Canadian Journal of Gastroenterology and Hepatology
Volume 2017 (2017), Article ID 7942489, 6 pages
https://doi.org/10.1155/2017/7942489

Research Article

Helicobacter pylori Pathogenicity Factors Related to Gastric Cancer

Kianoosh Dadashzadeh,¹ Maikel P. Peppelenbosch,² and Akyala Ishaku Adamu²

¹Department of Medical Laboratory Sciences, Marand Branch, Islamic Azad University, Marand, Iran
²Erasmus MC Cancer Institute, Erasmus University Rotterdam, Rotterdam, Netherlands

Correspondence should be addressed to Kianoosh Dadashzadeh; drkianoosh@gmail.com

Received 24 July 2017; Revised 23 November 2017; Accepted 29 November 2017; Published 17 December 2017

Academic Editor: Yousuke Nakai

Copyright © 2017 Kianoosh Dadashzadeh et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. Although the causal relationship between Helicobacter pylori infection and the development of gastric cancer is firmly established, the exact nature of the pathogenicity factors of H. pylori that predispose to gastric oncogenesis remains incompletely characterized. We investigated the association between H. pylori virulence genotypes and disease in a well-characterized cohort consisting of 109 H. pylori isolates from gastric biopsies originating from patients. Methods. The prevalence of genotype was assessed by PCR and related to clinical histopathological parameters. Results. The relation of babA2 and babB negative and iceA1 positive genotype as a single genotype and the development of cases to GC was statistically significant (). The cagE, cagA, and iceA1 were found more commonly in patients with GC as compared with the other groups. The relation of the presence of iceA1 and the development of cases to GC was statistically significant (), but babA2 and babB alleles were not detected in these patients. These apparent negative associations were still statically significant (  and 0.005). Conclusion. Our results show an elevated prevalence of infection with H. pylori strains carrying known virulence genotypes with high genetic diversity. This highlights the importance of identifying gene variants for an early detection of virulent genotypes.

1. Introduction

Gastric cancer remains a prevalent disease worldwide with a poor prognosis. Helicobacter pylori plays a major role in gastric carcinogenesis. H. pylori colonization leads to chronic gastritis, which predisposes to atrophic gastritis, intestinal metaplasia, dysplasia, and eventually gastric cancer. Screening, treatment, and prevention of H. pylori colonization can reduce the incidence of gastric cancer [1]. Other interventions that may yield a similar effect, although of smaller magnitude, include promotion of a healthy lifestyle including dietary measures, nonsmoking, low alcohol intake, and sufficient physical activity [2]. Furthermore, increasing evidence suggests that host factors, including genetic make-up, are also important determinants for carcinogenesis in H. pylori infection [3]. Colonization of H. pylori has been associated with chronic gastritis because it can trigger fulminant inflammatory response which can lead to pathological conditions such as gastric carcinoma and peptic ulcer disease [4]. Consequently a clinical need exists to stratify H. pylori-infected patients with respect to their propensity to develop H. pylori-related pathology; especially for GC this is felt as a pressing concern. The importance of H. pylori virulence factors is evident from the serious clinical outcome associated with bacteria positive for the vacillating cytotoxic (vacA) and the cytotoxin-associated gene A (cagA) antigen [5]. However, these two virulence factors are insufficient to explain the variety in clinical presentation of pathology associates with H. pylori infection [6, 7]. A potential H. pylori virulence factor possibly important to explain this variance in clinical outcome is the cag pathogenicity island (cag-PAI). The cagA gene is a marker for the presence of the cag-PAI of approximately 40 kb, whose presence is associated with the more severe clinical outcomes [8, 9]. A type IV secretion system translocates cagA protein into gastric epithelial cells, where it is phosphorylated. When this modification occurs, cagA affects various cellular processes and signal transduction pathways, such as disruption of tight and adherent junctions that lead to proinflammatory and mitogenic responses: effects [8, 10]. One of the six cag-PAI genes is cagE, located in the right half of the cag-PAI, that has been shown to induce secretion of interleukin- (IL-) 8, from infected host epithelial cells [11, 12].

Another putative virulence factor is iceA, whose gene has two main allelic variants, iceA1 and iceA2. The expression of iceA1 is upregulated on contact of H. pylori with human epithelial cells and may be linked with peptic ulcer disease [16, 17]. The blood group antigen binding adhesin (babA), a 78 KDa outer membrane protein encoded by the babA2 gene, binds to Lewis b antigens and ABO antigen [18, 19]. Although three bab alleles have been identified (babA1, babA2, and babB), only the babA2 gene product is functionally active [20]. Studies in Western populations have associated the presence of the babA2 gene with gastric cancer [19, 21]. The aim of this study is to assess the genotype of H. pylori strains infecting patients with chronic gastritis through the evaluation of the prevalence of several genes coding for virulence factors.

2. Materials and Methods

This research was approved by the regional Medical Research Ethics Committee of Azad University of Medical Science on 19 Jul 2016 (number 1311/28772) and all patients provided written informed consent for this research.

This study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki as reflected in a prior approval by the institution’s human research committee.

2.1. Patients, Bacterial Strains, and Cultivation

Our cohort consisted of 109 clinical isolates of H. pylori; 49 (45%) were from females and 60 from males (55%).

From male patients (sex ratio F/M: 0.82), the average age of the patients from which the isolates were obtained was years. H. pylori was isolated employing gastric biopsies of patients presenting with gastritis, peptic ulcer, or gastric cancer. Patients were not exposed to antimicrobial agents at least one week before endoscopy was performed. Following collection, gastric biopsy samples were homogenized and cultured onto Brucella agar supplanted with 5% sheep blood and antibiotics (vancomycin, amphotericin B, and trimethoprim). Culture plates were incubated at microaerophilic condition, 37°C and high humidity for 5–7 days. Organisms were identified as H. pylori based on colony morphology, gram staining, and positive oxidase, catalase, and urease tests.

2.2. DNA Extraction from Culture

Genomic DNA of total H. pylori isolates was extracted using the QiAamp DNA mini kit (QIAGEN, Hilden, Germany) according to manufacturer’s protocol and stored at −20°C until use.

2.3. Detection of Genes

In this study, PCR was used to detect the H. pylori specific ureC gene for confirming that the cultures represented a bona-fide H. pylori isolate, and the same technique was employed to establish presence or absence of cagE, cagA, iceA1, iceA2 babA2, and babB genes.

All primer sets were selected from published literature (listed in Table 1). PCR reactions were performed in a volume of 50 μL containing 10 mmol/L Tris-HCl, 1.5 mmol/L MgCl₂, 0.2 mmol/L of each deoxynucleotide, 25 pmol of each primer, and 2.5 units of Taq polymerase (Geneone, Germany) [22, 23]. The thermal cycler program used consisted of the following steps: initial denaturation at 94°C for 3 min followed by 35 cycles of 30 seconds at 94°C (denaturation); 30 seconds at 58°C for cagA and glmM [24]; 30 seconds at 53°C for cagE; 48°C for babA2; 49°C for babB; 57°C for iceA1; and 48°C and for iceA2 all annealing steps, followed by 30 seconds at 72°C (extension step); and a final extension step was 3 min at 72°C [25].

Table 1: Primer sequences for polymerase chain reaction.

Gene
Primer
Nucleotide sequence
Size (bp)
Reference

ureC (glmM)
Hp-F
GGATAAGCTTTTAGGGGTGTTAGGGG
294
[13]

HP-R
GCTTACTTTCTAACACTAACGCGC

cagE
cagE-F
TTGAAAACTTCAAGGATAGGATAGAGC
508
[12]

cagE-R
GCCTAGCGTAATATCACCATTACCC

babA2
babA2-F
CCAAACGAAACAAAAAGCGT
271
[6]

babA2-R
GCTTGTGTAAAAGCCGTCGT

babB
babB -F
ATGAAAAAAACCCTTTTAC
496
[14]

babB-R
CGAATTGCAAGTGATGGT

cagA
cagA-F
AGGGATAACAGGCAAGCTTTTGA
352
[15]

cagA-R
CTGCAAAAGATTGTTTGGCAGA

iceA1
iceA1-F
GTGTTTTTAACCAAAGTATC
247
[13]

iceA1-R
CTATAGCCASTYTCTTTGCA

iceA2
iceA2-F
GTTGGGTATATCACAATTTAT
229
[13]

iceA2-R
TTRCCCTATTTTCTAGTAGGT

2.4. Statistics Analysis

Data were analyzed by SPSS version 16. Fisher’s exact test or the Chi-square test was used for analysis of categorical data. A value of <0.05 was considered statistically significant.

3. Results

3.1. Description of the Patient Cohort and Isolation of Study Samples

A total of 109 H. pylori samples were isolated from an initial number of 359 biopsies included in this study (yielding an apparent infection rate of 30.4%), of which 60 (55%) were derived from male patients and 49 (45%) isolates came from female patients (sex ratio F/M: 0.82). The average patients’ age at the time of endoscopy was years. From the 109 patients with established H. pylori infection, 81 patients had presented with a nonulcer dyspepsia, nineteen patients with a peptic ulcer dyspepsia, and nine patients with GC (Signet Ring Cell Carcinoma (SRCC)). There was no significant difference between the mean age and sex of patients with and without ulcers and cancer. We concluded that our cohort would enable analysis of the link between H. pylori virulence factors and clinical presentation.

3.2. The Presence of Virulence Factors Is Common in the Clinical Cohort

The PCR-based amplification showed that the cagE, babA2, and babB positive strains had a prevalence of, respectively, 55.9%, 71.7%, and 61.3% in our cohort, whereas cagA, iceA1, and iceA2 were detected in, respectively, 70.6%, 42.2%, and 13.2% of the patients included in this study (Table 2). Thus, the virulence factors selected for this study are commonly detected in our patient cohort and allow statistical analysis as to their relation to disease manifestation.

Table 2: Relationship between clinical outcome and status of cagE, babA2, babB, iceA1, iceA2, and CagA.

Genotypes
Number (%) of isolates
Total )
value

NUD
PUD
GC ()

cagE
40 (49.4%)
13 (68.4%)
8 (88.9%)
61 (55.9%)
0.198

babA2
60 (74%)
16 (84.2%)
0
76 (71.7%)
0.001

babB
53 (65.4%)
12 (63.1%)
0
65 (61.3%)
0.005

iceA1
29 (35.8%)
8 (42.1%)
9 (100%)
46 (42.2%)
0.008

iceA2
11 (13.6%)
3 (15.8%)
0
14 (13.2%)
0.779

cagA
53 (65.4%)
15 (78.9%)
9 (100%)
77 (70.6%)
0.134

NUD: nonulcer dyspepsia; PUD: peptic ulcer disease; GC: gastric cancer; Pv: value.

3.3. Specific H. pylori Virulence Factors Show Trends of Being Positively or Negatively Associated with Patient’s Clinical Presentation

In our study the frequency of cagE-positive isolates obtained from patients with nonulcer dyspepsia, peptic ulcer dyspepsia, or GC patients was 49.4%, 68.4%, and 88.9%, respectively, but this apparent positive association with more severe disease did not reach statistical significance (). The babA2 genotype was detected in 74%, 84.2%, and 0% of isolates from NUD, PUD, and GC patients. The percentage of babA2⁻ genotype within GC patients was significantly higher than that of cagA⁺ genotype ().

Also the percentage of babB⁺ was 65.4% and 63.1% for NUD and PUD cases, respectively, but for isolates from patients with GC (0%), this apparent negative association was statistically significant (). Conversely the prevalence of the iceA2 allele was observed in NUD patients (13.6%) and in PUD (15.8%) and in GC patients (0%), but no significant association was observed between iceA2 genotype and GC (). Similarly, in this study the distribution of iceA1 and clinical outcome was analyzed statistically and it was observed that the frequency of iceA1-positive isolates in NUD, PUD, and GC patients was 35.8%, 42.1%, and 100%, respectively. The relation of the presence of iceA1 and the development of cases to gastric cancer was statistically significant ().

Although the cagA allele was observed in NUD (65.4%) cases and in PUD patients (78.9%) and in GC patients (100%), there was not statistically significant association between cagA and the gastric outcomes (). A full overview of all virulence factors studied and their linkage to specific clinical manifestations is provided through Table 2.

It is apparent from our data that cagE, cagA, and iceA1 are more common in patients with gastric cancer than in the other patient groups, whereas babA2 and babB alleles were absent in patients with GC.

3.4. Combining Different Virulence Factors Allows Stratification of the Patient Cohort with respect to Patient Stratification

We examined eight different combinations based on analysis of babA2, babB, and iceA1 genotypes (positive and negative) in patients as a single genotype (Table 3). We were able to identify an association between these genotypes and clinical outcome. The frequency distributions of the combination genotypes of H. pylori showed the relation of babA2 and babB negative and iceA1 positive genotype and the development of cases to gastric cancer was statistically significant () among the patient groups. But there was not statistically significant association between other genotype combinations and the gastric cancer ().

Table 3: Combination of babA2, babB, and iceA1 genotypes and clinical outcome.

babA2
babB
iceA1
GC ()
NUD ()
PUD ()
Total ()
value

Positive
Positive
Positive
0
19
6
25
0.113

Positive
Positive
Negative
0
15
3
18
0.121

Positive
Negative
Positive
0
12
2
14
0.136

Positive
Negative
Negative
0
9
4
13
0.196

Negative
Positive
Positive
3
7
1
11
0.216

Negative
Positive
Negative
0
11
2
13
0.157

Negative
Negative
Positive
6
3
1
10
0.001

Negative
Negative
Negative
0
5
0
5
0.253

Presence of a gene = positive; absence of a gene = negative; Pv: value.

The apparent absence of babA2 and babB alleles in GC patients raises, however, hopes that larger studies may establish the usefulness of these alleles in guiding patient management.

4. Discussion

Various studies have observed substantial differences in incidence and/or severity of gastroduodenal pathologies related to H. pylori which may vary according to geographical regions [26]. Although many factors may contribute to these differences, an obvious contributing factor is the different distribution of pathogenic markers in circulating strains [27]. The clinical relevance of the putative virulence-associated genes of H. pylori and geographical region remains controversial. Other factors that influence the risks for atrophy and cancer in the presence of infection may be related to the time when infection occurred, to other environmental factors, and to the host genetic variation [28]. In particular single nucleotide polymorphisms in genes that influence bacterial handling via pattern recognition receptors appear to be involved, further strengthening the link between host risk factors, H. pylori incidence, and cancer [29]. In the present study we exploited this situation to study the relationship between selected virulence genes of H. pylori and the clinical status. Our results clearly support the notion that further studies aimed at establishing the negative predictive value of the presence of babA2 and babB alleles for GC development are warranted.

The cagE is a pathogenicity biomarker of H. pylori. A survey of previous studies suggested that the cagE prevalence is different around the world [30]. The general importance of cagE is best illustrated by its high frequency in GC patients as demonstrated by studies performed in patient populations derived from India (100%), Turkey (81.8%), and Thailand (93.8%) [31]. However, the prevalence of cagE gene in this study was only 55.9%, markedly different from the results obtained in the aforementioned countries [32]. In the present study cagE-positive isolates were slightly more detected in isolates from peptic ulcer dyspepsia (PUD) patients (68.4%), but the potential significance of this finding, if any, remains to be established. The prevalence of cagA gene in our cohort is 70.6%, which resembles the situation in Western countries (Yamaoka et al., 2002), but is markedly lower than that observed in East Asian countries where cagA is present in more than 90% of cases [32]. Like cagE, cagA-positive isolates were enriched in samples obtained from peptic ulcer dyspepsia patients, albeit not in a statistically significant manner. Nevertheless, our findings support previous studies [32] (Wu et al., 2003) and should prove interesting in including our data in a meta-analysis of virulence genes in this respect. Our results show that the prevalence of iceA1 and iceA2 genes in isolates was 42.2% and 13.2%, respectively. These results are in agreement with previous studies showing that the iceA1 gene is prevalent in Japanese, Korean, and Dutch patients [13] (Ito et al., 2000; Shiota et al., 2013); conversely the iceA2 allele was predominant in the United States and Colombia. In our cohort, the relation of the presence of iceA1 and the development of cases to gastric cancer was statistically significant (). But our data showed that there was no significant association between iceA2 and GC compared with PUD or NUD. However, several studies have reported different results, as the iceA2 gene was detected to be predominant genotype in these studies (Aghdam et al., 2014; Biernat et al., 2014).

The babA is one of the mediators for the attachment to gastric cells by H. pylori [33]. More recent analysis of babA2 as a virulence marker has produced conflicting data on the usefulness of babA2 expression in predicting clinical outcome, which is most likely dependent on the geographic origin of the H. pylori strains. Survey of previous studies on Portuguese, Thai, and India populations showed that babA2 is not a marker for peptic ulcer disease or gastric cancer [12, 26, 34]. However, several studies have reported different results for strains isolated from Turkey or Germany [26, 35]. Our study suggests that babA2, “although quite prevalent,” is associated with reduced propensity to develop GC and is thus associated with less oncogenic H. pylori. Similar results were obtained concerning babB.

Our results showed the relation of babA2 and babB negative and iceA1 positive genotype and the development of cases to gastric cancer was statistically significant. Further studies are required to determine the functions of babA2 and babB and their relationship with disease outcome and whether the presence of these alleles indicates the presence of bacteria unlikely to confer progression towards GC.

Disclosure

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

Conflicts of Interest

The authors certify that they report no conflicts of interest.

Acknowledgments

The authors would like to acknowledge Marand Branch, Islamic Azad University, and Erasmus MC Cancer Institute, Erasmus University Rotterdam, Netherlands, for their support of this research.

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