Functional association between the Helicobacter pylori virulence factors VacA and CagA

被引:92
作者
Argent, Richard H. [1 ,2 ]
Thomas, Rachael S. [1 ,2 ]
Letley, Darren P. [1 ,2 ]
Rittig, Michael G. [3 ]
Hardie, Kim R. [1 ]
Atherton, John C. [1 ,2 ]
机构
[1] Univ Nottingham, Ctr Biomol Sci, Inst Infect Immun & Inflammat, Nottingham NG7 2RD, England
[2] Univ Nottingham, Queens Med Ctr, Wolfson Digest Dis Ctr, Nottingham NG7 2UH, England
[3] Univ Nottingham, Queens Med Ctr, Ctr Biochem & Cell Biol, Nottingham NG7 2UH, England
基金
英国医学研究理事会;
关键词
D O I
10.1099/jmm.0.47465-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Helicobacter pylori virulence factors CagA and VacA are implicated in the development of gastroduodenal diseases. Most strains possessing CagA also possess the more virulent vacuolating form of VacA. This study assessed the significance of possession of both virulence factors in terms of their effect on gastric epithelial cells, using a set of minimally passaged, isogenic VacA, CagA and CagE mutants in H. pylori strains 60190 and 84-183. The cagA and cagE mutants were found to significantly increase VacA-induced vacuolation of epithelial cells, and the vacA mutants significantly increased CagA-induced cellular elongations, compared with wild-type strains, indicating that CagA reduces vacuolation and VacA reduces hummingbird formation. Although epithelial cells incubated with the wild-type H. pylori strains may display both vacuolation and hummingbird formation, it was found that (i) hummingbird length was significantly reduced in vacuolated cells compared with those without vacuolation; (ii) the number of vacuoles was significantly reduced in vacuolated cells with hummingbird formation compared with those without hummingbirds; and (iii) cells displaying extensive vacuolation did not subsequently form hummingbirds and vice versa. VacA did not affect the phosphorylation of CagA. These data show that VacA and CagA downregulate each other's effects on epithelial cells, potentially allowing H. pylori interaction with cells whilst avoiding excessive cellular damage.
引用
收藏
页码:145 / 150
页数:6
相关论文
共 27 条
[1]   Determinants and consequences of different levels of CagA phosphorylation for clinical isolates of Helicobacter pylori [J].
Argent, RH ;
Kidd, M ;
Owen, RJ ;
Thomas, RJ ;
Limb, MC ;
Atherton, JC .
GASTROENTEROLOGY, 2004, 127 (02) :514-523
[2]   Brefeldin A enhances Helicobacter pylori vacuolating cytotoxin-induced vacuolation of epithelial cells [J].
Argent, RH ;
McGarr, C ;
Atherton, JC .
FEMS MICROBIOLOGY LETTERS, 2004, 237 (01) :163-170
[3]   Helicobacter pylori CagA containing ITAM-like sequences localized to lipid rafts negatively regulates VacA-induced signaling in vivo [J].
Asahi, M ;
Tanaka, Y ;
Izumi, T ;
Ito, Y ;
Naiki, H ;
Kersulyte, D ;
Tsujikawa, K ;
Saito, M ;
Sada, K ;
Yanagi, S ;
Fujikawa, A ;
Noda, M ;
Itokawa, Y .
HELICOBACTER, 2003, 8 (01) :1-14
[4]   Helicobacter pylori CagA protein can be tyrosine phosphorylated in gastric epithelial cells [J].
Asahi, M ;
Azuma, T ;
Ito, S ;
Ito, Y ;
Suto, H ;
Nagai, Y ;
Tsubokawa, M ;
Tohyama, Y ;
Maeda, S ;
Omata, M ;
Suzuki, T ;
Sasakawa, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (04) :593-602
[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]   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
[7]   Helicobacter pylori supernatants cause epithelial cytoskeletal disruption that is bacterial strain and epithelial cell line dependent but not toxin VacA dependent [J].
Bebb, JR ;
Letley, DP ;
Rhead, JL ;
Atherton, JC .
INFECTION AND IMMUNITY, 2003, 71 (06) :3623-3627
[8]   Nucleotide-binding oligomerization domain-1 and epidermal growth factor receptor -: Critical regulators of β-defensins during helicobacter pylori infection [J].
Boughan, PK ;
Argent, RH ;
Body-Malapel, M ;
Park, JH ;
Ewings, KE ;
Bowie, AG ;
Ong, SJ ;
Cook, SJ ;
Sorensen, OE ;
Manzo, BA ;
Inohara, N ;
Klein, NJ ;
Nuñez, G ;
Atherton, JC ;
Bajaj-Elliott, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (17) :11637-11648
[9]   NF-κB activation and potentiation of proinflammatory responses by the Helicobacter pylori CagA protein [J].
Brandt, S ;
Kwok, T ;
Hartig, R ;
König, W ;
Backert, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (26) :9300-9305
[10]   cag, a pathogenicity island of Helicobacter pylori, encodes type I-specific and disease-associated virulence factors [J].
Censini, S ;
Lange, C ;
Xiang, ZY ;
Crabtree, JE ;
Ghiara, P ;
Borodovsky, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14648-14653