Vanittanakom Nongnuch, Supabandhu Jitwadee, Khamwan Chantana, Praparattanapan Jutarut, Thirach Sophit, Prasertwitayakij Narawudt, Louthrenoo Worawit, Chiewchanvit Siri, Tananuvat Napaporn
Department of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
J Clin Microbiol. 2004 Sep;42(9):3970-4. doi: 10.1128/JCM.42.9.3970-3974.2004.
Pythium insidiosum is a pathogen that causes disease in both animals and humans. Human infection is rare; however, when it does occur, most patients, especially those having underlying hemoglobinopathy syndromes, such as thalassemia, exhibit a severe form. We identified four isolates of P. insidiosum. Two were recovered from tissue biopsy specimens from thalassemic and leukemic patients, one was derived from brain tissue from a thalassemic patient, and another was isolated from a corneal ulcer from a fourth patient. Western blotting and an enzyme-linked immunosorbent assay (ELISA) were performed with a serum sample derived from one thalassemic patient. The methods used to identify the P. insidiosum isolates were based on morphology, nucleic acid sequencing, and a PCR assay. To confirm the identification, portions of the 18S rRNA genes of these four isolates were sequenced. The sequences were shown to be homologous to previously described P. insidiosum DNA sequences. In addition, PCR amplification of the internal transcribed spacer region specific for P. insidiosum was positive for all four isolates. The ELISA with the serum sample from the thalassemic patient gave a positive result from a serum dilution of 1:800. Finally, Western immunoblotting with this serum sample showed positive immunoglobulin G recognition for proteins of 110, 73, 56, 42 to 35, 30 to 28, 26, and 23 kDa. The results of this study show that both molecularly based diagnostic and serodiagnostic techniques are useful for the rapid identification of human pythiosis. The predominant antigens recognized by Western blotting may be useful in the development of a more sensitive and specific diagnostic tool for this disease.
隐孢子虫是一种可导致动物和人类患病的病原体。人类感染较为罕见;然而,一旦发生感染,大多数患者,尤其是那些患有潜在血红蛋白病综合征(如地中海贫血)的患者,会表现出严重的症状。我们鉴定出了四株隐孢子虫分离株。其中两株从地中海贫血和白血病患者的组织活检标本中分离得到,一株来自一名地中海贫血患者的脑组织,另一株从第四名患者的角膜溃疡中分离得到。我们使用一名地中海贫血患者的血清样本进行了蛋白质印迹法和酶联免疫吸附测定(ELISA)。用于鉴定隐孢子虫分离株的方法基于形态学、核酸测序和聚合酶链反应(PCR)测定。为了确认鉴定结果,对这四株分离株的18S rRNA基因部分进行了测序。结果显示这些序列与先前描述的隐孢子虫DNA序列同源。此外,针对隐孢子虫特异性的内部转录间隔区的PCR扩增对所有四株分离株均呈阳性。对该地中海贫血患者血清样本进行的ELISA在血清稀释度为1:800时给出了阳性结果。最后,用该血清样本进行的蛋白质免疫印迹显示对110、73、56、42至35、30至28、26和23 kDa的蛋白质有阳性免疫球蛋白G识别反应。本研究结果表明,基于分子的诊断和血清学诊断技术对于快速鉴定人类腐皮病均有用。蛋白质印迹法识别的主要抗原可能有助于开发针对该疾病更敏感和特异的诊断工具。