Isolation of Bacillus siamensis B-612, a Strain That Is Resistant to Rice Blast Disease and an Investigation of the Mechanisms Responsible for Suppressing Rice Blast Fungus

Rice yield can be significantly impacted by rice blast disease. In this investigation, an endophytic strain of Bacillus siamensis that exhibited a potent inhibitory effect on the growth of rice blast was isolated from healthy cauliflower leaves. 16S rDNA gene sequence analysis showed that it belongs to the genus Bacillus siamensis. Using the rice OsActin gene as an internal control, we analyzed the expression levels of genes related to the defense response of rice. Analysis showed that the expression levels of genes related to the defense response in rice were significantly upregulated 48 h after treatment. In addition, peroxidase (POD) activity gradually increased after treatment with B-612 fermentation solution and peaked 48 h after inoculation. These findings clearly demonstrated that the 1-butanol crude extract of B-612 retarded and inhibited conidial germination as well as the development of appressorium. The results of field experiments showed that treatment with B-612 fermentation solution and B-612 bacterial solution significantly reduced the severity of the disease before the seedling stage of Lijiangxintuan (LTH) was infected with rice blast. Future studies will focus on exploring whether Bacillus siamensis B-612 produces new lipopeptides and will apply proteomic and transcriptomic approaches to investigate the signaling pathways involved in its antimicrobial effects.


Introduction
Rice (Oryza sativa L.) is one of the most significant food crops in the world and provides 21% of all calories consumed globally [1]. Rice blast, often known as rice cancer, is the most dangerous disease that can affect rice on a global level. Thus far, rice blast disease has been reported in 85 nations, with the worst incidence occurring in Asia and Africa [2]. Magnaporthe oryzae (M. oryzae) is a filamentous ascomycete fungus and is ranked as one of the ten most important plant pathogens; this fungus is spread aerially by conidia during an epidemic [3].
There are several methods used to combat rice blast disease at present, including the selection and breeding of disease-resistant types, chemical control, and biological control. Although infections prefer adaption to overcome host plant resistance, the formation of resistant types takes significant time; furthermore, resistance is not universal nor permanent. As a result, the breakdown of rice resistance is caused by the quick development of new strains. There are several long-term consequences associated with the careless use of chemical fertilizers and pesticides, including environmental damage, higher production costs,

Isolation and Identification of Endophytes
As shown in Figure 1a, B-612 showed a strong inhibitory effect against M. oryzae Guy11. The endophytic bacterium B-612, which was isolated from cauliflower leaves, inhibited the growth of M. oryzae by up to 79.76% according to tests for mycelial growth inhibition. When inoculated with ring picking bacteria, we found that endophyte B-612 could develop normally on beef paste peptone plate, and that the colonies were round, white, and opaque. The surface of the colonies was flat, dry, and wrinkled, and the interior was mucilaginous (Figure 1b). Bacillus siamensis KCTC 13613 and strain B-612 were found to be almost identical by 16S rRNA sequencing analysis. Figure 1c shows a phylogenetic tree illustrating the link between strain B-612 and other strains. Thus, strain B-612 was identified as Bacillus siamensis.

B-612 Fermentation Solution Enhanced the Resistance of Rice to M. oryzae
In order to detect the expression of peroxidase (POD) and genes related to the defense response in rice, we used rice OsActin genes as internal references. These genes fell into three main categories: first, genes related to disease-course, such as the OsPR1a, OsPR5a, and OsPR10a families; second, genes related to rice signal transduction, such as the salicylic acid (SA) signaling receptor gene OsNH1, chitin signaling receptor genes OsCEBiP and OsLYP6, and mitogen-activated protein kinase (MAPK) pathway genes; and third, genes encoding transcription factors, including OsWRKY45, OsWRKY89, OsWRKY53, and OsEREBP [11][12][13][14][15][16]. Between 24 and 48 h after inoculation, rice defense genes were activated to varying degrees ( Figure 3). All of these genes showed a significant upregulation at 48 h after treatment, with the expression levels of OsCEBiP and OsNH1 peaking at 24 h and the remaining genes peaking at 48 h. Comparing the B-612 fermentation broth-treated group to the control group at 48 h, OsPR1a expression was upregulated by approximately 60-fold, OsPR5 expression by approximately 150-fold, and OsLYP6 expression by approximately 40-fold. POD activity increased gradually and peaked at 48 h after inoculation, exhibiting an approximately 80-fold rise in POD levels in comparison to 0 h. After 48 h, it was evident that the group treated with B-612 fermentation broth had POD expression levels that had been upregulated by approximately 20-fold when compared to the control group. These data showed that the significant biocontrol action of B-612 was caused by the increased expression of defense-related genes and that this plays a crucial role in the defense of rice against rice blast.

B-612 Fermentation Solution Enhanced the Resistance of Rice to M. oryzae
In order to detect the expression of peroxidase (POD) and genes related to the defense response in rice, we used rice OsActin genes as internal references. These genes fell into three main categories: first, genes related to disease-course, such as the OsPR1a, OsPR5a, and OsPR10a families; second, genes related to rice signal transduction, such as the salicylic acid (SA) signaling receptor gene OsNH1, chitin signaling receptor genes OsCEBiP and OsLYP6, and mitogen-activated protein kinase (MAPK) pathway genes; and third, genes encoding transcription factors, including OsWRKY45, OsWRKY89, OsWRKY53, and OsEREBP [11][12][13][14][15][16]. Between 24 and 48 h after inoculation, rice defense genes were activated to varying degrees ( Figure 3). All of these genes showed a significant upregulation at 48 h after treatment, with the expression levels of OsCEBiP and OsNH1 peaking at 24 h and the remaining genes peaking at 48 h. Comparing the B-612 fermentation broth-treated group to the control group at 48 h, OsPR1a expression was upregulated by approximately 60fold, OsPR5 expression by approximately 150-fold, and OsLYP6 expression by approximately 40-fold. POD activity increased gradually and peaked at 48 h after inoculation, exhibiting an approximately 80-fold rise in POD levels in comparison to 0 h. After 48 h, it was evident that the group treated with B-612 fermentation broth had POD expression

H 2 O 2 Accumulation
The main function of superoxide dismutases (SODs) is to scavenge cellular superoxide radicals (O 2− ). However, the production of SOD can provide additional protection against pathogenic infections in plants, and increased SOD activity has previously been shown to lead to the accumulation of H 2 O 2 [17,18]. In this study, we used 3,3 -diaminobenzidine tetrahydrochloride (DAB) staining to detect H 2 O 2 accumulations, as depicted in  Multiple compariso were used to analyze significant differences, p < 0.01.* difference is significant at the 0.05 level; Figure 3. Effect of B-612 on the expression of genes related to rice defense. Multiple comparisons were used to analyze significant differences, p < 0.01. * difference is significant at the 0.05 level; ** difference is significant at the 0.01 level; *** difference is significant at the 0.001 level; **** difference is significant at the 0.0001 level.
The main function of superoxide dismutases (SODs) is to scavenge cellular superoxide radicals (O 2− ). However, the production of SOD can provide additional protection against pathogenic infections in plants, and increased SOD activity has previously been shown to lead to the accumulation of H2O2 [17,18]. In this study, we used 3,3′-diaminobenzidine tetrahydrochloride (DAB) staining to detect H2O2 accumulations, as depicted in Figure 4. The concentration of H2O2 in the rice leaves treated with fermentation broth increased over time, and peaked at 48 h.

Detection of Lipopeptide Biosynthetic Genes
Our PCR analysis indicated that strain B-612 expressed many relevant and functional genes, including fengycin (fenB, fenD), iturin (ituD), surfactin (srfAA), bacillomycin (bmyB), and biotene (bioA). These genes were amplified using primer pairs and generated PCR products with the predicted sizes of 1400, 293, 1203, 273, 395, and 210 base pairs (Figure 5). BLASTX analysis revealed a 96.26% amino acid sequence similarity between strain B-612 and Bacillus subtilis with regards to bacillin synthase, thus indicating that B-612 is able to successfully generate bacillomycin synthase and bacillomycin. The amino acid sequence similarity between strain B-612 and fengycin synthase B of Bacillus amyloliquefaciens and Bacillus velezensis was 100%, while the amino acid sequence similarity between fengycin synthase D of Bacillus subtilis was 98.68%. This shows that B-612 is able to synthesize fengycin synthetase B and fungogenin synth. Strain B-612 and Bacillus subtilis share 100% of amino acid identified for surfactin synthase; this suggests that B-612 may generate surfactin synthase on its own. Bacillus sp. and strain B-612 shared an amino acid sequence that was more than 98% similar with regards to iturin synthase, thus showing that B-612 can synthesize iturin synthase to make iturin. Thus, strain B-612 has the potential to prevent the growth of M. oryzae by producing key lipopeptide antibiotics, including fengycin, iturin, surfactin, or bacillomycin.

Detection of Lipopeptide Biosynthetic Genes
Our PCR analysis indicated that strain B-612 expressed many relevant and functional genes, including fengycin (fenB, fenD), iturin (ituD), surfactin (srfAA), bacillomycin (bmyB), and biotene (bioA). These genes were amplified using primer pairs and generated PCR products with the predicted sizes of 1400, 293, 1203, 273, 395, and 210 base pairs ( Figure 5). BLASTX analysis revealed a 96.26% amino acid sequence similarity between strain B-612 and Bacillus subtilis with regards to bacillin synthase, thus indicating that B-612 is able to successfully generate bacillomycin synthase and bacillomycin. The amino acid sequence similarity between strain B-612 and fengycin synthase B of Bacillus amyloliquefaciens and Bacillus velezensis was 100%, while the amino acid sequence similarity between fengycin synthase D of Bacillus subtilis was 98.68%. This shows that B-612 is able to synthesize fengycin synthetase B and fungogenin synth. Strain B-612 and Bacillus subtilis share 100% of amino acid identified for surfactin synthase; this suggests that B-612 may generate surfactin synthase on its own. Bacillus sp. and strain B-612 shared an amino acid sequence that was more than 98% similar with regards to iturin synthase, thus showing that B-612 can synthesize iturin synthase to make iturin. Thus, strain B-612 has the potential to prevent the growth of M. oryzae by producing key lipopeptide antibiotics, including fengycin, iturin, surfactin, or bacillomycin.

The Effects of Antifungal Substances Generated by Strain B-612 on M. oryzae Conidia Germination and the Formation of Appressorium
M. oryzae conidia were treated with either distilled water or a crude extract of B-612. The conidia in the control group began to develop budding tubes after two hours, as shown in Figure 6. The creation rate was 72.33% when the budding tubes extended and connected cells formed at the other end after 8 h. After being exposed to B-612 crude extract, the spores had hardly begun to develop budding tubes at 2 h; at 8 h, very few of the spores had generated budding tubes. The budding tube germination rate remained below 10% during the observation period of 48 h, and breakage of the connected cells was evident at both 24 and 48 h. Throughout the experiment, the development of normally linked cells was not apparent. At both 24 and 48 h, it was evident that the budding tubes had broken, and that generally, the normal development of adherent cells was not apparent.  The conidia in the control group began to develop budding tubes after two hours, as shown in Figure 6. The creation rate was 72.33% when the budding tubes extended and connected cells formed at the other end after 8 h. After being exposed to B-612 crude extract, the spores had hardly begun to develop budding tubes at 2 h; at 8 h, very few of the spores had generated budding tubes. The budding tube germination rate remained below 10% during the observation period of 48 h, and breakage of the connected cells was evident at both 24 and 48 h. Throughout the experiment, the development of normally linked cells was not apparent. At both 24 and 48 h, it was evident that the budding tubes had broken, and that generally, the normal development of adherent cells was not apparent.
Germination and the Formation of Appressorium M. oryzae conidia were treated with either distilled water or a crude extract of B-612. The conidia in the control group began to develop budding tubes after two hours, as shown in Figure 6. The creation rate was 72.33% when the budding tubes extended and connected cells formed at the other end after 8 h. After being exposed to B-612 crude extract, the spores had hardly begun to develop budding tubes at 2 h; at 8 h, very few of the spores had generated budding tubes. The budding tube germination rate remained below 10% during the observation period of 48 h, and breakage of the connected cells was evident at both 24 and 48 h. Throughout the experiment, the development of normally linked cells was not apparent. At both 24 and 48 h, it was evident that the budding tubes had broken, and that generally, the normal development of adherent cells was not apparent.

Biocontrol Efficacy of Strain B-612 and Its Culture Filtrate
Field tests were carried out to assess the ability of strain B-612 to prevent rice blast. Before being exposed to rice blast at the seedling stage in Lijiangxintuan (LTH), the treatment groups were administered B-612 filter fermentation solution and B-612 bacterial solution treatments; the administration of water and LB medium treatments served as positive controls while the administration of carbendazim treatments served as negative controls. Analysis revealed large spots in the positive control group (water and LB) with yellowish edges and dark brown centers and obvious signs of dieback; the spots in the positive control group (carbendazim) were small and less susceptible while the spots in the B-

Biocontrol Efficacy of Strain B-612 and Its Culture Filtrate
Field tests were carried out to assess the ability of strain B-612 to prevent rice blast. Before being exposed to rice blast at the seedling stage in Lijiangxintuan (LTH), the treatment groups were administered B-612 filter fermentation solution and B-612 bacterial solution treatments; the administration of water and LB medium treatments served as positive controls while the administration of carbendazim treatments served as negative controls. Analysis revealed large spots in the positive control group (water and LB) with yellowish edges and dark brown centers and obvious signs of dieback; the spots in the positive control group (carbendazim) were small and less susceptible while the spots in the B-612 filtrate fermentation solution and B-612 mycorrhizal solution treatment groups were brown in color without signs of dieback. The group treated with fermentation solution was less susceptible than the other two groups. Counting the number of spots within 5 cm of the leaf length, we found that there were significantly fewer spots in the treated group than in the negative control group (Figure 7) (p < 0.01). Thus, it appears that B-612 can be employed as a biocontrol bacterium for the control of rice blast in the field and that its mycorrhizal and filter fermentation solutions are more efficient in preventing rice blast on rice leaves.

Discussion
According to previous research, endophytic bacteria directly produce bioactive secondary metabolites that help protect their host plants from pathogenic microbes, thus im-

Discussion
According to previous research, endophytic bacteria directly produce bioactive secondary metabolites that help protect their host plants from pathogenic microbes, thus improving the fitness of their hosts [19]. One benefit of a genus for biological control is its capacity to produce spores and endure harsh environments. Endophytic Bacillus species offer a variety of advantages to plants, including defense against insects, nematodes, and pathogenic microbes; they can also induce resistance and foster plant growth without harming the environment [20]. Bacillus siamensis has been reported to reduce the incidence of a variety of plant diseases, including tobacco brown spot, rice leaf blight, and spike blight [21][22][23][24]. In a previous study, Xu et al. purified iturin A and bacillomycin F from Bacillus siamensis JFL15 to inhibit the growth of M. oryzae but did not investigate the precise mechanism involved. In the present study, a Bacillus siamensis B-612 endophytic strain was isolated from healthy cauliflower leaves and showed a potent inhibitory effect on the growth of rice fungus. However, it was also responsive to various antibiotics. Thus, Bacillus siamensis B-612 has the potential to be employed as a biocontrol bacterium to control rice disease.
Airborne conidia generated by M. oryzae play a significant role in the spread and severity of rice blast. The conidia germinate after touching a suitable host surface, thus creating an attachment cell, a dome-shaped infection structure at the end of the germ tube [25][26][27]. A variety of Bacillus species have been shown to inhibit the conidial germination of M. oryzae [28,29]. Yet, the conidia germination test findings performed in our present study showed that the germination process had been evidently reduced or even postponed. These findings clearly demonstrated that the 1-butanol crude extract of B-612 retarded and inhibited conidial germination as well as the development of appressorium. As a result, we can infer that the crude 1-butanol extract of B-612 can prevent M. oryzae from forming infectious structures in vitro. This is the first study showing that Bacillus siamensis can inhibit the spore germination and cell attachment formation of M. oryzae.
The biocontrol ability of Bacillus strains and their capability for global adaptation in their natural habitat, including settlement and biofilm development, depend on efficient lipopeptide production. Among plant-associated Bacillus isolates, the biocontrol agents (BCA) genes bmyB, srfAA, and fenD are most frequently observed [30]. It has been reported that when distinct lipopeptide families are synthesized together, their interactions can become synergistic and improve the activity of each individual family member [31][32][33]. Experimental results showed that B-612 may suppress M. oryzae growth by secreting antimicrobial lipopeptides such as bacillomycin, fengycin, iturin, or surface activator; however, these compounds still need to be further identified and purified.
The production of antibiotics, competition, the promotion of plant development, and the induction of systemic acquired resistance (SAR) and induced systemic resistance (ISR) are among the primary processes of BCA [30]. Following the production of SA, the coordinated activation of several PR proteins, and resistance-associated enzymes, SAR can initiate defense responses in response to the detection of pathogenic invasion [34]. BCA-induced SOD synthesis can provide plants with enhanced defense against harmful diseases [18]. Pathogen-sensing signaling molecules, MAPK, and transcription factors all contribute to the defense response of plants [13]. In a previous study, Awan et al. reported that Bacillus siamensis reduced cadmium toxicity in wheat plants by enhancing the antioxidant defense system [35]. In another study, Zhou et al. reported that Bacillus siamensis YC-9 increased the activities of defense enzymes such as POD, polyphenol oxidase (PPO), and phenylalanine aminolase (PAL) in the roots of diseased cucumber, thus resulting in increased levels of resistance [36]. In the present study, we showed, for the first time, that Bacillus siamensis can enhance systemic resistance in rice by inducing the expression of defense genes. These findings demonstrated that one of the primary mechanisms of action of B-612 fermentation broth was to induce SAR; more specifically, when B-612 fermentation broth was administered, free SA was created and the expression levels of SA-dependent PR family genes were markedly elevated. B-612 fermentation broth significantly increased the expression of rice defense genes 48 h after treatment, thus indicating that these genes and the products they produce may be important in the control of resistance during the late stages of M. oryzae infestation. During treatment, POD activity gradually increased, peaking 48 h after inoculation; these outcomes were in line with H 2 O 2 buildup. The enzymatic activity of POD contributes to its role in disease resistance and can stop the oxidation of damaged plant tissues. Inhibiting the growth of rice blast and minimizing the oxidative damage produced by rice blast may have been achieved by treating rice with B-612 fermentation solution.
In conclusion, B-612 can activate the defensive system of rice plants, thus suppressing rice blast, although further research into the metabolic pathway of activation is necessary. Field tests were used to further investigate the ability of B-612 to prevent rice blast disease. These findings demonstrated that disease severity was significantly reduced following treatment with B-612 fermentation solution and B-612 bacterial solution at the seedling stage of LTH prior to infection with rice blast disease, and that the effects of this treatment were comparable to carbendazim spraying. In order to effectively prevent rice blast disease in the field, B-612 fermentation solution could be sprayed during the pre-susceptible stage. Collectively, these results suggest that Bacillus siamensis B-612 is a promising biocontrol agent for the effective control of rice blast disease. Future studies will focus on exploring whether Bacillus siamensis B-612 produces new lipopeptides and will apply proteomic and transcriptomic approaches to investigate the signaling pathways involved in its antimicrobial effects. In the meantime, the B-612 genome will be sequenced to confirm that this is not the previously characterized Bacillus siamensis strain.

Isolation and Cultivation of Endophytic Bacteria
Fresh, healthy cauliflower leaves were collected, cleaned with distilled water, and placed in sterile 50 mL centrifuge tubes for storage. Then, we sterilized the leaves by submerging them two-to-three times in 75% ethanol for 3 min. Then, the leaves were placed in a solution of 1% sodium hypochlorite and soaked for two minutes; the leaves were then rinsed repeatedly with sterile distilled water to remove sodium hypochlorite from their surfaces. After drying the leaves and storing them in a 10 mL sterile centrifuge tube, a volume of sterile distilled water was added and the mixture was ground until it was homogeneous. Next, we spread 150-200 µL of leaf homogenate on a solid beef paste peptone substrate following the preparation of a gradient of dilutions with sterile distilled water. The dishes were incubated for 24-36 h at 37 • C in a constant temperature incubator. Individual colonies on the plates were chosen, transferred with clean toothpicks into LB liquid medium, and then incubated at 37 • C at 200 rpm for 36-48 h in a constant temperature shaking isolator. The endophytic bacterial solution was provided with the appropriate quantity of glycerol and kept as a backup at −80 • C. The dishes were coated with sterile distilled water for 48 h to prevent non-endophytic bacteria from adhering to the surface of the leaves and thus influencing test outcomes. To ascertain whether all of the non-endophytic bacteria on the surface of the leaves had been eliminated, we monitored the surfaces of the plates for the development of bacteria.

Rice Blast Pathogen (M. oryzae Guy11) and Culture Conditions
The Plant Pathogenic Laboratory of Sichuan Agriculture University provided us with the rice blast pathogenic fungus M. oryzae Guy11. This fungus was cultured on potato dextrose agar (PDA) at 28 • C.

Fungal Antagonism Assay
For fungal antagonism assays, 100 mL of LB liquid medium was combined with endophytic bacterial broth that had been kept at −80 • C and cultured for 72 h at 37 • C and 200 rpm in a constant temperature shaker. To create the endophytic filtered bacterial fermentation broth, the fully fermented endophytic bacterial broth was centrifuged at 4 • C at 11,000 r/min for 20 min. The supernatant was then filtered and sterilized with a 0.22 µm filter. Next, the plate was shaken and 5 mL of the filtrate fermentation solution was poured into 100 mL of chilled, uncoagulated PDA medium. To create drug-containing PDA plates, the filtrate fermentation solution-containing PDA plates were chilled and blown dry. A hole punch (7 mm diameter) was used to create a number of M. oryzae cakes from the M. oryzae plates. These M. oryzae cakes were smeared onto the medication-containing plates and cultured in a constant light incubator for 7 days at 28 • C with alternating light and dark conditions. The growth of M. oryzae was monitored and recorded throughout this period. Endophytic bacteria with strong activity levels were chosen as reference strains for further research based on the inhibition rate of each endophytic fermentation broth against M. oryzae, as determined by growth diameter. The inhibition rate (%) = [1−(diameter of M. oryzae in the treatment group-diameter of M. oryzae cake in the treatment group)/(diameter of M. oryzae in the control group-diameter of M. oryzae cake in the control group)] × 100. The strongest antifungal endophytic bacterium, designated B-612, was chosen for additional research.

Identification of Strain B-612
Standard procedures were used to recover genomic DNA from overnight B-612 cultures [37]. The gene encoding 16S rDNA can be used to distinguish bacterial species because it is the corresponding DNA sequence on the bacterial chromosome that encodes rRNA. 16S rDNA is extremely conserved in structure and function and is the most helpful and widely used molecular clock used in the systematic classification studies of bacteria [38]. Genomic DNA from strain B-612 was extracted using the sodium dodecyl sulfonate (SDS) technique for molecular characterization. We used forward primer 27F (5-AGAGTTTGATCCTGGCTCAG) and reverse primer 1492R

Antibiotic Susceptibility Assay
The susceptibility of the isolate to probiotics was investigated by applying the procedure outlined by the Clinical and Laboratory Standards [39]. The fresh endophytic bacterial solution was evenly applied to the surface of a beef paste peptone plate; after the bacterial solution was dried, drug-sensitive tablets containing different antibiotics were taken and applied to the surface of the medium. The plates were incubated in a constant temperature incubator for 24 h at 28 • C to observe the sensitivity of bacteria to various antibiotics and to measure the diameter of the inhibition circle. The drug-sensitive tablets of the antibiotics used were purchased from Hangzhou Microbiological Reagent Co. The product name and the corresponding product item number are shown in Table 1. Table 1. The product name and the product number.

Defense-Related Gene Expression
LTH plants were grown in a growth chamber (18 h of light at 28 • C and 6 h of darkness at 2 • C) to the three-leaf stage. Using distilled water with conidial suspension (concentration of 1 × 10 5 conidia/mL) as the control group, B-612 fermentation solution and conidial suspension (concentration of 1 × 10 5 conidia/mL) were mixed in a 1:1 ratio by volume and sprayed equally onto rice leaves. The rice leaves were collected at 0, 24, 48, and 72 h [40]. A Thermofisher NanoDROP was used to determine the quantity and quality of total RNA after it had been extracted using the Trizol technique. Then, we synthesized cDNA using a Primescript RT reagent kit from Takara (Beijing, China) in accordance with the manufacturer's instructions. The qRT-PCRs were conducted using a BIO-RAD connect and OsActin expression levels were used as an internal standard for normalization. Table 2 shows the primer sequences used for key defense genes and the internal reference gene. SYBR Premix Ex TaqTM (TransGen Biotech, Beijing, China) was used for real-time PCR and each reaction was carried out three times.  LTH rice leaves were collected at 0, 24, 48, and 72 h and stained for 12 h in the dark at pH = 3.8 with DAB, 1 mg/mL [41]. The stained leaves were then washed with distilled water after being destained with 95% ethanol until translucent. A ZEISS stereomicroscope was then used to track the accumulation of H 2 O 2 in the leaves.

Detection of Lipopeptide Biosynthetic Genes
The template used for the detection of lipopeptide biosynthetic genes was endophytic genomic DNA that had been kept at −20 • C. We amplified surfactin, iturin, fengycin, and bacillomycin biosynthetic genes from genomic DNA by PCR. After being recovered, the target strips were delivered to DynaScience Biotech for sequencing evaluation. The primers used were described previously. The temperature protocol for the PCR was 94 • C for 5 min, 94 • C for 30 s, 55 • C for 45 s, and 72 • C for 90 s for 30 cycles, with a final 10 min extension at 72 • C. Table 3 shows the primer sequences used to identify the lipopeptide genes.

B-612 Fermentation Broth Crude Extraction
Under reduced pressure and at 40 • C, the culture filtrate (10 L) was concentrated to a dark-brown tarry residue. Thereafter, 30 L of each of the following were used to remove the dark-brown tarry residue: n-hexane, dichloromethane, ethyl acetate, and 1-butanol. Three extractions of each organic solvent were performed. Each organic extract was then processed through a rotating vacuum evaporator to create a paste, which was then dissolved in sterile distilled water to test for antifungal activity. The organic extract with the most potent antifungal properties was then chosen for the next stage of experimentation.

Germination Testing of M. oryzae Conidia and the Formation of Appressorium
The State Key Laboratory of Agricultural Gene Exploration and Utilization in Southwest China kindly contributed to M. oryzae Guy11. The conidia originated from Guy11, a 9-day-old plant raised on complete medium (CM). Using the 1-butanol crude extract of B-612 and distilled water, the spore concentration was adjusted to approximately 1 × 10 5 conidia/mL [42]. Then, 50 µL of spore suspension was dropped onto the hydrophobic slide and kept at room temperature. With 100 conidia randomly chosen for observation, the germination rate of conidia and the development of appressorium were examined under a ZEISS fluorescence microscope at 2, 8, 12, 24, and 48 h. The experiment was repeated three times. The germination rate was calculated using the formula: Germination rate (%) = (A1/A2) × 100, where A1 represents the total number of conidia and A2 represents the number of conidia that had germinated. The developmental rate of appressorium was determined as follows: Appressorium formation rate (%) = (B1/B2) ×100 where B1 represents the number of conidia that formed appressorium and B2 represents the total number of conidia [43].

In Vivo Experiments with Living Leaves
An experimental paddy field was divided into many plots, each with an area of 1 m 2 . A film was employed to divide each plot to minimize the impact of various treatments. One-hundred LTH rice seeds were distributed uniformly throughout each plot before a 30-day cultivation period. Then, 150 mL of water, LB medium, carbendazim, B-612 bacterial solution, or B-612 filter fermentation solution, were sprayed into the plots. Each solution contained 0.1% of Tween 20 and each plot received 150 mL of M. oryzae conidia suspension containing 1 × 10 5 conidia/mL, after one day.