Reduced intracellular survival of Helicobacter pylori vacA mutants in comparison with their wild-types indicates the role of VacA in pathogenesis

被引:30
作者
Petersen, AM
Sorensen, K
Blom, J
Krogfelt, KA [1 ]
机构
[1] Statens Serum Inst, Dept Gastrointestinal Infect, DK-2300 Copenhagen S, Denmark
[2] Statens Serum Inst, Dept Virol, DK-2300 Copenhagen, Denmark
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2001年 / 30卷 / 02期
关键词
Helicobacter pylori; VacA; intracellular;
D O I
10.1111/j.1574-695X.2001.tb01556.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The vacuolating cytotoxin VacA of Helicobacter pylori plays an important but yet unknown role in pathogenesis. We studied the impact of the vacuolating cytotoxin on Ii. pylori invasion of and survival within AGS cells (human gastric cell line derived from an antral adenocarcinoma). Isogenic vacA and cagA mutants were constructed in a wild-type clinical isolate H. pylori. AF4. An H. pylori VacA-deficient mutant, AF4(vacA::kan). was cultured in significantly lower numbers fi om AGS cells after 24 h incubation with gentamicin added to the culture medium than were the type I wild-type strain AF4 (P<0.03) and an isogenic cagA mutant (P<0.01). Complementation of the AF4 vacA mutant with broth culture supernatant from wild-type AF4 improved the intracellular survival of the vacA mutant. We conclude that H. pylori's vacuolating cytotoxin improves the intracellular survival of H. pylori within AGS cells, suggesting the role of the vacuolating cytotoxin in II. pylori pathogenesis. (C) 2001 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:103 / 108
页数:6
相关论文
共 43 条
[1]
GROWTH-RATE PARADOX OF SALMONELLA-TYPHIMURIUM WITHIN HOST MACROPHAGES [J].
ABSHIRE, KZ ;
NEIDHARDT, FC .
JOURNAL OF BACTERIOLOGY, 1993, 175 (12) :3744-3748
[2]
Intracellular niches for extracellular bacteria:: lessons from Helicobacter pylori [J].
Allen, LAH .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 66 (05) :753-756
[3]
Phagocytosed live Listeria monocytogenes influences rab5-regulated in vitro phagosome-endosome fusion [J].
AlvarezDominguez, C ;
Barbieri, AM ;
Beron, W ;
WandingerNess, A ;
Stahl, PD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (23) :13834-13843
[4]
POSSIBLE EVIDENCE OF INVASIVENESS OF HELICOBACTER-(CAMPYLOBACTER)-PYLORI [J].
ANDERSEN, LP ;
HOLCK, S .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1990, 9 (02) :135-138
[5]
SURVIVAL AND ULTRASTRUCTURAL-CHANGES OF HELICOBACTER-PYLORI AFTER PHAGOCYTOSIS BY HUMAN POLYMORPHONUCLEAR LEUKOCYTES AND MONOCYTES [J].
ANDERSEN, LP ;
BLOM, J ;
NIELSEN, H .
APMIS, 1993, 101 (01) :61-72
[6]
REGRESSION OF PRIMARY GASTRIC LYMPHOMA OF MUCOSA-ASSOCIATED LYMPHOID-TISSUE TYPE AFTER CURE OF HELICOBACTER-PYLORI INFECTION [J].
BAYERDORFFER, E ;
NEUBAUER, A ;
RUDOLPH, B ;
THIEDE, C ;
LEHN, N ;
EIDT, S ;
STOLTE, M .
LANCET, 1995, 345 (8965) :1591-1594
[7]
In vitro models to study attachment and invasion of Helicobacter pylori [J].
Birkness, KA ;
Gold, BD ;
White, EH ;
Bartlett, JH ;
Quinn, FD .
MICROBIAL PATHOGENESIS AND IMMUNE RESPONSE II, 1996, 797 :293-295
[8]
PATHOGENETIC IMPLICATIONS OF ULTRASTRUCTURAL FINDINGS IN CAMPYLOBACTER-PYLORI RELATED GASTRODUODENAL DISEASE [J].
BODE, G ;
MALFERTHEINER, P ;
DITSCHUNEIT, H .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1988, 23 :25-39
[9]
INVASION OF CAMPYLOBACTER-LIKE ORGANISMS IN THE DUODENAL MUCOSA IN PATIENTS WITH ACTIVE DUODENAL-ULCER [J].
BODE, G ;
MALFERTHEINER, P ;
DITSCHUNEIT, H .
KLINISCHE WOCHENSCHRIFT, 1987, 65 (03) :144-146
[10]
INHIBITION OF MACROPHAGE PHAGOSOME-LYSOSOME FUSION BY SALMONELLA-TYPHIMURIUM [J].
BUCHMEIER, NA ;
HEFFRON, F .
INFECTION AND IMMUNITY, 1991, 59 (07) :2232-2238