Agroécologie, AgroSup Dijon, INRA, Univ.de Bourgogne Franche Comté, 17 rue Sully, Dijon, France.
University of Thessaly, Department of Biochemistry and Biotechnology, Laboratory of Plant and Environmental Biotechnology, Viopolis, 41500 Larissa, Greece.
Sci Total Environ. 2019 Feb 15;651(Pt 1):1189-1198. doi: 10.1016/j.scitotenv.2018.09.255. Epub 2018 Sep 21.
Modern agricultural practices largely rely on pesticides to protect crops against various pests and to ensure high yields. Following their application to crops a large amount of pesticides ends up in soil where they may affect non-target organisms, among which microorganisms. We assessed the effects of the carbamate nematicide oxamyl on the whole bacterial diversity of an agricultural soil exhibiting enhanced biodegradation of oxamyl through 16S rRNA amplicon next generation sequencing (NGS) and on the oxamyl-degrading bacterial community through cehA q-PCR analysis and C-oxamyl mineralization assays. Oxamyl was rapidly mineralized by the indigenous microorganisms reaching >70% within a month. Concomitantly, a significant increase in the number of oxamyl-degrading microorganisms was observed. NGS analysis of the total (DNA) and active (RNA) bacterial community showed no changes in α-diversity indices in response to oxamyl exposure. Analysis of the β-diversity revealed significant changes in the composition of the soil bacterial community after 13 and 30 days of oxamyl exposure only when the active fraction of the bacterial community was considered. These changes were associated with seven OTUs related to Proteobacteria (5), Acidobacteria (1) and Actinobacteria (1). The relative abundance of the dominant bacterial phyla were not affected by oxamyl, except of Bacteroidetes and Gemmatimonadetes which decreased after 13 and 30 days of oxamyl exposure respectively. To conclude, oxamyl induced changes in the abundance of oxamyl-degrading microorganisms and on the diversity of the soil bacterial community. The latter became evident only upon RNA-based NGS analysis emphasizing the utility of such approaches when the effects of pesticides on the soil microbial community are explored.
现代农业实践在很大程度上依赖于农药来保护作物免受各种害虫的侵害,并确保高产量。在将农药应用于作物之后,大量的农药最终会进入土壤中,在那里它们可能会影响到非目标生物,其中包括微生物。我们评估了氨基甲酸酯类杀线虫剂氧乐果对具有增强的氧乐果生物降解能力的农业土壤中整个细菌多样性的影响,方法是通过 16S rRNA 扩增子下一代测序 (NGS) 评估,以及通过 cehA q-PCR 分析和 C-氧乐果矿化测定评估氧乐果降解细菌群落。土壤中的土著微生物可迅速将氧乐果矿化,在一个月内达到>70%。同时,观察到氧乐果降解微生物的数量显著增加。对总(DNA)和活性(RNA)细菌群落的 NGS 分析表明,α多样性指数没有因氧乐果暴露而发生变化。β多样性分析表明,只有在考虑到细菌群落的活性部分时,在氧乐果暴露 13 和 30 天后,土壤细菌群落的组成才会发生显著变化。这些变化与 7 个与变形菌门(5)、酸杆菌门(1)和放线菌门(1)相关的 OTUs 有关。氧乐果没有影响主要细菌门的相对丰度,除了在氧乐果暴露 13 和 30 天后,拟杆菌门和芽单胞菌门的相对丰度分别下降。总之,氧乐果诱导了氧乐果降解微生物的丰度变化,并改变了土壤细菌群落的多样性。只有在基于 RNA 的 NGS 分析中才能发现后者的变化,这强调了当研究农药对土壤微生物群落的影响时,这种方法的实用性。