High-sensitivity detection of Mycobacterium tuberculosis DNA in tongue swab samples.

IF 6.1 2区 医学 Q1 MICROBIOLOGY
Journal of Clinical Microbiology Pub Date : 2025-02-19 Epub Date: 2024-12-31 DOI:10.1128/jcm.01140-24
Alaina M Olson, Rachel C Wood, Kris M Weigel, Alexander J Yan, Katherine A Lochner, Rane B Dragovich, Angelique K Luabeya, Paul Yager, Mark Hatherill, Gerard A Cangelosi
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引用次数: 0

Abstract

Tongue swab (TS) sampling combined with quantitative PCR (qPCR) to detect Mycobacterium tuberculosis (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 IS6110 and IS1081. 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 microbiological reference standard (MRS; 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.

舌拭子结核分枝杆菌DNA的高灵敏度检测。
舌拭子(TS)取样结合定量PCR (qPCR)检测结核分枝杆菌(MTB) DNA是一种有前景的替代痰液检测结核病(TB)诊断方法。在以往的研究中,舌拭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。其中一种方法是从高容量泡沫拭子样品中洗脱的2毫升悬浮液中离心浓缩舌背细菌。将微球重悬为500µL悬液,然后进行机械裂解,然后进行双目标qPCR检测MTB插入元件IS6110和IS1081。分离实验表明,临床拭子样本中大部分MTB DNA信号(99.22%±1.46%)存在于可沉积部分。当应用于从124名南非推定结核病患者收集的存档泡沫拭子时,该策略相对于痰微生物参考标准(MRS;痰培养和/或Xpert Ultra)。第二种策略使用序列特异性磁捕获(SSMaC)来浓缩从结核分枝杆菌细胞释放的DNA。对从128名推定患有结核病的南非参与者收集的Copan FLOQSwabs存档棉签样本对该方案进行了评估。材料洗脱到500µL缓冲液中进行机械裂解。用蛋白酶K消化,杂交到生物素化的双靶点寡核苷酸探针上,然后用磁分离浓缩~20倍。在浓缩物的双目标qPCR检测中,该策略相对于痰mrs显示出90%的灵敏度(83/92)和97%的特异性(35/36)。这些结果为ts中检测MTB DNA的自动化、高灵敏度方法指明了方向。使用比痰液更容易获得的样本类型可能能够发现更多病例,但至关重要的是对替代样本进行适当检测。在这里,我们描述了两种新的、高度准确的检测舌拭子结核DNA的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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