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...
Autores principales: | , , , , , |
---|---|
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 |