L. crispatus strain CCTCC M206119 was isolated from human feces in the Division of Digestive Disease of the Second XiangYa Hospital (Changsha, Hunan, China), and kept at China Center for Type Culture Collection (CCTCC, Wuhan, China). Lactobacillus strains were grown at 37 °C in de Man, Rogosa and Sharpe (MRS) medium (Difco, MD, United States) without shaking.

Eight-week-old BALB/c mice of either sex were purchased from Hunan Agricultural University [SCXK (Xiang 2002-003)], and then bred under specific pathogen-free conditions. Mice were kept in ventilated and filtered cages, fed an irradiated diet, and housed on irradiated bedding. Food and water were supplied ad libitum. All animal experiments were performed in compliance with the guidelines of the Chinese government approved by the College BioResources ethical review board.

Bacterial strains were grown to an optical density at 600 nm of 3 to 4 (early stationary phase) at 37 °C in MRS medium anaerobically, harvested by centrifugation, washed with sterile neutral saline, and resuspended at 10⁹ colony forming units (CFU)/mL in neutral saline. Three hundred microliters of this daily-prepared suspension was fed daily to the mice via intragastric gavage, whereas the controls (both UC-induced and healthy mice) received 300 μL neutral saline via the same procedure.

Eight-week-old Balb/c mice (20 ± 2 g) were divided into a healthy control group, negative control (normal saline) group, positive control (5-ASA, 6 mg/20 g) group, and investigation (CCTCC M206119 strain) group, with 10 mice in each. Normal saline (300 μL), sulfasalazine, CCTCC M206119 strain were administered intragastrically once daily for 2 d before starting DSS and continued for 7 d after DSS induction. Colitis was induced by 5% (w/v) DSS (molecular weight 35  000-50  000; MP Biomedicals, Solon, OH, United States) dissolved in drinking water for 7 d (Table 1). The healthy control group received no DSS. Severity of colitis was assessed daily using a disease activity index (DAI). After the seventh day of induction of colitis, animals were euthanized by CO₂ asphyxiation. The colon lengths and weight were measured. Under aseptic technique, 300 mg stools and mesenteric lymph nodes (MLNs) were collected for bacterial microflora analysis. All the samples were placed immediately in sterile tubes containing 5 mL of transport medium. One centimeter of the proximal colon, middle colon and distal colon was collected and fixed in 10% buffered formalin, dehydrated in ethanol, and embedded in paraffin. The remaining tissues were immediately snap-frozen and stored at -80 °C[23,24].

The severity of colitis was assessed daily using a DAI based on the scoring system of Hamamoto et al[25], which scores body weight loss, stool consistency and occult/gross fecal bleeding (Table 2). Occult blood in feces was evaluated by means of Hemoccult II test (Beckman Coulter, Palo Alto, CA, United States).

Tissue fixed with 4% (w/v) paraformaldehyde in phosphate buffered solution (PBS) was prepared for light microscopy, and 5-µm-thick sections were stained with hematoxylin and eosin to study histological changes. Grading of intestinal inflammation was determined as follows (Table 3)[26]. All scores were obtained in a blinded fashion by two independent investigators.

Three-hundred-microgram fecal samples were dispersed in 2 mL PBS. Each pooled sample (0.1 mL) was serially diluted via 10-fold dilutions (from 10^-1 to 10^-10). Eosin methylene blue agar, KULB agar, TTC azide dextrose agar and mannitol salt agar were used for the enumeration of Enterobacteriaceae, Bacteroides, Enterococcus and Staphylococcus spp., respectively. Standard Nutrient Agar was used for the enumeration of total aerobic bacteria. All the plates were incubated at 37 °C, aerobically, for 24-48 h and the number of colonies were counted. Brain-heart infusion agar and LAMVAB agar were used to enumerate bifidobacteria and lactobacteria, respectively. Anaerobic incubation was carried out in anaerobic jars (Oxoid, Basingstoke, Hants, United Kingdom) at 37 °C for 48-72 h. Anaerobic conditions were obtained using Anaerogen (Oxoid) and were checked using methyl blue strips as oxidation reduction indicator. CFUs were counted and expressed per gram of sample[27,28].

The extent of neutrophil infiltration was determined by myeloperoxidase (MPO) assay[29]. Briefly, 500 mg colon was homogenized in 1 mL iced 0.5% hexadecyltrimethylammonium bromide buffer. The aliquot was centrifuged (4000 g, 15 min) and the supernatant was diluted into 5% homogenates. A mixture of 0.1 mL 0.05% hydrogen peroxide and 0.9 mL 5% homogenates was vortexed to release MPO from the tissue. After incubation in 37 °C for 15 min, 0.2 mL mixture was added to 3 mL O-dianisidine reaction mixture and incubated for 30 min at 37 °C. Sodium azide (50 μL, 2.0%) was added and incubated at 60 °C for 10 min. Absorbance of the reaction mixture was measured at 460 nm by spectrophotometer. Saline was used as a control. MPO activity was expressed as U/g tissue.

HT-29 cells (purchased from Y-Y Chemical Reagent Co. Ltd., Shanghai, China) were cultured in RPMI 1640 medium (Gibco, Rockville, MD, United States) supplemented with 10% fetal calf serum under 5% CO₂ at 37 °C and divided into negative control, TNF-α (10 ng/mL) and CCTCC M206119 groups. CCTCC M206119 was diluted to 10⁹ CFU/mL with RPMI 1640 medium. HT-29 (3 × 10⁶ cells) were cultured in 24-well tissue culture plates for 72 h and TNF-α or CCTCC M206119 was added. After 4 h of incubation, HT-29 cells were fixed in cold methanol for 5-15 min. The fixed cells were blocked in 5% bovine serum albumin (BSA)/PBS for 1 h on ice. We remove the blocking buffer and added primary antibody anti-nuclear factor (NF)-κB p65 (10 µg/mL) (MBL, Woods Hole, MA, United States; clone 8F11, rat IgG2a) diluted in PBS/0.3% Triton X100/1%BSA/1% serum overnight at 4 °C in a humidified chamber. After washing three times for 10 min with PBS on ice, the cells were incubated with anti-rabbit Cy3 (10 µg/mL) (Abcam, Cambridge, United Kingdom; polyclonal rabbit IgG) for 1 h at room temperature. The cells were mounted in Vectashield mounting medium (Vector Laboratories, Burlingame, CA, United States) with 4',6'-diamidino-2-phenylindole hydrochloride after three washes in PBS at room temperature, and analyzed by a Nikon ECLIPSE E600 fluorescent microscope. The ratio of positive nuclear cells to total cells represented the nuclear translocation of NF-κB. The average number of positive stained cells within at least nine independent high power fields (400 × magnification) were determined microscopically and subjected to statistical analysis as indicated.

Total tissue RNA was isolated using TRIzol reagent following the manufacturer’s instructions For each sample, first-strand cDNA was synthesized using 1.0 µg total RNA with oligo dT23VN primer and M-MuLVuLV reverse transcriptase (Gibco). Five milliliters cDNA samples were amplified in 25 μL of a reaction mixture containing 10 × Taq buffer, 1.5 mmol MgCl₂, 5 μmol dNTPs (each), 10 μmol of each 5′ and 3′ primers, and 2 U TaqGold polymerase (Perkin-Elmer Cetus, Waltham, MA, United States). Polymerase chain reaction (PCR) was performed in a thermal cycler (GeneAmp Model 2400; Perkin-Elmer Cetus) for 22 cycles (94 °C for 30 s, 55 °C for 30 s, and 72 °C for 1 min), followed by a 10-min extension at 72 °C. The PCR products (5 μL) were subjected to electrophoresis on 1.5% agarose gels and stained with 0.5 μg/mL ethidium bromide. Primers used in this paper are illustrated in Table 4.

Colon extracts (40 μg total protein) from each group of mice were resolved by SDS-PAGE under reducing conditions and transferred to a nitrocellulose membrane (Bio-Rad Laboratories, Hercules, CA, United States). The membrane was blocked with 5% nonfat dry milk overnight and incubated with a rabbit polyclonal antibody to zonula occludens (ZO)-1, β-defensin 2 (Lab Version, Fremont, CA, United States), with a rabbit polyclonal antibody to IL-1β, IL-6 or TNF-α (Santa Cruz Biotechnology, Santa Cruz, CA, United States), with a mouse monoclonal antibody to IL-10 (BD Biosciences, Franklin Lakes, NJ, United States), or with an anti β-actin or glyceraldehyde-3-phosphate dehydrogenase (GAPDH) antibody (Affinity BioRegents, Golden, CO, United States) for loading control. Antigen-antibody binding was detected with horseradish-peroxidase-conjugated anti-rabbit or mouse IgG (Vector Laboratories) using enhanced chemiluminescence (Amersham Biosciences, Piscataway, NJ, United States).

To investigate the characterization of CCTCC M206119 strain, 10⁸ CFU/mL bacteria were grown for 18 h in MRS (Difco), washed with PBS and fixed with 2.5% glutaraldehyde. After two washings with PBS, samples were dehydrated with ethanol to the critical point, coated with 20 nm of gold in the scanning electron microscopy (SEM) coating unit, and examined by a XL30 ESEM scanning electron microscope (Philips, Eindhoven, Netherlands).

CCTCC M206119 strain were grown on MRS agar and incubated under anaerobic conditions at 37 °C for 24-48 h. All isolates were visualized by Gram staining. Biochemical testing was performed with API 20A strips (BioMerieux, Hazelwood, MO, United States) according to the manufacturer’s instructions. Catalase and SPOR tests were performed according to the supplier’s recommendations (Becton Dickinson). G + C percentage was determined using high-performance liquid chromatography (HPLC) method in the Chemistry College of Central South University (China). Ten microliters base standard and 10 μL DNA hydrolase were injected into the HPLC sample injector and analyzed three times. The separating conditions used were as follows: 250 mm Zonbax-C18 column, 0.05 mol/L NH₄H₂PO₄ (pH 4.0) and acetonitrile mixture (20:1) as washing solution, 1 mL/min, moving phase: 2% acetonitrile, 98% 50 mmol/L NaH₂PO₄ buffered solution (pH 3.94), room temperature, detecting wavelength 254 nm and 270 nm, 0.1 mg/mL dA, dT, dG, dC solution used as external standard.

Approximately 700 bp of the 16S rRNA gene were amplified with primers 16S-F (5’-AGA GTT TGA TCA TGG CTC AG-3’) and 16S-R (5’-CAC CGC TAC ACA TGG AG-3’) under the following PCR conditions: 95 °C for 5 min; 10 cycles of 94 °C for 30 s, 70 °C for 30 s, and 72 °C for 40 s; 26 cycles of 94 °C for 30 s, 60 °C for 30 s, and 72 °C for 1 min; and 72 °C for 10 min. 16S rDNA amplicons were gel purified by using SDS-PAGE and a gel band purification kit (Amersham Biosciences). The 5’ terminus of the 16S rRNA gene was sequenced with primers 16S-F and 16S-R by using an ABI Prism 3100 (Applied Biosystems) sequencing system and an ABI Prism BigDye Terminator cycle sequencing ready reaction kit (version 2.0, Applied Biosystems). Sequencing traces of amplicons containing ambiguous signals were resubmitted for sequencing. rDNA sequences were analyzed by using Lasergene (version 5.0, DNAStar, Madison, WI, United States). Contigs were generated by using SeqMan. Isolates were identified by using the nucleotide-nucleotide Basic Local Alignment Search Tool (BLASTn) (http://www.ncbi.nlm.nih.gov/blast).

Data were analyzed by Student’s t test or analysis of variance (ANOVA). The Wilcoxon signed-rank test was used to compare data that did not satisfy Student’s t test. P < 0.05 was considered significant.

Survival rate of DSS-colitis mice reduced to 80% from day 5 after CCTCC M206119 treatment changes, which differed from other groups significantly (Figure 1A). Body weight loss, stool consistency, and occult/gross fecal bleeding were evaluated and scored individually for each animal according (Table 2). The scores were evaluated statistically by χ² test and Monte Carlo exact test. CCTCC-M206119-treated DSS-colitis animals showed much higher DAI scores compared with 5-ASA- and saline-treated DSS-colitis mice, starting from day 3 after 5% DSS treatment (Figure 1B).

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Figure 1 Colonic inflammation was aggravated in dextran sulfate sodium-colitis mice after China Center for Type Culture Collection M206119 treatment. A: Survival rate changes of four age- and sex-matched BALB/c mouse groups (n = 10) [〇: Healthy controls; ●: 5% dextran sulfate sodium (DSS) plus saline treatment; △: 5% DSS plus 5-aminosalicylic acid (5-ASA) treatment; ▲: 5% DSS plus China Center for Type Culture Collection M206119] at the indicated time points; B: Disease activity index (DAI) changes among groups in (A) after 7 d 5% DSS treatment at the indicated time points. Each point represents the mean ± SE (n = 10); C: Mean colon length (cm) for the mice in (A); D: Histological analysis of representative colons from the mice in (A) (original magnification, hematoxylin and eosin staining, 100 ×); E: Summarized histological scores from colons of (D); F: Summarized myeloperoxidase (MPO) activities of colons from mice in (D).

After 7 d of treatment, all DSS-colitis mice showed a significant reduction in their colon length compared with the healthy controls. CCTCC-M206119-strain-treated DSS-colitis mice had the shortest length (8.2 ± 0.68 cm), followed by saline- (9.8 ± 0.56 cm) or 5-ASA- (10.0 ± 0.89 cm) treated DSS-colitis mice (P < 0.05, Figure 1C). CCTCC-M206119-treated DSS-colitis mice had markedly more severe disease, with greater weight loss, diarrhea, fecal bleeding, and shortened colon length.

The histological lesions were examined blindly and the average scores were evaluated statistically by ANOVA. In the acute study, CCTCC-M206119-treated DSS-colitis mice presented scores of 10.9 ± 0.5 that differed statistically from those in the 5-ASA-treated DSS-colitis mice. It became evident that the CCTCC-M206119-treated DSS-colitis group had comparatively higher DAI scores than the saline controls (P < 0.01, Figure 1D and E).

Furthermore, there was significant difference in MPO enzymatic activity detected in the colons control mice (1.038 ± 0.012 U/g tissue), DSS plus saline group (18.368 ± 1.226 U/g tissue), DSS plus 5-ASA group (8.369 ± 0.652 U/g tissue), and DSS plus CCTCC M206119 group (24.565 ± 2.006 U/g tissue) (Figure 1F). This indicated that more neutrophils infiltrated DSS-colitis mice after CCTCC M206119 treatment.

To characterize the role of CCTCC M206119 strain on potential gut flora shifts during DSS-induced barrier damage, we performed a bacterial-culture-based survey of the gut flora in DSS-colitis mice treated with saline, 5-ASA, or CCTCC M206119 strain. No significant differences in total aerobic bacteria or Enterococcus were obtained for any of the groups. Bacterial counts of all fecal aerobic [Escherichia coli (E. coli), Staphylococcus, Bacteroides, or total aerobic bacteria] cultured in DSS-colitis mice increased significantly compared to the healthy group. Also, both E. coli and Staphylococcus increased in the saline group, whereas 5-ASA rebalanced the bacterial counts of Staphylococcus to normal levels (Figure 2A). In contrast, Lactobacillus in the colon lumen was reduced significantly in all DSS-colitis groups, with no significant changes in Bifidobacterium or Enterococcus spp. (Figure 2B).

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Figure 2 Alteration of fecal microflora in DSS-colitis mice after China Center for Type Culture Collection M206119 treatment. Bacterial counts of (A) aerobic (Escherichia coli, Staphylococcus, Bacteroides, total aerobic bacteria) and (B) anaerobic (Bifidobacterium, Lactobacillus, Enterococcus spp.) in colon luminal contents from healthy animals and dextran sulfate sodium (DSS)-colitis mice treated by saline, 5-aminosalicylic acid (5-ASA), or China Center for Type Culture Collection (CCTCC) M206119 strain at day 2 and day 7 after DSS-treatment, as determined by culture. The data sets were pooled from two independent experiments. Significance levels were determined by U test. Underlined P values shown in black were calculated from comparisons of healthy vs diseased animals; C: Zonula occludens (ZO)-1 and defensin 2 expression from colons of DSS-colitis mice treated with saline or CCTCC M206119 and healthy mice was measured by western blotting at indicated time points; GAPDH was used as a loading control. The data represent at least three experiments. ^aP < 0.05 vs healthy group. GAPDH: Glyceraldehyde-3-phosphate dehydrogenase.

To determine whether the changes in gut flora after CCTCC M206119 treatment were due to alteration of the epithelial junction or antagonistic agents, we measured the expression levels of ZO-1 and β-defensin 2 from colons of DSS-colitis mice treated with saline or CCTCC M206119 and healthy mice, by western blotting. Expression of ZO-1 in healthy mice remained at an abundant level compared to all DSS-colitis mice. Treatment of mice for 5 d with 5% DSS plus saline reduced ZO-1 expression significantly compared to healthy mice, whereas 5% DSS plus CCTCC M206119 strain reduced ZO-1 expression dramatically at day 3. In contrast, no β-defensin 2 expression was detected in the healthy mice, with relatively high expression of β-defensin 2 detected in the colons in mice that were treated with 5 d of either 5% DSS plus saline or 5% plus CCTCC M206119. After 5 d exposure to 5% DSS plus CCTCC M206119, there was a significant (P < 0.05) decrease in β-defensin 2 level in the colons of mice relative to 5% DSS plus saline treatment (Figure 2C).

Nuclear translocation of NF-κB p65 represents increased inflammation at the initiation stage. To investigate whether the aggravation of DSS-colitis after CCTCC M206119 strain treatment was due to the initiation of inflammation-related transcription, we detected the translocation of NF-κB p65 in HT-29 cells inoculated with CCTCC M206119 strain. TNF-α was used as a control. In the blank control, no positive staining for NF-κB p65 was detected. Both TNF-α and CCTCC M206119 strain upregulated the translocation of NF-κB p65 in vitro, with more positively stained cells in the latter group (P < 0.05, Figure 3A and B).

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Figure 3 Effects of China Center for Type Culture Collection M206119 strain on epithelial injury and translocation of nuclear factor-κB in vitro. Immunofluorescence staining for nuclear factor (NF)-κB p65 (red) and 4',6'-diamidino-2-phenylindole hydrochloride (DAPI) (blue) in HT-29 cells treated either by tumor necrosis factor (TNF)-α or China Center for Type Culture Collection (CCTCC) M206119 (scale bars, 10 mm). A: Increased positive NF-κB p65 staining after CCTCC M206119 treatment; B: Positive staining areas were quantified as pixels per high-power microscopic field (400 ×) using Photoshop. Error bars indicate mean ± SD (n = 3).

To investigate if CCTCC M206119 administration affected the expression of colonic cytokines, we first screened the mRNA levels of the major colonic proinflammatory cytokines by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). We observed increased mRNA levels for IL-1 β, IL-6 and TNF-α from the colons of DSS-colitis mice treated with CCTCC M206119 strain or saline for 3 d. Also, it was evident that mRNA levels of IL-1 β, IL-6 and TNF-α from colons of CCTCC-M206119-treated DSS-colitis mice were significantly higher than those from colons of saline-treated DSS-colitis mice (Figure 4A). Next, we confirmed the changes in expression of the above cytokines at the protein level, suggesting that DSS treatment resulted in increased expression of proinflammatory cytokines, whereas DSS plus CCTCC M206119 strain treatment resulted in significantly higher expression of the cytokines mentioned above (Figure 4B).

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Figure 4 Colonic cytokines changes in China Center for Type Culture Collection M206119 or vehicle-treated dextran sulfate sodium-colitis mice. Expression of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α from the colons of dextran sulfate sodium (DSS)-colitis mice treated with China Center for Type Culture Collection (CCTCC) M206119 or saline was measured by (A) RT-PCR and (B) western blotting at indicated time points; GAPDH was used as a loading control; C: IL-10 expression from colons of DSS-colitis mice treated with saline, 5-aminosalicylic acid (5-ASA), or CCTCC M206119 was measured by western blotting at indicated time points; β-actin was used as a loading control. The data represent at least three experiments. GAPDH: Glyceraldehyde-3-phosphate dehydrogenase.

Anti-inflammatory cytokine IL-10 expression from colons of DSS-colitis mice treated with saline, 5-ASA, or CCTCC M206119 was measured by western blotting. IL-10 expression was dramatically downregulated in saline- and CCTCC-M206119-treated DSS-colitis mice, with more significant changes in the latter group. In contrast, 5-ASA upregulated IL-10 expression compared to saline-treated DSS-colitis mice (Figure 4C). It indicated that CCTCC M206119 treatment inhibited the expression of anti-inflammatory cytokine in DSS-colitis mice.

Distinct microscopic morphological features were observed after Gram staining of broth-grown CCTCC M206119 strain. Gram-positive, rod-shaped morphology could be distinguished (Figure 5A). Under SEM, CCTCC M206119 strain showed exclusively smooth rod- or fork-shaped morphology, without spores, flagella or capsules (Figure 5A). Based on analysis of the peak and data of base C, G, T and A, G + C mol% of CCTCC M206119 strain was determined as 58.64% (Figure 5B). All CCTCC M206119 strains tested were unable to utilize indepamide, urea enzymes and gelatin. All strains tested were able to utilize glucose, mannitol, lactose, saccharose, maltose, salicin, L-xylose, arabitol, esculin, glycerol, cellobiose, MNC, melezitose, D-raffinose, sorbitol, rhamnose, and trehalose. All strains were found to be catalase negative [at 3% (v/v) H₂O₂]. With discriminant and factorial analyses of data from all biochemical tests, a presumptive identification scheme for CCTCC M206119 strain was formulated based on biochemical properties. In conjunction with Gram stain morphology, biochemical profiling can be used to differentiate among major groups of lactobacilli (up to 95% confidence interval). In our abbreviated identification scheme, CCTCC M206119 strain can be presumptively grouped into lactobacilli when biochemical tests are combined with microscopic morphology (Figure 5C). To verify the identities of the reference strains used in this study, 16S rRNA genes were amplified and sequenced. With BLASTn, CCTCC M206119 strain was determined as L. crispatus at the 16S rRNA gene level (Figure 5D).

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Figure 5 Characteristics of China Center for Type Culture Collection M206119 strain. China Center for Type Culture Collection (CCTCC) M206119 strain was identified by (A) microscopy (Gram staining, oil 1000 ×) and scanning electron microscopy (10  000 ×); (B) Gas chromatography ratio (high performance liquid chromat); (C) biochemical reaction; and (D) sequence analyses of 16S rRNA gene fragments amplified from DNA eluted from CCTCC M206119 genomic DNA.

It is widely accepted that a combination of genetic factors, immune disorders and environmental factors could be involved in the etiology of inflammatory bowel disease (IBD). Recent research has illustrated that some commensal and pathogenic bacteria are closely related to IBD. However, to date, the role of bacteria in the pathogenesis of IBD, or the efficacy of probiotics is still controversial.

The efficiency of probiotics in controlling IBD is still controversial. Thus, it is difficult to draw a definitive conclusion in evaluating the role of microflora in the pathogenesis of IBD, and subsequently, the efficacy in controlling IBD. Some published data have also questioned the safety of probiotics.

Microflora considered beneficial to the host include the genera Bifidobacterium and Lactobacillus. In this context, several candidate strains were screened to find some probiotics as therapeutics using dextran sodium sulfate (DSS)-induced colitis in mice, and China Center for Type Culture Collection (CCTCC) M206119 strain led to an exacerbated phenotype of DSS-colitis mice. Expression of protective factors zonula occludens-1 and β-defensin 2 was downregulated after CCTCC M206119 treatment. There was an increase in the nuclear translocation of nuclear factor-κB in epithelial cells. Then, intestinal proinflammatory and anti-inflammatory cytokine responses were evaluated. Proinflammatory colonic cytokines [interleukin (IL)-1β, IL-6 and tumor necrosis factor-α] levels were clearly increased in CCTCC-M206119-treated animals, whereas anti-inflammatory colonic cytokine (IL-10) level was lowered compared with saline- or 5-ASA-treated DSS-colitis mice. Next, CCTCC M206119 strain was identified as Lactobacillus crispatus, so it was concluded that not all lactobacilli strains have beneficial effects on intestinal inflammation and that Lactobacillus crispatus (L. crispatus) CCTCC M206119 is involved in exacerbation of intestinal inflammation in DSS-colitis mice.

The study results suggest that some probiotics such as L. crispatus CCTCC M206119 strain might act as an aggravating factor in the pathogenesis of ulcerative colitis (UC). They also highlight the importance of selecting well-characterized probiotic strains and in delivering intact pharmaceutical formulations at an appropriate dose level to the inflamed regions of the intestine.

IBD is a group of inflammatory conditions of the colon and small intestine, including Crohn’s disease and UC, which are characterized by abnormal activation of the gut-associated immune system, resulting in chronic inflammation of the digestive tract. Lactobacillus is a genus of Gram-positive facultative anaerobic or microaerophilic rod-shaped bacteria. They are a major part of the lactic acid bacteria group, named as such because most of its members convert lactose and other sugars to lactic acid. They are common and usually benign.

In this study, the authors investigated the role of CCTCC M206119 strain on intestinal inflammation using a DSS-induced colitis mice model. They showed that CCTCC M206119 strain was identified as L. crispatus, but this strain was involved in the exacerbation of intestinal inflammation in DSS-colitis mice. From these results, the authors concluded that not all lactobacilli strains have beneficial effects on intestinal inflammation. This paper has been well written and the results are interesting.