Clarithromycin-resistant H. pylori primary strains and virulence genotypes in the Northeastern region of Brazil

ABSTRACT

The increase of H. pylori resistance to clarithromycin is a concern. This study evaluated the prevalence of H. pylori’s primary resistance to clarithromycin and its association with virulence factors in adult dyspeptic patients and asymptomatic children. The gastric mucosa from patients (153 gastritis, 24 gastric cancer, 21 peptic ulcer) and gastric juice obtained by string test from 24 H. pylori and 23S rRNA positive asymptomatic children were included. The clarithromycin resistance was assessed by TaqMan RT-PCR 23S rRNA point mutations, A2142G and/or A2143G, and H. pylori virulence markers by PCR. Overall, the clarithromycin resistance was 14.4% (32/222), 14.2% in adults, and 12% in children, whereas origin, gender, and disease were not distinctive factors. The most prevalent point mutation was A2143G (62.5%). The point mutation was significantly less frequent in cagA-positive (11.4%) than in cagA-negative (23.6%) strains (p=0.03 OR = 0.4 95%CI = 0.19 - 0.91) as well as in cagE-positive (10.2%), cagE-negative (21.2%) (p=0.03 OR: 0.4 I.C:0.20-0.91). No difference was found in iceA or vacA alleles genotypes. Primary resistance to clarithromycin was lower than that reported in Southeast Brazil. The cagA and cagE positive H. pylori samples have few point mutations suggesting that individuals infected with virulent strains may be more susceptible to anti-H. pylori treatment.

H; pylori; Virulence factors; Clarithromycin-resistance

INTRODUCTION

The Helicobacter pylori (H. pylori) infection causes chronic gastritis, peptic ulcer disease, gastric adenocarcinoma, and MALT (mucosa-associated lymphoid tissue) lymphoma¹.

The efficacy of H. pylori eradication rates following the standard first-line therapy that includes clarithromycin and metronidazole has been declining due to the increasing resistance to antimicrobial agents in several countries². The prevalence of clarithromycin resistance varies among different geographical regions², indicating that studies on this subject are required. Notably, it has been considered that resistance to clarithromycin has predicted treatment failure³.

The main cause of clarithromycin therapeutic failure lies in key mutations of the ribosomal 23S subunit⁴. Among the three main 23S rRNA point mutations, A2146C, A2146G, and A2147G, formerly described as A2142C, A2142G, and A2143G, are predicted to be responsible for more than 90% of clarithromycin resistance cases in Western countries⁵.

PCR-based (polymerase chain reaction) molecular methods can detect the mutations, either in bacterial culture samples or in gastric mucosa fragments⁵, in addition to stool samples and gastric juice obtained by less-invasive string test⁶ procedures. The molecular methods may have an important role in the prompt detection of resistance to clarithromycin in clinical practice⁷. Several studies have demonstrated that the existence of mutations identified by molecular tests has a direct correlation with culture-based susceptibility testing⁵.

Virulence factors of H. pylori have an important role in the pathogenicity of the bacteria⁸. However, its influence on drug resistance has not been well outlined yet⁹.

The main H. pylori virulence factors are encoded by the vacuolating cytokine-associated gene (vacA) and the cytotoxin-associated gene A (cagA). There are at least 4 variable regions in the vacA: in the signal region, s1 and s2 alleles, and in the middle region, m1 or m2 alleles. These variable regions show diverse levels of toxicity to host cells, with the vacA s1/m1 being the most cytotoxin producer, followed by s1/m2, and s2/m2 genotypes that induce little or no toxicity⁸. The cagA and cagE are located in the cag Pathogenicity Island (PAI), which encodes a type IV secretion system. Patients colonized by strains carrying the cagE and cagA genes as well as the vacA s1m1 alleles have a greater risk to develop severe gastrointestinal diseases¹⁰. Another virulence marker, the iceA (gene induced by contact with gastric epithelial cells), has two alleles, iceA1, and iceA2¹¹. In some regions¹², it has been reported that the iceA1 genotype is associated with gastric disease.

Although several studies evaluate clarithromycin resistance in Brazil, there is no study in the Ceara State, the Northeast part of the country. It should be noted that the prevalence of H. pylori infection is high, the children are infected earlier by the bacterium¹³,¹⁴ and the infection is significantly associated with gastric cancer in this region¹⁴. Furthermore, few studies evaluated the association of H. pylori virulence genotypes with clarithromycin resistance.

This study aimed to evaluate the prevalence of primary resistance of H. pylori to clarithromycin, using RT-PCR in adult patients with gastric disease as well as asymptomatic children from an urban community in the Northeast region of Brazil. We also investigated the association between the resistance profiles and a panel of H. pylori virulence genotypes.

MATERIALS AND METHODS

This study was performed in the tertiary care Hospital Universitario Walter Cantidio (HUWC, Federal University of Ceara) and an urban community, the Parque Universitario. The study protocol was approved by the Research Ethics Committee of HUWC, Nº 628.750, and performed in accordance with the ethical standards set out in an appropriate version of the Declaration of Helsinki, as revised in Brazil 2013. The informed consent was obtained from all subjects and/or their legal guardians.

Patients undergoing upper gastrointestinal endoscopy to investigate dyspeptic symptoms were invited to participate. The diagnosis of gastric cancer was confirmed by histopathology according to the Classification of Lauren¹⁵.

H. pylori-positive patients who had never been treated for H. pylori infection were included. Patients were excluded if they had taken proton-pump inhibitors or antibiotics during the 8 weeks before endoscopy. Patients with renal, hepatic, or hematological diseases, as well as pregnant women, were also excluded from the study. All patients answered a questionnaire about clinical symptoms, and demographic data such as age, gender, and residence area. Patients were recruited from August 2015 to August 2017.

The gastric mucosa fragments were obtained through endoscopy, and gastric juices by enterotest¹⁴. All samples were processed to obtain DNA in order to perform molecular biology studies.

Patients

The calculation of the sample size was performed by using a formula for infinite populations (higher than 100,000) considering a confidence level of 95%, with a 5.0% of maximum error. Taking into account that the clarithromycin resistance rate is approximately 14.0% in the Northeast region of Brazil¹⁶,¹⁷, it was necessary to include at least 185 samples.

In total, 300 H. pylori-positive samples were evaluated, 260 gastric mucosa fragments were obtained through endoscopy and 40 gastric juice samples were collected by enterotest. Of these, 222 (74.0%) were 23S rRNA positive; 76.1% (198/260) of the gastric mucosa, and 60.0% (24/40) of the gastric juice.

Enterotest

A gelatin capsule containing a 90 cm long absorbent cotton thread was swallowed along with a max of 200 mL of water. 20 cm of the string’s length was attached to the patient’s cheek. After an hour, the string was removed, and the proximal 30 cm was discarded. The segment of the thread with the gastric mucus impregnated with juice was washed with 5 ml of saline solution and then placed in sterile vials containing 3 ml of brain heart infusion broth (BHI) and sent to the laboratory to be processed. The liquid in the flask was centrifuged at 13000 rpm for 10 min and processed for DNA extraction. The samples were stored at -70 ºC. The method was improved and previously validated by our group¹⁴.

Genomic DNA extraction

The H. pylori DNA was extracted from gastric mucosa and gastric juice samples, as well as from the bacterium isolated by culture. H. pylori DNA was obtained using the QIAamp DNA extraction kit (QIAgen^®, Hilden, Germany) by following the manufacturer’s guidelines. The DNA samples were stored at -20 ºC until used for gene amplification.

Detection of the virulence factors

The virulence markers were determined by PCR performed in a Thermal Cycler 2400 (Perkin Elmer Applied Biosystems, Foster City, California, USA). Briefly, the “Master mix” solution for gene amplification consisted of 5.5 μL of distilled H2O, 12.5 μL of the enzyme Taq-DNA polymerase (GoTaq green - Promega^®, Madison, Wisconsin, USA), 1.0 μL of the “primers” (Carlsbad, California, USA) specific to each gene, starting from the 5’ to the 3’ termination, in both directions (Forward and Reverse Primer). The reactions occurred separately for each gene. In each microtube, 5.0 μL of the extracted DNA was added in specific 200 μL microtubes. The amplified fragments were developed on a 1% agarose gel stained with ethidium bromide. For the amplification of the 23S gene¹⁸ as well as cagA¹⁴,¹⁸, cagE¹⁹, vacAs1, vacAs2, vacAm1, vacAm2⁸, and iceA1/iceA2¹¹ genotypes, primers were used as previously described in the literature.

Optimizing the amount of DNA per sample

The DNA was quantified by ultraviolet absorbance at 260 nm. To determine the ideal amount of DNA for the assay, serial dilutions between 10 ng and 50 ng were made to evaluate the best reading profile of the device. The amount of DNA for each sample was adjusted to 30 ng, based on the observations already made by previous studies²⁰,²¹.

Characterization of positive and negative controls

The H.pylori 23S rRNA fragment used as positive and negative controls was obtained by PCR amplification of H. pylori DNA-extracted from homogenates of bacterial cultures (strains with and without clarithromycin resistance evaluated by phenotypic method) using Hp23-F (5-CCACAGCGAT GTG GTCTCAG-3) and Hp23-R (5-CTCCATAAGAGCCAAAGCCC-3) as primers, according to conventional PCR assay¹⁷.

Assay for RT-PCR and allele discrimination

The point mutations of H. pylori 23S rRNA (A2142G and A2143G) were performed by the real-time polymerase chain reaction (RT-PCR) reported by Oleastro et al.²⁰.

The assays were performed by using a 7500 RT-PCR system^® device (Applied Biosystems, inc. Foster City, CA, USA). The reactions were prepared using Universal PCR Master Mix kit (Applied Biosystems, inc. Foster City, California, USA) optimized for reactions with the TaqMan^® assay probe containing the AmpliTaq Gold DNA polymerase. The preparation and storage of the materials were carried out according to the manufacturer’s guidelines, except for the final volume of each reaction optimized for 10 µL. The mixture prepared for RT-PCR consisted of 5.0 µL of Universal Master Mix plus 4.5 µL of DNA solution containing 30 ng and 0.5 µl of prepared assay containing: 36 µM (Forward and Reverse Primer, Table 1) and a concentration of 8 µM TaqMan MGB probes (FAM and VIC)²¹. After that, the reaction plates were centrifuged for 1 min at 4500 rpm. The amplification conditions for PCR were: preheating at 50 ºC for 2 min, polymerase activation at 95 ºC for 10 min and 40 denaturation cycles of 15 s at 92 ºC and 1 min at 60 °C for extension and annealing. The polypropylene reaction plates for 96 reactions (MicroAmp 96-Well plates, Applied Biosystems, Foster City, California, USA) were covered with adhesives for high temperature and alcohol-resistant optical microplates (Optical adhesive film, Applied Biosystems, Foster City, California, USA). In all steps, the samples were immersed in ice under little exposure to light. Each sample was evaluated in duplicate and only samples whose amplification differences did not exceed 0.8 cycles (Δ Cq ≤ 0.8) were considered for analysis²². In all samples, negative and positive controls were performed. The increase in fluorescence of the FAM or VIC dye indicates a homozygous genotype (mutation or wild), while an increase in both signals indicates a heterozygous genotype²³.

Table 1
Primers and probes used for point mutations.

23SA2142G-2142F	TCAGTGAAATTGTAGTGGAGGTGAAAA
23SA2142G-2142R	CAGTGCTAAGTTGTAGTAAAGGTCCA
	VIC: AAGACGGAAAGACC	Wild DNA probe
	FAM: AAGACGGGAAGACC	Mutant DNA probe
23SA2143G-2143F	TCAGTGAAATTGTAGTGGAGGTGAAAA
23SA2143G-2143R	CAGTGCTAAGTTGTAGTAAAGGTCCA
	VIC: AAGACGGAAAGACC	Wild DNA probe
	FAM: CAAGACGGAGAGACC	Mutant DNA probe

Statistical analysis

The SPSS Statistics for Windows (version 21.0, IBM Corp, Armonk, New York, USA) was used to perform all statistical analyses. Chi-square and Fisher’s exact tests were used to determine the statistical significance of association between categorical variables, when applicable. The mean value and standard deviation were used to describe numeric variables. A p-value of less than 0.05 was considered statistically significant.

RESULTS

Characteristics of the patients

Overall, 222 H. pylori 23S rRNA positive samples were evaluated, from 198 adult patients and 24 asymptomatic subjects residing in the community. The demographic and clinical data of the 198 adult patients are shown in Table 2.

Table 2
Distribution of 198 adult patients by age, gender, origin and gastric diseases.

Age	47.95 ± 14.53 (19 to 89 years)
Gender
Male	43.4% (86)
Female	56.5% (112)
Origin
Rural	60.6% (120)
Urban	39.40% (68)
Gastric disease
Gastric Cancer	12.1% (24)
Peptic Ulcer Disease	10.6% (21)
Gastritis	77.3% (153)

Of the 24 asymptomatic subjects living in the community, 50% (12/24) were females, with a mean age and standard deviation of 12.92 ± 3.04, ranging from 8 to 18 years old, all of them from the urban area.

Prevalence of clarithromycin resistance

Overall, the primary prevalence of H. pylori clarithromycin resistance, based on the presence of 23S rRNA point mutations A2142G and/or A2143G, was 14.4% (32/222), being 14.6% (29/198) in adult patients and 12.5% (3/24) in children living in the community. The A2142G and A2143G mutations were observed in 37.5% (12/32) and in 62.5% (20/32) of the H. pylori-positive samples, respectively. In 4 of 32 (12.5%) samples, a double point mutation, A2142G plus A2143G, was observed. Samples containing simultaneously susceptible wild and resistant mutant strains (heteroresistant samples) were observed in 19 among 32 (59.4%) samples.

The prevalence of resistant did not significantly differ between the origin of the patients (31.5% rural vs 23.3% urban area, p=0.17), adults and children (14.6% vs 12%, p=0.77) male and female (14% vs 18%, p=0.87), gastritis and peptic ulcer disease (12.5% vs 14.6%, p=0.29) as well as between gastritis and gastric cancer (12.5% vs 14.6%, p=0.86) (Table 3).

Table 3
Susceptibility of H. pylori to clarithromycin using RT-PCR according to gender, origin and gastro duodenal diseases in 198 adults.

	Resistance, n (%)	Susceptible, n (%)	p value
Gender
Male (86)	13 (15.1)	73 (84.8)	0.87
Female (112)	16 (14.2)	96 (85.7)
Origin
Inland (113)	19 (16.8)	94 (83.2)	0.32
Capital (85)	10 (11.8)	75 (88.2)
Gastric Cancer vs. Gastritis
Gastric Cancer (24)	3 (12.5)	21 (87.5)	0.86
Gastritis (153)	25 (16.3)	128 (83.6)
Peptic ulcer vs. Gastritis
Peptic ulcer (21)	1 (4.8)	20 (95.2)	0.29
Gastritis (153)	25 (16.3)	128 (83.6)

H. pylori-genotypes of virulence

The cagA was identified in 75.2% (167/222) of the samples. The prevalence of point mutation conferring clarithromycin resistance was significantly less frequent (p=0.03 OR = 0.4 95%CI = 0.19 - 0.91) in cagA-positive (19/167 - 11.4%) than in cagA-negative (13/55 - 23.6%) strains. The most prevalent point mutation was A2143G (20/32-62.5%) (9/167-5.4% of cagA positive and 11/55-20% of cagA negative strains).

The cagE was observed in 137 of 222 samples (61.7%). Among them, 14 (10.2%) had a point mutation. Point mutations were observed in 18 of 85 (21.2%) cagE-negative samples. The difference between cagE-positive and cagE-negative samples was statistically significant (p=0.03 OR: 0.4 I.C:0.20-0.91). A2143G was the most prevalent mutation, being present in 7 of the 14 cagE-positive samples and in 13 of the 18 negative ones (Table 4).

Table 4
Profile of point mutations in the 23S rRNA gene by the TaqMan RT-PCR method and association with H. pylori genotypes cagA, cagE, and iceA1, iceA2 (N = 222)

	General Mutation	Mutation A2142G	Mutation A2143G	Double Mutation
cagA +(167)	19 (11.4%)	7 (4.1%)	9 (5.4%)	3 (1.8%)
cagA -(55)	13 (23.6%)	1 (1.8%)	11 (20%)	1 (1.8%)
p value	0.025	0.413	0.003	0.992
OR (IC 95%)	0.7(0.567-1.025)	-	-	-
cagE+ (137)	14 (10.2%)	4 (2.9%)	7 (5.1%)	3 (2.1%)
cagE- (85)	18 (21.2%)	4 (4.7%)	13 (15.2%)	1 (1.1%)
p value	0.03	0.754	0.021	0.968
OR (IC 95%)	0.4 (0.20-1.91)	-	-	-
IceA1+(33)	2 (6.0%)	0 (0%)	2 (6.0%)	0 (0%)
IceA1- (189)	30 (15.8%)	8 (4.2%)	18 (9.5%)	4 (2.1%)
p value	0.139	0.485	0.755	0.893
IceA2+ (155)	22 (14.1%)	5 (3.2%)	13 (8.3%)	4 (2.5%)
IceA2- (67)	10 (14.9%)	3 (4.5%)	7 (10.4%)	0 (0%)
p value	0.887	0.646	0.813	0.437

The prevalence of iceA1 and iceA2 alleles was 14.9% (33/222) and 69.8% (155/222), respectively. A higher prevalence of mutant strains was observed in iceA1-negative (30/189, 15.8%) than in iceA1-positive (2/33, 6.0%) samples, without statistical significance (p=0.13) (Table 4). In respect to iceA2 genotype, no difference in the prevalence of the point mutation was observed between iceA2-positive (22/155-14.1%) and iceA2-negative (10/67-14.9%) samples (Table 4).

No significant difference was observed between the vacA genotypes and the point mutation conferring H. pylori resistance, regarding vacAs1-positive and negative samples, s1m1-positive and -negative genotypes and s2m2 -positive and -negative genotypes (Table 5).

Table 5
Profile of point mutations in the 23s rRNA gene by the RT-PCR method and association with vacA alleles (N = 222).

	General Mutation	Mutation A2142G	Mutation A2143G	Double Mutation
VacAs1+(173)	24 (13.8%)	7 (4.0%)	13 (7.5%)	4 (2.3%)
VacAs1-(49)	8 (16.3%)	1 (2.0%)	7 (14.2%)	0 (0%)
p value	0.67
VacAs2+(26)	4 (15.3%)	0 (0%)	4(15.3%)	0 (0%)
VacAs2-(196)	28 (14.2%)	8 (4.0%)	16 (8.1%)	4 (2.0%)
p value	0.99
VacAm1+(178)	25 (14.0%)	6 (3.3%)	15 (8.4%)	4 (2.2%)
VacAm1-(44)	7 (15.9%)	2 (4.5%)	5 (11.3%)	0 (0%)
p value	0.94
VacAm2+(42)	5 (11.9%)	0 (0%)	5(11.9%)	0 (0%)
VacAm2-(180)	27 (15.0%)	8 (4.5%)	15 (8.3%)	4 (2.2%)
p value	0.79
VacAs1m1 +(145)	19 (13.1%)	6 (4.1%)	9 (6.2%)	4 (2.7%)
VacAs1m1 -(77)	13 (16.8%)	2 (2.6%)	11 (14.2%)	0 (0%)
p value	0.57
VacAs1m2+(30)	4 (13.3%)	0 (0%)	4(13.3%)	0 (0%)
VacAs1m2 -(192)	28 (14.5%)	8 (4.1%)	16 (8.3%)	4 (2.0%)
p value	0.99
VacAs2m1 +(20)	3 (15.0%)	1 (5.0%)	1 (5.0%)	1 (5.0%)
VacAs2m1 -(202)	29 (14.4%)	7 (3.5%)	19 (9.4%)	3 (2.6%)
p value	0.99
VacAs2m2+(18)	3 (16.6%)	0	3 (16.6%)	0
VacAs2m2 -(204)	29 (14.2%)	8 (3.9%)	17 (8.3%)	4 (2%)
p value	0.99

DISCUSSION

This study aimed to evaluate H. pylori resistance to clarithromycin by using RT-PCR in gastric mucosa samples from adult patients and gastric juice sample obtained by string test from asymptomatic children resident in the community of the Northeastern region of Brazil. Furthermore, we assessed the association of cagA, cagE, vacA and iceA virulence factors of H. pylori and resistance to clarithromycin.

In this study, we used the TaqMan^® RT-PCR to detect resistance of H. pylori to clarithromycin, a low-cost test that avoids reading errors, allowing analysis of many samples. In fact, RT-PCR has been used to detect clarithromycin resistance in gastric mucosa samples, in feces, as well as in gastric juice, with good accuracy when compared with culture and antibiogram⁶,²¹,²⁴.

The overall prevalence of H. pylori clarithromycin resistance in this study was 14.4%, a ratio that is acceptable for the empirical use of clarithromycin-based regimens²⁵. Several studies have used genotypic methods to detect primary clarithromycin resistance in Brazil, without major variations among them. A National study that evaluated samples from four different regions using GenoType HelicoDR showed an overall prevalence of 16.9%¹⁶. A primary resistance rate of 14.5% using phenotypic and genotypic methods was reported in the Northeast and 16.6% in the North of Brazil¹⁶.

In our cohort, the resistance to clarithromycin was more prevalent in patients with gastritis when compared to patients with peptic ulcer or gastric cancer, but without statistical significance, which may be explained by the low number of patients with peptic ulcer. On the other hand, a study from Turkey found a higher prevalence of clarithromycin resistance in the patients with peptic ulcer 40.9% when compared to those with gastritis. 24.6%²⁶.

This study was the first to evaluate the resistance to clarithromycin in gastric juice from asymptomatic children, which showed no difference between adults and children with a lower prevalence when compared to those reported in studies conducted in São Paulo, the Southeast region of Brazil, where a resistance rate of 27% was found in samples from children and adolescents who underwent endoscopy due to gastrointestinal symptoms in 2010, 26.7%²⁷ in 2011²⁴, and 19.5% in 2014²⁸. A higher prevalence of resistance to clarithromycin in children has been attributed to the greater use of antibiotics in this age group. It is possible that the lower prevalence found in our study is due to the fact that we evaluated asymptomatic children from a low-income community.

Among the resistant strains, the A2143G mutation was the most frequently observed, in accordance with researches from Europe, Japan, Spain, Australia, France and Brazil¹⁶,¹⁷,²⁹-³¹. Conversely, studies from Egypt reported that the A2142G mutation was more frequent than the A2143G³².

Heteroresistance to clarithromycin (samples that have a simultaneous presence of wild and mutant strains) were observed in 59.4% of our samples, a finding that has also been reported in other studies in Brazil, such as in Recife (77.8%)¹⁷ and in a national multi-center study (73.5%)¹⁶. High rates of clarithromycin heteroresistance were also detected in samples from Spain (51.3%)³³ and Italy (76.3%)³⁴.

The association between H. pylori virulence factors and clarithromycin resistance has been evaluated in several researches with divergent results³⁵. In this study, the overall prevalence of cagA positivity was 75.5%, 23S rRNA point mutation of clarithromycin was found in 11 % of these strains with a significant association with cagA-negative strains. The low prevalence of primary resistance to clarithromycin in H. pylori cagA-positive strains coincides with studies reported from the Southeast region of Brazil³⁶. On the contrary, other studies demonstrated that cagA positivity was not associated with resistance status³¹,³²,³⁷.

A meta-analysis study showed that the treatment efficacy was lower in patients infected by cagA-negative and vacAs2-positive strains and concluded that the treatment success is higher in subjects colonized with highly virulent strains⁹. It has been postulated that infection with cagA-positive strains, a more virulent genotype, is associated with high gastric epithelium lesions, which may facilitate the antimicrobials to reach higher concentrations in inflamed mucosa³⁸.

In this study, the absence of cagE gene was significantly associated with the resistance of clarithromycin. Conversely, a study from Turkey reported that the presence of cagE gene was associated with clarithromycin resistance³⁹ while other studies, such as that the one reported by Godoy et al.³⁶ in the Southeast region of Brazil, have demonstrated no association. These differences among regions point that further evaluation is needed.

Regarding the iceA, our results showed a high prevalence of iceA2 -positive strains, in accordance with the study of Yamaoka et al.⁴⁰ which demonstrated a higher prevalence of iceA1 than iceA2 strains in Asian countries, while the opposite was observed in the Western countries. Similarly to that observed in the Southeast region of Brazil³⁶ we did not observe an association between iceA genotypes and clarithromycin point mutations.

This study has several limitations; first we did not compare clarithromycin resistance by using RT-PCR with phenotypic methods; however, the accuracy of RT-PCR to detect clarithromycin resistance has been widely evaluated in other studies. In addition, RT-PCR was properly standardized using H. pylori strains resistant and sensitive to clarithromycin by phenotypic method. Second, the number of included samples of children is small, which may be explained by the fact that we studied asymptomatic children from a specific community.

CONCLUSION

In conclusion, the H. pylori resistance rate to clarithromycin we observed (14.41%) is an acceptable rate to empirically use the standard scheme for anti-H. pylori containing clarithromycin. The H. pylori cagA and cagE positive-samples have few punctual mutations that confer resistance to clarithromycin. Possibly the subjects infected with virulent strains are more susceptible to anti-H. pylori treatment containing clarithromycin.

ACKNOWLEDGMENTS

This work was supported by Fundacao de Apoio ao Desenvolvimento Cientifico e Tecnologico do Ceara, grant Nº 13506715-4. We wish to thank Antonio B. Viana Junior for the statistical analysis.

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Publication Dates

• Publication in this collection
  13 July 2022
• Date of issue
  2022

History

• Received
  23 Mar 2022
• Accepted
  16 May 2022