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Development of a PNA Probe for Fluorescence In Situ Hybridization Detection of Prorocentrum donghaiense

机译:东海原虫荧光原位杂交检测PNA探针的研制

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摘要

Prorocentrum donghaiense is a common but dominant harmful algal bloom (HAB) species, which is widely distributed along the China Sea coast. Development of methods for rapid and precise identification and quantification is prerequisite for early-stage warning and monitoring of blooms due to P. donghaiense. In this study, sequences representing the partial large subunit rDNA (D1–D2), small subunit rDNA and internal transcribed spacer region (ITS-1, 5.8S rDNA and ITS-2) of P. donghaiense were firstly obtained, and then seven candidate DNA probes were designed for performing fluorescence in situ hybridization (FISH) tests on P. donghaiense. Based on the fluorescent intensity of P. donghaiense cells labeled by the DNA probes, the probe DP0443A displayed the best hybridization performance. Therefore, a PNA probe (PP0443A) analogous to DP0443A was used in the further study. The cells labeled with the PNA probe displayed more intensive green fluorescence than that labeled with its DNA analog. The PNA probe was used to hybridize with thirteen microalgae belonging to five families, i.e., Dinophyceae, Prymnesiophyceae, Raphidophyceae, Chlorophyceae and Bacillariophyceae, and showed no visible cross-reaction. Finally, FISH with the probes PP0443A and DP0443A and light microscopy (LM) analysis aiming at enumerating P. donghaiense cells were performed on the field samples. Statistical comparisons of the cell densities (cells/L) of P. donghaiense in the natural samples determined by FISH and LM were performed using one-way ANOVA and Duncan's multiple comparisons of the means. The P. donghaiense cell densities determined by LM and the PNA probe are remarkably higher than (p<0.05) that determined by the DNA probe, while no significant difference is observed between LM and the PNA probe. All results suggest that the PNA probe is more sensitive that its DNA analog, and therefore is promising for the monitoring of harmful algal blooms of P. donghaiense in the future.
机译:东海原螯虾是常见但占主导地位的有害藻华(HAB)物种,在中国海沿岸广泛分布。开发快速,准确的鉴定和定量方法是对东海疫病引起的开花进行早期预警和监测的前提。在这项研究中,首先获得了东海假单胞菌的部分大亚基rDNA(D1-D2),小亚基rDNA和内部转录间隔区(ITS-1、5.8S rDNA和ITS-2)的序列,然后有七个候选序列设计了DNA探针,用于对东海疟原虫进行荧光原位杂交(FISH)测试。根据DNA探针标记的东海假单胞菌细胞的荧光强度,探针DP0443A显示出最佳的杂交性能。因此,在进一步研究中使用了与DP0443A类似的PNA探针(PP0443A)。用PNA探针标记的细胞比用其DNA类似物标记的细胞显示更强的绿色荧光。 PNA探针用于与属于五个科的13个微藻杂交,所述五个藻是迪科藻科,霸王藻科,树突藻科,绿藻科和芽孢杆菌科,并且没有可见的交叉反应。最后,在野外样本上进行了带有探针PP0443A和DP0443A的FISH以及旨在枚举东海道疟原虫细胞的光学显微镜(LM)分析。使用单向方差分析和方法的邓肯氏多重比较,对通过FISH和LM测定的天然样品中东海疟原虫的细胞密度(cells / L)进行统计比较。 LM和PNA探针测定的东海假单胞菌细胞密度显着高于DNA探针测定的(p <0.05),而LM和PNA探针之间无明显差异。所有结果表明,PNA探针比其DNA类似物更灵敏,因此有望在将来用于监测东海疫杆菌的有害藻华。

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