Diverse vacA allelic types of Helicobacter pylori in Korea and clinical correlation

被引:12
作者
Choe, YH
Kim, PS
Lee, DH
Kim, HK
Kim, YS
Shin, YW
Hwang, TS
Kim, HJ
Song, SU
Choi, MS
机构
[1] Inha Univ Hosp, Div Gastroenterol, Dept Internal Med, Jung Gu, Inchon 400103, South Korea
[2] Inha Univ, Coll Med, Dept Pathol, Inchon, South Korea
[3] Inha Univ Hosp, Clin Res Ctr, Inchon, South Korea
[4] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul, South Korea
关键词
Helicobacter pylori; vacA; allele; signal sequence; mid-region;
D O I
10.3349/ymj.2002.43.3.351
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Helicobacter pylori has a diversity of vacA allelic types. The purpose of this study was to correlate the vacA status and the clinical outcome. After constructing specific primers for the vacA signal sequence, H. pylori-positive antral biopsy specimens were examined for the vacA status in 25 gastric ulcers, 31 duodenal ulcers, 22 gastric cancers, 42 chronic gastritis, and 8 gastroduodenal ulcers. The relationship between the vacA allele and the clinical disease was examined. The vacA genotype s1c/m1 is predominant in Korea (71/128, 55.5%). Other strains including s1b or s2 were not found in this study. slc/nil was more prominent in duodenal ulcers, than in gastric ulcers (p=0.041) and cancer (p=0.029). Seven out of 8 patients with gastric and coexistent duodenal ulcers had the slc/ml allele. No statistical differences in the positive rates of the s1a/m1, s1a/m2, and s1c/m2 alleles among the disease groups were found. In conclusion, s1c/m1 is the main vacA allele in Korea and it is particularly associated with duodenal ulcers.
引用
收藏
页码:351 / 356
页数:6
相关论文
共 23 条
[11]   CYTO-TOXIC ACTIVITY IN BROTH-CULTURE FILTRATES OF CAMPYLOBACTER-PYLORI [J].
LEUNK, RD ;
JOHNSON, PT ;
DAVID, BC ;
KRAFT, WG ;
MORGAN, DR .
JOURNAL OF MEDICAL MICROBIOLOGY, 1988, 26 (02) :93-99
[12]   Major virulence factors, VacA and CagA, are commonly positive in Helicobacter pylori isolates in Japan [J].
Maeda, S ;
Ogura, K ;
Yoshida, H ;
Kanai, F ;
Ikenoue, T ;
Kato, N ;
Shiratori, Y ;
Omata, M .
GUT, 1998, 42 (03) :338-343
[13]   Equally high prevalences of infection with cagA-positive Helicobacter pylori in Chinese patients with peptic ulcer disease and those with chronic gastritis-associated dyspepsia [J].
Pan, ZJ ;
vanderHulst, RWM ;
Feller, M ;
Xiao, SD ;
Tytgat, GNJ ;
Dankert, J ;
vanderEnde, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (06) :1344-1347
[14]   Prevalence of vacuolating cytotoxin production and distribution of distinct vacA alleles in Helicobacter pylori from China [J].
Pan, ZJ ;
Berg, DE ;
van der Hulst, RWM ;
Su, WW ;
Raudonikiene, A ;
Xiao, SD ;
Dankert, J ;
Tytgat, GNJ ;
van der Ende, A .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (01) :220-226
[15]   Helicobacter pylori infection in Korea [J].
Park, IS ;
Lee, YC ;
Park, HJ ;
Kim, TI ;
Lee, SI ;
Kim, H ;
Chung, KS ;
Lee-Kim, YC .
YONSEI MEDICAL JOURNAL, 2001, 42 (04) :457-470
[16]   CYTOTOXIN PRODUCTION BY HELICOBACTER-PYLORI FROM PATIENTS WITH UPPER GASTROINTESTINAL-TRACT DISEASES [J].
TEE, W ;
LAMBERT, JR ;
DWYER, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (05) :1203-1205
[17]   Clinical relevance of the cagA, vacA, and iceA status of Helicobacter pylori [J].
van Doorn, LJ ;
Figueiredo, C ;
Sanna, R ;
Plaisier, A ;
Schneeberger, P ;
De Boer, W ;
Quint, W .
GASTROENTEROLOGY, 1998, 115 (01) :58-66
[18]   Expanding allelic diversity of Helicobacter pylori vacA [J].
van Doorn, LJ ;
Figueiredo, C ;
Sanna, R ;
Pena, S ;
Midolo, P ;
Ng, EKW ;
Atherton, JC ;
Blaser, MJ ;
Quint, WGV .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (09) :2597-2603
[19]   Geographic distribution of vacA allelic types of Helicobacter pylori [J].
van Doorn, LJ ;
Figueiredo, C ;
Mégraud, F ;
Pena, S ;
Midolo, P ;
Queiroz, DMD .
GASTROENTEROLOGY, 1999, 116 (04) :823-830
[20]   Heterogeneous Helicobacter pylori isolates from members of a family with a history of peptic ulcer disease [J].
vanderEnde, A ;
Rauws, EAJ ;
Feller, M ;
Mulder, CJJ ;
Tytgat, GNJ ;
Dankert, J .
GASTROENTEROLOGY, 1996, 111 (03) :638-647