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开发一种新型聚合酶链反应检测方法,该方法能够检测从钉螺中回收的单只日本血吸虫尾蚴。

Development of a novel PCR assay capable of detecting a single Schistosoma japonicum cercaria recovered from Oncomelania hupensis.

作者信息

Driscoll A J, Kyle J L, Remais J

机构信息

Center for Occupational and Environmental Health, School of Public Health, University of California at Berkeley, 140 Warren Hall #7360, Berkeley, CA 94720, USA.

出版信息

Parasitology. 2005 Oct;131(Pt 4):497-500. doi: 10.1017/S0031182005007961.

Abstract

Location and time-specific variability in Schistosoma japonicum cercarial density has been shown to be high in the mountainous regions of Sichuan Province, China. A polymerase chain reaction (PCR) assay for the detection of schistosome cercariae in these environments would aid in the determination of environmental risk, and the identification of individual-level risk factors. Here the authors present a highly sensitive and specific PCR assay for the detection of S. japonicum cercariae in laboratory samples. As few as 1 and as many as 300 cercariae, from both laboratory and field-collected S. japonicum strains, produced positive amplification results, and repeated assays showed no positive result for S. mansoni nor for non- japonicum cercariae isolated from infected snails collected in Sichuan Province. There was no difference found between the Chinese and Philippine S. japonicum strains. The results presented demonstrate the successful PCR amplification of a target sequence within the SjR2 retrotransposon from samples of S. japonicum cercariae, with the potential for application to natural water samples from endemic areas.

摘要

在中国四川省的山区,日本血吸虫尾蚴密度呈现出明显的地点和时间特异性变化。在这些环境中,用于检测血吸虫尾蚴的聚合酶链反应(PCR)检测方法将有助于确定环境风险,并识别个体层面的风险因素。在此,作者展示了一种高度灵敏且特异的PCR检测方法,用于检测实验室样本中的日本血吸虫尾蚴。来自实验室和野外采集的日本血吸虫菌株的尾蚴数量少至1条、多至300条,均产生了阳性扩增结果,且重复检测显示,曼氏血吸虫以及从四川省采集的受感染钉螺中分离出的非日本血吸虫尾蚴均未出现阳性结果。中国和菲律宾的日本血吸虫菌株之间未发现差异。所呈现的结果表明,成功从日本血吸虫尾蚴样本中扩增出了SjR2反转录转座子内的目标序列,具有应用于流行地区天然水样检测的潜力。

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