Abdel-Hamid Magda Youssef, Badawy Abeer Fathy, Ibrahim Ayman Nabil
Parasitology Department, Faculty of Medicine, Ain-Shams University, Cairo, Egypt.
Parasitol Res. 2015 Feb;114(2):453-6. doi: 10.1007/s00436-014-4202-4. Epub 2014 Oct 29.
Microsporidia spp. are obligate intracellular parasites which are very minute with sizes ranging from 1 to 10 μm. They have been increasingly recognized as human pathogens in AIDS and immunocompromised patients, mainly associated with life-threatening chronic diarrhea and systemic disease. For accurate identification of Microsporidia, permanent staining techniques are used to enable the examiner to use the ×100 objective which reveals the important details needed for diagnosis. On the other hand, ×10 and ×40 objectives are of no value in detection of such a minute organism. Until now, there is no study that demonstrates a rapid satisfactory technique for routine examination of wet mount by the oil-immersion lens. Glycerol jelly (GJ) reagent was previously studied for its benefit in fixing the cover slide of direct wet mounts instantly enabling the use of oil-immersion lens in examination that magnifies its role as a rapid technique for direct examination. The aim of this research is to identify Microsporidia by wet mounts immediately, using GJ reagent that enables the examiner to use the ×100 objective and to evaluate GJ wet mount as a method of identification. Glycerol jelly reagent was prepared (7 g gelatin dissolved in 50 ml boiling water was added to 10 ml glycerol) and added to fecal wet mounts stained by iodine and methylene blue. Wet mounts were examined using the ×100 objective. Satisfactory results were achieved in spite of the small size of Microsporidia, as both iodine and methylene blue stained the cytological structures; GJ reagent fixed the cover slide, maintained the high translucency of the films, and enabled the examiner to use the ×100 oil-immersion objective. We also compared fecal wet mounts stained by iodine and methylene blue + GJ with a stool sample stained by permanent stain modified Ziehl-Neelsen without GJ, and we found that fecal wet mounts stained by iodine and methylene blue + GJ were more clear. We concluded that glycerol jelly wet mount is an easy, fast, reliable, and cheap technique for identification of Microsporidia in direct smear, using the ×100 oil-immersion objective.
微孢子虫属是专性细胞内寄生虫,非常微小,大小在1至10微米之间。它们越来越被认为是艾滋病患者和免疫功能低下患者的人类病原体,主要与危及生命的慢性腹泻和全身性疾病有关。为了准确鉴定微孢子虫,采用永久染色技术,使检查人员能够使用100倍物镜,该物镜可揭示诊断所需的重要细节。另一方面,10倍和40倍物镜在检测这种微小生物时毫无价值。到目前为止,尚无研究证明有一种快速且令人满意的技术可用于油镜常规检查湿片。甘油明胶(GJ)试剂此前曾因其有助于立即固定直接湿片的盖玻片,从而使油镜检查成为可能,扩大了其作为直接检查快速技术的作用而得到研究。本研究的目的是使用GJ试剂通过湿片立即鉴定微孢子虫,该试剂使检查人员能够使用100倍物镜,并评估GJ湿片作为一种鉴定方法。制备了甘油明胶试剂(将7克明胶溶解在50毫升沸水中,加入10毫升甘油),并添加到经碘和亚甲蓝染色的粪便湿片中。使用100倍物镜检查湿片。尽管微孢子虫体积小,但仍取得了满意的结果,因为碘和亚甲蓝都能对细胞结构进行染色;GJ试剂固定了盖玻片,保持了涂片的高透明度,并使检查人员能够使用100倍油镜物镜。我们还将经碘和亚甲蓝+GJ染色的粪便湿片与未经GJ处理的改良齐-尼永久染色粪便样本进行了比较,发现经碘和亚甲蓝+GJ染色的粪便湿片更清晰。我们得出结论,甘油明胶湿片是一种简单、快速且可靠的廉价技术,可使用100倍油镜物镜在直接涂片中鉴定微孢子虫。