» Articles » PMID: 23418476

Functional Assays and Metagenomic Analyses Reveals Differences Between the Microbial Communities Inhabiting the Soil Horizons of a Norway Spruce Plantation

Overview
Journal PLoS One
Date 2013 Feb 19
PMID 23418476
Citations 57
Authors
Affiliations
Soon will be listed here.
Abstract

In temperate ecosystems, acidic forest soils are among the most nutrient-poor terrestrial environments. In this context, the long-term differentiation of the forest soils into horizons may impact the assembly and the functions of the soil microbial communities. To gain a more comprehensive understanding of the ecology and functional potentials of these microbial communities, a suite of analyses including comparative metagenomics was applied on independent soil samples from a spruce plantation (Breuil-Chenue, France). The objectives were to assess whether the decreasing nutrient bioavailability and pH variations that naturally occurs between the organic and mineral horizons affects the soil microbial functional biodiversity. The 14 Gbp of pyrosequencing and Illumina sequences generated in this study revealed complex microbial communities dominated by bacteria. Detailed analyses showed that the organic soil horizon was significantly enriched in sequences related to Bacteria, Chordata, Arthropoda and Ascomycota. On the contrary the mineral horizon was significantly enriched in sequences related to Archaea. Our analyses also highlighted that the microbial communities inhabiting the two soil horizons differed significantly in their functional potentials according to functional assays and MG-RAST analyses, suggesting a functional specialisation of these microbial communities. Consistent with this specialisation, our shotgun metagenomic approach revealed a significant increase in the relative abundance of sequences related glycoside hydrolases in the organic horizon compared to the mineral horizon that was significantly enriched in glycoside transferases. This functional stratification according to the soil horizon was also confirmed by a significant correlation between the functional assays performed in this study and the functional metagenomic analyses. Together, our results suggest that the soil stratification and particularly the soil resource availability impact the functional diversity and to a lesser extent the taxonomic diversity of the bacterial communities.

Citing Articles

Fungal Diversity in an Undisturbed Andean Páramo Soil in Quimsacocha (Ecuador).

Delgado-Fernandez E, Nicola L, Covarrubias S, Girometta C, Valdez-Tenezaca A J Fungi (Basel). 2024; 10(9).

PMID: 39330383 PMC: 11432993. DOI: 10.3390/jof10090623.


Decoding the microbiome and metabolome of the -An indigenous fermented bio-formulation.

Muthukapalli Krishnareddy P, Hirehally Basavarajegowda M, Perumal Buela P, Devanna P, Makali Eregowda P, Sarangi A Imeta. 2024; 1(4):e63.

PMID: 38867902 PMC: 10989784. DOI: 10.1002/imt2.63.


Multidisciplinary evaluation of plant growth promoting rhizobacteria on soil microbiome and strawberry quality.

Nam J, Thibodeau A, Qian Y, Qian M, Park S AMB Express. 2023; 13(1):18.

PMID: 36795258 PMC: 9935790. DOI: 10.1186/s13568-023-01524-z.


Treatment with organic manure inoculated with a biocontrol agent induces soil bacterial communities to inhibit tomato wilt disease.

Tang T, Sun X, Liu Q, Dong Y, Zha M Front Microbiol. 2023; 13:1006878.

PMID: 36687620 PMC: 9849813. DOI: 10.3389/fmicb.2022.1006878.


Effects of Tree Composition and Soil Depth on Structure and Functionality of Belowground Microbial Communities in Temperate European Forests.

Prada-Salcedo L, Prada-Salcedo J, Heintz-Buschart A, Buscot F, Goldmann K Front Microbiol. 2022; 13:920618.

PMID: 35910637 PMC: 9328770. DOI: 10.3389/fmicb.2022.920618.


References
1.
Suen G, Scott J, Aylward F, Adams S, Tringe S, Pinto-Tomas A . An insect herbivore microbiome with high plant biomass-degrading capacity. PLoS Genet. 2010; 6(9):e1001129. PMC: 2944797. DOI: 10.1371/journal.pgen.1001129. View

2.
Tyson G, Chapman J, Hugenholtz P, Allen E, Ram R, Richardson P . Community structure and metabolism through reconstruction of microbial genomes from the environment. Nature. 2004; 428(6978):37-43. DOI: 10.1038/nature02340. View

3.
Will C, Thurmer A, Wollherr A, Nacke H, Herold N, Schrumpf M . Horizon-specific bacterial community composition of German grassland soils, as revealed by pyrosequencing-based analysis of 16S rRNA genes. Appl Environ Microbiol. 2010; 76(20):6751-9. PMC: 2953013. DOI: 10.1128/AEM.01063-10. View

4.
Cantarel B, Coutinho P, Rancurel C, Bernard T, Lombard V, Henrissat B . The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics. Nucleic Acids Res. 2008; 37(Database issue):D233-8. PMC: 2686590. DOI: 10.1093/nar/gkn663. View

5.
Fierer N, Lauber C, Ramirez K, Zaneveld J, Bradford M, Knight R . Comparative metagenomic, phylogenetic and physiological analyses of soil microbial communities across nitrogen gradients. ISME J. 2011; 6(5):1007-17. PMC: 3329107. DOI: 10.1038/ismej.2011.159. View