Novi Vinni Thekkudan, Aboubakr Hamada A, Moore Melanie J, Zarouri Akli, Juzwik Jennifer, Abbas Abdennour
Department of Bioproducts and Biosystems Engineering, University of Minnesota, 55108, St. Paul, MN, U.S.A.
USDA Forest Service, Northern Research Station, 55108, St. Paul, MN, U.S.A.
Plant Methods. 2024 Aug 6;20(1):119. doi: 10.1186/s13007-024-01254-8.
Oak wilt disease, caused by Bretziella fagacearum is a significant threat to oak (Quercus spp.) tree health in the United States and Eastern Canada. The disease may cause dramatic damage to natural and urban ecosystems without management. Early and accurate diagnosis followed by timely treatment increases the level of disease control success.
A rapid assay based on loop mediated isothermal amplification (LAMP) was first developed with fluorescence detection of B. fagacearum after 30-minute reaction time. Six different primers were designed to specifically bind and amplify the pathogen's DNA. To simplify the use of this assay in the field, gold nanoparticles (AuNPs) were designed to bind to the DNA amplicon obtained from the LAMP reaction. Upon inducing precipitation, the AuNP-amplicons settle as a red pellet visible to the naked eye, indicative of pathogen presence. Both infected and healthy red oak samples were tested using this visualization method. The assay was found to have high diagnostic sensitivity and specificity for the B. fagacearum isolate studied. Moreover, the developed assay was able to detect the pathogen in crude DNA extracts of diseased oak wood samples, which further reduced the time required to process samples.
In summary, the LAMP assay coupled with oligonucleotide-conjugated gold nanoparticle visualization is a promising method for accurate and rapid molecular-based diagnosis of B. fagacearum in field settings. The new method can be adapted to other forest and plant diseases by simply designing new primers.
由栎枯萎病菌(Bretziella fagacearum)引起的栎枯萎病对美国和加拿大东部的栎树(Quercus spp.)健康构成重大威胁。如果不加以管理,这种疾病可能会对自然和城市生态系统造成巨大破坏。早期准确诊断并及时治疗可提高疾病控制成功率。
首先开发了一种基于环介导等温扩增(LAMP)的快速检测方法,在30分钟反应时间后对栎枯萎病菌进行荧光检测。设计了六种不同的引物,以特异性结合并扩增病原体的DNA。为了简化该检测方法在现场的使用,设计了金纳米颗粒(AuNPs)与从LAMP反应获得的DNA扩增子结合。诱导沉淀后,AuNP-扩增子沉淀为肉眼可见的红色颗粒,表明病原体存在。使用这种可视化方法对感染和健康的红橡树样本进行了检测。结果发现该检测方法对所研究的栎枯萎病菌分离株具有高诊断敏感性和特异性。此外,所开发的检测方法能够在患病橡木样本的粗DNA提取物中检测到病原体,这进一步缩短了样本处理所需的时间。
总之,LAMP检测方法与寡核苷酸偶联金纳米颗粒可视化相结合,是一种在现场环境中对栎枯萎病菌进行准确、快速分子诊断的有前景的方法。通过简单设计新的引物,这种新方法可适用于其他森林和植物疾病。