Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
Microb Ecol
2011 Jan 01;611:201-13. doi: 10.1007/s00248-010-9740-4.
Show Gene links
Show Anatomy links
The impact of biofumigation and chemical fumigation methods on the structure and function of the soil microbial community.
Omirou M
,
Rousidou C
,
Bekris F
,
Papadopoulou KK
,
Menkissoglou-Spiroudi U
,
Ehaliotis C
,
Karpouzas DG
.
Abstract
Biofumigation (BIOF) is carried out mainly by the incorporation of brassica plant parts into the soil, and this fumigation activity has been linked to their high glucosinolate (GSL) content. GSLs are hydrolyzed by the endogenous enzyme myrosinase to release isothiocyanates (ITCs). A microcosm study was conducted to investigate the effects induced on the soil microbial community by the incorporation of broccoli residues into soil either with (BM) or without (B) added myrosinase and of chemical fumigation, either as soil application of 2-phenylethyl ITC (PITC) or metham sodium (MS). Soil microbial activity was evaluated by measuring fluorescein diacetate hydrolysis and soil respiration. Effects on the structure of the total microbial community were assessed by phospholipid fatty acid analysis, while the impact on important fungal (ascomycetes (ASC)) and bacterial (ammonia-oxidizing bacteria (AOB)) guilds was evaluated by denaturating gradient gel electrophoresis (DGGE). Overall, B, and to a lesser extent BM, stimulated microbial activity and biomass. The diminished effect of BM compared to B was particularly evident in fungi and Gram-negative bacteria and was attributed to rapid ITC release following the myrosinase treatment. PITC did not have a significant effect, whereas an inhibitory effect was observed in the MS-treated soil. DGGE analysis showed that the ASC community was temporarily altered by BIOF treatments and more persistently by the MS treatment, while the structure of the AOB community was not affected by the treatments. Cloning of the ASC community showed that MS application had a deleterious effect on potential plant pathogens like Fusarium, Nectria, and Cladosporium compared to BIOF treatments which did not appear to inhibit them. Our findings indicate that BIOF induces changes on the structure and function of the soil microbial community that are mostly related to microbial substrate availability changes derived from the soil amendment with fresh organic materials.
Brown,
Brassicaceae tissues as inhibitors of nitrification in soil.
2009, Pubmed
Brown,
Brassicaceae tissues as inhibitors of nitrification in soil.
2009,
Pubmed
Chang,
Impact of herbicides on the abundance and structure of indigenous beta-subgroup ammonia-oxidizer communities in soil microcosms.
2001,
Pubmed
Clegg,
The impact of grassland management regime on the community structure of selected bacterial groups in soils.
2003,
Pubmed
Fahey,
The chemical diversity and distribution of glucosinolates and isothiocyanates among plants.
2001,
Pubmed
Ibekwe,
Microbial diversity along a transect of agronomic zones.
2002,
Pubmed
Ibekwe,
Impact of fumigants on soil microbial communities.
2001,
Pubmed
Infantino,
Molecular and physiological characterization of Italian isolates of Pyrenochaeta lycopersici.
2003,
Pubmed
Karpouzas,
Effect of continuous olive mill wastewater applications, in the presence and absence of nitrogen fertilization, on the structure of rhizosphere-soil fungal communities.
2009,
Pubmed
Kowalchuk,
Ammonia-oxidizing bacteria: a model for molecular microbial ecology.
2001,
Pubmed
Kowalchuk,
Analysis of ammonia-oxidizing bacteria of the beta subdivision of the class Proteobacteria in coastal sand dunes by denaturing gradient gel electrophoresis and sequencing of PCR-amplified 16S ribosomal DNA fragments.
1997,
Pubmed
Kurola,
Activity, diversity and population size of ammonia-oxidising bacteria in oil-contaminated landfarming soil.
2005,
Pubmed
Larena,
Design of a primer for ribosomal DNA internal transcribed spacer with enhanced specificity for ascomycetes.
1999,
Pubmed
Larkin,
Effects of different 3-year cropping systems on soil microbial communities and rhizoctonia diseases of potato.
2006,
Pubmed
Mahmood,
Comparison of PCR primer-based strategies for characterization of ammonia oxidizer communities in environmental samples.
2006,
Pubmed
Matthiessen,
Biofumigation: environmental impacts on the biological activity of diverse pure and plant-derived isothiocyanates.
2005,
Pubmed
McCaig,
Numerical analysis of grassland bacterial community structure under different land management regimens by using 16S ribosomal DNA sequence data and denaturing gradient gel electrophoresis banding patterns.
2001,
Pubmed
McCaig,
Molecular analysis of enrichment cultures of marine ammonia oxidisers.
1994,
Pubmed
Osono,
Roles of diverse fungi in larch needle-litter decomposition.
2003,
Pubmed
Phillips,
Effects of agronomic treatments on structure and function of ammonia-oxidizing communities.
2000,
Pubmed
Prosser,
Relative contributions of archaea and bacteria to aerobic ammonia oxidation in the environment.
2008,
Pubmed
Purkhold,
Phylogeny of all recognized species of ammonia oxidizers based on comparative 16S rRNA and amoA sequence analysis: implications for molecular diversity surveys.
2000,
Pubmed
Saitou,
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
1987,
Pubmed
Spyrou,
Do botanical pesticides alter the structure of the soil microbial community?
2009,
Pubmed
Viebahn,
Assessment of differences in ascomycete communities in the rhizosphere of field-grown wheat and potato.
2005,
Pubmed
Webster,
Grassland management regimens reduce small-scale heterogeneity and species diversity of beta-proteobacterial ammonia pxidizer populations.
2002,
Pubmed
Wittstock,
Glucosinolate research in the Arabidopsis era.
2002,
Pubmed
Zelenev,
Short-term wavelike dynamics of bacterial populations in response to nutrient input from fresh plant residues.
2005,
Pubmed