Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico

Detalhes bibliográficos
Ano de defesa: 2010
Autor(a) principal: Cavalcante, Meyssa Quezado de Figueiredo
Orientador(a): Braga, Lúcia Libanêz Bessa Campelo
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Não Informado pela instituição
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://www.repositorio.ufc.br/handle/riufc/10647
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 Cavalcante, Meyssa Quezado de FigueiredoBraga, Lúcia Libanêz Bessa Campelo2015-02-19T11:58:29Z2015-02-19T11:58:29Z2010CAVALCANTE, Meyssa Quezado de Figueiredo. Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico. 2010. 87 f. Dissertação (Mestrado em Cirurgia) - Universidade Federal do Ceará, Faculdade de Medicina, Fortaleza, 2010.http://www.repositorio.ufc.br/handle/riufc/10647The 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 espécie bacteriana Helicobacter pylori está intimamente correlacionado com o desenvolvimento das principais afecções gástricas e do câncer de estômago. As cepas que apresentam genótipo mais patogênico são as mais implicadas na virulência da bactéria. O objetivo deste trabalho foi caracterizar as cepas de H. pylori provenientes de pacientes portadores de gastrite, úlcera gastroduodenal e câncer gástrico quanto aos genes cagA e vacA e alelos através da técnica de PCR. A genotipagem das cepas de H. pylori foi realizada através da técnica de PCR. Foram avaliadas 134 cepas, sendo 76 de portadores de gastrite, 28 de úlcera péptica e 30 de câncer gástrico. 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 híbridas e 8,2% apresentaram somente o alelo da sequência sinal(s). Nos portadores de gastrite a distribuição dos alelos vacA foi: 46,1% s1m1, 22,4% s1m2, 5,3% s2m1, 11,8% s2m2, 3,9% cepas híbridas e 10,5% somente com alelo s. Nos casos de úlcera achou-se: 50% s1m1, 21,4% s1m2, 17,8% s2m1, 3,6% s2m2, 7,2% cepas híbridas. Nos portadores de câncer encontrou-se: 53,3% s1m1, 16,7% s1m2, 3,3% s2m2, 16,7% cepas híbridas 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 úlcera péptica e 96,7% portavam câncer gástrico com positividade para este gene. O alelo vacAs1m1 foi o mais prevalente observado nos três grupos estudados. Também foram encontradas cepas com alelos múltiplos desse gene, o que sugere um polimorfismo genético advindo de infecção por mais de um tipo de cepa em um mesmo indivíduo. O gene cagA também foi altamente prevalente nos grupos estudados. A presença do cagA foi estatisticamente significante no grupo de pangastrite e câncer gástrico. A relação do gene cagA com o alelo vacAs1m1 também foi significante nos grupos de pangastrite e câncer gástrico, o que corrobora a maior patogenicidade das cepas presentes nos indivíduos estudados.Helicobacter pyloriNeoplasias GástricasGastriteGenótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástricoGenotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancerinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisporreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccessLICENSElicense.txtlicense.txttext/plain; charset=utf-81786http://repositorio.ufc.br/bitstream/riufc/10647/2/license.txt8c4401d3d14722a7ca2d07c782a1aab3MD52ORIGINAL2010_dis_mqfcavalcante.pdf2010_dis_mqfcavalcante.pdfapplication/pdf2039790http://repositorio.ufc.br/bitstream/riufc/10647/1/2010_dis_mqfcavalcante.pdf22b9b8ce8cedcbdd53a754d52a85c7ecMD51riufc/106472018-12-13 15:56:38.114oai:repositorio.ufc.br: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Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2018-12-13T18:56:38Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.pt_BR.fl_str_mv Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
dc.title.en.pt_BR.fl_str_mv Genotypes cagA, vacA and alleles of H. pylori in patients gastritis, peptic ulcer and gastric cancer
title Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
spellingShingle Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
Cavalcante, Meyssa Quezado de Figueiredo
Helicobacter pylori
Neoplasias Gástricas
Gastrite
title_short Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
title_full Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
title_fullStr Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
title_full_unstemmed Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
title_sort Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico
author Cavalcante, Meyssa Quezado de Figueiredo
author_facet Cavalcante, Meyssa Quezado de Figueiredo
author_role author
dc.contributor.author.fl_str_mv Cavalcante, Meyssa Quezado de Figueiredo
dc.contributor.advisor1.fl_str_mv Braga, Lúcia Libanêz Bessa Campelo
contributor_str_mv Braga, Lúcia Libanêz Bessa Campelo
dc.subject.por.fl_str_mv Helicobacter pylori
Neoplasias Gástricas
Gastrite
topic Helicobacter pylori
Neoplasias Gástricas
Gastrite
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
dc.date.accessioned.fl_str_mv 2015-02-19T11:58:29Z
dc.date.available.fl_str_mv 2015-02-19T11:58:29Z
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dc.identifier.citation.fl_str_mv CAVALCANTE, Meyssa Quezado de Figueiredo. Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico. 2010. 87 f. Dissertação (Mestrado em Cirurgia) - Universidade Federal do Ceará, Faculdade de Medicina, Fortaleza, 2010.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufc.br/handle/riufc/10647
identifier_str_mv CAVALCANTE, Meyssa Quezado de Figueiredo. Genótipos cagA, vacA e alelos de H. pylori em pacientes portadores de gastrite, úlcera péptica e câncer gástrico. 2010. 87 f. Dissertação (Mestrado em Cirurgia) - Universidade Federal do Ceará, Faculdade de Medicina, Fortaleza, 2010.
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