Measurements of Antibacterial Activity of Seed Crude Extracts in Cultivated Rice and Wild Oryza Species
Rice volume 15, Article number: 63 (2022)
Seeds are continuously exposed to a wide variety of microorganisms in the soil. In addition, seeds contain large amounts of carbon and nitrogen sources that support initial growth after germination. Thus, seeds in the soil can easily promote microbial growth, and seeds are susceptible to decay. Therefore, seed defense against microorganisms is important for plant survival. Seed-microbe interactions are also important issues from the perspective of food production, in seed quality and shelf life. However, seed-microbe interactions remain largely unexplored. In this study, we established a simple and rapid assay system for the antibacterial activity of rice seed crude extracts by colorimetric quantification methods by the reduction of tetrazolium compound. Using this experimental system, the diversity of effects of rice seed extracts on microbial growth was analyzed using Escherichia coli as a bacterial model. We used collections of cultivated rice, comprising 50 accessions of Japanese landraces, 52 accessions of world rice core collections, and of 30 wild Oryza accessions. Furthermore, we attempted to find genetic factors responsible for the diversity by genome-wide association analysis. Our results demonstrate that this experimental system can easily analyze the effects of seed extracts on bacterial growth. It also suggests that there are various compounds in rice seeds that affect microbial growth. Overall, this experimental system can be used to clarify the chemical entities and genetic control of seed-microbe interactions and will open the door for understanding the diverse seed-microbe interactions through metabolites.
Plants are exposed to a wide variety of microorganisms throughout their life cycle and constantly interact with these microorganisms. Among the microorganisms that interact with plants, symbiotic microorganisms such as mycorrhizal fungi absorb nutrients from the soil and supply them to plants, thereby positively affecting plant growth. On the other hand, infection and proliferation by microorganisms can negatively affect plant growth. It is known that plants prevent infection by releasing a group of compounds with antimicrobial activity against pathogenic microorganisms (Bednarek and Osbourn 2009). Many of these compound groups are secondary metabolites, and plants have acquired the ability to produce a variety of antimicrobial secondary metabolites in their interactions with microorganisms. Phytoanticipin and phytoalexin are antimicrobial compounds that are synthesized inducibly or not, respectively, and the same compound may act as a phytoanticipin or phytoalexin depending on plant type and organs (VanEtten et al. 1994; Morrissey and Osbourn 1999; Jeandet 2018).
Plant chemical defense using these antimicrobial secondary metabolites has been extensively studied, and to date, numerous antimicrobial secondary metabolites have been found in various plant species. Saponins are well known as phytoanticipins, with α-tomatin in tomatoes and avenacin in oats (Oros and Kállai 2019). For phytoalexins, their bioactivity, synthetic pathways, and induction mechanisms have been analyzed in various plant species (Liu et al. 2010; Schmelz et al. 2011; Ube et al. 2021).
Seed defense against microorganisms is especially important because seeds store sufficient nutrients for seedling establishment, and these seed reserves are also a source of nutrients for microorganisms. Seed defense mechanisms against soil microorganisms can be broadly classified into physical, biochemical, and chemical defenses (Dalling et al. 2020). In physical defense, the seed coat and pericarp serve as a physical barrier between the seed, including the embryo, and its external environment, and suppress microbial invasion (Gergerich and Dolja 2006). Polyphenol oxidase (PPO) is a known defense enzyme involved in biochemical defense, which accumulates in wild oat and wheat glumes (Jerkovic et al. 2010; Fuerst et al. 2011, 2018). PPO catalyzes the conversion of phenolic compounds to quinones, and the quinones may protect seeds from microbes by damaging microbial cell walls (Baltas et al. 2017; Alibi et al. 2021).
Various antimicrobial secondary metabolites identified in studies with rhizosphere and aboveground parts of plants (leaves) have also been identified in seeds (Dalling et al. 2011; Ben-Abu and Itsko 2021; Ishihara 2021). This suggests that chemical defense against microorganisms via antimicrobial secondary metabolites may also operate in seeds.
Momilactones, well-known antimicrobial secondary metabolites of rice, have been studied not only for their functions as phytoalexins but also for their biosynthetic pathways and diversity (Kato et al. 1973; Izawa and Shimamoto 1996; Cartwright et al. 1981; Peters 2006; Schmelz et al. 2014). More than 20 phytoalexins have been reported to accumulate in rice (Kodama et al. 1992; Yamane 2013; Park et al. 2013, 2014; Ishihara et al. 2008; Morimoto et al. 2018; Kariya et al. 2020). The World Rice Core Collection (WRC) (Kojima et al. 2005) and the Rice Core Collection of Japanese Landraces (JRC) (Ebana et al. 2008), which are provided by the National Agriculture and Food Research Organization (NARO, Japan), cover a wide range of genetic diversity of landraces in rice, and they are useful material for the isolation of related quantitative trait loci by GWAS (genome-wide association studies) and for the elucidation of loci associated with phenotypic diversity (Tanaka et al. 2020, 2021). Analysis using the WRC revealed that the amount and type of phytoalexins induced in stress-treated leaves differ between accessions, and novel antimicrobial secondary metabolites have been found in the leaves of several accessions (Kariya et al. 2019, 2020; Murata et al. 2020). In addition, Friedman (2013) reported that different rice secondary metabolites are produced in specific organs and tissues.
The genus Oryza consists of 23 species, of which 2 are cultivated and the remaining 21 are wild species, with 11 genome types (AA, BB, CC, BBCC, CCDD, EE, FF, GG, KKLL, HHJJ, HHKK) (Lu et al. 2009; Jacquemin et al. 2013; Nonomura et al. 2010; Sato et al. 2021; Kajiya-Kanegae et al. 2021). Remarkable differences have been observed between metabolite diversity in wild and cultivated Oryza species (Atwell et al. 2014). Among the wild Oryza species, momilactones are produced in species with AA genome (O. barthii, O. glumaepatula, O. meridionalis and O. rufipogon) and BB genome (O. punctata), but not in O. brachyantha with FF genome, and phytocasans are produced in species with AA genome but not in species with BB genome or FF genome (Miyamoto et al. 2016). These findings suggest that the composition and the amount of secondary metabolites produced by wild and cultivated Oryza species are different. Therefore, wild Oryza species may accumulate antimicrobial secondary metabolites that are not present in cultivated species, and wild Oryza species are attractive materials to search for novel and useful secondary metabolites.
Disk diffusion method is the most common method for measuring the antimicrobial activity. However, quantification of antimicrobial activity is difficult with this method. To overcome these issues, we performed colorimetric assays using tetrazolium salts, which are widely used to measure cell growth, mainly for mammalian cells but also for bacteria (Eloff 1998; Tsukatani et al. 2009; Haase et al. 2017; Grela et al. 2015; Benov 2021).
To understand the chemical defense of seeds mediated by antimicrobial secondary metabolites, we developed a simple and rapid assay system to evaluate the antibacterial activity of rice seed crude extracts using disk diffusion and colorimetric quantification methods (Fig. 1). Furthermore, we investigated the diversity of antibacterial activity of rice seeds using the rice core collection of landraces WRC, JRC and wild Oryza species, and searched for genetic factors associated with the diversity of antibacterial activity in the landraces using GWAS. Here we demonstrate a colorimetric assay system that can detect antibacterial activity of rice seed crude extracts with higher sensitivity than the disk diffusion method. The results of the measurements of antibacterial activity of rice seeds of landraces and wild Oryza species using this assay system suggest that the antibacterial activity differs between accessions and that several types of antibacterial secondary metabolites are extracted with different solvents. Through comparing the antibacterial activity of husk and brown rice extracts, different types and amounts of antibacterial compounds are suggested to accumulate in these organs. Furthermore, GWAS using the antibacterial activity of husk and brown rice extracts measured by our assay system detected several genomic regions related to the diversity of antibacterial activity. The assay system established in this study using diverse genetic resources is expected to serve as a stepping stone to explore seed-microbe interactions and antibacterial secondary metabolites produced by seeds and to contribute to the elucidation of their genetic basis.
Materials and Methods
The seeds of World Rice Core Collection (WRC) (Kojima et al. 2005) and Rice Core Collection of Japanese landraces (JRC) (Ebana et al. 2008) were obtained from the National Agriculture and Food Research Organization Genebank (NARO gene bank, Japan, http://www.gene.affrc.go.jp/index_j.php). The seeds of cultivated rice (Oryza sativa L. ‘T65’) and wild Oryza species were provided by the National Institute of Genetics (NIG, Japan, https://www.nig.ac.jp/nig/ja/). Plants were grown under natural light condition in a green-house and transplanted to paddy fields at NIG in Mishima, Japan, and the collected seeds were analyzed in this study.
Preparation of Seed Crude Extracts
The collected seeds were separated into husks and brown rice using testing rice husker (Fujiwara factory, Tokyo, Japan). The weight of husks and brown rice in 10 grains were measured (Additional file 1: Table S1). Because the weight of husks and brown rice in one accession are constant among grains, we use fix number of grains in all experiments so that weight of tissues used for extraction become constant in replicated experiments. To prepare husk and brown rice crude extracts, rice husks of 20 grains and 10 grains of brown rice were pulverized in 5 mL microtubes, respectively, by a multi-beads shocker (Yasui Kikai Corporation, Japan). Powdered samples in 5 mL microtubes were immersed in 4 mL of four different solvents (80% MeOH, diethyl ether, acetone, and sterilized water, respectively) under two different temperature (room temperature for diethyl ether and acetone extraction, 80 °C for 80% MeOH and sterilized water extraction) for 24 h. For brown rice crude extracts, diethyl ether was not used as solvent. After filter-sterilization using 0.22 μm membrane filters (Membrane Solution Limited, USA), solvents were removed by a centrifugal concentrator and each crude extracts was stored at − 20 °C for further analysis.
Antibacterial Activity Test by Disk Diffusion Method
Antibacterial activity of the rice husk crude extract was determined against Eschelicia coli DH5α by disk diffusion method according to Fukuta et al. (2007), with some modifications. Muller-Hinton (MH) broth medium was used to grow the bacteria. Single colony of E. coli were inoculated to 4 mL of MH broth and incubated at 37 °C for overnight at 180 rpm in the shaker. Cell density of overnight cultures of E. coli was determined by spectrophotometer (Bio-Rad Laboratories, USA) and suspended in 0.9% sterilized saline to 2.0 × 105 cell/mL. 500 μL of the bacteria suspension was spread evenly on each MH agar plate (9 cm diameter). Crude extracts of 20 grains of rice husk (solvents: MeOH, acetone, and sterilized water, respectively) and 80 grains of rice husk (solvent: diethyl ether) were dried and dissolved in 30 μL of 100% dimethyl sulfoxide (DMSO). The crude extracts of 20 grains of rice husk, and only diethyl ether crude extracts were equal to 80 grains. Sterilized paper disks (6 mm diameter, ADVANTEC) were impregnated by 30 μL of each extract dissolved in 100% DMSO and laid on the surface of MH agar plates. Ampicillin (10 μg/mL) and 100% DMSO were used as positive and negative control, respectively. The plates were incubated for 24 h at 37 °C and inhibition zone was measured.
Antibacterial Activity Test by Colorimetric Quantification Assay
Antibacterial activity of rice husk and brown rice crude extracts was determined by microtiter plate bioassay method using the tetrazolium compound [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS)] as a color indicator (CellTiter 96® AQueous One Solution Cell Proliferation Assay, Promega, USA) according to the manufacture’s instructions. Relative growth rate of E. coli, which represents the antibacterial activity of the sample extracts, were measured for each sample extracts. DMSO and antibiotics (ampicillin and kanamycin) are negative and positive controls of antibacterial activity.
Concentration-Dependent Growth Inhibitory Effect of Seed Crude Extracts on Escherichia coli
Rice husk crude extracts were prepared from accessions that showed antibacterial activity by the disk diffusion method and their concentration-dependent growth inhibitory effect on E. coli was investigated. To determine concentration-dependent effects, rice husk crude extracts were prepared from 20 grains of rice husk. The extracts were dried and dissolved in 40 μL DMSO for 80% MeOH extracts, 20 μL DMSO for acetone extracts and 10 μL DMSO for sterilized water extracts, respectively, as stock solutions. Brown rice crude extracts were prepared from 10 grains of brown rice. The extracts were dried and dissolved in 10 μL of DMSO as stock solution.
20 μL rice crude extracts were transferred to the first well of 96-well plate and serial dilution was done by transferring 10 μL mixture via multichannel pipette. Then, 180 μL of MH broth was poured into each of the 96 wells of the assay plate. Bacterial cells were added at a density of 4.0 × 106 cells/mL (10 μL) in 96 wells. Ampicillin and kanamycin were used as a positive control. A growth control with 10 μL suspension solvent and blank control without bacteria were also loaded in the assay plate. The assay plates were incubated at 37 °C for 5 h in a humid environment. After incubation, 40 μL of MTS solution was added to each well and mixed. The plates were then centrifuged at 600 × g for 5 min and 100 μL of the supernatant was transferred to a new 96-well plate and the absorbance at 450 nm at 0 h was measured using a microplate reader. The assay plates were incubated again at 37 °C for 4 h. After the second incubation, the plate proceeded to centrifugation at 600 × g for 5 min and 100 μL of the supernatant was transferred to a new plate and the absorbance of after 4 h was measured. Relative growth rates of bacteria treated with antibiotics and/or crude extracts were calculated by taking the increase in absorbance of the growth control wells as 1. Relative growth rate was calculated as the change in absorbance after 4 h in wells treated with antibiotics and/or seed crude extract. The increase in absorbance after 4 h in wells of the growth control was set as 100%.
Evaluation of Antibacterial Activity of Seeds of Cultivated and Wild Rice Core Collections
Antibacterial activity assays for cultivated and wild Oryza species were analyzed in the same way using certain dilutions of each crude extract as described above. Based on the results of the measurements of concentration-dependent antibacterial activity, the dilution factors that showed stronger activity than the value of 50% of maximum inhibitory concentration (IC50) in the rice husk and brown rice crude extracts using three different solvents were used in the subsequent assays.
Construction of Genetic Map
Sequence data for JRC and WRC derived from the previous study in Tanaka et al. (2020) and Tanaka et al. (2021) were downloaded from DNA Data Bank of Japan Sequence Read Archive. Trimming of raw paired-end reads and subsequent mapping against Os-Nipponbare-Reference-IRGSP-1.0 (Kawahara et al. 2013) were performed using Galaxy/NAAC, a web-based platform for a bioinformatics analysis (https://galaxy.dna.affrc.go.jp/nias/static/register_en.html). “Trimmomatic” function (Galaxy Version 0.36.3) and “BWA mapping Illumina” workflow were used for the removal of low quality reads and mapping against the reference sequence, respectively. Obtained bam files were used to create gVCF files using GATK (ver.126.96.36.199) HaplotypeCaller (McKenna et al. 2010; DePristo et al. 2011), and then gVCF files were consolidated with CombineGVCFs. Variants called with GenotypeGVCFs were then filtered using “view” function in bcftools (Li 2011) with the following parameters: -m2 -M2 -g ^het --output-type z --exclude-uncalled -e "MAF < 0.05 || N_MISSING > 17 || QD < 2.0 || QUAL < 30.0 || SOR > 3.0 || FS > 60.0 || MQ < 40.0 || MQRankSum < -12.5 || ReadPosRankSum < -8.0" to obtain 1,213,105 variants with the maximum minor allele frequency of 5% and the minimum call rate of 85% without heterozygous haplotype.
The Weighted Mixed Linear Model in TASSEL (Bradbury et al. 2007) was used for the GWAS with the option of Re-estimate after each marker. The visualization of manhattan plots and qq plots were performed with R package qqman (Turner 2014). The false discovery rate (FDR) was calculated with Benjamini–Hochberg procedure (Benjamini and Hochberg 1995), and SNPs (Single nucleotide polymorphisms) with FDR of less than 5% were considered as significant association. Genomic linkage disequilibrium (LD) decay was estimated based on the coefficients of determination (r2) between all pairs of loci using PopLDdecay (ver. 3.41) (Zhang et al. 2019) in a 2000 kb distance, and it was considered that LD was decayed at 940 kb in our genetic map since r2 was less than 0.25 at this genetic distance. Therefore, subsequent LD analysis was performed within this distance using R package LDheatmap (Shin et al. 2006), and the continuous markers with r2 more than 0.5 were considered to belong to the same LD block.
Detection of Antibacterial Activity of Rice Seeds Crude Extracts by Disk Diffusion Methods
In order to elucidate the defense mechanism against microorganisms, we aimed to establish assay systems for the antibacterial activity of rice seeds (Fig. 1). First, a crude extract prepared in 80% MeOH from the husks of cultivated rice T65 was used to determine the antibacterial activity against Escherichia coli (E. coli) (Fig. 2a). We adopted the disk diffusion method where growth inhibition circles were formed around paper disks containing antibacterial substances. Ampicillin, a commonly used antibiotic, was selected as a positive control for antibacterial activity. Growth inhibition circles were formed around discs containing ampicillin, and similarly, growth inhibition circles were observed around discs containing rice husk crude extract. From this result, we concluded that the disc diffusion method can detect antibacterial activity derived from rice husks.
Next, the antibacterial activity of rice husk crude extract was analyzed by the disk diffusion method in 52 cultivars from the World Rice Core Collection (WRC) (Kojima et al. 2005) and 50 cultivars from the Rice Core Collection of Japanese Landraces (JRC) (Ebana et al. 2008). The crude extracts used to detect antibacterial activity were prepared from 20 seeds of rice husks, and 80% MeOH, diethyl ether, acetone, and water were used as extraction solvents. The diethyl ether crude extract was prepared from 80 seed husks.
Of a total of 106 cultivars tested, 43 showed antibacterial activity in extracts prepared from any of the solvents (Fig. 2b–e, Tables 1, 2). The cultivated rice core collection is classified into four subspecies: indica, aus, temperate japonica, and tropical japonica (Tanaka et al. 2020, 2021). Of the 43 cultivars that showed antibacterial activity, 12 (43%), 9 (45%), 8 (21%), and 14 (70%) belonged to indica, aus, temperate japonica, and tropical japonica, respectively (Fig. 3a). Extracts from many of the 43 varieties showed antibacterial activity in one of the four solvents (Fig. 3b). On the other hand, extracts from several varieties showed antibacterial activity in two or more solvents. These varieties may contain multiple antibacterial compounds extracted by different solvents (Fig. 3b).
Quantitative Measurements of Antibacterial Activity of Rice Seed Crude Extracts
Since it is difficult to quantify antibacterial activity by the disk diffusion method, we developed a simple and rapid assay system for the quantitative measurement of antibacterial activity (Fig. 1). In living cells, the tetrazolium salt, MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt), is reduced to form formazan. In the MTS assay, the production of formazan by bacterial growth is measured by its specific absorbance and thus effects addition of seed crude extracts on the bacterial growth can be quantified in small-scale culture with high sensitivity. The growth inhibition of bacteria cultured in the presence of the antibiotics ampicillin or kanamycin was examined by the MTS assay and we successfully detected a concentration-dependent decrease in the growth of E. coli (Fig. 4a).
Next, we selected four varieties whose antibacterial activity was detected by the disk diffusion method in extracts in each solvent and confirmed the detection of antibacterial activity by the MTS method. As a result, we were able to confirm the growth inhibition effect in extracts from three solvents other than diethyl ether (Fig. 4b). It may be possible that, due to the extremely low solubility of ether extract in DMSO, antibacterial activity is not detected in the MTS assay from diethyl ether extracts. For the above reasons, extracts from three extraction solvents were used for subsequent assays: 80% MeOH, acetone, and water. The dose dependence on bacterial growth inhibition was then examined using husk extracts with the strongest antibacterial activity in each solvent. The half-maximal inhibitory concentrations (IC50) were between two- and three-fold dilutions for 80% MeOH extracts, and around four-fold dilution for acetone and 16-fold dilutions for water extracts, that are equivalent to the amounts of extracts from 2.5, 5, and 2.5 grains dissolved in 10 ul of DMSO, respectively (Fig. 4c–e). Based on these results, we decided to dilute the extracts used in the subsequent assays to fourfold and eightfold for 80% MeOH and acetone, and for water extracts.
Quantification of Antibacterial Activity in Extracts from Husk and Brown Rice Using Collections of Cultivated Rice
The MTS assay was used to quantify the antibacterial activity of husk extracts derived from 107 cultivated rice varieties (106 core collection varieties + T65) (Fig. 5a–c). 80% MeOH extracts from most of the 107 varieties inhibited bacterial growth to less than 50%, with extracts from 15 cultivars inhibited to less than 20% (Fig. 5a). Acetone extracts from 7 of the 107 cultivars inhibited growth to less than 50%, with extracts from 3 cultivars inhibited growth to less than 20%. (Fig. 5b). Water extracts from most of the 107 cultivars inhibited growth to less than 50%, with extracts from 36 cultivars inhibited growth to less than 20%. (Fig. 5c). Extracts with antibacterial activities in disk diffusion methods also showed strong antibacterial activities in the MTS assay and the MTS assay detect antibacterial activities in a broader range of cultivars. Thus, the MTS assay seems more sensitive in detecting antibacterial activities.
The antibacterial activity exhibited by rice seeds is not only derived from the husks but brown rice is also known to possess antimicrobial activity (Gianinetti et al. 2018; Pumirat and Luplertlop 2013). Therefore, we attempted to detect the antibacterial activity of brown rice by MTS assay using 107 cultivated rice varieties (106 core collection varieties + T65). 80% MeOH extracts from 28 of the 107 varieties inhibited bacterial growth to less than 50% and extracts from none of cultivars inhibited to less than 20% (Fig. 6a). Acetone extracts from 17 of the 107 cultivars inhibited growth to less than 50%, with extracts from 9 cultivars inhibited growth to less than 20% (Fig. 6b). Water extracts from 44 of the 107 cultivars inhibited growth to less than 50%, with extracts from 7 cultivars inhibited growth to less than 20% (Fig. 6c). Brown rice extracts from several varieties promoted the growth of bacteria (Fig. 6a–c). Since brown rice is rich in carbon sources such as starch and sugar, it is possible that these compounds in the brown rice extract promoted the growth of bacteria.
Genome-Wide Association Study to Detect Genetic Factors Causing the Diversity of Bacterial Growth by Extracts from Husk and Brown Rice from Collections of Cultivated Rice
Genome-wide association study was conducted to detect genetic factors causing the diversity of bacterial growth by extracts from husks and brown rice from collections of cultivated species of rice using the effect of bacterial growth measured by the MTS assay as phenotype data. SNPs significantly associated with the phenotype at a − log10(p) value greater than 5 were detected in the phenotype data of 80% MeOH rice hull extract, acetone brown rice extract, and 80% MeOH brown rice extract (Fig. 7a–c, Additional file 2: Fig. S1). Among these SNPs, a total of 499 SNPs were selected based on filters of FDR < 0.05 and significant associations below the p-values, and these SNPs were located in 42 linkage disequilibrium (LD) blocks (Table 3). Next, we examined the effect of each haplotype on the bacterial growth at five SNPs with the lowest p-values in an LD block, we found significant differences in bacterial growth among haplotypes for four of the five SNPs (Fig. 7 d–g). The linkage disequilibrium regions where the four SNPs locate cover the 43 kb, 206 kb, 161 kb, and 28 kb regions on chromosomes 3, 4, 7, and 9, respectively. This suggests that there are single or multiple genetic factors affecting bacterial growth by seed extracts in these regions. Thus, the quantitative measurement of antibacterial activity using the MTS method can be used to approach the genetic basis of the production of seed-derived chemicals that affect bacterial growth using GWAS and possibly other methods such as biparental QTL analysis.
Quantification of Antibacterial Activity in Extracts of Husk and Brown Rice from Collections of Wild Oryza Species
In order to understand the diversity of seed defense against environmental microorganisms among wild Oryza species, we measured antibacterial activity in extracts of husk and brown rice from 30 accessions covering 15 wild Oryza species with 8 genome types by MTS assay (Kurata et al. 2010; Nonomura et al. 2010). As reference, we also measured antibacterial activity in two cultivars, Nipponbare (NP) and Kasalath (KS). 80% MeOH extracts of husks from 15 of the 30 accessions inhibited bacterial growth to less than 50% and extracts from two of them inhibited to less than 20% (Fig. 8a). Acetone extracts of husks from 8 of the 30 accessions inhibited growth to less than 50%, with extracts from one accession inhibited growth to less than 20% (Fig. 8b). Water extracts of husk from all 30 accessions inhibited growth to less than 50%, with extracts from 10 of them inhibited growth to less than 20% (Fig. 8c). 80% MeOH extracts of brown rice from none of the 30 accessions inhibited bacterial growth to less than 50% (Fig. 8d). Acetone extracts of brown rice from most of the 30 accessions inhibited growth to less than 50%, with extracts from 10 accessions inhibited growth to less than 20% (Fig. 8e). Water extracts of brown rice from all 30 accessions inhibited growth to less than 50%, with extracts from 16 of them inhibited growth to less than 20% (Fig. 8f). Surprisingly, the growth-promoting effect which was often observed in brown rice acetone extracts from cultivated species was barely observed in wild Oryza, instead, brown rice 80% MeOH extracts from several wild Oryza promoted bacterial growth compared to cultivated species. Another important finding in the analysis using wild Oryza is that there are several accessions whose seed extracts from two or more solvents show strong bacterial growth inhibition. For example, both water and 80% MeOH extracts of husks of W1169 (O. glumaepatula) showed strong bacterial growth inhibition. Similarly, brown rice extracts with two different solvents from W1166 (O. latifolia) and W1921 (O. rufipogon) showed strong growth inhibition. In addition, brown rice extracts from all three solvents in W1401 (O. brachyantha) showed very strong (undetectable levels of bacterial growth) or relatively strong growth inhibition. These results suggest that some of wild Oryza accumulate multiple growth inhibitory substances in grains. Overall, the MTS assay is also applicable to assess the effects on bacterial growth by the seed extracts prepared from wild Oryza.
Seeds interact with a variety of microorganisms in the environment, and microbial infection and proliferation can cause seed rot and non-germination (Mizobuchi et al. 2018; Fuerst et al. 2014, 2018). Although the interactions between plants and the microorganisms that infect them have been studied mainly in the aboveground plant body and rhizosphere, much is not known about the interactions between seeds and microorganisms, especially the defense mechanisms of seeds against microorganisms. It is known that defense against microorganisms in the environment is important for seeds to germinate. One of the defense mechanisms of seeds is chemical defense by antimicrobial compounds. Rice produces antimicrobial compounds such as momilactones are known to accumulate in the husks of cultivated rice (Kato et al. 1973; Minh et al. 2018). This suggests that momilactones may contribute to the chemical defense of rice seeds. On the other hand, much remains unknown about whether compounds other than momilactones contribute to rice seed chemical defense. To address these issues, we established two bioassay systems suitable for simple and rapid determination of seed-derived antibacterial activity in a variety of materials, including landraces and wild Oryza species.
The results of seed antibacterial activity measurements using cultivated rice accessions by the disk diffusion and colorimetric quantification methods established in this study showed generally consistent trends, but overall, the colorimetric method with MTS was able to detect antibacterial activity in a wider range of accessions (Fig. 5a–c). The growth inhibition circle of the disk diffusion method is often affected by the extent of the diffusion of compounds into the medium. Therefore, even if the crude extract contains compounds with antimicrobial activity, the activity may not be detected by the disk diffusion method (Valgas et al. 2007; Bubonja-Sonje et al. 2011). Furthermore, in cases where antimicrobial compounds do not inhibit but slow down the growth of bacteria, it is conceivable that the disk diffusion method may not be able to observe growth inhibition circles. These may be the reasons why antibacterial activity could be detected in more accessions than in the MTS assay.
In this study, the cultivated rice core collections, which cover a wide range of genetic diversity, were used to determine the strength of the seed defense mechanisms against microbial infection. These materials include 28 indica and 58 japonica lines. Seed antibacterial activity of these subspecies was measured in a crude extract of 80% methanol from rice husks, from which momilactones are efficiently extracted (Lee et al. 1999), by the disk diffusion method, and 42.9% and 37.9% of indica and japonica, respectively, showed growth inhibition circles (Tables 1, 2). Since it is known that momilactones tend to accumulate more in japonica than in indica (Kariya et al. 2020), it is likely that other antibacterial compounds are present in addition to momilactones at least in indica seeds. In fact, momilactones have been reported to exhibit antibacterial activity against E. coli at 400 μg/disc in the disk diffusion assay (Fukuta et al. 2007). However, the amount of momilactones contained in rice husk is extremely small, on the order of ng per hull, and is far less than the concentration that shows a growth inhibitory effect against E. coli (Quan et al. 2019a, 2019b; Kakar et al. 2019). This suggests that compounds other than momilactones are involved in the antibacterial activity of the seeds. Furthermore, Minh et al. (2018) focused on rice husk as a material including biochemicals and analyzed the metabolites in rice husks. They found that rice husks of Koshihikari contain momilactones, phenolic acids, phenols, and long-chain fatty acids, and exhibit antimicrobial activity against bacteria. Taken together, it is suggested that several antibacterial compounds other than momilactones may contribute to the antibacterial activity in several cultivated rice varieties used in this study. If momilactones function as antibacterial compounds in seeds, it may be due to the combined action of momilactones and other antibacterial compounds rather than momilactones alone.
Both in cultivated and wild Oryza species, antibacterial activities were detected either in husks or brown rice and in both. This suggests that the defense mechanism against microorganisms by seeds may operate both in husks and brown rice and that the defense by the husks and brown rice may function independently. In fact, components of rice bran derived from the outermost layer of brown rice aleurone have been reported to exhibit antibacterial activity against bacteria (Arpan et al. 2013; Castanho et al. 2019; Ferdes et al. 2009).
The GWAS performed in this study revealed several genomic regions that are strongly associated with the inhibition of bacterial growth. Among them, several SNPs showed a strong association with the growth inhibition induced by acetone extracts of brown rice. This suggests that the genetic factors responsible for the production of substances inhibiting bacterial growth, which is contained in brown rice, may be located near these SNPs. Because these SNPs were located in a relatively large linkage disequilibrium region, we could not identify the exact genetic factors through this analysis. In the future, genetic factors can be identified through QTL analysis using the progenies of crossed plants between two cultivars with different haplotypes identified from our GWAS analysis. The simple and high throughput seed antibacterial activity assay developed in this study is a possible significance tool to identify genetic factors related to seed antibacterial activity.
In this study, we comprehensively analyzed the antibacterial activity of seeds from a wide range of wild Oryza genetic resources. It is known that some wild Oryza accessions do not produce known phytoalexins, such as momilactones (Miyamoto et al. 2016; Kariya et al. 2020). Thus, the wild Oryza accessions with strong antibacterial activity could be useful materials for understanding seed defense and interactions with microorganisms and for searching for novel compounds related to these interactions. The quantitative assay of seed antibacterial activity through MTS method developed in this study can be used for analyzing materials with a limited number of seeds, such as wild Oryza species because this method can measure antibacterial activity with a limited amount of samples. Therefore, in the future, this method can be applied for GWAS analysis using wild Oryza genetic resources and for measurement of antibacterial activity after transformation experiments of wild Oryza in the process of identifying loci involved in antibacterial substance production (Shimizu-Sato et al. 2020). It is surprising that the growth-promoting effect seen in the acetone extracts is specific to cultivated species. It is intriguing that, during the process of domestication of rice, cultivated rice strains become to accumulate chemicals with a positive effect on bacterial growth.
Effectiveness and easiness of the bioassay system we developed in this study was confirmed with Gram-negative bacteria, E. coli. There is a possibility that this assay system is applicable to other microorganisms including Gram-positive bacteria and fungi. Furthermore, it can be used to investigate antibacterial activity against seed-decaying microorganisms and vertically transmitted pathogenic microorganisms. The use of this bioassay to search for varieties that exhibit potent seed antibacterial activity is expected to accelerate the breeding of varieties resistant to vertically transmitted seed-borne diseases, and with high seed quality after storage, and advance the identification of novel antibacterial compounds.
Availability of Data and Materials
All datasets are available from the corresponding author on reasonable request.
3-(4,5-Dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt
Genome-wide association study
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Seeds of World Rice Core Collection and Rice Core Collection of Japanese Landraces were obtained from National Agriculture and Food Research Organization. The wild Oryza accessions used in this study were distributed from the National Institute of Genetics supported by the National Bioresource Project, MEXT, Japan.
This work was supported by JSPS KAKENHI Grant No. JP20H00424 to YS, and by the Japan Science and Technology Agency (JST) ACT-X Grant No. JPMJAX20BJ to YY.
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. Weight of husks and brown rice from 10 grains of WRC, JRC and wild Oryza used in this study.
. Genome-wide association study using antibacterial activities of rice seed crude extracts from 107 accessions of landraces from WRC and JRC as phenotype data. (a–c) Manhattan and Quantile–quantile plots of SNPs associated with antibacterial activity in acetone extracts from husk (a), sterilized water extracts from husk (b), and sterilized water extracts from brown rice (c).
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Yoshida, Y., Nosaka-T, M., Yoshikawa, T. et al. Measurements of Antibacterial Activity of Seed Crude Extracts in Cultivated Rice and Wild Oryza Species. Rice 15, 63 (2022). https://doi.org/10.1186/s12284-022-00610-3