PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/16813 |
Resumo: | Triple therapy is the gold standard treatment for Helicobacter pylori eradication from the human stomach, but increased resistance to clarithromycin became the main factor of treatment failure. Until now, fastidious culturing methods are generally the method of choice to assess resistance status. In this study, a new genotypic method to detect clarithromycin resistance in clinical samples, based on fluorescent in situ hybridization (FISH) using a set of peptide nucleic acid probes (PNA), is proposed. Results: The set of probes targeting the point mutations responsible for clarithromycin resistance was applied to H. pylori suspensions and showed 100% sensitivity and specificity (95% CI, 79.9-100 and 95% CI, 71.6-100 respectively). This method can also be amenable for application to gastric biopsy samples, as resistance to clarithromycin was also detected when histological slides were tested. Conclusions: The optimized PNA-FISH based diagnostic method to detect H. pylori clarithromycin resistance shown to be a very sensitive and specific method for the detection of clarithromycin resistance in the H. pylori smears and also proved to be a reliable method for the diagnosis of this pathogen in clinical samples and an alternative to existing plating methods. |
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PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pyloriScience & TechnologyTriple therapy is the gold standard treatment for Helicobacter pylori eradication from the human stomach, but increased resistance to clarithromycin became the main factor of treatment failure. Until now, fastidious culturing methods are generally the method of choice to assess resistance status. In this study, a new genotypic method to detect clarithromycin resistance in clinical samples, based on fluorescent in situ hybridization (FISH) using a set of peptide nucleic acid probes (PNA), is proposed. Results: The set of probes targeting the point mutations responsible for clarithromycin resistance was applied to H. pylori suspensions and showed 100% sensitivity and specificity (95% CI, 79.9-100 and 95% CI, 71.6-100 respectively). This method can also be amenable for application to gastric biopsy samples, as resistance to clarithromycin was also detected when histological slides were tested. Conclusions: The optimized PNA-FISH based diagnostic method to detect H. pylori clarithromycin resistance shown to be a very sensitive and specific method for the detection of clarithromycin resistance in the H. pylori smears and also proved to be a reliable method for the diagnosis of this pathogen in clinical samples and an alternative to existing plating methods.The authors would like to thank Dr. Rainer Haas (Max von Pettenkofer Institute for Hygiene and Medical Microbiology, Ludwig Maximilians University of Munich, Germany), Dr. Guillermo Perez-Perez (NYU Langone Medical Center, New York, USA), and Dr. Monica Oleastro (National Institute of Health, Lisbon, Portugal) for kindly providing most of the H. pylori strains used in this study and Endoclab (Porto, Portugal). This work was supported by the Portuguese Institute Fundacao para a Ciencia e a Tecnologia (Ph.D. grant SFRH/BD/38124/2007).BioMed Central (BMC)Universidade do MinhoFernandes, R. M.Cerqueira, L.Ferreira, Rui M.Carneiro, FátimaRibeiro, Mário DinisFigueiredo, C.Keevil, C. W.Azevedo, N. F.Vieira, M. J.2011-112011-11-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/16813eng1471-218010.1186/1471-2180-11-10121569555info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-05-11T05:31:14Zoai:repositorium.sdum.uminho.pt:1822/16813Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-05-11T05:31:14Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori |
title |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori |
spellingShingle |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori Fernandes, R. M. Science & Technology |
title_short |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori |
title_full |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori |
title_fullStr |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori |
title_full_unstemmed |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori |
title_sort |
PNA-FISH as a new diagnostic method for the determination of clarithromycin resistance of Helicobacter pylori |
author |
Fernandes, R. M. |
author_facet |
Fernandes, R. M. Cerqueira, L. Ferreira, Rui M. Carneiro, Fátima Ribeiro, Mário Dinis Figueiredo, C. Keevil, C. W. Azevedo, N. F. Vieira, M. J. |
author_role |
author |
author2 |
Cerqueira, L. Ferreira, Rui M. Carneiro, Fátima Ribeiro, Mário Dinis Figueiredo, C. Keevil, C. W. Azevedo, N. F. Vieira, M. J. |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Fernandes, R. M. Cerqueira, L. Ferreira, Rui M. Carneiro, Fátima Ribeiro, Mário Dinis Figueiredo, C. Keevil, C. W. Azevedo, N. F. Vieira, M. J. |
dc.subject.por.fl_str_mv |
Science & Technology |
topic |
Science & Technology |
description |
Triple therapy is the gold standard treatment for Helicobacter pylori eradication from the human stomach, but increased resistance to clarithromycin became the main factor of treatment failure. Until now, fastidious culturing methods are generally the method of choice to assess resistance status. In this study, a new genotypic method to detect clarithromycin resistance in clinical samples, based on fluorescent in situ hybridization (FISH) using a set of peptide nucleic acid probes (PNA), is proposed. Results: The set of probes targeting the point mutations responsible for clarithromycin resistance was applied to H. pylori suspensions and showed 100% sensitivity and specificity (95% CI, 79.9-100 and 95% CI, 71.6-100 respectively). This method can also be amenable for application to gastric biopsy samples, as resistance to clarithromycin was also detected when histological slides were tested. Conclusions: The optimized PNA-FISH based diagnostic method to detect H. pylori clarithromycin resistance shown to be a very sensitive and specific method for the detection of clarithromycin resistance in the H. pylori smears and also proved to be a reliable method for the diagnosis of this pathogen in clinical samples and an alternative to existing plating methods. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-11 2011-11-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/1822/16813 |
url |
http://hdl.handle.net/1822/16813 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1471-2180 10.1186/1471-2180-11-101 21569555 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
BioMed Central (BMC) |
publisher.none.fl_str_mv |
BioMed Central (BMC) |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
mluisa.alvim@gmail.com |
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1817544648884748288 |