开发、验证和试点应用高通量分子异种监测测定法,以检测淡水蜗牛宿主体内的曼氏血吸虫和其他吸虫物种

IF 1.7 Q3 PARASITOLOGY
John Archer , Shi Min Yeo , Grace Gadd , Tom Pennance , Lucas J. Cunningham , Alexandra Juhàsz , Sam Jones , Priscilla Chammudzi , Donales R. Kapira , David Lally , Gladys Namacha , Bright Mainga , Peter Makaula , James E. LaCourse , Sekeleghe A. Kayuni , Janelisa Musaya , J. Russell Stothard , Bonnie L. Webster
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引用次数: 0

摘要

血吸虫病是一种被忽视的热带疾病(NTD),由血吸虫属寄生性吸虫感染引起,可导致衰弱的发病率和死亡率。世界卫生组织建议对曼氏血吸虫的淡水蜗牛中间宿主 Biomphalaria spp 进行分子异种监测,以确定高度集中的肠血吸虫病传播地点并监测疾病传播,特别是在低流行率地区。然而,这需要一个标准化的方案。在此,我们选择了两组以前发表的引物,开发并验证了一种多重分子异种监测终点 PCR 检测方法,该方法能够检测因蛔虫脱落而漏检的个体 Biomphalaria 中的曼森氏杆菌感染。事实证明,该检测方法在检测和扩增曼森氏杆菌 DNA 方面具有高灵敏度和高特异性,在检测和扩增非曼森氏杆菌吸虫 DNA 方面也具有高灵敏度。优化后的检测方法随后被用于筛查从曼氏沙门氏菌流行区采集的生物脑虫,并成功检测出了因蛛网膜脱落而漏检的曼氏沙门氏菌感染以及非曼氏沙门氏菌吸虫感染。继续开发和使用类似的分子异种监测检测方法将有助于改善疾病控制工作,从而大大降低血吸虫病流行地区居民与疾病相关的发病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development, validation, and pilot application of a high throughput molecular xenomonitoring assay to detect Schistosoma mansoni and other trematode species within Biomphalaria freshwater snail hosts

Development, validation, and pilot application of a high throughput molecular xenomonitoring assay to detect Schistosoma mansoni and other trematode species within Biomphalaria freshwater snail hosts

Schistosomiasis is a neglected tropical disease (NTD) caused by infection with parasitic trematodes of the genus Schistosoma that can lead to debilitating morbidity and mortality. The World Health Organization recommend molecular xenomonitoring of Biomphalaria spp. freshwater snail intermediate hosts of Schistosoma mansoni to identify highly focal intestinal schistosomiasis transmission sites and monitor disease transmission, particularly in low-endemicity areas. A standardised protocol to do this, however, is needed. Here, two previously published primer sets were selected to develop and validate a multiplex molecular xenomonitoring end-point PCR assay capable of detecting S. mansoni infections within individual Biomphalaria spp. missed by cercarial shedding. The assay proved highly sensitive and highly specific in detecting and amplifying S. mansoni DNA and also proved highly sensitive in detecting and amplifying non-S. mansoni trematode DNA. The optimised assay was then used to screen Biomphalaria spp. collected from a S. mansoni-endemic area for infection and successfully detected S. mansoni infections missed by cercarial shedding as well as infections with non-S. mansoni trematodes. The continued development and use of molecular xenomonitoring assays such as this will aid in improving disease control efforts, significantly reducing disease-related morbidities experienced by those in schistosomiasis-endemic areas.

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