Coyne C P, Brake D
Veterinary Pharmacology Research Laboratory, Veterinary Research Program, College of Veterinary Medicine, Mississippi State University 39762, Mississippi, MS, USA.
Int J Parasitol. 2001 Apr;31(4):359-76. doi: 10.1016/s0020-7519(01)00116-3.
Cell populations derived from viable Haemonchus contortus L(3) larvae were propagated in vitro in a tissue culture environment for a prolonged period (>48 months). Microscopic evaluation of H. contortus-derived cell populations revealed gross morphological characteristics highly analogous to those described for cell types originating from species of plant nematodes propagated in vitro in a tissue culture environment for a briefer period of time (<6 months). The characterisation of extracts harvested from tissue culture populations of H. contortus-derived cells by SDS-PAGE analysis detected molecular fractions of approximately 29, 45, 55, and 200-kDa that closely correlated with reports for preparations obtained from intact/viable H. contortus larvae. Complementary investigations detected the dual biochemical expression of phosphohydrolase and aminopeptidase-M activities based on the hydrolysis of the synthetic enzyme-specific substrates, para-nitrophenylphosphate and leucine-para-nitroanaline, respectively. The identification of phosphohydrolase and aminopeptidase-M-like biochemical activity in fractions harvested from H. contortus-derived cell populations and propagated in vitro in tissue culture served as evidence validating their parasitic-origin. Further validation of H. contortus-derived cell populations propagated in tissue culture entailed the formulation of Triton X-100 extracts containing potential immunoprotective antigens with SEAM adjuvant and its administration by intramuscular injection (100 microg total protein) to healthy sheep (n=8) on day 0 (left rear-limb) and day +14 (right rear-limb). Animals on day 28 subsequently received a single oral challenge of 10,000 infective L(3)-stage H. contortus larvae. Applying ELISA methodologies, increases in antigen-specific IgM and IgG were detected in ovine serum samples. Interpretation of experimental findings revealed that sheep with the greatest antigen-specific humoral immune responses (IgG titre 1/3125) also demonstrated a degree of reduced abomasal H. contortuslarvae burdens (60% reduction). Polyclonal antibody from immunoprotected sheep was subsequently found to recognise both the: (i), digestive tract; and (ii), antigen extracts associated with intact/viable H. contortus larvae. These experimental findings reveal the potential feasibility of propagating parasite-derived cell populations in an in vitro tissue culture environment in a manner that retains their ability to express immunoprotective antigenic fractions.
源自活捻转血矛线虫L(3)幼虫的细胞群体在组织培养环境中进行了长时间(>48个月)的体外培养。对捻转血矛线虫来源的细胞群体进行显微镜评估,发现其总体形态特征与在组织培养环境中体外培养较短时间(<6个月)的植物线虫物种来源的细胞类型所描述的特征高度相似。通过SDS-PAGE分析对从捻转血矛线虫来源细胞的组织培养群体中收获的提取物进行表征,检测到分子量约为29、45、55和200 kDa的分子组分,这与从完整/活的捻转血矛线虫幼虫获得的制剂的报道密切相关。补充研究分别基于合成酶特异性底物对硝基苯磷酸酯和亮氨酸对硝基苯胺的水解,检测到磷酸水解酶和氨肽酶-M活性的双重生化表达。在从捻转血矛线虫来源的细胞群体中收获并在组织培养中体外培养的组分中鉴定出磷酸水解酶和氨肽酶-M样生化活性,作为验证其寄生虫来源的证据。对在组织培养中培养的捻转血矛线虫来源的细胞群体的进一步验证包括用SEAM佐剂配制含有潜在免疫保护抗原的Triton X-100提取物,并在第0天(左后肢)和第+14天(右后肢)通过肌肉注射(总蛋白100μg)给予健康绵羊(n = 8)。随后在第28天,动物接受了10,000条感染性L(3)期捻转血矛线虫幼虫的单次口服攻击。应用ELISA方法,在绵羊血清样本中检测到抗原特异性IgM和IgG增加。对实验结果的解释表明,具有最大抗原特异性体液免疫反应(IgG滴度1/3125)的绵羊也表现出一定程度的皱胃捻转血矛线虫幼虫负担减轻(减少60%)。随后发现来自免疫保护绵羊的多克隆抗体能够识别:(i)消化道;以及(ii)与完整/活的捻转血矛线虫幼虫相关的抗原提取物。这些实验结果揭示了以保留其表达免疫保护抗原组分能力的方式在体外组织培养环境中培养寄生虫来源细胞群体的潜在可行性。