ORIGINAL RESEARCH article
Musca domestica Cecropin (Mdc) Alleviates Salmonella typhimurium-Induced Colonic Mucosal Barrier Impairment: Associating With Inflammatory and Oxidative Stress Response, Tight Junction as Well as Intestinal Flora
- 1Guangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangdong Pharmaceutical University, Guangzhou, China
- 2Intensive Care Unit, Shenzhen Second People’s Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, China
Salmonella typhimurium, a Gram-negative food-borne pathogen, induces impairment in intestinal mucosal barrier function frequently. The injury is related to many factors such as inflammation, oxidative stress, tight junctions and flora changes in the host intestine. Musca domestica cecropin (Mdc), a novel antimicrobial peptide containing 40 amino acids, has potential antibacterial, anti-inflammatory, and immunological functions. It remains unclear exactly whether and how Mdc reduces colonic mucosal barrier damage caused by S. typhimurium. Twenty four 6-week-old male mice were divided into four groups: normal group, control group (S. typhimurium-challenged), Mdc group, and ceftriaxone sodium group (Cs group). HE staining and transmission electron microscopy (TEM) were performed to observe the morphology of the colon tissues. Bacterial load of S. typhimurium in colon, liver and spleen were determined by bacterial plate counting. Inflammatory factors were detected by enzyme linked immunosorbent assay (ELISA). Oxidative stress levels in the colon tissues were also analyzed. Immunofluorescence analysis, RT-PCR, and Western blot were carried out to examine the levels of tight junction and inflammatory proteins. The intestinal microbiota composition was assessed via 16s rDNA sequencing. We successfully built and evaluated an S. typhimurium-infection model in mice. Morphology and microcosmic change of the colon tissues confirmed the protective qualities of Mdc. Mdc could inhibit colonic inflammation and oxidative stress. Tight junctions were improved significantly after Mdc administration. Interestingly, Mdc ameliorated intestinal flora imbalance, which may be related to the improvement of tight junction. Our results shed a new light on protective effects and mechanism of the antimicrobial peptide Mdc on colonic mucosal barrier damage caused by S. typhimurium infection. Mdc is expected to be an important candidate for S. typhimurium infection treatment.
Salmonella typhimurium is an important Gram-negative food-borne pathogen with a broad host range including humans and animals, and causes diseases ranging from gastroenteritis and diarrhea to life-threatening systemic infections (Wan et al., 2018), resulting in one million human deaths annually (Balasundaram et al., 2017). Owing to their metabolic versatility, Salmonella can colonize as multicellular aggregates on various surfaces, enhancing virulence levels through biofilm formations that often resist antibiotic therapy (Faccone et al., 2018; Kuang et al., 2018; Ridge et al., 2018; Wan et al., 2018).
Salmonella typhimurium challenge induces impairment in intestinal mucosal barrier function (Zhang et al., 2012; Boyer et al., 2015). The epithelial barrier is one of the most important components of the intestinal mucosal barrier against macromolecular transmission (Collado-Romero et al., 2012). The epithelial cells form a continuous intact physical epithelial barrier with interspersing tight junctions (TJs) between each cell. Disruption of TJs results in increased permeability to luminal antigens and bacteria, degrading mucosal barrier function. TJs can be altered by several bacterial pathogens through modification of TJ proteins such as occludin, claudin-1, and ZO-1. Infection of polarized epithelial cell monolayers by S. typhimurium may disrupt TJ structure and function, and subsequently disrupts epithelial barrier integrity (Zhang et al., 2012). Inflammation and oxidative stress are considered as the essential mechanism underlying the pathophysiology of intestinal injury (Di Sabatino et al., 2016). A relative increase in some inflammatory factors may attenuate zonula occluding protein expression, leading to intestinal barrier dysfunction, and promotion of intestinal inflammation in the colonic mucosa (Ogawa et al., 2018).
Intestinal microflora play a crucial role in host defense as demonstrated by their ability to modulate both innate and acquired immunity at the local as well as systemic levels (Colliou et al., 2017). Intestinal flora may also contribute to the development and progression of cancer (Loo et al., 2017). Most importantly, changes in microbe populations may be closely related to the degree of intestinal inflammation (Frank et al., 2011), which is one of the characteristics of S. typhimurium infection (Bronner et al., 2018). Host microbiota likely play a role in resistance to, and may also be indirectly responsible for some of the consequences of S. typhimurium infection (Argüello et al., 2018). Resistance to S. typhimurium by adjusting intestinal flora was reported long ago or recently (Baba et al., 1991; Deriu et al., 2013). Oral administration of probiotics has been demonstrated to increase paneth cells and intestinal antimicrobial activity, which is the main intestinal cell responsible for the immunoreactive antimicrobial peptide (AMP) production. This peptide helps to stabilize the intestinal barrier, while promoting the stability of intestinal microbial flora (Cazorla et al., 2018). It was also reported that the enhanced activity of AMPs by statins in Salmonella-infected IECs could protect the host against infection, and modulation of pro-inflammatory responses could prevent the detrimental effects of severe inflammation in the host (Huang and Huang, 2018). AMPs serve to protect the intestinal barrier, but the mechanism of AMP activity remains unclear, especially for regulating intestinal flora.
Housefly (Musca domestica) larvae have been used clinically to treat ecthyma, decubital necrosis, lip boil, and osteomyelitis since 1368 Anno Domini (Ming/Qing Danysty) in China (Hou et al., 2007). Musca domestica cecropin (Mdc), a novel AMP containing 40 amino acids, has been cloned and characterized from housefly larvae, and was found to have a significant potency against S. typhimurium in our previous studies (Lu et al., 2010). However, it is unclear whether Mdc has potent protection against the intestinal barrier impairment in mice colonic mucosal. Moreover, the precise protective mechanism(s) of Mdc remain unknown. Thus, the present study aimed to investigate the effect and mechanisms of Mdc on colonic mucosal barrier damage caused by S. typhimurium infection.
Materials and Methods
Peptide and Material
Musca domestica cecropin (Mdc) (Purity 97.15%; molecular weight: 4301.59 Da) was chemically synthesized by conventional Fmoc solid-phase synthetic method (Beijing Scilight Biotechnology Ltd., Beijing, China) (Lu et al., 2015). Streptomycin sulfate was purchased from Amresco Inc, United States. Ceftriaxone sodium (1 g/bottle) was obtained from Guangdong succhi pharmaceutical (group) Ltd. All other chemicals were standard commercial products with analytical reagent grade.
Microorganisms and Medium
Salmonella typhimurium GIM1.237 was obtained from Guangdong culture collection center. The compositions of medium from Guangdong Huankai Microbial Sci. & Tech. Co., Ltd in this work are as follows: Luria-Bertani (LB) medium [0.5% yeast extract (w/v), 1% tryptone, and 1% NaCl] and tryptone soybean broth (TSB) medium [1.7% Pancreatic digest of casein (w/v), 0.3% Enzymatic digest of soya bean, and 0.5% Sodium chloride, 0.25% Dipotassium hydrogen phosphate, 0.25% Glucose] were employed for pre-incubation of the test bacteria. The bacteria were grown overnight to an optical density at 600 nm (OD600) of 0.8–1.0 prior to appropriate dilution. The streptomycin resistant S. typhimurium suspension with a concentration of 0.7–0.75 × 109 CFU/mL was prepared and the mice were given gavage with a dose of 300 μL each.
Animals and Experimental Design
C57BL6 mice, male, were obtained from Center for Experimental Animals, Guangdong Province [Guangzhou, China approval number SCXK (Yue) 2013-0002]. Twenty four 6-week-old male mice were housed (eating and drinking ad libitum) under controlled conditions (room temperature 23 ± 2°C; relative humidity 55 ± 5%; 12-h dark/12-h light cycle) for 1 week. The use of the animals and experimental protocols were approved by the Guidelines for the Care and Use of Experimental Animals, the Guangdong Pharmaceutical University [SYXK (Yue) 2012-0125] and the Guangdong Pharmaceutical University Animal Care and Use Committee, China. All the mice were randomly divided into four groups of six each: the normal group, the control group, the Mdc group, and the Cs group. Animal grouping design is shown in Figure 1. One day before the start of the trial, the mice in each group were given water containing 5 g/L streptomycin, and then returned to normal drinking water after 24 h. During the seven-day experiment, the mice were given medicine (Mdc i.p in the Mdc group and Cefatriaxone sodium i.m in the Cs group, respectively) every morning for a fixed time. From the second to the fourth day, except the normal group, the rest of the groups were given gavage with a dose of 300 μL streptomycin resistant S. typhimurium suspension twice a day, morning and night. Blood and a variety of tissues were removed for the follow-up experiments. All animals were weighed and recorded at fixed times every day during the whole animal feeding period. Image-Pro Plus 6.0 was used for the analysis of intestinal thickness.
Bacterial Load of S. typhimurium in Colon and Analysis of Bacterial Translocation in Liver and Spleen
A stool of 20 mg from each mouse’s colon was taken and homogenized in 1 mL sterile PBS solution. Then the homogenate was diluted and homogenate diluent of 100 μL was coated on the LB agar plate containing 50 μg/mL streptomycin. After 24 h incubation at 37°C, the total number of colonies on the plate and the content of S. typhimurium in every gram of feces were calculated. To investigate bacterial translocation after S. typhimurium infection, the bactrial load in the liver and spleen was determined separately. Liver and spleen tissues were washed with normal saline immediately after removal from mice and stuck dry with filter paper. A tissue of 100 mg from the same site was placed in a centrifugal tube containing pre-cooled 1 mL PBS solution and homogenized. Homogenate of 100 μL was coated on the normal LB agar plate. After incubation at 37°C for 24 h, the actual bacterial content in each gram of tissue was counted.
Analysis of Colonic Morphology
Intestinal tissues of the middle colon from six mice in each group were examined. To evaluate the histological changes in the intestines, full thickness sections of the middle colon were excised, irrigated gently to dislodge intestinal contents with normal saline, immediately fixed in 4% paraformaldehyde solution, and embedded in paraffin. Samples were crosscut and stained with hematoxylin-eosin (H&E). Photomicrographs of sections were observed with a light microscope and taken with a digital camera (DFC495 Digital camera Leica, German), scored in a blinded fashion by three investigators. Histological damage was scored using the criteria of Appleyard and Wallace (Appleyard and Wallace, 1995), including loss of mucosal architecture [0, 1, 2, or 3 (absent, mild and severe)], cellular infiltration [0, 1, 2, or 3 (absent, mild and severe)], muscle thickening [0, 1, 2, or 3 (absent, mild and severe)], crypt abscess formation (0 or 1 (absent or present)], and goblet cell depletion [0 or 1 (absent or present)]. The sum of scores in each area is the final score and the final scores of the three investigators were averaged. Based on the average scores, the statistics data for histological damage were obtained.
Transmission Electron Microscopy (TEM)
To investigate the shape changes of intestinal mucosa after treatment with Mdc, we observed the ultrastructure of the colonic epithelium obtained by TEM. Distal colonic tissues were sliced into 1-mm3 cubes and immediately fixed in 0.1 M phosphate buffer containing 2.5% glutaraldehyde at 4°C for 12 h. After washing samples with 0.1 M phosphate buffer three times for 30 min, we fixed them in 1% osmium tetroxide for 2 h, and subsequently treated with 2% uranyl acetate for 1 h before dehydration in an ethanol series and embedded in epoxy resin. Finally, the embedded samples was sectioned and examined in a JEM1400 (Jeol, Japan) TEM. Microphotographs were taken with a digital camera Bioscan 792 (Gatan Inc., United States) and scored in a blinded fashion by three investigators. For the convenience of presentation, according to damage degree of microvilli, tight junction and epithelial cells, the mucosal changes in TEM are graded as follwing: (1) The score of complete and homogeneous microvilli is 0; the scores of short, sparse and curled microvilli in varying degrees are 1 (slight), 2 (moderate) and 3 (severe), respectively; the scores of microvilli falling off are 4 (mild) and 5 (severe), respectively. (2) The score of complete tight connection is 0 (close interconnection between cells); the scores of damaged tight junction are 1 (mild) and 2 (severe), respectively; the score of loss of tight junction is 3. (3) The score of normal epithelial cells is 0; the scores of structural damage of epithelial cells are 1 (slight), 2 (moderate) and 3 (severe), respectively. The sum of scores in each area is the final score and the final scores of the three investigators were averaged. Based on the average scores, the statistics data for histological damage were obtained.
Enzyme Linked Immunosorbent Assay (ELISA)
To determine the concentration of TNF-α, IFN-γ, IL-6, and IL-10 in serum of all groups, ELISA Kits (Beijing 4A Biotech Co., Ltd) was used. The kit assays were carried out according to the manufacturer’s instructions.
Detection of MPO, NAG, MDA, and GSH-Px in Colon
Colonic MPO, NAG, MDA, and GSH-Px activities were determined by using MPO Detection Kit, NAG Detection Kit, MDA Detection Kit, and GSH-Px Detection Kit, respectively. All the Kits were acquired from Nanjing Jiancheng Bioengineering Institute. The colon tissues were homogenized using 0.86% of cold saline as homogenizing medium before testing the samples complying with the instructions.
The distal colon samples were fixed in 4% paraformaldehyde solution, embedded in paraffin and cut into slices transversely, the steps before dewaxing were the same as those of hematoxylin-eosin (H&E) dyeing. For immunofluorescence analysis of Claudin-1 (Abcam UK), Occludin (Abcam UK), and ZO-1 (Abcam UK), COX-2 (Abcam UK), INOS (Abcam UK), P65 (Abcam UK), antigen retrieval was performed by heating the slices for 20 min in boiling water and non-specific binding sites were blocked with PBS containing 1% w/v BSA for 1 h at 37°C. The primary antibodies (1:200) above were added to the corresponding samples to incubate overnight at 4°C. After washing with PBS for three times, sections were incubated with the secondary antibody, Alexa Fluor 488-conjugated or Cy3-conjugated goat anti-rabbit IgG (1:200; Beyotime, China) at room temperature for 1 h in darkness. Eventually, DAPI was used to stain the nucleus. Images were taken under a fluorescence microscope (Leica, German) immediately. Fluorescence intensity was analyzed by using Image J.
Real-Time Quantitative PCR Detection
RNA samples were extracted from the distal colon. Total RNA isolation and cDNA synthesis by reverse transcription were conducted using Trizol reagent (Invitrogen Corporation, United States) and PrimeScriptTM RT reagent Kit with gDNA Eraser (Takara Biotechnology Co. Ltd., Japan), respectively. The mRNA levels of individual genes were measured by real-time PCR using the SYBR Premix Ex Taq Kit (Takara Biotechnology Co. Ltd., Japan) in the CFX Connect fluorescence quantitative PCR detection system (BIO-RAD, United States). The 25 μL PCR reaction mixture per reaction consists of 12.5 μL SYBR Premix Ex Taq II (Tli RNaseH Plus) (2×), 1 μL Forward Primer (10 μM), 1 μL Reverse Primer (10 μM), 2 μL reaction solution (cDNA), and 8.5 μL Sterilized purified water. Shuttle PCR standard protocol is as following: Stage 1 is the initial denaturation of one cycle at 95°C for 30 s; Stage 2 is the PCR reaction of 40 cycles at 95°C for 5 s and 60°C for 30 s; Stage 3 is the Dissociation. Data were analyzed according to the comparative threshold cycle (Cq) method and normalized to an endogenous reference, β-actin. The primers used in this experiment were listed in Table 1. Relative expression levels of inflammation related (INOS, COX-2, P65) and barrier function related genes (ZO-1, Claudin-1, Occludin) were analyzed in colon tissues.
Western Blot Analysis
Distal colons were ground and lysed with RIPA lysis buffer (Beyotime, China) with 1 mM PMSF (Beyotime, China). The protein content of each tissue was quantified and diluted and 20 μg of protein was loaded in each lane of a 5/12% or a 5/8% SDS-PAGE gel. The protein was separated by SDS-PAGE and transferred to nitrocellulose membrane. The membrane was blocked with 5% (w/v) defatted milk in TBS and incubated with a primary antibody, P65 (1:1000), COX-2 (1:1000), INOS (1:1000), ZO-1 (1:1500), Claudin-1 (1;1000), Occludin (1:50000), and overnight at 4°C. The above-mentioned primary antibodies were from Abcam and the manufacturer’s instructions were referred to when determining the appropriate dilution for each antibody. HRP-conjugated secondary antibody (1:1000) (Beyotime, China) was applied before the proteins were visualized via chemiluminescence. Images were collected with Tanon-5200 (Shanghai Tanon Technology Co., Ltd, China), for quantification of protein levels, appropriate film exposures were scanned and the density of bands was determined with Image J and normalized to band intensity for GAPDH.
Intestinal Flora Analysis
On the eighth day of the experiment, the three fecal samples from six mice in each group were collected and marked for sequencing, respectively, and the sequencing work was completed by the Novogene Corporation (Beijing, China).
Data were analyzed with the use of a 2-tailed unpaired Student’s t test. P ≤ 0.05 was considered to be significant. Each mouse was considered as an experimental unit. Data are expressed as means ± SEMs. Statistical analysis was performed using GraphPad Prism version 7.00.
Model Building Evaluation
The infection model was established successfully by intragastric administration of streptomycin resistant S. typhimurium (Figure 1), which laid the foundation for the following experiments. After modeling, some of the mice developed loose hair, poor spirits, and soft stools. From the beginning to the end of modeling, we recorded the weight changes of all the mice. At the time of sampling, photographs of the intestines in the experimental animals were made; comparisons between treatment and negative controls were noted. As shown in Figure 2A, the mice in control group were significantly lower in weight. In Figures 2B,C, the intestine of the control group (b) was thinner than in the normal group (a). After Mdc administration (c) and ceftriaxone sodium treatment (d), intestinal tissue of infected animals appeared to improve significantly.
Figure 2. Mdc could significantly improve weight loss and intestinal thinning after infection. Changes in body weight of mice during modeling period (A), comparison of intestinal appearance among normal group, control group, Mdc group, and Cs group (B), and statistical analysis for thickness of intestines (C). Values are means ± SEMs, n = 6, ∗p ≤ 0.05.
Musca domestica Cecropin (Mdc) Decreases Bacterial Translocation
Figure 3A showed that there was no significant difference in the number of S. typhimurium in feces between MDC group and Control group, indicating that intraperitoneal injection of Mdc did not affect bacterial load of S. typhimurium in colon contents. However, in Figures 3B,C, Mdc significantly reduced the number of bacterial translocation in liver and spleen.
Figure 3. The bacterial load of Salmonella typhimurium in the colon and the bactrial load in the liver and spleen were analyzed. Mdc couldn’t decrease bacterial load of S. typhimurium in the colon (A). But Mdc significantly ameliorated the bacterial translocation after S. typhimurium infection in the liver (B) and spleen (C). Values are means ± SEMs, n = 6. ns, no significant difference, ∗∗∗∗p ≤ 0.0001.
Mdc Reduces Colonic Mucosal Barrier Damage
As Figure 4 shows, microscopically, the colonic epithelial cells of normal group (Figure 4A) had a normal appearance, the glands of lamina propria were compact and regular, the mucosa and submucosa were clear and goblet cells were abundant; no inflammatory cell infiltration or ulcer formation was observed. In control (Figure 4B) and Mdc groups (Figure 4C), the epithelial cells of colonic mucosa were exfoliated, the glands were arranged in a disorderly fashion, inflammatory cells infiltrated the mucosa and submucosa, and erosion, destruction of glands, structural disorder, damage of epithelial integrity, loss of goblet cells were observed. The pathological signs in colon mucosa of Mdc group animals were less pronounced than those in the infection (positive) control group; however, intestinal tissues in the former group did show visible signs of infection (Figure 4D). The damage score (Figure 4E) intuitively summarizes the contents of the above four photos. These results show that while Mdc treatment can mitigate the severity of S. typhimurium-induced mucosa damage, its application does not completely reverse S. typhimurium-caused physiopathology.
Figure 4. Representative micrographs of HE staining show the colon of normal group (A), control group (B), Mdc group (C), and Cs group (D). Histological damage was scored using the criteria of Appleyard and Wallace. The damage score (E) intuitively indicates that Mdc could reduce colon tissue damage. Values are means ± SEMs, n = 6, ∗∗p ≤ 0.01.
In order to further observe the effects of Mdc on colonic mucosa damage caused by S. typhimurium, TEM was performed. It could be seen very intuitively from Figure 5 that the microvilli in the colonic epithelium of the normal group (Figure 5A) were well-distributed, and the size of cells was basically the same and the arrangement was compact, forming a complete tight junction. The control group (Figure 5B) showed widespread damage to microvilli as well as tight junction structure disruption, and epithelial cell death. Microphotographs corresponding to the Mdc group and Cs group were shown in Figures 5C,D, in which clearly show that Mdc application reduces the level of S. typhimurium induced colonic epithelial damage. Furthermore, the damage score (Figure 5E) from ultrastructure of colon tissues also shows the positive effect of Mdc on colon tissue damage.
Figure 5. The ultrastructure of the colonic epithelium of mice in the normal group (A), control group (B), Mdc group (C), and Cs group (D) under the transmission electron microscope. The red arrows indicate tight junctions (TJs) and the colonic microvilli are surrounded by red outline. The damage score (E) from ultrastructure of colon tissues shows the positive effect of Mdc on colon tissue damage. Values are means ± SEMs, n = 6, ∗∗∗∗p ≤ 0.0001.
Inhibition of Inflammatory Response
The contents of inflammatory factors in the serum of mice were conducted to evaluate the anti-inflammatory activity of Mdc. The results of TNF-α, IFN-γ, IL-6, and IL-10 concentrations in mice serum are shown in Figure 6. TNF-α, IFN-γ, IL-6, and IL-10 concentrations in serum were significantly decreased by exposure to Mdc than in the control group.
Figure 6. The concentrations of TNF-α (A), IFN-γ (B), IL-6 (C), and IL-10 (D) in the serum of 4 groups’ different mice. Values are means ± SEMs, n = 6. ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001, ∗∗∗∗p ≤ 0.0001.
Suppression of Oxidative Stress in Colon
Measuring intestinal tissue indicators was the basis for determining intestinal epithelial health, and colon was the most suitable with regard to our model. MPO, NAG, MDA, and GSH-Px in colon were measured. Figure 7 shows that Mdc could greatly promote GSH-Px and NAG activity as compared with the control group. Furthermore, Mdc largely depressed MPO activity and MDA levels.
Figure 7. The activities of MPO (A), NAG (B), GSH-Px (D), and the level of MDA (C) in the colon of 4 groups’ different mice. Values are means ± SEMs, n = 6. ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001, ∗∗∗∗p ≤ 0.0001.
Three Different Methods Jointly Verify Increasing Tight Junctions and Reducing Inflammation in Colon Induced by Mdc
The expression of ZO-1, Claudin-1, Occludin, P65, COX-2, and INOS proteins in colon were examined using immunofluorescence analysis. It could been seen clearly from Figures 8–10 that while comparing with the control group, the ZO-1, Claudin-1 and Occludin proteins in Mdc group showed increased significantly. On the contrary, the P65, COX-2 and INOS proteins expressed less in Mdc group. It was shown that the normal group had the highest expressions of the ZO-1, Claudin-1 and Occludin. The normal group also showed the lowest expression levels of P65, COX-2, and INOS proteins. There were notable increases in the expression levels of the ZO-1, Claudin-1 and Occludin proteins with significant decreases of P65, COX-2, and INOS proteins in the Mdc treated group as compared to the control group.
Figure 8. Immunofluorescence analysis of ZO-1 and Claudin-1 in colon of 4 groups. Values are means ± SEMs, n = 3, ∗∗p ≤ 0.01.
Figure 9. Immunofluorescence analysis of Occludin and P65 in colon of 4 groups. Values are means ± SEMs, n = 3. ∗p ≤ 0.05, ∗∗∗p ≤ 0.001.
Figure 10. Immunofluorescence analysis of COX-2 and INOS in colon of 4 groups. Values are means ± SEMs, n = 3, ∗∗p ≤ 0.01.
mRNA expression levels of ZO-1, Claudin-1, Occludin, P65, COX-2, and INOS in colon were examined through Real-time quantitative PCR. As shown in the Figure 11, the normal group possessed the highest expression level of ZO-1 (Figure 11A), Claudin-1 (Figure 11B), and Occludin (Figure 11C) as well as the lowest expression levels of P65 (Figure 11D), COX-2 (Figure 11E), and INOS (Figure 11F), followed by the Cs group, the Mdc group and the control group. The results of Real-time quantitative PCR detection were consistent with the results of immunofluorescence analysis.
Figure 11. Real-time quantitative PCR detection of ZO-1 mRNA (A), Claudin-1 mRNA (B), Occludin mRNA (C), P65 mRNA (D), COX-2 mRNA (E), and INOS mRNA (F) in colon of 4 groups. Values are means ± SEMs, n = 6. ∗∗p ≤ 0.01, ∗∗∗∗p ≤ 0.0001, ns, no significant difference.
In order to further verify the results of immunofluorescence analysis and Real-time quantitative PCR detection, we carried out western blot analysis. The results were shown in Figure 12 represented protein band and protein expression in relative to GAPDH (fold of control group), respectively. The results of western blot analysis showed the changes in the expression levels of ZO-1, Claudin-1, Occludin, P65, COX-2, and INOS similar to the results of immunofluorescence analysis.
Figure 12. Western blot analysis of ZO-1,Claudin-1, Occludin, P65, COX-2, INOS protein expression in relative to GAPDH in the colon of 4 groups (A,B). Values are means ± SEMs, n = 3. ∗p ≤ 0.05, ∗∗p ≤ 0.01,∗∗∗p ≤ 0.001, ∗∗∗∗p ≤ 0.0001, ns = no significant difference.
Mdc Ameliorates Intestinal Flora Imbalance Closely Related to Tight Junctions
In order to test whether Mdc regulated gut microbiota and characterize the modifications in the intestinal microbiota composition, we performed 16S rDNA sequencing in fecal samples of mice. The regulatory role of Mdc on the intestinal microecological system was indicated by the α, β diversity and OTUs analysis of the fecal samples. Unweighted unifrac-based PCoA analysis revealed a distinct clustering of microbiota composition for each group (Figure 13A). Closer lower sample distance implied a similar species composition; the normal group was relatively distant from the other three group cluster. From the UPGMA clustering tree (Figure 13B), the community structure of the Mdc group was more similar to the Cs group and the normal group than the control group, thus indicating that Mdc exerted considerable effects on the intestinal flora. The 10 most abundant bacterium in the level of genus were compared among groups (Figure 13C). The composition of intestinal bacterial species of Mdc group was dramatically changed compared with the other groups. Abundance of Bacteroides was decreased in the Mdc group with same trend as the normal group and Cs group. Interestingly, unlike the Cs group and normal group, Mdc treatment increased the abundance of Akkermansia and Parabacteroides. Heatmap and cluster analysis of the 35 most abundant genera were conducted based on the abundance of species annotation information (Figure 13D). Shannon and Simpson (Figure 13E), important components of alpha diversity index, are used to estimate the diversity of microbial communities in the samples. Compared with Shannon and Simpson indices of four groups, the two indices in the normal group were the biggest, and the second was the Cs group near the tertiary Mdc group. These results indicated that the Mdc could significantly increase species diversity compared with the control group. In order to study the species with significant difference among groups, the p value was obtained by hypothesis testing based on the phylum level species abundance table, and the q value was obtained by correcting the p value. Finally, the species with significant difference were selected according to the q value. As shown in Figure 13F, Verrucomicrobia and Lentisphaerae in the phylum level displayed significant differences among 4 groups. LEfSe (LDA Effect Size) analysis (Figure 13G, Left) demonstrated that Mdc increased the relative proportions of bacteria from the class Verrucomicrobiae, phylum Verrucomicrobia, family Verrucomicrobiaceae, genus Akkermansia, order Verrucomicrobiales, while the bacteria from the genus Bacteroides and family Bacteroidaceae had the greatest growth in the control group. The cladogram (Figure 13G, Right) showed that organisms in phylum Verrucomicrobia were mainly enriched in the Mdc group. For the normal group and Cs group, the cladogram also corroborated the LEfSe analysis results.
Figure 13. Microbiota composition in the feces were analyzed using 16s rDNA sequencing (n = 3 for each group). Unweighted unifrac-based PCoA analysis, each point in the graph represents a sample and the same group of samples is represented in the same color (A). Unweighted unifrac-based UPGMA clustering tree (B). Relative abundance of each group at the genus level (C). Species richness on the level of genus, the horizontal axis represents the sample information, and the vertical axis represents species annotation information, the left side of the cluster tree represents the species cluster tree, the corresponding value of the intermediate thermal map is the Z value obtained after normalization of the relative abundance of each row species (D). Analysis of Alpha diversity index (shannon and simpson) among groups (E). MetaStat analysis to find species with significant difference among groups in the phylum level (F). ∗q ≤ 0.05, ∗∗q ≤ 0.01. Linear discriminant analysis (LDA) plots highlighting significantly different characteristic taxons among 4 groups’ microbiota, only taxa with a value of LDA score of more than 4 are shown (G, Left). Taxonomic cladogram of 4 groups’ bacterial fecal samples (G, Right).
To further investigate how intestinal flora affected colonic mucosal injury caused by S. typhimurium, correlation analysis including Spearman sequential correlation analysis and Mantel test were conducted. IL-6, INOS, COX-2, P65, TNF-α, IFN-γ and MPO were positively correlated with phylum Verrucomicrobia and Lentisphaerae enriched in the control group, with which ZO-1, while Claudin-1 and Occludin were negatively correlated. There was a positive correlation between ZO-1, Claudin-1, Occludin and phylum Tenericutes and Firmicutes, and IL-6, INOS, COX-2, P65, TNF-α, IFN-γ, and MPO were negatively correlated with these clades. At the genus level, it should be noted that genus Akkermansia and genus Bacteroides, parabacteroides had a positive correlation with IL-6, INOS, COX-2, P65, TNF-α, IFN-γ and MPO (Figure 14).
Figure 14. Spearman correlation analysis was conducted to determine the relationship between various factors and species at the phylum level (A) as well as genus level (B). The corresponding value of the intermediate thermogram is Spearman correlation coefficient r, between -1 and 1, r < 0 is negative correlation, r > 0 is positive correlation. ∗p ≤ 0.05, ∗∗p ≤ 0.01.
Mantel test was used to calculate correlation between combination factors and microbial community data. As shown in Table 2, Mantel Test based on relative abundance in the level of genus and OTUs illustrated that the combination factors of IL-10 + ZO-1 + Occludin + Claudin-1 and ZO-1 + Occludin + Claudin-1 played the greatest role in the genus relative abundance and microbial species composition.
There is an impressive amount of literature on how AMPs maintain intestinal homeostasis such as stimulation of mucus synthesis, promoting the production of tight junction proteins and immune modulation (Brown et al., 2012; Ma et al., 2012; Tang et al., 2013; Kiatsurayanon et al., 2014). However, only very limited even no information is available on how AMPs affect intestinal microflora to maintain intestinal mucosal barrier with normal function (Pound et al., 2015; Fusco et al., 2017). Here, we elucidate how AMP Mdc improve the damage of colonic mucosal barrier by regulating intestinal flora for the first time, meanwhile other common functions of AMPs have also been verified. The present study provided convincing evidence that Mdc could markedly alleviate intestinal mucosal injury by not only depressing inflammatory response and oxidative stress response but also more importantly ameliorating zonula occludens and bacterial flora distribution.
Salmonella enterica is one of the leading causes of zoonotic foodborne disease worldwide. S. typhimurium had always been the top three pathogens isolated from foodborne diseases and food poisoning cases in China, among which S. typhimurium has the highest detection rate (Yang et al., 2013). It is an invasive bacterium that mainly invades small intestine and colon (Winter et al., 2010). Intestinal mucosal barrier injury frequently occurs following S. typhimurium challenge (Pohl et al., 2018). Although there are many Salmonella infection models that can be used to study different types of intestinal injury (Santos et al., 2001), the S. typhimurium infection model used in this experiment is usually used to establish colonic mucosal lesions (Manja et al., 2003). Therefore, the colonic mucosal damage caused by S. typhimurium infection was discussed in this study. In addition, according to Xia’s et al. (2015) research and preliminary experimental results, AMP Mdc may also improve ileal injury induced by S. typhimurium, which will be performed further in the future experiments. This model was very stable that symptoms of S. typhimurium infection were found in mice of model group and there was no death in mice. In the present study, H&E staining and intestinal TEM showed that Mdc significantly improved intestinal mucosal barrier damage induced by S. typhimurium. Furthermore, the decrease of bacterial translocation also fully demonstrated this role of Mdc.
There are many connections between intestinal mucosal epithelial cells, in which TJs are the most important, and the most important components of TJs are tight junction proteins such as ZO-1, Claudin-1 and Occludin (Betanzos et al., 2013). These proteins play pivotal roles in maintaining the integrity of tight junction between cells and the normal function of epithelial cell barriers. Abnormal expression of these protein cause barrier dysfunction, leading to dysfunction of tight junction and increased tissue permeability, which is one of the characteristics of inflammatory bowel disease (Walsh-Reitz et al., 2005; Förster, 2008; Mir et al., 2016; Li et al., 2018; Lucke et al., 2018). In the present study, the results of immunofluorescence analysis, Real-time quantitative PCR detection and western blot analysis demonstrated that Mdc could improve diseased intestinal tight junction by up-regulating the level of tight junction proteins ZO-1, Occludin and Claudin-1.
The intestinal mucosa has a variety of mechanisms for maintaining homeostasis, preventing excessive inflammatory responses (Wang and Colgan, 2017). Intestinal mucosal barrier injury could stimulate the occurrence of proinflammatory events (Turner, 2009; Capaldo et al., 2017). The intestinal epithelium is central to coordinating both inflammation and resolution (Ivanov et al., 2010). A recent study reported that the regulation of epithelial barrier function could inhibit intestinal inflammation (Shi et al., 2018). In addition, inflammation is also a key factor affecting intestinal mucosal barrier (Kamekura et al., 2015). Therefore, the decreases of TNF-α, IFN-γ and IL-6 induced by Mdc in our study could not only reflect its anti-inflammatory activity but also serve to protect the mucosal barrier. IL-10 is a multicellular and multifunctional cytokine and recognized as an inflammatory and immunosuppressive factor, which regulates cell growth and differentiation, participates in inflammatory and immune responses (Huang et al., 2018). Normal, Mdc and Cs group did not increase IL-10, which may be related to the intensive immune status of mice. In addition, IL-17 is an important component of the inflammatory response to infection with Salmonella serotypes. There will be a marked upregulation of IL-17 expression with the Salmonella infection (Manuela et al., 2007). IL-1β also greatly contributes to innate immune defenses against S. typhimurium infection (Bärbel et al., 2006). These important Salmonella infectious related cytokines will be further studied in the follow-up of this research.
Antioxidant activity is one of the likely mechanisms involved in amelioration of gut barrier dysfunction (Assimakopoulos et al., 2004; Chaudhry et al., 2016). Myeloperoxidase (MPO) is a constituent enzyme found principally in neutrophils that results in the formation of hypochlorous acid. Its presence in neutrophils allows it to be extracted from tissues; levels of this acid is directly proportional to neutrophil numbers (Liu et al., 2010). Maleic dialdehyde (MDA), a reliable marker of lipid peroxidation, has a positive correlation with levels of oxidative stress. Glutathione peroxidase (GSH-Px) is an important peroxide decomposing enzyme widely found in the body. After Mdc administration, MPO activity and MDA levels were significantly decreased, while the GSH-Px activity had a corresponding increase, indicating that Mdc had the ability to increase the anti-oxidative capacity to prevent intestinal barrier dysfunction, if only to a limited degree.
It has been reported that intestinal permeability and colitis severity are altered by the intestinal microbiota in mice (Llewellyn et al., 2018). Furthermore, previous studies suggested that the composition of the gut microbiota shapes the colon mucosal barrier (Jakobsson et al., 2015). 16S rDNA sequencing indicated that Mdc possessed considerable regulatory effects on the intestinal flora; its application brought the flora of diseased intestines to profiles more similar to that in normal group. Mdc treatment improved the abundances of Akkermansia and Parabacteroides and species composition diversity and decreased the abundance of Bacteroides, indicating reduction of intestinal inflammation and injury (Ramanan et al., 2016; Neyrinck et al., 2017). The increased phylum Verrucomicrobia and decreased phylum Lentisphaerae induced by Mdc showed significant differences compared with the control group. Although increase of phylum Verrucomicrobia was not in line with the expected trend to normal, we suspected that this may be one of the manifestations of Mdc’s unique role. Spearman sequential correlation analysis showed the apparent opposite between tight junction and inflammation. Moreover, the Mantel test also proved that tight junction proteins were closely related to intestinal flora. So the intestinal flora regulation of Mdc was mainly achieved by regulating tight junction. Tight junction dysfunction has been linked to a variety of local and systemic diseases (Buckley and Turner, 2018), which may have a decisive effect on intestinal flora disorder, inflammatory response and oxidative stress induced by S. typhimurium.
Increased epithelial permeability is observed in inflammatory states, and Matthias Bruewer clarified that IFN-γ produces a leaky epithelial barrier by inducing macropinoytosis of TJ proteins (Bruewer et al., 2005). In DSS colitis, the loss of tight junction proteins and increased permeability preceded the development of significant intestinal inflammation suggesting that alterations in the TJ complex occur before the intestinal inflammation and not as a consequence of it (Poritz et al., 2007). Oxidative stress is also one of the ways to alter tight junction proteins, thereby enhancing intestinal dysfunction (Ha et al., 2016). The reduction of oxidative stress may upregulate tight junction protein expression (Wu et al., 2018). Intestinal inflammation and oxidative stress may be partly caused by intestinal bacteria, but they also affect the environment, and changes bacterial population profiles (Ren et al., 2018). In our study, the results also showed that both inflammatory factors and tight junction proteins are closely related to intestinal flora. Altogether, there is a complex interrelationship among them (Tlaskalová-Hogenová et al., 2011).
In conclusion, these data suggested that Mdc had an obvious protective effect on S. typhimurium induced colonic mucosal barrier injury in mice. The mechanism may be through inhibiting colonic inflammation and oxidative stress, up-regulating the expression of tight junction proteins ZO-1, Occludin, Claudin-1 in colonic epithelial cells, improving intestinal flora imbalance, reducing the damage of colonic epithelium and intestinal permeability, protecting the tight junction structure of colon mucosa and ameliorating the function of colon mucosal barrier. These findings could enhance our understanding on the effect and mechanism of Mdc on colonic mucosal barrier damage caused by S. typhimurium infection and contribute to developing effective therapies in the future.
LZ and XL performed the research and wrote the manuscript. SG and ZL collected and analyzed the data. FC, XJ, and JZ participated in the design of the study. AL, ZC, YT, MX, and WL prepared the tissue sections. All authors approved the final version of the manuscript.
This work was financially supported by National Key R&D Program of China (No. 2018YFC1603900); National Natural Science Foundation of China (No. 31501894); Natural Science Foundation of Guangdong Province of China (No. 2018A030313461); Special Foundation of Public Welfare Research and Capacity Building of Guangdong Province (No. 2016A030303060 and 2017A010105012); and Scientific Research Project of Shenzhen Health and Family Planning System (No. SZXJ2017022).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Argüello, H., Estellé, J., Zaldívar-López, S., Jiménez-Marín,Á., Carvajal, A., López-Bascón, M. A., et al. (2018). Early Salmonella typhimurium infection in pigs disrupts microbiome composition and functionality principally at the ileum mucosa. Sci. Rep. 8:7788. doi: 10.1038/s41598-018-26083-3
Assimakopoulos, S., Vagianos, C., Patsoukis, N., Georgiou, C., Nikolopoulou, V., and Scopa, C. (2004). Evidence for intestinal oxidative stress in obstructive jaundice-induced gut barrier dysfunction in rats. Acta Physiol. Scand. 180, 177–185. doi: 10.1046/j.0001-6772.2003.01229.x
Baba, E., Nagaishi, S., Fukata, T., and Arakawa, A. (1991). The role of intestinal microflora on the prevention of Salmonella colonization in gnotobiotic chickens. Poult. Sci. 70, 1902–1907. doi: 10.3382/ps.0701902
Balasundaram, P., Veerappapillai, S., and Karuppasamy, R. (2017). Quinolones and fluoroquinolones to treat Salmonella typhimurium: a review of metabolism and pharmacokinetics. Curr. Drug Metab. 18, 1085–1094. doi: 10.2174/1389200218666170710185032
Bärbel, R., Soo-Kyung, P., Monack, D. M., and Arturo, Z. (2006). Caspase-1-mediated activation of interleukin-1beta (IL-1beta) and IL-18 contributes to innate immune defenses against Salmonella enterica serovar typhimurium infection. Infect. Immun. 74, 4922–4926. doi: 10.1128/IAI.00417-06
Betanzos, A., Javier-Reyna, R., García-Rivera, G., Bañuelos, C., González-Mariscal, L., Schnoor, M., et al. (2013). The EhCPADH112 complex of entamoeba histolytica interacts with tight junction proteins occludin and claudin-1 to produce epithelial damage. PLoS One 8:e65100. doi: 10.1371/journal.pone.0065100
Boyer, P., D’Costa, S., Edwards, L., Milloway, M., Susick, E., Borst, L., et al. (2015). Early life dietary spray dried plasma influences immunological and intestinal injury responses to later life Salmonella typhimurium challenge. Br. J. Nutr. 113, 783–793. doi: 10.1017/S000711451400422X
Bronner, D., Faber, F., Olsan, E., Byndloss, M., Sayed, N., Xu, G., et al. (2018). Genetic ablation of butyrate utilization attenuates Gastrointestinal Salmonella disease. Cell Host Microbe 23, 266–273.e4. doi: 10.1016/j.chom.2018.01.004
Brown, T. H., David, J., Acosta-Ramirez, E., Moore, J. M., Lee, S., Zhong, G., et al. (2012). Comparison of immune responses and protective efficacy of intranasal prime-boost immunization regimens using adenovirus-based and CpG/HH2 adjuvanted-subunit vaccines against genital Chlamydia muridarum infection. Vaccine 30, 350–360. doi: 10.1016/j.vaccine.2011.10.086
Bruewer, M., Utech, M., Ivanov, A. I., Hopkins, A. M., Parkos, C. A., and Nusrat, A. (2005). Interferon-γ induces internalization of epithelial tight junction proteins via a macropinocytosis-like process. FASEB J. 19, 923–933. doi: 10.1096/fj.04-3260com
Cazorla, S. I., Maldonado-Galdeano, C., Weill, R., De Paula, J., and Perdigón, G. D. (2018). Oral administration of probiotics increases Paneth cells and intestinal antimicrobial activity. Front. Microbiol. 9:736. doi: 10.3389/fmicb.2018.00736
Chaudhry, K. K., Shukla, P. K., Mir, H., Manda, B., Gangwar, R., Yadav, N., et al. (2016). Glutamine supplementation attenuates ethanol-induced disruption of apical junctional complexes in colonic epithelium and ameliorates gut barrier dysfunction and fatty liver in mice. J. Nutr. Biochem. 27, 16–26. doi: 10.1016/j.jnutbio.2015.08.012
Collado-Romero, M., Martins, R., Arce, C., Moreno,Á., Lucena, C., Carvajal, A., et al. (2012). An in vivo proteomic study of the interaction between Salmonella typhimurium and porcine ileum mucosa. J. Proteomics 75, 2015–2026. doi: 10.1016/j.jprot.2012.01.001
Colliou, N., Ge, Y., Sahay, B., Gong, M., Zadeh, M., Owen, J. L., et al. (2017). Commensal propionibacterium strain UF1 mitigates intestinal inflammation via Th17 cell regulation. J. Clin. Invest. 127, 3970–3986. doi: 10.1172/JCI95376
Deriu, E., Liu, J. Z., Pezeshki, M., Edwards, R. A., Ochoa, R. J., Contreras, H., et al. (2013). Probiotic bacteria reduce Salmonella typhimurium intestinal colonization by competing for iron. Cell Host Microbe 14, 26–37. doi: 10.1016/j.chom.2013.06.007
Di Sabatino, A., Santilli, F., Guerci, M., Simeone, P., Ardizzone, S., Massari, A., et al. (2016). Oxidative stress and thromboxane-dependent platelet activation in inflammatory bowel disease: effects of anti-TNF-α treatment. Thromb. Haemost. 116, 486–495. doi: 10.1160/TH16-02-0167
Faccone, D., Lucero, C., Albornoz, E., Petroni, A., Ceriana, P., Campos, J., et al. (2018). Emergence of azithromycin resistance mediated by the mph (A) gene in Salmonella typhimurium clinical isolates in Latin America. J. Glob. Antimicrob. Resist. 13, 237–239. doi: 10.1016/j.jgar.2018.04.011
Frank, D. N., Robertson, C. E., Hamm, C. M., Kpadeh, Z., Zhang, T., Chen, H., et al. (2011). Disease phenotype and genotype are associated with shifts in intestinal-associated microbiota in inflammatory bowel diseases. Inflamm. Bowel. Dis. 17, 179–184. doi: 10.1002/ibd.21339
Fusco, A., Savio, V., Cammarota, M., Alfano, A., Schiraldi, C., and Donnarumma, G. (2017). Beta-defensin-2 and beta-defensin-3 reduce intestinal damage caused by Salmonella typhimurium modulating the expression of cytokines and enhancing the probiotic activity of enterococcus faecium. J. Immunol. Res. 2017:6976935. doi: 10.1155/2017/6976935
Ha, T., Park, H., Seong, S., and Ahn, H. (2016). Puromycin aminonucleoside increases podocyte permeability by modulating ZO-1 in an oxidative stress-dependent manner. Exp. Cell Res. 340, 139–149. doi: 10.1016/j.yexcr.2015.12.001
Hou, L., Shi, Y., Zhai, P., and Le, G. (2007). Antibacterial activity and in vitro anti-tumor activity of the extract of the larvae of the housefly (Musca domestica). J. Ethnopharmacol. 111, 227–231. doi: 10.1016/j.jep.2006.11.015
Huang, F.-C., and Huang, S.-C. (2018). Differential effects of statins on inflammatory interleukin-8 and antimicrobial peptide human β-defensin 2 responses in Salmonella-infected intestinal epithelial cells. Int. J. Mol. Sci. 19:1650. doi: 10.3390/ijms19061650
Huang, Y., Kim, B. Y., Chan, C. K., Hahn, S. M., Weissman, I. L., and Jiang, W. (2018). Improving immune–vascular crosstalk for cancer immunotherapy. Nat. Rev. Immunol. 18, 195–203. doi: 10.1038/nri.2017.145
Jakobsson, H. E., Rodríguez-Piñeiro, A. M., Schütte, A., Ermund, A., Boysen, P., Bemark, M., et al. (2015). The composition of the gut microbiota shapes the colon mucus barrier. EMBO Rep. 16, 164–177. doi: 10.15252/embr.201439263
Kamekura, R., Nava, P., Feng, M., Quiros, M., Nishio, H., Weber, D. A., et al. (2015). A highlights from MBoC selection: inflammation-induced desmoglein-2 ectodomain shedding compromises the mucosal barrier. Mol. Biol. Cell 26, 3165–3177. doi: 10.1091/mbc.E15-03-0147
Kiatsurayanon, C., Niyonsaba, F., Smithrithee, R., Akiyama, T., Ushio, H., Hara, M., et al. (2014). Host defense (Antimicrobial) peptide, human β-defensin-3, improves the function of the epithelial tight-junction barrier in human keratinocytes. J. Invest. Dermatol. 134, 2163–2173. doi: 10.1038/jid.2014.143
Kuang, D., Zhang, J., Xu, X., Shi, W., Chen, S., Yang, X., et al. (2018). Emerging high-level ciprofloxacin resistance and molecular basis of resistance in Salmonella enterica from humans, food and animals. Int. J. Food Microbiol. 280, 1–9. doi: 10.1016/j.ijfoodmicro.2018.05.001
Li, C., Cai, Y., and Yan, Z. (2018). Brain-derived neurotrophic factor preserves intestinal mucosal barrier function and alters gut microbiota in mice. Kaohsiung J. Med. Sci. 34, 134–141. doi: 10.1016/j.kjms.2017.11.002
Liu, S.-H., Ma, K., Xu, X.-R., and Xu, B. (2010). A single dose of carbon monoxide intraperitoneal administration protects rat intestine from injury induced by lipopolysaccharide. Cell Stress Chaperones 15, 717–727. doi: 10.2307/20799965
Llewellyn, S., Britton, G., Contijoch, E., Vennaro, O., Mortha, A., Colombel, J., et al. (2018). Interactions between diet and the intestinal microbiota alter intestinal permeability and colitis severity in mice. Gastroenterology 154, 1037–1046.e2. doi: 10.1053/j.gastro.2017.11.030
Loo, T., Kamachi, F., Watanabe, Y., Yoshimoto, S., Kanda, H., Arai, Y., et al. (2017). Gut microbiota promotes obesity-associated liver cancer through PGE2-mediated suppression of antitumor immunity. Cancer Discov. 7, 522–538. doi: 10.1158/2159-8290.CD-16-0932
Lu, X., Jin, X., and Zhu, J. (2015). Flow cytometry and electron microscopy study of staphylococcus aureus and Escherichia coli treated with Mdc-Hly. Microsc. Microanal. 21, 351–357. doi: 10.1017/S1431927615000203
Lu, X.-M., Jin, X.-B., Zhu, J.-Y., Mei, H.-F., Ma, Y., Chu, F.-J., et al. (2010). Expression of the antimicrobial peptide cecropin fused with human lysozyme in Escherichia coli. Appl. Microbiol. Biotechnol. 87, 2169–2176. doi: 10.1007/s00253-010-2606-3
Lucke, A., Böhm, J., Zebeli, Q., and Metzler-Zebeli, B. U. (2018). Dietary deoxynivalenol and oral lipopolysaccharide challenge differently affect intestinal innate immune response and barrier function in broiler chickens. J. Anim. Sci. 96, 5134–5143. doi: 10.1093/jas/sky379
Ma, X., Fan, P. X., Li, L., Qiao, S., Zhang, G., and Li, D. (2012). Butyrate promotes the recovering of intestinal wound healing through its positive effect on the tight junctions. J. Anim. Sci. 90, 266–268. doi: 10.2527/jas.50965
Manja, B., Siegfried, H., Leticia, Q. M., Marcus, K., Manfred, R., Michael, H., et al. (2003). Pretreatment of mice with streptomycin provides a Salmonella enterica serovar typhimurium colitis model that allows analysis of both pathogen and host. Infect. Immun. 71, 2839–2858. doi: 10.1128/IAI.71.5.2839-2858.2003
Manuela, R., Santos, R. L., Daniela, C., Paul, W. R., Winter, S. E., Rossetti, C. A., et al. (2007). The capsule encoding the viaB locus reduces interleukin-17 expression and mucosal innate responses in the bovine intestinal mucosa during infection with Salmonella enterica serotype Typhi. Infect. Immun. 75, 4342–4350. doi: 10.1128/IAI.01571-06
Mir, H., Meena, A. S., Chaudhry, K. K., Shukla, P. K., Gangwar, R., Manda, B., et al. (2016). Occludin deficiency promotes ethanol-induced disruption of colonic epithelial junctions, gut barrier dysfunction and liver damage in mice. Biochim. Biophys. Acta 1860, 765–774. doi: 10.1016/j.bbagen.2015.12.013
Neyrinck, A. M., Etxeberria, U., Taminiau, B., Daube, G., Van Hul, M., Everard, A., et al. (2017). Rhubarb extract prevents hepatic inflammation induced by acute alcohol intake, an effect related to the modulation of the gut microbiota. Mol. Nutr. Food Res. 61:1500899. doi: 10.1002/mnfr.201500899
Ogawa, M., Osada, H., Hasegawa, A., Ohno, H., Yanuma, N., Sasaki, K., et al. (2018). Effect of interleukin-1β on occludin mRNA expression in the duodenal and colonic mucosa of dogs with inflammatory bowel disease. J. Vet. Intern. Med. 32, 1019–1025. doi: 10.1111/jvim.15117
Pohl, C. S., Lennon, E. M., Li, Y., DeWilde, M. P., and Moeser, A. J. (2018). S. Typhimurium challenge in juvenile pigs modulates the expression and localization of enteric cholinergic proteins and correlates with mucosal injury and inflammation. Auton. Neurosci. 213, 51–59. doi: 10.1016/j.autneu.2018.05.009
Poritz, L., Garver, K., Green, C., Fitzpatrick, L., Ruggiero, F., and Koltun, W. (2007). Loss of the tight junction protein ZO-1 in dextran sulfate sodium induced colitis. J. Surg. Res. 140, 12–19. doi: 10.1016/j.jss.2006.07.050
Pound, L. D., Patrick, C., Eberhard, C. E., Mottawea, W., Wang, G.-S., Abujamel, T., et al. (2015). Cathelicidin antimicrobial peptide: a novel regulator of islet function, islet regeneration and selected gut bacteria. Diabetes 64, 4135–4147. doi: 10.2337/db15-0788
Ramanan, D., Bowcutt, R., Lee, S. C., San Tang, M., Kurtz, Z. D., Ding, Y., et al. (2016). Helminth infection promotes colonization resistance via type 2 immunity. Science 352, 608–612. doi: 10.1126/science.aaf3229
Ren, Y., Geng, Y., Du, Y., Li, W., Lu, Z., Xu, H., et al. (2018). Polysaccharide of Hericium erinaceus attenuates colitis in C57BL/6 mice via regulation of oxidative stress, inflammation-related signaling pathways and modulating the composition of the gut microbiota. J. Nutr. Biochem. 57, 67–76. doi: 10.1016/j.jnutbio.2018.03.005
Ridge, Y., Landini, P., and Thompson, A. (2018). High throughput screening of a collection of known pharmacologically active small compounds for inhibitors of Salmonella invasion and intracellular replication. J. Appl. Microbiol. 125, 724–730. doi: 10.1111/jam.13890
Santos, R. L., Zhang, S., Tsolis, R. M., Kingsley, R. A., Adams, L. G., and Baumler, A. J. (2001). Animal models of Salmonella infections: enteritis versus typhoid fever. Microbes Infect. 3, 1335–1344. doi: 10.1016/S1286-4579(01)01495-2
Shi, Y., He, C., Ma, C., Yu, T., Cong, Y., Cai, W., et al. (2018). Smad nuclear interacting protein 1 (SNIP1) inhibits intestinal inflammation through regulation of epithelial barrier function. Mucosal Immunol. 11, 835–845. doi: 10.1038/mi.2017.95
Tang, Z., Deng, H., Zhang, X., Zen, Y., Xiao, D., Sun, W., et al. (2013). Effects of orally administering the antimicrobial peptide buforin II on small intestinal mucosal membrane integrity, the expression of tight junction proteins and protective factors in weaned piglets challenged by enterotoxigenic Escherichia coli. Anim. Feed Sci. Technol. 186, 177–185. doi: 10.1016/j.anifeedsci.2013.10.012
Tlaskalová-Hogenová, H., Štìpánková, R., Kozáková, H., Hudcovic, T., Vannucci, L., Tuèková, L., et al. (2011). The role of gut microbiota (commensal bacteria) and the mucosal barrier in the pathogenesis of inflammatory and autoimmune diseases and cancer: contribution of germ-free and gnotobiotic animal models of human diseases. Cell Mol. Immunol. 8, 110–120. doi: 10.1038/cmi.2010.67
Walsh-Reitz, M. M., Huang, E. F., Musch, M. W., Chang, E. B., Martin, T. E., Kartha, S., et al. (2005). AMP-18 protects barrier function of colonic epithelial cells: role of tight junction proteins. Am. J. Physiol. Gastrointest. Liver Physiol. 289, G163–G171. doi: 10.1152/ajpgi.00013.2005
Wan, M. L. Y., Forsythe, S. J., and El-Nezami, H. (2018). Probiotics interaction with foodborne pathogens: a potential alternative to antibiotics and future challenges. Crit. Rev. Food Sci. Nutr. 1–14. doi: 10.1080/10408398.2018.1490885
Wang, R. X., and Colgan, S. P. (2017). Special pro-resolving mediator (SPM) actions in regulating gastrointestinal inflammation and gut mucosal immune responses. Mol. Aspects Med. 58, 93–101. doi: 10.1016/j.mam.2017.02.002
Winter, S. E., Parameth, T., Winter, M. G., Butler, B. P., Huseby, D. L., Crawford, R. W., et al. (2010). Gut inflammation provides a respiratory electron acceptor for Salmonella. Nature 467, 426–429. doi: 10.1038/nature09415
Wu, H., Luo, T., Li, Y., Gao, Z., Zhang, K., Song, J., et al. (2018). Granny smith apple procyanidin extract upregulates tight junction protein expression and modulates oxidative stress and inflammation in lipopolysaccharide-induced Caco-2 cells. Food Funct. 9, 3321–3329. doi: 10.1039/c8fo00525g
Xia, X., Zhang, L., and Wang, Y. (2015). The antimicrobial peptide cathelicidin-BF could be a potential therapeutic for Salmonella typhimurium infection. Microbiol. Res. 171, 45–51. doi: 10.1016/j.micres.2014.12.009
Yang, B., Qiao, L., Zhang, X., Cui, Y., Xia, X., Cui, S., et al. (2013). Serotyping, antimicrobial susceptibility, pulse field gel electrophoresis analysis of Salmonella isolates from retail foods in Henan Province. China. Food Control 32, 228–235. doi: 10.1016/j.foodcont.2012.11.022
Zhang, B., Shao, Y., Liu, D., Yin, P., Guo, Y., and Yuan, J. (2012). Zinc prevents Salmonella enterica serovar Typhimurium-induced loss of intestinal mucosal barrier function in broiler chickens. Avian Pathol. 41, 361–367. doi: 10.1080/03079457.2012.692155
Keywords: Musca domestica cecropin, Salmonella typhimurium, colonic mucosal barrier, inflammation, oxidative stress, tight junctions, intestinal flora
Citation: Zhang L, Gui S, Liang Z, Liu A, Chen Z, Tang Y, Xiao M, Chu F, Liu W, Jin X, Zhu J and Lu X (2019) Musca domestica Cecropin (Mdc) Alleviates Salmonella typhimurium-Induced Colonic Mucosal Barrier Impairment: Associating With Inflammatory and Oxidative Stress Response, Tight Junction as Well as Intestinal Flora. Front. Microbiol. 10:522. doi: 10.3389/fmicb.2019.00522
Received: 16 December 2018; Accepted: 28 February 2019;
Published: 15 March 2019.
Edited by:George Grant, University of Aberdeen, United Kingdom
Reviewed by:Alessandra Fusco, University of Campania Luigi Vanvitelli, Italy
Wenkai Ren, South China Agricultural University, China
Copyright © 2019 Zhang, Gui, Liang, Liu, Chen, Tang, Xiao, Chu, Liu, Jin, Zhu and Lu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xuemei Lu, email@example.com
†These authors have contributed equally to this work as first authors