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小鼠针对刚地弓形虫(S-273)感染产生的免疫球蛋白M和G抗体及其在感染后不同天数的蛋白质印迹中的抗原识别模式。

Immunoglobulin M and G antibodies in mice in response to Toxoplasma gondii (S-273) infection and their antigen recognition patterns in western blotting on various post-infection days.

作者信息

Rai S K, Shibata H, Kubota K, Sumi K, Matsuoka A, Uga S, Matsumura T, Shrestha H G

机构信息

Department of Pathology, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.

出版信息

Kansenshogaku Zasshi. 1994 Nov;68(11):1318-23. doi: 10.11150/kansenshogakuzasshi1970.68.1318.

Abstract

Immunoglobulin M and G antibody responses in mice experimentally infected with Toxoplasma gondii (S-273) and the reaction patterns with T. gondii (RH) tachyzoite antigens were studied on various post-infection days (PIDs) (2nd to 36th PIDs) using a commercially available IgM and IgG enzyme linked immunosorbent assay (ELISA) test systems and Western blotting (WB) technique. IgM antibody in ELISA test appeared to be positive on 12th PID (absorbance 0.764) and reached its peak level on 16th PID (absorbance 1.338) showing a slow decline thereafter with an absorbance of 0.800 even on 36th PID. Positivity of IgM was confirmed by WB except for 36th PID. IgG appeared on 16th PID with an absorbance of 0.248 and showed a steady increasing tendency even on 36th PID (absorbance 1.747). However, IgG positivity on WB was observed only on 29th PID and afterwards. On Western blots, both IgM and IgG showed interesting antigen recognition patterns on various PIDs. At the most IgM recognised seven antigens of 14kDa to 53kDa while IgG recognised eight antigens of 17kDa to 53kDa. Major antigens recognised by IgM were of 53kDa and 21kDa while the major band recognised by IgG was of 19kDa. The major bands, however, showed variability in their consistency during various PIDs. All the antigens recognised by IgM and IgG were not identical.

摘要

利用市售的 IgM 和 IgG 酶联免疫吸附测定(ELISA)测试系统以及蛋白质印迹法(WB)技术,研究了实验感染刚地弓形虫(S - 273)的小鼠体内免疫球蛋白 M 和 G 的抗体反应,以及在感染后不同天数(PID,第 2 天至第 36 天)与刚地弓形虫(RH)速殖子抗原的反应模式。ELISA 测试中,IgM 抗体在感染后第 12 天呈阳性(吸光度 0.764),并在第 16 天达到峰值水平(吸光度 1.338),此后缓慢下降,即使在第 36 天吸光度仍为 0.800。除第 36 天外,WB 证实了 IgM 的阳性。IgG 在第 16 天出现,吸光度为 0.248,即使在第 36 天(吸光度 1.747)仍呈稳定上升趋势。然而,WB 上 IgG 阳性仅在第 29 天及之后观察到。在蛋白质印迹上,IgM 和 IgG 在不同 PID 显示出有趣且不同的抗原识别模式。IgM 最多识别出 7 种分子量在 14kDa 至 53kDa 的抗原,而 IgG 识别出 8 种分子量在 17kDa 至 53kDa 的抗原。IgM 识别的主要抗原为 53kDa 和 21kDa,而 IgG 识别的主要条带为 19kDa。然而,这些主要条带在不同 PID 期间的一致性存在差异。IgM 和 IgG 识别的所有抗原并不相同。

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