Persistence of Helicobacter pylori infection in patients with peptic ulcer perforation

被引:8
作者
Andreson, Helena
Sillakivi, Toomas
Peetsalu, Margot
Peetsalu, Ants
Mikelsaar, Marika
机构
[1] Univ Tartu, Dept Microbiol, EE-50411 Tartu, Estonia
[2] Univ Tartu, Dept Surg, EE-50411 Tartu, Estonia
关键词
cagA; Helicobacter pylori; perforated peptic ulcer; persistent infection; vacA; virulence;
D O I
10.1080/00365520600930859
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective. In patients with perforated peptic ulcer (PPU) the convergence between the high eradication rate of Helicobacter pylori infection and low rates of ulcer relapse after treatment has been associated with reinfection by non-virulent strains. The objective of this study was to evaluate the persistence of infection by virulent H. pylori strains and ulcer recurrence in 33 patients with PPU one year after surgery and antimicrobial treatment. Material and methods. The histological evaluation and molecular detection of H. pylori cagA and ureA genes, vacA allelic types and the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analyses of the glmM gene products from antral mucosa specimens were performed initially, 2-5 months and 1 year after therapy. Results. The density of H. pylori colonization was temporarily decreased ( p < 0.05) 2 - 5 months after therapy. After one year, complete eradication was achieved in only 7 patients (23%) at histological examination and recurrent ulcers were found in 3/33 ( 9%) patients. The vacA s1a allelic type of cagA-positive strains persisted in 19/33 (58%) PPU patients with identical PCR-RFLP fingerprints in 8/9 (89%) of the patients. Conclusions. In PPU patients with a low eradication rate of H. pylori infection after surgical and antimicrobial treatment, the frequent recrudescence of the infection is mostly caused by the persisting virulent strains of the cagA and vacA s1a subtypes. In the 1-year follow-up period the recurrent ulceration can be postponed just by the lowered colonization density of H. pylori after eradicative therapy.
引用
收藏
页码:324 / 329
页数:6
相关论文
共 25 条
[1]
Association of cagA and vacA genotypes of Helicobacter pylori with gastric diseases in Estonia [J].
Andreson, H ;
Loivukene, K ;
Sillakivi, T ;
Maaroos, HI ;
Ustav, M ;
Peetsalu, A ;
Mikelsaar, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (01) :298-300
[2]
MOSAICISM IN VACUOLATING CYTOTOXIN ALLELES OF HELICOBACTER-PYLORI - ASSOCIATION OF SPECIFIC VACA TYPES WITH CYTOTOXIN PRODUCTION AND PEPTIC-ULCERATION [J].
ATHERTON, JC ;
CAO, P ;
PEEK, RM ;
TUMMURU, MKR ;
BLASER, MJ ;
COVER, TL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :17771-17777
[3]
Clinical and pathological importance of heterogeneity in vacA, the vacuolating cytotoxin gene of Helicobacter pylori [J].
Atherton, JC ;
Peek, RM ;
Tham, KT ;
Cover, TL ;
Blaser, MJ .
GASTROENTEROLOGY, 1997, 112 (01) :92-99
[4]
Björkholm N, 2000, HELICOBACTER, V5, P148
[5]
SENSITIVE DETECTION OF HELICOBACTER-PYLORI BY USING POLYMERASE CHAIN-REACTION [J].
CLAYTON, CL ;
KLEANTHOUS, H ;
COATES, PJ ;
MORGAN, DD ;
TABAQCHALI, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (01) :192-200
[6]
Covacci A, 1996, HELICOBACTER PYLORI, P94
[7]
DEBONGNIE JC, 1995, ACTA GASTRO-ENT BELG, V58, P208
[8]
CYTO-TOXIN PRODUCTION BY CAMPYLOBACTER-PYLORI STRAINS ISOLATED FROM PATIENTS WITH PEPTIC-ULCERS AND FROM PATIENTS WITH CHRONIC GASTRITIS ONLY [J].
FIGURA, N ;
GUGLIELMETTI, P ;
ROSSOLINI, A ;
BARBERI, A ;
CUSI, G ;
MUSMANNO, RA ;
RUSSI, M ;
QUARANTA, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (01) :225-226
[9]
The recurrence of Helicobacter pylori infection:: Incidence and variables influencing it.: A critical review [J].
Gisbert, JP .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (09) :2083-2099
[10]
Helicobacter pylori infection and perforated peptic ulcer prevalence of the infection and role of antimicrobial treatment [J].
Gisbert, JR ;
Pajares, JM .
HELICOBACTER, 2003, 8 (03) :159-167