Prevalence of CagA and antimicrobial sensitivity of H. pylori isolates of patients with gastric cancer in Egypt

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorAl-Eraky D.M.
dc.contributor.authorHelmy O.M.
dc.contributor.authorRagab Y.M.
dc.contributor.authorAbdul-Khalek Z.
dc.contributor.authorEl-Seidi E.A.
dc.contributor.authorRamadan M.A.
dc.contributor.otherDepartment of Microbiology and Immunology
dc.contributor.otherOctober University for Modern Sciences and Arts
dc.contributor.otherCairo
dc.contributor.otherEgypt; Department of Microbiology and Immunology
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherCairo University
dc.contributor.otherCairo
dc.contributor.otherEgypt; Department of Medical Microbiology and Immunology
dc.contributor.otherFaculty of Medicine
dc.contributor.otherCairo University
dc.contributor.otherCairo
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:40:54Z
dc.date.available2020-01-09T20:40:54Z
dc.date.issued2018
dc.descriptionScopus
dc.description.abstractBackground: Helicobacter pylori (H. pylori) infection has been recognized as a significant threat for gastric cancer. However, studies that investigated the oncogenic factors and antimicrobial resistance of H. pylori in Egyptian isolates with gastric cancer are rare. The current study aimed to examine: (1) The pattern of antimicrobial resistance of H. pylori isolates of Egyptian gastric cancer patients, and (2) the prevalence of Cytotoxin-associated gene A (CagA). Methods: Samples were collected from patients with gastric cancer. Isolation of H. pylori was performed using Columbia blood agar supplemented with 10% horse blood, and selective supplement of H. pylori for 3 to 5 days at 37 �C under microaerophilic condition. Isolates were identified by biochemical traits of H. pylori: oxidase, urease and catalase tests. Antimicrobial susceptibility of H. pylori isolates was examined against five antimicrobial agents using disc diffusion method. After that, extraction of DNA and Polymerase Chain Reaction (PCR) were performed to amplify the target genes. Results: Twelve samples were collected from six males and six females Egyptian patients with cancer with an age range from 22 to 65 years. These cases are scarce and samples were collected over a period of almost eleven months. All isolates were confirmed as positive H. pylori through colony morphology and biochemical tests. The most effective antibiotic found was ciprofloxacin whereas all isolates showed resistance to metronidazole and erythromycin. The target CagA oncogene gene with expected product size was reported and seven (out of twelve) isolates (58%) were identified as CagA positive. Conclusion: The current study is unique in two main aspects. First, it reported the pattern of antimicrobial susceptibility and prevalence of CagA gene in H. pylori from Egyptian patients. Second, it exclusively recruited isolates from gastric cancer patients which were confirmed by clinical and laparoscopic examination. The moderately high prevalence of CagA gene in Egyptian cancer patients calls for more vigilance against that oncogene. � 2018 The Author(s).en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=5700191215&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.1186/s13027-018-0198-1
dc.identifier.doiPubMed ID :
dc.identifier.issn17509378
dc.identifier.otherhttps://doi.org/10.1186/s13027-018-0198-1
dc.identifier.otherPubMed ID :
dc.identifier.urihttps://t.ly/epML3
dc.language.isoEnglishen_US
dc.publisherBioMed Central Ltd.en_US
dc.relation.ispartofseriesInfectious Agents and Cancer
dc.relation.ispartofseries13
dc.subjectAntimicrobial sensitivityen_US
dc.subjectCagAen_US
dc.subjectEgypten_US
dc.subjectGastric canceren_US
dc.subjectH. pylorien_US
dc.subjectamoxicillinen_US
dc.subjectciprofloxacinen_US
dc.subjectcytotoxin associated gene Aen_US
dc.subjecterythromycinen_US
dc.subjectmetronidazoleen_US
dc.subjectoncoproteinen_US
dc.subjecttetracyclineen_US
dc.subjectunclassified drugen_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectalertnessen_US
dc.subjectantibiotic resistanceen_US
dc.subjectantibiotic sensitivityen_US
dc.subjectArticleen_US
dc.subjectbacterial strainen_US
dc.subjectbacterium colonyen_US
dc.subjectbacterium isolateen_US
dc.subjectbiochemical analysisen_US
dc.subjectCagA geneen_US
dc.subjectclinical articleen_US
dc.subjectcontrolled studyen_US
dc.subjectdisease eradicationen_US
dc.subjectdisk diffusionen_US
dc.subjectDNA extractionen_US
dc.subjectEgypten_US
dc.subjectfemaleen_US
dc.subjectgene amplificationen_US
dc.subjectgene identificationen_US
dc.subjectgene sequenceen_US
dc.subjectHelicobacter pylorien_US
dc.subjecthumanen_US
dc.subjectmaleen_US
dc.subjectoncogeneen_US
dc.subjectpolymerase chain reactionen_US
dc.subjectprevalenceen_US
dc.subjectpriority journalen_US
dc.subjectstomach canceren_US
dc.titlePrevalence of CagA and antimicrobial sensitivity of H. pylori isolates of patients with gastric cancer in Egypten_US
dc.typeArticleen_US
dcterms.isReferencedByEusebi, L.H., Zagari, R.M., Bazzoli, F., Epidemiology of Helicobacter pylori Infection (2014) Helicobacter., pp. 1-5; Nagy, P., Johansson, S., (2016) Molloy-bland M, , Systematic review of time trends in the prevalence of Helicobacter pylori infection in China and the USA Gut Pathog; Khalifa, M.M., Sharaf, R.R., Aziz, R.K., (2010) Helicobacter Pylori: A Poor Man's Gut Pathogen? Gut Pathog; Ahmed, N., Tenguria, S., Nandanwar, N., Helicobacter pylori - A seasoned pathogen by any other name (2009) Gut Pathog., 1, p. 24. , 20030808 2806874; Hunt, R.H., Xiao, S.D., Megraud, F., Leon-Barua, R., Bazzoli, F., Van Der Merwe, S., Helicobacter pylori in developing countries. World gastroenterology organisation global guideline (2011) J. Gastrointest. Liver Dis., pp. 299-304; Wang, F., Meng, W., Wang, B., Qiao, L., Helicobacter pylori-induced gastric inflammation and gastric cancer (2014) Cancer Lett., pp. 196-202; Wroblewski, L.E., Peek, R.M., Wilson, K.T., Helicobacter pylori and gastric cancer: Factors that modulate disease risk (2010) Clin. Microbiol. Rev., pp. 713-739; Kienesberger, S., Perez-Perez, G.I., Rivera-Correa, J.L., (2012) Gut Pathog, 4, p. 9; Kusters, J.G., Van Vliet, A.H.M., Kuipers, E.J., Pathogenesis of helicobacter pylori infection (2006) Clin Microbiol Rev, 19, pp. 449-490. , 16847081 1539101; Busler, V.J., Torres, V.J., McClain, M.S., Tirado, O., Friedman, D.B., Cover, T.L., Protein-protein interactions among helicobacter pylori cag proteins (2006) J Bacteriol, 188, pp. 4787-4800. , 16788188 1482994; Vannini, A., Roncarati, D., Spinsanti, M., Scarlato, V., Danielli, A., In depth analysis of the Helicobacter pylori cag pathogenicity island transcriptional responses (2014) PLoS One [Internet], 9, p. e98416. , http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0098416; Delgado-Rosado, G., Dominguez-Bello, M., Massey, S.E., Positive selection on a bacterial oncoprotein associated with gastric cancer (2011) Gut Pathog. [Internet]. BioMed Central, 3, p. 18. , http://gutpathogens.biomedcentral.com/articles/10.1186/1757-4749-3-18, [cited 2018 Jan 19]; Safavi, M., Sabourian, R., Foroumadi, A., Treatment of helicobacter pylori infection: Current and future insights (2016) World J Clin Cases, 4, pp. 5-19. , 26798626 4714294; Michel, A., Pawlita, M., Boeing, H., Gissmann, L., Waterboer, T., Helicobacter pylori antibody patterns in Germany: A cross-sectional population study (2014) Gut Pathog., 6, p. 10; De, R., Kundu, P., Swarnakar, S., Ramamurthy, T., Chowdhury, A., Nair, G.B., Antimicrobial activity of curcumin against helicobacter pylori isolates from India and during infections in mice (2009) Antimicrob Agents Chemother, 53, pp. 1592-1597. , 19204190 2663130; De, O.J.G., Cht, F., Acs, C., Rota, C.A., Meurer, L., Silveira, T.R., Prevalence of infection with cagA-positive Helicobacter pylori strains among children and adolescents in southern Brazil Arq. Gastroenterol. [Internet], 51, pp. 180-185. , http://www.ncbi.nlm.nih.gov/pubmed/25296076, [cited 2018 Jan 14]; Bonacorsi, C., Da Fonseca, L.M., Msg, R., Kitagawa, R.R., Vilegas, W., Comparison of Brazilian Plants Used to Treat Gastritis on the Oxidative Burst of Helicobacter pylori-Stimulated Neutrophil (2013) Evid. Based. Complement. Alternat. Med. [Internet], 2013, p. 851621. , http://www.hindawi.com/journals/ecam/2013/851621/, [cited 2018 Jan 14]; Contreras, M., Abrante, L., Salazar, V., Reyes, N., Garc�a-Amado, M.A., Fern�ndez-Delgado, M., Heterogeneity of cag genotypes of helicobacter pylori in the esophageal mucosa of dyspeptic patients and its relation to histopathological outcomes (2014) Int J Infect Dis, 26, pp. 91-95. , 25016039; Toledo, H., L�pez-Sol�s, R., Tetracycline resistance in Chilean clinical isolates of helicobacter pylori (2009) J Antimicrob Chemother, 65, pp. 470-473. , 20035020; Guti�rrez-Escobar, A.J., Trujillo, E., Acevedo, O., Bravo, M.M., Phylogenomics of Colombian helicobacter pylori isolates (2017) Gut Pathog, 9, p. 52; Talebi Bezmin Abadi, A., Mohabbati Mobarez, A., High Prevalence of Helicobacter pylori hopQ II Genotype Isolated from Iranian Patients with Gastroduodenal Disorders (2014) J. Pathog. [Internet], 2014, p. 842469. , https://doi.org/10.1155/2014/842469; Miftahussurur, M., Tuda, J., Suzuki, R., Kido, Y., Kawamoto, F., Matsuda, M., Extremely low helicobacter pylori prevalence in North Sulawesi (2014) Indonesia and Identification of A Maori-tribe Type Strain: A Cross Sectional Study Gut Pathog, 6, p. 42; Rasheed, F., Campbell, B.J., Alfizah, H., Varro, A., Zahra, R., Yamaoka, Y., Analysis of clinical isolates of helicobacter pylori in Pakistan reveals high degrees of pathogenicity and high frequencies of antibiotic resistance (2014) Helicobacter, 19, pp. 387-399. , 24827414 4162849; Alfaresi, M.S., Elkoush, A.A., Characterization of clarithromycin resistance in isolates of helicobacter pylori from the UAE (2010) Indian J Gastroenterol, 29, pp. 116-120. , 20658326; Alazmi, W.M., Siddique, I., Alateeqi, N., Al-Nakib, B., Prevalence of Helicobacter pylori infection among new outpatients with dyspepsia in Kuwait (2010) BMC Gastroenterol. [Internet], p. 10. , https://bmcgastroenterol.biomedcentral.com/articles/10.1186/1471-230X-10-14; Siddique, I., Al-Qabandi, A., Al-Ali, J., Alazmi, W., Memon, A., Mustafa, A.S., Association between helicobacter pylori genotypes and severity of chronic gastritis, peptic ulcer disease and gastric mucosal interleukin-8 levels: Evidence from a study in the Middle East (2014) Gut Pathog., 6, p. 41; Ghaith, D., Elzahry, M., Mostafa, G., Mostafa, S., Elsherif, R., Ramzy, I., Mutations affecting domain v of the 23S rRNA gene in Helicobacter pylori from Cairo, Egypt (2016) J. Chemother. [Internet], 28, pp. 367-370. , https://www.tandfonline.com/doi/full/10.1179/1973947815Y.0000000067, [cited 2018 Jun 14]; Mohammad, M.A., Hussein, L., Coward, A., Jackson, S.J., Prevalence of helicobacter pylori infection among Egyptian children: Impact of social background and effect on growth (2008) Public Health Nutr, 11, pp. 230-236. , 17666124; Hanafy, A.S., El Hawary, A.T., Hamed, E.F., Hassaneen, A.M., Impact of Helicobacter pylori eradication on refractory thrombocytopenia in patients with chronic HCV awaiting antiviral therapy (2016) Eur. J. Clin. Microbiol. Infect. Dis. [Internet], 35, pp. 1171-1176. , http://link.springer.com/10.1007/s10096-016-2650-8, Springer Berlin Heidelberg; [cited 2018 Jun 14]; El-Fakhry, A.A., Ma, E., Badr, R.I., El-Nady, G.M., Mesbah, M.R., Youssef, T., Association of the CagA gene positive Helicobacter pylori and tissue levels of interleukin-17 and interleukin-8 in gastric ulcer patients (2012) Egypt. J. Immunol. [Internet], 19, pp. 51-62. , http://www.ncbi.nlm.nih.gov/pubmed/23888551, [cited 2018 Jun 14]; Said Essa, A., Alaa Eldeen Nouh, M., Mohammed Ghaniam, N., Graham, D.Y., Said Sabry, H., Prevalence of cagA in relation to clinical presentation of Helicobacter pylori infection in Egypt (2008) Scand. J. Infect. Dis. [Internet], 40, pp. 730-733. , http://www.tandfonline.com/doi/full/10.1080/00365540802023725, [cited 2018 Jun 14]; El-Mashad, N., El-Emshaty, W.M., Arfat, M.S., Koura, B.A., Metwally, S.S., Relation of Cag-A-positive Helicobacter pylori strain and some inflammatory markers in patients with ischemic heart diseases (2009) Egypt. J. Immunol. [Internet], 16, pp. 39-47. , http://www.ncbi.nlm.nih.gov/pubmed/20726321, [cited 2018 Jun 14]; Diab, M., El-Shenawy, A., El-Ghannam, M., Salem, D., Abdelnasser, M., Shaheen, M., Detection of antimicrobial resistance genes of helicobacter pylori strains to clarithromycin, metronidazole, amoxicillin and tetracycline among Egyptian patients. Egypt (2018) J. Med. Hum. Genet.; Fathi, M.S., El-F, R.F., Hassan, R.A., El-Arab, M.E., Genotypic and phenotypic patterns of antimicrobial susceptibility of Helicobacter pylori strains among Egyptian patients. Egypt (2013) J. Med. Hum. Genet; Siu, L.K., Leung, W.K., Cheng, A.F., Sung, J.Y., Ling, T.K., Ling, J.M., Evaluation of a selective transport medium for gastric biopsy specimens to be cultured for Helicobacter pylori (1998) J. Clin. Microbiol. [Internet], 36, pp. 3048-3050. , http://www.ncbi.nlm.nih.gov/pubmed/9738066, [cited 2018 Jan 14]; Yamaoka, Y., Kodama, T., Gutierrez, O., Kim, J.G., Kashima, K., Graham, D.Y., Relationship between Helicobacter pylori iceA, cagA, and vacA status and clinical outcome: Studies in four different countries (1999) J. Clin. Microbiol. [Internet], 37, pp. 2274-2279. , http://www.ncbi.nlm.nih.gov/pubmed/10364597, [cited 2018 Jan 14]; Oskouei, D.D., Bekmen, N., Ellidokuz, H., Yllmaz, O., Evaluation of different cryoprotective agents in maintenance of viability of Helicobacter pylori in stock culture media (2010) Braz. J. Microbiol. [Internet], 41, pp. 1038-1046. , http://www.ncbi.nlm.nih.gov/pubmed/24031584, [cited 2018 Jan 14]; Owen, R.J., Slater, E.R., Xerry, J., Peters, T.M., Teare, E.L., Grant, A., Development of a scheme for genotyping Helicobacter pylori based on allelic variation in urease subunit genes (1998) J. Clin. Microbiol. [Internet], 36, pp. 3710-3712. , http://www.ncbi.nlm.nih.gov/pubmed/9817904, [cited 2018 Jan 14]; Ogata, S.K., Gales, A.C., Kawakami, E., Antimicrobial susceptibility testing for Helicobacter pylori isolates from Brazilian children and adolescents: Comparing agar dilution, E-test, and disk diffusion. Braz (2014) J. Microbiol. [Internet], 45, pp. 1439-1448. , http://www.ncbi.nlm.nih.gov/pubmed/25763052, [cited 2018 Jan 14]; Ozbey, G., Bahcecioglu, I.H., Acik, M.N., Prevalence of helicobacter pylori in children in eastern Turkey and molecular typing of isolates (2015) Braz J Microbiol, 46, pp. 505-511. , 26273266 4507543; Tanih, N.F., Okeleye, B.I., Naidoo, N., Clarke, A.M., Mkwetshana, N., Green, E., Marked susceptibility of South African Helicobacter pylori strains to ciprofloxacin and amoxicillin: Clinical implications (2010) S Afr Med J., 100, pp. 49-52. , https://www.ncbi.nlm.nih.gov/pubmed/20429489, [cited 2010 Jan 1]; Hafez, R., Hasanein, W., Elsayd, H., Basha, O., Elsayd, M.A., Antibiotic Resistance and Failure of Eradication of Helicobacter Pylori in Egypt (2011) Egypt. J. Med. Microbiol, 20 (2), pp. 149-154; Al-Qurashi, A.R., El-Morsy, F., Al-Quorain, A.A., Evolution of metronidazole and tetracycline susceptibility pattern in Helicobacter pylori at a hospital in Saudi Arabia (2001) Int. J. Antimicrob. Agents [Internet], 17, pp. 233-236. , http://www.ncbi.nlm.nih.gov/pubmed/11282271, [cited 2018 Jun 19]; Bindayna, K.M., Antibiotic susceptibilities of Helicobacter pylori (2001) Saudi Med. J. [Internet], 22, pp. 53-57. , http://www.ncbi.nlm.nih.gov/pubmed/11255612, [cited 2018 Jun 19]; Khedmat, H., Karbasi-Afshar, R., Agah, S., Taheri, S., Helicobacter pylori Infection in the general population: A Middle Eastern perspective (2013) Casp. J. Intern. Med. [Internet], 4, pp. 745-753. , http://www.ncbi.nlm.nih.gov/pubmed/24294467, Babol University of Medical Sciences; [cited 2018 Jun 19]; Khademi, F., Poursina, F., Hosseini, E., Akbari, M., Safaei, H.G., Helicobacter pylori in Iran: A systematic review on the antibiotic resistance [internet] (2015) Iran. J. Basic Med. Sci., pp. 2-7. , http://www.ncbi.nlm.nih.gov/pubmed/25810869, Mashhad University of Medical Sciences; [cited 2018 Jun 19]; Yousefi-Avarvand, A., Vaez, H., Tafaghodi, M., Sahebkar, A.H., Arzanlou, M., Khademi, F., Antibiotic Resistance of Helicobacter pylori in Iranian Children: A Systematic Review and Meta-Analysis (2017) Microb. Drug Resist. [Internet]. Mary Ann Liebert, Inc. 140, , http://www.liebertpub.com/doi/10.1089/mdr.2017.0292, Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA; [cited 2018 Jun 19];mdr.2017.0292; Kim, S.Y., Choi, D.J., Chung, J.-W., Antibiotic treatment for helicobacter pylori: Is the end coming? (2015) World J Gastrointest Pharmacol Ther [Internet], 6, pp. 183-198. , http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=4635158&tool=pmcentrez&rendertype=abstract; El-Khlousy, M., Rahman, E.A., Mostafa, S., Bassam, A., Elgawad, H.A., Elnasr, M.S., Study of the clinical relevance of Helicobacter pylori virulence genes to gastric diseases among Egyptian patients (2016) Arab J. Gastroenterol. [Internet], 17, pp. 90-94. , http://linkinghub.elsevier.com/retrieve/pii/S1687197916300259, [cited 2018 Jun 14]; Amf, A., Abdelattef, R.S., Abdel-Hady, A.A., Omran, F.H., El-Korashi, L.A., Abdel-Aziz El-Hady, H., Prevalence of Helicobacter pylori cagA and iceA genes and their association with gastrointestinal diseases (2018) Int J Microbiol [Internet], 2018, pp. 1-7. , http://www.ncbi.nlm.nih.gov/pubmed/29849647%0Ahttp://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC5907521%0Ahttps://www.hindawi.com/journals/ijmicro/2018/4809093/; Al, Q.A., Mustafa, A.S., Siddique, I., Khajah, A.K., Madda, J.P., Junaid TA Distribution of vacA and cagA genotypes of Helicobacter pylori in Kuwait (2005) Acta Trop, 93, pp. 283-288; Nimri, L.F., Matalka, I., Hani, K.B., Ibrahim, M., Helicobacter pylori genotypes identified in gastric biopsy specimens from Jordanian patients (2006) BMC Gastroenterol, 6, p. 27. , 17018159 1599735; Salih, B.A., Bolek, B., Yildiz, M., Arikan, S., Phylogenetic analysis of Helicobacter pylori cagA gene of Turkish isolates and the association with gastric pathologyGut Pathog (2013) [Internet]. BioMed Central, 5, p. 33. , http://gutpathogens.biomedcentral.com/articles/10.1186/1757-4749-5-33, [cited 2018 Jan 20]; Rom�n-Rom�n, A., Mart�nez-Carrillo, D.N., Atrisco-Morales, J., Az�car-Heziquio, J.C., Cuevas-Caballero, A.S., Casta��n-S�nchez, C.A., Helicobacter pylori vacA s1m1 genotype but not cagA or babA2 increase the risk of ulcer and gastric cancer in patients from Southern Mexico (2017) Gut Pathog. [Internet]. BioMed Central, 9, p. 18. , http://gutpathogens.biomedcentral.com/articles/10.1186/s13099-017-0167-z, [cited 2018 Jan 21]; Mgc, E., Vazquez, R.G., Mendez, I.M., Vargas, C.R., Cerezo, S.G., Detection of the glmM gene in Helicobacter pylori isolates with a novel primer by PCR (2011) J. Clin. Microbiol. [Internet], 49, pp. 1650-1652. , http://www.ncbi.nlm.nih.gov/pubmed/21289140, American Society for Microbiology (ASM); [cited 2018 Jan 21]; Izadi, F., Ahmadi, A., Ghourchian, S., Daneshi, A., Memari, F., Khadivi, E., Detection of helicobacter pylori in benign laryngeal lesions by polymerase chain reaction: A cross sectional study (2012) Infect. Agent. Cancer [Internet]. BioMed Central, 7, p. 10. , http://infectagentscancer.biomedcentral.com/articles/10.1186/1750, [cited 2018 Jan 21]
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