Co-occurrence Network Reveals the Higher Fragmentation of the Bacterial Community in Kaidu River Than Its Tributaries in Northwestern China
- PMID: 29794413
- PMCID: PMC6031398
- DOI: 10.1264/jsme2.ME17170
Co-occurrence Network Reveals the Higher Fragmentation of the Bacterial Community in Kaidu River Than Its Tributaries in Northwestern China
Abstract
Rivers and their tributaries sculpt the earth's surface, and play an important role in substance circulation and energy flow. Bacteria are involved in most biogeochemical processes in the fluvial ecosystem; however, their pattern distribution in a river and its tributaries has not yet been investigated in detail. In the present study, high-throughput sequencing was employed to examine bacterial communities and their co-occurrence networks between Kaidu River and its nine tributaries in northwestern China. The results obtained demonstrated that both bacterial communities shared a similar dominant sub-community, mainly consisting of Actinobacteria, Bacteroidetes, and Proteobacteria, with Limnohabitans and Variovorax as the dominant genera. In spite of these commonalities, bacterial community structures still significantly differed between these two habitats, which may be related to the distance-related dispersal limitation. Their co-occurrence networks were generally both positively structured. The structural analysis showed that OTUs from the same phyla were more likely to co-occur. Although the keystone genera were taxonomically different between Kaidu River and its tributaries, they both shared common trophic properties in exploiting niches under oligotrophic conditions. We noted that their relative abundances were less than 1%, indicating the over-proportional roles of rare genera in the bacterial community. In addition, the inferred networks showed less nodes and edges, but higher modularity in Kaidu River than its tributaries, suggesting the higher fragmentation of the bacterial community in the mainstream.
Keywords: Kaidu River; bacterial community; co-occurrence network; tributaries.
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References
-
- Abou-Shanab R.A.I., van Berkum P., Angle J.S. Heavy metal resistance and genotypic analysis of metal resistance genes in gram-positive and gram-negative of bacteria present in Ni-rich serpentine soil and in the rhizosphere of Alyssum murale. Chemosphere. 2007;68:360–367. - PubMed
-
- Altermatt F. Diversity in riverine metacommunities: A network perspective. Aquat Ecol. 2013;47:365–377.
-
- Aschenbrenner I.A., Cernava T., Erlacher A., et al. Differential sharing and distinct co-occurrence networks among spatially close bacterial microbia of bark, mosses and lichens. Mol Ecol. 2017;26:2826–2838. - PubMed
-
- Banerjee S., Baah-Acheamfour M., Carlyle C.N., et al. Determinants of bacterial communities in Canadian agroforestry systems. Environ Microbiol. 2015;18:1805–1816. - PubMed
-
- Banerjee S., Kirkby C.A., Schmutter D., et al. Network analysis reveals functional redundancy and keystone taxa amongst bacterial and fungal communities during organic matter decomposition in an arable soil. Soil Biol Biochem. 2016;97:188–198.
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