Article (Scientific journals)
Real-time PCR to quantify composition of arbuscular mycorrhizal fungal communities--marker design, verification, calibration and field validation.
Thonar, Cécile; Erb, A; Jansa, J
2012In Molecular Ecology Resources, 12 (2), p. 219 - 232
Peer Reviewed verified by ORBi
 

Files


Full Text
Thonar2012.pdf
Author postprint (465.59 kB)
Download

All documents in ORBi are protected by a user license.

Send to



Details



Keywords :
DNA Primers; DNA, Fungal; Calibration; DNA Primers/genetics; DNA, Fungal/genetics; Fungi/classification; Fungi/genetics; Fungi/isolation & purification; Molecular Sequence Data; Mycorrhizae/classification; Mycorrhizae/genetics; Mycorrhizae/isolation & purification; Phylogeny; Real-Time Polymerase Chain Reaction/methods; Real-Time Polymerase Chain Reaction/standards; Soil Microbiology; Field validation; Marker design; Nuclear large ribosomal subunit (nLSU, 28S); Specificity; Taxon-specific sequence motifs; Biotechnology; Ecology, Evolution, Behavior and Systematics; Genetics
Abstract :
[en] Quantitative real-time PCR (qPCR) is slowly becoming established as a tool to quantify abundance of different arbuscular mycorrhizal fungal (AMF) taxa in roots and in soil. Here, we describe the development and field validation of qPCR markers (i.e. primers with associated hydrolysis probes), targeting taxon-specific motifs in the nuclear large ribosomal subunit RNA genes. Design of such markers is complicated by the multinuclear and multigenomic cellular organization of these fungi and the high DNA sequence diversity within the smallest biologically relevant units (i.e. single-spore isolates). These limitations are further compounded by inefficient biomass production of these fungi, resulting in limited availability of pure genomic DNA (gDNA) of well-defined isolates for cross-specificity testing of the markers. Here we demonstrate, using a number of AMF isolates, the possibility to establish stringent qPCR running conditions allowing quantification of phylogenetically disjunctive AMF taxa. Further, we show that these markers can more generally be used to quantify abundance (i.e. number of target gene copies or amount of gDNA) of what is usually considered the level of AMF species, regardless of the isolate identities. We also illustrate the range of variation within qPCR signal strength across different AMF taxa with respect to the detected number of gene copies per unit amount of gDNA. This information is paramount for interpretation of the qPCR analyses of field samples. Finally, the field validation of these markers confirmed their potential to assess composition of field AMF communities and monitor the changes owing to agricultural practices such as soil tillage.
Disciplines :
Agriculture & agronomy
Phytobiology (plant sciences, forestry, mycology...)
Author, co-author :
Thonar, Cécile  ;  Université de Liège - ULiège > Département GxABT > Plant Sciences ; ETH Zürich, Institute of Agricultural Sciences, Eschikon 33, 8315 Lindau, Switzerland FiBL, Research Institute for Organic Agriculture, Ackerstrasse 1, 5070 Frick, Switzerland. cecile.thonar@fibl.org
Erb, A;  ETH Zürich, Institute of Agricultural Sciences, 8315 Lindau, Switzerland
Jansa, J;  ETH Zürich, Institute of Agricultural Sciences, 8315 Lindau, Switzerland
Language :
English
Title :
Real-time PCR to quantify composition of arbuscular mycorrhizal fungal communities--marker design, verification, calibration and field validation.
Publication date :
March 2012
Journal title :
Molecular Ecology Resources
ISSN :
1755-098X
eISSN :
1755-0998
Publisher :
Wiley, England
Volume :
12
Issue :
2
Pages :
219 - 232
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 14 March 2023

Statistics


Number of views
30 (0 by ULiège)
Number of downloads
80 (0 by ULiège)

Scopus citations®
 
106
Scopus citations®
without self-citations
64
OpenCitations
 
97

Bibliography


Similar publications



Contact ORBi