Jakub Dobrzyński
Zuzanna Jakubowska- Institute of Technology and Life Sciences—National Research Institute, Falenty, Poland
Plant Growth-Promoting Bacteria (PGPB) are a promising alternative to conventional fertilization. One of the most interesting PGPB strains, among the spore-forming bacteria of the phylum Firmicutes, is Bacillus pumilus. It is a bacterial species that inhabits a wide range of environments and shows resistance to abiotic stresses. So far, several PGPB strains of B. pumilus have been described, including B. pumilus LZP02, B. pumilus JPVS11, B. pumilus TUAT-1, B. pumilus TRS-3, and B. pumilus EU927414. These strains have been shown to produce a wide range of phytohormones and other plant growth-promoting substances. Therefore, they can affect various plant properties, including biometric traits, substance content (amino acids, proteins, fatty acids), and oxidative enzymes. Importantly, based on a study with B. pumilus WP8, it can be concluded that this bacterial species stimulates plant growth when the native microbiota of the inoculated soil is altered. However, there is still a lack of research with deeper insights into the structure of the native microbial community (after B. pumilus application), which would provide a better understanding of the functioning of this bacterial species in the soil and thus increase its effectiveness in promoting plant growth.
Introduction
Bacillus pumilus is a Gram-positive, spore-forming bacteria, which commonly occurs in various environments including marine water, deep-sea sediments, and soil (Priest, 1993; Shivaji et al., 2006; Liu et al., 2013; Pudova et al., 2022; Yakovleva et al., 2022; Zhang et al., 2022). This species exhibits significant resistance to environmental stresses, e.g., low or no nutrient availability, drought, irradiation, UV radiation, chemical disinfectants, or oxidizing enzymes (Nicholson et al., 2000). Previously, Bacillus pumilus was included in the Bacillus subtilis group. Currently, Bacillus pumilus belongs to the Bacillus pumilus group which also includes B. altitudinis, B. australimaris, B. safensis, B. xiamenensis, and B. zhangzhouensis (Chen et al., 2016).
Progressive climate change and environmental pollution are intensifying the development of eco-friendly fertilizers (Čimo et al., 2020; Dobrzyński et al., 2021; Kasperska-Wołowicz et al., 2021; Wierzchowski et al., 2021; Zielewicz et al., 2021; Heyi et al., 2022). One of the best solutions for safe fertilization appears to be fertilizers based on plant growth-promoting bacteria (Čimo et al., 2020). Due to its properties, Bacillus pumilus is classified as a plant growth-promoting bacteria (PGPB; Gutiérrez-Mañero et al., 2001; De-Bashan et al., 2010; Kaushal et al., 2017). PGPB can stimulate plant growth either directly or indirectly. Mechanisms of direct action are defined as the use of bacterial traits that result in the direct promotion of plant growth, including the production of auxins, e.g., indole-3-acetic acid (IAA), 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase, cytokinins, gibberellins, atmospheric nitrogen fixation (nitrogenase production), phosphorus solubilization, and iron sequestration (by production bacterial siderophores). In contrast, indirect mechanisms relate to the properties of bacteria that inhibit the functioning of one or more plant pathogenic organisms. Indirect mechanisms include, e.g., the production of antibiotics (e.g., cyclic lipopeptides), enzymes that degrade the cell wall of fungi (including chitinases and β-1,3 glucanases), and production of hydrogen cyanide (HCN) inducing plant resistance (e.g., against fungal phytopathogens; Joo et al., 2005; Cuong and Hoa, 2021; Lipková et al., 2021; Shahid et al., 2021; Bessai et al., 2022; Mirskaya et al., 2022)
The mini-review aims to summarize the current state of knowledge on the Bacillus pumilus plant growth promotion properties and highlight the lack in the literature on this issue.
Overall potential of Bacillus pumilus
Bacillus pumilus is one of the most studied bacterial strains in terms of promoting the growth of bacteria from the genus Bacillus. So far, it has been found that B. pumilus is capable of producing several phytohormones. Gutiérrez-Mañero et al. (2001) detected a few gibberellins (GA1, GA3, GA4, and GA20) in the culture of B. pumilus using full-scan gas chromatography and mass spectrometry assays. Joo et al. (2005) found other gibberellins derived from this species (strain no. CJ-69), including a few new ones such as GA5, GA8, GA34, GA44, and GA5. B. pumilus is also able to produce other traits that directly promote plant growth. Isolated from the tea rhizosphere, B. pumilus TRS-3 showed the production of indole 3-acetic acid (IAA), siderophore, and phosphate solubilization (Chakraborty et al., 2013). Besides, B. pumilus JPVS11 is capable of producing ACC deaminase which contributes to decreasing ethylene levels in the plants by degrading ACC (Kumar et al., 2021). Importantly, B. pumilus is also capable of fixing atmospheric N2 by nitrogenase production which reduces this nitrogen form to ammonia (Masood et al., 2020). Other authors also detected these plant growth-promoting traits in B. pumilus (Hafeez et al., 2006; Murugappan et al., 2013; Upadhyay et al., 2019).
Promoting plant growth under different growing conditions
To date, several papers have been published on the effect of various B. pumilus strains on plant growth parameters. The inoculation efficiency of B. pumilus was studied in various conditions including in vitro, growth chambers, greenhouses, and in-field conditions. A lot of these studies focus on rice growth promotion and deal mainly with biometric parameters and chemical properties of shoots and roots (Win et al., 2018; Ngo et al., 2019; Liu et al., 2020) Importantly, both commercial strains and soil isolates are used to study on the effects of bacteria on the efficiency in promoting plant growth.
The research based on growing plants on Murashige and Skoog liquid medium has proven that the strain B. pumilus LZP02 is able to promote rice growth by increasing the root length, root surface area, number of nodes, root tips, forks, and chlorophyll content (Liu et al., 2020). In addition, the application of B. pumilus LZP02 also caused an increase in nitrogen, phosphorus, calcium, and magnesium contents in rice roots (Liu et al., 2020). Previously, it was proven that B. pumilus promotes rice growth under growth chamber conditions (Ngo et al., 2019) B. pumilus TUAT1 significantly enhanced growth, root development, and nutrient absorption in 21-day-old rice seedlings compared to the control. Interestingly, significantly better efficiency of the studied strain was obtained after inoculating plants with spores than vegetative cells (Ngo et al., 2019).
As well, it has been reported that B. pumilus may be a good growth promoter of other plants, including grasses, trees, and others. For instance, after the application of B. pumilus of Alnus glutinosa, higher values of parameters linked with root system (in both studied soil types) and an increase in shoot surface (in one of the studied soil types) was documented compared to control (Ramos et al., 2003). Subsequently, the application of B. pumilus caused an increase in plant height, number of leaves and branches in Chinese tea under in vivo conditions (Chakraborty et al., 2013). Moreover, after inoculation of lentils (Lens culinaris Medik.) by B. pumilus, Siddiqui et al. (2007) noted an increase in plant length and plant fresh weight. Ahmad et al. (2012) also noted that inoculation B. pumilus of Lollium multiflorum led to increased biomass and growth of plants. Inoculation of wheat (var. Orkhon) by B. pumilus led to increasing root length, root area, shoot dry weight, and P and N contents in aboveground plants (Hafeez et al., 2006).
Interestingly, B. pumilus can also be an endophytic bacteria. This species was isolated from tissue surfaces of Ocimum sanctum and its ability to colonize tissues was confirmed by scanning electron microscopy (SEM; Murugappan et al., 2013). Importantly, the inoculation of Octimum sanctum by this species also caused an increase in root and shoot length and leaves number compared to non-inoculated treatment (Murugappan et al., 2013).
Recently it has been suggested that B. pumilus promotes plant growth better in combination with nitrogen fertilizers (Win et al., 2018; Masood et al., 2020). Strain B. pumilus TUAT-1 with added nitrogen fertilization increased the height, biomass, and chlorophyll content of 21-day-old rice seedlings); (what is important, this study was conducted under field conditions (Win et al., 2018). Next, Masood et al. (2020) carried out a study to determine the main mechanisms relating to PGPB-improved N nutrition in tomatoes under greenhouse conditions. The authors recorded an interesting pattern, namely B. pumilus improves tomato growth and N uptake only under N fertilization. Moreover, B. pumilus inoculation under nitrogen fertilization increased leaf chlorophyll contents, plant height, shoot fresh weight, and shoot dry weight in comparison with only bacteria inoculation treatment.
It was also documented that Bacillus pumilus is able to enhance the activity of a few antioxidant enzymes from the oxidoreductase class, including peroxidase, ascorbate peroxidase, superoxide dismutase, catalase, glutathione reductase, and adenosine triphosphatase in inoculated plants (Liu et al., 2020); (Shahzad et al., 2021). Besides, B. pumilus may cause an increase in soil enzyme activity such as alkaline phosphatase, acid phosphatase, urease, and β-glucosidase (Kumar et al., 2021).
Promoting plant growth under plant stress conditions
Bacillus pumilus has also been shown to promote plant growth under abiotic stress conditions (Kumar et al., 2021; Shahzad et al., 2021). Recently, it was found that B. pumilus can promote plant growth under salinity stress (Kumar et al., 2021). Positive effects of rice inoculation by B. pumilus JPVS11 (pot experiment) such as the enhancement of plant height, root length, and plant fresh weight were observed at the various values of NaCl concentration (0, 50, 100, 200, and 300 mM). Furthermore, B. pumilus also may promote plant growth in conditions of Cd contamination; maize seeds inoculation with B. pumilus contributed to an increase in the germination percentage, shoot length, leaf length, number of leaves, and plant fresh weight at different concentrations of CdSO4 (Shahzad et al., 2021). In addition, Khan et al. (2016) conducted a study on plant growth-promoting properties of rice seedlings by B. pumilus under saline and high boron (B) conditions. In non-inoculated treatment, they observed high values of B and salt toxic ions in leaves. On the other hand, there are also studies that show the lack of plant growth promotion by B. pumilus under abiotic stress conditions. This phenomenon was found in a study on several plants of the Brassica genus under caesium-contaminated conditions (Aung et al., 2015).
Mechanisms of promoting plant growth
Importantly, inoculation of plants by B. pumilus may affect the expression of genes related to root development, for instance, this bacteria increased transcript abundance CRL5 (Murugappan et al., 2013), which regulates crown root formation by expression activation of the OsRR1. It is a gene of rice which encodes a negative regulator of cytokinin signaling (Radhakrishnan et al., 2017). Moreover, B. pumilus may decrease transcript abundance WOX11 (Ngo et al., 2019), which contributes to the repression of OsRR2 (Cheng et al., 2016). This fact indicates that the impact of B. pumilus on the expression of previously mentioned rice genes may be one of its mechanisms of plant growth promotion (Ngo et al., 2019).
Plant growth promotion by Bacillus pumilus in co-inoculation
There are also results describing the potential to promote plant growth in consortia with other microorganisms. A consortium composed of B. pumilus EU927414, Pseudomonas medicona EU927412, and Arthrobacter sp. EU927410 led to a 24% increase in wheat yield compared to the control under field conditions (Upadhyay et al., 2019). In addition, it has been documented that the application of the consortium of B. pumilus and Bacillus subtilis increased values of crude protein, dry matter, fat, and carbohydrate in amaranth grains. Besides, in this study, a significant increase in a few amino acid values including methionine lysine and tryptophan was recorded in the studied sample (Pandey et al., 2018). Also dos Santos et al. (2018) used a combined application of B. pumilus and B. subtilis, however, in sugarcane cultivation. There, together with mineral fertilization and filter cake compost, the solution improved shoot and root growth, as well as increased phosphorus content in soil up to 13% compared to untreated control. Another example of co-inoculation is the application of B. pumilus CECT 5105 in combination with Bacillus licheniformis CECT 5106 and mycorrhizal fungus Pisolithus tinctorius to enhance Pinus pinea seedlings growth (Probanza et al., 2001). In this study, authors did not observe a synergic effect with mycorrhizal infection, however, the inoculation by various consortiums showed an increase in a few biometric parameters of the studied plant. For example, B. pumilus and Pisolithus tinctorius combination led to an increase in aerial and root system parameters.
Effect of Bacillus pumilus on native soil microbiota and post-inoculation tracking of its abundance
A very important aspect related to the application of PGPB is their impact on the indigenous microbiota of the inoculated soil or rhizosphere. Assessing the impact of plant growth-promoting bacteria on the soil microbiota can be crucial to its effectiveness. So far, there are several papers considering the B. pumilus effect on the formation of native microbial communities. For instance, (De-Bashan et al., 2010) revealed that inoculation with B. pumilus may shift the bacterial community over 60 days under greenhouse conditions and documented that B. pumilus prefers to colonize the roots tips and root elongation area (FISH analysis). Besides, using denaturing gradient gel electrophoresis (PCR-DGGE), Kang et al. (2013) conducted a study on the reaction of soil bacterial community soil under fava beans to B. pumilus WP8 and its post-inoculation monitoring in soil. Their results indicated that the studied strain survived in large numbers up to 40 days in bulk soil and shifted the bacterial community, especially dominant taxon populations. However, despite the short-lived studied strain in soil, it exhibits the ability to promote fava bean seedlings for at least 90 days; the inoculation of B. pumilus WP8 enhanced shoot length, aboveground dry weight, root length, and root dry weight. Interestingly, in the case of another Bacillus strain, Bacillus amyloliquefaciens NJN-6, using the qPCR technique, (Fu et al., 2017) recorded its stable abundance in the rhizosphere soil of banana plantation within 3 years of inoculation (in the range of 2.5–3.0 log copies of 16S rRNA gene per gram of soil). Also, it is worth mentioning that the survival rate of bacterial inoculants in the soil largely depends on the indigenous soil microbiota; the survival of PGPB in the soil is high when the diversity of native microbiota is low and vice versa (Mallon et al., 2015; Manfredini et al., 2021). In addition, (Bueno et al., 2022) carried out an interesting study on the persistence of B. subtilis in the endosphere of soybean roots, showing that after the application of concentrations of 1 × 104 CFU ml−1 and 1 × 1010 ml−1, a higher abundance of this strain was recorded a few weeks after inoculation compared to B. subtilis abundance in treatment: B. subtilis + mineral fertilization (the study based on transformed B. subtilis with ampicillin resistance gene).
The PLFA (phospholipid fatty acid) technique was also used to assess the response of native soil microbiota to B. pumilus application. The introduction of a consortium composed of B. pumilus and B. licheniformis shifted the rhizosphere microbiota, despite the low abundance of both strains in the final phase of the study (Probanza et al., 2001). Another example of using PLFA to evaluate native microbiota reaction to B. pumilus inoculation is a study conducted by (Ramos et al., 2003). The authors observed changes in the rhizosphere microbial community in one of the studied soil types from Alnus glutinosa cultivation (Ramos et al., 2003).
The only study assessing the status of the native microbiota following the application of B. pumilus (strain TUAT-1) was conducted by (Win et al., 2020) using Next-Generation Sequencing (NGS). The researchers studied B. pumilus TUAT-1 effect on the microbiota of bulk soil, rhizosphere, and root endosphere in forage rice 2 and 5 weeks after transplantation under greenhouse conditions. B. pumilus TUAT-1 shifted the microbial community of rhizosphere and roots endosphere, e.g., this bacterial strain significantly contributed to an increase in the Desulfuromonadales abundance and a decrease of the abundance of Xanthomonadales 5 weeks after transplantation of rice. While in the bacterial community of root endosphere, B. pumilus TUAT-1 significantly enhanced the relative abundance of Acidobacteriales, Saprospirales, and Alteromonadales 2 weeks after transplanting in comparison with control treatment. However, in bulk soil, the author did not note such a significant alteration in native microbiota after the introduction of the above-mentioned PGPB. Moreover, compared to the control, B. pumilus TUAT-1 enhanced bacterial biodiversity, including Shannon diversity in the rhizosphere and root endosphere 2 weeks after transplanting. Importantly, using qPCR techniques, the researchers also demonstrated that B. pumilus TUAT-1 persisted in the rhizosphere soil 2 and 5 weeks after transplanting of rice (Win et al., 2020). Different patterns after the introduction of B. subtilis into the soil were noted by dos (Dos Santos et al., 2022). The authors showed that B. subtilis application did not affect the root endophytic microbial community of soybean (greenhouse conditions), which was also evaluated by alpha diversity metrics. Importantly, it is still unclear whether the PGPB effect on native microbiota can be long-term. This phenomenon may depend on many factors, including the soil’s chemical properties, the stage of plant development, plant root exudates, or indeed the biodiversity and composition of the native microbial community. Hence, there is a need for further studies on the effects of PGPB on indigenous endophytic microbiota and soil microbiota, both for B. pumilus and other strains of the Bacillus genus (Manfredini et al., 2021).
Conclusion
Bacillus pumilus is a very interesting PGPB strain that has already been incorporated into the commercial circuit. Despite that, there are deficiencies in the literature in several areas. There is still a lot to be understood about the reaction of various plants to the inoculation of B. pumilus. The need for further research in this field is determined by the specificity of the plant rhizosphere microbiome, which can interact differently with B. pumilus strains and vice versa. In addition, it is vital to test the effectiveness of this bacterium on different soil types with different physicochemical properties. Importantly, there is a very small number of studies assessing the impact of B. pumilus on the native microbiota using NGS (only one paper to date). NGS offers the possibility of a more detailed analysis of the bacterial community structure than DGGE or PLFA. Hence, it is possible to find the abundance of important taxa involved in biochemical changes in the soil. e.g. whether the abundance of oligotrophic bacteria, including Acidobacteria, decreased after inoculation with the B. pumilus strain. Also, in order to test the effect of alterations in the native microbiota under the influence of PGPB, studies of this type should be conducted over a long period of time (even up to several years) and under field conditions. Finally, it is worth mentioning that there is also a lack of studies on the tracking of B. pumilus strains in soil (bulk and rhizosphere soil) or plant tissues after its introduction, especially in the long term aspect.
Author contributions
JD contributed to conception of the minireview. JD, ZJ, and BD wrote the first draft of the manuscript. All authors contributed to manuscript revision, read, and approved the submitted version.
Acknowledgments
Many thanks to Katarzyna Rafalska for English proofreading.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
Ahmad, F., Iqbal, S., Anwar, S., Afzal, M., Islam, E., Mustafa, T., et al. (2012). Enhanced remediation of chlorpyrifos from soil using ryegrass (Lollium multiflorum) and chlorpyrifos-degrading bacterium Bacillus pumilus C2A1. J. Hazard. Mater. Lett. 237-238, 110–115. doi: 10.1016/j.jhazmat.2012.08.006
Aung, H. P., Djedidi, S., Oo, A. Z., Aye, Y. S., Yokoyama, T., Suzuki, S., et al. (2015). Growth and 137Cs uptake of four brassica species influenced by inoculation with a plant growth-promoting rhizobacterium Bacillus pumilus in three contaminated farmlands in Fukushima prefecture. Japan. Sci. Total. Environ. 521-522, 261–269. doi: 10.1016/j.scitotenv.2015.03.109
Bessai, S. A., Bensidhoum, L., and Nabti, E. H. (2022). Optimization of IAA production by telluric bacteria isolated from northern Algeria. Biocatal. Agric. Biotechnol. 41:102319. doi: 10.1016/j.bcab.2022.102319
Bueno, C. B., Dos Santos, R. M., de Souza Buzo, F., and Rigobelo, E. C. (2022). Effects of chemical fertilization and microbial inoculum on Bacillus subtilis colonization in soybean and maize plants. Front. Microbiol. 13:901157. doi: 10.3389/fmicb.2022.901157
Chakraborty, U., Chakraborty, B. N., and Roychowdhury, P. (2013). Plant growth promoting activity of Bacillus pumilus in tea (Camellia sinensis) and its biocontrol potential against Poria hypobrunnea. Indian. Phytopathol. 66, 387–396.
Chen, L., Liu, Y., Wu, G., Veronican Njeri, K., Shen, Q., Zhang, N., et al. (2016). Induced maize salt tolerance by rhizosphere inoculation of bacillus amyloliquefaciens SQR9. Physiol. Plant. 158, 34–44. doi: 10.1111/ppl.12441
Cheng, S., Zhou, D. X., and Zhao, Y. (2016). WUSCHEL-related homeobox gene WOX11 increases rice drought resistance by controlling root hair formation and root system development. Plant Signal. Behav. 11:e1130198. doi: 10.1080/15592324.2015.1130198
Čimo, J., Šinka, K., Tárník, A., Aydin, E., Kišš, V., and Toková, L. (2020). Impact of climate change on vegetation period of basic species of vegetables in Slovakia. J. Water Land Dev. 47, 38–46. doi: 10.24425/jwld.2020.135030
Cuong, P. V., and Hoa, N. P. (2021). Optimization of culture condition for iaa roduction by Bacillus sp. isolated from cassava field of Vietnam. Vietnam. J. Sci. Technol. 59, 312–323. doi: 10.15625/2525-2518/59/3/15600
De-Bashan, L. E., Hernandez, J. P., Bashan, Y., and Maier, R. M. (2010). Bacillus pumilus ES4: candidate plant growth-promoting bacterium to enhance establishment of plants in mine tailings. Environ. Exp. Bot. 69, 343–352. doi: 10.1016/j.envexpbot.2010.04.014
Dobrzyński, J., Wierzchowski, P. S., Stępień, W., and Górska, E. B. (2021). The reaction of cellulolytic and potentially cellulolytic spore-forming bacteria to various types of crop management and farmyard manure fertilization in bulk soil. Agronomy 11:772. doi: 10.3390/agronomy11040772
Dos Santos, R. M., Cueva-Yesquén, L. G., Garboggini, F. F., Desoignies, N., and Rigobelo, E. C. (2022). Inoculum concentration and mineral fertilization: effects on the endophytic microbiome of soybean. Front. Microbiol. 13:900980. doi: 10.3389/fmicb.2022.900980
Dos Santos, R. M., Kandasamy, S., and Rigobelo, E. C. (2018). Sugarcane growth and nutrition levels are differentially affected by the application of PGPR and cane waste. MicrobiologyOpen. 7:e00617. doi: 10.1002/mbo3.617
Fu, L., Penton, C. R., Ruan, Y., Shen, Z., Xue, C., Li, R., et al. (2017). Inducing the rhizosphere microbiome by biofertilizer application to suppress banana Fusarium wilt disease. Soil Biol. Biochem. 104, 39–48. doi: 10.1016/j.soilbio.2016.10.008
Gutiérrez-Mañero, F. J., Ramos-Solano, B., Probanza, A. N., Mehouachi, J., R. Tadeo, F., and Talon, M. (2001). The plant-growth-promoting rhizobacteria Bacillus pumilus and bacillus licheniformis produce high amounts of physiologically active gibberellins. Physiol. Plan. 111, 206–211. doi: 10.1034/j.1399-3054.2001.1110211.x
Hafeez, F. Y., Yasmin, S., Ariani, D., Renseigné, N., Zafar, Y., and Malik, K. A. (2006). Plant growth-promoting bacteria as biofertilizer. Agron. Sustain. Dev. 26, 143–150. doi: 10.1051/agro:2006007
Heyi, E. A., Dinka, M. O., and Mamo, G. (2022). Assessing the impact of climate change on water resources of upper Awash River sub-basin. Ethiopia. J. Water Land Dev. 52, 232–244. doi: 10.24425/jwld.2022.140394
Joo, G. J., Kim, Y. M., Kim, J. T., Rhee, I. K., Kim, J. H., and Lee, I. J. (2005). Gibberellins-producing rhizobacteria increase endogenous gibberellins content and promote growth of red peppers. J. Microbiol. 43, 510–515.
Kang, Y., Shen, M., Wang, H., and Zhao, Q. (2013). A possible mechanism of action of plant growth-promoting rhizobacteria (PGPR) strain Bacillus pumilus WP8 via regulation of soil bacterial community structure. J. Gen. Appl. Microbiol. 59, 267–277. doi: 10.2323/jgam.59.267
Kasperska-Wołowicz, W., Rolbiecki, S., Sadan, H. A., Rolbiecki, R., Jagosz, B., Stachowski, P., et al. (2021). Impact of the projected climate change on soybean water needs in the Kuyavia region in Poland. J. Water. Land. Dev. 51, 199–207. doi: 10.24425/jwld.2021.139031
Kaushal, M., Kumar, A., and Kaushal, R. (2017). Bacillus pumilus strain YSPMK11 as plant growth promoter and biocontrol agent against Sclerotinia sclerotiorum. 3 Biotech 7, 90–99. doi: 10.1007/s13205-017-0732-7
Khan, A., Zhao, X. Q., Javed, M. T., Khan, K. S., Bano, A., Shen, R. F., et al. (2016). Bacillus pumilus enhances tolerance in rice (Oryza sativa L.) to combined stresses of NaCl and high boron due to limited uptake of Na+. Environ. Exp. Bot. 124, 120–129. doi: 10.1016/j.envexpbot.2015.12.011
Kumar, A., Singh, S., Mukherjee, A., Rastogi, R. P., and Verma, J. P. (2021). Salt-tolerant plant growth-promoting Bacillus pumilus strain JPVS11 to enhance plant growth attributes of rice and improve soil health under salinity stress. Microbiol. Res. 242:126616. doi: 10.1016/j.micres.2020.126616
Lipková, N., Cinkocki, R., Maková, J., Medo, J., and Javoreková, S. (2021). Characterization of endophytic bacteria of the genus bacillus and their influence on the growth of maize (Zea mays) in vivo. J. Microbiol. Biotechnol. Food Sci. 10:e3602. doi: 10.15414/jmbfs.3602
Liu, Y., Lai, Q., Dong, C., Sun, F., Wang, L., Li, G., et al. (2013). Phylogenetic diversity of the Bacillus pumilus group and the marine ecotype revealed by multilocus sequence analysis. PLoS One 8:e80097. doi: 10.1371/journal.pone.0080097
Liu, H., Wang, Z., Xu, W., Zeng, J., Li, L., Li, S., et al. (2020). Bacillus pumilus LZP02 promotes rice root growth by improving carbohydrate metabolism and phenylpropanoid biosynthesis. Mol. Plant-Microbe Interact. 33, 1222–1231. doi: 10.1094/MPMI-04-20-0106-R
Mallon, C., Poly, F., Le Roux, X., Marring, I., van Elsas, J. D., and Salles, J. F. (2015). Resource pulses can alleviate the biodiversity – invasion relationship in soil microbial communities. Ecology 96, 915–926. doi: 10.1890/14-1001.1
Manfredini, A., Malusà, E., Costa, C., Pallottino, F., Mocali, S., Pinzari, F., et al. (2021). Current methods, common practices, and perspectives in tracking and monitoring bioinoculants in soil. Front. Microbiol. 12:698491. doi: 10.3389/fmicb.2021.698491
Masood, S., Zhao, X. Q., and Shen, R. F. (2020). Bacillus pumilus promotes the growth and nitrogen uptake of tomato plants under nitrogen fertilization. Sci. Hortic. 272:109581. doi: 10.1016/j.scienta.2020.109581
Mirskaya, G. V., Khomyakov, Y. V., Rushina, N. A., Vertebny, V. E., Chizhevskaya, E. P., Chebotar, V. K., et al. (2022). Plant development of early-maturing spring wheat (Triticum aestivum L.) under inoculation with bacillus sp. V2026. Plan. Theory 11:1817. doi: 10.3390/plants11141817
Murugappan, R. M., Begum, S. B., and Roobia, R. R. (2013). Symbiotic influence of endophytic Bacillus pumilus on growth promotion and probiotic potential of the medicinal plant Ocimum sanctum. Symbiosis 60, 91–99. doi: 10.1007/s13199-013-0244-0
Ngo, N. P., Yamada, T., Higuma, S., Ueno, N., Saito, K., Kojima, K., et al. (2019). Spore inoculation of Bacillus pumilus TUAT1 strain, a biofertilizer microorganism, enhances seedling growth by promoting root system development in rice. Soil Sci. Plant Nutr. 65, 598–604. doi: 10.1080/00380768.2019.1689795
Nicholson, W. L., Munakata, N., Horneck, G., Melosh, H. J., and Setlow, P. (2000). Resistance of bacillus endospores to extreme terrestrial and extraterrestrial environments. Mol. Biol. Rev. 64, 548–572. doi: 10.1128/MMBR.64.3.548-572.2000
Pandey, C., Bajpai, V. K., Negi, Y. K., Rather, I. A., and Maheshwari, D. K. (2018). Effect of plant growth promoting bacillus spp. on nutritional properties of Amaranthus hypochondriacus grains. Saudi J. Biol. Sci. 25, 1066–1071. doi: 10.1016/j.sjbs.2018.03.003
Priest, F. G. (1993). “Systematics and ecology of bacillus”, in Bacillus subtilis and Other Gram-Positive Bacteria. eds. A. L. Sonenshein, J. A. Hoch, and R. Losick (Washington, DC: American Society for Microbiology Press). 1–16.
Probanza, A., Mateos, J. L., Lucas Garcia, J. A., Ramos, B., De Felipe, M. R., and Gutierrez Manero, F. J. (2001). Effects of inoculation with PGPR bacillus and Pisolithus tinctorius on Pinus pinea L. growth, bacterial rhizosphere colonization, and mycorrhizal infection. Microb. Ecol. 41, 140–148. doi: 10.1007/s00248000008
Pudova, D. S., Toymentseva, A. A., Gogoleva, N. E., Shagimardanova, E. I., Mardanova, A. M., and Sharipova, M. R. (2022). Comparative genome analysis of two Bacillus pumilus strains producing high level of extracellular hydrolases. Genes. 13:409. doi: 10.3390/genes13030409
Radhakrishnan, R., Hashem, A., and Abd Allah, E. F. (2017). Bacillus: a biological tool for crop improvement through bio-molecular changes in adverse environments. Front. Physiol. 8, 1–14. doi: 10.3389/fphys.2017.00667
Ramos, B., Lucas García, J. A., Probanza, A., Domenech, J., and Javier Gutierrez Mañero, F. (2003). Influence of an indigenous European alder (Alnus glutinosa (L.) Gaertn) rhizobacterium (Bacillus pumilus) on the growth of alder and its rhizosphere microbial community structure in two soils. New For. 25, 149–159. doi: 10.1023/A:1022688020897
Shahid, I., Han, J., Hanooq, S., Malik, K. A., Borchers, C. H., and Mehnaz, S. (2021). Profiling of metabolites of bacillus spp. and their application in sustainable plant growth promotion and biocontrol. Front. Sustain. Food. Syst. 5:605195. doi: 10.3389/fsufs.2021.605195
Shahzad, A., Qin, M., Elahie, M., Naeem, M., Bashir, T., Yasmin, H., et al. (2021). Bacillus pumilus induced tolerance of maize (Zea mays L.) against cadmium (cd) stress. Sci. Rep. 11, 17196–17111. doi: 10.1038/s41598-021-96786-7
Shivaji, S., Chaturvedi, P., Suresh, K., Reddy, G. S., Dutt, C. B., Wainwright, M., et al. (2006). Bacillus aerius sp. nov., Bacillus aerophilus sp. nov., bacillus stratosphericus sp. nov. and Bacillus altitudinis sp. nov., isolated from cryogenic tubes used for collecting air samples from high altitudes. Int. J. Syst. Evol. Microbiol. 56, 1465–1473. doi: 10.1099/ijs.0.64029-0
Siddiqui, Z. A., Baghel, G., and Akhtar, M. S. (2007). Biocontrol of Meloidogyne javanica by rhizobium and plant growth-promoting rhizobacteria on lentil. World J. Microbiol. Biotechnol. 23, 435–441. doi: 10.1007/s11274-006-9244-z
Upadhyay, S. K., Saxena, A. K., Singh, J. S., and Singh, D. P. (2019). Impact of native ST-PGPR (Bacillus pumilus; EU927414) on PGP traits, antioxidants activities, wheat plant growth and yield under salinity. CABI Agric. Biosci 7, 157–168. doi: 10.5958/2320-642X.2019.00021.8
Wierzchowski, P. S., Dobrzyński, J., Mazur, K., Kierończyk, M., Wardal, W. J., Sakowski, T., et al. (2021). Chemical properties and bacterial community reaction to acidified cattle slurry fertilization in soil from maize cultivation. Agronomy 11:601. doi: 10.3390/agronomy11030601
Win, K. T., Okazaki, K., Ohkama-Ohtsu, N., Yokoyama, T., and Ohwaki, Y. (2020). Short-term effects of biochar and Bacillus pumilus TUAT-1 on the growth of forage rice and its associated soil microbial community and soil properties. Biol. Fertil. Soils 56, 481–497. doi: 10.1007/s00374-020-01448-x
Win, K. T., Oo, A. Z., Ohkama-Ohtsu, N., and Yokoyama, T. (2018). Bacillus Pumilus strain TUAT-1 and nitrogen application in nursery phase promote growth of Rice plants under field conditions. Agron. J. 8:216. doi: 10.3390/agronomy8100216
Yakovleva, G., Kurdy, W., Gorbunova, A., Khilyas, I., Lochnit, G., and Ilinskaya, O. (2022). Bacillus pumilus proteome changes in response to 2, 4, 6-trinitrotoluene-induced stress. Biodegradation 33, 593–607. doi: 10.1007/s10532-022-09997-8
Zhang, Q., Lin, Y., Shen, G., Zhang, H., and Lyu, S. (2022). Siderophores of Bacillus pumilus promote 2-keto-L-gulonic acid production in a vitamin C microbial fermentation system. J. Basic Microbiol. 62, 833–842. doi: 10.1002/jobm.202200237
Zielewicz, W., Swędrzyński, A., Dobrzyński, J., Swędrzyńska, D., Kulkova, I., Wierzchowski, P. S., et al. (2021). Effect of forage plant mixture and biostimulants application on the yield, changes of botanical composition, and microbiological soil activity. Agronomy 11:1786. doi: 10.3390/agronomy11091786
Keywords: spore-forming bacteria, plant growth stimulation, phytohormones, sustainable agriculture, eco-friendly, soil microbiota
Citation: Dobrzyński J, Jakubowska Z and Dybek B (2022) Potential of Bacillus pumilus to directly promote plant growth. Front. Microbiol. 13:1069053. doi: 10.3389/fmicb.2022.1069053
Edited by:
José David Flores Félix, Universidade da Beira Interior, PortugalReviewed by:
Everlon Cid Rigobelo, São Paulo State University, BrazilCopyright © 2022 Dobrzyński, Jakubowska and Dybek. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jakub Dobrzyński, j.dobrzynski@itp.edu.pl