Lactobacillus rhamnosus GR-1 alleviates Escherichia coli-triggered bovine endometrial epithelial cells damage via the reactive oxygen species-mitochondrial pathway
Article information
Abstract
Objective
The objective of this study was to evaluate the function of the reactive oxygen species (ROS)-mitochondrial pathway in attenuating Escherichia coli (E. coli) induced apoptosis in bovine endometrial epithelial cells (BENDs) by Lactobacillus rhamnosus (L. rhamnosus) GR-1.
Methods
The BENDs were exposed to preincubation with and without L. rhamnosus GR-1 for 3 hours (h) and they were later subject to E. coli for 6 h. The release of lactate dehydrogenase (LDH), the expression of oxidative factors, adhesion and invasion of E. coli, the expression of mitochondrial membrane potential (MMP), apoptotic rate and apoptosis-associated protein expression were observed. Then, ROS expression, MMP level and cell rate apoptosis rate were further detected after the intervention of antioxidant n-acetyl-l-cysteine (NAC).
Results
L. rhamnosus GR-1 was capable of obviously alleviating the content of LDH, ROS expression, E. coli adhesion and invasion, the apoptotic rate and MDA concentrations in BENDs induced by E. coli (p<0.01). In addition, L. rhamnosus GR-1 could notably promote the levels of antioxidant factors (SOD, GSH, T-AOC) (p<0.01), inhibit the depolarization of MMP (p<0.01), and levels of apoptosis-related factors (Bax, Caspase-3 and Cyt-c), and promote anti-apoptosis factor (Bcl-2) (p<0.01). Moreover, after the intervention of antioxidant NAC, ROS expression, MMP depolarization, and apoptotic rate induced by E. coli in BENDs were decreased (p<0.01).
Conclusion
In E. coli-induced apoptosis in BENDs, therapeutic strategies aimed at down-regulating ROS and MDA and up-regulating antioxidant factors may maintain mitochondrial function and provide theoretical support for the use of probiotics in bovine endometritis.
INTRODUCTION
Bovine endometritis is a postpartum uterine inflammation of dairy cows, resulting in infertility, reduced milk production, and increased treatment costs, causing significantly economic losses [1,2]. Escherichia coli is one of the main pathogens leading to bovine endometritis [3]. Antibiotics have commonly been adopted for treating bovine endometritis, but due to antibiotic overuse, the problem of antibiotic resistance is becoming more serious, also posing a tremendous threat to dairy health [4]. Hence, it is critical to elucidate the underlying mechanisms of endometritis and to identify alternative treatments to prevent and manage bovine endometritis.
E. coli infection can be recognized by receptors expressed in bovine endometrial epithelial cells (BENDs), triggering an inflammatory response [5]. The progression of several inflammatory diseases has been linked to reactive oxygen species (ROS). Studies have shown that E. coli significantly elevates ROS levels, suppresses antioxidant enzyme expression, enhances lipid peroxidation, and ultimately triggers oxidative stress [6]. It is generally accepted that elevated ROS levels contribute to abnormalities in mitochondrial membrane potential (MMP) [7]. Then, pro-apoptotic proteins Cytochrome c (Cyt-c) is capable of releasing from mitochondria to the cytoplasm, with recruitment as well as the activation of procaspase-9. Next, the cleaved caspase-9 enzyme is found to activate the executioner procaspase-3, leading to the induction of apoptosis through the formation of cleaved caspase-3 [8]. Therefore, inhibition of ROS-mediated apoptosis may be an effective treatment for inflammatory diseases such as bovine endometritis.
As the alternative to antibiotics, probiotics have attracted particular attention. They are referred to as “living microorganisms that, when given in sufficient quantities, delivers host health advantages” [9]. Probiotics are widely used to address animal diseases resulting from bacterial infections. There are many kinds of probiotics widely used in endometritis, including Lactobacillus, Bifidobacterium and Streptococcus etc. [10,11]. Lactobacillus has anti-inflammatory, antioxidant, anti-apoptotic and antibacterial properties [12,13]. Previous studies have found that L. plantarum KSFY06 reduces liver injury by exerting antioxidant and anti-inflammatory effects [14], and Lactobacillus rhamnosus ameliorates BENDs inflammatory response as well as apoptosis caused by B. cereus [15]. Meanwhile, according to our previous research, L. rhamnosus GR-1 has demonstrated the ability to reduce apoptosis in the BENDs infected with E. coli [16]. However, the mechanism of L. rhamnosus GR-1 in attenuating the apoptosis of BENDs triggered by E. coli still needs to be clarified.
Therefore, we hypothesized that L. rhamnosus GR-1 had the capability of hindering the apoptosis of BENDs through inhibiting the mitochondrial apoptosis pathway and speculated that ROS exerted a vital role during this process. The current work was to investigate the inhibitory mechanistic function of L. rhamnosus GR-1 on the pathogenic effect in BENDs triggered by E. coli and to provide new insights for L. rhamnosus GR-1 to mitigate E. coli-induced injury in BENDs.
MATERIALS AND METHODS
Cell and bacterial strains
BENDs (BNCC340413, BNCC, Beijing, China) were incubated in 89% DMEM/F12 (Procell, Wuhan, China) supplemented with 10% concentration of fetal bovine serum (MeliunBio, Dalian, China), and 1% concentration of penicillin/streptomycin (Solarbio, Beijing, China), and passaged at a density of 1×106/well in 6-well plates for subsequent experiments.
L. rhamnosus GR-1 strain (ATCC 55826) was provided by the Laboratory of Clinical Nutrition and Immunology of the College of Veterinary Medicine of the China Agricultural University. The L. rhamnosus GR-1 was grown in MRS medium (AOBOX, Beijing, China) at 37°C and it was diluted in DMEM/F12 basic medium (Procell) to a density of 5×106 CFU/mL for follow-up tests.
E. coli strain O111: K58 (CVCC1450) was provided by the Laboratory of Clinical Nutrition and Immunology of the College of Veterinary Medicine of the China Agricultural University. The E. coli was grown in LB broth (AOBOX) with 180 rpm at 37°C and it was diluted in DMEM/F12 basic medium (Procell) to a density of 5×105 CFU/mL for infecting the cells.
Cell treatment in different experiments
BENDs were seeded in a 6-well plate at a density of 1×106 and incubated at 37°C for 24 h to reach 90%–100% density, then washed twice with PBS. BENDs were pretreated with L. rhamnosus GR-1 (5×106 CFU/mL) for 3 h and then infected with E. coli (5×105 CFU/mL) for 6 h [5]. After treatment, cell samples were collected for subsequent experimental analysis.
BENDs were inoculated into 6-well plates at a density of 1×106 cells/well and incubated at 37°C for 24 h to reach 90%–100% density, then washed twice with PBS. After ROS scavenger NAC (10 μM) pretreatment for 3 h. Subsequently, the cells were co-incubated with E. coli for 6 h in order to determine the effect of ROS deletion on the oxidative stress and apoptotic response of BENDs. After treatment, cell samples were collected for subsequent experimental analysis.
Cytotoxic lactate dehydrogenase release assay
BENDs were added 5×106 CFU/mL of L. rhamnosus GR-1 for 3 h, followed by the action of 5×105 CFU/mL of E. coli for 6 h. The cytotoxic effects of L. rhamnosus GR-1 on E. coli-infected BENDs were assessed using a lactate dehydrogenase (LDH) assay kit (Jiancheng Bioengineering Institute, Nanjing, China). The supernatant was collected according to manufacturer’s instructions. The optical density was measured at 450 nm with a Microplate Spectrophotometer (Bio Tek, Winooski, VT, USA).
Adhesion and invasion
Adhesion and invasion were measured following the method described by Wu [17]. Briefly, BENDs were pretreated with L. rhamnosus GR-1 for 3 h and then exposed to E. coli treatment for 6 h. Cells were washed three times with PBS to remove non-adherent bacteria and then harvested by treatment with 0.25% trypsin for 3 min at 37°C. The cells were then incubated with DMEM/F12 medium to determine the number of bacteria adhering to the surface of BENDs. Cell suspensions were diluted with DMEM/F12 medium and then incubated on EMB Agar plates to determine the number of bacteria attached to the surface of BENDs.
To evaluate the number of E. coli invading BENDs, the cells were washed with PBS and treated with 1 mL of DMEM/F12 containing Gentamicin (100 μg/mL) for 2 h. After that, the cells were lysed with 0.5% Triton X-100. The lysate was diluted and cultured on EMB Agar plate plate as described above. The colonies were counted, and the invasion rate of E. coli into BENDs was calculated.
Measurement of the levels of intracellular reactive oxygen species
Intracellular levels of ROS were measured using 2,7-dichlorofluorescein diacetate (DCFH-DA) (Beyotime, Beijing, China). After treating the cells, 1 mL of 10 μmol/L DCFH-DA was added and incubated at 37°C for 20 min. The cells were then washed three times with a medium devoid of FBS and and observed under a fluorescence microscope (IX51; Olympus, Tokyo, Japan).
Detection of oxidation-related factor
Oxidation-related factors including SOD, GSH, T-AOC and MDA were assessed in the cells using a kit (Jiancheng Bioengineering Institute, Nanjing, China). After modeling was completed, cell suspensions were collected according to the manufacturer’s instructions and then centrifuged at 1,000 r/min for 10 min. The optical density was measured with a Microplate Spectrophotometer (synergyLX, Bio Tek).
Assessment of mitochondrial membrane potential (ΔΨm)
The MMP of different groups of cells were assessed using the Enhanced Mitochondrial MMP Detection Kit (JC-1) (Beyotime). The degree of mitochondrial depolarization was assessed by calculating the relative ratio of red (JC-1 aggregate) to green (JC-1 monomer) fluorescence. After completing the modeling, 2 mL of JC-1 staining working solution was added to each group, and subsequently, the cells were rinsed twice with 2 mL of JC-1 staining buffer, and, finally, 2 mL of complete DMEM/F12 medium was added and the cells were visualized using fluorescence microscopy (IX51; Olympus).
Measurement of cell apoptosis
The apoptosis rate of BENDs were assessed using the Annexin V-FITC/PI Apoptosis Detection Kit (4ABioteece, Beijing, China). Cells were collected by adding 1× binding buffer and 5 μL of Annexin V/FITC, followed by a 5 min incubation at room temperature away from light. Then, 10 μL of 20 μg/mL propidium iodide solution and 400 μL of PBS were added. Finally, the samples were analysed using a flow cytometer (BD, Franklin Lakes, NJ, USA).
Real-time quantitative polymerase chain reaction
The total RNA was extracted from BENDs using Triquick Reagent (Solarbio). The RNA quality of all samples was assessed by NanoDrop ND-2000 spectrophotometer. The RevertAid First Strand cDNA Synthesis Kit was used to synthesize first-strand cDNA (Tiangen, Beijing, China). Primer-BLAST software was used to design primers (Table 1). The real-time polymerase chain reaction (RT–PCR) was conducted on a LightCycler 480 system using SuperReal PreMix Plus (Tiangen). The reaction conditions were set at 95°C for 15 min, followed by 40 cycles consisting of denaturation at 95°C for 10 s and annealing/elongation at 60°C for 30 s. Moreover, relative transcript expression levels were calculated via the 2−ΔΔCT.
The primer sequences, amplified fragment length, and sequence number of four target genes used in this study
Western blot
The total protein was extracted from cells using a whole protein extraction kit (Solarbio). Determination of group protein concentrations using the BCA Protein Concentration Assay Kit (Solarbio). Subsequently, proteins were separated by SDS-PAGE on a 12.5% gel and transferred to a PVDF membrane. The membrane was blocked with 5% skimmed milk for 60 min at 37°C, and then incubated overnight at 4°C with primary antibodies, including rabbit anti-Bcl-2 (1:500), rabbit anti-Bax (1:500), rabbit anti-caspase-3 (1:500), mouse β-actin (1:1,000) (Bioss, Beijing, China), and rabbit anti-Cyt-c (1:1,000) (Cell Signaling Technology, Danvers, MA, USA). After this, the membrane was incubated with secondary antibodies at 37°C for 1 h: goat anti-rabbit IgG (Bioss) and goat anti-mouse IgG (1:1,000) (Proteintech, Wuhan, China), followed by ultrasensitive ECL chemiluminescence development. The relative intensity of each band was assessed by Image J 1.47 v software.
Statistical analyses
The experimental results were derived from three independent experiments, each performed in triplicate. The experimental unit of investigation for each variable was a cell well. Values were expressed as means±standard errors of means (SEMs). Statistical significance was calculated using one-way ANOVA, followed by the Duncan and LSD multiple tests, using SPSS 27.0 (SPSS, Chicago, IL, USA), A p-value<0.05 was considered statistically significant. GraphPad Prism 8.0 software was used for all analyses.
RESULTS
Effect of Lactobacillus rhamnosus GR-1 on the activity of bovine endometrial epithelial cells infected with Escherichia coli
The effect of L. rhamnosus GR-1 on the rate of LDH release in E. coli infected BENDs is shown in Figure 1, where the rate of LDH release was significantly higher in the E. coli infected group (p<0.01), while pretreatment with L. rhamnosus GR-1 significantly reduced the rate of LDH release (p<0.01).
Effect of Lactobacillus rhamnosus GR-1 on the activity of BENDs infected with Escherichia coli. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. Cell activity was assessed by assaying the LDH release rate, using a Microplate Spectrophotometer to measure absorbance at 450 nm. The LDH release rate was calculated and expressed as a percentage of cells in CONT group (received no L. rhamnosus GR-1 and E. coli). Data represented are means± standard errors of means (SEMs) from triplicate experiments. a–c If the same letter appears on the bars, the difference is not significant (p>0.05). If there is no common letter among the bars, the difference is significant (p<0.05). LDH, lactate dehydrogenase; BENDs, bovine endometrial epithelial cells.
Effect of Lactobacillus rhamnosus GR-1 pretreatment on adhesion and invasion of bovine endometrial epithelial cells by Escherichia coli
The results of the effect of L. rhamnosus GR-1 pretreatment on the adhesion and invasion of BENDs by E. coli are shown in Figure 2. Pretreatment with L. rhamnosus GR-1 could significantly reduce the adhesion and invasion of BENDs by E. coli (p<0.01).
Effect of Lactobacillus rhamnosus GR-1 on the activity of BENDs infected with Escherichia coli. BENDs (90%–100%) were treated with E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. (A) Adhesion of E. coli-infected bMECs in pretreatment of L. rhamnosus GR-1. (B) invasion of E. coli-infected bMECs in pretreatment of L. rhamnosus GR-1. Data represented are means±standard errors of means (SEMs) from triplicate experiments. a,b If there is no common letter among the bars, the difference is significant (p<0.05). BENDs, bovine endometrial epithelial cells.
Effect of Lactobacillus rhamnosus GR-1 on oxidative stress induced by Escherichia coli in bovine endometrial epithelial cells
The results of the effect of L. rhamnose GR-1 on ROS levels in E. coli-infected BENDs are shown in Figure 3. The results showed a highly significant increase in cellular ROS expression in the E. coli infection group (p<0.01). Whereas, L. rhamnosus pretreatment reduced ROS expression extremely significantly (p<0.01) (Figure 3).
Effects of Lactobacillus rhamnosus GR-1 on ROS levels in Escherichia coli-treated BENDs. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. (A) Representative micrographs show DCF fluorescence of control cells, cells treated with L. rhamnosus GR-1 or E. coli alone, and cells co-treated with L. rhamnosus GR-1 and E. coli. (B) Quantification of DCF fluorescence was based on the images in Figure 3A. ROS generation was calculated and expressed as a percentage of fluorescence intensity for the CONT group (not receiving L. rhamnosus GR-1 and E. coli). Data represented are means±standard errors of means (SEMs) from triplicate experiments. a–d If there is no common letter among the bars, the difference is significant (p<0.05). ROS, reactive oxygen species; BENDs, bovine endometrial epithelial cells; DCF, dichlorofluorescein.
The results of the effect of L. rhamnosus GR-1 on the expression of oxidation-related factors in E. coli infected BENDs are shown in Figure 4. The L. rhamnosus pretreatment significantly repressed the E. coli-induced activity of oxidation factors (MDA), while the activity of antioxidant (SOD, GSH and T-AOC) was significantly increased (p<0.01).
Effects of Lactobacillus rhamnosus GR-1 on oxidative factors levels in Escherichia coli-treated BENDs. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. (A) MDA content. (B) SOD content. (C) GSH content. (D) T-AOC content. Absorbance was measured using a Microplate Spectrophotometer and content was calculated. Data represented are means±standard errors of means (SEMs) from triplicate experiments. a–d If the same letter appears on the bars, the difference is not significant (p>0.05). If there is no common letter among the bars, the difference is significant (p<0.05). MDA, malondialdehyde; SOD, superoxide dismutase; GSH, glutathione; T-AOC, total antioxidant capacity; BENDs, bovine endometrial epithelial cells.
Effect of Lactobacillus rhamnosus GR-1 on mitochondrial membrane potential of bovine endometrial epithelial cells induced by Escherichia coli
The results of the effect of L. rhamnosus GR-1 on MMP levels in E. coli-infected BENDs are shown in Figure 5. The results showed that MMP levels were highly significantly lower (p< 0.01) in the cells of the E. coli infected group. Whereas, MMP levels were highly significantly elevated (p<0.01) in the cells of L. rhamnosus pretreated group.
Effects of Lactobacillus rhamnosus GR-1 on MMP levels in Escherichia coli-treated BENDs. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. (A) Representative micrographs show JC-1 fluorescence of control cells, cells treated with L. rhamnosus GR-1 or E. coli alone, and cells co-treated with L. rhamnosus GR-1 and E. coli. (B) Quantification of JC-1 fluorescence was based on the images in Figure 5A. J-aggregayes/J-monomer was calculated and expressed as a percentage of fluorescence intensity for the CONT group (not receiving L. rhamnosus GR-1 and E. coli). Data represented are means±standard errors of means (SEMs) from triplicate experiments. a–d If there is no common letter among the bars, the difference is significant (p<0.05). MMP, mitochondrial membrane potential; BENDs, bovine endometrial epithelial cells.
Effect of Lactobacillus rhamnosus GR-1 on apoptosis of bovine endometrial epithelial cells induced by Escherichia coli
The results of the effect of L. rhamnosus GR-1 on apoptosis in E. coli-infected BENDs are shown in Figure 6. The results showed that the apoptosis rate was highly significantly increased (p<0.01) in the E. coli infected group, whereas L. rhamnosus GR-1 pretreatment resulted in a highly significant decrease in the apoptosis rate (p<0.01).
Effects of Lactobacillus rhamnosus GR-1 on apoptosis in Escherichia coli-treated BENDs. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. (A) Determination of apoptosis rates using flow cytometry. (B) Quantitative analysis of apoptosis rates was based on the images in Figure 6A. Cell apoptosis rate was calculated and expressed as a percentage of fluorescence intensity for the CONT group (not receiving L. rhamnosus GR-1 and E. coli). Data represented are means±standard errors of means (SEMs) from triplicate experiments. a–d If there is no common letter among the bars, the difference is significant (p<0.05). BENDs, bovine endometrial epithelial cells.
Subsequently, mRNA and protein expression levels of mitochondria-dependent apoptosis-related factors were further analyzed. The results are shown in Figures 7, 8. mRNA and protein levels of Bax and Caspase-3 were extremely significantly increased and Cyt-c protein expression was extremely significantly increased in E. coli infected group of cells (p< 0.01), whereas the mRNA and protein levels of Bax and Caspase-3 were significantly decreased after L. rhamnosus GR-1 pretreatment (p<0.05), Cyt-c protein expression was highly significantly reduced (p<0.01). mRNA and protein expression of Bcl-2 was highly significantly decreased (p<0.01) in E. coli infected group and increased (p<0.05) after L. rhamnosus GR-1 pretreatment.
Effects of Lactobacillus rhamnosus GR-1 on the mRNA levels of Bcl-2, Bax and Caspase-3 in Escherichia coli-treated BENDs. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. (A) mRNA levels of the Bax were assessed by RT-qPCR. Relative transcript expression was calculated using the 2−ΔΔCt method and presented as values relative to the CONT group (not receiving L. rhamnosus GR-1 and E. coli). (B) mRNA levels of the Bcl-2 were assessed by RT-qPCR. Relative transcript expression was calculated using the 2−ΔΔCt method and presented as values relative to the CONT group (not receiving L. rhamnosus GR-1 and E. coli). (C) mRNA levels of the Caspase-3 were assessed by RT-qPCR. Relative transcript expression was calculated using the 2−ΔΔCt method and presented as values relative to the CONT group (not receiving L. rhamnosus GR-1 and E. coli). Data represented are means±standard errors of means (SEMs) from triplicate experiments. a–d If the same letter appears on the bars, the difference is not significant (p>0.05). If there is no common letter among the bars, the difference is significant (p<0.05). Bax, Bcl-2-associated X protein; Bcl-2, B-cell lymphoma-2; BENDs, bovine endometrial epithelial cells; RT-qPCR, real-time quantitative polymerase chain reaction.
Effects of Lactobacillus rhamnosus GR-1on the expression of mitochondrial-mediated apoptosis pathway protein in Escherichia coli-treated BENDs. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL) for 9 h. (A) Bcl-2, Bax, Caspase-3 and Cyt-c and β-actin (internal control) protein levels were detected using Western blot. (B) Quantification of Bcl-2 expression of three independent experiments and normalized to β-actin and represented in the bar graph. (C) Quantification of Bax expression of three independent experiments and normalized to β-actin and represented in the bar graph. (D) Quantification of Caspase-3 expression of three independent experiments and normalized to β-actin and represented in the bar graph. (E) Quantification of Cyt-c expression of three independent experiments and normalized to β-actin and represented in the bar graph. Data represented are means±standard errors of means (SEMs) from triplicate experiments. a,b If the same letter appears on the bars, the difference is not significant (p>0.05). If there is no common letter among the bars, the difference is significant (p<0.05). BENDs, bovine endometrial epithelial cells.
Effect of reactive oxygen species signaling in Lactobacillus rhamnosus GR-1 on alleviating Escherichia coli induced-apoptosis in bovine endometrial epithelial cells
The results of the effect of NAC on alleviating E. coli-induced apoptosis in BEND cells are shown in Figure 9. The results showed that ROS level, MMP depolarization level and apoptosis rate were significantly reduced (p<0.05) in the E. coli group reinfected after NAC pretreatment.
Lactobacillus rhamnosus GR-1 alleviates ROS-dependent apoptosis of BENDs induced by Escherichia coli. BENDs (90%–100%) were treated with L. rhamnosus GR-1 (5×106 CFU/mL), E. coli (5×105 CFU/mL), NAC (10 μM) alone or a combination of L. rhamnosus GR-1 (5×106 CFU/mL) and E. coli (5×105 CFU/mL), NAC (10 μM) and E. coli (5×105 CFU/mL) for 9 h. (A) Representative micrographs show DCF fluorescence of control cells, cells treated with L. rhamnosus GR-1 or E. coli alone, and cells co-treated with L. rhamnosus GR-1 and E. coli. (B) Quantification of DCF fluorescence was based on the images in Figure 9A. ROS generation was calculated and expressed as a percentage of fluorescence intensity for the CONT group (not receiving L. rhamnosus GR-1 and E. coli). (C) Representative micrographs show JC-1 fluorescence of control cells, cells treated with L. rhamnosus GR-1 or E. coli alone, and cells co-treated with L. rhamnosus GR-1 and E. coli. (D) Quantification of JC-1 fluorescence was based on the images in Figure 9C. J-aggregayes/J-monomer was calculated and expressed as a percentage of fluorescence intensity for the CONT group (not receiving L. rhamnosus GR-1 and E. coli). (E) Determination of apoptosis rates using flow cytometry. (F) Quantitative analysis of apoptosis rates was based on the images in Figure 9E. Cell apoptosis rate was calculated and expressed as a percentage of fluorescence intensity for the CONT group (not receiving L. rhamnosus GR-1 and E. coli). Data represented are means±standard errors of means (SEMs) from triplicate experiments. a–f If the same letter appears on the bars, the difference is not significant (p>0.05). If there is no common letter among the bars, the difference is significant (p<0.05). ROS, reactive oxygen species; BENDs, bovine endometrial epithelial cells; DCF, dichlorofluorescein.
DISCUSSION
Bovine endometritis is a disease caused by postpartum bacterial infection. E. coli is one of the main pathogens which causes serious economic losses [18]. Our previous study found that L. rhamnosus GR-1 inhibited the inflammatory damage via NF-κB/MAPK pathway of bovine endometritis epithelial cells induced by E. coli [5]. Additionally, L. rhamnosus GR-1 has an anti-apoptotic effect in bovine endometritis epithelial cells induced by E. coli [16], but its molecular mechanism is unclear. In the current study, we found L. rhamnosus GR-1 improved the antioxidant effect in E. coli-infected BENDs. Meanwhile, ROS-mitochondrial pathway plays an important role in anti-apoptotic effects of L.rhamnosus GR-1 in E. coli-infected BENDs.
LDH is a stable intracellular cytoplasmic enzyme that is rapidly released into the cell culture supernatant when the cytoplasmic membrane is disrupted, which is a major feature of cells undergoing apoptosis or other forms of cellular damage [19]. LDH release assays are often used as complementary assays to assess cell membrane integrity [20]. Our study found that L. rhamnosus GR-1 alone did not cause cellular damage, while pretreatment with L. rhamnosus GR-1 attenuated E. coli-induced LDH release.
Bacterial adhesion to host epithelial cells is a critical step in initiating infection [21]. In contrast, the surface proteins and exopolysaccharides of probiotics can inhibit the formation of pathogenic biofilms by inhibiting adhesion, thus playing an important role in promoting pre-colonization and repelling pathogenic bacteria [22]. In the present study, L. rhamnosus GR-1 were able to significantly reduce the adhesion and colonization of E. coli, a result that is consistent with other studies, suggesting that L. rhamnosus GR-1 are effective in inhibiting the adhesion and invasion of E. coli [17], which may be due to the inhibition of adhesion and the blocking of the binding site of the pathogen to the cell-surface receptor to prevent formation of pathogenic biofilm.
Excess ROS lead to increased lipid peroxidation products and decreased antioxidant indices [23], the imbalance between the oxidation system and the antioxidant systems is an important factor leading to oxidative stress in dairy cows. After invasion of E. coli to the endometrium, E. coli can stimulate cells to cause oxidative stress in the cells [24]. In this study, we confirmed that E. coli could elevate ROS levels, increased the expression of MDA, and suppressed the expression of SOD, GSH and T-AOC, consistent with previous finding [25]. Lactic acid bacteria can regulate the expression of antioxidant enzymes, thereby alleviating oxidative stress [26,27]. In this study, L. rhamnosus GR-1 effectively reduced ROS levels. Subsequently, we observed that L. rhamnosus GR-1 significantly inhibited MDA activity while enhancing the activity of SOD, GSH and T-AOC. Therefore, L. rhamnosus GR-1 can effectively inhibit the oxidative damage of cells caused by E. coli.
Mitochondria are the energy center of the cell and are critical to cell survival. Studies have shown that excessive production of ROS can impair mitochondrial function, cause increased mitochondrial membrane permeability, and disrupt membrane integrity, leading to a decrease in MMP [28]. Song et al [29] found that excess ROS induced mitochondrial damage and decreased MMP levels in BEECs. Li et al [30] also found that E. coli could cause mitochondrial damage in MAC-T cells, and L. rhamnosus GR-1 could attenuate E. coli-induced mitochondrial damage. In agreement with our results of evaluating MMP levels in BENDs, E. coli infection significantly decreased MMP levels, and MMP levels in BENDs were significantly reduced with L. rhamnosus GR-1 Pretreatment significantly increased MMP levels in BENDs.
Apoptosis plays an important role in cellular physiological processes. Studies have shown that ROS overproduction leads to apoptosis and induces mitochondria-mediated production of endogenous apoptosis-associated protein Bax [31], which leads to the release of Cyt-c from the mitochondria to activate Caspase-3 leading to apoptosis [32]. In the present study, L. rhamnosus GR-1 significantly attenuated E. coli-induced apoptosis by decreasing Bax, Caspase-3 and Cyt-c expression and increasing Bcl-2 expression. Zhang et al [33] found that ROS overproduction induced apoptosis with an increase in the BAX to BCL-2 ratio and an increase in Caspase-3 content. Zheng et al [34] found that L. rhamnosus CY12 could alleviate LPS-induced apoptosis, and Zhang et al [35] found that L. plantarum Lp2 inhibited the mitochondria-mediated apoptosis pathway. Our data further confirm these studies and reinforce the important role of probiotics in regulating apoptosis.
ROS is produced by xenobiotic exposure and physiological metabolism, which can induce cell apoptosis [36,37]. ROS function as “redox messengers” involved in intracellular modulation and signal transduction, whereas elevated levels of ROS lead to oxidative modification of cellular macromolecules, suppression of protein activities, and promotion of cell apoptosis [38]. Mechanisms of ROS-induced apoptosis include caspase activation and mitochondrial damage among others [39].
In light of this, we hypothesized that ROS are required for E. coli to induce mitochondrial damage and apoptosis. Therefore, we therefore explored the importance of ROS for E. coli-induced mitochondrial damage and apoptosis by treating cells with NAC, a ROS scavenger. The results showed that NAC significantly reduced ROS expression and apoptosis and increased MMP levels, which is consistent with previous findings [40]. The observations suggest that ROS release is required for E. coli-induced mitochondrial damage. Meanwhile, L. rhamnosus GR-1 could attenuate E. coli-induced ROS activation and apoptosis. Therefore, we hypothesized that L. rhamnosus GR-1 has the ability to scavenge ROS. Together, our findings suggest that ROS-mediated mitochondrial apoptosis is one of the pathways by which L. rhamnosus GR-1 protects cells from E. coli-induced cellular injury.
In this study, only BEND was used as an in vitro infection model to explore the protective effects of L. rhamnosus GR-1 against endometritis in dairy cows, therefore, we must emphasize that this is only a preliminary exploration of the protective effects of L. rhamnosus GR-1 through the ROS-mediated mitochondrial pathway. Future studies need to establish in vivo infection models to further elucidate the protective effects of L. rhamnosus GR-1 in animals.
CONCLUSION
In conclusion, our findings suggest that L. rhamnosus GR-1 pretreatment attenuates E. coli-induced cellular damage, in part by inhibiting the damaging effects of E. coli by inhibiting its adhesion and invasion with BENDs and by modulating the ROS-mediated mitochondria-dependent apoptotic pathway. These findings deepen the understanding of probiotic immunoprotection and contribute to its application in the prevention and treatment of endometritis in dairy cows. However, studies on the in vivo protective mechanisms and probiotic routes of administration are necessary.
Notes
CONFLICT OF INTEREST
No potential conflict of interest relevant to this article was reported.
AUTHORS’ CONTRIBUTION
Conceptualization: Feng X, Wen X.
Data curation: Li Y, Feng M, Sun Y.
Formal analysis: Feng X, Li Y.
Methodology: Jin T.
Software: Shahid M.
Validation: Liu J, Liu B.
Investigation: Cheng J, Liu M.
Writing - original draft: Feng X.
Writing - review & editing: Feng X, Li Y, Wen X, Feng M, Jin T, Shahid M, Sun Y, Liu J, Liu B, Cheng J, Liu M.
FUNDING
This work was supported by the current project was obtained from the National Natural Science Foundation of China (No. 32373077), the National Natural Science Foundation of China (No. 31902328), the Basic Scientific Research Funds of Provincial Universities in Hebei Province (No. KY2021008), and the Introduction of Talent Research Start-up Fund of Hebei Agricultural University (No. 3118133).
ACKNOWLEDGMENTS
The authors want to deliver our thanks to laboratory members who assisted us to enhance the paper with their professional technical assistance, helpful comments and advice.
SUPPLEMENTARY MATERIAL
Not applicable.
DATA AVAILABILITY
Upon reasonable request, the datasets of this study can be available from the corresponding author.
ETHICS APPROVAL
Not applicable.
DECLARATION OF GENERATIVE AI
No AI tools were used in this article.