http://orcid.org/0000-0002-7523-7905
Figures
Abstract
The aim of this study was to compare the effect of Lactobacillus acidophilus on the attachment, invasion, and interaction of Shigella sonnei and Vibrio cholerae with Caco-2 epithelial cells. Also, the anti-apoptotic and anti-inflammatory effect of L. acidophilus was investigated on S. sonnei and V. cholerae interaction with Caco-2 cells as the representatives of invasive and non-invasive intestinal bacteria. It was found that pretreatment with L. acidophilus significantly prevented from adherence and internalization of S. sonnei/V. cholerae and reduced the expression of tumour necrosis factor-α and interleukin-8 in host cells. No significant difference was observed in inhibitory effect of Lactobacilli in V. cholerae and S. sonnei attachment, emphasizing on the role of lactobacilli as a physical barrier in inhibiting direct contact with host cell by competitive exclusion, which may affect attachment and subsequent internalization of both invasive and non-invasive pathogenic bacteria in a same scale. The evaluation of early and late apoptosis in Caco-2 cells exposed to V. cholerae/S. sonnei and pretreated by L. acidophilus indicated no remarkable difference in L. acidophilus anti-apoptotic effect on Caco-2 cells against invasive and non-invasive bacterial infection. Moreover, L. acidophilus by itself showed no apoptotic effect on Caco-2 cells. Statistical analysis revealed that L. acidophilus in S. sonnei infected cells was able to reduce pro-inflammatory immune responses (TNF-α, IL-8 and IL-1β) and NO and PGE2 secretion more strongly compared with V. cholerae infected cells. These data showed for the first time that the protective effect of Lactobacilli, as a probiotic bacterium, in interaction suppression was more in invasive bacteria including S. sonnei than in non-invasive V. cholerae.
Citation: Alamdary SZ, Bakhshi B, Soudi S (2018) The anti-apoptotic and anti-inflammatory effect of Lactobacillus acidophilus on Shigella sonnei and Vibrio cholerae interaction with intestinal epithelial cells: A comparison between invasive and non-invasive bacteria. PLoS ONE 13(6): e0196941. https://doi.org/10.1371/journal.pone.0196941
Editor: Irving Coy Allen, Virginia Polytechnic Institute and State University, UNITED STATES
Received: October 13, 2017; Accepted: April 23, 2018; Published: June 6, 2018
Copyright: © 2018 Alamdary et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The author(s) received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Shigellosis is an acute infectious colitis caused by shigella spp. organisms. This diarrheal disease is a global human health problem in both developing and industrialized countries, and it is estimated that shigellosis causes over than one million deaths per year, most of which are patient children under 5 years old. Shigella sonnei are rod-shape, non-motile, non-flagellated, facultative anaerobic, Gram-negative, and lactose-fermenting bacteria that cause dysentery by invading the colonic mucosa from the basolateral surface; multiplying within colonic epithelial cells; causing cell death; spreading laterally; infecting and killing adjacent epithelial cells; causing mucosal ulceration, inflammation, and bleeding. These organisms are typically confined to the epithelial layer of the colonic mucosa [1–3].
With a different mode of action, Vibrio cholerae causes a fetal diarrheal disease which is manifested with acute watery diarrhea. V. cholerae is halophilic, highly motile, curved and Gram-negative rod. During the course of disease, V. cholerae is ingested and survives the low pH of the stomach to colonize the host small intestine. During colonization, V. cholerae uses motility and mucinase to penetrate the mucus layer of the intestine and gain access to the underlying epithelial cell layer. Indeed, V. cholerae as a classical agent of secretory diarrhea [4] and S. sonnei as an agent of inflammatory diarrhea produce choleratoxin and shigatoxin [3], respectively, by colonizing to epithelial surface, they are responsible for inflammatory destruction and simultaneously the extent of the elicited innate responses. Although the use of various antimicrobial agents is the first step to reduce illness duration and possibly the transmission of these pathogens, high rates of drug resistance have limited the choice of antimicrobial agents. Lactobacilli as non-spore-forming, Gram-positive, non-motile rods are recognized as natural components of the colonic microbiota and as probiotic and friendly bacteria. They have been tested in the prevention and treatment of gastrointestinal diseases [5, 6]. Since intestinal epithelial cells can respond to intestinal pathogens by producing an array of cytokines and chemokines which are associated with host immune responses [7], some strains of lactobacilli have been investigated for their cytoprotective effects on intestinal epithelial cells by regulating cytokine and chemokine production [5, 8, 9].
Indeed, this study allows for a better understanding of how the commensal Lactobacilli contribute to the homeostasis of the host intestinal tract. Indeed, the main goals of this research were (i) investigating the protective effect of L. acidophilus on viability of Caco-2 cells (human colon adenocarcinoma cells which are broadly known as a model of absorptive and defensive properties of the intestinal mucosa) infected by V. cholerae (as a non-invasive small intestine pathogen model) and S. sonnei (as an invasive colon pathogen model), (ii) enumerating the inhibitory role of L. acidophilus in V. cholerae adherence to Caco-2 cells in comparison with S. sonnei, (iii) comparison of the relative apoptosis levels induced in L. acidophilus-treated Caco-2 cells following V. cholerae and S. sonnei exposure, (iv) exploring the effect of L. acidophilus on pro-inflammatory markers expression (IL-8, TNF-α and IL-1β) and NO and PGE2 releases in V. cholerae infected Caco-2 cells in comparison with S. sonnei.
Results
Protective effect of L. acidophilus in Caco-2 cells infected with S. sonnei/V. cholerae
According to the experimental groups, Caco-2 cells were plated in 96-well plate and exposed to 107 L. acidophilus for 2 hours before 4 h exposure to S. sonnei and V. cholerae. After 4 h, the cells were assayed for cell viability with MTT. Based on the results shown in (Fig 1A), pretreatment with L. acidophilus increased cell viability to 51.81 and 58.72% against S. sonnei and V. cholerae infections, respectively. Moreover, L. acidophilus alone did not have any cytotoxic effect on Caco-2 cells. Statistical significant increase (p < .001) in Caco-2 cells viability was observed in both test groups (L.a+V.c and L.a+S.s) compared to control group with no significant difference between the 2 test groups. The protective effect of L. acidophilus was further confirmed by morphological observation (Fig 1B).
(A) cell viability of Caco-2 cells infected by V. colarae/ S. sonnei was determined by MTT assay, Each value represents the mean ±SEM (n = 3). ***p < 0.001 compared with control (untreated Caco-2cells) by one way ANOVA with Tukey’s post hoc test. ###p < 0.001 significantly different of L.a+V.c+Caco-2 group from V.c+Caco-2 group. †††p < 0.001 significantly different between L.a+S.s+Caco-2 group with S.s+Caco-2 (by unpaired two-tailed Student’s t test). All experiments were repeated three times. L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei, ns: none significant. (B) Morphological evaluation of Caco-2 cells under the above-mentioned treatment by light microscopic observation. L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei.
Effect of L. acidophilus pretreatment on attachment and internalization of S. sonnei /V. cholerae to Caco-2 cells
Pretreatment of Caco-2 cells with L. acidophilus significantly (p < .001) decreased the adherence of both S. sonnei /V. cholerae to Caco-2 cells compared to control group. In cells pretreated with L. acidophilus, adherence rate of S. sonnei was decreased from 89.72 to 36.91%. This decrease was from 89.17 to 48.54% for cells infected with V. cholerae after pretreatment step. (Fig 2A). No significant difference was observed between attachment reductions for the 2 pathogenic bacteria. Pretreatment of Caco-2 cells with L. acidophilus decreased significantly (p < .001) the internalization of S. sonnei from 92 (control) to 36% (test). No internalization was observed for V. cholerae in test or control group (Fig 2B).
(A and B) Effect of pretreatment of L. acidophilus on its ability to inhibit V. colarae/ S. sonnei adherence and invasion to Caco-2 cells. ND means Not Detectable. Each value indicates the mean±SEM from three independent experiments and three replicates (n = 3). ###p < 0.001 significantly different of L.a+V.c+Caco-2 group from V.c+Caco-2 group. †††p < 0.001 significant difference between L.a+S.s+Caco-2 group and S.s+Caco-2 (by unpaired two-tailed Student’s t test). L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei.
Assessment of apoptosis in V. cholerae/ S. sonnei infected Caco-2 cells pretreated with L. acidophilus by flow cytometry
The Caco-2 cells pre-treated with L. acidophilus (2 hours) before exposure to S. sonnei /V. cholerae showed lower apoptotic cells (56 and 43%, respectively) compared with un-treated S. sonnei /V. cholerae infected Caco-2 cells (89 and 90%, respectively) (p < .001) (Fig 3). No significant difference was observed in protectivity role of L. acidophilus against apoptosis of Caco-2 cells exposed to V. cholerae and S. sonnei.
Images showed the typical morphologies of cells in the different regions. (A) Q1: Necrotic cells, Q2: Late apoptotic cells, Q2: Early apoptotic cells and Q4: Viable cells. L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei. (B)The pretreatment with L. acidophilus on Caco-2 cells exposed to V. colarae/ S. sonnei resulted in decreased apoptosis. Statistical analysis of representative images was performed with three independent experiments. The statistical significances were achieved when P <0.05 (***P <0.001). *** significantly different from control cells. ### significantly different of L.a+V.c+Caco-2 from V.c+Caco-2 cells. ††† significantly different of L.a+S.s+Caco-2 from S.s+Caco-2 cells L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei. ns: none significant.
Real time-PCR for pro-inflammatory markers (IL-8, TNF-α and IL-1β)
In L. acidophilus pretreated Caco-2 cells followed by S. sonnei /V. cholerae infection, the expression of IL-8, TNF- α, and IL-1β markers was down regulated compared to un-treated S. sonnei /V. cholerae infected Caco-2 cells (p < .001) (Fig 4A, 4B and 4C). As shown in (Fig 4A), in test group (L.a+V.c/L.a+S.s), IL-8 level was decreased by 2.3 and 1.5 fold, respectively, compared to untreated S. sonnei /V. cholerae infected controls (V.c/S.s). Moreover, TNF-α expression in Caco-2 cells was decreased by 2.7 and 1.5 fold, respectively, when cells were treated with L. acidophilus in comparison to S. sonnei /V. cholerae infected Caco-2 cells (Fig 4B). In (Fig 4C), IL-1β level was decreased by 2.2 and 1.6 fold, respectively, compared to controls (V.c/S.s) (S1 Table). The inhibitory effect of L. acidophilus on pro-inflammatory markers expression in S. sonnei infected Caco-2 cells was more significant than in V. cholerae infected Caco-2 cells (†p < .05).
The fold-changes in expression of (A)IL-8, (B)TNF-α and (C)IL-1β after treatment by L. acidophilus was normalized to GAPDH and compared in infected and uninfected Caco-2 cells. The fold-changes in genes expression were represented from at least 3 independent experiments. The statistical results were remarkable when P <0.05. (***P <0.001) significantly different from control cells. ## or ### significant difference between L.a+V.c+Caco-2 and V.c+Caco-2 cells. ††† or †††† significant difference between L.a+S.s+Caco-2 and S.s+Caco-2 cells L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei.
The effect of L. acidophilus on nitric oxide (NO) release in Caco-2 cells
The level of NO production in supernatants of Caco-2 cells was increased 10.15 and 9.52 μM in response to V. cholerae and S. sonnei infection compared to un-infected Caco-2 cells (Fig 5). Pre-treatment of Caco-2 cells with L. acidophilus decreased the level of NO production 6.8 and 4.3 μM in response to V. cholerae and S. sonnei infections, respectively. Nitric oxide secretion in S. sonnei infected Caco-2 cells pretreated by L. acidophilus decreased 1.4 fold while this level was 2.2 fold in V. cholerae infected Caco-2 cells (Fig 5). The decreasing role of L. acidophilus on NO expression in S. sonnei infected Caco-2 cells was more significant than in V. cholerae infected Caco-2 cells (†p < .05).
NO production after 24h, significantly decreased in comparison with V.cholerae/ S. sonnei infected cells alone. The mean of three independent experiments is shown. The significant differences were notabled when P <0.05. (***P <0.001) significantly different from control cells. ##significantly different of L.a+V.c+Caco-2 from V.c+Caco-2 cells. ††† significantly different of L.a+S.s+Caco-2 from S.s+Caco-2 cells L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei. ns: none significant.
Caco-2 epithelial cell lines and PGE2 release in response to V. cholerae and S. sonnei infection
The level of PGE2 secretion in infected Caco-2 cells with/without pretreatment by L. acidophilus are shown in (Fig 6). Caco-2 cells produced high level of PGE2 in response to V. cholerae/S. sonnei infection (6.25 and 5.78 pg, respectively), which was decreased to 4.8 and 3.1 pg in response to L. acidophilus pretreatment. Statistical analysis showed that inhibitory effect of L. acidiphilus on PGE2 production in S. sonnei infected Caco-2 cells was more significant than in V. cholerae infected Caco-2 cells (†p < .05).
PGE2 secretion was significantly elevated following infection with V. cholerae/ S. sonnei and this effect was abolished when the cells were pretreated by L. acidophilus. The data are presented as mean ±SEM. The statistical data (by unpaired two-tailed Student’s t test) were signed when P <0.05. ##significantly different of L.a+V.c+Caco-2 from V.c+Caco-2 cells. ††† significantly different of L.a+S.s+Caco-2 from S.s+Caco-2 cells L.a: Lactobacillus acidophilus, V.c: Vibrio cholerae and S.s: Shigella sonnei. ND: None Detectable.
Discussion
Lactobacilli are normal commensal flora of the gut and as beneficial microbes are used in the therapy of gastrointestinal diseases and enhancement of intestinal health [10]. In the current study, we have investigated the protective effect of L. acidophilus in inhibition of interaction of S. sonnei as a colon-invasive pathogen and V. cholerae as a non-invasive pathogen of small intestine with Caco-2 intestinal epithelial cells.
Our results indicated that pretreatment of Caco-2 cells with L. acidophilus followed by V. cholerae/S. sonnei infection was resulted in a significant increase in viability of Caco-2 intestinal epithelial cells (2.9 and 3.3 folds, respectively). These data suggest that L. acidophilus has a strong protective effect on Caco-2 intestinal epithelial cells against V. cholerae/S. sonnei induced cell death with no significant difference between invasive and non-invasive bacteria under study.
The adherence and invasion of V. cholerae/S. sonnei to Caco-2 cells was reduced following pretreatment by L. acidophilus. Previous researchers established that L. acidophilus had the ability to bind to brush borders of human epithelial cells [11], in which calcium cations act as an ion bridge to connect the surface of epithelial cells and L. acidophilus[12]. Also, adherence of lactobacilli to the intestinal epithelial cells is considered to be essential for the exertion of the protective effect against enteropathogenic bacteria[13, 14]. Moorthy et al (2010) has indicated that treatment of epithelial cells by lactobacilli would reduce adherence and invasion of S. dysenteriae to epithelial cells, but the interaction remained to be understood and compared for S. sonnei and V. cholerae regarding their increasing occurrence in developed and developing countries[15] and considering their different mode of action and consequences. No significant difference was observed in inhibitory role of Lactobacilli in V. cholerae and S. sonnei attachment. The probable explanation is i) the role of lactobacilli as a physical barrier to inhibit direct contact with host cell by competitive exclusion, which may affect attachment and subsequent internalization of both colon-invasive and non-invasive pathogens of small intestine in a same scale, ii) bacteriocin production by Lactobacilli may have direct inhibitory effect on adherence of both invasive and non-invasive pathogenic bacteria to epithelial cells [16, 17], and iii) immunomodulation of cellular mechanisms by Lactobacillus probably interferes with pathogen adhesion to epithelium probably through induction of primary apoptosis [18, 19]; however, late apoptosis which is supposed to be induced by pathogenic bacteria is inhibited by anti-inflammatory role of Lactobacilli, applied by suppression of TNF-α production.
Although many studies have dealt with the role of lactobacilli, as a part of the intestinal microflora, in modulation of host immunological responses, L. acidophilus has showed dual manner in apoptosis proceeding of epithelial cells. The study by Shumei Wang (2014) showed that cell walls and cytoplasm extracted from Lactobacilli induced DNA damage and apoptosis in HT-29 cells [20]. Russo et al in 2007 showed that L. rhamnosus strain GG homogenate showed apoptotic induction action in human gastric cancer cells [21]. In addition, a research by Chandra et al in 2008 showed supernatant of Lactobacillus reuteri regulated cell proliferation in myeloid leukemia-derived cells by promoting apoptosis and enhancing pro-apoptotic MAPK signaling [22]. Moreover, Soltan Dallal et al. (2015) indicated that treatment of Caco-2 cell line with either L. acidophilus or L. Casei supernatants and extracts was able to increase apoptosis, and consequently, to hinder the cancer cell migrations and invasions [23]. Controversially, some other studies revealed that L. acidophillus S-layer proteins in Caco-2 cells infected by Salmonella protected cells against apoptosis [24]. In the present study, the process of early and late apoptosis was evaluated in Caco-2 cells exposed to V. cholerae/S. sonnei and pretreated by L. acidophilus. The obtained data indicated that L. acidophilus pretreatment caused 2.1 and 1.5 fold reduction in apoptosis rate of V. cholerae and S. sonnei infected Caco-2 cells, respectively. Moreover, the results revealed that L. acidophilus by itself had no apoptotic effect on Caco-2 cells. Furthermore, statistical comparisons showed no remarkable difference in L. acidophilus anti-apoptotic effect on Caco-2 cells between invasive and non-invasive bacterial infection.
One of the toxic chemical species elaborated by the host epithelial cells during bacterial infection is nitric oxide (NO) which acts as an early signal to activate an acute mucosal inflammatory response and enhance the ability of epithelial cells to produce cytokines that regulate mucosal immune responses [25, 26]. In parallel, it is stated that Lactobacilli could reduce nitric oxide release [27]. Upon stimulation by proinflammatory cytokines such as IL-1β and TNF-α, as an important lipit mediator, PGE2 synthesis is upregulated following Gram-negative and Gram-positive bacterial infection [28–31]. Statistical comparisons between V. cholerae and S. sonnei infected Caco-2 cells pretreated by L. acidophilus surprisingly established significant difference in reduction of proinflammatory markers (TNF-α, IL-8 and IL-1β) expression and NO and PGE2 secretion (P-value < .05). Considering the critical role of TNF-α in modulating host immune responses, subsequent decrease in cell apoptotic responses can be attributed to inhibitory role of Lactobacilli in TNF-α production. Apoptosis was decreased but not missed, suggesting that the remaining apoptotic cells themselves reduce proinflammatory cytokines production which was considered to be an active process mediated by the production of PGE2 and NO [32, 33]; However, the role of remaining apoptotic cells in reducing TNF-α production should not be ignored[34–36].
In conclusion, statistical analysis revealed that L. acidophilus in S. sonnei infected cells could reduce pro-inflammatory immune responses more strongly compared with V. cholerae infected cells. These data show for the first time the more protective effect of Lactobacilli, as a beneficial bacterium, in suppression of colon-invasive bacteria including S. sonnei compared with V. cholerae, the non-invasive pathogen of small intestine. It can be suggested that i) the invasive nature of S. sonnei is the notable point for explaining the more efficient contribution of L. acidophilus in protection of intestinal epithelial cells, ii) attachment and invasion is a more critical step affecting subsequent inflammatory responses in S. sonnei infection than in V. cholerae, or iii) the anti-inflammatory properties of Lactobacilli may affect the apoptotic response of epithelial cells probably through the reduction of TNF-α.
Materials and methods
Bacterial strains and growth conditions
This study was approved by Medical Ethics Committee of Tarbiat Modares University (Code: IR.MODARES.REC) before the study began. S. sonnei ATCC9290, kindly provided by WHO, Lactobacillus acidophilus ATCC314, obtained from Pasteur Institute of Iran as a gift, and Vibrio cholerae ATCC14035, obtained from archive of our laboratory, were used in this study. S. sonnei and V. cholerae were routinely grown on Brain Heart Infusion (BHI) Broth at 37°C for 18–20 h before use. L. acidophilus was grown on Man–Rogosa–Sharpe (MRS) agar at 37°C under microaerophilic condition with 5% CO2 for 18–20 h before use.
Cell culture condition
Caco-2 cells purchased from Pasteur Institute of Iran were cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Sigma, Aldrich) supplemented with 5% fetal bovine serum and 1% antibiotic mixture of penicillin-streptomycin and incubated in a humidified atmosphere at 37°C with 5% CO2. Towards confluency, Caco-2 cells started to polarize, acquiring a characteristic apical brush border with microvilli. Tight junctions were formed between adjacent cells, and macromolecules were sorted and maintained between apical and basolateral surfaces of confluent cells. However, markers of colonocytes are also present in Caco-2 cells [37].
Culture of intestinal epithelial cells on 3D chambers (Transwell) is similar to in vivo environments, and cells are better polarized with sorted distribution of certain molecules exposed, at the apical surface and basolateral surface only. But, intestinal epithelial cells in ordinary tissue culture (2D medium culture) have surface molecules distributed all around the cell. Since cells in monolayer culture with full confluency can form polarized and tight monolayers with sorting and maintaining of cell surface molecules, we explored cells in full confluency (90% confluent) for all trials.
Design of cell groups for treatment
Intact untreated Caco-2 cells were served as control group (Group 1), cells incubated with L. acidophilus as Group 2, cells infected with V. cholerae as Group 3, cells incubated for 2 hours with L. acidophilus followed by the addition of V. cholerae as Group 4, cells infected with S. sonnei as Group 5, and cells pretreated for 2 hours with L. acidophilus followed by the infection with S. sonnei as Group 6.
Measurement of cell viability
Cell viability was evaluated by the conventional MTT (3-[4, 5-dimethylthiazol-2-yl]-2, 5-diphenyl tetrazolium bromide) reduction assay. This was tested to assess the viability of Caco-2 cells after the infection time. Approximately, 2 × 104 of Caco-2 cells per well were seeded into a 96-well plate for MTT assay. Cells were exposed to each of 3 bacterial species, separately, at varying MOIs of 1, 10, 20, 30, 40, 100 at 24, 48, and 72h exposure times. The dark blue formazan crystals formed in cells were dissolved using dimethyl sulfoxide (DMSO), and the absorbance was measured at 570 nm with an ELISA reader after 30 min. The cellular viability was calculated as the percentage of survival relative to the control cells, showing the best results at the MOI of 10, where 80–90% of the cells were found to be infected, with a cell viability of >80% at the 24h time point.
Enumeration of L. acidophilus, S. sonnei and V. cholerae for attachment and invasion experiments, apoptosis and cytokine assays
One colony of Lactobacillus culture on MRS agar was added to 5 mL MRS broth and incubated in 37°C under microaerophilic condition for overnight. Approximately, 300μL of overnight culture of Lactobacillus on MRS broth was added to 5mL fresh MRS broth and incubated at 37°C. After 2, 3, 4, 6 and 8 h incubation, the optical density (OD) was measured at 625nm wavelength, and 10μL of culture was simultaneously serially diluted and cultured on MRS agar and incubated in 37°C for overnight. The plates with 30–300 colonies per plate were counted and the Colony forming unit (CFU) was calculated as: number of colony × 100× inverse dilution factor. A growth curve was plotted for CFU based on OD625. The same procedure was applied for calculating the CFU of S. sonnei /V. cholerae on BHI agar plate under aerobic condition, as well.
The attachment and invasion experiments and apoptosis and cytokine assays were performed in 6-well plates and seeded with approximately 7 × 105 of Caco-2 cells per well to reach the confluency of 90%. All test groups were inoculated with 1×107 CFU.mL-1 of L. acidophilus 2 hours before addition of 1×107 CFU.mL-1 S. sonnei or V. cholerae. The 1×107 CFU.mL-1 of each bacterial species was related to OD 0.8 and fulfilled the MOI 10. Accordingly, 1 × 107 CFU L. acidophillus, S. sonnei or V. cholerae per mL (the OD625 of 1 ×107 bacteria/mL was 0.8, approximately) was centrifuged at 3500 × g for 5 min. Each supernatant was poured off and the pellet was resuspended in DMEM (without penicillin and streptomycin) after two washing steps with DMEM solution. All experiments were repeated three times and the average value was recorded.
Enumeration of S. sonnei and V. cholerae invasion to Caco-2 cells
The confluent Caco-2 cells in 6 well plates were prepared in 2 parallel sets, each set consisted of the six designed groups to enumerate the adherent and internalized S. sonnei and V. cholerae. After incubation of cells with 107 CFU of L. acidophilus for 2 hours (MOI = 10), followed by infection with 107 CFU of S. sonnei or 107 CFU of V. cholerae for 5 h, one set of groups of 6-well plates were washed twice with DMEM medium and treated with gentamicin (250 μg.mL-1) for 1 h to kill the extra cellular bacteria. Subsequently, the wells were washed by PBS for three times and lysed with 0.5% Triton-X 100 in PBS. Cell lysates were harvested and cultured onto BHI agar after serial dilution and incubated at 37°C for 18–24 h to assess the number of internalized S. sonnei or V. cholerae strains. The percentage of internalization was calculated based on following formula: total count of internalized pathogenic bacteria/ total number of inoculated pathogenic bacteria (107 CFU)×100.
Enumeration of adherent S. sonnei and V. cholerae to Caco-2 cells
The second set of 6-well plates were washed by PBS for three times to remove un-adhered bacteria. The cells were lysed with 0.5% Triton-X 100 in PBS and the lysed cells were plated onto BHI agar and incubated at 37°C for 18–24 h to enumerate total of adherent plus internalized bacteria.
Number of internalized S. sonnei or V. cholerae was subtracted from the total number of intracellular plus adherent S. sonnei or V. cholerae to assess the adherent pathogenic bacteria. The percentage of adherence was calculated by formula: total count of adherent pathogenic bacteria/ total number of inoculated pathogenic bacteria (107 CFU)×100.
Flow cytometry-based quantification of apoptosis in Caco-2 cells by annexin V/propidium iodide staining
Annexin V is a member of the annexin family of intracellular proteins that binds to phosphatidyl serine (PS) in a calcium-dependent manner. In viable and healthy cells, PS is located in the inner membrane leaflet, but during early apoptosis, it is translocated to the external leaflet and becomes available for annexin V binding. Annexin V binding alone cannot differentiate between apoptotic and necrotic cells. The addition of PI enabled viable, early apoptotic, late apoptotic, and necrotic cells to be distinguished. All the operations were performed according to the manufacturer’s instructions (FITC Annexin V Apoptosis Detection kit, BioLegend, USA). Briefly, the cells in 6 designed groups were rinsed with PBS and resuspended in a binding buffer [4]. Then 5 mL of Annexin V (20 mg.mL-1) and 10 mL of propidium iodide (PI, 50 mg.mL-1) were added to the suspension and incubated for 15 min at room temperature and analyzed by flow cytometer.
Total RNA isolation and cDNA synthesis
Confluent Caco-2 cells were incubated at 37°C for the infection period (6 designed groups). At the end of the infection, medium was removed and cells were washed by PBS for 3 times. The cell monolayers were lysed with Trizol reagent (Sigma Aldrich), after which chloroform was added. The resulting mixture was centrifuged, and the aqueous phase was added to a fresh tube to which 2-propanol was added and centrifuged. Total RNA was washed twice with 70% ethanol, dried, and solubilized in Diethyl pyrocarbonate (DEPC treated water). RNA was quantified by absorbance at OD260/280 and only samples with a ratio of 1.8–2.0 were used for cDNA synthesis.
Easy™ cDNA Synthesis Kit (ParsTous, IRAN) was used for synthesis of cDNA. According to protocol manual, template RNA, Random hexamer, DEPC treated water, and RT Premix (2X) were mixed and incubated for 10 minutes at 25°C, 1 hour at 50°C, and five minutes at 65°C. The resulting cDNA samples were stored at -20°C until required for later investigation.
Real-time RT-PCR analysis
The real-time RT-PCRs were performed by Rotor-Gene Q (Qiagen, Germany). Each PCR reaction contained 10μL 5x Real-time PCR Master Mix (Ampliqon, Denmark), 2 μL cDNA template, 1 μL of each primer and 6 μL distilled water in a total reaction volume of 20 μL. PCR reactions were performed according to annealing temperature of each primer pairs (Table 1). Conventional SYBR green based real-time PCR was used for gene quantification. Equal amounts of RNA were converted into cDNA in each sample and pipetting errors was avoided. GAPDH mRNA expression was quantified as the normalizer in each sample and the ΔCt of each sample was calculated (CT target−CT reference).
GAPDH is one of the most commonly used reference genes and a great majority of the most important scientific journals concerns its use through what is often referred as “classical” [38]. We used un-treated control (intact caco-2) culture, as the calibrator and ΔΔCt method was used to calculate the difference between treated and controls. Finally, the gene expression data were presented as the fold change relative to untreated control group after normalization with an endogenous reference gene (GAPDH). The manuscript was edited as suggested. Each real-time PCR reaction was performed in triplicate.
Nitric oxide assay
Nitric oxide (NO) is a diatomic free radical that is extremely short lived in biological systems and produced by various epithelial cells in response to the inflammatory functions. NO concentration in the supernatant was determined by a method based on the Griess reagent (Sigma Aldrich). The Griess reagent is made up of a 1% solution of sulfanilamide in 5% phosphoric acid and 0.1% naphthyl ethylenediamine dihydrochloride in distilled water. The supernatants of experimental cell groups (6 designed groups) were collected after infection period. The NO was assayed by mixing the equal volumes of supernatants and the Griess reagent. The absorption at 540 nm was read by an ELISA reader, and calibration curve was generated by different concentrations of sodium nitrite.
Prostaglandin E2 (PGE2) immunoassay
PGE2 concentration was assessed by immunoassay using the PGE2 ELISA Kit (Invitrogen, USA). According to the manufacturer instructions, a serial dilution was prepared from standards, and the supernatants from 6 designed groups were added into the appropriate wells, and blue PGE2-AP conjugate and yellow PGE2 antibody were added into each well and incubated at room temperature. Substrate solution was added to every well and incubated after the wells were rinsed with wash buffer for 2 times. Finally, stop solution was added to each well, and the absorbance of reaction mixture was detected at 405 nm.
Data analysis
Data were presented as the mean±standard error of the mean (S.E.M.). Statistical significance was assessed using GraphPad Prism 5 (GraphPad Software, San Diego, CA, www.graphpad.com). One-way analysis of variance (ANOVA) with Tukey’s post hoc test were performed for multiple comparisons, Statistical significance for L. acidophilus imaging data was assessed by unpaired two-tailed Student’s t test. The statistical significances were achieved when P < .05 (*or # or †P < .05, ** or ## or ††P < .01, *** or ### or †††P < .001 and **** or #### or ††††P < .0001).
Supporting information
S1 Table. Quantitative expression of IL-8, TNF-ɑ and IL-β.
https://doi.org/10.1371/journal.pone.0196941.s001
(DOCX)
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