The Decrease of Soil Microbial Community Diversity and Network Complexity Results in the Increase of Soil-Borne Diseases With Monocultural Years in Greenhouse Tomato Production Systems
Jing Hu, Li Wan, Yafang Wang, Kuai Dai, Klaus Butterbach-Bahl, Shan Lin
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Abstract
The excessive use of water and fertiliser, along with long-term monocultivation in greenhouse vegetable fields, has led to a decrease in soil quality and an imbalance in the soil microflora, which may contribute to worsening soil-borne diseases. To examine the associations between the soil microbial community composition and disease-suppressing microorganisms under different years of cultivation shifting from croplands to greenhouses, we collected soil samples from fields continuously planted with tomatoes for 5, 10 and 20 years, as well as from nearby maize–wheat fields (MW). The soil physicochemical properties, microbial community composition, putative plant pathogens and putative antagonistic bacteria were analysed. The results indicated that (1) the diversity and richness of soil bacteria and fungi significantly decreased with longer cultivation years; (2) bacterial and fungal diversity indices were negatively associated with soil nutrient content and positively associated with soil pH and NO3−-N content, the latter being identified as the main factor contributing to the decline in microbial diversity; (3) the complexity of the soil bacterial network initially increased, peaking after 5 years of continuous monoculture, and then decreased, whereas fungal network complexity gradually declined over time; (4) the relative abundance of putative pathogens such as Fusarium, Alternaria and Cladosporium (associated with tomato wilt and leaf mould) increased significantly with longer cultivation, whereas the relative abundance of the bacterial genera associated with putative antagonism Bacillus, Paenibacillus and Streptomyces decreased. In conclusion, after 10 years of continuous monocultivation, a marked reduction in soil microbial diversity and putative antagonistic bacteria was observed, along with an increase in putative pathogenic fungi. These changes likely contributed to the worsening of soil-borne diseases, threatening the sustainability of greenhouse vegetable production.
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.