Research Article | | Peer-Reviewed

Evaluation of Growth Promotion and Pathogenicity of Endophytic Fungi from the Root of Chenopodium Quinoa Willd

Received: 24 November 2024     Accepted: 23 December 2024     Published: 9 January 2025
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Abstract

Symbiotic associations between endophytic fungi and Chenopodium quinoa have been reported to be beneficial for increasing tolerance to drought and soil salinity, being this the only crop grown in the Southern Altiplano of Bolivia. The symbiotic interaction of endophytic fungi was investigated, considering their detrimental and mutualistic effects. 38 strains of endophytic fungi from the fungal collection of the Faculty of Agronomy were used. The percentage of germination and root length were measured in vitro (4 days). The percentage of emergence (7 days) and plant height (14 days) in pots were also evaluated. The fungi that did not impair germination were strains VP42, VP44, Alternaria sp. VP37, Fusarium sp. VP05 and Fusarium sp. VP30. Fungi that stimulated a significant increase in radicle longitudinal growth were Fusarium sp. VP35, Alternaria sp. VP37 and strain VP18. Fungi that caused a high mortality rate during the emergence phase were strain VP01, Alternaria sp. VP15, Fusarium sp. VP02, Fusarium sp. VP07, Fusarium sp. VP08, Fusarium sp. VP12, Fusarium sp. VP23 and Fusarium sp. VP36. The endophytic strains Alternaria sp. VP37, Fusarium sp. VP35 and strain VP18 stimulated superior seedling growth. The present research work reveals that some endophytic fungi of the Alternaria and Fusarium genera can behave as pathogens during the germination stage, while others have the function of promoting quinoa growth.

Published in American Journal of BioScience (Volume 13, Issue 1)
DOI 10.11648/j.ajbio.20251301.11
Page(s) 1-10
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2025. Published by Science Publishing Group

Keywords

Alternaria, Fusarium, Endophytic Fungus, Pathogenesis, Quinoa

1. Introduction
Quinoa (Chenopodium quinoa Willd.), is an annual dicotyledonous plant belonging to Amaranthaceae family . Currently, it is cultivated in more than 125 countries around the world, due to its genetic diversity of seeds preserved by generations of farmers in the Andes . It is the only crop adapted for thousands of years to the adverse conditions of the Southern Altiplano of Bolivia .
Plant-fungus interactions date back 400-500 million years . Plants do not thrive isolated, as constantly interact closely with various microorganisms, mainly bacteria and fungi . Their symbiotic relationship with plants attracts attention for its benefits in agriculture.
Fungi benefits to their host, existing a wide variety of plant-fungal symbiotic interactions . Favorable interactions, for example, allow plants to adapt to various ecosystems . For quinoa, endophytic fungi (EF) perform various functions that improve its resistance to adverse conditions, mitigating abiotic stress .
Associations can be beneficial, for example, promoting the adaptation and growth of plants in extreme conditions . Most plants interact with microorganisms , EF have been reported in plants that inhabit the Arctic, Antarctic, desert, ocean, tropical forests and agricultural fields . Growth promoting fungi can protect against plant pathogens by increasing tolerance to abiotic stress, such as drought, salinity and high temperatures through the production of secondary metabolites and hydrolytic enzymes . This study evaluated the influence of EF inoculated in roots and its effects on germination, emergence, root development and growth promotion in quinoa. Understanding the effect of applying EF in agriculture can offer innovative solutions to increase quinoa crop productivity by mitigating the conditions of the Southern Altiplano of Bolivia.
2. Materials and Methods
2.1. Study Area
The trials were carried out at the Plant Science Laboratory of the Faculty of Agronomy of the Technical University of Oruro. The HE strains used in this study were partially identified and are part of the mycological collection of the Faculty of Agronomy, whose specific details are presented in Table 1.
2.2. Fungal Cultivation and Biomass Production
For in vitro evaluation, axenic culture of EF were prepared in Potato Dextrose Agar (PDA) medium at 25°C for 14 days. Subsequently, mycelia discs (5 mm) of EF were collected to evaluate their promoting or pathogenic effect on quinoa germination. For pot tests, EF biomass was produced in 250 mL flasks inoculating 10 mycelia discs in 50 g of sugarcane bagasse.
2.3. In Vitro Germination and Root Length
Seeds of quinoa (Pandela rosada variety) were disinfested according to González-Teuber et al. . In vitro evaluation of EF effect on quinoa germination and root length, consisted of applying a mycelia disk in a 100 mm Petri dish with Murashige and Skoog (MS) medium (38 HE with 3 replicates + uninoculated Petri dishes) along with 10 desinfested quinoa seeds located around the disk. Petri dishes were incubated at 16°C for 4 days, with daily monitoring. Finally, germination (%) and root length (cm) were evaluated after the incubation period .
Table 1. Endophytic fungi in the current study.

Specimens

Strain code

Host

Place

Alternaria sp.

VP15

Quinoa root

Southern Alti-plano - Bolivia

Alternaria sp.

VP24

Quinoa root

Southern Altiplano - Bolivia

Alternaria sp.

VP37

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP12

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP11

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP16

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP02

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP21

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP22

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP23

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP03

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP30

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP35

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP36

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP39

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP40

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP41

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP43

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP05

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP06

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP07

Quinoa root

Southern Altiplano - Bolivia

Fusarium sp.

VP08

Quinoa root

Southern Altiplano - Bolivia

Penicillium sp.

VP32

Quinoa root

Southern Altiplano - Bolivia

Penicillium sp.

VP38

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP01

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP14

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP18

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP19

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP20

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP28

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP29

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP31

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP33

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP34

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP04

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP42

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP44

Quinoa root

Southern Altiplano - Bolivia

Unknown

VP09

Quinoa root

Southern Altiplano - Bolivia

2.4. Pots Assay: Emergence and Plant Length
Inoculation of EF in pot experiments consisted of: i) 15 g of sugarcane bagasse colonized with the fungus was placed at the bottom, ii) 600 g of sterile soil (collected from fallow quinoa plots in Southern Altiplano, commonly sandy) into 1 L plastic pot (38 pots with 3 replicates + uninoculated pots). Then, all pots were covered with sterile plastic bags until sowing. 10 disinfested quinoa seeds were sown at the surface and covered again with sterile plastic bags until germination. The pots were kept at room temperature (14°C) with relative humidity of 37%. The emergence percentage (%) was evaluated at 7 days and the plant length (cm) at 14 days after sowing.
2.5. Statistical Analysis
A complete randomized design (CRD) was used for the in vitro evaluation and a complete randomized block design (RBD) for the pots assay. Analysis of variance (ANOVA) was determined using R 4.2.3 software (R Development Core 2023) and Tukey test was used post-hoc.
3. Results
In vitro assay. There were significant differences in germination of quinoa seeds subjected to 38 EF (p<0.05). EF such as Alternaria sp. VP37, Alternaria sp. VP24, Fusarium sp. VP05, Fusarium sp. VP30, strains VP44 and VP42 applied to quinoa seeds promoted 100% of germination. In contrast, EF as Alternaria sp. VP15, Fusarium sp. VP12, Fusarium sp. VP23, Fusarium sp. VP02, Fusarium sp. VP08, Fusarium sp. VP07, strain VP01 and Fusarium sp. VP36 inhibited the germination completely, but Fusarium sp. VP21, strain VP14, Fusarium sp. VP43, Fusarium sp. VP39, strain VP31, Fusarium sp. VP22 and Fusarium sp. VP16 inhibited 93.33% of germination. Other strains showed intermediate values (Figure 1). On the other hand, there were significant differences in root length among the 38 EF (p<0.05). Growth promoting fungi based on longitudinal development of roots were Fusarium sp. VP35, Alternaria sp. VP37 and strain VP18 that reached 49.85, 49.73 and 48.85 mm respectively, followed by Alternaria sp. VP24, Fusarium sp. VP05, strains VP29 and VP42 and VP44 that promote relatively similar quinoa roots varying from 46.43 to 46.12 mm. In contrast, the strain VP14 and Fusarium sp. VP43 affected root development with 23.28 and 21.98 mm, respectively (Figures 2, 3).
Figure 1. Quinoa germination can be influenced by inoculation with endophytic fungi.
Figure 2. Root development of quinoa can be influenced by inoculation with endophytic fungi.
Figure 3. In vitro test: Endophytic fungi effect on quinoa root length. (A) Fungus observed to be beneficial as it promotes root growth, (B) Fungi has a moderately detrimental effect on root development, and (C) certain endophytic fungi are detrimental to root development.
Emergence and height of potted plants. Fully emerged cotyledons were statistically different in the presence of EF (p<0.05). The endophytic fungi that did not cause damage were strains VP18, VP19, VP29, VP42, VP44, Fusarium sp. VP35, Alternaria sp. VP37, Fusarium sp. VP05, Alternaria sp. VP24 and Fusarium sp. VP30, which only limited emergence by 3.33%. EF that presented less emergence of cotyledons and caused high mortality were Alternaria sp. VP15, Fusarium sp. VP07, Fusarium sp. VP08, Fusarium sp. VP02, Fusarium sp. VP12, Fusarium sp. VP36, strain VP01 and Fusarium sp. VP23 with 96.67% (Figure 4).
Plant height was statistically significant (p<0.05). Endophytic strains Alternaria sp. VP37, Fusarium sp. VP35 and strain VP18 promoted higher plant development reaching 55.98, 54.95 and 53.58 mm respectively, followed by strains VP44, VP42, VP19 and Fusarium sp. VP05 with developments 44.91, 44.86, 41.52 and 41.62 mm, respectively. Fusarium sp. VP03, Fusarium sp. VP06, as well as strains VP04, VP31 and VP33, showed a development similar to that of plants free of infection by endophytic fungi (control). Other endophytic strains had negative effects on plant height compared to the control (Figures 5, 6).
4. Discussion
Some EF from quinoa roots have positive effects on germination, root length, emergence and plant height. However, the vast majority caused detrimental effects including death. Several studies have described the positive effect of the association between EF and several crops . The HEs that were isolated from the quinoa root of the Atacama Desert, had their positive effect on the morphological and physiological characteristics of quinoa by inoculation of Talaromyces minioluteus and Penicillium murcianum under drought and salinity conditions .
Figure 4. Effect of inoculation with endophytic fungi in the emergence phase of quinoa.
Figure 5. The effect of inoculation with endophytic fungi on the height growth of quinoa plants.
EF from quinoa root such as Alternaria sp. VP37, Fusarium sp. VP05, Fusarium sp. VP30, strains VP44 and VP42 promoted 100% of in vitro (MS and PDA medium) germination compared to other endophytes. Moreover, under controlled conditions in pots assay, strains Fusarium sp. VP35, Fusarium sp. VP05, Alternaria sp. VP37, strains VP18, VP19, VP42 and VP44 promoted 100% of plant emergence (Figure 4). The symbiosis between EF and plants can increase or reduce certain phytohormones, for example, by secreting indole acetic acid (IAA) and gibberellic acid (GA) that affect longitudinal growth of roots and phylosphere .
Figure 6. Impact of endophytic fungi inoculation on quinoa growth. In (A), a positive boost in development is evident due to the mutualistic strain. On the other hand, in (B), it is observed that the endophytic fungus has a moderate detrimental effect, while in (C), it is shown that this strain is highly detrimental due to its pathogenic behavior.
Three EF that promoted greatest root elongation were Fusarium sp. VP35, Alternaria sp. VP37 and strain VP18, reaching a plant height of 55.98, 54.95 and 53.58 mm (Figure 5). These results reveal that fungi of the Fusarium genus may promote plant growth, probably by producing IAA, nitrogen fixation, phosphate solubilization and production of siderophores such as F. annulatum and F. proliferatum . Nevertheless, the relationship between plant-fungus can be beneficial and/or pathogenic , for example, those symbionts that do not cause any disease symptoms can colonize host plants tissues and there are benefits for both parties . In contrast, harmful aspects are described to interfere in transport of nutrients and water , abnormal metabolism in different stages of plant growth . These negative effects can be controlled by other EF , for example, A. fumigatus that has the ability to control pathogens by producing aflatoxins . Based upon the above described, the results of the initial vegetative development in this study showed that EF can be harmful and/or beneficial on the development of quinoa (Figure 6). For example, the strains Alternaria sp. VP37, Fusarium sp. VP35 and strain VP18 promoted seedling growth, but Fusarium sp. VP02 and Fusarium sp. VP07 are the strains that affected longitudinal elongation of the seedlings. In root development, 25.92% of EF promoted growth and the rest restricted elongation. These results are similar to those of other authors such as who reported that there are pathogenic fungi of the genus Penicillium. In contrast, there are studies that highlighted how EF stimulate the root growth to promote nutrients absorption , in exchange the plants synthesize several hydrolytic enzymes such as xylanase, pectinase, cellulase and proteinase that favor the fungi to access plant tissues . Understanding the dynamics of interaction between endophytic fungi and crop plants is essential to take advantage of the positive effects and mitigate the risks of potential pathogenic effects. That is essential for the development of agricultural management strategies that optimize the use of endophytic fungi in the improvement of crops such as quinoa, especially under abiotic stress conditions, such as drought and salinity.
5. Conclusion
Some strains of EF significantly promote key processes such as germination, root growth, emergence and height development of quinoa plants. However, other strains exert inhibitory effects on these processes, which could be detrimental.
EF with growth-promoting capacity represent a resource with great potential for implementation as biostimulants in sustainable agricultural systems. However, it is imperative to carry out a rigorous and precise selection of strains before proceeding with their application in field conditions.
Abbreviations

EF

Endophytic Fungi

MS

Murashige and Skoog

PDA

Potato Dextrose Agar

IAA

Indole Acetic Acid

GA

Gibberellic Acid

Source of Financing
This research did not receive external funding.
Acknowledgments
We would like to thank the director of the Agricultural Engineering Program at the Faculty of Agricultural and Natural Sciences at the Technical University of Oruro, National Institute of Agricultural and Forestry Innovation, the Peasant Academic Unit of Tiahuanacu – Bolivian Catholic University “San Pablo”, and the quinoa producers from different municipalities of the Southern Altiplano in Bolivia.
Ethical Considerations
This work was carried out according to the recommendations of related authors.
Research Limitations
There were no limitations in the present research.
Author Contributions
Victor Paco Pérez, conceived the idea and wrote the initial draft of the manuscript, Carla Crespo Melgar and Fernando Pacasa Quisbert, edited and revised the manuscript and Edwin Marcelo Gonzales Torrico, collaborated at microbiology laboratory.
Conflicts of Interest
The authors declare no conflicts of interest.
References
[1] A. Vega-Gálvez, M. Miranda, J. Vergara, E. Uribe, L. Puente, y E. A. Martínez, «Nutrition facts and functional potential of quinoa (Chenopodium quinoa willd.), an ancient Andean grain: a review», J. Sci. Food Agric., vol. 90, n.o 15, pp. 2541-2547, dic. 2010,
[2] D. Bazile, «Global Trends in the Worldwide Expansion of Quinoa Cultivation», Biol. Life Sci. Forum, vol. 15, n.o 1, p. 13, 2023, [En línea]. Disponible en:
[3] D. Bazile, S.-E. Jacobsen, y A. Verniau, «The Global Expansion of Quinoa: Trends and Limits», Front. Plant Sci., vol. 7, p. 622, 2016,
[4] M. Walsh-Dilley, «Resilience compromised: Producing vulnerability to climate and market among quinoa producers in Southwestern Bolivia», Glob. Environ. Chang., vol. 65, p. 102165, 2020,
[5] F. Lutzoni et al., «Contemporaneous radiations of fungi and plants linked to symbiosis», Nat. Commun., vol. 9, n.o 1, p. 5451, 2018,
[6] C. Strullu-Derrien, M. A. Selosse, P. Kenrick, y F. M. Martin, «The origin and evolution of mycorrhizal symbioses: from palaeomycology to phylogenomics», New Phytol., vol. 220, n.o 4, pp. 1012-1030, 2018,
[7] N. Vigneron, G. V. Radhakrishnan, y P. M. Delaux, «What have we learnt from studying the evolution of the arbuscular mycorrhizal symbiosis?», Curr. Opin. Plant Biol., vol. 44, pp. 49-56, 2018,
[8] M. A. Hassani, P. Durán, y S. Hacquard, «Microbial interactions within the plant holobiont», Microbiome, pp. 6-58, 2018,
[9] J. Mercado-Blanco, «Life of Microbes Inside the Plant», en Principles of Plant-Microbe Interactions: Microbes for Sustainable Agriculture, B. Lugtenberg, Ed. Springer, 2015, pp. 25-32.
[10] W. K. Mousa y M. N. Raizada, «The diversity of anti-microbial secondary metabolites produced by fungal endophytes: an interdisciplinary perspective», Front. Microbiol., vol. 4, p. 65, 2013,
[11] Z.-L. Yuan, C.-L. Zhang, y F.-C. Lin, «Role of Diverse Non-Systemic Fungal Endophytes in Plant Performance and Response to Stress: Progress and Approaches», J. Plant Growth Regul., vol. 29, n.o 1, pp. 116-126, 2010,
[12] P. Bonfante y A. Genre, «Mechanisms underlying beneficial plant - Fungus interactions in mycorrhizal symbiosis», Nat. Commun., p. 1: 48, 2010,
[13] F. A. Decunta, L. I. Pérez, D. P. Malinowski, M. A. Molina-Montenegro, y P. E. Gundel, «A Systematic Review on the Effects of Epichloë Fungal Endophytes on Drought Tolerance in Cool-Season Grasses», Front. Plant Sci., vol. 12, p. 644731, 2021,
[14] K. M. Thambugala, D. A. Daranagama, A. J. L. Phillips, S. D. Kannangara, y I. Promputtha, «Fungi vs. Fungi in Biocontrol: An Overview of Fungal Antagonists Applied Against Fungal Plant Pathogens», Front. Cell. Infect. Microbiol., vol. 10, n.o November, p. 604923, 2020,
[15] P. Trivedi, J. E. Leach, S. G. Tringe, T. Sa, y B. K. Singh, «Plant-microbiome interactions: from community assembly to plant health», Nat. Rev. Microbiol., vol. 18, n.o 11, pp. 607-621, 2020,
[16] A. E. Fadiji y O. O. Babalola, «Exploring the potentialities of beneficial endophytes for improved plant growth», Saudi J. Biol. Sci., vol. 27, n.o 12, pp. 3622-3633, 2020,
[17] P. R. Hardoim et al., «The Hidden World within Plants: Ecological and Evolutionary Considerations for Defining Functioning of Microbial Endophytes», Microbiol. Mol. Biol. Rev., vol. 79, n.o 3, pp. 293-320, 2015,
[18] K. Selim, «Biology of Endophytic Fungi», Curr. Res. Environ. Appl. Mycol., vol. 2, n.o 1, pp. 31-82, 2012,
[19] V. V. Kumar, «Plant Growth-Promoting Microorganisms: Interaction with Plants and Soil», en Plant, Soil and Microbes, vol. 1, K. R. Hakeem, M. S. Akhtar, y S. N. A. Abdullah, Eds. Springer International Publishing Switzerland, 2016, pp. 1-16.
[20] M. González-Teuber, R. A. Contreras, G. E. Zúñiga, D. Barrera, y L. Bascuñán-Godoy, «Synergistic Association With Root Endophytic Fungi Improves Morpho-Physiological and Biochemical Responses of Chenopodium quinoa to Salt Stress», Front. Ecol. Evol., vol. 9, p. 787318, 2022,
[21] M. González-Teuber, C. Vilo, y L. Bascuñán-Godoy, «Molecular characterization of endophytic fungi associated with the roots of Chenopodium quinoa inhabiting the Atacama Desert, Chile», Genomics Data, vol. 11, pp. 109-112, 2017,
[22] G. Berg, P. Kusstatscher, A. Abdelfattah, T. Cernava, y K. Smalla, «Microbiome Modulation-Toward a Better Understanding of Plant Microbiome Response to Microbial Inoculants», Front. Microbiol., vol. 12, p. 650610, 2021,
[23] Y. A. Millet et al., «Innate immune responses activated in Arabidopsis roots by microbe-associated molecular patterns», Plant Cell, vol. 22, n.o 3, pp. 973-990, 2010,
[24] A. C. Perez, J. S. Rojas, y H. M. Vale, «Biologia y perspectiva de microorganismos endófitos asociados a plantas», Rev. Colomb. Cienc. Anim. - RECIA, vol. 1, n.o 2, pp. 286-301, 2009,
[25] A. Zuccaro et al., «Endophytic life strategies decoded by genome and transcriptome analyses of the mutualistic root symbiont Piriformospora indica», PLoS Pathog., vol. 7, n.o 10, p. e1002290, 2011,
[26] I. Khalmuratova, D. H. Choi, H. J. Yoon, T. M. Yoon, y J. G. Kim, «Diversity and plant growth promotion of fungal endophytes in five halophytes from the buan salt marsh», J. Microbiol. Biotechnol., vol. 31, n.o 3, pp. 408-418, 2021,
[27] A. E. Arnold y F. Lutzoni, «Diversity and host range of foliar fungal endophytes: are tropical leaves biodiversity hotspots?», Ecology, vol. 88, n.o 3, pp. 541-549, 2007,
[28] S. Kusari, S. P. Pandey, y M. Spiteller, «Untapped mutualistic paradigms linking host plant and endophytic fungal production of similar bioactive secondary metabolites», Phytochemistry, vol. 91, pp. 81-87, 2012,
[29] N. M. Chauhan, A. D. Gutama, y A. Aysa, «Endophytic fungal diversity isolated from different agro-ecosystem of Enset (Ensete ventericosum) in Gedeo zone, SNNPRS, Ethiopia», BMC Microbiol., vol. 19, n.o 1, p. 172, 2019, [En línea]. Disponible en:
[30] J. G. Harrison y E. A. Griffin, «The diversity and distribution of endophytes across biomes, plant phylogeny and host tissues: how far have we come and where do we go from here?», Environ. Microbiol., vol. 22, n.o 6, pp. 2107-2123, 2020,
[31] L. Jin et al., «Diversity and Biocontrol Potential of Culturable Endophytic Fungi in Cotton», Front. Microbiol., vol. 12, p. 698930, 2021,
[32] K. L. Rana et al., «Endophytic microbes: biodiversity, plant growth-promoting mechanisms and potential applications for agricultural sustainability», Antonie Van Leeuwenhoek, vol. 113, n.o 8, pp. 1075-1107, 2020,
[33] R. E. Sánchez-Fernández et al., «Hongos endófitos: fuente potencial de metabolitos secundarios bioactivos con utilidad en agricultura y medicina», Tip Rev. Espec. en Ciencias Químico-Biológicas, vol. 16, n.o 2, pp. 132-146, 2013,
[34] J. A. Castillo, G. Conde, M. Claros, y N. Ortuño, «Diversity of cultivable microorganisms associated with Quinoa (Chenopodium quinoa) and their potential for plant growth-promotion», Bionatura, vol. 7, n.o 2, p. 61, 2022,
[35] J. O. de Carvalho, V. Broll, A. H. S. Martinelli, y F. C. Lopes, «Endophytic fungi: positive association with plants», en Molecular Aspects of Plant Beneficial Microbes in Agriculture, V. Sharma, R. Salwan, y L. K. Tawfeeq Al-Ani, Eds. India: Academic Press, 2020, pp. 321-332. [En línea]. Disponible en:
[36] N. Ortuño, J. A. Castillo, y M. Claros, «Symbiotic Native Microorganisms of Quinoa in the Bolivian Altiplano», en Biology and Biotechnology of Quinoa, A. Varma, Ed. Springer Nature Singapore, 2021, pp. 131-151. [En línea]. Disponible en:
[37] P. W. Crous et al., «Fusarium: more than a node or a foot-shaped basal cell», Stud. Mycol., vol. 98, p. 100116, 2021,
[38] M. R. Panuccio, S. E. Jacobsen, S. S. Akhtar, y A. Muscolo, «Effect of saline water on seed germination and early seedling growth of the halophyte quinoa», AoB Plants, vol. 6, p. plu047, 2014,
[39] A. Naureen, F. ul H. Nasim, M. S. Choudhary, M. Ashraf, F. M. W. Grundler, y A. S. S. Schleker, «A new endophytic fungus CJAN1179 isolated from the Cholistan desert promotes lateral root growth in Arabidopsis and produces IAA through tryptophan-dependent pathway», Arch. Microbiol., vol. 204, n.o 3, p. 181, 2022,
[40] N. C. Baron, A. de Souza Pollo, y E. C. Rigobelo, «Purpureocillium lilacinum and Metarhizium marquandii as plant growth-promoting fungi», PeerJ, n.o 8, p. e9005, 2020,
[41] G. Berg, «Plant-microbe interactions promoting plant growth and health: Perspectives for controlled use of microorganisms in agriculture», Appl. Microbiol. Biotechnol., vol. 84, n.o 1, pp. 11-18, 2009,
[42] L. R. Jaber y J. Enkerli, «Fungal entomopathogens as endophytes: can they promote plant growth?», Biocontrol Sci. Technol., vol. 27, n.o 1, pp. 28-41, 2017,
[43] A. L. Khan, J. Hussain, A. Al-Harrasi, A. Al-Rawahi, y I.-J. Lee, «Endophytic fungi: resource for gibberellins and crop abiotic stress resistance», Crit. Rev. Biotechnol., vol. 35, pp. 62-74, 2015.
[44] N. C. Baron y E. C. Rigobelo, «Endophytic fungi: a tool for plant growth promotion and sustainable agriculture», Mycology, vol. 13, n.o 1, pp. 39-55, 2022,
[45] L. Yan, J. Zhu, X. Zhao, J. Shi, C. Jiang, y D. Shao, «Beneficial effects of endophytic fungi colonization on plants», Appl. Microbiol. Biotechnol., vol. 103, n.o 8, pp. 3327-3340, 2019,
[46] M. González-Teuber, A. Urzuá, P. Plaza, y L. Bascuñán-Godoy, «Effects of root endophytic fungi on response of Chenopodium quinoa to drought stress», Plant Ecol., vol. 219, pp. 231-240, 2018,
[47] L. Bilal et al., «Plant growth promoting endophytic fungi Asprgillus fumigatus TS1 and Fusarium proliferatum BRL1 produce gibberellins and regulates plant endogenous hormones», Symbiosis, vol. 76, pp. 117-127, 2018, [En línea]. Disponible en:
[48] S. Roy, A. Sarma, S. Paul, D. K. Jha, y K. Tayung, «Plant growth-promoting traits and activation of defense enzymes intraditional rice variety by fungal endophytes isolated from seeds ofindigenous rice cultivars of Northeast India», South African J. Bot., vol. 160, pp. 483-492, 2023, [En línea]. Disponible en:
[49] N. A. Elhamouly et al., «The hidden power of secondary metabolites in plant-fungi interactions and sustainable phytoremediation», Front. Plant Sci., vol. 13, p. 1044896, 2022,
[50] P. Tiwari y H. Bae, «Endophytic Fungi: Key Insights, Emerging Prospects, and Challenges in Natural Product Drug Discovery», Microorganisms, vol. 10, p. 360, 2022,
[51] S. E. Smith, E. Facelli, S. Pope, y F. A. Smith, «Plant performance in stressful environments: interpreting new and established knowledge of the roles of arbuscular mycorrhizas», Plant Soil, vol. 326, pp. 3-20, 2010,
[52] H. A. Bruns, «Controlling Aflatoxin and Fumonisin in Maize by Crop Management», J. Toxicol., vol. 22, n.o 2-3, pp. 153-173, 2003,
[53] M. Kottb, T. Gigolashvili, D. K. Großkinsky, y B. Piechulla, «Trichoderma volatiles effecting Arabidopsis: from inhibition to protection against phytopathogenic fungi», Front. Microbiol., vol. 6, p. 995, 2015,
[54] A. M. Abdelaziz, D. A. El-Wakil, M. S. Attia, O. M. Ali, H. AbdElgawad, y A. H. Hashem, «Inhibition of Aspergillus flavus Growth and Aflatoxin Production in Zea mays L. Using Endophytic Aspergillus fumigatus», J. Fungi, vol. 8, n.o 5, p. 482, 2022,
[55] J. P. Louw y L. Korsten, «Pathogenic Penicillium spp. on apple and pear», Plant Dis., vol. 98, n.o 5, pp. 590-598, 2014,
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    Pérez, V. P., Fabiana, C. M. C., Quisbert, F. P. (2025). Evaluation of Growth Promotion and Pathogenicity of Endophytic Fungi from the Root of Chenopodium Quinoa Willd. American Journal of BioScience, 13(1), 1-10. https://doi.org/10.11648/j.ajbio.20251301.11

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    Pérez, V. P.; Fabiana, C. M. C.; Quisbert, F. P. Evaluation of Growth Promotion and Pathogenicity of Endophytic Fungi from the Root of Chenopodium Quinoa Willd. Am. J. BioScience 2025, 13(1), 1-10. doi: 10.11648/j.ajbio.20251301.11

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    AMA Style

    Pérez VP, Fabiana CMC, Quisbert FP. Evaluation of Growth Promotion and Pathogenicity of Endophytic Fungi from the Root of Chenopodium Quinoa Willd. Am J BioScience. 2025;13(1):1-10. doi: 10.11648/j.ajbio.20251301.11

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  • @article{10.11648/j.ajbio.20251301.11,
      author = {Victor Paco Pérez and Crespo Melgar Carla Fabiana and Fernando Pacasa Quisbert},
      title = {Evaluation of Growth Promotion and Pathogenicity of Endophytic Fungi from the Root of Chenopodium Quinoa Willd
    },
      journal = {American Journal of BioScience},
      volume = {13},
      number = {1},
      pages = {1-10},
      doi = {10.11648/j.ajbio.20251301.11},
      url = {https://doi.org/10.11648/j.ajbio.20251301.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajbio.20251301.11},
      abstract = {Symbiotic associations between endophytic fungi and Chenopodium quinoa have been reported to be beneficial for increasing tolerance to drought and soil salinity, being this the only crop grown in the Southern Altiplano of Bolivia. The symbiotic interaction of endophytic fungi was investigated, considering their detrimental and mutualistic effects. 38 strains of endophytic fungi from the fungal collection of the Faculty of Agronomy were used. The percentage of germination and root length were measured in vitro (4 days). The percentage of emergence (7 days) and plant height (14 days) in pots were also evaluated. The fungi that did not impair germination were strains VP42, VP44, Alternaria sp. VP37, Fusarium sp. VP05 and Fusarium sp. VP30. Fungi that stimulated a significant increase in radicle longitudinal growth were Fusarium sp. VP35, Alternaria sp. VP37 and strain VP18. Fungi that caused a high mortality rate during the emergence phase were strain VP01, Alternaria sp. VP15, Fusarium sp. VP02, Fusarium sp. VP07, Fusarium sp. VP08, Fusarium sp. VP12, Fusarium sp. VP23 and Fusarium sp. VP36. The endophytic strains Alternaria sp. VP37, Fusarium sp. VP35 and strain VP18 stimulated superior seedling growth. The present research work reveals that some endophytic fungi of the Alternaria and Fusarium genera can behave as pathogens during the germination stage, while others have the function of promoting quinoa growth.
    },
     year = {2025}
    }
    

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  • TY  - JOUR
    T1  - Evaluation of Growth Promotion and Pathogenicity of Endophytic Fungi from the Root of Chenopodium Quinoa Willd
    
    AU  - Victor Paco Pérez
    AU  - Crespo Melgar Carla Fabiana
    AU  - Fernando Pacasa Quisbert
    Y1  - 2025/01/09
    PY  - 2025
    N1  - https://doi.org/10.11648/j.ajbio.20251301.11
    DO  - 10.11648/j.ajbio.20251301.11
    T2  - American Journal of BioScience
    JF  - American Journal of BioScience
    JO  - American Journal of BioScience
    SP  - 1
    EP  - 10
    PB  - Science Publishing Group
    SN  - 2330-0167
    UR  - https://doi.org/10.11648/j.ajbio.20251301.11
    AB  - Symbiotic associations between endophytic fungi and Chenopodium quinoa have been reported to be beneficial for increasing tolerance to drought and soil salinity, being this the only crop grown in the Southern Altiplano of Bolivia. The symbiotic interaction of endophytic fungi was investigated, considering their detrimental and mutualistic effects. 38 strains of endophytic fungi from the fungal collection of the Faculty of Agronomy were used. The percentage of germination and root length were measured in vitro (4 days). The percentage of emergence (7 days) and plant height (14 days) in pots were also evaluated. The fungi that did not impair germination were strains VP42, VP44, Alternaria sp. VP37, Fusarium sp. VP05 and Fusarium sp. VP30. Fungi that stimulated a significant increase in radicle longitudinal growth were Fusarium sp. VP35, Alternaria sp. VP37 and strain VP18. Fungi that caused a high mortality rate during the emergence phase were strain VP01, Alternaria sp. VP15, Fusarium sp. VP02, Fusarium sp. VP07, Fusarium sp. VP08, Fusarium sp. VP12, Fusarium sp. VP23 and Fusarium sp. VP36. The endophytic strains Alternaria sp. VP37, Fusarium sp. VP35 and strain VP18 stimulated superior seedling growth. The present research work reveals that some endophytic fungi of the Alternaria and Fusarium genera can behave as pathogens during the germination stage, while others have the function of promoting quinoa growth.
    
    VL  - 13
    IS  - 1
    ER  - 

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