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用于检测和评估蓝氏贾第鞭毛虫活力的流式细胞术方案的优化。

Optimization of a flow cytometry protocol for detection and viability assessment of Giardia lamblia.

作者信息

Barbosa Joana, Costa-de-Oliveira Sofia, Rodrigues Acácio Gonçalves, Pina-Vaz Cidália

机构信息

Department of Microbiology, School of Medicine, University of Porto, Porto, Portugal.

出版信息

Travel Med Infect Dis. 2008 Jul;6(4):234-9. doi: 10.1016/j.tmaid.2008.01.004. Epub 2008 Mar 4.

Abstract

Giardia lamblia is responsible for causing diarrhoeal diseases in humans. Infection occurs by fecal-oral route and is considered an important water pathogen, since many water surfaces are infected by cysts. Most studies involve cyst concentration procedures, followed by conventional microscopy, but are often tedious and influenced by fatigue. Our main objective was to optimize a specific flow cytometric (FC) protocol for detection of G. lamblia, to establish its sensibility limit and also the cyst viability. G. lamblia cysts (Waterborne, Inc., USA) were used for protocol optimization. FC analysis was performed using cyst suspensions stained with serial concentrations of a fluorescein-labelled mouse monoclonal antibody (Giardia-a-Glo, Waterborne). Serial concentrations (2 x 10(5), 1 x 10(5), 2 x 10(4), 1 x 10(4), 2 x 10(3), 1 x 10(3), 2 x 10(2) and 1 x 10(2)cysts/ml) were stained with the optimized antibody concentration and analysed by FC. Specificity and sensibility limit of the method were established using both prokaryotic (Escherichia coli, Staphylococcus aureus) and eukaryotic microorganisms (Candida albicans, Cryptosporidium parvum oocysts). Dead cysts were stained with 5.0 microg/ml of propidium iodide (PI, Sigma), with and without the specific fluorescent antibody. As the antibody concentration decreased, a decline of peak intensity was registered; 1.5 microg/ml was considered as the optimal antibody concentration, yielding a histogram clearly separated. We established a threshold of detection of 2 x 10(2)cysts/ml. Below threshold limit fluorescence was not enough to allow the discrimination of cysts. The staining procedure was shown to be specific, no cross-reaction occurring with bacteria, fungi or parasites. When using both antibody and PI, we could distinguish the viable cyst. With the use of specific antibodies, a distinct cellular population corresponding to cysts could be represented in the FC histogram.

摘要

蓝氏贾第鞭毛虫可导致人类腹泻疾病。感染通过粪-口途径发生,由于许多水体表面被包囊污染,它被视为一种重要的水生病原体。大多数研究涉及包囊浓缩程序,随后进行传统显微镜检查,但这些操作通常很繁琐且受疲劳影响。我们的主要目标是优化一种用于检测蓝氏贾第鞭毛虫的特定流式细胞术(FC)方案,确定其灵敏度极限以及包囊活力。使用蓝氏贾第鞭毛虫包囊(美国Waterborne公司)进行方案优化。使用用系列浓度的荧光素标记小鼠单克隆抗体(Giardia-a-Glo,Waterborne)染色的包囊悬液进行FC分析。将系列浓度(2×10⁵、1×10⁵、2×10⁴、1×10⁴、2×10³、1×10³、2×10²和1×10²个包囊/毫升)用优化后的抗体浓度染色,并通过FC进行分析。使用原核生物(大肠杆菌、金黄色葡萄球菌)和真核微生物(白色念珠菌、微小隐孢子虫卵囊)确定该方法的特异性和灵敏度极限。死包囊用5.0微克/毫升的碘化丙啶(PI,Sigma)染色,有无特异性荧光抗体均可。随着抗体浓度降低,峰值强度下降;1.5微克/毫升被视为最佳抗体浓度,产生明显分开的直方图。我们确定检测阈值为2×10²个包囊/毫升。低于阈值极限时,荧光不足以区分包囊。染色程序显示具有特异性,与细菌、真菌或寄生虫无交叉反应。同时使用抗体和PI时,我们可以区分活包囊。使用特异性抗体时,FC直方图中可呈现对应于包囊的独特细胞群体。

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