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Development and field application of a quantitative method for examining natural assemblages of protists with oligonucleotide probes.

机译:开发和现场应用定量方法检测寡核苷酸探针天然存在的原生生物的方法。

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摘要

A fluorescent in situ hybridization method that uses rRNA-targeted oligonucleotide probes for counting protists in cultures and environmental water samples is described. Filtration, hybridization, and enumeration of fixed cells with biotinylated eukaryote-specific probes and fluorescein isothiocyanate-conjugated avidin were performed directly on 0.4-microns-pore-size polycarbonate filters of Transwell cell culture inserts (Costar Corp., Cambridge, Mass.). Counts of various species of cultured protists by this probe hybridization method were not significantly different from counts obtained by the 4',6-diamidino-2-phenylindole (DAPI) and acridine orange (AO) staining methods. However, counts of total nanoplankton (TNAN) based on probe hybridizations in several field samples and in samples collected from a mesocosm experiment were frequently higher than TNAN counts obtained by staining with DAPI or AO. On the basis of these results, 25 to 70% of the TNAN determined with probes were not detectable by DAPI or AO staining. The underestimation of TNAN abundances in samples stained with DAPI or AO was attributed to the existence of small nanoplanktonic cells which could be detected with probes but not DAPI or AO and the difficulty associated with distinguishing DAPI- or AO-stained protists attached to or embedded in aggregates. We conclude from samples examined in this study that enumeration of TNAN with oligonucleotide probes provides estimates of natural TNAN abundances that are at least as high as (and in some cases higher than) counts obtained with commonly employed fluorochrome stains. The quantitative in situ hybridization method we have described here enables the direct enumeration of free-living protists in water samples with oligonucleotide probes. When combined with species-specific probes, this method will enable quantitative studies of the abundance and distribution of specific protistan taxa.
机译:描述了一种荧光原位杂交方法,该方法使用靶向rRNA的寡核苷酸探针对培养物和环境水样品中的原生生物计数。直接在Transwell细胞培养插入物(Costar Corp.,Cambridge,Mass。)的0.4微米孔径的聚碳酸酯滤膜上进行生物素化的真核生物特异性探针和荧光素异硫氰酸酯缀合的亲和素的固定细胞的过滤,杂交和计数。通过这种探针杂交方法得到的各种原生生物的计数与通过4',6-二6-基-2-苯基吲哚(DAPI)和a啶橙(AO)染色方法获得的计数没有显着差异。但是,基于探针杂交的几个田间样品和中观实验收集的样品中的总纳米浮游生物(TNAN)计数通常高于通过DAPI或AO染色获得的TNAN计数。根据这些结果,用DAPI或AO染色无法检测到用探针测定的TNAN的25%至70%。 DAPI或AO染色的样品中TNAN丰度的低估归因于存在小的纳米浮游细胞,可以用探针检测到,但不能检测到DAPI或AO,并且难以区分附着或嵌入在其中的DAPI或AO染色的原生生物聚集体。我们从本研究中检查的样品得出结论,用寡核苷酸探针对TNAN进行计数可以提供自然TNAN丰度的估计值,该估计值至少与通常使用的荧光染料获得的计数一样高(在某些情况下高于)。我们在此描述的定量原位杂交方法可利用寡核苷酸探针直接枚举水样品中的自由生物。当与特定物种的探针结合使用时,该方法将能够定量研究特定原生动物类群的丰度和分布。

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