This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Abdelhai MH, Awad FN, Yang Q, Mahunu GK, Godana EA, Zhang H. Enhancement the biocontrol efficacy of Sporidiobolus pararoseus Y16 against apple blue mold decay by glycine betaine and its mechanism. Biol Control. 2019 Dec;139:104079. https://doi.org/10.1016/j.biocontrol.2019.104079AbdelhaiMHAwadFNYangQMahunuGKGodanaEAZhangHEnhancement the biocontrol efficacy of Sporidiobolus pararoseus Y16 against apple blue mold decay by glycine betaine and its mechanismBiol Control2019Dec139104079https://doi.org/10.1016/j.biocontrol.2019.104079Search in Google Scholar
Abdel-Kader M, El-Mougy N, Lashin S. Essential oils and Trichoderma harzianum as an integrated control measure against faba bean root rot pathogens. J Plant Prot Res. 2011 Jul;51(3):306–313. https://doi.org/10.2478/v10045-011-0050-8Abdel-KaderMEl-MougyNLashinSEssential oils and Trichoderma harzianum as an integrated control measure against faba bean root rot pathogensJ Plant Prot Res2011Jul513306313https://doi.org/10.2478/v10045-011-0050-8Search in Google Scholar
Ahsan T, Chen J, Zhao X, Irfan M, Wu Y. Extraction and identification of bioactive compounds (eicosane and dibutyl phthalate) produced by Streptomyces strain KX852460 for the biological control of Rhizoctonia solani AG-3 strain KX852461 to control target spot disease in tobacco leaf. AMB Express. 2017 Dec;7(1):54. https://doi.org/10.1186/s13568-017-0351-zAhsanTChenJZhaoXIrfanMWuYExtraction and identification of bioactive compounds (eicosane and dibutyl phthalate) produced by Streptomyces strain KX852460 for the biological control of Rhizoctonia solani AG-3 strain KX852461 to control target spot disease in tobacco leafAMB Express2017Dec7154https://doi.org/10.1186/s13568-017-0351-zSearch in Google Scholar
Al-Askar AA, Saber WIA, Ghoneem KM, Hafez EE, Ibrahim AA. Crude citric acid of Trichoderma asperellum: tomato growth promotor and suppressor of Fusarium oxysporum f. sp. lycopersici. Plants. 2021 Jan;10(2):222. https://doi.org/10.3390/plants10020222Al-AskarAASaberWIAGhoneemKMHafezEEIbrahimAACrude citric acid of Trichoderma asperellum: tomato growth promotor and suppressor of Fusarium oxysporum f. sp. lycopersiciPlants2021Jan102222https://doi.org/10.3390/plants10020222Search in Google Scholar
Arai M, Han C, Yamano Y, Setiawan A, Kobayashi M. Aaptamines, marine spongean alkaloids, as anti-dormant mycobacterial substances. J Nat Med. 2014 Apr;68(2):372–376. https://doi.org/10.1007/s11418-013-0811-yAraiMHanCYamanoYSetiawanAKobayashiMAaptamines, marine spongean alkaloids, as anti-dormant mycobacterial substancesJ Nat Med2014Apr682372376https://doi.org/10.1007/s11418-013-0811-ySearch in Google Scholar
Bae H, Sicher RC, Kim MS, Kim SH, Strem MD, Melnick RL, Bailey BA. The beneficial endophyte Trichoderma hamatum isolate DIS 219b promotes growth and delays the onset of the drought response in Theobroma cacao. J Exp Bot. 2009 Jul;60(11):3279–3295. https://doi.org/10.1093/jxb/erp165BaeHSicherRCKimMSKimSHStremMDMelnickRLBaileyBAThe beneficial endophyte Trichoderma hamatum isolate DIS 219b promotes growth and delays the onset of the drought response in Theobroma cacaoJ Exp Bot2009Jul601132793295https://doi.org/10.1093/jxb/erp165Search in Google Scholar
Bae SJ, Park YH, Bae HJ, Jeon J, Bae H. Molecular identification, enzyme assay, and metabolic profiling of Trichoderma spp. J Microbiol Biotechnol. 2017 Jun;27(6):1157–1162. https://doi.org/10.4014/jmb.1702.02063BaeSJParkYHBaeHJJeonJBaeHMolecular identification, enzyme assay, and metabolic profiling of Trichoderma sppJ Microbiol Biotechnol2017Jun27611571162https://doi.org/10.4014/jmb.1702.02063Search in Google Scholar
Bañados MP. Blueberry production in South America. Acta Hortic. 2006;715:165–172 https://doi.org/10.17660/ActaHortic.2006.715.24BañadosMPBlueberry production in South AmericaActa Hortic200671516517https://doi.org/10.17660/ActaHortic.2006.715.24Search in Google Scholar
Behiry S, Soliman SA, Massoud MA, Abdelbary M, Kordy AM, Abdelkhalek A, Heflish A.Trichoderma pubescens elicit induced systemic resistance in tomato challenged by Rhizoctonia solani. J Fungi (Basel). 2023 Jan 27;9(2):167. https://doi.org/10.3390/jof9020167BehirySSolimanSAMassoudMAAbdelbaryMKordyAMAbdelkhalekAHeflishATrichoderma pubescens elicit induced systemic resistance in tomato challenged by Rhizoctonia solaniJ Fungi (Basel)2023Jan2792167https://doi.org/10.3390/jof9020167Search in Google Scholar
Benítez T, Rincón AM, Limón MC, Codón AC. Biocontrol mechanisms of Trichoderma strains. Int Microbiol. 2004 Dec;7(4):249–260.BenítezTRincónAMLimónMCCodónACBiocontrol mechanisms of Trichoderma strainsInt Microbiol2004Dec74249260Search in Google Scholar
Bhutia DD, Zhimo Y, Kole R, Saha J. Antifungal activity of plant extracts against Colletotrichum musae, the post harvest anthracnose pathogen of banana cv. Martaman. Nutr Food Sci. 2016 Feb;46(1):2–15. https://doi.org/10.1108/NFS-06-2015-0068BhutiaDDZhimoYKoleRSahaJAntifungal activity of plant extracts against Colletotrichum musae, the post harvest anthracnose pathogen of banana cv. MartamanNutr Food Sci2016Feb461215https://doi.org/10.1108/NFS-06-2015-0068Search in Google Scholar
Bigirimana J, De Meyer G, Poppe J, Elad Y, Höfte M. Induction of systemic resistance on bean (Phaseolus vulgaris) by Trichoderma harziamum. Meded – Fac Landbouwkd Toegepaste Biol Wet (Univ Gent). 1997;62:1001–1007.BigirimanaJDe MeyerGPoppeJEladYHöfteMInduction of systemic resistance on bean (Phaseolus vulgaris) by Trichoderma harziamumMeded – Fac Landbouwkd Toegepaste Biol Wet (Univ Gent)19976210011007Search in Google Scholar
Calonje M, Novaes-Ledieu M, Bernardo D, Ahrazem O, Mendoza CG. Chemical components and their locations in the Verticillium fungicola cell wall. Can J Microbiol. 2000 Feb;46(2):101–109. https://doi.org/10.1139/w99-120CalonjeMNovaes-LedieuMBernardoDAhrazemOMendozaCGChemical components and their locations in the Verticillium fungicola cell wallCan J Microbiol2000Feb462101109https://doi.org/10.1139/w99-120Search in Google Scholar
Chet I, Inbar J. Biological control of fungal pathogens. Appl Biochem Biotechnol. 1994 Jul;48(1):37–43. https://doi.org/10.1007/BF02825358ChetIInbarJBiological control of fungal pathogensAppl Biochem Biotechnol1994Jul4813743https://doi.org/10.1007/BF02825358Search in Google Scholar
Chong KP, Rossall S, Atong M.In vitro antimicrobial activity and fungitoxicity of syringic acid, caffeic acid and 4-hydroxybenzoic acid against Ganoderma boninense. J Agric Sci. 2009;1(2):15. https://doi.org/10.5539/jas.v1n2p15ChongKPRossallSAtongMIn vitro antimicrobial activity and fungitoxicity of syringic acid, caffeic acid and 4-hydroxybenzoic acid against Ganoderma boninenseJ Agric Sci20091215https://doi.org/10.5539/jas.v1n2p15Search in Google Scholar
da Silva JAT, de Medeiros EV, da Silva JM, Tenório DA, Moreira KA, Nascimento TCES, Souza-Motta C.Trichoderma aureoviride URM 5158 and Trichoderma hamatum URM 6656 are Biocontrol agents that act against cassava root rot through different Mechanisms. J Phytopathol. 2016 Dec;164(11–12):1003–1011. https://doi.org/10.1111/jph.12521da SilvaJATde MedeirosEVda SilvaJMTenórioDAMoreiraKANascimentoTCESSouza-MottaCTrichoderma aureoviride URM 5158 and Trichoderma hamatum URM 6656 are Biocontrol agents that act against cassava root rot through different MechanismsJ Phytopathol2016Dec16411–1210031011https://doi.org/10.1111/jph.12521Search in Google Scholar
de França SKS, Cardoso AF, Lustosa DC, Ramos EMLS, de Filippi MCC, da Silva GB. Biocontrol of sheath blight by Trichoderma asperellum in tropical lowland rice. Agron Sustain Dev. 2015 Jan;35(1):317–324. https://doi.org/10.1007/s13593-014-0244-3de FrançaSKSCardosoAFLustosaDCRamosEMLSde FilippiMCCda SilvaGBBiocontrol of sheath blight by Trichoderma asperellum in tropical lowland riceAgron Sustain Dev2015Jan351317324https://doi.org/10.1007/s13593-014-0244-3Search in Google Scholar
de los Santos-Villalobos S, Guzmán-Ortiz DA, Gómez-Lim MA, Délano-Frier JP, de-Folter S, Sánchez-García P, Peña-Cabriales JJ. Potential use of Trichoderma asperellum (Samuels, Liechfeldt et Nirenberg) T8a as a biological control agent against anthracnose in mango (Mangifera indica L.). Biol Control. 2013 Jan;64(1):37–44. https://doi.org/10.1016/j.biocontrol.2012.10.006de los Santos-VillalobosSGuzmán-OrtizDAGómez-LimMADélano-FrierJPde-FolterSSánchez-GarcíaPPeña-CabrialesJJPotential use of Trichoderma asperellum (Samuels, Liechfeldt et Nirenberg) T8a as a biological control agent against anthracnose in mango (Mangifera indica L.)Biol Control2013Jan6413744https://doi.org/10.1016/j.biocontrol.2012.10.006Search in Google Scholar
Dihazi A, Jaiti F, WafaTaktak, kilani-Feki O, Jaoua S, Driouich A, Baaziz M, Daayf F, Serghini MA. Use of two bacteria for biological control of bayoud disease caused by Fusarium oxysporum in date palm (Phoenix dactylifera L) seedlings. Plant Physiol Biochem. 2012 Jun; 55:7–15. https://doi.org/10.1016/j.plaphy.2012.03.003DihaziAJaitiFTaktakWafakilani-FekiOJaouaSDriouichABaazizMDaayfFSerghiniMAUse of two bacteria for biological control of bayoud disease caused by Fusarium oxysporum in date palm (Phoenix dactylifera L) seedlingsPlant Physiol Biochem2012Jun55715https://doi.org/10.1016/j.plaphy.2012.03.003Search in Google Scholar
El Komy MH, Saleh AA, Eranthodi A, Molan YY. Characterization of novel Trichoderma asperellum isolates to select effective biocontrol agents against tomato Fusarium wilt. Plant Pathol J. 2015 Mar; 31(1):50–60. https://doi.org/10.5423/PPJ.OA.09.2014.0087El KomyMHSalehAAEranthodiAMolanYYCharacterization of novel Trichoderma asperellum isolates to select effective biocontrol agents against tomato Fusarium wiltPlant Pathol J2015Mar3115060https://doi.org/10.5423/PPJ.OA.09.2014.0087Search in Google Scholar
Elshahawy IE, El-Mohamedy RS. Biological control of Pythium damping-off and root-rot diseases of tomato using Trichoderma isolates employed alone or in combination. J Plant Pathol. 2019 Aug; 101(3):597–608. https://doi.org/10.1007/s42161-019-00248-zElshahawyIEEl-MohamedyRSBiological control of Pythium damping-off and root-rot diseases of tomato using Trichoderma isolates employed alone or in combinationJ Plant Pathol2019Aug1013597608https://doi.org/10.1007/s42161-019-00248-zSearch in Google Scholar
Faria A, Oliveira J, Neves P, Gameiro P, Santos-Buelga C, de Freitas V, Mateus N. Antioxidant properties of prepared blueberry (Vaccinium myrtillus) extracts. J Agric Food Chem. 2005 Aug; 53(17):6896–6902. https://doi.org/10.1021/jf0511300FariaAOliveiraJNevesPGameiroPSantos-BuelgaCde FreitasVMateusNAntioxidant properties of prepared blueberry (Vaccinium myrtillus) extractsJ Agric Food Chem2005Aug531768966902https://doi.org/10.1021/jf0511300Search in Google Scholar
Fei NY, Qi YB, Meng TT, Fu JF, Yan XR. First report of root rot caused by Calonectria ilicicola on blueberry in Yunnan Province, China. Plant Dis. 2018 May;102(5):1036–1036. https://doi.org/10.1094/PDIS-09-17-1337-PDNFeiNYQiYBMengTTFuJFYanXRFirst report of root rot caused by Calonectria ilicicola on blueberry in Yunnan Province, ChinaPlant Dis2018May102510361036https://doi.org/10.1094/PDIS-09-17-1337-PDNSearch in Google Scholar
Guo R, Wang Z, Zhou C, Huang Y, Fan H, Wang Y, Liu Z. Biocontrol potential of Trichoderma asperellum mutants T39 and T45 and their growth promotion of poplar seedlings. J For Res. 2020 Jun; 31(3):1035–1043. https://doi.org/10.1007/s11676-018-0797-0GuoRWangZZhouCHuangYFanHWangYLiuZBiocontrol potential of Trichoderma asperellum mutants T39 and T45 and their growth promotion of poplar seedlingsJ For Res2020Jun31310351043https://doi.org/10.1007/s11676-018-0797-0Search in Google Scholar
Hahn M. The rising threat of fungicide resistance in plant pathogenic fungi: Botrytis as a case study. J Chem Biol. 2014 Oct;7(4): 133–141. https://doi.org/10.1007/s12154-014-0113-1HahnMThe rising threat of fungicide resistance in plant pathogenic fungi: Botrytis as a case studyJ Chem Biol2014Oct74133141https://doi.org/10.1007/s12154-014-0113-1Search in Google Scholar
Haran S, Schickler H, Chet I. Molecular mechanisms of lytic enzymes involved in the biocontrol activity of Trichoderma harzianum. Microbiology. 1996 Sep;142(9):2321–2331. https://doi.org/10.1099/00221287-142-9-2321HaranSSchicklerHChetIMolecular mechanisms of lytic enzymes involved in the biocontrol activity of Trichoderma harzianumMicrobiology1996Sep142923212331https://doi.org/10.1099/00221287-142-9-2321Search in Google Scholar
Harman GE. Overview of mechanisms and uses of Trichoderma spp. Phytopathology. 2006 Feb;96(2):190–194. https://doi.org/10.1094/PHYTO-96-0190HarmanGEOverview of mechanisms and uses of Trichoderma sppPhytopathology2006Feb962190194https://doi.org/10.1094/PHYTO-96-0190Search in Google Scholar
He W, Megharaj M, Wu CY, Subashchandrabose SR, Dai CC. Endophyte-assisted phytoremediation: Mechanisms and current application strategies for soil mixed pollutants. Crit Rev Biotechnol. 2020 Jan;40(1):31–45. https://doi.org/10.1080/07388551.2019.1675582HeWMegharajMWuCYSubashchandraboseSRDaiCCEndophyte-assisted phytoremediation: Mechanisms and current application strategies for soil mixed pollutantsCrit Rev Biotechnol2020Jan4013145https://doi.org/10.1080/07388551.2019.1675582Search in Google Scholar
Herrera Cano N, Ballari MS, López AG, Santiago AN. New synthesis and biological evaluation of benzothiazole derivates as antifungal agents. J Agric Food Chem. 2015 Apr;63(14):3681–3686. https://doi.org/10.1021/acs.jafc.5b00150Herrera CanoNBallariMSLópezAGSantiagoANNew synthesis and biological evaluation of benzothiazole derivates as antifungal agentsJ Agric Food Chem2015Apr631436813686https://doi.org/10.1021/acs.jafc.5b00150Search in Google Scholar
Jiang H, Zhang L, Zhang J, Ojaghian MR, Hyde KD. Antagonistic interaction between Trichoderma asperellum and Phytophthora capsici in vitro. J Zhejiang Univ Sci B. 2016 Apr;17(4):271–281. https://doi.org/10.1631/jzus.B1500243JiangHZhangLZhangJOjaghianMRHydeKDAntagonistic interaction between Trichoderma asperellum and Phytophthora capsici in vitroJ Zhejiang Univ Sci B2016Apr174271281https://doi.org/10.1631/jzus.B1500243Search in Google Scholar
Keswani C, Bisen K, Chitara MK, Sarma BK, Singh HB. Exploring the role of secondary metabolites of Trichoderma in tripartite interaction with plant and pathogens. In Singh J, Seneviratne G, editors. Agro-environmental sustainability. Cham (Germany): Springer; 2017. p. 63–79. https://doi.org/10.1007/978-3-319-49724-2_4KeswaniCBisenKChitaraMKSarmaBKSinghHBExploring the role of secondary metabolites of Trichoderma in tripartite interaction with plant and pathogensInSinghJSeneviratneGeditors.Agro-environmental sustainabilityCham (Germany)Springer20176379https://doi.org/10.1007/978-3-319-49724-2_4Search in Google Scholar
Kong P, Hong C. Biocontrol of boxwood blight by Trichoderma koningiopsis Mb2. Crop Prot. 2017 Aug;98:124–127. https://doi.org/10.1016/j.cropro.2017.03.015KongPHongCBiocontrol of boxwood blight by Trichoderma koningiopsis Mb2Crop Prot2017Aug98124127https://doi.org/10.1016/j.cropro.2017.03.015Search in Google Scholar
Kumar S, Stecher G, Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for bigger datasets. Mol Biol Evol. 2016 Jul; 33(7):1870–1874. https://doi.org/10.1093/molbev/msw054KumarSStecherGTamuraKMEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for bigger datasetsMol Biol Evol2016Jul33718701874https://doi.org/10.1093/molbev/msw054Search in Google Scholar
Li M, Ma G, Lian H, Su X, Tian Y, Huang W, Mei J, Jiang X. The effects of Trichoderma on preventing cucumber fusarium wilt and regulating cucumber physiology. J Integr Agric. 2019 Mar;18(3):607–617. https://doi.org/10.1016/S2095-3119(18)62057-XLiMMaGLianHSuXTianYHuangWMeiJJiangXThe effects of Trichoderma on preventing cucumber fusarium wilt and regulating cucumber physiologyJ Integr Agric2019Mar183607617https://doi.org/10.1016/S2095-3119(18)62057-XSearch in Google Scholar
Li S, Hou R, Zhang F, Shang X. First report of Fusarium commune causing root rot of blueberry plants in Guizhou Province, China. Plant Dis. 2023 Apr;107(4):1227. https://doi.org/10.1094/PDIS-06-22-1305-PDNLiSHouRZhangFShangXFirst report of Fusarium commune causing root rot of blueberry plants in Guizhou Province, ChinaPlant Dis2023Apr10741227https://doi.org/10.1094/PDIS-06-22-1305-PDNSearch in Google Scholar
Liu YH, Lin T, Ye CS, Zhang CQ. First report of Fusarium wilt in blueberry (Vaccinium corymbosum) caused by Fusarium oxysporum in China. Plant Dis. 2014 Aug;98(8):1158–1158. https://doi.org/10.1094/PDIS-02-14-0167-PDNLiuYHLinTYeCSZhangCQFirst report of Fusarium wilt in blueberry (Vaccinium corymbosum) caused by Fusarium oxysporum in ChinaPlant Dis2014Aug98811581158https://doi.org/10.1094/PDIS-02-14-0167-PDNSearch in Google Scholar
Loc NH, Huy ND, Quang HT, Lan TT, Thu Ha TT. Characterisation and antifungal activity of extracellular chitinase from a biocontrol fungus, Trichoderma asperellum PQ34. Mycology. 2020 Jan 02;11(1):38–48. https://doi.org/10.1080/21501203.2019.1703839LocNHHuyNDQuangHTLanTTThu HaTTCharacterisation and antifungal activity of extracellular chitinase from a biocontrol fungus, Trichoderma asperellum PQ34Mycology2020Jan021113848https://doi.org/10.1080/21501203.2019.1703839Search in Google Scholar
Mathivanan N, Prabavathy VR, Vijayanandraj VR. The effect of fungal secondary metabolites on bacterial and fungal pathogens. In Karlovsky P, editor. Secondary metabolites. Soil ecology. Berlin, Heidelberg (Germany): Springer; 2008. p. 129–140. https://doi.org/10.1007/978-3-540-74543-3_7MathivananNPrabavathyVRVijayanandrajVRThe effect of fungal secondary metabolites on bacterial and fungal pathogensInKarlovskyPeditor.Secondary metabolites. Soil ecologyBerlin, Heidelberg (Germany)Springer2008129140https://doi.org/10.1007/978-3-540-74543-3_7Search in Google Scholar
Meena M, Swapnil P, Zehra A, Dubey MK, Upadhyay RS. Antagonistic assessment of Trichoderma spp. by producing volatile and non-volatile compounds against different fungal pathogens. Arch Phytopathol Pflanzenschutz. 2017 Aug;50(13–14):629–648. https://doi.org/10.1080/03235408.2017.1357360MeenaMSwapnilPZehraADubeyMKUpadhyayRSAntagonistic assessment of Trichoderma spp. by producing volatile and non-volatile compounds against different fungal pathogensArch Phytopathol Pflanzenschutz2017Aug5013–14629648https://doi.org/10.1080/03235408.2017.1357360Search in Google Scholar
Mischke S. A quantitative bioassay for extracellular metabolites that antagonize growth of filamentous fungi, and its use with biocontrol fungi. Mycopathologia. 1997;137(1):45–52. https://doi.org/10.1023/A:1006814521872MischkeSA quantitative bioassay for extracellular metabolites that antagonize growth of filamentous fungi, and its use with biocontrol fungiMycopathologia199713714552https://doi.org/10.1023/A:1006814521872Search in Google Scholar
Mu J, Li X, Jiao J, Ji G, Wu J, Hu F, Li H. Biocontrol potential of vermicompost through antifungal volatiles produced by indigenous bacteria. Biol Control. 2017 Sep;112:49–54. https://doi.org/10.1016/j.biocontrol.2017.05.013MuJLiXJiaoJJiGWuJHuFLiHBiocontrol potential of vermicompost through antifungal volatiles produced by indigenous bacteriaBiol Control2017Sep1124954https://doi.org/10.1016/j.biocontrol.2017.05.013Search in Google Scholar
Mukherjee PK, Raghu K. Effect of temperature on antagonistic and biocontrol potential of Trichoderma sp. on Sclerotium rolfsii. Mycopathologia. 1997;139(3):151–155. https://doi.org/10.1023/A:1006868009184MukherjeePKRaghuKEffect of temperature on antagonistic and biocontrol potential of Trichoderma sp. on Sclerotium rolfsiiMycopathologia19971393151155https://doi.org/10.1023/A:1006868009184Search in Google Scholar
Muniroh MS, Nusaibah SA, Vadamalai G, Siddique Y. Proficiency of biocontrol agents as plant growth promoters and hydrolytic enzyme producers in Ganoderma boninense infected oil palm seedlings. Curr Plant Biol. 2019 Dec;20:100116. https://doi.org/10.1016/j.cpb.2019.100116MunirohMSNusaibahSAVadamalaiGSiddiqueYProficiency of biocontrol agents as plant growth promoters and hydrolytic enzyme producers in Ganoderma boninense infected oil palm seedlingsCurr Plant Biol2019Dec20100116https://doi.org/10.1016/j.cpb.2019.100116Search in Google Scholar
Nakkeeran S, Priyanka R, Rajamanickam S, Sivakumar U.Bacillus amyloliquefaciens alters the diversity of volatile and non-volatile metabolites and induces the expression of defence genes for the management of Botrytis leaf blight of Lilium under protected conditions. J Plant Pathol. 2020 Nov;102(4):1179–1189. https://doi.org/10.1007/s42161-020-00602-6NakkeeranSPriyankaRRajamanickamSSivakumarUBacillus amyloliquefaciens alters the diversity of volatile and non-volatile metabolites and induces the expression of defence genes for the management of Botrytis leaf blight of Lilium under protected conditionsJ Plant Pathol2020Nov102411791189https://doi.org/10.1007/s42161-020-00602-6Search in Google Scholar
Nawrocka J, Małolepsza U. Diversity in plant systemic resistance induced by Trichoderma. Biol Control. 2013 Nov;67(2):149–156. https://doi.org/10.1016/j.biocontrol.2013.07.005NawrockaJMałolepszaUDiversity in plant systemic resistance induced by TrichodermaBiol Control2013Nov672149156https://doi.org/10.1016/j.biocontrol.2013.07.005Search in Google Scholar
Neto CC. Cranberry and blueberry: evidence for protective effects against cancer and vascular diseases. Mol Nutr Food Res. 2007 Jun; 51(6):652–664. https://doi.org/10.1002/mnfr.200600279NetoCCCranberry and blueberry: evidence for protective effects against cancer and vascular diseasesMol Nutr Food Res2007Jun516652664https://doi.org/10.1002/mnfr.200600279Search in Google Scholar
Nguyen TTT, Lee HB. Isolation and characterization of three Zygomycetous fungi in Korea: Backusella circina, Circinella muscae, and Mucor ramosissimus. Mycobiology. 2018 Dec 21;46(4):317–327. https://doi.org/10.1080/12298093.2018.1538071NguyenTTTLeeHBIsolation and characterization of three Zygomycetous fungi in Korea: Backusella circina, Circinella muscae, and Mucor ramosissimusMycobiology2018Dec21464317327https://doi.org/10.1080/12298093.2018.1538071Search in Google Scholar
Papavizas GC, Lumsden RD. Biological control of soilborne fungal propagules. Annu Rev Phytopathol. 1980 Sep;18(1):389–413. https://doi.org/10.1146/annurev.py.18.090180.002133PapavizasGCLumsdenRDBiological control of soilborne fungal propagulesAnnu Rev Phytopathol1980Sep181389413https://doi.org/10.1146/annurev.py.18.090180.002133Search in Google Scholar
Podile AR, Laxmi VDV. Seed Bacterization with Bacillus subtilis AF 1 increases phenylalanine ammonia-lyase and reduces the incidence of Fusarial Wilt in Pigeonpea. J Phytopathol. 1998 Jul;146(5–6):255–259. https://doi.org/10.1111/j.1439-0434.1998.tb04687.xPodileARLaxmiVDVSeed Bacterization with Bacillus subtilis AF 1 increases phenylalanine ammonia-lyase and reduces the incidence of Fusarial Wilt in PigeonpeaJ Phytopathol1998Jul1465–6255259https://doi.org/10.1111/j.1439-0434.1998.tb04687.xSearch in Google Scholar
Ruangwong OU, Wonglom P, Suwannarach N, Kumla J, Thaochan N, Chomnunti P, Pitija K, Sunpapao A. Volatile organic compound from Trichoderma asperelloides TSU1: impact on plant pathogenic fungi. J Fungi. 2021 Mar;7(3):187. https://doi.org/10.3390/jof7030187RuangwongOUWonglomPSuwannarachNKumlaJThaochanNChomnuntiPPitijaKSunpapaoAVolatile organic compound from Trichoderma asperelloides TSU1: impact on plant pathogenic fungiJ Fungi2021Mar73187https://doi.org/10.3390/jof7030187Search in Google Scholar
Sahebani N, Hadavi N. Biological control of the root-knot nematode Meloidogyne javanica by Trichoderma harzianum. Soil Biol Biochem. 2008 Aug;40(8):2016–2020. https://doi.org/10.1016/j.soilbio.2008.03.011SahebaniNHadaviNBiological control of the root-knot nematode Meloidogyne javanica by Trichoderma harzianumSoil Biol Biochem2008Aug40820162020https://doi.org/10.1016/j.soilbio.2008.03.011Search in Google Scholar
Saravanakumar K, Yu C, Dou K, Wang M, Li Y, Chen J. Synergistic effect of Trichoderma-derived antifungal metabolites and cell wall degrading enzymes on enhanced biocontrol of Fusarium oxysporum f. sp. cucumerinum. Biol Control. 2016 Mar;94:37–46. https://doi.org/10.1016/j.biocontrol.2015.12.001SaravanakumarKYuCDouKWangMLiYChenJSynergistic effect of Trichoderma-derived antifungal metabolites and cell wall degrading enzymes on enhanced biocontrol of Fusarium oxysporum f. sp. cucumerinumBiol Control2016Mar943746https://doi.org/10.1016/j.biocontrol.2015.12.001Search in Google Scholar
Sid Ahmed A, Ezziyyani M, Pérez Sánchez C, Candela ME. Effect of chitin on biological control activity of Bacillus spp. and Trichoderma harzianum against root rot disease in pepper (Capsicum annuum) plants. Eur J Plant Pathol. 2003;109(6):633–637. https://doi.org/10.1023/A:1024734216814Sid AhmedAEzziyyaniMPérez SánchezCCandelaMEEffect of chitin on biological control activity of Bacillus spp. and Trichoderma harzianum against root rot disease in pepper (Capsicum annuum) plantsEur J Plant Pathol20031096633637https://doi.org/10.1023/A:1024734216814Search in Google Scholar
Sundar D, Perianayaguy B, Reddy AR. Localization of antioxidant enzymes in the cellular compartments of sorghum leaves. Plant Growth Regul. 2004;44(2):157–163. https://doi.org/10.1023/B:GROW.0000049418.92833.d6SundarDPerianayaguyBReddyARLocalization of antioxidant enzymes in the cellular compartments of sorghum leavesPlant Growth Regul2004442157163https://doi.org/10.1023/B:GROW.0000049418.92833.d6Search in Google Scholar
Takahashi Y, Kubota T, Shibazaki A, Gonoi T, Fromont J, Kobayashi J. Nakijinamines C–E, new heteroaromatic alkaloids from the sponge Suberites species. Org Lett. 2011 Jun;13(12):3016–3019. https://doi.org/10.1021/ol2008473TakahashiYKubotaTShibazakiAGonoiTFromontJKobayashiJNakijinamines C–E, new heteroaromatic alkaloids from the sponge Suberites speciesOrg Lett2011Jun131230163019https://doi.org/10.1021/ol2008473Search in Google Scholar
Vinale F, Sivasithamparam K, Ghisalberti EL, Marra R, Woo SL, Lorito M.Trichoderma-plant-pathogen interactions. Soil Biol Biochem. 2008 Jan;40(1):1–10. https://doi.org/10.1016/j.soilbio.2007.07.002VinaleFSivasithamparamKGhisalbertiELMarraRWooSLLoritoMTrichoderma-plant-pathogen interactionsSoil Biol Biochem2008Jan401110https://doi.org/10.1016/j.soilbio.2007.07.002Search in Google Scholar
Wang LJ, Wu J, Wang HX, Li SS, Zheng XC, Du H, Xu YJ, Wang LS. Composition of phenolic compounds and antioxidant activity in the leaves of blueberry cultivars. J Funct Foods. 2015 Jun; 16:295–304. https://doi.org/10.1016/j.jff.2015.04.027WangLJWuJWangHXLiSSZhengXCDuHXuYJWangLSComposition of phenolic compounds and antioxidant activity in the leaves of blueberry cultivarsJ Funct Foods2015Jun16295304https://doi.org/10.1016/j.jff.2015.04.027Search in Google Scholar
Ward NA. Blueberry root rot. Extension Plant Pathologist. 2013; PPFS-FR-S-19.WardNABlueberry root rot. Extension Plant Pathologist2013PPFS-FR-S-19.Search in Google Scholar
Wu Q, Sun R, Ni M, Yu J, Li Y, Yu C, Dou K, Ren J, Chen J. Identification of a novel fungus, Trichoderma asperellum GDFS1009, and comprehensive evaluation of its biocontrol efficacy. PLoS One. 2017 Jun;12(6):e0179957. https://doi.org/10.1371/journal.pone.0179957WuQSunRNiMYuJLiYYuCDouKRenJChenJIdentification of a novel fungus, Trichoderma asperellum GDFS1009, and comprehensive evaluation of its biocontrol efficacyPLoS One2017Jun126e0179957https://doi.org/10.1371/journal.pone.0179957Search in Google Scholar
Xie Y, Peng Q, Ji Y, Xie A, Yang L, Mu S, Li Z, He T, Xiao Y, Zhao J, et al. Isolation and identification of antibacterial bioactive compounds from Bacillus megaterium L2. Front Microbiol. 2021 Mar; 12:645484. https://doi.org/10.3389/fmicb.2021.645484XieYPengQJiYXieAYangLMuSLiZHeTXiaoYZhaoJIsolation and identification of antibacterial bioactive compounds from Bacillus megaterium L2Front Microbiol2021Mar12645484https://doi.org/10.3389/fmicb.2021.645484Search in Google Scholar
Yi HW, Chi YJ. Biocontrol of Cytospora canker of poplar in northeast China with Trichoderma longibrachiatum. For Pathol. 2011 Aug; 41(4):299–307. https://doi.org/10.1111/j.1439-0329.2010.00704.xYiHWChiYJBiocontrol of Cytospora canker of poplar in northeast China with Trichoderma longibrachiatumFor Pathol2011Aug414299307https://doi.org/10.1111/j.1439-0329.2010.00704.xSearch in Google Scholar
Zhang D, Bi W, Kai K, Ye Y, Liu J. Effect of chlorogenic acid on controlling kiwifruit postharvest decay caused by Diaporthe sp. LWT. 2020 Oct;132:109805. https://doi.org/10.1016/j.lwt.2020.109805ZhangDBiWKaiKYeYLiuJEffect of chlorogenic acid on controlling kiwifruit postharvest decay caused by Diaporthe spLWT2020Oct132109805https://doi.org/10.1016/j.lwt.2020.109805Search in Google Scholar
Zhou Y, Yang L, Wang J, Guo L, Huang J. Synergistic effect between Trichoderma virens and Bacillus velezensis on the control of tomato bacterial wilt disease. Hortic. 2021 Nov 01;7(11):439. https://doi.org/10.3390/horticulturae7110439ZhouYYangLWangJGuoLHuangJSynergistic effect between Trichoderma virens and Bacillus velezensis on the control of tomato bacterial wilt diseaseHortic2021Nov01711439https://doi.org/10.3390/horticulturae7110439Search in Google Scholar