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海藻酸假单胞菌对细菌与小鼠巨噬细胞结合的抑制作用。

Inhibition of bacterial binding to mouse macrophages by Pseudomonas alginate.

作者信息

Oliver A M, Weir D M

出版信息

J Clin Lab Immunol. 1983 Apr;10(4):221-4.

PMID:6408261
Abstract

Alginate, an acetylated polymer of D-mannuronic and L-guluronic acid obtained from a mucoid strain of Pseudomonas aeruginosa was shown to inhibit the binding of an isogenic non-mucoid revertant to mouse peritoneal and pulmonary macrophages. Inhibition of bacterial binding by the alginate was also demonstrated in tests with other non-mucoid P. aeruginosa strains and a strain of Staphylococcus albus. Since the mucoid form of P. aeruginosa eventually predominates in chronic P. aeruginosa infection in patients with cystic fibrosis, it is postulated that the alginate's inhibition of binding gives mucoid forms a selective advantage over non-mucoid forms against macrophage defence mechanisms in the lung.

摘要

藻酸盐是从铜绿假单胞菌的黏液样菌株中获得的D-甘露糖醛酸和L-古洛糖醛酸的乙酰化聚合物,已证明它能抑制同基因非黏液样回复突变体与小鼠腹腔和肺巨噬细胞的结合。在用其他非黏液样铜绿假单胞菌菌株和一株白色葡萄球菌进行的试验中,也证实了藻酸盐对细菌结合的抑制作用。由于铜绿假单胞菌的黏液样形式最终在囊性纤维化患者的慢性铜绿假单胞菌感染中占主导地位,因此推测藻酸盐对结合的抑制作用使黏液样形式相对于非黏液样形式在抵抗肺部巨噬细胞防御机制方面具有选择性优势。

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