| Abstract|| |
Introduction: The aim of the study is relative proportion of cytotoxin-associated gene A (cagA) virulence marker in Helicobacter pylori isolates and gastric biopsy samples by polymerase chain reaction (PCR). Methods: This cross-sectional study was conducted at a tertiary care hospital setting. Gastric biopsy tissues from 200 patients, suffering from upper gastrointestinal tract disorders, were examined for H. pylori infection using methods, such as hematoxylin and eosin (H and E) staining, 16S rRNA (Ribosomal ribonucleic acid), and cagA gene PCR. Chi-square and kappa statistics were used to find the association and agreement between the tests, respectively; P ≤ 0.05 was considered statistically significant. Screening tests' accuracy was calculated in terms of sensitivity and specificity along with positive and negative predictive values. Results: Out of 200 patients, H. pylori was detected in 14.5%, 48.5%, and 31% patients by H and E staining, 16S rRNA, and cagA PCR, respectively. Sensitivity and specificity of cagA PCR as compared to H and E staining were 89.6% and 78.9%, respectively. Conclusions: CagA detection directly from biopsy specimen by PCR can potentially and rapidly determine the patient's status, especially when at a higher risk of peptic ulcer.
Keywords: Culture, cytotoxin-associated gene A, diagnosis, gastric biopsy, Helicobacter pylori, polymerase chain reaction
|How to cite this article:|
Vagarali MA, Metgud SC, Bannur H, Dodamani SS. A cross-sectional study on molecular detection of Helicobacter pylori cytotoxin-associated gene A and 16SrRNA gene from gastric biopsy specimens. J Global Infect Dis 2021;13:120-5
|How to cite this URL:|
Vagarali MA, Metgud SC, Bannur H, Dodamani SS. A cross-sectional study on molecular detection of Helicobacter pylori cytotoxin-associated gene A and 16SrRNA gene from gastric biopsy specimens. J Global Infect Dis [serial online] 2021 [cited 2021 Oct 17];13:120-5. Available from: https://www.jgid.org/text.asp?2021/13/3/120/325214
| Introduction|| |
Helicobacter pylori (H. pylori) is a fastidious, Gram-negative, microaerophilic, spiral-shaped bacterium present in gastric mucosa of the 50% human beings across the world population and 70%–90% of human population in developing countries., About 20% of H. pylori-infected individuals tend to develop gastrointestinal disorders, during their lifetime.
H. pylori plays a significant role in chronic gastritis and peptic ulcer disease development and is a potential risk factor for mucosa-associated lymphoid tissue lymphoma and gastric adenocarcinoma. The consortium between H. pylori and gastroduodenal diseases reveals a necessity for diagnosing the H. pylori presence in acid peptic disease. Despite a number of diagnostic methods available for H. pylori detection, such as smear examinations, rapid urease test, serological, urea breaths, and fecal antigen tests along with bacteriological culture and its identification, none of the method individually meets the requirement of sensitivity and specificity for its identification. Therefore, a combination of the tests is required to get the highest positive results.
Researchers have made multiple attempts previously to implement molecular diagnostic tests for early diagnosis of H. pylori to prevent further complications.,, They pointed out that molecular diagnostic tests such as polymerase chain reaction (PCR) are preferable choice due to higher sensitivity and specificity even at low bacterial load., Different genes, such as urease A (ureA),,16S rRNA, 23S rRNA,, cytotoxin-associated gene A (cagA), and vacuolating toxin A (vacA), have been targeted by researchers to improve the detection of H. pylori. However, cagA and vacA can determine the clinical consequence of H. pylori infections.
cagA gene, a marker of pathogenicity island and indicator of severity due to various manifestation, is not possessed by all strains. Moreover, cagA gene polymorphism is evident in H. pylori isolates from different geographical regions. Although majority of H. pylori isolates from peptic ulcer cases are cagA+, there are very few studies directly investigating cagA gene presence using stomach biopsy., Therefore, we have evaluated PCR technique for detecting cagA gene presence in H. pylori isolates from both stomach biopsies and their corresponding H. pylori culture isolates.
| Methods|| |
This was a cross-sectional study involving gastric mucosal biopsies from 200 subjects with acid peptic disease, which were obtained aseptically during endoscopy.
Sample size calculation
Two hundred gastric tissue biopsies from the study subjects were enrolled. Estimation of sample size was done based on the following formula:
where N = sample size
p = sensitivity (70%),
q = 100-p,
d = absolute error which is 10%
N = 200
Error = 10%, sensitivity = 70%, 95% confidence interval
The study was conducted in the Microbiology department of a tertiary care hospital in accordance with the Declaration of Helsinki and was approved by the local ethics committee of the institute. Written informed consent was obtained from all patients before their enrollment in this study. The data were collected from October 2012 to 2014.
Subjects included in the study were from both the genders, comprised different age groups, suffering from gastric and duodenal diseases only, and having upper gastrointestinal disease complaints, such as upper abdominal pain, vomiting, and epigastric pain, immediately after food, empty stomach, and 2 h after food. However, subjects on analgesics, antibiotics, and proton-pump inhibitors before 48 h of endoscopic procedure and/or having prior history of gastric surgery or active bleeding ulcers were excluded from the study. Informed consent was taken from the subjects before their enrollment into the study.
Endoscopic samples were collected from the overnight-fasted subjects using a fiberoptic endoscope. Endoscope and biopsy forceps were soaked in 2% glutaraldehyde for 30 min before endoscopy and rinsed thoroughly with sterile saline just before the specimen collection. All the biopsy samples were immediately transferred to 10% buffered formalin solution that was used for bacteriological culture using Columbia agar and PCR.
Hematoxylin and eosin staining
Gastric tissue sections of antral part from 10% buffered formalin were processed for hematoxylin and eosin (H and E) staining by following the standard protocol. Identification of H. pylori was done under a microscope (×400) by observing pink, curved bacilli on luminal surface of gastric epithelium. H and E staining was taken as a reference method in order to compare other methods.
Molecular characterization of 16S r RNA and cytotoxin-associated gene A genes
PCR was used to detect H. pylori with the help of primers specific for 16S rRNA and cagA genes. 16SrRNA gene was used for reclassification of the organism and cagA gene acts as virulence marker; hence, a combination of genes was used to identify pathogenic H. pylori.
Primers for 16S rRNA and cytotoxin-associated gene A genes
16S rRNA primers
Forward: JW 21:5′-GCGACCTGCTGGAACATTAC-3′ and
Reverse: JW 22: 5′-CGTTAGCTGCATTACTGGAGA-3′
Product size: 139 bp
Cytotoxin-associated gene A primers
cag A Forward: 5′-AGACAACTTGAGCGAGAAAG-3′ and
cag A Reverse: 5′-TATTGGGATTCTTGGAGGCG-3′,
Product size-320 bp
DNA was extracted from the gastric biopsy tissues and their corresponding bacterial isolates along with reference strains of H. pylori – ATCC 13629 and ATCC 43504 (procured from IMTECH Chandigarh) using the modified proteinase K method as per the standard protocol. Deparaffinization of tissue was done before DNA extraction using the protocol of Gohar and Mohammadi. DNA was extracted from both biopsy samples and their corresponding bacterial isolates and amplified using PCR by following the standard protocols. Further, all the samples were kept at −20°C, until further use.
Polymerase chain reaction protocol
Primer and target combination were optimized and the same was used throughout the study. Following DNA extraction, PCR reaction mix was prepared in a sterile microcentrifuge PCR tubes by adding 10 μl master mix, 1.5 μl DNA, 0.5 μl forward primer (10 pM), 0.5 μl reverse primer (10 pM), and 7.5 μl nuclease-free water, to make up the final volume of 20 μl. This was followed by mixing and centrifugation for 5 s at <2000 rpm/min.
PCR reaction mix was amplified using a thermocycler (Veriti, Applied Biosystems, USA), with initial denaturation (1 cycle at 95°C for 5 min), followed by denaturation (35 cycles, 95°C, 1 min), annealing, and extension cycles (55°C and 72°C for 1 min each). Final extension for 1 cycle was performed at 72°C for 10 min. Amplified samples were kept at 4°C until use.
Identification on gel
Electrophoresis of 10 μl amplified product was done using 2% agarose along with standard molecular weight markers, followed by DNA staining with 0.5 μg/ml ethidium bromide solution. The bright fluorescent bands of amplified PCR products (product size – 16S r RNA: 139 bp and cag A: 320 bp) and 100 base pair DNA molecular marker were visualized under ultraviolet light using Syngene G Box image analysis system.
SPSS software version 12 (Chicago, USA) was used for the data analysis. Sensitivity and specificity along with positive and negative predictive values were calculated to assess the accuracy for screening tests. Chi-square test and kappa statistics were applied to find association and agreement between the tests, respectively. P ≤ 0.05 was considered statistically significant.
| Results|| |
As per the demographic distribution of the subjects, 50.5% belonged to the age group of <40 years, while 20.5%, 17.5%, and 11.5% were from the age group of 51–60 years, 41–50 years, and >61 years, respectively. Male predominance was observed to be 76%. H. pylori was detected in biopsy samples by observing the pink, curved bacilli on luminal surface of gastric epithelium (×400) using H and E method, as presented in [Figure 1].
|Figure 1: Hematoxylin and eosin staining showing curved bacilli over luminal surface of gastric epithelium (×400)|
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Out of 200 subjects, 29 were H. pylori-positive cases identified using H and E method, out of which 21 and 8 were cases of chronic gastritis and peptic ulcer, respectively. However, only five subjects were found to be positive for cultures, out of which two had chronic gastritis and three suffered from peptic ulcer [Table 1]. Representative images of gene identification on gel of 16S rRNA and cagA genes are presented in [Figure 2] and [Figure 3], respectively. 16S rRNA PCR detected 97 positive H. pylori cases, out of which 87 were chronic gastritis and 10 were peptic ulcer cases, whereas cagA PCR identified 62 H. pylori positive cases, of which 53 cases were chronic gastritis and 9 were peptic ulcer, respectively. All the methods were found to be statistically significant (P < 0.05) in evaluating the H. pylori-positive cases, as tabulated in [Table 1]. Moreover, all the positive cultures and their corresponding gastric biopsy samples showed positive results for cagA gene and 16S rRNA by PCR.
|Figure 2: Gel electrophoresis of the polymerase chain reaction amplified product of Helicobacter pylori16S rRNA|
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|Figure 3: Gel electrophoresis of Helicobacter pylori cytotoxin-associated gene A gene|
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The comparative account of 16S rRNA PCR and cag A PCR showed 48.5% and 31% positive cases, respectively, when compared with H and E staining, which yielded 14.5% positive cases [Table 2]. However, the sensitivity and specificity of 16S rRNA PCR were found to be 96.55% and 59.65%, respectively, while cag A PCR sensitivity and specificity were found to be 89.66% and 78.95%, on comparing with H and E staining, respectively [Table 3]. The kappa values were found to be 0.2848 and 0.4659, thus showing moderate agreement on comparing the H and E staining results with 16S rRNA PCR and cagA PCR results, respectively [Table 3].
|Table 2: Comparative account of hematoxylin and eosin stain versus 16S ribosomal ribonucleic acid polymerase chain reaction and hematoxylin and eosin stain versus cagA polymerase chain reaction|
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|Table 3: Statistics of diagnostic tests in terms of sensitivity, specificity and κ values|
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| Discussion|| |
In this study, H and E staining was taken as reference method as it is a popular and practical diagnostic method with an added advantage of providing histopathologic features of stomach epithelium, such as degree of inflammation and mucosal changes and compared with PCR results of 16S rRNA and cagA gene to calculate accuracy in terms of sensitivity, specificity, and predictive values (positive and negative). Similar approach of H. pylori detection using H and E staining was done by Mehmood et al.
H. pylori is usually seen in active chronic gastritis due to prolonged colonization and inflammation of epithelial lining of stomach in most of the individuals. Conversely, only 2% of patients were noticed with minimal or no mucosal inflammation when suffering from H. pylori infection in the present study.
Our observation showed 14.5% positivity with H and E staining of gastric tissue sections; however, different degrees of positivity were reported by researchers, which were not accorded with our results.,,, Adlekha et al. found that H and E staining resulted in 62% of positive cases out of 530 specimens collected from gastric endoscopic examinations. Whereas, Akanda et al. and Ahmad et al. reported 45.6% and 34% positive cases by H and E staining, respectively. On the contrary, Kaur et al. reported 8% prevalence on histological examinations of biopsies.
Furthermore, sensitivity and specificity of the histology were reported to be affected due to various reasons: expertise or trained personnel and the levels at which the sections were taken may affect the positivity of the H and E staining. For example, in some cases of gastric atrophy where the bacterial density is less because of deprivation of nutrients, resulting in less chance of H. pylori-positive cases from biopsies. These changes led to decreased stomach bacterial load, owing to scarcity of nutrients for H. pylori and may lead to false negative test by H and E method.
We used JW 21 and 22 primers, which showed specificity for H. pylori DNA detection by the presence of a 139-bp fragment of 16S rRNA gene and was in accordance with the findings of Samra et al. where they detected 139-bp fragment in 10 biopsies samples out of 18. They detected an amplified 16S rRNA gene segment of 139 bp from drinking water and vomiting fluids, thereby confirming that direct detection of H. pylori positive samples can be possible by PCR. Moreover, PCR specificity is useful in ruling out the cross-reaction with other bacteria, such as E. coli and other important organism, such as Campylobacter and Helicobacters (H. cinnaedi, H. fenelliae, and H. muselae) species. Recent studies showed that PCR analysis had improved sensitivity to detect DNA, encoded from 16S rRNA gene of H. pylori from gastric tissue samples and possessed a higher degree of positivity and accuracy (55% and 80%) to demonstrate H. pylori presence, as compared to H and E method. However, variations in PCR detection rates could be possible due to low bacterial load in biopsies.
Till date, only few studies had analyzed such a large sample number and our study was among one of them where we studied 200 subjects and analyzed the biopsy samples by PCR for 16S rRNA and cagA genes. We observed that 97/200 (48.50%) cases were positive for 16S rRNA PCR with 96.55% sensitivity and 59.65% specificity. Hence, our observations showed the importance of PCR for H. pylori detection from stomach biopsies. Smith et al. reported that 52.38% of cases were found to be of H. pylori positive with 100% sensitivity and 68% specificity for 16S rRNA on comparing with H and E staining. In western regions 60%-70% of H. pylori strains were cagA positive and were associated with gastric cancer and duodenal ulcer. Thus, we also detected the cagA presence by PCR, a pathogenicity indicator using gastric biopsies and 62 (31%) subjects were cagA positive with 89.66% sensitivity and 78.95% specificity. Similar results were reported by Smith et al. detection of 35% cagA positive (19/42) of the biopsy specimens of H. pylori were among Nigerian people with 92.9% sensitivity and 78.6% specificity on comparing with histological examinations (H and E staining and Giemsa staining). Conversely, higher occurrence of cagA was reported by Bindayna et al. in biopsy samples (59%) and clinical isolates (62%).
The present study also demonstrated the existence of a good association of cagA+ strains between biopsies with endoscopic findings, which correlates with observations of Bindayna et al. Our finding of 85.48% subjects of chronic gastritis and 14.52% of peptic ulcer pointed toward the important findings of cagA gene positivity among different clinical conditions suffering from gastric problems and were in accordance with the results of Bindayna et al. having cagA positivity of 80% and 100% for duodenal ulcer and chronic gastritis cases, respectively. Therefore, cagA presence may be associated with increased manifestations of complications. Thus, the presence of certain genotype, such as cagA in isolates, can be closely related to cause severe inflammation of stomach mucosa, leading to severe gastritis and peptic ulcer.
Furthermore, five H. pylori positive cultures were isolated out of 200 biopsy samples that were grown on culture media. All the five cultures along with their corresponding gastric biopsy samples were tested and noted to be 100% cagA positive in accordance with the results of Mishra et al. where 54 bacterial isolates along with their respective biopsy tissues were cagA positive, out of which majority of patients suffered from duodenal ulcer and chronic gastritis. Furthermore, cagA gene identification by PCR directly from samples of gastric biopsy carries more value as H. pylori is microaerophilic and fastidious organism and its culturing is difficult, which takes longer time for culturing and identification. Therefore, cagA gene typing helps in identifying strains that are associated with pathogenicity and disease severity. However, geographical, environmental, and agent determinants together determine disease outcome.
Thus, H. pylori diagnosis using PCR can detect H. pylori DNA that can act as an indicator of infections. Importance of PCR is due to its specificity, rapid test outcome, and detecting DNA from nonviable cells. However, every method has certain disadvantages and the major disadvantages of PCR include practicability and cost factor along with false negativity due to the presence of inhibitors, thereby affecting the result of PCR., Our observation on PCR for 16S rRNA gene detection from biopsies was found to be quite sensitive, thereby establishing its high prognostic value where it can detect bacteria even at very low number that were usually missed by other methods, including culture. Furthermore, genotypic level variability exhibited by H. pylori strains has got importance in the molecular biology research field. Combination of 16S rRNA and cagA PCR can detect H. pylori, belonging to virulent species, owing to its specificity, thereby confirming the presence of pathogenic H. pylori. Hence, our study showed the importance of PCR for studying 16S rRNA and cagA directly from gastric biopsies, thereby allowing rapid detection of patients who are prone to develop peptic ulcer and infection detection at early stage is crucial for preventing further complications. In future, this study can be extended to other virulence-associated genes.
| Conclusion|| |
Detection of cagA directly from biopsy specimen helps in rapid diagnosis of H pylori infections.
Research quality and ethics statement
This study was approved by the Institutional Review Board/Ethics Committee of K.L.E. University, Belgaum, India. IRB No 2494 (A) 2012-13. The authors followed applicable EQUATOR Network (“http:// www.equator-network.org/) guidelines during the conduct of this research project.
The authors gratefully thank Dr. Santosh Hazare, Professor of Gastroenterology, for providing endoscopic gastric biopsy samples to carry out the study. We are also thankful to all faculty and facilities rendered in KLE University's Dr. Prabhakar Kore Basic Science Research Centre, Belagavi.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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Dr. Manjula A Vagarali
Department of Microbiology, JNMC, KAHER, Belagavi, Karnataka
Source of Support: None, Conflict of Interest: None
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2], [Table 3]