A case–control study on the association of intestinal flora with ulcerative colitis

The association between intestinal flora and ulcerative colitis (UC) was studied in order to provide a basis and method for clinical treatment. Fresh fecal samples were collected from 30 active UC patients and 10 healthy controls. The intestinal flora DNA from each sample was extracted and 16S rRNA gene sequencing was carried out using HiSeq platform to identify the intestinal flora in fecal samples. The richness and diversity of intestinal flora in UC patients were significantly lower than those in healthy control group (P < 0.05). Significant differences were observed between the intestinal flora-species of UC patients and healthy controls. Synergistetes (P < 0.01) and Firmicutes (P < 0.05), along with probiotics Veillonella (P < 0.01), Ruminococcus and Coprococcus (P < 0.05) in the UC patients were lower than that in the healthy controls significantly. Furthermore, compared with the control group, Tenericutes (P < 0.01) and intestinal pathogenic bacteria, including Bacteroides (P < 0.01), Escherichia and Sutterella (P < 0.05) were significantly increased. The incidence of UC is significantly associated with the changes in intestinal flora. Changes in intestinal flora may lead to a decrease in the diversity of intestinal flora or to the enrichment of a particular intestinal flora. Supplementary Information The online version contains supplementary material available at 10.1186/s13568-021-01267-9.


Introduction
Ulcerative colitis (UC) is a chronic non-specific intestinal inflammatory disease of unknown etiology. Its main symptoms include abdominal pain, diarrhea and mucus, pus and blood. Some UC patients have extra-intestinal manifestations and complications, which affect their daily lives, and even their health (Whitehead 2016;Sykora et al. 2018). An epidemiological survey reported higher prevalence of UC among the people of 20-40 years, and higher prevalence in males than females (Lewin et al. 2019). The incidence rate of UC fluctuates from 5.5 to 24.3 per million people worldwide with significant regional and ethnic specificity. Statistically, the prevalence of UC in China is about 11.6 per million (Whitesides 1985;Molodecky et al. 2012;Ng et al. 2013;Cui et al. 2018). The pathogenesis of UC has been reported to be associated with environmental, genetic, immune and intestinal flora-factors (Cui et al. 2018). Among them, the barrier, metabolic and nutritive function of intestinal flora, immune system function, and the regulation of the balance of intestinal flora play a key role in the pathogenesis of UC.
The intestinal flora is currently considered to be a complex ecosystem, which is (Ahlawat et al. 2021b) composed of 500-1000 different species, accounting for 10 14 bacterial cells, which is 10 times more than that of the total number of human cells (Domingo and Sanchez 2018). The genome of all intestinal microorganisms is known as "microbiome", which is more than 100-times larger than the human nuclear genome (Huang et al. 2019). Intestinal microflora is increasingly recognized as a key factor of human health. Several studies have shown that many human chronic diseases are associated with intestinal microecological disorders (Tripathi et al. 2018;Zhang et al. 2018;Ma et al. 2019;Ahlawat et al. 2021a). The intestinal flora is an important environmental factor, which has been reported to be associated with a series of metabolic diseases, including obesity (Machiels et al. 2014) and diabetes . It is crucial for human beings to maintain a good symbiotic relationship between human body and intestinal flora.
Although the specific pathogenesis of UC remains unclear, the interactions of genetic abnormalities, immune system dysfunction, intestinal barrier dysfunction and microbiological infection are thought to be the early risk factors of UC (Deng et al. 2019;Lewin et al. 2019;Lee et al. 2020). The microbiological factor has been recognized as the most potent environmental factor in the UC progression, which is possibly associated with the harmful mucosal invasion, activation of carcinogens, or inflammatory responses (Zheng et al. 2019). Moreover, the inflammatory cytokines and/or mixed inflammatory infiltrates in the intestinal mucosa may also be responsible for the development of UC (Kopecki et al. 2019). Therefore, a better understanding of the gastrointestinal microflora and inflammatory cytokines in the progression of UC has been of great significance.
This study provides a new basis and method for the clinical assessment of UC by analyzing the association between changes in intestinal flora and UC. It is of great importance to fully understand the changes of intestinal flora in UC. This study provides a theoretical basis for the regulation of intestinal flora in the treatment of UC and its complications.

Materials and methods
We have uploaded the data to the NCBI Sequence Read Archive database (Accession Number: PRJNA695366).

Materials
Agencourt AMPure XP magnetic beads and Elution Buffer were purchased from MGI Tech Co., Ltd. Inhibi-tEX Buffer and Qubit ® dsDNA BR Assay Kit were purchased from Shanghai Haoran Biotechnology Co., Ltd. Two wash buffers, including Buffer AW1 and Buffer AW2 were purchased from Shanghai Beinuo Biotechnology Co., Ltd. Buffer AL and Buffer ATE were purchased from Shanghai Limin Industrial Co., Ltd. KAPA HiFi HotStart DNA Polymerase was purchased from Shanghai HiFi Biotech Co., Ltd.

Sample collections and setting participants
According to the revised standards of "Consensus Opinions on Diagnosis and Treatment of Inflammatory Bowel Disease" formulated by the Inflammatory Bowel Disease Group of the Chinese Medical Association Gastroenterology Branch in 2018, 30 patients with ulcerative colitis were recruited from the First Affiliated Hospital, Harbin Medical University from January to December 2019. There were no gender restrictions. The inclusion criteria for the recruitment of patients included: (1) region, Heilongjiang province; (2) age, 30-65 years; (3) past history of ulcerative colitis, the ulcerative colitis active period; and (4) the patients are not treated with antibiotics and microecological agents or not treated with these drugs 4 weeks before the onset. The core standards included: (a) hematology tests, such as hemoglobin (Hb), white blood cells (WBC), erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP); (b) colonoscopy report showing ulcerative colitis; and (c) pathology report showing moderate to severe mucosal chronic inflammation or suggesting crypt abscess. The exclusion criteria of the UC patients included: (a) incomplete clinical data; (b) patients with severe heart, liver, lung, and kidney diseases; (c) patients with diabetes and severe infections; (d) patients with pregnancy and lactation; (e) patients with UC complications; (f) patients with extra-intestinal manifestations; and (g) patients with other autoimmune diseases. In addition, 10 healthy controls in the physical examination center of the First Affiliated Hospital, Harbin Medical University were recruited, regardless of gender. For the inclusion criteria of the recruitment of healthy controls, the region, age, and drugs usage were same as that of UC patients. Other inclusion criteria parameters included: (1) no history of chronic gastrointestinal diseases and routine physical examination and stool examination showed no abnormalities; and (2) information collection such as hematological tests, such as Hb, WBC, ESR, and CRP. The sample collection was reviewed by the Ethics Committee of the First Affiliated Hospital of Harbin Medical University.
Fresh stool samples of 1-10 g were collected in a medical stool collection vessels (the surface of the vessels had sample numbers) from the patients and healthy controls, and stored in a − 80 °C low-temperature freezer after one hour of sampling.

DNA extraction and sequencing
The intestinal floras from the fecal samples were homogenized and genomic DNA was extracted using QIAamp Fast DNA Stool Mini Kit (QIAGEN China (Shanghai) Co., Ltd.). The quality and integrity of the DNA extraction were evaluated using micro spectrophotometer and gel electrophoresis.
The extracted DNA samples and corresponding fusion primers were mixed in order to configure the PCR reaction system. The PCR reaction parameters were set for PCR amplification. Agencourt AMPure XP magnetic beads were used to purify the PCR amplification products, which were then dissolved in Elution Buffer, and labeled. The metagenomic library was prepared and the fragment range and concentration were analyzed using Agilent 2100 Bioanalyzer. The prepared colonies were selected for sequencing on HiSeq platform based on insert size.

Data filtering
The original sequencing data was processed to remove low-quality, low-complexity, pollution and N-terminal sequences and obtain clean data. FLASH (Fast Length Adjustment of Short reads, v1.2.11) software was used to sequence paired-end sequences using overlapping relationships The obtained paired-end sequences were assembled into a sequence to obtain the tags of hypervariable region. USEARCH (v7.0.1090) software was used to perform clustering and splicing at 97% similarity. The spliced tags were clustered as OUT (Operational Taxonomic Units) and compared with the database and species annotations. The statistics table of OTU abundance for each sample was obtained, and the samples were analyzed on the basis of OTU and species annotation results.

Statistical analysis
Statistical analysis was carried out using Excel spreadsheets and SPSS statistical software. The differences in the species diversity and richness between the UC patients' samples and that of healthy controls were analyzed. The rank sum test was used, and the results were analyzed using OTU Rank curve, alpha diversity box plot and beta diversity box plot. The similarity in the species of both the groups was analyzed by OTU PLS-DA (Partial Least Squares Discriminant Analysis) method. The RDP classifier Bayesian algorithm was used for species composition analysis and statistics. The histogram and heat map of species richness and the comparison histogram of key species difference were used for the analysis of species composition between two groups. U test was used to calculate the average relative abundance of species between the two groups and to analyze the significance of the difference test. The statistical differences of P < 0.05 and P < 0.01 were considered as significant and extremely significant, respectively. FastTree is used to construct evolutionary tree by selecting OTU or sequence corresponding to classification information at a certain level.

Comparison of species diversity and richness
The comparison of species diversity between the UC patients and the healthy controls is shown in Figs. 1, 2, 3. Shannon index, simpson index and unweighted UniFrac Fig. 1 Comparison of Alpha diversity box between disease group (UC patients) and normal group (healthy controls). Red and blue colored boxes show the richness of microflora in disease and control samples, respectively for all the statistical analysis mentioned with each graph. Clear significant differences were observed in all the statistical analyses Beta diversity box plot were used to reflect the diversity of bacterial community in the samples (Fig. 1). The species diversity in the UC patients was significantly lower than that in the health controls (P < 0.05). The comparison of species richness between the UC patients and the healthy controls is shown in Figs. 1, 3. The observed species index, chao index, and ACE index reflected the community richness between the two groups of samples. The species richness in the UC patients was significantly lower than that of the healthy controls (P < 0.05). The biodiversity statistics between the two groups are listed in Table 1.

Comparison of species similarity
The species similarities between the samples of the UC patients and healthy controls were analyzed on the basis of two sets of OTU data and OTU PLS-DA analysis chart. As shown in Fig. 2B, the intestinal flora clustering of the UC patients and healthy controls showed distinct distribution from each other, without showing any intersection, which showed significant differences in the species diversity between the two sets of samples.

Species level composition analysis
The histogram and heat map of the species richness of the UC patients and healthy controls are shown in Figs. 4, 5, respectively. The average relative abundance and the significance of difference test are shown in Fig. 6 and provided in Additional file 1: Table S1. The probabilities of species distribution of the two groups are listed in Table 2. Synergistetes and Firmicutes were decreased in the UC patients as compared to the healthy control with statistical significance (P < 0.01 and P < 0.05), respectively. Compared with healthy controls, patients with UC showed a significant increase in Tenericutes (P < 0.01). There were no significant differences in Bacteroides, Proteobacteria, Actinomycetes, Fusobacteria, Verrucomicrobia, Lentisphaerae, Euryarchaeota between the UC patients and healthy controls.

Genus level composition analysis
The average relative abundance of species in the UC patients and healthy controls is shown in Fig. 7 and provided in Additional file 1: Table S2. The beneficial bacteria Veillonella were significantly reduced in the UC patients Firmicutes were also reduced in the UC patients as compared to the healthy controls with statistical significance of P < 0.05. The differences in Bacteroides, Proteobacteria, Actinomycetes, Fusobacteria, Verrucomicrobia, Lentisphaerae, Euryarchaeota between the UC patients and healthy controls were insignificant.

Phylogenetic analysis of species
The phylogenetic analysis of species level was studied as follows. Firmicutes and Proteobacteria were the two largest intestinal microbial species, which also the fastest growing species. Second, Actinobacteria and Bacteroidetes have more branches than other species. Euryarchaeota, Fusobacteria, Lentisphaerae, and Verrucomicrobia have less species evolution (Fig. 8).

Discussion
In this study, a case-control experimental method was adopted and 16S rRNA gene sequencing technology using Illumina HiSeq 2500 sequencing platform was applied to explore the relationship between changes in intestinal flora of UC patients and healthy controls. The results showed that the species richness and diversity of the intestinal flora in the UC patients were significantly lower than those of healthy controls. Consistent with the domestic and foreign studies, significant differences in the species diversity of the intestinal flora between UC patients and healthy controls were observed (Ruili et al. 2012;Min et al. 2015). It has been reported that the UC recurrence in the patients in UC remission period is associated with the aggravation of intestinal flora imbalance. It also found that the status of intestinal flora of UC patients is closely associated with the development of the disease by testing intestinal flora in the stool samples of UC active period, UC remission period and healthy controls (Min et al. 2015). Another study have also revealed that the diversity of intestinal flora in patients with active UC is lower than that in UC remission and healthy controls, analyzed by ERIC-PCR (enterobacterial repetitive intergenic consensus PCR) technology (Ruili et al. 2012). It was found that the synergistetes and firmicutes decreased significantly, and the Soft-walled bacteria significantly increased in the UC patients as compared to healthy controls. The current research showed that the alterations in the intestinal flora of UC patients were mainly attributable to decrease in Firmicutes and increase in Proteobacteria. The trend of changes in Actinobacteria and Bacteroides has not been confirmed yet (Hold et al. 2014). Following these differences, the differences in the composition of intestinal flora in UC patients and healthy controls at genus level were analyzed, which showed that Escherichia and Sutterella were significantly increased in UC patients. The increase in Escherichia has been reported to disrupt the balance and integrity of intestinal environment and promote inflammation. A study reported that Helicobacter is a major flora in intestinal infections (Li et al. 2017). When the distribution of the flora changes, it can cause biliary infections, urinary tract infections, and intra-abdominal infections, and even life-threatening. Sutterella sp. may cause digestive disorders (Sartor and Wu 2017), which may be another factor that affect the aggravation and complications of UC patients. Coprococcus, a major flora found in the intestines of humans and animals, decreased significantly in the intestinal flora of UC patients, which can produce natural antibiotics, enhance intestinal function, and also benefit the body. Coprococcus, not only produce bacteriostatic substances, such as bacteriocins, that inhibit the growth of pathogenic bacteria, but they can also inhibit the reproduction of urease-producing bacteria and spoilage bacteria in the intestinal tract. Through these mechanisms it improves the protection of the intestinal microenvironment and reduces endotoxin and inflammation. Ruminococcus are the main fiber-degrading bacteria Our research showed a higher number of Bacteroides in UC patients than the healthy controls, which was consistent with a previous study (Furusawa et al. 2013). In our present study, the number of Faecalibacterium genus was relatively high as compared to the healthy controls, which was inconsistent with previous studies. One of the representative species of Clostridium prausnitzii is Faecalibacterium prausnitzii. Clostridium prausnitzii is a major probiotic in the gastrointestinal tract. It plays vital role in the formation of intestinal mucosal barrier, reduction of intestinal inflammation, competitive inhibition of pathogenic bacteria and reduction of pathogenic bacterial colonization. An early study showed that the number of Clostridium prasmoides in UC patients was significantly lower than healthy controls (Machiels et al. 2014). Man et al. (Man et al. 2013) compared the number of Bacteroides, Clostridium tenuiens and Bifidobacteria in UC patients and healthy controls. They showed an increased number of Bacteroides in UC patients, which could promote inflammation, and a decreased number of Clostridium tenuis and Bifidobacterium, which could inhibit inflammation (Man et al. 2013). We speculated that the UC patients who participated in this study did not take medication within 4 weeks. The accuracy of this experiment on the effect of medication was not studied in this study. The long course of UC patients, repeated symptoms and long-term use of aminosalicylic acid, biological agents, glucocorticoids, microecological agents, etc. might have impact on the results of this study. The degree of inflammation in UC patients is also an important factor that affect intestinal flora. This study did not strictly distinguish among patients having mild, moderate, and severe UC. Therefore, the role of these factors Heat map showing horizontal species richness between UC patients and healthy controls (normal). The relative abundance of bacteria is shown in terms of color intensities (denoted by the scale given in upper left corner). The differences in the color intensities between disease and normal samples show differences in the number of respective species still needs to be studied in more detail. In addition, the age, gender, and living habits of the study participants can lead to different research conclusions. This requires the sample size to be expanded and refined and the sample variables to be specified as much as possible.
This study explored the feasibility of using intestinal flora to guide the treatment of UC by studying the intestinal flora of UC patients. Probiotics, such as Clostridium prasylvia, can positively regulate the stability of intestinal flora by increasing the permeability of intestinal mucosa and producing butyrate to reduce intestinal inflammation (Jinli et al. 2019); Lactobacillus regulates the balance of intestinal flora by promoting digestion and inhibiting the growth of potential pathogenic bacteria. Faecococcus can decompose nutrients to produce lactic acid, enhance intestinal function and inhibit the growth and reproduction of pathogenic bacteria. Fecal bacteria transplantation is another application of