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[对接种刚地弓形虫的兔子的血清学研究]

[Serological studies on rabbits inoculated with Toxoplasma gondii].

作者信息

Lee Ok Ran, Choi Won Young

机构信息

Department of Parasitology and Institute of Parasitic Diseases, Catholic Medical College, Korea.

出版信息

Kisaengchunghak Chapchi. 1975 Jun;13(1):7-18. doi: 10.3347/kjp.1975.13.1.7.

Abstract

Serological studies on toxoplasmosis were conducted with rabbits sera that were immunized with RH strain or infected with Beverley strain of Toxoplasma gondii. Complement fixation tests, agar-gel double diffusion tests and agar-gel immunoelectrophoresis were performed. Toxoplasma crude antigen was prepared from the organisms in mice peritoneal fluids, which were infected with RH strain of Toxoplasma gondii. The organisms were suspended in saline volume originally exudated and counted in hemocytometer for purity of the organisms over 99%. These suspended organisms were prepared by sonication, and the solution was centrifuged for 30 min. at 10,000 rpm in 4 degrees C. These supernatant fluids were used as crude antigen. On the other hand, purified antigens were fractionated on Sephadex G-200 gel filtration. A Sephadex G-200 column, 80 by 4 cm, equilibrated with Tris-HCl-(0.1M)-NaCl (1.0M) buffer, pH 8.0 was used. The eluate fractions were collected in 3 ml per hour and the absorbance at 280 nm was measured with a Beckman Du-2 spectrophotometer. Each tube is pooled into 6 fractions by protein density graph. For immunization of rabbits, crude antigen of RH strain was emulsified with an equal amount of incomplete Freund's adjuvant and l ml of mixture was injected subcutaneously into them once a week for 5 successive weeks. Antisera were obtained at an interval of a week, beginning the first week after the last immunization, while several rabbits were infected with Beverley strain of Toxoplasma gondii by inoculating about 200 cysts and antisera were obtained from them serially at a week interval. The results were as follows: 1. The sera from the rabbits immunized with the RH strain or infected with Beverley strain of Toxoplasma gondii againist the crude antigen showed the first positive reactions in 2 or 3 weeks after the administration or immunization in complement fixation tests. Maximum titers appeared in 4 or 5 weeks after immunization with RH strain and in 7 or 9 weeks after infection with Beverley strain respectively. 2. Complement fixation tests showed the positive reactions in the rabbits sera immunized with RH strain against the purified antigens II, III, IV, V and VI: moreover, antigen IV fraction showed the highest titer. On the other hand in the rabbits sera infected with Beverley strain against the purifed antigens II, III and IV fractions showed the positive reaction; especially, antigen fraction IV showed the highest titer. 3. In immuno-diffusion tests, the sera from the rabbits immunized with RH strain and infected with Beverley strain, against the crude antigen appeared the precipitin bands 2 weeks after the immunization or infection. And the former showed the 2 or 5 precipitin bands after 5-8 weeks and the latter showed the l or 2 precipitin bands after 6 weeks. 4. The sera from the rabbits immunized with RH strain against the purified antigens II, III, IV,V and VI showed the precipitin bands, and the sera from the rabbits infected with Beverley strain against the purified antigens II, III and IV showed the precipitin bands in the immuno-diffusion tests. Especially antigen IV was the strongest reaction against the sera from RH strain and Beverley strain. 5. In agar-gel immunoelectrophoresis, the immunized sera against the crude antigen showed 8 arcs. But the infected sera against the crude antigen showed 4 or 5 arcs. 6. The immunized sera against the fractionated antigens II, III, IV, V, VI showed arcs, but against the fractionated antigen IV showed 6 arcs and in the antigens II, III, V, VI showed l or 2 arcs only. On the other hand, the infected sera against the fractionated antigens IV showed 4 arcs, II and III showed the l arcs, which was the most weak of all.

摘要

用经刚地弓形虫RH株免疫或感染贝弗利株的兔血清进行了弓形虫病的血清学研究。进行了补体结合试验、琼脂凝胶双向扩散试验和琼脂凝胶免疫电泳。弓形虫粗抗原由感染刚地弓形虫RH株的小鼠腹腔液中的虫体制备。将虫体悬浮于最初渗出的盐溶液体积中,并在血细胞计数器中计数,以确保虫体纯度超过99%。将这些悬浮的虫体通过超声处理制备,然后将溶液在4℃下以10000转/分钟离心30分钟。这些上清液用作粗抗原。另一方面,通过Sephadex G - 200凝胶过滤对纯化抗原进行分级分离。使用一根80×4 cm的Sephadex G - 200柱,用pH 8.0的Tris - HCl -(0.1M)- NaCl(1.0M)缓冲液平衡。以每小时3 ml的速度收集洗脱液馏分,并用贝克曼Du - 2分光光度计在280 nm处测量吸光度。根据蛋白质密度图将每个管合并为6个馏分。为了免疫兔,将RH株粗抗原与等量的不完全弗氏佐剂乳化,每周一次皮下注射1 ml混合物,连续注射5周。从最后一次免疫后的第一周开始,每隔一周采集抗血清,同时几只兔通过接种约200个包囊感染刚地弓形虫贝弗利株,并每隔一周连续从它们身上采集抗血清。结果如下:1. 在补体结合试验中,用RH株免疫或感染贝弗利株的兔血清针对粗抗原在给药或免疫后2或3周出现首次阳性反应。用RH株免疫后4或5周以及感染贝弗利株后7或9周出现最高滴度。2. 补体结合试验显示,用RH株免疫的兔血清针对纯化抗原II、III、IV、V和VI呈阳性反应;此外,抗原IV馏分显示的滴度最高。另一方面,感染贝弗利株的兔血清针对纯化抗原II、III和IV馏分呈阳性反应;特别是,抗原馏分IV显示的滴度最高。3. 在免疫扩散试验中,用RH株免疫和感染贝弗利株的兔血清针对粗抗原在免疫或感染后2周出现沉淀带。前者在5 - 8周后出现2或5条沉淀带,后者在6周后出现1或2条沉淀带。4. 在免疫扩散试验中,用RH株免疫的兔血清针对纯化抗原II、III、IV、V和VI显示沉淀带,感染贝弗利株的兔血清针对纯化抗原II、III和IV显示沉淀带。特别是抗原IV对RH株和贝弗利株血清的反应最强。5. 在琼脂凝胶免疫电泳中,针对粗抗原的免疫血清显示8条弧。但针对粗抗原的感染血清显示4或5条弧。6. 针对分级分离抗原II、III、IV、V、VI的免疫血清显示弧,但针对分级分离抗原IV显示6条弧,而在抗原II、III、V、VI中仅显示1或2条弧。另一方面,针对分级分离抗原IV的感染血清显示4条弧,针对抗原II和III显示1条弧,这是所有反应中最弱的。

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