Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer

Detalhes bibliográficos
Autor(a) principal: Meyssa Quezado Cavalcante Braga
Data de Publicação: 2010
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UFC
Texto Completo: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13463
Resumo: The bacterial species H. pylori is closely correlated with the development of major diseases and gastric cancer of the stomach. The strains that have more pathogenic genotype are more involved in bacterial virulence. The objective was to genotype strains of H. pylori from patients with gastritis, gastroduodenal ulcer and gastric cancer as the cagA and vacA genes and alleles by PCR technique. The genotyping of strains of H. pylori was performed by PCR technique. We evaluated 134 strains, 76 of patients with gastritis, 28 peptic ulcer and 30 gastric cancer. As a result of this research it was found that all strains subtyped were vacA positive, and 48.5% with the allele s1m1 vacA, vacA s1m2 20.9% and 6.7% s2m1 vacA, vacA s2m2 8.2%; 7 5% were hybrid strains and 8.2% had only the allele of the sequence signal (s). Gastritis in the distribution of vacA alleles were: 46.1% s1m1, s1m2 22.4%, 5.3% s2m1, s2m2 11.8%, 3.9% and 10.5% hybrid strains only with allele s. In cases of ulcer was found: 50% s1m1, s1m2 21.4%, 17.8% s2m1, s2m2 3.6%, 7.2% hybrid strains. In patients with cancer met: s1m1 53.3%, 16.7% s1m2, s2m2 3.3%, 16.7% and 10.0% hybrid strains with allele only s. The cagA gene was observed in 82.8% of strains, where 73.7% had gastritis and cagA positive, 96.4% had peptic ulcer and gastric cancer harbored 96.7% were positive for this gene. Allele vacAs1m1 was the most prevalent observed in the three groups. We have also found strains with multiple alleles of this gene, suggesting a genetic polymorphism arising from infection by more than one type of strain in the same individual. The cagA gene was also highly prevalent in both groups. The presence of cagA was statistically significant in the group of pangastritis and gastric cancer. The relationship of the cagA gene with allele vacAs1m1 was also significant in the groups of pangastritis and gastric cancer, which supports the higher pathogenicity of strains of the studied individuals.
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spelling info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisGenotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancerGenÃtipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, Ãlcera pÃptica e cÃncer gÃstrico 2010-08-13LÃcia LibanÃz Bessa Campelo Braga20891342320http://lattes.cnpq.br/6795261152083416MÃrcia Maria de Negreiros Pinto Rocha46546529300http://lattes.cnpq.br/2888374721836380 Paulo Roberto LeitÃo de Vasconcelos11852844353http://buscatextual.cnpq.br/buscatextual/servletrecuperafoto?id=K4787736J667622602368http://lattes.cnpq.br/8475145074093902Meyssa Quezado Cavalcante BragaUniversidade Federal do CearÃPrograma de PÃs-GraduaÃÃo em CirurgiaUFCBRENFERMAGEMThe bacterial species H. pylori is closely correlated with the development of major diseases and gastric cancer of the stomach. The strains that have more pathogenic genotype are more involved in bacterial virulence. The objective was to genotype strains of H. pylori from patients with gastritis, gastroduodenal ulcer and gastric cancer as the cagA and vacA genes and alleles by PCR technique. The genotyping of strains of H. pylori was performed by PCR technique. We evaluated 134 strains, 76 of patients with gastritis, 28 peptic ulcer and 30 gastric cancer. As a result of this research it was found that all strains subtyped were vacA positive, and 48.5% with the allele s1m1 vacA, vacA s1m2 20.9% and 6.7% s2m1 vacA, vacA s2m2 8.2%; 7 5% were hybrid strains and 8.2% had only the allele of the sequence signal (s). Gastritis in the distribution of vacA alleles were: 46.1% s1m1, s1m2 22.4%, 5.3% s2m1, s2m2 11.8%, 3.9% and 10.5% hybrid strains only with allele s. In cases of ulcer was found: 50% s1m1, s1m2 21.4%, 17.8% s2m1, s2m2 3.6%, 7.2% hybrid strains. In patients with cancer met: s1m1 53.3%, 16.7% s1m2, s2m2 3.3%, 16.7% and 10.0% hybrid strains with allele only s. The cagA gene was observed in 82.8% of strains, where 73.7% had gastritis and cagA positive, 96.4% had peptic ulcer and gastric cancer harbored 96.7% were positive for this gene. Allele vacAs1m1 was the most prevalent observed in the three groups. We have also found strains with multiple alleles of this gene, suggesting a genetic polymorphism arising from infection by more than one type of strain in the same individual. The cagA gene was also highly prevalent in both groups. The presence of cagA was statistically significant in the group of pangastritis and gastric cancer. The relationship of the cagA gene with allele vacAs1m1 was also significant in the groups of pangastritis and gastric cancer, which supports the higher pathogenicity of strains of the studied individuals. A espÃcie bacteriana Helicobacter pylori està intimamente correlacionado com o desenvolvimento das principais afecÃÃes gÃstricas e do cÃncer de estÃmago. As cepas que apresentam genÃtipo mais patogÃnico sÃo as mais implicadas na virulÃncia da bactÃria. O objetivo deste trabalho foi caracterizar as cepas de H. pylori provenientes de pacientes portadores de gastrite, Ãlcera gastroduodenal e cÃncer gÃstrico quanto aos genes cagA e vacA e alelos atravÃs da tÃcnica de PCR. A genotipagem das cepas de H. pylori foi realizada atravÃs da tÃcnica de PCR. Foram avaliadas 134 cepas, sendo 76 de portadores de gastrite, 28 de Ãlcera pÃptica e 30 de cÃncer gÃstrico. Como resultado desta pesquisa obteve-se que, todas as cepas genotipadas foram vacA positivas, sendo 48,5% com o alelo vacA s1m1; 20,9% vacA s1m2; 6,7% vacA s2m1; 8,2% vacA s2m2; 7,5% eram cepas hÃbridas e 8,2% apresentaram somente o alelo da sequÃncia sinal(s). Nos portadores de gastrite a distribuiÃÃo dos alelos vacA foi: 46,1% s1m1, 22,4% s1m2, 5,3% s2m1, 11,8% s2m2, 3,9% cepas hÃbridas e 10,5% somente com alelo s. Nos casos de Ãlcera achou-se: 50% s1m1, 21,4% s1m2, 17,8% s2m1, 3,6% s2m2, 7,2% cepas hÃbridas. Nos portadores de cÃncer encontrou-se: 53,3% s1m1, 16,7% s1m2, 3,3% s2m2, 16,7% cepas hÃbridas e 10,0% somente com alelo s. O gene cagA foi observado em 82,8% das cepas, onde 73,7% tinham gastrite e cagA positivo, 96,4% tinham Ãlcera pÃptica e 96,7% portavam cÃncer gÃstrico com positividade para este gene. O alelo vacAs1m1 foi o mais prevalente observado nos trÃs grupos estudados. TambÃm foram encontradas cepas com alelos mÃltiplos desse gene, o que sugere um polimorfismo genÃtico advindo de infecÃÃo por mais de um tipo de cepa em um mesmo indivÃduo. O gene cagA tambÃm foi altamente prevalente nos grupos estudados. A presenÃa do cagA foi estatisticamente significante no grupo de pangastrite e cÃncer gÃstrico. A relaÃÃo do gene cagA com o alelo vacAs1m1 tambÃm foi significante nos grupos de pangastrite e cÃncer gÃstrico, o que corrobora a maior patogenicidade das cepas presentes nos indivÃduos estudados.CoordenaÃÃo de AperfeÃoamento de Pessoal de NÃvel Superior http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13463application/pdfinfo:eu-repo/semantics/openAccessporreponame:Biblioteca Digital de Teses e Dissertações da UFCinstname:Universidade Federal do Cearáinstacron:UFC2019-01-21T11:26:42Zmail@mail.com -
dc.title.en.fl_str_mv Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
dc.title.alternative.pt.fl_str_mv GenÃtipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, Ãlcera pÃptica e cÃncer gÃstrico
title Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
spellingShingle Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
Meyssa Quezado Cavalcante Braga
ENFERMAGEM
title_short Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
title_full Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
title_fullStr Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
title_full_unstemmed Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
title_sort Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
author Meyssa Quezado Cavalcante Braga
author_facet Meyssa Quezado Cavalcante Braga
author_role author
dc.contributor.advisor1.fl_str_mv LÃcia LibanÃz Bessa Campelo Braga
dc.contributor.advisor1ID.fl_str_mv 20891342320
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/6795261152083416
dc.contributor.referee1.fl_str_mv MÃrcia Maria de Negreiros Pinto Rocha
dc.contributor.referee1ID.fl_str_mv 46546529300
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/2888374721836380
dc.contributor.referee2.fl_str_mv Paulo Roberto LeitÃo de Vasconcelos
dc.contributor.referee2ID.fl_str_mv 11852844353
dc.contributor.referee2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/servletrecuperafoto?id=K4787736J6
dc.contributor.authorID.fl_str_mv 67622602368
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/8475145074093902
dc.contributor.author.fl_str_mv Meyssa Quezado Cavalcante Braga
contributor_str_mv LÃcia LibanÃz Bessa Campelo Braga
MÃrcia Maria de Negreiros Pinto Rocha
Paulo Roberto LeitÃo de Vasconcelos
dc.subject.cnpq.fl_str_mv ENFERMAGEM
topic ENFERMAGEM
dc.description.sponsorship.fl_txt_mv CoordenaÃÃo de AperfeÃoamento de Pessoal de NÃvel Superior
dc.description.abstract.por.fl_txt_mv The bacterial species H. pylori is closely correlated with the development of major diseases and gastric cancer of the stomach. The strains that have more pathogenic genotype are more involved in bacterial virulence. The objective was to genotype strains of H. pylori from patients with gastritis, gastroduodenal ulcer and gastric cancer as the cagA and vacA genes and alleles by PCR technique. The genotyping of strains of H. pylori was performed by PCR technique. We evaluated 134 strains, 76 of patients with gastritis, 28 peptic ulcer and 30 gastric cancer. As a result of this research it was found that all strains subtyped were vacA positive, and 48.5% with the allele s1m1 vacA, vacA s1m2 20.9% and 6.7% s2m1 vacA, vacA s2m2 8.2%; 7 5% were hybrid strains and 8.2% had only the allele of the sequence signal (s). Gastritis in the distribution of vacA alleles were: 46.1% s1m1, s1m2 22.4%, 5.3% s2m1, s2m2 11.8%, 3.9% and 10.5% hybrid strains only with allele s. In cases of ulcer was found: 50% s1m1, s1m2 21.4%, 17.8% s2m1, s2m2 3.6%, 7.2% hybrid strains. In patients with cancer met: s1m1 53.3%, 16.7% s1m2, s2m2 3.3%, 16.7% and 10.0% hybrid strains with allele only s. The cagA gene was observed in 82.8% of strains, where 73.7% had gastritis and cagA positive, 96.4% had peptic ulcer and gastric cancer harbored 96.7% were positive for this gene. Allele vacAs1m1 was the most prevalent observed in the three groups. We have also found strains with multiple alleles of this gene, suggesting a genetic polymorphism arising from infection by more than one type of strain in the same individual. The cagA gene was also highly prevalent in both groups. The presence of cagA was statistically significant in the group of pangastritis and gastric cancer. The relationship of the cagA gene with allele vacAs1m1 was also significant in the groups of pangastritis and gastric cancer, which supports the higher pathogenicity of strains of the studied individuals.
A espÃcie bacteriana Helicobacter pylori està intimamente correlacionado com o desenvolvimento das principais afecÃÃes gÃstricas e do cÃncer de estÃmago. As cepas que apresentam genÃtipo mais patogÃnico sÃo as mais implicadas na virulÃncia da bactÃria. O objetivo deste trabalho foi caracterizar as cepas de H. pylori provenientes de pacientes portadores de gastrite, Ãlcera gastroduodenal e cÃncer gÃstrico quanto aos genes cagA e vacA e alelos atravÃs da tÃcnica de PCR. A genotipagem das cepas de H. pylori foi realizada atravÃs da tÃcnica de PCR. Foram avaliadas 134 cepas, sendo 76 de portadores de gastrite, 28 de Ãlcera pÃptica e 30 de cÃncer gÃstrico. Como resultado desta pesquisa obteve-se que, todas as cepas genotipadas foram vacA positivas, sendo 48,5% com o alelo vacA s1m1; 20,9% vacA s1m2; 6,7% vacA s2m1; 8,2% vacA s2m2; 7,5% eram cepas hÃbridas e 8,2% apresentaram somente o alelo da sequÃncia sinal(s). Nos portadores de gastrite a distribuiÃÃo dos alelos vacA foi: 46,1% s1m1, 22,4% s1m2, 5,3% s2m1, 11,8% s2m2, 3,9% cepas hÃbridas e 10,5% somente com alelo s. Nos casos de Ãlcera achou-se: 50% s1m1, 21,4% s1m2, 17,8% s2m1, 3,6% s2m2, 7,2% cepas hÃbridas. Nos portadores de cÃncer encontrou-se: 53,3% s1m1, 16,7% s1m2, 3,3% s2m2, 16,7% cepas hÃbridas e 10,0% somente com alelo s. O gene cagA foi observado em 82,8% das cepas, onde 73,7% tinham gastrite e cagA positivo, 96,4% tinham Ãlcera pÃptica e 96,7% portavam cÃncer gÃstrico com positividade para este gene. O alelo vacAs1m1 foi o mais prevalente observado nos trÃs grupos estudados. TambÃm foram encontradas cepas com alelos mÃltiplos desse gene, o que sugere um polimorfismo genÃtico advindo de infecÃÃo por mais de um tipo de cepa em um mesmo indivÃduo. O gene cagA tambÃm foi altamente prevalente nos grupos estudados. A presenÃa do cagA foi estatisticamente significante no grupo de pangastrite e cÃncer gÃstrico. A relaÃÃo do gene cagA com o alelo vacAs1m1 tambÃm foi significante nos grupos de pangastrite e cÃncer gÃstrico, o que corrobora a maior patogenicidade das cepas presentes nos indivÃduos estudados.
description The bacterial species H. pylori is closely correlated with the development of major diseases and gastric cancer of the stomach. The strains that have more pathogenic genotype are more involved in bacterial virulence. The objective was to genotype strains of H. pylori from patients with gastritis, gastroduodenal ulcer and gastric cancer as the cagA and vacA genes and alleles by PCR technique. The genotyping of strains of H. pylori was performed by PCR technique. We evaluated 134 strains, 76 of patients with gastritis, 28 peptic ulcer and 30 gastric cancer. As a result of this research it was found that all strains subtyped were vacA positive, and 48.5% with the allele s1m1 vacA, vacA s1m2 20.9% and 6.7% s2m1 vacA, vacA s2m2 8.2%; 7 5% were hybrid strains and 8.2% had only the allele of the sequence signal (s). Gastritis in the distribution of vacA alleles were: 46.1% s1m1, s1m2 22.4%, 5.3% s2m1, s2m2 11.8%, 3.9% and 10.5% hybrid strains only with allele s. In cases of ulcer was found: 50% s1m1, s1m2 21.4%, 17.8% s2m1, s2m2 3.6%, 7.2% hybrid strains. In patients with cancer met: s1m1 53.3%, 16.7% s1m2, s2m2 3.3%, 16.7% and 10.0% hybrid strains with allele only s. The cagA gene was observed in 82.8% of strains, where 73.7% had gastritis and cagA positive, 96.4% had peptic ulcer and gastric cancer harbored 96.7% were positive for this gene. Allele vacAs1m1 was the most prevalent observed in the three groups. We have also found strains with multiple alleles of this gene, suggesting a genetic polymorphism arising from infection by more than one type of strain in the same individual. The cagA gene was also highly prevalent in both groups. The presence of cagA was statistically significant in the group of pangastritis and gastric cancer. The relationship of the cagA gene with allele vacAs1m1 was also significant in the groups of pangastritis and gastric cancer, which supports the higher pathogenicity of strains of the studied individuals.
publishDate 2010
dc.date.issued.fl_str_mv 2010-08-13
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
status_str publishedVersion
format masterThesis
dc.identifier.uri.fl_str_mv http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13463
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dc.publisher.none.fl_str_mv Universidade Federal do CearÃ
dc.publisher.program.fl_str_mv Programa de PÃs-GraduaÃÃo em Cirurgia
dc.publisher.initials.fl_str_mv UFC
dc.publisher.country.fl_str_mv BR
publisher.none.fl_str_mv Universidade Federal do CearÃ
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UFC
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instname_str Universidade Federal do Ceará
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