- Research article
- Open Access
Dietary rice bran promotes resistance to Salmonella enterica serovar Typhimurium colonization in mice
© Kumar et al.; licensee BioMed Central Ltd. 2012
- Received: 15 October 2011
- Accepted: 14 May 2012
- Published: 4 July 2012
Dietary rice bran consists of many bioactive components with disease fighting properties; including the capacity to modulate the gut microbiota. Studies point to the important roles of the gut microbiota and the mucosal epithelium in the establishment of protection against enteric pathogens, such as Salmonella. The ability of rice bran to reduce the susceptibility of mice to a Salmonella infection has not been previously investigated. Therefore, we hypothesized that the incorporation of rice bran into the diet would inhibit the colonization of Salmonella in mice through the induction of protective mucosal responses.
Mice were fed diets containing 0%, 10% and 20% rice bran for one week prior to being orally infected with Salmonella enterica serovar Typhimurium. We found that mice consuming the 10 and 20% rice bran diets exhibited a reduction in Salmonella fecal shedding for up to nine days post-infection as compared to control diet fed animals (p < 0.05). In addition, we observed decreased concentrations of the pro-inflammatory cytokines, TNF-alpha, IFN-gamma, and IL-12 (p < 0.05) as well as increased colonization of native Lactobacillus spp. in rice bran fed mice (p < 0.05). Furthermore, in vitro experiments revealed the ability of rice bran extracts to reduce Salmonella entry into mouse small intestinal epithelial cells.
Increasing rice bran consumption represents a novel dietary means for reducing susceptibility to enteric infection with Salmonella and potentially via induction of native Lactobacillus spp.
- Rice Bran
- MacConkey Agar
- Oral Challenge
- Enteric Infection
- Rice Bran Extract
Salmonella outbreaks are a major health challenge and medical problem around the world. Of the ~2,200 strains, Salmonella enterica and enteridis cause 75% of total disease incidence . Disease occurrence has resulted in economic burdens of $0.5 to $2.3 billion due to healthcare costs and productivity loss . Emergence of drug resistant Salmonella strains is a strong rationale for the development of easily implemented dietary strategies to reduce susceptibility to infection [3, 4]. Evidence suggests that presence of some indigestible saccharides and polyphenols in the diet can affect survival and maintenance of gut microflora as well as help prevention of colonization by enteric pathogens [5–7]. For example, non-digestible carbohydrates can be fermented by native gut Lactobacillus spp. which results in the production of organic acids, such as bacteriocins and hydrogen peroxides. These byproducts are associated with reduced growth of Salmonella[8, 9]. Therefore, dietary supplementation represents a novel approach to aid in the induction of protective responses against enteric infections.
Little is known regarding the potential impact of whole foods on the colonization of Salmonella in the small intestine because traditional biomedical research methods focus on the effect of single nutrients or isolated dietary small molecules . Rice is an important staple food worldwide and the bran portion is typically removed, making rice bran widely available for human and animal consumption. Rice bran contains prebiotic components , and is a rich source of bioactive polyphenols, fatty acids and peptides [12–16]. Dietary rice bran intake has been shown to increase the fecal IgA and native gut Lactobacillus spp. in mice . Also, rice bran has been found to control gastrointestinal cancers, hyperlipidemia and diabetes in rats [18–21] as well as hypercholesterolemia in humans .
The primary goal of this study was to examine the effect of dietary rice bran intake on susceptibility of mice to oral challenge with Salmonella. The Salmonella enterica serovar Typhimurium strain 14028s was chosen for these studies because it is a translational model of non-lethal, infection in female 129 S6/SvEvTac mice . The protective effect of rice bran against Salmonella infection in mice was measured by decreased fecal shedding following oral challenge. These novel findings of rice bran bioactivity have practical implications for developing accessible, affordable and effective dietary public health intervention strategies to reduce Salmonella infections worldwide.
Effect of dietary rice bran intake on Salmonella fecal shedding
Effect of dietary rice bran on serum cytokines
Effect of dietary rice bran on fecal Lactobacillus spp
Rice bran extract inhibited Salmonella entry and replication in vitro
We next assessed the ability of RBE to inhibit the intracellular replication of Salmonella in MSIE cells (Figure 4B). After infection and incubation, extracellular bacteria were removed by washing and antibiotic treatment, and kept for 24 h with RBE. The 2 mg/ml dose of RBE reduced intracellular Salmonella replication by 30% (p < 0.05) in comparison to control. No direct effect of RBE on Salmonella extracellular growth and replication was detected (data not shown). These results suggest that the rice bran extract contains bioactive compounds that block Salmonella entry into MSIE cells as well as inhibit intracellular Salmonella replication in in vitro model.
We next assessed the ability of RBE to inhibit the intracellular replication of Salmonella in MSIE cells (Figure 3B). After infection and incubation, extracellular bacteria were removed by washing and antibiotic treatment, and kept for 24 h with RBE. The 2 mg/ml dose of RBE reduced intracellular Salmonella replication by 30% (p < 0.05) in comparison to control. No direct effect of RBE on Salmonella extracellular growth and replication was detected (data not shown). These results suggest that the rice bran extract contains bioactive compounds that block Salmonella entry into MSIE cells as well as inhibit intracellular Salmonella replication in in vitro model.
Rice bran diet components and weight of animals
Composition of control (AIN93-M) and Rice Bran supplemented mice diets
Rice Bran (RB)
In this study, we examined the ability of dietary rice bran to protect mice against an oral challenge with Salmonella. Decreased Salmonella fecal shedding is a reliable marker for reduced susceptibility to infection [28–30] and was used herein to determine whether dietary rice bran supplementation reduced susceptibility to Salmonella infection. Fecal shedding of Salmonella from orally challenged mice fed 10 and 20% rice bran diets was significantly reduced as compared to control diet (Figure 1). Consistent with previous research, the highest number of fecal Salmonella in the control diet fed mice was observed on day 7, followed by a reduction in Salmonella numbers on days 8–13 (Figure 1) . Salmonella fecal shedding in rice bran fed mice was consistently lower than control diet fed mice until day 9-post infection.
We chose this mouse model of Salmonella infection over other models because the 129 S6/SvEvTac mice do not die from disseminated Salmonella infection due to presence of both functional copies of the nramp1 gene whereas other strains would die within 7–14 days of inoculation . Although our data suggested that rice bran supplementation decreased Salmonella invasion in the ileum, Peyer’s patches and mesenteric lymph node of the rice bran fed mice, these values were not significant ( Additional file 1: Figure S1). Thus, the rice bran diet reduced Salmonella fecal shedding may be a result of the induction of increased colonization resistance in the intestinal lumen as opposed to the increased horizontal transfer of Salmonella into the tissues .
Gut inflammation resulting from Salmonella presence favors the colonization and growth of the Salmonella because of changes in gut ecology and environment . Local inflammation in the intestine occurs in conjunction with a massive systemic release of TNF-α, IFN-γ and IL-12 [24, 32, 33]. The rice bran fed mice showed a significant reduction in serum inflammatory cytokines associated with Salmonella infection, namely TNF-α, IFN-γ and IL-12 (Figure 2A-C). The presence of Salmonella antigens in the lumen is in part responsible for inducing the inflammatory cytokines in control diet fed animals. Therefore, a reduced Salmonella antigen load in the lumen of rice bran fed mice may have diminished this inflammatory response. Determining the mucosal immune cells involved in the development of local and systemic inflammation by Salmonella in these mice will be important for understanding the mechanisms by which rice bran modulates the inflammatory response.
Given that Salmonella induces changes in the gut microbiome [25, 34], we next explored differences in the gut microbial communities between control and rice bran fed mice as a plausible mechanism for the reduced colonization of Salmonella (Figure 1). Our exploratory data showed increased Firmicutes in rice bran diet fed animals as compared to control animals before infection (Data not shown). The phylum Firmicutes contains the genus Lactobacillus and rice bran fed animals demonstrated a ~170 fold increase in fecal Lactobacillus spp. content as compared to control before infection (Figure 3). Probiotic Lactobacillus spp. protect against Salmonella infection through production of lactic acid that modulates bacterial virulence gene expression and can help maintain tight junctions of mucosal epithelial cells [35–37]. Changes in the gut microbiota by dietary rice bran warrant a separate study to explore this novel mechanism for prevention and reduced susceptibility to Salmonella infection.
Our study has indicated a potential use for dietary rice bran to mitigate Salmonella infection. Increasing consumption of rice bran represents a promising and novel means for reducing susceptibility to enteric infection with Salmonella, potentially through the modulation of native gut Lactobacillus spp. Further investigation in animal models and human clinical studies will be necessary to elucidate mechanisms of action and physiological importance of dietary rice bran supplementation against enteric infections.
Animals and feeding schedule
Four-to-six weeks-old female 129 S6/SvEvTac (Taconic Farms, Germantown, NY) mice were randomly divided into 3 groups (n = 5 in each group) and housed with a 12-hour light/dark cycle at 20–25°C. Animals were provided water and fed a maintenance diet AIN-93 M (Harlan Teklad, Madison, WI) ad libido for three weeks. After 3 weeks, mice were randomized into Group 1- AIN-93 M control diet, Group 2–10% rice bran diet, or Group 3–20% rice bran diet. The Animal Care and Use Committee at Colorado State University approved all mouse protocols (Protocol number 09-1457A).
Salmonella enterica serovar Typhimurium strain 14028s was a generous gift from Dr. Andres Vazquez-Torres (University of Colorado). Salmonella was grown in LB broth (Sigma Aldrich) at 37°C overnight to obtain stationary phase cultures, 15% glycerol (Fisher Scientific) was added and stocks were stored at −80°C. Frozen Salmonella stock was thawed and diluted with PBS to a final concentration of 2 × 107 CFU/ml. Mice were infected with ~2 × 107 CFU in a total volume of 200 μl using a 25-gauge gavage needle. Each inoculum used for oral infection was plated on MacConkey agar (BD Biosciences) to confirm bacterial concentration.
Rice bran used in these studies was provided as a gift from Dr. Anna McClung at USDA-ARS Dale Bumpers National Rice Research Center (Stuttgart, AK). Diets were formulated to match macronutrients (e.g. protein, carbohydrates) across groups. Differences in macronutrient composition were balanced using purified diet components. The percent of rice bran incorporated into the diet is expressed as g/100 g of diet. Harlan mixed and made pellets of rice bran containing diets using AIN-93 M purified components. The composition of rice bran containing diets was calculated based on published reports [41–43] that demonstrated chronic disease fighting activity. Diet formulations are shown in Table 1. The Neptune rice variety was chosen for its availability.
Fecal collection and processing
Fecal pellets were collected and body weights were recorded on day 0 before oral challenge, and on days 2, 5, 7, 9, 12 and 14-post infection. Mice were kept in Tupperware for 30 minutes and pellets from each mouse were weighed and diluted with PBS. After homogenization, fecal matter was serially diluted and plated on MacConkey agar (BD Biosciences) with 50 μg/ml of kanamycin (Fisher Scientific). Agar plates were incubated at 37°C under humid conditions for 24 hours and bacteria were counted as CFU/g of fecal matter. Feces from rice bran fed, uninfected mice were plated on MacConky agar with kanamycin and no Salmonella CFU was detected in the plates. Morphology of Salmonella colony in pure culture and infected feces were similar.
Blood and tissue collection
Blood was collected by tail vein (before infection) or cardiac puncture (before necropsy) using 4% Isoflurane (Attane Isoflurane USP, Minard Inc) in anesthesia machine with oxygen at a flow rate of 0.1 L/min. Serum separator tubes (BD Microtainer) were centrifuged at 7500 g for 10 minutes and stored at −20°C. Spleen, liver, ileum (distal 10 cm), mesenteric lymph nodes and Peyer’s patches were harvested, thoroughly washed with PBS, weighed and transferred to bags (Whirl-Pack, Nasco) and homogenized in stomacher (Seward Stomacher 80, Biomaster Lab Systems). Serial dilutions of homogenized tissues were plated on MacConkey agar with 50 μg/ml of kanamycin.
Serum cytokine analysis
Serum cytokines (TNF-α, IFN-γ and IL-12) were analyzed by cytometric bead array assay using the mouse inflammation kit (BD Biosciences) and the assay was performed according to the manufacturer’s instructions. Flow cytometry was performed using a Cyan ADP flow cytometer and Summit software (Beckman Coulter), and FlowJo software (TreeStar Inc) was used for analysis and quantification of serum cytokine data.
Cell culture conditions
Mouse small intestine epithelial cells (MSIE) were a generous gift from Dr. Robert Whitehead at Vanderbilt University and the Ludwig Institute for Cancer Research . Briefly, MSIE cells were grown using published methods in RPMI 1640 media supplemented with 2.05 mM L-Glutamine (Hyclone Laboratories). RPMI media was also supplemented with heat inactivated 10% FBS (Atlas Biologicals), 1% antibiotic (Penicillin and Streptomycin) and antimycotic (Amphotericin) solution (Cellgro, Mediatech Inc), 0.1% Thioglycerol Hydrocortisone (Sigma), 0.004% IFN-γ (Peprotech USA), 0.023% Insulin (Regular Human Insulin, Novo Nordik). Cells were grown in 75 cm2 flasks and trypsinized at 80% confluence. Cells were seeded overnight in a 6 well plate at a density of 2 × 105 cell/well. After 12 hours media was aspirated and fresh media was added with rice bran extracts for 24 hours at 37°C and 5% CO2 and 95% humidity.
Rice bran extraction
Crude rice bran cannot be reliably tested in cellular assays, and was therefore extracted with 80% methanol to obtain a mixture of rice bran phytochemicals and called a rice bran extract (RBE). Briefly, rice bran (Neptune variety) was removed from the grain and heat stabilized at 110°C for 3 minutes. Ice-cold, 80% methanol was added, vortexed and incubated at −80°C for one hour. Following centrifugation at 1500 g for 5 minutes, the supernatant was removed. Methanol was dried by vacuum centrifugation (SpeedVac Concentrator, Thermo Savant Model RT-100). Dried rice bran extract was weighed and then re-suspended with cell culture media to the appropriate doses for treatment of MSIE cells.
Salmonella entry and replication
Salmonella entry assay was done according to previously published protocol . This assay measures the total number of Salmonella (the bacteria that is surface attached plus the Salmonella internalized in the cell). MSIE cells were grown and treated with RBE for 24 hours. Media was aspirated and cells were re-incubated with fresh media containing Salmonella and RBE. Frozen stock of Salmonella was mixed in RPMI media at a Multiplicity of Infection (MOI) of 100–120 in the presence (co-incubation with Salmonella) or absence of RBE. After 30 minutes of incubation, media was aspirated, and MSIE cell monolayer was washed with PBS twice to remove extracellular bacteria. Fresh media was added to cells for additional 1 hour. There were 2 additional cycles of washing with fresh media plus 50 μg/ml of gentamicin (Sigma-Aldrich) following 1-hour incubations under the same conditions with 5 μg/ml of gentamicin. Media was aspirated and cell monolayer was washed with PBS twice to remove extracellular gentamicin. The cell monolayer was placed in 1 ml of buffer (PBS containing 1% TritonX-100 and 0.1% SDS) for 5 minutes. The contents were mixed by pipetting and serially diluted on MacConkey agar plates (BD Biosciences) with 50 μg/ml of kanamycin (Fisher Scientific) and incubated at 37°C for 24 hours. Colonies were counted and presented per ml of cell lysate. Intracellular Salmonella replication was measured in cells incubated with 5 μg/ml of gentamycin and RBE for 24 hours. Cells were lysed and plated on agar media to enumerate the total CFU count .
Cell viability was determined using alamarBlue (Invitrogen). Briefly, cells were seeded in a 96 well plate at 2x105/ml. After 6 hours of cell adherence, cells were treated in the presence and absence of RBE for 24 hours at 37°C, 5% CO2 in maintenance media. Supernatant was removed and alamarBlue was added to media (20 μg/ml). Fluorescence was detected at excitation: 530/25; emission: 590/35 in ELISA plate reader (Bio-Tek Synergy HT, Winooski, VT).
RBE doses of 0, 1, 2, 5 and 10 mg/ml were tested for direct effects on Salmonella viability. Bacteria was added to media at a concentration of 2 × 107 CFU/ml and incubated for 6 hours at 37°C. Bacterial suspension was serially diluted, plated on agar plates and counted after 24 hours incubation.
Quantitative PCR for Lactobacillus spp
DNA was extracted from fecal pellets of control and rice bran fed mice before and after Salmonella challenge using a MoBio Powersoil DNA extraction kit (MoBio, Carlsbad, CA). A dilution of DNA from pure cultures of Lactobacillus rhamnosus was used to generate standard curves and DNA from Pseudomonas aeruginosa were run as a negative control to ensure primer specificity. DNA was quantified by Nanodrop (Thermo Fisher Scientific) and diluted to 5 ng/μl. Real time PCR primers were used from Malinen et al.  for amplification of Lactobacillus spp. Samples were run on an ABI Prism 310 thermocycler (Applied Biosystems) using the following program: 95°C for 3 min 30 s followed by 30 cycles of 95°C for 15 s, 58°C for 20 s 72°C for 30 s and melt curves were generated by 95°C for 1 min followed by eighty 10 s repeats at set point temperatures incrementally decreasing by 0.5°C.
Data was analyzed using Graphpad Prism5 Software. Experiments were repeated a minimum of three times. Raw data were log transformed into a log10 scale for CFU analysis and repeated measures ANOVA and post hoc Tukey’s test were used for Salmonella fecal shedding and fecal Lactobacilli measures. Inflammatory cytokines were analyzed using two -way ANOVA and Bonferroni post hoc test. A nonparametric ANOVA (Kruskal Wallis) was performed, followed by Dunn’s test for in vitro Salmonella assays. Significance was determined for all studies at P <0.05.
We would like to thank Dr. Andres Vazquez-Torres for providing the strain of Salmonella used in these studies, and Dr. Anna McClung from the USDA-ARS Dale Bumpers Rice Research Center for providing rice bran from the single Neptune variety. We also thank Dr. Daniel Manter from USDA-ARS-Soil Plant Nutrient Research, Brittany Barnett for for assistance with qPCR of Lactobacillus spp. and Adam Heuberger and Caleb Schmidt for their technical assistance.
A Grand Explorations in Global Health Grant from the Bill and Melinda Gates Foundation (OPP1015267) and the Shipley Foundation supported this work.
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