Lack of a relationship between Lewis antigen expression and cagA, CagA, vacA and VacA status of Irish Helicobacter pylori isolates

被引:37
作者
Marshall, DG
Hynes, SO
Coleman, DC
O'Morain, CA
Smyth, CJ
Moran, AP [1 ]
机构
[1] Natl Univ Ireland Univ Coll Galway, Dept Microbiol, Galway, Ireland
[2] Trinity Coll, Sch Dent Sci, Dept Oral Med & Pathol, Dublin, Ireland
[3] Meath Adelaide Hosp, Dept Clin Med & Gastroenterol, Dublin, Ireland
[4] Trinity Coll, Moyne Inst Prevent Med, Dept Microbiol, Dublin, Ireland
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 1999年 / 24卷 / 01期
关键词
Helicobacter pylori; cagA; vacA; lipopolysaccharide; Lewis antigens; virulence;
D O I
10.1111/j.1574-695X.1999.tb01268.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The cagA gene, vacA gene, CagA (cytotoxin-associated gene A product) and VacA (vacuolating cytotoxin) status of a collection of Helicobacter pylori isolates from the geographically distinct Irish population was determined, the potential association of these traits with Lewis (Le) antigen expression was assessed, and the relationship between these bacterial properties and the pathology associated with H. pylori infection was evaluated. Of the 57 isolates, a higher proportion from ulcer than from non-ulcer patients expressed VacA (71% vs. 53%). H. pylori isolates which were cagA-positive were no more significantly associated with peptic ulcers than non-ulcer disease (71% vs. 67%, P = 0.775), nor were CagA-positive isolates (57% vs. 50%, P = 0.783), but 80% of the isolates from duodenal ulcer patients were cagA-positive. Thirty-seven of the 57 isolates were tested for Le antigen expression. No statistically significant relationship (P>0.05) was found between the occurrence and level of expression of Le(x) or Le(y) and cagA, vacA, or VacA status. This lack of an association in the Irish H. pylori isolates contrasts with that previously reported for predominantly North American isolates, and may be attributable to the adaptation of H. pylori strains with differing attributes to different human populations. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 90
页数:12
相关论文
共 57 条
[1]   Potential role of molecular mimicry between Helicobacter pylori lipopolysaccharide and host Lewis blood group antigens in autoimmunity [J].
Appelmelk, BJ ;
SimoonsSmit, I ;
Negrini, R ;
Moran, AP ;
Aspinall, GO ;
Forte, JG ;
DeVries, T ;
Quan, H ;
Verboom, T ;
Maaskant, JJ ;
Ghiara, P ;
Kuipers, EJ ;
Bloemena, E ;
Tadema, TM ;
Townsend, RR ;
Tyagarajan, K ;
Crothers, JM ;
Monteiro, MA ;
Savio, A ;
DeGraaff, J .
INFECTION AND IMMUNITY, 1996, 64 (06) :2031-2040
[2]  
ASPINALL GO, 1994, CARBOHYDR LETT, V0001
[3]   Lipopolysaccharide of the Helicobacter pylori type strain NCTC 11637 (ATCC 43504): Structure of the O antigen chain and core oligosaccharide regions [J].
Aspinall, GO ;
Monteiro, MA ;
Pang, H ;
Walsh, EJ ;
Moran, AP .
BIOCHEMISTRY, 1996, 35 (07) :2489-2497
[4]   Lipopolysaccharides of Helicobacter pylori strains P466 and MO19: Structures of the O antigen and core oligosaccharide regions [J].
Aspinall, GO ;
Monteiro, MA .
BIOCHEMISTRY, 1996, 35 (07) :2498-2504
[5]   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
[6]  
ATHERTON JC, 1997, PATHOGENESIS HOST RE, P76
[7]  
Ausubel FM, 1995, SHORT PROTOCOLS MOL
[8]  
Blaser MJ, 1997, EUR J GASTROEN HEPAT, V9, pS3
[9]   HELICOBACTER-PYLORI PHENOTYPES ASSOCIATED WITH PEPTIC-ULCERATION [J].
BLASER, MJ .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1994, 29 :1-5
[10]   Evidence for ethnic tropism of Helicobacter pylori [J].
Campbell, S ;
Fraser, A ;
Holliss, B ;
Schmid, J ;
OToole, PW .
INFECTION AND IMMUNITY, 1997, 65 (09) :3708-3712