一种针对克氏锥虫HSP70基因的特异性、稳定性和可获得的LAMP检测方法。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Sneider Alexander Gutierrez Guarnizo, Beth Jessy Condori, Luciana Basma, Shirley Equilia, Edith Malaga, Siena Defazio, Emily Arteaga, Jean Karla Velarde, Martín Obregón, Anshule Takyar, Carolina Duque, Jill Hakim, Freddy Tinajeros, Robert H Gilman, Natalie Bowman, Monica R Mugnier
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引用次数: 0

摘要

诊断延误使大多数恰加斯病患者无法在治疗有效的急性期得到及时治疗。基于定量PCR (qPCR)的诊断方法在这一阶段提供了高灵敏度,但需要专门的设备和复杂的方案。迫切需要更简单和更具成本效益的工具,以便在低收入流行地区扩大恰加斯病的早期诊断。在这里,我们提出了一种环介导的等温扩增(LAMP),其目标是恰加斯病的病原体克氏锥虫HSP70基因的高度保守区域。该试验证明了多种寄生虫遗传谱系的物种特异性扩增,同时在1小时的孵育和至少8个月的-20°C储存后保持稳定。此外,该检测方法比目前常规用于急性恰加斯病诊断的TaqMan qPCR便宜至少12倍,并且与低成本的基于ctab的DNA提取方法兼容。与针对卫星DNA的TaqMan qPCR相比,在玻利维亚圣克鲁斯的100名恰加斯阳性母亲所生的婴儿中进行的基于人群的验证产生了100%的特异性和超过77%的灵敏度。这种具有成本效益的DNA提取方法和LAMP测定显示了在资源有限的流行地区诊断恰加斯病的潜力,特别是在无法获得qPCR的地区。重要性:由克氏锥虫寄生虫引起的恰加斯病是一种威胁生命的疾病,对资源有限的社区造成不成比例的影响。如果早期诊断出先天性恰加斯病,将提供独特的干预机会,因为对新生儿的治疗非常有效,副作用最小。然而,在流行地区,高昂的费用和有限的现有分子诊断方法阻碍了早期诊断。本研究介绍了一种简单、低成本、高特异性的针对克氏锥虫HSP70基因的LAMP检测方法。该分析是用户友好的,在不同的储存和孵育条件下稳定,并设计用于服务不足地区的可及性。通过提供详细的、开放获取的协议和引物,我们的目标是促进这种诊断分析的广泛采用,使早期发现和治疗成为可能。这一分析为一种新的南美锥虫病管理方法奠定了基础,有可能减少南美锥虫病的传播,并改善全球弱势群体的公共卫生结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A specific, stable, and accessible LAMP assay targeting the HSP70 gene of Trypanosoma cruzi.

Diagnostic delays prevent most Chagas disease patients from receiving timely therapy during the acute phase when treatment is effective. Quantitative PCR (qPCR)-based diagnostic methods provide high sensitivity during this phase but require specialized equipment and complex protocols. More simple and cost-effective tools are urgently needed to expand early Chagas disease diagnosis in low-income endemic regions. Here, we present a loop-mediated isothermal amplification (LAMP) that targets a highly conserved region in the HSP70 gene of Trypanosoma cruzi, the causative agent of Chagas disease. This assay demonstrates species-specific amplification across multiple parasite genetic lineages while maintaining stability after 1 hour of incubation and at least 8 months of storage at -20°C. Moreover, the assay is at least 12 times less expensive than the TaqMan qPCR that is currently routinely used for acute Chagas diagnostics and is compatible with a low-cost CTAB-based DNA extraction method. Population-based validation in 100 infants born to Chagas-positive mothers in Santa Cruz, Bolivia, yielded a specificity of 100% and sensitivity exceeding 77% when compared to a TaqMan qPCR that targets satellite DNA. This cost-effective DNA extraction method and LAMP assay demonstrate potential for diagnosing Chagas disease in resource-limited endemic regions, particularly where qPCR is unavailable.

Importance: Chagas disease, caused by the parasite Trypanosoma cruzi, is a life-threatening illness that disproportionately affects resource-limited communities. Congenital Chagas disease, if diagnosed early, presents a unique opportunity for intervention, as treatment in newborns is highly effective with minimal side effects. However, early diagnosis is hindered by the high cost and limited availability of current molecular diagnostic methods in endemic regions. Our study introduces a simple, low-cost, and highly specific LAMP assay targeting the HSP70 gene of T. cruzi. This assay is user-friendly, stable under varying storage and incubation conditions, and designed for accessibility in underserved areas. By providing a detailed, open-access protocol and primers, we aim to facilitate the widespread adoption of this diagnostic assay, enabling earlier detection and treatment. This assay lays the groundwork for a new approach to Chagas disease management, potentially reducing the spread of Chagas disease and improving public health outcomes in vulnerable populations globally.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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