Beetle Gut Research Articles

Trichosporon vanderwaltii sp. nov., an asexual basidiomycetous yeast isolated from soil and beetles

During a survey of unidentified yeast isolates deposited in the UNESCO-MIRCEN Biotechnological Yeast Culture Collection housed at the Department of Microbial, Biochemical and Food Biotechnology of the University of the Free State, one isolate obtained from soil in South Africa showed 100 % identity in D1/D2 rDNA sequence with undescribed basidiomycetous yeasts isolated from the gut of beetles from the United States of America and forest soil from Taiwan in the NCBI sequence database. Phylogenetic analyses using sequences of the D1/D2 rDNA and ITS regions indicated that all these isolates form a well-supported sub-clade that is the sister clade to the Brassicae plus Porosum clades of Trichosporon in the order Trichosporonales. Subsequent phenotypic tests revealed that asexual reproduction by budding is rare but dominated by arthroconidia resulting from segmentation of hyphae and that fusiform giant cells are characterized by budding from a broad base. These findings further suggest that these isolates belong to a single tremellomycetous yeast species for which the name Trichosporon vanderwaltii CBS 12124(T) (=NRRL Y-48732(T), =UOFS Y-1920(T)) is proposed.

The bacterium Pantoea stewartii uses two different type III secretion systems to colonize its plant host and insect vector.

Plant- and animal-pathogenic bacteria utilize phylogenetically distinct type III secretion systems (T3SS) that produce needle-like injectisomes or pili for the delivery of effector proteins into host cells. Pantoea stewartii subsp. stewartii (herein referred to as P. stewartii), the causative agent of Stewart's bacterial wilt and leaf blight of maize, carries phylogenetically distinct T3SSs. In addition to an Hrc-Hrp T3SS, known to be essential for maize pathogenesis, P. stewartii has a second T3SS (Pantoea secretion island 2 [PSI-2]) that is required for persistence in its flea beetle vector, Chaetocnema pulicaria (Melsh). PSI-2 belongs to the Inv-Mxi-Spa T3SS family, typically found in animal pathogens. Mutagenesis of the PSI-2 psaN gene, which encodes an ATPase essential for secretion of T3SS effectors by the injectisome, greatly reduces both the persistence of P. stewartii in flea beetle guts and the beetle's ability to transmit P. stewartii to maize. Ectopic expression of the psaN gene complements these phenotypes. In addition, the PSI-2 psaN gene is not required for P. stewartii pathogenesis of maize and is transcriptionally upregulated in insects compared to maize tissues. Thus, the Hrp and PSI-2 T3SSs play different roles in the life cycle of P. stewartii as it alternates between its insect vector and plant host.

Identification of proteases from leaf beetle (Oulema spp.) by selective protease inhibitorsIdentyfikacja proteaz skrzypionek (Oulema spp.) za pomocą selektywnych inhibitorów proteaz

Summary The aim of the study was the identification of gut proteases of leaf beetle Oulema spp. Leaf beetles like aphids or saddle gall midge belong to main cereal pests in Poland. Two species of leaf beetles are common in Poland: cereal leaf beetle (Oulema melanopus, Linnaeus 1758) and grey leaf beetle (Oulema gallaeciana, Heydel 1870). The larvae of both species damage the assimilation surface of plant leaves. Leaf beetles were collected from the fields. The larvae of leaf beetles were immobilized on ice and then homogenized. For identification of different gut proteases polyacrylamide gel separation (in-gel protease assay condition) and selective inhibitors E-64 (trans-epoxysuccinyl-L-leucylamido(4-guanidino)butane) for cysteine protease and PMSF (Phenylmethylsulfonyl fluoride) for serine protease were used. Two kind of proteases: serine and cysteine were identified in guts of leaf beetles. This aspect is very important because insects utilize proteases to digest plant material and to gain exogenous amino acids.

Erwinia typographi sp. nov., isolated from bark beetle (Ips typographus) gut

Gram-negative-staining bacteria that were resistant to monoterpene myrcene (7-methyl-3-methylene-1.6-octadiene, C10H16, at concentrations of up to 10 µl ml(-1) in TSB) were isolated from the gut contents of adult bark beetles Ips typographus (Coleoptera, Scolytidae). The beetles were collected from the bark of Norway spruce (Picea abies) in Lithuania. Bark beetles feed on conifers, which produce myrcene among many other defensive compounds. It has been suggested that the micro-organisms present within the beetles' guts could be involved in their resistance towards this plant defensive compound. The most resistant bacterial strains were isolated and characterized by phenotypic assays as well as fatty acid analysis, 16S rRNA gene sequencing, multilocus sequence analyses (MLSA) based on the rpoB, atpD and infB genes and DNA-DNA hybridization. Biochemical characterization indicated that the bacteria belonged to the family Enterobacteriaceae. Phylogenetic analyses of the 16S rRNA gene sequences and MLSA of the novel strains revealed that they belonged to the genus Erwinia, but represented a novel species. The dominant cellular fatty acids were C16:0 and C17:0 cyclo. The DNA G+C content was 49.1 mol%. The results obtained in this study indicated that these bacteria from the bark beetle gut represented a novel species, for which the name Erwinia typographi sp. nov. is proposed, with the type strain DSM 22678T (=Y1T=LMG 25347T).

Herbiconiux moechotypicola sp. nov., a xylanolytic bacterium isolated from the gut of hairy long-horned toad beetles, Moechotypa diphysis (Pascoe)

A novel Gram-positive, non-motile, rod-shaped bacterium, designated strain RB-62(T), was isolated during a study of culturable bacteria from the gut of Moechotypa diphysis (Pascoe) and its taxonomic position was investigated. Strain RB-62(T) grew at 15-30 °C and pH 5.0-8.5. The isoprenoid quinones were menaquinones MK-11 (77.1%), MK-10 (11.7%) and MK-12 (11.2%). The major cellular fatty acids were anteiso-C(15:0) (34.6%), anteiso-C(17:0) (29.8%), iso-C(16:0) (17.0%) and cyclohexyl-C(17:0) (11.4%). The diagnostic diamino acid of the cell-wall peptidoglycan was 2,4-diaminobutyric acid. The G+C content of the genomic DNA of strain RB-62(T) was 70.3 mol%. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain RB-62(T) was affiliated with the genus Herbiconiux cluster within the family Microbacteriaceae, and was related most closely to Herbiconiux ginsengi wged11(T) (98.08% similarity). The level of DNA-DNA relatedness between strain RB-62(T) and H. ginsengi wged11(T) was 43.2% (reciprocal 66.7%). Phenotypic and phylogenetic characteristics clearly distinguished strain RB-62(T) from recognized species of the genus Herbiconiux. Based on data from the present polyphasic study, strain RB-62(T) is considered to represent a novel species of the genus Herbiconiux, for which the name Herbiconiux moechotypicola sp. nov. is proposed. The type strain is RB-62(T) (=KCTC 19653(T)=JCM 16117(T)).

Endozoochory by beetles: a novel seed dispersal mechanism

Due in part to biophysical sized-related constraints, insects unlike vertebrates are seldom expected to act as primary seed dispersers via ingestion of fruits and seeds (endozoochory). The Mediterranean parasitic plant Cytinus hypocistis, however, possesses some characteristics that may facilitate endozoochory by beetles. By combining a long-term field study with experimental manipulation, we tested whether C. hypocistis seeds are endozoochorously dispersed by beetles. Field studies were carried out over 4 years on six populations in southern Spain. We recorded the rate of natural fruit consumption by beetles, the extent of beetle movement, beetle behaviour and the relative importance of C. hypocistis fruits in beetle diet. The tenebrionid beetle Pimelia costata was an important disperser of C. hypocistis seeds, consuming up to 17·5 % of fruits per population. Forty-six per cent of beetles captured in the field consumed C. hypocistis fruits, with up to 31 seeds found in individual beetle frass. An assessment of seeds following passage through the gut of beetles indicated that seeds remained intact and viable and that the proportion of viable seeds from beetle frass was not significantly different from that of seeds collected directly from fruits. A novel plant-animal interaction is revealed; endozoochory by beetles may facilitate the dispersal of viable seeds after passage through the gut away from the parent plant to potentially favourable underground sites offering a high probability of germination and establishment success. Such an ecological role has until now been attributed only to vertebrates. Future studies should consider more widely the putative role of fruit and seed ingestion by invertebrates as a dispersal mechanism, particularly for those plant species that possess small seeds.

Diversity of Beetle Genes Encoding Novel Plant Cell Wall Degrading Enzymes

Plant cell walls are a heterogeneous mixture of polysaccharides and proteins that require a range of different enzymes to degrade them. Plant cell walls are also the primary source of cellulose, the most abundant and useful biopolymer on the planet. Plant cell wall degrading enzymes (PCWDEs) are therefore important in a wide range of biotechnological processes from the production of biofuels and food to waste processing. However, despite the fact that the last common ancestor of all deuterostomes was inferred to be able to digest, or even synthesize, cellulose using endogenous genes, all model insects whose complete genomes have been sequenced lack genes encoding such enzymes. To establish if the apparent “disappearance” of PCWDEs from insects is simply a sampling problem, we used 454 mediated pyrosequencing to scan the gut transcriptomes of beetles that feed on a variety of plant derived diets. By sequencing the transcriptome of five beetles, and surveying publicly available ESTs, we describe 167 new beetle PCWDEs belonging to eight different enzyme families. This survey proves that these enzymes are not only present in non-model insects but that the multigene families that encode them are apparently undergoing complex birth-death dynamics. This reinforces the observation that insects themselves, and not just their microbial symbionts, are a rich source of PCWDEs. Further it emphasises that the apparent absence of genes encoding PCWDEs from model organisms is indeed simply a sampling artefact. Given the huge diversity of beetles alive today, and the diversity of their lifestyles and diets, we predict that beetle guts will emerge as an important new source of enzymes for use in biotechnology.

Trichosporon xylopini sp. nov., a hemicellulose-degrading yeast isolated from the wood-inhabiting beetle Xylopinus saperdioides

Four arthroconidium-producing yeasts were isolated from the gut of wood-inhabiting tenebrionid and passalid beetles. The rRNA genes of these yeast strains were sequenced, compared and analysed. The sequence results and other taxonomic characterizations placed two of the strains into Trichosporon porosum, and the remaining strains, EH024(T) and EH026 which were isolated from Xylopinus saperdioides (Coleoptera: Tenebrionidae), into a novel species of the genus Trichosporon in the Porosum clade. Strain EN6S23 was independently isolated from forest soil in Taiwan and was identified as the same novel species based on identical sequences in the internal transcribed spacers (ITS) and the D1/D2 region of the LSU rRNA gene and similar physiological characteristics to those of strains EH024(T) and EH026. The three strains can assimilate cellulose and xylan as sole carbon source, and are clearly distinguished from their closest taxon, T. porosum, by 14 nt differences in the ITS and D1/D2 region. These strains did not reproduce sexually under the laboratory conditions tested. The novel species is proposed as Trichosporon xylopini sp. nov. (type strain EH024(T) = ATCC MYA-4670(T) = CBS 11841(T)).

Yeasts in the Sugiyamaella clade associated with wood-ingesting beetles and the proposal of Candida bullrunensis sp. nov.

During a survey of yeasts associated with wood-ingesting insects, six strains of the Sugiyamaella clade were isolated from the gut of passalid and tenebrionid beetles and the decayed wood inhabited by them. Phylogeny based on rRNA gene sequences placed these yeasts as members of Sugiyamaella smithiae, Sugiyamaella americana, Candida lignohabitans and a novel species closely related to Su. americana. The only strain of the novel species, EH008(T), could be unquestionably distinguished from its relatives by DNA sequences and other taxonomic characteristics. Ascospore production was not observed under the laboratory conditions tested. Therefore, this novel species is proposed as Candida bullrunensis sp. nov. (type strain EH008(T) = ATCC MYA-4660(T) = CBS 11840(T)).

Intramolecular proteolytic nicking and binding of Bacillus thuringiensis Cry8Da toxin in BBMVs of Japanese beetle

Bacillus thuringiensis (Bt) Cry8D insecticidal proteins are unique among Cry8 family proteins in terms of its insecticidal activity against adult Scarab beetles, such as Japanese beetle ( Popillia japonica Newman). From the sequence homology with other Bt Cry proteins especially those active against beetles, such as Cry3Aa whose 3D structure is available, the structure of the Cry8D protein has been predicted to be a typical three-domain Cry protein type. In addition, the activation process of Cry8D in gut juice of susceptible insects is presumed to be similar to that of Cry3A ( Yamaguchi et al., 2008). In this study, the activation process of Cry8Da in insect gut juice was closely examined. Japanese beetle gut juice proteases digested the 130 kDa Cry8Da protein to produce a 64 kDa protein. This 64 kDa protein was active against both adult and larval Japanese beetle and considered to be an activated toxin. N-terminal sequencing of this 64 kDa protein revealed that the Cry8Da leader sequence consisting of 63 amino acid residues from M 1 to F 63 was removed. As in the case of Cry3Aa, the proteases further digested the 64 kDa protein to two 8 kDa and 54 kDa fragments. N-terminal amino acid analysis of these smaller fragments indicated that the proteases digested the loop between Alpha Helix (Alpha for short) 3 and Alpha 4. This means that the 8 kDa fragment consists of Alpha 1–3 of Domain I and that the 54 kDa fragment contains the remaining Domain I and full Domain II and Domain III. Size exclusion chromatography and anion exchange chromatography could not separate these 64, 54 and 8 kDa proteins suggesting that the 54 kDa and 8 kDa fragments are still forming the toxin complex equivalent to the 64 kDa protein by size and ionic charge. The sequencing and chromatography results suggest that the gut juice proteases merely nicked the loop between Alpha 3 and Alpha 4. This nicking process appeared to be essential for receptor binding of the Cry8Da toxin. BBMV binding assay revealed that the Cry8Da toxin bound to BBMV preparations from both adult and larval Japanese beetle only after the loop was nicked. Only the 54 kDa fragment bound to the BBMV preparations but not the 64 kDa protein. Ligand blot showed that the protease activated Cry8Da toxin, presumably the 54 kDa fragment, bound to specific BBMV proteins, one or more of those would be receptor(s). The sizes and binding affinities of these Cry8Da-bound proteins of Japanese beetle BBMV differed between larvae and adults.

Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle

BackgroundObligate bacterial symbionts alter the diets of host animals in numerous ways, but the ecological roles of facultative bacterial residents that colonize insect guts remain unclear. Carabid beetles are a common group of beneficial insects appreciated for their ability to consume insect prey and seeds, but the contributions of microbes to diet diversification in this and similar groups of facultative granivores are largely unknown.Methodology and Principal FindingsUsing 16S rRNA gene clone libraries and terminal restriction fragment (tRF) length polymorphism analyses of these genes, we examined the bacterial communities within the guts of facultatively granivorous, adult Harpalus pensylvanicus (Carabidae), fed one of five dietary treatments: 1) an untreated Field population, 2) Seeds with antibiotics (seeds were from Chenopodium album), 3) Seeds without antibiotics, 4) Prey with antibiotics (prey were Acheta domesticus eggs), and 5) Prey without antibiotics. The number of seeds and prey consumed by each beetle were recorded following treatment. Harpalus pensylvanicus possessed a fairly simple gut community of approximately 3-4 bacterial operational taxonomic units (OTU) per beetle that were affiliated with the Gammaproteobacteria, Bacilli, Alphaproteobacteria, and Mollicutes. Bacterial communities of the host varied among the diet and antibiotic treatments. The field population and beetles fed seeds without antibiotics had the closest matching bacterial communities, and the communities in the beetles fed antibiotics were more closely related to each other than to those of the beetles that did not receive antibiotics. Antibiotics reduced and altered the bacterial communities found in the beetle guts. Moreover, beetles fed antibiotics ate fewer seeds, and those beetles that harbored the bacterium Enterococcus faecalis consumed more seeds on average than those lacking this symbiont.Conclusions/SignificanceWe conclude that the relationships between the bacterium E. faecalis and this factultative granivore's ability to consume seeds merit further investigation, and that facultative associations with symbiotic bacteria have important implications for the nutritional ecology of their hosts.

Conjugative plasmid transfer between Salmonella enterica Newport and Escherichia coli within the gastrointestinal tract of the lesser mealworm beetle, Alphitobius diaperinus (Coleoptera: Tenebrionidae)

The objective of this study was to determine if conjugative transfer of antimicrobial resistance plasmids could occur between donor and recipient bacteria within the gastrointestinal tract of lesser meal-worm beetles, a common pest in poultry production facilities. In 3 replicate studies (n = 40 overall), beetles were allowed to feed for 2 h on brain heart infusion agar inoculated with a multidrug-resistant Salmonella enterica serotype Newport strain (SN11 that carried plasmid replicons A/C and N) at 1.0 × 108 cfu/mL. Beetles were surface-disinfected and allowed to feed for 16 h on brain heart infusion agar inoculated with nalidixic acid- and rifampicin-resistant Escherichia coli JM109 at 9.0 × 106 cfu/mL. After bacterial exposure, beetles were surface-disinfected, homogenized, and selectively plated for transconjugants. Serial dilutions were done for conjugation frequencies. In vitro filter conjugations were performed simultaneously with beetle conjugations. Transconjugants were produced in all beetles exposed to both donor and recipient bacteria. Ninety-five percent of the beetle and 100% of the in vitro filter transconjugants were positive for the N plasmid replicon. The A/C replicon, which was also detected in the SN11 donor strain, did not transfer in any of the conjugation studies. None of the transconjugants displayed resistance to extended-spectrum cephalosporins. The geometric mean conjugation frequency in the beetle gut was 1.07 × 10−1. The average conjugation frequencies for the beetle gut were 2 logs higher than those for the filter conjugations 4.1 × 10−3. This study demonstrates that horizontal transfer of antimicrobial resistance plasmids can occur between Salmonella and E. coli within the gut of beetles and that beetles may be used as an in vivo model to study resistance gene transfer.

Four novel Candida species in the Candida albicans/Lodderomyces elongisporus clade isolated from the gut of flower beetles

Flower-visiting beetles belonging to three species of Cetoniidae were collected on three mountains near Beijing, China, and yeasts were isolated from the gut of the insects collected. Based on the 26S rDNA D1/D2 domain and internal transcribed spacer (ITS) region sequence analysis and phenotypic characterization, four novel anamorphic yeast species located in the Candida albicans/Lodderomyces elongisporus clade were identified from 18 of the strains isolated. The new species and type strains are designated as Candida blackwellae AS 2.3639(T) (=CBS 10843(T)), Candida jiufengensis AS 2.3688(T) (=CBS 10846(T)), Candida oxycetoniae AS 2.3656(T) (=CBS 10844(T)), and Candida pseudojiufengensis AS 2.3693(T) (=CBS 10847(T)). C. blackwellae sp. nov. was basal to the branch formed by C. albicans and C. dubliniensis with moderately strong bootstrap support. The closest relative of C. oxycetoniae was L. elongisporus. C. jiufengensis sp. nov. and C. pseudojiufengensis sp. nov. were closely related with each other and formed a branch in a subclade represented by C. parapsilosis and L. elongisporus.

Monoclonal antibodies reveal changes in predator efficiency with prey spatial pattern

Spatially explicit predator-prey interactions can alter the predatory potential of natural enemies augmented through conservation biological control. To test hypotheses regarding such interactions and predatory efficiency, we used a combination of molecular techniques and mark-release-recapture to study the foraging behaviour of a generalist carabid predator, Poecilus cupreus, in response to spatial patterns of its cereal aphid prey (Metapolophium dirhodum and Sitobion avenae). Beetle and aphid numbers were measured across two grids of sampling locations, within which aphid spatial pattern had been manipulated to generate patchy and more homogenous distributions. Aphid consumption was measured by enzyme-linked immunosorbent assays (ELISA) of beetle gut contents, using an aphid-specific monoclonal antibody. Movement and distribution patterns suggest that P. cupreus does not aggregate at, nor instigate prey-taxis within, aphid patches. However, more than two-thirds of the 2169 P. cupreus tested by ELISA had consumed aphids and the proportion of beetles containing aphid proteins was positively related to aphid density. Against expectation, the proportion of predators feeding on aphids was greatest where prey were homogenously distributed, and this was attributed to the loss of partial refuges for prey in aphid patches. The functional value of this type of uniform foraging strategy is ideally suited to early colonization of the crop habitat, when aphid numbers are low, before populations build up and form strong spatial patterns.

Five novel Candida species in insect-associated yeast clades isolated from Neuroptera and other insects

Ascomycete yeasts are found commonly in the guts of basidioma-feeding beetles but little is known about their occurrence in the gut of other insects. In this study we isolated 95 yeasts from the gut of adult insects in five neuropteran families (Neuroptera: Corydalidae, Chrysopidae, Ascalaphidae, Mantispidae and Hemerobiidae) and a roach (Blattodea: Blattidae). Based on DNA sequence comparisons and other taxonomic characteristics, they were identified as more than 15 species of Saccharomycetes as well as occasional Cryptococcus-like basidiomycete yeasts. Yeast species such as Lachancea fermentati, Lachancea thermotolerans and Hanseniaspora vineae were isolated repeatedly from the gut of three species of corydalids, suggesting a close association of these species and their insect hosts. Among the yeasts isolated in this study 12 were identified as five novel Candida species that occurred in three phylogenetically distinct clades. Molecular phylogenetic analyses showed that Candida chauliodes sp. nov. (NRRL Y-27909T) and Candida corydali sp. nov. (NRRL Y-27910T) were sister taxa in the Candida albicans/ Lodderomyces elongisporus clade. Candida dosseyi sp. nov. (NRRL Y-27950T) and Candida blattae sp. nov. (NRRL Y-27698T) were sister taxa in the Candida intermedia clade. Candida ascalaphidarum sp. nov. (NRRL Y-27908T) fell on a basal branch in a clade containing Candida membranifaciens and many other insect-associated species. Descriptions of these novel yeast species are provided as well as discussion of their ecology in relation to their insect hosts.

Five novel Candida species in insect-associated yeast clades isolated from Neuroptera and other insects

Ascomycete yeasts are found commonly in the guts of basidioma-feeding beetles but little is known about their occurrence in the gut of other insects. In this study we isolated 95 yeasts from the gut of adult insects in five neuropteran families (Neuroptera: Corydalidae, Chrysopidae, Ascalaphidae, Mantispidae and Hemerobiidae) and a roach (Blattodea: Blattidae). Based on DNA sequence comparisons and other taxonomic characteristics, they were identified as more than 15 species of Saccharomycetes as well as occasional Cryptococcus-like basidiomycete yeasts. Yeast species such as Lachancea fermentati, Lachancea thermotolerans and Hanseniaspora vineae were isolated repeatedly from the gut of three species of corydalids, suggesting a close association of these species and their insect hosts. Among the yeasts isolated in this study 12 were identified as five novel Candida species that occurred in three phylogenetically distinct clades. Molecular phylogenetic analyses showed that Candida chauliodes sp. nov. (NRRL Y-27909T) and Candida corydali sp. nov. (NRRL Y-27910T) were sister taxa in the Candida albicans/ Lodderomyces elongisporus clade. Candida dosseyi sp. nov. (NRRL Y-27950T) and Candida blattae sp. nov. (NRRL Y-27698T) were sister taxa in the Candida intermedia clade. Candida ascalaphidarum sp. nov. (NRRL Y-27908T) fell on a basal branch in a clade containing Candida membranifaciens and many other insect-associated species. Descriptions of these novel yeast species are provided as well as discussion of their ecology in relation to their insect hosts.

Isolation and Characterization of Xylitol-Producing Yeasts from the Gut of Colleopteran Insects

A total of 35 yeasts were isolated from the gut of beetles collected from Hyderabad city, India. Twenty of these yeasts utilized xylose as a sole carbon source but only 12 of these converted xylose to xylitol. The ability to convert xylose to xylitol varied among the isolates and ranged from 0.12 to 0.58 g/g xylose. Based on the phenotypic characteristics and phylogenetic analysis of the D1/D2 domain sequence of 26S rRNA gene, these isolates were identified as members of Pichia, Candida, Issatchenkia, and Clavispora. Strain YS 54 (CBS 10446), which was phylogenetically similar to Pichia caribbica and which formed hat-shaped ascospore characteristics of the genus Pichia, was the best xylitol producer (0.58 g xylitol/g xylose). YS 54 was also capable of producing xylitol from sugarcane bagasse hydrolysate and the efficiency of conversion was 0.32 g xylitol/g xylose after 20 cycles of adaptation in medium containing sugarcane bagasse hydrolysate.

Characterization of Gut-Associated Bacteria in Larvae and Adults of the Southern Pine Beetle, <I>Dendroctonus frontalis</I> Zimmermann

We report the Þrst study of gut-associated bacteria of bark beetles using both culture- dependent and culture-independent methods. These insects are major pests of pine trees but also contribute to important ecological functions such as nutrient cycling. We found members of the - and -Proteobacteria and Firmicutes in larvae of the southern pine beetle, Dendroctonus frontalis Zimmermann. Sequences from three larval guts were grouped into one to three operational taxonomic units (OTUs) at 3% difference among sequences. Communities in adult southern pine beetle guts consisted solely of members of the -Proteobacteria. These could be grouped into three to Þve OTUs at 3% difference between sequences. These gut communities have relatively low species richness, which may resect the specialization needed to exploit a nutrient-poor food source, colonize a chemically complex habitat, and maintain consistent associations with mutualistic fungi. However, there is considerable variation in gut microbiota composition among individual insects, suggesting the need for additional studies on sources of variation and potential substitutability among species performing similar functions.

Gene expression in the gut of keratin-feeding clothes moths ( Tineola) and keratin beetles ( Trox) revealed by subtracted cDNA libraries

Few lineages of insects are able to feed on keratin (hair, feathers) and it remains unknown which genes enable this metabolism and what is their evolutionary origin. We conducted a transcriptomic study of two keratin-feeding insects, the clothes moth Tineola bisselliella (Lepidoptera) and the keratin beetle Trox sp. (Coleoptera). Using subtracted cDNA libraries enriched for gut-expressed transcripts, a total of 672 clones sequenced per library resulted in >150 tentative unique sequences for each species. Sequence similarity predictions identified 22.4% ( Tineola) and 6.8% ( Trox) of the ESTs as proteases, and mainly as serine proteases of the trypsin and chymotrypsin type, while lacking cysteine proteases. None of the sequences showed similarity to subtilisin type proteases that confers keratinolytic activities in prokaryotes and fungi. Neighbor-Joining trees grouped Tineola and Trox serine proteases near other lepidopteran and coleopteran sequences, respectively, but distant from each other. A few abundant ESTs had no database matches but their presence suggests a role specific to these keratin-feeding insects. While high expression of specific serine proteases appears linked to keratin digestion in both species, it remains to be established if their action requires additional enzymatic or physiological functions to initiate the degradation of the abundant cysteine bonds of keratins. These catabolic pathways are of great interest in the leather industry for the removal of hair, while proteinase inhibitors could prevent damage from clothes moths.

Detailed Analysis of Modifications in Lignin After Treatment With Cultures Screened for Lignin Depolymerizing Agents

Termites, beetles, and other arthropods can digest living and decaying wood plus other lignocellulosic plant litter. Microbial sources like other wood-eating insect guts and wastewater treatment sludge were screened for lignin depolymerization. Near infrared spectroscopy and atomic force microscopy (AFM) along with high-performance liquid chromatography (HPLC), were used to track changes in functional groups, size, shape, and molecular weight of lignin molecules during incubations. Odontotaenius disjunctus (Betsy beetle) guts dissected whole or separately as midgut, foregut, and hindgut, consumed corn stover but did not show lignin depolymerization. The sludge-treated lignin did show some reduction in molecular weight on the HPLC, particle size (350-650 nm initially to 135-220 nm by day 30) and particles per field on AFM. pH and the presence of nutrients had a substantial effect on the extent of depolymerization. Cultures in lignin and nutrients showed higher growth than cultures with lignin only. Colony characteristics within the beetle gut and the sludge were also evaluated.