Development of a multiplex Q-PCR to detect Trichoderma harzianum Rifai strain T22 in plant roots

• Published in: Journal of microbiological methods 2016-02, Vol.121, p.44-49
• Main Authors: Horn, Ivo R., van Rijn, Menno, Zwetsloot, Tom J.J., Basmagi, Said, Dirks-Mulder, Anita, van Leeuwen, Willem B., Ravensberg, Willem J., Gravendeel, Barbara
• Format: Article
• Language: English
• Subjects: aox1; Base Sequence; Biological control agent; DNA, Fungal - analysis; DNA, Fungal - genetics; Genes, Fungal; Hydrolysis probes; Lycopersicon esculentum; Lycopersicon esculentum - microbiology; Molecular Sequence Data; Multiplex Polymerase Chain Reaction - methods; Mycological Typing Techniques - economics; Mycological Typing Techniques - methods; Plant roots; Plant Roots - microbiology; Q-PCR; Soil Microbiology; Symbiosis; Trichoderma; Trichoderma - genetics; Trichoderma - isolation & purification
• ISSN: 0167-7012; 1872-8359
• DOI: 10.1016/j.mimet.2015.12.014

The fungal species Trichoderma harzianum is widely used as a biological agent in crop protection. To verify the continued presence of this fungus on plant roots manually inoculated with T. harzianum strain T22, a Q-PCR was designed using specific probes for this particular strain. To develop these molecular diagnostic tools, genome mining was first carried out to retrieve putative new regions by which different strains of T. harzianum could be distinguished. Subsequently, Sanger sequencing of the L-aminoacid oxidase gene (aox1) in T. harzianum was applied to determine the mutations differing between various strains isolated from the Trichoderma collection of Koppert Biological Systems. Based on the sequence information obtained, a set of hydrolysis probes was subsequently developed which discriminated T. harzianum T22 strains varying in only a single nucleotide. Probes designed for two strains uniquely recognized the respective strains in Q-PCR with a detection limit of 12,5ng DNA. Titration assays in which T. harzianum DNA from distinct strains was varied further underscored the specificity of the probes. Lastly, fungal DNA extracted from roots of greenhouse cultured tomato plants was analyzed using the probe-based assay. DNA from T. harzianum strain T22 could readily be identified on roots of greenhouse reared tomato plants inoculated with varying concentrations up to one week after treatment with a detection limit of 3e6 colony forming units of T. harzianum T22. We conclude that the Q-PCR method is a reliable and robust method for assessing the presence and quantity of T. harzianum strain T22 in manually inoculated plant material. Our method provides scope for the development of DNA based strain specific identification of additional strains of Trichoderma and other fungal biological control agents. [Display omitted] •Tomato roots were inoculated manually with Trichoderma harzianum strain T22.•A multiplex Q-PCR detection method was developed for strain T22.•Both the presence and quantity of T. harzianum strain T22 could be assessed.•This method enables cost effective treatment of plants in greenhouses with biological control agents.