A Ready-to-Use Single- and Duplex-TaqMan-qPCR Assay to Detect and Quantify the Biocontrol Agents Trichoderma asperellum and Trichoderma gamsii
Author(s) -
Donato Gerin,
Stefania Pollastro,
Celeste Raguseo,
Rita Milvia De Miccolis Angelini,
F. Faretra
Publication year - 2018
Publication title -
frontiers in microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.701
H-Index - 135
ISSN - 1664-302X
DOI - 10.3389/fmicb.2018.02073
Subject(s) - biology , biological pest control , trichoderma , taqman , conidium , microbiology and biotechnology , real time polymerase chain reaction , horticulture , botany , gene , biochemistry
Trichoderma asperellum strain icc012 and Trichoderma gamsii strain icc080, the microbial active ingredients of Remedier TM (ISAGRO, Novara, Italy), are biocontrol agents (BCAs) employable for crop protection against a wide range of fungal pathogens, including soil-borne pathogens and fungi involved in grapevine trunk disease. In this study, single and duplex real-time quantitative PCR (qPCR) methods to detect and quantify T. asperellum and T. gamsii were developed. Primers/probe sets were designed on the T. asperellum and T. gamsii rpb2 genes and tested for specificity on a panel of microorganisms commonly associated with grape wood and soil. No differences were observed comparing single- and duplex-qPCR assays on different BCAs, 1 pg of target DNA was detected approximately at C q = 34. R 2 -values and the efficiency were always equal to 0.99 and >80%, respectively. The detection limit of the duplex-qPCR assay on artificially inoculated samples was 2 × 10 3 and 4 × 10 4 conidia g -1 of grape wood tissue and soil, respectively. The methods will be useful to better schedule BCA application in the field and in grapevine nurseries, as well as for investigating the dynamic of BCA populations.
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