Molecular diagnostic toolkit for Rhizophagus irregularis isolate DAOM-197198 using quantitative PCR assay targeting the mitochondrial genome

• Published in: Mycorrhiza 2016-10, Vol.26 (7), p.721-733
• Main Authors: Badri, Amine, Stefani, Franck O. P., Lachance, Geneviève, Roy-Arcand, Line, Beaudet, Denis, Vialle, Agathe, Hijri, Mohamed
• Format: Article
• Language: English
• Subjects: Agriculture; Biofertilizers; Biomedical and Life Sciences; DNA, Fungal - genetics; Ecology; Forestry; Genetic Markers; Genome, Fungal - genetics; Genome, Mitochondrial - genetics; Glomeromycota - genetics; Glomus; Life Sciences; Microbiology; Mycorrhizae - genetics; Original Article; Plant Sciences; Quality control; Real-Time Polymerase Chain Reaction - methods; Research institutions; Rhizophagus; Taxa
• ISSN: 0940-6360; 1432-1890
• DOI: 10.1007/s00572-016-0708-1

Rhizophagus irregularis (previously named Glomus irregulare ) is one of the most widespread and common arbuscular mycorrhizal fungal (AMF) species. It has been recovered worldwide in agricultural and natural soils, and the isolate DAOM-197198 has been utilized as a commercial inoculant for two decades. Despite the ecological and economical importance of this taxon, specific markers for quantification of propagules by quantitative real-time PCR (qPCR) are extremely limited and none have been rigorously validated for quality control of manufactured products such as biofertilizers. From the sequencing of 14 complete AMF mitochondrial (mt) genomes, a qPCR assay using a hydrolysis probe designed in the single copy cox3-rnl intergenic region was tested and validated to specifically and accurately quantify the spores of R. irregularis isolate DAOM-197198. Specificity tests were performed using standard PCR and qPCR, and results clearly showed that the primers specifically amplified the isolate DAOM-197198, yielding a PCR product of 106 bp. According to the qPCR analyses on spores produced in vitro, the average copy number of mt genomes per spore was 3172 ± 304 SE ( n  = 6). Quantification assays were successfully undertaken on known and unknown samples in liquid suspensions and commercial dry formulations to show the accuracy, precision, robustness, and reproducibility of the qPCR assay. This study provides a powerful molecular toolkit specifically designed to quantify spores of the model AMF isolate DAOM-197198. The approach of molecular toolkit used in our study could be applied to other AMF taxa and will be useful to research institutions and governmental and industrial laboratories running routine quality control of AMF-based products.