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Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers

Although the type 4 secretion system of the integrating and conjugative elements (tfs ICE) is common in Helicobacter pylori, its clinical association with the cag pathogenicity island (cagPAI) have not yet been well-investigated. In this study, Vietnamese patient H. pylori samples (46 duodenal ulcer...

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Autores principales: Phuc, Bui Hoang, Tuan, Vo Phuoc, Dung, Ho Dang Quy, Binh, Tran Thanh, Tung, Pham Huu, Tri, Tran Dinh, Thuan, Ngo Phuong Minh, Van Khien, Vu, Trang, Tran Thi Huyen, Akada, Junko, Matsumoto, Takeshi, Yamaoka, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907105/
https://www.ncbi.nlm.nih.gov/pubmed/33633144
http://dx.doi.org/10.1038/s41598-021-83862-1
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author Phuc, Bui Hoang
Tuan, Vo Phuoc
Dung, Ho Dang Quy
Binh, Tran Thanh
Tung, Pham Huu
Tri, Tran Dinh
Thuan, Ngo Phuong Minh
Van Khien, Vu
Trang, Tran Thi Huyen
Akada, Junko
Matsumoto, Takeshi
Yamaoka, Yoshio
author_facet Phuc, Bui Hoang
Tuan, Vo Phuoc
Dung, Ho Dang Quy
Binh, Tran Thanh
Tung, Pham Huu
Tri, Tran Dinh
Thuan, Ngo Phuong Minh
Van Khien, Vu
Trang, Tran Thi Huyen
Akada, Junko
Matsumoto, Takeshi
Yamaoka, Yoshio
author_sort Phuc, Bui Hoang
collection PubMed
description Although the type 4 secretion system of the integrating and conjugative elements (tfs ICE) is common in Helicobacter pylori, its clinical association with the cag pathogenicity island (cagPAI) have not yet been well-investigated. In this study, Vietnamese patient H. pylori samples (46 duodenal ulcer (DU), 51 non-cardia gastric cancer (NCGC), 39 chronic gastritis (CG)) were fully sequenced using next-generation sequencing and assembled into contigs. tfs3, tfs4, and cagPAI genes were compared with the public database. Most (94%) H. pylori strains possessed a complete cagPAI, which was the greatest risk factor for clinical outcomes, while the prevalences of tfs3 and tfs4 were 45% and 77%, respectively. Complete tfs3 and tfs4 were found in 18.3% and 17.6% of strains, respectively. The prevalence of H. pylori strains with complete tfs3 ICE in DU patients was significantly higher than that in NCGC patients (30.4% vs 11.7%, P < 0.05). In addition, the prevalence of strains with complete tfs3 ICE and cagPAI was significantly higher in DU patients than that in NCGC (28.4% vs 9.8%, P = 0.038) and CG patients (28.2% vs 7.7%, P = 0.024). cagPAI and complete tfs3 increased the risk of DU compared to NCGC (OR = 3.56, 95%CI: 1.1–14.1, P = 0.038) and CG (OR = 4.64, 95%CI: 1.1–27.6, P = 0.024). A complete cluster of tfs3 ICE was associated with gastroduodenal diseases in Vietnam. However, there was a low prevalence of the dupA/complete dupA cluster (15.4%) in the Vietnam strains. The prevalence of cagPAI in Vietnam strains was significantly higher than in US (P = 0.01) and Indonesia (P < 0.0001); the prevalence of the dupA cluster was also higher in the Vietnam strains than in the Indonesian strains (P < 0.05). In addition, the prevalence of ctkA, an accessory gene of tfs3, was significantly different between Vietnam and US strains (28% vs 2%, P = 0.0002). In summary, the acquisition of tfs3/4 ICE was common in H. pylori strains in patients with gastroduodenal disease in Vietnam, and the complete cluster of tfs3 ICE was a reliable marker for the severity of disease in the H. pylori infected population.
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spelling pubmed-79071052021-02-26 Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers Phuc, Bui Hoang Tuan, Vo Phuoc Dung, Ho Dang Quy Binh, Tran Thanh Tung, Pham Huu Tri, Tran Dinh Thuan, Ngo Phuong Minh Van Khien, Vu Trang, Tran Thi Huyen Akada, Junko Matsumoto, Takeshi Yamaoka, Yoshio Sci Rep Article Although the type 4 secretion system of the integrating and conjugative elements (tfs ICE) is common in Helicobacter pylori, its clinical association with the cag pathogenicity island (cagPAI) have not yet been well-investigated. In this study, Vietnamese patient H. pylori samples (46 duodenal ulcer (DU), 51 non-cardia gastric cancer (NCGC), 39 chronic gastritis (CG)) were fully sequenced using next-generation sequencing and assembled into contigs. tfs3, tfs4, and cagPAI genes were compared with the public database. Most (94%) H. pylori strains possessed a complete cagPAI, which was the greatest risk factor for clinical outcomes, while the prevalences of tfs3 and tfs4 were 45% and 77%, respectively. Complete tfs3 and tfs4 were found in 18.3% and 17.6% of strains, respectively. The prevalence of H. pylori strains with complete tfs3 ICE in DU patients was significantly higher than that in NCGC patients (30.4% vs 11.7%, P < 0.05). In addition, the prevalence of strains with complete tfs3 ICE and cagPAI was significantly higher in DU patients than that in NCGC (28.4% vs 9.8%, P = 0.038) and CG patients (28.2% vs 7.7%, P = 0.024). cagPAI and complete tfs3 increased the risk of DU compared to NCGC (OR = 3.56, 95%CI: 1.1–14.1, P = 0.038) and CG (OR = 4.64, 95%CI: 1.1–27.6, P = 0.024). A complete cluster of tfs3 ICE was associated with gastroduodenal diseases in Vietnam. However, there was a low prevalence of the dupA/complete dupA cluster (15.4%) in the Vietnam strains. The prevalence of cagPAI in Vietnam strains was significantly higher than in US (P = 0.01) and Indonesia (P < 0.0001); the prevalence of the dupA cluster was also higher in the Vietnam strains than in the Indonesian strains (P < 0.05). In addition, the prevalence of ctkA, an accessory gene of tfs3, was significantly different between Vietnam and US strains (28% vs 2%, P = 0.0002). In summary, the acquisition of tfs3/4 ICE was common in H. pylori strains in patients with gastroduodenal disease in Vietnam, and the complete cluster of tfs3 ICE was a reliable marker for the severity of disease in the H. pylori infected population. Nature Publishing Group UK 2021-02-25 /pmc/articles/PMC7907105/ /pubmed/33633144 http://dx.doi.org/10.1038/s41598-021-83862-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Phuc, Bui Hoang
Tuan, Vo Phuoc
Dung, Ho Dang Quy
Binh, Tran Thanh
Tung, Pham Huu
Tri, Tran Dinh
Thuan, Ngo Phuong Minh
Van Khien, Vu
Trang, Tran Thi Huyen
Akada, Junko
Matsumoto, Takeshi
Yamaoka, Yoshio
Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers
title Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers
title_full Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers
title_fullStr Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers
title_full_unstemmed Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers
title_short Helicobacter pylori type 4 secretion systems as gastroduodenal disease markers
title_sort helicobacter pylori type 4 secretion systems as gastroduodenal disease markers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907105/
https://www.ncbi.nlm.nih.gov/pubmed/33633144
http://dx.doi.org/10.1038/s41598-021-83862-1
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