McOrist S, Jasni S, Mackie R A, Berschneider H M, Rowland A C, Lawson G H
Department of Veterinary Pathology, University of Edinburgh, Veterinary Field Station, Easter Bush, Midlothian.
Res Vet Sci. 1995 Nov;59(3):255-60. doi: 10.1016/0034-5288(95)90013-6.
Separate suspensions of two strains of ileal symbiont (IS) intracellularis, an obligate intracellular bacterium and the causative agent of porcine proliferative enteropathy, were added to 40 or 80 per cent confluent monolayers of established cultures of rat (IEC-18) or pig enterocytes (IPEC-J2). Peak numbers of intracellular organisms were detected within the enterocytes six days later, but no cytopathic effects were evident. After an initial close association with the cell membrane of the enterocytes, single bacteria were internalised after three hours within membranes-bound vacuoles. The formation of an electron-dense projection between cell membranes and external bacteria was only evident if the bacterial suspensions were centrifuged on to the monolayers. The release of internalised bacteria into the cytoplasm, with the breakdown and loss of membrane-bound vacuoles, was also evident three hours after infection. Internalised bacteria were associated with, but not observed within, coated membrane pits. Mitochondria were closely associated with internalised vacuoles and with released bacteria. Two to six days after infection, multiplication of the bacteria free in the cytoplasm was frequently observed. In infected cells six days after the inoculation of monolayers, groups of bacteria were found within large, balloon-like, cytoplasmic protrusions, and the subsequent release of bacteria from the monolayer provided a means of bacterial exit from the cells. Many events in the in vitro culture model closely resembled events observed at the cellular level in animals infected with IS intracellularis and the model provides a useful basis for investigating the pathogenetic mechanisms of this bacterium.
将猪增生性肠炎的病原体——专性胞内菌两株回肠共生菌(IS)细胞内菌的单独悬液,添加到已建立的大鼠(IEC-18)或猪肠上皮细胞(IPEC-J2)培养物的40%或80%汇合单层细胞中。六天后在肠上皮细胞内检测到细胞内菌的峰值数量,但未观察到明显的细胞病变效应。在最初与肠上皮细胞膜紧密结合后,单个细菌在三小时内被内化到膜结合的液泡中。只有当细菌悬液离心到单层细胞上时,细胞膜与外部细菌之间才会明显形成电子致密突起。感染三小时后,内化细菌释放到细胞质中,膜结合液泡破裂并消失也很明显。内化细菌与包被膜小窝相关,但未在其中观察到。线粒体与内化液泡和释放的细菌紧密相关。感染后两到六天,经常观察到细胞质中游离细菌的增殖。在单层细胞接种六天后的感染细胞中,在大的、气球状的细胞质突起内发现了细菌群,随后细菌从单层细胞中释放为细菌从细胞中排出提供了一种方式。体外培养模型中的许多事件与感染IS细胞内菌的动物在细胞水平上观察到的事件非常相似,该模型为研究这种细菌的致病机制提供了有用的基础。