Suppr超能文献

舌拭子样本中DNA的高灵敏度检测。

High-sensitivity detection of DNA in tongue swab samples.

作者信息

Olson Alaina M, Wood Rachel C, Weigel Kris M, Yan Alexander J, Lochner Katherine A, Dragovich Rane B, Luabeya Angelique K, Yager Paul, Hatherill Mark, Cangelosi Gerard A

机构信息

Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.

Department of Bioengineering, University of Washington, Seattle, Washington, United States of America.

出版信息

medRxiv. 2024 Jul 27:2024.07.26.24311064. doi: 10.1101/2024.07.26.24311064.

Abstract

UNLABELLED

Tongue swab (TS) sampling combined with qPCR to detect (MTB) DNA is a promising alternative to sputum testing for tuberculosis (TB) diagnosis. In prior studies, the sensitivity of tongue swabbing has usually been lower than sputum. In this study, we evaluated two strategies to improve sensitivity. In one, centrifugation was used to concentrate tongue dorsum bacteria from 2-mL suspensions eluted from high-capacity foam swab samples. The pellets were resuspended as 500-μL suspensions, and then mechanically lysed prior to dual-target qPCR to detect MTB insertion elements IS and IS. Fractionation experiments demonstrated that most of the MTB DNA signal in clinical swab samples (99.22% ± 1.46%) was present in the sedimentable fraction. When applied to archived foam swabs collected from 124 South Africans with presumptive TB, this strategy exhibited 83% sensitivity (71/86) and 100% specificity (38/38) relative to sputum MRS (microbiological reference standard; sputum culture and/or Xpert Ultra). The second strategy used sequence-specific magnetic capture (SSMaC) to concentrate DNA released from MTB cells. This protocol was evaluated on archived Copan FLOQSwabs flocked swab samples collected from 128 South African participants with presumptive TB. Material eluted into 500 μL buffer was mechanically lysed. The suspensions were digested by proteinase K, hybridized to biotinylated dual-target oligonucleotide probes, and then concentrated ~20-fold using magnetic separation. Upon dual-target qPCR testing of concentrates, this strategy exhibited 90% sensitivity (83/92) and 97% specificity (35/36) relative to sputum MRS. These results point the way toward automatable, high-sensitivity methods for detecting MTB DNA in TS.

IMPORTANCE

Improved testing for tuberculosis (TB) is needed. Using a more accessible sample type than sputum may enable the detection of more cases, but it is critical that alternative samples be tested appropriately. Here, we describe two new, highly accurate methods for testing tongue swabs for TB DNA.

摘要

未标注

舌拭子(TS)采样结合定量聚合酶链反应(qPCR)检测结核分枝杆菌(MTB)DNA是一种很有前景的替代痰液检测用于结核病(TB)诊断的方法。在之前的研究中,舌拭子采样的敏感性通常低于痰液。在本研究中,我们评估了两种提高敏感性的策略。一种策略是使用离心法从大容量泡沫拭子样本洗脱的2毫升悬浮液中浓缩舌背细菌。将沉淀重悬为500微升悬浮液,然后在进行双靶点qPCR检测MTB插入元件IS和IS之前进行机械裂解。分级实验表明,临床拭子样本中大部分MTB DNA信号(99.22%±1.46%)存在于可沉淀部分。当应用于从124名疑似结核病的南非人收集的存档泡沫拭子时,相对于痰液微生物参考标准(MRS,痰液培养和/或Xpert Ultra),该策略表现出83%的敏感性(71/86)和100%的特异性(38/38)。第二种策略是使用序列特异性磁捕获(SSMaC)来浓缩MTB细胞释放的DNA。该方案在从128名疑似结核病的南非参与者收集的存档Copan FLOQSwabs植绒拭子样本上进行了评估。洗脱到500微升缓冲液中的物质进行机械裂解。悬浮液用蛋白酶K消化,与生物素化的双靶点寡核苷酸探针杂交,然后使用磁分离浓缩约20倍。对浓缩物进行双靶点qPCR检测时,相对于痰液MRS,该策略表现出90%的敏感性(83/92)和97%的特异性(35/36)。这些结果为在舌拭子中检测MTB DNA的可自动化、高灵敏度方法指明了方向。

重要性

需要改进结核病(TB)检测方法。使用比痰液更容易获取的样本类型可能能够检测到更多病例,但对替代样本进行适当检测至关重要。在此,我们描述了两种用于检测舌拭子中TB DNA的新型、高度准确的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c207/11302704/8063846f5d01/nihpp-2024.07.26.24311064v1-f0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验