A Note On Survival Of Infective Stage Larva Of Gnathostoma Spp. In BME Culture Medium

S. Soogarun, J. Suwansaksri, V. Wiwanitkit
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Abstract

Dear editor, human gnathostomiasis in an important tropical parasitic infection ( 1). The major manifestation as nodular migratory eosinophilic panniculitis is suggested for this disease. More severe presentations, resulting from visceral larva migran, such as ocular and CNS gnathostomiasis are also reported. The diagnosis is confirmed by identification of the parasite from the pathological specimen. However, it is difficult to get the histological diagnosis, therefore, the immunological diagnosis for this infection is necessary. At present, Gnathostoma spinigerum third stage larvae (L3) antigen is necessary for Western blot analysis in the diagnosis of Gnathostomiasis ( 2 , 3). Acid pepsin solution is required for digestion of eel's liver (Fluta alba) to yield the larvae for antigen preparation. However, the specific antigen is excretion secretory (ES) antigen, which can be derived from viable larva. Since the larva start to degenerate within a short period, therefore, the larva derived from digestion must be used before its death. Here, we reported our result in using the BME culture medium for cultivation of the derived larva to prolong the period of usage of the harvested larva in antigen preparation.
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颌口蝇侵染期幼虫在BME培养基中的存活研究
尊敬的编辑,人类颌口病是一种重要的热带寄生虫感染(1)。该病的主要表现为结节性迁移性嗜酸性泛膜炎。更严重的表现,由内脏幼虫迁移引起,如眼部和中枢神经系统颌口病也有报道。病理标本中寄生虫的鉴定证实了诊断。然而,很难得到组织学诊断,因此,对这种感染的免疫学诊断是必要的。目前,在诊断颌口病时,需要使用棘齿颌口病第三期幼虫(L3)抗原进行Western blot分析(2,3)。酸性胃蛋白酶溶液需要消化鳗鱼肝脏(Fluta alba)以产生用于抗原制备的幼虫。然而,特异性抗原是排泄分泌(ES)抗原,可以从活的幼虫中提取。由于幼虫在短时间内开始退化,因此,消化后的幼虫必须在其死亡之前使用。本文报道了用BME培养基培养衍生幼虫的结果,以延长收获的幼虫在抗原制备中的使用时间。
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