 2017. <https://link.springer.com/article/10.1007%2Fs11738-017-2421-x> Accessed: Mar. 26, 2018.
https://link.springer.com/article/10.100...
) verified the effect of salinity on wheat and reported an increase in chlorophyll content in inoculated plants submitted to 200mM of NaCl. This result may be associated with the better condition of water in the leaves in the inoculated plants under high salinity (Figure 1C). The lower water content in leaves is a signal of salts stress (FAHAD et al., 2015FAHAD, S. et al. Phytohormones and plant responses to salinity stress: a review. Plant Growth Regulation, v.75, p.391-404, 2015. <https://link.springer.com/article/10.1007/s10725-014-0013-y>. Accessed: Aug. 13, 2017. doi: 10.1007/s10725-014-0013-y.
https://link.springer.com/article/10.100...
), and B. subtilis could ameliorate this condition contributing for increasing water in leaves. It agrees with VARDHARAJULA et al. (2011VARDHARAJULA, S. et al. Drought-tolerant plant growth promoting Bacillus spp: effect on growth, osmolytes, and antioxidant status of maize under drought stress. Journal of Plant Interaction, v.6, p.1-14, 2011. <https://www.tandfonline.com/doi/abs/10.1080/17429145.2010.535178> Accessed: Mar. 26, 2018.
https://www.tandfonline.com/doi/abs/10.1...
) who reported that the inoculation of maize with Bacillus spp. alleviates the negative effect of drought stress by increasing relative water content in plants.

At the highest salinity concentration (200mM) there was an increase in the concentration of proline in treatment without B. subtilis as compared with the presence of Bacillus. Its accumulation in plants provides protection against salinity and drought stress (SINGH et al., 2014SINGH, M. et al. Proline and salinity tolerance in plants. Biochemical Pharmacology, v.3, e170, 2014. <https://www.omicsonline.org/open-access/proline-and-salinity-tolerance-in-plants-2167-0501.1000e170.pdf>. Accessed: Mar. 25, 2018.
https://www.omicsonline.org/open-access/...
). It can be associated with content of water in leaves since there is a strong correlation between water potential in leaves and the concentration of proline (NADEEM et al., 2010NADEEM, S.M. et al. Rhizobacteria capable of producing ACC-deaminase may mitigate salt stress in wheat. Soil Science Society American Journal, v.74, p.533-542, 2010. <https://dl.sciencesocieties.org/publications/sssaj/abstracts/74/2/533?access=0&view=pdf>. Accessed: Aug. 15, 2017. doi: 10.2136/sssaj2008.0240.
https://dl.sciencesocieties.org/publicat...
). It means that proline is important for maintenance of water in leaves. However, the presence of B. subtilis decreased the concentration of proline under highest salinity concentration and it was also observed by NADEEM et al. (2010)NADEEM, S.M. et al. Rhizobacteria capable of producing ACC-deaminase may mitigate salt stress in wheat. Soil Science Society American Journal, v.74, p.533-542, 2010. <https://dl.sciencesocieties.org/publications/sssaj/abstracts/74/2/533?access=0&view=pdf>. Accessed: Aug. 15, 2017. doi: 10.2136/sssaj2008.0240.
https://dl.sciencesocieties.org/publicat...
in wheat under salts stress. In this study, there was an increase in the peroxidase activity when the plants were submitted to salts stress. However, there was not reported positive effect of B. subtilis on the peroxidase activity under salts stress. Although, results showed lower activity of peroxidase in inoculated plants in soil without salinity, it confirms that PGPBs can collaborate with plants in the decrease in peroxidase activity, so decreasing the oxidative damages, as also reported in maize inoculated with Pseudomonas spp. (SANDHYA et al., 2010SANDHYA, V. et al. Effect of plant growth promoting Pseudomonas spp. on compatible solutes. antioxidant status and plant growth of maize under drought stress. Plant Growth Regulation, v.62, p.21-30, 2010. <https://link.springer.com/article/10.1007/s10725-010-9479-4>. Accessed: Aug. 12, 2017. doi: 10.1007/s10725-010-9479-4.
https://link.springer.com/article/10.100...
). Results suggested that B. subtilis presents significant positive influence on growth and biochemical activity of plants under salts stress. This study showed that the inoculation of B. subtilis promoted better plant growth under salinity condition. Amelioration of biochemical damages in maize with inoculation of B. subtilis indicates that this PGPB present potential for promoting tolerance of plants to salinity.

REFERENCES:

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    CR-2017-0910.R2

Publication Dates

  • Publication in this collection
    2018

History

  • Received
    14 Dec 2017
  • Accepted
    01 July 2018
  • Reviewed
    14 July 2018
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