Cargando…

Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont

Many ecological and evolutionary processes in animals depend upon microbial symbioses. In spiders, the role of the microbiome in these processes remains mostly unknown. We compared the microbiome between populations, individuals, and tissue types of a range-expanding spider, using 16S rRNA gene sequ...

Descripción completa

Detalles Bibliográficos
Autores principales: Sheffer, Monica M., Uhl, Gabriele, Prost, Stefan, Lueders, Tillmann, Urich, Tim, Bengtsson, Mia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023434/
https://www.ncbi.nlm.nih.gov/pubmed/31861544
http://dx.doi.org/10.3390/microorganisms8010008
_version_ 1783498249051570176
author Sheffer, Monica M.
Uhl, Gabriele
Prost, Stefan
Lueders, Tillmann
Urich, Tim
Bengtsson, Mia M.
author_facet Sheffer, Monica M.
Uhl, Gabriele
Prost, Stefan
Lueders, Tillmann
Urich, Tim
Bengtsson, Mia M.
author_sort Sheffer, Monica M.
collection PubMed
description Many ecological and evolutionary processes in animals depend upon microbial symbioses. In spiders, the role of the microbiome in these processes remains mostly unknown. We compared the microbiome between populations, individuals, and tissue types of a range-expanding spider, using 16S rRNA gene sequencing. Our study is one of the first to go beyond targeting known endosymbionts in spiders and characterizes the total microbiome across different body compartments (leg, prosoma, hemolymph, book lungs, ovaries, silk glands, midgut, and fecal pellets). Overall, the microbiome differed significantly between populations and individuals, but not between tissue types. The microbiome of the wasp spider Argiope bruennichi features a novel dominant bacterial symbiont, which is abundant in every tissue type in spiders from geographically distinct populations and that is also present in offspring. The novel symbiont is affiliated with the Tenericutes, but has low sequence identity (<85%) to all previously named taxa, suggesting that the novel symbiont represents a new bacterial clade. Its presence in offspring implies that it is vertically transmitted. Our results shed light on the processes that shape microbiome differentiation in this species and raise several questions about the implications of the novel dominant bacterial symbiont on the biology and evolution of its host.
format Online
Article
Text
id pubmed-7023434
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-70234342020-03-12 Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont Sheffer, Monica M. Uhl, Gabriele Prost, Stefan Lueders, Tillmann Urich, Tim Bengtsson, Mia M. Microorganisms Article Many ecological and evolutionary processes in animals depend upon microbial symbioses. In spiders, the role of the microbiome in these processes remains mostly unknown. We compared the microbiome between populations, individuals, and tissue types of a range-expanding spider, using 16S rRNA gene sequencing. Our study is one of the first to go beyond targeting known endosymbionts in spiders and characterizes the total microbiome across different body compartments (leg, prosoma, hemolymph, book lungs, ovaries, silk glands, midgut, and fecal pellets). Overall, the microbiome differed significantly between populations and individuals, but not between tissue types. The microbiome of the wasp spider Argiope bruennichi features a novel dominant bacterial symbiont, which is abundant in every tissue type in spiders from geographically distinct populations and that is also present in offspring. The novel symbiont is affiliated with the Tenericutes, but has low sequence identity (<85%) to all previously named taxa, suggesting that the novel symbiont represents a new bacterial clade. Its presence in offspring implies that it is vertically transmitted. Our results shed light on the processes that shape microbiome differentiation in this species and raise several questions about the implications of the novel dominant bacterial symbiont on the biology and evolution of its host. MDPI 2019-12-19 /pmc/articles/PMC7023434/ /pubmed/31861544 http://dx.doi.org/10.3390/microorganisms8010008 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sheffer, Monica M.
Uhl, Gabriele
Prost, Stefan
Lueders, Tillmann
Urich, Tim
Bengtsson, Mia M.
Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont
title Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont
title_full Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont
title_fullStr Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont
title_full_unstemmed Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont
title_short Tissue- and Population-Level Microbiome Analysis of the Wasp Spider Argiope bruennichi Identified a Novel Dominant Bacterial Symbiont
title_sort tissue- and population-level microbiome analysis of the wasp spider argiope bruennichi identified a novel dominant bacterial symbiont
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023434/
https://www.ncbi.nlm.nih.gov/pubmed/31861544
http://dx.doi.org/10.3390/microorganisms8010008
work_keys_str_mv AT sheffermonicam tissueandpopulationlevelmicrobiomeanalysisofthewaspspiderargiopebruennichiidentifiedanoveldominantbacterialsymbiont
AT uhlgabriele tissueandpopulationlevelmicrobiomeanalysisofthewaspspiderargiopebruennichiidentifiedanoveldominantbacterialsymbiont
AT proststefan tissueandpopulationlevelmicrobiomeanalysisofthewaspspiderargiopebruennichiidentifiedanoveldominantbacterialsymbiont
AT luederstillmann tissueandpopulationlevelmicrobiomeanalysisofthewaspspiderargiopebruennichiidentifiedanoveldominantbacterialsymbiont
AT urichtim tissueandpopulationlevelmicrobiomeanalysisofthewaspspiderargiopebruennichiidentifiedanoveldominantbacterialsymbiont
AT bengtssonmiam tissueandpopulationlevelmicrobiomeanalysisofthewaspspiderargiopebruennichiidentifiedanoveldominantbacterialsymbiont