Leong J M, Moitoso de Vargas L, Isberg R R
Department of Medicine, Tufts-New England Medical Center Hospital, Boston, Massachusetts.
Infect Immun. 1992 Feb;60(2):683-6. doi: 10.1128/iai.60.2.683-686.1992.
The invasin protein of Yersinia pseudotuberculosis binds to integrin receptors on mammalian cells and promotes cellular penetration. We demonstrate here that the cell attachment activity of invasin can be detected in bacterial colonies that have been immobilized on filter membranes. Invasin expressed in either Escherichia coli K-12 or Y. pseudotuberculosis mediated binding to membranes, and as few as 10(5) Y. pseudotuberculosis resulted in detectable attachment of cultured epithelial cells. A similar binding activity was detected in clinical isolates of the related pathogen Y. enterocolitica but not in environmental isolates. Although there exist multiple mechanisms for the binding of wild-type organisms to host cells, efficient mammalian cell binding to immobilized Y. pseudotuberculosis required expression of a functional invasin protein. Several pathogens that are known to bind or penetrate mammalian cells were also tested, and only one of these bound cultured mammalian cells efficiently.
假结核耶尔森菌的侵袭蛋白与哺乳动物细胞上的整合素受体结合并促进细胞穿透。我们在此证明,侵袭蛋白的细胞附着活性可在固定于滤膜上的细菌菌落中检测到。在大肠杆菌K-12或假结核耶尔森菌中表达的侵袭蛋白介导与膜的结合,仅10⁵个假结核耶尔森菌就能使培养的上皮细胞产生可检测到的附着。在相关病原体小肠结肠炎耶尔森菌的临床分离株中检测到了类似的结合活性,但在环境分离株中未检测到。虽然野生型生物体与宿主细胞结合存在多种机制,但哺乳动物细胞与固定化假结核耶尔森菌的有效结合需要功能性侵袭蛋白的表达。还测试了几种已知能结合或穿透哺乳动物细胞的病原体,其中只有一种能有效结合培养的哺乳动物细胞。