Juvenile hormone regulates the reproductive diapause through Methoprene-tolerant gene in Galeruca daurica.

Juvenile hormone (JH) signalling plays an important role in regulation of reproductive diapause in insects. However, its underlying molecular mechanism has been unclear. Methoprene-tolerant (Met), as a universal JH receptor, is involved in JH action. To gain some insight into its function in the reproductive diapause of Galeruca daurica, a serious pest on the Inner Mongolia grasslands undergoing obligatory summer diapause at the adult stage, we cloned the complete open-reading frame (ORF) sequences of Met and other 7 JH signalling-related genes, including JH acid methyltransferase (JHAMT), JH esterase (JHE), JH epoxide hydrolase (JHEH), Krüppel homologue 1 (Kr-h1), vitellogenin (Vg), forkhead box O (FOXO) and fatty acid synthase 2 (FAS2), from this species. GdMet encoded a putative protein, which contained three domains typical of the bHLH-PAS family. Expression patterns of these eight genes were developmentally regulated during adult development. Topical application of JH analogue (JHA) methoprene into the 3-day-old and 5-day-old adults induced the expression of GdMet. Silencing GdMet by RNAi inhibited the expression of JHBP, JHE, Kr-h1 and Vg, whereas promoted the FAS2 expression, which enhanced lipid accumulation and fat body development, and finally induced the adults into diapause ahead. Combining with our previous results, we conclude that JH may regulate reproductive diapause through a conserved Met-dependent pathway in G. daurica.

Molecular cloning of heat shock protein 10 (Hsp10) and 60 (Hsp60) cDNAs from Galeruca daurica (Coleoptera: Chrysomelidae) and their expression analysis.

Galeruca daurica (Joannis) is a new outbreak pest in the Inner Mongolia grasslands in northern China. Heat shock protein 10 and 60 (Hsp10 and Hsp60) genes of G. daurica, designated as GdHsp10 and GdHsp60, were cloned by rapid amplification of cDNA ends techniques. Sequence analysis showed that GdHsp10 and GdHsp60 encoded polypeptides of 104 and 573 amino acids, respectively. Sequence alignment and phylogenetic analysis clearly revealed that the amino acids of GdHsp10 and GdHsp60 had high homology and were clustered with other Hsp10 and Hsp60 genes in insects which are highly relative with G. daurica based on morphologic taxonomy. The mRNA expression analysis by real-time PCR revealed that GdHsp10 and GdHsp60 were expressed at all development stages and in all tissues examined, but expressed highest in eggs and in adults' abdomen; both heat and cold stresses could induce mRNA expression of GdHsp10 and GdHsp60 in the 2nd instar larvae; the two Hsp genes were expressed from high to low with the extension of treatment time in G. daurica eggs exposed to freezing point. Overall, our study provides useful information to understand temperature stress responses of Hsp60 and Hsp10 in G. daurica, and provides a basis to further study functions of Hsp60/Hsp10 relative to thermotolerance and cold hardiness mechanism.

Identification of odorant-binding protein genes in Galeruca daurica (Coleoptera: Chrysomelidae) and analysis of their expression profiles.

Odorant-binding proteins (OBPs) play a fundamental role in insect olfaction. In recent years, Galeruca daurica (Joannis) (Coleoptera: Chrysomelidae) has become one of the most important insect pests in the Inner Mongolian grasslands of China. This pest only feeds on the species of Allium plants, implying the central role of olfaction in its search for specific host plants. However, the olfaction-related proteins have not been investigated in this beetle. In this study, we identified 29 putative OBP genes, namely GdauOBP1-29, from the transcriptome database of G. daurica assembled in our laboratory by using RNA-Seq. All 29 genes had the full-length open reading frames except GdauOBP29, encoding proteins in length from 119 to 202 amino acids with their predicted molecular weights from 12 to 22 kDa with isoelectric points from 3.88 to 8.84. Predicted signal peptides consisting of 15-22 amino acid residues were found in all except GdauOBP6, GdauOBP13 and GdauOBP29. The amino acid sequence identity between the 29 OBPs ranged 8.33-71.83%. GdauOBP1-12 belongs to the Classic OBPs, while the others belong with the Minus-C OBPs. Phylogenetic analysis indicated that GdauOBPs are the closest to CbowOBPs from Colaphellus bowringi. RT-PCR and qRT-PCR analyses showed that all GdauOBPs were expressed in adult antennae, 11 of which with significant differences in their expression levels between males and females. Most GdauOBPs were also expressed in adult heads (without antennae), thoraxes, abdomens, legs and wings. Moreover, the expression levels of the GdauOBPs varied during the different development stages of G. daurica with most GdauOBPs expressed highly in the adult antennae but scarcely in eggs and pupae. These results provide insights for further research on the molecular mechanisms of chemical communications in G. daurica.

Reference gene selection and evaluation for expression analysis using qRT-PCR in Galeruca daurica (Joannis).

Quantitative real-time PCR (qRT-PCR) has been used extensively to analyze gene expression and decipher gene function. To obtain the optimal and stable normalization factors for qRT-PCR, selection and validation of reference genes should be conducted in diverse conditions. In insects, more and more studies confirmed the necessity and importance of reference gene selection. In this study, eight traditionally used reference genes in Galeruca daurica (Joannis) were assessed, using qRT-PCR, for suitability as normalization genes under different experimental conditions using four statistical programs: geNorm, Normfinder, BestKeeper and the comparative ΔC t method. The genes were ranked from the most stable to the least stable using RefFinder. The optimal suite of recommended reference genes was as follows: succinate dehydrogenase (SDHA) and tubulin-alpha (TUB-α) for temperature-treated larvae; ribosomal protein L32, SDHA and glutathione S-transferase were best for all developmental stages; ACT and TUB-α for male and female adults; SDHA and TUB-α were relatively stable and expressed in different tissues, both diapause and non-diapause adults. Reference gene evaluation was validated using expression of two target genes: the P450 CYP6 gene and the heat shock protein gene Hsp70. These results confirm the importance of custom reference gene selection when studies are conducted under diverse experimental conditions. A standardized qRT-PCR analysis procedure for gene functional studies is provided that could be useful in studies on other insect species.

Effects of Tetracycline and Rifampicin Treatments on the Fecundity of the Wolbachia -Infected Host, Tribolium confusum (Coleoptera: Tenebrionidae).

We examined the effects of Wolbachia bacteria on the reproduction of the flour beetle Tribolium confusum (Coleoptera: Tenebrionidae) using different antibiotics and across generations. We first removed infections by rearing insects on a diet with tetracycline (T; 1.0, 2.0, 3.0, 5.0, 10.0 mg/g) or rifampicin (R; 0.1, 0.2, 0.3, 0.5, 1.0 mg/g). We then performed experimental crosses using adults two generations (G2) and four generations (G4) removed from antibiotic treatments. Results showed that use of rifampicin more readily cured infections. Egg hatch from crosses of uninfected females and infected males was 0, but averaged 84 to 91% for eggs from all other crosses. Elevated fecundity was observed for T-G2 females, but not for T-G4, R-G2, or R-G4 females. Cross type had little or no effect on the sex of F 1 offspring, which averaged 52% female. These collective results support previous findings that show that Wolbachia in T. confusum causes 100% cytoplasmic incompatibility and emphasize that the antibiotic treatment used to remove infections may have additional consequences (e.g., elevated fecundity) that may not be apparent in subsequent generations.

RELATIONSHIP BETWEEN SUPERCOOLING CAPABILITY AND CRYOPROTECTANT CONTENT IN EGGS OF PARARCYPTERA MICROPTERA MERIDIONALIS (ORTHOPTERA: ACRYPTERIDAE).

BACKGROUND: Grasshoppers are major agricultural pests throughout the world. The egg stage is important for the low temperature resistance, and almost all grasshoppers overwinter in the egg stage. OBJECTIVE: To study the relationship between cold hardiness and cryoprotectant content in Pararcyptera microptera meridionalis eggs. MATERIALS AND METHODS: The supercooling point (SCP) of the eggs was measured, along with the contents of water, fat, amino acids, low molecular sugars and polyols. RESULTS: SCP, water content and glucose concentration decreased during egg development, whereas the contents of fat, trehalose, glycerol, inositol and sorbitol increased. SCP is negatively correlated with the concentrations of fat, trehalose, glycerol, inositol and sorbitol, but positively with water content and glucose concentration. Among low molecular weight sugars and polyols tested in eggs, trehalose concentration was highest, followed by glycerol. Although total content of free amino acids did not change much, of the tested 17 free amino acids in eggs, proline and glutamine had increased by 46.3 % and 13.2 %, respectively, and both showed a negative correlation with SCP. Stepwise regression analysis showed that proline, glycerol, trehalose and inositol contribute most to the SCP depression. Cold acclimation at 0 degree C increased the contents of trehalose and glycerol, and decreased SCP. CONCLUSION: The increase of the supercooling capacity in P. microptera meridionalis eggs during development could be attributed mainly to proline, glycerol, trehalose and inositol. Cold acclimation enhances supercooling capacity via glycerol and trehalose.