DOI QR코드

DOI QR Code

Virulence Genes of Helicobacter pylori in Gastritis, Peptic Ulcer and Gastric Cancer in Laos

  • Vannarath, Sengdao (Department of Gastroenterology, Mahosot Hospital) ;
  • Vilaichone, Ratha-Korn (Gastroenterology Unit, Department of Medicine, Thammasat University Hospital) ;
  • Rasachak, Bouachanh (Department of Gastroenterology, Mahosot Hospital) ;
  • Mairiang, Pisaln (Department of Gastroenterology, Srinagarind Hospital, Khonkaen University) ;
  • Yamaoka, Yoshio (Department of Medicine, Michael E. Debakey Veterans Affairs Medical Center and Baylor College of Medicine) ;
  • Shiota, Seiji (Department of Environmental and Preventive Medicine, Oita University Faculty of Medicine) ;
  • Binh, Tran Thanh (Department of Environmental and Preventive Medicine, Oita University Faculty of Medicine) ;
  • Mahachai, Varocha (Division of Gastroenterology, Department of Medicine, Chulalongkorn University Hospital)
  • Published : 2014.11.06

Abstract

Background: Helicobacter pylori (H. pylori) infection is an established cause of peptic ulcers and gastric cancer. The aim of this study was to identify H. pylori genotypes and to examine their associations with geographical regions and gastritis, peptic ulcers and gastric cancer in Laos. Materials and Methods: A total of 329 Lao dyspeptic patients who underwent gastroscopy at Mahosot Hospital, Vientiane, Laos during December 2010 - March 2012 were enrolled. Two biopsy specimens (one each from the antrum and corpus) were obtained for CLO testing and only CLO test-positive gastric tissue were used to extract DNA. PCR and sequencing were identified for variants of the cagA and vacA genotypes. Results: Some 119 Laos patients (36.2%) were found to be infected with H. pylori including 83 with gastritis, 13 with gastric ulcers (GU), 20 with duodenal ulcers (DU) and 3 with gastric cancer. cagA was detected in 99.2%. East-Asian-type cagA (62%) and vacA s1c (64.7%) were predominant genotypes in Laos. vacA s1c-m1b was significantly higher in GU than gastritis (53.8% vs. 24.1%; P-value=0.04) whereas vacA s1a-m2 was significantly higher in DU than gastritis (40.0% vs. 16.9%; P-value=0.03). East-Asian-type cagA and vacA s1c were significantly higher in highland than lowland Lao (100% vs. 55.8%; P-value=0.001 and 88.2% vs. 61.5%, P-value=0.03 respectively). Conclusions: H. pylori is a common infection in Laos, as in other countries in Southeast Asia. The cagA gene was demonstrated in nearly all Laos patients, cagA and vacA genotypes being possible important factors in explaining H. pylori infection and disease outcomes in Laos.

Keywords

References

  1. Andreson H, Loivukene K, Sillakivi T, et al (2002). Association of cagA and vacA genotypes of Helicobacter pylori with gastric diseases in Estonia. J Clin Microbiol, 40, 298-300. https://doi.org/10.1128/JCM.40.1.298-300.2002
  2. Atherton JC, Cao P, Peek RM Jr et al (1995). Mosaicism in vacuolating cytotoxin alleles of Helicobacter pylori. Association of specific vacA types with cytotoxin production and peptic ulceration. J Biol Chem, 270, 17771-7. https://doi.org/10.1074/jbc.270.30.17771
  3. Atherton JC, Peek RM Jr, Tham KT, et al (1997). Clinical and pathological importance of heterogeneity in vacA, the vacuolating cytotoxin gene of Helicobacter pylori. Gastroenterol, 112, 92-99. https://doi.org/10.1016/S0016-5085(97)70223-3
  4. Atherton JC (2000). CagA: a role at last. Gut, 47, 330-1. https://doi.org/10.1136/gut.47.3.330
  5. Atherton JC (2006). The pathogenesis of Helicobacter pyloriinduced gastro-duodenal diseases. Annu Rev Patholo, 1, 63-96. https://doi.org/10.1146/annurev.pathol.1.110304.100125
  6. Azuma T, Yamakawa A, Yamazaki S, et al (2004). Association between diversity in the Src homology 2 domain-containing tyrosine phosphatase binding site of Helicobacter pylori CagA protein and gastric atrophy and cancer Helicobacter pylori strains in Japan. J Infect Dis, 189, 820-7. https://doi.org/10.1086/381782
  7. Basiri Z, Safaralizadeh R, Bonyadi MJ, et al (2014). Helicobacter pylori vacA d1 genotype predicts risk of gastric adenocarcinoma and peptic ulcers in northwestern Iran. Asian Pac J Cancer Prev, 15, 1575-9. https://doi.org/10.7314/APJCP.2014.15.4.1575
  8. Blaser MJ, Perez-Perez GI, Kleanthous H, et al (1995). Infection with Helicobacter pylori strains possessing cagA is associatedwith an increased risk of developing adenocarcinoma of the stomach. Cancer Res, 55, 2111-5.
  9. Breurec S, Guillard B, Hem S et al (2011). Expansion of European vacA and cagA alleles to East-Asian Helicobacter pylori strains in Cambodia. Infection, Genetics Evolution, 11, 1899-905 https://doi.org/10.1016/j.meegid.2011.08.007
  10. Cittelly DM, Huertas MG, Martinez JD, et al (2002). Helicobacter pylori genotypes in non atrophic gastritis are different of the found in peptic ulcer, pre-malig nant lesions and gastric cancer in colombia. Rev Med Chil, 130, 143-51.
  11. Cover TL, Blaster MJ (1992). Purification and characterization of the vacuolating toxin form Helicobacter pylori. J Biol Chem, 267, 10570-5
  12. Dixon MF (1991). Helicobacter pylori and peptic ulceration: Histopathological aspect. J Gastroenterol Hepatol, 6, 125-30. https://doi.org/10.1111/j.1440-1746.1991.tb01451.x
  13. Ghose C, Perez-Perez GI, Dominguez-Bello MG, et al (2002). East Asian genotypes of Helicobacter pylori strains in Amerindians provide evidence for its ancient human carriage. Proc Natl Acad Sci USA, 99, 15107-11. https://doi.org/10.1073/pnas.242574599
  14. Hamajima N, Goto Y, Nishio K, et al (2004). Helicobacter pylori eradication as a preventive tool against gastric cancer. Asian Pac J Cancer Prev, 5, 246-52
  15. Hamlet A, Thoreson AC, Nilsson O, et al (1999). Duodenal Helicobacter pylori infection differs in cagA genotype between asymptomatic subjects and patients with duodenal ulcers. Gastroenterol, 116, 259-68. https://doi.org/10.1016/S0016-5085(99)70121-6
  16. Hussein NR (2014). Helicobacter pylori vacA d1 genotype is associated with gastric cancer but not peptic ulcers in Kurdistan region, northern Iraq. Asian Pac J Cancer Prev, 15, 5965-6. https://doi.org/10.7314/APJCP.2014.15.14.5965
  17. Karami N, Talebkhan Y, Saberi S, et al (2013). Seroreactivity to Helicobacter pylori antigens as a risk indicator of gastric cancer. Asian Pac J Cancer Prev, 14, 1813-7. https://doi.org/10.7314/APJCP.2013.14.3.1813
  18. Kersulyte D, Mukhopadhyay AK, Velapatino B, et al (2000). Differences in genotypes of Helicobacter pylori from different human populations. J Bacteriol, 182, 3210-8. https://doi.org/10.1128/JB.182.11.3210-3218.2000
  19. Kim SY, Woo CW, Lee YM, et al (2001). Genotyping cagA, vacA subtype, iceA1, and babA of Helicobacter pylori isolates from Korean patients, and their association with gastroduodenal diseases. J Korean Med Sci, 16, 579-84. https://doi.org/10.3346/jkms.2001.16.5.579
  20. Letley DP, Rhead JL, Twells RJ, et al (2003): Determinant of non-toxicity in the gastric pathogen Helicobacter pylori. J Biol Chem, 278, 26734-41. https://doi.org/10.1074/jbc.M304071200
  21. Maeda S,Ogura K,Yoshida H, et al (1998). Major virulence factors, VacA and CagA, are commonly posi-tive in Helicobacter pylori isolates in Japan. Gut, 42, 338-43. https://doi.org/10.1136/gut.42.3.338
  22. Mukhopadhyay AK, Kersulyte D, Jeong JY et al (2000). Distinctiveness of genotypes of Helicobacter pylori in Calcutta, India. J Bacteriol, 182, 3219-27. https://doi.org/10.1128/JB.182.11.3219-3227.2000
  23. Nguyen LT, Mai HB, Ta L (2011). Helicobacter pylori infection and gastroduodenal diseases in Vietnam. Helicobacter Research, 15, 220-7.
  24. Nguyen TL, Nguyen DC, Nguyen TH, et al (2011). Surveybased Cancer Mortality in Lao PDR, 2007-2008. Asian Pac J Cancer Prev, 12, 2495-8.
  25. Pandey R, Misra V, Misra SP, Dwivedi, et al (2010). Helicobacter pylori and gastric cancer. Asian Pac J Cancer Prev, 11, 583-8.
  26. Park S, Bae J, Nam BH, et al (2008). Aetiology of cancer in Asia. Asian Pac J Cancer Prev, 9, 371-80.
  27. Parsonnet J, Friedman GD Orentrich N, et al (1997). Risk for gastric cancer in people with Cag A positive for cag A negative Helicobacter pylori infection. Gut, 40, 297-310. https://doi.org/10.1136/gut.40.3.297
  28. Parsonnet J, Friedman GD, Vandersteen DP, et al (1999). Helicobacter pylori infection and the risk of gastric carcinomar. N Eng J Med, 325, 1127-31.
  29. Podzorski RP, Podzorski DS, Wuerth A, et al (2003). Analysis of the vacA, cagA, cagE, iceA and babA2 genes in Helicobacter pylori from sixty-one pediatric patients from the Midwestern United States. Diagn Microbiol Infect Dis, 46, 83-8. https://doi.org/10.1016/S0732-8893(03)00034-8
  30. Rasachak B, Sihavonb B (2000). Epidemiologic and endoscopic aspects of Helicobacter pylori infection in Vientian Laos. Bull Soc Pathol Exot, 93, 91-4.
  31. Rudi J, Kolb C, Maiwald M, et al (1998). Diversity of Helicobacter pylori vac A and cag A genes and relationship to Vac A and CagA protein expression, cytotoxin production and associated diseases. J Clin Microbiol, 36, 944-8
  32. Sriamporn S, Setiawan V, Pisani P, et al (2002). Gastric cancer: the roles of diet, alcohol drinking, smoking and Helicobacter pylori in Northeastern Thailand. Asian Pac J Cancer Prev, 3, 345-52.
  33. Suerbaum S, Michetti P (2002). Helicobacter pylori infection. N Engl J Med, 347, 1175-86. https://doi.org/10.1056/NEJMra020542
  34. Tokudome S, Hosono A, Suzuki S,et al (2006). Helicobacter pylori infection as an essential factor for stomach cancer. Asian Pac J Cancer Prev, 7, 163.
  35. Tytgat GNJ, Noach LA, Rauws EAJ (1993). Helicobacter pylori infection and duodenal ulcer disease. Gastroenterol Clin North Am, 22, 127-39.
  36. Uchida T, Nguyen TL, Takayama A et al (2009). Analysis of virulence factors of Helicobacter pylori isolated from a Vietnamese population. BMC Microbiology, 9, 175. https://doi.org/10.1186/1471-2180-9-175
  37. Valliani A, Khan F, Chagani B, et al (2013). Factors associated with Helicobacter pylori infection, results from a developing country - Pakistan. Asian Pac J Cancer Prev, 14, 53-6. https://doi.org/10.7314/APJCP.2013.14.1.53
  38. Van Doorn LJ, Figueiredo C, Megraud F, et al (1999). Geographic distribution of vacA allelic types of Helicobacter pylori. Gastroenterol, 116, 823-30. https://doi.org/10.1016/S0016-5085(99)70065-X
  39. van Doorn LJ, Figueiredo C, Sanna R et al (1998). Expanding allelic diversity of Helicobacter pylori vacA. J Clin Microbiol, 36, 2597-603.
  40. van Doorn LJ, Figueiredo C, Sanna R, et al (1998). Clinical relevance of the cagA, vacA, and iceA status of Helicobacter pylori. Gastroenterol, 115, 58-66. https://doi.org/10.1016/S0016-5085(98)70365-8
  41. Vilaichone RK, Mahachai V, Tumwasorn S et al (2004). Molecular epidemiology and outcome of Helicobacter pylori infection in Thailand: a cultural cross roads. Helicobacter, 9, 453-9. https://doi.org/10.1111/j.1083-4389.2004.00260.x
  42. Wang HJ, Kuo CH, Amy A. M et al (1998). Vacuolating Toxin Production in Clinical Isolates of Helicobacter pylori with Different vacA Genotypes. J Infect Di, 178, 207-12. https://doi.org/10.1086/515600
  43. Warren JR, Marshall BJ (1983). Unidentified curved bacilli on gastric epithelium in active chronic gastritis. Lancet, 1, 1273-5.
  44. Weel JF, van der Hulst RW, Gerrits Y, et al (1996). The interrelationship between cytotoxin associated gene A, vacuolating cytotoxin and Helicobacter pylori related disease. J Infec Dis, 173, 1171-5. https://doi.org/10.1093/infdis/173.5.1171
  45. Wotherspoon AC, Ortiz-Hidalgo C, Falzon MR, et al (1999). Helicobacter pylori associated gastritis and primary B-cell lymphoma. Lancet, 338, 1175-6.
  46. Xue FB, Xu YY, Wan Y, et al (2001). Association of H. pylori infection with gastric carcinoma: a meta analysis. World J Gastroenterol, 7, 801-4.
  47. Yamaoka Y, El-Zimaity HMT, Gutierrez O, et al (1999). Relationship between subtypes of the cagA-3 repeat region, gastric histology, and susceptibility to low pH. Gastroenterol, 117, 342-9. https://doi.org/10.1053/gast.1999.0029900342
  48. Yamaoka Y, Kodama T, Kashima K, et al (1998). Variants of the 3' region of the cagA gene in Helicobacter pylori isolates from different H. pylori associated diseases. J Clin Microbiol, 36, 2258-63.
  49. Yamaoka Y, Orito E, Mizokami M, et al (2002). Helicobacter pylor in North and South America before Columbus. FEBS Letter, 517, 180-4. https://doi.org/10.1016/S0014-5793(02)02617-0
  50. Yamaoka Y, Osato MS, Sepulveda AR, et al (2000). Molecular epidemiology of Helicobacter pylori: separation of H. pylori from East Asian and non-Asian countries. Epidemiol Infect, 124, 91-6. https://doi.org/10.1017/S0950268899003209
  51. Yamaoka Y (2010). Mechanisms of disease: Helicobacter pylori virulence factors. Nat Rev Gastroenterol Hepatol, 7, 629-41
  52. Zhao Y, Wang J, Tanaka T, et al (2012). Association between HLA-DQ genotypes and haplotypes vs Helicobacter pylori infection in an Indonesian population. Asian Pac J Cancer Prev, 13, 1247-51. https://doi.org/10.7314/APJCP.2012.13.4.1247
  53. Zheng RN, Li SR, Masahiro A (2012). Helicobacter pylori CagA and gastric carcinogenesis. Asian Pac J Cancer Prev, 13, 2481-4. https://doi.org/10.7314/APJCP.2012.13.6.2481
  54. Zhou J, Zhang J, Xu C et al (2004). cagA genotype and variants in Chinese Helicobacter pylori strain and relationship to gastroduodenal diseases. J Med Microbiol, 53, 231-5. https://doi.org/10.1099/jmm.0.05366-0

Cited by

  1. Effects of the CYP2C19 Genetic Polymorphism on Gastritis, Peptic Ulcer Disease, Peptic Ulcer Bleeding and Gastric Cancer vol.15, pp.24, 2014, https://doi.org/10.7314/APJCP.2014.15.24.10957
  2. Epidemic Trends of Upper Gastrointestinal Tract Abnormalities: Hospital-based study on Endoscopic Data Evaluation vol.16, pp.14, 2015, https://doi.org/10.7314/APJCP.2015.16.14.5741
  3. Resistance to clarithromycin and genotypes in Helicobacter pylori strains isolated in Sicily vol.64, pp.11, 2015, https://doi.org/10.1099/jmm.0.000163
  4. Antibiotic Resistant Pattern of Helicobacter Pylori Infection Based on Molecular Tests in Laos vol.17, pp.1, 2016, https://doi.org/10.7314/APJCP.2016.17.1.285
  5. Extremely High Prevalence of Metronidazole-Resistant Helicobacter pylori Strains in Mountain People (Karen and Hmong) in Thailand vol.94, pp.4, 2016, https://doi.org/10.4269/ajtmh.15-0449
  6. outer inflammatory protein A (OipA) suppresses apoptosis of AGS gastric cells in vitro vol.19, pp.12, 2017, https://doi.org/10.1111/cmi.12771
  7. management in ASEAN: The Bangkok consensus report vol.33, pp.1, 2018, https://doi.org/10.1111/jgh.13911
  8. Association between IL-1β polymorphisms and gastritis risk vol.96, pp.5, 2017, https://doi.org/10.1097/MD.0000000000006001
  9. Molecular Epidemiology of Helicobacter pylori Infection in a Minor Ethnic Group of Vietnam: A Multiethnic, Population-Based Study vol.19, pp.3, 2018, https://doi.org/10.3390/ijms19030708