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在透析袋中对成年曼氏血吸虫进行无血清培养以生产排泄/分泌抗原。

Serum-free culturing of adult Schistosoma mansoni in dialysis bags for the production of excretory/secretory antigens.

作者信息

Call J L, Pilcher J B, Freeman G L, Tsang V C

机构信息

Centers for Disease Control and Prevention, U.S. Department of Health and Human Services, Atlanta, Georgia 30341-3724, USA.

出版信息

J Parasitol. 1995 Oct;81(5):742-6.

PMID:7472866
Abstract

Antigenic excretory/secretory (E/S) products from Schistosoma mansoni are potentially important in the development of diagnostic assays used to detect circulating antigens in schistosomiasis. The E/S products to be used as antigen(s) for this development must, by necessity, be free of exogenous proteins. The ability to extend serum-free in vitro culture of adult worms is, therefore, essential. Adult worms were perfused from mice, washed in serum-free RPMI-1640 with antibiotics, and placed in sterile dialysis bags, molecular weight cut-off 10 kDa, at a concentration of 100 worms in 1 ml of serum-free, supplemented RPMI-1640. Each bag was then placed in a flask of supplemented RPMI-1640 with 10% fetal calf serum in a humidified incubator at 37 C, 7% CO2. At days 1, 3, 5, 8, and 12, worms were collected; E/S culture medium was analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis. Worm survival rates were 85% after 1 day in culture, dropping gradually to 65% on day 8, and then to 38% on day 12. Silver stain for total protein and immunoblot exposed to positive human infection serum showed E/S culture media from days 3 and 5 having the least complex banding pattern. The quantitative specific activity of E/S, as measured by antigen-limiting Falcon assay screening test system-enzyme-linked immunosorbent assays against human infection serum, indicates E/S antigenicity closely follows the attrition of worms and, therefore, may be directed against the release of somatic antigens by dead worms. Culturing S. mansoni in dialysis tubing is useful in deriving E/S products.

摘要

曼氏血吸虫的抗原性排泄/分泌(E/S)产物在用于检测血吸虫病循环抗原的诊断检测方法的开发中可能具有重要意义。用作该检测抗原的E/S产物必须不含外源蛋白。因此,延长成虫无血清体外培养的能力至关重要。将成虫从小鼠体内灌注出来,用含抗生素的无血清RPMI-1640洗涤,然后放入分子量截留值为10 kDa的无菌透析袋中,以每毫升无血清、补充了RPMI-1640的培养基中100条虫的浓度放置。然后将每个透析袋放入装有含10%胎牛血清的补充了RPMI-1640的培养基的烧瓶中,置于37℃、7%二氧化碳的湿润培养箱中。在第1、3、5、8和12天收集虫体;通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳分析E/S培养基。培养1天后虫体存活率为85%,在第8天逐渐降至65%,然后在第12天降至38%。总蛋白银染和与阳性人类感染血清杂交的免疫印迹显示,第3天和第5天的E/S培养基条带模式最不复杂。通过针对人类感染血清的抗原限量法尔肯检测筛选试验系统 - 酶联免疫吸附测定法测量的E/S定量比活性表明,E/S抗原性与虫体损耗密切相关,因此可能针对死虫释放的体抗原。在透析管中培养曼氏血吸虫有助于获得E/S产物。

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