Identification of Rhizospheric Actinomycete Streptomyces lavendulae SPS-33 and the Inhibitory Effect of its Volatile Organic Compounds against Ceratocystis fimbriata in Postharvest Sweet Potato (Ipomoea batatas (L.) Lam.)

Black spot disease, which is caused by the pathogenic fungal Ceratocystis fimbriata, seriously affects the production of sweet potato and its quality during postharvest storage. In this study, the preliminary identification of the rhizosphere actinomycete strain SPS-33, and its antifungal activity of volatiles in vitro and in vivo was investigated. Based on morphological identification and phylogenetic analysis of the 16S rRNA gene sequence, strain SPS-33 was identified as Streptomyces lavendulae. Volatile organic compounds (VOCs) emitted by SPS-33 inhibited mycelial growth and sporulation of C. fimbriata in vitro and also induced a series of observable hyphae morphological changes. In an in vivo pathogenicity assay, exposure to SPS-33 significantly decreased the lesion diameter and water loss rate in sweet potato tuberous roots (TRs) inoculated with C. fimbriata. It increased the antioxidant enzymes’ activities of peroxidase, catalase, and superoxide dismutase as well as decreased malondialdehyde and increased total soluble sugar. In the VOC profile of SPS-33 detected by a headspace solid-phase micro extraction (HS-SPME) and gas chromatography-mass spectrometry (GC-MS), heptadecane, tetradecane, and 3-methyl-1-butanol were the most abundant compounds. 2-Methyl-1-butanol, 3-methyl-1-butanol, pyridine, and phenylethyl alcohol showed strong antifungal effects against C. fimbriata. These findings suggest that VOCs from S. lavendulae SPS-33 have the potential for pathogen C. fimbriata control in sweet potato postharvest storage by fumigant action.


Introduction
Sweet potato [Ipomoea batatas (L.) Lam.] is one of the 10 most important crops in the world. It has the characteristics of low fat, low caloric, and high dietary fiber content. It is also a medicinal plant, which has many important biological activities, such as anti-tumor, antibacterial, and antioxidant factors [1,2]. At present, sweet potato is widely planted in more than 100 countries in the world, of which the largest cultivated area is the continent of Asia. This is followed by Africa and South America. China is the largest sweet potato planting country with an annual planting area of more than 5 million hm 2 , which accounts for about 65% of the world's total output [3]. Recently, sweet potato has and (3) identifying the VOC composition of SPS-33 and evaluating the antifungal effect of selected volatile compounds.

Microorganism, Plant Materials, and Chemicals
Strain SPS-33, which is a Streptomyces-like actinobacterium, was isolated from the sweet potato rhizosphere soil at the Sweet Potato Research Institute of Chinese Academy of Agricultural Sciences in Xuzhou, Jiangsu, China. SPS-33, which is grown on malt extract-yeast extract agar (ISP 2 medium) at 28 • C, was preserved in our laboratory. Ceratocystis fimbriata ACCC30008, obtained from the Agricultural Culture Collection of China, was cultured on potato dextrose agar (PDA) medium at 28 • C. Sweet potato TRs (cv. 'Tianmu') with a similar size (13-15 cm length and 5-7 cm width) and a healthy appearance were purchased from a local market (Xuzhou, China). In preparation for the pathogenicity test, the surface of TRs was sterilized with 2% sodium hypochlorite for 2 min, thoroughly washed with tap water, and air-dried at room temperature.

Identification of Strain SPS-33
Strain SPS-33 was identified by the combination of morphological observation, 16S RNA gene sequencing, and phylogenetic analysis methods. The colony and cultural characteristics were observed on ISP 2 agar [21]. The morphology of mycelia and the spore chain were observed by light microscopy (SA3300-PL) after being grown on ISP 2 medium for 7 days at 28 • C. Total genomic DNA extraction and PCR amplification of the 16S rRNA gene was carried out, according to the previously published procedures [22]. The 16S rRNA gene sequence alignment and similarity calculation was determined via the EzTaxon-e database (http://eztaxon-e.ezbiocloud.net/). Phylogenetic trees were constructed using the maximum-likelihood [23], maximum-parsimony [24], and the neighbor-joining [25] tree, which makes algorithms by MEGA 6.0 software [26]. The topologies of the trees were evaluated in a bootstrap analysis based on 1000 re-samplings [27]. The complete 16S rRNA gene sequence (1510 bp) of strain SPS-33 has been deposited in the GenBank under the accession number MN540709.

Antagonistic Test of VOCs Emitted by SPS-33
The antagonistic assay of VOCs produced by SPS-33 against C. fimbriata was determined according to the previous research [20] with minor modifications. Potato dextrose agar (PDA) medium was added to one side of the I-plates (diameter, 90 mm, volume, 0.07 L), and ISP 2 medium was added to the other side of the same plate. SPS-33 was inoculated on ISP 2 medium by streaking and incubated at 28 • C for 2 days until white aerial mycelium appeared. Then, C. fimbriata mycelial discs (5-mm diameter) were inoculated on PDA medium. I-plates with C. fimbriata on one half were used as controls. All of the I-plates were completely sealed with Parafilm to form a closed environment and incubated at 28 • C. Two vertical diameters of each C. fimbriata colony were measured daily with Vernier calipers until fungal mycelium reached the edge of the control plates. The inhibition rate was determined according to the formula: inhibition rate (%) = 1 − Dt−Dd Dc−Dd × 100%, where Dc is the average diameter of the mycelial in the control plate, Dt is that of the test plate, and Dd is that of the inoculated mycelium discs. Meanwhile, the sporulation capacity was counted every day with a hemocytometer. Mycelial morphology was observed after dyeing with lactophenol cotton blue [20].

Pathogenicity Assay
The postharvest in vivo experiment was performed similarly to the previous procedure [6] with minor modifications. Twenty micro-wounds (5-mm deep) were made using the sterile needle tip in the middle of one side of the sweet potato TRs to form a circle with a diameter of about 8 mm. Then, the sweet potato TRs and six ISP 2 agar plates containing 200 µL SPS-33 suspensions (cultured at 28 • C, 120 rpm for 5 days) were sealed in plastic boxes (volume, 0.75 L). Sweet potato TRs without SPS-33 treatment placed in plastic boxes were used as controls. After incubation at 28 • C for 20 days, a series of indicators for disease resistance and quality of sweet potato TRs were evaluated. The weight loss rate of TRs was detected by the weighing method. Evaluation of disease severity (DS) was based on a five-degree empirical scale: (1) 0 mm < lesion diameter ≤ 8 mm, (2) 8 mm < lesion diameter ≤ 16 mm, (3) 16 mm < lesion diameter ≤ 24 mm, (4) 24 mm < lesion diameter ≤ 32 mm, and (5) 32 mm < lesion diameter ≤ 40 mm. DS was calculated according to the formulas in the literature [20].
For antioxidant enzymes and malondialdehyde (MDA) analysis, 1.0 g of the sweet potato TRs was homogenized in 2 mL of 0.1 M phosphate buffer (pH 7.0) on ice. After centrifugation at 10,000 rpm for 20 min, the supernatant was collected for a subsequent detection. Activity of peroxidase (POD) was determined by a guaiacol colorimetric method [28], catalase (CAT) activity was measured spectrophotometrically at 240 nm [29], and superoxide dismutase (SOD) was measured by determining the scavenging degree for the superoxide anion radical using the nitro blue tetrazolium (NBT) method [30]. The MDA content was measured via the thiobarbituric (TBA) reaction on the basis of the previously described procedure [31]. An anthrone method was used to quantify the total soluble sugar (TSS) of sweet potato TRs [32].

Analysis of VOCs Emitted by SPS-33
The VOCs produced by SPS-33 were analyzed by headspace solid-phase micro extraction (HS-SPME) and gas chromatography-mass spectrometry (GC-MS). The extraction and detection method of VOCs were previously reported [16]. SPS-33 was incubated on ISP 2 medium in a headspace vial at 28 • C for 7 days. A blank ISP 2 medium served as the control. The HS-SPME fiber (DVB/CAR/PDMS, Supelco, Bellefonte, PA, USA) was used to extract the volatile compounds at 50 • C for 30 min. The GC-MS analyses were determined by the Agilent 7890B GC system and Agilent 5975C mass spectrometer. The GC-MS condition used for analysis was as mentioned according to the method described by Zhang et al. [20]. The Chroma TOF 4.3X software (LECO Corporation) was used for peaks extraction, filtering and calibration, and VOCs produced by strain SPS-33 were tentatively identified by the National Institute of Standards and Technology (NIST 14) database.

Inhibitory Effect of Selected Volatile Compounds on C. fimbriata
According to the test results of HS-SPME/GC-MS analysis, 15 volatile compounds with a similarity ≥800 and area ≥0.9% were selected for this antifungal assay. Components presented in both the control and SPS-33 treated groups were removed. Different volumes of volatile compounds sterilized by filter membranes were dropped on filter papers. Sterile water served as the control. C. fimbriata mycelial discs were placed on the other compartment of I-plates (diameter, 90 mm) containing PDA medium. The inhibition rate was calculated after being incubated at 28 • C for 7 days.

Statistical Analysis
All experiments were carried out at least three times. The data analysis and graphical drawing were performed using the Graphpad Prism 7.0 software, and differences among groups were identified by one-way analysis of variance. The results are expressed as the mean ± standard deviation.

Identification of Strain SPS-33
Strain SPS-33 grew well on the ISP 2 agar plates, and its colony was loose and grey ( Figure 1B). It also formed branched substrate and aerial hyphae, which broke into rods after maturation ( Figure 1C). Morphological observation revealed that strain SPS-33 had the typical colony and mycelial characteristics of the genus Streptomyces. 16S rRNA gene sequencing and analysis revealed that strain SPS-33 showed 100% sequence identity to Streptomyces lavendulae, and they formed a distinct subclade in the phylogenetic tree ( Figure 1A). Thus, strain SPS-33 was identified as a new strain of the species Streptomyces lavendulae. Strain SPS-33 grew well on the ISP 2 agar plates, and its colony was loose and grey ( Figure 1B). It also formed branched substrate and aerial hyphae, which broke into rods after maturation ( Figure  1C). Morphological observation revealed that strain SPS-33 had the typical colony and mycelial characteristics of the genus Streptomyces. 16S rRNA gene sequencing and analysis revealed that strain SPS-33 showed 100% sequence identity to Streptomyces lavendulae, and they formed a distinct subclade in the phylogenetic tree ( Figure 1A). Thus, strain SPS-33 was identified as a new strain of the species Streptomyces lavendulae.

Antagonistic Test of VOCs Produced by SPS-33
In the control group, the colony diameter of C. fimbriata increased significantly with the prolongation of culture time. The colony had grown to the edge of the plate on the 7 th day ( Figure  2A). However, the mycelial growth was significantly inhibited in the SPS-33 treated group. From the second day after inoculation, there was a significant difference in the colony diameter between two groups ( Figure 2B). The highest inhibition rate of mycelial growth was 54.92%, which appeared on the fourth day ( Figure 2C). Although the inhibition rate did not increase continuously, the morphology of the fungal colonies clearly changed. In the control group, the colonies were dense and coupled with a felt-like appearance, which indicates that the aerial mycelium were abundant. Colonies in the treatment group not only had a smaller size, but also displayed a sparse mycelial distribution (Figure 2A).
It was found that spores of C. fimbriata in the control group were produced from the second day after inoculation. The spore production continued to increase with the prolongation of incubation time with a sporulation capacity of 1.14×10 7 spores/mL. However, C. fimbriata in the treatment group did not produce spores within 7 days.
All of the hyphae in the control group were stained by lactophenol cotton blue. The hyphal interiors were fully filled with abundant cellular inclusions. Hyphae were connected together, similar to bamboo and displayed clear and visible septum. Short rod spores were observed around hyphae ( Figure 2D). Hyphae treated by SPS-33 were discontinuously stained, which showed many

Antagonistic Test of VOCs Produced by SPS-33
In the control group, the colony diameter of C. fimbriata increased significantly with the prolongation of culture time. The colony had grown to the edge of the plate on the 7 th day ( Figure 2A). However, the mycelial growth was significantly inhibited in the SPS-33 treated group. From the second day after inoculation, there was a significant difference in the colony diameter between two groups ( Figure 2B). The highest inhibition rate of mycelial growth was 54.92%, which appeared on the fourth day ( Figure 2C). Although the inhibition rate did not increase continuously, the morphology of the fungal colonies clearly changed. In the control group, the colonies were dense and coupled with a felt-like appearance, which indicates that the aerial mycelium were abundant. Colonies in the treatment group not only had a smaller size, but also displayed a sparse mycelial distribution (Figure 2A).
It was found that spores of C. fimbriata in the control group were produced from the second day after inoculation. The spore production continued to increase with the prolongation of incubation time with a sporulation capacity of 1.14×10 7 spores/mL. However, C. fimbriata in the treatment group did not produce spores within 7 days. All of the hyphae in the control group were stained by lactophenol cotton blue. The hyphal interiors were fully filled with abundant cellular inclusions. Hyphae were connected together, similar to bamboo and displayed clear and visible septum. Short rod spores were observed around hyphae ( Figure 2D). Hyphae treated by SPS-33 were discontinuously stained, which showed many uncolored areas and vacuoles. The septum was difficult to observe, and an abnormal enlargement occurred at the hyphal end ( Figure 2E). uncolored areas and vacuoles. The septum was difficult to observe, and an abnormal enlargement occurred at the hyphal end ( Figure 2E).

Pathogenicity Assay
The lesion diameter of the TR+CF group significantly expanded at the end of the 20 days of storage time. In the TR+CF+SPS-33 group, exposure to SPS-33 significantly decreased the lesion diameter caused by C. fimbriata compared with the TR+CF group. There were no lesions on the surfaces of the TR group and the TR + SPS-33 group without C. fimbriata inoculation. Furthermore, the black spot spread rapidly to the inside of the TRs in the transverse section of the TR + CF group. More than one-third of the transverse section turned black after 20 days. In particular, the surface of TRs sagged inward, and the lesions became dry and empty because of the large area of the lesions. Less lesion areas and milder symptoms were observed in the TR+CF+SPS-33 group. There were no black spots or other symptoms in the transverse section of the TR group and the TR+ SPS-33 group ( Figure 3A).
After incubation for 20 days, the weight loss rate of the TR+CF group was significantly higher than that of the TR+CF+SPS-33 group. There was no significant difference in the weight loss rate between the TR group and the TR+ SPS-33 group ( Figure 3B). Similar results were observed

Pathogenicity Assay
The lesion diameter of the TR+CF group significantly expanded at the end of the 20 days of storage time. In the TR+CF+SPS-33 group, exposure to SPS-33 significantly decreased the lesion diameter caused by C. fimbriata compared with the TR+CF group. There were no lesions on the surfaces of the TR group and the TR + SPS-33 group without C. fimbriata inoculation. Furthermore, the black spot spread rapidly to the inside of the TRs in the transverse section of the TR + CF group. More than one-third of the transverse section turned black after 20 days. In particular, the surface of TRs sagged inward, and the lesions became dry and empty because of the large area of the lesions. Less lesion areas and milder symptoms were observed in the TR+CF+SPS-33 group. There were no black spots or other symptoms in the transverse section of the TR group and the TR+ SPS-33 group ( Figure 3A). The results are presented as the mean values ± standard deviation. Means with different letters for each volume (a-d) denote differences (P < 0.05).

Analysis of VOCs Emitted by SPS-33
Based on the analysis of VOCs obtained by HS-SPME combined with GC-MS, 20 volatile compounds produced by S. lavendulae, SPS-33 with a relative area of more than 0.9% are listed ( Table 2). Heptadecane (16.73%) was the most abundant, which was followed by tetradecane (10.84%), 3-methyl-1-butanol (9.40%), acetone (5.41%), and pyridine (5.35%). Fifteen volatile compounds were selected for the antifungal assay, according to their physicochemical properties and antimicrobial activity reports. After incubation for 20 days, the weight loss rate of the TR+CF group was significantly higher than that of the TR+CF+SPS-33 group. There was no significant difference in the weight loss rate between the TR group and the TR+ SPS-33 group ( Figure 3B). Similar results were observed regarding the DS in Figure 3C. The DS of the TR+CF group was significantly higher than that of the TR+CF+SPS-33 group.
The effects of fumigation on the physiological indicators of TRs were evaluated by antioxidant enzymes and the content of MDA and TSS (Table 1). For antioxidant enzymes activity, there was no significant difference for the TR+SPS-33 groups. The SOD, POD, and CAT activities of the TR+CF+SPS-33 group were significantly higher than that of the control groups after 20 days. The MDA content of the TR+CF+SPS-33 group and the TR+SPS-33 group was significantly lower than the SPS-33 untreated groups. After 20 days of culturing, the TSS contents of the TR+SPS-33 and TR+CF+SPS-33 groups were significantly higher than that of the control.

Analysis of VOCs Emitted by SPS-33
Based on the analysis of VOCs obtained by HS-SPME combined with GC-MS, 20 volatile compounds produced by S. lavendulae, SPS-33 with a relative area of more than 0.9% are listed ( Table 2). Heptadecane (16.73%) was the most abundant, which was followed by tetradecane (10.84%), 3-methyl-1-butanol (9.40%), acetone (5.41%), and pyridine (5.35%). Fifteen volatile compounds were selected for the antifungal assay, according to their physicochemical properties and antimicrobial activity reports. a VOCs with an area of >0.9%. b The relative area of a single compound is the percentage of the total area of the chromatographic peak.

Inhibitory Effect of Selected Volatile Compounds on C. fimbriata
As shown in Table 3, 9 of the 15 compounds showed different inhibitory effects on C. fimbriata, and their antifungal activities were increased with the increase of volume. 2-Methyl-1-butanol and 3-methyl-1-butanol showed the strongest antifungal activities against C. fimbriata with an inhibition rate of 100% at 30 µL/plate concentration. The next was pyridine with an inhibition rate of 100% at 70 µL/plate concentration. Another alcohol, which is phenylethyl alcohol, also had strong antifungal activity against C. fimbriata with an inhibition rate of 88.38% at 50 µL/plate concentration. Six of the 15 volatile compounds, i.e., heptadecane, tetradecane, pentadecane, ethyl dodecanoate, hexadecane, and 2-pentadecanone, had no inhibitory effect on C. fimbriata at the tested volume range. Table 3. Inhibition effects of the VOCs on C. fimbriata mycelial growth.

Discussion
The genus Streptomyces, as a typical representative of actinomycetes, is known for producing a variety of antibiotics for the benefit of human health. In recent years, it has been found that many strains of streptomycetes also produce VOCs to inhibit fungi growth. Volatiles generated by S. alboflavus TD-1 showed wide-spectrum antimicrobial activity against Fusarium moniliforme Sheldon, Aspergillus flavus, A. ochraceus, A. niger, and Penicillum citrinum [33]. Volatile substances from S. globisporus JK-1 inhibited the development of P. italicum in vitro as well as on Citrus microcarpa [34]. VOCs produced by S. albulus NJZJSA2 significantly repressed mycelial growth of Sclerotinia sclerotiorum and F. oxysporum [35]. However, there is no report about VOCs produced by S. lavendulae to date. The original culture of S. lavendulae was isolated from soil by Waksman and Curtis in 1916 [36]. Since Waksman and Woodruff isolated streptothricin from it in 1942 [37], numerous reports explored the secondary metabolites and their further functions of S. lavendulae, including antibacterial, antifungal, antioxidant, cytotoxic, and antiviral activities [38][39][40][41][42][43]. For decades, the research on S. lavendulae that has focused on its fermentation broth. To our knowledge, this is the first report on the VOCs produced by the S. lavendulae strain.
In this study, the C. fimbriata colony fumigated by S. lavendulae SPS-33 was sparse and light in color, which indicated that the development of aerial mycelium was significantly inhibited. Fungal reproduction is mainly accomplished by producing a large number of spores. In artificial media, fungi usually produce asexual spores through the differentiation of aerial hyphae. Therefore, the healthy growth and development of aerial mycelium is directly related to the formation of spores, which explains why no sporulation was observed in the SPS-33 treated group. Dyeing photographs directly proved the damage of VOCs to mycelia. The results suggested that VOCs produced by S. lavendulae SPS-33 inhibited spore production by affecting the normal growth and development of mycelia. The fumigation of S. lavendulae SPS-33 clearly reduced the lesion diameter and disease severity in sweet potato TRs, and, thus, decreased the weight loss rate due to black spot disease. Oxidative burst is one of the earliest defense reactions in the plant to pathogenic infection, which leads to rapid production of high levels of reactive oxygen species (ROS). Recent studies considered that ROS plays a dual role in plant defense mechanisms [44]. Low concentration of ROS acts as an important signal molecule to participate in cell proliferation, differentiation, apoptosis, and adaptation to stress. However, a high concentration of ROS has strong oxidation ability, which can destroy many biological functional molecules, including the peroxidation of membranes. Antioxidants in plant defense systems, such as SOD, POD, and CAT, can reduce ROS and decrease cell damage [45]. The present results indicated that SOD, POD, and CAT activities were enhanced during the culture time after treatment. The reason may be that it takes time to synthesize antioxidant enzymes and increase the expression of antioxidant enzymes induced by VOCs. The MDA production is one of the indicators for identifying stress injury in plants [46]. Results showed that the fumigation of S. lavendulae SPS-33 decreased MDA content, which further verified the detection of antioxidant activities.
TSS is mainly composed of sucrose, glucose, and fructose. The high content of TSS in sweet potato TRs is associated with a sweet taste and good edible quality. Soluble sugar is also an important substance for plants to cope with salt stress, drought, and low temperature, which is related to drought resistance and freeze resistance of sweet potatoes [47]. Therefore, TSS is one of the most important indicators to measure the quality of sweet potatoes. In this study, we found that the TSS content of sweet potatoes fumigated by strain S. lavendulae SPS-33 were increased significantly with or without pathogen infection (Table 1). 'Tianmu,' which is used in the pathogenicity assay, is a very popular edible-type sweet potato TR known for their good taste in recent years. Fumigation treatment not only alleviated the symptoms of black spot disease, but also increased the TSS contents during storage. Thus, it is significant to maintain the quality of sweet potato during postharvest storage.
As the genus Streptomyces produces large quantities of antibiotics, so does its VOC production capacity. Of the 120 VOCs isolated from 26 Streptomyces spp. cultured on Emmerson's yeast starch agar, the most common compounds included isoprene, acetone, 3-methyl-1-butanol, 2-methyl-1-butanol, cyclopentanone, dimethyl disulfide, dimethyl trisulfide, phenylethyl alcohol, and geosmin [48]. It was indicated that some frequently produced VOCs may be the by-products of primary metabolism [49] like an earthy-smelling substance geosmin [34]. However, most of the VOCs are strain-specific, which means each strain produces a unique profile of VOCs [49]. The VOCs produced by streptomycetes generally include alcohols, esters, ketones, sulfur compounds, and terpenoid compounds [48]. As shown in Table 2, the main alcohols produced by S. lavendulae SPS-33 were 3-methyl-1-butanol, 2-methyl-1-butanol, and phenylethyl alcohol. These three volatiles have good antimicrobial activity and can be produced by a variety of microorganisms, such as S. fimicarius BWL-H1, different Actinobacteria isolates, and Pseudomonas chlororaphis subsp. aureofaciens SPS-41 [20,49,50]. It was found that alcohols showed a noticeably higher antimicrobial activity than esters and ketones in this study, which was consistent with other reports [9,20]. Ethyl decanoate, ethyl dodecanoate, and ethyl octanoate, classified into medium chain fatty acid ethyl esters, were relatively high-content esters produced by S. lavendulae SPS-33. These esters are commonly used as additives in the food industry for their excellent aroma characteristics [51]. Ethyl octanoate and ethyl decanoate showed antifungal activity against C. fimbriata to some extent, but ethyl dodecanoate did not. In this study, most ketones did not show an inhibition effect on C. fimbriata, except acetone. Ketones produced by Pseudomonas chlororaphis 449 inhibited the formation of biofilms of Agrobacterium tumefaciens and reduced the number of living cells in mature biofilms [52]. Volatile ketones may form Schiff bases with amino groups of proteins, which interferes with the normal functions of proteins [52]. Sulfur compounds and terpenoid compounds were not listed in the table because their content was very low. However, some sulfur VOCs, such as dimethyl disulfide produced by some Streptomyces spp., showed significantly antifungal activity against storage pathogens [33]. This indicated that microbially-mediated VOC compositions are affected by many factors, such as strains, growth media composition and proportion, and culture conditions. We noticed that heptadecane and tetradecane, which are the most abundant volatile compounds produced by SPS-33, had no clear inhibition activity against C. fimbriata. The following work is to change the VOC composition and improve the antimicrobial ability of S. lavendulae SPS-33 by optimizing the culture medium and conditions.

Conclusions
To our knowledge, this is the first study that focuses on the VOCs produced by S. lavendulae. VOCs emitted by S. lavendulae significantly inhibited the development of C. fimbriata in vitro as well as in postharvest sweet potato TRs. Furthermore, fumigation of SPS-33 caused a series of positive physiological reactions in TRs during storage. These results suggested that S. lavendulae SPS-33 could be a potential biological fumigant to control black spot disease in postharvest sweet potato. The fumigation activity of the strain needs to be further optimized and improved in a further study.
Author Contributions: K.X. and S.Q. conceived and designed the experiments. X.L., B.L., S.C., Y.Z., and M.X. performed the experiments. C.Z. and B.Y. contributed by preparing the materials/analysis tools. K.X. and S.Q. wrote the paper. All authors have read and agreed to the published version of the manuscript.