Abstract
This is a pioneering report on the metagenomic exploration of the bacterial diversity from a busy sea port in Paradip, Odisha, India. In our study, high-throughput sequencing of community 16S rRNA gene amplicon was performed using 454 GS Junior platform. Metagenome contain 34,121 sequences with 16,677,333 bp and 56.3% G + C content. Metagenome sequences data are now available at NCBI under the Sequence Read Archive (SRA) database with accession no. SRX897055. Community metagenome sequence revealed the presence of 11,705 species belonging to 40 different phyla. Bacteroidetes (23%), Firmicutes (19%), Proteobacteria (17%), Spirochaetes (10%), Nitrospirae (8%), Actinobacteria (7%) and Acidobacteria (3%) are the predominant bacterial phyla in this port soil. Analysis of metagenomic sequences unfolded the interesting distribution of several phyla which pointed to the significant anthropogenic intervention influencing the bacterial community character of this port.
Keywords: Pyrosequencing, Bacteria, Diversity, Paradip Port, Metagenomics
| Specifications | |
|---|---|
| Organism/cell line/tissue | Paradip Port soil sediment metagenome |
| Sex | Not applicable |
| Sequencer or array type | 454 GS junior platform |
| Data format | Sff file |
| Experimental factors | Environmental sample |
| Experimental features | 16S rRNA pyrosequencing and bacterial community structure diversity analysis using MG-RAST portal |
| Consent | Not applicable |
| Sample source location | Soil sediment from Paradip Port, Odisha, India |
1. Direct link to deposited data
http://www.ncbi.nlm.nih.gov/sra/SRX897055.
Microbial ecology deals with the dynamic relationship between microorganisms and their biotic and abiotic environments, predominantly comprising the analysis of abundance, composition and activity of microbial communities. This discipline is currently undergoing a paradigm shift, driven by the development and application of genomics, transciptomics and proteomics technologies, including metagenomic tools [1]. High-throughput pyrosequencing of PCR amplicons has emerged as a valuable technique to access the huge and diverse gene pool of unculturable bacteria which led to a ‘gold rush’ in the last decade [2]. Therefore, recently metagenomic approach has been implemented for divulging the microbial diversity worldwide.
Paradip Port (20° 3′ N; 86° 55′ E) is situated at Bay of Bengal, in Odisha at the east coast of India. It is an important port and a gateway of national and international coastal trades. Significant quantity of materials exported through Paradip Port includes iron ore, manganese ore, coal, chrome ore whereas the imported materials include coking coal, petroleum, sulphuric acid etc. For coastal fishing and deep sea fishing more than 600 small fishing trawlers and about seventy large fishing trawlers are engaged through Paradip Port day in and day out. Various activities in port and harbor affect the environment specially the coastal and estuarine water, soil, sediment and air quality. In consequence polluted coastal air and sediment further affect crop, marine plants, marine animals and their habitat, finally influencing the microbiota of the ecosystem [3].
Recent developments in molecular microbial ecology have provided means to identify microbial community in different ecosystems without the need to culture the microorganisms through metagenomic approaches. Next-generation sequencing technology is being successfully applied to study bacterial diversity in different ecosystem, which has been marked as a strong pillar for the development of microbial biotechnology [4].
We investigated the prokaryotic community structure in the soil sediment of the Paradip Port by metagenomic approach (Fig. 1). Soil sediment Samples were collected in triplicate from surface sediments of the Paradip Port (20° 15′ 26″ N; 86° 39′ 44″ E).
Fig. 1.
Bacterial community structure of Paradip Port sediment metagenome.
Total metagenomic DNA was extracted by the soil DNA isolation kit (MoBio Laboratories, Carlsbad, CA). To analyze bacterial diversity, amplification of the V1–V3 region of the 16S rRNA gene was performed according to Pramanik et al. 2015 [5]. High-throughput sequencing was performed by the Pyrosequencing on a Roche 454 GS-Junior sequencing platform according to the manufacturer's protocol (454 Life Sciences, USA). Sequences were processed and analyzed with MG-RAST on-line server [6]. Bacterial species present in metagenome sequences was explored by Genome Peek online tool [7].
Soil metagenome contained 47.8 Mb data consisting of 34,121 sequences with a G + C content of 56.3%. A total of 40 phyla were detected and the dominant phyla were Bacteroidetes (23%) followed by Firmicutes (19%), Proteobacteria (17%), Spirochaetes (10%), Nitrospirae (8%), Actinobacteria (7%) and Acidobacteria (3%). Dominating bacterial species Paludibacter propionicigenes was found in our metagenomic sample which belongs to phyla Bacteroidetes (Fig. 2).
Fig. 2.

Abundance comparison among the major bacterial species found in Paradip Port sediment metagenome.
This study is a de novo reporting of bacterial communities applying high-throughput pyrosequencing methods in Paradip Port soil. The phyla Bacteroidetes and Firmicutes are potential indicators of anthropogenic intervention in the soil sediment. The excessive abundance of these phyla supports the huge anthropogenic pressure in the Paradip Port and also indicates altered eco-dynamics due to cargo handling induced pollution.
2. Nucleotide sequence accession number
Metagenome sequence data from this study were submitted to the NCBI Sequence Read Archive (SRA) under accession numbers: SRR1825760 (Paradip Port).
Acknowledgments
This work was financially supported by the NCSCM (National Centre for Sustainable Coastal Management-grant no. 21/RCO/CR/CMR/2013) under the Ministry of Environment and Forests, Government of India. The authors express their sincere thanks to Mr. Niladri Shekher Majumdar, Roche Diagnostics, for his technical support in pyrosequencing work. We are grateful to ICZM project, World Bank for providing the 454 GS Junior pyrosequencer facility to this work and Mr. Tapas Paul, Environment Specialist, for his continuous encouragement.
Contributor Information
Sanghamitra Sengupta, Email: sanghamitrasg@yahoo.com.
Dhrubajyoti Chattopadhyay, Email: djcbcg@caluniv.ac.in.
Maitree Bhattacharyya, Email: bmaitree@gmail.com.
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