Skip to content

Advertisement

  • Research article
  • Open Access
  • Open Peer Review

The Helicobacter pylori duodenal ulcer promoting gene, dupAin China

  • 1,
  • 1,
  • 1,
  • 1,
  • 1 and
  • 1Email author
BMC Gastroenterology20088:49

https://doi.org/10.1186/1471-230X-8-49

©  Zhang et al; licensee BioMed Central Ltd. 2008

  • Received: 30 May 2008
  • Accepted: 25 October 2008
  • Published:
Open Peer Review reports

Abstract

Background

The prevalence of H. pylori is as high as 60–70% in Chinese population. Although duodenal ulcer and gastric cancer are both caused by H. pylori, they are at opposite ends of the spectrum and as such are considered mutually exclusive. Duodenal ulcer promoting (dupA) gene was reported to be associated with duodenal ulcer development. The aim of this study was to determine the prevalence of dupA gene of Helicobacter pylori in patients with various gastroduodenal diseases and to explore the association between the gene and other virulence factors.

Methods

H. pylori were isolated from gastric biopsies of patients with chronic gastritis, duodenal ulcer (DU), gastric ulcer (GU), or non-cardia gastric carcinoma. The dupA, cagA, vacA, iceA and babA2 genotypes were determined by polymerase chain reaction. Histological features of gastric mucosal biopsy specimens were graded based on the scoring system proposed by the updated Sydney system. IL-1β polymorphism was investigated using restriction fragment length polymorphism.

Results

Isolates from 360 patients including 133 with chronic gastritis, 101 with DU, 47 with GU, and 79 with non-cardia gastric carcinoma were examined. The dupA gene was detected in 35.3% (127/360) and the prevalence DU patients was significantly greater than that in gastric cancer or GU patients (45.5% vs. 24.1% and 23.4%, P < 0.05). Patients infected with dupA-positive strains had higher scores for chronic inflammation compared to those with dupA-negative strains (2.36 vs. 2.24, p = 0.058). The presence of dupA was not associated with the cagA, vacA, iceA and babA 2 genotypes or with IL-1β polymorphisms.

Conclusion

In China the prevalence of dupA gene was highest in DU and inversely related to GU and gastric cancer.

Keywords

  • Gastric Cancer
  • Gastritis
  • Duodenal Ulcer
  • Gastric Ulcer
  • Intestinal Metaplasia

Background

The morbility and mortality of gastric cancer rank the third in Chinese population and it accounts for around 0.3 million deaths per year. There is considerable interest in identifying virulence factors that are Helicobacter pylori disease specific (eg, related to duodenal ulcer and not gastric cancer). Several virulence factors such as the cag pathogenicity island, vacA, oipA and babA have been described and have been associated with an increase in the risk of both gastric cancer and duodenal ulcer disease [1–4]. They have also been associated with an increase in mucosal inflammation which is thought to underlie both duodenal ulcers and gastric cancer. Duodenal ulcer is associated with corpus sparing gastritis and gastric cancer with corpus atrophy and are clinically mutually exclusive diseases.

One problem that has possibly complicated identification of definite disease-specific H. pylori virulence factors is the considerable geographic diversity in the prevalence of H. pylori virulence factors. For example, in some regions, (ie, East Asia) the vast majority of strains have similar if not identical patterns of virulence factors such that potentially important factors can best be identified in regions where there is considerable diversity among strains. For example, the associations between the cag pathogenicity island, vacA, oipA and babA and enhanced mucosal inflammation, gastric cancer and peptic ulcer were identified and confirmed in Western countries where there is considerable strain diversity [5–9]. Polymorphism of interleukin-1β was reported to be an important host factor that increases the risk gastric cancer [10, 11].

The duodenal ulcer promoting (dupA) gene was the first putative disease specific marker whose association was described using strains obtained from in both Asian (Japan and Korea) and Western (Colombia) regions [12]. dupA is though to be a vir homologue and the gene encompasses the sequences jhp917 and jhp918 as describe in strain J99. The original description of dupA reported that its presence was associated with increased mucosal neutrophil infiltration and its presence was inversely related to mucosal atrophy and gastric cancer. The aims of this study were to test the hypothesis regarding the association of dupA with the clinical outcome in a different population (ie, Chinese patients) as well as to test whether there were associations between dupA and previously described virulence factors or with proinflammatory interleukin-1β (IL-1β) polymorphisms.

Methods

Patients

Inclusion criteria included patients with documented H. pylori infection as evidence by positive H. pylori culture who underwent gastric endoscopy with biopsy specimens for H. pylori culture between January 2006 to August 2007 in the Department of Gastroenterology, Shanghai Renji Hospital, Shanghai, China. The patients involved were from 23 cities of China. All patients had simple H. pylori gastritis or a clinical H. pylori-related disease including: duodenal ulcer (DU), gastric ulcer (GU) or non-cardiac gastric adenocarcinoma. Simple H. pylori gastritis was defined as the presence of typical histological inflammation of gastric mucosa without peptic ulcer, gastric cancer or esophageal disease. Duodenal ulcers and gastric ulcers were identified endoscopically as active ulcers or ulcer scars. Exclusion criteria included negative results for culture, the presence of both duodenal and gastric ulcers or prior treatment for H. pylori infection. Patients with other primary malignancies, inflammatory diseases such as rheumatoid arthritis, or prior gastric surgery were also excluded. Written informed consent was obtained from all patients and the protocol was approved by the Institutional ethics committee of the Shanghai Renji Hospital based on the Helsinki Declaration.

Biopsy protocol

Three biopsy specimens were taken from the greater curvature of the antrum in patients of gastritis, DU and GU. One specimen was used for H. pylori culture and two for histological examination. For gastric cancer and GU group one normal-appearing biopsy was taken culture and other 3 or 4 biopsies for diagnosis.

H. pyloriculture from biopsy specimens

The biopsies was inoculated onto brain heart infusion agar plates (Difco Laboratories, Detroit, USA) supplemented with 7% sheep blood, vancomycin (10 mg/mL), trimethoprim lactate (5 mg/L), amphoteracin-B (5 mg/mL) and of polymixin-B (2500 units/mL) and incubated in a microaerobic atmosphere (10%CO2, 85%N2, 5%O2) at 37°C for 5–7 days with 95% humidity. The organisms were identified as H. pylori by Gram staining, colony morphology and positive oxidase, catalase and urease reactions. Bacteria were sub-cultured using the same conditions.

Histological evaluation

Gastric mucosal biopsy specimens were fixed in 10% buffered formalin, embedded in paraffin, cut in sequential 4-μm sections, stained with Haematoxylin & Eosin and modified Giemsa stain. One experienced pathologist blinded to the patient's clinical diagnosis examined the samples. Each specimen was scored for chronic inflammation, neutrophil infiltration, intestinal metaplasia and atrophy. Histological features were graded with the visual analog scale system graded from 0 (absent/normal) to 3 (maximal intensity) according to the scheme proposed by the updated Sydney system [13]. Each biopsy site was scored individually and the median score was determined for the all biopsy sites.

DNA Extraction and PCR amplification

Bacterial chromosomal DNA was isolated from confluent plate cultures expanded from a single colony using the QIAamp Tissue kit (QIAGEN Inc. Santa Clarita, CA) according to the manufacturer's instructions. The isolated DNA was used as the template for PCR amplification. The 16S rRNA gene was amplified to confirm the presence of the isolated H. pylori strains. For analyses of the presence of target genes, dupA, cagA, babA2, iceA and vacA genotypes, H. pylori DNA were amplified using specific oligonucleotide primers described previously [Table 1] [14–18]. Primers of jhp0917 yielded a fragment of approximately 307 bp and primers of jhp0918 yielded a fragment of approximately 276 bp. PCR amplification was performed with a DNA Engine (MJ Research Inc., Watertown, Mass.) for 35 cycles consisting of 1 min at 95°C, 1 minute at 52°C and 1 minute at 72°C. The final cycle included a 7 min extension step to ensure full extension of the PCR products. The products of amplification were subsequently electrophoresed in 1.5% agarose gel stained with ethidium bromide to visualize the presence of amplified genes. H. pylori strain 26695 (ATCC700392) and J99 (ATCC700824) were used as negative and positive controls. The presence of dupA gene was defined as positive PCR results for both jhp0917 (product of 307 bp) and jhp0918 (276 bp product). If the PCR results yielded negative results, the isolate was considered negative for dupA.
Table 1

Primers used in the study

Gene

Primer Sequences

Reference

16S rRNA

5'-GCGCAATCAGCGTCAGGTAATG-3' 5'-GCTAAGAGATCAGCCTATGTCC-3'

14

cagA-3'region

5'-ACC CTA GTC GGT AAT GGG TTA-3' 5'-GTA ATT GTC TAG TTT CGC-3'

15

babA2

5'-AAT CCA AAA AGG AGA AAA AGT ATG AAA-3' 5'-TGT TAG TGA TTT CGG TGT AGG ACA-3'

17

iceA1

5'-GTG TTT TTA ACC AAA GTA TC-3' 5'-CTA TAG CCA STY TCT TTG CA-3'

18

iceA2

5'-GTT GGG TAT ATC ACA ATT TAT-3' 5'-TTR CCC TAT TTT CTA GTA GGT-3'

18

vacAs1a

5'-GTC AGC ATC ACA CCG CAA C-3' 5'-CTG CTT GAA TGC GCC AAA C-3'

16

vacAs1b

5'-AGC GCC ATA CCG CAA GAG-3' 5'-CTG CTT GAA TGC GCC AAA C-3'

16

vacAs2

5'-GCT AAC ACG CCA AAT GAT CC-3' 5'-CTG CTT GAA TGC GCC AAA C-3'

16

vacAm1

5'-GGT CAA AAT GCG GTC ATG G-3' 5'-CCA TTG GTA CCT GTA GAA AC-3'

16

vacAm2

5'-GGA GCC CCA GCA AAC ATT G-3' 5'-CAT AAC TAG CGC CTT GCA C-3'

16

jhp0917

5'-TGG TTT CTA CTG ACA GAG CGC-3' 5'-AAC ACG CTG ACA GGA CAA TCT CCC-3'

12

jhp0918

5'-CCT ATA TCG CTA ACG CGC TCG C-3' 5'-AAG CTG AAG CGT TTG TAA CG-3'

12

IL-1β polymorphism

The genomic DNA was purified from 5 ml samples of peripheral bloods using Wizard Genomic DNA Purification kit (Promega) according to the manufacture's instruction. The polymorphisms (IL-1β-31 and IL-1β-511) were investigated using restriction fragment length polymorphism analysis of polymerase chain reaction products as previously studied [19]. PCR products were digested by restriction endonucleases (Alul for IL-1β-31 and Ava1 for IL-1β-511) and visualized by electrophoresis on a 2.5% agarose gel stained with 0.1% ethidium bromide.

Data analysis

Chi-squire test and Fisher's exact test was used for univariate analysis. The significance of differences in histological features between dupA positive and negative groups was determined by comparing individual grades using the Mann-Whitney U test. P < 0.05 was taken to denote significance.

Results

H. pylori isolates were obtained from 360 patients (235 men and 125 women; mean age of 53 years; range 17–90 years). The proportion of men was higher in the GU than in other three groups (p = 0.03) and the mean age of the patients with DU was lower than those with GU gastric cancer or gastritis (p = 0.03) (Table 2).
Table 2

Patients' characteristics in the study

 

Men (%)

Mean age (range, years)

DU (n = 101)

59 (58%)

41 (17–72)

Gastritis (n = 133)

80 (61%)

59 (18–81)

Gastric cancer (n = 79)

54(68%)

59 (34–90)

GU (n = 47)

42 (89%)

58 (32–83)

Detection of the dupAgene and clinical manifestations

Overall, the dupA gene was present in 35.3% (127/360, 95% confidence interval (CI), 30.3–40.2%) of H. pylori strains isolated and the prevalence of the dupA gene was significantly higher in strains from DU (46/101, 45.5%, 95%CI, 38.2–55.2%) compared to those from gastric cancer (19/79, 24.1%, 95%CI, 14.6–33.5%) or GU (11/47, 23.4%, 95%CI, 11.3–35.5%) (P < 0.05 for both) confirming the original observation that dupA was related to DU and protective against gastric cancer (Figure 1). Fifty-one (38.3%, 95%CI, 30–45.6%) of the 133 patients with gastritis had dupA-positive strains which was higher than among those with gastric cancer but the difference did not reach statistically significance (P = 0.06). There is no significant difference between DU group and gastritis group (P = 0.2). The result also showed that the presence of the jhp0917 and jhp0918 genes was strongly linked (P < 0.001). Nine strains (2.5%) possessed jhp0917 positive/jhp0918 negative genotype and were classified as dupA negative. A jhp0917 negative/jhp0918 positive genotype strain was not detected.
Figure 1
Figure 1

Prevalence of the dupA gene and clinical outcomes.

Association of dupAgene with histological findings

We compared the relationship between the present of dupA and the degree of chronic inflammation, neutrophil infiltration, atrophy and intestinal metaplasia in the antrum in the different groups except gastric cancer patients. Mann-Whitney U test showed that although patients infected with dupA-positive strains had higher scores for chronic inflammation compared to those with dupA-negative strains (2.36 vs. 2.24, p = 0.058), but the difference did not reach statistical significance (Table 3). The prevalence of the dupA gene was also independent of the scores of other histological variables including antral neutrophil infiltration, atrophy and intestinal metaplasia.
Table 3

Antral histological scores for the dupA matched groups

 

Chronic inflammation

Acute inflammation

Atrophy

Intestinal metaplasia

dupA+

    

   Mean

2.36

1.31

0.74

0.49

   Range

2–3

0–3

0–3

0–3

   Median

2

1

1

0

dupA-

    

   Mean

2.24

1.3

0.63

0.47

   Range

1–3

0–2

0–3

0–3

   Median

2

1

0

0

Z

-1.92

-0.066

-0.956

-0.06

P

0.058

0.948

0.339

0.952

The individual grades for each histological feature were used in a Mann-Whitney U test to explore difference

Association with other virulence factors

The only type of vacA signal sequence detected was s1a. Most (98%) strains were cagA-positive and 93% strains were vacA s1 genotype. The positive rate of vacA m1, vacA m2, iceA1, iceA2 and babA 2 of the 360 strains was 27%, 69%, 90%, 16%, and 64%, respectively (Table 4). The presence of dupA was not associated with any other virulence factors (P > 0.50 for all groups).
Table 4

Association between virulence factors and disease outcomes

Diseases

Patients No.

dupA

cagA

vacA s1a

vacAm1

vacAm2

babA2

iceA1

iceA2

DU

101

45.5%

98.0%

95.0%

18.0%

80.3%

60.6%

96.7%

19.8

Gastritis

133

38.3%

98.5%

90.9%

34.2%

64.3%

67.1%

88.6%

18.5

Gastric cancer

79

24.0%

97.5%

94.9%

34.2%

65.8%

68.4%

86.8%

21.0

GU

47

23.4%

97.8%

91.5%

20.0%

65.7%

60.0%

85.7%

14.2

Association of dupAgene with IL-1β polymorphism

There were no significant differences in IL-1β genotype distribution between patients with dupA positive strains and those with negative strains (P = 0.50 for the patients with IL-1β-31 C carriers and P = 0.68 for IL-1β-511 T carriers).

Discussion

Although DU and gastric cancer are both caused by H. pylori, they are at opposite ends of the spectrum and as such are considered mutually exclusive. DU is associated with sparing of the gastric corpus and high acid secretion whereas gastric cancer is associated with an atrophic pangastritis and low to absent acid secretion [20–22]. These different manifestations of the infection are thought to relate to as yet unexplained interactions between host and environmental factors and with bacteria virulence. Current virulence determinants including the cag-pathogenicity island, OipA, and BabA individually and together have been associated with an increased risk of ulcer or gastric cancer, however none has consistently shown specificity related to a specific pattern of gastritis or disease outcome.

The dupA gene is thought to be a homolog of the virB4 gene and is located in plasticity region of the H. pylori genome. Originally it was reported to be rare (9%) among patients with gastric cancer and common (42%) among patients with duodenal ulcer. As such, it appeared to be a marker for the presence of antral predominant gastritis and "protective" against the development of atrophic pangastritis. Using the same primers and primers of their own design, Arachchi et al. [23] confirmed that the dupA gene was present in approximately the same percentage of H. pylori strains isolated from DU patients (37%) in an Indian population as originally described [10]. They did not study patients with gastric cancer. A study in Brazilian adults [24] reported the dupA gene was present in 87% of patients with either DU or gastric cancer. They used their own primer set based on the sequences of Brazilian strains as well as the original primer sets. They subsequently reported identified two polymorphisms, an adenine deletion at the position 1311 and/or an adenine insertion after the position 1426 of the dupA gene in their isolates that led to different results [25]. They reported that the presence of wild dupA was significantly lower in gastric cancer (50%) than in gastritis (70%) or DU (78%). Finally, Argent et al. used the originally described primers and several other primer sets to examined H. pylori strains collected from Belgium (135 samples), South Africa (46 samples), China (31 samples) and the United States (46 samples) and reported that the prevalence of dupA gene was 50.6% of H. pylori strains isolated from DU patients and 71.1% from gastric cancer patients [26]. In this study, we evaluated Chinese isolates using the originally described primer sets. All patients had the typical East Asia type H. pylori genotype (ie, cagA+ve/vacA s1+ve) and dupA was present in 46% of strains from DU compared to 24% of patients with gastric cancer this confirming the original observations that dupA was commonly found in strains from patients with DU and infrequent among those with gastric cancer. The overall prevalence of dupA in Chinese isolates in study of Argent et al. was 32.3% which is similar to our result (35.3%). They only had one strain from a Chinese gastric cancer patient such that the DU: gastric cancer ratio could not be examined. In their study the results with China were lower than other three Western countries (43.5 to 84.8%). The difference between our studies and those of Argent et al. may be technical or relate to geographic variations circulation strains or difference in the definitions of patient groups [26]. In addition, we extended prior observations by showing that there was no relationship between dupA and previously proposed virulence factors (cagA, vacA,, iceA and babA2) or with host IL-1β polymorphisms.

Based on studies by the current author showing that presence of dupA appears to be associated with the absence of severe corpus gastritis or alternately with antral predominant gastritis, one can propose studies to directly test the hypothesis that dupA is associated with a particular pattern of gastritis. For example, the group of patients with H. pylori gastritis alone contains subgroups of patients some of whom will develop DU (ie, retain the antral predominant pattern), some destined to develop panatrophic gastritis and gastric cancer, and some who do neither. Thus, one would expect the presence of dupA to be inversely related to the severity of corpus gastritis. Unfortunately, the design of the current study did not allow us to test this hypothesis as we did not systematically collect corpus mucosal samples from the gastritis only group and we were only able to compare the severity of antral gastritis in relation to the presence of dupA. Patients infected with dupA-positive strains had higher scores for chronic inflammation compared to those with dupA-negative strains but the difference missed achieving statistical significance (p = 0.058). Initially dupA was identified in strain J99 where the gene was disrupted. Studies from Brazil have identified another truncation site [25] suggesting that PCR determination of functional dupA status may sometime provide misleading results. Interpretation of future studies would be improved if the presence of the DupA protein can be directly assessed as that would eliminate false positive PCR results which may as noted above fail to separate strains with a functionally inactive dupA from those that produce the DupA protein.

Conclusion

Our present study showed that dupA gene was associated with DU in Chinese population, but its protective effects against atrophy/gastric cancer could not be confirmed. Similar to the other virulence factors of H. pylori, regional differences exist in the distribution of this gene.

Declarations

Acknowledgements

This work was supported by Shanghai Pujiang Program (No. 06PJ14066) and the National Natural Science Foundation of China (30670940) both to Dr. Hong Lu.

Authors’ Affiliations

(1)
Department of Gastroenterology, Shanghai Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai Institute of Digestive Disease, Shanghai, P.R. China

References

  1. Graham DY, Yamaoka Y: Disease-specific Helicobacter pylori virulence factors: the unfulfilled promise. Helicobacter. 2000, 5: S3-9. 10.1046/j.1523-5378.2000.0050S1003.x.View ArticlePubMedGoogle Scholar
  2. Crabtree JE, Taylor JD, Wyatt JI, Heatley RV, Shallcross TM, Tompkins DS, Rathbone BJ: Mucosal IgA recognition of Helicobacter pylori 120 kDa protein, peptic ulceration, and gastric pathology. Lancet. 1991, 338: 332-5. 10.1016/0140-6736(91)90477-7.View ArticlePubMedGoogle Scholar
  3. Yamaoka Y, Kikuchi S, el-Zimaity HM, Gutierrez O, Osato MS, Graham DY: Importance of Helicobacter pylori oipA in clinical presentation, gastric inflammation, and mucosal interleukin 8 production. Gastroenterology. 2002, 123: 414-24. 10.1053/gast.2002.34781.View ArticlePubMedGoogle Scholar
  4. Olfat FO, Zheng Q, Oleastro M, Voland P, Borén T, Karttunen R, Engstrand L, Rad R, Prinz C, Gerhard M: Correlation of the Helicobacter pylori adherence factor BabA with duodenal ulcer disease in four European countries. FEMS Immunol Med Microbiol. 2005, 44: 151-6. 10.1016/j.femsim.2004.10.010.View ArticlePubMedGoogle Scholar
  5. Yamaoka Y, Kodama T, Gutierrez O, Kim JG, Kashima K, Graham DY: Relationship between Helicobacter pylori iceA, cagA, and vacA status and clinical outcome: studies in four different countries. J Clin Microbiol. 1999, 37: 2274-9.PubMedPubMed CentralGoogle Scholar
  6. Yamaoka Y, Souchek J, Odenbreit S, Haas R, Arnqvist A, Borén T, Kodama T, Osato MS, Gutierrez O, Kim JG, Graham DY: Discrimination between cases of duodenal ulcer and gastritis on the basis of putative virulence factors of Helicobacter pylori. J Clin Microbiol. 2002, 40: 2244-6. 10.1128/JCM.40.6.2244-2246.2002.View ArticlePubMedPubMed CentralGoogle Scholar
  7. Yamaoka Y, Kodama T, Kita M, Imanishi J, Kashima K, Graham DY: Relationship of vacA genotypes of Helicobacter pylori to cagA status, cytotoxin production, and clinical outcome. Helicobacter. 1998, 3: 241-53. 10.1046/j.1523-5378.1998.08056.x.View ArticlePubMedGoogle Scholar
  8. Ende van der A, Pan ZJ, Bart A, Hulst van der RW, Feller M, Xiao SD, Tytgat GN, Dankert J: cagA-positive Helicobacter pylori populations in China and The Netherlands are distinct. Infect Immun. 1998, 66: 1822-6.PubMedPubMed CentralGoogle Scholar
  9. Pan ZJ, Hulst van der RW, Feller M, Xiao SD, Tytgat GN, Dankert J, Ende van der A: Equally high prevalences of infection with cagA-positive Helicobacter pylori in Chinese patients with peptic ulcer disease and those with chronic gastritis-associated dyspepsia. J Clin Microbiol. 1997, 35: 1344-7.PubMedPubMed CentralGoogle Scholar
  10. El-Omar EM, Carrington M, Chow WH, McColl KE, Bream JH, Young HA, Herrera J, Lissowska J, Yuan CC, Rothman N, Lanyon G, Martin M, Fraumeni JF, Rabkin CS: Interleukin-1 polymorphisms associated with increased risk of gastric cancer. Nature. 2000, 404: 398-402. 10.1038/35006081.View ArticlePubMedGoogle Scholar
  11. Furuta T, El-Omar EM, Xiao F, Shirai N, Takashima M, Sugimura H: Interleukin 1beta polymorphisms increase risk of hypochlorhydria and atrophic gastritis and reduce risk of duodenal ulcer recurrence in Japan. Gastroenterology. 2002, 123: 92-105. 10.1053/gast.2002.34156.View ArticlePubMedGoogle Scholar
  12. Lu H, Hsu PI, Graham DY, Yamaoka Y: Duodenal ulcer promoting gene of Helicobacter pylori. Gastroenterology. 2005, 128: 833-48. 10.1053/j.gastro.2005.01.009.View ArticlePubMedPubMed CentralGoogle Scholar
  13. Dixon MF, Genta RM, Yardley JH, Correa P: Classification and grading of gastritis. The updated Sydney System. International Workshop on the Histopathology of Gastritis, Houston 1994. Am J Surg Pathol. 1996, 20: 1161-81. 10.1097/00000478-199610000-00001.View ArticlePubMedGoogle Scholar
  14. Ho SA, Hoyle JA, Lewis FA, Secker AD, Cross D, Mapstone NP, Dixon MF, Wyatt JI, Tompkins DS, Taylor GR: Direct polymerase chain reaction test for detection of Helicobacter pylori in humans and animals. J Clin Microbiol. 1991, 29: 2543-9.PubMedPubMed CentralGoogle Scholar
  15. Yamaoka Y, Kodama T, Kashima K, Graham DY, Sepulveda AR: Variants of the 3' region of the cagA gene in Helicobacter pylori isolates from patients with different H. pylori-associated diseases. J Clin Microbiol. 1998, 36: 2258-63.PubMedPubMed CentralGoogle Scholar
  16. Atherton JC, Cao P, Peek RM, Tummuru MK, Blaser MJ, Cover TL: Mosaicism in vacuolating cytotoxin alleles of Helicobacter pylori. Association of specific vacA types with cytotoxin production and peptic ulceration. J Biol Chem. 1995, 270: 17771-7. 10.1074/jbc.270.30.17771.View ArticlePubMedGoogle Scholar
  17. Mizushima T, Sugiyama T, Komatsu Y, Ishizuka J, Kato M, Asaka M: Clinical relevance of the babA2 genotype of Helicobacter pylori in Japanese clinical isolates. J Clin Microbiol. 2001, 39: 2463-5. 10.1128/JCM.39.7.2463-2465.2001.View ArticlePubMedPubMed CentralGoogle Scholar
  18. van Doorn LJ, Figueiredo C, Rossau R, Jannes G, van Asbroek M, Sousa JC, Carneiro F, Quint WG: Typing of Helicobacter pylori vacA gene and detection of cagA gene by PCR and reverse hybridization. J Clin Microbiol. 1998, 36: 1271-6.PubMedPubMed CentralGoogle Scholar
  19. Zhang D, Zheng H, Zhou Y, Tang X, Yu B, Li J: Association of IL-1beta gene polymorphism with cachexia from locally advanced gastric cancer. BMC Cancer. 2007, 7: 45-10.1186/1471-2407-7-45.View ArticlePubMedPubMed CentralGoogle Scholar
  20. Faber K: Chronic gastritis: its relation to achylia and ulcer. Lancet. 1927, 2: 902-7.Google Scholar
  21. Tarpila S, Kekki M, Samloff IM, Sipponen P, Siurala M: Morphology and dynamics of the gastric mucosa in duodenal ulcer patients and their first-degree relatives. Hepato-Gastroenterology. 1983, 30: 198-201.PubMedGoogle Scholar
  22. Graham DY: Helicobacter pylori infection in the pathogenesis of duodenal ulcer and gastric cancer: a model. Gastroenterology. 1997, 113: 1983-91. 10.1016/S0016-5085(97)70019-2.View ArticlePubMedGoogle Scholar
  23. Arachchi HS, Kalra V, Lal B, Bhatia V, Baba CS, Chakravarthy S, Rohatgi S, Sarma PM, Mishra V, Das B, Ahuja V: Prevalence of duodenal ulcer-promoting gene (dupA) of Helicobacter pylori in patients with duodenal ulcer in North Indian population. Helicobacter. 2007, 12: 591-7.View ArticlePubMedGoogle Scholar
  24. Gomes LI, Rocha GA, Rocha AM, Soares TF, Oliveira CA, Bittencourt PF, Queiroz DM: Lack of association between Helicobacter pylori infection with dupA-positive strains and gastroduodenal diseases in Brazilian patients. Int J Med Microbiol. 2008, 298: 223-30. 10.1016/j.ijmm.2007.05.006.View ArticlePubMedGoogle Scholar
  25. Queiroz DM, Rocha GA, Gomes LI, Soares TF, Melo FF, Rocha AA, Moura SB, Oliveira CA: Dupa Polymorphisms and Risk of Distal Gastric Carcinoma. Gastroenterology. 2008, 134: A610-Google Scholar
  26. Argent RH, Burette A, Miendje Deyi VY, Atherton JC: The presence of dupA in Helicobacter pylori is not significantly associated with duodenal ulceration in Belgium, South Africa, China, or North America. Clin Infect Dis. 2007, 45: 1204-6. 10.1086/522177.View ArticlePubMedGoogle Scholar

    27. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/8/49/prepub

Copyright

© Zhang et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Advertisement

BMC Gastroenterology

ISSN: 1471-230X

Contact us