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. 2014 May 13;2014:142980. doi: 10.1155/2014/142980

Prevalence and Correlation with Clinical Diseases of Helicobacter pylori cagA and vacA Genotype among Gastric Patients from Northeast China

Faisal Aziz 1, Xin Chen 2, Xuesong Yang 1, Qiu Yan 1,*
PMCID: PMC4052682  PMID: 24949419

Abstract

Helicobacter pylori vacA and cagA genes have significant genetic heterogenicity, resulting in different clinical outcomes. Northeast part of China has reported high prevalence of H. pylori infections and gastric cancer. Hence, we investigated the H. pylori cagA and vacA genotypes with clinical outcomes in Northeast China. Gastric tissue samples (n = 169), chronic gastritis (GIs), gastric ulcer (GU), and gastric cancer (GC) were analysed for 16S rRNA ureA, cagA, and cagA genotypes by PCR. A total of 141 (84%) cases were found positive for H. pylori by 16S rRNA and ureA. GC showed high H. pylori infection (93%) compared with GIs (72%) and GU (84%). The vacAs1am1 was highly found in GC (40%) and GU (36%), vacAs1am2 in GIs (33%), vacAs1bm1 (14%) and vacAs1bm2 (8%) in GU cases, and s2m1 in normal cases (33%), while vacAs1cm1 showed low frequency in GIs (2%) and GU (3%) and GC showed negative result. The East-Asian cagA strain was highly observed in GC (43%), as compared to GIs (41%) and GU (20%). The East-Asian cagA/vacAs1am1 was significantly higher in GC (23%) than in GU (22%) and GIs (145) patients. The East-Asian type cagA with vacAs1a and vacAm1 is the most predominant genotype in H. pylori strains of Northeast China.

1. Introduction

Helicobacter pylori is a causative agent of gastritis (GIs) and gastric ulcer (GU) diseases, which leads to the development of gastric cancer (GC). Hence it is classified as class I carcinogen by the World Health Organization. Developing countries have H. pylori prevalence rate of 80% as compared to developed countries (20–50%) [1, 2]. Genetic diversity may play an important role in genotypic variation of H. pylori, which makes it more virulent with diverse pathogenicity [3]. H. pylori carries different virulence factors, such as urease, flagellar, vacuolating cytotoxin A (VacA), and cytotoxin-associated gene A (CagA), that play an important role in invasion, colonization, and cell proliferation [4, 5]. High genetic variations of cagA and vacA gene are associated with more severe infectionsof H. pylori [6].

VacA toxin encoded by vacA gene induces cytoplasmic vacuoles and increases permeability, which leads to the damage of gastric epithelial cells [7]. The vacA gene exhibits significant allelic variation in the signal (s) and middle (m) regions. The s-region consists of two major subtypes (s1 and s2) and s1-region has further three subtypes (s1a, s1b, and s1c), whereas m-region designates m1 and m2 subtypes [8, 9]. A pleomorphic combination of s and m regions affects the vacuolating activity of vacA gene [10]. Different genotypic combination of vacA region results in different pathogenicity level as follows: s1am1 and s1bm1 produce high amount of toxin and are considered the most virulent as compared to s1m2, which produces moderate vacuolating toxins [11, 12]. However, s2m1 and s2m2 are considered less toxic because of their inability to form vacuoles [9]. The s1am1 and s1bm1 subtypes are frequently reported in acute gastritis (GIs), peptic ulcer, and gastric cancer patients, while s2m1 and s2m2 have been reported in the gastric ulcer (GU) patients [9, 13].

Cytotoxin-associated gene A (CagA) is a cytotoxin-associated protein, linked with peptic ulcer and gastric cancer [6]. H. pylori strains can be grouped as Western and East-Asian subtypes based on polymorphism in 3′ repeat region of the cagA gene, which results in the variation of clinical outcome in East-Asian and Western countries. 3′ region of the cagA gene consists of two types of repeat regions as 57 bp regions (first repeat region; FR region) and 102 bp regions (Western-type second repeat region; WSR region) [14]. The FR region of East-Asian strains has similar 57 bp region to Western type, but the repeat region of 162 bp was completely different [15]. East-Asian type of cagA is more prevalent in East-Asian countries and is more commonly associated with gastric cancer mortality worldwide than Western subtypes [16].

China has high rate of H. pylori infections. Some studies reported high prevalence of the vacA and cagA genotypes from South China. There is little data present regarding the H. pylori vacA and cagA genotypes and their association with clinical outcomes in Northeast China, where the prevalence of H. pylori infection and gastric cancer is much higher than in the south part of China [17]. The cagA and vacA genotyping is useful to determine molecular epidemiological status of H. pylori strain in the northeast part of China. Hence, we aim to evaluate the frequency of vacA and cagA genotypes with their clinical outcomes in gastric patients from the northeast part of China. This study helps to characterize the more prevalent strain of H. pylori in Northeast China, which is useful in diagnosis and treatment of gastric patients.

2. Materials and Methods

2.1. Patients and Gastroendoscopy

All gastric patients underwent gastroendoscopy and examination at Dalian 1st & 2nd Affiliated Hospital, Dalian, China. Gastric tissues were obtained from the antral and corpus part of the stomach during gastrointestinal endoscopy. Gastric patient's tissue samples were characterized as chronic gastritis (GIs), gastric ulcer (GU), and gastric cancer (GC). Clinical diseases were diagnosed by endoscopic appearance as “normal” in cases of intact mucosa, chronic gastritis, gastric ulcer, and gastric cancer. All the samples were processed and frozen at −20°C until tested. Fresh surgical gastric cancer tissues were collected in transport media and analyzed in laboratory. All gastric samples collected from the patients and the research protocols were in accordance with the Institutional Review Board of Dalian Medical University.

2.2. DNA Extraction

The SDS-PK method was adopted to extract DNA from gastric patient's tissues. Gastric tissues were crushed manually and resuspended in 20 μL of 10% SDS, 80 μL of proteinase K buffer (0.5 M EDTA and 4 M NaCl, pH 7.5), 40 μL of proteinase K (10 mg/mL) and make final volume up to 380 μL with sterile water. The mixture was incubated at 55°C overnight. The following day, 100 μL of 6 M NaCl was added, followed by centrifugation at 14,000 rpm for 5 min and the supernatant was separated in new tube. To precipitate the DNA, 500 μL of absolute isopropanol was added, mixed well and centrifuged for 5 minutes at 9000 rpm. DNA pellet was washed with 70% ethanol and air dried. The pellet was resuspended in 50 μL of TE buffer (10 mM Tris and 1 mM EDTA; pH 8.0). Samples were stored at −20°C until used.

2.3. Polymerase Chain Reaction (PCR)

PCR was performed to detect H. pylori by using specific primers. Target gene, amplicon size, primer names, and sequences are shown in Table 1. For PCR amplification, 1-2 μg of DNA samples was added to a PCR mixture containing 20 pmol forward and reverse primers, 1.5 mM MgCl2, 1.5 U of Taq polymerase (Takara, Japan), 2.5 μL PCR buffer, and 200 μM of dNTPs to the total volume of 25 μL. PCR amplification was performed under the following conditions: initial denaturation at 95°C for 3 min followed by 30 cycles of denaturation at 95°C for 30 s, annealing for 30 s (Table 1), polymerization at 72°C for 30 s, and final polymerization at 72°C for 5 min (Bio-Rad Thermocycler). The PCR reaction products were electrophoresed on 1.5% agarose gel with 2000 bp DNA ladder (Takara, Japan) and the bands were visualized by ethidium bromide staining, followed by analysis with Quantity One software (Bio-Rad, USA). H. pylori strain was detected by using specific primers targeting 16S rRNA and ureA genes (Table 1). The cagA and vacA statuses were determined from H. pylori positive samples by PCR using their respective primers as described in Table 1.

Table 1.

Primer sets used for genotyping H. pylori by PCR.

Target site Amplicon size (bp) Primer names and sequences Annealing temperature References
16S rRNA 138 HP-F (5-GCGACCTGCTGGAACATTAC-3)
HP-R (5-CGTTAGCTGCATTACTGGAGA-3) 		60°C Gramley et al., 1999 [18]
UreA 411 HPU1-F (5-GCCAATGGTAAATTAGTT-3)
HPU1-R (5-CTCCTTAATTGTTTTTAC-3) 		45°C Smith et al., 2004 [19]
vacAs1a 190 AA1-F (5-GTCAGCATCACACCGCAAC-3)
AA1-R (5-TGCTTGAATGCGCCAAAC-3) 		56°C Atherton et al., 1995 [9]
vacAs1b 187 SS3-F (5-AGCGCCATACCGCAAGAG-3)
SS3-R (5-CTGCTTGAATGCGCCAAAC-3) 		56°C Atherton et al., 1995 [9]
vacAs1c 213 S1C-F (5-CTCGCTTTAGTGGGGCTA-3)
S1C-R (5-CTGCTTGAATGCGCCAAAC-3) 		56°C Yamaoka et al., 1999 [20]
vacAs2 199 SS2-F (5-GCTAACACGCCAAATGATCC-3)
SS2-R (5-CTGCTTGAATGCGCCAAAC-3) 		56°C Atherton et al., 1995 [9]
vacAm1/m2 570/645 VAG-F (5-CAATCTGTCCAATCAAGCGAG-3)
VAG-R (5-GCGTCTAAATAATTCCAAGG-3) 		57°C Yamaoka et al., 1999 [20]
cagA 189 CAGA-F (5-TTGACCAACAACCACAAACCGAAG-3)
CAGA-R (5-CTTCCCTTAATTGCGAGATTCC-3) 		62°C van Doorn et al., 1998 [21]
Western type cagA Variable CAGT-F (5-ACCCTAGTCGGTAATGGG-3)
CAGW-R (5-TGCCCTACAMCACCSAAACCAC-3)
CAGW-F (5-AAAAATTGACCRACTCAATC-3)
CAGT-R (5-GCTTTAGCTTCTGAYACYGC-3)		 61°C Yamaoka et al., 1999 [22]
East-Asian type cagA Variable CAGT-F (5-ACCCTAGTCGGTAATGGG-3)
CAGJ-R (5-GCAATTTTGTTAATCCGGTC-3)
CAGJ-F (5-GCATCAGCAGGTAAAGGAGT-3)
CAGT-R (5-GCTTTAGCTTCTGAYACYGC-3)		 52°C Yamaoka et al., 2000 [14]
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2.4. Statistical Analysis

Categorical data were analysed by using chi-square test. P value of less than 0.05 was regarded as significant. The statistical software GraphPad prism 5.03 was used for analyzing the data.

3. Results

3.1. Gastric Patients History

This study was designed to determine the frequency of cagA and vacA genotypes in gastritis (GIs), gastric ulcer (GU), and gastric cancer (GC) patients from the northeast part of China. A total of 169 gastric patients, 63 males and 106 females ranging in age from 10 to 80 years (average age of 56.32 ± 2.394), were included in the study. Among 169 cases, 51 (30.17%) were diagnosed as GIs, 36 (21.30%) were diagnosed as GU, and 73 (43.19%) samples were regarded as GC, while 9 (5.32%) were normal cases.

3.2. Detection of H. pylori Infection

Helicobacter pylori specific genes (ureA and 16S rRNA) revealed that (141) 84% of samples were H. pylori positive. These included 6 (54%) normal, 37 (72%) GIs cases, 30 (84%) GU and 68 (93%) of the H. pylori positive GC cases (Table 2).

Table 2.

Distribution of cagA and vacA genotypes with diseases outcomes.

Description Total n = 169 Normal n = 9 Chronic gastritis n = 51 Gastric ulcer n = 36 Gastric cancer n = 73
N % N % N % N % N %
H. pylori positive 141 84 6 54 37 72 30 84 68 93
cagA positive 86 61 1 11 21 41 18 50 46 63
(i) Western type cagA 27 19 1 11 2 4 11 31 13 18
(ii) East-Asian type cagA 59 42 0 0 21 41 7 20 31 43
vacAs1am1 51 36 0 0 9 18 13 36 29 40
vacAs1am2 24 17 1 11 17 33 2 6 4 6
vacAs1bm1 7 5 0 11 1 2 5 14 1 1
vacAs1bm2 7 5 0 0 2 4 3 8 2 3
vacAs1cm1 2 2 0 0 1 2 1 3 0 0
vacAs2m1 12 6 3 33 9 18 0 0 0 0
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3.3. Detection of the H. pylori vacA Genotyping and Clinical Manifestations

Among 141 H. pylori positive gastric tissues, we determined six different allelic variants of the vacA gene in H. pylori positive gastric tissues. Among H. pylori positive gastric tissues, 51 (36%) were positive for vacAs1am1, 24 (17%) for vacAs1am2, and 7 (5%) for vacAs1bm1, whereas 7 (5%) were vacAs1bm2, 2 (2%) were vacAs1cm1, and 12 (6%) were positive for vacAs2 m1. As shown in Table 2, detailed analysis revealed that 29 (40%) of the GC cases had s1am1 genotype (P < 0.05), which was significantly higher than GIs (9) (18%), GU (13) (36%), and normal cases (P < 0.05). Respective percentages in GIs, GU, and GC tissue samples of s1am2 were high (33%, 6%, and 6%) as compared to s1mb1 (2%, 14%, and 1%) and s1bm2 (4%, 8%, and 3%) vacA genotype. s1cm1 was observed in GIs and GU, while s2m1 was found only in normal and GIs cases (Table 2).

3.4. H. pylori cagA Genotyping with Clinical Association

We found that the prevalence of cagA gene was 86 (61%), out of which 27 (19%) were Western types and 59 (42%) were East-Asian types (Table 2). All negative tissues for 16S rRNA gene were also negative for cagA and vacA genes. In detailed analysis, Western-type cagA gene was observed in 4% of the patients with GIs, 31% with GU, and 18% with GC (P < 0.05), whereas 11% of the normal cases were also positive. East-Asian type strains were observed in 41% of the patients with GIs, 20% with GU, and 43% with GC (P < 0.05) (Table 2).

3.5. Combinational Study of H. pylori vacA with cagA Genotype

In combinational analysis of vacA strain with Western type of cagA, as shown in Table 3, we found that 17 (20%) of the H. pylori strains have vacAs1am1/cagA combination, while 7 (8%) of H. pylori strains have vacAs1am2/cagA. In contrast, vacAs1bm1/cagA and vacAs1bm2/cagA showed low number of H. pylori strains of 2 (2%) and 1 (1%), respectively. The vacAs1cm1/cagA and vacAs2cm1/cagA were not found in H. pylori positive strains. In detailed analysis, 6 (17%) of GU patients have vacAs1am1, 2 (6%) vacAs1am2, 1 (3%) vacAs1bm1, and 1 (3%) vacAs1bm2. Gastric cancer patients showed a number of H. pylori strains as follows: 9 (12%) have vacAs1am1, 5 (7%) vacAs1am2, and 1 (1%) vacAs1bm1, and vacAs1bm2 has no case reported. GIs patients showed only 1 (2%) vacAs1am1 combinational H. pylori strain (Table 3). In contrast, combinational analysis of East-Asian type of cagA with vacA genes demonstrated more frequently H. pylori strains of vacAs1am1/cagA 32 (37%) and vacAs1bm2/cagA 19 (22%) than vacAs1bm1/cagA 6 (7%) and vacAs1bm2/cagA 2 (2%) (P < 0.05). However, vacAs1cm1/cagA and vacAs2cm1/cagA were not found in H. pylori positive strains. Distribution analysis further showed that GIs patients have 7 (14%) s1am1/cagA, 4 (18%) vacAs1am2/cagA, and 3 (6%) vacAs1bm1/cagA H. pylori positive strains. In GU patients, we found 8 (22%) vacAs1am1/cagA and 2 (6%) vacAs1am2/cagA combinations in H. pylori positive strain. In contrast, GC patients showed high number of vacAs1am1/cagA 17 (23%) and vacAs1am2/cagA 13 (18%) H. pylori positive strains. However, combinations of vacAs1bm1/cagA and vacAs1bm2/cagA in GC were found in low percentages as 3 (4%) and 2 (3%), respectively (P < 0.05) (Table 3).

Table 3.

Combinational study between cagA and vacA genotypes with diseases outcomes.

Description Total n = 169 Normal n = 9 Chronic gastritis n = 51 Gastric ulcer n = 36 Gastric cancer n = 73
N % N % N % N % N %
Total H. pylori positive 141 84 6 67 37 73 30 83 68 93
Total cagA positive 86 61 1 11 21 41 18 50 46 63
Western cagA/vacAs1am1 17 20 1 11 1 2 6 17 9 12
Western cagA/vacAs1am2 7 8 0 0 0 0 2 6 5 7
Western cagA/vacAs1bm1 2 2 0 0 0 0 1 3 1 1
Western cagA/vacAs1bm2 1 1 0 0 0 0 1 3 0 0
Western cagA/vacAs1cm1 0 0 0 0 0 0 0 0 0 0
Western cagA/vacAs2m1 0 0 0 0 0 0 0 0 0 0
East-Asian cagA/vacAs1am1 32 37 0 0 7 14 8 22 17 23
East-Asian cagA/vacAs1am2 19 22 0 0 4 18 2 6 13 18
East-Asian cagA/vacAs1bm1 6 7 0 0 3 6 0 0 3 4
East-Asian cagA/vacAs1bm2 2 2 0 0 0 0 0 0 2 3
East-Asian cagA/vacAs1cm1 0 0 0 0 0 0 0 0 0 0
East-Asian cagA/vacAs2m1 0 0 0 0 0 0 0 0 0 0
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4. Discussion

Several studies have focused on the diversity of the H. pylori vacA and cagA virulence genotypes. However, there is little information available related to the frequency of H. pylori vacA and cagA genotypes in Northeast China. In the present study, we determined the vacA and cagA statuses among gastritis (GIs), gastric ulcer (GU), and gastric cancer (GC) patients' samples. The prevalence of H. pylori was found to be considerably high in the Pacific Asian countries: for example, China has high prevalence of H. pylori infection and gastric cancer compared to the rest of the world [23]. In this study, we observed high prevalence of H. pylori infection (84%) in gastric patients from 2011 to 2013 (Table 2). Previous studies from the northern and central part of China reported H. pylori prevalence rate of 58% from 1990 to 2002 [24]. In comparison, other countries in the same region such as Singapore, Malaysia, Taiwan, and Vietnam showed low H. pylori prevalence [23]. These results indicate that H. pylori infections have epidemiological diversity, which show different prevalence in different geographical locations.

Genetic variations of the vacA genotype make the requirement to investigate clinical outcomes, which is directly linked with the virulence status of H. pylori. vacA gene shows variation in the signal and midregion that determine H. pylori cytotoxin activity. In our study, we predominantly found vacA subtypes of s1a, m1, and m2, while s1b and s1c were found in low frequency (Table 2). Our results showed comparable vacA frequency rates in China with those from other reported data; for example, Hou et al. reported that s1a and m2 were more prevalent vacA genes in China [25], while Mishra et al. found that vacAs1a and vacA m1 were major subtypes in India [26]. Previously, studies carried out on the Chinese population have reported high prevalence of s1a subtype, while s1b subtype is rarely found in East-Asian countries [27–29]. In another study, s1b subtype was not detected in Hong Kong vacA positive H. pylori infected patients, while m2 subtype was found in high frequency of 67%. Similarly, we also rarely observed s1c subtype, while s1c was exclusively found from East-Asian isolates [30]. In our study, we found that vacAs1am1 (36%) is a more prevalent genotype as compared to the vacAs1am2 (17%), while slbm1 (5%), s1bm2 (5%), s1 cm1 (2%), and s2 m1 (6%) genotypes were found in low frequency (Table 2). Previous study showed high prevalence of vacA genotype; Ahmad et al. reported the prevalence of s1b/m2 (54.5%) in adult dyspeptic patients from Pakistan [8]. According to Mishra et al., vacAs1a/m1 (53.2%) has predominant genotype in India [26]. However, Hou et al. reported high (90.5%) frequency of vacA genotype in China [25]. vacAs1a and s1b genotypes are prominently associated with high toxin activity and linked to clinical outcome of the diseases. In a detailed analysis of vacA genotype, we found high frequency of s1am1 in GU (36%) and GC (40%) patients, while s1am2 was highly found in GIs (33%) and normal cases (11%). s1bm1 and s1bm2 showed high frequency in GU (14%) and (8%), respectively, while s2m1 was found only in normal (33%) and GIs patients (18%) (Table 2). Our results indicate diverse epidemiology of gastritis patients containing vacAs2 m1 genotype in the northeast part of China. The vacAs1 and vacAm1 bearing H. pylori strains have been associated with increased virulence capability and higher gastric epithelial damage and ulceration than s2 and m2 strains [31].

H. pylori CagA induces pathological alterations, which is closely associated with development of gastritis, gastric ulcer, and gastric cancer. H. pylori cagA-positive strains are more virulent causing higher levels of gastric mucosal inflammation in gastritis and gastric cancer [32, 33]. In present study, about 61% of strains were cagA positive, which comprises 19% Western-type cagA and 42% East-Asian type cagA strain. Conversely, our results showed low prevalence of cagA gene in gastric patients from Northeast China (Table 2). Previous studies reported high prevalence (93.9%) of cagA-positive H. pylori strain in China [34–36]. According to Hou et al., H. pylori cagA has high prevalence of 93.2% in Shanghai (the southern part of China) [25]. The neighboring countries of China were also reported to have high prevalence of cagA; for example, India has high cagA prevalence of 96.2% [26]. Rasheed et al. reported that 52% of H. pylori strains carried cagA gene with the positivity rate of 80% in GC, 74% in GU, 63% in duodenal ulcer (DU), and 11% in normal cases from Pakistan [37]. Conversely, in Western Europe, cagA-positive strains are less prevalent and more frequently found in GU or GC patients [38].

In combinational analysis of vacA and cagA genotypes, we found that H. pylori strains have high frequency of vacAs1am1 (37%) or vacAs1am2 (22%) with East-Asian type cagA genotype (Table 3). Rasheed et al. reported high frequency of cagA (61.9%) with predominant vacAs1a/m2 genotype in H. pylori infected gastric tissues of Pakistani children [37]. A previous study reported significantly higher percentages of cagA-positive and vacAs1 and vacAm1 genotypes with high risk for GC [39]. A recent study conducted in China found no differences in the distribution of cagA-positive and vacAm genotypes [40]. Our results showed high prevalence of vacAs1 m1 and East-Asian type cagA-positive H. pylori strain in gastric cancer patients.

These results might have useful roles in clinical appreciation so as to categorize the specific and most prevalent biomarkers of H. pylori strains in the northeast part of China that will be helpful to precisely diagnose large population of gastric cancer patients. H. pylori has high capability of developing antibiotic resistance, which make difficult to treat H. pylori by conventional antibiotics; however, targeted marker therapy leads to effective H. pylori treatment and helps reduce antibiotic resistance.

In conclusion, the present study showed high diversity of the H. pylori vacA and cagA genotyping. We have reported high frequency of East-Asian type cagA with predominant vacAs1am1 and vacAs1am2 genotypes in gastric ulcer, gastritis, and gastric cancer patients. This study helps to effectively diagnose and treat gastric patients by understanding the trend of H. pylori infection in Northeast China.

Acknowledgments

The project was supported by the China 973 Grant no. 2012CB822100 and the National Natural Science Foundation of China Research Grants nos. 30672753 and 31270866.

Ethical Approval

The project was approved by the Dalian Medical University Ethics Committee in China.

Conflict of Interests

The authors declare that they have no conflict of interests.

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