Cargando…

Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host

Recent characterization of the obligate episymbiont Saccharibacteria (TM7) belonging to the candidate phyla radiation (CPR) has expanded the extent of microbial diversity. However, the episymbiotic lifestyle of TM7 is still underexploited due to the deficiency of cultivated representatives. Here, we...

Descripción completa

Detalles Bibliográficos
Autores principales: Xie, Bingliang, Wang, Jian, Nie, Yong, Tian, Jing, Wang, Zerui, Chen, Dongwei, Hu, Beiyu, Wu, Xiao-Lei, Du, Wenbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894109/
https://www.ncbi.nlm.nih.gov/pubmed/36454763
http://dx.doi.org/10.1073/pnas.2215990119
_version_ 1784881672305508352
author Xie, Bingliang
Wang, Jian
Nie, Yong
Tian, Jing
Wang, Zerui
Chen, Dongwei
Hu, Beiyu
Wu, Xiao-Lei
Du, Wenbin
author_facet Xie, Bingliang
Wang, Jian
Nie, Yong
Tian, Jing
Wang, Zerui
Chen, Dongwei
Hu, Beiyu
Wu, Xiao-Lei
Du, Wenbin
author_sort Xie, Bingliang
collection PubMed
description Recent characterization of the obligate episymbiont Saccharibacteria (TM7) belonging to the candidate phyla radiation (CPR) has expanded the extent of microbial diversity. However, the episymbiotic lifestyle of TM7 is still underexploited due to the deficiency of cultivated representatives. Here, we describe gene-targeted TM7 cultivation guided by repurposing epicPCR (emulsion, paired isolation, and concatenation PCR) to capture in situ TM7‒host associations. Using this method, we obtained a novel Saccharibacteria isolate TM7i and its host Leucobacter aridicollis J1 from Cicadae Periostracum, the castoff shell of cicada. Genomic analyses and microscopic characterizations revealed that TM7i could bind to J1 through twitching-like motility mediated by type IV pili (T4P). We further showed that the inhibition of T4P extrusion suppressed the motility and host adherence of TM7i, resulting in its reduced growth. However, the inactivation of T4P had little effect on the growth of TM7i that had already adhered to J1, suggesting the essential role of T4P in host recognition by TM7i. By capturing CPR‒host association and elaborating the T4P-dependent episymbiotic association mechanism, our studies shed light on the distinct yet widespread lifestyle of CPR bacteria.
format Online
Article
Text
id pubmed-9894109
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-98941092023-02-03 Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host Xie, Bingliang Wang, Jian Nie, Yong Tian, Jing Wang, Zerui Chen, Dongwei Hu, Beiyu Wu, Xiao-Lei Du, Wenbin Proc Natl Acad Sci U S A Biological Sciences Recent characterization of the obligate episymbiont Saccharibacteria (TM7) belonging to the candidate phyla radiation (CPR) has expanded the extent of microbial diversity. However, the episymbiotic lifestyle of TM7 is still underexploited due to the deficiency of cultivated representatives. Here, we describe gene-targeted TM7 cultivation guided by repurposing epicPCR (emulsion, paired isolation, and concatenation PCR) to capture in situ TM7‒host associations. Using this method, we obtained a novel Saccharibacteria isolate TM7i and its host Leucobacter aridicollis J1 from Cicadae Periostracum, the castoff shell of cicada. Genomic analyses and microscopic characterizations revealed that TM7i could bind to J1 through twitching-like motility mediated by type IV pili (T4P). We further showed that the inhibition of T4P extrusion suppressed the motility and host adherence of TM7i, resulting in its reduced growth. However, the inactivation of T4P had little effect on the growth of TM7i that had already adhered to J1, suggesting the essential role of T4P in host recognition by TM7i. By capturing CPR‒host association and elaborating the T4P-dependent episymbiotic association mechanism, our studies shed light on the distinct yet widespread lifestyle of CPR bacteria. National Academy of Sciences 2022-12-01 2022-12-06 /pmc/articles/PMC9894109/ /pubmed/36454763 http://dx.doi.org/10.1073/pnas.2215990119 Text en Copyright © 2022 the Author(s). Published by PNAS.2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Xie, Bingliang
Wang, Jian
Nie, Yong
Tian, Jing
Wang, Zerui
Chen, Dongwei
Hu, Beiyu
Wu, Xiao-Lei
Du, Wenbin
Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host
title Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host
title_full Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host
title_fullStr Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host
title_full_unstemmed Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host
title_short Type IV pili trigger episymbiotic association of Saccharibacteria with its bacterial host
title_sort type iv pili trigger episymbiotic association of saccharibacteria with its bacterial host
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894109/
https://www.ncbi.nlm.nih.gov/pubmed/36454763
http://dx.doi.org/10.1073/pnas.2215990119
work_keys_str_mv AT xiebingliang typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT wangjian typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT nieyong typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT tianjing typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT wangzerui typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT chendongwei typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT hubeiyu typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT wuxiaolei typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost
AT duwenbin typeivpilitriggerepisymbioticassociationofsaccharibacteriawithitsbacterialhost