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从大鼠肠道中分离和纯化贾第虫滋养体。

Isolation and purification of Giardia trophozoites from rat intestine.

作者信息

Feely D E, Erlandsen S L

出版信息

J Parasitol. 1981 Feb;67(1):59-64.

PMID:7229820
Abstract

A method for the isolation of Giardia trophozoites based on their ability to attach to warm surfaces has been developed. Mucosal scrapings were obtained from the small intestine of rats infected with Giardia and suspended in Hanks' balanced salt solution (HBSS). Trophozoites were concentrated by centrifugation and allowed to attach to the surfaces of polystyrene petri dishes incubated at 37 C. Incubation temperature significantly affected the recovery of trophozoites. After attachment at 37 C, trophozoites were separated from contaminating intestinal debris by incubation at cold temperature. The trophozoites detach at 4 C, whereas the intestinal debris remain adherent. Then the detached trophozoites were isolated by reattachment at 37 C. Examination by scanning electron microscopy revealed a marked reduction in contamination of attached trophozoites and dish surfaces after the use of cold temperature detachment and reattachment at 37 C. Viability of trophozoites as measured by erythrosin-B dye exclusion, remained above 90% up to 120 min after isolation. This method of isolation facilitates the recovery of this protozoan directly from small intestine for morphological and experimental study.

摘要

一种基于贾第虫滋养体附着于温暖表面的能力来分离它们的方法已被开发出来。从感染贾第虫的大鼠小肠获取黏膜刮片,并将其悬浮于汉克斯平衡盐溶液(HBSS)中。通过离心浓缩滋养体,然后让其附着于在37℃孵育的聚苯乙烯培养皿表面。孵育温度显著影响滋养体的回收率。在37℃附着后,通过在低温下孵育将滋养体与污染的肠道碎片分离。滋养体在4℃时脱落,而肠道碎片仍保持附着。然后通过在37℃重新附着来分离脱落的滋养体。扫描电子显微镜检查显示,在使用低温脱附和37℃重新附着后,附着的滋养体和培养皿表面的污染显著减少。通过赤藓红-B染料排除法测定,滋养体的活力在分离后长达120分钟仍保持在90%以上。这种分离方法便于直接从小肠中回收这种原生动物用于形态学和实验研究。

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