Department of Microbiology and Immunology, The University of Melbourne at The Doherty Institute for Infection and Immunity, Victoria, Australia.
Department of Infectious Diseases, Monash Health, Clayton, Victoria, Australia.
Appl Environ Microbiol. 2024 Oct 23;90(10):e0102124. doi: 10.1128/aem.01021-24. Epub 2024 Sep 10.
In Australia, native possums are a major wildlife reservoir for , the causative agent of the neglected tropical skin disease Buruli ulcer (BU). Large-scale possum excreta surveys that use PCR to detect in 100-1,000 s of excreta specimens are an important tool that can inform geospatial modeling and predict locations of future human BU risk. However, the significant expense of commercial kits used to extract DNA from specimens is a major barrier to routine implementation. Here, we developed a low-cost method for DNA extraction from possum excreta, possum tissue, and pure mycobacterial cultures, using a guanidinium isothiocyanate lysis solution and paramagnetic beads. In a 96-well plate format for high-throughput processing, the paramagnetic bead DNA extraction method was threefold less sensitive but only 1/6 the cost of a commonly used commercial kit. Applied to tissue swabs, the method was fourfold more sensitive and 1/5 the cost of a commercial kit. When used for preparing DNA from pure mycobacterial cultures, the method yielded purified genomic DNA with quality metrics comparable to more lengthy techniques. Our paramagnetic bead method is an economical means to undertake large-scale environmental surveillance that will directly inform efforts to halt the spread of BU in Victoria, Australia, with potential for applicability in other endemic countries.
Buruli ulcer (BU) is a neglected tropical skin disease, with an incidence that has dramatically increased in temperate southeastern Australia over the last decade. In southeastern Australia, BU is a zoonosis with native possums the major wildlife reservoir of the causative pathogen, . Infected possums shed in their excreta, and excreta surveys using PCR to screen for the presence of pathogen DNA are a powerful means to predict future areas of Buruli ulcer risk for humans. However, excreta surveys across large geographic areas require testing of many thousands of samples. The cost of commercial DNA extraction reagents used for preparing samples for PCR testing can thus become prohibitive to effective surveillance. Here, we describe a simple, low-cost method for extracting DNA from possum excreta using paramagnetic beads. The method is versatile and adaptable to a variety of other sample types including swabs collected from possum tissues and pure cultures of mycobacteria.
在澳大利亚,本地负鼠是造成被忽视的热带皮肤疾病——布鲁里溃疡(BU)的病原体的主要野生动物宿主。使用聚合酶链反应(PCR)检测 100-1000 份粪便标本中的 ,对大规模负鼠粪便检测来说是一种重要的工具,可以为地理空间建模提供信息,并预测未来人类 BU 风险的地点。然而,商业试剂盒用于从标本中提取 DNA 的高昂费用是常规实施的主要障碍。在这里,我们开发了一种从负鼠粪便、负鼠组织和纯分枝杆菌培养物中提取 DNA 的低成本方法,使用异硫氰酸胍裂解溶液和超顺磁珠。在高通量处理的 96 孔板格式中,超顺磁珠 DNA 提取方法的灵敏度降低了三倍,但成本仅为常用商业试剂盒的 1/6。应用于组织拭子,该方法的灵敏度提高了四倍,成本仅为商业试剂盒的 1/5。当用于从纯分枝杆菌培养物中制备 DNA 时,该方法产生的纯化基因组 DNA 的质量指标与更冗长的技术相当。我们的超顺磁珠方法是进行大规模环境监测的经济手段,这将直接为阻止澳大利亚维多利亚州 BU 的传播提供信息,并且有可能适用于其他流行国家。
布鲁里溃疡(BU)是一种被忽视的热带皮肤疾病,在过去十年中,澳大利亚东南部的温带地区发病率显著上升。在澳大利亚东南部,BU 是一种人畜共患病,本地负鼠是主要的野生动物宿主,也是病原体的主要宿主。受感染的负鼠会在粪便中排出 ,使用 PCR 筛查病原体 DNA 存在情况的粪便检测是预测未来人类布鲁里溃疡风险的有力手段。然而,在大面积的地理区域进行粪便检测需要测试数千份样本。用于准备用于 PCR 检测的样品的商业 DNA 提取试剂的成本可能会对有效的监测造成阻碍。在这里,我们描述了一种简单、低成本的方法,使用超顺磁珠从负鼠粪便中提取 DNA。该方法具有通用性,可以适应从负鼠组织采集的拭子和纯分枝杆菌培养物等各种其他样本类型。