Zweygarth E, Josemans A I
Onderstepoort Veterinary Institute, Private Bag X5, Onderstepoort 0110, South Africa.
Ann N Y Acad Sci. 2003 Jun;990:573-80. doi: 10.1111/j.1749-6632.2003.tb07429.x.
The Welgevonden stock of Ehrlichia ruminantium was propagated in eight nonendothelial cell cultures derived from different animal species, both ruminants and nonruminants. The origins of the cells were: bovine fetal testis (BFT), cat ovary (COC), donkey fibroblasts (DFC), sheep fibroblasts (E(2)), horse testis (HTC), lamb fetal testis (LFT), mouse connective tissue (L), and African green monkey kidney (Vero). Four cell culture types (BFT, E(2), LFT and Vero) required supplementation of the medium with cycloheximide for suitable growth of E. ruminantium, whereas the other four (COC, DFC, HTC, and L) did not. Three other stocks of E. ruminantium, Senegal, Ball 3, and Gardel, were also propagated, either in LFT cultures only or in both E(2) and LFT cell cultures. The Welgevonden stock was successfully initiated using E(2) and LFT cell cultures.
反刍兽埃立克体的韦尔格冯登毒株在源自不同动物物种(包括反刍动物和非反刍动物)的8种非内皮细胞培养物中进行传代培养。细胞的来源分别是:牛胎儿睾丸(BFT)、猫卵巢(COC)、驴成纤维细胞(DFC)、绵羊成纤维细胞(E(2))、马睾丸(HTC)、羔羊胎儿睾丸(LFT)、小鼠结缔组织(L)和非洲绿猴肾(Vero)。四种细胞培养类型(BFT、E(2)、LFT和Vero)需要在培养基中添加放线菌酮以促进反刍兽埃立克体的适宜生长,而其他四种(COC、DFC、HTC和L)则不需要。反刍兽埃立克体的其他三个毒株,即塞内加尔毒株、鲍尔3毒株和加德尔毒株,也进行了传代培养,要么仅在LFT培养物中,要么在E(2)和LFT细胞培养物中。使用E(2)和LFT细胞培养物成功启动了韦尔格冯登毒株的传代培养。