通讯机构：
[Guo-Hua Huang] H;Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Hunan Agricultural University, Changsha, Hunan 410128, China<&wdkj&>College of Plant Protection, Hunan Agricultural University, Changsha, Hunan 410128, China
摘要：
<jats:p>Asian species of the genus Vespina Davis, 1972 (Lepidoptera, Incurvariidae) are mainly reviewed. Vespina meridiana Hirowatari & Yagi sp. nov. from the Ryukyu Islands, Japan, and Vespina sichuana Hirowatari, Huang & Wang sp. nov. from Sichuan, China, are described. The previously known Vespina species are associated with plants from the Fagaceae family on the western coast of the USA and East Asia and with Sapindaceae (Aceraceae) in eastern Europe. The two new species described here are associated with Fagaceae and Myricaceae, respectively, in warm temperate areas in Asia. Vespina nielseni Kozlov, 1987, which was only known from East Asia, is newly recorded from South China. A checklist for the genus is provided herein. Morphological information of the immature stages of the two new species is partially provided. The absence or reduction of a female frenulum and presence of approximately 20 thin pseudofrenular bristles, the dorsoventrally flattened pupa, and the minute tergal spines scattered on abdominal segments 3–8 are considered as possible autapomorphies of Vespina.</jats:p>
摘要：
Identifying novel biocontrol agents and developing new strategies are urgent goals in insect pest biocontrol. Ascoviruses are potential competent insect viruses that may be developed into bioinsecticides, but this aim is impeded by their poor oral infectivity. To improve the per os infectivity of ascovirus, Bacillus thuringiensis kurstaki (Btk) was employed as a helper to damage the midgut of lepidopteran larvae (Helicoverpa armigera, Mythimna separata, Spodoptera frugiperda, and S. litura) in formulations with Heliothis virescens ascovirus isolates (HvAV-3h and HvAV-3j). Btk and ascovirus mixtures (Btk/HvAV-3h and Btk/HvAV-3j) were fed to insect larvae (3rd instar). With the exception of S. frugiperda larvae, which exhibited low mortality after ingesting Btk, the larvae of the other tested species showed three types of response to feeding on the formulas: type I, the tested larvae (H. armigera) were killed by Btk infection so quickly that insufficient time and resources remained for ascoviral invasion; type II, both Btk and the ascovirus were depleted by their competition, such that neither was successfully released or colonized the tissue; type III, Btk was eliminated by the ascovirus, and the ascovirus achieved systemic infection in the tested larvae. The feeding of Btk/ascovirus formulas led to a great reduction in larval diet consumption and resulted in a significant decrease in the emergence rate of H. armigera, M. separata, and S. litura larvae, which suggested that the formulas exerted marked oral control effects on both the contemporary individuals and the next generation of these tested pest species.
摘要：
Melanization is an important innate immune defense mechanism of insects, which can kill invading pathogens. Most pathogens, for their survival and reproduction, inhibit the melanization of the host. Interestingly, our results suggested that after infection with Heliothis virescens ascovirus 3h (HvAV-3h), the speed of melanization in infected Spodoptera exigua larval hemolymph was accelerated and that the phenoloxidase (PO) activity of hemolymph in larvae infected with HvAV-3h increased significantly (1.20-fold at 96 hpi, 1.52-fold at 120 hpi, 1.23-fold at 144 hpi, 1.12-fold at 168 hpi). The transcription level of the gene encoding S. exigua prophenoloxidase-1 (SePPO-1 gene) was upregulated dramatically in the fat body during the middle stage of infection. In addition, when melanization was inhibited or promoted, the replication of HvAV-3h was inhibited or promoted, respectively. In conclusion, infection with HvAV-3h can markedly induce melanization in the middle stage of infection, and melanization is helpful for HvAV-3h viral replication.
摘要：
Apoptosis play critical roles in multiple biological processes in multicellular organisms. Caspases are known as important participator and regulator of apoptosis. Here, four novel caspase genes of Spodoptera exigua were cloned and characterized, which were designated as SeCasp-1, SeCasp-6, SeCasp-7 and SeCasp-8. Analysis of the putative encoded protein sequences of these SeCasps indicated that SeCasp-1 and SeCasp-7 were possible homologues of executor caspases; SeCasp-8 was a possible homologue of initiator caspases; and SeCasp-6 was a unique caspase of S. exigua that shares low similarity with all the identified insect caspases. Based on baculovirus expression system analyses, SeCasp-1 exhibited similar caspase activity to human caspase-1, -3, -4, -6, -8 and -9; SeCasp-6 presented similar caspase activity to human caspase-2, -3, -4, -6, -8 and -9; SeCasp-7 exhibited similar caspase activity to human caspase-2, -3 and -6; and SeCasp-8 presented similar caspase activity only to human caspase-8. Induction with different chemicals revealed that SeCasp-1 showed extreme upregulation after 24 h in the treated fat body cell line (IOZCAS-Spex-II) of S. exigua. Developmental expression analysis revealed that SeCasp-1 was highly transcribed in the larval stages, while SeCasp-6, SeCasp-7, SeCasp-8 were down-regulated. The in vivo detection of the relative expression levels of SeCasps in S. eixgua larvae inoculated with different pathogens suggested that SeCasp-1 was sensitive to Bacillus thuringiensis infection and that SeCasp-6 was sensitive to baculovirus infection. SeCasp-7 and SeCasp-8 showed slight changes under either in vitro chemical apoptosis induction or in vivo pathogen infection. This article is protected by copyright. All rights reserved.
摘要：
So far, ascoviruses have only been identified from Lepidoptera host insects and their transmission vectors-endoparasitic wasps. Here, we reported the first finding of a complete novel ascovirus genome from a Diptera insect, Dasineura jujubifolia. Initially, sequence fragments with homology to ascoviruses were incidentally identified during metagenomic sequencing of the mitochondria of D. jujubifolia (Cecidomyiidae, Diptera) which is a major pest on Ziziphus jujuba. Then a full circular viral genome was assembled from the metagenomic data, which has an A+T percentage of 74% and contains 142,600 bp with 141 open reading frames (ORFs). Among the 141 ORFs, 37 were conserved in all sequenced ascoviruses (core genes) including proteins predicted to participate in DNA replication, gene transcription, protein modification, virus assembly, lipid metabolism and apoptosis. Multi-gene families including those encode for baculovirus repeated open reading frames (BROs), myristylated membrane proteins, RING/U-box E3 ubiquitin ligases, and ATP-binding cassette (ABC) transporters were found in the virus genome. Phylogenetic analysis showed that the newly identified virus belongs to genus Toursvirus of Ascoviridae, and is therefore named as Dasineura jujubifolia toursvirus 2 (DjTV-2a). The virus becomes the second reported species of the genus after Diadromus pulchellus toursvirus 1 (DpTV-1a). The genome arrangement of DjTV-2a is quite different from that of DpTV-1a, suggesting these two viruses separated in an early time of evolution. The results suggest that the ascoviruses may infect a much broader range of hosts than our previous knowledge, and shed lights on the evolution of ascoviruses and particularly on that of the toursviruses.
摘要：
<jats:title>Abstract</jats:title><jats:p><jats:italic>Microplitis similis</jats:italic> (Hymenoptera: Braconidae) is a solitary endoparasitoid of <jats:italic>Spodoptera litura</jats:italic> larvae (Lepidoptera: Noctuidae). Here, the effects of constant temperature (18, 21, 24, 27, 30, 33 and 36 °C) on the development and fecundity of <jats:italic>M. similis</jats:italic> developing in <jats:italic>S. litura</jats:italic> were studied in the laboratory to clarify the range of its potential distribution and better understand its potential as a biological control agent. The developmental duration of <jats:italic>M. similis</jats:italic> varied from 10.6 (33 °C) to 27.9 days (18 °C). The developmental threshold temperature and effective accumulative temperature of <jats:italic>M. similis</jats:italic> were 9.96 °C and 231.14 Degree‐days, respectively. The average adult longevity of <jats:italic>M. similis</jats:italic> ranged from 5.1 (33 °C) to 26.8 days (18 °C). The maximum fecundity of the parasitoid was observed at 27 and 30 °C, which were 43.07 and 39.73 eggs, respectively. The minimum fecundity of the parasitoid was observed at 18 °C, which was 8.27 eggs. The intrinsic rate of increase (<jats:italic>r</jats:italic><jats:sub><jats:italic>m</jats:italic></jats:sub>) and finite rate of increase (<jats:italic>λ</jats:italic>) of <jats:italic>M. similis</jats:italic> were the highest at 30 °C. The net reproduction rate (<jats:italic>R</jats:italic><jats:sub>0</jats:sub>) was the highest at 27 °C and 30 °C, which were 44.34 and 40.39, respectively. We concluded that temperatures in the range 27–30 °C are the most suitable for development and reproduction of <jats:italic>M. similis</jats:italic>. Our study provides detailed basic information for development and reproduction of <jats:italic>M. similis</jats:italic> under different temperature conditions.</jats:p>
摘要：
The open reading frame 117 (3h-117) of Heliothis virescens ascovirus 3h (HvAV-3h), which is a conserved coding region present in all completely sequenced ascovirus members, was characterized in this study. By RT-PCR detection, 3h-117 transcription began at 6-h post-infection (hpi) and remained stable until 168 hpi in HvAV-3h-infected Helicoverpa armigera (Hubner) (Lepidoptera: Noctuidae) larvae. In addition, 3h-117 putatively encodes a 21.5-kDa protein (3H-117) predicted to be a CTD-like phosphatase. Western blot analysis using a prepared rabbit polyclonal antibody specific to 3H-117 showed that the product could be detected at 24 hpi, which remained stably detectable until 168 hpi. The same analysis also demonstrated that the 3H-117 protein localized in the virions of HvAV-3h. Immunofluorescence analysis showed that at 24 hpi, 3H-117 was mainly located in the nuclei of H. armigera larval fat body cells and later spread into the cytoplasm. In summary, our results indicate that 3H-117 is a structural protein of HvAV-3h.
摘要：
The family Bombycidae (sensu Minet, 1994) is a diverse group of species belonging to the superfamily Bombycoidea. It is an economically important group of moth species, containing well-known silk-producing insects, as well as many pests of agriculture and forestry. The morphology-based hypothesis of Minet (1994) on the composition of Bombycidae is in conflict with subsequent phylogenetic hypotheses for the superfamily based on nuclear genes. In this paper, the complete mitochondrial genomes of nine species of Bombycidae are presented for the first time. Based on these genomes, four dataset partitions and three gblocks parameter settings, phylogenetic relationships among Bombycidae were reconstructed using maximum likelihood and Bayesian inference methods. Bombycidae was confirmed as a polyphyletic group, with the traditional subfamilies Prismostictinae and Oberthueriinae forming a single well-supported clade that is distant to Bombycinae. The phylogenetic relationships within Bombycoidea were supported as ((((Bombycinae, Sphingidae), Saturniidae), (Prismostictinae, Oberthueriinae)), Eupterotidae).
摘要：
As specific pathogens of noctuid pests, including Spodoptera exigua, S. litura, Helicoverpa armigera, and Mythimna separata, ascoviruses are suitable for the development of bioinsecticides. In this study, the infectivity of Heliothis virescens ascovirus 3j (HvAV-3j) on insect and mammalian cells was evaluated. HvAV-3j infection induced drastic morphological changes in Sf9, HzAM1, SeFB, and HaFB cells, including swelling and detachment. Notably, the latter phenomena did not occur in HvAV-3j-inoculated mammalian cells (HEK293, 7402, HePG2, PK15, ST, and TM3). MTT assays indicated that HvAV-3j inhibited the growth of host insect cells from the 6th hpi, but no effects were detected in the HvAV-3j-inoculated mammalian cells. Furthermore, viral DNA replication, gene transcription, and protein expression were investigated, and the results consistently suggested that HvAV-3j viruses were not able to replicate their genomic DNA, transcribe, or express their proteins in the non-target vertebrate cells. The HvAV-3j genes were only transcribed and expressed in the four insect cell lines. These results indicated that HvAV-3j was infectious to cells derived from S. frugiperda, S. exigua, H. armigera, and H. zea but not to cells derived from human, pig, and mouse, suggesting that ascoviruses are safe to non-target vertebrate cells.
关键词：
Lepidoptera, DNA barcoding, co1, Gnathospinosa, new taxa
摘要：
The genus Gnathospinosa Liao Huang, gen. nov., belonging to the subfamily Euplocaminae, is described with a new species G. qinlingensis Liao Huang, sp. nov. from China as its type species. The new species was illustrated with photographs of the adults and male genitalia. A preliminary phylogenetic study based on mitochondrial cytochrome c oxidase subunit I gene (co1) sequence data of the new species and Psecadioides cuneus are presented.
