A new bacterial consortia for management of Fusarium head blight in wheat.
Fusarium
Bacterial consortium
Chlorophyll fluorescence
DON
Wheat
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
02 May 2024
02 May 2024
Historique:
received:
13
10
2023
accepted:
22
04
2024
medline:
3
5
2024
pubmed:
3
5
2024
entrez:
2
5
2024
Statut:
epublish
Résumé
Fusarium head blight (FHB) is a significantly important disease in cereals primarily caused by Fusarium species. FHB control is largely executed through chemical strategies, which are costlier to sustainable wheat production, resulting in leaning towards sustainable sources such as resistance breeding and biological control methods for FHB. The present investigation was aimed at evaluating newly identified bacterial consortium (BCM) as biocontrol agents for FHB and understanding the morpho-physiological traits associated with the disease resistance of spring wheat. Preliminary evaluation through antagonistic plate assay and in vivo assessment indicated that BCM effectively inhibited Fusarium growth in spring wheat, reducing area under disease progress curve (AUDPC) and deoxynivalenol (DON), potentially causing type II and V resistance, and improving single spike yield (SSPY). Endurance to FHB infection with the application of BCM is associated with better sustenance of spike photosynthetic performance by improving the light energy harvesting and its utilization. Correlation and path-coefficient analysis indicated that maximum quantum yield (QY_max) is directly influencing the improvement of SSPY and reduction of grain DON accumulation, which is corroborated by principal component analysis. The chlorophyll fluorescence traits identified in the present investigation might be applied as a phenotyping tool for the large-scale identification of wheat sensitivity to FHB.
Identifiants
pubmed: 38698085
doi: 10.1038/s41598-024-60356-4
pii: 10.1038/s41598-024-60356-4
doi:
Substances chimiques
deoxynivalenol
JT37HYP23V
Trichothecenes
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
10131Subventions
Organisme : Formas
ID : # 2020-01828
Organisme : Formas
ID : # 2020-01828
Organisme : Formas
ID : # 2020-01828
Organisme : Formas
ID : # 2020-01828
Organisme : Formas
ID : # 2020-01828
Informations de copyright
© 2024. The Author(s).
Références
FAOSTAT. ( https://www.fao.org/faostat/en/#data , 2022).
Parry, D., Jenkinson, P. & McLeod, L. Fusarium ear blight (scab) in small grain cereals—a review. Plant Pathol. 44, 207–238 (1995).
doi: 10.1111/j.1365-3059.1995.tb02773.x
Sutton, J. Epidemiology of wheat head blight and maize ear rot caused by Fusarium graminearum. Can. J. Plant Pathol. 4, 195–209 (1982).
doi: 10.1080/07060668209501326
Wang, Y. & Miller, J. in Wheat Production Constraints in Tropical Environments 19–23 (Chiang Mai, 1987).
Bai, G. & Shaner, G. Management and resistance in wheat and barley to Fusarium head blight. Annu. Rev. Phytopathol. 42, 135–161 (2004).
pubmed: 15283663
doi: 10.1146/annurev.phyto.42.040803.140340
Johnson, D. D., Flaskerud, G. K., Taylor, R. D. & Satyanarayana, V. Quantifying economic impacts of Fusarium head blight in wheat. Fusarium Head Blight Wheat Barley 461–483, 1 (2003).
Bottalico, A. & Perrone, G. Toxigenic Fusarium species and mycotoxins associated with head blight in small-grain cereals in Europe. Mycotoxins in Plant Disease: Under the aegis of COST Action 835 ‘Agriculturally Important Toxigenic Fungi 1998–2003’, EU project (QLK 1-CT-1998–01380), and ISPP ‘Fusarium Committee’, 611–624 (2002).
Yi, X. et al. Genetic analysis of Fusarium head blight resistance in CIMMYT bread wheat line C615 using traditional and conditional QTL mapping. Front. Plant Sci. 9, 573 (2018).
pubmed: 29780395
pmcid: 5946024
doi: 10.3389/fpls.2018.00573
Khan, M. K. et al. Fusarium head blight in wheat: contemporary status and molecular approaches. 3 Biotech 10, 1–17 (2020).
doi: 10.1007/s13205-020-2158-x
Logrieco, A., Bottalico, A., Mulé, G., Moretti, A. & Perrone, G. Epidemiology of toxigenic fungi and their associated mycotoxins for some Mediterranean crops. Epidemiology of Mycotoxin Producing Fungi: Under the aegis of COST Action 835 ‘Agriculturally Important Toxigenic Fungi 1998–2003, EU project (QLK 1-CT-1998–01380), 645–667 (2003).
Desjardins, A. E. Fusarium mycotoxins: chemistry, genetics, and biology. (American Phytopathological Society (APS Press), 2006).
Maresca, M. From the gut to the brain: Journey and pathophysiological effects of the food-associated trichothecene mycotoxin deoxynivalenol. Toxins 5, 784–820 (2013).
pubmed: 23612752
pmcid: 3705292
doi: 10.3390/toxins5040784
Mielniczuk, E. & Skwaryło-Bednarz, B. Fusarium head blight, mycotoxins and strategies for their reduction. Agronomy 10, 509 (2020).
doi: 10.3390/agronomy10040509
Terzi, V., Tumino, G., Stanca, A. M. & Morcia, C. Reducing the incidence of cereal head infection and mycotoxins in small grain cereal species. J. Cereal Sci. 59, 284–293 (2014).
doi: 10.1016/j.jcs.2013.10.005
Wang, L. et al. Effect of deoxynivalenol detoxification by ozone treatment in wheat grains. Food Control 66, 137–144 (2016).
doi: 10.1016/j.foodcont.2016.01.038
Goswami, S. K., Singh, V., Chakdar, H. & Choudhary, P. Harmful effects of fungicides-Current status. Int. J. Agric. Environ. Biotechnol. 11, 1011–1019 (2018).
Palazzini, J. M., Ramirez, M. L., Torres, A. M. & Chulze, S. N. Potential biocontrol agents for Fusarium head blight and deoxynivalenol production in wheat. Crop Prot. 26, 1702–1710 (2007).
doi: 10.1016/j.cropro.2007.03.004
Xiao, Z., Zhao, Q., Li, W., Gao, L. & Liu, G. Strain improvement of Trichoderma harzianum for enhanced biocontrol capacity: Strategies and prospects. Front. Microbiol. 13(14), 1146210 (2023).
doi: 10.3389/fmicb.2023.1146210
O’Brien, P. A. Biological control of plant diseases. Australas. Plant Pathol. 46, 293–304 (2017).
doi: 10.1007/s13313-017-0481-4
Köhl, J., Kolnaar, R. & Ravensberg, W. J. Mode of action of microbial biological control agents against plant diseases: relevance beyond efficacy. Front. Plant Sci. 19(10), 454982 (2019).
Hashem, A., Tabassum, B. & Abdallah, E. F. Bacillus subtilis: A plant-growth promoting rhizobacterium that also impacts biotic stress. Saudi J. Biol. Sci. 26(6), 1291–1297 (2019).
pubmed: 31516360
pmcid: 6734152
doi: 10.1016/j.sjbs.2019.05.004
Tiwari, S., Prasad, V. & Lata, C. In New and future developments in microbial biotechnology and bioengineering 43–55 (Elsevier, 2019).
Uwaremwe, C. et al. An endophytic strain of Bacillus amyloliquefaciens suppresses Fusarium oxysporum infection of chinese wolfberry by altering its rhizosphere bacterial community. Front. Microbiol. 12, 3927 (2022).
doi: 10.3389/fmicb.2021.782523
Sato, I. et al. Cryptococcus nodaensis sp nov, a yeast isolated from soil in Japan that produces a salt-tolerant and thermostable glutaminase. J. Ind. Microbiol. Biotechnol. 22, 127–132 (1999).
doi: 10.1038/sj.jim.2900623
Schisler, D. A., Khan, N. I. & Boehm, M. J. Biological control of Fusarium head blight of wheat and deoxynivalenol levels in grain via use of microbial antagonists. Mycotoxins Food Safety 53–69, 1 (2002).
Schisler, D. et al. Selection and evaluation of the potential of choline-metabolizing microbial strains to reduce Fusarium head blight. Biol. Control 39, 497–506 (2006).
doi: 10.1016/j.biocontrol.2006.08.007
Khan, M. R. & Doohan, F. M. Bacterium-mediated control of Fusarium head blight disease of wheat and barley and associated mycotoxin contamination of grain. Biol. Control 48, 42–47 (2009).
doi: 10.1016/j.biocontrol.2008.08.015
Araus, J., Brown, H., Febrero, A., Bort, J. & Serret, M. Ear photosynthesis, carbon isotope discrimination and the contribution of respiratory CO2 to differences in grain mass in durum wheat. Plant Cell Environ. 16, 383–392 (1993).
doi: 10.1111/j.1365-3040.1993.tb00884.x
Chen, W., Zhang, J. & Deng, X. The spike weight contribution of the photosynthetic area above the upper internode in a winter wheat under different nitrogen and mulching regimes. Crop J. 7, 89–100 (2019).
doi: 10.1016/j.cj.2018.10.004
Shi, B., Qu, Y., Li, H., Wan, M. & Zhang, J. Pseudomonas simiae augments the tolerance to alkaline bauxite residue in Atriplex canescens by modulating photosynthesis, antioxidant defense enzymes, and compatible osmolytes. Environ. Sci. Pollut. Res. 29, 24370–24380 (2022).
doi: 10.1007/s11356-022-19031-2
Win, K. T., Tanaka, F., Okazaki, K. & Ohwaki, Y. The ACC deaminase expressing endophyte Pseudomonas spp. enhances NaCl stress tolerance by reducing stress-related ethylene production, resulting in improved growth, photosynthetic performance, and ionic balance in tomato plants. Plant Physiol. Biochem. 1(127), 599–607 (2018).
doi: 10.1016/j.plaphy.2018.04.038
Yang, S. et al. Wheat resistance to fusarium head blight is associated with changes in photosynthetic parameters. Plant Dis. 100, 847–852 (2016).
pubmed: 30688616
doi: 10.1094/PDIS-04-14-0398-RE
Kemp, N. D., Vaughan, M. M., McCormick, S. P., Brown, J. A. & Bakker, M. G. Sarocladium zeae is a systemic endophyte of wheat and an effective biocontrol agent against Fusarium head blight. Biol. Control 149, 104329 (2020).
doi: 10.1016/j.biocontrol.2020.104329
Rojas, E. C. et al. The fungal endophyte Penicillium olsonii ML37 reduces Fusarium head blight by local induced resistance in wheat spikes. J. Fungi 8, 345 (2022).
doi: 10.3390/jof8040345
Whitaker, B. K., Vaughan, M. M. & McCormick, S. P. Biocontrol impacts on wheat physiology and fusarium head blight outcomes are bacterial endophyte strain and cultivar specific. Phytobiomes J. 7(1), 55–64 (2023).
doi: 10.1094/PBIOMES-08-22-0056-R
Hue, A. et al. Biological control of fusarium head blight of wheat with Clonostachys rosea strain ACM941. Can. J. Plant Pathol. 31, 169–179 (2009).
doi: 10.1080/07060660909507590
Rojas, E. C. et al. Selection of fungal endophytes with biocontrol potential against Fusarium head blight in wheat. Biol. Control 144, 104222 (2020).
doi: 10.1016/j.biocontrol.2020.104222
Hu, W. et al. Potential of Pseudomonas chlororaphis subsp. aurantiaca strain Pcho10 as a biocontrol agent against Fusarium graminearum. Phytopathology 104, 1289–1297 (2014).
pubmed: 24941327
doi: 10.1094/PHYTO-02-14-0049-R
Huang, R. et al. Pyrrolnitrin is more essential than phenazines for Pseudomonas chlororaphis G05 in its suppression of Fusarium graminearum. Microbiol. Res. 215, 55–64 (2018).
pubmed: 30172309
doi: 10.1016/j.micres.2018.06.008
Guo, Z. et al. In vitro inhibitory effect of the bacterium Serratia marcescens on Fusarium proliferatum growth and fumonisins production. Biol. Control 143, 104188 (2020).
doi: 10.1016/j.biocontrol.2020.104188
Schroeder, H. & Christensen, J. Factors affecting resistance of wheat to scab caused by Gibberella zeae. Phytopathology 53, 831–838 (1963).
Cantoro, R., Palazzini, J. M., Yerkovich, N., Miralles, D. J. & Chulze, S. N. Bacillus velezensis RC 218 as a biocontrol agent against Fusarium graminearum: Effect on penetration, growth and TRI5 expression in wheat spikes. BioControl 66, 259–270 (2021).
doi: 10.1007/s10526-020-10062-7
Khan, N., Schisler, D., Boehm, M. J., Slininger, P. & Bothast, R. Selection and evaluation of microorganisms for biocontrol of Fusarium head blight of wheat incited by Gibberella zeae. Plant Dis. 85, 1253–1258 (2001).
pubmed: 30831786
doi: 10.1094/PDIS.2001.85.12.1253
Suárez, J. C. et al. Chlorophyll fluorescence imaging as a tool for evaluating disease resistance of common bean lines in the Western Amazon Region of Colombia. Plants 11, 1371 (2022).
pubmed: 35631796
pmcid: 9143997
doi: 10.3390/plants11101371
Shin, Y. K. et al. Response to salt stress in lettuce: Changes in chlorophyll fluorescence parameters, phytochemical contents, and antioxidant activities. Agronomy 10, 1627 (2020).
doi: 10.3390/agronomy10111627
Acosta-Motos, J. R. et al. Plant responses to salt stress: adaptive mechanisms. Agronomy 7, 18 (2017).
doi: 10.3390/agronomy7010018
Hasan, A. K., Herrera, J., Lizana, C. & Calderini, D. F. Carpel weight, grain length and stabilized grain water content are physiological drivers of grain weight determination of wheat. Field Crops Res. 123, 241–247 (2011).
doi: 10.1016/j.fcr.2011.05.019
Leiva, F. et al. Phenotyping Fusarium head blight through seed morphology characteristics using RGB imaging. Front. Plant Sci. 13, 1010249 (2022).
pubmed: 36330238
pmcid: 9623152
doi: 10.3389/fpls.2022.1010249
Lambers, H. & Poorter, H. in Advances in ecological research Vol. 23 187–261 (Elsevier, 1992).
Maphosa, L. et al. Genetic control of grain yield and grain physical characteristics in a bread wheat population grown under a range of environmental conditions. Theor. Appl. Genet. 127, 1607–1624 (2014).
pubmed: 24865506
doi: 10.1007/s00122-014-2322-y
Bauriegel, E., Giebel, A. & Herppich, W. Rapid Fusarium head blight detection on winter wheat ears using chlorophyll fluorescence imaging. J. Appl. Bot. Food Qual 83, 196–203 (2010).
Bolton, M. D. Primary metabolism and plant defense—fuel for the fire. Mol. Plant-Microbe Interact. 22, 487–497 (2009).
pubmed: 19348567
doi: 10.1094/MPMI-22-5-0487
Murchie, E. H. & Lawson, T. Chlorophyll fluorescence analysis: a guide to good practice and understanding some new applications. J. Exper. Bot. 64, 3983–3998 (2013).
doi: 10.1093/jxb/ert208
Pineda, M., Pérez-Bueno, M. L. & Barón, M. Detection of bacterial infection in melon plants by classification methods based on imaging data. Front. Plant Sci. 9, 164 (2018).
pubmed: 29491881
pmcid: 5817087
doi: 10.3389/fpls.2018.00164
Leslie, J. F. & Summerell, B. A. The Fusarium laboratory manual. (John Wiley & Sons, 2008).
Zakieh, M. et al. Characterizing winter wheat germplasm for fusarium head blight resistance under accelerated growth conditions. Front. Plant Sci. 12, 705006 (2021).
pubmed: 34512690
pmcid: 8425451
doi: 10.3389/fpls.2021.705006
Siddiqui, I. & Shaukat, S. Combination of Pseudomonas aeruginosa and Pochonia chlamydosporia for control of root-infecting fungi in tomato. J. Phytopathol. 151, 215–222 (2003).
doi: 10.1046/j.1439-0434.2003.00708.x
Santiago, C. D. et al. Bacterial compatibility in combined inoculations enhances the growth of potato seedlings. Microbes Environ. 32, 14–23 (2017).
pubmed: 28163278
pmcid: 5371070
doi: 10.1264/jsme2.ME16127
Nishino, S. et al. 1-Phenyl-3-pentanone, a volatile compound from the edible mushroom Mycoleptodonoides aitchisonii active against some phytopathogenic fungi. J. Phytopathol. 161, 515–521 (2013).
doi: 10.1111/jph.12100
Li, Z. et al. Effects of bacteria-free filtrate from Bacillus megaterium strain L2 on the mycelium growth and spore germination of Alternaria alternata. Biotechnol. Biotechnol. Equip. 29, 1062–1068 (2015).
doi: 10.1080/13102818.2015.1068135
Daroodi, Z., Taheri, P. & Tarighi, S. Direct antagonistic activity and tomato resistance induction of the endophytic fungus Acrophialophora jodhpurensis against Rhizoctonia solani. Biol. Control 160, 104696 (2021).
doi: 10.1016/j.biocontrol.2021.104696
Stack, R. W. & McMullen, M. P. A visual scale to estimate severity of Fusarium head blight in wheat. (1998).
Schisler, D., Khan, N., Boehm, M. J. & Slininger, P. Greenhouse and field evaluation of biological control of Fusarium head blight on durum wheat. Plant Dis. 86, 1350–1356 (2002).
pubmed: 30818440
doi: 10.1094/PDIS.2002.86.12.1350
Baker, N. R. & Rosenqvist, E. Applications of chlorophyll fluorescence can improve crop production strategies: an examination of future possibilities. Journal of experimental botany 55, 1607–1621 (2004).
pubmed: 15258166
doi: 10.1093/jxb/erh196
Cgrain, A. B. Cgrain value TM, the new standard for analysis grain quality. Available at: www.cgrain.se.
Team, R. C. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. @@@@ (2013).
De Mendiburu, F. Agricolae: Statistical procedures for agricultural research. R package version 1.1–3. Comprehensive R Arch. Network, Vienna. @@@@ (accessed 25 July 2019) (2012).
Madden, L. V., Hughes, G. & Van Den Bosch, F. The study of plant disease epidemics. (2007).
Dewey, D. R. & Lu, K. A correlation and path-coefficient analysis of components of crested wheatgrass seed production 1. Agron. J. 51, 515–518 (1959).
doi: 10.2134/agronj1959.00021962005100090002x
Akintunde, A. Path analysis step by step using excel. J. Tech. Sci. Technol. 1, 09–15 (2012).