Abstract

Growing evidence points out that the capacity of organisms to acclimate or adapt to new habitat conditions basically depends on their phenomic plasticity attributes, of which their gut commensal microbiota might be an essential impact factor. Especially in aquatic organisms, which are in direct and continual contact with the aquatic environment, the complex and dynamic microbiota have significant effects on health and development. However, an understanding of the relative contribution of internal sorting (host genetic) and colonization (environmental) processes is still unclear. To understand how microbial communities differ in response to rapid environmental change, we surveyed and studied the environmental and gut microbiota of native and habitat-exchanged shrimp (Macrobrachium nipponense) using 16S rRNA amplicon sequencing on the Illumina MiSeq platform. Corresponding with microbial diversity of their living water areas, the divergence in gut microbes of lake-to-river shrimp (CK) increased, while that of river-to-lake shrimp (KC) decreased. Importantly, among the candidate environment specific gut microbes in habitat-exchanged shrimp, over half of reads were associated with the indigenous bacteria in native shrimp gut, yet more candidates presented in CK may reflect the complexity of new environment. Our results suggest that shrimp gut microbiota has high plasticity when its host faces environmental changes, even over short timescales. Further, the changes in external environment might influence the gut microbiome not just by providing environment-associated microbes directly, but also by interfering with the composition of indigenous gut bacteria indirectly.

Highlights

  • ObjectivesWe aimed to determine whether the microbial diversity in gut, which potentially reflects the host phenomic plasticity, varies in response to the environmental type

  • Animals live in intimate association with diverse communities of symbiotic microorganisms [1, 2]

  • We found that when shrimp were exposed to a new habitat with higher microbial biodiversity, both environmental and indigenous gut microbes contribute to the plasticity of shrimp gut microbiome, leading to higher composition variation and divergence among individuals; yet when shrimp were transplanted to an environment with lower microbial diversity, only indigenous gut microbiota function as a major contributor, leading to a convergence of between-host diversity

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Summary

Objectives

We aimed to determine whether the microbial diversity in gut, which potentially reflects the host phenomic plasticity, varies in response to the environmental type

Methods
Results
Conclusion
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