POTENTIAL PATHOGEN WITH TROPHISM FOR GASTRIC MUCIN
POTENTIAL PATHOGEN WITH TROPHISM FOR GASTRIC MUCIN
批准号:
6107256
负责人:
DAVID CALHOUN
金额:
$2.57万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-02-01 至 2000-01-31
关键词:
Staphylococcus infection adhesin bacteria infection mechanism catalase duodenum disorder endoscopy enzyme linked immunosorbent assay gastritis gastrointestinal infection gram positive bacteria human tissue microorganism classification microorganism culture molecular cloning mucins nucleic acid sequence peptic ulcer protein purification serotyping swine
中文摘要
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英文摘要
Description (Adapted from Application): A large proportion of a variety
of gastric disorders occurring in the industrialized countries have been
attributed to infections by Helicobacter pylori. However, some patients
suffering these symptoms are culture negative and antibody negative for
H. pylori, and these disorders are often attributed to other causes,
such as the habitual use of certain drugs. There have been reports of
uncharacterized coccoid organisms proposed as the causative agent for
gastric inflammation in some patients, and coccoid forms have been
detected in gastric biopsy samples. Experimental proof of a role of the
coccoid forms in the transmission of infection has not been possible
because the coccoid forms could not be cultivated in the laboratory. A
coccoid organism was recently cultivated from biopsy material obtained
from patients suffering gram gastritis. The prototype isolate,
designated strain SL-100, infects the porcine gastric antrum and binds
to porcine gastric mucin in vitro. These observations suggest that the
coccoid organisms isolated from these gastric patients may be human
pathogens. Major goals of the proposed research are to (1) further
characterize strain SL-100 and related isolated, and (2) determine the
incidence, in this country and abroad, of infection or disease due to
this species. The PI will test serum samples from normal and infected
individuals to test for antibodies specific for this organism. He
currently has clinical collaborators in the New York area, and the
initial goal will be to attempt to cultivate the organism from biopsy
material and to determine if antibodies directed against specific
microbial proteins are correlated with infection or disease.
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