http://orcid.org/0000-0003-3733-4197
Figures
Abstract
The role of rhizosphere microbial communities in the degradation of hydrocarbons remains poorly understood and is a field of active study. We used high throughput sequencing to explore the rhizosphere microbial diversity in the alfalfa and barley planted oil contaminated soil samples. The analysis of 16s rRNA sequences showed Proteobacteria to be the most enriched (45.9%) followed by Bacteriodetes (21.4%) and Actinobacteria (10.4%) phyla. The results also indicated differences in the microbial diversity among the oil contaminated planted soil samples. The oil contaminated planted soil samples showed a higher richness in the microbial flora when compared to that of untreated samples, as indicated by the Chao1 indices. However, the trend was different for the diversity measure, where oil contaminated barley planted soil samples showed slightly lower diversity indices. While the clustering of soil samples grouped the oil contaminated samples within and across the plant types, the clean sandy soil samples formed a separate group. The oil contaminated rhizosphere soil showed an enrichment of known oil-degrading genera, such as Alcanivorax and Aequorivita, later being specifically enriched in the contaminated soil samples planted with barley. Overall, we found a few well known oil-degrading bacterial groups to be enriched in the oil contaminated planted soil samples compared to the untreated samples. Further, phyla such as Thermi and Gemmatimonadetes showed an enrichment in the oil contaminated soil samples, indicating their potential role in hydrocarbon degradation. The findings of the current study will be useful in understanding the rhizosphere microflora responsible for oil degradation and thus can help in designing appropriate phytoremediation strategies for oil contaminated lands.
Citation: Kumar V, AlMomin S, Al-Aqeel H, Al-Salameen F, Nair S, Shajan A (2018) Metagenomic analysis of rhizosphere microflora of oil-contaminated soil planted with barley and alfalfa. PLoS ONE 13(8): e0202127. https://doi.org/10.1371/journal.pone.0202127
Editor: Ulrich Melcher, Oklahoma State University, UNITED STATES
Received: January 29, 2018; Accepted: July 27, 2018; Published: August 9, 2018
Copyright: © 2018 Kumar et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The raw data is deposited in NCBI database (SRA: SRP127607; BioProject: PRJNA427666).
Funding: This work was supported by Kuwait Foundation for the Advancement of Sciences (Grant No. 2013-4401-01) to VK. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Microorganisms are probably associated with every living organism on earth. They have been found to play an active role in both animal and plant physiology. Diverse microorganisms live in association with plants, both below and above the ground [1, 2]. They are found within the plants as endophytes and on plant surface as epiphytes. The interaction between the microbial populations can have beneficial and detrimental effects on the plant development and growth [3]. The microbial community residing in the soil has been shown to benefit the plants to a more significant extent. One gram of forest soil contains an estimated 4 X 107 prokaryotic cells [4], which is found to be more than the known catalog of prokaryotes [5]. Soil is one of the major reservoirs of organic carbon, and prokaryotes are an essential part of the soil decomposition system [6]. The biologically active zone of the soil around the plant roots is known as rhizosphere. The rhizosphere harbors soil-borne microbes including bacteria and fungi, which influence the roots through their biological, physical, and chemical interactions. Hence, it is imperative to study the interactions between plants and these soil microorganisms for understanding various plant related processes. However, many groups of microorganisms residing in the soil are not cultivable in the standard laboratory conditions [7]. With the birth of sequencing, and more recently next-generation sequencing (NGS), it has been possible to explore the microbial diversity by using specific genomic regions, such as 16s-rRNA gene. With NGS, it is possible to assess the microbial population from an environmental sample without the need of isolation and culture. This approach termed as metagenomics is a rapidly growing field of microbiology. Metagenomics approach has been used to study the microbial diversity in various contexts in both plants and animals.
The NGS technology has been extensively used to study the human gut microbiome, revealing the interplay between the microorganisms and host metabolism [8, 9]. The approach has also been employed to explore the microbial diversity in plants. In a recent study [10], Mendes et al. used shotgun metagenomics approach to explore the microbial communities in the bulk soil and the rhizosphere of soybean plants, showing an apparent selection at both taxonomic and functional levels. In another study [11], the metagenomic analysis revealed changes in the relative abundance of the bacterial groups, which include strains that promote plant growth and phytic acid utilization, and some genes associated with phytic acid utilization, such as alkaline phosphatase and citrate synthase. Bai et al., [12] assessed the microbial community composition and function in a constructed wetland receiving surface water. The results indicated that the diversity of the rhizosphere soil was found to be significantly higher than that of the wetland influent water, likely due to the availability of diverse habitats and nutrients provided by the wetland plants. The study shows that the use of metagenomic approach can also provide new insights for the study of wetland ecosystems. Metagenomic analysis by Chen et al., [13] showed the importance of microbial population in the phytoremediation of cadmium-contaminated soils. The role of the microbial community has also been established in the degradation of hydrocarbons. A recent study [14] showed the influence of polycyclic aromatic hydrocarbons (PAHs) concentration on the microbial communities in the rice rhizosphere. The microbial population was also affected depending on the distance from the root surface during PAHs degradation. The study also showed that the relative abundance of genes involved in defense mechanisms, replication, and recombination was significantly higher in samples with high PAHs degrading potentials. A study by Koshlaf et al., [15] showed a shift in bacterial communities when pea straw was added to the diesel-contaminated soil. The metagenomic analysis indicated that the original soil contained hydrocarbon degraders (e.g., Pseudoxanthomonas spp.), however, treatment with the biostimulant (pea straw) made them active, and accelerated the process of degradation.
Exploring the bacterial communities in aged oil contaminated soil can provide insights into the microbial species involved in bioremediation of oil. Further, different plant species may support different bacterial communities in their rhizosphere as a result of different root exudates. In the current study, we have used NGS technology to explore the microbial communities in different plant species grown in aged oil contaminated soil.
Materials and methods
Experimental setup
Seeds of alfalfa cv Regen SY was procured from USDA-WRPIS, Agriculture Research Station, USA. Barley seeds were procured from the local market in Kuwait. The seeds were washed and seeded on moistened potting soil mix and were allowed to germinate and grow for ten days. The seedlings were then transferred to half gallon pots containing aged oil contaminated soil from a site which was contaminated with crude oil during the 90s gulf war. Physical properties of the oil contaminated soil used in the experiments were as follows, pH 7.95±0.01; electrical conductivity 852±17 (μS); salinity 545±11 (ppm); soluble SO4 (mg/kg) 4425±218; TPHs 1.33±0.06 (%). Clean sandy-soil from the nearest location of the oil contaminated site was used as a control. Two seedlings were transferred to each pot, and five pots for each treatment were maintained. All the pots were watered daily and fertilized at the end of every two weeks (N:P:K 20:20:20 with trace metals). The plants were maintained in a plant growth chamber set at 25°C and 14:10 light regime. The seedlings were allowed to grow for two months. At the end of two months duration, the plants were removed from the soil and gently shaken to remove excess soil. The rhizospheric soil was collected from the root zone, within five mm from the root surface of the plants from three pots for each treatment using brush and tweezers. Non-rhizospheric control bulk soil samples were also collected for comparative analysis using a cork borer. The soil samples were used for the study of microbial community structure and diversity using 16S rRNA metagenome analysis. DNA was extracted from 0.5 to 2.0 g of the soil using the PowerMax Soil DNA Isolation kit (MoBio, Carlsbad, CA, USA) following manufacturer’s instructions.
Sequencing of 16s rRNA gene
The 16S rRNA gene variable region V4 PCR primers 515/806 with barcode on the forward primer were used in a 30 cycle PCR (5 cycles used on PCR products) using the HotStarTaq Plus Master Mix Kit (Qiagen, USA) under the following conditions: 94°C for 3 minutes, followed by 28 cycles of 94°C for 30 seconds, 53°C for 40 seconds and 72°C for 1 minute, after which a final elongation step at 72°C for 5 minutes was performed. After amplification, the PCR products were checked in 2% agarose gel to determine the success of amplification and the relative intensity of bands. Multiple samples were pooled together in equal proportions based on their molecular weight and DNA concentrations. Pooled samples were purified using calibrated Ampure XP beads. Then the pooled and purified PCR product was used to prepare DNA library by following Illumina TruSeq DNA library preparation protocol. Sequencing was performed on a MiSeq sequencing platform following the manufacturer’s guidelines. Each sample was sequenced as a paired-end set of reads with a read length of 300 bp. The sequencing was performed at Beijing Genomics Institute (BGI), Hong Kong. The raw data is deposited in NCBI database (SRA: SRP127607; BioProject: PRJNA427666).
Analysis of high throughput sequencing data
The raw sequence data obtained as paired-end fastq files were checked for quality before and after trimming, using FastQC v0.10.1 tool (https://www.bioinformatics.babraham.ac.uk/projects/fastqc/). The raw data was trimmed for barcode and primer sequences, any ambiguous bases, and homopolymers >6 bases. Reads shorter than 150 bp and with an average Phred quality score of <20 were removed. All the trimming and filtering steps were performed using Quantitative Insights Into Microbial Ecology (QIIME) version 1.9.0 [16].
The trimmed sequences were checked for chimeric sequences by using both de-novo and reference based methods. The RDP Gold database v9 reference was used for the reference based detection of chimeric sequences using USEARCH program [17]. The detected chimeric sequences were removed and only the non-chimeric sequences were considered for further analysis. The chimera filtered sequences were used for the identification of operational taxonomic unit (OTU) clusters with a minimum similarity of 97% using UCLUST [17], and the clusters were used for generating representative sequences. The representative sequences were further filtered to remove any singletons using QIIME. The filtered representative sequences were aligned using PyNAST [18], a method for performing pair-wise alignment. The alignment file was further filtered for positions with gaps, and outliers (sequences dissimilar to the alignment consensus). The filtered representative sequences were mapped against the greengenes database [19] with a similarity of 80% using Ribosomal Database Project (RDP) classifier [20]. All the data analysis steps were performed using the tools implemented within QIIME [16].
Filtered alignments were considered for various statistical analysis and phylogenetic tree construction. Alpha diversity representing the diversity and richness of each sample was calculated by rarefying a small percentage of randomly picked sequences, and considering 10 iterations each time. The rarefaction analysis was performed by considering the sampling depth of 55,000 sequences per sample. The Shannon index indicating the diversity and Chao1 index indicating the richness of microbial population were calculated using the taxonomic classifications and phylogenetic tree. Beta diversity indicating the diversity across samples was calculated using the weighted and unweighted UniFrac [21] distance matrix. Principal Coordinate Analysis (PCoA) was performed using the UniFrac results. All the statistical analyses were performed using QIIME tool [16]. Significant differential abundance of taxonomic assignments across samples was identified using t-test. Phyla and genera having a p-value of < 0.05 were considered as significantly enriched.
Unweighted Pair Group Method with Arithmetic mean (UPGMA) clustering was performed using the biom table in QIIME. Heatmap was generated using METAGENassist [22], with genus level counts across samples. Reads that were unassigned or unmapped, and the genus with over 50% zeros (across samples) were excluded while generating the heatmap.
Results
Quality analysis, raw data trimming, and chimera detection
The sequencing of 16s r-RNA gene from 15 samples resulted in 1,628,728 reads. The paired-end raw data obtained in fastq files was subjected to stringent trimming and filtering. Around 91% of the data was retained after various quality filtering steps, Table 1. The counts of filtered reads per sample after the quality filtering are shown in Table 2. Approximately 3% of the raw reads were removed because of the mismatches in primer sequence. A total of 66,414 chimeric sequences corresponding to 4.08% of the raw reads were detected and excluded from further analysis, Table 3. Reference based chimera analysis detected more number of chimeric sequences than the de-novo method.
OTU generation, filtering and alignment
The filtered reads were grouped into OTU clusters. A total of 154,254 OTUs were identified across all the samples, of which 29,894 were retained after filtering the singletons. Singleton OTUs are the clusters containing only one read sequence. The filtered OTUs represented 1,368,497 sequences from all samples, corresponding to an average number of 91,233 sequences per sample, Table 4. A single representative sequence was obtained from each OTU cluster and subjected to alignment. All the representative sequences except 69 produced alignment hits. After filtering alignments with gaps, and removing outliers, 29,630 aligned sequences were obtained.
Taxonomic classification
Around 1.3 million sequences were assigned to various taxa with at least 80% similarity. A total of 36 taxa at phylum level were identified across samples, of which 11 are represented by at least 0.5% of total reads. Phylum level distribution across samples for these 11 taxa is presented in Fig 1. The distribution of all the phyla can be found in S1 File. Major percentage of the sequences were assigned to Proteobacteria (45.9%), followed by Bacteriodetes (21.4%) and Actinobacteria (10.4%). However, we found bacterial population from the phylum Proteobacteria to be comparatively low in the clean sandy soil (common control) group. Ninety seven percent of the total sequences were assigned to the top 10 phyla, S1 File. The oil contaminated soil showed a decreased population of Proteobacteria compared to the untreated soil, in both the plants groups. The clean sandy soil was found to be enriched with the bacterial population from the phylum Actinobacteria. Further, the oil contaminated soil sample showed a slight increase in the microbial population from the phylum Actinobacteria compared to the clean soil samples, Fig 1. The microbial population from the phylum Gemmatimonadetes showed enrichment specifically in the oil contaminated planted soil samples. However, Firmicutes were shown to be specifically enriched in the clean sandy soil samples.
Phyla represented by at least 0.5% of the total assigned sequences (11 of total 36 phyla) are shown here. CS: Clean sandy soil; BC: Control oil contaminated bulk soil without barley plants; BO: Barley planted oil contaminated rhizosphere soil; AC: Control oil contaminated bulk soil without alfalfa plants; AO: Alfalfa planted oil contaminated rhizosphere soil.
A total of 657,190 sequences were assigned to 372 genera. There were 26 genera covering 72% of the total assigned sequences and represented by at least 1% of the total assigned sequences. Flavobacterium was the most enriched genus among the classified genera, representing 9.6% of the total assigned sequences, followed by Pseudomonas (7.0%) and Thermomonas (6.3%). Genus level distribution for the taxa with at least 2% abundance is shown in Fig 2. The distribution of all the genera can be found in S1 File. The distribution of Pseudomonas across the oil contaminated soil samples planted with barley or alfafa was shown to be comparatively more than in the untreated or clean sandy soil samples. In contrast, the distribution of Flavobacterium was found to be decreased comparatively in the oil contaminated soil samples than in the untreated groups. We found similar correlation with the microbial population from the genus Thermomonas. The oil contaminated soil samples planted with barley and alfalfa were found to be specifically enriched in the genera Alcanivorax, Nitrosomonas and B-42 (Fig 2).
Genera with at least 2% of the total assigned sequences (12 of total 372 genera) are represented here. CS: Clean sandy soil; BC: Control oil contaminated bulk soil without barley plants; BO: Barley planted oil contaminated rhizosphere soil; AC: Control oil contaminated bulk soil without alfalfa plants; AO: Alfalfa planted oil contaminated rhizosphere soil.
Significance enrichment analysis also indicated a difference in the distribution of microbial population across the treated and untreated groups, with a p-value <0.05, Table 5 and S2 File. The phyla Gemmatimonadetes (p-value 5.6E-05), BRC1 (p value 6.99E-05) and Chloroflexi (p-value 1.72E-04) were the top 3 that showed significant differences between the oil contaminated soil planted with alfalfa or barley and the untreated soil samples. Bacteria from the phyla Armatimonadetes, TM6, and TM7 were found to be significantly enriched only in barley planted oil contaminated soil samples compared to the untreated. SBR1093 and Armatimonadetes were found to be the most significant phyla in oil contaminated soil samples planted with alfalfa and barley respectively compared to their untreated counterparts. Interestingly, microbial population from a few phyla were also found to be enriched in all the planted soil samples compared to the clean sandy soil samples, with Verrucomicrobia being the most significant.
Among the 372 genera compared, Halorhodospira was found to be the most significantly (p-value 2.30E-06) enriched in planted oil contaminated soil group compared to the untreated soil sample group. When the planted oil contaminated and untreated soil sample groups were compared with the clean sandy soil sample group, Rubellimicrobium was found to be the most significantly enriched genus.
Analysis of sample diversity and clustering
The microbial diversity of different soil samples was studied using Alpha and Beta diversity indices. Alpha diversity indices are used to estimate the diversity within a sample, whereas, Beta diversity is used to estimate the microbial diversity across the communities or samples. Chao1 and Shannon indices were calculated using the rarefaction sampling to estimate the Alpha diversity of different soil samples. The Chao1 index is commonly used to estimate the species richness of a sample, and is based upon the number of rare classes (i.e. OTUs) found in a sample, Fig 3 and Table 6. Overall, clean sandy soil samples showed the highest richness. The species richness was also shown to be increased with increasing number of sequences for all the soil samples. The Chao1 index overall indicated a slight increase in the richness of species in oil contaminated samples planted with alfalfa or barley compared to the untreated sample groups.
CS: Clean sandy soil; BC: Control oil contaminated bulk soil without barley plants; BO: Barley planted oil contaminated rhizosphere soil; AC: Control oil contaminated bulk soil without alfalfa plants; AO: Alfalfa planted oil contaminated rhizosphere soil.
The Shannon index used to estimate the sample diversity indicated enough sampling depth at 12,000 sequences, Fig 4. The microbial diversity was found to be highest for the clean sandy soil samples, similar to sample richness index, Table 6. The diversity of the oil contaminated samples planted with barley was lower compared to the untreated soil samples, which was found to be opposite to the Chao1 richness index. For alfalfa planted soil samples the difference between the planted and untreated control was shown to be negligible.
CS: Clean sandy soil; BC: Control oil contaminated bulk soil without barley plants; BO: Barley planted oil contaminated rhizosphere soil; AC: Control oil contaminated bulk soil without alfalfa plants; AO: Alfalfa planted oil contaminated rhizosphere soil.
Beta diversity was used to estimate the sample diversity across the soil samples. To estimate the beta diversity, weighted and unweighted UniFrac distance matrix was used. PCoA plots using the unweighted UniFrac results indicated that the samples from same group clustered together, Fig 5. The oil contaminated soil samples planted with barley and alfalfa plants clustered together indicating the existence of common microorganisms. Clean sandy soil samples as expected formed a separate cluster indicating a different microbial diversity compared to other soil samples. These results were further corroborated by the UPGMA clustering, Fig 6. Heatmap using the top 25 enriched genera showed a similar pattern in oil contaminated soil samples planted with barley and alfalfa plants, Fig 7. Genera such as, Mycobacterium, Nocardia, and Halorhodospira were shown to be specifically enriched in these sample groups. Clean sandy soil clearly showed a distinct enrichment of genera such as, Afifella, Euzebya, Geodermatophilus, and Modestobacter. We found enrichment of genera Lacibacter in rhizosphere soil samples planted with barley plants. Genus Mesorhizobium was found to be specifically enriched in the oil contaminated soil samples planted with alfalfa.
CS: Clean sandy soil; BC: Control oil contaminated bulk soil without barley plants; BO: Barley planted oil contaminated rhizosphere soil; AC: Control oil contaminated bulk soil without alfalfa plants; AO: Alfalfa planted oil contaminated rhizosphere soil.
CS: Clean sandy soil; BC: Control oil contaminated bulk soil without barley plants; BO: Barley planted oil contaminated rhizosphere soil; AC: Control oil contaminated bulk soil without alfalfa plants; AO: Alfalfa planted oil contaminated rhizosphere soil.
CS: Clean sandy soil; BC: Control oil contaminated bulk soil without barley plants; BO: Barley planted oil contaminated rhizosphere soil; AC: Control oil contaminated bulk soil without alfalfa plants; AO: Alfalfa planted oil contaminated rhizosphere soil.
Discussion
The plant rhizosphere actively secretes a number of compounds that are used by the microbial communities present in the soil around the plant roots. These microorganisms help in the growth and development of the plants. Contamination of the soil with different contaminants, such as petroleum hydrocarbons may affect the microbial composition of the rhizosphere, which in turn may have adverse effects on the plant development. The use of plants in the removal of contaminants, also called as phytoremediation, has been a subject of interest among many microbiologists. Microorganisms involved in hydrocarbon degradation are well-studied microbial groups. Many bacterial, algal, and fungal genera indeed have been recognized as capable hydrocarbon degraders [23, 24]. In the current study, we used high throughput sequencing technology to explore the microbial diversity of oil contaminated soil planted with barley and alfalfa plants. We compared the microbial composition of the oil contaminated soil planted with barley and alfalfa with their untreated counterparts and clean sandy soil to understand the effect of aged crude oil on the microbial diversity of rhizosphere. The analysis clearly differentiates the microbial composition and abundance between both the soil sample groups. Study by Lupatini et. al., [25], showed that the soil samples of different farming systems are dominated by phyla such as, Proteobacteria, Bacteroidetes and Actinobacteria. The soil samples in the current study, irrespective of the treatments showed a similar microbial dominance of these phyla. However, the abundance of Proteobacteria and Bacteroidetes was comparatively more in the untreated oil contaminated soil samples in case of both the plant types.
Alfalfa plant has been used to remove contaminants in many studies [26, 27]. Kim et. al., [26] explored the rhizosphere of diesel-contaminated soils planted with alfalfa, and showed that the total microbial activity was highest in diesel-contaminated rhizosphere soils. Further, significantly more hydrocarbon-degraders were found in diesel-contaminated rhizosphere soil compared to unplanted and uncontaminated soil. Our study showed similar results for both barley and alfalfa planted rhizosphere soil samples. Oil contaminated barley planted soil showed an average increase of 45 fold, and alfalfa planted soil showed an average increase of 40 fold for the bacterial species from genus Alcanivorax, a known oil degrader. A slight increase in microbial strains of Pseudomonas was also seen in the barley planted oil contaminated soil samples. Muratova et. al., [27] showed that the changes in the microbial community under bitumen contamination does not depend only on the presence of the plant, but also on the type of plant. They also showed that the rhizosphere microflora of alfalfa had a higher degradative potential. However, our study showed a higher increase in the number of hydrocarbon degraders in the barley planted soil. The genus Aequorivita has also been proposed to have hydrocarbon degradation potential in culture media [28]. Our study showed around 52 fold enrichment of bacterial species from Aequorivita genus in the barley planted oil contaminated soil compared to the untreated samples, indicating the degradative potential of the genus in barley rhizosphere. However, the same genus was shown to be decreased by around 2 fold in the alfalfa planted oil contaminated soil. Nitrosomonas, a nitrifying bacterial genus was found to be enriched by more than 25 fold in both barley and alfalfa planted oil contaminated soil samples indicating its possible role in oil degradation. A low abundant phylum Thermi (~1.2%) showed higher fold enrichment in the oil contaminated soil samples compared to the control clean soil. In contaminated soil planted with alfalfa and barley, the enrichment was shown to be 59 and 67 fold respectively compared to their untreated counterparts. Genus B-42 from the same phylum showed a high fold enrichment of around 150 in the oil contaminated planted soil samples compared to the untreated soil samples. A few studies [29, 30] have also shown the presence of Deinococcus, a class of Thermi group, in the oil contaminated samples, however their role in oil degradation has not been established. A study by An et. al., [31] showed the role of organisms from phylum Chloroflexi in anaerobic hydrocarbon degradation. Our study indicated around 11 fold increase in the population of this phylum in the oil contaminated planted soil samples compared to the untreated samples.
Our study explored the microbial diversity of clean desert soil and untreated oil contaminated soil with oil contaminated rhizosphere soil planted with barley and alfalfa plants. We observed differences in the diversity and enrichment of microflora in the planted soil samples compared to the untreated samples. Further, the results showed variation based on the type of plant used. We identified a few known oil degrading bacterial genera, such as Alcanivorax and Aequorivita to be enriched in the oil contaminated planted soil samples. Gemmatimonadetes, a well abundant phyla across the samples, was found to be significantly enriched (p value 5.6E-05), with a high fold increase (average fold of ~25) in the oil contaminated planted soil samples compared to the untreated counterparts. A similar trend was observed with a low abundant phylum Thermi, which showed significant enrichment (p value 0.001239) with an increase of 63 fold on an average. Though a casual association of these phyla with hydrocarbon degradation cannot be ruled out, their exact role in the oil remediation needs to be evaluated further. The findings of the current study will be useful in understanding the microbial population responsible for oil degradation, and hence can be helpful in designing appropriate phytoremediation strategies for oil contaminated lands.
Supporting information
S1 File. Distribution of the microbial population at phylum and genus level across all the sequenced samples.
Number indicates the read count for a phylum/genus in each sample.
https://doi.org/10.1371/journal.pone.0202127.s001
(XLS)
S2 File. Statistically significant (student t-test, p <0.05) phylum and genus across the sample groups.
https://doi.org/10.1371/journal.pone.0202127.s002
(XLS)
Acknowledgments
The team thanks Dr. M.T. Balba for providing oil contaminated soil for the research work. We thank Dr. Kshitish Acharya and his team from Shodhaka for their contribution in the analysis of the next generation sequencing data. We thank USDA, Agriculture Research Station, WRPIS for providing alfalfa seeds for research purpose. The support lent by the management and other departments of KISR is gratefully acknowledged.
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