Psychrotolerant strains of the genus Trichoderma from bottom sediments of Lake Baikal as promising biopesticides’ producers
- Authors: Roshka Y.A.1,2, Kurakov A.V.2, Fedorova M.D.2, Sadykova V.S.1
-
Affiliations:
- Gause Institute of New Antibiotics
- Moscow State University, Faculty of Biology, Department of Mycology and Algology
- Issue: Vol 59, No 4 (2025)
- Pages: 313-325
- Section: ФИЗИОЛОГИЯ, БИОХИМИЯ, БИОТЕХНОЛОГИЯ
- URL: https://bakhtiniada.ru/0026-3648/article/view/304806
- DOI: https://doi.org/10.31857/S0026364825040052
- EDN: https://elibrary.ru/benyxe
- ID: 304806
Cite item
Abstract
About the authors
Y. A. Roshka
Gause Institute of New Antibiotics; Moscow State University, Faculty of Biology, Department of Mycology and Algology
Email: roshkajulia@gmail.com
Moscow, Russia; Moscow, Russia
A. V. Kurakov
Moscow State University, Faculty of Biology, Department of Mycology and Algology
Email: kurakov57@mail.ru
Moscow, Russia
M. D. Fedorova
Moscow State University, Faculty of Biology, Department of Mycology and AlgologyMoscow, Russia
V. S. Sadykova
Gause Institute of New Antibiotics
Email: sadykova_09@mail.ru
Moscow, Russia
References
- Al-Surhanee A. A. Protective role of antifusarial eco-friendly agents (Trichoderma and salicylic acid) to improve resistance performance of tomato plants. Saudi J. Biol. Sci. 2022. V. 29 (4). P. 2933–2941. https://doi.org/10.1016/j.sjbs.2022.01.020
- Babich O., Shevchenko M., Ivanova S. et al. Antimicrobial potential of microorganisms isolated from the bottom sediments of lake Baikal. Antibiotics (Basel). 2021. V. 10 (8). P. 927. https://doi.org/10.3390/antibiotics10080927
- Bashenkhaeva M., Yeletskaya Y., Tomberg I. et al. Free-living and particle-associated microbial communities of lake Baikal differ by season and nutrient intake. Diversity. 2023. V. 15 (4). P. 572. https://doi.org/10.3390/d15040572
- BLAST – Basic Local Alignment Search Tool. 2025. https://blast.ncbi.nlm.nih.gov/Blast.cgi. Accessed 02.02.2025.
- Czajkowski R., Kaczyńska N., Jafra S. et al. Temperature-responsive genetic loci in pectinolytic plant pathogenic Dickeya solani. Plant Pathol. 2017. V. 66 (4). P. 584–594. https://doi.org/10.1111/ppa.12618
- De Hoog G. S., Guarro J., Gené J., et al. Atlas of clinical fungi. CBS-KNAW, Fungal Biodiversity Centre, 3rd edn. Utrecht, 2011.
- Domsch K. H., Gams W., Anderson T.-H. Compendium of soil fungi. IHW-Verlag et Verlagsbuchhandlung, 2nd edn. Eching, 2001.
- Dutta P., Mahanta M., Singh S. B. et al. Molecular interaction between plants and Trichoderma species against soil-borne plant pathogens. Front. Plant. Sci. 2023. V. 14. Art. 1145715. https://doi.org/10.3389/fpls.2023.1145715
- Egorov N. S. Fundamentals of the doctrine of antibiotics. Nauka, Moscow, 2004. (In Russ.).
- Ephytia, INRAE portal. 2025. Pectobacterium carotovorum subsp. carotovorum (Jones 1901) Hauben et al. (1999). https://ephytia.inra.fr/en/C/27040/Eggplant-Pectobacterium-carotovorum. Accessed 20.05.2025.
- Fedorova M. D., Kurakov A. V. Microbiota of bottom sediments in the coastal zone of lake Baikal. Contemp. Probl. Ecol. 2023. V. 16. P. 492–508. https://doi.org/10.1134/S1995425523040030
- Fontana D. C., de Paula S., Torres A. G. et al. Endophytic fungi: biological control and induced resistance to phytopathogens and abiotic stresses. Pathogens. 2021. V. 10 (5). P. 570. https://doi.org/10.3390/pathogens10050570
- Furhan J. Adaptation, production, and biotechnological potential of cold-adapted proteases from psychrophiles and psychrotrophs: recent overview. J. Genet. Eng. Biotechnol. 2020. V. 18 (1). P. 36. https://doi.org/10.1186/s43141-020-00053-7
- Galachyants A. D., Krasnopeev A. Y., Podlesnaya G. V. et al. Diversity of aerobic anoxygenic phototrophs and rhodopsin-containing bacteria in the surface microlayer, water column and epilithic biofilms of lake Baikal. Microorganisms. 2021. V. 9 (4). P. 842. https://doi.org/10.3390/microorganisms9040842
- GenBank. 2025. https://www.ncbi.nlm.nih.gov/genbank. Accessed 12.02.2025.
- Goyer C., Ullrich M. S. Identification of low-temperature-regulated genes in the fire blight pathogen Erwinia amylovora. Can. J. Microbiol. 2006. V. 52 (5). P. 468–475. https://doi.org/10.1139/w05-153
- GOST 12038-84. Agricultural seeds. Methods for determination of germination. 1984. (In Russ.).
- GOST 33777-2016. Surface active agent. Method for the determination of phytotoxicity on seeds of higher plants. 2016. (In Russ.).
- Hagestad O. C., Andersen J. H., Altermark B. et al. Cultivable marine fungi from the Arctic Archipelago of Svalbard and their antibacterial activity. Mycology. 2020. V. 11 (3). P. 230–242. https://doi.org/10.1080/21501203.2019.1708492
- Hassan N., Rafiq M., Hayat M. et al. Psychrophilic and psychrotrophic fungi: a comprehensive review. Rev. Environ. Sci. Biotechnol. 2016. V. 15 (2). P. 147–172. https://doi.org/10.1007/s11157-016-9395-9
- Hitora Y., Sejiyama A., Honda K. et al. Fluorescent image-based high-content screening of extracts of natural resources for cell cycle inhibitors and identification of a new sesquiterpene quinone from the sponge, Dactylospongia metachromia. Bioorg. Med. Chem. 2021. V. 31. Art. 115968. https://doi.org/10.1016/j.bmc.2020.115968
- Ibrar M., Ullah M. W., Manan S. et al. Fungi from the extremes of life: an untapped treasure for bioactive compounds. Appl. Microbiol. Biotechnol. 2020. V. 104. P. 2777–2801. https://doi.org/10.1007/s00253-020-10399-0
- Index Fungorum. 2025. http://www.indexfungorum.org/Names/Names.asp. Accessed 20.03.2025.
- Khuong N. Q., Nhien D. B., Thu L. T.M. et al. Using Trichoderma asperellum to Antagonize Lasiodiplodia theobromae Causing Stem-End Rot Disease on Pomelo (Citrus maxima). J. Fungi. 2023. V. 9 (10). P. 981. https://doi.org/10.3390/jof9100981
- Krasnopeev A. Y., Ziemens E. A., Sukhanova E. V. et al. Bacterial community seasonal dynamics in lake Baikal littoral zone. Microbiology. 2024. V. 93 (Suppl 1). P. 40–44. https://doi.org/10.1134/S0026261724609151
- Kulikova N. N., Suturin A. N., Boyko S. M. et al. The role of water lichens in the biogeochemical processes in the lake Baikal stony littoral. Inland Water Biol. 2009. V. 2 (2). P. 144–148.
- Kurakov A. V., Fedorova M. D. Mycobiota of bottom sediments of lake Baikal. In: T. K. Antal, E. A. Bonch-Osmolovskaya, N. V. Pimenov (eds). Proceedings of the III Russian Microbiological Congress. Pskov, 2023, pp. 214–215.
- Kuznetsov E. A. Fungi of aquatic ecosystems. Dr. Sci. Thesis. Moscow, 2003. (In Russ.).
- Lanham P. G., Mcllravey K. I., Perombelon M. C.M. Production of cell wall dissolving enzymes by Erwinia carotovora subsp. atroseptica in vitro at 27° and 30.5°. J. Appl. Microbiol. 1991. V. 70 (1). P. 20–24. https://doi.org/10.1111/j.1365-2672.1991.tb03781.x
- Mincheva E. V., Peretolchina T. E., Kravtsova L. S. et al. Hidden diversity of microeukaryotes in lake Baikal: a metagenomic approach. Limnol. Freshwater Biol. 2019. V. 1. P. 150–154. https://doi.org/10.31951/2658-3518-2019-A-1-150
- Ogaki M. B., Coelho L. C., Vieira R. et al. Cultivable fungi present in deep-sea sediments of Antarctica: taxonomy, diversity, and bioprospecting of bioactive compounds. Extremophiles. 2020. V. 24 (2). P. 227–238. https://doi.org/10.1007/s00792-019-01148-x
- Ogaki M. B., Teixeira D. R., Vieira R. et al. Diversity and bioprospecting of cultivable fungal assemblages in sediments of lakes in the Antarctic Peninsula. Fungal Biol. 2020. V. 124 (6). P. 601–611. https://doi.org/10.1016/j.funbio.2020.02.015
- Palafox-Leal N.L., Castillo Batista J. Ch., Santos-Cervantes M.E. et al. Pectobacterium punjabense causing soft rot and blackleg of potato in Sinaloa, Mexico. Eur. J. Plant. Pathol. 2024. V. 168. P. 29–37. https://doi.org/10.1007/s10658-023-02725-9
- Pandey A., Dhakar K., Jain R. et al. Cold adapted fungi from Indian Himalaya: untapped source for bioprospecting. Proc. Natl. Acad. Sci., India, Sect. B Biol. Sci. 2019. V. 89 (4). P. 1125–1132. https://doi.org/10.1007/s40011-018-1002-0
- Polyakova M. S., Mincheva Е. V., Pudovkina Т.А et al. The first data on fungi and fungus-like organisms in Lake Baikal. Limnol. Freshwater Biol. 2020. V. 3 (4). P. 741–742. https://doi.org/10.31951/2658-3518-2020-a-4-741
- Rabosky D. L. Evolutionary time and species diversity in aquatic ecosystems worldwide. Biol. Rev. 2022. V. 97 (6). P. 2090–2105. https://doi.org/10.1111/brv.12884
- Rifai M. A. A revision on the genus Trichoderma. Mycol. Pap. 1969. V. 116. P. 1–56.
- Rojo F. G., Reynoso M. M., Ferez M. et al. Biological control by Trichoderma species of Fusarium solani causing peanut brown root rot under feld conditions. Crop. Prot. 2007. V. 26 (4). P. 549–555. https://doi.org/10.1016/j.cropro.2006.05.006
- Roshka Yu. A., Markelova N. N., Mashkova S. D. et al. Antimicrobial Potential of Secalonic Acids from Arctic-Derived Penicillium chrysogenum INA 01369. Antibiotics. 2025. V. 14 (88). https://doi.org/10.3390/antibiotics14010088
- Senthil-Nathan S. A Review of biopesticides and their mode of action against insect pests. In: Thangavel P., Sridevi G. (eds). Environmental Sustainability. Springer, New Delhi, 2015, pp. 49–63.
- Sharma A., Gupta B., Verm S. et al. Unveiling the biocontrol potential of Trichoderma. Eur. J. Plant. Pathol. 2023. V. 167. P. 569–591. https://doi.org/10.1007/s10658-023-02745-5
- Smadja B., Latour X., Trigui S. et al. Thermodependence of growth and enzymatic activities implicated in pathogenicity of two Erwinia carotovora subspecies (Pectobacterium spp.). Can. J. Microbiol. 2004. V. 50 (1). P. 19–27. https://doi.org/10.1139/w03-099
- Smirnova A., Li H., Weingart H. et al. Thermoregulated expression of virulence factors in plant-associated bacteria. Arch. Microbiol. 2001. V. 176 (6). P. 393–399. https://doi.org/10.1007/s002030100344
- Sonkar S. S., Bhatt J., Meher J. et al. Bio-efficacy of Trichoderma viride against the root-knot nematode (Meloidogyne incognita) in tomato plant. J. Pharmacogn. Phytochem. 2018. V. 7 (6). P. 2010–2014.
- Sparks T.C, Sparks J.M, Duke S. O. Natural product-based crop protection compounds – origins and future prospects. J. Agric. Food. Chem. 2023. V. 71 (5). P. 2259–2269. https://doi.org/10.1021/acs.jafc.2c06938
- Ullrich M. S., Schergaut M., Boch J. et al. Temperature-responsive genetic loci in the plant pathogen Pseudomonas syringae pv. glycinea. Microbiology. 2000. V. 146 (10). P. 2457–2468. https://doi.org/10.1099/00221287-146-10-2457
- Yi Z., Berney C., Hartikainen H. et al. High-throughput sequencing of microbial eukaryotes in Lake Baikal reveals ecologically differentiated communities and novel evolutionary radiations. FEMS Microbiol. Ecol. 2017. V. 93 (8). https://doi.org/10.1093/femsec/fix073
- Zemskaya T. I., Cabello-Yeves P. J., Pavlova O. N. et al. Microorganisms of Lake Baikal – the deepest and most ancient lake on Earth. Appl. Microbiol. Biotechnol. 2020. V. 104. P. 6079–6090. https://doi.org/10.1007/s00253020-10660-6
- Zenteno-Alegría C.O., Yarzábal Rodríguez L. A., Ciancas Jiménez J. et al. Fungi beyond limits: The agricultural promise of extremophiles. Microb Biotechnol. 2024. V. 17 (3). e14439. https://doi.org/10.1111/1751-7915.14439
- Zhan X., Wang R., Zhang M. et al. Trichoderma-derived emodin competes with ExpR and ExpI of Pectobacterium carotovorum subsp. carotovorum to biocontrol bacterial soft rot. Pest. Manag. Sci. 2024. V. 80. P. 1039–1052. https://doi.org/10.1002/ps.7835
- ГОСТ 12038-84. (GOST) Семена сельскохозяйственных культур. Методы определения всхожести. М., 1984.
- ГОСТ 33777-2016. (GOST) Поверхностно-активные вещества. Метод определения фитотоксичности на семенах высших растений. М., 2016.
- Егоров Н. С. (Egorov) Основы учения об антибиотиках. М.: Наука, 2004. 450 с.
- Кузнецов Е. А. (Kuznetsov) Грибы водных экосистем. Дисс. … докт. биол. наук. М.: МГУ, 2003. 865 с.
Supplementary files
