Wang Wei-ping, Chai A-li, Shi Yan-xia, Xie Xue-wen, Li Bao-ju
Guang Pu Xue Yu Guang Pu Fen Xi. 2015 May;35(5):1243-7.
Clubroot, caused by Plasmodiophora brassicae, is considered the most devastating soilborne disease in Brassica crops. It has emerged as a serious disease threatening the cruciferous crop production industry in China. Nowadays, the detection techniques for P. brassicae are laborious, time-consuming and low sensitivity. Rapid and effective detection methods are needed. The objective of this study is to develop a Fourier transform infrared spectrometer (FTIR) technique for detection of P. brassicae effectively and accurately. FTIR and Real-time PCR techniques were applied in quantitative detection of P. brassicae. Chinese cabbages were inoculated with P. brassicae. By analyzing the FTIR spectra of P. brassicae, infected clubroots and healthy roots, three specific bands 1 105, 1 145 and 1 228 cm-1 were selected. According to the correlation between the peak areas at these sensitive bands and Real-time PCR Ct value, quantitative evaluation model of P. brassicae was established based on FTIR y=34. 17 +12. 24x - 9. 81x2 - 6. 05x3, r=0. 98 (p<0. 05). To validate accuracy of the model, 10 clubroot samples were selected randomly from field, and detected by FTIR spectrum model, the results showed that the average error is 1. 60%. This demonstrated that the FTIR technology is an available one for the quantitative detection of P. brassicae in clubroot, and it provides a new method for quantitative and quickly detection of Chinese cabbage clubroot.
由芸薹根肿菌引起的根肿病被认为是十字花科作物中最具毁灭性的土传病害。它已成为威胁中国十字花科作物生产行业的一种严重病害。目前,对芸薹根肿菌的检测技术费力、耗时且灵敏度低。需要快速有效的检测方法。本研究的目的是开发一种傅里叶变换红外光谱仪(FTIR)技术,以有效、准确地检测芸薹根肿菌。FTIR和实时荧光定量PCR技术被应用于芸薹根肿菌的定量检测。用芸薹根肿菌接种大白菜。通过分析芸薹根肿菌、感病根肿和健康根的FTIR光谱,选择了1 105、1 145和1 228 cm-1这三个特定波段。根据这些敏感波段的峰面积与实时荧光定量PCR Ct值之间的相关性,建立了基于FTIR的芸薹根肿菌定量评价模型y=34. 17 +12. 24x - 9. 81x2 - 6. 05x3,r=0. 98(p<0. 05)。为验证模型的准确性,从田间随机选取10个根肿样本,用FTIR光谱模型进行检测,结果表明平均误差为1. 60%。这表明FTIR技术可用于根肿病中芸薹根肿菌的定量检测,为大白菜根肿病的定量快速检测提供了一种新方法。