Thiagarajan D, Saeed M, Turek J, Asem E
Department of Veterinary Pathobiology, School of Veterinary Medicine, Purdue University, West Lafayette, Indiana 47907, USA.
Infect Immun. 1996 Dec;64(12):5015-21. doi: 10.1128/iai.64.12.5015-5021.1996.
The attachment and invasion of chicken ovarian granulosa cells by Salmonella enteritidis was examined in vitro. The attachment was inhibited by preincubation of granulosa cells with anti-chicken fibronectin antibody (approximately 70% reduction in attachment) or preincubation with a 14-kDa fimbrial protein isolated from S. enteritidis (68% reduction in attachment). Treatment of bacterial cells with the tetrapeptide RGDS before addition to granulosa cells resulted in inhibition of attachment (60% inhibition when 2 x 10(7) CFU of bacteria was treated with 500 microg of peptide). Treatment with the peptide GRGD resulted in similar magnitude of inhibition, indicating that extracellular matrix proteins play significant roles in the interaction of S. enteritidis with granulosa cells. In contrast, treatment of the bacterial cells with the peptide GRAD did not result in significant inhibition of attachment to the granulosa cells. S. enteritidis was found to attach specifically to fibronectin, collagen IV, and laminin-coated microtiter plate wells, with the rank order of attachment as follows: fibronectin > laminin > collagen IV. Light and transmission electron micrographs of S. enteritidis invasion of granulosa cells showed organisms with or without a surrounding membrane in the cytoplasm of granulosa cells. In some instances, dividing bacterial cells were observed in the cytoplasm. Results of this study demonstrated that S. enteritidis interacts with granulosa cells in a specific manner and can invade and multiply in these cells. The granulosa cell layer of the preovulatory follicles may be a preferred site for the colonization of the chicken ovaries by invasive strains of S. enteritidis.
在体外检测了肠炎沙门氏菌对鸡卵巢颗粒细胞的黏附和侵袭情况。用抗鸡纤连蛋白抗体预孵育颗粒细胞可抑制黏附(黏附减少约70%),或者用从肠炎沙门氏菌分离的14 kDa菌毛蛋白预孵育也可抑制黏附(黏附减少68%)。在向颗粒细胞中添加细菌之前,用四肽RGDS处理细菌细胞会导致黏附受到抑制(当用500 μg肽处理2×10⁷ CFU细菌时,抑制率为60%)。用肽GRGD处理也产生了类似程度的抑制,这表明细胞外基质蛋白在肠炎沙门氏菌与颗粒细胞的相互作用中发挥着重要作用。相比之下,用肽GRAD处理细菌细胞并未导致对颗粒细胞黏附的显著抑制。发现肠炎沙门氏菌能特异性地黏附于纤连蛋白、IV型胶原和层粘连蛋白包被的微量滴定板孔,黏附顺序如下:纤连蛋白>层粘连蛋白>IV型胶原。肠炎沙门氏菌侵袭颗粒细胞的光镜和透射电镜图像显示,在颗粒细胞的细胞质中,细菌周围有或没有包膜。在某些情况下,可观察到细胞质中有正在分裂的细菌细胞。本研究结果表明,肠炎沙门氏菌以特定方式与颗粒细胞相互作用,并且能够在这些细胞中侵袭和繁殖。排卵前卵泡的颗粒细胞层可能是侵袭性肠炎沙门氏菌菌株在鸡卵巢中定植的首选部位。