Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root Microbiome

Plant-associated microbes are critical for plant growth and survival under natural environmental conditions. To date, most plant microbiome studies involving high-throughput amplicon sequencing have focused on the relative abundance of microbial taxa. However, this technique does not assess the tota...

Full description

Bibliographic Details
Main Authors: Xiaoxuan Guo, Xiaoning Zhang, Yuan Qin, Yong-Xin Liu, Jingying Zhang, Na Zhang, Kun Wu, Baoyuan Qu, Zishan He, Xin Wang, Xinjian Zhang, Stéphane Hacquard, Xiangdong Fu, Yang Bai
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:Plant Communications
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2590346219300033
id doaj-5f92ffa278f64e51b8c7843085afe40e
record_format Article
collection DOAJ
language English
format Article
sources DOAJ
author Xiaoxuan Guo
Xiaoning Zhang
Yuan Qin
Yong-Xin Liu
Jingying Zhang
Na Zhang
Kun Wu
Baoyuan Qu
Zishan He
Xin Wang
Xinjian Zhang
Stéphane Hacquard
Xiangdong Fu
Yang Bai
spellingShingle Xiaoxuan Guo
Xiaoning Zhang
Yuan Qin
Yong-Xin Liu
Jingying Zhang
Na Zhang
Kun Wu
Baoyuan Qu
Zishan He
Xin Wang
Xinjian Zhang
Stéphane Hacquard
Xiangdong Fu
Yang Bai
Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root Microbiome
Plant Communications
microbial load
host-associated quantitative abundance profiling
root microbiome
author_facet Xiaoxuan Guo
Xiaoning Zhang
Yuan Qin
Yong-Xin Liu
Jingying Zhang
Na Zhang
Kun Wu
Baoyuan Qu
Zishan He
Xin Wang
Xinjian Zhang
Stéphane Hacquard
Xiangdong Fu
Yang Bai
author_sort Xiaoxuan Guo
title Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root Microbiome
title_short Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root Microbiome
title_full Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root Microbiome
title_fullStr Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root Microbiome
title_full_unstemmed Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root Microbiome
title_sort host-associated quantitative abundance profiling reveals the microbial load variation of root microbiome
publisher Elsevier
series Plant Communications
issn 2590-3462
publishDate 2020-01-01
description Plant-associated microbes are critical for plant growth and survival under natural environmental conditions. To date, most plant microbiome studies involving high-throughput amplicon sequencing have focused on the relative abundance of microbial taxa. However, this technique does not assess the total microbial load and the abundance of individual microbes relative to the amount of host plant tissues. Here, we report the development of a host-associated quantitative abundance profiling (HA-QAP) method that can accurately examine total microbial load and colonization of individual root microbiome members relative to host plants by the copy-number ratio of microbial marker gene to plant genome. We validate the HA-QAP method using mock experiments, perturbation experiments, and metagenomic sequencing. The HA-QAP method eliminates the generation of spurious outputs in the classical method based on microbial relative abundance, and reveals the load of root microbiome to host plants. Using the HA-QAP method, we found that the copy-number ratios of microbial marker genes to plant genome range from 1.07 to 6.61 for bacterial 16S rRNA genes and from 0.40 to 2.26 for fungal internal transcribed spacers in the root microbiome samples from healthy rice and wheat. Furthermore, using HA-QAP we found that an increase in total microbial load represents a key feature of changes in root microbiome of rice plants exposed to drought stress and of wheat plants with root rot disease, which significantly influences patterns of differential taxa and species interaction networks. Given its accuracy and technical feasibility, HA-QAP would facilitate our understanding of genuine interactions between root microbiome and plants.
topic microbial load
host-associated quantitative abundance profiling
root microbiome
url http://www.sciencedirect.com/science/article/pii/S2590346219300033
work_keys_str_mv AT xiaoxuanguo hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT xiaoningzhang hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT yuanqin hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT yongxinliu hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT jingyingzhang hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT nazhang hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT kunwu hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT baoyuanqu hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT zishanhe hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT xinwang hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT xinjianzhang hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT stephanehacquard hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT xiangdongfu hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
AT yangbai hostassociatedquantitativeabundanceprofilingrevealsthemicrobialloadvariationofrootmicrobiome
_version_ 1724721393575133184
spelling doaj-5f92ffa278f64e51b8c7843085afe40e2020-11-25T02:54:24ZengElsevierPlant Communications2590-34622020-01-0111Host-Associated Quantitative Abundance Profiling Reveals the Microbial Load Variation of Root MicrobiomeXiaoxuan Guo0Xiaoning Zhang1Yuan Qin2Yong-Xin Liu3Jingying Zhang4Na Zhang5Kun Wu6Baoyuan Qu7Zishan He8Xin Wang9Xinjian Zhang10Stéphane Hacquard11Xiangdong Fu12Yang Bai13State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, China; College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100039, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, China; College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100039, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, China; College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100039, ChinaState Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, China; College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100039, ChinaState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, ChinaShandong Provincial Key Laboratory of Applied Microbiology, Ecology Institute, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250014, ChinaMax Planck Institute for Plant Breeding Research, Cologne 50829, GermanyState Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China; Corresponding authorState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences (CAS), Beijing 100101, China; CAS-JIC Centre of Excellence for Plant and Microbial Science (CEPAMS), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences (CAS), Beijing 100101, China; College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100039, China; Corresponding authorPlant-associated microbes are critical for plant growth and survival under natural environmental conditions. To date, most plant microbiome studies involving high-throughput amplicon sequencing have focused on the relative abundance of microbial taxa. However, this technique does not assess the total microbial load and the abundance of individual microbes relative to the amount of host plant tissues. Here, we report the development of a host-associated quantitative abundance profiling (HA-QAP) method that can accurately examine total microbial load and colonization of individual root microbiome members relative to host plants by the copy-number ratio of microbial marker gene to plant genome. We validate the HA-QAP method using mock experiments, perturbation experiments, and metagenomic sequencing. The HA-QAP method eliminates the generation of spurious outputs in the classical method based on microbial relative abundance, and reveals the load of root microbiome to host plants. Using the HA-QAP method, we found that the copy-number ratios of microbial marker genes to plant genome range from 1.07 to 6.61 for bacterial 16S rRNA genes and from 0.40 to 2.26 for fungal internal transcribed spacers in the root microbiome samples from healthy rice and wheat. Furthermore, using HA-QAP we found that an increase in total microbial load represents a key feature of changes in root microbiome of rice plants exposed to drought stress and of wheat plants with root rot disease, which significantly influences patterns of differential taxa and species interaction networks. Given its accuracy and technical feasibility, HA-QAP would facilitate our understanding of genuine interactions between root microbiome and plants.http://www.sciencedirect.com/science/article/pii/S2590346219300033microbial loadhost-associated quantitative abundance profilingroot microbiome