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用于粪便中微生物检测的简易侧向流动分析方法。

Simple lateral flow assays for microbial detection in stool.

作者信息

Henderson Wendy A, Xiang Lichen, Fourie Nicolaas H, Abey Sarah K, Ferguson Eric G, Diallo Ana F, Kenea Natnael D, Kim Chang Hee

机构信息

Division of Intramural Research , National Institute of Nursing Research , National Institutes of Health , Department of Health and Human Services , Bethesda , MD 20892 , USA . Email:

GoDx , 510 Charmany Drive, Suite 257 , Madison , WI 53719 , USA . Email:

出版信息

Anal Methods. 2018 Dec 7;10(45):5358-5363. doi: 10.1039/c8ay01475b. Epub 2018 Sep 20.

Abstract

Diarrheal diseases claim the lives of 1300 children daily, mostly in the developing world. We have developed a simple lateral flow assay capable of detecting and EPEC DNA and RNA rapidly (<15 minutes) at the point-of-need, directly from stool without nucleic acid extraction or molecular amplification. The limit of detection of the method is 1 nM using synthetic DNA target substrates spiked into stool. However, due to the endogenous amplification of the 23S rRNA targets, we were able to detect the endogenous EPEC in pea-sized (5 mg) stool without labor-intensive and time-consuming nucleic acid purification or target amplification using enzymes. The significance of this method is that it is rapid (<15 minutes) and simple (without nucleic acid purification or molecular amplification) and does not require instrumentation, or access to a laboratory, cold chain or electric power. Thus, it is well-suited for point-of-need use in remote and/or resource-limited settings in the developing world where the mortality due to diarrheal diseases is especially high. The rapid testing of stool pathogens in real time at the point-of-need will decrease the loss of patients to follow-up, and enable patients to be treated earlier with the appropriate therapeutics in both the developed and developing world settings.

摘要

腹泻疾病每天导致1300名儿童死亡,其中大多数发生在发展中世界。我们开发了一种简单的侧向流动检测方法,能够在现场(无需核酸提取或分子扩增)直接从粪便中快速(<15分钟)检测肠致病性大肠杆菌(EPEC)的DNA和RNA。使用添加到粪便中的合成DNA靶标底物,该方法的检测限为1 nM。然而,由于23S rRNA靶标的内源性扩增,我们能够在豌豆大小(5 mg)的粪便中检测到内源性EPEC,而无需使用酶进行费力且耗时的核酸纯化或靶标扩增。该方法的意义在于它快速(<15分钟)且简单(无需核酸纯化或分子扩增),不需要仪器设备,也无需进入实验室、冷链或电力供应。因此,它非常适合在腹泻疾病死亡率特别高的发展中世界的偏远和/或资源有限地区进行现场使用。在现场实时快速检测粪便病原体将减少失访患者的数量,并使发达国家和发展中国家的患者都能更早地接受适当的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a86/6253687/ebc1095297a7/c8ay01475b-f1.jpg

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