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DNA-based species level detection of Glomeromycota: one PCR primer set for all arbuscular mycorrhizal fungi
被引:335
作者:
Krueger, Manuela
[1
]
Stockinger, Herbert
[1
]
Krueger, Claudia
[1
]
Schuessler, Arthur
[1
]
机构:
[1] Univ Munich, Dept Biol 1, D-82152 Planegg Martinsried, Germany
关键词:
arbuscular mycorrhizal fungi (AMF);
DNA barcoding;
ITS region;
LSU rRNA gene;
molecular community analyses;
rDNA;
species level resolution;
specific primers;
RIBOSOMAL-RNA GENE;
MOLECULAR DIVERSITY;
GLOMUS-INTRARADICES;
COMMUNITY STRUCTURE;
NESTED PCR;
ROOTS;
IDENTIFICATION;
AMPLIFICATION;
SEQUENCES;
PHYLOGENY;
D O I:
10.1111/j.1469-8137.2009.02835.x
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
At present, molecular ecological studies of arbuscular mycorrhizal fungi (AMF) are only possible above species level when targeting entire communities. To improve molecular species characterization and to allow species level community analyses in the field, a set of newly designed AMF specific PCR primers was successfully tested. Nuclear rDNA fragments from diverse phylogenetic AMF lineages were sequenced and analysed to design four primer mixtures, each targeting one binding site in the small subunit (SSU) or large subunit (LSU) rDNA. To allow species resolution, they span a fragment covering the partial SSU, whole internal transcribed spacer (ITS) rDNA region and partial LSU. The new primers are suitable for specifically amplifying AMF rDNA from material that may be contaminated by other organisms (e.g., samples from pot cultures or the field), characterizing the diversity of AMF species from field samples, and amplifying a SSU-ITS-LSU fragment that allows phylogenetic analyses with species level resolution. The PCR primers can be used to monitor entire AMF field communities, based on a single rDNA marker region. Their application will improve the base for deep sequencing approaches; moreover, they can be efficiently used as DNA barcoding primers. New Phytologist (2009) 183: 212-223doi: 10.1111/j.1469-8137.2009.02835.x.
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页码:212 / 223
页数:12
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