Abstract

BackgroundTermites and their microbial gut symbionts are major recyclers of lignocellulosic biomass. This important symbiosis is obligate but relatively open and more complex in comparison to other well-known insect symbioses such as the strict vertical transmission of Buchnera in aphids. The relative roles of vertical inheritance and environmental factors such as diet in shaping the termite gut microbiome are not well understood.ResultsThe gut microbiomes of 66 specimens representing seven higher and nine lower termite genera collected in Australia and North America were profiled by small subunit (SSU) rRNA amplicon pyrosequencing. These represent the first reported culture-independent gut microbiome data for three higher termite genera: Tenuirostritermes, Drepanotermes, and Gnathamitermes; and two lower termite genera: Marginitermes and Porotermes. Consistent with previous studies, bacteria comprise the largest fraction of termite gut symbionts, of which 11 phylotypes (6 Treponema, 1 Desulfarculus-like, 1 Desulfovibrio, 1 Anaerovorax-like, 1 Sporobacter-like, and 1 Pirellula-like) were widespread occurring in ≥50% of collected specimens. Archaea are generally considered to comprise only a minority of the termite gut microbiota (<3%); however, archaeal relative abundance was substantially higher and variable in a number of specimens including Macrognathotermes, Coptotermes, Schedorhinotermes, Porotermes, and Mastotermes (representing up to 54% of amplicon reads). A ciliate related to Clevelandella was detected in low abundance in Gnathamitermes indicating that protists were either reacquired after protists loss in higher termites or persisted in low numbers across this transition. Phylogenetic analyses of the bacterial communities indicate that vertical inheritance is the primary force shaping termite gut microbiota. The effect of diet is secondary and appears to influence the relative abundance, but not membership, of the gut communities.ConclusionsVertical inheritance is the primary force shaping the termite gut microbiome indicating that species are successfully and faithfully passed from one generation to the next via trophallaxis or coprophagy. Changes in relative abundance can occur on shorter time scales and appear to be an adaptive mechanism for dietary fluctuations.Electronic supplementary materialThe online version of this article (doi:10.1186/s40168-015-0067-8) contains supplementary material, which is available to authorized users.

Highlights

  • Termites and their microbial gut symbionts are major recyclers of lignocellulosic biomass

  • Using culture-independent small subunit (SSU) small subunit ribosomal RNA (rRNA)-based community profiling, Ley et al [3,4] found that both host phylogeny and diet shape gut microbiomes in many mammalian species and Ochman et al concluded that vertical inheritance of gut microbiota in primates is discernable over evolutionary time scales [5]

  • All other cytochrome oxidase II (COII) sequences obtained from the collected specimens, including cockroach outgroups, are grouped with reference sequences belonging to the expected genera predicted by morphology (Additional file 2: Figure S1)

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Summary

Introduction

Termites and their microbial gut symbionts are major recyclers of lignocellulosic biomass This important symbiosis is obligate but relatively open and more complex in comparison to other well-known insect symbioses such as the strict vertical transmission of Buchnera in aphids. Termites are thought to have evolved from a cockroach-like ancestor into strictly eusocial insects that feed exclusively on lignocellulosic biomass [7] Such recalcitrant substrates are digested through an obligate symbiosis with specialized gut microbiota comprising bacteria and protists in lower termites (classified into eight families) and bacteria only, in more recently evolved higher termites (classified in a single family, the Termitidae) [8]. To determine whether vertical inheritance is the dominant force shaping termite gut communities more broadly, we used SSU rRNA gene amplicon pyrosequencing to profile the gut microbiomes of 66 termite samples, representing 16 genera, obtained in Australia and North America. These data expand current knowledge of termite gut microbiome diversity and represent the first gut community profiles for three higher (Tenuirostritermes, Drepanotermes, Gnathamitermes) and two lower (Marginitermes, Porotermes) termite genera

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