Nine land types in the northern mining area (BKQ) (mining land, smelting land, living area), the old mining area (LKQ) (whole-ore heap, wasteland, grassland), and southern mining area (NKQ) (grassland, shrubs, farmland) of Xikuang Mountain were chosen to explore the composition and functions of soil bacterial communities under different habitats around mining areas. The composition and functions of soil bacterial communities were compared among the sampling sites using 16S rRNA high-throughput sequencing and metagenomic sequencing. α diversity analysis showed the soil bacterial diversity and abundance in the old mining area were significantly higher than those in the northern mining area. β diversity analysis demonstrated that the soil bacterial community composition was highly similar among different vegetation coverages in the southern mining area. Microbial community function analysis showed the annotated KEGG function pathways and eggNOG function composition were consistent between the grassland of the old mining area and the grassland of the southern mining area. This study uncovers the soil bacterial community composition and functions among different habitats in the mining areas of Xikuang Mountain and will underlie soil ecosystem restoration in different habitats under heavy metal pollution around the mining areas there.
Xikuang or Tin Deposit Mountain, located near Lengshuijiang City of Hunan Province, China, is named "the capital of antimony" and is one of major antimony ores worldwide [[
As the soil habitats in the mining areas are complex and diverse, some environmental factors affect microbial community distributions among different soil habitats [[
High-throughput sequencing has been applied to analyze microbial communities in seawater, soils, human hand surface, and human distal intestinal tract [[
The experimental sites were located at the Xikuang Mountain, Lengshuijiang City, Hunan Province. Mining and smelting activities have resulted in the pollution of soil and water with Sb. The average annual rainfall and temperature are 1222 mm and 18.6°C, respectively. The northern mining area (BKQ), the old mining area (LKQ), and the southern mining area (NKQ) of Xikuang Mountain were chosen. At each mining area, 3 sampling sites were set, which led to totally 9 sampling sites (Table 1). At each sampling site, 6 soil samples were collected from the topsoil (0–5 cm). The total number of samples is 54. The samples were all put into aseptic sealing bags, and stored in a cooler (with ice bags). The samples were immediately taken back to the laboratory. All procedures were performed in aseptic conditions as much as possible. All samples were processed with 16S rRNA high-throughput sequencing. Samples LKQ6 and NKQ7 were also tested with metagenomics analysis. The described study complied with all relevant regulations and our non-invasive sampling method required no specific research permits.
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Table 1 Details of sampling sites.
Sampling site Latitude and longitude Land use Details BKQ1 27°46'6.09"N;111°29'24.20"E Mining land 0.01 km away from the mining plant BKQ2 27°46'24.28"N;111°29'36.15"E Smelting land near the mining plant BKQ3 27°46'40.73"N;111°29'58.23"E Living area 4 km away from the smelting land LKQ4 27°47'38.71"N;111°29'47.69"E Whole-ore heap land near the abandoned ore heap LKQ5 27°47'19.41"N;111°29'53.41"E Wasteland near the smelting plant LKQ6 27°47'28.97"N;111°30'4.55"E Grassland 2.5 km from the smelting plant NKQ7 27°44'18.13"N;111°27'56.00"E Grassland about 3 km from the mining area NKQ8 27°44'2.23"N;111°27'47.63"E Shrubs 0.5 km from the mining plant NKQ9 27°44'17.43"N;111°27'42.51"E Farmland 1 km from the smelting plant
Total DNA extraction, PCR amplification, and Illumina HiSeq. DNA from each sample was extracted using MN NucleoSpin 96 Soil kits, and DNA quality was detected via agarose gel electrophoresis. The V3—V4 region of bacterial 16S rRNA genes were amplified via polymerase chain reaction (PCR) using forward primer 338F and reverse primer 806R. The PCR amplification system was 10 μL, including 50 ng ± 20% genomic DNA, 0.3 μL of each of forward and reverse primers (10 μM), KOD FX Neo Buffer 5 μL, dNTP (2 mM each) 2 μL, and KOD FX Neo 0.2 μL, which were diluted by ddH
Sequencing data processing. With the original data, the reads of the samples were spliced on FLASH 1.2.11 [[
The tags were clustered on Usearch [[
After genomic DNA detection showed the samples were qualified, DNA was fragmented ultrasonically. Then the DNA fragments were purified, end-repaired, and 3'-end added with A, followed by sequencing connection. Next, a sequence library was created via PCR amplification, and its quality was tested. The qualified library was sequenced on Illumina.
The raw tags after sequencing were filtered on Trimmomatic to form clean reads. The clean reads were metagenomically assembled on MEGAHIT [[
The α diversity index of the samples was calculated on Mothur 1.30, and a rarefaction curve was plotted. The β diversity index was calculated on QIIME. Results were analyzed in R v.4.0.3, by principal co-ordinates analysis (PCoA) and analysis of similarities (ANOSIM), which are based on unweighted unifrac. The homogeneity of variance was compared using the least significant difference method (LSD) in one-factor analysis of variance. In case of variance heterogeneity, the microbial α diversity index and bacterial community relative abundance were compared among different mining areas using Dunnett's T3 test. PCoA curves were plotted in R v.4.0.3 and analyzed. With silva as the reference database, taxonomic annotations were done using a naive Bayesian classifier. Then the microbe names were updated with LPSN (
The library coverage rates of the samples were all above 99% (Table 2), indicating this sequencing result is valuable for analysis. The ACE, Chao1, Simpson, and Shannon indices were used to evaluate species richness and diversity. According to Table 2, the diversity and richness of bacterial communities in LKQ samples were significantly higher than those in BKQ samples (P<0.05).
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Table 2 Microbial α diversity index in soils of different mining areas.
Sample ACE Chao1 Simpson Shannon Coverage/% BKQ 652.84±157.42a 654.37±170.13b 0.9880±0.0047b 7.51±0.54b 99.51±0.09a LKQ 898.22±55.30a 926.46±69.84a 0.9948±0.0011a 8.50±0.28a 99.24±0.18b NKQ 832.73±20.38a 846.76±28.43ab 0.9911±0.0004ab 8.19±0.07ab 99.45±0.03ab ANOVE F 5.142 5.085 4.449 6.031 4.512
The different lowercases indicate significantly different in the same column indicate the α diversity index is significantly different among the mining areas (P<0.05).
One-factor analysis of variance (ANOVA) showed the α diversity index of soil microbes was different among mining areas. The ACE index was not significantly different among the three mining areas (P > 0.05). The Chao1, Simpson and Shannon indices were all significantly different between BKQ and LKQ (F = 6.57, 5.96, and 7.79, respectively; all P < 0.05). Hence, significant differences in the abundance and diversity of soil bacterial communities only exist between the northern mining area and the old mining area.
Beta diversity is a comparative analytical measure of the microbial community composition among the different samples. In this study, β diversity was calculated using principal coordinates analysis (PCoA) and Analysis of similarities (ANOSIM) based on unweighted UniFrac metric.
PCoA showed that the BKQ microbiome differed significantly from those of the LKQ and NKQ groups (Fig 1a). The results of ANOSIM indicated that inter-group differences were greater than intra-group differences, indicating that the soil bacterial community structure differed significantly among the different samples (R = 0.630, P = 0.006) (Fig 1b). PCoA plot and ANOSIM analysis together showed that the community composition of soil bacteria significantly differed among the different mining areas.
Graph: Fig 1 (a) PCoA and (b) ANOSIM based on unweighted UniFrac metric.
The relative abundance of soil bacteria at the phylum level was shown in Fig 2a. The top 10 phyla ranked by relative abundance were Pseudomonadota (20.13%–40.15%), Acidobacteriota (9.91%–35.48%), Actinomycetota (4.54%–26.87%), Chloroflexota (6.97%–18.82%), Gemmatimonadota (3.16%–12.63%), Bacteroidota (0.28%–5.09%), Cyanobacteriota (0.14%–4.93%), Nitrospirota (0.59%–4.46%), Candidatus Rokubacteria (0.13%–4.00%), and Planctomycetota (0.13%–2.87%).
Graph: Fig 2 (a) Relative abundance of predominant bacterial at phyla and (b) class level.
The top 10 bacterial phyla were sent to one-factor ANOVA to compare the differences in relative abundance of soil bacterial communities among different mining areas. Compared with the relative abundance of Bacteroidota (0.43% ± 0.22%) in BKQ, the relative abundance of Bacteroidota in LKQ (3.54% ± 1.66%) and NKQ (3.54% ± 0.74%) was significantly higher (F = 10.30, F = 48.44, both P < 0.05).
In the northern mining area, the predominant soil bacterial phyla were basically consistent among different habitats, but the relative abundance was significantly different. The top 4 dominant bacterial phyla in the soils of the mining land are Pseudomonadota (39.28%) > Acidobacteriota (23.97%) > Gemmatimonadota (12.63%) > Chloroflexota (6.97%). The top 4 dominant bacterial phyla in the soils of the smelting land are Acidobacteriota (30.01%) > Pseudomonadota (23.16%) > Chloroflexota (18.82%) > Actinomycetota (11.75%). The top 4 dominant bacterial phyla in the soils of the living area are Acidobacteriota (35.48%) > Pseudomonadota (20.13%)> Chloroflexota (18.79%) > Actinomycetota (9.83%). The relative abundance of Pseudomonadota, and Gemmatimonadota in the soils of mining land was far higher than in the other two habitats, and the relative abundance of Acidobacteriota and Chloroflexota in the soils of mining areas was far lower than in the two habitats.
In the old mining area, the predominant soil bacterial phyla were different among the sampling sites. The bacterial communities of whole-ore heap soils were dominated by Pseudomonadota and Acidobacteriota, and the sum of relative abundance was up to 63.46%. The bacterial communities of wasteland soils were dominated by Pseudomonadota, Acidobacteriota, Actinomycetota and Chloroflexota, and the sum of relative abundance was up to 81.63%. The bacterial communities of grassland soils were dominated by Pseudomonadota, Actinomycetota, Chloroflexota and Gemmatimonadota, and the sum of relative abundance was up to 84.73%. The relative abundance of Acidobacteriota in grassland soils was far lower than it in whole-ore heap soils, but the relative abundance of Actinomycetota was far higher than it in whole-ore heap or wasteland soils.
In the southern mining area, the predominant soil bacterial phyla were basically consistent among different habitats, and the difference in the relative abundance of the same phylum was low. The top 4 dominant bacterial phyla in the soils of the grasslands are Pseudomonadota (33.46%) > Acidobacteriota (20.99%) > Actinomycetota (17.99%) > Chloroflexota (12.43%). The top 4 dominant bacterial phyla in the soils of the shrubs are Pseudomonadota (34.77%) > Actinomycetota (22.55%) > Acidobacteriota (16.63%) > Chloroflexota (12.34%). The top 4 dominant bacterial phyla in the soils of the farmlands are Pseudomonadota (35.63%) > Acidobacteriota (23.89%) > Actinomycetota (17.80%) > Chloroflexota (9.16%). The top 4 dominant bacterial phyla were consistent among the soils of grassland, shrubs, and farmland in the southern mining area, including Pseudomonadota, Acidobacteriota, Actinomycetota, and Chloroflexota.
The relative abundance of soil bacteria at the class level was shown in Fig 2b. The top 10 bacterial classes ranked by relative abundance were Others(19.02% -30.13%), Alphaproteobacteria (10.18%–25.49%), Gammaproteobacteria (6.56%–21.85%), Acidobacteria (1.46%–35.20%), Acidimicrobiia (2.24%–17.21%), Gemmatimonadota (2.82%–12.62%), Actinomycetes (1.23%–11.75%), Deltaproteobacteria (1.42%–8.81%), Blastocatellia_Subgroup_4 (0.02%–7.48%), and Anaerolineae (1.99%–5.57%).
The top 10 bacterial classes were sent to one-factor ANOVA to compare the differences in pair relative abundance of soil bacterial communities among different mining areas. The relative abundance of Alphaproteobacteria (22.40% ± 2.91%), Acidimicrobiia (7.26% ± 0.59%) and Blastocatellia_Subgroup_4 (6.40% ± 1.83%) in the soils of NKQ was significantly higher than that of BKQ (F = 11.16, 46.97, and 29.61, respectively; all P < 0.05). The relative abundance of Blastocatellia_Subgroup_4 (6.40% ± 1.83%) in the soils of NKQ was significantly higher than compared with BKQ and LKQ (F = 29.61, F = 4.62, both P < 0.05).
In the northern mining area, the predominant soil bacterial classes were basically consistent among different habitats, but the relative abundance was different slightly. The top 4 dominant bacterial classes in the soils of the mining land are Alphaproteobacteria (17.45%) > Acidobacteria (16.07%) > Gammaproteobacteria (13.02%) > Gemmatimonadota (12.62%). The top 4 dominant bacterial classes in the soils of the smelting land are Acidobacteria (29.49%) > Alphaproteobacteria (11.68%) > Gammaproteobacteria (10.06%) > Gemmatimonadota (5.24%). The top 4 dominant bacterial classes in the soils of the living region are Acidobacteria (35.20%) > Alphaproteobacteria (10.18%) > Gammaproteobacteria (7.39%) > Gemmatimonadota (5.88%). The relative abundance of Alphaproteobacteria, Gammaproteobacteria and Gemmatimonadota in the soils of mining areas was far higher than in the other two habitats, and the relative abundance Acidobacteria and Others of in the soils of mining areas was far lower than in the two habitats.
In the old mining area, the predominant soil bacterial classes were basically consistent among different habitats, but the relative abundance was different. The top 4 dominant bacterial classes in the soils of the whole-ore heap are Gammaproteobacteria (21.85%) > Subgroup_6 (13.88%) > Alphaproteobacteria (11.74%) > Gemmatimonadota (6.43%). The top 4 dominant bacterial classes in the soils of the wasteland are Alphaproteobacteria (16.51%) > Gammaproteobacteria (13.62%) > Subgroup_6 (8.75%) > Acidimicrobiia (6.37%). The top 4 dominant bacterial classes in the soils of the grassland are Alphaproteobacteria (22.61%) > Acidimicrobiia (17.21%) > Gammaproteobacteria (10.23%) > Gemmatimonadota (9.36%). The relative abundance of Alphaproteobacteria, Acidimicrobiia in the soils of grassland was far higher than in the other two habitats, and the relative abundance Gammaproteobacteria in the soils of grassland was far lower than in the two habitats.
In the southern mining area, the predominant soil bacterial classes were different among the sampling sites. The soil bacterial communities of grassland were dominated by Alphaproteobacteria, as the relative abundance was up to 21.98%. The soil bacterial communities of shrubs were dominated by Alphaproteobacteria and Actinomycetes, as the sum of relative abundance was up to 37.24%. The soil bacterial communities of farmland were dominated by Alphaproteobacteria, Gammaproteobacteria and Subgroup_6, as the sum of relative abundance was up to 44.74%. The relative abundance of Actinomycetes in the soils of shrubs was far higher than in the other two habitats, and the relative abundance of Gammaproteobacteria, or Subgroup_6 of farmland soils was far higher than in the other two habitats. Relatively, the predominant soil bacterial classes were consistent among different habitats in the southern mining area.
The eggNOG functions of LKQ6 and NKQ7 were annotated (Fig 3a). The results indicate the compositions of the annotated functions are consistent between the 2 sampling sites, and the relative abundance is almost insignificantly different among the function clusters. It is suggested the compositions of annotated eggNOG function clusters are not significantly different between the grassland of the old mining area and the grassland of the southern mining area. The annotated eggNOG function cluster with the highest relative abundance is 'unknown', followed by function prediction, amino acid transport and metabolism, and energy generation and conversion.
Graph: Fig 3 (a) Relative abundance matched with eggNOG database and (b) KEGG database.
The KEGG functions of LKQ6 and NKQ7 were annotated (Fig 3b). The annotated KEGG function pathways from the 2 samples were very consistent, and nearly no significant difference in the relative abundance of any metabolic pathway was found. It is suggested the compositions of annotated KEGG function clusters are not significantly different between the grassland of the old mining area and the grassland of the southern mining area. The most annotated KEGG function type in the 2 sampling sites was 'global and review', followed by carbohydrate metabolism, metabolism of amino acid, and energy metabolism.
The above results indicate the microbial community functions in the soils were consistent between the 2 sampling sites (grassland of the old mining area and grassland of the southern mining area).
Soil bacterial communities are complex and diverse among different mining areas and different habitats, which shall be discussed by combining environment variables [[
The absolutely dominant bacterial phyla in the soils polluted by heavy metals around the antimony mining area were Pseudomonadota, Acidobacteriota, Actinomycetota, Chloroflexota, and Gemmatimonadota, and the sum of relative abundance reached 82.11%–94.64%. Wang et al. found Pseudomonadota, Acidobacteriota, Chloroflexota, Bacteroidota, Actinomycetota, Gemmatimonadota and Cyanobacteriota were predominance in the communities of Sb-polluted soils(Xikuangshan Sb mine area, Lengshuijiang, Hunan Province) [[
Kenarova et al. reported that the predominant bacteria in the soils of mining areas under heavy metal pollution may be tolerant against heavy metals to some extent [[
Moreover, the functional pathways of soil microbial communities were almost not different between LKQ6 and NKQ7. The above results indicate the functions of soil microbial communities may be consistent among different mining areas of the same habitat. Ezeokoli et al. found bacterial communities were affected by the differences in soil history and location, but the abundance of bacterial communities differed among different types of soils [[
The diversity and functions of soil bacterial communities among different habitats around the mining areas of Xikuang Mountain were analyzed, which will help with biological remediation of heavy-metal-polluted soils in the periphery of mining areas. However, we only preliminarily studied the functions of bacterial communities, so further research is needed to uncover the functions of bacterial communities, and even the existence and expressions of functional genes.
Generally, the soil bacterial communities of the 3 sampling sites were largely different. The soil bacterial community compositions varied significantly among different land use types in the northern mining area and the old mining area. In comparison, the soil bacterial community compositions did not vary significantly among different vegetation types in the southern mining area. The diversity and abundance of soil bacterial communities in LKQ are significantly higher than in BKQ (P<0.05). The relative abundance of some predominant bacterial phyla and classes are significantly different in the soils among different mining areas. The functions of bacterial communities are basically consistent between the grassland of the old mining area and the grassland of the southern mining area, indicating the functions of soil bacterial communities are redundant. The findings are expected to theoretically underlie ecosystem restoration in soils under heavy metal pollution around the mining areas.
By Jiao Yue; Dongpeng Zhang; Miaomiao Cao; Yukui Li; Qianwen Liang; Fei Liu and YuQiang Dong
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