2013
DOI: 10.1007/s10531-013-0527-z
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Land use and host neighbor identity effects on arbuscular mycorrhizal fungal community composition in focal plant rhizosphere

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Cited by 41 publications
(24 citation statements)
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“…A semi-nested PCR protocol was used to amplify the %630 bp-long small subunit (SSU) region of the AMF 18S rDNA via pyrosequencing analysis (454 GS-FLX, Roche). In the first PCR run (PCRI) a Glomeromycota-specific region was amplified with the primer set GLOMERWT0/GLOMER1536 (Wubet et al, 2006), followed by the semi-nested second PCR reaction with the forward general fungal primer NS31 (Simon et al, 1992) including the A adaptor and a 10 bp multiplex identifier (1 of 60 different MIDs), and the B adaptor including the reverse modified AMF primer AM1a and AM1b (Morris et al, 2013). The first PCR was carried out at a 25 μl reaction volume with 0.5 μl of diluted DNA template (5-20 ng μl −1 ), 12.5 μl GoTaq Green Mastermix 2× (Promega, Mannheim, Germany), 1 μl of each primer (25 μM) on an Eppendorf Mastercycler DNA Engine Thermal Cycler PCR (Eppendorf, Hamburg, Germany) with the following PCR conditions: 98 C for 30 s, 5 cycles of 94 C for 30 s, 60 C (−1 C/cycle, 4 cycles) for 30 s, 72 C for 1 min and 25 cycles of 94 C for 30 s, 55 C for 30 s, 72 C for 1 min, and for extension 72 C for 5 min.…”
Section: Dna Extraction and Pyrosequencing Of Amf Ampliconsmentioning
confidence: 99%
“…A semi-nested PCR protocol was used to amplify the %630 bp-long small subunit (SSU) region of the AMF 18S rDNA via pyrosequencing analysis (454 GS-FLX, Roche). In the first PCR run (PCRI) a Glomeromycota-specific region was amplified with the primer set GLOMERWT0/GLOMER1536 (Wubet et al, 2006), followed by the semi-nested second PCR reaction with the forward general fungal primer NS31 (Simon et al, 1992) including the A adaptor and a 10 bp multiplex identifier (1 of 60 different MIDs), and the B adaptor including the reverse modified AMF primer AM1a and AM1b (Morris et al, 2013). The first PCR was carried out at a 25 μl reaction volume with 0.5 μl of diluted DNA template (5-20 ng μl −1 ), 12.5 μl GoTaq Green Mastermix 2× (Promega, Mannheim, Germany), 1 μl of each primer (25 μM) on an Eppendorf Mastercycler DNA Engine Thermal Cycler PCR (Eppendorf, Hamburg, Germany) with the following PCR conditions: 98 C for 30 s, 5 cycles of 94 C for 30 s, 60 C (−1 C/cycle, 4 cycles) for 30 s, 72 C for 1 min and 25 cycles of 94 C for 30 s, 55 C for 30 s, 72 C for 1 min, and for extension 72 C for 5 min.…”
Section: Dna Extraction and Pyrosequencing Of Amf Ampliconsmentioning
confidence: 99%
“…In a study on Arbuscular Mycorrhizal Fungi (AMF), effects of land use, host plant neighbourhood and spatial arrangement on the AMF composition was tested over 67 grassland plots spread across the three German Biodiversity Exploratories (Morris et al 2013). The authors show that the diversity of AMF react similar sensitive at both, large-and small scales; for example, the ability of AMF to provide protection from pathogens declined under high land-use intensity (Morris et al 2013). …”
Section: Effects Of Abiotic and Biotic Factors On Species Diversitymentioning
confidence: 99%
“…we would expect a similar pattern for phyllosphere bacterial communities, becoming more dissimilar with 40 increasing geographic distances between sites. Furthermore, it has to be considered that anthropogenic 41 influences on intensities of land use management types like fertilization, grazing and mowing can have 42 strong effects on soil properties and on plant pheno-and chemotypic characteristics, and therefore may 43 also shape flower and leaf microbiomes (Estendorfer et al, 2017; Li et al, 2018; E. K. Morris et al, 2013; were constructed and differences in relative abundance between groups were tested with t-tests. To 140 identify chosen individual ASVs at the species level, 16S rDNA sequences were compared with available 141 rDNA sequences in GenBank, using the NCBI BLASTN program (Zhang et al, 2000).…”
mentioning
confidence: 99%