Novel bacteriocyte-associated pleomorphic symbiont of the grain pest beetle Rhyzopertha dominica (Coleoptera: Bostrichidae)
© The Author(s). 2017
Received: 7 July 2017
Accepted: 7 August 2017
Published: 19 August 2017
The lesser grain borer Rhyzopertha dominica (Coleoptera: Bostrichidae) is a stored-product pest beetle. Early histological studies dating back to 1930s have reported that R. dominica and other bostrichid species possess a pair of oval symbiotic organs, called the bacteriomes, in which the cytoplasm is densely populated by pleomorphic symbiotic bacteria of peculiar rosette-like shape. However, the microbiological nature of the symbiont has remained elusive.
Here we investigated the bacterial symbiont of R. dominica using modern molecular, histological, and microscopic techniques. Whole-mount fluorescence in situ hybridization specifically targeting symbiotic bacteria consistently detected paired bacteriomes, in which the cytoplasm was full of pleomorphic bacterial cells, in the abdomen of adults, pupae and larvae, confirming previous histological descriptions. Molecular phylogenetic analysis identified the symbiont as a member of the Bacteroidetes, in which the symbiont constituted a distinct bacterial lineage allied to a variety of insect-associated endosymbiont clades, including Uzinura of diaspidid scales, Walczuchella of giant scales, Brownia of root mealybugs, Sulcia of diverse hemipterans, and Blattabacterium of roaches. The symbiont gene exhibited markedly AT-biased nucleotide composition and significantly accelerated molecular evolution, suggesting degenerative evolution of the symbiont genome. The symbiotic bacteria were detected in oocytes and embryos, confirming continuous host–symbiont association and vertical symbiont transmission in the host life cycle.
We demonstrate that the symbiont of R. dominica constitutes a novel bacterial lineage in the Bacteroidetes. We propose that reductive evolution of the symbiont genome may be relevant to the amorphous morphology of the bacterial cells via disruption of genes involved in cell wall synthesis and cell division. Genomic and functional aspects of the host-symbiont relationship deserve future studies.
Many insects harbor symbiotic bacteria in their gut, body cavity, and/or cells . Some bacterial symbionts are indispensable for the growth, survival, and reproduction of their insect hosts through synthesizing essential nutrients [2, 3], assisting food digestion [4, 5], or providing food sources [6, 7]. Other bacterial symbionts are not essential, but nonetheless influence a variety of host biological traits, such as susceptibility to natural enemies [8, 9], tolerance to environmental stresses [10, 11], resistance to noxious chemicals [12, 13], adaptation to specific food plants [14, 15], or sex ratios and related reproductive traits [16, 17]. The most intimate host–symbiont associations often involve development of a specific symbiotic organ, called the bacteriome, consisting of specialized cells for symbiosis, called the bacteriocytes, the cytoplasm of which harbors symbiotic bacteria [1, 18, 19].
Beetles, comprising the largest insect order Coleoptera, are characterized by sclerotized exoskeleton, including thick and hard forewings, known as elytra . Some beetles cause significant damage to stored cereals, beans, seeds, spices, dried fruits, and other durable commodities, and are thus regarded as stored-product pests [21, 22]. Probably relevant to their peculiar ecological niche, namely continuous living on non-fresh and monotonous food sources under low-humidity conditions, many, if not all, stored-product pest beetles are associated with symbiotic microorganisms (reviewed in ). Relatively well-studied examples are the grain weevils Sitophilus oryzae, S. granarius and allied species (Curculionidae), which harbors the γ-proteobacterial endosymbiont, “Candidatus Sodalis pierantonius” in its bacteriome [23–25]; the cigarette beetle Lasioderma serricorne and the drugstore beetle Stegobium paniceum (Anobiidae) associated with yeast-like symbiotic fungi, Symbiotaphrina spp., which are found both endocellularly in intestinal epithelial cells and extracellularly in the intestinal cavity [26–28]; and the flour beetle Tribolium confusum (Tenebrionidae) infected with an α -proteobacterial Wolbachia endosymbiont that infects a variety of cells and tissues and causes reproductive phenotypes such as cytoplasmic incompatibility [29–31]. Pioneering early research also provided detailed descriptions of well-developed bacteria-containing symbiotic organs in other stored-product pests belonging to such beetle families as the Silvanidae and the Bostrichidae [32–36], but the microbiological aspects of these symbiotic relationships have remained unstudied in the decades since the original descriptions.
In the present study, we investigated the microbiological nature, fine structure, intra-host localization, and infection dynamics of the peculiar bacterial symbiont of R. dominica in detail, using modern molecular, histological and microscopic techniques.
Insect and rearing
A long-lasting laboratory strain of R. dominica RdNFRI, which is of unknown origin and has been maintained on unpolished rice grains for over 20 years, was reared at 25 °C under constant darkness and used in this study. Collection of undamaged larvae, pupae and teneral adults of R. dominica from infested rice grains is difficult (Fig. 1b), so we developed an artificial diet rearing system for that purpose. Using an electric coffee mill, 90 g of unpolished rice grains were ground into a coarse powder, which we combined with 10 g of whole wheat flour and kneaded with 100 ml of water. The resultant dough was poured into about 3 cm × 3 cm square box-shaped molds made of aluminum foil, the poured molds were dried in an heating incubator at 65 °C for two days, and biscuit-like artificial diet pieces were obtained (Fig. 1c). Adult insects fed on, dug into, oviposited on and reproduced in the artificial nutriment, and we were readily able to obtain larvae, pupae and teneral adults by breaking apart the substrate (Fig. 1d, e). In the present study, 10% whole wheat flour was used as a binding agent as well as a food substrate. The insects readily accepted nutriment pieces containing either 0% or 50% whole wheat flour. However, the 0% wheat pieces were so fragile that the insect’s feeding activity resulted in their disintegration, whereas the 50% wheat pieces were too hard to be broken by hand for the purpose of obtaining larvae and pupae. Sexing of adult insects was conducted by a squeezing method as described previously [42, 43]. The abdomen of each adult insect was gently pressed and squeezed with forceps from anterior to posterior, exposing the genitalia from the abdominal tip. Squeezing was unnecessary to discern some, if not all, adult females, as the tips of their genitalia are always slightly exposed.
Adult insects were individually dissected in 70% ethanol, and the dissected bacteriomes were subjected to DNA extraction using QIAamp DNA Mini Kit (Qiagen). A 1.5 kb region of bacterial 16S rRNA gene was amplified from the DNA samples by PCR using the primers 10FF (5′-AGT TTG ATC ATG GCT CAG GAT-3′) and 1515R (5′-GTA CGG CTA CCT TGT TAC GAC TTA G-3′)  under the temperature profile of 94 °C for 5 min followed by 35 cycles of 94 °C for 30 s, 55 °C for 30 s and 72 °C for 1 min and a final incubation at 72 °C for 5 min. A smaller 0.6 kb region of bacterial 16S rRNA gene was also amplified by PCR using the primers 16SA2 (5′-GTG CCA GCA GCC GCG GTA ATA C-3′) and 16SB2 (5′-CGA GCT GAC GAC ARC CAT GCA-3′)  under the same temperature profile. The PCR products were electrophoresed in agarose gels and stained with ethidium bromide, and the amplified bands were excised from the gels and subjected to DNA extraction using the QIAquick Gel Extraction Kit (Qiagen). The purified PCR products were cloned using pT7Blue T-vector (Novagen) and Escherichia coli competent cells, and subjected to DNA sequencing using BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems) and 3130xl Genetic Analyzer (Applied Biosystems).
Molecular phylogenetic and evolutionary analyses
Nucleotide sequences were multiple-aligned using Clustal W  implemented in MEGA v7.0.26 . The alignment was then inspected and corrected manually. Molecular phylogenetic analyses were conducted by neighbor-joining, maximum-likelihood, and Bayesian methods. Neighbor-joining phylogenies were constructed using MEGA v7.0.26  with 1000 bootstrap replicates. The best-fit substitution model for the aligned sequences was evaluated by Kakusan v4 , which selected the GTR Gamma model for both the maximum-likelihood and Bayesian methods. Maximum-likelihood phylogenies were constructed using MEGA v7.0.26  with 1000 bootstrap replicates. Bayesian phylogenies were inferred using MrBayes v3.2.6 . Relative rate tests were performed by RRTree .
For observing fresh cell images of the symbiont, the bacteriomes were dissected from teneral adult insects using fine forceps in PBS [0.8% NaCl, 0.02% KCl, 0.115% Na2HPO4 and 0.02% KH2PO4 (w/v)], placed on a glass slide with a drop of SYTOX Green (Thermo Fisher Scientific) solution (1/1000 dilution), smashed with a coverslip, and observed under an epifluorescence microscope (Axiophot, Zeiss). For whole-mount fluorescence in situ hybridization, the insect samples were processed in 70% ethanol under a dissection microscope in order to facilitate infiltration of hybridization reagents. For adult insects, all wings were removed by forceps, and a side of the abdomen was cut with a razor. As for larvae and pupae, several holes were made by a needle at the anterior and posterior regions of the body. Eggs were treated with 50% bleach for 2 min followed by thorough washing with distilled water. These pre-treated insect samples were fixed in Carnoy’s solution (60% ethanol, 30% chloroform and 10% acetic acid) for at least 1 h at room temperature, washed thoroughly with 70% ethanol, and stored in 70% ethanol at 4 °C until use.
Fluorescence in situ hybridization
Fluorescence in situ hybridization specifically targeting 16S rRNA of the symbiont was conducted essentially as described . Briefly, the samples were rehydrated with PBT [PBS containing 0.1% Tween 20 (v/v)], and hybridized with hybridization buffer [20 mM Tris-HCl (pH 8.0), 0.9 M NaCl, 0.01% sodium dodecyl sulfate and 30% formamide (w/v)] containing 100 pmol/ml probe (5′-AlexaFluor555-TAT AGT TAC CTA CTC GCA AC-3′) at room temperature overnight. After washing with PBT three times for 10 min each at room temperature, the samples were placed on glass slides, mounted in 90% glycerol, and observed under a fluorescence dissection microscope (M165FC, Leica) and/or a laser scanning confocal microscope (LSM710, Zeiss). Digital images were merged and adjusted manually using Gimp Ver. 2.8 (GNU project).
Teneral adult insects were dissected in 2.5% glutaraldehyde in 0.1 M phosphate buffer (pH 7.4), and the dissected bacteriomes were pre-fixed with the fixative at 4 °C overnight. Subsequently, the samples were post-fixed with 2% osmium tetroxide in 0.1 M phosphate buffer (pH 7.4) at 4 °C for 60 min, dehydrated through a water-ethanol series, embedded in Epon812 resin, processed into ultrathin sections (around 80 nm thick) by an ultramicrotome (EM UC7, Leica), mounted on copper meshes, stained with uranyl acetate and lead citrate, and observed under a transmission electron microscope (H-7600, Hitachi).
Results and discussion
Rosette-shaped symbiont in paired bacteriomes
In dissected teneral adult insects, paired oval bacteriomes were found in association with an anterior region of the midgut (Fig. 1f). When the dissected bacteriomes were crushed on a glass slide and observed under an epifluorescence microscope with DNA-staining fluorochrome, numerous symbiont cells of peculiar shape, flower- or rosette-like in appearance with radially connected lobes, were observed as clusters (Fig. 1g, h). It was difficult to determine whether each lobe represented a bacterial cell, each rosette constitutes a bacterial cell, or multiple rosettes are connected by thin DNA-positive filaments (presumable cytoplasmic bridges across rosettes; arrowheads in Fig. 1i, j) forming an extremely extended bacterial cell. The very peculiar morphology of these symbionts is thus consistent with early histological descriptions of the endosymbiotic system of R. dominica and other bostrichid species [34–36].
Bacterial 16S rRNA gene of the symbiont
From the dissected bacteriomes, DNA was extracted and subjected to PCR, cloning and sequencing of bacterial 16S rRNA gene, which yielded identical 1578 bp sequences from three insects (sequence accession number LC310894). BLASTN searches against the DNA databases using the sequence as query retrieved 16S rRNA gene sequences of Sulcia mulleri, the ancient endosymbiont clade associated with diverse hemipteran insects (ex. sequence accession numbers AB772235, AB772237 and AB772238) [44, 52], as the top hits. In addition, a shorter segment of 16S rRNA gene was amplified by PCR and cloned from two insects. When 12 clones from each insect were sequenced, all 24 sequences, 583 bp in size, were identical. These results indicate that a single bacterial species dominates the endosymbiotic microbiota of R. dominica.
Phylogenetic placement of the symbiont
In vivo localization and morphology of the symbiont
Infection dynamics of the symbiont
Molecular evolutionary aspects of the symbiont
Relative rate tests of 16S rRNA gene sequences of the symbiont of Rhyzopertha dominica in comparison with Sulcia symbionts and Blattabacterium symbionts
P value c
Symbiont of Rhyzopertha dominica [LC310894]
Sulcia symbionts d
Flavobacterium columnare [AB010952]
2.5 × 10−6
Symbiont of Rhyzopertha dominica [LC310894]
Blattabacterium symbionts e
Flavobacterium columnare [AB010952]
1.0 × 10−7
Sulcia symbionts d
Blattabacterium symbionts e
Flavobacterium columnare [AB010952]
Independent evolutionary origins of rosette-shaped insect symbionts
Apart from the rosette-shaped endosymbionts of the bostrichid beetles including R. dominica [34–36], an old histological study on endosymbionts of leaf beetles described a rosette-shaped bacterial symbiont associated with gut symbiotic organs and female genital accessory organs of Bromius obscurus (Coleoptera: Chrysomelidae) . The similarity of the peculiar symbiont morphology, despite the phylogenetically distant insect hosts, raises the question of whether the rosette-shaped symbiotic bacteria of bostrichid beetles are phylogenetically related to those of the chrysomelid beetle . Recently, molecular phylogenetic analyses showed that the symbiont of B. obscurus is a member of the class γ-Proteobacteria [70, 71]. We show in the present study that the symbiont of R. dominica belongs to the Bacteroidetes, which is phylogenetically distant from the γ-Proteobacteria (see Fig. 2). These results strongly suggest that the rosette-shaped pleomorphic symbionts have evolved independently from different bacterial groups in the Bostrichidae and the Chrysomelidae. Such amorphous bacterial morphology, known as the L-form, has been reported to occur when bacterial genes involved in cell wall synthesis and/or cell division are disrupted [72, 73]. Considering that both the rosette-shaped symbionts of R. dominica and B. obscurus exhibit remarkably AT-biased nucleotide compositions and significantly accelerated rates of molecular evolution  (see Fig. 2 and Table 1), the parallelism giving rise to the rosette-like bacterial shape may be attributable to degenerative evolution of the symbiont genomes.
In this study, we demonstrated that the pleomorphic symbiont of R. dominica, whose microbiological affiliation has been obscure for decades, constitutes a distinct bacterial lineage in the Bacteroidetes. The Bacteroidetes embraces a variety of endosymbiont clades associated with plant-sucking insects (Uzinura, Walczuchella and Brownia of scale insects; Sulcia of diverse hemipterans) and omnivorous/xylophagous insects (Blattabacterium of cockroaches, woodroaches and termites) . Here we add the endosymbiont of the grain-feeding insect, R. dominica, to the list of endosymbiont lineages that have evolved in the Bacteroidetes.
The peculiar rosette-like morphology of the symbiont of R. dominica is of particular interest. We found that the symbiont gene exhibits remarkably AT-biased nucleotide composition and significantly accelerated molecular evolution, which are suggestive of degenerative evolution of the symbiont genome. A morphologically similar bacterial symbiont was also reported from a chrysomelid leaf beetle , but that symbiont was recently shown to be a member of the γ-Proteobacteria [70, 71], suggesting that these rosette-shaped bacterial symbionts have independent evolutionary origins. The rosette-shaped symbiont of the leaf beetle also exhibited a remarkably AT-biased nucleotide composition and a significantly accelerated rate of molecular evolution . We speculate that the reductive genome evolution, which is universally observed in bacteriocyte-associated endosymbionts of diverse insects [2, 64], may have resulted in disruption of bacterial genes involved in cell wall synthesis and/or cell division, which may be causative of the L-form-like amorphous morphology of the symbiont cells. Genome sequencing of the symbiont of R. dominica will provide information essential to addressing this intriguing evolutionary question. Biological roles of the symbiont for R. dominica are currently unknown and to be investigated in the future, for which the symbiont genome information, in combination with physiological data on experimentally generated symbiotic and aposymbiotic insects, will provide essential clues.
In addition to R. dominica, early histological studies described diverse bostrichid species, including Apate degener, A. monachus, Bostrychoplites zickeli, Scobicia chevrieri, Sinoxylon ceratoniae and S. sexdentatus, possessing similar paired bacteriomes and pleomorphic symbiotic bacteria therein [34, 35], raising the possibility that endosymbiotic association may have been inherited from a common ancestor. Surveys of these and other diverse bostrichid species for their endosymbiotic bacteria and co-phylogenetic analysis of the host-symbiont relationships would help to provide an integrated picture of the host–symbiont co-evolutionary history in the Bostrichidae.
We thank Minoru Moriyama for insect photos.
This study was supported by JSPS Kakenhi Grant Number JP25221107 to TF.
Availability of data and materials
The nucleotide sequence determined in this study was deposited in the DNA Data Bank of Japan (http://www.ddbj.nig.ac.jp/index-e.html) under accession number LC310894.
GO contributed centrally to most of the experimental work, including molecular phylogenetic and histological characterization of the symbiont of R. dominica. RK assisted in the fluorescence in situ hybridization of the symbiont. TH and YN participated in microbiological characterization of the symbiont. XYM conducted transmission electron microscopy. NN performed molecular evolutionary analyses. AM maintained and supplied the laboratory colony of R. dominica. TF supervised the entire research project and wrote the manuscript. All authors read and approved the final manuscript.
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