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Baur Hannes - One of the best experts on this subject based on the ideXlab platform.

Qi Fang - One of the best experts on this subject based on the ideXlab platform.

  • venom α amylase of the endoparasitic wasp Pteromalus puparum influences host metabolism
    Pest Management Science, 2020
    Co-Authors: Beibei Wang, Qi Fang, Lei Yang, Chaodu Ren, Qisheng Song
    Abstract:

    Background Pteromalus puparum (Hymenoptera: Pteromalidae) is an endoparasitoid wasp that parasitizes many butterfly species, including a Brassicaceae pest, Pieris rapae (Lepidoptera: Pieridae), the small white cabbage butterfly. P. puparum females inject venom along with their eggs into hosts to ensure successful parasitism. The venom regulates host development and behavior, suppresses host immunity, and influences host metabolism. It has been shown that the venom contains α-amylases, a group of hydrolytic enzymes that act in insect sugar metabolism. So far, three α-amylases have been identified in P. puparum (Pteromalus puparum α-amylases, PpAmys) and the function of PpAmy1 has been reported. However, the functions of PpAmy2 and PpAmy3 remain unknown. Results We studied the functions of an α-amylase highly expressed in muscle-rich tissues (PpAmy2) and an α-amylase highly expressed in venom apparatus (PpAmy3) using RNAi and GC-TOF-MS techniques. Knockdown of PpAmy3 by RNAi reduced the body length and weight of 1-day old larval offspring while there was no significant effect when PpAmy2 was knocked down. Compared to the control injected with siGFP, many metabolites in P. puparum changed when PpAmy2 was knocked down, while the injection of PpAmy3 recombinant protein into host induced metabolite changes in the P. rapae hemolymph. Conclusion Our study demonstrated that PpAmy2 acts in metabolism in the muscles of the parasitoid while PpAmy3 could influence the host metabolism and may support the development of parasitic wasp offspring. © 2020 Society of Chemical Industry.

  • genes acting in longevity related pathways in the endoparasitoid Pteromalus puparum
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Shijiao Xiong, Qi Fang, Fei Wang, Beibei Wang, Zhichao Yan, Lei Yang, Shan Xiao, Fang Wang, Yi Deng, Qisheng Song
    Abstract:

    Among insects, lifespans vary over a broad range, from the short-lived mayflies to the 17-year periodical cicadas. Generally, lifespans are determined by a phase in life, the reproductive lifespan, which varies among species. Numerous pathways, such as the insulin/insulin-like growth factor signaling pathway, the target of rapamycin pathway and the mitogen-activated protein kinase/extracellular signal-regulated kinases pathways, influence aging and lifespan. Components of these pathways were identified as lifespan-related genes, including genes mediating growth, metabolism, development, resistance, and other processes. Many age-related genes have been discovered in fruit flies, honeybees, and ants among other insect species. Studies of insect aging and longevity can help understand insect biology and develop new pest management technologies. In this paper, we interrogated the new Pteromalus puparum genome, from which we predicted 133 putative lifespan-related genes based on their homology with known lifespan-related genes of Drosophila melanogaster. These genes function in five signaling pathways and three physiological processes. The conserved domain structures of these genes were predicted and their expression patterns were analyzed. Amino acid sequence alignments and domain structure analysis indicate that most components remain conserved across at least six insect orders. The data in this paper will facilitate future work on parasitoid lifespans, which may have economic value in biocontrol programs.

  • genome wide identification and analysis of genes encoding cuticular proteins in the endoparasitoid wasp Pteromalus puparum hymenoptera pteromalidae
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Jiale Wang, Qisheng Song, Hongxia Jin, Lei Yang, Shan Xiao, David Stanley, Qi Fang
    Abstract:

    The multifunctional insect cuticle serves as the exoskeleton, determines body shape, restricts water loss, provides attachment sites for muscles and internal organs and is a formidable barrier to invaders. It is morphologically divided into three layers, including envelope, epicuticle, and procuticle and is composed of chitin and cuticular proteins (CPs). Annotation of CPs and their cognate genes may help understand the structure and functions of insect cuticles. In this paper, we interrogated the genome of Pteromalus puparum, an endoparasitoid wasp that parasitizes Pieris rapae and Papilio xuthus pupae, and identified 82 genes encoding CPs belonging to six CP families, including 62 in the CPR family, 8 in CPAP3, 5 in CPF/CPFL, 2 low complexity proteins, 2 in TWDL, and 3 in Apidermin. We used six RNA-seq libraries to determine CP gene expression profiles through development and compared the cuticle hydrophobicity between the P. puparum and the ectoparasitoid Nasonia vitripennis based on GRAVY values of CPR sequences. In the Nasonia-Pteromalus comparison, we found in both N. vitripennis and P. puparum, the peak of their CPR hydrophobicity displayed at their pupal stage, whereas their adult stage showed the lowest level. Except at the adult stage, the CPR hydrophobicity in N. vitripennis is always higher than P. puparum. Finally, we identified three novel Apidermin genes, a family found solely in Hymenoptera and revealed a new sequence feature of this family. This new information contributes to a broader understanding of insect CPs generally.

  • genome wide characterization and transcriptomic analyses of neuropeptides and their receptors in an endoparasitoid wasp Pteromalus puparum
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Ziwen Teng, Qi Fang, Fei Wang, Qisheng Song, Shan Xiao, Fang Wang, Lei Guo, David Stanley
    Abstract:

    In insects, neuropeptides constitute a group of signaling molecules that act in regulation of multiple physiological and behavioral processes by binding to their corresponding receptors. On the basis of the bioinformatic approaches, we screened the genomic and transcriptomic data of the parasitoid wasp, Pteromalus puparum, and annotated 36 neuropeptide precursor genes and 33 neuropeptide receptor genes. Compared to the number of precursor genes in Bombyx mori (Lepidoptera), Chilo suppressalis (Lepidoptera), Drosophila melanogaster (Diptera), Nilaparvata lugens (Hemiptera), Apis mellifera (Hymenoptera), and Tribolium castaneum (Coleoptera), P. puparum (Hymenoptera) has the lowest number of neuropeptide precursor genes. This lower number may relate to its parasitic life cycle. Transcriptomic data of embryos, larvae, pupae, adults, venom glands, salivary glands, ovaries, and the remaining carcass revealed stage-, sex-, and tissue-specific expression patterns of the neuropeptides, and their receptors. These data provided basic information about the identity and expression profiles of neuropeptides and their receptors that are required to functionally address their biological significance in an endoparasitoid wasp.

  • genomic and transcriptomic analyses of glutathione s transferases in an endoparasitoid wasp Pteromalus puparum
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Ziwen Teng, Qi Fang, Fei Wang, Beibei Wang, Qisheng Song, Jiale Wang, Shan Xiao, Fang Wang, Lei Guo, David Stanley
    Abstract:

    Pteromalus puparum is a gregarious pupal endoparasitoid with a wide host range. It deposits eggs into pierid and papilionid butterfly pupae. Glutathione S-transferases (GSTs) are a family of multifunctional detoxification enzymes that act in xenobiotic metabolism in insects. Insect genome projects have facilitated identification and characterization of GST family members. We identified 20 putative GSTs in the P. puparum genome, including 19 cytosolic and one microsomal. Phylogenetic analysis showed that P. puparum GSTs are clustered into Hymenoptera-specific branches. Transcriptomic data of embryos, larvae, female pupae, male pupae, female adults, male adults, venom glands, carcass, salivary glands, and ovaries revealed stage-, sex-, and tissue-specific expression patterns of GSTs in P. puparum. This is the most comprehensive study of genome-wide identification, characterization, and expression profiling of GST family in hymenopterans. Our results provide valuable information for understanding the metabolic adaptation of this wasp.

Qisheng Song - One of the best experts on this subject based on the ideXlab platform.

  • venom α amylase of the endoparasitic wasp Pteromalus puparum influences host metabolism
    Pest Management Science, 2020
    Co-Authors: Beibei Wang, Qi Fang, Lei Yang, Chaodu Ren, Qisheng Song
    Abstract:

    Background Pteromalus puparum (Hymenoptera: Pteromalidae) is an endoparasitoid wasp that parasitizes many butterfly species, including a Brassicaceae pest, Pieris rapae (Lepidoptera: Pieridae), the small white cabbage butterfly. P. puparum females inject venom along with their eggs into hosts to ensure successful parasitism. The venom regulates host development and behavior, suppresses host immunity, and influences host metabolism. It has been shown that the venom contains α-amylases, a group of hydrolytic enzymes that act in insect sugar metabolism. So far, three α-amylases have been identified in P. puparum (Pteromalus puparum α-amylases, PpAmys) and the function of PpAmy1 has been reported. However, the functions of PpAmy2 and PpAmy3 remain unknown. Results We studied the functions of an α-amylase highly expressed in muscle-rich tissues (PpAmy2) and an α-amylase highly expressed in venom apparatus (PpAmy3) using RNAi and GC-TOF-MS techniques. Knockdown of PpAmy3 by RNAi reduced the body length and weight of 1-day old larval offspring while there was no significant effect when PpAmy2 was knocked down. Compared to the control injected with siGFP, many metabolites in P. puparum changed when PpAmy2 was knocked down, while the injection of PpAmy3 recombinant protein into host induced metabolite changes in the P. rapae hemolymph. Conclusion Our study demonstrated that PpAmy2 acts in metabolism in the muscles of the parasitoid while PpAmy3 could influence the host metabolism and may support the development of parasitic wasp offspring. © 2020 Society of Chemical Industry.

  • genome wide identification and analysis of genes encoding cuticular proteins in the endoparasitoid wasp Pteromalus puparum hymenoptera pteromalidae
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Jiale Wang, Qisheng Song, Hongxia Jin, Lei Yang, Shan Xiao, David Stanley, Qi Fang
    Abstract:

    The multifunctional insect cuticle serves as the exoskeleton, determines body shape, restricts water loss, provides attachment sites for muscles and internal organs and is a formidable barrier to invaders. It is morphologically divided into three layers, including envelope, epicuticle, and procuticle and is composed of chitin and cuticular proteins (CPs). Annotation of CPs and their cognate genes may help understand the structure and functions of insect cuticles. In this paper, we interrogated the genome of Pteromalus puparum, an endoparasitoid wasp that parasitizes Pieris rapae and Papilio xuthus pupae, and identified 82 genes encoding CPs belonging to six CP families, including 62 in the CPR family, 8 in CPAP3, 5 in CPF/CPFL, 2 low complexity proteins, 2 in TWDL, and 3 in Apidermin. We used six RNA-seq libraries to determine CP gene expression profiles through development and compared the cuticle hydrophobicity between the P. puparum and the ectoparasitoid Nasonia vitripennis based on GRAVY values of CPR sequences. In the Nasonia-Pteromalus comparison, we found in both N. vitripennis and P. puparum, the peak of their CPR hydrophobicity displayed at their pupal stage, whereas their adult stage showed the lowest level. Except at the adult stage, the CPR hydrophobicity in N. vitripennis is always higher than P. puparum. Finally, we identified three novel Apidermin genes, a family found solely in Hymenoptera and revealed a new sequence feature of this family. This new information contributes to a broader understanding of insect CPs generally.

  • genes acting in longevity related pathways in the endoparasitoid Pteromalus puparum
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Shijiao Xiong, Qi Fang, Fei Wang, Beibei Wang, Zhichao Yan, Lei Yang, Shan Xiao, Fang Wang, Yi Deng, Qisheng Song
    Abstract:

    Among insects, lifespans vary over a broad range, from the short-lived mayflies to the 17-year periodical cicadas. Generally, lifespans are determined by a phase in life, the reproductive lifespan, which varies among species. Numerous pathways, such as the insulin/insulin-like growth factor signaling pathway, the target of rapamycin pathway and the mitogen-activated protein kinase/extracellular signal-regulated kinases pathways, influence aging and lifespan. Components of these pathways were identified as lifespan-related genes, including genes mediating growth, metabolism, development, resistance, and other processes. Many age-related genes have been discovered in fruit flies, honeybees, and ants among other insect species. Studies of insect aging and longevity can help understand insect biology and develop new pest management technologies. In this paper, we interrogated the new Pteromalus puparum genome, from which we predicted 133 putative lifespan-related genes based on their homology with known lifespan-related genes of Drosophila melanogaster. These genes function in five signaling pathways and three physiological processes. The conserved domain structures of these genes were predicted and their expression patterns were analyzed. Amino acid sequence alignments and domain structure analysis indicate that most components remain conserved across at least six insect orders. The data in this paper will facilitate future work on parasitoid lifespans, which may have economic value in biocontrol programs.

  • genomic and transcriptomic analyses of glutathione s transferases in an endoparasitoid wasp Pteromalus puparum
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Ziwen Teng, Qi Fang, Fei Wang, Beibei Wang, Qisheng Song, Jiale Wang, Shan Xiao, Fang Wang, Lei Guo, David Stanley
    Abstract:

    Pteromalus puparum is a gregarious pupal endoparasitoid with a wide host range. It deposits eggs into pierid and papilionid butterfly pupae. Glutathione S-transferases (GSTs) are a family of multifunctional detoxification enzymes that act in xenobiotic metabolism in insects. Insect genome projects have facilitated identification and characterization of GST family members. We identified 20 putative GSTs in the P. puparum genome, including 19 cytosolic and one microsomal. Phylogenetic analysis showed that P. puparum GSTs are clustered into Hymenoptera-specific branches. Transcriptomic data of embryos, larvae, female pupae, male pupae, female adults, male adults, venom glands, carcass, salivary glands, and ovaries revealed stage-, sex-, and tissue-specific expression patterns of GSTs in P. puparum. This is the most comprehensive study of genome-wide identification, characterization, and expression profiling of GST family in hymenopterans. Our results provide valuable information for understanding the metabolic adaptation of this wasp.

  • genome wide characterization and transcriptomic analyses of neuropeptides and their receptors in an endoparasitoid wasp Pteromalus puparum
    Archives of Insect Biochemistry and Physiology, 2020
    Co-Authors: Ziwen Teng, Qi Fang, Fei Wang, Qisheng Song, Shan Xiao, Fang Wang, Lei Guo, David Stanley
    Abstract:

    In insects, neuropeptides constitute a group of signaling molecules that act in regulation of multiple physiological and behavioral processes by binding to their corresponding receptors. On the basis of the bioinformatic approaches, we screened the genomic and transcriptomic data of the parasitoid wasp, Pteromalus puparum, and annotated 36 neuropeptide precursor genes and 33 neuropeptide receptor genes. Compared to the number of precursor genes in Bombyx mori (Lepidoptera), Chilo suppressalis (Lepidoptera), Drosophila melanogaster (Diptera), Nilaparvata lugens (Hemiptera), Apis mellifera (Hymenoptera), and Tribolium castaneum (Coleoptera), P. puparum (Hymenoptera) has the lowest number of neuropeptide precursor genes. This lower number may relate to its parasitic life cycle. Transcriptomic data of embryos, larvae, pupae, adults, venom glands, salivary glands, ovaries, and the remaining carcass revealed stage-, sex-, and tissue-specific expression patterns of the neuropeptides, and their receptors. These data provided basic information about the identity and expression profiles of neuropeptides and their receptors that are required to functionally address their biological significance in an endoparasitoid wasp.

Gongyin Ye - One of the best experts on this subject based on the ideXlab platform.

  • insights into the venom composition and evolution of an endoparasitoid wasp by combining proteomic and transcriptomic analyses
    Scientific Reports, 2016
    Co-Authors: Qi Fang, Lei Wang, Fei Wang, Fei Li, John H Werren, Gongyin Ye
    Abstract:

    Parasitoid wasps are abundant and diverse hymenopteran insects that lay their eggs into the internal body (endoparasitoid) or on the external surface (ectoparasitoid) of their hosts. To make a more conducive environment for the wasps’ young, both ecto- and endoparasitoids inject venoms into the host to modulate host immunity, metabolism and development. Endoparasitoids have evolved from ectoparasitoids independently in different hymenopteran lineages. Pteromalus puparum, a pupal endoparasitoid of various butterflies, represents a relatively recent evolution of endoparasitism within pteromalids. Using a combination of transcriptomic and proteomic approaches, we have identified 70 putative venom proteins in P. puparum. Most of them show higher similarity to venom proteins from the related ectoparasitoid Nasonia vitripennis than from other more distantly related endoparasitoids. In addition, 13 venom proteins are similar to venoms of distantly related endoparasitoids but have no detectable venom matches in Nasonia. These venom proteins may have a role in adaptation to endoparasitism. Overall, these results lay the groundwork for more detailed studies of venom function and adaptation to the endoparasitic lifestyle.

  • venom of the parasitoid wasp Pteromalus puparum contains an odorant binding protein
    Archives of Insect Biochemistry and Physiology, 2015
    Co-Authors: Lei Wang, Qi Fang, Cen Qian, Gongyin Ye
    Abstract:

    Odorant binding proteins (OBPs) are crucial for insects to detect food, mates, predators, or other purposes. They are mostly located on antennae and other olfactory sensilla. In this study, we identified an OBP from the venom of Pteromalus puparum, designated as PpOBP. The cDNA of PpOBP is 517 bp in length, encoding 132 amino acids. Phylogenetic analysis revealed that PpOBP was clustered with OBP68 and OBP67 of Nasonia vitripennis. PpOBP was highly expressed in the venom apparatus at the transcriptional and translational levels. PpOBP was located in all parts of venom apparatus including venom gland, venom reservoir, and Dufour's gland. During 0-6 days post adult eclosion, the PpOBP mRNA level peaked at 2 days in the venom apparatus, whereas the protein remained at a high level. In the venom apparatus, the PpOBP mRNA was significantly upregulated following feeding with honey and parasitization. We propose that PpOBP is involved in parasitoid-host interactions. Language: en

  • heat shock protein genes hsp20 hsp75 and hsp90 from pieris rapae molecular cloning and transcription in response to parasitization by Pteromalus puparum
    Insect Science, 2013
    Co-Authors: Guoxing Wu, Gongyin Ye, Cui Hu
    Abstract:

    Abstract  Most molecular work on the roles of heat shock proteins (hsps) in host-parasite interaction has focused on vertebrates, rather than invertebrates. Here the full length complementary DNA (cDNA) sequences of three hsp genes (hsp20, hsp75 and hsp90) were amplified from Pieris rapae, and their transcriptional responsiveness to parasitization by the endoparasitic wasp Pteromalus puparum were investigated. The cDNA sequence analysis of hsp20, hsp75 and hsp90 revealed open reading frames of 531, 2 328 and 2 157 bp in length, which encode proteins with calculated molecular weights of 19.5, 75.48 and 82.7 kDa, respectively. The comparison of amino acid sequences showed that P. rapae hsp20 shared highly divergent homology to that of other insects, while hsp75 and hsp90 showed high homology to their counterparts of other species. The expression analysis indicated that these three genes were influenced in response to parasitization by P. puparum. The hsp20 transcripts in parasitized pupae were higher compared to non-parasitized pupae. The expression of hsp75 and hsp90 were down-regulated following parasitization. The results indicate that hsps are involved in host-parasitoid interactions.

  • proteome changes in the plasma of pieris rapae parasitized by the endoparasitoid wasp Pteromalus puparum
    Journal of Zhejiang University-science B, 2011
    Co-Authors: Qi Fang, Gongyin Ye, Cui Hu
    Abstract:

    Parasitism by the endoparasitoid wasp Pteromalus puparum causes alterations in the plasma proteins of Pieris rapae. Analysis of plasma proteins using a proteomic approach showed that seven proteins were differentially expressed in the host pupae after 24-h parasitism. They were masquerade-like serine proteinase homolog (MSPH), enolase (Eno), bilin-binding protein (BBP), imaginal disc growth factor (IDGF), ornithine decarboxylase (ODC), cellular retinoic acid binding protein (CRABP), and one unknown function protein. The full length cDNA sequences of MSPH, Eno, and BBP were successfully cloned using rapid amplification of cDNA ends-polymerase chain reaction (RACE-PCR). Reverse transcriptase-polymerase chain reaction (RT-PCR) analysis indicated that the transcript levels of MSPH and BBP in the fat bodies of host pupae were inducible in response to the parasitism and their variations were consistent with translational changes of these genes after parasitism, while the transcript levels of Eno and IDGF were not affected by parasitism. This study will contribute to the better understanding of the molecular bases of parasitoidinduced host alterations associated with innate immune responses, detoxification, and energy metabolism.

  • proteomic analysis of the venom from the endoparasitoid wasp Pteromalus puparum hymenoptera pteromalidae
    Archives of Insect Biochemistry and Physiology, 2010
    Co-Authors: Qi Fang, Cui Hu, Lei Wang, Gongyin Ye
    Abstract:

    Parasitoid venom is a complex mixture of active substances with diversified biological functions. Because of its range of activities, venom is an important resource with respect to potential application in agriculture and medicine. Only a limited number of peptides, proteins, and enzymes have been identified and characterized from parasitoid venom. Here we describe a proteomic analysis of the venom from the endoparasitoid wasp Pteromalus puparum (Hymenoptera: Pteromalidae). Venom resolved by two-dimensional electrophoresis yielded 56 protein spots with major proteins in the pI range 4–7 and molecular mass range of 25–66.2 kDa. The amino acid sequences of the proteins were identified by mass spectrometry. Several venom proteins such as calreticulin, venom acid phosphatase, serine protease, arginine kinase, serine protease homolog, aminotransferase-like venom protein, and heat shock protein 70, were identified in silico based on their amino acid sequences. The full-length cDNAs of calreticulin and arginine kinase were cloned. Calreticulin showed 62% identity with calreticulin in the venom of Cotesia rubecula. Arginine kinase showed a high level of sequence identity (92%) with its counterpart in the venom of Cyphononyx dorsalis. RT-PCR analysis revealed that the transcript levels of calreticulin and arginine kinase were developmentally changed, suggesting a possible correlation with the oviposition process. This study contributes to our appreciation of a parasitoid wasp venom composition. © 2010 Wiley Periodicals, Inc.

Hany K M Dweck - One of the best experts on this subject based on the ideXlab platform.

  • antennal sensory receptors of Pteromalus puparum female hymenoptera pteromalidae a gregarious pupal endoparasitoid of pieris rapae
    Micron, 2009
    Co-Authors: Hany K M Dweck
    Abstract:

    The external morphology of the antennal sensilla of Pteromalus puparum females (Hymenoptera: Pteromalidae) is described using scanning electron microscopy. The antennae of P. puparum females are geniculate in shape, formed from a large, cylindrical scape with a basal radicel fitting into the antennal socket, a shorter, barrel-shaped pedicel and a flagellum composed of 12 subsegments. Eight morphologically distinct types of sensilla were found on the female antennae. These are: nonporous sensilla trichodea types 1 and 2, which are putative mechanosensilla, nonporous sensilla chaetica, which may function as proprioceptors, uniporous sensilla trichodea types 3 and 4, which are presumably contact chemosensilla, basiconic capitate peg sensilla, which probably function in thermo-hygro reception, multiporous sensilla trichodea, and multiporous sensilla placodea which are all presumed to be olfactory sensilla.

  • antennal sensory receptors of Pteromalus puparum female hymenoptera pteromalidae a gregarious pupal endoparasitoid of pieris rapae
    Micron, 2009
    Co-Authors: Hany K M Dweck
    Abstract:

    The external morphology of the antennal sensilla of Pteromalus puparum females (Hymenoptera: Pteromalidae) is described using scanning electron microscopy. The antennae of P. puparum females are geniculate in shape, formed from a large, cylindrical scape with a basal radicel fitting into the antennal socket, a shorter, barrel-shaped pedicel and a flagellum composed of 12 subsegments. Eight morphologically distinct types of sensilla were found on the female antennae. These are: nonporous sensilla trichodea types 1 and 2, which are putative mechanosensilla, nonporous sensilla chaetica, which may function as proprioceptors, uniporous sensilla trichodea types 3 and 4, which are presumably contact chemosensilla, basiconic capitate peg sensilla, which probably function in thermo-hygro reception, multiporous sensilla trichodea, and multiporous sensilla placodea which are all presumed to be olfactory sensilla.