Foliar Endophytic Fungi Inhabiting an Annual Grass Along an Aridity Gradient.
Journal
Current microbiology
ISSN: 1432-0991
Titre abrégé: Curr Microbiol
Pays: United States
ID NLM: 7808448
Informations de publication
Date de publication:
May 2021
May 2021
Historique:
received:
14
05
2020
accepted:
01
03
2021
pubmed:
26
3
2021
medline:
15
5
2021
entrez:
25
3
2021
Statut:
ppublish
Résumé
Mutualistic fungi are known to increase plant tolerance to abiotic and biotic stress. Therefore, it is expected that along aridity gradients the diversity and composition of symbiotic fungal community will be associated with climate. We examined the diversity of foliar endophytic fungi, inhabiting an annual grass, growing in three different climates (arid, Mediterranean, and wet Mediterranean) along the Israeli aridity gradient. Among the identified endophyte taxa, some were unique to each site, some were common to the two sites located in the extremes of the gradient, but none was common to all sites. Although most fungal endophyte taxa identified were not related to stress adaptation, we detected two that are considered to benefit plants by mitigating stress: Cladosporium and Trichoderma. Cladosporium is highly osmotolerant, frequently found in saline environments. Trichoderma is a biocontrol agent, frequently found in mesic environments. These findings support the hypothesis that species composition of foliar endophytic fungi is associated with stress adaptation of plants.
Identifiants
pubmed: 33765191
doi: 10.1007/s00284-021-02437-5
pii: 10.1007/s00284-021-02437-5
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2080-2090Références
Rodriguez RJ, White JF Jr, Arnold AE, Redman RS (2008) Fungal endophytes: diversity and functional roles. New Phytol 182(2):314–330
doi: 10.1111/j.1469-8137.2009.02773.x
Ofek-Lalzar M, Gur Y, Ben-Moshe S, Sharon O, Kosman E, Mochli E, Sharon A (2016) Diversity of fungal endophytes in recent and ancient wheat ancestors Triticum dicoccoides and Aegilops sharonensis. FEMS Microbiol Ecol 92:1–11
doi: 10.1093/femsec/fiw152
Sadeghi F, Samsampour D, Seyahooei MA, Bagheri A, Soltani J (2019) Diversity and spatiotemporal distribution of fungal endophytes associated with Citrus reticulata cv Siyahoo. Curr Microbiol 76:279–289
doi: 10.1007/s00284-019-01632-9
Gagné-Bourque F, Mayer BF, Charron J-B, Vali H, Bertrand A, Jabaji S (2015) Accelerated growth rate and increased drought stress resilience of the model grass Brachypodium distachyon colonized by Bacillus subtilis B26. PLoS One 10(6):e0130456
doi: 10.1371/journal.pone.0130456
Kigel J, Konsens I, Rosen N, Rotem G, Kon A, Fragman-Sapir O (2011) Relationships between flowering time and rainfall gradients across Mediterranean-desert transects. Israel J Ecol Evol 57:91–109
doi: 10.1560/IJEE.57.1-2.91
Black E, Brayshaw DJ, Rambeau CMC (2010) Past, present and future precipitation in the Middle East: insights from models and observations. Philos Trans Royal Soc A Math Phys Eng Sci 368:5173–5184
doi: 10.1098/rsta.2010.0199
Penner S, Dror B, Aviezer I, Bar-Lev Y, Salman-Minkov A, Mandakova T, Šmarda P, Mayrose I, Sapir Y (2019) Phenology and polyploidy in annual Brachypodium species (Poaceae) along the aridity gradient in Israel. J Syst Evol 58:189–199
doi: 10.1111/jse.12489
Rysavy A, Seifan M, Sternberg M, Tielbörger K (2014) Shrub seedling survival under climate change–comparing natural and experimental rainfall gradients. J Arid Environ 111:14–21
doi: 10.1016/j.jaridenv.2014.07.004
Mur LAJ, Allainguillaume J, Catalán P, Hasterok R, Jenkins G, Lesniewska K, Thomas I, Vogel J (2011) Exploiting the Brachypodium tool box in cereal and grass research. New Phytol 191(2):334–347
doi: 10.1111/j.1469-8137.2011.03748.x
Cenis JL (1992) Rapid extraction of fungal DNA for PCR amplification. Nucleic Acids Res 20:2380
doi: 10.1093/nar/20.9.2380
Drori M, Rice A, Einhorn M, Chay O, Glick L, Mayrose I (2018) OneTwoTree: An online tool for phylogeny reconstruction. Mol Ecol Resour, 1–8.
Heberle H, Meirelles GV, da Silva FR, Telles GP, Minghim R (2015) InteractiVenn: a web-based tool for the analysis of sets through Venn diagrams. BMC Bioinformatics 16:169
doi: 10.1186/s12859-015-0611-3
Wang M, Liu F, Crous PW, Cai L (2017) Phylogenetic reassessment of Nigrospora: ubiquitous endophytes, plant and human pathogens. Persoonia 39:118–142
doi: 10.3767/persoonia.2017.39.06
Yagame T, Funabiki E, Nagasawa E, Fukiharu T, Iwase K (2013) Identification and symbiotic ability of Psathyrellaceae fungi isolated from a photosynthetic orchid, Cremastra appendiculata (Orchidaceae). Am J Bot 100:1823–1830
doi: 10.3732/ajb.1300099
Harman GE, Howell CR, Viterbo A, Chet I, Lorito M (2004) Trichoderma species—opportunistic, avirulent plant symbionts. Nat Rev Microbiol 2(1):43–56
doi: 10.1038/nrmicro797
Kendrick B, Risk MJ, Michaelides J, Bergman K (1982) Amphibious microborers: bioeroding fungi isolated from live corals. Bull Mar Sci 32(4):862–867
Samson RA, Visagie CM, Houbraken J, Hong SB, Hubka V, Klaassen CHW, Perrone G, Seifert KA, Susca A, Tanney JB et al (2014) Phylogeny, identification and nomenclature of the genus Aspergillus. Stud Mycol 78:141–173
doi: 10.1016/j.simyco.2014.07.004
Woudenberg JHC, Groenewald JZ, Binder M, Crous PW (2013) Alternaria redefined. Stud Mycol 75:171–212
doi: 10.3114/sim0015
Väre H, Vestberg M, Eurola S (1992) Mycorrhiza and root-associated fungi in Spitsbergen. Mycorrhiza 1(3):93–104
doi: 10.1007/BF00203256
Stchigel AM, Calduch M, Guarro J, Zaror L (2002) A new species of Podospora from soil in Chile. Mycologia 94(3):554–558
doi: 10.1080/15572536.2003.11833221
Syvertsen JP, Garcia-Sanchez F (2014) Multiple abiotic stresses occurring with salinity stress in citrus. Environ Exp Bot 103:128–137
doi: 10.1016/j.envexpbot.2013.09.015
Leuchtmann A, Schardl CL (1998) Mating compatibility and phylogenetic relationships among two new species of Epichloë and other congeneric European species. Mycol Res 102(10):1169–1182
doi: 10.1017/S0953756298006236
Wang XW, Houbraken J, Groenewald JZ, Meijer M, Andersen B, Nielsen KF, Crous PW, Samson RA (2016) Diversity and taxonomy of Chaetomium and chaetomium-like fungi from indoor environments. Stud Mycol 84:145–224
doi: 10.1016/j.simyco.2016.11.005
Ariyawansa HA, Kang JC, Alias SA, Chukeatirote E, and Hyde KD (2014) Pyrenophora Mycosphere 5: 351–362
Câmara MPS, O’Neill NR, van Berkum P (2002) Phylogeny of Stemphylium spp. based on ITS and glyceraldehyde-3-phosphate dehydrogenase gene sequences. Mycologia 94(4):660–672
doi: 10.1080/15572536.2003.11833194
Manamgoda DS, Rossman AY, Castlebury LA, Crous PW, Madrid H, Chukeatirote E, Hyde KD (2014) The genus Bipolaris. Stud Mycol 79:221–288
doi: 10.1016/j.simyco.2014.10.002
Inui T, Takeda Y, Iizuka H (1965) Taxonomical studies on genus Rhizopus. J Gen Appl Microbiol 11:1–121
doi: 10.2323/jgam.11.Supplement_1
Giraldo A, Gené J, Sutton DA, Madrid H, De Hoog GS, Cano J, Guarro J (2015) Phylogeny of Sarocladium (Hypocreales). Persoonia Mol Phylogeny Evol Fungi 34:10
doi: 10.3767/003158515X685364
Goh YK, Vujanovic V (2010) Sphaerodes quadrangularis biotrophic mycoparasitism on Fusarium avenaceum. Mycologia 102(4):757–762
doi: 10.3852/09-171
McTaggart AR, Shivas RG, Boekhout T, Oberwinkler F, Vánky K, Pennycook SR, Begerow D (2016) Mycosarcoma (Ustilaginaceae), a resurrected generic name for corn smut (Ustilago maydis) and its close relatives with hypertrophied, tubular sori. IMA Fungus 7(2):309–315
doi: 10.5598/imafungus.2016.07.02.10