Aebi, H. (1984). Catalase in vitro.
Methods in Enzymology,
105, 121-126. doi:
10.1016/s0076-6879(84)05016-3.##Ahangar, L., Babaeizad, V., Ranjbar, G. A., NajafiZarrini, H., & Biabani, A. (2016). Study of
PR gene expression pattern related to induced resistance to powdery mildew in susceptible wheat genotype after treating with salicylic acid.
Journal of Crop Breeding,
17(42), 208–217. [In Persian]. doi:
10.18869/acadpub.jcb.8.17.218.##Allario, T., Fourquez, A., Magnin-Robert, M., Siah, A., Maia-Grondard, A., Gaucher, M., & Baltenweck, R. (2023). Analysis of defense-related gene expression and leaf metabolome in wheat during the early infection stages of
Blumeria graminis f. sp.
tritici.
Phytopathology,
113(8), 1537-1547. doi:
10.1094/PHYTO-10-22-0364-R.##Barna, B., Abdou, S., Manninger, K., & Király, Z. (1998). Systemic acquired resistance in wheat against stem and leaf rusts.
Acta Phytopathologica et Entomologica Hungarica,
33, 31-36.##Barna, B., Máté, G., Preuss, J., Harrach, B. D., Gullner, G., Manninger, K., & Fodor, J. (2022). Defence responses triggered by
Blumeria graminis f. sp. hordei in non‐host wheat genotypes results in a decrease in
Puccinia triticina infection.
Journal of Phytopathology,
170(2), 82-90. doi:
10.1111/jph.13057.##Benítez, T., Rincón, A. M., Limón, M. C., & Codon, A. C. (2004). Biocontrol mechanisms of
Trichoderma strains.
International Microbiology,
7(4), 249-260.##Bi, Q., Lu, F., Wu, J., Liu, X., Han, X., & Zhao, J. (2025). The control effect and induced disease resistance mechanism of
Bacillus tequilensis on wheat powdery mildew.
Biological Control, 105698. doi:
10.1016/j.biocontrol.2025.105698.##Boamah, S., Zhang, S., Xu, B., Li, T., & Calderón-Urrea, A. (2021).
Trichoderma longibrachiatum (TG1) enhances wheat seedlings tolerance to salt stress and resistance to
Fusarium pseudograminearum.
Frontiers in Plant Science,
12, 741231. doi:
10.3389/fpls.2021.741231.##Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
Analytical Biochemistry,
72(1-2), 248-254.##Chen, X., Koumoutsi, A., Scholz, R., Schneider, K., Vater, J., Süssmuth, R., Piel, J., & Borriss, R. (2009). Genome analysis of
Bacillus amyloliquefaciens FZB42 reveals its potential for biocontrol of plant pathogens.
Journal of Biotechnology,
140(1-2), 27-37. doi:
10.1016/j.jbiotec.2008.10.011.##Choudaker, K. R., Singh, V. K., Kashyap, A. S., Patel, A. V., Sameriya, K. K., Yadav, D., Manzar, N., Kamil, D., Prasad, L., & Saharan, M. (2024). Evaluating the efficacy of microbial antagonists in inducing resistance, promoting growth, and providing biological control against powdery mildew in wheat.
Frontiers in Microbiology,
15, 1419547. doi:
10.3389/fmicb.2024.1419547.##Dangl, J. L., & Jones, J. D. (2001). Plant pathogens and integrated defence responses to infection.
Nature,
411(6839), 826-833. doi:
10.1038/35081161.##Dean, R., Van Kan, J. A., Pretorius, Z. A., Hammond‐Kosack, K. E., Di Pietro, A., Spanu, P. D., Rudd, J. J., Dickman, M., Ellis, J., & Foster, G. D. (2012). The Top 10 fungal pathogens in molecular plant pathology.
Molecular Plant Pathology,
13(4), 414-430. doi:
10.1111/j.1364-3703.2011.00783.x.##Deshmukh, S., & Kogel, K. H. (2007).
Piriformospora indica protects barley from root rot caused by
Fusarium graminearum/
Piriformospora indica schützt Gerste vor der von
Fusarium graminearum verursachten Wurzelfäule.
Journal of Plant Diseases & Protection, 114, 263-268. doi:
10.1007/BF03356227.##Dumanović, J., Nepovimova, E., Natić, M., Kuča, K., & Jaćević, V. (2021). The significance of reactive oxygen species and antioxidant defense system in plants: A concise overview.
Frontiers in Plant Science,
11, 552969. doi:
10.3389/fpls.2020.552969.##Egusa, M., Miwa, T., Kaminaka, H., Takano, Y., & Kodama, M. (2013). Nonhost resistance of
Arabidopsis thaliana against
Alternaria alternata involves both pre-and postinvasive defenses but is collapsed by AAL-toxin in the absence of LOH2.
Phytopathology,
103(7), 733-740. doi:
10.1094/PHYTO-08-12-0201-R.##El-Sayed, W. S., Akhkha, A., El-Naggar, M. Y., & Elbadry, M. (2014). In vitro antagonistic activity, plant growth promoting traits and phylogenetic affiliation of
rhizobacteria associated with wild plants grown in arid soil.
Frontiers in Microbiology,
5, 651. doi:
10.3389/fmicb.2014.00651.##Gao, H., Niu, J., & Li, S. (2018). Impacts of wheat powdery mildew on grain yield & quality and its prevention and control methods.
American Journal of Agriculture & Forestry,
6(5), 141-147. doi:
10.11648/j.ajaf.20180605.14.##Gerhardson, B. (2002). Biological substitutes for pesticides.
Trends in Biotechnology,
20(8), 338-343. doi:
10.1016/S0167-7799(02)02021-8.##Hafez, Y. M., El-Nagar, A. S., Elzaawely, A. A., Kamel, S., & Maswada, H. F. (2018). Biological control of
Podosphaera xanthii the causal agent of squash powdery mildew disease by upregulation of defense-related enzymes.
Egyptian Journal of Biological Pest Control,
28, 1-8. doi:
10.1186/s41938-018-0058-8.##He, J., Liu, Y., Yuan, D., Duan, M., Liu, Y., Shen, Z., Yang, C., Qiu, Z., Liu, D., Wen, P., Huang, J., Fan, D., Xiao, S., Xin, Y., Chen, X., Jiang, L., Wang, H., Yuan, L., & Wan, J. (2020). An R2R3 MYB transcription factor confers brown planthopper resistance by regulating the phenylalanine ammonia-lyase pathway in rice. Proceedings of the National Academy of Sciences of the United States of America,
117(1), 271-277. doi:
10.1073/pnas.1902771116.##He, P., Cui, W., & Peng, L. (2022). Biocontrol efficacy of
Bacillus velezensis HC-8 against powdery mildew of honeysuckle caused by
Erysiphe lonicerae var. Lonicerae.
Biological Control,
166, 104834. doi:
10.1016/j.biocontrol.2021.104834.##Hou, L., Wang, L. N., Wu, X. L., Gao, W., Zhang, J. X., & Huang, C. Y. (2019). Expression patterns of two
PAL genes of
Pleurotus ostreatus across developmental stages and under heat stress.
BMC Microbiology, 19(1), 231. doi:
10.1186/s12866-019-1618-4.##Hu, Z., Qiuxia, Z., Ling, H., Huajun, Z., Zuohua, R., & Erming, L. (2019). Isolation and identification of
Bacillus tequilensis JN-369 and antimicrobial substance analysis.
Chinese Journal of Pesticide Science,
21(1), 52-58. doi:
10.16801/j.issn.1008-7303.2019.0007.##Ivanov, S., Miteva, L., Alexieva, V., Karjin, H., & Karanov, E. (2005). Alterations in some oxidative parameters in susceptible and resistant wheat plants infected with
Puccinia recondita f. sp.
tritici.
Journal of Plant Physiology,
162(3), 275-279. doi:
10.1016/j.jplph.2004.07.010.##Kashyap, A. S., Manzar, N., Nebapure, S. M., Rajawat, M. V. S., Deo, M. M., Singh, J. P., Kesharwani, A. K., Singh, R. P., Dubey, S. C., & Singh, D. (2022). Unraveling microbial volatile elicitors using a transparent methodology for induction of systemic resistance and regulation of antioxidant genes at expression levels in chili against bacterial wilt disease.
Antioxidants,
11(2), 404. doi:
10.3390/antiox11020404.##Kazerooni, E. A., Maharachchikumbura, S. S., Al-Sadi, A. M., Kang, S.-M., Yun, B.-W., & Lee, I.-J. (2021). Biocontrol potential of
Bacillus amyloliquefaciens against
Botrytis pelargonii and
Alternaria alternata on
Capsicum annuum.
Journal of Fungi,
7(6), 472. doi:
10.3390/jof7060472.##Kogel, K. H., & Langen, G. (2005). Induced disease resistance and gene expression in cereals.
Cellular Microbiology,
7(11), 1555-1564. doi:
10.1111/j.1462-5822.2005.00592.x.##Kthiri, Z., Jabeur, M. B., Machraoui, M., Gargouri, S., Hiba, K., & Hamada, W. (2020). Coating seeds with
Trichoderma strains promotes plant growth and enhance the systemic resistance against
Fusarium crown rot in durum wheat.
Egyptian Journal of Biological Pest Control,
30, 1-10. doi:
10.1186/s41938-020-00338-6.##Li, L., Guo, N., Feng, Y., Duan, M., & Li, C. (2022). Effect of
Piriformospora indica-induced systemic resistance and basal immunity against
Rhizoctonia cerealis and
Fusarium graminearum in wheat.
Frontiers in Plant Science,
13, 836940. doi:
10.3389/fpls.2022.836940.##Liu, H., Jiang, W., Bi, Y., & Luo, Y., (2005). Postharvest BTH treatment induces resistance of peach (
Prunus persica L. cv. Jiubao) fruit to infection by
Penicillium expansum and enhances activity of fruit defense mechanisms.
Postharvest Biology & Technology,
35(3), 263-269. doi:
10.1016/j.postharvbio.2004.08.006.##Liu, M., Braun, U., Takamatsu, S., Hambleton, S., Shoukouhi, P., Bisson, K. R., & Hubbard, K. (2021). Taxonomic revision of
Blumeria based on multi-gene DNA sequences, host preferences and morphology.
Mycoscience,
62(3), 143-165. doi:
10.47371/mycosci.2020.12.003.##Liu, R., Lv, X., Wang, X., Yang, L., Cao, J., Dai, Y., Wu, W., & Wu, Y. (2023). Integrative analysis of the multi-omics reveals the stripe rust fungus resistance mechanism of the
TaPAL in wheat.
Frontiers in Plant Science,
14, 1174450. doi:
10.3389/fpls.2023.1174450.##Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. M
ethods,
25(4), 402-408. doi:
10.1006/meth.2001.1262.##Makarewicz, O., Farouk, A., Rosner, K., Greiner, R., Bochow, H., & Borriss, R. (2002). Extracellular phytase activity of
Bacillus amyloliquefaciens FZB45 contributes to its plant-growth-promoting effect.
Microbiology,
148(7), 2097-2109. doi:
10.1099/00221287-148-7-2097.##Manzar, N., Singh, Y., Kashyap, A. S., Sahu, P. K., Rajawat, M. V. S., Bhowmik, A., Sharma, P. K., & Saxena, A. K. (2021). Biocontrol potential of native
Trichoderma spp. against anthracnose of great millet (
Sorghum bicolour L.) from Tarai and Hill regions of India.
Biological Control,
152, 104474. doi:
10.1016/j.biocontrol.2020.104474.##Mapuranga, J., Chang, J., & Yang, W. (2022). Combating powdery mildew: Advances in molecular interactions between
Blumeria graminis f. sp.
tritici and wheat.
Frontiers in Plant Science,
13, 1102908. doi:
10.3389/fpls.2022.1102908.##Martinelli, J., Brown, J., & Wolfe, M. (1993). Effects of barley genotype on induced resistance to powdery mildew.
Plant Pathology,
42(2), 195-202. doi:
10.1111/j.1365-3059.1993.tb01491.x.##McDonald, B. A., & Linde, C. (2002). Pathogen population genetics, evolutionary potential, and durable resistance.
Annual Review of Phytopathology,
40(1), 349-379. doi:
10.1146/annurev.phyto.40.120501.101443.##Narusaka, Y., Narusaka, M., Seki, M., Ishida, J., Shinozaki, K., Nan, Y., Park, P., Shiraishi, T., & Kobayashi, M. (2005). Cytological and molecular analyses of non-host resistance of
Arabidopsis thaliana to
Alternaria alternata.
Molecular Plant Pathology,
6(6), 615-627. doi:
10.1111/j.1364-3703.2005.00310.x.##Niu, J., Cao, Y., Lin, X., Leng, Q., Chen, Y., & Yin, J. (2018). Field and laboratory screening of anthurium cultivars for resistance to foliar bacterial blight and the induced activities of defence-related enzymes.
Folia Horticulturae,
30(1), 129-137. doi:
10.2478/fhort-2018-0013.##Otani, H., Kohmoto, K., Kodama, M., & Nishimura, S. (1991). Role of host-specific toxins in the pathogenesis of
Alternaria alternata. In: Patil, S. S. (Ed.). Molecular Strategies of Pathogens and Host Plants. Springer, New York. pp. 139-149. doi:
10.1007/978-1-4612-3084-7_12.##Panstruga, R., & Kuhn, H. (2019). Mutual interplay between phytopathogenic powdery mildew fungi and other microorganisms.
Molecular Plant Pathology,
20(4), 463-470. doi:
10.1111/mpp.12771.##Paul, R., Basandrai, A. K., & Tyagi, P. (1999). Identification of resistance genes against
Erysiphe graminis tritici in Indian and exotic wheats .
Indian Journal of Genetics & Plant Breeding,
59(02), 125-134. ##Paul, R., Basandrai, A. K., & Tyagi, P. (2000). Virulence spectrum of
Erysiphe graminis f. sp.
tritici in Himachal Pradesh.
Indian Phytopathology,
53(4), 415-418. ##Pazarlar, S., Cetinkaya, N., Bor, M., & Ozdemir, F. (2017). Ozone triggers different defence mechanisms against powdery mildew (
Blumeria graminis DC. Speer f. sp.
tritici) in susceptible and resistant wheat genotypes.
Functional Plant Biology,
44(10), 1016-1028. doi:
10.1071/FP17038.##Pina, A., Errea, P. (2008). Differential induction of phenylalanine ammonia-lyase gene expression in response to in vitro callus unions of
Prunus spp.
Plant Physiology,
165(7), 705-714. doi:
10.1016/j.jplph.2007.05.015.##Qiang, X., Weiss, M., Kogel, K. H., & Schäfer, P. (2012).
Piriformospora indica—a mutualistic basidiomycete with an exceptionally large plant host range.
Molecular Plant Pathology,
13(5), 508-518. doi:
10.1111/j.1364-3703.2011.00764.x.##Reuveni, R. (2017). Biochemical markers for disease resistance. In: Singh, U. S., & Singh, R. P. (Eds.). Molecular Methods in Plant Pathology. pp. 99-114. CRC Press. doi:
10.1201/9780203746523.##Reyad, N. E. H. A., Azoz, S. N., Ali, A. M., & Sayed, E. G. (2022). Mitigation of powdery mildew disease by integrating biocontrol agents and shikimic acid with modulation of antioxidant defense system, anatomical characterization, and improvement of squash plant productivity.
Horticulturae,
8(12), 1145. doi:
10.3390/horticulturae8121145.##Saadaoui, M., Faize, M., Bonhomme, L., Benyoussef, N. O., Kharrat, M., Chaar, H., Label, P., & Venisse, J. S. (2023). Assessment of
Tunisian trichoderma isolates on wheat seed germination, seedling growth and fusarium seedling blight suppression.
Microorganisms,
11(6), 1512. doi:
10.3390/microorganisms11061512.##Safaei, M., Jorkesh, A., & Olfati, J. (2022). Chemical and biological products for control of powdery mildew on cucumber.
International Journal of Vegetable Science,
28(3), 233-238. doi:
10.1080/19315260.2021.1935388.##Sahay, N., & Varma, A. (1999).
Piriformospora indica: A new biological hardening tool for micropropagated plants.
FEMS Microbiology Letters,
181(2), 297-302. doi:
10.1111/j.1574-6968.1999.tb08858.x.##Samobor, V., Vukobratović, M., & Marijan, J. (2006). Effect of powdery mildew attack on quality parameters and experimental bread baking of wheat.
Acta Agriculturae Slovenica,
87(2), 381-391. doi:
10.14720/aas.2006.87.2.15116.##Savary, S., Willocquet, L., Pethybridge, S. J., Esker, P., McRoberts, N., & Nelson, A. (2019). The global burden of pathogens and pests on major food crops.
Nature Ecology & Evolution,
3(3), 430-439. doi:
10.1038/s41559-018-0793-y.##Singh, U. B., Malviya, D., Singh, S., Kumar, M., Sahu, P. K., Singh, H. V., Kumar, S., Roy, M., Imran, M., Rai, J. P., Sharma, A. K., & Saxena, A. K. (2019).
Trichoderma harzianum- and methyl jasmonate-induced resistance to
Bipolaris sorokiniana through enhanced phenylpropanoid activities in bread wheat (
Triticum aestivum L.).
Frontiers in Microbiology,
10, 1697. doi:
10.3389/fmicb.2019.01697.##Van Eck, L., Schultz, T., Leach, J. E., Scofield, S. R., Peairs, F. B., Botha, A. M., & Lapitan, N. L. V. (2010). Virus-induced gene silencing of
WRKY53 and an inducible phenylalanine ammonia-lyase in wheat reduces aphid resistance.
Plant Biotechnology Journal,
8(9), 1023-1032. doi:
10.1111/j.1467-7652.2010.00539.x.##Yuan, M., Huang, Y., Ge, W., Jia, Z., Song, S., Zhang, L., & Huang, Y. (2019). Involvement of jasmonic acid, ethylene and salicylic acid signaling pathways behind the systemic resistance induced by
Trichoderma longibrachiatum H9 in cucumber.
BMC Genomics,
20, 1-13. doi:
10.1186/s12864-019-5513-8.##Zhan, C., Li, Y., Li, H., Wang, M., Gong, S., Ma, D., & Li, Y. (2022). Phylogenomic analysis of phenylalanine ammonia-lyase (PAL) multigene family and their differential expression analysis in wheat (
Triticum aestivum L.) suggested their roles during different stress responses.
Frontiers in Plant Science,
13, 982457. doi:
10.3389/fpls.2022.982457.##Zhang, S., Liu, J., Xu, B., & Zhou, J. (2021). Differential responses of
Cucurbita pepo to
Podosphaera xanthii reveal the mechanism of powdery mildew disease resistance in pumpkin.
Frontiers in Plant Science,
12, 633221. doi:
10.3389/fpls.2022.982457.##Zhu, M., Riederer, M., & Hildebrandt, U. (2017). Very-long-chain aldehydes induce appressorium formation in ascospores of the wheat powdery mildew fungus
Blumeria graminis.
Fungal Biology,
121(8), 716-728. doi:
10.1016/j.funbio.2017.05.003.##