Kao C M, Chen S C, Chen Y S, Lin H M, Chen Y L
Institute of Environmental Engineering, National Sun Yat-Sen University, Kaohsiung, Taiwan.
Folia Microbiol (Praha). 2003;48(4):521-4. doi: 10.1007/BF02931334.
Burkholderia pseudomallei Ara- in rice fields was detected using PCR-based techniques with 16S RNA and flagella gene primer sets. The sensitivity of these PCRs was at least 1 CFU/mL of B. pseudomallei Ara- preincubated into Ashdown's medium for 6 h. B. pseudomallei Ara- DNA from watery soil were more detectable than from dry soil. The distribution of this DNA was mainly found at a depth of 300-600 mm under crop-covered fields, but not detected in the location of soil close to the land surface. The results suggest that PCR based on 16S RNA and flagella gene primer sets can be applied to investigate the presence of B. pseudomallei Ara- in contaminated soil of rice fields.
利用基于PCR技术的16S RNA和鞭毛基因引物组,检测稻田中的类鼻疽伯克霍尔德菌Ara-。这些PCR检测的灵敏度为预培养在阿什当培养基中6小时的每毫升至少1个类鼻疽伯克霍尔德菌Ara-菌落形成单位(CFU)。来自水田土壤中的类鼻疽伯克霍尔德菌Ara-DNA比来自旱地土壤的更易检测到。该DNA的分布主要在作物覆盖田地下300 - 600毫米深处发现,但靠近地表的土壤位置未检测到此类DNA。结果表明,基于16S RNA和鞭毛基因引物组的PCR可用于调查稻田污染土壤中类鼻疽伯克霍尔德菌Ara- 的存在情况。