Antagonistic Strains of  Pantoea brenneri  as Plant Protectors

D. S. Bulmakova; Бульмакова Д. С.; G. I. Shagieva; Шагиева Г. И.; D. L. Itkinaa; Иткина Д. Л.; O. A. Leninа; Ленина О. А.; M. R. Sharipova; Шарипова М. Р.; A. D. Suleimanova; Сулейманова А. Д.

doi:10.31857/S0026364823050033

Antagonistic Strains of Pantoea brenneri as Plant Protectors

Authors: Bulmakova D.S.¹, Shagieva G.I.¹, Itkinaa D.L.¹, Leninа O.A.², Sharipova M.R.¹, Suleimanova A.D.¹
Affiliations:
1. Kazan Federal University
2. Institute of Organic and Physical Chemistry, Kazan Scientific Center, Russian Academy of Sciences
Issue: Vol 57, No 5 (2023)
Pages: 352-361
Section: ГРИБЫ – ВОЗБУДИТЕЛИ БОЛЕЗНЕЙ РАСТЕНИЙ
URL: https://journals.rcsi.science/0026-3648/article/view/138088
DOI: https://doi.org/10.31857/S0026364823050033
EDN: https://elibrary.ru/UHEADW
ID: 138088

Cite item

Full Text

Open Access
Restricted Access

Access granted
Restricted Access

Subscription Access

Abstract
About the authors
References
Supplementary files
Statistics

Abstract

The antagonistic activity of Pantoea brenneri strains against a wide range of phytopathogenic threats was studied. It has been established that the strains are characterized by fungicidal activity against the micromycetes Fusarium sambucinum, F. oxysporum, F. solani, Rhizoctonia solani, Alternaria sp., Ascochyta kamchatica, Colletotrichum coccodes as well as antibacterial activity against the phytopathogen Erwinia amylovora, which causes bacterial burn of fruit trees. It has been shown that the cell suspension and supernatant of the culture liquid of Pantoea brenneri strains suppress Fusarium on potato tubers during storage. Pantoea brenneri strains have been found to be safe for model animals. A conclusion was made about the prospects of using P. brenneri strains as objects for the creation of environmentally friendly plant protection products against phytopathogens.

Keywords

biocontrol, biosafety, Erwinia amylovora, phytopathogenic microorganisms, rhizospheric bacteria

References

Barbetti M.J., Khan T.N., Pritchard I. et al. Challenges with managing disease complexes during application of different measures against foliar diseases of field pea. Plant Dis. 2021. V. 105. P. 616–627. https://doi.org/10.1094/PDIS-07-20-1470-RE
Chernyavskaya M.I., Sidorenko A.V., Golenchenko S.G. et al. Ecological microbiology: textbook.-method. allowance. Izdatelstvo BGU, Minsk, 2016. (in Russ.)
Dubrovsky J.G., Guttenberger M., Saralegui A. et al. Neutral red as a probe for confocal laser scanning microscopy studies of plant roots. Ann. Bot. 2006. V. 97. P. 1127–1138. https://doi.org/10.1093/aob/mcl045
Egorov N.S. Fundamentals of the doctrine of antibiotics. Nauka, Moscow, 2004 (in Russ.).
Etesami H., Jeong B.R., Glick B.R. Contribution of arbuscular mycorrhizal fungi, phosphate-solubilizing bacteria, and silicon to p uptake by plant. Front. Plant Sci. 2021. V. 12. Art. 699618. https://doi.org/10.3389/fpls.2021.699618
Evans H.M., Schulemann W. The action of vital stains belonging to the benzidine group. Science. 1914. V. 39. P. 443–454. https://doi.org/10.1126/science.39.1004.443
Förster H., McGhee G.C., Sundin G.W. et al. Characterization of streptomycin resistance in isolates of Erwinia amylovora in California. Phytopathology. 2015. V. 105. P. 1302–1310. https://doi.org/10.1094/PHYTO-03-15-0078-R
Itkina D.L., Suleimanova A.D., Sharipova M.R. Pantoea brenneri AS3 and Bacillus ginsengihumi M2.11 as potential biocontrol and plant growth-promoting agents. Mikrobiologiya. 2021. V. 90. P. 204–214 (in Russ.). https://doi.org/10.31857/S0026365621020063
Jiang L., Jeong J.C., Lee J.S. et al. Potential of Pantoea dispersa as an effective biocontrol agent for black rot in sweet potato. Sci. Rep. 2019. V. 9. Art. 16354. https://doi.org/10.1038/s41598-019-52804-3
Johnson K.B. Effect of antagonistic bacteria on establishment of honey bee-dispersed Erwinia amylovora in pear blossoms and on fire blight control. Phytopathology. 1993. V. 83. P. 995–1002.
Khan A., Singh P., Srivastava A. Synthesis, nature and utility of universal iron chelator – siderophore: a review. Microbiol. Res. 2018. V. 212. P. 103–111. https://doi.org/10.1016/j.micres.2017.10.012
Lahlali T., Berke J. M., Vergauwen K. et al. Novel potent capsid assembly modulators regulate multiple steps of the hepatitis B virus life cycle. Agents Chemother. 2018. V. 62. P. 672–615. https://doi.org/10.1128/AAC.00835-18
Lastochkina O., Pusenkova L., Garshina D. et al. The effect of endophytic bacteria Bacillus subtilis and salicylic acid on some resistance and quality traits of stored Solanum tuberosum L. tubers infected with Fusarium dry rot. Plants. 2020. V. 9. Art. 738. https://doi.org/10.3390/plants9060738
Li D., Li S., Wei S. et al. Strategies to manage rice sheath blight: lessons from interactions between rice and Rhizoctonia solani. Rice (NY). 2021. V. 14. Art. 21. https://doi.org/10.1186/s12284-021-00466-z
Mejdoub-Trabelsi B., Aydi Ben Abdallah R., Ammar N. et al. Antifungal potential of extracellular metabolites from Penicillium spp. and Aspergillus spp. naturally associated to potato against Fusarium species causing tuber dry rot. J. Microb. Biochem. Technol. 2017. V. 9. P. 181–190. https://doi.org/10.4172/1948-5948.1000364
Mikiciński A., Puławska J., Molzhigitova A. et al. Bacterial species recognized for the first time for its biocontrol activity against fire blight (Erwinia amylovora). Eur. J. Plant Pathol. 2020. V. 156. P. 257–272. https://doi.org/10.1007/s10658-019-01885-x
Netrusov F.I. Workshop on microbiology. Moscow, 2005 (in Russ.).
Ordax M., Piquer-Salcedo J.E., Santander R.D. et al. Medfly Ceratitis capitata as potential vector for fire blight pathogen Erwinia amylovora : survival and transmission. PLOS One. 2015. V. 10. Art. e0127560. https://doi.org/10.1371/journal.pone.0127560
Rochlani A., Dalwani A., Shaikh N.B. et al. Plant growth promoting rhizobacteria as biofertilizers: application in agricultural sustainability. Acta Scientific Microbiology. 2022. V. 5. P. 12–21. https://doi.org/10.1016/B978-0-12-815879-1.00003-3
Santoyo G., Guzman-Guzman P., Parra-Cota F.I. et al. Plant growth stimulation by microbial consortia. Agronomy. 2021. V. 11. Art. 219. https://doi.org/10.3390/agronomy11020219
Sellem I., Triki M.A., Elleuch L. et al. The use of newly isolated Streptomyces strain TN258 as potential biocontrol agent of potato tubers leak caused by Pythium ultimum. J. Basic Microbiol. 2017. V. 57 (5). P. 393–401. https://doi.org/10.1002/jobm.201600604
Smith D.D.N., Nickzad A., Stavrinides J. A novel glycolipid biosurfactant confers grazing resistance upon Pantoea ananatis BRT175 against the social amoeba Dictyostelium discoideum. ASM J. 2016. V. 1. Art. e00075–15. https://doi.org/10.1128/mSphere.00075-15
Suleimanova A.D., Beinhauer A., Valeeva L. R. et al. Novel glucose-1-phosphatase with high phytase activity and unusual metal ion activation from soil bacterium Pantoea sp. strain 3.5.1. Appl. Environ. Microbiol. 2015. V. 81. P. 6790–6799. https://doi.org/10.1128/AEM.01384-15
Suleimanova A.D., Itkina D.L., Pudova D.S. et al. Identification of Pantoea phytate-hydrolyzing rhizobacteria based on their phenotypic features and multilocus sequence analysis (MLSA). Mikrobiologiya. 2021. V. 90. P. 100–109 (in Russ.). https://doi.org/10.31857/S0026365621010122
Tan Y.N., Li Q. Microbial production of rhamnolipids using sugars as carbon sources. Microb. Cell Fact. 2018. V. 17. P. 89–92. https://doi.org/10.1186/s12934-018-0938-3
Titova Yu.A., Krasnobaeva I.L. Multiconversion biopreparations for plant protection and the possibility of their use in organic farming. Tekhnologii i tekhnicheskie sredstva mekhanizirovannogo proizvodstva produkcii rastenievodstva i zhivotnovodstva. 2019. V. 2. P. 164–183 (in Russ.).
Town J., Audy P., Boyetchko S.M. et al. High-quality draf genome sequence of biocontrol strain Pantoea sp. Oxwo6b1. Genome Announc. 2016. V. 4. Art. e00582-16. https://doi.org/10.1128/genomeA.00582-16
Walterson A.M., Smith D.D.N., Stavrinides J. Identification of a Pantoea biosynthetic cluster that directs the synthesis of an antimicrobial natural product. PLoS One. 2014. V. 9. Art. e96208. https://doi.org/10.1371/journal.pone.0096208
Zhang Y., Sun W., Ning P. et al. First report of anthracnose of papaya (Carica papaya L.) caused by Colletotrichum siamense in China. Plant Dis. 2021. V. 105. Art. 2252. https://doi.org/10.1094/PDIS-10-20-2154-PDN