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Microbial Communities in the Rhizosphere Analyzed by Cultivation-Independent DNA-Based Methods

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Principles of Plant-Microbe Interactions

Abstract

The development of methods to extract nucleic acids directly from the rhizosphere or from microbial cells detached by a mechanical treatment from roots opened new dimensions to study the rhizosphere microbiome and to overcome limitations of cultivation-dependent methods. This chapter summarizes the potentials and limitations of cultivation-independent methods used by our group in the last 15 years to investigate microbial communities in the rhizosphere and their response to changing environmental conditions. We showed that rhizosphere microbial communities are highly dynamic, and that their composition is mainly shaped by the plant and the soil type and factors influencing these drivers of microbial diversity in the rhizosphere.

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References

  • Adesina MF, Grosch R, Lembke A et al (2009) In vitro antagonists of Rhizoctonia solani tested on lettuce: rhizosphere competence, biocontrol efficiency and rhizosphere microbial community response. FEMS Microbiol Ecol 69:62–74

    Google Scholar 

  • Bent SJ, Forney LJ (2008) The tragedy of the uncommon: understanding limitations in the analysis of microbial diversity. ISME J 2:689–695

    Google Scholar 

  • Berendsen RL, Pieterse CMJ, Bakker PAHM (2012) The rhizosphere microbiome and plant health. Trends Plant Sci 17:478–486

    Google Scholar 

  • Berg G, Smalla K (2009) Plant species and soil type cooperatively shape the structure and function of microbial communities in the rhizosphere. FEMS Microbiol Ecol 68:1–13

    Google Scholar 

  • Berg G, Roskot N, Steidle A et al (2002) Plant-dependent genotypic and phenotypic diversity of antagonistic rhizobacteria isolated from different Verticillium host plants. Appl Environ Microbiol 68:3328–3338

    Google Scholar 

  • Bulgarelli D, Schlaeppi K, Spaepen S et al (2013) Structure and functions of the bacterial microbiota of plants. Annu Rev Plant Biol 64:807–838

    Google Scholar 

  • Costa R, Götz M, Mrotzek N et al (2006a) Effects of site and plant species on rhizosphere community structure as revealed by molecular analysis of microbial guilds. FEMS Microbiol Ecol 56: 236–249

    Google Scholar 

  • Costa R, Salles JF, Berg G et al (2006b) Cultivation-independent analysis of Pseudomonas species in soil and in the rhizosphere of field-grown Verticillium dahliae host plants. Environ Microbiol 8:2136–2149

    Google Scholar 

  • Costa R, Gomes NCM, Krögerrecklenfort E et al (2007) Pseudomonas community structure and antagonistic potential in the rhizosphere: insights gained by combining phylogenetic and functional gene-based analyses. Environ Microbiol 9:2260–2273

    Google Scholar 

  • DeSantis TZ, Brodie EL, Moberg JP, et al (2007) High-density universal 16 S rRNA microarray analysis reveals broader diversity than typical clone library when sampling the environment. Microb Ecol 53:371–383

    Google Scholar 

  • Eltlbany N, Prokscha Z-Z, Castaneda-Ojeda MP et al (2012) A new bacterial disease on Mandevilla sanderi, caused by Pseudomonas savastanoi: Lessons learned for bacterial diversity studies. Appl Environ Microbiol 78:8492–8497

    Google Scholar 

  • Gomes NCM, Heuer H, Schönfeld J et al (2001) Bacterial diversity of the rhizosphere of maize (Zea mays) grown in tropical soil studied by temperature gradient gel electrophoresis. Plant Soil 232:167–180

    Google Scholar 

  • Gomes NCM, Fagbola O, Costa R et al (2003) Dynamics of fungal communities in bulk and maize rhizosphere soil in the tropics. Appl Environ Microbiol 69:3758–3766

    Google Scholar 

  • Götz M, Gomes NCM, Dratwinski A et al (2006) Survival of gfp-tagged antagonistic bacteria in the rhizosphere of tomato plants and their effects on the indigenous bacterial community. FEMS Microbiol Ecol 56:207–218

    Google Scholar 

  • Grosch R, Dealtry S, Schreiter S et al (2012) Biocontrol of Rhizoctonia solani: complex interaction of biocontrol strains, pathogen and indigenous microbial community in the rhizosphere of lettuce shown by molecular methods. Plant Soil 361:343–357

    Google Scholar 

  • Heuer H, Smalla K (2012) Plasmids foster diversification and adaptation of bacterial populations in soil. FEMS Microbiol Rev 36:1083–1104

    Google Scholar 

  • Heuer H, Krsek M, Baker P et al (1997) Analysis of actinomycete communities by specific amplification of genes encoding 16 S rRNA and gel-electrophoretic separation in denaturing gradients. Appl Environ Microbiol 63:3233–3241

    Google Scholar 

  • Heuer H, Kroppenstedt RM, Lottmann J et al (2002) Effects of T4 lysozyme release from transgenic potato roots on bacterial rhizosphere relative to communities are negligible natural factors. Appl Environ Microbiol 68:1325–1335

    Google Scholar 

  • Jechalke S, Schreiter S, Wolters B et al (2014) Widespread dissemination of class 1 integron components in soils and related ecosystems as revealed by cultivation-independent analysis. Front Microbiol 4:420

    Google Scholar 

  • Klappenbach JA, Dunbar JM, Schmidt TM (2000) rRNA operon copy number reflects ecological strategies of bacteria. Appl Environ Microbiol 66:1328–1333

    Google Scholar 

  • Kropf S, Heuer H, Gruening M et al (2004) Significance test for comparing complex microbial community fingerprints using pairwise similarity measures. J Microbiol Meth 57:187–195

    Google Scholar 

  • Marques JM, Da Silva TF, Vollu RE et al (2014) Plant age and genotype affect the bacterial community composition in the tuber rhizosphere of field-grown sweet potato plants. FEMS Microbiol Ecol 88:424–435

    Google Scholar 

  • Neumann G, Bott S, Ohler M et al (2014) Root exudation and root development of lettuce (Lactuca sativa L. cv. Tizian) as affected by different soils. Front Microbiol 5:2

    Google Scholar 

  • Nübel U, Engelen B, Felske A et al (1996) Sequence heterogeneities of genes encoding 16 S rRNAs in Paenibacillus polymyxa detected by temperature gradient gel electrophoresis. J Bacteriol 178:5636–5643

    Google Scholar 

  • Schreiter S, Ding G, Heuer H et al (2014a) Effect of the soil type on the microbiome in the rhizosphere of field-grown lettuce. Front Microbiol 5:144

    Google Scholar 

  • Schreiter S, Sandmann M, Smalla K et al (2014b) Soil type dependent rhizosphere competence and biocontrol of two bacterial inoculant strains and their effects on the rhizosphere microbial community of field-grown lettuce. Plos ONE:9:e103726

    Google Scholar 

  • Smalla K, Wieland G, Buchner A et al (2001) Bulk and rhizosphere soil bacterial communities studied by denaturing gradient gel electrophoresis: plant-dependent enrichment and seasonal shifts revealed. Appl Environ Microbiol 67:4742–4751

    Google Scholar 

  • Smalla K, Oros-Sichler M, Milling A et al (2007) Bacterial diversity of soils assessed by DGGE, T-RFLP and SSCP fingerprints of PCR-amplified 16 S rRNA gene fragments: Do the different methods provide similar results? J Microbiol Meth 69:470–479

    Google Scholar 

  • Weinert N, Meincke R, Gottwald C et al (2009) Rhizosphere communities of genetically modified zeaxanthin-accumulating potato plants and their parent cultivar differ less than those of different potato cultivars. Appl Environ Microbiol 75:3859–3865

    Google Scholar 

  • Weinert N, Piceno Y, Ding G, et al (2011) PhyloChip hybridization uncovered an enormous bacterial diversity in the rhizosphere of different potato cultivars: many common and few cultivar-dependent taxa. FEMS Microbiol Ecol 75:497–506

    Google Scholar 

  • Xue Q, Ding G, Li S et al (2013) Rhizocompetence and antagonistic activity towards genetically diverse Ralstonia solanacearum strains—an improved strategy for selecting biocontrol agents. Appl Microbiol Biotechnol 97:1361–1371

    Google Scholar 

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Correspondence to Kornelia Smalla .

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Schreiter, S., Eltlbany, N., Smalla, K. (2015). Microbial Communities in the Rhizosphere Analyzed by Cultivation-Independent DNA-Based Methods. In: Lugtenberg, B. (eds) Principles of Plant-Microbe Interactions. Springer, Cham. https://doi.org/10.1007/978-3-319-08575-3_30

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