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Metagenomics and vegetative growth of Salvia hispanica inoculated with Trichoderma harzianum

Metagenômica e crescimento vegetativo de Salvia hispanica inoculada com Trichoderma harzianum

Abstract

The soil is a dynamic environment, influenced by abiotic and biotic factors, which can result in changes in plant development. This study aimed to assess the impact on vegetative growth of chia (Salvia hispanica L) inoculated with Trichoderma harzianum and on the rhizosphere microbiome. The experimentation was conducted in a greenhouse under controlled conditions growing chia plants in pots containing soil with a clayey texture. Different concentrations of T. harzianum (0; 2.5; 5.0; 10.0; 20.0 µL. g-1 of seed) were applied to the chia seeds before planting. Morphological parameters, including plant height (cm), number of branches, stem diameter (mm), number of days to flowering and shoot and root dry masses (g) were quantitatively assessed. After the cultivation period, soil samples from the rhizosphere region were collected for subsequent chemical and metagenomic analyses. These samples were also compared with the control soil, collected before installing the experiment. The results showed that increasing doses of T. harzianum promoted a significant increase in the diameter of the stem, number of branches, dry biomass of the root system and the number of days to flowering, without modifying the overall height of the plants. Soil metagenomics indicated that T. harzianum inoculation modified the microbial diversity of the rhizosphere environment, with more pronounced effects observed in samples treated with higher concentrations of the inoculant. Furthermore, there were changes in the chemical composition and enzymes related to soil quality in correlation with the concentrations of the applied inoculant. This study demonstrated that inoculating chia seeds with T. harzianum not only promotes specific morphogenetic characteristics of the plant, but it also has a significant impact on the microbial diversity and biochemical functionality of the soil, including an observed increase in the populations of T. harzianum and T. asperellum.

Keywords:
chia; growth promotion; microbiome; antagonists; phytopathogens

Resumo

O solo é um ambiente dinâmico, influenciado por fatores abióticos e bióticos, e que pode resultar em modificações do desenvolvimento vegetal. Este estudo teve como objetivos avaliar o impacto da inoculação de sementes de chia (Salvia hispanica L) com Trichoderma harzianum sobre o desenvolvimento vegetativo, e verificar a influência desta inoculação no microbioma rizosférico. O estudo consistiu no cultivo de plantas de chia em solo com textura argilosa contido em vasos sob condições controladas de casa-de-vegetação. Para tal, diferentes concentrações de T. harzianum (0; 2.5; 5.0; 10.0; 20.0 µL.g-1 de semente) foram aplicadas às sementes antes do plantio. Parâmetros morfológicos, incluindo altura das plantas (cm), número de ramos, diâmetro do caule (mm), número de dias para florescimento e para massas secas da parte aérea e radicular (g) foram quantitativamente avaliados. Após o período de cultivo, amostras de solo da região rizosferica foram coletadas para posterior análises química e de metagenômica. Essas amostras foram comparadas também com o solo controle, coletado antes da instalação do experimento. Os resultados revelaram que doses crescentes de T. harzianum promoveram um aumento significativo do diâmetro do caule, do número de ramificações, da biomassa seca do sistema radicular e do número de dias para o florescimento, sem modificar a altura global das plantas. A metagenômica do solo indicou que a inoculação de T. harzianum alterou a diversidade microbiana do ambiente rizosférico, com efeitos mais pronunciados observados nas amostras tratadas com maiores concentrações do inoculante. Além disso, verificou-se alterações na composição química e em enzimas relacionadas a qualidade do solo em correlação com as concentrações do inoculante aplicado. Em síntese, este estudo sugere que a inoculação de sementes de chia com T. harzianum não apenas promove características morfogenéticas específicas da planta, mas também exerce um impacto significativo sobre a diversidade microbiana e a funcionalidade bioquímica do solo, incluindo um incremento observado nas populações de T. harzianum e T. asperellum.

Palavras-chave:
chia; promoção do crescimento; microbioma; antagonistas; fitopatógenos Introduction

1. Introduction

Plants and the soil microbiome are in dynamic interaction and are directly or indirectly influenced by abiotic factors and by other organisms. This interaction ends up determining physical-chemical and biological characteristics of the soil, which can result in changes in plant growth. In this context, in recent years, studies have been intensified to prove the relevance of plant-microorganism interaction in crop yield (Fu et al., 2020FU, J., XIAO, Y., LIU, Z., ZHANG, Y., WANG, Y. and YANG, K., 2020. Trichoderma asperellum improves soil microenvironment in different growth stages and yield of maize in saline-alkaline soil of the Songnen Plain. Plant, Soil and Environment, vol. 66, no. 12, pp. 639-647. http://doi.org/10.17221/456/2020-PSE.
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; Hang et al., 2022HANG, X., MENG, L., OU, Y., SHAO, C., XIONG, W., ZHANG, N., LIU, H., LI, R., SHEN, O. and KOWALCHUK, G.A., 2022. Trichoderma-amended biofertilizer stimulates soil resident Aspergillus population for joint plant growth promotion. NPJ Biofilms and Microbiomes, vol. 8, no. 1, pp. 57. http://doi.org/10.1038/s41522-022-00321-z PMid:35831320.
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) which can contribute to more sustainable agriculture (Antoszewski et al., 2022ANTOSZEWSKI, M., MIEREK-ADAMSKA, A. and DĄBROWSKA, G.B., 2022. The importance of microorganisms for sustainable agriculture: a review. Metabolites, vol. 12, no. 11, pp. 1100. http://doi.org/10.3390/metabo12111100 PMid:36422239.
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).

The culture of chia (Salvia hispanica) is quite widespread among farmers in countries such as Argentina and Paraguay (Orona-Tamayo et al., 2017ORONA-TAMAYO, D., VALVERDE, M.E., PAREDES-LÓPEZ, O., 2017. Chia — the new golden seed for the 21st century: nutraceutical properties and technological uses. In: S.R. NADATHUR, L. SCANLIN and J.P.D. WANASUNDARA, eds. Sustainable protein sources. London: Academic Press. p. 265-281. http://doi.org/10.1016/B978-0-12-802778-3.00017-2.
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). In Brazil, chia cultivation is recent (Radke et al., 2018RADKE, A.K., XAVIER, F.D.M., EBERHARDT, P.E.R., VILLELA, F.A. and MENEGHELLO, G.E., 2018. Methodological adjustment of the accelerated aging test to evaluate the vigor of chia seeds. Journal of Seed Science, vol. 40, no. 2, pp. 173-178. http://doi.org/10.1590/2317-1545v40n2188348.
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; Costa et al., 2022COSTA, A.A., PAIVA, E.P., TORRES, S.B., SOUZA NETA, M.L., PEREIRA, K.T.O., LEITE, M.S., SÁ, F.V.S. and BENEDITO, C.P., 2022. Osmoprotection in Salvia hispanica L. seeds under water stress attenuators. Brazilian Journal of Biology = Revista Brasileira de Biologia, vol. 82, pp. e233547. http://doi.org/10.1590/1519-6984.233547 PMid:34105656.
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), occurring in the West of Paraná and Northwest of Rio Grande do Sul (Migliavacca et al., 2014MIGLIAVACCA, R.A., SILVA, T.R.B., VASCONCELOS, A.L.S., MOURÃO FILHO, W. and BAPTISTELLA, J.L.C., 2014. O cultivo da chia no Brasil: futuro e perspectivas. Journal of Agronomic Sciences, vol. 3, pp. 161-179.). It has seeds with nutraceutical importance that are rich in fatty acids, proteins, fiber, vitamins (Jamboonsri et al., 2012JAMBOONSRI, W., PHILLIPS, T., GENEVE, R., CAHILL, J. and HILDEBRAND, D., 2012. Extending the range of an ancient crop,Salvia hispanicaL. - a new ω3 source. Genetic Resources and Crop Evolution, vol. 59, no. 2, pp. 171-178. http://doi.org/10.1007/s10722-011-9673-x.
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; Knez Hrnčič et al., 2019KNEZ HRNČIČ, M., IVANOVSKI, M., CÖR, D. and KNEZ, Ž., 2019. Chia Seeds (Salvia hispanica L.): an overview—phytochemical profile, isolation methods, and application. Molecules (Basel, Switzerland), vol. 25, no. 1, pp. 11. http://doi.org/10.3390/molecules25010011 PMid:31861466.
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) and substances with antioxidant effect (Pellegrini et al., 2018PELLEGRINI, M., LUCAS-GONZALEZ, R., SAYAS-BARBERÁ, E., FERNÁNDEZ-LÓPEZ, J., PÉREZ-ÁLVAREZ, J.A. and VIUDA-MARTOS, M., 2018. Bioaccessibility of phenolic compounds and antioxidant capacity of chia (Salvia hispanica L.) seeds. Plant Foods for Human Nutrition, vol. 73, no. 1, pp. 47-53. http://doi.org/10.1007/s11130-017-0649-7 PMid:29188413.
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).

Chia plants are highly influenced by temperature and photoperiod conditions and planting time and/or latitude can substantially limit grain production (Jamboonsri et al., 2012JAMBOONSRI, W., PHILLIPS, T., GENEVE, R., CAHILL, J. and HILDEBRAND, D., 2012. Extending the range of an ancient crop,Salvia hispanicaL. - a new ω3 source. Genetic Resources and Crop Evolution, vol. 59, no. 2, pp. 171-178. http://doi.org/10.1007/s10722-011-9673-x.
http://doi.org/10.1007/s10722-011-9673-x...
; Rodríguez-Abello et al., 2018RODRÍGUEZ-ABELLO, D.C., NAVARRO-ALBERTO, J.A., RAMÍREZ-AVILÉS, L. and ZAMORA-BUSTILLOS, R., 2018. The effect of sowing time on the growth of chia (Salvia hispanica L.): what do nonlinear mixed models tell us about it? PLoS One, vol. 13, no. 11, pp. e0206582. http://doi.org/10.1371/journal.pone.0206582 PMid:30383782.
http://doi.org/10.1371/journal.pone.0206...
). According to Jamboonsri et al. (2012)JAMBOONSRI, W., PHILLIPS, T., GENEVE, R., CAHILL, J. and HILDEBRAND, D., 2012. Extending the range of an ancient crop,Salvia hispanicaL. - a new ω3 source. Genetic Resources and Crop Evolution, vol. 59, no. 2, pp. 171-178. http://doi.org/10.1007/s10722-011-9673-x.
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, chia is a short-day plant with a critical photoperiod for floral induction of approximately 12 h. In Western Paraná, chia produces inflorescences at the beginning of April (autumn) (Pereira et al. 2020PEREIRA, D., SCHUELTER, A.R., DEMBOCURSKI, D., PASSOS, F.R., MAESTRE, K.L., SILVA, E.A. and KLEN, M.R.F., 2020. Componentes do rendimento e composição química de grãos de genótipos de Salvia hispanica L. cultivados no Oeste do Paraná sob diferentes densidades populacionais.Research. Social Development, vol. 9, no. 12, pp. e10591210798. http://doi.org/10.33448/rsd-v9i12.10798.
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). Therefore, plantings at the beginning of autumn can result in a reduction in the vegetative growth period, leading to a reduction in productivity, while those carried out in summer result in taller and more productive plants (Pereira et al., 2020PEREIRA, D., SCHUELTER, A.R., DEMBOCURSKI, D., PASSOS, F.R., MAESTRE, K.L., SILVA, E.A. and KLEN, M.R.F., 2020. Componentes do rendimento e composição química de grãos de genótipos de Salvia hispanica L. cultivados no Oeste do Paraná sob diferentes densidades populacionais.Research. Social Development, vol. 9, no. 12, pp. e10591210798. http://doi.org/10.33448/rsd-v9i12.10798.
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). Nevertheless, chia lodging is recurrent, especially in taller plants, making harvesting difficult and facilitating exposure to the occurrence of microorganisms in the seeds (Goergen et al., 2018GOERGEN, P.C.H., NUNES, U.R., STEFANELLO, R., LAGO, I., NUNES, A.R. and DURIGON, A., 2018. Yield and physical and physiological quality of Salvia hispanica L. seeds grown at different sowing dates. Journal of Agricultural Science, vol. 10, no. 8, pp. 182-191. http://doi.org/10.5539/jas.v10n8p182.
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).

Different studies showed the presence of fungal contaminants in chia seeds, some of which are phytopathogenic fungi that can be transmitted to seedlings, such as Fusarium sp. (Witkovski et al., 2021WITKOVSKI, A., STEFENI, A., POSSENTI, J.C., BORIN, M.D.S.R., DEUNER, C. and FAVORETTO, V.R., 2021. Incubation period and fungi identification in seeds of Salvia hispanica L. Comunicata Scientiae, vol. 12, pp. e3535-e3535. http://doi.org/10.14295/cs.v12.3535.
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), Penicillium sp. and Aspergillus sp (Jermnak et al., 2020JERMNAK, U., YURAYART, C., POAPOLATHEP, A., POAPOLATHEP, S., IMSILP, K., TANHAN, P. and LIMSIVILAI, O., 2020. Evaluation of aflatoxin concentrations and occurrence of potentially toxigenic fungi in imported chia seeds consumed in Thailand. Journal of Food Protection, vol. 83, no. 3, pp. 497-502. http://doi.org/10.4315/0362-028X.JFP-19-316 PMid:32068855.
http://doi.org/10.4315/0362-028X.JFP-19-...
; Witkovski et al., 2021WITKOVSKI, A., STEFENI, A., POSSENTI, J.C., BORIN, M.D.S.R., DEUNER, C. and FAVORETTO, V.R., 2021. Incubation period and fungi identification in seeds of Salvia hispanica L. Comunicata Scientiae, vol. 12, pp. e3535-e3535. http://doi.org/10.14295/cs.v12.3535.
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), and a larger part made up of non-phytopathogenic species, but which can cause problems to human health due to the production of mycotoxins (Freire et al., 2007FREIRE, F.D.C.O., VIEIRA, I.G.P., GUEDES, M.I.F. and MENDES, F.N.P., 2007 [viewed 23 Apr 2024]. Micotoxinas: importância na alimentação e na saúde humana e animal.Fortaleza: Embrapa Agroindústria Tropical, Documento 110, 48p. Available from: https://www.infoteca.cnptia.embrapa.br/bitstream/doc/427374/1/Dc110.pdf.
https://www.infoteca.cnptia.embrapa.br/b...
). In the absence of the main host these fungi have different survival strategies associated with resistance structures and permanence in alternative hosts or in soil organic matter for long periods (Kerdraon et al., 2019KERDRAON, L., LAVAL, V. and SUFFERT, F., 2019. Microbiomes and pathogen survival in crop residues, an ecotone between plant and soil. Phytobiomes Journal, vol. 3, no. 4, pp. 246-255. http://doi.org/10.1094/PBIOMES-02-19-0010-RVW.
http://doi.org/10.1094/PBIOMES-02-19-001...
). The reduction in microbial diversification of soils, caused by conventional cultivation systems, tends to increase vulnerability to the invasion of these phytopathogens (Samaddar et al., 2021SAMADDAR, S., KARP, D.S., SCHMIDT, R., DEVARAJAN, N., MCGARVEY, J.A., PIRES, A.F. and SCOW, K., 2021. Role of soil in the regulation of human and plant pathogens: soils’ contributions to people. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, vol. 376, no. 1834, pp. 20200179. http://doi.org/10.1098/rstb.2020.0179 PMid:34365819.
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).

Different strategies to control these soil microorganisms have been suggested, including crop rotation, soil solarization, use of resistant cultivars and biological control agents (Panth et al., 2020PANTH, M., HASSLER, S.C. and BAYSAL-GUREL, F., 2020. Methods for management of soilborne diseases in crop production. Agriculture, vol. 10, no. 1, pp. 16. http://doi.org/10.3390/agriculture10010016.
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). In this context, several antagonistic fungi have great potential for use in biocontrol (Sood et al., 2020SOOD, M., KAPOOR, D., KUMAR, V., SHETEIWY, M.S., RAMAKRISHNAN, M., LANDI, M., ARANITI, F. and SHARMA, A., 2020. Trichoderma: the “secrets” of a multitalented biocontrol agent. Plants, vol. 9, no. 6, pp. 762. http://doi.org/10.3390/plants9060762 PMid:32570799.
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; Nascimento et al., 2022NASCIMENTO, V.C., RODRIGUES-SANTOS, K.C., CARVALHO-ALENCAR, K.L., CASTRO, M.B., KRUGER, R.H. and LOPES, F.A.C., 2022. Trichoderma: biological control efficiency and perspectives for the Brazilian Midwest states and Tocantins. Brazilian Journal of Biology = Revista Brasileira de Biologia, vol. 82, pp. e260161. http://doi.org/10.1590/1519-6984.260161 PMid:35946640.
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), such as species of the genus Trichoderma, especially T. harzianum, which has been widely used in the biocontrol of several phytopathogens (Fraceto et al., 2018FRACETO, L.F., MARUYAMA, C.R., GUILGER, M., MISHRA, S., KESWANI, C., SINGH, H.B. and DE LIMA, R., 2018. Trichoderma harzianum‐based novel formulations: potential applications for management of Next‐Gen agricultural challenges. Journal of Chemical Technology and Biotechnology, vol. 93, no. 8, pp. 2056-2063. http://doi.org/10.1002/jctb.5613.
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). Furthermore, different strains can adopt different antagonism mechanisms, which include antibiosis, competition and mycoparasitism (Asad, 2022ASAD, S.A., 2022. Mechanisms of action and biocontrol potential of Trichoderma against fungal plant diseases-A review. Ecological Complexity, vol. 49, pp. 100978. http://doi.org/10.1016/j.ecocom.2021.100978.
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), and could stimulate growth (Stewart and Hill, 2014STEWART, A. and HILL, R., 2014. Applications ofTrichodermain plant growth promotion. In V. GUPTA, M. SCHMOLL, A. HERRERA-ESTRELLA, R. UPADHYAY, I. DRUZHININA, and M. TUOHY, eds. Biotechnology and Biology of Trichoderma. Amsterdam: Elsevier, pp. 415-428. http://doi.org/10.1016/B978-0-444-59576-8.00031-X.
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; Fu et al., 2020FU, J., XIAO, Y., LIU, Z., ZHANG, Y., WANG, Y. and YANG, K., 2020. Trichoderma asperellum improves soil microenvironment in different growth stages and yield of maize in saline-alkaline soil of the Songnen Plain. Plant, Soil and Environment, vol. 66, no. 12, pp. 639-647. http://doi.org/10.17221/456/2020-PSE.
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; Hang et al., 2022HANG, X., MENG, L., OU, Y., SHAO, C., XIONG, W., ZHANG, N., LIU, H., LI, R., SHEN, O. and KOWALCHUK, G.A., 2022. Trichoderma-amended biofertilizer stimulates soil resident Aspergillus population for joint plant growth promotion. NPJ Biofilms and Microbiomes, vol. 8, no. 1, pp. 57. http://doi.org/10.1038/s41522-022-00321-z PMid:35831320.
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) or induce plant systemic resistance to diseases (Meyer et al., 1998MEYER, G., BIGIRIMANA, J., ELAD, Y. and HÖFTE, M., 1998. Induced systemic resistance in Trichoderma harzianum T39 biocontrol of Botrytis cinerea. European Journal of Plant Pathology, vol. 104, no. 3, pp. 279-286. http://doi.org/10.1023/A:1008628806616.
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).

Studies using Trichoderma spp in chia crops are scarce (El-Kaed et al., 2021EL-KAED, S.A., MERGAWY, M.M., HASSANIN, M.M.H., 2021. Management of the most destructive diseases of chia plant and its impact on the yield. Egyptian Journal of Phytopathology, vol. 49, no. 1, 37-48. http://doi.org/10.21608/ejp.2021.61936.1023.
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; Witkovski et al., 2021WITKOVSKI, A., STEFENI, A., POSSENTI, J.C., BORIN, M.D.S.R., DEUNER, C. and FAVORETTO, V.R., 2021. Incubation period and fungi identification in seeds of Salvia hispanica L. Comunicata Scientiae, vol. 12, pp. e3535-e3535. http://doi.org/10.14295/cs.v12.3535.
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; Abdel-Aty et al., 2022ABDEL-ATY, A.M., BARAKAT, A.Z., BASSUINY, R.I. and MOHAMED, S.A., 2022. Improved production of antioxidant-phenolic compounds and certain fungal phenolic-associated enzymes under solid-state fermentation of chia seeds with Trichoderma reesei: response surface methodology-based optimization. Journal of Food Measurement and Characterization, vol. 16, no. 5, pp. 3488-3500. http://doi.org/10.1007/s11694-022-01447-6.
http://doi.org/10.1007/s11694-022-01447-...
), not having been published to date research that verifies the effect of its inoculation in seeds on the growth and development of this crop, and its rhizosphere.

This research aims studying the effect of inoculating chia seeds with T. harzianum on the growth of plants and the diversity of their rhizosphere microbiome.

2. Material and Methods

2.1. Genetic material

The Chia cultivar CH03 (MaisGenes Sementes LTDA, Toledo, Paraná, Brazil) was used in the experiments conducted under laboratory and greenhouse conditions at Faculdade Educacional de Medianeira (UDC Medianeira), Medianeira, Paraná, Brazil.

2.2. Seed sanitary analysis

The sanitary analysis was performed according to the Brasil (2009)BRASIL. Ministério da Agricultura, Pecuária e Abastecimento, 2009. Regras para Análise de Sementes. Brasília, DF: Mapa/AC, 395p. protocol, consisting of four replications with 100 seeds each. The seeds were placed on two sheets of sterile germtest paper, previously moistened with an autoclaved solution of dichlorophenoxyacetic acid (2,4-D) at a concentration of 5 ppm. These preparations were placed in Gerbox-type polypropylene boxes and subjected to asepsis with 70% alcohol. Subsequently, the boxes were hermetically sealed with parafilm and incubated in a BOD chamber under controlled conditions of 25°C and a photoperiod of 12:00 h, at intervals of 7 and 14 days. The taxonomic identification of microorganisms associated with the seeds was carried out through morphological assessment with the aid of an optical microscope. Fungi belonging to the genera Aspergillus, Penicillium and Rhizopus were identified in 1%, 0.25% and 0.75% of the seeds, respectively.

2.3. Inoculation with Trichoderma harzianum and installation of the experiment

Chia seeds were inoculated with doses of Trichoderma harzianum, using the commercial strain CCT 7589, which contained 1x109 UFC.L-1 of the fungi. The treatments consisted of T1 (control), T2 (2.5 µL.g-1 seed), T3 (5.0 µL.g-1 seed), T4 (10.0 µL.g-1 seed) and T5 (20.0 µL.g-1 seed), having as reference the spray volume of 20 mL. kg-1 of seeds.

For treatments with the fungi, inoculation was carried out using 1 g of chia seeds placed in a becker filled with 20 µL of the solution, followed by homogenization for 15 s. After that the seeds were removed from the solution, dried at room temperature (25ºC) for 15 min and sowed at a depth of 1 cm using four seeds per pot containing substrate. Thinning was performed seven days after sowing, leaving one plant per pot.

The substrate used to cultivate the plants in pots (20 L capacity) was made up of a mixture of soil, sand, and poultry litter in a volumetric ratio of 3:2:1, respectively. After mixing, substrate samples were collected to perform chemical and metagenomic analyses. The fertilization of the substrate was prescribed based on its chemical composition (LABAGRO, Serranópolis do Iguaçu, PR, Brazil), 20 kg.ha-1 of N, 80 kg.ha-1 of P2O5 and 40 kg.ha-1 of K2O.

2.4. Experimental design

The experiment was conducted in a greenhouse with controlled temperature conditions, 28 ± 4ºC, and water regime of 10 mm.day-1. The experimental design used was completely randomized (DIC) with five treatments, which are described above, and ten replications. The experimental unit consisted of one plant per pot.

Plant height was measured periodically from 14 days after sowing until the beginning of flowering. The following characteristics were evaluated: number of days to flowering (NDF), number of branches (NB), stem diameter (SD), dry mass of the shoot (MSA), and root system (RDM).

At the same time of the final experimental evaluation, a soil sample was taken from the rhizosphere region, from each of the five treatments. These samples were placed in plastic bags and subjected to freezing at a temperature of -20ºC, until they were sent for chemical and metagenomic analyses.

2.5. Metagenomics analysis

For this analysis, soil samples derived from T1 to T5 treatments were collected at the end of the experiment, plus the sample obtained before the start of cultivation, providing a temporal comparison regarding the microbial composition of the soil. The metagenomics analyzes were carried out by the company LAGBio – Análises Genômicas e Biotecnologia (Toledo, PR, Brazil). For this purpose, the samples were initially subjected to total DNA extraction, using the extraction kit DNEASY PowerSoil Pro – Qiagen, and the total DNA concentration and quality was verified using the dsDNA HS Assay Kit Qubit® - Life Technologies. With the use of 1 µg of DNA per soil sample, metagenomic libraries were constructed using the Nextera XT kit (Illumina, San Diego, CA, USA). Sequencing was carried out using MiSeq equipment (Illumina, San Diego, CA, USA).

After complete sequencing, the sequence reads were pre-processed using the FastQC program (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/). To check the quality of sequence readings and remove low-quality ones, the Sickle software was used (Joshi and Fass, 2011JOSHI, N.A. and FASS, J., 2011. Sickle: A sliding-window, adaptive, quality-based trimming tool for FastQ files (Version 1.33). Sickle.). In this process, all sequences smaller than 50 bp and with a Phred score lower than 20 were removed from the data set. In this way, all sequence readings with undetermined bases were removed.

To analyze the structure of microbial communities, including the study of taxonomic diversity, the Kraken 2 program was used (Wood et al., 2019WOOD, D.E., LU, J. and LANGMEAD, B., 2019. Improved metagenomic analysis with Kraken 2.Genome Biology, vol. 20, pp. 1-13.). For functional analysis of the sequences, the MG-RAST online platform (version 4.0.3) was used (Keegan et al., 2016KEEGAN, K.P., GLASS, E.M. and MEYER, F., 2016. MG-RAST, a metagenomics service for analysis of microbial community structure and function. Microbial Environmental Genomics, vol. 1399, pp. 207-233. http://doi.org/10.1007/978-1-4939-3369-3_13. [MEG] PMid:26791506.
http://doi.org/10.1007/978-1-4939-3369-3...
). The sequences were submitted to the platform and processed using the standard pipeline, which consisted of E-value 105 and cut-off with a minimum of 60% of similarity between sequences. To verify the possible metabolic routes present in the set of microorganisms in this study, the SEED Subsystems level 1 function was used, with direct plugging to the KEGG Pathway (Kanehisa and Goto, 2000KANEHISA, M. and GOTO, S., 2000. KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Research, vol. 28, no. 1, pp. 27-30. http://doi.org/10.1093/nar/28.1.27 PMid:10592173.
http://doi.org/10.1093/nar/28.1.27...
). The results obtained from MG-RAST were subsequently analyzed using the Statistical Analysis of Metagenomic Profiles program, STAMP (version 2.1.3) (Parks et al., 2014PARKS, D.H., TYSON, G.W., HUGENHOLTZ, P. and BEIKO, R.G., 2014. STAMP: statistical analysis of taxonomic and functional profiles. Bioinformatics, vol. 30, no. 21, pp. 3123-3124. http://doi.org/10.1093/bioinformatics/btu494 PMid:25061070.
http://doi.org/10.1093/bioinformatics/bt...
).

2.6. Statistical analysis

The data collected throughout the development of chia plants, except for growth analysis, were subjected to normality and homogeneity of variance tests, followed by analysis of variance for regression, considering the 5% of probability by using the F test.

For the plant height variable, whose measurements were collected until flowering, the data were analyzed using Generalized Linear Mixed Models (GLMM). The gamma distribution was the best representation of the data. The quality of the models was assessed using the values of AIC (Akaike’s information criterion) or QIC (Quasi likelihood under Independence model Criterion) as selection criteria. It was also verified that the individual (ID) is a random factor according to the AIC criterion. Therefore, the model with the best adherence considers data with gamma distribution, ID as a random factor and use of the AR1 covariance matrix. All parametric statistical analyzes were performed using the SPSS programs (IBM Corp. Released, 2020), JAMOVI (Navarro et al., 2020NAVARRO, D., FOXCROFT, D. and MEUNIER, J., 2020 [viewed 23 Apr 2024].Learning statistics with Jamovi. Available from: https://hal.science/hal-02335912/.
https://hal.science/hal-02335912/...
) and SISVAR (Ferreira, 2011FERREIRA, D.F., 2011. Sisvar: um sistema computacional de análise estatística. Ciência e Agrotecnologia, vol. 35, pp. 1039-1042. http://doi.org/10.1590/S1413-70542011000600001.
http://doi.org/10.1590/S1413-70542011000...
).

3. Results and Discussion

3.1. Growth and development of chia plants

Under greenhouse temperature conditions, 28 ± 4ºC, the emergence of chia seedlings occurred between 3 and 4 DAP (days after planting), regardless of the dose of T. harzianum. The first lateral shoots occurred from 36 DAP, while the first inflorescences, also called clusters or spikes, were observed between 62 and 73 days after planting. The plants reached an average height of 116 ± 3.8 cm at the end of the vegetative stage. The emergence of seedlings between 3 and 4 DAP demonstrates the seed vigor and the capacity for rapid initial establishment, essential for short-cycle crops.

The GLMM analysis for the plant height variable showed a significant increase over time as indicated by the AIC criterion (-473.974) and F value of 4921.787; (p < 0.001), however, it was not found any effects of the Trichoderma dose or Time x Trichoderma interaction (Figure 1). The lack of effect of the Trichoderma dose suggests that the influence of this fungus is not necessarily manifested in terms of height in chia plants. This strain is recommended for the biocontrol of Rhizoctonia solani and Sclerotinia sclerotiorum, with root growth stimulation being one of its modes of action (Bettiol et al., 2019BETTIOL, W., PINTO, Z.V., SILVA, J.C., FORNER, C., FARIA, M.R., PACIFICO, M.G. and COSTA, L.S.A.S., 2019. Produtos comerciais à base de Trichoderma. In: M. C. MEYER, S. M. MAZARO, and J. C. SILVA, eds. Trichoderma: uso na agricultura. Brasília, DF: Embrapa, p. 45-160.). Generally, there is strong evidence for the influence of indole acetic acid (IAA) synthesized by microorganisms on plants. For Trichoderma, Stewart and Hill (2014)STEWART, A. and HILL, R., 2014. Applications ofTrichodermain plant growth promotion. In V. GUPTA, M. SCHMOLL, A. HERRERA-ESTRELLA, R. UPADHYAY, I. DRUZHININA, and M. TUOHY, eds. Biotechnology and Biology of Trichoderma. Amsterdam: Elsevier, pp. 415-428. http://doi.org/10.1016/B978-0-444-59576-8.00031-X.
http://doi.org/10.1016/B978-0-444-59576-...
suggest that growth stimulation may be associated with the establishment of a balance of hormones such as IAA, gibberellic acid, and ethylene. Thus, the absence of a dose effect of CCT 7589 on the growth of chia plants' aerial parts is likely associated with genetic-environmental factors not investigated in the present study. This observation is relevant and highlights the need for future research as to explore the underlying mechanisms of this relation.

Figure 1
Marginal averages estimated for: A: Height of chia plants as a function of inoculant dose and assessment period in days after planting (D); A: Height of chia plants as a function of time. This variable was not affected by the inoculant dose.

Although the treatment of chia seeds with T. harzianum did not result in changes in plant height, it was found a linear increase in the magnitude of the variables: number of days to flowering (NDF), number of branches per plant (NB) and stem diameter (SD) up to the maximum dose (20 µL.g-1 seed) of the inoculant (Figures 2A, 2B and 2D). For the variable root dry mass (RDM), a quadratic regression equation was adjusted, in which the maximum estimated point for root biomass accumulation was reached with the application of 17.08 µL.g-1 seed (Figure 2C), suggesting that inoculant doses above this may not offer additional benefits. Furthermore, by avoiding excessive doses, the risk of possible adverse effects on the soil ecosystem is minimized, contributing to a more sustainable agriculture.

Figure 2
Regression analysis of the variables number of days to flowering (NDF), root dry mass (RDM), number of branches per plant (NB) and stem diameter (SD) of chia as a function of inoculant dose (T. harzianum).

The stimulation of root growth of chia plants promoted by T. harzianum is of great relevance for the crop, since this species has an incipient root system with frequent occurrence of lodging (Pereira et al., 2020PEREIRA, D., SCHUELTER, A.R., DEMBOCURSKI, D., PASSOS, F.R., MAESTRE, K.L., SILVA, E.A. and KLEN, M.R.F., 2020. Componentes do rendimento e composição química de grãos de genótipos de Salvia hispanica L. cultivados no Oeste do Paraná sob diferentes densidades populacionais.Research. Social Development, vol. 9, no. 12, pp. e10591210798. http://doi.org/10.33448/rsd-v9i12.10798.
http://doi.org/10.33448/rsd-v9i12.10798...
). Studies carried out with different plant species have revealed that the Trichoderma-plant interaction causes changes in the root system (Contreras-Cornejo et al., 2009CONTRERAS-CORNEJO, H.A., MACÍAS-RODRÍGUEZ, L., CORTÉS-PENAGOS, C. and LÓPEZ-BUCIO, J., 2009. Trichoderma virens, a plant beneficial fungus, enhances biomass production and promotes lateral root growth through an auxin-dependent mechanism in Arabidopsis. Plant Physiology, vol. 149, no. 3, pp. 1579-1592. http://doi.org/10.1104/pp.108.130369 PMid:19176721.
http://doi.org/10.1104/pp.108.130369...
; Harman et al., 2012HARMAN, G.E., HERRERA-ESTRELLA, A.H., HORWITZ, B.A. and LORITO, M., 2012. Trichoderma–from basic biology to biotechnology. Microbiology, vol. 158, no. 1, pp. 1-2. http://doi.org/10.1099/mic.0.056424-0 PMid:22210803.
http://doi.org/10.1099/mic.0.056424-0...
; Chagas et al., 2017CHAGAS, L.F.B., CHAGAS JUNIOR, A.F., SOARES, L.P. and FIDELIS, R.R., 2017. Trichoderma na promoção do crescimento vegetal. Revista de Agricultura Neotropical, vol. 4, no. 3, pp. 97-102. http://doi.org/10.32404/rean.v4i3.1529.
http://doi.org/10.32404/rean.v4i3.1529...
), which can lead to improvement in the carrying capacity of the aerial part (Contreras-Cornejo et al., 2009CONTRERAS-CORNEJO, H.A., MACÍAS-RODRÍGUEZ, L., CORTÉS-PENAGOS, C. and LÓPEZ-BUCIO, J., 2009. Trichoderma virens, a plant beneficial fungus, enhances biomass production and promotes lateral root growth through an auxin-dependent mechanism in Arabidopsis. Plant Physiology, vol. 149, no. 3, pp. 1579-1592. http://doi.org/10.1104/pp.108.130369 PMid:19176721.
http://doi.org/10.1104/pp.108.130369...
). In addition, compounds produced by the fungus induce the formation of a greater volume of root cells, thus maximizing the absorption of water and nutrients by the plant, as well as participating in the decomposition of organic matter, consequently contributing to the availability of nutrients (Vergara et al., 2019VERGARA, C., ARAUJO, K.E.C., SOUZA, S.R.D., SCHULTZ, N., SAGGIN JÚNIOR, O.J., SPERANDIO, M.V.L. and ZILLI, J.É., 2019. Plant-mycorrhizal fungi interaction and response to inoculation with different growth-promoting fungi. Pesquisa Agropecuária Brasileira, vol. 54, pp. e25140. http://doi.org/10.1590/s1678-3921.pab2019.v54.25140.
http://doi.org/10.1590/s1678-3921.pab201...
).

Recent studies by Fu et al. (2020)FU, J., XIAO, Y., LIU, Z., ZHANG, Y., WANG, Y. and YANG, K., 2020. Trichoderma asperellum improves soil microenvironment in different growth stages and yield of maize in saline-alkaline soil of the Songnen Plain. Plant, Soil and Environment, vol. 66, no. 12, pp. 639-647. http://doi.org/10.17221/456/2020-PSE.
http://doi.org/10.17221/456/2020-PSE...
and Hang et al. (2022)HANG, X., MENG, L., OU, Y., SHAO, C., XIONG, W., ZHANG, N., LIU, H., LI, R., SHEN, O. and KOWALCHUK, G.A., 2022. Trichoderma-amended biofertilizer stimulates soil resident Aspergillus population for joint plant growth promotion. NPJ Biofilms and Microbiomes, vol. 8, no. 1, pp. 57. http://doi.org/10.1038/s41522-022-00321-z PMid:35831320.
http://doi.org/10.1038/s41522-022-00321-...
revealed that inoculation with fungi of the genus Trichoderma promoted changes in the soil microbiome, and that depending on the strain, they favored plant growth in maize and cucumber plants, respectively. However, to date, there are no research results available on chia.

The data obtained in this study show that the T. harzianum had no dose influence on the characteristics of germination and plant height. However, it had a significant impact, especially in optimizing root biomass. These results expand the understanding of plant-fungus interactions in chia cultures, highlighting the potential of T. harzianum as a growth-promoting agent. Identification of the effectiveness threshold of T. harzianum provides a basis for more sustainable and cost-effective agricultural practices. Nevertheless, it is imperative that further research is needed to understand the mechanisms of these interactions, and to verify the applicability of these findings in different agricultural contexts.

3.2. Metagenomics analysis

Through the exploratory analysis of metagenome data from soil samples from the rhizosphere region, we found a wide variability both in the number of obtained sequences, as well as in the diversity of genera and identified species. Nonetheless, it was verified that, independently of the soil sample, approximately 98% of sequences belonged to the Bacteria domain, with a predominance of the phyla Proteobacteria (52.94 to 65.77%), Actinobacteria (10.35 to 24.08%), Bacteroidetes (2.35 to 13.74%), Firmicutes (3.16 to 7.21%) and Plantomycetes (1.68 to 3.45%). For the Eukaria domain, which represents approximately 1% of the biological diversity of the samples, were predominantly detected the organisms from the phyla Ascomycota (0.23 to 0.63%), Streptophyta (0.12 to 0.19%) and Chordata. (0.1 to 0.13%).

In relation to the diversity of bacteria and fungi (Tables 1 and 2), it was found that, regardless of the soil sample analyzed, highly diverse microbial taxa were detected, which according to Igiehon and Babalola (2018)IGIEHON, N.O. and BABALOLA, O.O., 2018. Below-ground-above-ground plant-microbial interactions: focusing on soybean, rhizobacteria and mycorrhizal fungi. The Open Microbiology Journal, vol. 12, no. 1, pp. 261-279. http://doi.org/10.2174/1874285801812010261 PMid:30197700.
http://doi.org/10.2174/18742858018120102...
may be involved in neutral, beneficial as well as phytopathogenic associations. In the metagenomic analysis of a soil sample pre-cultivation of chia, a prevalence of DNA sequences associated with the genera Pseudomonas, Streptomyces and Mesorhyzobium was found, involved, respectively, in growth promotion (Sah et al., 2021SAH, S., KRISHNANI, S. and SINGH, R., 2021. Pseudomonas mediated nutritional and growth promotional activities for sustainable food security. Current Research in Microbial Sciences, vol. 2, pp. 100084. http://doi.org/10.1016/j.crmicr.2021.100084 PMid:34917993.
http://doi.org/10.1016/j.crmicr.2021.100...
), antagonism (Pengproh et al., 2023PENGPROH, R., THANYASIRIWAT, T., SANGDEE, K., KAWICHA, P. and SANGDEE, A., 2023. Antagonistic ability and genome mining of soil Streptomyces spp. against Fusarium oxysporum f. sp. lycopersici. European Journal of Plant Pathology, vol. 167, no. 2, pp. 251-270. http://doi.org/10.1007/s10658-023-02698-9.
http://doi.org/10.1007/s10658-023-02698-...
) and atmospheric nitrogen fixation (Knežević et al., 2022KNEŽEVIĆ, M., BERIĆ, T., BUNTIĆ, A., JOVKOVIĆ, M., AVDOVIĆ, M., STANKOVIĆ, S., DELIC, D. and STAJKOVIĆ-SRBINOVIĆ, O., 2022. Native Mesorhizobium strains improve yield and nutrient composition of the common bird’s-foot trefoil grown in an acid soil. Rhizosphere, vol. 21, pp. 100487. http://doi.org/10.1016/j.rhisph.2022.100487.
http://doi.org/10.1016/j.rhisph.2022.100...
). As for fungi, there was a predominance of the biological control agent Trichoderma spp. and the genera related to etiological agents of plant diseases such as Fusarium, Rhizoctonia, Sclerotium, Macrophomina and Aspergillus.

Table 1
Diversity of bacteria for the main genera of agronomic importance in different soil samples: Before (BC) and after (T1 to T5) cultivation with chia, in the % of reading sequence of DNA per gram of soil.
Table 2
Diversity of fungi and oomycetes for the main genera of agronomic importance in different soil samples: Before (BC) and after (T1 to T5) cultivation with chia, in the % of reading sequence of DNA per gram of soil.

In relation to the fungus Trichoderma spp, a greater number of sequence readings were detected in the T2 sample (2.5 µL. g-1 seed) when compared to the other treatments (Table 2). Through the analyzes of the Trichoderma species present in the soil (Table 3), there was a predominance of T. reesei and T. virens, followed by T. asperellum and T. harzianum in all samples. In the T1 treatment, soil without seed inoculation with T. harzianum, it was detected a lower percentage of Trichoderma DNA sequences (1.06%), in relation to other treatments, as well as for the species that was inoculated to the seeds (11.3%). The increase in readings of Trichoderma spp. in the T2 sample suggests a positive response to the applied treatment, which may provide strategies for crop management. However, the lower reading of T1 sequences in relation to other treatments demonstrates the importance of inoculation in ensuring the presence and activity of this beneficial fungus.

Table 3
Diversity analysis of Trichoderma spp. (% of sequence of DNA/g of soil) in different soil samples before and after inoculation with T. harzianuam: BC: Before cultivation; T1: control; T2: 2.5 µL. g-1 seed; T3: 5.0 µL. g-1 seed; 10.0 µL. g-1 seed; 20.0 µL. g-1 seed.

The diversity of the genus species of Trichoderma revealed in this research (Table 3), associated with the role of this biological control agent as an antagonist and/or growth promoter presented in the literature, allows us to suggest a probable influence on the growth and development of chia plants by modifying the soil microbiome.

Through the comparison of the bacteria genera in rhizospheric soil after plant cultivation (Table 1), there was a wide variation between treatments for Mesorhyzobium, Pseudomonas and Streptomyces. For the genus Pseudomonas, it was originally detected 6.6%, being that after cultivation with chia there was a wide variation between treatments T5 (1.75%) and T2 (7.4%). In relation to the genus Mesorhyzobium, T1 (4.1%) and T5 (1.7%) had, respectively, the highest and lowest abundance among all treatments. For the genus Streptomyces, the opposite occurred, that is, T5 (6.2%) was higher than T1 (2.1%). The variation observed between the treatments for bacteria after chia cultivation highlights the dynamic intervention of agricultural practices on the soil microbiome. Chia, as a crop, may be influencing the abundance of specific bacterial genera, which could have repercussions on soil health and plant productivity. For example, fluctuations in Pseudomonas and Mesorhyzobium may reflect changes in nutrient availability or in the plant-microbe interactions (Nadarajah and Abdul Rahman, 2021NADARAJAH, K. and ABDUL RAHMAN, N.S.N., 2021. Plant–microbe interaction: aboveground to belowground, from the good to the bad. International Journal of Molecular Sciences, vol. 22, no. 19, pp. 10388. http://doi.org/10.3390/ijms221910388 PMid:34638728.
http://doi.org/10.3390/ijms221910388...
).

Using the estimated Pearson correlation coefficients, we detected no association between the abundance of Mesorhyzobium, Pseudomonas, Streptomyces and Trichoderma and the increase in doses of the inoculant based on T. harzianum. Yet, a strong negative correlation was estimated between the abundance of Trichoderma and microorganisms of the genera Ralstonia (r = - 0.94; p-value = 0.012) and Nigrospora (r= - 0.89; p-value = 0.04). In this context, different studies have revealed antagonistic action of Trichoderma spp. against Ralstonia (Konappa et al., 2018KONAPPA, N., KRISHNAMURTHY, S., SIDDAIAH, C.N., RAMACHANDRAPPA, N.S. and CHOWDAPPA, S., 2018. Evaluation of biological efficacy of Trichoderma asperellum against tomato bacterial wilt caused by Ralstonia solanacearum. Egyptian Journal of Biological Pest Control, vol. 28, no. 1, pp. 63. http://doi.org/10.1186/s41938-018-0069-5.
http://doi.org/10.1186/s41938-018-0069-5...
; Okinda, 2022OKINDA, C., 2022.Abundance of Trichoderma species in different habitats and their efficacy in the management of bacterial wilt of tomato. Nairobi: University of Nairobi. Dissertação de Mestrado em Proteção de Plantas.) and Nigrospora (Talapatra et al., 2016TALAPATRA K., DAS A.R., SAHA A.K. and DAS P., 2016 In vitro antagonistic activity of a root endophytic fungus towards plant pathogenic fungi. Journal of Applied Biology and Biotechnology, vol. 5, no. 2, pp. 68-71. http://doi.org/10.7324/JABB.2017.50210.
http://doi.org/10.7324/JABB.2017.50210...
; Hamdia et al., 2020HAMDIA, Z.A., WAFAA, H.H., HUTHAM, M.S., ABDUL RAHMAN, A.A. and HADI, M.A., 2020. Efficiency of 10 compatible isolates of Trichoderma spp. against rice pathogens under laboratory conditions. Trends in Applied Sciences Research, vol. 15, pp. 1-13.; Zhang et al., 2021ZHANG, W., YANG, J.Y., LU, X., LIN, J.M. and NIU, X.L., 2021. A preliminary study of the antifungal activity and antagonism mechanisms of Trichoderma spp. against turfgrass pathogens. Caoye Xuebao, vol. 30, pp. 137. http://doi.org/10.11686/cyxb2020333.
http://doi.org/10.11686/cyxb2020333...
), suggesting a possible influence of this biological control agent.

Although limited statistically significant associations were detected in this study, a pronounced increase in the abundance of Trichoderma was found in treatments with inoculation, especially T2 with a prevalence of 5.47% compared to the control treatment, 1.06%. According to Kaul et al. (2021)KAUL, S., CHOUDHARY, M., GUPTA, S. and DHAR, M.K., 2021. Engineering host microbiome for crop improvement and sustainable agriculture. Frontiers in Microbiology, vol. 12, pp. 635917. http://doi.org/10.3389/fmicb.2021.635917 PMid:34122359.
http://doi.org/10.3389/fmicb.2021.635917...
, microorganisms introduced into the agroecosystem modify the soil microbiome in a targeted manner. This statement is corroborated by studies developed by Fu et al. (2020)FU, J., XIAO, Y., LIU, Z., ZHANG, Y., WANG, Y. and YANG, K., 2020. Trichoderma asperellum improves soil microenvironment in different growth stages and yield of maize in saline-alkaline soil of the Songnen Plain. Plant, Soil and Environment, vol. 66, no. 12, pp. 639-647. http://doi.org/10.17221/456/2020-PSE.
http://doi.org/10.17221/456/2020-PSE...
and Hang et al. (2022)HANG, X., MENG, L., OU, Y., SHAO, C., XIONG, W., ZHANG, N., LIU, H., LI, R., SHEN, O. and KOWALCHUK, G.A., 2022. Trichoderma-amended biofertilizer stimulates soil resident Aspergillus population for joint plant growth promotion. NPJ Biofilms and Microbiomes, vol. 8, no. 1, pp. 57. http://doi.org/10.1038/s41522-022-00321-z PMid:35831320.
http://doi.org/10.1038/s41522-022-00321-...
, who investigated the inoculation of fungi of the genus Trichoderma.

Based on metagenomic analyzes focused on genes associated with cellular metabolism using the UPGMA method (Figure 3), greater genetic similarity was found between T3, T4 and T5 in relation to treatments T1 (control) and T2. These results suggest the existence of high genetic divergence of T1 (control) in relation to the other treatment samples after cultivation with Salvia hispanica, suggesting potential implications for the vegetative growth of the plant.

Figure 3
UPGMA analysis for genes related to metabolic pathways of metagenomes from soil samples using the Stamp program.

When applying principal component analysis (PCA) with the metagenomic data of the arylsulfatase enzymes (AS), beta-glucosidase (BG) and alkaline phosphatase (FA), which act as bioindicators and are crucial in evaluating soil health with the chemical parameters of soil samples, it was verified a wide dispersion of treatments in the graph (Figure 4a). The variables Ca, S and MO content were identified as the main contributions to this variation (Figure 4b).

Figure 4
Main components of metagenomic analysis for the enzymes arylsulfatase (AS), beta-glucosidase (BG) and alkaline phosphatase (FA) and soil chemical parameters. A: Graphical dispersion of scores in relation to the first two main components (PC1 and PC2) resulting from the condensation of abundance data for 67 genera of agronomic importance; B: Relative contribution of the variables analyzed based on the first two main components (PC1 and PC2).

In relation to the biplot graph, the distribution of treatments demonstrated distinct relations with the variables studied. The samples from treatment T5 were distinctively characterized by high levels of Ca, Mg, K and P, in addition to presenting a high number of copies of metagenomic DNA associated with the arylsulfatase enzyme (Figure 4a), a key enzyme in sulfur metabolism (Tabatabai and Bremner, 1970TABATABAI, M.A. and BREMNER, J.M., 1970. Arylsulfatase activity of soils. Soil Science Society of America Journal, vol. 34, no. 2, pp. 225-229. http://doi.org/10.2136/sssaj1970.03615995003400020016x.
http://doi.org/10.2136/sssaj1970.0361599...
; Ganeshamurthy and Nielsen, 1990GANESHAMURTHY, A.N. and NIELSEN, N.E., 1990. Arylsulfatase and the biochemical mineralization of soil organic sulphur. Soil Biology & Biochemistry, vol. 22, no. 8, pp. 1163-1165. http://doi.org/10.1016/0038-0717(90)90045-2.
http://doi.org/10.1016/0038-0717(90)9004...
). Treatments T1 (control) and T4, which are close together in the biplot graphical dispersion, were predominantly associated with high iron contents, and showed weaker correlations with the levels of copper, boron, organic matter, and sulfur. Treatments T2 and T3 exhibited weak associations with the alkaline phosphatase and beta-glucosidase enzymes, which are involved in hydrolysis reactions of organic phosphorus (Nannipieri et al., 2011NANNIPIERI, P., GIAGNONI, L., LANDI, L. and RENELLA, G. 2011. Role of phosphatase enzymes in soil. In: E. BÜNEMANN, A. OBERSON, and E. FROSSARD, eds. Phosphorus in action. Soil Biology. Springer: Berlin, Heidelberg, vol. 26. http://doi.org/10.1007/978-3-642-15271-9_9.) and glycosidic bonds (Bhatia et al., 2002BHATIA, Y., MISHRA, S. and BISARIA, V.S., 2002. Microbial β-glucosidases: cloning, properties, and applications. Critical Reviews in Biotechnology, vol. 22, no. 4, pp. 375-407. http://doi.org/10.1080/07388550290789568 PMid:12487426.
http://doi.org/10.1080/07388550290789568...
), respectively. It is interesting to note that these enzymes did not show a direct association with the nutrients analyzed. This suggests the complexity and multifunctionality of the soil microbiome, where certain enzymatic functions can be influenced by factors beyond traditionally measured nutrients, reinforcing the need for more in-depth studies to understand their interactions and impacts on the edaphic ecosystem.

In the joint analyzes of the results of metagenomics and soil chemistry, it is possible to suggest that there was a differential modification of the environment with the cultivation of chia (Salvia hispanica). Several studies reveal that microbial diversity is associated with soil multifunctionality (Wagg et al., 2014WAGG, C., BENDER, S.F., WIDMER, F. and VAN DER HEIJDEN, M.G., 2014. Soil biodiversity and soil community composition determine ecosystem multifunctionality. Proceedings of the National Academy of Sciences of the United States of America, vol. 111, no. 14, pp. 5266-5270. http://doi.org/10.1073/pnas.1320054111 PMid:24639507.
http://doi.org/10.1073/pnas.1320054111...
; Li et al., 2019LI, J., DELGADO-BAQUERIZO, M., WANG, J.T., HU, H.W., CAI, Z.J., ZHU, Y.N. and SINGH, B.K., 2019. Fungal richness contributes to multifunctionality in boreal forest soil. Soil Biology & Biochemistry, vol. 136, pp. 107526. http://doi.org/10.1016/j.soilbio.2019.107526.
http://doi.org/10.1016/j.soilbio.2019.10...
). However, this diversity does not in itself guarantee edaphic functionality (Shade, 2017SHADE, A., 2017. Diversity is the question, not the answer. The ISME Journal, vol. 11, no. 1, pp. 1-6. http://doi.org/10.1038/ismej.2016.118 PMid:27636395.
http://doi.org/10.1038/ismej.2016.118...
). According to Zhao et al. (2020)ZHAO, Z.B., HE, J.Z., QUAN, Z., WU, C.F., SHENG, R., ZHANG, L.M. and GEISEN, S., 2020. Fertilization changes soil microbiome functioning, especially phagotrophic protists. Soil Biology & Biochemistry, vol. 148, pp. 107863. http://doi.org/10.1016/j.soilbio.2020.107863.
http://doi.org/10.1016/j.soilbio.2020.10...
, the soil microbiome plays a crucial role in crop production and drives nutrient cycling. Soil interventions such as fertilization can lead to changes in the microbial community. Notably, microbial predators, when affecting the genetic variability of others, have substantial influence on the dynamics and functioning of soil. Through the metagenomic analysis for Trichoderma of soil samples collected before (AC) and after cultivation with chia, without seed inoculation with T. harzianum (T1), it was found that the predominant native species T. asperellum, T. harzianum, T. virens and T. reesei, represented respectively 67.1% and 69% of the total sequences per gram of soil for this microbial predator (Table 3). With the inoculation of seeds with T. harzianum, there was an increase in the contribution of the predominant species to 85.4% in T2, 87.6% in T3, 88.6% in T4 and 81.2% in T5. Thus, although there was no association detected between doses of the inoculant applied to the seeds and the abundance of species of this fungus present in the soil, significant correlations were found between T. asperellum (r = -0.96 p-value = 0.009) and T. harzianum (r = - 0.96 p-value = 0.02) with the contribution of other Trichoderma species. These results make it possible to suggest that the increase in T. asperellum and T. harzianum populations influenced reducing the contribution of other Trichoderma species.

The Trichoderma species, which include T. asperellum and T. harzianum, have the ability to cooperate with other beneficial soil microorganisms, thus promoting modification of the soil microbiome, which can result in growth promotion (Stewart and Hill, 2014STEWART, A. and HILL, R., 2014. Applications ofTrichodermain plant growth promotion. In V. GUPTA, M. SCHMOLL, A. HERRERA-ESTRELLA, R. UPADHYAY, I. DRUZHININA, and M. TUOHY, eds. Biotechnology and Biology of Trichoderma. Amsterdam: Elsevier, pp. 415-428. http://doi.org/10.1016/B978-0-444-59576-8.00031-X.
http://doi.org/10.1016/B978-0-444-59576-...
; Fu et al., 2020FU, J., XIAO, Y., LIU, Z., ZHANG, Y., WANG, Y. and YANG, K., 2020. Trichoderma asperellum improves soil microenvironment in different growth stages and yield of maize in saline-alkaline soil of the Songnen Plain. Plant, Soil and Environment, vol. 66, no. 12, pp. 639-647. http://doi.org/10.17221/456/2020-PSE.
http://doi.org/10.17221/456/2020-PSE...
; Hang et al., 2022HANG, X., MENG, L., OU, Y., SHAO, C., XIONG, W., ZHANG, N., LIU, H., LI, R., SHEN, O. and KOWALCHUK, G.A., 2022. Trichoderma-amended biofertilizer stimulates soil resident Aspergillus population for joint plant growth promotion. NPJ Biofilms and Microbiomes, vol. 8, no. 1, pp. 57. http://doi.org/10.1038/s41522-022-00321-z PMid:35831320.
http://doi.org/10.1038/s41522-022-00321-...
) and to induce systemic plant resistance to diseases (De Meyer et al., 1998; Sabbagh et al., 2017SABBAGH, S.K., ROUDINI, M. and PANJEHKEH, N., 2017. Systemic resistance induced by Trichoderma harzianum and Glomus mossea on cucumber damping-off disease caused by Phytophthora melonis. Archiv für Phytopathologie und Pflanzenschutz, vol. 50, no. 7-8, pp. 375-388. http://doi.org/10.1080/03235408.2017.1317953.
http://doi.org/10.1080/03235408.2017.131...
; Ilham et al., 2019ILHAM, B., NOUREDDINE, C., PHILIPPE, G., MOHAMMED, E.G., BRAHIM, E., SOPHIE, A., MARTINE, N. and MURIEL, M., 2019. Induced systemic resistance (ISR) in Arabidopsis thaliana by Bacillus amyloliquefaciens and Trichoderma harzianum used as seed treatments. Agriculture, vol. 9, no. 8, pp. 166. http://doi.org/10.3390/agriculture9080166.
http://doi.org/10.3390/agriculture908016...
). In relation to the present study, a substantial increase in the root biomass of chia plants (Figure 2B) and in the populations of T. asperellum and T. harzianum (Table 3) was detected in the samples that received inoculant in relation to the control treatment (T1). Metagenomic analyzes revealed the significant presence of the phytopathogenic genera Macrophomina, Rhizoctonia and Sclerotinia in soil samples (Table 2). Despite this, no disease symptoms were observed in plants, although such pathogens have been associated with infection in chia (El-Kaed et al., 2021EL-KAED, S.A., MERGAWY, M.M., HASSANIN, M.M.H., 2021. Management of the most destructive diseases of chia plant and its impact on the yield. Egyptian Journal of Phytopathology, vol. 49, no. 1, 37-48. http://doi.org/10.21608/ejp.2021.61936.1023.
http://doi.org/10.21608/ejp.2021.61936.1...
). In this way, it is plausible to state that the presence of Trichoderma species, particularly T. asperellum and T. harzianum, had a significant contribution to the dynamics of the soil microbiome, and favored plant growth during the vegetative stage.

4. Conclusions

The inoculation of the T. harzianum strain into chia seeds promotes an increase in the number of branches per plant, stem diameter, root dry mass and the number of days to flowering. Besides, there is a change in soil microbial diversity after chia cultivation, and the soil in which plants were grown from seeds inoculated with T. harzianum result in a greater number of genera and species in relation to the control (T1). Metagenomic analysis reveals that, regardless of the sample analyzed, the soil is made up of beneficial and phytopathogenic microorganisms. Based on the results of the multivariate analysis of taxonomic data and genes related to metagenome metabolic pathways, it is possible to suggest that seeds inoculated with higher doses of T. harzianum (T3 to T5) result in the formation of a soil microbial community with greater genetic similarity than those of T1 (control) and T2 (lowest dose). Besides, the inoculation with a higher dose of T. harzianum resulted in a higher content of Ca, Mg, K, P, and in the number of soil metagenomic DNA copies for the arylsulfase enzyme. T. asperellum, T. harzianum, T. virens and T. reesei were the Trichoderma species in the soil sample, having occurred after the cultivation of plants that received inoculum, an increase in the abundance of T. asperellum and T. harzianum and a reduction in less relevant native species present in the soil. Finally, it is concluded that the community of Trichoderma species in the soil, especially T. asperellum and T. harzianum, has a significant contribution to the dynamics of the soil microbiome, and to the growth of chia plants during the vegetative stage.

Acknowledgements

The authors would like to give special thanks to LAGBIO – Análises genômicas e biotecnologia and UDC for the financial support, and to Ph.D. Cássia Renata Pinheiro for assisting in the analysis and interpretation of metagenomics data.

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Publication Dates

  • Publication in this collection
    20 Sept 2024
  • Date of issue
    2024

History

  • Received
    23 Mar 2024
  • Accepted
    03 July 2024
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