Antifungal Activity, Identication and Biosynthetic Potential Analysis of Fungi Against Rhizoctonia Cerealis

Purpose: Wheat sheath blight mainly infected by Rhizoctonia cerealis is one of the soil-borne fungal diseases of wheat worldwide and prevalent in major wheat growing areas in China at present. This study aimed to evaluate the antifungal activity of 163 endophytic fungi on R. cerealis. Antifungal strains were identied and their biosynthetic potential was analysed. Methods: The antifungal activity of the strains was evaluated via dual-culture antagonism assay. The antifungal strains were identied on the basis of morphological characteristics and internal transcribed spacer gene sequencing. The polyketide synthases (PKSs) and nonribosomal peptide synthetase (NRPS) genes in antifungal strains were detected via specic amplication of chromosomal DNA. Result: Twelve out of 163 fungal strains, including seven strains with matrix competition and ve strains with antibiosis, were obtained. The 12 antifungal strains belonged to four genera: Alternaria, Ascochyta, Botryosphaeria and Talaromyces. The inhibition rate of the seven strains with matrix competition was greater than 50%, with that of Botryosphaeria dothidea S2-33 being the highest at 84.6%. The inhibition zone of Talaromyces assiutensis R-03 amongst the ve strains with antibiosis was the widest at up to 7 mm. Among the 12 antifungal strains, the strain S2-16 contained all the genes tested, ve B. dothidea strains contained PKS-II and NRPS genes, two Alternaria alternate strains only contained PKS-II gene and the remaining four strains did not contain any. Conclusion: Results demonstrated 12 potential strains for the biocontrol of wheat sheath blight. In particular, T. assiutensis R-03 was determined as a promising agent. The active substances secreted by antifungal strains may be produced by other biosynthetic pathways.


Introduction
Wheat is one of the major food crops in the world and it plays an important role in ensuring food security. The control of wheat disease is one of the main measures to improve wheat yield. Wheat sheath blight, also known as wheat sharp eyespot, is a widespread worldwide soil-borne fungal disease caused by Rhizoctonia cerealis and Rhizoctonia solani Guo et al. 2012. Wheat sheath blight destroys guiding and mechanical tissues in the stem and other parts of the wheat, leading to necrosis of the stem wall and eventually hindrance in the transportation of nutrients and water, which results in the absence of seed in the ear of wheat Cromey et al. 2006. This disease seriously reduces wheat quality and yield at the mild reduction of 5-20%, heavy reduction of more than 50% or even without grain harvest Cromey et al. 2002.
Wheat sheath blight was rst identi ed in 1978 in China and the incidence area of the disease has been increasing year by year, accounting for 60-80% of the total wheat planting area in severe cases, which result in an annual yield loss of approximately 50,000 tons Yang et al. 2010. At present, wheat sheath blight mainly infected by R. cerealis is prevalent in major wheat growing areas in China; it results in severe losses and has become one of the important factors restricting the high and stable yield of wheat.
The prevention and control of wheat sheath blight mainly consists of chemical agents and eld management at present. However, the prevention and control effects are not ideal because of the unavailability of chemical pesticides with good control effect, the pathogen's natural persistence in soils and various changeable factors in eld management. Moreover, wheat varieties resistant to R. cerealis have not been cultivated. With the pollution from chemical pesticides becoming increasingly prominent and the people's awareness of environmental protection becoming strong, biological control becomes a promising alternative to prevent plant diseases. Biological control refers to using one or more organisms or their secondary metabolites to reduce the damage from pests Straub et al. 2008. In particular, using microorganisms in nature to control plant diseases is an important biological approach Yuan et al. 2017.
In the last few decades, researchers have been working hard to nd methods to prevent and control plant diseases from microorganisms or their secondary metabolites and many successful cases have been reported. Validamycin, which is an aminoglycoside antibiotic produced by Streptomyces hygroscopicus, has been extensively used for the control of crop diseases caused by Rhizoctonia spp. in many countries Guirao-Abad et al. 2013. It also could control Fusarium head blight caused by Fusarium graminearum by inhibiting deoxynivalenol biosynthesis and inducing host resistance Li et al. 2019.
In previous studies, 163 endophytic fungi, which were isolated from medicinal plant Cornus o cinalis, were obtained. The present study aimed to evaluate the activity of these 163 strains against R. cerealis via dual culture-plate antagonism and identify the strain with antifungal activity. The polyketide synthases (PKSs) and nonribosomal peptide synthases (NRPS) genes in antagonistic strains were detected to evaluate the biosynthetic potential of strains in terms of natural product discovery. PKS-I, PKS-II and NRPS are multi-enzymatic and multi-domain megasynthases involved in the biosynthesis of polyketides and non-ribosomal peptides with a remarkable range of biological activities, such as antifungal, antitumor, antiparasitic, antimicrobial and immunosuppressive Ansari  University of Science and Technology, China. The hyphae or spores of these strains were stored in an aqueous glycerol solution (30%, v/v) at − 80°C. The fungal inoculum used in the assays was prepared from these frozen stocks by transferring the hyphae or spores onto potato dextrose agar (PDA) media.

Evaluation of antifungal activity
The antifungal potential of the 163 endophytic fungi against R. cerealis was evaluated by modifying the dual culture-plate antagonism assay described previously Zhang et al. 2014. All fungi were cultured on PDA media at 26°C for 7 d. Then, 5 mm plugs of each endophyte and R. cerealis were co-cultured in 90 mm-sterile Petri dishes, with approximately 28 mL of PDA yielding a nal depth of 5 mm, and incubated at 26°C ± 0.5°C. The plugs were placed on the opposite sides of the centre of the Petri dishes, with a distance of 4 cm between them. R. cerealis alone was inoculated as controls. The growth radii of endophyte and R. cerealis and the production of an inhibition zone were monitored at regular intervals every day and recorded until the R. cerealis stopped growing or the size of the control colony was close to that of the plate. All control and test plates were run in triplicate.
Relative growth inhibitions (% antagonism) were calculated as percentage of inhibition of radial growth (PIRG): where R1 is the radial growth of fungi in control plates and R2 is the radial growth of fungi in tested plates.

Morphological identi cation of antagonistic strains
The fungi with antifungal activity against R. cerealis were cultured on PDA media at 26°C for approximately 10 d to observe their colony characteristics, including colour, texture, topography, border type, radial growth rate, the presence of aerial mycelia and substrate mycelia and distinctive reverse colony colour. Meanwhile, the production of spores was monitored regularly every day until the morphology and size of conidia were clearly observed under the light microscope. All the results obtained were compared with taxonomic keys Kim et al. 1990; Wei 1979.

DNA extraction, PCR ampli cation and ITS sequencing
The antagonistic isolates were subjected to DNA extraction, ampli cation and sequencing of the ITS region of rRNA gene. The genomic DNA was extracted using the CTAB method Kim, Mauthe, Hausner and Klassen 1990. Universal primers ITS1 (5′-TCCGTAGGTGAACCTGCGG-3′, forward) and ITS4 (5′-TCCTCCGCTTATTGATATGC-3′, reverse) were used for ampli cation of the ITS region, which consisted of ITS1, 5.8S and ITS2 regions of the rDNA. PCR reaction  was performed in a total volume of 25 µL containing 12.5 µL of 2 × Taq PCR Green Mix, 0.5 µL of ITS1 (10 µM), 0.5 µL of ITS4 (10 µM), 1 µL of template DNA and 10.5 µL of sterile double-distilled water. The PCR cycling protocol Kusari, Kusari, Spiteller and Kayser 2013 consisted of an initial denaturation at 94°C for 4 min and 35 cycles of denaturation, annealing and elongation at 94°C for 30 s, 55°C for 30 s and 72°C for 40 s, which was followed by a nal elongation step of 72°C for 10 min. As a negative control, the template DNA was replaced by sterile double-distilled water. After ampli cation, an aliquot was analysed by running on a 1% (w/v) TAE agarose gel stained with nucleic acid fuel Goldview, which was added at the volume ratio of 1/20 and visualized under UV light if a clear and bright band was present. The PCR products were compared to a molecular size standard 2 kb plus DNA ladder. All the molecular reagents were purchased from Sangon Biotech (Shanghai, China).
When the ampli cation product was detected as a single bright band, it was sent to Sangon Biotech (Shanghai, China) for sequencing. For the identi cation of screened fungal isolates, the ITS sequences were matched with the nucleotide database by using the Basic Local Alignment Search Tool (BLAST) of the US National Centre for Biotechnology Information (NCBI). The sequences were aligned using CLUSTAL W software packaged with MEGA 7.0 under default setting. When the similarity between a particular problem sequence and a phylogenetically associated reference sequence was ≥ 99%, only then the sequences were considered to be conspeci c Yuan et al. 2010. The phylogenetic tree was reconstructed and the evolutionary history was inferred using the neighbour-joining method. The robustness of the internal branches was also assessed with 1000 bootstrap replications. The evolutionary distances were computed using the Maximum Composite Likelihood method and calculated in the units of the number of base substitutions per site.
Taxonomic assignment was based on similarity with reference sequences retrieved from GenBank and in consultation with observed colony and spore morphology. The ITS sequences of the screened fungal isolates were deposited in the NCBI GenBank and accession numbers were obtained.

Detection of PKS-I, PKS-II and NRPS gene sequences
The screened fungal isolates, which showed good antifungal activity, were selected for the detection of genes encoding PKS-I, PKS-II and NRPSs. Three sets of primers were used to amplify these three genes

Antifungal activity of testing fungal isolates
The main three types of antagonism are matrix competition, mycoparasitism and antibiosis . In the present study, the antagonistic effects of the testing strains on R. cerealis exhibited matrix competition and antibiosis. (1) In matrix competition, the living space and the availability of nutrients for R. cerealis was compressed and reduced because of the rapid growth of testing strains. (2) In antibiosis, a clear halo (inhibition zone) emerged around the biomass of the testing strains because they could inhibit the growth of R. cerealis by secreting secondary metabolites before their mycelia come in physical contact. Amongst the 163 strains tested, ve showed antibiosis and the other 158 showed matrix competition. In terms of matrix competition, the inhibition rate of the testing strains on R. cerealis ranged from negative to 72%. Given that only when the inhibition rate is greater than 50% could the competitive effect be further studied, seven strains with inhibition rate of greater than 50% are listed in Table 1. The inhibition rates increased from 53-84.6%; amongst them, the strain S2-33 was the highest (Table 1 and Fig. 1). With regard to antibiosis, all the ve antibiotic strains had clear and obvious inhibition zones ranging from 2 mm to 7 mm after 5-10 d of confrontation culture, of which the inhibition zone of strain R-03 was the widest (Table 1 and Fig. 1).  2 The numbers in parentheses after MC and AB represent "inhibition rate%" and "width of the inhibition zone (mm)" respectively.
3 The signs + and -represent the presence and absence of the corresponding gene, respectively.

Identi cation of isolates with antifungal activity
A total of 12 strains were screened via antagonism assay and identi ed on the basis of morphological characteristics and ITS (ITS1, intervening 5.8S and ITS2) sequence alignments. All the ITS sequence length of the antagonistic strains spanned around 500-600 bp. These sequences were matched with those of the most closely related fungal species (identity values higher than 99%) in the NCBI database (http://www.ncbi.nlm.nih.gov/) through the BLAST program, combining with the morphology of colonies and spores. The similarity between the antagonistic strain sequence and the reference sequence was all above 99%. The detailed descriptions of the antagonistic strains with respective codes, GenBank accession numbers and closest sequence homologs are summarised in Tables 1.
As for the seven strains with competition for substrate (Table 1), they belonged to genera Alternaria, Ascochyta and Botryosphaeria. Amongst them, Alternaria contained three strains of two species, Botryosphaeria contained three strains of one species, Ascochyta had only one strain Ascochyta medicaginicola and the strain S2-33 Botryosphaeria dothidea had the highest inhibition rate of up to 84.6%. As for the ve strains with antibiosis (Table 1), three belonged to genus Talaromyces, including two species, whilst the other two belonged to B. dothidea. The antifungal activity of Talaromyces was generally higher than that of Botryosphaeria. Given that the T. assiutensis strain R-03 with the strongest antibiosis had the greatest potential for further development, it was used as an example and a phylogenetic tree was constructed in detail, which showed the relationship of strain R-03 to closer species with the genus Talaromyces and Trichocoma paradoxa as an outgroup (Fig. 2).

Detection of PKS-I, PKS-II and NRPS gene sequences
Twelve antagonistic strains exhibiting good or moderate activity against R. cerealis were selected for the detection of PKS-I, PKS-II and NRPS genes ( Table 1). The Ascochyta medicaginicola strain S2-16 was detected to have these genes. With regard to ve strains of Botryosphaeria dothidea, whether they had matrix competition or antibiosis, they were detected to have the PKS-II and NRPS genes but without the PKS-I gene. In terms of the two strains of Alternaria alternate with competition for substrate, they only had the PKS-II gene. However, as for the A. arborescens strain S2-12 and three strains belonging to genus Talaromyces, they did not possess any of the genes mentioned.

Discussion
In using microorganisms to control wheat sheath blight, most of the reported biocontrol strains were bacteria. Nanjing Agricultural University of China reported the effects of using Bacillus subtilis B3 to control R. cerealis and the optimization scheme of fermentation conditions (Zhang et al., 1995). Endophytic fungi are present in every plant through long-term co-evolution with host plants; they not only do not cause plant diseases but also promote plant growth, improve plant stress resistance and produce some secondary metabolites to resist and inhibit the invasion of pathogens Zheng et al. 2016. Therefore, starting from endophytic fungi is an important method to search for biocontrol fungi with antibiosis. In the present study, ve strains with antibiosis against R. cerealis were selected from 163 cornel endophytic fungi with biocontrol potential to their host. Amongst them, T. assiutensis strain R-03 had the strongest antibiosis. During the process of culture, this strain grew slowly at a growth rate of only 1/4-1/3 of that of R. cerealis. However, even under such adverse circumstances, a 7 mm-inhibition zone was produced (Fig. 1). By contrast, R. cerealis had no effect on the growth of strain R-03. Meanwhile, when the colony radius of strain R-03 no longer changed over time, a circle of secretion around the edge of its colony was observed. Moreover, with the accumulation of the secretion, the inhibition zone tended to broaden. Therefore, T. assiutensis strain R-03 could continuously produce secondary metabolites with inhibitory effect on R. cerealis.
The genus Talaromyces is a sexual type of Penicillium found widely in terrestrial and marine climates. Sea, a fungus T. assiutensis JTY2 was obtained from the leaves of Ceriops tagal. The ethyl acetate extract of a solid rice fermentation of the fungus exhibited antimicrobial and anti-in ammatory activities. Bioassay-guided fractionation of the bioactive extract led to the isolation of four compounds with inhibitory activities against NO production induced by lipopolysaccharide in mouse macrophage RAW 264.7 cells in vitro and one compound with broad spectrum antibacterial activity against six terrestrial pathogenic bacteria Cai et al. 2019. No studies are available on the application of fungus T. assiutensis in the control of fungal diseases at present. Therefore, the T. assiutensis strain R-03 with antibiosis obtained in the present study could be further evaluated and selected for suppressing R. cerealis in pot and eld experiments.
In the present study, some of the 12 strains that showed good inhibitory activity against R. cerealis, contained three functional genes, whilst some contained two, only one and even none. This nding indicated no direct correlation between the antifungal activity and the three target genes, which was consistent with the results from previous reports Kampapongsa

Conclusion
In this study, 12 antagonistic strains against R. cerealis, including seven strains with matrix competition and ve strains with antibiosis, were screened and identi ed from 163 endophytic fungi. In particular, T. assiutensis R-03 with antibiosis was determined as a promising agent for the biocontrol of wheat sheath blight. Screening of PKSs and NRPS genes in the 12 antifungal strains revealed that the active substances secreted by antifungal strains may be produced by other biosynthetic pathways. The results showed the potential strains for the biocontrol of the wheat sheath blight.

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Competing interests
The authors declare that there are no con icts of interest. Funding