Figures
Abstract
Olfaction plays a fundamental role in insect survival through resource location and intra and interspecific communications. We used RNA-Seq to analyze transcriptomes for odorant-binding proteins (OBPs) from major stink bug pest species in Brazil, Euschistus heros, Chinavia ubica, and Dichelops melacanthus, and from their egg parasitoid, Telenomus podisi. We identified 23 OBPs in E. heros, 25 OBPs in C. ubica, 9 OBPs in D. melacanthus, and 7 OBPs in T. podisi. The deduced amino acid sequences of the full-length OBPs had low intraspecific similarity, but very high similarity between two pairs of OBPs from E. heros and C. ubica (76.4 and 84.0%) and between two pairs of OBPs from the parasitoid and its preferred host E. heros (82.4 and 88.5%), confirmed by a high similarity of their predicted tertiary structures. The similar pairs of OBPs from E. heros and C. ubica may suggest that they have derived from a common ancestor, and retain the same biological function to bind a ligand perceived or produced in both species. The T. podisi OBPs similar to E. heros were not orthologous to any known hymenopteran OBPs, and may have evolved independently and converged to the host OBPs, providing a possible basis for the host location of T. podisi using E. heros semiochemical cues.
Citation: Farias LR, Schimmelpfeng PHC, Togawa RC, Costa MMC, Grynberg P, Martins NF, et al. (2015) Transcriptome-Based Identification of Highly Similar Odorant-Binding Proteins among Neotropical Stink Bugs and Their Egg Parasitoid. PLoS ONE 10(7): e0132286. https://doi.org/10.1371/journal.pone.0132286
Editor: J Joe Hull, USDA-ARS, UNITED STATES
Received: February 20, 2015; Accepted: June 11, 2015; Published: July 10, 2015
Copyright: © 2015 Farias et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: MB received CNPq/Embrapa grant (code 562307/201-9). SNB received FAPDF/PRONEX grant (code 193.000.583/2009). LRF and PHCS received post-graduation fellowships from CNPq and CAPES, respectively. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The phytophagous stink bugs, Euschistus heros (Fabricius, 1794), Chinavia ubica (Rolston, 1983) and Dichelops melacanthus (Dallas, 1851) (Hemiptera: Pentatomidae), are responsible for severe damage to important crops in the Neotropical region, mostly soybean in the reproductive stage [1–4]. They locate their host plants through constitutive plant volatiles [5], and signal within their own species through pheromones (e.g. sexual and alarm) [6,7]. These stink bugs also have natural enemies in common, of which the most prominent is the Neotropical egg parasitoid Telenomus podisi (Ashmead, 1893) (Hymenoptera: Scelionidae) [8–12]. It locates its stink bug hosts mainly by using olfactory cues, such as plant volatiles released during stink bug oviposition or feeding (synomones) [5,13–16], as well as stink bug pheromones (kairomones) [11,17–28].
In insects, it is well known that olfaction occurs in olfactory sensilla, mostly found in the antenna, through a complex of proteins, in which the odorant binding proteins (OBPs) have been the most studied because of their key role in the first step of olfaction [29,30]. They act as a semiochemical solubilizer, transporter, and ligand-specific selector for mediating the activation of the olfactory receptors enabling insect olfactory perception [30–39]. They were first obtained through biochemical protein isolation from crude antennal extracts (e.g., [40]) and were characterized as small globular water-soluble acidic proteins (about 120–150 amino acids) with a signal peptide in the N-terminal region, six cysteine (Cys) residues in conserved positions, and a predominant alpha-helical secondary structure (e.g., [40,41]). With the application of cDNA libraries (EST-based) and massive DNA parallel sequencing (e.g., [42,43]) OBPs had been found to comprise a multigene family found in 10 different orders, including 32 hemipteran and 43 hymenopteran species (National Center for Biotechnology Information-NCBI). Since then, OBPs have been classified into subfamilies based on the number of conserved Cys: classical OBPs (six), plus-C (more than six and a conserved proline, and according to Ji et al. [44] with a C-terminal extension), minus-C (less than six), and OBP dimers (two complete OBP domains each with six conserved Cys) [37,41,43,45–50].
The pattern of six conserved cysteines (Cys motif) has been used as a signature for OBP identification (e.g., [37,43,48,51,52]). The Cys motif forms three disulphide bridges [47], which, in combination with the amino acid sequence and the physicochemical environment, generate the tertiary structure with a binding pocket that reversibly binds a particular ligand. This OBP domain comprises more than 70% of the amino acid sequence, with a general pattern of low similarity within and among species [41]. Exceptions were observed in some cases intraspecifically, such as in splice variants [53], and interspecifically in some closely related species with known similar ligands [33,54,55]. Such OBP diversity suggests selective binding of odorants in a given species (e.g., [34,55,56]), and may reflect the diversity of chemosensory behavior among the insects [56].
In this work, we analyzed transcriptomes from the main stink bug pest species of soybean in Brazil (E. heros, C. ubica and D. melacanthus), and from one of their main natural enemies, the egg parasitoid T. podisi to identify and characterize OBP transcripts. Finally, the similarity and phylogeny among these and other available OBPs were analyzed to determine if closely related species share similar OBPs, and if hosts and their natural enemy also share similar OBPs, suggesting they may respond to similar chemical signals/cues.
Materials and Methods
Insects
The three stink bugs species, E. heros, C. ubica and D. melacanthus, and the parasitoid T. podisi were obtained from laboratory colonies in Embrapa Genetic Resources and Biotechnology (Brasília, Distrito Federal, Brazil), and reared according to Borges et al. [57] and Moraes et al. [7] on raw peanuts (Arachis hypogaea), soybeans (Glycine max), sunflower (Helianthus annuus), fresh green beans (Phaseolus vulgaris), and water. Insects were kept in 8 L plastic containers (50–60 insects/container) with the food supply renewed three times per week. Unmated male and female adults were placed in separate cages, and after 12 days when the sex pheromone is produced at a consistently high level [58], their antennae were removed using entomological scissors, and immediately used for RNA extraction. Telenomus podisi was reared according to Borges et al. [11] in 25 cm3 plastic cages, fed with pure honey and provided E. heros eggs to be used as hosts. When the parasitoids were 20 days-old, they were used for RNA extraction.
RNA-Seq Construction and Sequencing
A total of 50 pairs of antennae from stink bug males and females (1:1) from each species and 300 T. podisi, mostly females, were ground in TRIzol reagent (Invitrogen, Life Technologies, Carlsbad, California, USA) and total RNA was obtained according to the method described by Chomczynski and Sacchi [59]. Immediately after extraction, 1 μg of the total RNA of each sample was individually placed in RNAstable tubes (Biomatrica, San Diego, California, USA) and shipped to Beijing Genomics Institute (BGI, China) for sequencing. The integrity/quality of the RNA samples was evaluated using the 2100 Bioanalyzer (Agilent Technologies, Santa Clara, California, USA) and as the RNA Integrity Numbers were ≥ 7.0, the RNA samples were used for RNA-Seq library construction and sequencing using the Illumina GAIIx platform (one lane/sample, 100 bp paired-end).
De novo Transcriptome Assembly and Annotation
The four transcriptome datasets were received in Fastq format. Quality control was performed by Trimmomatic (http://etal.usadellab.org/cms/?page=trimmomatic) using leading 3, trailing 3, sliding window 4:15 and minimum length 36. Before assembly, the high quality paired and unpaired reads were run through VelvetOptimiser 2.2.5 (http://bioinformatics.net.au/software.velvetoptimiser.shtml) to find the best k-mer per dataset in the interval 15 to 47 k-mers. The assembly was first made using Velvet (version 1.2.0.7), and then Oases (version 0.2.0.8) was applied to the output from Velvet (both K-mers). CEGMA software (Core Eukaryotic Genes Mapping Approach) was used (default parameters) to assess the completeness of the transcriptome assemblies, and identify the presence of a core consisting of 248 highly conserved proteins that are found in a wide range of eukaryotes, mostly housekeeping genes, that can be expected to be expressed [60].
To search for related olfaction transcripts, the assembled transcripts (contigs) were annotated using a BLASTx search against a non-redundant protein database from NCBI (E-value≤ 1e-5) and the results were loaded into Blast2GO software version 2.7.0 [61]. The Blast2GO annotation and mapping steps added the gene ontology terms and the transcripts were categorized into biological processes and molecular functions. For each species, the 15 most common biological processes or molecular functions were identified and combined, resulting in a total of 24 biological processes or molecular functions for the four species. Then, the number of annotated sequences in each process or function was normalized by the total number of sequences for each species and the normalized proportions were ranked for statistical analyses with the Cochran-Mantel-Haenszel (CMH) test (Chi-square statistic) on ranks (SAS version 9.3). The species distribution charts of the four species were compared with the Kruskal-Wallis (H) test for independence of ranks.
The putative OBP contigs were screened for open reading frames (ORFs) using the software ORF Finder (http://www.ncbi.nlm.nih.gov/gorf/gorf.html) to identify the coding region. In addition, the OBP domain (SM00708) and gene family (PF01395) were checked by InterProScan 5 [62]. We have named the mined putative OBP ORFs by the first letter of the genus followed by the first three letters of the species name followed by a number in increasing scaffold order. The only exception is for the putative OBP found for D. melacanthus, which we named using the first two letters of the genus, so that it is not confused with Drosophila melanogaster OBPs. The raw sequence transcriptome data were deposited in the Sequence Read Archive (SRA) at DDBJ/EMBL/GenBank database and can be accessed under BioProject PRJNA246320. The assembly results were deposited in the Transcriptome Shotgun Assembly (TSA) and can be accessed as first versions: GBER01000000 for E. heros, GBFA01000000 for C. ubica, GBES01000000 for D. melacanthus, and GBEU01000000 for T. podisi.
In silico Characterization
The full-length putative OBPs were submitted to a series of in silico analyses to predict: the deduced amino acid sequences (Expasy Translate Tool, http://web.expasy.org/translate/); the isoeletric point (pI) and molecular weight (MW) (Compute pI/Mw, http://web.expasy.org/compute_pi/); the signal peptide presence (SignalP 4.1, http://etal.cbs.dtu.dk/services/SignalP/) [63]; as well as tertiary structure and alignment (I-TASSER server 4.2) [64]. To predict the tertiary structure, a query sequence was first threaded by LOMETS through the nr Protein Data Bank (PDB) library to identify structural templates, which were adopted for further structural reassembly, model selection and refinement, following the I-TASSER Suite pipeline [65], which was especially designed for proteins with unknown structure and with low identity (≤25%) with known structures (Table A in S2 File).
Similarity Analyses
The deduced amino acid sequences of the putative full-length OBPs were aligned with the OBPs from other species available at GenBank using MAFFT 7.017 [66] with the algorithm auto, scoring matrix BLOSUM62, gap opening penalty 1.53, and offset value of 0.123 using Geneious 7.0.5. The OBP sequence orthologs were selected by BLASTx using the criteria of: minimum similarity of E-value< 10e-20 with identity higher than 35% in query coverage of at least 70% for the alignment with the parasitoid putative OBPs, and E-value< 10e-7 with identity higher than 26% in query coverage of at least 77% for the alignment with the target stink bug putative OBPs. We also constructed phylogenetic trees with the mined OBPs from the target stink bugs and the 185 hemipteran OBPs, and with the mined OBPs from the target parasitoid and the 215 hymenopteran OBPs, all available at DDBJ/EMBL/GenBank. First we used the MEGA 6.06 program [67] to find the best Maximum Likelihood (ML) model using the BIC and AICc. Both phylogenetic trees were constructed using the LG+G+I model with 1,000 bootstrap replications, partial deletion of gaps, coverage cutoff 95%, and Nearest-Neighbor Interchange (NNI) ML heuristic method, with strong branch swap filter, to generate an unrooted tree.
Results and Discussion
Library Statistics and Transcriptome Assembly, Annotation and Completeness
Transcriptome data of four important economic species in soybean in Brazil were generated and compared for the first time: the phytophagous stink bugs E. heros, C. ubica and D. melacanthus, and their biological control agent the egg parasitoid T. podisi. The total number of reads obtained after quality control in the stink bug and parasitoid libraries is presented in Table 1, as well as the number and maximum length of contigs. The total number of reads before quality control for the four libraries was similar (data not showed). However, after quality control, the number was uneven, resulting in uneven assembly with 19,697 contigs for E. heros (3,812 transcripts annotated), 41,860 for C. ubica (4,594 annotated), 8,647 for D. melacanthus (1,680 annotated), and 51,106 for T. podisi (5,540 annotated) (Table B in S2 File). As the RNA samples had similar quality scores (RIN≥ 7.0) and the total number of reads was similar in the four libraries before quality control, the lower number of high quality reads for D. melacanthus could have occurred due to some bias, possibly in library construction or sequencing. Similarly, regarding the transcriptome completeness assessments, we identified 223 out of 248 constitutive genes indicated by CEGMA for T. podisi, i.e. 89.9% completeness, while for the stink bugs it was 50.0% for C. ubica, 44.35% for E. heros, and 14.9% for D. melacanthus (Table C in S2 File). One factor that may have influenced the completeness was that the parasitoid T. podisi transcriptome was extracted from the whole body, while the transcriptomes from the stinkbugs were from a specialized tissue (antennae). The uneven number of annotated contigs obtained from the four target species reflected both the BLASTx results and annotation process: 5,540 annotations out of 22,926 BLASTx results for T. podisi, 4,594 annotations out of 7,370 for C. ubica, 3,812 out of 5,142 for E. heros, and 1,680 out of 2,346 for D. melacanthus. The predicted olfaction related transcripts are indicated in Tables D to G in S2 File. The total number of putative olfaction related transcripts was similar for the stink bugs E. heros (23 OBPs, with four full-length) and C. ubica (25 OBPs, with four full-length), but lower for the stink bug D. melacanthus (9 OBPs, with one full-length) and for the parasitoid T. podisi (7 OBPs, with three full-length). We previously identified two other putative full-length E. heros OBPs (EherOBP1 and EherOBP2, GenBank codes ADJ18275.1 and ADO24165.1, respectively) [68] through antennal cDNA library screening, so the total number of putative OBPs for E. heros is actually 25, the same as found for C. ubica. The lower number of putative olfaction transcripts from D. melacanthus compared to the other stink bugs might be related to its lower transcriptome coverage, although it could also be related to a biological reason. Studies on D. melacanthus have shown that they produce a similar blend of defensive compounds identified in other stink bugs [58,69,70], but there is currently no report identifying its sex or aggregation pheromone. It is not yet possible to determine if this species has or does not have similar chemical communication as other stink bugs, i.e, this species may also use non-chemical cues to locate host and partners, such as vibrational or visual signals, which could explain why they have fewer putative OBPs [7]. Regardless, the number of OBPs identified could have been higher by using a higher performance sequencing or increasing the number of lanes used.
The minimum contig length was 300 bp for all samples. QC: quality control.
Gu et al. [71] constructed cDNA libraries from the male and female antennae of the lucerne plant bug, Adelphocoris lineolatus (Hemiptera: Miridae), and selecting 2,915 ESTs they obtained 1,423 unigenes (with 215 contigs) with an average length of 532 bp and 549 bp for ESTs from the male and the female libraries, respectively, from which were annotated 14 putative OBPs. In the antennal cDNA library from the green plant bug Apolygus lucorum (Hemiptera: Miridae), Ji et al. [44] obtained 5,018 ESTs, which assembled into 3,881 unigenes (with 783 contigs) with an average length of 144 bp, from which were annotated 12 putative OBPs that also had a molecular function of putative binding proteins.
The number of putative OBPs found in the antennae of the stink bugs E. heros and C. ubica was higher than that found in the lucerne and green plant bugs, however, the plant bug studies produced the transcriptome through Sanger sequencing instead of high throughput sequencing and had a much smaller number of unigenes/contigs from which to search for putative OBP transcripts. The heterogeneity of OBPs mined from the Neotropical stink bugs E. heros and C. ubica was also higher than that identified for other hemipterans, including the aphids Acyrthosiphon pisum, with 15 putative OBPs identified through its genome sequence [41], and Aphis gossypii, with 10 OBPs identified using a high throughput sequencing platform (from total of 54,547 unigenes) [72], the human body louse, with five genes obtained from its genome project [73], and the white-backed planthopper Sogatella furcifera, with 12 OBPs obtained from a transcriptome analysis [74]. The only exception was the tarnished plant bug Lygus lineolaris, from which 33 putative OBPs were found using a high throughput sequencing platform; however, instead of a single life stage, the researchers sequenced all developmental stages to generate the libraries [53]. No comparison was possible with other Pentatomidae species because we were the first group to identify putative OBPs in this family [68].
In the parasitoid wasp, Cotesia vestalis, using transcriptome pyrosequencing of antennae, Nishimura et al. [75] obtained 17,238 contigs (average size 549 bp) and 31,921 singletons, which had a similar species distribution as that found for the target parasitoid T. podisi. They annotated 22 putative OBPs, a higher number of OBPs than mined from the whole body of T. podisi. The number of OBPs from T. podisi was also smaller than that obtained from genome analyses of other hymenoptera, e.g., 12 putative OBPs mined from the fire ant Solenopsis invicta [76], 21 from Apis mellifera [48], and 90 from the parasitoid Nasonia vitripennis [50]. Despite the high transcriptome coverage of T. podisi (51,106 contigs), the smaller number of OBPs mined from it compared to these other hymenopteran species might be related to having analyzed the whole body, instead of a tissue specialized in olfaction, such as the antenna. However, in the solitary bee Osmia cornuta, Yin et al. [77] annotated only six putative OBPs from a transcriptome analysis of the antennae using high throughput sequencing, which assembled 85,143 contigs (average length of 914.5 bp).
Transcriptome Comparisons
The BLASTx search using the transcripts reconstituted from the transcriptome of the target stink bugs and the parasitoid matched homologous sequences in other species (Fig 1, BLASTx top 5 hits in S1 File). Of the 40 species with the highest number of matches, 21 matched with all four target species, and these were retained for statistical analysis. The 19 species that did not have matches with all four target species were Coleoptera (Dendroctonus ponderosae), Diptera (Anopheles darling, Drosophila virilis, Dr. willistoni), Hemiptera (Cimex lectularius, L. lineolaris, Rhodnius prolixus, Triatoma infestans), Hymenoptera (Trissolcus basalis), Ixodida (Ixodes scapularis), Lepidoptera (Papilio xuthus), Chordata (Anolis carolinensis, Danio rerio, Mus musculus), Hemichordata (Saccoglossus kowalevskii), Echinodermata (Strongylocentrotus purpuratus), Mollusca (Biomphalaria glabrata), Cnidaria (Hydra magnipapillata), and Proteobacteria (Bradyrhizobiaceae bacterium). The Hemiptera species matched with the target stink bugs, whereas T. podisi had higher matches with hymenopteran species, especially with the parasitoid N. vitripennis, and with the egg parasitoid Tr. basalis.
Distribution of species with the highest number of hits with similarity to contigs from antennae of 12 day-old virgin adults of stink bugs and whole body of 20 day-old parasitoid: (a) E. heros (n = 11,035 top BLASTx hits, 10.8% total BLASTx hits), (b) C. ubica (n = 14,869, 11.02%), (c) D. melacanthus (n = 4,789, 11.1%) and (d) T. podisi (n = 31,619, 10.4%).
The retained 21 match species were ranked among the three target stink bugs and parasitoid data (Table 2). The distribution of species matches was significantly different among the three target stink bug hosts and their parasitoid (H = 146.803, df = 60, P< 0.0001). As expected, most matches were with species in the same order as the target species. For the stink bugs the main species were Hemiptera, and for the parasitoid the main species were Hymenoptera. Six species were significantly different among the four target species. Acyrthosiphon pisum, Tri. castaneum, P. humanus, and Bombyx mori were similarly ranked among the three stink bugs, but ranked significantly lower in the parasitoid. The first three species were also the most similar to the antennal transcriptome of the 3 day-old adult hemipteran A. lineolatus (Miridae) [71]. Bombus terrestris and N. vitripennis were significantly higher ranked in the parasitoid compared to the stink bugs, and the parasitoid top-hits species distribution was similar to that found for the antennal transcriptome of 24 h adult wasps Co. vestalis (Braconidae) [75]. Based on this initial result, data were analyzed for the three stink bugs only. There was no difference in match species among these three species (H = 5.994, df = 40, P = 1.000).
Match species in bold are significantly different among the target stink bugs and parasitoid.
Overall, comparing the BLASTx results between the stink bug species and the parasitoid, the number of hits found for the parasitoid was more than twice that for the stink bug species. This may reflect the difference in the starting number of contigs (more from T. podisi) or indicate that the transcriptome of a specific tissue (antenna) may have poorer representation in the public databases. The list of matching species should be considered carefully, as it could be related to the proportion and representation of species in the public databases (and the particular physiologic condition of the insects from which the transcriptomes were obtained) rather than having a phylogenetic meaning.
The relative abundance of the transcripts was also analyzed based on Gene Ontology (GO) classifications for biological process and molecular function (Fig 2). Some of the most common biological processes differed quantitatively among the target species (CMH = 58.34, df = 21, P< 0.0001). The three most common of these were oxidation-reduction processes, regulation of transcription DNA-dependent, and translation. Of the 24 most common biological processes in the four target species, C. ubica had the highest richness and differed from the others in ribosome biogenesis, electron transport, serine family amino acid metabolic process, signal transduction, sodium ion transport and proton transport. Telenomus podisi differed from the others in ion transport, and all four species differed from each other in microtubule-based movement.
The number of transcripts for a particular GO term (at lower hierarchy level) in each category was normalized by the total number of classified transcripts.
The molecular functions had a rich representation of binding activities (such as to ATP, nucleic acids and ions). The most common molecular functions also differed quantitatively among the species (CMH = 81.67, df = 21, P< 0.0001). Of the 24 most common molecular functions in the four target species, D. melacanthus differed from the others in RNA binding; T. podisi differed from the others in catalytic activity, and sequence-specific DNA binding (GO:0043565 and GO:0003700). All four species differed from each other in protein serine/threonine kinase activity.
The biological processes diverged more among the target species than the molecular functions, as can be observed in Fig 3. More biological processes were identified in the antennae of C. ubica (n = 160, 70 exclusive), than in T. podisi (n = 121, 43 exclusive), E. heros (n = 87, 13 exclusive) and D. melacanthus (n = 39, 1 exclusive). In total, 32 biological processes were shared among the four species, but only two were exclusive to the three stink bug species. More molecular functions were identified in the whole body of T. podisi (n = 121, 39 exclusive), than in the stink bugs C. ubica (n = 107, 14 exclusive), E. heros (n = 99, 7 exclusive), and D. melacanthus (n = 49, none exclusive). The stink bugs shared more molecular functions among themselves than with the parasitoid T. podisi.
A species was considered to have the category if it had more than 10 transcripts. The radii of the circles are proportional to the number of categories.
Overall, the transcriptome composition of the stink bugs and the parasitoid was similar to other hemipteran and hymenopteran species. In the antenna of 3 day-old adult hemipterans A. lineolatus [71] and Ap. lucorum [44], the relative abundance of the transcripts also had higher representation of binding and catalytic activity in the molecular function ontology, and cellular process in the biological process ontology. In the 24 h emerged adult wasps Co. vestalis, the genes expressed in the antennae were also mostly associated with molecular binding activity or categorized as catalysts [75].
In silico Characterization
The full-length putative OBPs (Table 3) revealed OBPs with physicochemical properties similar to other OBPs [31,33,78]. They are small (136–212 residues and 14,627.8–23,783.1 Da), have an amino terminal signal peptide (from position 1 to around 20) followed by the OBP domain until a few residues prior to the carboxyl terminal end, and have an acidic pI< 6, except for DimelOBP1 with a pI of 6.57 and TpodOBP3 with an unusual basic pI of 9.41. The predicted tertiary structures had five to seven alpha-helixes (Fig 4), held together by three disulfide bridges between Cys1-Cys3, Cys2-Cys5, and Cys4-Cys6, as expected for an OBP structure [38].
AA: Amino acid residue number; pI: Isoelectric point; MW: molecular weight (Da); Cys: cysteine; SignalP: signal peptide amino acid location. InterPro domains IPR023316 and SM00708, and families IPR006170 and PF01395. Unless otherwise indicated the “Conserved Cys” is six classical.
Blue shows structural similarities and red shows dissimilarities according to the matrix Blosum60 for: (a) within EherOBPs; (b) within CubiOBPs; (c) between EherOBP3 and CubiOBP3; (d) between EherOBP6 and CubiOBP1; (e) within TpodOBPs; (f) between TpodOBP1 and EherOBP2; (g) between TpodOBP2 and EherOBP1. The structures were generated by I-TASSER server 4.2 and were oriented with the N-terminal to the right side.
Regarding the C-pattern, the putative OBPs from the target stink bugs and parasitoid had six cysteines (Cys) in conserved positions, as in a classical OBP, except for DimelOBP1 with five Cys (minus C6), which would be classified as a minus-C OBP [43]. In this work, all putative OBPs have the strictly conserved three residues between C2-C3, and most of them (9 of 14) have the expected Cys motif-pattern for Hemiptera (C1-X22-32-C2-X3-C3-X36-46-C4-X8-14-C5-X8-C6) [52], except for EherOBP1 and EherOBP5 with C1-X41-C2, EherOBP5 and EherOBP6 and CubiOBP1 with C4-X22-C5, EherOBP6 and CubiOBP1 with C5-X9-C6, and TpodOBP2 with C3-X46-C4. In addition, EherOBP6 and CubiOBP1 have additional conserved Cys: C1a, C1b, C1c, C6a, C6b and C6c, a proline (P) after the C6a, and an extended C-terminal end. These characteristics indicate that EherOBP6 and CubiOBP1 are OBP Plus-C [43]. Therefore, of the six putative OBPs found for E. heros, five are classical OBPs and one is a Plus-C OBP, and of the four found for C. ubica, three are classical OBPs and one is a Plus-C OBP.
The number of Plus-C OBPs found was less than that from other Hemiptera species, e.g., two from A. lineolatus [71]; four-six from Ap. lucorum [44,71]; 12 from L. lineolaris [53]; two from pea aphid A. pisum [41] and three from S. furcifera [74]. For the parasitoid, all three full-length putative OBPs had the classical C-pattern, no other OBP category was found, similar to the parasitoid N. vitripennis, with a large number (90) of putative OBPs identified [50], and for Co. vestalis [75].
According to Xu et al. [52], in most insects the typical OBP motif C-pattern has three amino acids between the second (C2) and third (C3) Cys, and eight residues between the fifth (C5) and sixth (C6) Cys. They hypothesized the existence of an order-specific Cys motif-pattern for OBPs, such that in Hemiptera the pattern would be C1-X22-32-C2-X3-C3-X36-46-C4-X8-14-C5-X8-C6, and in Hymenoptera it would be C1-X23-35-C2-X3-C3-X27-45-C4-X7-14-C5-X8-C6, where X stands for any amino acid. Of the 14 putative OBPs mined, four of the stink bug OBPs and one of the parasitoid OBPs do not completely fit this hypothesized order-specific Cys motif-pattern, although all putative OBPs have the strictly conserved three residues between C2-C3.
OBP Similarity
The similarity analysis of the mined hypothetical OBPs from the target stink bugs and parasitoid (Fig 4) with other orthologous OBPs from different insect species is represented in Figs 5 and 6 and in Table H in S2 File. The predicted tertiary structure of the stinkbug and parasitoid full-length putative OBPs are individually presented in Figure A in S2 File. In all the alignments the most conserved regions were around the conserved Cys. The sequence similarity among EherOBPs ranged from 5.1 to 25.2%, among CubiOBPs from 9.3 to 25.3%, and among TpodOBPs from 16.3 to 27.5%.
Similarity is scored by matrix Blosum62 where the black color indicates 100% identity, darker grey 100% > identity ≥ 80%, lighter grey 80% > identity ≥ 60% and white color identity <60%. The sequence logo is at the top of the alignment. The amino acid percentage identity matrix is presented in Table H in S2 File. The conserved Cys are indicated by sequence logo. The species names are abbreviated with four letters, and their full names with all accession numbers of the OBP amino acid sequences are provided in Table I in S2 File.
Alignment of the deduced amino acid sequences of OBPs from the parasitoid T. podisi and the most similar OBPs obtained from GenBank by BLASTx: (a) TpodOBP1; (b) TpodOBP2; (c) TpodOBP3. Similarity is scored by matrix Blosum62 where the black color indicates 100% identity, darker grey 100% > identity ≥ 80%, lighter grey 80% > identity ≥ 60% and white color identity <60%. The sequence logo is at the top of the alignment. The amino acid percentage identity matrix is presented in Table H in S2 File. The conserved Cys are indicated by sequence logo. The species names are abbreviated with four letters, and their full names with all accession numbers of the OBP amino acid sequences are provided in Table I in S2 File.
The highest sequence similarities were obtained from four interspecific comparisons. Euschistus heros and C. ubica had two cases of high similarity across their OBPs: between EherOBP6 and CubiOBP1 with 84% similarity, and between EherOBP3 and CubiOBP3 with 76.4% similarity. The most interesting findings of this work were the high similarities of OBPs between the preferred stink bug host and its natural enemy: TpodOBP1 & EherOBP2 (88.5%) and TpodOBP2 & EherOBP1 (82.4%). TpodOBP1 also had similarity to OBPs from the Coleoptera, Hemiptera, Orthoptera, and Thysanoptera (ranging from 29.4 to 49.3%), and TpodOBP2 only with hemipteran OBPs (ranging from 28.6 to 44.2%). TpodOBP3 was the only one similar to hymenopteran OBPs, although at no more than 30% similarity. The alignment of the predicted tertiary structure between these four pairs also presented high similarity, especially among the α-helixes (Fig 4). As expected, the loops were the most variable regions.
Previous studies have generally found low OBP similarities among species, typically < 40% [71], with a few exceptions among related species. Lepidopteran Pheromone Binding Proteins (PBPs) and general OBPs have 31–91% and 47–100% similarities respectively [33]. The OBPs from 12 aphid species all cluster to 10 groups with 81.2% similarity within groups compared to an overall similarity of only 20.0% [72]. High interspecific similarity was not common within the Heteroptera and only two pairs of mirid OBPs had high similarity, 89% and 74% [44,71]. The high similarities observed between EherOBP6 & CubiOBP1 and EherOBP3 & CubiOBP3 are consistent with these reports. Only Yin et al. [77] report similarities of OBPs from insects of different families, and the highest observed similarity was 65%. The observed similarity across insect orders between TpodOBP1 & EherOBP2, and TpodOBP2 & EherOBP1 was much higher than previously reported for phylogenetically unrelated species.
The phylogenic analysis (Fig 7) for the target stink bug OBPs with the other 185 hemipteran sequences from 28 species confirmed the intraspecific divergence of their putative OBPs. The OBP phylogeny did not correspond to the known hemipteran phylogeny. The intraspecific OBPs did not form a single clade, and for both E. heros and C. ubica, their OBPs mapped to different clades. At the same time, the phylogeny showed the convergence or shared derived character of the two pairs of similar putative OBPs across E. heros and C. ubica. EherOBP6 and CubiOBP1 were sisters with high (99) bootstrap support. They had three mirid OBPs as their closest outgroup with high (92) bootstrap support, but the next closest outgroup was unclear (bootstrap support 12). EherOBP3 and CubiOBP3 were sisters with high (98) bootstrap support, but they were not clearly linked to any outgroup (bootstrap support 0).
The trees were constructed with MEGA 6.06 using a LG+G+I model. Values indicated at the nodes are bootstrap values based on 1,000 replicates presented with 50% cut-off bootstrap value for (a) and no cut-off for (b). The species names are abbreviated with four letters, and their full names with all accession numbers of the OBP amino acid sequences are provided in Table I in S2 File.
The phylogenetic relations of the other stink bug OBPs revealed two patterns. The first was monophyly with early divergence from other OBPs. EherOBP1 was monophyletic with one reduviid and 7 mirid OPBs with high (96) bootstrap support (Fig 7B), EherOBP5 was monophyletic with four mirid, one delphacid, and seven aphidid OBPs (bootstrap support 93), and DimelOBP1 was monophyletic with three mirid and one reduviid OBPs (bootstrap support 94). The EherOBP6 & CubiOBP1 pair mentioned above was also a part of a monophyletic group of three mirids (bootstrap support 92). As the database is enriched with more species of Heteroptera, these clades are likely to remain monophyletic, but the phylogenetic pattern within the clade will become clarified.
The second pattern was exhibited by EherOBP2, EherOBP4, CubiOBP2, CubiOBP4, and the EherOBP3/CubiOBP3 pair, which had uncertain phylogenetic position, probably because there were no similar OBPs among the Hemiptera in the database. EherOBP2 was distantly related to two mirids and delphacids (bootstrap support 45). CubiOBP2 was distantly related to other hemipteran OBPs (bootstrap support 23). EherOBP4 and CubiOBP4 may be related to three reduviid OBPs (bootstrap support 50 and 69, respectively). The EherOBP3/CubiOBP3 pair mentioned above also had uncertain phylogenetic position (bootstrap support 0). Database enrichment will clarify the phylogenetic relationships of these OBPs.
These results support the hypothesis that within the Heteroptera there has been extensive duplication and differentiation of OBPs [50] especially compared to the conservative evolution in the aphids [69] and Lepidoptera [43]. We found no intraspecific orthologues in the stink bugs, unlike the mirid studies [44,53,71], but a slightly higher rate of orthologues between related species. The absence of intraspecific orthologues might be related to the comparatively lower number of full-length OBPs characterized in the three stink bugs species studied. Additionally, as indicated by the alignment and phylogenetic analyses, the stink bug OBPs are probably not splice variants, which according to Hull et al. [53] can generate intraspecific orthologous OBP clades.
The phylogenetic relation of the target parasitoid putative OBPs was made with 215 hymenopteran putative OBPs from 36 species, with a rich representation of Solenopsis spp. (18 species), N. vitripennis putative OBPs (90 units), and Apis spp. putative OBPs (42 units) (Fig 8). The OBP phylogeny did not correspond to the known hymenopteran phylogeny. The three TpodOBPs mapped to different parts of the OBP phylogeny and probably are products of different genes for recognition of different odors. None of them are closely related to any of the other hymenopteran OBPs (bootstrap support < 17), and all diverged early from their closest sister OBP. TpodOBP1 and TpodOBP3 were related to OBPs in different hymenopteran families, but with low (5) bootstrap support. TpodOBP2 is most closely related to five other OBPs with low (17) bootstrap support. The phylogenetic pattern for the T. podisi OBPs differs from other hymenopteran OBPs, which generally have more intra- and interspecific orthologues [50,77], suggesting that evolutionary history of the T. podisi OBP genes may have been independent of the other identified hymenopteran OBPs.
The trees were constructed with MEGA 6.06 using a LG+G+I model. Values indicated at the nodes are bootstrap values based on 1,000 replicates presented with 50% cut-off bootstrap value for (a) and no cut-off for (b). The species names are abbreviated with four letters, and their full names with all accession numbers of the OBP amino acid sequences are provided in Table I in S2 File.
The high similarities in the primary and tertiary predicted structures indicate that the pairs of OBPs EherOBP3 & CubiOBP3, EherOBP6 & CubiOBP1, TpodOBP1 & EherOBP2, and TpodOBP2 & EherOBP1 might recognize similar odors. The phylogenetic analyses support these inferences. The monophyly between EherOBP3 and EherOBP6 with CubiOBP3 and CubiOBP1, respectively, may imply that they detect similar odors, and that these are different from the odors recognized by the other hemipteran OBPs presently in GenBank. The corresponding parasitoid OBPs, TpodOBP2 and TpodOBP1, have low relatedness to other hymenopteran OBPs, suggesting that they have evolved independent of phylogenetic constraint, and therefore may have evolved to capture host semiochemical cues.
In 2009, Qiao et al. [79] demonstrated that different aphid species shared some highly conserved OBPs, for instance OBP3, which has affinity to sequisterpene (E)-β-farnesene (EβF), an aphid alarm pheromone that is released by most aphid species. In addition, lepidopteran PBPs are also similar and monophyletic [43] supporting a hypothesis that OBPs with shared semiochemical ligands are conserved through evolution [54]. Steinbrecht [80] tested the reactivity of an antiserum against the PBP of Antheraea polyphemus in pheromone-sensitive sensilla tricodea in nine moth species belonging to six families and three superfamilies of Lepidoptera and concluded that the observed cross-reactivity was related to the chemical relatedness of the pheromones used by the tested species rather than their taxonomic relatedness. The similar OBPs in the two closely related stink bug species, which have broadly overlapping host plant ranges and have similar ecological niches, could suggest that these species can recognize a pheromone component of the other species, such as defense compounds [7,81], to avoid resource competition with the other species, or use it as a cue to locate host plants for mating, feeding and laying eggs. Borges et al. [21,22,82] have shown in field studies that E. heros sex pheromone baited traps captured not only E. heros, but also other pentatomids, such as Edessa meditabunda and Piezodorus guildinii, and platygastrid egg parasitoids. The shared OBP would not be species-specific but rather ligand-specific, which would imply that species sharing a similar ecological niche (such as host plants, natural enemies, defence compounds), could have a similar OBP, no matter how those species are phylogenetically related.
The similar OBPs in the parasitoid and its host could suggest that the parasitoid can recognize a host pheromone, or some other scent that the stink bug uses in its chemical communication. Laboratory bioassays and field tests showed that T. podisi uses the sex pheromone of E. heros to locate its hosts [21,22,82]. Therefore, TpodOBP1 and TpodOBP2 might be involved in recognizing a pheromone of E. heros. Vandermoten et al. [83] found an OBP in the aphid Sitobion avenae (SaveOBP3), and two of its predators, the syrphid fly Episyrphus balteatus (EbalOBP3) and the ladybird beetle Harmonia axyridis (HaxyOBP3), with amino acid sequence similarities ≥ 94%. Both SaveOBP3 and EbalOBP3 recognized a component of the aphid alarm pheromone EβF, which was acting as a kairomone for the natural enemies.
The high primary and tertiary structure similarities between the two pairs of similar OBPs in the stink bugs E. heros and C. ubica, may indicate that they have derived from a common ancestor, retaining the same biological function to bind to a ligand perceived or produced in both species. In the case of the parasitoid and host, the parasitoid OBPs may have evolved to become similar to the host OBPs to recognize host semiochemicals. Hence the parasitoid may be eavesdropping on stink bug chemical communication to find suitable hosts to parasitize. Such convergent evolution of a parasitoid OBP would be expected in the tertiary structure, specifically in the OBP domain. However, the OBP domain in insects comprises a uniquely large portion of the protein, so convergent evolution must also act on the OBP primary structure. Overall, these results reinforce that OBP similarity could be more related to specificity to a ligand than to species relatedness. Highly similar OBPs among species might occur via multiple evolutionary processes and provide one pathway to a refined and selective interspecific semiochemical signaling via allomones, kairomones and synomones.
Conclusion
The transcriptomes of E. heros, C. ubica and D. melacanthus stink bugs were similar to that of other hemipteran species and the transcriptome of T. podisi parasitoid was similar to other hymenopteran species. Overall, the biological processes and molecular functions were similar among the four species. The most common biological process was related to oxidation-reduction, and the most common molecular function was related to ATP-binding, which have been commonly reported for other insect transcriptomes. Transcriptome analyses enabled the mining of putative OBPs, with a similar number identified from E. heros and C. ubica stink bugs, which was higher than from other Hemiptera in the Miridae, Aphididae and Delphacidae families. The lone exception was the mirid L. lineolaris. Fewer OBPs were identified from D. melacanthus compared to the other stink bugs, and fewer were from their parasitoid compared to most other Hymenoptera. The full-length putative OBPs had physicochemical properties expected of OBPs, except for an unusual basic pI for one T. podisi OBP. They largely exhibited the classical Cys-motif pattern, except one minus-C in D. melacanthus and one plus-C in E. heros and C. ubica. High similarity (> 75%) in the 1D and 3D predicted structures were found between two pairs of E. heros and C. ubica OBPs, and also between two pairs of E. heros and its egg parasitoid OBPs, for which the latter had much lower similarity (< 28%) to other hymenopteran OBPs. The 1D and 3D alignments and phylogenetic analyses suggest that these highly similar OBPs might bind to similar semiochemicals. For species sharing a similar ecological niche, such as the stink bugs, this might function for finding shared host plants or recognizing alarm pheromones to shared threats (e.g., natural enemies). For the parasitoid, this might function for recognizing host semiochemical cues to help find hosts.
Supporting Information
S2 File. Containing Tables A to I and Figure A.
https://doi.org/10.1371/journal.pone.0132286.s002
(DOCX)
Acknowledgments
We thank David A. Andow for English revisions and statistical analyses, and the editor J Joe Hull for his helpful revisions. This work was supported by a CNPq/Embrapa grant (code 562307/201-9) and FAPDF/PRONEX grant (code 193.000.583/2009). L.R.F and P.H.C.S received post-graduation fellowship from CNPq and CAPES, respectively.
Author Contributions
Conceived and designed the experiments: DPP MB. Performed the experiments: LRF PHCS. Analyzed the data: DPP RCT MMCC PG NFM. Contributed reagents/materials/analysis tools: SNB DPP RCT MMCC PG NFM. Wrote the paper: MB MCBM RAL SNB DPP.
References
- 1.
Schuh RT, Slater JA (1995) The bugs of the world (Hemiptera: Heteroptera). Classification and natural history. Cornell University Press, Ithaca, New York, USA. 336p.
- 2.
Corrêa-Ferreira BS, Panizzi AR (1999) Percevejos da soja e seu manejo. Londrina: EMBRAPA-CNPSo, Circular Técnica 24. 45p.
- 3.
Panizzi AR, McPherson JE, James DG, Javahery M, McPherson RM (2000) Stink bugs (Pentatomidae). In: Heteroptera of economic importance. Edt: Schaefer CW and Panizzi AR.
- 4.
Corrêa-Ferreira BS, Krzyzanowski FC, Minami CA (2009) Percevejos e a qualidade da semente da soja. Circular Técnica 67 –Embrapa. ISSN 1516-7860.
- 5. Michereff MFF, Laumann RA, Borges M, Michereff-Filho M, Diniz IR, (2011) Volatiles mediating a plant-herbivore-natural enemy interaction in resistant and susceptible soybean cultivars. J Chem Ecol 37:273–285. pmid:21318397
- 6. Borges M, Jepson PC, Howse PE (1987) Long-range mate location and close-range courtship behaviour of the green stink bug, Nezara viridula and its mediation by sex pheromones. Entomol Exp Appl 44:205–212.
- 7. Moraes MCB, Pareja M, Laumann RA, Borges M (2008) The chemical volatiles (Semiochemicals) produced by neotropical stink bugs (Hemiptera: Pentatomidae). Neo Entomol 37:489–505.
- 8. Corrêa-Ferreira BS, Moscardi F (1995) Seasonal occurrence and host spectrum of egg parasitoids associated with soybean stink bugs. Biol Control 5:196–202.
- 9. Medeiros MA, Loiácono MS, Borges M, Schimidt FVG (1998) Incidência natural de parasitóides em ovos de percevejos (Hemiptera: Pentatomidae) encontrados na soja no Distrito Federal. PAB 33:1431–1435.
- 10. Pacheco DJP, Corrêa-Ferreira BS (1998) Potencial reprodutivo e longevidade do parasitoide Telenomus podisi Ashmead, em ovos de diferentes espécies de percevejos. An Soc Entomol Brasil 27 (4):585–591.
- 11. Borges M, Costa MLM, Sujii ER, Cavalcanti MG, Redígolo GF, Resck IS et al. (1999) Semiochemical and physical stimuli involved in host recognition by Telenomus podisi (Hymenoptera: Scelionidae) toward Euschistus heros (Heteroptera: Pentatomidae). Physiol Entomol 24:227–233.
- 12. Sujii ER, Costa MLM, Pires CSS, Colazza S, Borges M (2002) Inter and intra-guild interactions in egg parasitoid species of the soybean stink bug complex. PAB 37 (11):1541–1549.
- 13. Moraes MCB, Laumann RA, Sujii ER, Pires CSS, Borges M (2005) Induced volatiles in soybean and pigeon pea plants artificially infested with the neotropical brown stink bug, Euschistus heros, and their effect on the egg parasitoid, Telenomus podisi. Entomol Exp Appl 115:227–237.
- 14. Moraes MCB, Pareja M, Laumann RA, Hoffmann-Campo CB; Borges M (2008) Response of the parasitoid Telenomus podisi to induced volatiles from soybean damaged by stink bug herbivory and oviposition. J Plant Interact 3 (2):1742–1756.
- 15. Moraes MCB, Laumann RA, Pareja M, Sereno FTPS, Michereff MFF, Birkett MA et al. (2009) Attraction of the stink bug egg parasitoid Telenomus podisi to defence signals from soybean activated by treatment with cis-jasmone. Entomol Exp Appl 131:178–188.
- 16. Michereff MFF, Michereff-Filho M, Blassioli-Moraes MC, Laumann RA, Diniz IR, Borges M (2014) Effect of resistant and susceptible soybean cultivars on the attraction of egg parasitoids under field conditions. J Appl Entomol 139 (3):207–216.
- 17. Borges M, Aldrich JR (1992) Instar-specific defensive secretions of stink bugs (Heteroptera: Pentatomidae). Experientia 48:893–896.
- 18. Bin FSB, Vinson MRS, Colazza S, Jones WAJr (1993) Source of an egg kairomone for Trissolcus basalis, a parasitoid of Nezara viridula. Physiol Entomol 18:7–15.
- 19. Mattiacci L, Vinson SB, Williams HJ, Aldrich JR, Bin F (1993) A long-range attractant kairomone for egg parasitoid Trissolcus basalis, isolated from defensive secretion of its host, Nezara viridula. J Chem Ecol 19 (6):1167–1181. pmid:24249135
- 20. Aldrich JR (1995) Testing the "new associations" biological control concept with a tachinid parasitoid (Euclytia flava). J Chem Ecol 21 (7):1031–1042. pmid:24234417
- 21. Borges M, Schmidt FGV, Sujii ER, Medeiros MA, Mori K, Zarbin PHG, Ferreira JTB (1998) Field responses of stink bugs to the natural and synthetic pheromone of the Neotropical brown stink bug, Euschistus heros (Heteroptera: Pentatomidae). Physiol Entomol 23 (3):202–207.
- 22. Borges M, Mori K, Costa MLM, Sujii ER (1998) Behavioural evidence of methyl-2,6,10-trimethyltridecanoate as a sex pheromone of Euschistus heros (Het., Pentatomidae). J Appl Entomol 122 (6):335–338.
- 23. Colazza S, Salerno G, Wajnberg E (1999) Volatile and contact chemicals released by Nezara viridula (Heteroptera: Pentatomidae) have a kairomonal effect on the egg parasitoid Trissolcus basalis (Hymenoptera: Scelionidae). Biol Control 16 (3):310–317.
- 24. Bruni R, Sant'Ana J, Aldrich JR, Bin F (2000) Influence of host pheromone on egg parasitism by scelionid wasps: Comparison of phoretic and non-phoretic parasitoids. J Insect Behav 13 (2):165–172.
- 25. Conti E, Salerno G, Bin F, Williams HJ, Vinson SB (2003) Chemical cues from Murgantia histrionica eliciting host location and recognition in the egg parasitoid Trissolcus brochymenae. J Chem Ecol 29 (1):115–130. pmid:12647857
- 26. Silva CC, Moraes MCB, Laumann RA, Borges M (2006) Sensory response of the egg parasitoid Telenomus podisi to stimuli from the bug Euschistus heros. PAB 41 (7):1093–1098.
- 27. Laumann RA, Aquino MFS, Moraes MCB, Pareja M, Borges M (2009) Response of the egg parasitoids Trissolcus basalis and Telenomus podisi to compounds from defensive secretions of stink bugs. J Chemical Ecol 35:8–19.
- 28. Laumann RA, Cokl A, Lopes APS, Fereira JBC, Moraes MCB, Borges M (2011) Silent singers are not safe: selective response of a parasitoid to substrate-borne vibratory signals of stink bugs. Anim Behav 82:1175–1183.
- 29. Matsuo T, Sugaya S, Yasukawa J, Aigaki T, Fuyama Y (2007) Odorant-binding proteins OBP57d and OBP57e affect taste perception and host-plant preference in Drosophila sechellia. PLoS Biology 5 (5):e118. pmid:17456006
- 30. Laughlin JD, Ha TS, Jones DN, Smith DP (2008) Activation of pheromone-sensitive neurons is mediated by conformational activation of pheromone-binding protein. Cell 133 (7):1255–1265. pmid:18585358
- 31. Vogt RG, Prestwich GD, Lerner MR (1991) Odorant-binding-protein subfamilies associate with distinct classes of olfactory receptor neurons in insects. J Neurobiol 22 (1):74–84. pmid:2010751
- 32. Pelosi P (1994) Odorant-binding proteins. Crit. Rev. Biochem. Mol Biol 29:199–228. pmid:8070277
- 33. Pelosi P, Maida R (1995) Odorant-binding proteins in insects. Comp Biochem Physiol 111B:503e514.
- 34. Prestwich GD, Du G, LaForest S (1995) How is pheromone specificity encoded in proteins? Chem Senses 20: 461e469.
- 35. Danty E, Briand L, Michard-Vanhée D, Perez V, Arnold G, Gaudemer O et al. (1999) Cloning and expression of a queen pheromone-binding protein in the honeybee: An olfactory-specific, developmentally regulated protein. J Neurosci 19:7468–7475. pmid:10460253
- 36. Plettner E, Lazar J, Prestwich EG, Prestwich GD (2000) Discrimination of pheromone-enantiomers by two pheromone-binding proteins from the gypsy moth Lymantria dispar. Biochemistry 2000:8953–8962.
- 37. Zhou JJ, Huang WS, Zhang GA, Pickett JA, Field LM (2004) “Plus-C” odorant- binding protein genes in two Drosophila species and the malaria mosquito Anopheles gambiae. Gene 327:117e129.
- 38. Fan J, Francis F, Liu Y, Chen JL, Cheng DF (2011) An overview of odorant-binding protein functions in insect peripheral olfactory reception. Genet Mol Res 10 (4):3056–3069. pmid:22180039
- 39. Schultze A, Schymura D, Forstner M, Krieger J (2012) Expression pattern of a ‘Plus-C’ class odorant binding protein in the antenna of the malaria vector Anopheles gambiae. Insect Mol Biol 21 (2):187–195. pmid:22211989
- 40. Vogt RG, Riddiford LM (1981) Pheromone binding and inactivation by moth antennae. Nature 293 (5828):161–163. pmid:18074618
- 41. Zhou JJ, Vieira FG, He XL, Smadja C, Liu RH, Rozas J et al. (2010) Genome annotation and comparative analyses of the odorant-binding proteins and chemosensory proteins in the pea aphid Acyrthosiphon pisum. Insect Mol Biol 19 (Suppl. 2):113e122.
- 42. Liu RH, Lehane S, He XL, Lehane M, Hertz-Fowler C, Berriman M et al. (2010) Characterizations of odorant-binding proteins in the tsetse fly Glossina morsitans morsitans. Cell Mol Life Sci 67:919e929.
- 43. Hekmat-Scafe DS, Scafe CR, McKinney AJ, Tanouye MA (2002) Genome-wide analysis of the odorant-binding protein gene family in Drosophila melanogaster. Genome Res 12 (9):1357–1369. pmid:12213773
- 44. Ji P, Gu S-H, Liu J-T, Zhu X-Q, Guo Y-Y, Zhou J-J et al. (2013) Identification and expression profile analysis of odorant-binding protein genes in Apolygus lucorum (Hemiptera: Miridae). Appl Entomol Zool 48:301–311.
- 45. Xu PX, Zwiebel LJ, Smith DP (2003) Identification of a distinct family of genes encoding atypical odorant-binding proteins in the malaria vector mosquito, Anopheles gambiae. Insect Mol Biol 12:549e560.
- 46. Zhou JJ, He XL, Pickett JA, Field LM (2008) Identification of odorant-binding proteins of the yellow fever mosquito Aedes aegypti: genome annotation and comparative analyses. Insect Mol Biol 17 (2):147–163. pmid:18353104
- 47. Pelosi P, Zhou JJ, Ban LP, Calvello M (2006) Soluble proteins in insect chemical communication. Cell Mol Life Sci 63:1658e1676.
- 48. Forêt S, Maleszka R (2006) Function and evolution of a gene family encoding odorant binding-like proteins in a social insect, the honey bee (Apis mellifera). Genome Res 16:1404–1413. pmid:17065610
- 49. Lagarde A, Spinelli S, Qiao H, Tegoni M, Pelosi P, Cambillau C (2011) Crystal structure of a novel type of odorant binding protein from Anopheles gambiae belonging to the C-Plus class. Biochem J 437:423–430. pmid:21561433
- 50. Vieira FG, Forêt S, He X, Rozas J, Field LM, Zhou J-J (2012) Unique features of odorant-binding proteins of the parasitoid wasp Nasonia vitripennis revealed by genome annotation and comparative analyses. PLoS ONE 7 (8):e43034. pmid:22952629
- 51. Li Z-X, Pickett JA, Field LM, Zhou J-J (2005) Identification and expression of odorant-binding proteins of the malaria-carrying mosquitoes Anopheles gambiae and Anopheles arabiensis. Arch Insect Biochem Physiol 58:175–189. pmid:15717318
- 52. Xu YL, He P, Zhang L, Fang SQ, Dong SL, Zhang YJ et al. (2009) Large-scale identification of odorant-binding proteins and chemosensory proteins from expressed sequence tags in insects. BMC Genomics 10:632e645.
- 53. Hull JJ, Perera OP, Snodgrass GL (2014) Cloning and expression profiling of odorant- binding proteins in the tarnished plant bug, Lygus lineolaris. Insect Mol Biol 23:78–97. pmid:24224606
- 54. Vogt RG, Rybczynski R, Lerner MR (1991) Molecular cloning and sequencing of General Odorant-binding Proteins GOBPI and GOBP2 from the tobacco hawk moth Manduca sexta: comparisons with other insect OBPs and their signal peptides. J Neurosci 17(10): 2972–2984.
- 55. Vogt RG, Köhne AC, Dubnau JT, Prestwich GD (1989) Expression of pheromone binding proteins during atennal development in the gypsy moth Lymantria dispar. J Neurosci 9:3332–3346. pmid:2795166
- 56. Vogt RG, Callahan FE, Rogers ME, Dickens JC (1999) Odorant binding protein diversity and distribution among the insect orders, as indicated by LAP, an OBP-related protein of the true bug Lygus lineolaris (Hemiptera, Heteroptera). Chem Senses 24 (5):481–495. pmid:10576256
- 57. Borges M, Milar J, Laumann RA, Moraes MCB (2007) A male-produced sex pheromone from the neotropical redbanded stink bug, Piezodorus guildinii (westwood) (Hemiptera: Pentatomidae). J Chem Ecol 33:1235–1248. pmid:17453323
- 58. Moraes MCB, Borges M, Pareja MF, Vieira HG, Souza Sereno FTP, Laumann RA (2008) Food and humidity affect pheromone rations in the stink bug, Euschistus heros. Physiol Entomol 33:43–50.
- 59. Chomczynski P, Sacchi N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156–159. pmid:2440339
- 60. Parra G, Bradnam K, Ning Z, Keane T, Korf I (2009) Assessing the gene space in draft genomes. Nucleic Acids Res 37(1):289–297. pmid:19042974
- 61. Conesa A, Götz S, Garcia-Gomez JM, Terol J, Talon M, Robles M (2005) Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics 21:3674–3676. pmid:16081474
- 62. Jones P, Binns D, Chang H-Y, Fraser M, Li W, McAnulla C et al. (2014) InterProScan 5: genome-scale protein function classification. Bioinformatics 30 (9):1236–1240. pmid:24451626
- 63. Petersen TN, Brunak S, Heijne G, Nielsen H (2011) SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat Methods 8:785–786. pmid:21959131
- 64. Zhang Y (2008) I-TASSER server for protein 3D structure prediction. BMC Bioinformatics 9:40–48. pmid:18215316
- 65. Yang J, Yan R, Roy A, Xu D, Poisson J, Zhang Y (2015) The I-TASSER Suite: protein structure and function prediction. Nat Methods 12 (1):7–8. pmid:25549265
- 66. Katoh K, Misawa K, Kuma K, Miyata T (2002) MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res 30:3059–3066. pmid:12136088
- 67. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S (2013) MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol Biol Evol 30: 2725–2729. pmid:24132122
- 68. Farias LR, Paula DP, Zhou J-J, Liu R, Pappas GJ, Moraes MCB et al. (2014) Identification and expression profile of two putative odorant-binding proteins from the neotropical brown stink bug, Euschistus heros (Fabricius) (Hemiptera: Pentatomidae). Neo Entomol 43:106–114.
- 69. Marques FA, Wendler EP, Maia BHLNS, Ventura MU, Arruda-Gatti ICA (2007) Identification of defensive compounds in metathoracic glands of adults of the stink bug Dichelops melacanthus (Hemiptera: Pentatomidae). J Braz Chem Soc 18 (6):1242–1246.
- 70. Pareja M, Borges M, Laumann RA, Moraes MCB (2007) Inter- and intraspecific variation in defensive compounds produced by five neotropical stink bug species (Hemiptera: Pentatomidae). J Insect Physiol 53:639–648. pmid:17574569
- 71. Gu S-H, Wang S-P, Zhang X-Y, Wu K-M, Guo Y-Y, Zhou J-J et al. (2011) Identification and tissue distribution of odorant binding protein genes in the lucerne plant bug Adelphocoris lineolatus (Goeze). Insect Biochem Mol Biol 41:254e263.
- 72. Gu S-H, Wu K-M, Guo Y-Y, Field LM, Pickett JA, Zhang Y-J et al. (2013) Identification and expression profiling of odorant binding proteins and chemosensory proteins between two wingless morphs and a winged morph of the cotton aphid Aphis gossypii Glover. PLoS One 8:e73524. pmid:24073197
- 73. Kirkness EF, Haas BJ, Sun W, Braig HR, Perotti MA, Clark JM et al. (2010) Genome sequences of the human body louse and its primary endosymbiont provide insights into the permanent parasitic lifestyle. Proc Natl Acad Sci USA 107:12168–12173. pmid:20566863
- 74. He M, He P (2014) Molecular characterization, expression profiling, and binding properties of odorant binding protein genes in the whitebacked planthopper, Sogatella furcifera. Comp Biochem Physiol Part B 174:1–8.
- 75. Nishimura O, Brillada C, Yazawa S, Maffei ME, Arimura G-I (2012) Transcriptome pyrosequencing of the parasitoid wasp Cotesia vestalis: genes involved in the antennal odorant-sensory system. PLoS ONE 7 (11):e50664. pmid:23226348
- 76. Wurm Y, Wang J, Riba-Grognuz O, Coronaa M, Nygaardd S, Hunte BG et al. (2011) The genome of the fire ant Solenopsis invicta. Proc Natl Acad Sci USA 108 (14):5679–5684. pmid:21282665
- 77. Yin X-W, Iovinella I, Marangoni R, Cattonaro F, Flamini G, Sagona S et al. (2013) Odorant-binding proteins and olfactory coding in the solitary bee Osmia cornuta. Cell Mol Life Sci 70:3029–3039. pmid:23512006
- 78. Pikielny CW, Hasan G, Rouyer F, Rosbash M (1994) Members of a family of Drosophila putative odorant-binding proteins are expressed in different subsets of olfactory hairs. Neuron 12:35–49. pmid:7545907
- 79. Qiao H, Tuccori E, He X, Gazzano A, Field L, Zhou JJ et al. (2009) Discrimination of alarm pheromone (E)-beta-farnesene by aphid odorant-binding proteins. Insect Biochem Mol Biol 39:414–419. pmid:19328854
- 80. Steinbrecht RA (1996) Are odorant-binding proteins involved in odorant discrimination? Chem Senses 21:719–727. pmid:8985600
- 81. Pareja MF, Borges M, Laumann RA, Moraes MCB (2007) Inter- and intraspecific variation in defensive compounds produced by five Neotropical stink bug species (Hemiptera: Pentatomidae). J Insect Physiol 53:639–648. pmid:17574569
- 82. Borges M, Moraes MCB, Peixoto MF, Pires CSS, Sujii ER, Laumann RA (2011) Monitoring the neotropical brown stink bug Euschistus heros (F.) (Hemiptera: Pentaomidae) with pheromone baited-traps in soybean fields. J App Entomol 135:68–80.
- 83. Vandermoten S, Francis F, Haubruge E, Leal WS (2011) Conserved odorant-binding proteins from aphids and eavesdropping predators. PLoS ONE 6 (8):e23608. pmid:21912599