Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.

Although blattid cockroaches and termites share a common ancestor, their diets are distinctly different. While termites consume a highly specialized diet of lignocellulose, cockroaches are omnivorous and opportunistic feeders. The role of the termite gut microbiota has been studied intensively, but...

Full description

Bibliographic Details
Main Authors: Christine Schauer, Claire Thompson, Andreas Brune
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3893267?pdf=render
id doaj-2be74760d3ed4fca9a04719c5e830acd
record_format Article
spelling doaj-2be74760d3ed4fca9a04719c5e830acd2020-11-25T01:23:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8586110.1371/journal.pone.0085861Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.Christine SchauerClaire ThompsonAndreas BruneAlthough blattid cockroaches and termites share a common ancestor, their diets are distinctly different. While termites consume a highly specialized diet of lignocellulose, cockroaches are omnivorous and opportunistic feeders. The role of the termite gut microbiota has been studied intensively, but little is known about the cockroach gut microbiota and its function in digestion and nutrition, particularly the adaptation to different diets. Our analyses of the bacterial gut microbiota of the blattid cockroach Shelfordella lateralis combining terminal restriction fragment length polymorphism of their 16S rRNA genes with physiological parameters (microbial metabolites, hydrogen and methane emission) indicated substantial variation between individuals but failed to identify any diet-related response. Subsequent deep-sequencing of the 16S rRNA genes of the colonic gut microbiota of S. lateralis fed either a high- or a low-fiber diet confirmed the absence of bacterial taxa that responded to diet. Instead, we found a small number of abundant phylotypes that were consistently present in all samples and made up half of the community in both diet groups. They varied strongly in abundance between individual samples at the genus but not at the family level. The remaining phylotypes were inconsistently present among replicate batches. Our findings suggest that S. lateralis harbors a highly dynamic core gut microbiota that is maintained even after fundamental dietary shifts, and that any dietary effects on the gut community are likely to be masked by strong individual variations.http://europepmc.org/articles/PMC3893267?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Christine Schauer
Claire Thompson
Andreas Brune
spellingShingle Christine Schauer
Claire Thompson
Andreas Brune
Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.
PLoS ONE
author_facet Christine Schauer
Claire Thompson
Andreas Brune
author_sort Christine Schauer
title Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.
title_short Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.
title_full Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.
title_fullStr Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.
title_full_unstemmed Pyrotag sequencing of the gut microbiota of the cockroach Shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.
title_sort pyrotag sequencing of the gut microbiota of the cockroach shelfordella lateralis reveals a highly dynamic core but only limited effects of diet on community structure.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Although blattid cockroaches and termites share a common ancestor, their diets are distinctly different. While termites consume a highly specialized diet of lignocellulose, cockroaches are omnivorous and opportunistic feeders. The role of the termite gut microbiota has been studied intensively, but little is known about the cockroach gut microbiota and its function in digestion and nutrition, particularly the adaptation to different diets. Our analyses of the bacterial gut microbiota of the blattid cockroach Shelfordella lateralis combining terminal restriction fragment length polymorphism of their 16S rRNA genes with physiological parameters (microbial metabolites, hydrogen and methane emission) indicated substantial variation between individuals but failed to identify any diet-related response. Subsequent deep-sequencing of the 16S rRNA genes of the colonic gut microbiota of S. lateralis fed either a high- or a low-fiber diet confirmed the absence of bacterial taxa that responded to diet. Instead, we found a small number of abundant phylotypes that were consistently present in all samples and made up half of the community in both diet groups. They varied strongly in abundance between individual samples at the genus but not at the family level. The remaining phylotypes were inconsistently present among replicate batches. Our findings suggest that S. lateralis harbors a highly dynamic core gut microbiota that is maintained even after fundamental dietary shifts, and that any dietary effects on the gut community are likely to be masked by strong individual variations.
url http://europepmc.org/articles/PMC3893267?pdf=render
work_keys_str_mv AT christineschauer pyrotagsequencingofthegutmicrobiotaofthecockroachshelfordellalateralisrevealsahighlydynamiccorebutonlylimitedeffectsofdietoncommunitystructure
AT clairethompson pyrotagsequencingofthegutmicrobiotaofthecockroachshelfordellalateralisrevealsahighlydynamiccorebutonlylimitedeffectsofdietoncommunitystructure
AT andreasbrune pyrotagsequencingofthegutmicrobiotaofthecockroachshelfordellalateralisrevealsahighlydynamiccorebutonlylimitedeffectsofdietoncommunitystructure
_version_ 1725123305676996608