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Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales

It has been widely accepted that there is a distance‐decay pattern in the soil microbiome. However, few studies have attempted to interpret the microbial distance‐decay pattern from the perspective of quantifying underlying processes. In this study, we examined the processes governing bacterial comm...

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Autores principales: Feng, Maomao, Tripathi, Binu M., Shi, Yu, Adams, Jonathan M., Zhu, Yong‐Guan, Chu, Haiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741136/
https://www.ncbi.nlm.nih.gov/pubmed/31074596
http://dx.doi.org/10.1002/mbo3.851
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author Feng, Maomao
Tripathi, Binu M.
Shi, Yu
Adams, Jonathan M.
Zhu, Yong‐Guan
Chu, Haiyan
author_facet Feng, Maomao
Tripathi, Binu M.
Shi, Yu
Adams, Jonathan M.
Zhu, Yong‐Guan
Chu, Haiyan
author_sort Feng, Maomao
collection PubMed
description It has been widely accepted that there is a distance‐decay pattern in the soil microbiome. However, few studies have attempted to interpret the microbial distance‐decay pattern from the perspective of quantifying underlying processes. In this study, we examined the processes governing bacterial community assembly at multiple spatial scales in maize fields of Northeast China using Illumina MiSeq sequencing. Results showed that the processes governing spatial turnover in bacterial community composition shifted regularly with spatial scale, with homogenizing dispersal dominating at small spatial scales and variable selection dominating at larger scales, which in turn explained the distance‐decay pattern that closer located sites tended to have higher community similarity. Together, homogenizing dispersal and dispersal limitation resulting from geographic factors governed about 33% of spatial turnover in bacterial community composition. Deterministic selection processes had the strongest influence, at 57%, with biotic factors and abiotic environmental filtering (mainly imposed by soil pH) respectively contributing about 37% and 63% of variation. Our results provided a novel and comprehensive way to explain the distance‐decay pattern of soil microbiome via quantifying the assembly processes at multiple spatial scales, as well as the method to quantify the influence of abiotic, biotic, and geographic factors in shaping microbial community structure, thus enabling understanding of widely acknowledged microbial biogeographic patterns and microbial ecology.
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spelling pubmed-67411362019-09-13 Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales Feng, Maomao Tripathi, Binu M. Shi, Yu Adams, Jonathan M. Zhu, Yong‐Guan Chu, Haiyan Microbiologyopen Original Articles It has been widely accepted that there is a distance‐decay pattern in the soil microbiome. However, few studies have attempted to interpret the microbial distance‐decay pattern from the perspective of quantifying underlying processes. In this study, we examined the processes governing bacterial community assembly at multiple spatial scales in maize fields of Northeast China using Illumina MiSeq sequencing. Results showed that the processes governing spatial turnover in bacterial community composition shifted regularly with spatial scale, with homogenizing dispersal dominating at small spatial scales and variable selection dominating at larger scales, which in turn explained the distance‐decay pattern that closer located sites tended to have higher community similarity. Together, homogenizing dispersal and dispersal limitation resulting from geographic factors governed about 33% of spatial turnover in bacterial community composition. Deterministic selection processes had the strongest influence, at 57%, with biotic factors and abiotic environmental filtering (mainly imposed by soil pH) respectively contributing about 37% and 63% of variation. Our results provided a novel and comprehensive way to explain the distance‐decay pattern of soil microbiome via quantifying the assembly processes at multiple spatial scales, as well as the method to quantify the influence of abiotic, biotic, and geographic factors in shaping microbial community structure, thus enabling understanding of widely acknowledged microbial biogeographic patterns and microbial ecology. John Wiley and Sons Inc. 2019-05-10 /pmc/articles/PMC6741136/ /pubmed/31074596 http://dx.doi.org/10.1002/mbo3.851 Text en © 2019 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Feng, Maomao
Tripathi, Binu M.
Shi, Yu
Adams, Jonathan M.
Zhu, Yong‐Guan
Chu, Haiyan
Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
title Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
title_full Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
title_fullStr Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
title_full_unstemmed Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
title_short Interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
title_sort interpreting distance‐decay pattern of soil bacteria via quantifying the assembly processes at multiple spatial scales
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741136/
https://www.ncbi.nlm.nih.gov/pubmed/31074596
http://dx.doi.org/10.1002/mbo3.851
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