This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Ashe S, Maji UJ, Sen R, Mohanty S, Maiti NK. Specific oligonucleotide primers for detection of endoglucanase positive Bacillus subtilis by PCR. 3 Biotech. 2014 Oct;4(5):461–465. https://doi.org/10.1007/s13205-013-0177-6AsheSMajiUJSenRMohantySMaitiNK. Specific oligonucleotide primers for detection of endoglucanase positive Bacillus subtilis by PCR. 2014Oct; 4(5):461–465. https://doi.org/10.1007/s13205-013-0177-6Search in Google Scholar
Aslani MA, Harighi B, Abdollahzadeh J. Screening of endofungal bacteria isolated from wild growing mushrooms as potential biological control agents against brown blotch and internal stipe necrosis diseases of Agaricus bisporus. Biol Control. 2018 Apr;119:20–26. https://doi.org/10.1016/j.biocontrol.2018.01.006AslaniMAHarighiBAbdollahzadehJ. Screening of endofungal bacteria isolated from wild growing mushrooms as potential biological control agents against brown blotch and internal stipe necrosis diseases of Agaricus bisporus. 2018Apr;119:20–26. https://doi.org/10.1016/j.biocontrol.2018.01.006Search in Google Scholar
Bhatti SK, Thakur M. An overview on orchids and their interaction with endophytes. Bot Rev. 2022 Feb;88(4):485–504. https://doi.org/10.1007/s12229-022-09275-5BhattiSKThakurM. An overview on orchids and their interaction with endophytes. 2022Feb; 88(4):485–504. https://doi.org/10.1007/s12229-022-09275-5Search in Google Scholar
Bhutani N, Maheshwari R, Negi M, Suneja P. Optimization of IAA production by endophytic Bacillus spp. from Vigna radiata for their potential use as plant growth promoters. Isr J Plant Sci. 2018 Jun; 65(1–2):83–96. https://doi.org/10.1163/22238980-00001025BhutaniNMaheshwariRNegiMSunejaP. Optimization of IAA production by endophytic Bacillus spp. from Vigna radiata for their potential use as plant growth promoters. 2018Jun; 65(1–2):83–96. https://doi.org/10.1163/22238980-00001025Search in Google Scholar
Büttner E, Gebauer AM, Hofrichter M, Liers C, Kellner H. Draft genome sequence of Xylaria longipes DSM 107183, a saprotrophic ascomycete colonizing hardwood. Microbiol Resour Announc. 2019 Mar;8(12):e00157-19. https://doi.org/https://doi.org/10.1128/MRA.00157-19BüttnerEGebauerAMHofrichterMLiersCKellnerH. Draft genome sequence of Xylaria longipes DSM 107183, a saprotrophic ascomycete colonizing hardwood. 2019Mar; 8(12):e00157-19. https://doi.org/https://doi.org/10.1128/MRA.00157-19Search in Google Scholar
Chen XM, Dong HL, Hu KX, Sun ZR, Chen J, Guo SX. Diversity and antimicrobial and plant-growth-promoting activities of endophytic fungi in Dendrobium loddigesii Rolfe. J Plant Growth Regul. 2010 Sep;29(3):328–337. https://doi.org/10.1007/s00344-010-9139-yChenXMDongHLHuKXSunZRChenJGuoSX. Diversity and antimicrobial and plant-growth-promoting activities of endophytic fungi in Dendrobium loddigesii Rolfe. 2010Sep; 29(3):328–337. https://doi.org/10.1007/s00344-010-9139-ySearch in Google Scholar
Cheng S, Jiang JW, Tan LT, Deng JX, Liang PY, Su H, Sun ZX, Zhou Y. Plant growth-promoting ability of mycorrhizal Fusarium strain KB-3 enhanced by its IAA producing endohyphal bacterium, Klebsiella aerogenes. Front Microbiol. 2022 Apr;13:855399. https://doi.org/10.3389/fmicb.2022.855399ChengSJiangJWTanLTDengJXLiangPYSuHSunZXZhouY. Plant growth-promoting ability of mycorrhizal Fusarium strain KB-3 enhanced by its IAA producing endohyphal bacterium, Klebsiella aerogenes. 2022Apr;13:855399. https://doi.org/10.3389/fmicb.2022.855399Search in Google Scholar
Cock PJ, Fields CJ, Goto N, Heuer ML, Rice PM. The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants. Nucleic Acids Res. 2010 Apr;38(6):1767–1771. https://doi.org/10.1093/nar/gkp1137CockPJFieldsCJGotoNHeuerMLRicePM. The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants. 2010Apr; 38(6):1767–1771. https://doi.org/10.1093/nar/gkp1137Search in Google Scholar
Desirò A, Hao Z, Liber JA, Benucci GMN, Lowry D, Roberson R, Bonito G.Mycoplasma-related endobacteria within Mortierellomycotina fungi: diversity, distribution and functional insights into their lifestyle. ISME J. 2018 Jun;12(7):1743–1757. https://doi.org/10.1038/s41396-018-0053-9DesiròAHaoZLiberJABenucciGMNLowryDRobersonRBonitoG. Mycoplasma-related endobacteria within Mortierellomycotina fungi: diversity, distribution and functional insights into their lifestyle. 2018Jun; 12(7):1743–1757. https://doi.org/10.1038/s41396-018-0053-9Search in Google Scholar
Galkiewicz JP, Kellogg CA. Cross-kingdom amplification using Bacteria-specific primers: complications for studies of coral microbial ecology. Appl Environ Microbiol. 2008 Dec;74(24):7828–7831. https://doi.org/10.1128/AEM.01303-08GalkiewiczJPKelloggCA. Cross-kingdom amplification using Bacteria-specific primers: complications for studies of coral microbial ecology. 2008Dec; 74(24):7828–7831. https://doi.org/10.1128/AEM.01303-08Search in Google Scholar
Ghignone S, Salvioli A, Anca I, Lumini E, Ortu G, Petiti L, Cruveiller S, Bianciotto V, Piffanelli P, Lanfranco L, et al. The genome of the obligate endobacterium of an AM fungus reveals an interphylum network of nutritional interactions. ISME J. 2012 Jan; 6(1):136–145. https://doi.org/10.1038/ismej.2011.110GhignoneSSalvioliAAncaILuminiEOrtuGPetitiLCruveillerSBianciottoVPiffanelliPLanfrancoLThe genome of the obligate endobacterium of an AM fungus reveals an interphylum network of nutritional interactions. 2012Jan; 6(1):136–145. https://doi.org/10.1038/ismej.2011.110Search in Google Scholar
Gholamalizadeh R, Khodakaramian G, Ebadi AA. Assessment of rice associated bacterial ability to enhance rice seed germination and rice growth promotion. Braz Arch Biol Techn. 2017 Aug; 60:e17160410. https://doi.org/10.1590/1678-4324-2017160410GholamalizadehRKhodakaramianGEbadiAA. Assessment of rice associated bacterial ability to enhance rice seed germination and rice growth promotion. 2017Aug; 60:e17160410. https://doi.org/10.1590/1678-4324-2017160410Search in Google Scholar
Gutiérrez RMP. Orchids: a review of uses in traditional medicine, its phytochemistry and pharmacology. J Med Plants Res. 2010 Apr; 4(8):592–638. https://doi.org/10.5897/JMPR10.012GutiérrezRMP. Orchids: a review of uses in traditional medicine, its phytochemistry and pharmacology. 2010Apr; 4(8):592–638. https://doi.org/10.5897/JMPR10.012Search in Google Scholar
Hoffman MT, Arnold AE. Diverse bacteria inhabit living hyphae of phylogenetically diverse fungal endophytes. Appl Environ Microbiol. 2010 Jun;76(12):4063–4075. https://doi.org/10.1128/AEM.02928-09HoffmanMTArnoldAE. Diverse bacteria inhabit living hyphae of phylogenetically diverse fungal endophytes. 2010Jun; 76(12):4063–4075. https://doi.org/10.1128/AEM.02928-09Search in Google Scholar
Hoffman MT, Gunatilaka MK, Wijeratne K, Gunatilaka L, Arnold AE. Endohyphal bacterium enhances production of indole-3-acetic acid by a foliar fungal endophyte. PLoS One. 2013 Sep;8(9):e73132. https://doi.org/10.1371/journal.pone.0073132HoffmanMTGunatilakaMKWijeratneKGunatilakaLArnoldAE. Endohyphal bacterium enhances production of indole-3-acetic acid by a foliar fungal endophyte. 2013Sep; 8(9):e73132. https://doi.org/10.1371/journal.pone.0073132Search in Google Scholar
Jiang JW, Zhang K, Cheng S, Nie QW, Zhou SX, Chen QQ, Zhou JL, Zhen X, Li XT, Zhen TW, et al.Fusarium oxysporum KB-3 from Bletilla striata: an orchid mycorrhizal fungus. Mycorrhiza. 2019a Oct; 29(5):531–540. https://doi.org/10.1007/s00572-019-00904-3JiangJWZhangKChengSNieQWZhouSXChenQQZhouJLZhenXLiXTZhenTWFusarium oxysporum KB-3 from Bletilla striata: an orchid mycorrhizal fungus. 2019aOct; 29(5):531–540. https://doi.org/10.1007/s00572-019-00904-3Search in Google Scholar
Jiang Q, Lou Z, Wang H, Chen C. Antimicrobial effect and proposed action mechanism of cordycepin against Escherichia coli and Bacillus subtilis. J Microbiol. 2019b Apr;57(4):288–297. https://doi.org/10.1007/s12275-019-8113-zJiangQLouZWangHChenC. Antimicrobial effect and proposed action mechanism of cordycepin against Escherichia coli and Bacillus subtilis. 2019bApr; 57(4):288–297. https://doi.org/10.1007/s12275-019-8113-zSearch in Google Scholar
Kashyap BK, Solanki MK, Pandey AK, Prabha S, Kumar P, Kumari B.Bacillus as plant growth promoting rhizobacteria (PGPR): a promising green agriculture technology. In: Ansari R, Mahmood I, editors. Plant health under biotic stress: Volume 2: Microbial interactions. Singapore: Springer Singapore; 2019. p. 219–236. https://doi.org/10.1007/978-981-13-6040-4_11KashyapBKSolankiMKPandeyAKPrabhaSKumarPKumariB. Bacillus as plant growth promoting rhizobacteria (PGPR): a promising green agriculture technology. In: AnsariRMahmoodIeditors. . Singapore: Springer Singapore; 2019. p. 219–236. https://doi.org/10.1007/978-981-13-6040-4_11Search 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/msw054KumarSStecherGTamuraK. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. 2016Jul; 33(7):1870–1874. https://doi.org/10.1093/molbev/msw054Search in Google Scholar
Li T, Yang W, Wu S, Selosse MA, Gao J. Progress and prospects of mycorrhizal fungal diversity in orchids. Front Plant Sci. 2021 May; 12:646325. https://doi.org/10.3389/fpls.2021.646325LiTYangWWuSSelosseMAGaoJ. Progress and prospects of mycorrhizal fungal diversity in orchids. 2021May; 12:646325. https://doi.org/10.3389/fpls.2021.646325Search in Google Scholar
Li XS, Sato T, Ooiwa Y, Kusumi A, Gu JD, Katayama Y. Oxidation of elemental sulfur by Fusarium solani strain THIF01 harboring endobacterium Bradyrhizobium sp. Microb Ecol. 2010 Jul;60(1):96–104. https://doi.org/10.1007/s00248-010-9699-1LiXSSatoTOoiwaYKusumiAGuJDKatayamaY. Oxidation of elemental sulfur by Fusarium solani strain THIF01 harboring endobacterium Bradyrhizobium sp. 2010Jul; 60(1):96–104. https://doi.org/10.1007/s00248-010-9699-1Search in Google Scholar
Lin YL, Huang RL, Don MJ, Kuo YH. Dihydrophenanthrenes from Spiranthes sinensis. J Nat Prod. 2000 Dec;63(12):1608–1610. https://doi.org/10.1021/np000170pLinYLHuangRLDonMJKuoYH. Dihydrophenanthrenes from Spiranthes sinensis. 2000Dec; 63(12):1608–1610. https://doi.org/10.1021/np000170pSearch in Google Scholar
Miljaković D, Marinković J, Balešević-Tubić S. The significance of Bacillus spp. in disease suppression and growth promotion of field and vegetable crops. Microorganisms. 2020 Jul;8(7):1037. https://doi.org/10.3390/microorganisms8071037MiljakovićDMarinkovićJBalešević-TubićS. The significance of Bacillus spp. in disease suppression and growth promotion of field and vegetable crops. 2020Jul; 8(7):1037. https://doi.org/10.3390/microorganisms8071037Search in Google Scholar
Naumann M, Schüssler A, Bonfante P. The obligate endobacteria of arbuscular mycorrhizal fungi are ancient heritable components related to the Mollicutes. ISME J. 2010 Jul;4(7):862–871. https://doi.org/10.1038/ismej.2010.21NaumannMSchüsslerABonfanteP. The obligate endobacteria of arbuscular mycorrhizal fungi are ancient heritable components related to the Mollicutes. 2010Jul; 4(7):862–871. https://doi.org/10.1038/ismej.2010.21Search in Google Scholar
Obasa K, Adesemoye A, Obasa R, Moraga-Amador D, Shinogle H, Alvarez S, Kelley K. Endohyphal bacteria associated with virulence, increased expression of fumonisin biosynthetic genes, and production of fumonisin and macroconidia in Fusarium fujikuroi W343. Plant Pathol. 2020 Jan;69(1):87–100. https://doi.org/10.1111/ppa.13107ObasaKAdesemoyeAObasaRMoraga-AmadorDShinogleHAlvarezSKelleyK. Endohyphal bacteria associated with virulence, increased expression of fumonisin biosynthetic genes, and production of fumonisin and macroconidia in Fusarium fujikuroi W343. 2020Jan; 69(1):87–100. https://doi.org/10.1111/ppa.13107Search in Google Scholar
Obasa K, White FF, Fellers J, Kennelly M, Liu S, Katz B, Tomich J, Moore D, Shinogle H, Kelley K. A dimorphic and virulence-enhancing endosymbiont bacterium discovered in Rhizoctonia solani. Phytobiomes J. 2017 Jan;1(1):14–23. https://doi.org/10.1094/Pbiomes-08-16-0005-RObasaKWhiteFFFellersJKennellyMLiuSKatzBTomichJMooreDShinogleHKelleyK. A dimorphic and virulence-enhancing endosymbiont bacterium discovered in Rhizoctonia solani. 2017Jan; 1(1):14–23. https://doi.org/10.1094/Pbiomes-08-16-0005-RSearch in Google Scholar
Pakarian P, Pawelek PD. Intracellular co-localization of the Escherichia coli enterobactin biosynthetic enzymes EntA, EntB, and EntE. Biochem Biophys Res Commun. 2016 Sep;478(1):25–32. https://doi.org/10.1016/j.bbrc.2016.07.105PakarianPPawelekPD. Intracellular co-localization of the Escherichia coli enterobactin biosynthetic enzymes EntA, EntB, and EntE. 2016Sep; 478(1):25–32. https://doi.org/10.1016/j.bbrc.2016.07.105Search in Google Scholar
Pakvaz S, Soltani J. Endohyphal bacteria from fungal endophytes of the Mediterranean cypress (Cupressus sempervirens) exhibit in vitro bioactivity. For Path. 2016 Apr;46(6):569–581. https://doi.org/10.1111/efp.12274PakvazSSoltaniJ. Endohyphal bacteria from fungal endophytes of the Mediterranean cypress (Cupressus sempervirens) exhibit in vitro bioactivity. 2016Apr; 46(6):569–581. https://doi.org/10.1111/efp.12274Search in Google Scholar
Partida-Martinez LP, Hertweck C. Pathogenic fungus harbours endosymbiotic bacteria for toxin production. Nature. 2005 Oct; 437(7060):884–888. https://doi.org/10.1038/nature03997Partida-MartinezLPHertweckC. Pathogenic fungus harbours endosymbiotic bacteria for toxin production. 2005Oct; 437(7060):884–888. https://doi.org/10.1038/nature03997Search in Google Scholar
Pei DF, Wu QQ, Luo H, Paul NC, Deng JX, Zhou Y. Diversity and antifungal activity of endophytes associated with Spiranthes sinensis (Orchidaceae, Magnoliophyta) in China. Int J Appl Microbiol Biotechnol Res. 2019;7:7–17. https://doi.org/10.33500/ijambr.2019.07.002PeiDFWuQQLuoHPaulNCDengJXZhouY. Diversity and antifungal activity of endophytes associated with Spiranthes sinensis (Orchidaceae, Magnoliophyta) in China. 2019; 7:7–17. https://doi.org/10.33500/ijambr.2019.07.002Search in Google Scholar
Peng J, Xu Q, Xu Y, Qi Y, Han X, Xu L. A new anticancer dihydroflavanoid from the root of Spiranthes australis (R. Brown) Lindl. Nat Prod Res. 2007 Jun;21(7):641–645. https://doi.org/10.1080/14786410701371165PengJXuQXuYQiYHanXXuL. A new anticancer dihydroflavanoid from the root of Spiranthes australis (R. Brown) Lindl. 2007Jun; 21(7):641–645. https://doi.org/10.1080/14786410701371165Search in Google Scholar
Peng JY, Han X, Xu LN, Qi Y, Xu YW, Xu QW. Two new prenylated coumarins from Spiranthes sinensis (Pers.) Ames. J Asian Nat Prod Res. 2008 Mar–Apr;10(3–4):279–283. https://doi.org/10.1080/10286020701605182PengJYHanXXuLNQiYXuYWXuQW. Two new prenylated coumarins from Spiranthes sinensis (Pers.)2008Mar–Apr;10(3–4):279–283. https://doi.org/10.1080/10286020701605182Search in Google Scholar
Ruiz-Herrera J, León-Ramírez C, Vera-Nuñez A, Sánchez-Arreguín A, Ruiz-Medrano R, Salgado-Lugo H, Sánchez-Segura L, Peña-Cabriales JJ. A novel intracellular nitrogen-fixing symbiosis made by Ustilago maydis and Bacillus spp. New Phytol. 2015 Aug; 207(3):769–777. https://doi.org/10.1111/nph.13359Ruiz-HerreraJLeón-RamírezCVera-NuñezASánchez-ArreguínARuiz-MedranoRSalgado-LugoHSánchez-SeguraLPeña-CabrialesJJ. A novel intracellular nitrogen-fixing symbiosis made by Ustilago maydis and Bacillus spp. 2015Aug; 207(3):769–777. https://doi.org/10.1111/nph.13359Search in Google Scholar
Salvioli A, Ghignone S, Novero M, Navazio L, Venice F, Bagnaresi P, Bonfante P. Symbiosis with an endobacterium increases the fitness of a mycorrhizal fungus, raising its bioenergetic potential. ISME J. 2016 Jan;10(1):130–144. https://doi.org/10.1038/ismej.2015.91SalvioliAGhignoneSNoveroMNavazioLVeniceFBagnaresiPBonfanteP. Symbiosis with an endobacterium increases the fitness of a mycorrhizal fungus, raising its bioenergetic potential. 2016Jan; 10(1):130–144. https://doi.org/10.1038/ismej.2015.91Search in Google Scholar
Santos-Beneit F. The Pho regulon: a huge regulatory network in bacteria. Front Microbiol. 2015 Apr;6:402. https://doi.org/10.3389/fmicb.2015.00402Santos-BeneitF. The Pho regulon: a huge regulatory network in bacteria. 2015Apr;6:402. https://doi.org/10.3389/fmicb.2015.00402Search in Google Scholar
Sarsaiya S, Shi J, Chen J. A comprehensive review on fungal endophytes and its dynamics on Orchidaceae plants: current research, challenges, and future possibilities. Bioengineered. 2019 Dec; 10(1): 316–334. https://doi.org/10.1080/21655979.2019.1644854SarsaiyaSShiJChenJ. A comprehensive review on fungal endophytes and its dynamics on Orchidaceae plants: current research, challenges, and future possibilities. 2019Dec; 10(1): 316–334. https://doi.org/10.1080/21655979.2019.1644854Search in Google Scholar
Seemann T. Prokka: rapid prokaryotic genome annotation. Bioinformatics. 2014 Jul;30(14):2068–2069. https://doi.org/10.1093/bioinformatics/btu153SeemannT. Prokka: rapid prokaryotic genome annotation. 2014Jul; 30(14):2068–2069. https://doi.org/10.1093/bioinformatics/btu153Search in Google Scholar
Shaffer JP, Sarmiento C, Zalamea PC, Gallery RE, Davis AS, Baltrus DA, Arnold AE. Diversity, specificity, and phylogenetic relationships of endohyphal bacteria in fungi that inhabit tropical seeds and leaves. Front Ecol Evol. 2016 Oct;4:116. https://doi.org/10.3389/fevo.2016.00116ShafferJPSarmientoCZalameaPCGalleryREDavisASBaltrusDAArnoldAE. Diversity, specificity, and phylogenetic relationships of endohyphal bacteria in fungi that inhabit tropical seeds and leaves. 2016Oct;4:116. https://doi.org/10.3389/fevo.2016.00116Search in Google Scholar
Shaffer JP, U’Ren JM, Gallery RE, Baltrus DA, Arnold AE. An endohyphal bacterium (Chitinophaga, Bacteroidetes) alters carbon source use by Fusarium keratoplasticum (F. solani species complex, Nectriaceae). Front Microbiol. 2017 Mar 14;8:350. https://doi.org/10.3389/fmicb.2017.00350ShafferJPU’RenJMGalleryREBaltrusDAArnoldAE. An endohyphal bacterium (Chitinophaga, Bacteroidetes) alters carbon source use by Fusarium keratoplasticum (F. solani species complex, Nectriaceae). 2017Mar14;8:350. https://doi.org/10.3389/fmicb.2017.00350Search in Google Scholar
Shie PH, Huang SS, Deng JS, Huang GJ.Spiranthes sinensis suppresses production of pro-inflammatory mediators by down-regulating the NF-κB signaling pathway and up-regulating HO-1/Nrf2 anti-oxidant protein. Am J Chin Med. 2015;43(5):969–989. https://doi.org/10.1142/S0192415X15500561ShiePHHuangSSDengJSHuangGJ. Spiranthes sinensis suppresses production of pro-inflammatory mediators by down-regulating the NF-κB signaling pathway and up-regulating HO-1/Nrf2 anti-oxidant protein. 2015;43(5):969–989. https://doi.org/10.1142/S0192415X15500561Search in Google Scholar
Singh P, Singh RK, Guo DJ, Sharma A, Singh RN, Li DP, Malviya MK, Song XP, Lakshmanan P, Yang LT, et al. Whole Genome analysis of sugarcane root-associated endophyte Pseudomonas aeruginosa B18-A plant growth-promoting bacterium with antagonistic potential against Sporisorium scitamineum. Front Microbiol. 2021 Feb;12:628376. https://doi.org/10.3389/fmicb.2021.628376SinghPSinghRKGuoDJSharmaASinghRNLiDPMalviyaMKSongXPLakshmananPYangLTWhole Genome analysis of sugarcane root-associated endophyte Pseudomonas aeruginosa B18-A plant growth-promoting bacterium with antagonistic potential against Sporisorium scitamineum. 2021Feb;12:628376. https://doi.org/10.3389/fmicb.2021.628376Search in Google Scholar
Stenglein SA, Balatti PA. Genetic diversity of Phaeoisariopsis griseola in Argentina as revealed by pathogenic and molecular markers. Physiol Mol Plant Pathol. 2006 Apr–Jun;68(4–6):158–167. https://doi.org/10.1016/j.pmpp.2006.10.001StengleinSABalattiPA. Genetic diversity of Phaeoisariopsis griseola in Argentina as revealed by pathogenic and molecular markers. 2006Apr–Jun;68(4–6):158–167. https://doi.org/10.1016/j.pmpp.2006.10.001Search in Google Scholar
Tian F, Liao XF, Wang LH, Bai XX, Yang YB, Luo ZQ, Yan FX. Isolation and identification of beneficial orchid mycorrhizal fungi in Paphiopedilum barbigerum (Orchidaceae). Plant Signal Behav. 2022 Dec;17(1):2005882. https://doi.org/10.1080/15592324.2021.2005882TianFLiaoXFWangLHBaiXXYangYBLuoZQYanFX. Isolation and identification of beneficial orchid mycorrhizal fungi in Paphiopedilum barbigerum (Orchidaceae). 2022Dec; 17(1):2005882. https://doi.org/10.1080/15592324.2021.2005882Search in Google Scholar
Wang T, Chi M, Guo L, Liu D, Yang Y, Zhang Y. The diversity of root-associated endophytic fungi from four epiphytic orchids in China. Diversity. 2021 Apr;13(5):197. https://doi.org/10.3390/d13050197WangTChiMGuoLLiuDYangYZhangY. The diversity of root-associated endophytic fungi from four epiphytic orchids in China. 2021Apr; 13(5):197. https://doi.org/10.3390/d13050197Search in Google Scholar
Xie J, Shi H, Du Z, Wang T, Liu X, Chen S. Comparative genomic and functional analysis reveal conservation of plant growth promoting traits in Paenibacillus polymyxa and its closely related species. Sci Rep. 2016 Feb;6:21329. https://doi.org/10.1038/srep21329XieJShiHDuZWangTLiuXChenS. Comparative genomic and functional analysis reveal conservation of plant growth promoting traits in Paenibacillus polymyxa and its closely related species. 2016Feb;6:21329. https://doi.org/10.1038/srep21329Search in Google Scholar
Zettler LW, Corey LL. Orchid mycorrhizal fungi: isolation and identification techniques. In: Lee YI, Yeung ET, editors. Orchid propagation: From laboratories to greenhouses – methods and protocols. New York (USA): Humana Press; 2018. p. 27–59. https://doi.org/10.1007/978-1-4939-7771-0_2ZettlerLWCoreyLL. Orchid mycorrhizal fungi: isolation and identification techniques. In: LeeYIYeungETeditors. . New York (USA): Humana Press; 2018. p. 27–59. https://doi.org/10.1007/978-1-4939-7771-0_2Search in Google Scholar
Zhao DK, Selosse MA, Wu L, Luo Y, Shao SC, Ruan YL. Orchid reintroduction based on seed germination-promoting mycorrhizal fungi derived from protocorms or seedlings. Front Plant Sci. 2021 Jun;12:701152. https://doi.org/10.3389/fpls.2021.701152ZhaoDKSelosseMAWuLLuoYShaoSCRuanYL. Orchid reintroduction based on seed germination-promoting mycorrhizal fungi derived from protocorms or seedlings. 2021Jun;12:701152. https://doi.org/10.3389/fpls.2021.701152Search in Google Scholar