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一种确定贾第虫包囊活力的新方法:荧光素二乙酸酯和碘化丙啶染色与动物感染性的相关性。

A new method to determine Giardia cyst viability: correlation of fluorescein diacetate and propidium iodide staining with animal infectivity.

作者信息

Schupp D G, Erlandsen S L

出版信息

Appl Environ Microbiol. 1987 Apr;53(4):704-7. doi: 10.1128/aem.53.4.704-707.1987.

Abstract

The viability of Giardia muris cysts was studied with the fluorogenic dyes fluorescein diacetate (FDA) and propidium iodide (PI). G. muris cysts were seen to fluoresce intensely green with FDA at an excitation wavelength of 450 to 490 nm. Cysts stained with PI fluoresced bright orange at an excitation wavelength of 450 to 490 nm and bright red at 545 to 546 nm. Examination of isolated G. muris cyst preparations stained with FDA-PI revealed that greater than 85% of the cysts stained green with FDA and less than 15% stained orange-red with PI. Using the mouse model for giardiasis, we inoculated FDA- or PI-stained cysts into neonatal mice. Feces were examined at days 3, 5, 8, and 11 postinoculation for the presence of cysts. Using 1,000 FDA-stained cysts as the inoculum, we detected cysts at days 5, 8, and 11 postinoculation in 19 of 19 mice, whereas a 50-fold greater dose of cysts produced infection in 27 of 27 mice at day 3 as well as at days 5, 8, and 11 postinoculation. Inoculation of mice with either 5,000 or 50,000 PI-stained G. muris cysts did not produce infection in any of the animals. Necropsy of mice infected with FDA-stained cysts showed trophozoites within the intestines. No trophozoites were detected within animals inoculated with PI-stained cysts. These results demonstrate that FDA-positive cysts are viable, as determined by infectivity, while PI-positive cysts are nonviable and incapable of producing G. muris infections in vivo.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用荧光染料荧光素二乙酸酯(FDA)和碘化丙啶(PI)研究了微小贾第虫包囊的活力。在激发波长为450至490nm时,微小贾第虫包囊被FDA染成强烈的绿色荧光。用PI染色的包囊在激发波长为450至490nm时发出亮橙色荧光,在545至546nm时发出亮红色荧光。对用FDA-PI染色的分离微小贾第虫包囊制剂进行检查发现,超过85%的包囊被FDA染成绿色,不到15%被PI染成橙红色。利用贾第虫病小鼠模型,将用FDA或PI染色的包囊接种到新生小鼠体内。在接种后第3、5、8和11天检查粪便中是否存在包囊。以1000个用FDA染色的包囊作为接种物,在接种后第5、8和11天,19只小鼠中有19只检测到包囊,而剂量大50倍的包囊在接种后第3天以及第5、8和11天在27只小鼠中有27只引发感染。用5000个或50000个用PI染色的微小贾第虫包囊接种小鼠,没有任何动物发生感染。对感染用FDA染色包囊的小鼠进行尸检发现肠道内有滋养体。在用PI染色包囊接种的动物体内未检测到滋养体。这些结果表明,通过感染性确定,FDA阳性包囊是有活力的,而PI阳性包囊是无活力的,并且在体内不能引发微小贾第虫感染。(摘要截短为250字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1f/203740/ad3b4ae0ea14/aem00121-0097-a.jpg

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