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  • Monthly, Founded in 1950
    Supervisor:Chinese Academy of Sciences
    Sponsor:Institute of Zoology,Chinese Academy of Sciences
    The Entomological Society of China
    Domestic postal code: 2-153
    Foreign issuance code: Q61
    ISSN 0454-6296
    CN 11-1832/Q
Table of Content
20 September 2023, Volume 66 Issue 9
For Selected: View Abstracts Toggle Thumbnails
  • RESEARCH PAPERS
    Spatiotemporal expression of WntA during the embryonic development in Locusta migratoria manilensis (Orthoptera: Locustidae)
    SONG Jia, MA Yu-Jie, PU Xue, JI Rong, KABAK Iliya, YUAN Liang
    2023, 66(9):  1139-1149.  doi:10.16380/j.kcxb.2023.09.001
    Abstract ( 281 )   PDF (28116KB) ( 306 )   PDF(mobile) (28116KB) ( 70 )     
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     【Aim】 To explore the sequence characteristics of WntA-encoding protein in the Wnt gene family of Locusta migratoria manilensis and its spatiotemporal expression profile during the embryonic development, and lay a foundation for the further functional research of LmmWntA and mining other Wnt gene family members of L. migratoria manilensis. 【Methods】 The Wnt gene family gene LmmWntA of L. migratoria manilensis was cloned by PCR and identified by neighbor-joining (NJ) method. The amino acid sequence characteristics of LmmWntA were analyzed by homologous sequence multiple alignment. Whole-mount in situ hybridization was used to screen the transcriptional signals of LmmWntA in 17 consecutive embryonic developmental stages of L. migratoria manilensis after egg laying (AEL) to 12, 24, 35, 46, 56 and 65 h, and 3, 3.5, 4, 4.5, 5, 5.5, 6.5, 8, 8.5, 9.5 and 11 d. 【Results】 The full-length CDS of LmmWntA (GenBank accession number: MW052768) of L. migratoria manilensis was cloned and is 1 101 bp, encoding 336 amino acids. LmmWntA and WntA proteins of cephalochordates, insects, clawed animals and annelids were clustered into a monophyletic group of WntA subfamily. The middle region and C-terminus of LmmWntA maintain high homology with the WntA protein sequences of the corresponding species, except for the difference in the N-terminal signal peptide region, and LmmWntA was clustered with the AmWntA protein of Apis mellifera in Hymenoptera as a sister group with the amino acid sequence identity of 59.05%. LmmWntA was first expressed in the terminal growth region of the 35 h AEL and continued to be expressed in this region until the 4 d AEL, forming stripe expression in the abdomen of each segment of the neonatal segment, and continued to be expressed in the posterior half of the optic lobe, which develops into compound eyes in the future, from the 46 h AEL to the 8.5 d AEL of L. migratoria manilensis. LmmWntA was continuously expressed in the brain from the 56 h AEL to the 5.5 d AEL. At the 65 h AEL, the stripe-like expression signal of LmmWntA in each segment of the abdomen was gradually transferred to both sides of the midline of the abdomen, and there was a clear expression signal at the base of the antennae. At the 5.5 d AEL, the expression signal of LmmWntA was further transferred to the abdominal nerve. From the 3 d AEL, LmmWntA was expressed at the distal end of the ventral somite, and later transferred to the palate, foot joint and end. As the end of the 4.5 d AEL embryo began to invaginate to form proctodeum, LmmWntA was expressed in the ventral and anterior end of the invaginated proctodeum, and most of them invaginated to the 7th somite of the abdomen. At the 9.5 d AEL, LmmWntA was expressed at the wing germ disc. 【Conclusion】 LmmWntA was dynamically expressed during the embryonic development of L. migratoria manilensis, speculating that LmmWntA is involved in the development and formation of important tissues and organs such as the posterior segment growth of embryo, nervous system (brain and abdominal nerve), compound eye, antennae, posterior end of digestive system (proctodeum), jaw, chest appendages (leg and wing) of L. migratoria manilensis. The results of this study lay the foundation of developmental biology for further research on LmmWntA deficiency.
    Identification and localization analysis of intestinal mucin AcMucin5AC-1 in Apis cerana cerana (Hymenoptera: Apidae)
    LI Xiao-Qing, GUO Yue, ZHANG Jie, ZHOU Ze-Yang, DANG Xiao-Qun
    2023, 66(9):  1150-1160.  doi:10.16380/j.kcxb.2023.09.002
    Abstract ( 167 )   PDF (24465KB) ( 143 )   PDF(mobile) (24465KB) ( 21 )     
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    【Aim】 The purpose of this study is to identify the structure, distribution and effect of intestinal mucin AcMucin5AC-1 on the midgut of Apis cerana cerana, so as to provide a theoretical basis for analyzing the physiological function of the honeybee midgut. 【Methods】 Bioinformatics was used to compare and analyze the sequence characteristics of Mucin5AC protein in A. cerana cerana. RT-qPCR was used to detect the expression levels of AcMucin5AC-1 in the midgut and cuticle of the 4-day-old larva of A. cerana cerana and in the midgut of the 2-day-old larva of A. cerana cerana at 0, 12, 24, 48 and 72 h after infection with Chinese sacbrood virus (CSBV). The prokaryotic expression system was used to express AcMucin5AC-1. The recombinant AcMucin5AC-1 was purified by Ni2+ affinity column and the polyclonal antibody to AcMucin5AC-1 was prepared. Western blot was used to detect the expression of AcMucin5AC-1 in the 3-6-day-old larvae, and the midgut, cuticle and peritrophic membrane of the 4-day-old larva of A. cerana cerana. Using indirect immunofluorescence assay, the localization of AcMucin5AC-1 in the 4-day-old larva of A. cerana cerana was analyzed. The interference efficiency of RNAi was analyzed at 12, 24, 48 and 72 h after silencing AcMucin5AC-1 in the 2-day-old A. cerana cerana larva by RNAi through feeding method. Hematoxylin-eosin (HE) staining method was used to explore the effects at 24, 48 and 72 h after silencing AcMucin5AC-1 in the 2-day-old larva by RNAi on the overall histomorphology of A. cerana cerana larva.【Results】 There are eight AcMucin5AC genes in the genome of A. cerana cerana, and their amino acid sequences all contain mucin domains. The results of RT-qPCR showed that the expression level of AcMucin5AC-1 was higher in the midgut of the 4-day-old larva of A. cerana cerana than in the cuticle, and was significantly down-regulated in the midgut of the 2-day-old larva at 12 and 72 h after infection with CSBV as compared to that in the control group. The recombinant protein AcMucin5AC-1 about 50 kD and polyclonal antibody were successfully obtained. Western blot result showed that AcMucin5AC-1 could be detected in the total protein of the 3-6-day-old larvae, and the midgut, cuticle and peritrophic membrane of the 4-day-old larva of A. cerana cerana. Indirect immunofluorescence experiment result showed that AcMucin5AC-1 was mainly localized in the midgut and peritrophic membrane of the 4-day-old larva. The detection result of RNAi efficiency showed that the expression level of AcMucin5AC-1 in A. cerana cerana was down-regulated by 92% at 24 h by 2.0 μg/individual dsAcMucin5AC-1 compared with the dsEGFP control group. HE staining detection result showed that the compactness between cells of the whole intestinal lumen of A. cerana cerana larva was weakened, and the morphological structure was disordered at 72 h after RNAi. 【Conclusion】 AcMucin5AC-1 is characterized as a mucin located in the midgut and peritrophic membrane of A.cerana cerana larvae. Down-regulation of AcMucin5AC-1 affects the morphology of the midgut of A. cerana cerana larva, suggesting that this gene may play an important role in the development of the A. cerana cerana larval midgut.
    Cloning and identification of two GST genes in Pardosa astrigera (Araneae: Lycosidae) and their expression in response to deltamethrin stress
    JIAO Li-Ya-Lin, ZHAO Meng-Meng, WANG Mei, NIU Yue, WANG Xi, LI Rui
    2023, 66(9):  1161-1170.  doi:10.16380/j.kcxb.2023.09.003
    Abstract ( 165 )   PDF (2357KB) ( 352 )   PDF(mobile) (2357KB) ( 38 )     
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    【Aim】To clarify the spatiotemporal expression patterns of two genes of glutathione S-transferases (GSTs) in Pardosa astrigera and to investigate whether the two genes can respond to deltamethrin stress.【Methods】 Based on the transcriptome database of P. astrigera, the full-length cDNA sequences of the GST genes PaGSTd1 and PaGSTd2 of P. astrigera were cloned by PCR and bioinformatically analyzed. RT-qPCR was used to detect the expression levels of PaGSTd1 and PaGSTd2 in different developmental stages (2nd-6th instar nymphs and adult), female and male adult tissues (cephalothorax, abdomen and leg), and in male adult of P. astrigera stressed by deltamethrin at different concentrations [LC10(5.151 mg/L), LC30 (8.619 mg/L) and LC50 (12.311 mg/L)] for different time (6, 12, 18, 24 and 48 h)through residual film method.【Results】 The full-length cDNA sequence of PaGSTd1 (GenBank accession number: OR096398) of P. astrigera is 708 bp in length with an open reading frame of 645 bp in length, encoding 214 amino acids. The full-length cDNA sequence of PaGSTd2 (GenBank accession number: OR096399) of P. astrigerais 793 bp in length with an open reading frame of 645 bp in length, encoding 214 amino acids. The detection results of RT-qPCR showed that PaGSTd1 and PaGSTd2 were expressed in different developmental stages and adult tissues of P. astrigera, and the expression levels of PaGSTd1 and PaGSTd2 were the lowest in the 5th instar nymph. The expression level of PaGSTd1 was the highest in the 4th instar nymph of P. astrigera,and that of PaGSTd2 was the highest in adult of P. astrigera. The expression levels of PaGSTd1 and PaGSTd2 were the highest in the leg, and the expression levels in other tissues except for that in the abdomen were significantly higher in male adults than in female adults of P. astrigera. PaGSTd1 and PaGSTd2 in male adult of P. astrigera were induced at 24 h, and at 6 and 18 h, respectively, after stress by LC10 of deltamethrin. PaGSTd1 and PaGSTd2 in male adult of P. astrigera were induced at 18, 24 and 48 h, and at 18 h, respectively, after stress by LC30 of deltamethrin. Both PaGSTd1 and PaGSTd2 were induced in male adult of P. astrigera at 24 h after stress by LC50 of deltamethrin.【Conclusion】 In this study, two GST genes PaGSTd1 and PaGSTd2 were cloned from P. astrigera. Both PaGSTd1 and PaGSTd2 were most highly expressed in the leg of P. astrigera, suggesting that these two GST genes in the leg of P. astrigera play an important role in the detoxification of exogenous substances. These two GST genes could be induced to express by deltamethrin, suggesting that these two GST genes PaGSTd1 and PaGSTd2 may be involved in the stress response of P. astrigera to deltamethrin, providing clues for subsequent functional studies of GSTs.
    Study on the pathogenesis of jujube flower disease in Apis mellifera ligustica workers based on midgut metabolomics
    DU Ya-Li, XU Kai, ZHENG Li-Fang, LIU Yu-Ling, JIANG Yu-Suo
    2023, 66(9):  1171-1182.  doi:10.16380/j.kcxb.2023.09.004
    Abstract ( 127 )   PDF (2374KB) ( 119 )   PDF(mobile) (2374KB) ( 6 )     
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     【Aim】 Changes in midgut metabolites of the Italian honeybee, Apis mellifera ligustica workers suffering jujube flower disease were analyzed using metabolomics and important metabolic pathways related to jujube flower disease were excavated, so as to reveal the pathogenesis of jujube flower disease and provide a theoretical basis for the research and development of targeted medicine for jujube flower disease. 【Methods】 Liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-mass spectrometry (GC-MS) were used respectively to perform midgut non-targeted metabolomics detection on jujube flower disease-suffered and healthy A. m. ligustica workers. Through principal component analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA), the differential metabolites were screened by variable projection importance (VIP)>1.0, fold change (FC)>2.0, and P<0.05. KEGG annotation and pathway enrichment were conducted to all differential metabolites screened. The activities of superoxide dismutase (SOD) and catalase (CAT) in the midgut of A. m. ligustica workers were determined by biochemical methods, and the expression levels of antioxidant genes Sod1, Sod2 and CAT, and immune genes Defensin, Hymenoptaecin, Apidaecin and Abaecin in the midgut of A. m. ligustica workers were determined by qRT-PCR. 【Results】 According to the metabolomics detection by LC-MS, 49 and 43 differential metabolites between jujube flower disease-suffered and healthy A. m. ligustica workers were obtained, of which 33 and 30 could be identified in HMDB and KEGG databases under the positive ion mode and negative ion mode, respectively. Based on GC-MS metabolomics detection, 22 volatile differential metabolites between jujube flower disease-suffered and healthy A. m. ligustica workers were screened, among which 11 were identified in HMDB and KEGG databases. The contents of 28 of the 73 differential metabolites identified in the midgut of jujube flower disease-suffered A. m. ligustica workers increased, and those of 45 decreased as compared to those in healthy A. m. ligustica workers. Among them, geniposidic acid, indole-3-acetic acid, quinoline and raffinose accumulated in large quantities in the midgut of the jujube flower disease-suffered A. m. ligustica workers, while the contents of ursolic acid, L-threonic acid, gluconic acid, D-galactonic acid, threonic acid and rutin decreased most significantly. The analysis result of KEGG metabolic pathway enrichment showed that differential metabolites between jujube flower disease-suffered and healthy A. m. ligustica workers were significantly enriched in three carbohydrate metabolic pathways, namely ascorbate and aldarate metabolism, galactose metabolism, and butanoate metabolism. Enzyme activity determination and qRT-PCR results indicated that the activities of SOD and CAT in the midgut of jujube flower disease-suffered A. m. ligustica workers were significantly decreased, and the expression levels of Sod1, Sod2, CAT, Defensin, Hymenoptaecin and Apidaecin showed a downward trend as compared with those of healthy A. m. ligustica workers. 【Conclusion】 Both LC-MS and GC-MS non-targeted metabolomics can effectively analyze the changes of metabolites in the midgut of honeybees under the influence of jujube flower disease. The research results indicate that the abnormal carbohydrate metabolism in the honeybee midgut after collecting jujube flower caused a significant decline in the intestinal antioxidant and immune capacities, speculating that intestinal dysfunction may be the main cause of honeybee death. The research provides new insights into the pathogenesis of honeybee jujube flower disease.
    Relationship between the symbiotic microbial community and insecticide resistance in wild Anopheles sinensis (Diptera: Culicidae) 
    QIU Xin, MENG Chen, WANG Ming-Bin, CHEN Bin, ZHANG Yu-Juan
    2023, 66(9):  1183-1191.  doi:10.16380/j.kcxb.2023.09.005
    Abstract ( 213 )   PDF (4457KB) ( 200 )   PDF(mobile) (4457KB) ( 20 )     
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    【Aim】 To investigate the relationship between the symbiotic microbial communities in Anopheles sinensis and the insecticide resistance of An. sinensis in different regions of the wild environment. 【Methods】 Wild female adults of An. sinensis were collected from Chongqing, Yunnan, and Anhui in China. WHO standard in vitro bioassay and 0.05% deltamethrin impregnated paper were used to conduct insecticide susceptibility tests on the female adults of An. sinensis, classifying them as insecticide-sensitive (FS) or insecticide-resistant (FR) to perform high-throughput sequencing of the whole genomes through Illumina Hiseq 2000 platform. The sequences of 16S rRNA and 18S rRNA genes were aligned to identify symbiotic microbiota in the FS and FR An. sinensis. Alpha diversity analysis, beta diversity analysis, clustering analysis, principal coordinates analysis (PCoA) and analysis of symbiotic microbial community differences were conducted. 【Results】 A total of 3 284 species of 52 genera of 14 phyla of symbiotic microbiota were identified from the female adults of the FS and FR wild An. sinensis from Chongqing, Yunnan and Anhui. The diversity difference and community richness of the FR wild An. sinensis female adults from Anhui were the highest, and those of the FS wild An. sinensis female adults from Chongqing were the lowest. The symbiotic microbial communities in the female adults of wild An. sinensis were first clustered by region, and the diversity of the symbiotic microbial communities in the female adults of An. sinensis from Chongqing and Yunnan were more similar. A total of 10 strains including two strains of Cyanobacteria, three strains of Halobacteria, one strain of Haliangium, three strains of Ruminococcaceae and one strain of Streptococcus of bacteria in the symbiotic microbiota in the FR wild An. sinensis female adults were more abundant.【Conclusion】 The symbiotic microbial communities of the wild An. sinensis exhibit regional and resistance differences. The identified symbiotic microbiota play a positive role in the insecticide resistance of An. sinensis. The results of this study provide insights into understanding the insecticide resistance of An. sinensis.
    Life cycle and overwintering rules of Lissorhoptrus orvzophitus (Coleoptera: Curculionidae) in Guangdong province, South China
    YUAN Long-Yu, LEI Hao-Lin, LI Yan-Fang, XIAO Han-Xiang, WEI Hong-Yi, ZHANG Zhen-Fei
    2023, 66(9):  1192-1200.  doi:10.16380/j.kcxb.2023.09.006
    Abstract ( 160 )   PDF (15197KB) ( 114 )   PDF(mobile) (15197KB) ( 25 )     
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    【Aim】 To clarify the life cycle, overwintering habitats, occurrence regularity, host plant species and natural enemy species of the rice water weevil (Lissorhoptrus orvzophitus) in Guangdong province, South China, so as to provide scientific guidance for the prevention and control of this insect pest.【Methods】 We investigated the life cycle and overwintering habitats of L. orvzophitus in Guangdong through field surveys, cage observation experiments and ovary dissection from March, 2019 to April, 2021, identified its overwintering transitional host plants through molecular detection of the midgut contents in adults, and detected its main natural enemies using sequence characterized amplified region (SCAR) marker technology.【Results】 L. orvzophitus had two generations a year in the double cropping rice area of Guangdong province, and had overwintering and oversummering habits during March, 2019 and April, 2021. A complete generation of L. orvzophitus needed (140.86±1.05) d, and the larval duration was about 20 d in Guangdong. L. orvzophitus overwintered as adult in Guangdong province. The overwintering habitat pattern was paddy field, transitional zone (grassland), and swamp (abundant water grass). It was found that the ovary of L. orvzophitus adults during the overwintering period underwent diapause, and the ovarian grade was level Ⅰ. Through molecular detection of the midgut contents in L. orvzophitus adults, it was found that during the overwintering period, the main transitional host plants of L. orvzophitus were regenerated rice (Oryza sativa) and Leersia hexandra, and the main natural enemy was Pardosa laura, a nomadic spider, as revealed by the result of SCAR-based PCR.【Conclusion】 L. orvzophitus has two generations a year in Guangdong, and mainly overwinters in the swamp. The main transitional hosts during the overwintering period are Leersia hexandra and regenerated rice, and the main natural enemy in overwintering habits is P. laura. These findings have theoretical guiding significance for the accurate prevention and control of L. orvzophitus epidemic in Guangdong.
    Analysis on the stability and influencing factors of protogyny of Spodoptera frugiperda (Lepidoptera: Noctuidae)
    BI Si-Jia, HU Ben-Jin, HU Fei, XU Ting-Ting, XU Li-Na
    2023, 66(9):  1201-1209.  doi:10.16380/j.kcxb.2023.09.007
    Abstract ( 224 )   PDF (8224KB) ( 184 )   PDF(mobile) (8224KB) ( 27 )     
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    【Aim】 Protandry was more common in studies on developmental duration of sex dimorphic insects, and protogyny was less reported. The fall armyworm, Spodoptera frugiperda is a severe migratory pest on maize, and there is a phenomenon of protogyny in its developmental duration. The purpose of this study is to clarify the stability of this phenomenon and explore its influencing factors, so as to provide a theoretical basis for the accurate monitoring and early warning of S. frugiperda.【Methods】 The growth and development of S. frugiperda under three photoperiods (16L∶8D, 14L∶10D and 8L∶16D) and three food conditions (maize leaves, peanut leaves and artificial diet) were analyzed, and the ovaries of S. frugiperda reared under different photoperiods and food conditions were dissected. Moreover, the growth and development of Mythimna separata, S. litura and S. frugiperda in Noctuidae were compared to evaluate whether the protogyny was the commonness of Noctuidae insects with migratory habits.【Results】 In the comparison of three Noctuidae migratory insects, only the female adults of S. frugiperda eclosed significantly earlier (1.28 d ahead) than the male adults, and the eclosion phenomenon was stable under different photoperiods and food conditions, and only showed a weakening trend when S. frugiperda fed on peanut leaves. It was found that the ovaries of the newly eclosed adults of S. frugiperda were always immature under different photoperiods and food conditions, and did not change with external conditions. The development of female pupa of S. frugiperda was significantly faster than that of male pupa, which was the main reason for the difference in eclosion time between the two sexes of S. frugiperda, and the difference was positively correlated with the pupal weight of the two sexes: Compared with the female pupal weight, the male pupal weight of S. frugiperda increased significantly by 9.88%.【Conclusion】 The phenomenon of protogyny of S. frugiperda is relatively stable. Photoperiod and food will not change this phenomenon, but will affect the difference of eclosion time between the two sexes, and protogyny is not the commonness of Noctuidae insects with migratory habits.
    Morphology and development of the internal reproductive system of Monochamus alternatus (Coleoptera: Cerambycidae) adults
    CHEN Jin, LI Hui, HU Tian-Yi, YANG Hua-Lei, WEI Jia-Hang, JIN Lin, HAO De-Jun
    2023, 66(9):  1210-1220.  doi:10.16380/j.kcxb.2023.09.008
    Abstract ( 240 )   PDF (86405KB) ( 177 )   PDF(mobile) (86405KB) ( 29 )     
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    【Aim】To clarify the structure and developmental process of the internal reproductive system of Monochamus alternatus adults and provide a theoretical basis for its reproductive mechanism research and population dynamics monitoring.【Methods】The internal reproductive system of M. alternatus adults at different ages (day-old) was anatomically observed under optical microscope to clarify its structural characteristics and developmental classification criteria, and the developmental process of the internal reproductive system of female and male adults was determined by divison of developmental levels. 【Results】The female internal reproductive system of M. alternatus adults is composed of one pair of ovaries, one pair of lateral oviducts, common oviduct, copulatory pouch, spermathecal duct, spermatheca, spermathecal gland , ovipositor and genital cavity. According to the morphology and color of ovarioles and spermathecal glands, the sexual maturation process of female adults can be divided into the following stages: Transparent stage (stage Ⅰ), primary vitellogenesis stage (stage Ⅱ), secondary vitellogenesis stage (stage Ⅲ) and egg maturation stage (stage Ⅳ). Ovarioles grow continuously during the ovarian development, and the color changes from transparent milky white to yellow. The morphology and color of the spermathecal gland changes from flat and translucent to full and yellow. The male internal reproductive system of M. alternatus adults is composed of one pair of testes, two pairs of accessory glands, one pair of vas deferens, one pair of vesicula seminalis, one pair of ejaculatory ducts, circulator and aedeagus. According to the morphology and color of the testes, vesicula seminalis and accessory glands, the sexual maturation process of male adults can be divided into four stages including transparent stage (stage Ⅰ), initial stage of spermiogenesis (stage Ⅱ), peak period of spermiogenesis (stage Ⅲ) and maturing stage (stage Ⅳ). The testicular long diameter changes little. The color of the testis, vesicula seminalis and circulator changes from milky white and translucent to white. The morphology and color of the accessory gland changes from small and translucent to swollen and transparent. The development of the internal reproductive system of both female and male adults is mainly concentrated at the stages Ⅱ-Ⅲ. In terms of the developmental process of the internal reproductive system, male adults develop more rapidly and their internal reproductive system is already mature at the 12-day-old, while the internal reproductive system of female adults is mature at the 15-day-old. 【Conclusion】 This study has clarified the basic structure and developmental processes of the internal reproductive system of female and male adults of M. alternatus, not only providing a theoretical basis for further research on the reproductive mechanism of M. alternatus, but also providing a reference for predicting the peak ovioposition period of M. alternatus in production practice.
    Interspecific comparative analysis of transcriptome in the genus Sclomina
    DENG Mei-Jing, ZHAO Ping
    2023, 66(9):  1221-1232.  doi:10.16380/j.kcxb.2023.09.009
    Abstract ( 144 )   PDF (4857KB) ( 92 )   PDF(mobile) (4857KB) ( 9 )     
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    【Aim】To establish the transcriptome databases of three species of the genus Sclomina, analyze the expression differences of transcriptomes among related species, and investigate the interspecific divergence at the transcriptome level.【Methods】The Illumina HiSeqTM4000 high-throughput sequencing platform was used for transcriptome sequencing in the three Sclomina species, S. erinacea, S. xingrensis and S. guangxiensis. The gene function annotation was conducted by using Nr, Swiss-Prot, COG/KOG and KEGG databases. The GO functional annotation and KEGG pathway enrichment analysis were performed for the interspecific differentially expressed genes (DEGs).【Results】A total of 42 215 unigenes were obtained by transcriptome sequencing of S. erinacea, S. xingrensis and S. guangxiensis. A total of 21 117 genes were annotated in the above four databases (number of genes: Nr, 20 522; Swiss-Prot, 15 550; COG/KOG, 13 969, KEGG, 10 850). There were 3 390 DEGs (803 up-regulated, 2 587 down-regulated) in the S. xingrensis vs S. erinacea transcriptomes, 12 543 DEGs (6 639 up-regulated, 5 904 down-regulated) in the S. xingrensis vs S. guangxiensis transcriptomes, and 3 580 DEGs (2 485 up-regulated, 1 095 down-regulated) in the S. erinacea vs S. guangxiensis transcriptomes. GO functional annotation result showed that all of the above DEGs were annotated into three functional classes including biological process, cellular component and molecular function, and some functional subclasses. The DEGs in the S. xingrensis vs S. erinacea transcriptomes were annotated into 50 functional subclasses, such as metabolic process, cell and cell part, and more genes were down-regulated, and a few genes were up-regulated. The DEGs in the S. xingrensis vs S. guangxiensis transcriptomes were annotated into 54 functional subclasses, such as biological process, cell part and cell. The DEGs in the S. erinacea vs S. guangxiensis transcriptomes were annotated into 46 functional subclasses, such as cell part and metabolic process. A total of 6 254 DEGs were annotated to KEGG metabolic pathways involving several different metabolic pathways, including metabolic pathway, drug metabolism-cytochrome P450, ribosome, etc. A total of 702 DEGs in the S. xingrensis vs S. erinacea transcriptomes were enriched in 164 KEGG pathways. A total of 2 091 DEGs in the S. xingrensis vs S. guangxiensis transcriptomes were enriched to 201 KEGG pathways. A total of 865 DEGs in the S. erinacea vs S. guangxiensis transcriptomes were enriched to 129 KEGG pathways. The number of DEGs enriched in metabolic pathway, drug metabolism-cytochrome P450 and ribosome in the S. xingrensis vs S. guangxiensis transcriptomes was the highest.【Conclusion】This study results enrich the molecular biological data of the genus Sclomina. At the level of transcriptome, the interspecies difference in S. erinacea, S. xingrensis and S. guangxiensis, and the actual situation of species divergence in this genus Sclomina are explored.
    Sequencing and analysis of the complete mitochondrial genome of Eurytoma acutibialis (Hymenoptera: Eurytomidae), an important natural enemy insect of Bradybatus sp. (Coleoptera: Curculionidae) in China
    LIU Hui-Hui, LI En-Jie, CAO Liang-Ming, BAO Qing-Chun, WANG Xiao-Lin, XIN Xue-Bing, YANG Zhong-Qi
    2023, 66(9):  1233-1245.  doi:10.16380/j.kcxb.2023.09.010
    Abstract ( 153 )   PDF (4491KB) ( 170 )   PDF(mobile) (4491KB) ( 19 )     
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    【Aim】 Eurytoma acutibialis Yang, Liu et Cao is a parasitic wasp of Bradybatus sp., a serious seed-eating pest of Acer truncatum in China, and is a new species found during the investigation of Bradybatus sp. and can play an important role in controlling Bradybatus sp. To further understand the new parasitoid, the complete mitochondrial genome of E. acutibialis was sequenced and analyzed so as to provide molecular biological evidence for the systematic taxonomy and phylogenetic relationship of hymenopterous wasps (Hymenoptera: Chalcidoidea: Eurytomidae).【Methods】 The complete mitochondrial genome of E. acutibialis was sequenced on Illumina HiSeqTM4000 sequencing platform and then assembled, annotated and analyzed. Based on the nucleotide sequences of 13 protein-coding genes (PCGs) from 40 species of hymenopteran insects in the Chalcidoidea, the phylogenetic tree was constructed by Bayesian inference (BI) and maximum likelihood (ML) methods, and the phylogenetic relationship between E. acutibialis and other insects in the Chalcidoidea was analyzed.【Results】The mitochondrial genome of E. acutibialis is 15 849 bp in full-length, with the A+T content of 82.00%, and consists of 37 genes including 13 PCGs, 2 rRNA genes, 22 tRNA genes, and a control region (CR). Among the 13 PCGs, the amino acid usage frequencies from high to low are Leu,Ile, Met, Phe and Asn. All the 13 PCGs initiate with the standard start codons of ATN (ATT, ATG and ATA) and terminate with the typical stop codons TAA/TAG. Among the 22 tRNA genes, trnI lacks receptor arm, trnF lacks TΨC-arm, trnS1 lacks DHU arm and DHU arm of trnS2 forms a simple loop. The remaining tRNA genes have a typical cloverleaf structure. There is a significant gene rearrangement, with an inversion occurring in the nad2-nad1-cytb-nad6-nad4L-nad4-nad5 cluster and rearrangements of 16 tRNA genes. The phylogenetic analysis highly supported the monophyly of the subfamily Eurytomidae, and E. acutibialis was the closest to Eurytoma sp. ZJUH 2016013.【Conclusion】The complete mitochondrial genome sequence of E. acutibialis was firstly obtained, and the phylogenetic analysis based on the mitochondrial genome supported its taxonomic position in the genus Eurytoma in the family Eurytomidae in the order Hymenoptera and proved to be consistent with the morphological taxonomy.
    REVIEW ARTICLES
    Research advances in the structure and function of insect fat bodies and their application in human disease models
    MA Zhen-Gang, HE Yu-Bo, MA Qiang, WANG Jing-Lin, ZHOU Ze-Yang
    2023, 66(9):  1246-1257.  doi:10.16380/j.kcxb.2023.09.011
    Abstract ( 300 )   PDF (3559KB) ( 164 )   PDF(mobile) (3559KB) ( 22 )     
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    Insect fat bodies are widely distributed in the body of insects, and they are a dynamically loose tissue that includes peripheral fat bodies and visceral fat bodies. The structure and function of insect fat bodies are closely related, and their structure changes with the changes of different life stages, and their functions also change. However, the most basic function of insect fat bodies is to act as the core tissue of insect life metabolism to synthesize and store substances. In addition, fat bodies, which are the target organs of various hormones, have many important functions and are related to the innate immunity, longevity, growth and development of insects. Therefore, the study on insect fat body is very important for the analysis of the important life phenomena of insects. In recent years, a large number of studies have taken insect fat bodies as research models for human diseases and drug development, and applied them in many fields such as human immunology, pathogenesis of human diseases, and new drug research and development. Here, in order to systematically deepen the understanding of the structure and function of insect fat bodies, the morphological structure, formation and metamorphosis, biological function, and their application and prospect in the study of human disease models were reviewed. Insect fat bodies would have great application potential in the construction of major human disease models and the exploration of disease pathogenesis.
    Research progress of the population genetic differentiation and environmental adaptation mechanisms in Apis cerana cerana (Hymenoptera: Apidae)
    CHEN Bing, LUO Jia-Yu
    2023, 66(9):  1258-1270.  doi:10.16380/j.kcxb.2023.09.012
    Abstract ( 231 )   PDF (1849KB) ( 458 )   PDF(mobile) (1849KB) ( 21 )     
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     Apis cerana cerana is a critical and important pollinator in China. This bee species has a wide distribution in various habitats, and exhibits several advantages as pollinator, e.g., agility in flight, long nectar gathering period and strong adaptability. However, in recent years, A. c. cerana has been facing an unprecedented decline in population diversity. In order to protect the genetic resources of these specific populations, researchers studied the physiology and mechanism of genetic differentiation and environmental adaptation in A. c. cerana based on geometric morphology, molecular biology and genomics technologies. Meanwhile, the diverse populations of A. c. cerana in China provided rich materials for analyzing their adaptive evolution. In this article, we summarized the research progress from the four aspects: The correlation between population genetic differentiation and environmental changes, the morphological variation and environmental adaptation, the enviroment-adaptive physiological and behavioral changes, and the genetic mechanisms behind these phenotypic changes of A. c. cerana populations. Previous studies showed that changes in physical barriers and ecological environment, especially those related to altitude and latitude, were the main reasons for the differentiation of A. c. cerana populations. Among the climatic factors, temperature, oxygen, radiation and humidity had important effects on the morphological development and eco-physiological traits of A. c. cerana. The morphological changes were mainly explained by variation in body size and color. Changes in metabolic physiology and behaviors have been evolved as a crucial adaption strategy. Population genetics and genomics based on modern genomics and molecular biology techniques showed that genes and pathways related to social division of labor, learning and perceiving behavior, information perception, growth and development, thermal adaptation and metabolism are subject to natural selection. These findings provide molecular evidence for the ability of A. c. cerana to adapt to different habitats and the evolution of bee species. However, the specific molecular evolution mechanisms for the environmental adaption of bees await further investigation. Our review on the mechanisms of genetic differentiation and environmental adaption of A. c. cerana will deepen our understanding of the evolutionary history and genetic diversity of ancient bee species, and lay a foundation for further studies on the adaptive mechanisms of social insects to different environments and the development of effective conservation strategies.
    CONTENTS
    Contents of Vol. 66 Issue 9
    2023, 66(9):  1271-1271. 
    Abstract ( 95 )   PDF (493KB) ( 215 )   PDF(mobile) (493KB) ( 7 )     
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