Romano Ida, Ventorino Valeria, Pepe Olimpia
Department of Agricultural Sciences, University of Naples Federico II, Naples, Italy.
Task Force on Microbiome Studies, University of Naples Federico II, Naples, Italy.
Front Plant Sci. 2020 Jan 31;11:6. doi: 10.3389/fpls.2020.00006. eCollection 2020.
Issues concerning the use of harmful chemical fertilizers and pesticides that have large negative impacts on environmental and human health have generated increasing interest in the use of beneficial microorganisms for the development of sustainable agri-food systems. A successful microbial inoculant has to colonize the root system, establish a positive interaction and persist in the environment in competition with native microorganisms living in the soil through rhizocompetence traits. Currently, several approaches based on culture-dependent, microscopic and molecular methods have been developed to follow bioinoculants in the soil and plant surface over time. Although culture-dependent methods are commonly used to estimate the persistence of bioinoculants, it is difficult to differentiate inoculated organisms from native populations based on morphological characteristics. Therefore, these methods should be used complementary to culture-independent approaches. Microscopy-based techniques (bright-field, electron and fluorescence microscopy) allow to obtain a picture of microbial colonization outside and inside plant tissues also at high resolution, but it is not possible to always distinguish living cells from dead cells by direct observation as well as distinguish bioinoculants from indigenous microbial populations living in soils. In addition, the development of metagenomic techniques, including the use of DNA probes, PCR-based methods, next-generation sequencing, whole-genome sequencing and pangenome methods, provides a complementary approach useful to understand plant-soil-microbe interactions. However, to ensure good results in microbiological analysis, the first fundamental prerequisite is correct soil sampling and sample preparation for the different methodological approaches that will be assayed. Here, we provide an overview of the advantages and limitations of the currently used methods and new methodological approaches that could be developed to assess the presence, plant colonization and soil persistence of bioinoculants in the rhizosphere. We further discuss the possibility of integrating multidisciplinary approaches to examine the variations in microbial communities after inoculation and to track the inoculated microbial strains.
有害化学肥料和农药的使用对环境和人类健康产生了巨大负面影响,这使得人们越来越关注利用有益微生物来发展可持续农业食品系统。一种成功的微生物接种剂必须定殖于根系,建立积极的相互作用,并通过根际竞争能力特征在与土壤中天然微生物竞争的环境中持续存在。目前,已经开发了几种基于培养、显微镜和分子方法的途径,用于长期追踪土壤和植物表面的生物接种剂。虽然基于培养的方法通常用于估计生物接种剂的持久性,但基于形态特征很难将接种的生物体与天然种群区分开来。因此,这些方法应与非培养方法互补使用。基于显微镜的技术(明场、电子和荧光显微镜)能够以高分辨率获得植物组织内外微生物定殖的图像,但通过直接观察并不总是能够区分活细胞和死细胞,也无法区分生物接种剂与土壤中存在的本地微生物种群。此外,宏基因组技术的发展,包括使用DNA探针、基于PCR的方法、下一代测序、全基因组测序和泛基因组方法,提供了一种有助于理解植物-土壤-微生物相互作用的互补方法。然而,为了确保微生物分析取得良好结果,首要的基本前提是针对将要检测的不同方法进行正确的土壤采样和样品制备。在此,我们概述了目前使用的方法的优缺点以及可开发的新方法,以评估生物接种剂在根际的存在、植物定殖和土壤持久性。我们还进一步讨论了整合多学科方法来检查接种后微生物群落变化并追踪接种微生物菌株的可能性。