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首页> 外文期刊>Aquatic biosystems >Variation in spatial and temporal incidence of the crustacean pathogen Hematodinium perezi in environmental samples from Atlantic Coastal Bays
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Variation in spatial and temporal incidence of the crustacean pathogen Hematodinium perezi in environmental samples from Atlantic Coastal Bays

机译:大西洋沿岸海湾环境样品中甲壳类病原体Perezi的时空发生率变化

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Background Hematodinium perezi, a parasitic dinoflagellate, infects and kills blue crabs, Callinectes sapidus, along the Atlantic and Gulf coasts of the United States. The parasite proliferates within host hemolymph and tissues, and also produces free-swimming biflagellated dinospores that emerge from infected crabs. Infections in C. sapidus recur annually, and it is not known if biotic or environmental reservoirs contribute to reinfection and outbreaks. To address this data gap, a quantitative PCR assay based on the internal transcribed spacer 2 (ITS2) region of H. perezi rRNA genes was developed to asses the temporal and spatial incidence of the parasite in Delaware and Maryland coastal bays. Results A previously-used PCR assay for H. perezi, based on the small subunit rRNA gene sequence, was found to lack adequate species specificity to discriminate non-Hematodinium sp. dinoflagellate species in environmental samples. A new ITS2-targeted assay was developed and validated to detect H. perezi DNA in sediment and water samples using E. coli carrying the H. perezi rDNA genes. Application of the method to environmental samples identified potential hotspots in sediment in Indian River Inlet, DE and Chincoteague Bay, MD and VA. H. perezi DNA was not detected in co-occurring shrimp or snails, even during an outbreak of the parasite in C. sapidus. Conclusions H. perezi is present in water and sediment samples in Maryland and Delaware coastal bays from April through November with a wide spatial and temporal variability in incidence. Sampling sites with high levels of H. perezi DNA in both bays share characteristics of silty, organic sediments and low tidal currents. The environmental detection of H. perezi in spring, ahead of peak prevalence in crabs, points to gaps in our understanding of the parasite’s life history prior to infection in crabs as well as the mode of environmental transmission. To better understand the H. perezi life cycle will require further monitoring of the parasite in habitats as well as hosts. Improved understanding of potential environmental transmission to crabs will facilitate the development of disease forecasting.
机译:背景寄生性鞭毛虫Perezi感染并杀死了美国大西洋沿岸和墨西哥湾沿岸的蓝蟹Callinectes sapidus。寄生虫在宿主的血淋巴和组织内扩散,还产生从被感染的螃蟹中出来的自由游动的双鞭毛二孢子孢子。每年发生的C. sapidus感染均会再次发生,尚不清楚生物或环境贮藏库是否会造成再感染和暴发。为了解决这一数据缺口,开发了一种基于H. perezi rRNA基因内部转录间隔区2(ITS2)区域的定量PCR分析方法,以评估特拉华州和马里兰州沿海海湾的寄生虫的时空分布。结果发现基于小亚基rRNA基因序列的H. perezi先前使用的PCR分析方法缺乏足够的物种特异性来区分非血红素菌。环境样品中的鞭毛藻物种。开发了一种新的针对ITS2的检测方法,并经过验证,可以使用携带H. perezi rDNA基因的大肠杆菌检测沉积物和水样中的H. perezi DNA。该方法在环境样品中的应用确定了印度河入口,德州和钦科蒂格湾,马里兰州和弗吉尼亚州的沉积物中潜在的热点。在共生的虾或蜗牛中也未检测到H. perezi DNA,即使在C. sapidus的寄生虫暴发期间也是如此。结论从4月到11月,马里兰州和特拉华州沿海海湾的水和沉积物样本中都存在H. perezi,其发生时空变化很大。在两个海湾中,H。perezi DNA含量高的采样点具有粉质,有机沉积物和低潮流的特征。春季对H. perezi的环境检测早于螃蟹的流行高峰,这表明我们对螃蟹感染前寄生虫的生活史以及环境传播方式的理解存在差距。为了更好地了解H. perezi的生命周期,将需要进一步监测栖息地和寄主中的寄生虫。更好地了解对蟹的潜在环境传播,将有助于疾病预测的发展。

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