Biodiversity Data Journal : OMIC Data Paper
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OMIC Data Paper
Revealing the active microbiome connected with the rhizosphere soil of maize plants in Ventersdorp, South Africa
expand article infoOlubukola O. Babalola, Rebaona R. Molefe, Adenike E. Amoo
‡ Food Security and Safety Niche, Faculty of Natural and Agricultural Sciences, North-West University, Private Bag X2046, Mafikeng, South Africa
Open Access

Abstract

We conducted shotgun metagenomics sequencing of the maize rhizosphere and bulk soils in Ventersdorp, South Africa. Information on the structural composition and functional capabilities of microbial communities in the maize rhizosphere are provided by the data. Characterising the functional potentials of rhizosphere microbiomes gives an opportunity to link the microbiome to plant growth and health and provides the possibility of discovering new plant-beneficial genes that could enhance agricultural sustainability.

Keywords

Illumina sequencing, metagenomics, rhizosphere, maize plants

Introduction

Maize is one of South Africa's most economically-valuable crops. Globally, it fills the diets of billions of people with basic carbohydrates. Poor management practices, such as over-fertilisation, have gone up significantly due to the quest to feed the ever-increasing human population. Therefore, it is imperative to identify eco-friendly fertilisers that do not have adverse effects on soil and maize development. Plants establish associations with soil microorganisms for various functions including nutrient cycling, stress tolerance and pathogen immunity (Liu et al. 2019). Increased knowledge of these mechanisms is a productive and positive way for the improvement of sustainable agriculture (Babalola et al. 2021).

The rhizosphere, which is the medium between plants and soil, has been labelled a 'hotspot' for new genes and biomolecules (Babalola et al. 2020). Plant-root exudates generate nourishing conditions for microbial growth and easily attract a selection of soil microorganisms (Adedeji and Babalola 2020; Canarini et al. 2019; Chukwuneme et al. 2021). Microbial communities in the rhizosphere are recruited from the large and diverse pool of microbes in bulk soils through root exudate chemical signalling (Adedeji and Babalola 2020;Hartman and Tringe 2019). This has contributed to an increase in microbial activity and quantity in rhizosphere soils compared to bulk soils. In contrast, microbial diversity significantly reduces in the rhizosphere soil relative to bulk soil (Praeg et al. 2019; Hartman and Tringe 2019).

Rhizosphere microbes exist to protect against pathogens and improve growth by developing phytohormones. These organisms enable plants to handle environmental disruptions, such as irregular climate-related changes in temperature, drought and salinity (Lu et al. 2018). It has been shown that nitrogen-fixing rhizobia and the mycorrhizal fungi in the rhizosphere have significant impacts on plant nutrient status (Mendes et al. 2013; Lu et al. 2018). For example, symbiotics, such as mycorrhizal fungi, are important for the absorption of nutrients and minerals from the soil to plants. Therefore, studies on the rhizospheric microbes and their functions could open several appealing features, from alleviating several of the consequences of climate change and environmental stress on plants by modifying plant features using microbial inocula to enhancing crop production. Therefore, the discovery of new genes in the maize rhizosphere could be an incentive to fix food insecurity and promote agricultural sustainability.

Value of the dataset

The dataset contains raw sequences (FASTQ format files) obtained using shotgun metagenomic sequencing of the maize rhizosphere and bulk soils. Samples were collected from the maize rhizosphere (F3R1) and bulk (F3B1) soils to understand the microbial community structure, function and plant-beneficial genes in maize plantations. These data can be used alone or along with other datasets to achieve a larger scale view with more power for maize-associated microbiome research.

Methods

Sampling

Soil samples were collected from the rhizosphere soil (F3R1) and the bulk soil (F3B1) of maize plants on 16 June 2019 from a farm situated at Ventersdorp, South Africa. The rhizosphere soil samples were collected at 8 cm diameter, 15 cm depth of maize plants. The bulk soils were also collected within the maize farms.

Environmental profile

The maize field being investigated in this study is a private farm in Ventersdorp in the North West Province of South Africa. The farm was intentionally selected, based on the geographic location and the availability of maize plants. Ventersdorp has summer temperatures ranging from 17ºC to 31ºC and winter temperatures ranging from 3ºC to 21ºC. The annual rainfall ranges between 300 mm and 600 mm with more rain falling in summer than in winter.

Geographic range

Ventersdorp, North West Province (approximately 26°19'36.9''S, 26°53'19.1''E). Coordinates: -26°18'60.00''S; 26°48'59.99''E.

Sample processing

The soil samples were transported to the laboratory on ice and stored until further use. Genomic DNA extraction was conducted using the DNeasy PowerSoil® DNA isolation kit (MoBio Laboratories, Carlsbad, CA) in accordance with the manufacturer's directions. The extracted DNA was sent for shotgun metagenome sequencing to the Molecular Research Laboratory (www.mrdnalab.com) in Texas, USA. The initial concentration of DNA was evaluated using the Qubit® dsDNA HS Assay Kit (Life Technologies). The libraries were prepared using Nextera DNA Flex library preparation kit (Illumina), following the manufacturer's user guide. Using 50 ng of DNA from each sample, libraries were prepared according to the Illumina NovaSeq DNA library preparation protocol. The determination of library average insert size was determined using the Agilent 2100 Bioanalyzer (Agilent Technologies). The library insert size ranged from 617 bp to 873 bp. The libraries were pooled, diluted (to 0.6 nM) and sequenced paired-end for 300 cycles using the NovaSeq system (Illumina).

Data processing

The raw metagenome sequences were subjected to quality control using Metagenomic Rapid Annotations using Subsystems Technology (MG-RAST) online server (Meyer et al. 2008). This resulted in evacuation of artificial sequences generated by sequencing errors, exclusion of sequences of host-specific organisms, unclear base filtering (abolition of sequences of > 5 questionable base pairs with a cut-off score of 15 Q) and filtering of length (abolition of sequences of > 2 standard deviations from mean length). Following the quality control (QC), the sequences were annotated using the BLAT (the BLAST-like alignment tool) algorithm (Kent 2002) against the M5NR database (Wilke et al. 2012), which provides a non-redundant integration of many databases. For taxonomic profiling of microbial communities, the SEED subsystem was used and evaluation of their functional profiles was performed using SEED subsystem level 1. The subsystem database revealed bacteria (98.76%) had the highest taxonomical representation compared with eukaryote (0.72%) and archaea (0.73%). Annotation revealed that F3R1 had 15,713,893 sequences totalling 2,338,704,495 bp size and 64.11% G+C content. F3B1 had 12,463,113 sequences totalling 1,850,061,852 bp size and G+C 66.11%.

Technologies used

MG-RAST (https://mg-rast.org).

Source: The National Human Genome Research Institute (NHGRI)

Biodiversity scope

The maize rhizosphere soil sample had more microorganisms than the bulk soil sample.

Target

The rhizosphere microbiome and their functional potentials.

Taxonomic range

All soil microbiomes were identified to genus or species level. The study revealed that the most abundant phyla were Proteobacteria and Actinobacteria in the rhizosphere and bulk soils. Ascomycota and Basidiomycota were distributed fungal reads, while Thauarcheota and Euyarchaeota were distributed as archaeal reads, respectively, but with an abundance of < 1%.Table 1

Table 1.

Taxonomic classification of microorganisms in the maize rhizosphere and bulk soils

Domain

Phyla

F3R1

F3B1

Bacteria

Acidobacteria

368735

226709

Bacteria

Actinobacteria

2511153

2794515

Bacteria

Aquificae

15800

10882

Bacteria

Bacteroidetes

347509

261611

Bacteria

Candidatus Poribacteria

3480

1944

Bacteria

Chlamydiae

6644

4512

Bacteria

Chlorobi

35848

24915

Bacteria

Chloroflexi

203916

170908

Bacteria

Chrysiogenetes

2318

1452

Bacteria

Cyanobacteria

190459

138395

Bacteria

Deferribacteres

6452

4206

Bacteria

Deinococcus-Thermus

66466

56965

Bacteria

Dictyoglomi

4479

3216

Bacteria

Elusimicrobia

1759

1224

Bacteria

Fibrobacteres

1452

1021

Bacteria

Firmicutes

393062

304682

Bacteria

Fusobacteria

5707

4073

Bacteria

Gemmatimonadetes

153957

140020

Bacteria

Lentisphaerae

4635

3029

Bacteria

Nitrospirae

27120

15636

Bacteria

Planctomycetes

185528

121559

Bacteria

Proteobacteria

3443718

2362316

Bacteria

Spirochaetes

17790

12214

Bacteria

Synergistetes

9010

6373

Bacteria

Tenericutes

1687

1121

Bacteria

Thermotogae

15919

11866

Bacteria

Verrucomicrobia

179156

100394

Bacteria

unclassified (derived from Bacteria)

22169

18869

Fungi

Ascomycota

30221

31523

Fungi

Basidiomycota

3615

2657

Fungi

Blastocladiomycota

14

20

Fungi

Chytridiomycota

44

32

Fungi

Glomeromycota

38

6

Fungi

Microsporidia

121

57

Fungi

unclassified (derived from Fungi)

43

20

Archaea

Crenarchaeota

10423

7705

Archaea

Euryarchaeota

59001

45925

Archaea

Korarchaeota

728

451

Archaea

Nanoarchaeota

60

44

Archaea

Thaumarchaeota

6596

5229

Viruses

unclassified (derived from Viruses)

1244

1109

Functional range

The functional annotation using SEED subsystems revealed that reads were more ascribed to carbohydrates metabolism (15.76 to 15.90%), amino acids and derivatives (11.53 to 11.61%) and clustering-based systems (13.63 to 13.78%) in the maize rhizosphere and bulk soils samples.

Data Resources

Maize associated microbiome studies (Suppl. material 1).

Resource 1

Download URL

https://trace.ncbi.nlm.nih.gov/Traces/sra/?run=SRR12288319

Resource identifier

SRR12288319

Data format

FASTQ

Resource 2

Download URL

https://trace.ncbi.nlm.nih.gov/Traces/sra/?run=SRR12288317

Resource identifier

SRR12288317

Data format

FASTQ

Usage Rights

Creative Commons Public Domain Waiver (CC-Zero)

Acknowledgements

OOB would like to thank the National Research Foundation of South Africa for a grant (Grant Ref: UID123634; OOB) that has supported work in our laboratory. RRM would like to thank the North-West University for the postgraduate bursary that was granted during her MSc programme. AEA is grateful to the North-West University for postdoctoral bursary and research support.

Hosting institution

North-West University

Author contributions

All the mentioned authors contributed substantially and intellectually to the work. OOB designed the research, revised the work critically for important intellectual content, performed quality assurance, provided funding acquisition, project administration and resources. RRM was involved in data curation, formal analysis, investigation, visualisation of data and writing of the original draft of the manuscript. AEA was involved in data curation, visualisation of data, reviewing and thoroughly editing of the original draft, validation and formal analysis.

Conflicts of interest

The authors declare that they have no conflict of interest, either financial or commercial wise.

References

Supplementary material

Suppl. material 1: BioSample metadata file 
Authors:  Olubukola O. Babalola; Rebaona R. Molefe; Adenike E. Amoo
Data type:  Metagenomic data
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