Candidatus Helicobacter heilmannii from a cynomolgus monkey induces gastric mucosa-associated lymphoid tissue lymphomas in C57BL/6 mice

被引:63
作者
Nakamura, Masahiko
Murayama, Somay Yamagata
Serizawa, Hiroshi
Sekiya, Yukie
Eguchi, Masahiro
Takahashi, Shinichi
Nishikawa, Kaori
Takahashi, Tetsufumi
Matsumoto, Tsukasa
Yamada, Haruki
Hibi, Toshifumi
Tsuchimoto, Kanji
Matsui, Hidenori
机构
[1] Kitasato Univ, Sch Pharmaceut Sci, Minato Ku, Ctr Clin Pharm & Clin Sci, Tokyo 1088641, Japan
[2] Kitasato Inst Life Sci, Minato Ku, Tokyo 1088641, Japan
[3] Grad Sch Infect Control Sci, Minato Ku, Tokyo 1088641, Japan
[4] Kitasato Inst Hosp, Kitasato Inst, Ctr Basic Res, Minato Ku, Tokyo 1088642, Japan
[5] Kitasato Inst Hosp, Kitasato Inst, Dept Internal Med, Minato Ku, Tokyo 1088642, Japan
[6] Kyorin Univ, Dept Internal Med 3, Tokyo 1818611, Japan
[7] Keio Univ, Dept Internal Med, Sch Med, Shinjuku Ku, Tokyo 1608582, Japan
关键词
D O I
10.1128/IAI.01459-06
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Both Helicobacter pylori and "Candidatus Helicobacter heilmannii" infections are associated with peptic ulcers, gastric adenocarcinoma, and gastric mucosa-associated lymphoid tissue (MALT) lymphomas. However, good animal models of H. pylori clinical diseases are rare. In this study, we aimed to establish an animal model of "Candidatus Helicobacter heilmannii" gastric MALT lymphoma. We used a urease-positive gastric mucosal and mucus homogenate from a cynomolgus monkey maintained in C57BL/6 mouse stomachs. The bacterium in the homogenate was identified as "Candidatus Helicobacter heilmannii" based on a DNA sequence analysis of the 16S rRNA and urease genes. Mucosal and mucus homogenates were used to inoculate C57BL/6 mice, which were then examined for 24 months. We observed a gradual increase in the surface area of protrusive lesions in almost all infected C57BL/6 mouse fundic stomachs 6 months after infection. Light microscopic observations revealed an accumulation of B lymphocytes along with destruction of glandular elements and the presence of lymphoepithelial lesions consistent with low-grade MALT lymphomas. Electron microscopic observation revealed numerous "Candidatus Helicobacter heilmannii" bacilli in the fundic glandular lumen, the intracellular canaliculi, and the cytoplasm of intact cells, as well as damaged parietal cells. In conclusion, "Candidatus Helicobacter heilmannii" induced gastric MALT lymphomas in almost 100% of infected C57BL/6 mice after a 6-month period associated with the destruction of parietal cells.
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页码:1214 / 1222
页数:9
相关论文
共 30 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Isolation of a ''Helicobacter heilmanii''-like organism from the human stomach [J].
Andersen, LP ;
Norgaard, A ;
Holck, S ;
Blom, J ;
Elsborg, L .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1996, 15 (01) :95-96
[3]   Development and application of a novel screening PCR assay for direct detection of 'Helicobacter heilmannii'-like organisms in human gastric biopsies in Southeast England [J].
Chisholm, SA ;
Owen, RJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2003, 46 (01) :1-7
[4]  
DUBOIS AL, 1994, GASTROENTEROLOGY, V160, P1405
[5]   HELICOBACTER-PYLORI GASTRITIS AND PRIMARY GASTRIC NON-HODGKINS-LYMPHOMAS [J].
EIDT, S ;
STOLTE, M ;
FISCHER, R .
JOURNAL OF CLINICAL PATHOLOGY, 1994, 47 (05) :436-439
[6]  
ENNO A, 1995, AM J PATHOL, V147, P217
[7]  
Erdman SE, 1997, AM J PATHOL, V151, P273
[8]   CORRELATION OF PARIETAL-CELL STRUCTURE AND FUNCTION [J].
FORTE, JG ;
FORTE, TM ;
BLACK, JA ;
OKAMOTO, C ;
WOLOSIN, JM .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1983, 5 :17-27
[9]   Immunogenetic analysis of gastric MALT lymphoma-like lesions induced by Helicobacter pylori infection in neonatally thymectomized mice [J].
Fukui, T ;
Okazaki, K ;
Tamaki, H ;
Kawasaki, K ;
Matsuura, M ;
Asada, M ;
Nishi, T ;
Uchida, K ;
Iwano, M ;
Ohana, M ;
Hiai, H ;
Chiba, T .
LABORATORY INVESTIGATION, 2004, 84 (04) :485-492
[10]  
ITOH T, 1994, GASTROENTEROLOGY, V106, pA99