Skirpstunas Ramona T, Baldwin Thomas J
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington 99164, USA.
Dis Aquat Organ. 2002 Oct 4;51(3):161-7. doi: 10.3354/dao051161.
Invasion of Edwardsiella ictaluri into cultured mammalian, fish and enzymatically harvested catfish enteric epithelial cells is described. Gentamicin survival assays were used to demonstrate the ability of this catfish pathogen to invade IEC-6 (origin: rat small intestinal epithelium), Henle 407 (origin: human embryonic intestinal epithelium), fathead minnow (FHM, minnow epithelial cells) and trypsin/pepsin-harvested channel catfish enteric epithelial cells. Invasion of all cell types occurred within 2 h of contact at 26 degrees C, in contrast to Escherichia coli DH5 alpha, which did not invade cells tested. Eight Edwardsiella ictaluri isolates from diseased catfish and the ATCC (American Type Culture Collection) strain were evaluated for invasion efficiency using FHM cells. All isolates were invasive, but at differing efficiencies. Invasion blocking assays using chemical blocking agents were performed on a single isolate (LA 89-9) using IEC-6 epithelial cells. Preincubation of IEC-6 cells with cytochalasin D (microfilament depolymerizer) and monodansylcadaverine (blocks receptor-mediated endocytosis) significantly reduced invasion by E. ictaluri, whereas exposure to colchicine (microtubule depolymerizer) had no effect on bacterial internalization. Results indicate that actin polymerization and receptor-mediated endocytosis are involved in uptake of E. ictaluri by IEC-6 epithelial cells. Invasion trials using freshly harvested cells from the intestine of the natural host, Ictalurus punctatus, show that invasion occurs, but at a low efficiency. This is possibly due to loss of outer membrane receptors during enzymatic cell harvest. This study provides the first documentation of the invasion of cultured mammalian and fish cells by E. ictaluri, and identifies possible mechanisms used for intracellular access. Additionally, the study describes several functional in vitro invasion models using commercially available cell lines as well as cells from the natural host (channel catfish, I. punctatus).
本文描述了爱德华氏菌侵入培养的哺乳动物、鱼类以及经酶解收获的鲶鱼肠道上皮细胞的情况。采用庆大霉素存活试验来证明这种鲶鱼病原体侵入IEC-6细胞(来源:大鼠小肠上皮)、亨勒407细胞(来源:人胚胎肠上皮)、黑头呆鱼(FHM,米诺鱼上皮细胞)以及经胰蛋白酶/胃蛋白酶收获的沟鲶肠道上皮细胞的能力。与未侵入所测试细胞的大肠杆菌DH5α不同,在26℃接触2小时内,所有细胞类型均发生了爱德华氏菌的侵入。使用FHM细胞评估了从患病鲶鱼分离出的8株爱德华氏菌以及美国模式培养物集存库(ATCC)菌株的侵入效率。所有分离株均具有侵入性,但效率不同。使用化学阻断剂对单个分离株(LA 89-9)进行了IEC-6上皮细胞的侵入阻断试验。用细胞松弛素D(微丝解聚剂)和单丹磺酰尸胺(阻断受体介导的内吞作用)对IEC-6细胞进行预孵育,可显著降低爱德华氏菌的侵入,而暴露于秋水仙碱(微管解聚剂)对细菌内化没有影响。结果表明,肌动蛋白聚合和受体介导的内吞作用参与了IEC-6上皮细胞对爱德华氏菌的摄取。使用从天然宿主斑点叉尾鮰肠道新鲜收获的细胞进行的侵入试验表明,虽然发生了侵入,但效率较低。这可能是由于在酶解收获细胞过程中外膜受体丢失所致。本研究首次记录了爱德华氏菌对培养的哺乳动物和鱼类细胞的侵入,并确定了用于细胞内进入的可能机制。此外,该研究还描述了几种使用市售细胞系以及天然宿主(沟鲶,斑点叉尾鮰)细胞的功能性体外侵入模型。