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Article

Interaction between Trichoderma sp., Pseudomonas putida, and Two Organic Amendments on the Yield and Quality of Strawberries (Fragaria x annanasa cv. San Andreas) in the Huaral Region, Peru

by
Lucero Huasasquiche
1,
Thania Ccori
2,
Leonela Alejandro
2,
Héctor Cántaro-Segura
3,
Tomás Samaniego
1 and
Richard Solórzano
4,5,*
1
Estación Experimental Donoso, Dirección de Supervisión y Monitoreo de las Estaciones Experimentales, Instituto Nacional de Innovación Agraria (INIA), Lima 15200, Peru
2
Facultad de Agronomía, Universidad Nacional Agraria La Molina (UNALM), Lima 15024, Peru
3
Departamento de Fitotecnia, Facultad de Agronomía, Universidad Nacional Agraria La Molina (UNALM), Lima 15024, Peru
4
Centro Experimental La Molina, Dirección de Supervisión y Monitoreo de las Estaciones Experimentales Agrarias, Instituto Nacional de Innovación Agraria (INIA), Lima 15024, Peru
5
Facultad de Ciencias Ambientales, Universidad Científica del Sur (UCSUR), Lima 15067, Peru
*
Author to whom correspondence should be addressed.
Appl. Microbiol. 2024, 4(3), 1110-1123; https://doi.org/10.3390/applmicrobiol4030075
Submission received: 20 May 2024 / Revised: 20 June 2024 / Accepted: 27 June 2024 / Published: 22 July 2024
(This article belongs to the Special Issue Applied Microbiology of Foods, 2nd Edition)

Abstract

:
Strawberry cultivation holds significant economic and social promise within Peruvian fruit production. However, conventional management practices have led to the excessive use of agrochemicals in this crop. This study proposes an organic approach to strawberry production, integrating less environmentally harmful technologies. The aim was to assess microbial inoculation by using Trichoderma sp. and Pseudomonas putida and the application of organic amendments on strawberry seedlings of the commercial cultivar “San Andreas”. A field experiment was established with evaluations in the vegetative and productive stages. Results indicate that the co-inoculation of Trichoderma sp. and Pseudomonas putida increased leaf area by 7%, and enhanced the aerial part’s fresh and dry biomass by 13% and 28%, respectively, compared to treatment without microbial inoculation. Concurrently, compost application increased the leaf number and aerial dry biomass by 22% and 19% at the end of the vegetative stage, respectively, compared to treatment without organic amendment. In addition, it reduced the days for flowering, maintaining the fruit’s physicochemical attributes. Regarding yield, the amendments application significantly enhanced fruit weight per plant by 40%, especially when applied together with Trichoderma sp., and co-inoculation increased the number of fruits per meter square by 22%. These findings highlight the potential of technologies such as microbial inoculation and organic amendments to enhance strawberry yields and to gradually reduce the use of synthetic fertilizers.

1. Introduction

Strawberry (Fragaria sp.) is one of the most appreciated cultivated berries in the world due to its high economic and nutritional value [1]. In 2020, global strawberry production value reached USD 14 billion [2]. Moreover, strawberry consumption provides essential nutrients and high vitamin C and folate levels. In addition, strawberries are rich in bioactive compounds such as phenolic compounds, which together with vitamin C act as antioxidants in the human diet [3].
In 2022, more than 9.5 million tons were produced globally, with China and the United States leading production [2]. Latin America contributed 5% of the total production, with Peru being the third largest producer with almost 46,000 tons of volume [2]. Peruvian production value doubled during 2020–2022. Sowed areas are concentrated in the coastal regions, mainly in Lima and La Libertad, but in recent years cultivation has expanded to the Andes regions or inter-Andean valleys [4]. In addition, strawberry cultivation generates a considerable labor demand for harvesting, thus providing work opportunities throughout the year.
Most strawberry fields in Peru are managed by small producers, typically cultivating areas of no more than three hectares [4], and they often receive minimal technical and financial assistance [5]. The main source of information that strawberry growers have regarding chemical input use is through sales personnel in commercial houses [6], which in many cases causes the excessive use of agrochemicals. This global problem has negatively impacted the environment, leading to ecosystem degradation. In 2018, total global emissions from agriculture and related land use reached 9.3 billion tons of equivalent CO2 [7], which contributes the most to the greenhouse effect. N2O emissions are expected to increase between 30–60% until 2030 [8] and fertilizer consumption by developing countries will exceed 75% of world consumption in 2050 [9]. Furthermore, the excessive use of fertilizers has led to a significant reduction in the economic efficiency of strawberry production [10].
In this context, bio-input use emerges as an alternative to generate cleaner and more sustainable production systems [11]. Among practices associated with bio-input use, the incorporation of plant-growth-promoting microorganisms into the soil can provide nutrients to plants, stimulate their growth, or protect them from pathogen attack [12]. Thus, microbial inoculation reduces the need for fertilizers, an increasingly important strategy being adopted worldwide. Trichoderma is a genus widely known for its antagonistic capacity; however, some strains of Trichoderma spp. have beneficial effects on plant growth [13]. These strains operate through various mechanisms, including the biological control of phytopathogens, improvement in nutrient absorption, increased root hair formation, and the induction of systemic resistance in plants [14]. Likewise, Pseudomonas species influence plant growth due to their ability to produce siderophores, solubilizing phosphorus and secreting antagonistic compounds for plant pathogens [15].
Solid waste management through organic composting is also a potential alternative for agricultural system sustainability. Organic amendments are used to improve the physical, microbiological, and chemical conditions of soils thereby increasing plant nutrient availability [16]. Thus, compost is an excellent organic fertilizer because it provides essential nutrients and organic matter. Additionally, compost enhances the soil’s water retention capacity, improves tillage, promotes better aeration for seed germination, and consequently supports robust plant root development [17].
Undoubtedly, the strawberry is a crop with great export potential and profitability in Peru [18]. Still, there is a need to explore new technologies that are environmentally friendly to our soil integrity and human health. Therefore, the objective of this study is to evaluate the influence of microbial inoculation and the application of organic amendments on strawberry (Fragaria x ananassa cv. San Andreas) yield and quality, as organic alternatives for a more sustainable management of this crop.

2. Materials and Methods

2.1. Plant Material and Sowing

Strawberry plants (Fragaria sp. var. San Andreas) were obtained from the National Vegetable Research Program (PNIH) of the National Institute for Agrarian Innovation (INIA), as 3-month-old bare-root seedlings. Field installation was carried out in June 2023 at the Donoso Agricultural Experimental Station of INIA in Huaral Valley, and the experiment lasted seven months, from transplanting to harvest. The Huaral region is influenced by winter fogs and drizzles, creating a cool and humid environment in the middle of the desert. During the period from June to December 2023, the average temperature was 19.5 °C (max. 23.3 °C, min. 17.0 °C) and the relative humidity was 80.5%. The experimental area was 172.8 m2. The soil of the experimental plot was sandy clay–loam in texture, low in organic matter (0.7%), with 8.0 soil pH; the available N, P, and K were 15, 109, and 150 kg ha−1, respectively. The planting frame during transplanting was 0.8 m between furrows and 0.2 m between plants, with a total density of 62,500 plants per hectare. The field was irrigated 1–2 times per week, according to demand, and manual weeding was carried out every two weeks. No synthetic fertilizers or agrochemicals (for pest control) were used during the experimental area management.

2.2. Design and Treatments

A Completely Randomized Block Design (CRBD) experimental plot was set up with a 4 × 3 factorial scheme, involving four combinations of microorganisms and three organic amendments. A total of 12 treatments were used and considering that 3 blocks were installed in the plot, a total of 36 experimental units were managed during the whole research. The different treatments used in the experiment are described in Table 1.
The organic amendments application (compost and cow manure + avocado stubble) was carried out five days before sowing, at a 15 t ha−1 for compost, 7.5 t ha−1 for manure, and 7.5 t ha−1 for avocado stubble dose. The pH of the organic amendments was around 8.0 and the electrical conductivity was low for the manure and compost (<1 dS∙m−1) but high for the leaf litter (2.2 dS∙m−1). The C:N ratios for the compost, manure, and leaf litter were 10.0, 19.8, and 26.8, respectively. Microbial inoculation was carried out 4 times during the trial; the first at sowing and the remaining as complementary inoculations in the field at 21, 50, and 77 days after transplanting (dat). The first inoculation consisted of immersing the roots inside the inoculant for 15 min, and then transplanting the seedlings in the field [19], ensuring that the crown was at ground level. Complementary inoculations were carried out by adding 2 L of the inoculant to each plant’s neck [20].

2.3. Inoculant Preparation

For inoculation with Trichoderma sp., a spore suspension obtained by washing sporulated broken maize with this fungus (Soluciones Agrosostenibles S.A.C., Trujillo, Peru, 1 × 1012 conidia per kg concentration,) in non-chlorinated water at 40 g∙L−1 was prepared (Solution A, inoculant). For inoculation with Pseudomonas putida, a pure culture of P. putida strain PS168 (private collection) was prepared, from which a 1% (v/v) dilution was made for the inoculation. Pure culture was prepared by incubating the strain in nutrient broth for 4 days at 28 °C until a 109 CFU mL−1 concentration (Solution B) was obtained. Subsequently, Solution B was diluted by taking a 10 mL aliquot and mixing it with 1 L of non-chlorinated water (Solution C, inoculant). For treatments containing both microorganisms, the inoculant was prepared at a rate of 10 mL of pure culture of Pseudomonas putida (Solution B) for each 1 L of spore suspension (Solution A).

2.4. Biometric Parameters

The seedling mortality percentage was assessed at 30 dat. In addition, on five randomly marked plants per treatment, the leaf number, plant height (cm), and leaf area (cm2) were assessed monthly until 90 dat. The leaf number was assessed by manually counting the leaves on each plant; the height was measured from the plant’s crown to the last point of plant biomass, without spreading the leaves; and the leaf area was calculated by measuring the width and length of each leaf on the plant. Three plants were randomly removed to assess the fresh and dry biomass at 90 and 160 dat. For this, the root part was separated from the aerial part and the fresh weight of each one was recorded by a high precision balance (Axis Aka 4200, Gdañsk, Poland). They were then placed in paper bags and dried initially at room temperature for three weeks, followed by further drying in a drying oven (Yamato Scientific DS-64, Santa Clara, CA, USA) at 70 °C for 3 days [21].

2.5. Performance and Quality Parameters

From 90 dat onwards, plants were evaluated daily to observe the appearance of the first flower in each treatment, thereby calculating the number of days to flowering. In addition, in five randomly marked plants in each experimental unit, the number of flowers, the fresh weight (g), and the fruit dimensions (cm) were evaluated weekly. Additionally, the number of commercially ripe fruits (minimum 75% of the total fruit surface with red coloring) per experimental unit was recorded. At 160 dat, the fruits were harvested. The cell juice pH was evaluated using a multi-parameter meter (Hanna HI2020, Hanna Instruments, Leighton Buzzard, Bedfordshire, UK) by the AOAC 981.12 method; the acidity by titration with 0.1 N sodium hydroxide (AOAC 942.15 method); the Brix degrees by using a digital refractometer (PAL-1 Atago 3810, ATAGO, Tokyo, Japan); and the firmness by using a penetrometer (Lutron FR-5120, Lutron, New York City, NY, USA).

2.6. Statistical Analysis

The results were analyzed using R software version 4.3.1 (Lucent Technologies, Murray Hill, NJ, USA), employing the analysis of variance (ANOVA) with a significance level of 0.05, following verification of data normality assumptions and homogeneity of variances. Means were analyzed by the least significant difference test (LSD Fisher) with a p ≤ 0.05.

2.7. Principal Component Analysis

A principal component analysis (PCA) was conducted using PAST 3.24 software to assess the relationship between the studied parameters. Separate PCA analyses were performed for each factor: microbial inoculation and application of organic amendments.

3. Results

3.1. Strawberry Plant Rooting Percentage (Fragaria sp. var. San Andreas)

The results indicated no interaction between the study factors; however, a significant effect of microbial inoculation on the percentage of strawberry seedling mortality was observed. Plants inoculated with Trichoderma sp. and co-inoculated with Trichoderma sp. and Pseudomonas putida showed lower plant mortality (p-value 0.024) compared to non-inoculated plants (Figure 1).

3.2. Number of Leaves, Plant Height, and Leaf Area

A significant interaction of factors was observed in the initial evaluations for leaf area (p-value 0.048) and plant height (p-value 0.027) (Figure 2). The combined treatment of inoculation with Trichoderma sp. plus compost incorporation was the most significant interaction for both variables. It was also observed that, in both parameters, the organic amendments application has a very variable effect when interacting with Trichoderma sp. Figure 2 shows that Trichoderma sp. in combination with cow manure plus avocado stubble presents very low values; however, when combined with compost, the height and leaf area values increase. This significant interaction was not maintained until the end of the trial.
Regarding the individual effects of treatment on each parameter, it was observed in Table 2 that, for leaf number, microbial inoculation did not differ from the non-inoculated treatment; in fact, the treatment with Trichoderma sp. had the lowest value at 90 dat. In this period, it was observed that the compost application increased the number of leaves (p-value 0.047), differing from plants without the organic amendment. None of the factors had a significant effect on plant height at 90 dat.
The co-inoculated treatment (Trichoderma sp. + Pseudomonas putida) showed plants with greater leaf area compared to the other treatments (Figure 3); this result was significant at 60 (p-value 0.005) and 90 dat (p-value 0.012).

3.3. Fresh and Dry Biomass

A significant interaction of factors was observed in the aerial (p-value 0.040) and root (p-value 0.014) dry biomass parameters. The treatment whose seedlings were co-inoculated and had compost application stood out in both parameters (Table S1). This interaction was only significant in the first evaluation (90 dat) and was not maintained towards the end of the trial, so the results were analyzed according to each study factor.
It was observed that microbial inoculation had statistical differences in the fresh (p-value 0.029) and dry biomass (p-value 0.018) of the aerial part at 90 dat (Table 3). In both parameters, co-inoculated seedlings (Trichoderma sp. + Pseudomonas putida) presented higher aerial biomass, and in the specific case of aerial dry biomass, the co-inoculation treatment was statistically different from the treatment without inoculation. The organic amendments application, specifically compost, was able to increase the aerial dry biomass (p-value 0.008) at 90 dat (Table 3), compared to cow manure and the treatment without amendment (Table 3).

3.4. Flowering, Fruit, and Yield Analysis

The results showed that the plants with the compost application started flowering in a shorter time compared to the plants with treatment without amendment (p-value 0.007). Also, plants with inoculation with Pseudomonas putida (individual and co-inoculated) started fruiting in a shorter time compared to plants with the treatment without inoculation (p-value 0.012) (Figure 4).
Regarding flowers and fruits, it was observed that the compost application treatment increased the number of flowers per m2 (p-value 0.027), while co-inoculation increased the number of fruits per m2 (p-value 0.037) (Figure 5).
The fruit’s physical–chemical evaluation results are shown in Table 4. Statistical differences were only found in the titratable acidity of the fruits, where the treatment without organic amendment showed slightly more acid fruits (p-value 0.047). Concerning pH, firmness, Brix degrees, and fruit dimensions, it was observed that the study factors maintained the same fruit quality as the control treatments.
In terms of crop yield, the results showed that the organic amendments application, with either compost or manure, significantly increased the grams of fruit per plant (p-value 0.023). In the microbial inoculation cases, we did not find significant differences (Table 5).
Figure 6 and Figure 7 show the Principal Component Analysis (PCA) for microbial inoculation and the application of organic amendments, respectively. In both cases, the first two principal components explain over 80% of the total variance. The samples that are on the positive axis of PC1 have a greater influence on most of the variables evaluated (Figure 6b and Figure 7b). On this basis, we observed that co-inoculation (Figure 6a) and the compost application (Figure 7a) are the treatments that had the best results in the variables.

4. Discussion

Trichoderma sp. inoculation and the co-inoculation of Trichoderma sp. with Pseudomonas putida were found to be the treatments with the lowest mortality percentage, less than 7%. Similar results have been reported with the application of effective microorganisms supplemented with bokashi, where strawberries reached less than a 10% mortality rate [22]. In other studies, more than 98% of strawberry seedlings inoculated with Trichoderma sp. [23] were able to achieve rooting. However, Pseudomonas putida has a higher mortality rate, similar to the uninoculated treatment.
The difference between Trichoderma sp. and Pseudomonas putida is likely due to the greater efficacy in controlling root diseases and Trichoderma sp. causing greater root biostimulation. Root pathogens such as Phytophthora sp., Fusarium sp., and Rhizoctonia sp. are the main limiting factors in strawberry establishment [24]. These cause rotting of the crown and lateral roots. The mechanisms used by Trichoderma sp. to control root pathogens are antibiosis, mycoparasitism, induced resistance, and niche exclusion [25]. Previous research shows that glyotoxins, viridin, trichodermin, and furanone are the main metabolites that degrade the cell wall and cause pathogenic hyphae-programmed cell death [26].
Strawberry’s high sensitivity to salt stress could cause the low rotting percentage [27] obtained in this research (the maximum value was 93%). Osmotic and oxidative stress caused by a high level of salts inhibits strawberry root development in the early development stages [28]. Trichoderma sp. promotes root growth by releasing auxin intermediary metabolites such as indole 3-acetaldehyde acid (IAA) and indole 3-ethanol (IET) [29]. Furthermore, under salt stress conditions, Trichoderma sp. produces 6-pentyl-α-pyrone (6-PP), a volatile organic compound that inhibits primary root growth and induces lateral root growth [30]. However, to determine the influence of Trichoderma sp. on the mortality rate, more detailed studies should be carried out.
Regarding vegetative growth, it was found that the combination of Trichoderma sp. with compost resulted in the highest values for leaf number and plant height during the early growth stages. However, at 90 dat, only the compost explained the highest number of leaves and the co-inoculation of Trichoderma sp. and Pseudomonas putida explained the highest leaf area. Also, microbial co-inoculation and the compost application increased the aerial dry biomass.
Increased biomass expressed as greater leaf number and plant height is related to a major leaf photosynthetic activity [31]. Sucrolytic activity in Trichoderma sp. fungal cells, mediated by intracellular invertase, is known to direct the systemic induction of photosynthesis and sucrose partitioning to the roots [32]. In addition, Trichoderma sp. causes plant gene expression reprogramming to induce the rubisco activity and the oxygen-generating complex of the photosystem II [33]. The leaf area increase is likely due to an increased requirement for photosynthetic activity. In addition, synergistic action between T. harzianum and P. fluorescens in increasing nitrogen and phosphorus uptake has been reported, resulting in higher aerial biomass [34]. Both Pseudomonas sp. and Trichoderma sp. can exert beneficial and biocontrol effects on plants; however, studies show that combinations of the two are more effective than each individually [35,36]. This situation was observed in our results, as co-inoculated seedlings showed greater leaf area and aerial biomass, statistically different from those in which only one microorganism was inoculated. In addition, compost use as an organic amendment or substrate for Trichoderma sp. development resulted in greater plant growth stimulation. This positive effect of compost agrees with other studies, where the incorporation of organic amendments in strawberry cultivation increases the number of leaves [37].
The positive effect of co-inoculation could be associated with synergism between bioactive molecules or volatile organic compounds of both strains [38]. Biomass increase due to the integrated effect of different rhizospheric strains has been reported in strawberry cultivation [39]. Also, this response could be attributed to chlorophyll content increase, an indirect indicator of leaf photosynthetic activity [40]. This study revealed the positive effect of the interaction between compost and co-inoculation on biomass increase. There is scientific evidence justifying the increased nitrogen mineralization and phosphatase activity in the soil due to the inoculation effect of Trichoderma sp. supplemented with compost [41]. Also, studies indicate that the application of compost improves microbial activity and thus generates the production of growth regulators by microorganisms, which is reflected in an increase in biomass in the plant. [42]. This is supported by other studies with strawberry seedlings grown under greenhouse conditions, where it is shown that compost helps Trichoderma sp. populations to remain stable in the soil [43].
Inoculation with Pseudomonas putida (individual or co-inoculation with Trichoderma sp.) influenced the days to flowering, reducing the time by an average of 4 days. These results have been rarely reported in fruit crops; however, it has been found in the literature that Pseudomonas sp. influences flowering. In a study on the chrysanthemum, Pseudomonas sp. accelerated flowering by an average of 14 days compared to the control [44]. Another study on the chrysanthemum showed that two strains of Pseudomonas putida, characterized as indole acetic acid (IAA) producers, improved flowering [45]. So, it is likely that this influence is related to the improvement in nutrient absorption and the transport of growth-promoting substances, resulting in an early transformation of plant parts from the vegetative to the reproductive phase.
On the other hand, organic amendments not only provide nutrients to the plant but also contribute organic matter, thereby increasing soil fertility [46]. The addition of compost is known to stimulate microbial growth due to the increased amount of organic carbon it provides [47]. It can also have a direct effect on the plant due to the microorganisms present in it. Manure improves soil’s chemical and physical properties such as soil water, bulk density, erosion resistance, and nutrient status, among others, which can favor crop growth and productivity [48]. The benefits of the amendments application were reflected in the yield increase (g fruit plant−1) observed in our results, which correlates with what is found in the literature. Some studies conclude that the addition of vermicompost improved growth and yield levels in strawberries [49,50]. Also, significant differences in strawberry yield and fruit quality were found with the addition of chicken manure [51].

5. Conclusions

Pseudomonas putida inoculation accelerated the seedling’s flowering process and co-inoculation (Trichoderma sp. + Pseudomonas putida) increased the leaf area, fresh biomass, and dry biomass, both aerial and root, and the number of fruits per square meter. Concerning the organic amendments, only the compost treatment stood out, with higher values found in the number of leaves, the aerial dry biomass, the days to flowering, the number of flowers per square meter, and the fruit yield per plant. Under the conditions in which the experiments were carried out, these results show that compost application at 15 t∙ha−1 and co-inoculation of Trichoderma sp. and Pseudomonas putida have potential as organic technologies in Fragaria sp. cultivation; however, it is important to repeat these treatments in other seasons and regions to validate the effect observed in our study.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/applmicrobiol4030075/s1, Table S1: Aerial and root dry biomass at 90 dat based on the interactions of the two study factors.

Author Contributions

Conceptualization, H.C.-S. and R.S.; formal analysis, L.H.; investigation, L.H. and T.S.; methodology, L.H., T.C., L.A. and T.S.; project administration, R.S.; supervision, R.S.; writing—original draft, L.H.; writing—review and editing, R.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the INIA project “Mejoramiento de los servicios de investigación y transferencia tecnológica en el manejo y recuperación de suelos agrícolas degradados y aguas para riego en la pequeña y mediana agricultura en los departamentos de Lima, Áncash, San Martín, Cajamarca, Lambayeque, Junín, Ayacucho, Arequipa, Puno y Ucayali” CUI 2487112.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The authors appreciate the participation and logistical support of Pedro Nicho and José Cóndor Caro, research specialists in the EEA Donoso INIA.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Fernández-Lara, R.; Gordillo, B.; Rodríguez-Pulido, F.J.; Lourdes González-Miret, M.; del Villar-Martínez, A.A.; Dávila-Ortiz, G.; Heredia, F.J. Assessment of the Differences in the Phenolic Composition and Color Characteristics of New Strawberry (Fragaria x Ananassa Duch.) Cultivars by HPLC–MS and Imaging Tristimulus Colorimetry. Food Res. Int. 2015, 76, 645–653. [Google Scholar] [CrossRef] [PubMed]
  2. FAO. FAOSTAT Database. Available online: https://www.fao.org/faostat/en/#data/QCL (accessed on 1 March 2024).
  3. Giampieri, F.; Forbes-Hernandez, T.Y.; Gasparrini, M.; Alvarez-Suarez, J.M.; Afrin, S.; Bompadre, S.; Quiles, J.L.; Mezzetti, B.; Battino, M. Strawberry as a Health Promoter: An Evidence Based Review. Food Funct. 2015, 6, 1386–1398. [Google Scholar] [CrossRef] [PubMed]
  4. Parodi, G.; Benavides, M. Desarrollo Del Cultivo de Berries En Perú. In Avances en el Cultivo de las Berries en el Trópico; Sociedad Colombiana de Ciencias Hortícolas: Bogotá, Colombia, 2021; pp. 91–101. ISBN 978-958-59886-1-3. [Google Scholar]
  5. Flores-Bernedo, J.; Vásquez-Castro, J. Susceptibility to Spirodiclofen in field populations of Tetranychus urticae (Acari: Tetranychidae) from strawberry plantations in Lima region, Peru. Peruv. J. Agron. 2020, 4, 61–67. [Google Scholar] [CrossRef]
  6. Beyer Arteaga, A.A.; Rodríguez Quispe, P.; Collantes González, R.D.; Joyo Coronado, G. Factores Socioeconómicos, Productivos y Fuentes de Información Sobre Plaguicidas Para Productores de Fragaria x Ananassa En Cañete, Lima, Perú. Idesia Arica 2017, 35, 31–37. [Google Scholar] [CrossRef]
  7. FAO. Emissions Due to Agriculture Global, Regional and Country Trends 2000–2018. In FAOSTAT Analytical Brief Series N° 18; FAO: Rome, Italy, 2020; ISSN 2709-0078. [Google Scholar]
  8. FAO. World Agricultural towards 2015/2030. An FAO Perspective; FAO: Rome, Italy, 2003; ISBN 92-5-104835-5. [Google Scholar]
  9. Alexandratos, N.; Bruinsma, J. World Agriculture towards 2030/2050: The 2012 Revision. ESA Working Paper No. 12-03. 2012. Available online: https://www.fao.org/4/ap106e/ap106e.pdf (accessed on 13 June 2024).
  10. Anuradha; Goyal, R.; Sindhu, S. Response of Strawberry (Fragaria × Ananassa Duch.) to PGPR Inoculation. Bangladesh J. Bot. 2020, 49, 1071–1076. [Google Scholar] [CrossRef]
  11. Pulido-Blanco, V.C.; Insuasty-Burbano, O.I.; Sarmiento-Naizaque, Z.X.; Ramírez-Durán, J. Carmenta theobromae (Busck, 1910), Pest of Guava in Colombia: Biology, Life Cycle and Natural Enemies. Heliyon 2020, 6, e05489. [Google Scholar] [CrossRef] [PubMed]
  12. Ahmad, M.; Pataczek, L.; Hilger, T.H.; Zahir, Z.A.; Hussain, A.; Rasche, F.; Schafleitner, R.; Solberg, S.Ø. Perspectives of Microbial Inoculation for Sustainable Development and Environmental Management. Front. Microbiol. 2018, 9, 02992. [Google Scholar] [CrossRef] [PubMed]
  13. Hermosa, R.; Viterbo, A.; Chet, I.; Monte, E. Plant-beneficial effects of Trichoderma and of its genes. Microbiology 2012, 158, 17–25. [Google Scholar] [CrossRef]
  14. Cano, M.A. Interacción de microorganismos benéficos en plantas: Micorrizas, Trichoderma spp. y Pseudomonas spp. Una revision. Rev. UDCA Actual. Divulg. Científica 2011, 14, 15–31. [Google Scholar]
  15. Sah, S.; Krishnani, S.; Singh, R. Pseudomonas mediated nutritional and growth promotional activities for sustainable food security. Curr. Res. Microb. Sci. 2021, 2, 100084. [Google Scholar] [CrossRef]
  16. Murillo Montoya, S.A.; Mendoza Mora, A.; Fadul Vásquez, C.J. La importancia de las enmiendas orgánicas en la conservación del suelo y la producción agrícola. Rev. Colomb. Investig. Agroindustriales 2020, 7, 58–68. [Google Scholar] [CrossRef]
  17. Ajema, W. Effect of compost in Improving Soil Properties an Its Consequent Effect on crop production—A review. J. Nat. Sci. Res. 2021, 12, 15–25. [Google Scholar]
  18. Memenza, A.; Cauty, N.; Sotelo, F.; Ramos, E. Standardize Strawberry Crops by Applying the Quality Function Deployment in Huaura, Perú. In Proceedings of the 18th LACCEI International Multi-Conference for Engineering, Education, and Technology: Engineering, Integration, and Alliances for a Sustainable Development “Hemispheric Cooperation for Competitiveness and Prosperity on A Knowledge-Based Economy”, Virtual, 27–31 July 2020; Latin American and Caribbean Consortium of Engineering Institutions: Buenos Aires, Argentina, 2020. [Google Scholar]
  19. Lombardi, N.; Caira, S.; Troise, A.D.; Scaloni, A.; Vitaglione, P.; Vinale, F.; Marra, R.; Salzano, A.M.; Lorito, M.; Woo, S.L. Trichoderma Applications on Strawberry Plants Modulate the Physiological Processes Positively Affecting Fruit Production and Quality. Front. Microbiol. 2020, 11, 01364. [Google Scholar] [CrossRef] [PubMed]
  20. Martín, L.; Velázquez, E.; Rivas, R.; Mateos, P.F.; Martínez-Molina, E.; Rodríguez-Barrueco, C.; Peix, A. Effect of Inoculation with a Strain of Pseudomonas fragi in the Growth and Phosphorous Content of Strawberry Plants. In Proceedings of the First International Meeting on Microbial Phosphate Solubilization, Salamanca, Spain, 16–19 July 2002; Velázquez, E., Rodríguez-Barrueco, C., Eds.; Springer: Dordrecht, The Netherlands, 2007; pp. 309–315. [Google Scholar]
  21. Serret-López, M.; Espinosa-Victoria, D.; Gómez-Rodríguez, O.; Delgadillo-Martínez, J.; Serret-López, M.; Espinosa-Victoria, D.; Gómez-Rodríguez, O.; Delgadillo-Martínez, J. Tolerancia de plantas de fresa (Fragaria × ananassa Duch.) premicorrizadas con Rhizophagus intraradices e inoculadas con PGPR’s a Phytophthora capsici. Agrociencia 2016, 50, 1107–1121. [Google Scholar]
  22. Sarmiento, G.; Amézquita, M.; Mena, L. Use of bocashi and effective microorganisms as an ecological alternative in strawberry crops in arid zones. Sci. Agropecu. 2019, 10, 55–61. [Google Scholar] [CrossRef]
  23. Rosero Cisneros, N.G. Efectos de la Aplicación de Trichoderma Harzianum Sobre la Incidencia de “Damping off” en el Cultivo de Fresa (Fragaria vesca L.) en la Zona de el Quinche Provincia de Pichincha. Bachelor Thesis, UTB, Babahoyo, Ecuador, 2011. [Google Scholar]
  24. Kumari, N.; Thakur, A. Black Root Rot of Strawberry: A Disease Complex. Int. J. Econ. Plants 2022, 9, 158–163. [Google Scholar] [CrossRef]
  25. Admassie, M.; Alemu, T.; Mulatu, A. Microbial biocontrol by Trichoderma, its biological interactions and mode of actions. Pak. J. Phytopathol. 2019, 31, 123–146. [Google Scholar] [CrossRef]
  26. Jiang, H.; Zhang, L.; Zhang, J.; Ojaghian, M.R.; Hyde, K.D. Antagonistic Interaction between Trichoderma asperellum and Phytophthora capsici in Vitro. J. Zhejiang Univ. Sci. B 2016, 17, 271–281. [Google Scholar] [CrossRef]
  27. Faghih, S.; Zarei, A.; Ghobadi, C. Positive Effects of Plant Growth Regulators on Physiology Responses of Fragaria × Ananassa Cv. ‘Camarosa’ under Salt Stress. Int. J. Fruit Sci. 2019, 19, 104–114. [Google Scholar] [CrossRef]
  28. Demiral, M.A. Effect of Salt Stress on Concentration of Nitrogen and Phosphorus in Root and Leaf of Strawberry Plant. Eurasian J. Soil Sci. EJSS 2017, 6, 357–364. [Google Scholar] [CrossRef]
  29. Wang, Y.-F.; Hou, X.-Y.; Deng, J.-J.; Yao, Z.-H.; Lyu, M.-M.; Zhang, R.-S. Auxin Response Factor 1 Acts as a Positive Regulator in the Response of Poplar to Trichoderma asperellum Inoculation in Overexpressing Plants. Plants 2020, 9, 272. [Google Scholar] [CrossRef]
  30. Garnica-Vergara, A.; Barrera-Ortiz, S.; Muñoz-Parra, E.; Raya-González, J.; Méndez-Bravo, A.; Macías-Rodríguez, L.; Ruiz-Herrera, L.F.; López-Bucio, J. The Volatile 6-Pentyl-2H-Pyran-2-One from Trichoderma atroviride Regulates Arabidopsis thaliana Root Morphogenesis via Auxin Signaling and ETHYLENE INSENSITIVE 2 Functioning. New Phytol. 2016, 209, 1496–1512. [Google Scholar] [CrossRef]
  31. Vico, G.; Way, D.A.; Hurry, V.; Manzoni, S. Can Leaf Net Photosynthesis Acclimate to Rising and More Variable Temperatures? Plant Cell Environ. 2019, 42, 1913–1928. [Google Scholar] [CrossRef]
  32. Esparza-Reynoso, S.; Ruíz-Herrera, L.F.; Pelagio-Flores, R.; Macías-Rodríguez, L.I.; Martínez-Trujillo, M.; López-Coria, M.; Sánchez-Nieto, S.; Herrera-Estrella, A.; López-Bucio, J. Trichoderma atroviride-Emitted Volatiles Improve Growth of Arabidopsis Seedlings through Modulation of Sucrose Transport and Metabolism. Plant Cell Environ. 2021, 44, 1961–1976. [Google Scholar] [CrossRef] [PubMed]
  33. Harman, G.E.; Doni, F.; Khadka, R.B.; Uphoff, N. Endophytic Strains of Trichoderma Increase Plants’ Photosynthetic Capability. J. Appl. Microbiol. 2021, 130, 529–546. [Google Scholar] [CrossRef]
  34. Bononi, L.; Chiaramonte, J.B.; Pansa, C.C.; Moitinho, M.A.; Melo, I.S. Phosphorus-Solubilizing Trichoderma spp. from Amazon Soils Improve Soybean Plant Growth. Sci. Rep. 2020, 10, 2858. [Google Scholar] [CrossRef]
  35. Singh, R.; Ryu, J.; Kim, S.W. Microbial Consortia Including Methanotrophs: Some Benefits of Living Together. J. Microbiol. Seoul Korea 2019, 57, 939–952. [Google Scholar] [CrossRef] [PubMed]
  36. Youssef, S.; Tartoura, K.; Abdelraouf, G. Evaluation of Trichoderma harzianum and Serratia proteamaculans Effect on Disease Suppression, Stimulation of ROS-Scavenging Enzymes and Improving Tomato Growth Infected by Rhizoctonia solani. Biol. Control 2016, 100, 79–86. [Google Scholar] [CrossRef]
  37. Hossain, B.; Rashid, M.H.A. Efficiency of Using Different Organic Manures on Growth, Yield and Quality of Strawberry through Various Planting Media. Trends Sci. 2022, 19, 4484. [Google Scholar] [CrossRef]
  38. Poveda, J.; Eugui, D. Combined Use of Trichoderma and Beneficial Bacteria (Mainly Bacillus and Pseudomonas): Development of Microbial Synergistic Bio-Inoculants in Sustainable Agriculture. Biol. Control 2022, 176, 105100. [Google Scholar] [CrossRef]
  39. de Andrade, F.M.; de Assis Pereira, T.; Souza, T.P.; Guimarães, P.H.S.; Martins, A.D.; Schwan, R.F.; Pasqual, M.; Dória, J. Beneficial Effects of Inoculation of Growth-Promoting Bacteria in Strawberry. Microbiol. Res. 2019, 223–225, 120–128. [Google Scholar] [CrossRef]
  40. Rueda, D.; Valencia, G.; Soria, N.; Rueda Benítez, B.; Bangeppagari, M.; Kundapur, R.; Selvanayagam, M. Effect of Azospirillum spp. and Azotobacter spp. on the Growth and Yield of Strawberry (Fragaria vesca) in Hydroponic System under Different Nitrogen Levels. J. Appl. Pharm. Sci. 2016, 6, 48–54. [Google Scholar] [CrossRef]
  41. Asghar, W.; Kataoka, R. Effect of Co-Application of Trichoderma spp. with Organic Composts on Plant Growth Enhancement, Soil Enzymes and Fungal Community in Soil. Arch. Microbiol. 2021, 203, 4281–4291. [Google Scholar] [CrossRef] [PubMed]
  42. Liu, X.; Shi, Y.; Kong, L.; Tong, L.; Cao, H.; Zhou, H.; Lv, Y. Long-term application of bio-compost increased soil microbial community diversity and altered its composition and network. Microorganisms 2022, 10, 462. [Google Scholar] [CrossRef] [PubMed]
  43. Leao, L.F.S.; Guzman, T.; Ferguson, L.M.; Fernandez, G.E.; Louws, F.J. Population Dynamics of Trichoderma in Fumigated and Compost-Amended Soil and on Strawberry Roots. Appl. Soil Ecol. 2007, 35, 237–246. [Google Scholar] [CrossRef]
  44. Kumari, A.; Goyal, R.K.; Choudhary, M.; Sindhu, S.S. Effects of some plant growth promoting rhizobacteria (PGPR) strains on growth and flowering of chrysanthemum. J. Crop Weed 2016, 12, 7–15. [Google Scholar]
  45. Cipriano, M.A.P.; Freitas, S.S. Effect of Pseudomonas putida on chrysanthemum growth under greenhouse and field conditions. Afr. J. Agric. Res. 2017, 13, 302–310. [Google Scholar] [CrossRef]
  46. Scotti, R.; Bonanomi, G.; Scelza, R.; Zoina, A.; Rao, M.A. Organic Amendments as Sustainable Tool to Recovery Fertility in Intensive Agricultural Systems. J. Soil Sci. Plant Nutr. 2015, 15, 333–352. [Google Scholar] [CrossRef]
  47. Yang, Y.; Liu, H.; Dai, Y.; Tian, H.; Zhou, W.; Lv, J. Soil organic carbon transformation and dynamics of microorganisms under different organic amendments. Sci. Total Environ. 2021, 750, 141719. [Google Scholar] [CrossRef]
  48. Rayne, N.; Aula, L. Livestock Manure and the Impacts on Soil Health: A Review. Soil Syst. 2020, 4, 64. [Google Scholar] [CrossRef]
  49. Mehraj, H.; Ahsan, M.; Hussain, M.; Rahman, M.; Jamal ddin, A.U. Response of Different Organic Matters in Strawberry. Bangladesh Res. Publ. J. 2014, 10, 151–161. [Google Scholar]
  50. Apu, S.; Biswas, M.; Bhuiyan, M.; Gomasta, J.; Easmin, S.; Kayesh, E. Effect of Organic Amendments and Arbuscular Mycorrhizal Fungi on Plant Growth, Yield and Quality of Strawberry. Ann. Bangladesh Agric. 2023, 26, 71–82. [Google Scholar] [CrossRef]
  51. Sayğı, H. Effects of Organic Fertilizer Application on Strawberry (Fragaria vesca L.) Cultivation. Agronomy 2022, 12, 1233. [Google Scholar] [CrossRef]
Figure 1. Mortality rates in strawberry seedlings cv. San Andreas at 30 dat according to the microbial inoculation (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation). Means with different letters are statistically different (LSD Fisher, α = 0.05.)
Figure 1. Mortality rates in strawberry seedlings cv. San Andreas at 30 dat according to the microbial inoculation (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation). Means with different letters are statistically different (LSD Fisher, α = 0.05.)
Applmicrobiol 04 00075 g001
Figure 2. Interaction between microbial inoculation and the organic amendments application on the (a) leaf area at 30 dat and (b) plant height at 60 dat of strawberry plants cv. San Andreas at. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter.)
Figure 2. Interaction between microbial inoculation and the organic amendments application on the (a) leaf area at 30 dat and (b) plant height at 60 dat of strawberry plants cv. San Andreas at. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter.)
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Figure 3. Leaf area according to microbial inoculation from 30 to 90 dat. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation.). Means with different letters are statistically different (LSD Fisher, α = 0.05.); n.s. no significance.
Figure 3. Leaf area according to microbial inoculation from 30 to 90 dat. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation.). Means with different letters are statistically different (LSD Fisher, α = 0.05.); n.s. no significance.
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Figure 4. Days to flowering in strawberry seedlings cv. San Andreas based on microbial inoculation and organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter.) Means with different letters in the same factor are statistically different (LSD Fisher, α = 0.05).
Figure 4. Days to flowering in strawberry seedlings cv. San Andreas based on microbial inoculation and organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter.) Means with different letters in the same factor are statistically different (LSD Fisher, α = 0.05).
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Figure 5. Number of fruits and flowers per square meter in strawberry seedlings cv. San Andreas based on microbial inoculation and the organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter.) Means with different letters in the same factor in the same series are statistically different (LSD Fisher, α = 0.05).
Figure 5. Number of fruits and flowers per square meter in strawberry seedlings cv. San Andreas based on microbial inoculation and the organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter.) Means with different letters in the same factor in the same series are statistically different (LSD Fisher, α = 0.05).
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Figure 6. Principal Component Analysis (PCA) showing the interrelation of evaluated parameters in strawberries according to microbial inoculation. (a) Distribution of inoculation treatments in the principal components (Black = Without inoculation; Aqua = Inoculation with Trichoderma sp.; Purple: Inoculation with Pseudomonas putida; Green: Co-inoculation). (b) Distribution of the variables in the principal components (NL = Number of leaves; H = Height; LA = Leaf area; FW_a = Fresh weight aerial; FW_r = Root fresh weight; DW_a = Dry weight aerial; DW_r = Root dry weight; DtF = Days to fruiting; Fl = Number of flowers; Fr = Number or fruits; W_fr = Fruit weight; Y_gr = Yield expressed in grams of fruit per plant; Y_tn = Yield expressed in tons per hectare; pH = pH; S = Sugars; Ac = Acidity; Fir = Firmness).
Figure 6. Principal Component Analysis (PCA) showing the interrelation of evaluated parameters in strawberries according to microbial inoculation. (a) Distribution of inoculation treatments in the principal components (Black = Without inoculation; Aqua = Inoculation with Trichoderma sp.; Purple: Inoculation with Pseudomonas putida; Green: Co-inoculation). (b) Distribution of the variables in the principal components (NL = Number of leaves; H = Height; LA = Leaf area; FW_a = Fresh weight aerial; FW_r = Root fresh weight; DW_a = Dry weight aerial; DW_r = Root dry weight; DtF = Days to fruiting; Fl = Number of flowers; Fr = Number or fruits; W_fr = Fruit weight; Y_gr = Yield expressed in grams of fruit per plant; Y_tn = Yield expressed in tons per hectare; pH = pH; S = Sugars; Ac = Acidity; Fir = Firmness).
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Figure 7. Principal Component Analysis (PCA) showing the interrelation of evaluated parameters in strawberries according to the application of organic amendments. (a) Distribution of inoculation treatments in the principal components (Black: Without organic amendment; Aqua: with compost; Green: with manure and leaf litter). (b) Distribution of the variables in the principal components (NL = Number of leaves; H = Height; LA = Leaf area; FW_a = Fresh weight aerial; FW_r = Root fresh weight; DW_a = Dry weight aerial; DW_r = Root dry weight; DtF = Days to fruiting; Fl = Number of flowers; Fr = Number or fruits; W_fr = Fruit weight; Y_gr = Yield expressed in grams of fruit per plant; Y_tn = Yield expressed in tons per hectare; pH = pH; S = Sugars; Ac = Acidity; Fir = Firmness).
Figure 7. Principal Component Analysis (PCA) showing the interrelation of evaluated parameters in strawberries according to the application of organic amendments. (a) Distribution of inoculation treatments in the principal components (Black: Without organic amendment; Aqua: with compost; Green: with manure and leaf litter). (b) Distribution of the variables in the principal components (NL = Number of leaves; H = Height; LA = Leaf area; FW_a = Fresh weight aerial; FW_r = Root fresh weight; DW_a = Dry weight aerial; DW_r = Root dry weight; DtF = Days to fruiting; Fl = Number of flowers; Fr = Number or fruits; W_fr = Fruit weight; Y_gr = Yield expressed in grams of fruit per plant; Y_tn = Yield expressed in tons per hectare; pH = pH; S = Sugars; Ac = Acidity; Fir = Firmness).
Applmicrobiol 04 00075 g007
Table 1. Evaluated factors and treatments.
Table 1. Evaluated factors and treatments.
Treat.Factor 1. Microbial InoculationFactor 2. Organic Amendments Application
T1Without microbial inoculation (WM)Without amendments (WA)
T2Compost (C)
T3Manure + Leaf litter (M)
T4Trichoderma viride (T)Without amendments (WA)
T5Compost (C)
T6Manure + Leaf litter (M)
T7Pseudomonas putida (P)Without amendments (WA)
T8Compost (C)
T9Manure + Leaf litter (M)
T10Trichoderma viride + Pseudomonas putida (T + P)Without amendments (WA)
T11Compost (C)
T12Manure + Leaf litter (M)
Table 2. Number of leaves, plant height, and leaf area of strawberry seedlings cv. San Andreas at the end of the vegetative stage (90 dat). (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
Table 2. Number of leaves, plant height, and leaf area of strawberry seedlings cv. San Andreas at the end of the vegetative stage (90 dat). (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
Treatment Number of LeavesPlant HeightLeaf Area
per Plant(cm)(cm2)
Interactionn.s.n.s.n.s.
Factor 1. Microbial inoculation
WM13.06 ± 1.6 a11.89 ± 1.2 n.s.788 ± 128 ab
T10.44 ± 2.3 b10.73 ± 1.3630 ± 140 c
P13.24 ± 2.2 a11.26 ± 1.4686 ± 133 bc
T + P13.45 ± 3.4 a12.17 ± 1.2847 ± 164 a
Factor 2. Organic amendment application
WA11.53 ± 1.4 b11.16 ± 1.2 n.s.732 ± 158 n.s.
C14.12 ± 2.7 a11.82 ± 1.4780 ± 161
M12.00 ± 3.0 ab11.55 ± 1.4701 ± 167
Means with different letters in the same factor in the same column are statistically different (LSD Fisher, α = 0.05); n.s.: no significance.
Table 3. Fresh and dry biomass of the aerial part based on microbial inoculation and the organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
Table 3. Fresh and dry biomass of the aerial part based on microbial inoculation and the organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
Treatment Fresh BiomassDry Biomass
90 datHarvest90 datHarvest
Factor 1. Microbial inoculation
WM37.8 ± 9.7 ab90.3 ± 13.2 n.s.7.6 ± 2.3 b25.2 ± 5.8 n.s.
T34.3 ± 6.0 b92.2 ± 26.58.3 ± 1.4 b25.8 ± 5.3
P33.3 ± 6.2 b85.3 ± 26.68.1 ± 1.5 b23.9 ± 5.2
T + P42.7 ± 8.5 a109.4 ± 26.49.7 ± 1.5 a29 ± 6.1
Factor 2. Organic amendment application
WA34.5 ± 5.8 n.s.95.2 ± 16.9 n.s.7.9 ± 1.4 b25.0 ± 4.4 n.s
C40.7 ± 8.993.4 ± 24.19.5 ± 1.7 a27.2 ± 6.2
M35.5 ± 8.993.3 ± 34.67.6 ± 2.0 b25.8 ± 6.6
Means with different letters in the same factor in the same column are statistically different (LSD Fisher, α = 0.05); n.s.: no significance.
Table 4. Physical–chemical characteristics and fruit size based on microbial inoculation and organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
Table 4. Physical–chemical characteristics and fruit size based on microbial inoculation and organic amendments application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
TreatmentpHAciditySugarsFirmnessSize
(g Citric Acid∙100 mL−1)(Brix°)(kg)(cm2)
Interactionn.s.n.s.n.s.n.s.n.s.
Factor 1. Microbial inoculation
WM3.37 ± 0.06 n.s.0.71 ± 0.06 n.s.13.33 ± 1.80 n.s.0.14 ± 0.03 n.s.1471 ± 107 n.s.
T3.33 ± 0.100.76 ± 0.0812.84 ± 2.220.15 ± 0.031451 ± 55
P3.38 ± 0.120.73 ± 0.09 13.65 ± 1.830.13 ± 0.031541 ± 110
T + P3.40 ± 0.040.69 ± 0.0412.7 ± 2.220.16 ± 0.091435 ± 179
Factor 2. Organic amendments application
WA3.33 ± 0.09 n.s.0.76 ± 0.07 a12.99 ± 1.77 n.s.0.14 ± 0.03 n.s.1492 ± 169 n.s.
C3.39 ± 0.060.71 ± 0.06 ab13.33 ± 2.120.14 ± 0.041485 ± 88
M3.39 ± 0.090.69 ± 0.07 b13.08 ± 2.170.14 ± 0.081447 ± 102
Means with different letters in the same factor in the same column are statistically different (LSD Fisher, α = 0.05); n.s.: no significance.
Table 5. Strawberry crop yield cv. San Andreas based on microbial inoculation and the organic amendment application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
Table 5. Strawberry crop yield cv. San Andreas based on microbial inoculation and the organic amendment application. (WM = without microbial inoculation, T = inoculation with Trichoderma sp., P = inoculation with Pseudomonas putida, T + P = co-inoculation, WA = without organic amendments, C = with compost, M = with manure and leaf litter).
Treatment Fruit WeightYield
(g Fruit−1)(g Fruit Plant−1)(t ha−1)
Interactionn.s.n.s.n.s.
Factor 1. Microbial inoculation
WM21.29 ± 1.15 n.s.173.6 ± 65.3 n.s.9.3 ± 1.1 n.s.
T20.61 ± 1.23212.9 ± 45.79.8 ± 1.5
P20.96 ± 1.89183.7 ± 73.78.9 ± 3.0
T + P20.36 ± 1.32201.2 ± 84.310.3 ± 2.0
Factor 2. Organic amendment application
WA20.91 ± 1.60 n.s.152.7 ± 78.0 b9.3 ± 2.7 n.s.
C21.10 ± 1.52214.4 ± 48.8 a9.9 ± 1.6
M20.41 ± 1.09211.4 ± 58.4 a9.6 ± 1.7
Means with different letters in the same factor in the same column are statistically different (LSD Fisher, α = 0.05); n.s.: no significance.
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Huasasquiche, L.; Ccori, T.; Alejandro, L.; Cántaro-Segura, H.; Samaniego, T.; Solórzano, R. Interaction between Trichoderma sp., Pseudomonas putida, and Two Organic Amendments on the Yield and Quality of Strawberries (Fragaria x annanasa cv. San Andreas) in the Huaral Region, Peru. Appl. Microbiol. 2024, 4, 1110-1123. https://doi.org/10.3390/applmicrobiol4030075

AMA Style

Huasasquiche L, Ccori T, Alejandro L, Cántaro-Segura H, Samaniego T, Solórzano R. Interaction between Trichoderma sp., Pseudomonas putida, and Two Organic Amendments on the Yield and Quality of Strawberries (Fragaria x annanasa cv. San Andreas) in the Huaral Region, Peru. Applied Microbiology. 2024; 4(3):1110-1123. https://doi.org/10.3390/applmicrobiol4030075

Chicago/Turabian Style

Huasasquiche, Lucero, Thania Ccori, Leonela Alejandro, Héctor Cántaro-Segura, Tomás Samaniego, and Richard Solórzano. 2024. "Interaction between Trichoderma sp., Pseudomonas putida, and Two Organic Amendments on the Yield and Quality of Strawberries (Fragaria x annanasa cv. San Andreas) in the Huaral Region, Peru" Applied Microbiology 4, no. 3: 1110-1123. https://doi.org/10.3390/applmicrobiol4030075

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