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Antibiotic resistance pattern and frequency of cagA and vacA genes in Helicobacter pylori strains isolated from patients in Tabriz city, Iran

BMC Research Notes volume 14, Article number: 216 (2021) Cite this article

Abstract

Objective

Helicobacter pylori is one of the most common causes of gastric infections in humans. It is estimated that approximately 50% of people around the world are infected with this bacterium. This study aimed to determine the antibiotic resistance pattern, as well as the frequency of cagA and vacA genes in H. pylori isolates obtained from patients in the clinical centers in Tabriz city, Iran.

Results

The culture method detected 100 (45.25%) H. pylori isolates from 221 biopsy samples during 3 years. The results showed that 63% and 81% of the isolates were positive for cagA and vacA genes, respectively. The highest resistance of isolates was seen against metronidazole (79%) and amoxicillin (36%), respectively. Also, the isolates showed the least resistance to tetracycline (8%).

Introduction

Helicobacter pylori is a spiral Gram-negative bacterium and the causative agent of chronic gastric infections in about half of the world’s population [1]. The infections caused by this bacterium mostly progress from childhood and remain chronically (lifelong) without any symptoms. Acute gastric infections, however, may be developed in some patients [2]. The gastric mucus of humans is the most significant place for the colonization of H. pylori, but it is rarely observed in other Helicobacter species [3]. In 1994, the World Health Organization (WHO) classified H. pylori as a Class I carcinogen and declared that its eradication could reduce the risk of stomach cancer [4]. H. pylori has also been recognized as a major cause of many gastrointestinal infections such as gastritis, duodenal and gastric ulcers, as well as mucosa-associated lymphoid tissue (MALT) lymphoma [1].

The virulence factors responsible for establishing the pathogenesis of H. pylori encompass urease, flagella, adhesins, cytotoxin-associated gene A (cagA), and vacuolating cytotoxin A (vacA) [5]. It seems likely that these virulence factors contribute to tissue damage, bacterial resistance to the host immune system, bacterial adaptation, and survival in the acidic environment of the stomach [5, 6]. Surveys have suggested that cagA and vacA genes, as two important determinants of H. pylori pathogenicity, are mainly involved in the damage to epithelial cells and chronic inflammation, which possibly results in elevated risk of gastric cancer [5, 6]. The vacA toxin produced by H. pylori can induce the formation of pores in the host cellular membrane, giving rise to the development of vacuoles in host cells [7]. The presence of the cagA gene is associated with the development of gastrointestinal ulcers and severe gastritis, as well as precancerous and cancerous lesions [8, 9]. Moreover, the cagA-positive strains have more ability to develop gastric cancer compared to cagA-negative strains [9].

Recently, the standard multiple therapies by a proton pump inhibitor or ranitidine bismuth citrate, together with clarithromycin and amoxicillin or metronidazole, have become the most effective protocol for treating H. pylori infections [10]. However, the emergence of the antibiotic resistant bacteria, including methicillin-resistant Staphylococcus aureus, carbapenem-resistant Klebsiella pneumoniae, extended spectrum β-lactamases (ESBLs)-producing Enterobacteriaceae, and H. pylori isolates in various countries has emerged as a global problem [11,12,13,14]. Therefore, evaluating the antibiotic resistance pattern of H. pylori isolates is of great importance in the prospect of treatment. The current study aimed to assess the antibiotic resistance patterns as well as the frequency of cagA and vacA genes in H. pylori isolates collected from clinical centers in Tabriz city, Iran.

Main text

Methods

Sample collection

This cross-sectional study was conducted on 221 gastric biopsies of patients who were referred to clinics and endoscopy centers located in Tabriz city from April 2013 to June 2015. The Cochran's formula was used to determine the sample size. Patients (aged 15–90 years old) had several clinical symptoms, comprising abdominal pain, stomach sore, burping, flatulence, nausea, and vomiting. Exclusion criteria were as follows: non-cooperative patients who refused to give their consent or to participate in the study, patients with a history of H. pylori eradication treatment, and those with a history of consumption of antibiotics or proton pump inhibitory drugs within the last 1 month. The endoscopy was performed to obtain gastric biopsy samples. The collection of samples was carried out aseptically from the site of lesion or gastric antrum. After transferring in Stuart transport culture medium (Liofilchem, Italy), all the samples were analyzed in the microbiology laboratory within 4 h of preparation.

Culture of samples

The whole samples were cultured on selective Brucella agar (Liofilchem, Italy) plates, containing 5% sterile sheep blood, vancomycin (5 mg/L), trimethoprim (5 mg/L), and polymyxin B (2500 U/L). The plates were incubated under microaerophilic conditions (5% O2, 10% CO2, 85% N2) using the Anoxomat® jar system (USA) at 37 °C for 7 days. Isolates exhibiting Gram-negative curved rods, positive reaction for catalase, oxidase, and urease tests were considered as H. pylori. Confirmed isolates were suspended in Eppendorf tubes, comprising of brain heart infusion (BHI) broth supplemented with 5% horse serum and 20% glycerol. The tubes were stored at − 80 °C until future use [15]. A standard control strain, NCTC 11638, was used to confirm the identity of the isolates and to affirm antimicrobial assays.

Determination of antibiotic resistance

The antibiotic resistance pattern of the isolates was determined by the disc diffusion method according to the Clinical and Laboratory Standards Institute (CLSI) guidelines [16]. The antibiotics used included clarithromycin (15 µg), metronidazole (5 µg), amoxicillin (25 µg), tetracycline (30 µg), ciprofloxacin (5 µg), and furazolidone (100 µg), which were all procured from Mast Diagnostics Mast group Ltd., Merseyside, UK. After 2–3 days of incubation under microaerophilic conditions, the diameters of the growth inhibition zones were measured in millimeters.

DNA extraction and detection of vacA and cagA genes

For the molecular identification of vacA and cagA genes, DNA of all the isolates was extracted using a commercial extraction kit (Invitek Molecular, Berlin, Germany) according to the manufacturer’s instructions. The multiplex polymerase chain reaction (M-PCR) for the mentioned genes was conducted in a total volume of 25 µL using the primers listed in Table 1 [17]. For this purpose, 5.5 µL of PCR master mix (5×), consisting of Taq DNA polymerase (0.05 U/µL), MgCl2 (3 mM), dNTPs (0.4 mM), was admixed with 1 µL of each primer, 1 µL of template DNA, and 10.5 µL of distilled water. The temperature program was set to an initial denaturation at 94 °C for 4 min, followed by 35 cycles of denaturation at 94 °C for 45 s, annealing at 60 °C for 30 s, extension at 72 °C for 90 s, and the final extension at 72 °C for 4 min. The M-PCR products were separated by electrophoresis on 1% agarose gel and stained in a tank containing ethidium bromide for 15 min. The results were visualized under a UV light using a gel documentation system. H. pylori ATCC 43504 and Salmonella typhimurium ATCC 14028 strains were used as positive and negative controls, respectively.

Table 1 The primer sequences used for the identification of vacA and cagA genes in H. pylori isolates
Full size table

Statistical analysis

The descriptive statistical tests (numbers and percentages) were performed using SPSS version 20 (IBM®, New York, NY, USA) for the frequency rates of antibiotic resistance of vacA, and cagA gene. Fisher’s exact test was applied to compare the variables, and a p-value of less than 0.05 was deemed statistically important.

Results

Among 221 collected samples, 129 (58.37%) and 92 (41.63%) samples were from males and females, respectively. The mean age of the patients was 36.4 ± 29.7 years old. The culture method detected 100 (45.25%) H. pylori isolates from 221 biopsy samples. No statistically significant difference was detected in the distribution of H. pylori between different gender and age groups (p > 0.05). The highest resistance of the isolates was against metronidazole (79%), followed by amoxicillin (36%), clarithromycin (25%), furazolidone (20%), ciprofloxacin (10%), and tetracycline (8%). Besides, there was no statistically significant association of resistance to different antibiotics with gender and age (p > 0.05). Based on the molecular analysis, the frequencies of the cagA and vacA genes were 63% and 81%, respectively, and difference in the distribution of the two genes between different age and gender groups (p > 0.05) was insignificant.

Discussion

This study demonstrated the prevalence rate of 45.25% for H. pylori isolates in Tabriz, the most heavily developed town in the northwest of Iran. However, Navidifar et al. [15] reported a lower rate of prevalence (22.12%) in Yazd, Iran. The present study investigated the resistance rates of H. pylori isolates against six antibiotics, and the results indicated a high percentage (79%) of resistance to metronidazole among H. pylori isolates. Metronidazole is a prodrug activated by oxygen-insensitive nitroreductases in the bacterial cell, and the well-characterized mechanism of resistance to this antibiotic is mutations in the rdxA gene encoding RdxA [18]. Similar to our study, a number of other surveys have reported high resistance rates, ranging from 60 to 77.8%, to metronidazole among H. pylori isolates [15, 19,20,21]. In addition to H. pylori treatment, metronidazole is recommended for treating other infections such as parasitic, periodontal, and gynecological infections; the primary resistance to this antibiotic among H. pylori isolates may be due to the frequent use of this drug for treating the above-mentioned infections [15, 18].

In this study, there was no correlation (p > 0.05) between metronidazole resistance and female gender, as reported by other researchers [15, 22]; however, some others [23,24,25] explored a positive correlation between metronidazole resistance and female gender [23,24,25]. The reason for such relationship could be explained by the fact that metronidazole is frequently administered for treating gynecological infections. Following metronidazole, amoxicillin showed the highest percentage of resistance. A mutation in the pbp-1a gene has been found as a primary cause of bacterial resistance to amoxicillin [18]. In support of our results, only a few Iranian researchers have reported the relatively high rates of resistance to amoxicillin [26, 27], while several researchers opposed to this result and implied low resistance rates to this antibiotic [15, 28, 29]. Overall, the general resistance to amoxicillin is low worldwide, but owing to the disproportionate use of amoxicillin, particularly for treating common respiratory tract infections, bacteria can develop some mechanisms of resistance to this antibiotic [18].

Our results reflected that about 25% of H. pylori isolates were resistant to clarithromycin, an essential component of standard triple therapy for H. pylori and a member of macrolide family [30]. The main mechanism of action of macrolides is the inhibition of protein synthesis-dependent RNA by binding to receptors located in the 23S rRNA gene. Hence, the mutations in this region have been associated with the resistance of H. pylori to clarithromycin [31]. The resistance rate to this antibiotic in other regions of Iran has also been reported to be 14.6% to 53.4% [15, 27,28,29, 32, 33]. Nonetheless, due to the prolonged use of clarithromycin to treat other infectious diseases, which causes the expansion of resistant strains as a result of selection pressure, the effective treatment of H. pylori in regimes containing this antibiotic is decreasing [34]. Likewise, around 20% of H. pylori isolates were furazolidone-resistant. This antibiotic is a synthetic nitrofuran with a broad spectrum of antimicrobial activities widely recommended for treating bacterial and protozoal infectious diseases. However, some concerns recently arose from using furazolidone because of its potential carcinogenic effect [35]. Mutations occurring in the 2-oxoglutarate acceptor oxidoreductase (oorD) and pyruvate oxidoreductase (porD) genes are possibly related to the resistance to this antibiotic [36]. The resistance rates of furazolidone in other regions of Iran have mostly been reported to be different, ranging from 4.5 to 61.4% [27, 32, 37], while in some other regions, there was no furazolidone-resistant isolate [15, 38]. One of the main reasons for the emergence of resistance could be the use of furazolidone for the treatment of bacterial and protozoal infections [35].

In the current study, the lowest levels of resistance were shown against tetracycline and ciprofloxacin. The average percentage of the tetracycline resistance rate in Iran is 12.2%. In virtue of the selection pressure, resistance to tetracycline, the same as other antibiotics, is enhanced with the use of this drug [18]. In our study, the resistance rate of H. pylori isolates against tetracycline was 8%; however, other studies conducted in Iran have indicated varied rates (from 4.4 to 76.2%) against this antibiotic [15, 26, 32]. Besides, the resistance to ciprofloxacin was detected in 10% of the isolates. The resistance to ciprofloxacin has been studied in other research works, but was less than the rate stated in our study [15, 27, 32].

As mentioned above, the cagA and vacA genes are the most important determinants of gastric pathogenesis. The frequencies of the cagA and vacA genes were 63% and 81%, respectively. In previous studies from Iran, Molaei et al. [39], Doosti et al. [40], and Doraghi et al. [41] reported the frequency of 78.6%, 83.5%, and 82.2% for the cagA gene in H. pylori isolates, respectively, indicating a higher frequency than our study. The prevalence of vacA gene in this study was also lower than studies conducted in South Africa by Idowu et al. [42] and in India by Vadivel et al. [43] who reported the prevalence rates of 90.6% and 85.5% in H. pylori isolates, respectively. In another study by El Khadir et al. [44] in Morocco, vacA and cagA genes were detected in 99.5% (638/641) and 61.2% (392/641) of biopsies, respectively. However, Akeel et al. [45] reported the cagA gene in 49.2% (63/128) and the vacA gene in 100% (128/128) of Saudi patients.

Conclusion

This study showed the most resistance rates of H. pylori isolates against metronidazole, amoxicillin, and clarithromycin. Therefore, using such antibiotics require to be used with more caution. The present study also found a relatively high frequency rate of two main virulence genes (cagA and vacA) in H. pylori strains collected from the northwest of Iran. Moreover, there was no significant association between the prevalence of the two genes in different age and gender groups.

Limitation

In this study, the minimum inhibitory concentration (MIC) of antibiotics and also the association of different risk factors with H. pylori infection were not evaluated. Additionally, the genotyping of cagA and vacA genes was not performed.

Availability of data and materials

The data of the current study are available from the corresponding author on reasonable request.

Abbreviations

CLSI:

Clinical and Laboratory Standards Institute

ESBL:

Extended spectrum β-lactamases

cagA :

Cytotoxin-associated gene A

MALT:

Mucosa associated lymphoid tissue

MIC:

Minimum inhibitory concentration

M-PCR:

Multiplex polymerase chain reaction

oorD :

Oxoglutarate acceptor oxidoreductase

porD :

Pyruvate oxidoreductase

vacA :

Vacuolating cytotoxin A

WHO:

World Health Organization

References

  1. Gravina AG, Zagari RM, De Musis C, Romano L, Loguercio C, Romano M. Helicobacter pylori and extragastric diseases: a review. World J Gastroenterol. 2018;24:3204–21.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Blanchard TG, Czinn SJ. Identification of Helicobacter pylori and the evolution of an efficacious childhood vaccine to protect against gastritis and peptic ulcer disease. Pediatr Res. 2017;81:170–6.

    Article  PubMed  Google Scholar 

  3. Flahou B, Rossi M, Bakker J, et al. Evidence for a primate origin of zoonotic Helicobacter suis colonizing domesticated pigs. ISME J. 2018;12:77–86.

    Article  PubMed  Google Scholar 

  4. Moss SF. The clinical evidence linking Helicobacter pylori to gastric cancer. Cell Mol Gastroenterol Hepatol. 2016;3:183–91.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Chang WL, Yeh YC, Sheu BS. The impacts of H. pylori virulence factors on the development of gastroduodenal diseases. J Biomed Sci. 2018;25:68.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  6. Kao CY, Sheu BS, Wu JJ. Helicobacter pylori infection: an overview of bacterial virulence factors and pathogenesis. Biomed J. 2016;39(1):14–23.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Foegeding NJ, Caston RR, McClain MS, Ohi MD, Cover TL. An overview of Helicobacter pylori VacA toxin biology. Toxins (Basel). 2016;8:173.

    Article  CAS  Google Scholar 

  8. Conteduca V, Sansonno D, Lauletta G, Russi S, Ingravallo G, Dammacco F. H. pylori infection and gastric cancer: state of the art. Int J Oncol. 2013;42:5–18.

    Article  CAS  PubMed  Google Scholar 

  9. Yong X, Tang B, Li BS, et al. Helicobacter pylori virulence factor CagA promotes tumorigenesis of gastric cancer via multiple signaling pathways. Cell Commun Signal. 2015;13:30.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  10. Goderska K, Agudo Pena S, Alarcon T. Helicobacter pylori treatment: antibiotics or probiotics. Appl Microbiol Biotechnol. 2018;102:1–7.

    Article  CAS  PubMed  Google Scholar 

  11. Legese H, Kahsay AG, Kahsay A, et al. Nasal carriage, risk factors and antimicrobial susceptibility pattern of methicillin resistant Staphylococcus aureus among healthcare workers in Adigrat and Wukro hospitals, Tigray, Northern Ethiopia. BMC Res Notes. 2018;11(1):1–6.

    Article  Google Scholar 

  12. Indrajith S, Mukhopadhyay AK, Chowdhury G, et al. Molecular insights of carbapenem resistance Klebsiella pneumoniae isolates with focus on multidrug resistance from clinical samples. J Infect Pubic Health. 2021;14(1):131–8.

    Article  Google Scholar 

  13. Saravanan M, Ramachandran B, Barabadi H. The prevalence and drug resistance pattern of extended spectrum β-lactamases (ESBLs) producing Enterobacteriaceae in Africa. Microb Pathog. 2018;114:180–92.

    Article  PubMed  Google Scholar 

  14. Thung I, Aramin H, Vavinskaya V, et al. Review article: the global emergence of Helicobacter pylori antibiotic resistance. Aliment Pharmacol Ther. 2016;43:514–33.

    Article  CAS  PubMed  Google Scholar 

  15. Navidifar T, Eslami G, Akhondi M, Baghbanian M, Fallah Zadeh H, Zandi H. Antibacterial resistance patterns of Helicobacter pylori clinical isolates from gastric biopsy of patients in Yazd. Int J Enteric Pathog. 2014;2:1–4.

    Article  Google Scholar 

  16. Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing. Supplement M100. 25th ed. Wayne: CLSI; 2015.

    Google Scholar 

  17. Ahmadi E, Amini K, Sadeh M. Prevalence of cagA, cagT, cagE, vacA and hrgA genes in Helicobacter pylori strains isolated from patients with gastric cancer in Karaj city, 2016. Feyz. 2017;21:562–8.

    Google Scholar 

  18. Khademi F, Poursina F, Hosseini E, Akbari M, Safaei HG. Helicobacter pylori in Iran: a systematic review on the antibiotic resistance. Iran J Basic Med Sci. 2015;18:2–7.

    PubMed  PubMed Central  Google Scholar 

  19. Pourakbari B, Mahmoudi S, Parhiz J, Sadeghi RH, Monajemzadeh M, Mamishi S. High frequency of metronidazole and clarithromycin-resistant Helicobacter pylori in formalin-fixed, paraffin-embedded gastric biopsies. Br J Biomed Sci. 2018;75:61–5.

    Article  CAS  PubMed  Google Scholar 

  20. Mahmoudi S, Mamishi S, Banar M, et al. Antibiotic susceptibility of Helicobacter pylori strains isolated from Iranian children: high frequency of A2143G point mutationassociated with clarithromycin resistance. J Glob Antimicrob Resist. 2017;10:131–5.

    Article  PubMed  Google Scholar 

  21. Hamidi S, Badmasti F, Sadeghpour Heravi F, et al. Antibiotic resistance and clonal relatedness of Helicobacter pylori strains isolated from stomach biopsy specimens in northeast of Iran. Helicobacter. 2020;25:e12684.

    Article  PubMed  Google Scholar 

  22. Lui SY, Yeoh KG, Ho B. Metronidazole-resistant Helicobacter pylori is more prevalent in patients with nonulcer dyspepsia than in peptic ulcer patients in a multiethnic Asian population. J Clin Microbiol. 2003;41:5011–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Wu DC, Hsu PI, Wu JY, et al. Sequential and concomitant therapy with 4 drugs are equally effective for eradication of H. pylori infection. Clin Gastroenterol Hepatol. 2010;8:36–41.

    Article  CAS  PubMed  Google Scholar 

  24. Magalhães PP, Queiroz DM, Barbosa DV, et al. Helicobacter pylori primary resistance to metronidazole and clarithromycin in Brazil. Antimicrob Agents Chemother. 2002;46:2021–3.

    Article  CAS  Google Scholar 

  25. Boyanova L, Ilieva J, Gergova G, et al. Numerous risk factors for Helicobacter pylori antibiotic resistance revealed by extended anamnesis: a Bulgarian study. J Med Microbiol. 2012;61:85–93.

    Article  CAS  PubMed  Google Scholar 

  26. Maleknejad S, Mojtahedi A, Safaei-Asl A, Taghavi Z, Kazemnejad E. Primary antibiotic resistance to Helicobacter pylori strains isolated from children in Northern Iran: a single center study. Iran J Pediatr. 2015;25:e2661.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Saniee P, Hosseini F, Kadkhodaei S, Siavoshi F, Khalili-Samani S. Helicobacter pylori multidrug rResistance due to misuse of antibiotics in Iran. Arch Iran Med. 2018;21:283–8.

    PubMed  Google Scholar 

  28. Mirzaei N, Poursina F, Faghri J, et al. Prevalence of resistance of Helicobacter pylori strains to selected antibiotics in Isfahan, Iran. Jundishapur J Microbiol. 2013;6(5):e6342.

    Article  Google Scholar 

  29. Eslami G, Taheri S, Baseri N, et al. Prevalence of Helicobacter pylori and determination of antibiotic resistance in patients with gastritis referred to Shahid Beheshti University of Medical Sciences Hospitals in Tehran Between 2010 and 2011. Arch Clin Infect Dis. 2012;8:18–22.

    Article  Google Scholar 

  30. Coelho LG, Maguinilk I, Zaterka S, Parente JM, Passos MD, Moraes-Filho JP. 3rd Brazilian consensus on Helicobacter pylori. Arq Gastroenterol. 2013;50:81–96.

    Article  Google Scholar 

  31. Ménard A, Santos A, Mégraud F, Oleastro M. PCR-restriction fragment length polymorphism can also detect point mutation A2142C in the 23S rRNA gene, associated with Helicobacter pylori resistance to clarithromycin. Antimicrob Agents Chemother. 2002;46:1156–7.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  32. Farzi N, Yadegar A, Sadeghi A, Asadzadeh Aghdaei H, Marian Smith S, Raymond J, et al. High prevalence of antibiotic resistance in Iranian Helicobacter pylori isolates: importance of functional and mutational analysis of resistance genes and virulence genotyping. J Clin Med. 2019;17(8):2004.

    Article  CAS  Google Scholar 

  33. Amin M, Shayesteh AA, Serajian A, Goodarzi H. Assessment of metronidazole and clarithromycin resistance among Helicobacter pylori isolates of Ahvaz (Southwest of Iran) During 2015–2016 by phenotypic and molecular methods. Jundishapur J Microbiol. 2019;12:e80156.

    CAS  Google Scholar 

  34. Vianna JS, Ramis IB, Ramos DF, Von Groll A, Silva PE. Drug resistance in Helicobacter pylori. Arq Gastroenterol. 2016;53:215–23.

    Article  PubMed  Google Scholar 

  35. Zullo A, Ierardi E, Hassan C, De Francesco V. Furazolidone-based therapies for Helicobacter pylori infection: a pooled-data analysis. Saudi J Gastroenterol. 2012;18:11–7.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Zamani M, Rahbar A, Shokri-Shirvani J. Resistance of Helicobacter pylori to furazolidone and levofloxacin: a viewpoint. World J Gastroenterol. 2017;23:6920–2.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Siavoshi F, Saniee P, Latifi-Navid S, Massarrat S, Sheykholeslami A. Increase in resistance rates of Helicobacter pylori isolates to metronidazole and tetracycline-comparison of three 3-year studies. Arch Iran Med. 2010;13:177–87.

    CAS  PubMed  Google Scholar 

  38. Sirous M, Mehrabadi JF, Daryani NE, Eshraghi S, Hajikhani S, Shirazi MH. Prevalence of antimicrobial resistance in Helicobacter pylori isolates from Iran. Afr J Biotechnol. 2010;9:5962–5.

    Google Scholar 

  39. Molaei M, Foroughi F, Mashayekhi R, et al. CagA status and VacA subtypes of Helicobacter pylori in relation to histopathologic findings in Iranian population. Indian J Pathol Microbiol. 2010;53:24–7.

    Article  PubMed  Google Scholar 

  40. Dousti A, Gh R, Nasiri J, Yavari FP. Identification the frequency of cytotoxin associated gene in H. pylori strain isolated form biopsy samples in Shahrekord. J Armaghan Danesh. 2007;29:12–21.

    Google Scholar 

  41. Douraghi M, Mohamadi M, Shirazi MH, Esmaili M. Evaluation of cytotoxin associated gene with gastric disorders in H. pylori infected patients. Iran J Med Microbiol. 2008;2:31–6.

    Google Scholar 

  42. Idowu A, Mzukwa A, Harrison U, et al. Detection of Helicobacter pylori and its virulence genes (cagA, dupA, and vacA) among patients with gastroduodenal diseases in Chris Hani Baragwanath Academic Hospital, South Africa. BMC Gastroenterol. 2019;19:73.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Vadivel A, Kumar CP, Muthukumaran K, et al. Clinical relevance of cagA and vacA and association with mucosal findings in Helicobacter pylori-infected individuals from Chennai, South India. Indian J Med Microbiol. 2018;36:582–6.

    Article  PubMed  Google Scholar 

  44. El Khadir M, Alaoui Boukhris S, Benajah D-A, et al. vacA and cagA status as biomarker of two opposite end outcomes of Helicobacter pylori infection (gastric cancer and duodenal ulcer) in a Moroccan population. PLoS ONE. 2017;12(1):e0170616.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  45. Akeel M, Shehata A, Elhafey A, et al. Helicobacter pylori vacA, cagA and iceA genotypes in dyspeptic patients from southwestern region, Saudi Arabia: distribution and association with clinical outcomes and histopathological changes. BMC Gastroenterol. 2019;19(1):1–1.

    Article  Google Scholar 

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Acknowledgements

The authors acknowledge the Microbiology Laboratory personnel of Islamic Azad University of Ahar, Iran for their unwavering assistance in bacterial collection and identification.

Funding

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors and was conducted at personal expense.

Author information

Authors and Affiliations

  1. Department of Microbiology, Marand Branch, Islamic Azad University, Marand, Iran

    Farnaz Rasi-Bonab

  2. Department of Microbiology, School of Basic Sciences, Kazerun Branch, Islamic Azad University, Kazerun, Iran

    Abolfazl Jafari-Sales

  3. Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran

    Mohammad Amin Shaverdi

  4. Khuzestan Blood Transfusion Center, Abadan, Iran

    Mohammad Amin Shaverdi

  5. Shoushtar Faculty of Medical Sciences, Shoushtar, Iran

    Tahereh Navidifar

  6. Department of Microbiology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

    Morteza Saki & Atosa Ghorbani

  7. Student Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

    Morteza Saki

  8. Environmental Microbiology and Biotechnology Laboratory, Department of Microbiology, University of Ibadan, Ibadan, Nigeria

    Abimbola Olumide Adekanmbi

  9. Department of Microbiology, Ahar Branch, Islamic Azad University, Ahar, Iran

    Behboud Jafari & Sara Naebi

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Contributions

FRB, AJS, BJ, and SN conceived the project and designed the experiments. FRB, AJS, BJ, and SN collected the samples. AJS, BJ, and SN performed laboratory experiments. MS, TN, AG and AOA analyzed the data. MAS, MS, TN, AG and AOA wrote the primary manuscript. All authors reviewed manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Abolfazl Jafari-Sales or Mohammad Amin Shaverdi.

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Ethics approval and consent to participate

This study was approved by the Ahar Branch, Islamic Azad University, Ahar, Iran (no registered code). All procedures performed in studies involving human participants were in accordance with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. All patients were informed that their test results may be used anonymously for research purposes, and a written informed consent was received from each patient. For children under legal age, the consent was obtained from their parents or legal guardians.

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Rasi-Bonab, F., Jafari-Sales, A., Shaverdi, M.A. et al. Antibiotic resistance pattern and frequency of cagA and vacA genes in Helicobacter pylori strains isolated from patients in Tabriz city, Iran. BMC Res Notes 14, 216 (2021). https://doi.org/10.1186/s13104-021-05633-5

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  • DOI: https://doi.org/10.1186/s13104-021-05633-5

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BMC Research Notes

ISSN: 1756-0500

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