- Original article
- Open Access
Two-step genomic sequence comparison strategy to design Trichoderma strain-specific primers for quantitative PCR
AMB Express volume 9, Article number: 179 (2019)
Survival of inoculated fungal strains in a new environment plays a critical role in functional performance, but few studies have focused on strain-specific quantitative PCR (qPCR) methods for monitoring beneficial fungi. In this study, the Trichoderma guizhouense strain NJAU 4742 (transformed with the gfp gene and named gfp-NJAU 4742), which exhibits a growth-promoting effect by means of phytohormone production and pathogen antagonism, was selected as a model to design strain-specific primer pairs using two steps of genomic sequence comparison to detect its abundance in soil. After a second comparison with the closely related species T. harzianum CBS 226-95 to further differentiate the strain-specific fragments that had shown no homology to any sequence deposited in the databases used in the first comparison, ten primer pairs were designed from the whole genome. Meanwhile, 3 primer pairs, P11, P12 and P13, were also designed from the inserted fragment containing the gfp gene. After verification testing with three types of field soils, primer pairs P6, P7 and P8 were further selected by comparison with P11, P12 and P13. A practical test using a pot experiment showed that stable colonization of gfp-NJAU 4742 in pepper rhizosphere soil could be detected using primer pairs P6 and P7, showing no significant difference from the results of primers P11 and P12. Hence, the strategy described here for designing fungal-strain-specific primers may theoretically be used for any other fungi for which the whole genome sequence is available in a database, and the qPCR methodology developed can also be used to further monitor the population dynamics of different strains based on the designed primers.
Fungal species of the genus Trichoderma are widespread in soils and considered to be an ideal biocontrol agent, with specific biocontrol mechanisms including mycoparasitism, production of antibiotics, competition and induced resistance (Harman et al. 2004; Shoresh et al. 2010). Meanwhile, some Trichoderma strains with rhizosphere colonization deliver direct or indirect plant growth promotion benefits via enhancing nutrient uptake, as well as stimulating plant defence against biotic and abiotic damage (Martínezmedina et al. 2014; Trillas and Segarra 2009). In the past dozen years, to gain beneficial effects on a target plant, numerous studies have introduced different Trichoderma agents in large numbers by direct inoculation into soil or as soil amendments combined with organic fertilizers (Bal and Alti̇Ntas 2008; Haque et al. 2012; Puttanna et al. 2010). The survival of the inoculated strains in a new environment (Zhang et al. 2015, 2017), however, does play a critical role in functional performance, since effective colonization is necessary for the successful stimulation of plant growth or the soil microbial ecosystem by the target strain. In addition, in certain areas, such as Europe, a risk assessment for the biocontrol agent focusing on the persistence and multiplication of the inoculant in the environment is required (Savazzini et al. 2008). Thus, the lack of an effective, economical, fast and accurate quantitation strategy has obstructed the widespread application of beneficial fungi.
Selective medium has traditionally been utilized to detect or isolate beneficial probiotics in different environments (Azaizeh et al. 2003; Bashan and Gonzalez 1999), and one half-selective medium has also been developed for the isolation and quantification of the genus Trichoderma (Williams et al. 2003). However, the method has low sensitivity, requires the correct identification of conidia, cannot easily detect specific fungi that include morphologically similar strains, and is extremely time consuming (Ritz 2007). In addition, the current method cannot distinguish among different Trichoderma at the species level. Based on DNA analyses, quantitative PCR (qPCR), which can accurately quantify the abundance of numerous fungal species, is widely used for detecting different microbes (Atkins et al. 2003; Boyle et al. 2005) to investigate their ecology in soil and other environments, even at very low inoculation levels (Atkins et al. 2003; Bates et al. 2001; Böhm et al. 1999; Cullen et al. 2001; Renske et al. 2003; Winton et al. 2002). Primer sequences, in general, have been designed from regions of the genome with known or unknown functions (Carmen et al. 2007; Sarlin et al. 2006). For Trichoderma, detection and quantification have been performed in different soils based on a recognized genus-specific 600 bp internal transcribed spacer (ITS) region (Beaulieu et al. 2011; Hagn et al. 2007; López-Mondéjar et al. 2010); however, ITS, as a common region without enough specificity, cannot discriminate between different species, and sequence-characterized amplified region (SCAR) markers are mainly derived from randomly amplified polymorphic DNA (RAPD) analysis, leading to a long and laborious process to develop a specific SCAR marker.
Trichoderma guizhouense NJAU 4742, belonging to the Trichoderma harzianum species aggregate (Chenthamara et al. 2014; Zhang et al. 2016), is now commercialized in China and is widely used for the solid-state fermentation of commercial biological agents and the research and development of biological fertilizers (Patent Application Nos. 200910233576.1, CN201610003589.X and CN201610440785.3). A large number of previous studies have shown that this strain has a strong growth-promoting ability (Cai et al. 2013; Huang et al. 2011; Liu et al. 2017; Yang et al. 2011), as well as a variety of superior and advantageous genes, such as HFB7, a novel orphan hydrophobic protein, which is involved in response to biotic and abiotic stresses (Przylucka et al. 2017), and NMP1, a neutral metallopeptidase, required for mycotrophy and self-defence (Zhang et al. 2016). Therefore, it is particularly important to uncover the potential mechanisms underlying their use in agricultural practices.
In this study, the Trichoderma guizhouense strain NJAU 4742 transformed with the gfp gene and named gfp-NJAU 4742 was selected as a model to design strain-specific primer pairs using two stages of genomic sequence comparison to detect its abundance in soil. The sensitivity of the PCR assay was determined, and the PCR protocols were tested for their ability to detect strain gfp-NJAU 4742 in pepper rhizosphere soil and in soil samples collected in the field. It is hoped that the results will provide technical assistance to microbial ecology researchers of the species in the future and will be a reference for the quantitative study of other strains based on whole genome sequences.
Materials and methods
Trichoderma guizhouense NJAU 4742 wild (CGMCC accession No. 12166, China General Microbiology Culture Collection Center) and gfp-tagged (tagged with the gfp gene to express green fluorescent protein) transformed strains (gfp-NJAU 4742) were provided by the Jiangsu Provincial Key Laboratory of Organic Solid Waste Utilization, Nanjing, China. The mutation strain was labelled with the plasmid pCAMBIA-gfp (Additional file 1) in the wild-type strain, and the gfp sequence was fused with the hygromycin B resistance (hph) genewith the glyceraldehyde-3-phosphate dehydrogenase (gpdA) promoter from Aspergillus nidulans and the tryptophan C (trpC) transcription-termination signal (Additional file 1) (Zhang et al. 2016). Whole genome sequence of T. harzianum CBS 226-95 (sibling strain to NJAU 4742) was downloaded from the NCBI database, and T. harzianum CBS 226-95 was provided by Prof. Irina S. Druzhinina, Vienna University of Technology.
Primer pair design and evaluation of amplification efficiency
Strain-specific PCR primer were designed from the complete genome sequence of Trichoderma guizhouense strain NJAU 4742, which is available in NCBI GenBank with accession numbers of PRJNA314460. In brief, the complete genome sequence of T. guizhouense NJAU 4742 from the FASTA genome sequence was fragmented in silico using in-house scripts to produce non-overlapping fragments. For the first comparison, the fragments were subjected to a BLASTn search against the NCBI and Joint Genome Institute (JGI) databases, and four sequence fragments without any match in the two BLAST sequence analyses were obtained as putative strain-specific sequences (positions T37_S00003:2560926 to 2576741, T37_S00005:2001401 to 2006364, T37_S00007:2096560 to 2099766 and T37_S00017: 678513 to 681994) (Additional file 2: Table S1). Next, the genome sequence of T. harzianum CBS 226-95 (sibling strain to NJAU 4742) was used to build a local BLAST database, and putative strain-specific sequence fragments were used as queries for a BLASTn similarity search with default parameters for the second comparison; then, 10 specific primer pairs were designed (Table 1). Meanwhile, 3 primer pairs, Primer 11, Primer 12 and Primer 13 (the code “primer” is abbreviated as P, and the same is true below), were derived from the gfp fragment, the hygromycin fragment and a fragment including both gfp and hygromycin (Table 1 and Additional file 1). Because P11, P12 and P13 were designed from two fragments inserted in the whole genome with one copy (Zhang et al. 2016), the number of sequences detected was regarded as the standard amount and used as reference for the primers P1 to P10, which were designed from the genome sequence. The designed primer pairs were analysed using Oligo 6, synthesized by Nanjing GenScript Biotechnology Co., Ltd. (China) and qualitatively detected by conventional PCR. A pair of published primers for ITS1 (López-Mondéjar et al. 2010) was used as a positive amplification control (Table 1). Total DNA from fungal strains was extracted directly from 50 to 100 mg mycelia using the E.Z.N.A. Fungal RNA Kit (Omega Inc., USA).
Target plasmid construction and qPCR amplification
Thirteen fragments produced from the selected target genetic regions of the T. guizhouense gfp-NJAU 4742 and ITS1 primer pair were cloned into the pMD 19-T vector (TaKaRa). The plasmids were transformed into Escherichia coli TOP10 cells. The fragments in the plasmids were verified by a PCR test using the PMD-19T universal sequence primers M13-F (TGTAAAACGACGGCCAGT) and M13-R (CAGGAAACAGCTATGACC) and sequenced by Nanjing GenScript Biotechnology Co., Ltd. (China). The DNA concentration of the plasmid was measured using a spectrophotometer (NanoDrop 2000, Thermo Scientific Inc., USA). qPCR amplification was performed using gradient PCR analysis in a 20 μl reaction volume using SYBR®Premix Ex Taq™ (TaKaRa) on a 7500 Real-time PCR system (Applied Biosystems, USA) (Shen et al. 2017). The plasmids containing the different fragments were used to prepare tenfold dilution series (in triplicate). Sterile water was used as a negative control. The cycle threshold (CT) value was automatically determined for each sample. A standard curve was generated by plotting the CT value against the logarithm of the DNA concentration (data not shown) and used to calculate the amplification efficiency (E). Initial target gene copy numbers in unknown samples were calculated from the standard curves (all gene fragments are single copy).
Three soils with different physicochemical properties were collected from Hengxi, Nanjing (31° 43′ N, 118° 46′ E); Dafeng, Yancheng (32° 56′ N, 120° 13′ E); and Luquan, Kunming (25° 58′ N, 102° 45′ E), China. The soils were hand-picked to remove stones, larger plant residues and macroinvertebrates (earthworms, etc.) and then passed through a 2-mm sieve, slightly air-dried, and mixed thoroughly. The soil from Hengxi was characterized as yellow brown soil with a pH of 6.83, and it contained 2.19 mg kg−1 NH4–N, 15.5 mg kg−1 NO3–N, 120.01 mg kg−1 available P and 307.17 mg kg−1 available K; the soil from Dafeng was characterized as saline-alkali soil with a pH of 8.81, and it contained 7.72 mg kg−1 ammonium N, 24.34 mg kg−1 nitrate N, 2.36 mg kg−1 available P and 285.29 mg kg−1 available K; and the soil from Luquan was characterized as red soil with a pH of 5.0, and it contained 18.72 mg kg−1 ammonium N, 15.34 mg kg−1 nitrate N, 6.7 mg kg−1 available P and 42.6 mg kg−1 available K.
Inoculation of T. guizhouense NJAU 4742 into soils and qPCR assay
Spore suspensions of gfp-NJAU 4742 was prepared by flooding PDA medium plates containing 7-day-old cultures with sterile water and subsequently scraping with a sterile glass rod. The suspension was then filtered through a double layer of sterile cheesecloth. The conidial density of the suspension was assessed by counting on a haemocytometer. Soil samples of 20 g were loaded into 50-ml centrifuge tubes with six tubes for each soil (saline-alkali soil, red soil, and yellow brown soil), and the six tubes of each soil type were equally divided into the following one treatment and one control groups: the treatment was inoculated with 4 ml of gfp-NJAU 4742 spore suspension with concentration of approximately 106 conidia g−1 soil dry weight; and the control was combined with equal volumes of water. All soil samples were uniformly incubated in the dark for 7 days at 28 °C. Yellow brown soils inoculated with different gfp-NJAU 4742 spore concentrations of approximately 0, 103, 104, 105, 106, 107, and 108 conidia ml−1, respectively, were further examined to verify the specificity of the primer pairs. Each concentration was assessed in triplicate. Total soil genomic DNA was extracted from 0.5 g soil samples using the PowerSoil DNA Isolation Kit (MoBio) according to the prescribed protocol. The concentration and quality of the DNA were determined using a NanoDrop 2000 spectrophotometer (Thermo Scientific, Waltham, MA, USA).
Pot experiments and qPCR assay of strain NJAU 4742
The pepper pot experiment was performed in a greenhouse located in Huaian, China (32° 43′ N, 118° 12′ E), from April to June 2014. The pepper seedlings were cultivated in ordinary nursery substrate and bio-nursery substrate, respectively. Bio-nursery substrate was produced by adding gfp-NJAU 4742 to ordinary nursery substrate to obtain a spore concentration in the novel product of more than 107 conidia ml−1. The pot experiment included the following four treatments: (a) OF treatment, soil amended with chicken manure compost and transplanted pepper (Capsicum annuum L.) seedlings from ordinary nursery substrate. (b) OFBS treatment, soil amended with chicken manure compost and transplanted pepper seedlings cultured from bio-nursery substrate. (c) BF treatment, soil amended with chicken manure compost and fill the strain gfp-NJAU 4742 spore solution into bulk soil, the final spore concentration in the bulk soil was 106 conidia g−1 dry soil, and transplanted seedlings from ordinary nursery substrate. (d) BFBS treatment, soil amended with chicken manure compost and fill the strain gfp-NJAU 4742 spore solution into bulk soil, the final spore concentration in the bulk soil was 106 conidia g−1, and transplanted pepper seedlings cultured from bio-nursery substrate. Pepper seedlings or “bio-seedlings” were transferred into pots with 5 kg soil and supplemented with 1.5% (w/w DW) chicken manure compost fertilizer. Each treatment had ten random independent replications. The chicken manure compost was produced by Nantong Huinong Co. Ltd, Jiangsu, China by composting chicken manure at 30–70 °C for more than 20 days. Rhizosphere soil samples were obtained according to Bakker et al. (Bakker et al. 2015). Total numbers of gfp-NJAU 4742 were quantified by qPCR with primer pairs P6, P7, P11, and P12. Each sample was assessed in three replicates, and the results were expressed as lg (copies g−1) dry soil.
Statistical analysis was performed by using the IBM SPSS 18.0 software program (IBM Corporation, New York, USA). All statistical tests performed in this study were considered significant at P < 0.05. The data were subjected to analysis of variance (ANOVA) with means compared by the Tukey test.
Primer design and evaluation of amplification efficiency
The amplification of 14 cloned plasmids was tested using the PMD-19T universal sequence primer M13, and unique amplicons of the expected sizes were observed on agarose gel electrophoresis, indicating that all fragments produced from a total of 14 primer pairs, including ITS1, were successfully inserted (Additional file 3: Figure S1). The amplification efficiencies of all strain-specific primer pairs obtained in this study were tested by constructing a standard curve. The primer pairs P1, P2, P3, P4, P5 and P9 were excluded from further analysis because they showed low amplification efficiencies (data not shown). The standard curves obtained from primer pairs P6, P7, P8, P10, P11, P12, and P13 performed well, and their melting temperatures were approximately 76–83 °C with a single melting peak (Additional file 3: Figure S1). As expected, the melting curve obtained from primer ITS1 showed double peaks, suggesting that this primer is nonspecific in gfp-NJAU 4742 (Additional file 3: Figure S1). Thus, the remaining 7 pairs of primers, P6, P7, P8, P10, P11, P12 and P13, were used as candidates, and the optimal amplification conditions for each pair are shown in Table 2.
Quantification of NJAU 4742 in soils
As shown in Fig. 1, as expected, the primer pair ITS1, targeting ITS-encoding genes, showed higher copy numbers (Fig. 1), indicating that ITS1 produced a nonspecific amplification including other Trichoderma species existing in the original soil or amended externally. This result is consistent with the two peaks shown in the melting curve (Additional file 3: Figure S1). Meanwhile, the value of primer P10 is very close to that of ITS1, suggesting that nonspecific amplification was apparently also present in P10, which was discarded in subsequent experiments. Beyond that, there was no significant difference between the remaining 3 primer pairs (P6, P7, P8) and the 3 standard primer pairs (P11, P12, P13), which all showed a consistent range of copy numbers of gfp-NJAU 4742, indicating that these primers are specific for detecting strain gfp-NJAU 4742. Moreover, soil samples from the water control were also subjected to qPCR using primers P6–P8 and P10–P13, and the CT values were all above 32, indicating that no gfp-NJAU 4742 existed in the original soil (data not shown).
Quantitation of gfp-NJAU 4742 in soils with different inoculation concentrations
The primer pairs P7 and P12 were selected to quantify the amounts of gfp-NJAU 4742 in initial and after 10 days soils with different concentrations of spores. The two primers both showed increasing trends with the spore concentrations added, and no significant difference was observed between the two primers, demonstrating that both primer pairs are sensitive and capable of accurately distinguishing the copy number (Fig. 2). Similar to the above detection, the CT values for the soil with zero and 102 conidia ml−1 spore inoculations were both above 32 and thus were under the detection level (data not shown).
Practical application of the quantification method in the pot experiments
The copy number of gfp-NJAU 4742 was effectively detected using the primers P6, P7, P11, and P12 by qPCR in the OFBS, BF and BFBS treatments, respectively, and no copies were detected in the OF treatment (CT values were both above 32, data not shown) (Fig. 3). In the OFBS, BF and BFBS treatments, the copy number of gfp-NJAU 4742 in the rhizosphere was higher than that in the bulk soil, and the value in the OFBS treatment was the lowest among the three treatments regardless of rhizosphere or bulk soil. Copy numbers in the rhizosphere soils of the BFBS and BF treatments were similar, and the number in the bulk BFBS soil was slightly higher than that in BF. Furthermore, primers P6 and P7 showed similar copy numbers of the target strain, regardless of bulk or rhizosphere soil, in the OFBS, BF and BFBS treatments, and the values were consistent with those from primer pairs P11 and P12, showing that primer pairs P6 and P7 possessed the ability to effectively and sensitively monitor the target species in natural soil.
In this study, strain-specific qPCR primers were explored based on two steps of comparative genome analysis and protocol to quantify T. guizhouense NJAU 4742, a plant growth-promoting fungus chosen as a model species. A rapid, sensitive and diagnostic test to confirm the presence of Trichoderma spp. inoculants in different environments is essential, since an increasing number of farmers are recognizing the effects of Trichoderma not only in promoting plant root growth but also in protecting plant roots from soilborne pathogens (Cai et al. 2013, 2015; Chen et al. 2011; Xiong et al. 2017; Yang et al. 2011). Thus, the present study will provide a highly useful alternative for the detection of Trichoderma using strain-specific primers designed from the whole genome.
For strain-specific primer design, comparison of T. guizhouense NJAU 4742 whole genome with the NCBI and Joint Genome Institute (JGI) databases was performed to obtain nonoverlapping fragments (first comparison), which were further utilized to arrange a second comparison against the T. harzianum CBS 226-95 genome in a local database, resulting in 10 primer pairs. Whole genome sequences provide comprehensive information about an organism, and in the past decade, with advances in sequencing technology, the cost of sequencing has been greatly reduced; thus, genomics has become an important method in microbial research (Havlak et al. 2004). Similar to this study, strain-specific primer pairs were designed from specific regions of a bacterium, Azospirillum brasilense FP2, by aligning the draft genomic sequences of FP2 to the databases and a closely related strain, A. brasilense Sp245 (Stets et al. 2015). For Trichoderma, sequence characterized amplified region (SCAR) markers have mostly been used for designing specific primers for biocontrol Trichoderma strains (e.g., biocontrol strain T. harzianum 2413 and T. atroviride 11); however, this method is derived from randomly amplified polymorphic DNA (RAPD) analysis and is very complicated and time consuming (Hermosa et al. 2001). Therefore, our findings suggest that direct comparison of the genomic sequences of closely related organisms is a rapid and reliable approach to detect specific DNA regions.
Next, three representative soil types, saline-alkali soil, yellow brown soil and red soil, were further selected and inoculated with strain gfp-NJAU 4742 to verify the specificity of the designed primer pairs in soil conditions. The gfp-NJAU 4742 strain, an Agrobacterium-mediated fluorescent protein-tagged strain of T. guizhouense NJAU 4742, was provided by our laboratory, Zhang et al. (2016), and using its inserted single-copy foreign fragments to design PCR primers as a measure of the accuracy of the primers designed from the NJAU 4742 genomic sequence is an important experimental basis and innovation of this study. This method is often used to distinguish and identify target strains in biological research (Zhang et al. 2014). It is usually difficult to reproduce results from DNA extracted from soil compared to results obtained from pure DNA, which may be attributed to a number of factors, such as the presence of PCR inhibitors (e.g., tannins, humic acids, etc.) (Porteous and Armstrong 1991; Tsai and Olson 1992) and the large amount of DNA from other microorganisms in the soil. Thus, three soil types were selected in this study, and the results showed that gfp-NJAU 4742 could be detected and quantified in these three different soil types and that, indicating that the primers have a wide range of applicability and are sufficiently specific. In comparison to a previous study, which showed that T. harzianum could no longer be detected in soil using a strain-specific sequence characterized amplified region (SCAR) when the specific strain was introduced as part of a mixture of 27 Trichoderma spp. strains (Rubio et al. 2005), the results of the present study demonstrated the specificity of primer pairs P6-P8 and robust colonization by the target strain.
In natural soils with different concentrations of gfp-NJAU 4742 spores added to the soil, the results using primers P7 and P12 showed an increase in gfp-NJAU 4742 copy number with increasing concentrations of spores amended, regardless of initial soil or after 10 days soil, and no significant difference between the two primer pairs were observed. It was found that the PCR amplification of DNA extracted directly from soil samples could be problematic (Cullen and Hirsch 1998). The variability may be due to the patchy distribution of the strain in soil samples and/or the presence of PCR-inhibitory compounds in the soil. Thus, although it is difficult to ascertain a direct relationship between the amount of DNA present in the soil and the amount detectable by the assay given the inclusion of a biological amplification step (Lees et al. 2002), signal reflecting the concentrations still can be detected by real-time assays using these kind of strain-specific qPCR primers.
Similarly, in pepper root, the copy numbers of gfp-NJAU 4742 can be determined by comparing P6 and P7 with each other or with the reference primers, P11 and P12. The stable colonization ability of strain NJAU 4742 in rhizosphere and bulk soils were recognized by qPCR with nonspecific primers (Cai et al. 2013, 2015; Chen et al. 2011), while the present study demonstrated its colonization ability by strain-specific qPCR primers. In addition, in the OF, OFBS and BFBS treatments, there was a significant difference in the number of copies of gfp-NJAU 4742. This result is perhaps due to their individual soil ecological environments and physicochemical properties (Couillerot et al. 2010a, b).
In conclusion, three strain-specific primer pairs, P6, P7 and P8, were successfully designed by using available genome sequence information to detect the number of T. guizhouense NJAU 4742 inoculated into different soil types and to monitor its population fluctuation after inoculation into pepper roots during a pot experiment, demonstrating that the designed primer pairs can be utilized in practice. The results from the pot experiment also confirmed the stable colonization of T. guizhouense NJAU 4742 in plant roots after inoculation. Thus, the strategy for designing strain-specific primers described here may theoretically be used for any other microbes for which the whole genome sequence is available in a database, and the qPCR methodology developed in this work is a generally applicable tool that may be used to further monitor the population dynamics of different strains based on the designed primers.
Availability of data and materials
All data and material are fully available without restriction. And the dataset supporting the conclusions of this article is included within the article.
Atkins SD, Clark IM, Sosnowska D, Hirsch PR, Kerry BR (2003) Detection and quantification of Plectosphaerella cucumerina, a potential biological control agent of potato cyst nematodes, by using conventional PCR, real-time PCR, selective media, and baiting. Appl Environ Microbiol 69(8):4788–4793
Azaizeh HA, Salhani N, Sebesvari Z, Emons H (2003) The potential of rhizosphere microbes isolated from a constructed wetland to biomethylate selenium. J Environ Qual 32(1):55–62
Bakker MG, Chaparro JM, Manter DK, Vivanco JM (2015) Impacts of bulk soil microbial community structure on rhizosphere microbiomes of Zea mays. Plant Soil 392(1–2):115–126
Bal U, Alti̇Ntas S (2008) Effects of Trichoderma harzianum on lettuce in protected cultivation. J Cent Eur Agric 9(1):63–70
Bashan Y, Gonzalez LE (1999) Long-term survival of the plant-growth-promoting bacteria Azospirillum brasilense and Pseudomonas fluorescens in dry alginate inoculant. Appl Microbiol Biotechnol 51(2):262–266
Bates JA, Taylor EJA, Kenyon DM, Thomas JE (2001) The application of real-time PCR to the identification, detection and quantification of Pyrenophora species in barley seed. Mol Plant Pathol 2(1):49–57
Beaulieu R, Lópezmondéjar R, Tittarelli F, Ros M, Pascual JA (2011) qRT-PCR quantification of the biological control agent Trichoderma harzianum in peat and compost-based growing media. Bioresour Technol 102(3):2793–2798
Böhm J, Hahn A, Schubert R, Bahnweg G, Adler N, Nechwatal J, Oehlmann R, Obszwald W (1999) Real-time quantitative PCR: DNA determination in isolated spores of the mycorrhizal fungus Glomus mosseae and monitoring of Phytophthora infestans and Phytophthora citricola in their respective host plants. J Phytopathol 147(7–8):409–416
Boyle B, Hamelin RC, Séguin A (2005) In vivo monitoring of obligate biotrophic pathogen growth by kinetic PCR. Appl Environ Microbiol 71(3):1546–1552
Cai F, Yu G, Wang P, Wei Z, Fu L, Shen Q, Chen W (2013) Harzianolide, a novel plant growth regulator and systemic resistance elicitor from Trichoderma harzianum. Plant Physiol Biochem 73(6):106–113
Cai F, Chen W, Wei Z, Pang G, Li R, Ran W, Shen Q (2015) Colonization of Trichoderma harzianum strain SQR-T037 on tomato roots and its relationship to plant growth, nutrient availability and soil microflora. Plant Soil 388(1–2):337–350
Carmen G, Oscarmartínez DI, Federico P, Fuencisla MDC (2007) Assessment of real-time PCR as a method for determining the presence of Verticillium dahliae in different Solanaceae cultivars. Eur J Plant Pathol 118(3):199–209
Chen L, Yang X, Raza W, Li J, Liu Y, Qiu M, Zhang F, Shen Q (2011) Trichoderma harzianum SQR-T037 rapidly degrades allelochemicals in rhizospheres of continuously cropped cucumbers. Appl Microbiol Biotechnol 89(5):1653–1663
Chenthamara DIK, Atanasova L, Yang D, Kopchinskiy AG, Grigoriev I, Kubicek CP, Shen Q, Druzhinina IS (2014) Phylogenomics of Trichoderma. In: Conference: European conference of fungal genetics
Couillerot O, Bouffaud ML, Baudoin E, Muller D, Caballero-Mellado J, Moënne-Loccoz Y (2010a) Development of a real-time PCR method to quantify the PGPR strain Azospirillum lipoferum CRT1 on maize seedlings. Soil Biol Biochem 42(12):2298–2305
Couillerot O, Poirier MA, Prigent Combaret C, Mavingui P, Caballero-Mellado J, Moënne-Loccoz Y (2010b) Assessment of SCAR markers to design real-time PCR primers for rhizosphere quantification of Azospirillum brasilense phytostimulatory inoculants of maize. J Appl Microbiol 109:528–538
Cullen DW, Hirsch PR (1998) Simple and rapid method for direct extraction of microbial DNA from soil for PCR. Soil Biol Biochem 30:983–993
Cullen DW, Lees AK, Toth IK, Duncan JM (2001) Conventional PCR and real-time quantitative PCR detection of Helminthosporium Solani in soil and on potato tubers. Eur J Plant Pathol 107(4):387–398
Hagn A, Wallisch S, Radl V, Munch JC, Schloter M (2007) A new cultivation independent approach to detect and monitor common Trichoderma species in soils. J Microbiol Methods 69(1):86–92
Haque MM, Ilias GNM, Molla AH (2012) Impact of Trichoderma-enriched biofertilizer on the growth and yield of mustard (Brassica rapa L.) and tomato (Solanum lycopersicon Mill.). Agriculturists 10(2):109–119
Harman GE, Howell CR, Viterbo A, Chet I, Lorito M (2004) Trichoderma species—opportunistic, avirulent plant symbionts. Nat Rev Microbiol 2(1):43–56
Havlak P, Chen R, Durbin KJ, Egan A, Ren Y, Song XZ, Weinstock GM, Gibbs RA (2004) The atlas genome assembly system. Genome Res 14(4):721–732
Hermosa MR, Grondona I, Díaz-Mínguez JM, Iturriaga EA, Monte E (2001) Development of a strain-specific SCAR marker for the detection of Trichoderma atroviride 11, a biological control agent against soilborne fungal plant pathogens. Curr Genet 38(6):343–350
Huang X, Chen L, Ran W, Shen Q, Yang X (2011) Trichoderma harzianum strain SQR-T37 and its bio-organic fertilizer could control Rhizoctonia solani damping-off disease in cucumber seedlings mainly by the mycoparasitism. Appl Microbiol Biotechnol 91(3):741–755
Lees AK, Cullen DW, Sullivan L, Nicolson MJ (2002) Development of conventional and quantitative real-time PCR assays for the detection and identification of Rhizoctonia solani AG-3 in potato and soil. Plant Pathol 51(3):293–302
Liu QM, Chen X, Meng XH, Qi YE, Tuo LI, Liu DY, Shen QR (2017) Development of a new type of biological organic fertilizer and its effect on the growth promotion of tomato. Chin J Appl Ecol 28(10):3314–3322
López-Mondéjar R, Antón A, Raidl S, Ros M, Pascual JA (2010) Quantification of the biocontrol agent Trichoderma harzianum with real-time TaqMan PCR and its potential extrapolation to the hyphal biomass. Bioresour Technol 101(8):2888–2891
Martínezmedina A, Del MAM, Pascual JA, Van Wees SC (2014) Phytohormone profiles induced by Trichoderma isolates correspond with their biocontrol and plant growth-promoting activity on melon plants. J Chem Ecol 40(7):804–815
Porteous LA, Armstrong JL (1991) Recovery of bulk DNA from soil by a rapid, small-scale extraction method. Curr Microbiol 22(6):345–348
Przylucka A, Akcapinar GB, Chenthamara K, Cai F, Grujic M, Karpenko J, Livoi M, Shen Q, Kubicek CP, Druzhinina IS (2017) HFB7-A novel orphan hydrophobin of the Harzianum and Virens clades of Trichoderma, is involved in response to biotic and abiotic stresses. Fungal Genet Biol 102:63–76
Puttanna K, Rao EVSP, Parameswaran TN, Singh R, Kalra A (2010) Effect of organic and inorganic fertilizers and Trichoderma harzianum on patchouli (Pogostemon cablin) herb yield. J Med Aromat Plant Sci 32:50–52
Renske L, Christiaan V, Thom WK, Hannu F, Karel W, Eric S (2003) Quantification of ectomycorrhizal mycelium in soil by real-time PCR compared to conventional quantification techniques. FEMS Microbiol Ecol 45(3):283–292
Ritz K (2007) The plate debate: cultivable communities have no utility in contemporary environmental microbial ecology. FEMS Microbiol Ecol 60(3):358–362
Rubio MB, Hermosa MR, Keck E, Monte E (2005) Specific PCR assays for the detection and quantification of DNA from the biocontrol strain Trichoderma harzianum 2413 in soil. Microb Ecol 49(1):25–33
Sarlin T, Yli-Mattila T, Jestoi M, Rizzo A, Paavanen-Huhtala S, Haikara A (2006) Real-time PCR for quantification of Toxigenic Fusarium species in barley and malt. Eur J Plant Pathol 114(4):371–380
Savazzini F, Longa CM, Pertot I, Gessler C (2008) Real-time PCR for detection and quantification of the biocontrol agent Trichoderma atroviride strain SC1 in soil. J Microbiol Methods 73(2):185–194
Shen Z, Penton CR, Lv N, Xue C, Yuan X, Ruan Y, Li R, Shen Q (2017) Banana Fusarium wilt disease incidence is influenced by shifts of soil microbial communities under different monoculture spans. Microb Ecol 75(3):739–750
Shoresh M, Harman GE, Mastouri F (2010) Induced systemic resistance and plant responses to fungal biocontrol agents. Annu Rev Phytopathol 48(1):21–43
Stets MI, Alqueres SM, Souza EM, Pedrosa FO, Schmid M, Hartmann A, Cruz LM (2015) Quantification of Azospirillum brasilense FP2 bacteria in wheat roots by strain-specific quantitative PCR. Appl Environ Microbiol 81(19):6700–6709
Trillas MI, Segarra G (2009) Chapter 8 interactions between nonpathogenic fungi and plants. Advances in botanical research. Elsevier, London, pp 321–359
Tsai YL, Olson BH (1992) Detection of low numbers of bacterial cells in soils and sediments by polymerase chain reaction. Appl Environ Microbiol 58(2):754–757
Williams J, Clarkson JM, Mills PR, Cooper RM (2003) A selective medium for quantitative reisolation of Trichoderma harzianum from Agaricus bisporus compost. Appl Environ Microbiol 69(7):4190–4191
Winton LM, Stone JK, Watrud LS, Hansen EM (2002) Simultaneous one-tube quantification of host and pathogen DNA with real-time polymerase chain reaction. Phytopathology 92(1):112–116
Xiong W, Guo S, Jousset A, Zhao Q, Wu H, Li R, Kowalchuk GA, Shen Q (2017) Bio-fertilizer application induces soil suppressiveness against Fusarium wilt disease by reshaping the soil microbiome. Soil Biol Biochem 114:238–247
Yang X, Chen L, Yong X, Shen Q (2011) Formulations can affect rhizosphere colonization and biocontrol efficiency of Trichoderma harzianum SQR-T037 against Fusarium wilt of cucumbers. Biol Fertil Soils 47(3):239–248
Zhang JH, Liu Y, Han YT, Pan CQ, Wang ZY, Zhang LL, Cui KX (2014) GFP genetic transformation of Magnaporthe grisea mediated by Agrobacterium tumefaciens. J Northeast Agric Univ 45(11):1–7
Zhang Y, Wen CY, Zhao MQ, Zhang M, Gao Q, Li R, Shen QR (2015) Isolation of plant growth promoting rhizobacteria from pepper and development of bio-nursery substrates. J Nanjing Agric Univ 38(6):950–957
Zhang J, Bayram AG, Atanasova L, Rahimi MJ, Przylucka A, Yang D, Kubicek CP, Zhang R, Shen Q, Druzhinina IS (2016) The neutral metallopeptidase NMP1 of Trichoderma guizhouense is required for mycotrophy and self-defence. Environ Microbiol 18(2):580–597
Zhang Y, Wang T, Sun Y, Hu G, Li R, Yu P, Shen Q (2017) Screening of plant growth-promoting Rhizobacteria from watermelon and development of bio-nursery substrates. Acta Pedol Sin 54(3):702–712
The authors are thankful to Prof. Irina S. Druzhinina, Vienna University of Technology, for the gift of the T. harzianum CBS 226-95 strain.
This research was supported by the National Key Research and Development Program of China (2017YFD0200800), the National Key Basic Research Program of China (2015CB150500), the Natural Science Foundation of Jiangsu (BK20160710), the Priority Academic Program Development of the Jiangsu Higher Education Institutions (PAPD), the 111 project (B12009), the China Scholarship Council (award to Rong Li for 1 year’s abroad study), and Top-notch Academic Programs Project of Jiangsu Higher Education Institution (PPZY2015A061).
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Insertion sequence information used in this study.
Genome sequence information used in this study.
Agarose gel electrophoresis for conventional PCR amplification of 14 cloned plasmids using the universal primer M13 (above) and fluorescence melting curves for strain T. guizhouense NJAU 4742 using 7 primer pairs and primer ITS1 (below).
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Zhang, Y., Wang, X., Pang, G. et al. Two-step genomic sequence comparison strategy to design Trichoderma strain-specific primers for quantitative PCR. AMB Expr 9, 179 (2019). https://doi.org/10.1186/s13568-019-0904-4
- Quantitative PCR
- Strain-specific primers
- Complete genome sequence
- Number detection