Accessing inoculation methods of maize and wheat with Azospirillum brasilense
© Fukami et al. 2016
Received: 16 October 2015
Accepted: 11 December 2015
Published: 13 January 2016
The utilization of inoculants containing Azospirillum is becoming more popular due to increasing reports of expressive gains in grain yields. However, incompatibility with pesticides used in seed treatments represents a main limitation for a successful inoculation. Therefore, in this study we searched for alternatives methods for seed inoculation of maize and wheat, aiming to avoid the direct contact of bacteria with pesticides. Different doses of inoculants containing Azospirillum brasilense were employed to perform inoculation in-furrow, via soil spray at sowing and via leaf spray after seedlings had emerged, in comparison to seed inoculation. Experiments were conducted first under greenhouse controlled conditions and then confirmed in the field at different locations in Brazil. In the greenhouse, most parameters measured responded positively to the largest inoculant dose used in foliar sprays, but benefits could also be observed from both in-furrow and soil spray inoculation. However, our results present evidence that field inoculation with plant-growth promoting bacteria must consider inoculant doses, and point to the need of fine adjustments to avoid crossing the threshold of growth stimulation and inhibition. All inoculation techniques increased the abundance of diazotrophic bacteria in plant tissues, and foliar spray improved colonization of leaves, while soil inoculations favored root and rhizosphere colonization. In field experiments, inoculation with A. brasilense allowed for a 25 % reduction in the need for N fertilizers. Our results have identified alternative methods of inoculation that were as effective as the standard seed inoculation that may represent an important strategy to avoid the incompatibility between inoculant bacteria and pesticides employed for seed treatment.
KeywordsAzospirillum brasilense Biological nitrogen fixation Leaf spray Plant growth promoting bacteria Soil spray Triticum aestivum L. Zea mays L.
The bacterial genus Azospirillum encompasses bacteria associated with various plant species such as maize (Zea mays L.), wheat (Triticum aestivum L.) and sugarcane (Saccharum spp.) (Swedrzyńska and Sawicka 2001; Hungria et al. 2010; Moutia et al. 2010; Piccinin et al. 2011). Azospirillum spp. are by far the best-studied plant growth-promoting bacteria (PGPB) (Bashan and de-Bashan 2010). They are believed to stimulate plant growth by an array of mechanisms including, but not restricted to, production and secretion of phytohormones (Tien et al. 1979; Bottini et al. 1989), increase of nutrient availability (Rodriguez et al. 2004; Bashan and de-Bashan 2005; Hungria et al. 2010), and biological nitrogen fixation (BNF) (de-Bashan et al. 2012). In addition, Azospirillum spp. have been implicated in increasing plant resistance to pathogens (Romero et al. 2003; Tortora et al. 2011). Due to the wide array of mechanisms proposed for stimulation of plant growth by Azospirillum spp., Bashan and de-Bashan (2010) proposed a theory of multiple mechanisms that might act either in a cumulative or sequential pattern.
The analysis of results from a large number of field trials with various non-legume crops, conducted worldwide over 20 years, under different soil and weather conditions, has demonstrated that yield increases of up to 30 % could be obtained 70 % of the time (Okon and Labandera-Gonzalez 1994) in response to inoculation with Azospirillum. In addition, an extensive evaluation of wheat inoculated with a commercial liquid Azospirillum brasilense formulation at 297 locations in Argentina has demonstrated positive responses of up to 6 % increases in yield in 70 % of the cases, depending on the experimental conditions (Diaz-Zorita and Fernández-Canigia 2009). In Brazil, Hungria et al. (2010) observed increases of up to 30 and 18 % in the grain yields of maize and wheat, respectively, inoculated with elite strains of A. brasilense in field trials. In addition, there are also reports of grain yield increases by co-inoculation of legumes with A. brasilense and rhizobia, e.g. in soybean (Glycine max (L.) Merr.) and common bean (Phaseolus vulgaris L.) (Hungria et al. 2013, 2015).
Even though field inoculation with Azospirillum may promote crop yield increases, limitations related to strain compatibility with chemicals employed for seed treatment—mostly pesticides—may be expected (Puente et al. 2008), as is the case with other PGPB such as Bradyrhizobium (Campo et al. 2009). There is little information available about the toxicity of pesticides employed for seed treatment towards non-target microorganisms and PGPB, and their various modes of action may affect different aspects of such beneficial microorganisms, making it difficult to infer about compatibility between products and inoculants (Yang et al. 2011). Some chemicals have been shown to be very harmful to rhizobia (Hungria et al. 2005; Campo et al. 2009) and either harmless (Elslahi et al. 2014) or very toxic (Mohiuddin and Mohammed 2013) to Azospirillum.
Partial or total replacement of chemical fertilizers with PGPB may not only reduce costs, but also help to mitigate the negative environmental impacts of agricultural activities. There is much knowledge about formulations and inoculation technologies with PGPB (Bashan et al. 2014), but further studies are necessary to evaluate the ease and viability of large-scale inoculation strategies, taking into account that sowing is a critical phase of the agricultural activity due to weather and season constraints for each crop. In addition, since seed treatment with chemicals will continue to be practiced, and until more information on this subject is available, inoculation strategies should try to avoid damage to the bacteria. The hypothesis of our study is that it is possible to find alternatives methods to seed inoculation of cereals with A. brasilense, reducing or avoiding the negative impacts of chemicals applied to the seeds.
Materials and methods
Inoculants and inoculation methods
Inoculants consisted of a mixture of strains CNPSo 2083 (=Ab-V5) and CNPSo 2084 (=Ab-V6) of A. brasilense (from the Collection of Diazotrophic and Plant Growth-Promoting Bacteria of Embrapa Soja, WFCC # 1213, WDCM # 1054). Both strains derived from a selection program that evaluated N2-fixing capacity in vitro and under field conditions (Hungria et al. 2010). The strains were shown to be highly efficiency in promoting growth of wheat and maize in several trials in Brazil, mainly due to their capacity of producing plant hormones and increasing root growth and nutrients uptake. Both strains are currently employed for commercial production of Azospirillum inoculants in Brazil.
Four methods of inoculation were compared: (1) standard seed inoculation (SI) – control treatment; (2) inoculation in the planting furrow at sowing (IPF); (3) leaf spray inoculation at the V2.5 stage of the maize plant growth cycle (Hickman and Shroyer 1994) or 3rd tiller (Large 1954) for wheat (ILS); and (4) spray inoculation on the soil surface at the V2.5 stage of the maize plant growth cycle (Hickman and Shroyer 1994) or 3rd tiller (Large 1954) for wheat (ISS).
For the maize crop 1 dose of inoculant corresponded to the application of 1.0 × 105 cells seed−1 for seed inoculation (SI) and in-furrow (IPF) and to 1.0 × 105 cells plant−1 for leaf spray (ILS) and soil spray (ISS). For the wheat crop 1 dose of inoculant corresponded to the application of 1.74 × 104 cells seed−1 for SI and IPF and to 1.74 × 104 cells plant−1 for ILS and ISS. Different doses of inoculant were evaluated.
First, greenhouse experiments were performed aiming at screening the treatments for the field experiments and to obtain preliminary results about diazotrophic populations in plant tissues with different types of inoculation. We did not repeat the greenhouse experiments because, once the preliminary results were obtained, we went straight to the field experiments.
Chemical (before liming) and granulometric characteristics of the soil employed for greenhouse experiments
P (mg dm−3)
Al (cmolc dm−3)
H + Al (cmolc dm−3)
Ca + Mg (cmolc dm−3)
K (cmolc dm−3)
SB (cmolc dm−3)
CEC (cmolc dm−3)
Pots were arranged in a completely randomized design with 18 treatments and five replicates. Treatments consisted of combinations of varying doses of N fertilizer (100 % and 75 % N) and inoculants (1× and 2.5×), and different methods of inoculation (SI, IPF, ILS, and ISS).
When maize was planted, each pot received three seeds of the BRS 3010 hybrid (Embrapa). Seeds, which were not surface disinfected in order to mimic field conditions, were treated with fungicide Maxim™XL [active ingredient (a.i.: 2.5 % fludioxonil); 1.0 % metalaxyl − M] and insecticides Actellic™500 CE (a.i.: 50 % methyl pirimifos) and K-Obiol™25 CE (a.i.: 2.5 % deltametrine), according to technical recommendations for the crop in Brazil. Five days after emergence (DAE), one seedling was removed, leaving two plants per pot.
Wheat seeds were treated with Maxim™X, and each pot received four non-disinfected seeds of cultivar BRS Gaivota (Embrapa), leaving only two seedlings per pot at 6 DAE.
Seed inoculation was performed 1 h before sowing by evenly coating seeds with the appropriate amounts of inoculants. For the in-furrow inoculation, inoculant diluted in sterile distilled water [1:500 (v:v), for maize; 1:3000 (v:v) for wheat] was applied to the soil with the help of an adjustable pipetor, immediately before sowing, to simulate the action of a planting device. Here it is worth mentioning that although the dilution with water might not be ideal in terms of osmotic effect for the bacterium, we wanted to follow what the farmer does under field conditons, where he mixes the inoculant with water. For leaf and soil surface spray inoculation, an aerograph atomizer was employed to mimic the action of a spraying equipment. For leaf spray inoculation, the soil surface was covered with aluminum foil in order to avoid that the inoculant reached the soil. For soil surface spray inoculation, plant shoots were covered with plastic bags to make sure that the inoculant reached only the soil surface.
For the maize plants, N was supplied as NH4NO3 in order to provide 120 (100 %) and 90 (75 %) kg N ha−1. N was applied in equal amounts every 8 days.
For the wheat plants, N was supplied as NH4NO3 in order to provide 80 (100 %) and 60 (75 %) kg N ha−1. N was applied in equal amounts every 8 days.
Average temperatures in the greenhouse during the experiments were of 29/16 °C (day/night) for maize, and 27/15 °C (day/night) for wheat; light inside the greenhouse was very close to the regular light, with a decrease of only 10 % of the radiation.
Plants from maize treatments were harvested 52 DAE (end of vegetative stage) for measurements of plant components. Plants from wheat treatments were harvested 54 DAE (end of vegetative stage) for measurements of plant components.
Before plants were harvested, chlorophyll content (CC) was determined according to Kaschuk et al. (2009) and based on the SPAD (Soil Plant Analysis Development) index, with readings taken from the lowermost third of the +3 (Trani et al. 1983) leaf for maize, and of the last fully expanded leaf for wheat.
Biometric parameters such as plant height (cm; PH) and culm diameter (mm; CD) of maize plants were determined with the aid of a digital caliper. In the case of wheat, the number of tillers (NT) was determined. For both crops, root volume was determined by measuring water displacement caused by immersion of the root systems in a graduate cylinder with a known volume of water.
Shoot dry weight (SDW) and root dry weight (RDW) were determined after drying plant material at 60 °C for approximately 72 h, until constant weight. Dry shoots were then ground (18 mesh) and subjected to sulfuric digestion to determine total shoot N by the salicylate green method (Searle 1984).
The populations of diazotrophic bacteria inside the leaves, roots, and rhizosphere were estimated by the most probable number (MPN) technique, as described before (Hungria and Araujo 1994; Döbereiner et al. 1995), from dilutions (105 to 109) of soil or homogenized tissues. Diazotrophic populations in leaves and roots were always evaluated in superficially disinfected tissues (Döbereiner et al. 1995). We used the classical MPN method in our study because we wanted to be sure that the same strains would be evaluated in the field experiments. Brazilian soils carry very high populations of Azospirillum (usually >104 cells g−1), and there are so far no specific probes capable of distinguishing CNPSo 2083 and CNPSo 2084 from indigenous strains. The surface disinfection of leaves and roots should allow to access bacteria inside the tissues, including both obligatory and facultative endophytes, while the counting of bacteria in the rhizosphere would estimate the population of associative bacteria (Döbereiner et al. 1995). It is worth mentioning that despite the limitations of the NMP method, our goal was to have an indication if the bacteria could, or could not colonize tissues and to establish in the rhizosphere.
Agronomic and climatic information about the sites where the field experiments were planted
Number of seeds m−1
Plant population ha−1
Date of harvest
Area harvested (m2)
Cachoeira Dourada (18º29′31″ S; 49º28′29″ W)
Latossolo Vermelho Distrófico
Maize hybrid 2B707 HX
Luis E. Magalhães (12º05′31″ S; 45º48′18″ W)
Latossolo Amarelo Distrófico
Maize hybrid 2B707 HX
(25º13′ S; 50º1′ W)
Latossolo Vermelho-Escuro Distrófico
Maize hybrid P4285 H
Wheat cultivar BRS Pardela
Chemical and granulometric characteristics of 0–20 cm layer of the soils at the locations where field experiments were planted
P (mg dm−3)
Al (cmolc dm−3)
H + Al (cmolc dm−3)
Ca + Mg (cmolc dm−3)
K (cmolc dm−3)
SB (cmolc dm−3)
CEC (cmolc dm−3)
C (g dm−3)
Luis E. Magalhães
Experimental design and procedures
All field trials were set in a completely randomized block design comprising 11 treatments, with six replicates. Experiments were planted with commercial seeds and the maize and wheat genotypes used are listed in Table 2. Seeds were treated with fungicide Maxim®XL and insecticides Actellic®500 CE (a.i.: 50 % methyl pirimifos) and K-Obiol®25 CE (a.i.: 2.5 % deltametrine).
Maize plots measured 4 m (wide) × 8 m (long). The experiment received 300 kg ha−1 of NPK (08-20-20) fertilizer in the sowing furrow, to provide 24 kg N ha−1 immediately before sowing. Thirty-five DAE, plants received complementary doses of urea-N fertilizer, corresponding to 75 % N (67.5 kg ha−1) and 100 % N (90 kg ha−1) of the amount prescribed for the maize crop in Brazil. Therefore, when we mention 75 % of the dose, that refers to 75 % of the complementary dose of N-fertilizer, as the basal level of N was applied to all treatments. In Cachoeira Dourada, Spodoptera frugiperda insects were controlled with lufenuron (15 g a.i. ha−1).
Wheat plots measured 4.6 m (wide) × 6 m (long). The experiment received 70 kg P ha−1 (supplied as super triple phosphate), 40 kg K ha−1 (supplied as potassium chloride) and either 24 kg N (urea) ha−1 at sowing plus 67.5 kg N ha−1−as side dress (75 % N treatment) or 24 kg N ha−1 at sowing plus 90 kg N ha−1 as side dress (100 % N treatment). Therefore, again, when we mention 75 % of the dose, it refers to 75 % of the complementary dose of N-fertilizer, as the basal level of N was applied to all treatments.
Inoculation in the field compared standard seed inoculation (SI; control treatment) with the application of one, two or four doses of inoculants in the planting furrow (IPF), and leaf (ILS) and soil (ISS) spray inoculations, in the same concentrations specified in the greenhouse experiments
In the case of inoculation in-furrow, as well as of foliar and soil spray inoculations, inoculants were diluted with water to a final volume of 150 L ha−1. Seed and in-furrow inoculations were performed at sowing, whereas leaf and soil spray inoculation took place when maize plants were at the V2.5 (Hickman and Shroyer 1994) vegetative stage and when wheat plants were at tiller stage 3 (Large 1954). Spray applications were performed with a costal spray equipament (Herbicat), with air induction plan spray (VI-110.015), pression of 45 pounds, adjusted to the application of medium drops (200–400 µm). Other pertinent agronomic information about the experiments are presented in Table 2.
For maize, shoot dry weight (SDW), leaf N content (NC), total N in shoots (TNS), and grain yield at 13 % humidity (Y) were determined. For SDW, five plants were collected per plot 56, 61, and 30 DAE, in Cachoeira Dourada, Ponta Grossa and Luis Eduardo Magalhães, respectively. In addition, 15 leaves (middle third section of each leaf without the main nerve) were taken from each plot for determination of NC and TNS at 92, 96, and 84 DAE in Cachoeira Dourada, Luis Eduardo Magalhães, and Ponta Grossa, respectively. In the case of wheat, only grain yield at 13 % humidity was determined.
Data obtained from each experiment were first evaluated for normality and variance homogeneity, followed by the analysis of variance (ANOVA). In the case of greenhouse experiments, when p ≤ 0.05 was confirmed by the F test, Duncan’s post hoc multiple range test at p ≤ 0.05 was employed for multiple comparisons, followed by Dunnett’s test (p ≤ 0.05) for the comparisons of means relative to the control treatment. For the field experiment Duncan’s post hoc multiple range test at p ≤ 0.05 was employed for multiple comparisons (SAS Institute 2001).
Greenhouse experiment with maize
Shoot dry weight (SDW), root dry weight (RDW), N content (NC), total N accumulated in the shoots (TNS), chlorophyll content (CC), root volume (RV), culm diameter (CD), plant height (PH), and MPN (most probable number) of diazotrophic bacteria on leaves, roots and rhizosphere in a greenhouse experiment performed with hybrid maize BRS 3010 in response to different doses of inoculant, levels of N fertilization, and methods of inoculation
SDW (g pl−1)
RDW (g pl−1)
NC (mg g−1)
TNS (mg pl−1)
CC (µg cm−2)
RV (mL pl−1)
Leaves (n° cells g−1)
Roots (n° cells g−1)
Rhizosphere soil (n° cells g−1)
T1: C + 75 % Na
4.57 × 106 cde
1.73 × 108 e
1.55 × 106 b
T2: C + 100 % N
2.92 × 106 de
4.75 × 108 bcde
5.52 × 105 b
T3: SI + 1 doseb + 75 % N
2.47 × 106 de
6.24 × 108 abcde
6.12 × 105 b
T4: SI +1 dose + 100 % N
1.14 × 107 bcde
6.24 × 108 abcde
2.12 × 106 b
T5: SI + 2.5 doses + 75 % N
4.31 × 106 cde
6.86 × 108 abcde
5.10 × 105 b
T6: SI + 2.5 doses + 100 % N
1.16 × 108 b
2.83 × 108 cde
5.10 × 105 b
T7: IPF + 1 dose + 75 % N
1.22 × 108 b*
5.03 × 108 abcde
3.02 × 106 b
T8: IPF + 1 dose + 100 % N
2.70 × 107 bcd
4.58 × 108 abcde
2.52 × 107 a*
T9: IPF + 2.5 doses + 75 % N
2.18 × 107 bcd
1.25 × 109 a*
1.52 × 106 b
T10: IPF + 2.5 doses + 100 % N
2.40 × 109 a*
3.28 × 108 bcde
8.48 × 107 b
T11: ILS + 1 dose + 75 % N
2.05 × 109 a*
2.37 × 108 de
1.03 × 106 b
T12: ILS + 1 dose + 100 % N
7.38 × 107 bc
1.02 × 10 abc
4.65 × 106 ab
T13: ILS + 2.5 doses + 75 %N
7.50 × 106 bcde
9.18 × 108 abcd
1.54 × 106 b
T14: ILS + 2.5 doses + 100 % N
1.12 × 106 de
7.33 × 108 abcde
3.04 × 106 b
T15: ISS + 1 dose + 75 % N
4.07 × 106 cde
4.84 × 108 cde
1.34 × 106 b
T16: ISS + 1 dose + 100 % N
1.10 × 106 de
9.94 × 108 abc
1.40 × 106 b
T17: ISS + 2.5 doses + 75 % N
1.11 × 106 de
3.66 × 108 cde
1.50 × 106 b
T18: ISS + 2.5 doses + 100 % N
6.25 × 105 e
1.14 × 109 ab
1.65 × 106 b
Chlorophyll content (CC) and culm diameter (CD) were not affected by any of the treatments studied (Table 4). Root growth, as indicated by root volume (RV), responded positively to seed inoculation (SI) with 2.5 doses of inoculant and full N fertilization (T6) when compared to all treatments of inoculation in-furrow (T7–T10). Inoculation by soil spray with one dose of inoculant in addition to full N fertilization (T16) significantly increased plant height (PH) relative to all treatments with seed inoculation and to the non-inoculated control that received 75 % N (Table 4).
Internal leaf colonization by diazotrophs, as estimated by the most-probable number (MPN) technique, was significantly superior in plants from treatments 6, 7, 10, and 11, when compared to plants from the non-inoculated controls (T1 and T2) (Table 4). Higher internal leaf populations of diazotrophic bacteria were observed in plants from treatments in which one dose of inoculant was applied by leaf spraying at the V2.5 stage (T11 and T12), but also with 2.5 doses of inoculation in-furrow with 100 % of N (T10). Significantly increased internal root colonization by diazotrophic bacteria was observed in plants from T9, where 2.5 doses of inoculant were applied in-furrow with 75 % of N, in comparison to plants from the non-inoculated controls (T1 and T2). When rhizospheric soil was analyzed, the largest bacterial populations were observed in association with T8, which received a single dose of inoculant in-furrow and 100 % N (Table 4).
Greenhouse experiment with wheat
Shoot dry weight (SDW), root dry weight (RDW), N content (NC), total N accumulated in the shoots (TNS), chlorophyll content (CC), root volume (RV), number of tillers (NT), and MPN (most probable number) of diazotrophic bacteria on leaves, roots and rhizosphere soil in a greenhouse experiment with wheat cultivar the BRS Gaivota in response to different doses of inoculant, levels of N fertilization, and methods of inoculation
SDW (g pl−1)
RDW (g pl−1)
NC (mg g−1)
TNS (mg pl−1)
CC (µg cm−2)
RV (mL pl−1)
NT (n° pl−1)
Leaf (n° cells g−1)
Root (n° cells g−1)
Rhizosphere soil (n° cells g−1)
T1: C + 75 %Na
1.26 × 105 cd
2.64 × 108 abcd
3.30 × 106 bcd
T2: C + 100 %N
4.07 × 104 d
7.92 × 108 abcd
5.33 × 106 d
T3: SI + 1 doseb + 75 %N
8.94 × 105 cd
5.28 × 108 abcd
2.24 × 106 bcd
T4: SI +1 dose +100 %N
6.95 × 105 bcd
9.00 × 107 bcd
2.19 × 106 cd
T5: SI + 2.5 doses + 75 %N
3.98 × 105 cd
4.97 × 108 abcd
1.00 × 107 abcd
T6: SI + 2.5 doses + 100 %N
3.69 × 106 abc
6.26 × 107 cd
4.14 × 106 abcd
T7: IPF + 1 dose + 75 %N
5.04 × 106 abc*
5.42 × 108 abcd
1.38 × 107 abcd
T8: IPF + 1 dose + 100 %N
1.07 × 106 abcd
1.60 × 108 d
4.46 × 106 abcd
T9: IPF + 2.5 doses + 75 %N
2.09 × 106 abcd
1.03 × 109 ab
3.32 × 107 abc
T10: IPF + 2.5 doses + 100 %N
1.14 × 106 abcd
4.84 × 108 abcd
3.29 × 107 a*
T11: ILS + 1 dose + 75 %N
2.40 × 107 a*
4.17 × 108 abcd
1.12 × 108 ab
T12: ILS + 1 dose + 100 %N
20. 49 ab
2.74 × 106 abc
8.94 × 107 bcd
2.98 × 106 cd
T13: ILS + 2.5 doses + 75 %N
7.06 × 105 abcd
5.17 × 108 abcd
3.95 × 106 bcd
T14: ILS + 2.5 doses + 100 %N
3.82 × 107 a*
6.82 × 107 bcd
6.20 × 106 abcd
T15: ISS + 1 dose + 75 %N
9.72 × 106 ab*
9.92 × 108 abc
5.36 × 106 bcd
T16: ISS + 1 dose + 100 %N
1.04 × 106 abc
2.40 × 109 a*
2.42 × 106 cd
T17: ISS + 2.5 doses + 75 % N
1.45 × 106 abc
8.23 × 108 abcd
2.13 × 106 cd
T18: ISS + 2.5 doses + 100 % N
1.90 × 106 abc
1.21 × 109 abcd
1.77 × 106 d
Bacterial populations were significantly larger on the leaves (internal) of plants from treatments with foliar spray inoculation (T11 and T14), when compared to non-inoculated treatments (T1 and T2) (Table 5). In the case of the roots, diazotrophic bacteria were more numerous when a single dose of inoculant was sprayed on the soil with full N fertilization (T16), whereas for the rhizosphere significantly larger bacterial populations were observed for in-furrow application of 2.5 doses of inoculant (T10), compared to non-inoculated controls (T1 and T2) (Table 5).
These preliminary greenhouse experiments were performed to verify possible effects on plant growth and colonization of diazotrophic bacteria, aiming to obtain an indication of the treatments that could be taken to the field.
Field trials with maize and wheat
Shoot dry weight (SDW) and N content (NC) in maize plants from field experiments performed in three different regions of Brazil (Cachoeira Dourada, hybrid 2B707 HX, Luis Eduardo Magalhães, hybrid 2B707 HX, and Ponta Grossa, hybrid P4285 H), in response to different doses of N fertilizer, doses of inoculant and methods of inoculation with Azospirillum brasilens
Luis E. Magalhães
SDW (g pl−1)
NC (mg g−1)
SDW (g pl−1)
NC (mg g−1)
SDW (g pl−1)
NC (mg g−1)
T2: C + 100 % Na
T3: C + 75 % N
T4: SI + 1 doseb + 100 % N
T5: SI + 1 dose + 75 % N
T6: IPF + 2 doses + 75 % N
T7: IPF + 4 doses + 75 % N
T8: ILS + 2 doses + 75 % N
T9: ILS + 4 doses + 75 % N
T10: ISS + 2 doses + 75 % N
T11: ISS + 4 doses + 75 % N
Recent data indicate that about 25 million doses of Bradyrhizobium spp. inoculants for soybeans, and 2 million doses of A. brasilense inoculants, for maize and wheat, are sold annually in Brazil (Marks et al. 2013). Although the commercialization of products containing Azospirillum seems proportionally low, such inoculants only reached the Brazilian market about a half decade ago, while rhizobia have been in the market for over 60 years. In addition, very few field studies have been conducted under Brazilian conditions, and no options to avoid the incompatibility between the bacteria and the array of seed treatment agrichemicals are available. The results reported here are largely applicable to other important producing countries of South America and Africa.
Full replacement of N fertilizers for grasses by A. brasilense may not be feasible, because of the modest contribution of biological nitrogen fixation by the bacterium. However, the combination of all minor contributions by Azospirillum to plant growth may result in plants that are more efficient to absorb water and nutrients from soil, thus enhancing plant nutrition and growth (Stancheva et al. 1992; Dobbelaere et al. 2001, 2002; Bashan et al. 2004; Bashan and de-Bashan 2010; Hungria et al. 2010, 2013, 2015; Kouchebagh et al. 2012).
In our study, we observed that spray inoculation, either on the leaves or on the soil surface increased maize plant growth. In general, when inoculation with Azospirillum was associated to 75 % of the complementary dose of N, plant growth was superior to non-inoculated plants receiving 100 % N. Therefore, the replacement of 25 % of the N-fertilizer by Azospirillum is profitable for the farmer and the environment.
The efficiency of Azospirillum spp. may be negatively affected by the presence of high levels of N fertilizers, due to the rapid decrease in the activity of nitrogenase (Hartmann 1989), and in general such negative effects were also observed in our study. On the other hand, stimulation in response to the association between lower doses of N and Azospirillum are reported (Piccinin et al. 2013). For example, in our greenhouse experiment with wheat, shoot dry matter was not affected by inoculation, but foliar spray inoculation resulted in increased root systems and N accumulation in the shoots. Reports from literature show increases in root growth and N accumulation in the shoots of maize and Setaria grass inoculated with A. brasilense (Cohen et al. 1980), effect that has been attributed to morphological and physiological changes in the roots, promoting water and nutrient uptake by the plants (Dobbelaere et al. 2001, 2002).
Alterations in the root system are probably caused by the presence of plant growth hormones, especially indoleacetic acid (IAA) produced and secreted by Azospirillum, thus playing a major role in plant growth promotion (Bashan and Holguin 1997). In addition to IAA production, Azospirillum, as well as other PGPB have been implicated with an array of mechanisms that act simultaneously or sequentially and result in increased plant growth (Bashan and de-Bashan 2010), root formation, cell division and growth, and production of lateral and adventitious roots (Werner et al. 2003; Bhattacharyya and Jha 2012). Azospirillum has also been implicated with higher photosynthesis rates and photosynthetic pigments (Bashan et al. 2006; Barassi et al. 2008; Hungria et al. 2010).
In contrast to the satisfactory results of foliar spray inoculation that we observed in this study, in-furrow inoculation with elevated doses of Azospirillum was somewhat inhibitory to plant growth. Dobbelaere et al. (2002) suggested that high concentrations of plant hormones, which are stimulatory at low concentrations, may have negative effects on plant growth. The higher abundance of Azospirillum in the root environment may have increased the secretion of such hormones, thus inhibiting root growth. Similar negative effects of high concentrations of Azospirillum have been previously reported for wheat (Bashan 1986) and maize (Fallik et al. 1988). Hungria et al. (2013) observed benefits only at lower doses of inoculation, and growth inhibition with higher doses of Azospirillum when soybean and common bean were co-inoculated with rhizobia and the same strains of Azospirillum employed in our study. Inoculation with high concentrations of Azospirillum also decreased the N content of field-grown plants in Cachoeira Dourada and Ponta Grossa, but not in Luiz Eduardo Magalhães. Our results present strong evidence that field inoculation with PGPB must pay attention to inoculant doses, and point to the need of fine adjustments so as not to cross the threshold of growth stimulation and inhibition.
In this paper, we report positive effects of inoculation on maize root volume, in addition to increases in plant height when inoculant was sprayed on the soil, whereas foliar spray inoculation resulted in more tillers in wheat, probably related to plant growth hormones that might have been present in the inoculants or were produced by the bacteria. Azospirillum colonizes plant niches that are protected from oxygen and, as a result, nitrogenase is maintained functional (Dobbelaere et al. 2003). Colonization of intercellular spaces between the epidermis and the cortex, and of the outermost layers of the cortex of inoculated roots is frequently observed (Patriquin et al. 1983; Mostajeran et al. 2007). A. brasilense was predominantly located between the apoplast and the epidermal cells of wheat roots (Nabti et al. 2010). However, these bacteria can also colonize leaves (Bashan 1998). Even after surface disinfection, those authors observed that the bacteria were more frequent on the roots, followed by culms and leaves of maize plants. In this study, we observed higher numbers of bacteria on roots, but they were also recovered, although in 100-fold lower populations, from leaves.
Azospirillum survives well in Brazilian soils and can be found in association with plants even when no inoculation is done. For example, Pereyra et al. (2010) detected populations of A. brasilense of 3 × 103 colony forming units (CFU) g−1 of roots of non-inoculated cucumber (Cucumis sativus) plants, whereas the roots of inoculated plants contained as much as 8 × 106 CFU g−1. In our study, both maize and wheat plants showed improved rhizosphere and root colonization by diazotrophic bacteria in some treatments that received inoculation in-furrow. Bacterial abundances also showed some increase when non-inoculated treatments were considered, but responses were more expressive when inoculation was performed.
Inoculation by soil spraying resulted in increased internal colonization of aerial plant parts of wheat by Azospirillum, indicating high bacterial mobility through the plants. Several authors (Baldani et al. 1992; James et al. 1994; Souza et al. 2004) have suggested that the presence of diazotrophic bacteria in xylem vessels may indicate that this may be one route of bacterial migration to different plant parts. The internal colonization of both maize and wheat leaves also increased in response to foliar spray inoculation, suggesting that in this case the stomata acted as a passive doorway for bacteria, since for leaf sprays the soil was covered to avoid cross contamination and root colonization by inoculant bacteria. In fact, in a scan electron microscopy (SEM) study performed by Baldotto et al. (2011) to evaluate the colonization of pineapple [Ananas comosus (L.) Merril] by Herbaspirillum seropedicae, bacterial aggregates could be observed over trichomes and junctions of the epidermis cell walls, as well as on the external periclinal wall and near stomata complexes. Those authors suggested that their observations evidenced that bacterial penetration in the leaves occurred passively via stomata, and colonization began in the sub-stomata chamber and progressed on through the intercellular spaces of the spongy chlorenchyma of the leaf mesophyll. Similarly, Souza et al. (2004) have observed that bacterial distribution throughout maize leaves takes place via colonization of the epidermal cells of the adaxial face, with the formation of aggregates on the epidermis or near the stomata. Another evidence of leaf colonization obtained in our study is that our tests have indicate that Azospirillum can barely survive 2 h on the leaves, and far less under field conditions (data not shown), giving more support to the hypothesis that the increase in bacteria inside the leaves could be related to colonization associated with leaf spray. It is worth reinforcing that in our field experiments with maize in general yields of inoculated plants with maize and receiving 75 % of the complementary dose of N-fertilizer produced as much as non-inoculated plantas receiving 100 % of N.
Inoculation with A. brasilense may result in increases of wheat yield, or maintain actual yield standards but with a reduction in the amounts of N fertilizers applied (Rothballer et al. 2003; Hungria et al. 2010; Venieraki et al. 2011; Piccinin et al. 2013). Increased yield in wheat is generally attributed to an increase in the number of fertile tillers (Salantur et al. 2006), and inoculation with A. brasilense resulted in more tillers in wheat plants grown in disinfected soil (Saubidet et al. 2002). In our study, inoculation by both soil and leaf sprays also resulted in more tillers in the greenhouse experiment, strengthening the hypothesis of increased tillering as a mechanism of yield promotion in response to inoculation with Azospirillum. Although tillering was not evaluated in the field, our data confirmed the benefits of A. brasilense to wheat grain yield, since all treatments that received inoculants produced more grains than the non-inoculated controls, even when full N fertilization was performed. In addition, in our field trial with wheat in general the presence of the inoculant applied to the seeds, or by soil or leaf spray allowed a 25 % reduction in the rates of N fertilization with better yields than when 100 % N was employed without inoculation.
Grain yield of inoculated maize increased due to improved N nutrition, and part could be attributed to biological nitrogen fixation by Azospirillum spp. (Dobbelaere et al. 2003), but the magnitude of the response depended on the level of N fertilization practiced, as reported before (Piccinin et al. 2013). In studies of maize seed inoculation with different species (A. lipoferum and A. brasilense) and strains (including the two strains of the present study), Hungria et al. (2010) observed yield increases of up to 30 % (or 823 kg ha−1), which were attributed to improved N nutrition and to increased nutrient absorption by inoculated plants with larger root systems. In Cerrado region of Brazil, 29 % yield increases in maize were due to inoculation with Azospirillum (Ferreira et al. 2013).
In Brazil it is estimated that 70 % of the N fertilizers are imported from other countries, resulting in high costs for agricultural activities (Hungria et al. 2013). The increased yields obtained from treatments that receive adequate doses of inoculants, combined with a 25 % reduction in urea application present an attractive alternative to reduce costs in agriculture. For example, in the experiment performed in Cachoeira Dourada, inoculation by leaf spray with the highest inoculant dose promoted an increase of 773 kg ha−1 in grain yield of maize over the treatment that received the full dose of N fertilizer (100 % N), with no inoculation.
In conclusion, taking into account the search for more conservative agricultural systems, inoculation with A. brasilense stands as a promising strategy to contribute to increased sustainability. However, in times when more and more pesticides for seed treatment are released, and so little is known about their toxicity to inoculated Azospirillum bacteria, compatibility with inoculants applied to the seed can seriously limit microbial contribution. In our study we have identified alternative methods of inoculation to avoid the contact of Azospirillum with pesticides applied to the seeds, with an emphasis on leaf spray at the beginning of the vegetative phase. Alternative methods of inoculation may increase the utilization of such bacteria in the field and help reduce agricultural costs.
Conceived and designed the experiments: MAN, MH. Performed the experiments: JF, MAN, RSA. Analyzed the data: all authors. Contributed reagents/materials/analysis tools: MAN, RSA, MH. All authors read and approved the final manuscript.
Funded by Embrapa (02.13.08.003.00.00). J. Fukami acknowledges an MSc fellowship from CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Brazil). The microbiology group of Embrapa Soja is also supported by CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico, Brazil). M. Hungria and M.A. Nogueira are also research fellows from CNPq. Approved for publication by the Editorial Board of Embrapa Soja as manuscript number 283/2014.
The authors declare that they have no competing interests.
The author declares no ethical conflicts.
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