Construction and analysis of cDNA libraries from the antennae of Batocera horsfieldi and expression pattern of putative odorant binding proteins

Abstract A high-quality cDNA library was constructed from female and male antenna of the longhorned beetle, Batocera horsfieldi (Hope) (Coleoptera: Cerambycidae), a serious pest of Populus (Salicales: Salicaceae). The titer was approximately 2.37 × 106 pfu/mL, and this complies with the test requirement. From the libraries, 692 clones were selected randomly, sequenced, and further analyzed, and the recombinational efficiency reached 93.85%. By alignment and cluster analysis, we identified four odorant binding proteins, two pheromone-binding proteins (have the characteristic six conserved cysteine residues), four Minus-C odorant binding proteins (lost two conserved cysteines), and three chemosensory proteins. In this study, we describe the identification and characterization of four new cDNAs that encode Minus-C odorant binding proteins (Minus-C OBPs) from B. horsfieldi antennal cDNA libraries. Our investigation focused on the expression pattern of the Minus-C OBP genes in various tissues in both sexes at different developmental stages, using reverse transcription PCR (RT-PCR) and realtime PCR (qPCR) strategies. Minus-C OBP1, 2, and 3 were expressed in all tested tissues, with the exception of the head (without antenna, labial palps, and maxillary palps). Minus-C OBP4 was expressed in the antenna, legs, and abdomen, but not in the labial palps, maxillary palps, or head. The qPCR results revealed MinusC OBPs were expressed in the antenna throughout the adult life, and that the transcript levels of these genes depended on the sex, age, and mating status of adults.


Introduction
The sense of smell is vital in insect communication, and most insect species' chemoreception systems are extremely sensitive to environmental odors and tastes. Considerable progress has been made in understanding insect olfaction, and it is known that odorant binding proteins (OBPs) and odorant receptors play important roles in this process (Zwiebel and Takken 2004). There are a large number of OBPs present within a variety of insect species. Insect OBPs are small, globular, water-soluble proteins that are specifically expressed in both the olfactory and gustatory systems (Vogt and Riddiford 1981;Steinbrecht et al. 1996). OBPs of insects were first identified in the silkmoth, Antheraea polyphemus, where they are known as pheromone binding proteins (PBPs) (Vogt and Riddiford 1981). Subsequently, large families of similar but divergent OBPs have been identified in many other insect species (Pelosi and Maida 1995;Krieger et al. 1997;Vogt et al. 1999;Hekmat-Scafe et al. 2000;Ishida et al. 2002;Nagnan-Le Meillour 2004;Zhang et al. 2009a, b).
The features identifying genes encoding OBPs include the six-cysteine signature, a size of 15-20 kDa, the α -helix pattern, the globular water-soluble nature, and the presence of a signal peptide. A six-cysteine signature motif is the most typical, and generally diagnostic, feature of the classical insect OBPs (Pelosi and Maida 1995). The spacing pattern of the conserved cysteine residues in Coleoptera is typically C1-X 23-44 -C2-X 3 -C3-X 36-43 -C4-X 8-12 -C5-X 8 -C6, in which X is any amino acid (Xu et al. 2009). The OBPs of insect are a multigene family that includes a lot of members: most OBPs are classic OBPs (possessing all the features), seem to play a more general role in olfaction by carrying odorants (Vogt and Riddiford 1981;Vogt and Lerner 1989) and perceiving sex pheromonesVogt et al. 1991), dimer OBPs (having two six-cysteine signatures), plus-C OBPs (having two additional conserved cysteines plus 1 proline), Minus-C OBPs (having lost two conserved cysteines), and atypical OBPs (having nine to 10 cysteines and a long C-terminus) (Hekmat-Scafe et al. 2002;Xu et al. 2003;).
The longhorned beetle, Batocera horsfieldi (Hope) (Coleoptera: Cerambycidae), is an important pest of Populus (Salicales: Salicaceae) species. The larvae and pupae develop inside Populus, and every year in May in China the adults of B. horsfieldi eclose, and newly-emerged adults use semiochemicals from Rosa multiflora Thunb (Rosales: Rosaceae) to locate their feeding-plant. After mating, the females travel back to Populus for oviposition (Li et al. 2008;Zhuge et al. 2010). This process allows the development of pest control measures based on olfactory-mediated behavioral modification. Insect antennae contain a high concentration of OBPs, which are believed to be involved in the first step of olfactory molecular recognition and signal transduction by ferrying airborne host odorants across the sensillum lymph to the odorant receptors (ORs) (Vogt et al. 1981;Vogt et al. 1991;Pelosi et al. 2006). Expressed sequence tags (ESTs) are short, single-pass sequences generated from either the 5' or the 3' end of cDNAs. ESTs of several thousand randomly chosen clones from the cDNA library analyses of certain tissues or organs are useful in identifying a gene or protein system with a specific function, such as chemoreception (Robertson et al. 1999;Zhou et al. 2010). In this study, we constructed an antennal cDNA library of B. horsfieldi for EST sequencing. In order to exploit the molecular mechanism of the perception of volatile cues associated with Minus-C OBP genes, we investigated the ex-pression of Minus-C OBPs in different tissues and both sexes at different development stages in antennae. Phylogenetic relationships of the Minus-C OBPs in B. horsfieldi were also analyzed with other OBPs, and the evolution of Minus-C OBP genes was discussed.

Materials and Methods
Insect collection and tissue preparation B. horsfieldi adults were collected from their feeding-plant R. multiflora in Gong'an county of Hubei Province in China (112°23′E; 30°04′N). Adult B. horsfieldi were determined to be either mated or unmated based on the presence or absence of patch of sexuality. All the insects were individually maintained in clear plastic containers (5 cm in diameter, 8 cm in height) and fed twigs (without leaf) of R. multiflora. The antennae from male and female adults were mixed for constructing the cDNA library. For tissue profiling, the antennae, head (without antennae, labial palps, and maxillary palps), labial palps, maxillary palps, mid-abdomen, hind-abdomen, legs (separating foreleg, middle leg, and hind leg), and wings were dissected from the adults of mated males five days after eclosion. Also, for spatial expression, antennae were isolated from the adult virgin males and females and mated males and females at different development stages after eclosion. Tissues were stored at -70 o C until used.

RNA extraction and construction of the antennal cDNA library
For construction of the antennal cDNA library, antennae (1:1 male:female) were quickly ground in liquid nitrogen, then the powder was transferred into a 1.5 mL RNasefree tube and mixed with 1.0 mL Trizol Reagent (Invitrogen, Life Technologies, www.lifetechnologies.com), following the manufacturer's instructions. The isolated total RNA from B. horsfieldi was reverse transcribed to double-strand cDNA using a modification of the SMART cDNA method (Clontech, www.clontech.com). A primer containing an oligo (dT) and a unique SfiI site at the 3' end was used to prime the first cDNA strand. A second oligonucleotide containing a unique SfiI site was added to the 5' cap at the end of the first-strand synthesis. After firststrand cDNA synthesis, long-distance PCR was used for generating the double-strand cDNA. The amplified double-strand cDNA was digested using SfiI and size fractionation using CHROMA SPIN Columns (Clontech). In order to construct an antennal cDNA library containing as much of the target genes as possible, 300-1000 bp fragments were collected. Then the cDNA fragments were ligated into the SfiI predigested pDNR-LIB (Invitrogen) plasmid vector. The ligation mixture was transformed into competent DH10 cells and plated on the agar plates supplemented with chloramphenicol (34 µg/mL). The plate was then inverted and incubated at 37°C. The entire step follows the SMART cDNA library construction kit user manual (Clontech).
Total RNA was isolated from each tissue using the Trizol reagent (Invitrogen) and was treated with DNase I (Qiagen, www.qiagen.com). First-strand cDNA was synthesized using oligo (dT) primer and Re-vertAid M-MuLV Reverse Transcriptase (Thermo Scientific, www.thermoscientificbio.com) in a total volume of 20 µL. The mix was incubated at 42°C for 1 hr, and the reaction was terminated by heating at 70°C for 5 min (MBI Fermantas, Thermo Scientific). cDNA was stored at -20°C.

Clone detection and sequence annotation
The 692 randomly selected clones from the antennal cDNA libraries were amplified by colony PCR using the M13 universal primer. Sequences from the cDNA inserts were determined using ABI 3730 sequencer (Applied Biosystems, Life Technologies). Manually trimming the sequences to remove vector and primer sequences, a total of 402 informative ESTs (unigenes) were obtained. To search for homologous olfactory genes, all nucleotide sequences were subjected to the Basic Local Alignment Search Tool (BLASTx and BLASTn, NCBI, www.ncbi.nlm.nih.gov). Olfactory genes were identified by their characteristic features, containing six or four conserved cysteines. The signal peptides and cleavage sites were predicted using SignalP 4.0 (Center for Biological Sequence Analysis, Technical University of Denmark, www.cbs.dtu.dk/services/SignalP-4.0; Nielsen et al., 1997). In order to compare sequence similarity among homologous genes, Minus-OBP-related sequences from Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) and other species were initially identified using the NCBI BLAST network server and retrieved from GenBank (NCBI). All sequences were aligned using ClustalX (www.clustal.org; Thompson et al. 1994). The neighbor-joining method was used to con-struct the phylogenetic tree using MEGA version 4.0 (www.megasoftware.net; Tamura et al. 2007). Bootstrapping was performed to estimate the reliability of the branches using 1500 neighbor-joining replicates. The tree presented only includes nodes with 50% or higher bootstrap support.

Tissue specificity and spatial expression profiling of B. horsfieldi Minus-C OBPs
To investigate tissue and spatial expression profiling of Minus-C OBPs, adult tissue samples were dissected according to the methods described and prepared in triplicate. The samples used in RT-PCR were from mated males five days after eclosion. The RT-PCR primers ( Table 2) were designed using Primer Premier 5.0 (Premier Biosoft, www.premierbiosoft.com) based on the EST sequences from cDNA library of B. horsfieldi. The 18s rRNA was used as the reference gene. PCR experiments were carried out in a PTC-200 (Bio-Rad, www.bio-rad.com), and PCR reactions were performed in the following conditions: 94°C for 5 min, 35 cycles of 30 sec at 94°C, 30 sec at 60°C (the melting temperature of the Minus-C OBPs and 18S rRNA), 1 min at 72°C and 72°C for 10 min. The reactions were performed in 25 µL with 300 ng of single-stranded cDNA, 2.0 mM MgCl 2 , 0.5 mM dNTP, 0.4 µM for each pri- mer, and 1.25 U Taq polymerase (TaKaRa, www.takara-bio.com). PCR products were analyzed by electrophoresis on 1% agarose gel and stained with ethidium bromide to ensure the correct products were being amplified.
Real-time PCR (qPCR) was performed using the ABI 7500 Sequence Detection system (Applied Biosystems). The template cDNA was obtained from unmated or mated males and females of different ages. Specific primer pairs were designed to amplify the Minus-C OBP genes (Table 2). An endogenous control was needed in order to normalize the expression of the target genes and to correct for sample-to-sample variation. Because there are no 18S rRNA and β-actin gene sequences for B. horsfieldi in any database, two conserved sequences were selected among the 18S rRNA genes in the Cerambycidae aligned by DNAMAN (Lynnon, www.lynnon.com) for designing a primer pair for the B. horsfieldi 18S rRNA control. The target fragments of Minus-C OBP 1, 2, 3, and 4, and 18S rRNA were expected to be 246 bp, 241 bp, 152 bp, 184 bp, and 112 bp, respectively. The qPCR reaction conditions were 25 µL 2× QuantiTect SYBR Green PCR Master Mix (Qiagen), primer forward, primer reverse, RNase-free water (Millipore, www.millipore.com), and 500 ng cDNA template per reaction in a final volume of 50 µL. The thermo cycling conditions for qPCR were: 95°C for 3 min, followed by 35 cycles of 30 sec at 94°C, 30 sec at 60°C (the melting temperature of the Minus-C OBPs and 18S rRNA), and 30 sec at 72°C. PCR reactions were performed in triplicate, and the cDNA samples were serially diluted to C0 (1, 10 1 , 10 2 , 10 3 , and 10 4 ) times, and the CT values of the Minus-C OBPs and Bhor18S rRNA were measured by qPCR. The data were processed using the relative quanti-

EST sequencing and identification
An antennal cDNA library was constructed from a pool of total RNAs extracted from the antennae of male and female B. horsfieldi, and the titers of the library was approximately 2.37 × 10 6 pfu/mL, and the recombinational efficiency was 93.85%. 692 randomly selected clones were sequenced from this antennal cDNA library for further analysis. Of the 649 total clones, 88 clones (the length less than 100 bp) had no obvious ORF. 402 unigenes with an average length of 427 bp were identified. Of the 402 unigenes with an ORF, 106 clones did not produce a significant BLASTx match with a known protein sequence in GenBank. The functional categories of the 402 unigenes are classified and shown in Figure 1. 58.33% of the unigenes have the function of translation, ribosomal structure, and biogenesis; 13.1% have the function of posttranslational modification, protein turnover, and chaperones; 5.95% have the general  function; 5.95% have the function of energy production and conversion; and 3.57% have the function of chromatin structure and dynamics.

Isolation and characterization of OBP cDNAs from B. horsfieldi antennae
Following the prediction of their open reading frames and annotation of their biological functions, 68 clones (9.82%) displayed a strong similarity to OBPs or chemosensory proteins (CSPs) from a variety of insect species. After removal of the duplicated sequences, we identified 10 odorant binding proteins and three chemosensory proteins. As for OBPs in insect species, the six-cysteine signature (C 1 -C 6 pattern) is the most striking conservation of amino acids. However, four of the putative OBP genes lacking C2 and C5 (Figure 2) were classified into the Minus-C OBP group, following the naming system proposed by Hekmat-Scafe et al. (2002). The sequences for . Tissue-specific distribution of Minus-C OBPs. RT-PCRs were performed using cDNAs isolated and synthesized from the different tissues of mated male Batocera horsfieldi, five days after eclosion, to examine the expression patterns in the various tissues. Amplification products were analyzed on agarose gel and visualized by UV illumination after staining with ethidium bromide. The PCRproducts were 135 bp in size for Minus-C OBP1, 120 bp for Minus-C OBP2, 127 bp for Minus-C OBP3, 132 bp for Minus-C OBP4, and 112 bp for 18s rRNA (control). Lanes correspond to cDNA or control template derived from: At, antenna; Lp, labial palp; Mp, maxillary palp; H, head (devoid of antennae, labial palps and maxillary palps); FL, foreleg; ML, mid leg; HL, hind leg; MAb, mid abdomen; HAb, hind abdomen; W, wing; control, no template (negative control) to ensure the specificity of the amplification. Amplification of the expressed 18S rRNA cDNA provides an additional positive control for the quality of each cDNA template pool. High quality figures are available online.
the Minus-C OBP1-4 genes have been deposited in GenBank under the following accession numbers: GU575294, GU575295, GU584933, and GU584934. The ORFs of these four Minus-C OBPs were 387 bp, 432 bp, 408 bp, and 399 bp. The computed values of the hydrophobic signal peptides at the N terminus, the theoretical isoelectric point, and molecular mass of the four Minus-C OBPs agreed closely with those obtained for other OBPs (Table 1, Figure 2).
We aligned the deduced Minus-C OBP protein sequences with those from Monochamus alternatus Hope (Coleoptera: Cerambycidae), Rhynchophorus palmarum (L.) (Curculionidae), Tenebrio molitor L. (Tenebrionidae), and other insect species. The results showed that the deduced amino acid sequences of OBPs had only four conserved cysteines. Also, we found the amino acids behind the lacking second and fifth cysteine residues were conserved (Figure 2). Amino acid sequence alignments revealed that Minus-OBPs shared 45% identity with each other, and these Minus-C OBPs showed low similarity (28.17%) with OBPs from other insect species. Minus-C OBP1 sequence was homologous to a odorant binding protein of the Coleopteran T. molitor (AAO18185), Mi-nus-C OBP2 was homologous to an OBP of M. alternates (ABR53888), and Minus-C OBP3 and 4 were homologous to an OBP of T. castaneum (XP_975687) ( Table 1). In order to better understanding the relationships between these Minus-C OBPs, a phylogenetic tree was constructed using the deduced amino acid sequences (Figure 3). The cladogram indicates that Minus-C OBPs are divided into three separate groups. Minus-C OBP3 and Minus-C OBP4 belonged to a single cluster and were similar to some of the insect OBPs, such as TcasOBP; Minus-C OBP1 belonged to a different cluster and was similar to cluster Minus-C OBP3 and Minus-C OBP4; Minus-C OBP2 belonged to another cluster and was distant from the other three Minus-C OBPs ( Figure 2). This result is largely consistent with the alignment above.

Tissue specificity and spatial expression patterns of Minus-C OBPs
Reverse transcription PCR (RT-PCR) experiments were performed using specific primers to determine the distribution of Minus-C OBPs in the various tissues (Figure 4). The integrity of the cDNA templates prepared from different tissues was verified by 18S rRNA gene amplification as a positive control. RT-PCR products of the size predicted for Minus-C OBP1, 2 and 3 were observed in all tested tissues with the exception of the head (without antenna), and RT-PCR products of Minus-C OBP4 were expressed in the antenna, foreleg, middle leg, hind leg, middle abdomen, and hind abdomen, but not in the labial palp, maxillary palp, and head. The data suggested that the genes encoding these proteins are highly expressed in the olfactory tissues (antenna, labial palp, and maxillary palp), as well as in non-olfactory tissues such as the leg, wing, and abdomen. The transcript levels of Minus-OBPs varied between different tissues. Minus-OBP1 had the lowest transcription level in Mp, Minus-OBP2 had the lowest transcription level in the foreleg and hind leg, and Minus-OBP4 had the lowest transcription level in the wing. The transcript levels' diversity of Minus-OBPs indicate these genes may have various non-olfactory functions.
Real-time PCR (qPCR) was performed to compare the transcript levels of Minus-C OBPs in antennae of adults from emergence until death. The results show that in all four Minus-OBPs, the transcription level of fe-males was significantly higher than males at the same developmental stages ( Figure 5). This was most noticeable in mated females at five days and 15 days after eclosion and unmated females at five days and 20 days, respectively. This result indicated that the genes likely to be involved in olfaction are most highly expressed in the females. This phenomenon can be explained because females look for food and host plants. The expression levels of Minus-C OBP1 and 2 had the lowest transcript levels at five days after eclosion, had the highest level at 10 days, after which they decreased. Minus-C OBP2 had the lowest expression (0.06). Minus-C OBP3 had the highest level at 10 days, reaching 36.08, which was 601 times higher than Minus-C OBP2. The expression levels of Minus-C OBP1 and 2 reached their peak at 25 days, Minus-C OBP3 and 4 reached their peaks at 20 days, and Minus-C OBP2 had the highest expression level (6.52) in unmated males. The transcription levels of Minus-C OBP1 and 2 in mated female antennae had the highest level at five days, then decreased. Minus-C OBP3 and 4 had their highest levels of expression in the 15-day-old mated females, and Minus-C OBP4 had the highest level (203.12) at 15 days, which was 12.62 times higher than that at five days. Unmated females had a higher expression level at five days, then the level decreased and at 15 days they had the lowest level, then at 20 days their highest level was reach, and then levels decreased. Minus-C OBP3 had the highest overall expression level (254.7).

Discussion
An antennal cDNA library of B. horsfieldi was constructed for the first time, and 692 positive clones were sequenced. From approximately 692 clones, we found 296 independent clones that contained ORFs averaging 142 amino acids. All the 296 clones were used to search NCBI with BLASTN and BLASTX. The COG classification shows these clones have different functions: translation, ribosomal structure and biogenesis, posttranslational modification, and protein turnover ( Figure 1). As expected, 68 clones (22.97%) shared homologs to OBPs or CSPs from a variety of insect species. After discrimination and classification, we obtained four GOBP genes, two PBP genes, four Minus-C OBP genes, and three CSP genes from the libraries. In addition to an N-terminal signal peptide sequence, these Minus-C OBP genes had only four conserved cysteines, unlike other classical insect OBPs, which have a characteristic pattern of six cysteines. The Minus-C OBP subfamily of B. horsfieldi is part of a larger subfamily of insect OBPs that have been reported in some insects, such as Ceratitis capitata (Christophides et al. 2000), T. molitor (Graham et al. 2001), Anopheles gambiae (Biessmann et al. 2002), Apis mellifera (Forêt and Maleszka 2006), and Microplitis mediator (Zhang et al. 2009). In Drosophila melanogaster, the Minus-C subfamily includes seven members; three proteins carry all six conserved cysteines (OBP99a, OBP99d, and OBP83f), and four members of the subfamily (OBP8a, OBP44a, OBP99b, and OBP99c) are missing C2 and C5, indicating that the loss of cysteines C2 and C5 happened after the family diverged from the rest of the insect OBPs (Hekmat-Scafe et al. 2002). The diversity of the OBP gene family suggests that positive selection results in rapid evolutionary changes and functional diversification.
The OBPs of insects have been described as transport proteins that transfer hydrophobic semiochemicals in the sensillum cavity. However, no exact functions of OBPs have yet been clarified, except for the PBPs of moths, where binding studies have confirmed their role in pheromone recognition, specifically their interaction with female pheromones (Du and Prestwich 1995;Biessmann et al. 2002). The PBPs also appear to contribute to the excitation of the receptor neurons. Bombykal in combination with the expressed PBP of Bombyx mori failed to activate the corresponding receptor neuron of B. mori, but did so when combined with one of the PBPs of A. polyphemus (Pophof 2004). The OBP LUSH of D. melanogaster has been proved to be important in detecting alcohol, knocking out the LUSH gene results in an abnormal attraction to food sources with high concentrations of ethanol, propanol, and butanol (Kim et al. 1998;Kim and Smith 2001). In the Minus-C OBP of the moth Cactoblastis cactorum, the a10/OS-D has been found expressed in the labial palps (CO 2 -sensing organs). Some of the Drosophila Minus-C OBPs may also have adapted to a non-olfactory function (Maleszka and Stange 1997;Hekmat-Scafe et al. 2002), but their exact physiological function still requires further research.
The expression patterns of the Minus-C OBP genes in B. horsfieldi may help to characterize the function of these OBPs in future research. The results of the tissue specificity showed that Minus-C OBP1, 2, and 3 were expressed in all dissected tissues except the head (without antennae, labial palps, and maxillary palps), and Minus-C OBP4 was expressed in all tissues tested, except the labial palp, maxillary palp, and head. All Minus-C OBPs had high expression in non-olfactory tissues, such as the legs, wings, and abdomen, but also in olfactory tissues such as the antennae, labial palps, and maxillary palps, except that Minus-C OBP4 was only expressed in the antennae. As for the expression in wings and legs, some papers have reported that Minus-C OBPs are expressed in taste tissues, and these genes may play an important role in taste function and gustatory reorganization. The a10/OS-D, a Minus-C OBP of the moth C. cactorum, has been found expressed in the labial palps and can detect the CO 2 change in the air (Maleszka and Stange 1997). The distribution diversity of the Minus-OBPs also indicate they may have other functions, not just olfaction.
Real-time PCR was used to evaluate the expression levels and abundance of the identified Minus-C OBPs during various developmental stages and between the sexes. The results showed Minus-C OBPs of adult females expressed at a higher level than that of the males at the same developmental stage, no matter whether they were mated or unmated. The transcription levels of Minus-C OBPs did not change as the male beetle aged over a period of 20-25 days, with the exception of 10-day-old mated males. The data showed mating status had little effect on expression levels of these four genes in male beetles. The age and mating status did affect the expression levels of Minus-C OBPs 3 and 4 in females, with the highest expression levels of these two genes in mated and unmated female occurring on the 15 th or 20 th day after eclosion, respectively. This phenomenon may be because males look for females, while females look for food and an oviposition site. It has been reported that female insects release a blend of sex pheromones to attract males over long distances, and males detect the released pheromones with extreme sensitivity and selectivity (Kaissling et al. 1987;Baker et al. 2004). It also has been reported that age and mating status could affect the expression levels of the PBP gene PxylPBP1 in the diamondback moth, Plutella xylostella (Zhang et al. 2009). Other studies in A.gambiae and D. melanogaster also have shown a correlation between changes in expression of a specific set of genes and behavioral and physiological responses (Abrantes et al. 2008;Zhou et al. 2009). However, Merlin et al. (2007) examined expression of one OR and one PBP at nine time points during a 24-hr period post-eclosion in Spodoptera littoralis male antennae and found no drastic changes in transcript abundance throughout this period of time. In a study by Soques et al. (2010), the age and mating status had no effects on the expression levels of two OR genes in the male antenna of Heliothis virescens (HvOR13 and HvOR15) and H. subflexa (HsOR13 and HsOR15). Taken together, we think that developmental stage and mating status could affect the transcription level of Minus-C OBPs of the beetle, but the effect was different with the different genes.
B. horsfieldi adults emerge in the early summer and feed mainly on branches of R. multiflora until they are sexually mature. After copulation, the females deposit their eggs at night under the bark of poplar trees before returning to R. multiflora to feed again, while the males remain on R. multiflora (Yan et al. 1997). Our previous experiments in laboratory olfactometers using beetles deprived of vision have shown that volatiles from R. multiflora are attractive to all adults, while volatiles from Populus species are only attractive to mated females (Li et al. 2008). In this paper, a cDNA library was successfully constructed from B. horsfieldi antennae, and 10 putative OBPs and three CSPs were obtained. These proteins may play an important role in adult female B. horsfieldi behavior in looking for food and locating host trees for oviposition. The research on these OBPs may give us a better understanding of the insect olfactory system and possible targets for insect pest control. However, further research on the exact physiological functions and the structural characterization of these OBPs are needed.