Britton A P, Miller R B, Ruhnke H L, Johnson W M
Department of Pathology, Ontario Veterinary College, University of Guelph.
Can J Vet Res. 1989 Apr;53(2):172-5.
The object of this study was to develop a prefixation protein A gold labelling technique for Ureaplasma diversum and to apply this to bovine embryos. Sixteen hour cultures of Ureaplasma diversum strain 2312 were incubated with either specific antiserum or nonimmune serum, followed by exposure to protein A gold and negative staining. The ureaplasmas which were incubated with specific antiserum were labelled with gold particles while those ureaplasmas which were incubated with nonimmune serum were not labelled. Twenty-three unhatched, day 7 bovine embryos were then incubated in either embryo culture medium (ECM) alone, ECM with sterile ureaplasma broth added or ECM with 1.7 X 10(6) colony forming units of Ureaplasma diversum strain 2312 per embryo. After 16 hours, the embryos were washed twice and incubated with either specific antiserum or nonimmune serum. The embryos were then incubated with medium containing protein A gold and examined by electron microscopy. No ureaplasmas were identified on the zona pellucida of the control embryos. Ureaplasmas were identified on the outer surface of the zona pellucida of 13 of the 17 embryos which had been exposed to the organism. Of these, the embryos which were incubated with specific antiserum had labelled ureaplasmas while the embryos which were incubated with nonimmune serum had unlabelled ureaplasmas on the zona pellucida. It was concluded that the protein A gold method was a suitable technique for the identification of ureaplasmas in EM preparations. The presence of ureaplasmas on the outer surface of the bovine zona pellucida following in vitro exposure to the organism was confirmed.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究的目的是开发一种用于多样性脲原体的预固定蛋白A金标记技术,并将其应用于牛胚胎。将多样性脲原体2312菌株培养16小时,分别与特异性抗血清或非免疫血清孵育,随后用蛋白A金处理并进行负染色。与特异性抗血清孵育的脲原体被金颗粒标记,而与非免疫血清孵育的脲原体未被标记。然后将23个未孵化的第7天牛胚胎分别在单独的胚胎培养基(ECM)、添加无菌脲原体肉汤的ECM或每胚胎含有1.7×10⁶个多样性脲原体2312菌株菌落形成单位的ECM中孵育。16小时后,胚胎洗涤两次,分别与特异性抗血清或非免疫血清孵育。然后将胚胎与含有蛋白A金的培养基孵育,并通过电子显微镜检查。对照胚胎的透明带上未鉴定出脲原体。在暴露于该微生物的17个胚胎中的13个胚胎的透明带外表面鉴定出脲原体。其中,与特异性抗血清孵育的胚胎,其透明带上的脲原体被标记,而与非免疫血清孵育的胚胎,其透明带上的脲原体未被标记。结论是蛋白A金方法是在电子显微镜制剂中鉴定脲原体的合适技术。体外暴露于该微生物后,证实牛透明带外表面存在脲原体。(摘要截短至250字)