The experiment was set up in triplicate for each of the 36 variants (Figure 1) and the research material consisted of strawberry cv. Honeoye. Each strawberry plant was grown in a separate pot without undercutting or root curling in a greenhouse at 23°C. Each pot contained 4 kg of soil collected from an organic experimental field of the Institute of Soil Science and Plant Cultivation - State Research Institute (Puławy, Poland) located in Grabów (Poland) and it was subjected to chemical and microbiological analysis. The soil was characterized as Cambisol with a loamy sand texture. Clover was used as a pre-crop. The soil composition was as follows: humus 1.9%, P₂O₅ 10.1 mg 100 g^–1 soil, K₂O 5.0 mg 100 g^–1 soil, Mg 10.6 mg 100 g^–1 soil, N-NO₃ 8.92 mg kg^–1 DM of soil, N-NH₄ 2.29 mg kg^–1 DM of soil, pH 5.9. Keramzite was placed at the bottom of each pot in a volume of 0.5 l. The soil was fertilized in autumn with manure (pH = 8.6, nutrient content: N 5.06 mg kg^–1, P₂O₅ 2.47 mg kg^–1, K₂O 6.90 mg kg^–1, CaO 3.04 mg kg^–1, MgO 2.38 mg kg^–1, S 0.69 mg kg^–1) and potassium salt (LUVENA, 100 kg ha^–1). Bioilsa^® (NaturalCrop, Poland) fertilizer was applied in a quantity corresponding to a dose of 150 kg ha^–1.

Plants were treated with five consortia (C1, C2, C3, C4, and C5) and a control (C0) was prepared, in which no consortia were applied (Figure 1). The consortia consisted of the following bacterial strains: AF117AB (P. polymyxa), Sp115AD (Bacillus subtilis), AF75AB2, Sp115AD, AF75BC (Bacillus sp.), AF75AA, AF75AD (Streptomyces sp.), JAFGU (Lysobacter sp.), and AF70AC (Pseudomonas sp.). The bacterial strains used in the experiment originated from the SYMBIOBANK collection of the Research Institute of Horticulture in Skierniewice and were selected based on a previous study as microorganisms with potentially beneficial properties in terms of plant biostimulation and protection. The bacterial consortia, with a population size of 10⁸ cfu (colony-forming units) in 1 ml, were applied to the soil in a volume of 10 ml per pot directly to the roots at planting time and twice after planting at intervals of 3–4 weeks. The objects called “Consortium C0,” in which bacteria were not introduced, were the control for the ones containing bacterial consortia with their potential for plant biostimulation and protection, while NC objects constituted controls without pathogen contamination.

The next step was the infection of plants with five phytopathogenic fungi and fungus-like pathogens (BC, V, P, C, and MIX) and the submission of the control (NC) in which the plants were not treated with pathogens (Figure 1). Two days after plant inoculation with bacterial consortia, the plants were infected with the following pathogens: G277/18 (Botrytis cinerea), G296/18 (Verticillium sp.), G408/18 (Phytophthora sp.), G171/18 (Colletotrichum sp.). Strains of B. cinerea, Phytophthora sp., and Verticillium sp. were isolated from infected strawberry roots (Oszust et al., 2020), while Colletotrichum sp. was isolated from infected strawberry fruit (Malarczyk et al., 2020) at the Institute of Agrophysics of the Polish Academy of Sciences (Lublin, Poland). In the case of B. cinerea and Colletotrichum sp. the strawberry flowers were infected with 10 ml of pathogen suspension using an inoculum adjusted to 1,000 conidia in 1 ml. In contrast, Phytophthora sp. and Verticillium sp. were added to the soil as a pathogen inoculum suspension of 10⁵ cfu ml^–1 (10 ml was applied) and 10⁴ cfu g^–1 of soil, respectively.

At the harvest maturity stage, the strawberries (developed and grown, and the sepals easily detach from the stalk) were collected on March 23, 2019.

Firmness is one of main parameter of texture which determine overall quality evaluation by consumers (Harker et al., 2003). For soft fruit puncture test is the most common method used for determination of firmness (Døving and Måge, 2002). Fresh fruit firmness (n) was determined by a puncture test by using a universal test machine (Lloyd LRX, Lloyd Instruments). The strawberry was placed on the platform of the device and the aluminium probe (3 mm diameter) was lowered with a constant plunger speed (20 mm min^–1) to a constant depth (6 mm). The maximum force required to penetrate the strawberry to a set depth was a measure of tissue firmness (Fraeye et al., 2009). The test was carried out on twenty strawberries for each replicate of the variant. Average fruit firmness was expressed in terms of N.

The shape of the fruit is a hormone-regulated trait and many factors can alter the final shape including environmental conditions (Rey-Serra et al., 2021). The shape was determined in accordance with the method proposed by Ishikawa et al. (2018). The length (the longer dimension was measured from the fruit’s tip to the base) and width (the shorter dimension of the fruit, was measured as a transverse measurement at the thickest point) of the fruit were determined. The quotient of length and width was calculated. Fruits are classified as flattened (quotient < 1), round (quotient = 1), or oblong (quotient > 1). The test was carried out on fifteen strawberries for each replicate of the variant.

Fresh weight is the weight of the fruit on the day it is harvested. It is determined by a weight method to initially determine the size of the fruit (Reyes-Yanes et al., 2020). The purpose of determining the fresh weight is to obtain information on the effectiveness of the cultivation methods. Comparison the fresh weight, dry weight and shape provides information on the hydration level of the fruit and the tissue density (Miller et al., 2000). To determine the fresh weight of fruit (FWF), each fruit was weighed to three decimal places. The results were summed and averaged. The average fresh fruit weight was expressed in g.

The dry matter allows the determination of the product residue after the removal of water from it (Ozdemir and Topuz, 2004). The drying oven method is a validated standardized method that is readily available (International Organization for Standardization, 2000). Dry weight (DW) was determined according to the procedure described in standard PN ISO 1026:2000 (International Organization for Standardization, 2000). In Brief, 0.5 g of strawberries were taken from each variant in triplicate and weighed to the nearest 0.001 g. The strawberries were then placed in an oven at 105°C, after 24 h the fruit was weighed, placed in the oven for 2 h and weighed again. The procedure was repeated until no further weight loss was noted. The average dry weight of one fruit was expressed as a percentage of fresh weight.

The soluble solid content (SSC) is a measure of the total soluble solid, which includes sugars, organic acids, amino acids, and more, and it is associated with consumer preference for fruit (Crisosto et al., 2003). The refractometric method is used because of the optical properties of sugars and sugar alcohols which are majority of soluble solids of most fruit (Magwaza and Opara, 2015). SSC was determined using a refractometer (PAL-BX/RI, ATAGO, Japan) and expressed in percentage terms. A minimum of five fresh strawberries were picked and juiced. One drop of juice was applied to the refractometer glass and the measurement was performed; the soluble sugar content was expressed in percentage terms. The measurement was performed in triplicate for each variant of the experiment.

Due to the strong antioxidant activity of most phenolic compounds in fruits, the total polyphenol content is determined for the evaluation of health-promoting properties. The Folin-Ciocalteu method has been used for many years and is still relevant today due to its high accuracy (Carmona-Hernandez et al., 2021). Phenolic compounds (PC) were determined according to the procedure proposed by Folin and Ciocalteu (1927) and Nunes et al. (2001), with some modifications. From each variant of the experiment, five fruit were taken in triplicate and then juiced. Then, 0.5 ml of the clear juice was diluted by adding 9.5 ml of deionized water. The resulting solution was spiked with 5 ml of Folin-Ciocalteu reagent (1:9 dilution) and 4 ml of sodium carbonate (0.075 g ml^–1). The mixture was left to stand for 30 min at 30°C, and then transferred to an ice bath (0°C) for 30 min. The absorbance of the solutions was measured at 760 nm. The content of phenolic compounds was determined using gallic acid solution as a standard, and the phenol concentration was expressed in mg 100 g^–1 FW.

Anthocyanin is natural dye responsible for the color of the fruit and belongs to antioxidants which demonstrate health beneficial properties. The spectrophotometric method based on the reversible discoloration of anthocyanin depending on the pH is commonly used to measure the anthocyanin content (Johnson et al., 2020). The anthocyanins content (AC) was determined according to a previous procedure described by Nunes et al. (2001) and consisted of measuring the content of pelargonidin-3-glucoside [the main pigment in strawberries (Nunes et al., 2001)]. For each variant, 2 g of strawberry pulp was collected in triplicate. Subsequently, 18 ml of 0.5% (v/v) HCl in methanol was added to the pulp and the mixture was incubated in a refrigerator (4°C) for 1 h to extract the pigment. After incubation, the mixture was centrifuged and the supernatant was used to determine the anthocyanin content through the use of spectrophotometry at 520 nm. The anthocyanin content was calculated using the following formula: A₅₂₀ ^∗ dilution factor ^∗ [molecular weight of pelargonidin-3-glucoside (PGN)/molar extinction coefficient (MEC)], where PGN = 433.2, MEC = 2.908 ^∗ 10⁴. The result was expressed in terms of an average of three repetitions in terms of mg 100 g^–1 FW.

Pectin are one of the basic components of the cell wall. It has been shown that oxalate-soluble pectin play a significant role in shaping the texture of the fruit, which directly affects, among others, resistance to mechanical damage (Makarova and Shakhmatov, 2020). Strawberry pectin analysis was carried out according to the procedure proposed by Koubala et al. (2008) and Min et al. (2011) with some modifications. 1 g of pulp was taken in triplicate from each experimental variant. 35 ml of 0.25% ammonium oxalate (pH = 4.6) was added to the pulp and the mixture was transferred to a water bath (85°C) for 1 h. After incubation, the mixture was centrifuged (20,000 × g) for 10 min and the supernatant was collected. Three volumes of 96% ethanol were added to the supernatant and the solution was incubated in a refrigerator (4°C) for 24 h. The next step was to centrifuge (20,000 × g, 10 min) the solution and discard the supernatant. The remaining residue contained pectin, it was washed twice with 96% ethanol, dried and used to determine the D-galacturonic acid content.

Content of galacturonic acid as the main component of pectin determines suitability of fruit for processing (gelling, production of ascorbic acid) (Ben Abdallah et al., 2018). The content of D-galacturonic acid (GalA) in strawberries was determined using a continuous flow analyser (CFA), SanPlus (Skalar, Netherlands) according to the procedure recommended by the manufacturer. The applied automatic colorimetric method of measurement of GalA content is based on a color reaction, where the color intensity is measured at a wavelength of 520 nm (Ognyanov et al., 2021). 10 mg of dried pectin was dissolved in 12 ml of deionised water. The resulting solution was diluted 10 times and the D-galacturonic acid content was determined. The result is expressed in g kg^–1 DW.

The rheological properties, which demonstrate the relationship between the structural, mechanical and sensory properties, are among the basic parameters of pectin (Xie et al., 2021). The rheological properties were measured using a Discovery HR-1 hybrid rheometer (TA Instruments, United States) with a cone-plate sensor. In brief, 1% aqueous solutions of strawberry pectin extracted with ammonium oxalate were prepared according to a procedure described elsewhere (Koubala et al., 2008; Min et al., 2011). For each variant of the experiment, pectin solutions were prepared in triplicate and each measurement was carried out at a temperature of 20 ± 0.5°C. Viscosity was measured at a constant shear rate of 10 s^–1 (three repetitions), and the flow curves were determined based on measurements at variable shear rates of 10 and 600 s^–1. Flow curves were described using the Ostwald–de Waele model as represented by the following equation:

where σ is shear stress (Pa), k is consistency index (Pasⁿ), γ is shear rate (s⁻¹) and n is flow behaviour index.

Antagonistic properties of consortia against fungal pathogens are determined in order to test the effectiveness of the tested bacterial consortia in combating fungal and fungal-like pathogens in the strawberry (Win et al., 2021). In vitro confrontations of four separate bacterial consortia and their mixtures (C5) against four selected phytopathogenic fungi and fungal-like-pathogens were set up using the plate culture method (Petri dish diameter 90 mm) with potato dextrose agar (PDA). Paper discs (5 mm diameter) were surface sterilized with UV light, dipped in 30 μl of bacterial consortia suspension (10⁸ cfu ml^–1) and placed in duplicates on Petri dishes inoculated with fungal pathogens. The pathogen inoculation included 150 μl of inoculum of a 7-day old culture of B. cinerea G277/18, Phytophthora sp. G408/18, Verticillium sp. G296/18, and Colletotrichum sp. G171/18 suspended with 10 ml of sterile water. The concentration of B. cinerea and Colletotrichum sp. was 10³ jtk ml^–1, P. cactorum 10⁵ jtk ml^–1, and Verticillium sp. 10⁴ jtk g^–1. The pathogen-inoculated plates with discs soaked in bacterial consortia were incubated at 26°C in the dark. The observations were recorded 4 days after inoculation by measuring the fungal growth inhibition zone around the paper discs containing bacterial consortia.

Characteristics of soil used for strawberry cultivation is a source of information about the processes during the growth and development of plants, which can have a direct impact on the quality of the fruit. Methods determining the content of proteins, enzymes, carbon and nitrogen in soil provide information on the level of soil degradation and allow the assessment of the importance of the biological consortia used (Wang et al., 2017). Soil samples were taken by complete randomization from a depth of 0–15 cm. The soil was dried at 23°C and sieved through a sieve with a mesh diameter of 2 mm. Total glomalin content (TG), easily extractable fractions of glomalin (EEG) (Wrigth and Upadhyaya, 1998), soil enzyme activity (dehydrogenase DHA) (Klein et al., 1964), acidic phosphatase (ACP), alkaline phosphatase (ALP) (Tabatabai and Bremner, 1969), as well as the carbon and nitrogen content in the biomass were determined in the samples.

Principal component analysis (PCA) is used to discover regularities between variables. It consists in determining the components which are a linear combination of the examined variables. PCA enables the identification of those initial variables that have a significant impact on the appearance of individual principal components (Yagmur and Gunes, 2021). In order to assess the relationship between the studied parameters, PCA analysis was performed using STATISTICA software (Statistica v.12, StatSoft Inc., United States).

The obtained results were analysed with STATISTICA software (Statistica v.12, StatSoft Inc., United States) using a two-way analysis of variance (ANOVA) followed by the Tukey HSD test or Tuckey for different N, F-Welch and RIR Tuckey test for unequal numbers or ANOVA Kruskal–Wallis test; significant differences were determined at P < 0.05.

The shape of strawberries has a significant influence over visual quality and consumer interest. Based on previous findings, auxin derived from achene is responsible for cell division and expansion (Zahedipour-Sheshglani and Asghari, 2020), this changes the shape of the strawberry. Consumers prefer round strawberries (Zahedipour-Sheshglani and Asghari, 2020). The change in shape from oblong (in C0) to round after the use of the appropriate consortium was noted in strawberry P (C4 and C5) and (Figure 2D), which makes them the most attractive to the consumer. Strawberry V (C4), P (C3), and MIX (C2) were distinguished by their flattened shape (Figures 2C,D,F). The remaining fruits were characterized as oblong.

An important parameter for assessing the quality of strawberries is firmness. Ensuring the proper firmness of the fruit allows for longer storage periods and facilitates transport over greater distances (Liu et al., 2019). The highest increase in firmness was observed for MIX-infected strawberries treated with C2, the maximum load in this case was on average 2.4 times higher than in the control (C0) (Figure 2F). A statistically significant increase in the maximum load value as compared to the control was also observed in the NC (C1), P (C4), and C (C5) groups (Figures 2A,D,E). It is assumed that the reason for the increase in the firmness of strawberries infected with selected pathogens could be the activity of bacterial consortia associated with the production of metabolites limiting mycelium growth and leading to an improvement in the quality and firmness of the fruit. Strawberries soften during ripening, mainly by degrading the middle lamina of the cell wall of the cortical parenchyma cells (Qin et al., 2017). One of the reasons for this degradation may be the activity of fungal pathogens attacking the fruit during ripening and storage (Ahmadi-Afzadi et al., 2013). The treatment of strawberries with Hanseniaspora uvarum yeast and infection with B. cinerea has been shown to preserve fruit firmness as compared to the control (Qin et al., 2017). The impact of the investigated bacterial consortia and fungal and fungal-like pathogens on the firmness of strawberries has not yet been investigated. The production of various metabolites that dissolve mycelium might play a role (Olanrewaju and Babalola, 2019). It is known that treating strawberries with beneficial microorganisms can improve the quality and properties of the stored fruit, including firmness (Fan et al., 2009). The antifungal activity of Bacillus sp. isolates against C. acutatum (Moreira et al., 2014) and Phytophthora infestans (Caulier et al., 2018), Lysobacter sp. and Pseudomonas sp. against Colletotrichum sp. (Tang et al., 2019), S. griseus against P. capsici (Nguyen et al., 2015) and Lysobacter sp. against P. infestans (Lazazzara et al., 2017) have been confirmed.

Fruit firmness is closely related to the dry matter content. Their soft texture and high water content make strawberry fruit susceptible to mechanical and physical damage which facilitates the penetration of microorganisms (Siebeneichler et al., 2020). In General, fruit with a higher tissue density exhibits a higher dry matter content and a greater degree of firmness compared to fruit with a lower tissue density (Tarantino et al., 2018). This relationship was observed for the strawberries NC (C1) and C (C5), with an increase in firmness and dry matter compared to the control (Figures 2A,E, 3A,E). An inverse relationship was observed in samples P (C4) and MIX (C2), fruit with a higher degree of firmness had a lower or comparable to the control dry content (Figures 2D,F, 3D,F). It is assumed that the decrease in the firmness of fruit with a high dry matter content is caused by a relatively high cell fragility, low turgor pressure or a low degree of adhesion between the adjacent strawberry tissue cells (Harker et al., 2000). Tissue hydration has a great impact not only on firmness, but also on fresh fruit weight. Studies have shown that strawberries may contain 84–92% water, depending on the variety and cultivation method (Liu et al., 2019). Only the C3 bacterial consortium increased the fresh matter content over the no contaminated (NC) strawberry by 63% (Figure 3G) and C3 and C5 consortia increased the fresh matter content in MIX-infected strawberry by 21% on average (Figure 3L). The higher fresh weight combined with the lower dry weight values indicate a higher water content in the strawberries belonging to these groups.

One of the factors determining consumer interest in strawberries is the SSC content, which is defined as the aggregate concentration of sugars (80–90% of the SSC), acids and other solutes in the cell juice (Mackenzie et al., 2011). The average content of SSC in the tested fruits was 6% (Figures 2S–X), which is the same as other studies which reported the content of SSC in strawberries to be within the range of 4–10% (Chen H. et al., 2018). In most cases, the SSC content was greater than or comparable to the control (C0) in strawberries treated with the bacterial consortia. A statistically significant decrease in the SSC value by 0.9–3.4% compared to the control (C0) was observed in groups V (C4), C (C3), and MIX (C1 and C4) (Figures 2U,W,X). The occurrence of differences in the content of SSC in the tested strawberries is natural and may result from differences in the cultivation method (Cao et al., 2015) consisting of treating the fruit with different bacterial consortia. The SSC content is influenced by various factors, such as genetics, climate, water management and cultivation practices. Positive correlations between the nutrient content, e.g., phosphorus and an increase in SSC content was noted for the strawberries (Valentinuzzi et al., 2015). This effect may occur due to the ability of bacteria to dissolve phosphates, which lowers soil pH and increases phosphorus availability through the production of organic acids. Moreover, an increase in the content of phosphorus in the fruit was shown after the treatment of strawberry seedlings with Bacillus sp. and Klebsiella planticola (Tomic et al., 2015).

Polyphenols and anthocyanins are responsible for the bright red colour of strawberries and play a key role as bioactive ingredients (de Andrade et al., 2019). The mean content of polyphenols in the tested fruit was in the range of 93–115 mg 100 g^–1, while the anthocyanins content was in the range of 31–57 mg 100 g^–1. The increase in polyphenol content was only observed in the NC group (C2) and was 20% greater than in the control (C0) (Figure 2M). None of the preparations used caused a statistically significant decrease in the content of polyphenols in strawberry cv. Honeoye. Unlike the case of polyphenols, a decrease in the content of anthocyanins in strawberry NC (C2), V (C2), and MIX (C1) was noted (Figures 2M,O,R). However, an increase in anthocyanin content at the level of 25–51% compared to the control (C0) occurred only in the group of Phytophthora sp. infected strawberries treated with C2, C3, C4, and C5 consortia (Figure 2P). It is predicted that the changes to the level of total phenolic compounds and anthocyanins may be due to the presence of pathogenic fungi, and fungal-like-pathogens, and beneficial bacteria. The bacterial synthesis of plant hormones or amino acids may enter the shikimic acid metabolic pathway, thereby acting as the precursors of phenolic acids (Cisternas-Jamet et al., 2020). The increase in anthocyanin content may be attributed to the release of anthocyanins from degraded cellular components (López-Ortiz et al., 2019), the activity of the enzymes responsible for the synthesis of anthocyanins and also the activity of microorganisms. Lingua et al. (2013) demonstrated the positive effect of bacteria of the genus Pseudomonas on the anthocyanin (cyanidine-3-glucoside and pelargonidine-3-glucoside) concentration in strawberries. However, the anthocyanin content shows a high degree of variability with respect to species, varieties, growth conditions and the degree of fruit ripeness (Todeschini et al., 2018).

The content of galacturonic acid (Figure 2), which is the main component of pectin, is important in fruit processing. Pectins have stabilizing and gelling properties, which is why they are used in the production of jam, juice, drinks, and jellies (Ben Abdallah et al., 2018). In addition, galacturonic acid is extracted from fruit for the synthesis of ascorbic acid (Agius et al., 2003). The content of galacturonic acid may vary; in a previous study, a ripe strawberry of the cultivar Chandler was found to contain about 330 mg of galacturonic acid g^–1 DW (Paniagua et al., 2017). The use of consortia resulted in an increase in the galacturonic acid content of ≥400 mg g^–1 DW (>40%) for strawberry grown in the following variants: BC (C1), C (C2, C3, C4, and C5), and MIX (C1 and C2) (Figures 2T,W,X), which was greater than the control (C0). Relatively large fluctuations in the content of galacturonic acid confirms the complexity of the processes caused by the activity of microorganisms, which are affected by plant variety, growth conditions, pathogen infections and the consortia used.

The rheological properties of liquids determine the behaviour of the solution at all of the production stages, such as filling, mixing, packaging and removal from the package (Lee et al., 2009). Pectin solutions are used for the production of yoghurts, jelly, juices (Ke et al., 2020), paints, pastes and medicines (Jouini et al., 2018), due to their gelling, stabilizing and flavour-enhancing properties (Ke et al., 2020).

The viscosity of 1% solutions of strawberry pectin extracted with ammonium oxalate is shown in Table 1. The increase in viscosity as compared to the control (C0) occurred in NC (C3), BC (C1, C4, and C5), C (C2), and MIX (C2, C3, C4, and C5) strawberries. Also, contamination with pathogens (BC, V, C, and MIX) significantly lowered the viscosity of the strawberry pectin solutions in the controls (C0) as compared to the control of uninfected NC strawberries (C0). These results show that the use of appropriate consortia, dedicated to a specific pathogen, can increase the viscosity of pectin solutions. The decrease in viscosity may be attributed to the activity of microorganisms that soften the fruit cell walls though pectin degradation (Mierczyńska et al., 2014). Viscosity depends, among other factors, on the molecular weight of the pectin molecules, their degree of methylation and pH, which may be affected by fungi and bacteria associated with strawberries at all stages of growth and ripening. It has been proven that viscosity increases with increasing pectin concentration (Chan et al., 2017).

The rheological data of the 1% pectin solutions were suitably adjusted by the Ostwald–de Waele model with a high coefficient of determination of R² > 0.996. Higher values of the coefficient k correspond to the higher viscosity of the samples. Based on the k-factor analysis, pectin solutions were obtained with a viscosity higher than that of the control (C0) in the NC (C3) and BC (C4 and C5) groups (Table 1). The antagonistic interactions of the microorganisms used led to the modification of pectin, an increase in apparent viscosity and the coefficient k, which is associated with an increase in the molar mass of pectin (Fracasso et al., 2018). The high molar mass of pectin promotes the formation of a gel structure (O’Donoghue and Somerfield, 2008). However, for some applications a lower viscosity may be seen as a positive property of the solutions due to pelargonidine lower energy consumption during processing (Venzon et al., 2015).

Flow curves reveal pseudoplastic, non-Newtonian behaviour due to the melt flow index values n (n < 1). The 1% pectin solutions tested are classified as shear thinned. Their viscosity decreases as the shear rate increases. Based on a previous study, the lower the n coefficient, the greater the degree of pseudoplasticity (Lee et al., 2009). The values of n for the tested solutions were in the range of 0.713–0.996. In comparison, the n values for 2% strawberry pectin solutions were 0.52, while for 5% strawberry pectin solutions they were 0.54 (Mierczyńska et al., 2017). Pseudoplastic fluid behaviour is important in the food industry (gelatinization of jellies and jams, thickening of juices and purees, and stabilization of liquids) (Grassino et al., 2016) and in medicine production (thickening of syrups or ointment, encapsulation of preparations) (Jouini et al., 2018).

The differences in the values of viscosity and in the flow of pectin solutions refers to the molecular properties of the samples, such as the chemical composition of neutral sugars, galacturonic acid content and the degree of pectin esterification (Fracasso et al., 2018). Microorganisms may have an indirect effect on the chemical composition of the samples (Erturk et al., 2012). The use of beneficial microorganisms such as Pseudomonas sp., Bacillus sp., and Azospirillum sp. results in an increase in plant biomass and fruit yields (Erturk et al., 2012). In addition, it was found that beneficial fungi and plant growth-promoting bacteria show antagonism to the pathogens C. acutatum, Macrophomina phaseolina, and Fusarium solani in strawberry plants (Pastrana et al., 2016). Inoculation with beneficial bacteria in order to increase plant growth also has potential environmental benefits; it could reduce the use of agricultural chemicals and facilitate adaptation to sustainable management practices (Erturk et al., 2012).

In Petri dish-based assays carried out for the determination of the antifungal properties of the tested bacterial consortia, C4 and C5 did not show any clear zone of inhibition in the growth of the tested fungi, and fungal-like-pathogens or only indicated very weak inhibition (Table 2). The inhibitory effect was observed for C1, C2, and C3, with evident growth inhibition of all of the tested fungal pathogens in the case of C1 and C2, thereby confirming the antagonistic properties of the bacterial strains present in these consortia, which was observed in a greenhouse experiment. Other studies are consistent with the obtained results and confirm the antagonism of the tested bacterial consortia (contained Bacillus sp., P. polymyxa, and Streptomyces sp.) against strawberry pathogenic microorganisms (Chen P.H. et al., 2018; Li et al., 2021).

The content of nutrients, proteins, and soil enzyme activity plays a key role in the functioning of the ecosystem. The cultivation of plants is accompanied by a decrease in soil productivity related to the depletion of nutrients, the release of toxic metabolites, and the development of pathogenic fungi (Gałązka, 2013). Total glomalin (TG) is one of the glycoproteins produced by arbuscular mycorrhizal fungi that live in symbiosis with plants and facilitate the uptake of water and nutrients from the environment. Easily extractable glomalin (EEG) has a more immunoreactive fraction than TG (Wrigth and Upadhyaya, 1998). For this reason, an increase in TG and EEG levels is desirable in the context of promoting plant growth. An increase in the TG content as compared to the control (C0) was only observed in the strawberry NC (C5), while an increase in EEG content may be observed in the strawberry BC (C5) (Table 3).

The data shows the significant influence of the type of infectious pathogen and the bacterial consortium used on enzyme activity. The increase in acid phosphatase content as compared to the control (C0) characterized the strawberry fruit in the groups NC (C3, C4, and C5), BC (C2, C3, and C4), V (C1, C2, C3, and C4), and C (C2, C3, C4, and C5), while an increase in the content of alkaline phosphatase occurred in groups BC (C1 and C3), V (C3 and C4), P (C2, C3, C4, and C5), C (C4 and C5), and MIX (C2, C3, and C5) (Table 3). Increased phosphatase activity is associated with a higher content of organic matter in the soil (Singh et al., 2018). In contrast to phosphatase, a statistically significant increase in dehydrogenase content was observed in strawberry V (C1 and C3), C (C1, C2, C3, C4, and C5), and MIX (C2, C4, and C5) (Table 3). The increase in dehydrogenase activity may be explained by the greater availability of nutrients (Kanchikerimath and Singh, 2001).

The relationships between the parameters studied were analysed using the PCA method (Figure 3). The distribution of individual samples on the plane is shown in Figures 3A,C,E,G,I,K. The first two factors (PC1 and PC2) explain over 50% of the total variance among the analysed samples for all of the investigated variables. For all of the tested samples, the first axis (PC1) accounted for over 30% of the total variance. The samples that explain the PC1 and PC2 axis positively have the greatest impact on the tested infection factor. On this basis, we may distinguish C0 and C3 for the NC control (Figure 3A), C0 for BC (Figure 3C), C0 for V (Figure 3E), C5 for P (Figure 3G), C2 for C (Figure 3I), and C3 for MIX (Figure 3K). An analysis of the PCA1-PCA2 observation charts (Figures 3A,C,E,G,I,K) confirms the results of the analyses above; the need to select an appropriate consortium which acts antagonistically against individual pathogens in order to obtain the highest quality of fruit.

An analysis of the PCA variable charts allowed for the identification of certain dependencies between the examined parameters in all of the studied groups, a positive correlation was found between DW and SSC, which was consistent with the results of other studies (Jorquera-Fontena et al., 2014). The increase in the content of anthocyanins (AC) was accompanied by an increase in the content of phenols (PC) only in strawberries infected with Phytophthora sp. (Figure 3H). A positive correlation between the content of anthocyanins and polyphenols indicates a high antioxidant activity (Dembczyński et al., 2015). It was observed that an increase in total glomalin (TG) and easily extractable fractions of glomalin (EEG) in the soil were related to an increase in the level of nitrogen (NB) and carbon in biomass (CB) for the NC, V, and MIX groups (Figures 1B,F,L). Glomalin contains approximately 30% of soil carbon and is the main component of soil organic matter (Gałązka, 2013), which is associated with a positive correlation between TG and EEG and CB. The growth of glomalin-producing bacteria (TG and EEG) requires a sufficiently high nitrogen concentration thereby explaining the positive correlation between TG, EEG, and NB (Gałązka, 2013). On the other hand, it is believed that an excessively high nitrogen level in the soil leads to a significant reduction in the activity of dehydrogenases involved in the transformation of soil carbon. High dehydrogenase activity provides favourable conditions for the development of microorganisms in the soil environment (Koper and Siwik-Ziomek, 2006). A positive correlation between dehydrogenase activity (DHA) and CB was noted for the uninfected samples and those infected by Verticillium sp., Colletotrichum sp. and a mixture of pathogens (Figures 1B,F,J,L), which is consistent with the results of the studies by Turski and Wyczółkowski (2008). Our research confirms that there is only a positive correlation between acid phosphatase and alkaline phosphatase for the group infected with Colletotrichum sp. (Figure 3J). For the remaining groups studied, there is either a negative or an absence of any correlation between these enzymes. This situation may be explained by the development of soil microorganisms limiting the activity of certain enzymes. It is assumed that an excess of inorganic phosphorus inhibits the synthesis of phosphatases (Nahas et al., 1982).