Abstract
Objective
Microbial infections have been shown to contribute to gastric carcinogenesis, the knowledge of gastric microbiota alteration in this process may provide help in early diagnosis of gastric cancer. The aim of this study was to characterize the microbial changes and identify taxonomic biomarkers across stages of gastric carcinogenesis.
Methods
The gastric microbiota was investigated by 16S rRNA gene analysis in gastric mucosal specimens from 47 patients including superficial gastritis (SG), atrophic gastritis (AG), gastric intraepithelial neoplasia (GIN), and gastric cancer (GC). Differences in microbial composition across the disease stages, especially in GIN and GC were assessed using linear discriminant analysis effect size.
Results
There was no gradual changing trend in the richness or diversity of the gastric microbiota across stages of gastric carcinogenesis. The relative abundance of dominant taxa at phylum and genus levels didn’t show a gradual shift pattern, and the only four taxa that continuously enriched from SG to GC were Slackia, Selenomonas, Bergeyella, and Capnocytophaga, all of which were oral bacteria. The most representative taxa which were enriched in GC patients were oral bacteria including Parvimonas, Eikenella and Prevotella-2, and environmental bacteria including Kroppenstedtia, Lentibacillus, and Oceanobacillus. The gastric microbiota in GIN patients were characterized by enrichment of intestinal commensals including Romboutsia, Fusicatenibacter, Prevotellaceae-Ga6A1-group, and Intestinimonas. Gastric cardia cancer and non-cardia cancer patients had significantly different microbiota profiles characterized by a higher abundance of Helicobacter in the cardia cancer patients.
Conclusions
Our results provide insights on potential taxonomic biomarkers for gastric cancer and precancerous stages, and suggest that gastric microbiota might play different roles in the carcinogenesis of cardia cancer and non-cardia cancer.
Keywords: gastric carcinogenesis, microbiota, taxonomic biomarker, gastric cancer, gastric cardia cancer, gastric intraepithelial neoplasia
Introduction
Gastric cancer remains the second-leading cause of cancer-related deaths worldwide, which emphasizes the need for knowledge of the key changes in the process of carcinogenesis to make early diagnosis. According to Lauren’s histological classification, gastric cancer is classified into the diffuse type and the intestinal-type (Lauren, 1965). The current widely accepted biological model of intestinal-type gastric carcinogenesis can be described as a series of sequential stages: from superficial gastritis (SG) through atrophic gastritis (AG), intestinal metaplasia (IM), and gastric intraepithelial neoplasia (GIN) to gastric cancer (GC) (Correa, 2004). Other than genetic predisposition, environmental factors including microbial infections have been shown to contribute to gastric carcinogenesis. Chronic Helicobacter pylori (H. pylori) infection is considered to be the strongest risk factor for intestinal-type gastric cancer, but only 3% of people with H. pylori infection develop gastric cancer, implying that other factors also play a role (Björkholm et al., 2003).Studies have presented evidence that gastric carcinogenesis can be associated with enrichment in many non-H. pylori bacteria, as well as depletion in others (Emanuel et al., 2016), although there are inconsistent conclusions about the changing trend of a specific bacterium. The changes of gastric microbiome in the development of gastric cancer remains largely unknown. Previous studies have revealed a gradual shift in gastric microbiota profile from SG to IM to GC (Coker et al., 2018; Eun et al., 2014; Francisco et al., 2014). Gastric intraepithelial neoplasia, including low-grade and high-grade intraepithelial neoplasia, is the precancerous lesion of gastric cancer, and mainly develops based on atrophic gastritis with intestinal metaplasia. The prognosis of patients with gastric cancer can be greatly improved by early diagnosis and endoscopic resection of GIN. So far, the microbial profile of GIN in the process of gastric carcinogenesis is barely known. In this study, we investigate the microbial changes in mucosal biopsies of patients with progressive histological stages along gastric carcinogenesis—from SG, through AG and GIN to GC.
Materials and Methods
Patients
Gastric biopsies were collected from 47 patients during upper gastroenterology endoscopic examination or endoscopic submucosal dissection (ESD) due to precancerous mucosal lesions from August 2016 to March 2019 at Nanjing First Hospital, China. The pathological diagnosis was confirmed for each patient, and the results showed 17 patients of superficial gastritis (SG group), 10 patients of atrophic gastritis with intestinal metaplasia (AG group), five patients of gastric intraepithelial neoplasia (GIN group, including four patients of low-grade GIN and one patient of high-grade GIN), and 15 patients of intestinal-type gastric cancer (GC group), including 27 male patients and 20 female patients in total. For pathological diagnosis, two biopsies were taken from antrum and corpus in SG and AG group, if both tissues showed superficial gastritis, then it was classified into SG group, if atrophic gastritis was seen in either site, then it was classified into AG group. GIN specimens were obtained through ESD, GC was confirmed by the specimens from the lesion. For microbiological analyses, two mucosal biopsies were obtained from antrum for SG and AG, and biopsies were taken from relatively intact mucosa adjacent to the lesion, other than necrotic tissue on the lesion, for GIN and GC. The biopsies were stored at −80°C. The age of the patients in each group was increasing from SG to CG (56.00 ± 10.25, 63.58 ± 6.69, 64.80 ± 9.93, and 69.87 ± 11.57 for SG, AG, GIN, and GC groups, respectively, p=0.005). This study was approved by the Ethics Committee of Nanjing First Hospital. Written informed consent was obtained from all of the patients in accordance with the Declaration of Helsinki.
DNA Extraction
Bacterial genomic DNA was extracted with the E.Z.N.A ®Stool DNA Kit (Omega Bio-tek, Norcross, GA, U.S.), following the manual (Supplementary Text). The extracted DNA specimens were checked by NanoDrop for purity and quality, and stored at - 20°C.
PCR Amplification
The variable regions 3 and 4 of the bacterial 16S rRNA gene were amplified from purified DNA specimens with the primers 338F (5’-ACTCCTACGGGAGGCAGCAG-3’) and 806R (5’-GGACTACNNGGG TATCTAAT-3’). PCR was carried out on a Mastercycler Gradient (Eppendorf, Germany) using a reaction mixture containing 12.5 μl 2× Taq PCR MasterMix, 3 μl BSA(2ng/μl), 1 μl Forward Primer (5 uM), 1 μl Reverse Primer (5 uM), 30 ng DNA with ddH2O to make up to 25 μl, 12.5 μl 2×Taq Plus Master Mix, 3 μl BSA (2ng/μl). PCR cycling parameters were a 5-min denaturation cycle at 95°C, followed by 32 cycles of the following: 95°C for 45 s, 55°C for 50 s, and 72°C for 45 s, and finally a 10-min extension at 72°C. Three PCR products per specimen were pooled to mitigate reaction-level PCR biases. The PCR products were purified using QIAquick Gel Extraction Kit (QIAGEN, Hilden, Germany) and checked using 1% agarose gel electrophoresis.
Sequencing Processing
Paired-end sequencing was performed on Illumina Miseq PE300 platform (Illumina, San Diego, CA, USA), at Allwegene Company (Beijing, China). The raw data were filtered with QIIME (v 1.8.0), discarding the reads which were dereplicated or shorter than 150 bp. Filtered reads were clustered into operational taxonomic units (OTUs) assuming 97% similarity. Compared with the SILVA database (version 128), the species classification information of each OTU was obtained.
Data Analysis
Rarefaction curves were calculated using Mothur (version 1.31.2) and R language to determine sequencing depth (Wang et al., 2012). Alpha diversity analysis (including the indexes of Chao 1 and Shannon, which reflect the richness and biodiversity of gastric microbiota, respectively) was performed using QIIME (Caporaso et al., 2010). The dissimilarity of the microbial communities among groups was evaluated by partial least squares discrimination analysis (PLS-DA) using R (Li et al., 2012). Sample clustering in beta diversity analysis was tested using analysis of similarity (ANOSIM) using the vegan package in R (Ferreira et al., 2018). The heatmap of genus information was also created using the vegan package in R. Linear discriminant analysis (LDA) effect size (LEfSe) was applied to find significant metagenome markers of different groups (Xu and Jiang, 2017). Only taxa with LDA >2 at a P value <0.05 were considered significantly enriched.
Statistical significance among groups was determined by Students’ t-test and one-way analysis of variance. Wilcoxon tests and Kruskal-Wallis rank tests were conducted in R to compare data between each two groups. A P-value less than 0.05 was considered to be significant.
Results
Quality Control and Basic Analysis
After sequencing and quality filtering, more than 2.3 million tags and a total of 3,055 OTUs were obtained (Supplementary Table 1). The dominant length of tags was among 400-440bp, and the average number of OTUs was 473 per specimen. The average number of reads per specimen in the SG, AG, GIN, and GC groups was 460,588,423 and 428, respectively.
Richness and Diversity Analysis
The microbial α diversity and β diversity were measured to analyze the differences of microbiota structure among the four groups. Firstly, to test the sequencing depth, we created the rarefaction curves and showed a reasonable amount of sampling (Figure 1A). The Chao1 index and Shannon index were used to describe the α diversity of the bacterial community results. We found that the richness of microbiota was significantly higher in AG group than in SG and GC group (Chao1 index, p=0.032 and 0.003, respectively, Figure 1B) and there was no significant difference in microbial diversity among groups (Shannon index, Figure 1C). Partial least squares Discriminant Analysis (PLS-DA) at the OTU level revealed a statistically significant separation of the groups (ANOSIM, p = 0.037; Figure 1D), suggesting different microbial community structures.
The Changes of Gastric Microbiota Composition in Different Stages of Carcinogenesis
The Relative abundance of phyla in four groups was shown in Figure 2A. The top 5 phyla in stomach were Firmicutes, Proteobacteria, Bacteroidetes, Fusobacteria, and Actinobacteria, with an average relative abundance of 44.75%, 31.04%, 11.32%, 3.49%, and 2.51%, respectively, in all the specimens. There was no significant difference among the four groups for each phylum. None of the phyla showed a continuous increasing or a decreasing changing trend from SG to GC.
There were a total of 561 identifiable genera in all specimens (Supplementary Table 2). Twenty genera with the highest relative abundance were shown in Figure 2B. Helicobacter, Streptococcus, Bacillus, and Anaerobacillus were the most abundant genera. With the progressive disease stages from SG to GC, none of these genera presented a continuous and consistent trend of change in abundance. The only four genera that continuously increased from SG to GC group were Slackia, Selenomonas, Bergeyella, and Capnocytophaga, although they had a relatively low abundance in stomach (Table 1).
Table 1.
Relative abundance (%) | P# | ||||
---|---|---|---|---|---|
SG | AG | GIN | GC | ||
The genera enriched in GC compared with SG | |||||
Prevotella_2 | 0.014 | 0.317 | 0.299 | 0.135 | 0.006 |
Oceanobacillus | 0.011 | 0.362 | 0.000 | 0.472 | 0.006 |
Lentibacillus | 0.012 | 0.595 | 0.000 | 0.667 | 0.011 |
Kroppenstedtia | 0.018 | 0.608 | 0.001 | 0.846 | 0.012 |
Parvimonas | 0.076 | 0.177 | 0.500 | 0.178 | 0.020 |
Erysipelotrichaceae_UCG-007 | 0.194 | 0.248 | 0.258 | 0.242 | 0.021 |
Staphylococcus | 0.079 | 0.115 | 0.013 | 0.113 | 0.026 |
Eikenella | 0.024 | 0.015 | 0.022 | 0.232 | 0.028 |
Bifidobacterium | 0.108 | 0.190 | 0.002 | 0.327 | 0.038 |
The genera depleted in GC compared with SG | |||||
Prevotella_1 | 0.173 | 0.019 | 0.154 | 0.015 | 0.001 |
CL500-29_marine_group | 0.086 | 0.003 | 0.045 | 0.008 | 0.001 |
Rhodobacter | 0.285 | 0.011 | 0.063 | 0.014 | 0.003 |
Massilia | 0.419 | 0.065 | 0.085 | 0.048 | 0.003 |
Flavihumibacter | 0.153 | 0.001 | 0.055 | 0.013 | 0.003 |
Ensifer | 0.108 | 0.028 | 0.059 | 0.019 | 0.003 |
Hydrogenophaga | 0.073 | 0.004 | 0.026 | 0.005 | 0.003 |
Anaerobacillus | 15.208 | 7.702 | 9.883 | 6.744 | 0.004 |
Nitrospira | 0.176 | 0.014 | 0.047 | 0.017 | 0.004 |
Ferruginibacter | 0.148 | 0.000 | 0.026 | 0.014 | 0.004 |
Gemmobacter | 0.091 | 0.001 | 0.021 | 0.005 | 0.004 |
Denitratisoma | 0.101 | 0.005 | 0.092 | 0.011 | 0.007 |
Bacillus | 14.978 | 7.716 | 9.092 | 6.866 | 0.008 |
Brevundimonas | 0.091 | 0.034 | 0.001 | 0.002 | 0.038 |
Romboutsia | 0.156 | 0.011 | 0.609 | 0.136 | 0.043 |
The genera enriched in GIN | |||||
Romboutsia | 0.156 | 0.011 | 0.609 | 0.136 | |
Fusicatenibacter | 0.089 | 0.002 | 0.492 | 0.002 | |
Prevotellaceae_Ga6A1_group | 0.154 | 0.001 | 0.276 | 0.046 | |
Intestinimonas | 0.027 | 0.014 | 0.270 | 0.035 | |
The genera continuously enriched from SG to GC | |||||
Slackia | 0.0000 | 0.0004 | 0.0007 | 0.0058 | |
Selenomonas | 0.0280 | 0.0309 | 0.0393 | 0.0441 | |
Bergeyella | 0.0135 | 0.0240 | 0.0269 | 0.0434 | |
Capnocytophaga | 0.1540 | 0.2549 | 0.2727 | 0.4965 |
#P: SG vs. GC.
LEfSe analysis was applied to identify the most relevant taxa responsible for the differences among disease stages (Figure 2C). We focused observations on the bacterial taxa with different abundance at genus and species level. The SG-enriched genera include Anaerobacillus, Bacillus, Massilia, and Rhodobacter. The AG-enriched genera include Alloprevotella, Pelomonas, Ralstonia, Clocibacterium, Deinococcus, etc. In GIN group, an enrichment in the genera Romboutsia, Fusicatenibacter, Prevotellaceae-Ga6A1-group, and Intestinimonas were observed. In GC group, enriched genera Kroppenstedtia, Lentibacillus, Oceanobacillus, and Bifidobacterium, and enriched species Streptococcus pyogenes and Lactobacillus salivarius were observed.
Specific Bacterial Taxa Are Associated With Gastric Cancer and Gastric Intraepithelial Neoplasia
When GC was compared with SG alone, LEfSe analysis (LDA>2) showed the potential taxonomic biomarkers on genus level in the two groups (Figure 3A). Kroppenstedtia (p=0.012), Lentibacillus (p=0.011), Oceanobacillus (p=0.006), Prevotella-2 (p=0.006), etc. were more abundant in GC group, while Anaerobacillus (p=0.004), Bacillus (p=0.008), Rhodobacter (p=0.043), and Massilia (p=0.003), etc. were more abundant in SG group. We observed the changing trend of these genera along the disease stages and found that, none of them showed a continuous and consistent abundance change from SG to GC. However, Prevotella_1, Massilia, Ensifer, and Bacillus showed and a depleting trend from SG to GC with AG and GIN in between. Kroppenstedtia, Lentibacillus, Bifidobacterium, and Oceanobacillus showed an enriching trend in the groups of SG, AG, and GC (Table 1).
The gradual enriching pattern of some potential taxonomic biomarkers that were abundant in GC group seemed to be disturbed by GIN group. Were there specific changes in the microbiota community of GIN? LEfSe analysis revealed the taxa that differed GIN from other groups, and we focused on the genus level and noticed four GIN-enriched genera: Romboutsia, Fusicatenibacter, Prevotellaceae-Ga6A1-group, and Intestinimonas. Then we examined their changing pattern in the four disease stages (Table 1, Figure 3B). Wilcoxon test was used to compare the relative abundance of taxa between each two groups. All these four genera were significantly abundant in GIN group than in AG group, and Fusicatenibacter and Intestinimonas were significantly more abundance in GIN than in SG group. All of the four genera depleted significantly from GIN to GC group. This result suggested that the mucosal adjacent to GIN might provide a suitable growth environment for these bacteria, and their enrichment might be a marker of a precancerous condition.
The Gastric Microbiota Profile Differs in Cardia Cancer and Non-Cardia Cancer
When we examined the GC group, we found that gastric cardia cancer (GCC), including patients GC1-6, and gastric non-cardia cancer (GNCC), including patients GC7-15, showed an obvious different microbiota profile. We thus divided GC group into GCC group and GNCC group, and compared their microbial structures. The patients’ age of GCC and GNCC were 66.5 ± 6.87 and 72.11 ± 13.38, respectively (p=0.39). We found that there was no significant difference in microbial richness between the two groups (Chao1 index, p=0.52, Figure 4A), however, microbial diversity was significantly higher in GNCC group (Shannon index, p=0.003, Figure 4B). PLS-DA at the OTU level revealed a significant separation of the two groups (ANOSIM, p=0.002), suggesting a striking different microbial community structures (Figure 4C). At phylum level, the abundance of Proteobacteria in GCC was significantly higher than in GNCC (0.641 vs. 0.189, p=0.018), while the abundance of Bacteroidetes and Fusobacteria were significantly lower in GCC than in GNCC (0.045 vs. 0.164, p=0.049, 0.008 vs. 0.043, p=0.036, respectively, Figure 4D). The comparison at genus level revealed that the high abundance of Proteobacteria in GCC was mainly due to the significant enrichment of Helicobacter in this group (Figure 4E). Species under the genus Helicobacter were not furtherly identified in this study.
Discussion
The microbial structure in the stomach has been demonstrated changed during carcinogenesis. Most studies have found that gastric cancer is lower in both the microbial diversity and richness, compared with chronic gastritis (Francisco et al., 2014; Coker et al., 2018; Ferreira et al., 2018), while some other studies reported inconsistent results that the microbial diversity and richness increased in gastric cancer patients (Eun et al., 2014). In this study, no significant difference was found in the microbial diversity and richness between GC group and other groups, while the AG group showed the highest richness among the four groups. The different results of α diversity in different studies may be related to different age, gender and race of the patients. The results of β diversity in our study showed that SG, AG, and GC group could be separated well, which agreed with previous reports that there was a shift in the composition of microbial community along disease stages (Eun et al., 2014; Francisco et al., 2014; Coker et al., 2018).
We observed the microbial composition of the four disease stages. The five predominant phyla in all groups were Firmicutes, Proteobacteria, Bacteroidetes, fusobacteria, and Actinobacteria, and the major genera included Helicobacter, Streptococcus, Bacillus, Anaerobacillus, Fusobacterium, Prevotella, Lactobacillus, etc., which was consistent with the literature (Eun et al., 2014; Francisco et al., 2014; Emanuel et al., 2016; Coker et al., 2018).
To searching for potential taxonomic biomarkers that might related to carcinogenesis, we identified the most relevant taxa responsible for the differences among SG and GC by LEfSe analysis. At the level of genus, nine genera were abundant in GC, and 15 genera were depleted in GC. Among the GC-enriched genera, Parvimonas, Eikenella, and Prevotella-2 were oral bacteria. Parvimonas micra in feces has been found related to colorectal cancer (Yu et al., 2017), and it is enriched in gastric mucosa in gastric cancer (Coker et al., 2018). The genus Eikenella contains only one species, Eikenella corrodens, which usually cause pneumonia, intra-abdominal abscess, or purulent skin and soft tissue infections from bites. This is the first study to find it related with gastric cancer. Prevotella has relatively high abundance in stomach, and several species in this genus have been found enriched in GC patients (Emanuel et al., 2016; Coker et al., 2018). Kroppenstedtia, Lentibacillus, and Oceanobacillus, which were from the environment including soil and water area, were also the first time to be found enriched in GC, and their roles in gastric carcinogenesis remain unclear. Erysipelotrichaceae has been reported to enrich in inflammatory bowel disease and colon cancer (Kaakoush, 2015). Its enrichment in GC implies its potential contribution to gastric carcinogenesis. To investigate the roles of these genera in carcinogenesis, we observed their changing trend in abundances in the four groups, but did not find a continuous increasing or decreasing trend in any of them. The only four bacterial taxa showing continuous increasing trend were Slackia, Selenomonas, Bergeyella, and Capnocytophaga. Interestingly, all of them were oral bacteria. The relationship between oral bacteria and gastric cancer has attracted much attention (Mirjana et al., 2020). Olabisi et al. observed significant centralities of OTUs corresponding to oral microbes P. stomatis, Streptococcus anginosus, P. micra, S. exigua, and D. pneumosintes in GC microbial ecology network and suggested them to be used as biomarkers to distinguish GC from SG (Coker et al., 2018). Sun et al. designed a scoring system for screening suspected gastric cancer patients by oral microbiome detection (Sun et al., 2018). Our results highlighted the significance of oral bacteria in gastric carcinogenesis, that these oral bacteria markers may serve as potential diagnostic tissue markers for GC.
Our study put GIN into disease stages to observe the microbial change in gastric carcinogenesis. According to the degree of cell atypia and structural disorder, GIN was divided into low-grade GIN (equivalent to mild to moderate dysplasia) and high-grade GIN (equivalent to severe dysplasia and carcinoma in situ) (Hamilton and Aaltonen, 2000). Srivastava et al. reported that low-grade GIN disappeared in 38%–75% of patients, remained unchanged for a long time in 19%–50% of patients, and developed into advanced gastric cancer in only a few patients (Srivastava and Lauwers, 2008). The specimens of GIN in our study were mainly taken from low-grade GIN patients (4/5), and the lesions were resected endoscopically due to the high risk of progression assessed by endoscopy (>2cm and/or demarcation line with irregular microsurface pattern) (Endoscopic Classification Review Group, 2005; Kim et al., 2014; Hwang et al., 2016). According to our observation, the β diversity analysis showed that GIN group did not separate well from other groups. When we observed the changing trend of the potential biomarkers, we found five out of nine GC-enriched genera presented with continuous enriching trend along SG to AG and to GC, but the trend was disturbed by GIN. The incompatibility of GIN group may due to the various prognosis of low-grade GIN.
The LEfSe analysis identified four GIN-enriched genera, and we investigated their roles in gastric precancerous disease. All of the four genera were intestinal bacteria that usually show protective effects. Romboutsia depletes significantly in colorectal cancer, and its absence is a sign of intestinal mucosal damage (Mangifesta et al., 2018). Fusicatenibacter belongs to Clostridium. cluster XIVa and contains only one species, Fusicatenibacter saccharivorans (Takada et al., 2013). Takeshita’s study revealed that the prevalence of F.saccharivorans was strikingly lower in active ulcerative colitis than quiescent ones, and suggested that human-derived F.saccharivorans can suppress intestinal inflammation, probably through IL-10 induction (Takeshita et al., 2016). Prevotellaceae-Ga6A1-group, which belongs to the Prevotellaceae family, is a short chain fatty acids (SCFAs)-producing bacterium. Intestinimonas is a butyrate-producing bacterium isolated from intestine (Klaring et al., 2013). SCFAs, including butyrate, play an important role in maintaining the intactness of intestinal epithelial cells and the normal function of the intestine. The significant enrichment of these genera in GIN compared with SG and AG may be due to a gastric niche favoring their colonization, and their depletion in GC may follow a similar path as observed in inflammatory bowel disease and colorectal cancer. It should be noted that the number of high-grade GIN in this study was very small, and the results of low-grade GIN may not represent the situation of high-grade GIN. The potential of these bacteria to be indicators of precancerous disease needs to be verified by further studies with more cases and validated by real-time quantitative PCR.
When the GC group was divided into GCC and GNCC, we found that the bacterial composition of the two subgroups were totally separated on PLS-DA. The significant higher abundance of Helicobacter in the GCC group corelated with the lower microbial diversity in this group and resulted in the difference in the bacterial structure between the two groups. The genus of Helicobacter was not further identified into species in our study. Han et al. investigated the presence of Helicobacter DNA in gastric cancer patients and revealed that the majority was H. pylori in human stomach. H. cinaedi, H. mustelae, and C. hyointestinalis also existed but rarely occurred (Han et al., 2010). So in our study we considered that the genus Helicobacter could be represented by H. pylori. H. pylori has been reported to alter gastric microbiome structure (Kienesberger et al., 2016). The abundance of H. pylori was found decreased from SG to GC in most studies (Eun et al., 2014; Ferreira et al., 2018; Hsieh et al., 2018; Liu et al., 2019). In this study, we found it depleted from SG to AG to GIN, but enriched in GC, as a result of high H. pylori abundance in the GCC group. The incidence rate of GCC is increasing in western countries (Devesa and Fraumeni, 1999; Brown and Devesa, 2002). However, the relationship between H. pylori infection and increasing risk of GCC is controversial (Egi et al., 2007; Hansen et al., 2007; Kamangar et al., 2006; Kim et al., 2012; Wang et al., 2014). A meta-analysis concluded that studies conducted in western countries tend to show a neutral or even negative association, while in eastern populations with high GC incidence including China, Korea, and Japan, there is evidence of a higher risk of GCC among the infected (Marlene et al., 2011). Gao et al. concluded from a study conducted in Southeast China that H. pylori may affect the gastric microbial structure in the pathogenesis of gastric cardia adenocarcinoma (Gao et al., 2019). But the mechanisms of non-H. pylori bacteria’s influence on GCC are still needs to be investigated. In this study, the abundance of Helicobacter was significantly higher in GCC than in GNCC, we infer that this may be attributed to the fact that the boundary of atrophic gastritis usually extends from gastric antrum to cardia, and the site suitable for H. pylori colonization also retreats from antrum to cardia. Further studies with more cases are needed to verify this point of view.
Conclusions
Although our study is limited by the low number of patients with gastric intraepithelial neoplasia, we showed that the gastric microbial structure changed along SG-AG-GIN-GC stages. We found some bacterial taxa associated with GC and GIN, and their potential to be indicators of cancer and precancerous stages needs to be verified by further studies. We also found a significantly different microbial structure between the cardia cancer and non-cardia cancer groups characterized by a higher abundance of Helicobacter in the cardia cancer group, and suggested that gastric microbiota might play different roles in the carcinogenesis of cardia cancer and non-cardia cancer.
Data Availability Statement
The original contributions presented in the study are publicly available. This data can be found here: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA634837.
Ethics Statement
The studies involving human participants were reviewed and approved by the Ethics Committee of Nanjing First Hospital. The patients/participants provided their written informed consent to participate in this study.
Author Contributions
ZZ designed the study. XZ analyzed the data and wrote the initial manuscript. CL and WC performed sample collection and laboratory experiments. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the Medical Science and technology development Foundation and the Nanjing Municipality Health Bureau (Grant number YKK16135 and YKK18103).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
The authors are grateful to the Allwegene Company (Beijing, China) for assistance with DNA sequencing and delivering the data to us.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcimb.2021.559148/full#supplementary-material
Abbreviations
SG, Superficial gastritis; AG, Atrophic gastritis; IM, Intestinal metaplasia; GIN, Gastric intraepithelial neoplasia; GC, Gastric cancer; GCC, Gastric cardia cancer; GNCC, Gastric non-cardia cancer; H. pylori, Helicobacter pylori; ESD, Endoscopic submucosal dissection; OUT: Operational taxonomic unit; PLS-DA, Partial least squares discrimination analysis; ANOSIM, Analysis of similarity; LEfSe, Linear discriminant analysis effect size; LDA, Linear discriminant analysis.
References
- Björkholm B., Falk P., Engstrand L., Nyrén O. (2003). Helicobacter pylori: Resurrection of the cancer link. J. Intern. Med. 253, 102–119. 10.1046/j.1365-2796.2003.01119.x [DOI] [PubMed] [Google Scholar]
- Brown L. M., Devesa S. S. (2002). Epidemiologic trends in esophageal and gastric cancer in the United States. Surg. Oncol. Clin. N. Am. 11, 235–256. 10.1016/s1055-3207(02)00002-9 [DOI] [PubMed] [Google Scholar]
- Caporaso J. G., Kuczynski J., Stombaugh J., Bittinger K., Bushman F. D., Costello E. K., et al. (2010). QIIME allows analysis of high-throughput community sequencing data. Nat. Methods 7, 335–336. 10.1038/nmeth.f.303 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coker O. O., Dai Z., Nie Y., Zhao G., Cao L., Nakatsu G., et al. (2018). Muc osal microbiome dysbiosis in gastric carcinogenesis. Gut 67, 1024–1032. 10.1136/gutjnl-2017-314281 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Correa P. (2004). The biological model of gastric carcinogenesis. Iarc. Sci. Publ. 157, 301–310. [PubMed] [Google Scholar]
- Devesa S. S., Fraumeni J. F. J. (1999). The rising incidence of gastric cardia cancer. J. Natl. Cancer Inst. 91, 747–749. 10.1093/jnci/91.9.747 [DOI] [PubMed] [Google Scholar]
- Egi Y., Ito M., Tanaka S., Imagawa S., Takata S., Yoshihara M., et al. (2007). Role of Helicobacter pylori infection and chronic inflammation in gastric cancer in the cardia. Jpn. J. Clin. Oncol. 37, 365–369. 10.1093/jjco/hym029 [DOI] [PubMed] [Google Scholar]
- Emanuel D. J., Diogo L., Marta B. C., Ana G., Pedro P. N. (2016). Gastric microbiota and carcinogenesis: the role of non-Helicobacter pylori bacteria - A systematic review. Rev. Esp. Enferm. Dig. 108, 530–540. 10.17235/reed.2016.4261/2016 [DOI] [PubMed] [Google Scholar]
- Endoscopic Classification Review Group (2005). Update on the Paris classification of superficial neoplastic lesions in the digestive tract. Endoscopy 37, 570–578. 10.1055/s-2005-861352 [DOI] [PubMed] [Google Scholar]
- Eun C. S., Kim B. K., Han D. S., Kim S. Y., Kim K. M., Choi B. Y., et al. (2014). Differences in gastric mucosal microbiota profiling in patients with chronic gastritis, intestinal metaplasia, and gastric cancer using pyrosequencing methods. Helicobacter 19, 407–416. 10.1111/hel.12145 [DOI] [PubMed] [Google Scholar]
- Ferreira R. M., Pereira-Marques J., Pinto-Ribeiro I., Costa J. L., Carneiro F., Machado J. C., et al. (2018). Gastric microbial community profiling reveals a dysbiotic cancer-associated microbiota. Gut 67, 226–236. 10.1136/gutjnl-2017-314205 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Francisco A. J., Flor V. J., Rafael M. G., Alejandra M., Javier T. (2014). Stomach microbiota composition varies between patients with non-atrophic gastritis and patients with intestinal type of gastric cancer. Sci. Rep. 4, 4202. 10.1038/srep04202 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gao X., Wang J., Li Q., Yan T., Lin J. (2019). Correlation between gastric microflora and gastric cardia adenocarcinoma associated with Helicobacter pylori infection. Chin. J. Microecol. 31, 197–201. 10.13381/j.cnki.cjm.201902018 [DOI] [Google Scholar]
- Hamilton S. R., Aaltonen L. A. (2000). World Health Organization classification of tumours: Pathology and genetics of tumours of the digestive system (Lyon: IARC Press; ). [Google Scholar]
- Han H. S., Lee K. Y., Lim S. D., Kim W. S., Hwang T. S. (2010). Molecular identification of Helicobacter DNA in human gastric adenocarcinoma tissues using Helicobacter species-specific 16S rRNA PCR amplification and pyrosequencing analysis. Oncol. Lett. 1, 555–558. 10.3892/ol_00000098 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hansen S., Vollset S. E., Derakhshan M. H., Fyfe V., Melby K. K., Aase S., et al. (2007). Two distinct aetiologies of cardia cancer; evidence from premorbid serological markers of gastric atrophy and Helicobacter pylori status. Gut 56, 918–925. 10.1136/gut.2006.114504 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hsieh Y. Y., Tung S. Y., Pan H. Y., Yen C. W., Xu H. W., Lin Y. J., et al. (2018). Increased abundance of Clostridium and Fusobacterium in gastric microbiota of patients with gastric cancer in Taiwan. Sci. Rep. 8, 158. 10.1038/s41598-017-18596-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hwang J. W., Bae Y. S., Kang M. S., Kim J. H., Jee S. R., Lee S. H., et al. (2016). Predicting pre- and post-resectional histologic discrepancies in gastric low-grade dysplasia: A comparison of white-light and magnifying endoscopy. J. Gastroenterol. Hepatol. 31, 394–402. 10.1111/jgh.13195 [DOI] [PubMed] [Google Scholar]
- Kaakoush N. O. (2015). Insights into the role of Erysipelotrichaceae in the human host. Front. Cell Infect. Mi. 5, 84. 10.3389/fcimb.2015.00084 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kamangar F., Dawsey S. M., Blaser M. J., Perez-Perez G. I., Pietinen P., Newschaffer C. J., et al. (2006). Opposing risks of gastric cardia and noncardia gastric adenocarcinomas associated with Helicobacter pylori seropositivity. J. Natl. Cancer Inst. 98, 1445–1452. 10.1093/jnci/djj393 [DOI] [PubMed] [Google Scholar]
- Kienesberger S., Cox L. M., Livanos A., Zhang X. S., Chung J., Perez-Perez G. I., et al. (2016). Gastric Helicobacter pylori infection affects local and distant microbial populations and host responses. Cell Rep. 14, 1395–1407. 10.1016/j.celrep.2016.01.017 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kim J. Y., Lee H. S., Kim N., Shin C. M., Lee S. H., Park Y. S., et al. (2012). Prevalence and clinicopathologic characteristics of gastric cardia cancer in South Korea. Helicobacter 17, 358–368. 10.1111/j.1523-5378.2012.00958.x [DOI] [PubMed] [Google Scholar]
- Kim M. K., Jang J. Y., Kim J. W., Shim J. J., Lee C. K., Chang Y. W., et al. (2014). Is lesion size an independent indication for endoscopic resection of biopsy-proven low-grade gastric dysplasia? Dig. Dis. Sci. 59, 428–435. 10.1007/s10620-013-2805-8 [DOI] [PubMed] [Google Scholar]
- Klaring K., Hanske L., Bui N., Charrier C., Blaut M., Haller D., et al. (2013). Intestinimonas butyriciproducens gen. nov. sp. nov. a butyrate-producing bacterium from the mouse intestine. Int. J. Syst. Evol. Micr. 63, 4606–4612. 10.1099/ijs.0.051441-0 [DOI] [PubMed] [Google Scholar]
- Lauren P. (1965). The two histological main types of gastric carcinoma, diffuse and so-called intestinal-types carcinoma. Acta Pathol. Microbiol. Scand. 1965 64, 31–45. 10.1111/apm.1965.64.1.31 [DOI] [PubMed] [Google Scholar]
- Li F. T., Zhao J., Pang X. Y. (2012). The oral microbial fingerprint on the greasy tongue coating of patients with chronic gastritis. Chin. J. Integrated Tradit. Western Med. 32, 1331–1335. [PubMed] [Google Scholar]
- Liu X., Shao L., Liu X., Ji F., Mei Y., Cheng Y., et al. (2019). Alterations of gastric mucosal microbiota across different stomach microhabitats in a cohort of 276 patients with gastric cancer. EBioMedicine 40, 336–348. 10.1016/j.ebiom.2018.12.034 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mangifesta M., Mancabelli L., Milani C., Gaiani F., Angelis N., Angelis G. L., et al. (2018). Mucosal microbiota of intestinal polyps reveals putative biomarkers of colorectal cancer. Sci. Rep. 8, 13974. 10.1038/s41598-018-32413-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marlene C. P., Bárbara P., Nuno L., Henrique B. (2011). Helicobacter pylori infection and gastric cardia cancer: systematic review and meta-analysis. Cancer Cause Control. 22, 375–387. 10.1007/s10552-010-9707-2 [DOI] [PubMed] [Google Scholar]
- Mirjana R. S., Ceu F., Annemieke S., Richard H., Juozas K., Theo R., et al. (2020). Systematic review: gastric microbiota in health and disease. Aliment Pharmacol. Ther. 51, 582–602. 10.1111/apt.15650 [DOI] [PubMed] [Google Scholar]
- Srivastava A., Lauwers G. Y. (2008). Gastric epithelial dysplasia: the western perspective. Dig. Liver Dis. 40, 641–649. 10.1016/j.dld.2008.02.039 [DOI] [PubMed] [Google Scholar]
- Sun J. H., Li X. L., Yin J., Li Y. H., Hou B. X., Zhang Z. (2018). A screening method for gastric cancer by oral microbiome detection. Oncol. Rep. 39, 2217–2224. 10.3892/or.2018.6286 [DOI] [PubMed] [Google Scholar]
- Takada T., Kurakawa T., Tsuji H., Nomoto K. (2013). Fusicatenibacter saccharivorans gen. nov., sp. nov., isolated from human faeces. Int. J. Syst. Evol. Microbiol. 63, 3691–3696. 10.1099/ijs.0.045823-0 [DOI] [PubMed] [Google Scholar]
- Takeshita K., Mizuno S., Mikami Y., Sujino T., Saigusa K., Matsuoka K., et al. (2016). A single species of Clostridium subcluster XIVa decreased in ulcerative colitis patients. Inflammation Bowel Dis. 22, 2802–2810. 10.1097/MIB.0000000000000972 [DOI] [PubMed] [Google Scholar]
- Wang Y., Sheng H., He Y., Wu J., Jiang Y., Tam N. F., et al. (2012). Comparison of the levels of bacterial diversity in freshwater, intertidal wetland, and marine sediments by using millions of illumina tags. Appl. Environ. Microbiol. 78, 8264–8271. 10.1128/AEM.01821-12 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang Y., Liu S., Zhang Y., Bi C., Xiao Y., Lin R., et al. (2014). Helicobacter pylori infection and gastric cardia cancer in Chaoshan region. Microbes Infect. 16, 840–844. 10.1016/j.micinf.2014.06.009 [DOI] [PubMed] [Google Scholar]
- Xu K., Jiang B. (2017). Analysis of mucosa-associated microbiota in colorectal cancer. Med. Sci. Monit. 23, 4422–4430. 10.12659/msm.904220 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yu J., Feng Q., Wong S. H., Zhang D., Liang Q. Y., Qin Y., et al. (2017). Metagenomic analysis of faecal microbiome as a tool towards targeted non-invasive biomarkers for colorectal cancer. Gut 66, 70–78. 10.1136/gutjnl-2015-309800 [DOI] [PubMed] [Google Scholar]
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Supplementary Materials
Data Availability Statement
The original contributions presented in the study are publicly available. This data can be found here: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA634837.