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利用大规模测序和抗生素耐药性选择提高土壤中释放转基因细菌的微生物风险检测。

Improved detection of microbial risk of releasing genetically modified bacteria in soil by using massive sequencing and antibiotic resistance selection.

机构信息

School of Civil and Environmental Engineering and WCU Center for Green Metagenomics, Yonsei University, Seoul, South Korea.

出版信息

J Hazard Mater. 2012 Aug 15;227-228:172-8. doi: 10.1016/j.jhazmat.2012.05.031. Epub 2012 May 15.

Abstract

High-throughput 16S rRNA gene-targeted pyrosequencing was used with commonly used risk assessment techniques to evaluate the potential microbial risk in soil after inoculating genetically modified (GM) Corynebacterium glutamicum. To verify the risk, reference experiments were conducted in parallel using well-defined and frequently used GM Escherichia coli and wild-type strains. The viable cell count showed that the number of GM bacteria in the soil was reduced to below the detection limit within 10 days, while the molecular indicator for GM plasmids was detected throughout the experiment by using quantitative real-time polymerase chain reactions. Subsequent pyrosequencing showed an insignificant influence of the GM bacteria and/or their GM plasmids on the structure of the soil bacterial community this was similar to non-GM wild-type strains. However, pyrosequencing combined with kanamycin-resistant bacteria selection uncovered a potential risk of GM bacteria on the soil bacterial community and pathogens. The results of the improved methodology showed that the microbial risk attributable to GM C. glutamicum was relatively lower than that attributable to the reference GM E. coli.

摘要

高通量 16S rRNA 基因靶向焦磷酸测序与常用风险评估技术相结合,用于评估接种转基因(GM)谷氨酸棒杆菌后土壤中的潜在微生物风险。为了验证风险,使用定义明确且常用的 GM 大肠杆菌和野生型菌株进行了平行参考实验。活细胞计数表明,在 10 天内,土壤中 GM 细菌的数量减少到检测限以下,而通过定量实时聚合酶链反应,整个实验过程中都检测到了 GM 质粒的分子指标。随后的焦磷酸测序表明,GM 细菌和/或其 GM 质粒对土壤细菌群落结构的影响微不足道,与非 GM 野生型菌株相似。然而,焦磷酸测序结合卡那霉素抗性细菌选择揭示了 GM 细菌对土壤细菌群落和病原体的潜在风险。改进方法的结果表明,归因于 GM 谷氨酸棒杆菌的微生物风险相对低于归因于参考 GM 大肠杆菌的风险。

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