[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Indexing Sources::
Editorial Board::
Executive Members::
Articles Archive::
Instruction to Authors::
Peer-Review::
Contact Us::
Site Facilities::
::
Search in website

Advanced Search
Receive site information
Enter your Email in the following box to receive the site news and information.
:: Volume 20, Issue 3 (10-2018) ::
J Gorgan Univ Med Sci 2018, 20(3): 70-75 Back to browse issues page
Prevalence of s1, s2, m1 and m2 alleles of vacA Helicobacter pylori gene isolated from clinical specimen
Sasan Badi1 , Hami Kaboosi 2, Hossian Abbaspoor3
1- M.Sc in Genetic Biology, Damghan Branch, Islamic Azad University, Damghan, Iran
2- Assistant Professor, Department of Microbiology, Ayatollah Amoli Branch, Islamic Azad University, Amol, Iran. hkaboosi@gmail.com , hkaboosi@gmail.com
3- Associate Professor, Department of Biology, Damghan Branch, Islamic Azad University, Damghan, Iran
Abstract:   (6915 Views)
Background and Objective: Helicobacter pylori infection is a pathogenic agent of many stomach disorders, including peptic ulcer disease, stomach cancer and stomach lymphoma. The reasons for the variety of the outcomes of the infection resulting from Helicobacter pylori may be related to difference in genotype or expression of pathogenic bacterial-related factors, as well as environmental and host factors. This study was conducted to determine the frequency of s1, s2, m1 and m2 alleles of the vacA Helicobacter pylori gene isolated from clinical samples.
Methods: This descriptive-analytic study was conducted on 183 patients whom suffering from digestive disorders which referring to the endoscopic department of Kordkuy’s Amiralmomenin hospital in Golestan province, north of Iran during 2016. Two samples of biopsy from antrum region were taken from each patient. The first sample was evaluated by urease test and the second one was done with saline buffer phosphate solution. Urease test of 50 positive samples and DNA extraction was performed. The polymerase chain reaction was performed for vacA alleles and then the relationship between toxin secretion with the symptoms such as abdominal pain, stomachache, reflux, nausea, gastritis, bleeding, stomach ulcers, burning, anemia, and weight loss were evaluated.
Results: Frequency of s1, s2, m1, m2 vacA alleles of isolated strains was 88%, 6%, 38% and 70%, respectively. Also, the s1 / m1, s1 / m2, s2 / m1 and s2 / m2 genotypes of vacA Helicobacter pylori gene were determined 36%, 58%, 0% and 6%, respectively. Toxin secretion did not have significant relationship with digestive symptoms.
Conclusion: The dominant genotype of the patients with digestive disorders (58%) in this study was s1 / m2 and s2 / m1 genotype did not observe in clinical samples.
Keywords: Digestive diseases, Helicobacter pylori, vacA gene alleles
Full-Text [PDF 283 kb] [English Abstract]   (12540 Downloads) |   |   Abstract (HTML)  (274 Views)  
Type of Study: Original Articles | Subject: Microbiology
References
1. Mobaraki M, Roughanian R, AzamT, Zarkesh-Esfahani S, Daghaghzadeh H. [Simultaneous detection of caga gene and vaca alleles in Helicobacter pylori isolated from patients with gastrointestinal inflammations using multiplex PCR]. Iranian Biology Society. 2012; 24(6): 895-903. [Article in Persian]
2. Warren JR, Marshall B. Unidentified curved bacilli on gastric epithelium in active chronic gastritis. Lancet. 1983 Jun; 1(8336): 1273-75.
3. Mégraud F. Advantages and disadvantages of current diagnostic tests for the detection of Helicobacter pylori. Scand J Gastroenterol Suppl. 1996; 215: 57-62.
4. Ford AC, Axon AT. Epidemiology of Helicobacter pylori infection and public health implications. Helicobacter. 2010 Sep; 15 Suppl 1: 1-6. doi:10.1111/j.1523-5378.2010.00779.x
5. Tajbakhsh E, Shahve M, Tajbakhsh S, khamesipour F. Prevalence of Helicobacter pylori vacA allels and cagA gene in the feces of seroposetive children in Kermanshah city. Iran J Med Microbiol. 2015; 9(3): 54-65. [Article in Persian]
6. Nguyen AM, Engstrand L, Genta RM, Graham DY, el-Zaatari FA. Detection of Helicobacter pylori in dental plaque by reverse transcription-polymerase chain reaction. J Clin Microbiol. 1993 Apr; 31(4): 783-87.
7. Madinier IM, Fosse TM, Monteil RA. Oral carriage of Helicobacter pylori: a review. J Periodontol. 1997 Jan; 68(1): 2-6. doi:10.1902/jop.1997.68.1.2
8. Brown LM. Helicobacter pylori: epidemiology and routes of transmission. Epidemiol Rev. 2000; 22(2): 283-97.
9. Gramley WA, Asghar A, Frierson Jr HF, Powell SM. Detection of Helicobacter pylori DNA in fecal samples from infected individuals. J Clin Microbiol. 1999 Jul; 37(7): 2236-40.
10. Zhang L, Blot WJ, You WC, Chang YS, Kneller RW, Jin ML, et al. Helicobacter pylori antibodies in relation to precancerous gastric lesions in a high-risk Chinese population. Cancer Epidemiol Biomarkers Prev. 1996 Aug; 5(8): 627-30.
11. Havaei SA, Salehi R, Fazeli SA, Tavakkoli H, Mohajeri P. [Study of vac A genotypes of H.pylori Isolated from Patients with the Upper Gastrointestinal Diseases by PCR]. J Isfahan Med Sch. 2009; 27(93): 85-92. [Article in Persian]
12. Kargar M, Souod N, Doosti A, Ghorbani-Dalini S. [Prevalence of Helicobacter pylori vacuolating cytotoxin A gene as a predictive marker for different gastrodoudenal diseases]. Iran J Clin Infect Dis. 2011; 6(2): 85-89.
13. Rezaeian A, Karegar M, Souod N, Ghorbani Salini S. Genetic polymorphisms of CagA and VacA genes in Helicobacter pylori isolates from Chaharmahal and Bakhtiari province, Iran. J Isfahan Med Sch. 2012; 30(197): 1019-27. [Article in Persian]
14. Vinagre ID, Queiroz AL, Silva Júnior MR, Vinagre RM, Martins LC. Helicobacter pylori infection in patients with different gastrointestinal diseases from Northern Brazil. Arq Gastroenterol. 2015 Dec; 52(4): 266-71. doi:10.1590/S0004-28032015000400004
15. Honarmand-Jahromy S, Siavoshi F, Malekzadeh R, Nejad Sattari T, Latifi-Navid S. Reciprocal impact of host factors and Helicobacter pylori genotypes on gastric diseases. World J Gastroenterol. 2015 Aug; 21(31): 9317-27. doi:10.3748/wjg.v21.i31.9317
16. Latifi-Navid S, Mohammadi S, Maleki P, Zahri S, Yazdanbod A, Siavoshi F, Massarrat S. Helicobacter pylori vacA d1/-i1 genotypes and geographic differentiation between high and low incidence areas of gastric cancer in Iran. Arch Iran Med. 2013 Jun; 16(6): 330-37. doi:013166/AIM.005
17. Ozbey G, Dogan Y, Demiroren K. Prevalence of Helicobacter pylori virulence genotypes among children in Eastern Turkey. World J Gastroenterol. 2013 Oct; 19(39): 6585-89. doi:10.3748/wjg.v19.i39.6585
18. Kidd M, Lastovica AJ, Atherton JC, Louw JA. Heterogeneity in the Helicobacter pylori vacA and cagA genes: association with gastroduodenal disease in South Africa? Gut. 1999 Oct; 45(4): 499-502.
19. GoSciiziak G, Gasxewska-Mastalarz A, Przotido-Mordarska' A, Zakriezuska- Czenuiriska J, Iwahxak B, Poiiiezuierka E. Diversity of Helicobacter pylori vacA gene and cytotoxin production. Clin Microbiol Infect. 1999; 5: 662-67.
20. Erdogdu C, Saribas Z, Akyön Yilmaz Y. Detection of cagA and vacA genotypes of Helicobacter pylori isolates from a university hospital in Ankara region, Turkey. Turk J Med Sci. 2014; 44(1): 126-32.
21. Pajavand H, Alvandi A, Mohajeri P, Bakhtyari S, Bashiri H, Kalali B, et al. High frequency of vacA s1m2 genotypes among Helicobacter pylori isolates from patients with gastroduodenal disorders in Kermanshah, Iran. Jundishapur J Microbiol. 2015 Nov; 8(11): e25425. doi:10.5812/jjm.25425
22. Vaziri F, Najar Peerayeh S, Alebouyeh M, Mirzaei T, Yamaoka Y, Molaei M, et al. Diversity of Helicobacter pylori genotypes in Iranian patients with different gastroduodenal disorders. World J Gastroenterol. 2013 Sep; 19(34): 5685-92. doi:10.3748/wjg.v19.i34.5685
23. Nahaei MR, Sharifi Y, Akhi MT, Asgharzadeh M, Nahaei M, Fatahi E. Helicobacter pylori cagA and vacA genotypes and their relationships to peptic ulcer disease and non-ulcer dyspepsia. Research Journal of Microbiology. 2008; 3: 386-94.
24. Foroughi F, Molaei M, Mashayekhi R, Dabiri H, Shokrzadeh L, Zojaji H, et al. Helicobacter pylori cagA Status, vacA subtypes and histopathologic findings in Iranian patients with chronic gastritis. Iran J Pathol. 2009; 4(1): 19-25.
25. El-Toukhy N, Saeed AM, Emara NM. Clinical Relevance of the cagA,vacA and babA2 virulence factors of Helicobacter pylori in Egyptian patients with gastroduodenal diseases. International Journal of Advanced Research. 2016; 4: 1002-20. doi:10.21474/IJAR01/192
26. Shiota S, Cruz M, Abreu JA, Mitsui T, Terao H, Disla M, et al. Virulence genes of Helicobacter pylori in the Dominican Republic. J Med Microbiol. 2014 Sep; 63(Pt 9): 1189-96. doi:10.1099/jmm.0.075275-0
27. Rafeey M, Ghostaslou R, Milani M, Farokhi N, Ghojazadeh M. Association between Helicobacter pylori, cagA, and vacA status and clinical presentation in Iranian Children. Iran J Pediatr. 2013 Oct; 235: 551-56.
Send email to the article author


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Badi S, Kaboosi H, Abbaspoor H. Prevalence of s1, s2, m1 and m2 alleles of vacA Helicobacter pylori gene isolated from clinical specimen . J Gorgan Univ Med Sci 2018; 20 (3) :70-75
URL: http://goums.ac.ir/journal/article-1-3457-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 20, Issue 3 (10-2018) Back to browse issues page
مجله دانشگاه علوم پزشکی گرگان Journal of Gorgan University of Medical Sciences
Persian site map - English site map - Created in 0.04 seconds with 36 queries by YEKTAWEB 4645