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BACKGROUND: The Oriental tobacco budworm, Helicoverpa assulta, a specialist herbivorous insect that exclusively feeds on plants of the Solanaceae family, causes considerable damage to crops, such as tobacco and hot pepper. The absence of a genome sequence for this species hinders further research on its pest management and ecological adaptation. RESULTS: Here, we present a high‐quality chromosome‐level genome of a Korean strain of H. assulta (Pyeongchang strain, K18). The total assembly spans 424.4 Mb with an N50 length of 14.54 Mb and 37% GC content. The assembled genome (ASM2961881v1) comprises 31 chromosomes, similar to other congeneric generalist species including H. armigera and H. zea. In terms of genomic assembly quality, the complete BUSCOs and repeat content accounted for 98.3% and 33.01% of the genome, respectively. Based on this assembly, 19 485 protein‐coding genes were predicted in the genome annotation. A comparative analysis was conducted using the identified number of protein‐coding genes in H. armigera (24154) and H. zea (23696). Out of the 19 485 predicted genes, 137 genes in 15 orthogroups were found to have expanded significantly in H. assulta, while 149 genes in 95 orthogroups contracted rapidly. CONCLUSION: This study revealed specific gene expansions and contractions in H. assulta compared to those in its close relatives, indicating potential adaptations related to its specialized feeding habits. Also, the comparative genome analysis provides valuable insights for the integrated pest management of H. assulta and other globally significant pests in the Heliothinae subfamily. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Oriental tobacco budworm (Helicoverpa assulta) and cotton bollworm (Helicoverpa armigera) are two closely related species within the genus Helicoverpa. They have similar appearances and consistent damage patterns, often leading to confusion. However, the cotton bollworm is a typical polyphagous insect, while the oriental tobacco budworm belongs to the oligophagous insects. In this study, we used Nanopore, PacBio, and Illumina platforms to sequence the genome of H. assulta and used Hifiasm to create a haplotype-resolved draft genome. The Hi-C technique helped anchor 33 primary contigs to 32 chromosomes, including two sex chromosomes, Z and W. The final primary haploid genome assembly was approximately 415.19 Mb in length. BUSCO analysis revealed a high degree of completeness, with 99.0% gene coverage in this genome assembly. The repeat sequences constituted 38.39% of the genome assembly, and we annotated 17093 protein-coding genes. The high-quality genome assembly of the oriental tobacco budworm serves as a valuable genetic resource that enhances our comprehension of how they select hosts in a complex odour environment. It will also aid in developing an effective control policy. [ABSTRACT FROM AUTHOR]

The ATP-binding cassette (ABC) transporters are a superfamily of membrane proteins. These active transporters are involved in the export of different substances such as xenobiotics. ABC transporters from subfamily C (ABCC) have also been described as functional receptors for different insecticidal proteins from Bacillus thuringiensis (Bt) in several lepidopteran species. Numerous studies have characterized the relationship between the ABCC2 transporter and Bt Cry1 proteins. Although other ABCC transporters sharing structural and functional similarities have been described, little is known of their role in the mode of action of Bt proteins. For Heliothis virescens, only the ABCC2 transporter and its interaction with Cry1A proteins have been studied to date. Here, we have searched for paralogs to the ABCC2 gene in H. virescens, and identified two new ABC transporter genes: HvABCC3 and HvABCC4. Furthermore, we have characterized their gene expression in the midgut and their protein topology, and compared them with that of ABCC2. Finally, we discuss their possible interaction with Bt proteins by performing protein docking analysis. [ABSTRACT FROM AUTHOR]

The potential interaction of fluctuating temperature and the virulence of entomopathogens has implications for biological control. The objective of this study was to investigate the effect of entomopathogenic fungi (Metarhizium brunneum, Beauveria bassiana) on noctuid pest caterpillars (Spodoptera littoralis, Heliothis virescens) under constant and fluctuating temperature regimes. The results revealed similar virulence of entomopathogenic fungi under fluctuating temperature (20–30 °C or 15–35 °C) compared with constant temperature (25 °C). Experiments with cotton leaves as food confirmed that S. littoralis was less susceptible to entomopathogenic fungi (M. brunneum) than H. virescens. Results of additional experiments with H. virescens larvae, B. bassiana, and artificial diet were comparable to experiments with M. brunneum and cotton leaves, despite that susceptibility to B. bassiana was three orders of magnitude lower than to M. brunneum. The fact that both fungus species showed reduced growth on medium under fluctuating temperatures when compared to constant temperatures did not translate to an interaction of temperature regime and the virulence against noctuid larvae. Our study implies that virulence studies with noctuid larvae under constant temperatures using plant material or artificial diet might be fair models also for environments with fluctuating temperatures. [ABSTRACT FROM AUTHOR]

Heliothine moths represent some of the world's most important agricultural pest species. Helicoverpa zea (Corn Earworm) and Heliothis virescens (Tobacco Budworm) cause billions in damage and control costs worldwide each year. Given their economic importance, sex pheromones of many species have been studied for the development of management techniques such as trapping for population monitoring. The majority of pheromones identified and studied to date have been female‐produced sex pheromones. Less emphasis has been placed on male sex pheromones, associated with abdominal hairpencil structures that often function in courtship or to attract females. The present study examines the composition, detection and behavioural role of male H. zea hairpencil compounds in male autodetection and in courtship. Comparative examination of the hairpencil effluvia of H. zea and H. virescens did not reveal distinct differences in pheromone blend composition produced by males of these species. Electrophysiological testing demonstrated broad antennal neuron response in both males and females of H. zea to nine key stimuli, with sexual dimorphism present in each species. Behavioural assays suggested that odours released by male hairpencils are important in mate acceptance by female H. zea and may play a role in mate choice and species isolation. Wind tunnel observations indicated that key H. zea hairpencil odours (hexadecanyl acetate and octadecanyl acetate) also function in mate competition, antagonising responses of downwind conspecific males following a synthetic female sex pheromone plume. This finding provides insight regarding male–male detection and response to hairpencil compounds in H. zea. [ABSTRACT FROM AUTHOR]

Premise: Glandular trichomes are implicated in direct and indirect defense of plants. However, the degree to which glandular and non‐glandular trichomes have evolved as a consequence of herbivory remains unclear, because their heritability, their association with herbivore resistance, their trade‐offs with one another, and their association with other functions are rarely quantified. Methods: We conducted a phylogenetic comparison of trichomes and herbivore resistance against the generalist caterpillar, Heliothis virescens, among tarweed species (Asteraceae: Madiinae) and a genetic correlation study comparing those same traits among maternal half‐sibs of three tarweed species. Results: Within a tarweed species, we found no evidence that herbivore growth rate decreased on tarweed individuals or maternal sib groups with more glandularity or denser trichomes. However, tarweed species with more glandularity and fewer non‐glandular trichomes resulted in slower‐growing herbivores. Likewise, a trade‐off between glandular and non‐glandular trichomes was apparent among tarweed species, but not among individuals or sib groups within a species. Conclusions: Our results suggest that this key herbivore does not select for trichomes as a direct defense in tarweed species. However, trichomes differed substantially among species and likely affect herbivore pressure on those species. Our results demonstrate that trade‐offs among plant traits, as well as inference on the function of those traits, can depend on scale. [ABSTRACT FROM AUTHOR]

Sexual signals often function in species recognition and may also guide mate choice within a species. In noctuid moths, both males and females may exercise mate choice. Females of the tobacco budworm Chloridea virescens prefer to mate with larger males, but the signal(s) underlying female choice remain unknown. Male hairpencil volatiles are emitted during close range courtship displays. However, previously identified male hairpencil volatiles, namely acetate esters, aldehydes, alcohols, and fatty acids, are not associated with female choice. Recently, two new hairpencil compounds were identified that elicit strong electrophysiological responses in female antennae: methyl salicylate (MeSA) and δ-decalactone. In this study, we investigated the effect of larval diet and adult feeding on MeSA and δ-decalactone content in hairpencils and determined whether these compounds are involved in female choice. We found that larval diet affected MeSA content in hairpencils, but not δ-decalactone. Conversely, adult feeding affected the level of δ-decalactone, but not MeSA: sugar-water feeding increased δ-decalactone content compared to plain water. In two-choice assays, females mated more with males that had higher amounts of δ-decalactone, and less with males with higher amounts of MeSA. [ABSTRACT FROM AUTHOR]

The larval stages of the tobacco budworm, Heliothis virescens (Fabricius) (Lepidoptera: Noctuidae), are parasitized by the endophagous parasitoid wasp, Toxoneuron nigriceps (Viereck) (Hymenoptera: Braconidae). During the injections of eggs, this parasitoid wasp also injects into the host body the secretion of the venom gland and the calyx fluid, which contains a polydnavirus (T. nigriceps BracoVirus: TnBV) and the Ovarian calyx fluid Proteins (OPs). The effects of the OPs on the host immune system have recently been described. In particular, it has been demonstrated that the OPs cause hemocytes to undergo a number of changes, such as cellular oxidative stress, actin cytoskeleton modifications, vacuolization, and the inhibition of hemocyte encapsulation capacity, which results in both a loss of hemocyte functionality and cell death. In this study, by using a combined transcriptomic and proteomic analysis, the main components of T. nigriceps ovarian calyx fluid proteins were identified and their possible role in the parasitic syndrome was discussed. This study provides useful information to support the analysis of the function of ovarian calyx fluid proteins, to better understand T. nigriceps parasitization success and for a more thorough understanding of the components of ovarian calyx fluid proteins and their potential function in combination with other parasitoid factors. [ABSTRACT FROM AUTHOR]

The ATP-binding cassette (ABC) transporters are a superfamily of membrane proteins. These active transporters are involved in the export of different substances such as xenobiotics. ABC transporters from subfamily C (ABCC) have also been described as functional receptors for different insecticidal proteins from Bacillus thuringiensis (Bt) in several lepidopteran species. Numerous studies have characterized the relationship between the ABCC2 transporter and Bt Cry1 proteins. Although other ABCC transporters sharing structural and functional similarities have been described, little is known of their role in the mode of action of Bt proteins. For Heliothis virescens, only the ABCC2 transporter and its interaction with Cry1A proteins have been studied to date. Here, we have searched for paralogs to the ABCC2 gene in H. virescens, and identified two new ABC transporter genes: HvABCC3 and HvABCC4. Furthermore, we have characterized their gene expression in the midgut and their protein topology, and compared them with that of ABCC2. Finally, we discuss their possible interaction with Bt proteins by performing protein docking analysis.

Background: Herbivore‐induced plant volatiles (HIPVs) are important self‐defense outputs of pepper plants to resist insect pests. Ascoviruses are pathogenic to the larvae of most lepidopteran vegetable pests. However, whether Heliothis virescens ascovirus 3h (HvAV‐3h)‐infected Spodoptera litura larvae can change pepper leaf HIPVs is not well understood. RESULTS: Spodoptera litura larvae preferred S. litura‐infested leaves, and this preference was stronger with longer duration of S. litura infestation. In addition, S. litura larvae significantly chose pepper leaves damaged by HvAV‐3h‐infected S. litura over the healthy pepper leaves. Results also showed that S. litura larvae preferred leaves mechanically damaged and treated with oral secretions from HvAV‐3h infected‐S. litura larvae in a simulation test. We captured the volatiles emitted by leaves under six treatments. Results showed that the volatile profile changed with the different treatments. Testing of volatile blends, prepared to the proportion released showed that the blend from simulated HvAV‐3h‐infected S. litura larvae‐damaged plants was the most attractive to S. litura larvae. Further, we also found that some of the compounds significantly attracted S. litura larvae at specific concentrations. CONCLUSION: HvAV‐3h‐infected S. litura can alter the release of HIPVs in pepper plants and thus become more attractive to S. litura larvae. We speculate that this may be due to alterations in the concentration of some compounds (such as geranylacetone and prohydrojasmon) affecting the behavior of S. litura larvae. © 2023 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Ascoviruses are insect-specific viruses that are thought to utilize the cellular apoptotic processes of host larvae to produce numerous virion-containing vesicles. In this study, we monitored the in vivo infection processes of Heliothis virescens ascovirus 3h (HvAV-3h) to illustrate the regulated cell death (RCD) of host cells. Transmission electron microscopic observations did not reveal any morphological markers of apoptosis in the fat bodies or hemocytes of HvAV-3h-infected Helicoverpa armigera or Spodoptera exigua larvae. However, several hemocytes showed the morphological criteria for necrosis and/or pyroptosis. Further in vitro biochemical tests were performed to confirm the RCD type of host cells after infection with HvAV-3h. Different morphological characteristics were found between the early (prior to 24 hours post-infection, [hpi]) and later (48 to 120 hpi) stages in both HvAV-3h infected larval fat bodies and hemocytes. In the early stages, the virions could only be found in several adipohemocytes, and the fat bodies were cleaving their contained lipid inclusions into small lipid dots. In the later stage, both fat bodies and hemocytes were filled with numerous virions. According to the morphological characteristics of HvAV-3h infected larval fat bodies or hemocytes, the pathogenic characteristics and infection patterns of HvAV-3h in the host larvae were described, and the systematic pathogenic mode of ascovirus infection was refined in this study. This study details the complete infection process of ascoviruses, which provides insights into the relationship between a pathogenesis of an insect virus and the RCD of different host tissues at different stages of infection. IMPORTANCE Viruses and other pathogens can interrupt host cellular apoptosis to gain benefits, such as sufficient resources and a stable environment that enables them to complete their replication and assembly. It is unusual for viruses to code proteins with homology to caspases, which are commonly recognized as apoptosis regulators. Ascoviruses are insect viruses with special cytopathology, and they have been hypothesized to induce apoptosis in their host larvae via coding a caspase-like protein. This enables them to utilize the process of cellular apoptosis to facilitate vesicle formation and replication. However, our previous studies revealed different trends. The fat bodies and hemocytes of Heliothis virescens ascovirus 3h (HvAV-3h)-infected larvae did not show any morphological markers of apoptosis but did display necrosis and/or pyroptosis morphological characteristics. The pathogenic characteristics and infection patterns of HvAV-3h in the host larvae were described, which can help us understand the relationship between the pathogenesis of an insect virus and host RCD. [ABSTRACT FROM AUTHOR]

Copyright of Revista Colombiana de Entomología is the property of Universidad del Valle and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The bioinsecticide effect of two microencapsulated formulations of the entomopathogenic fungus Metarhizium anisopliae was evaluated on first-instar larvae of tobacco budworm, Chloridea virescens, a recurring pest of tomato and chickpea at Sinaloa, Mexico. Each microencapsulated contained M. anisopliae at 1×108 conidia/ml, MDF1 based on maltodextrin at 10%, GBF2 with bovine gelatin at 7%. Macrocystis pyrifera algal extract at 2% was added to each formulation as adjuvant. Fungus at 1×108 conidia/ml and distilled water was used as a check. The MDF1 microencapsulation measured 2 to 18 microns, had 2.95% of moisture, 87% of adherence, 85% of solubility, and conidia release time of 15 minutes; GBF2 measured 1 to 10 microns and had 3.1% of moisture, 79% of adherence, 82% of solubility, and release time of 28 minutes. The mortality of C. virescens was 68% in MDF1 and 54% in GBF2, and their lethal times were 4.5 and 4.9 days. M. pyrifera extract allowed release and germination of the conidia that adhere better to insect cuticle, making them more effective for control of C. virescens. [ABSTRACT FROM AUTHOR]

The use of insect-resistant transgenic crops producing Bacillus thuringiensis protein Cry toxins (Bt) to control caterpillars is wide-spread. Development of a mechanism to prevent Bt from reaching its target site in the digestive system could result in Bt resistance and resistance to other insecticides active per os. Increased feeding rates by increasing temperature in tobacco budworms, Chloridea virescens, and bollworms, Helicoverpa zea, decreased Bt Cry1Ac susceptibility and mortality. The same was found in C. virescens for Bollgard II plant extract containing Bt Cry1Ac and Cry2Ab2 toxins. Furthermore, H. zea from the same inbred laboratory colony that fed faster independent of temperature manipulation were less susceptible to Bt intoxication. A laboratory derived C. virescens Bt resistant strain demonstrated a higher feeding rate on non-Bt artificial diet than the parental, Bt susceptible strain. A laboratory-reared Bt resistant fall armyworm, Spodoptera frugiperda, strain also fed faster on non-Bt diet compared to Bt susceptible caterpillars of the same species, both originally collected from corn. The studies in toto and the literature reviewed support the hypothesis that increased feeding rate is a behavioral mechanism for reducing caterpillar susceptibility to Bt. Its possible role in resistance needs further study. [ABSTRACT FROM AUTHOR]

There are no standard protocols for assessing antibiosis in soybean, Glycine max (L.) (Fabaceae), cultivars to lepidopterans, including tobacco budworm, Chloridea virescens (Fabricius) (Lepidoptera: Noctuidae), an important species that causes damage to soybean crops in several production regions. This study was conducted to assess methodologies to determine the optimal combination of larval density, confinement container size, and plant structure in soybean antibiosis assays to C. virescens. In addition, primary and secondary metabolites in plant structures were analyzed to elucidate potential chemical resistance mechanisms against this lepidopteran. Antibiosis assays to C. virescens in resistant (IAC‐100) and susceptible (BR‐16) soybean cultivars were performed using three larval densities (one, two, and three larvae), two confinement container sizes (150 and 300 ml), and combinations of soybean plant structures (leaves, uncut pods, leaves + uncut pods, cut pods, and leaves + cut pods). Phenol, tannin, fiber, and lignin contents were quantified in the leaves, uncut pods, and grains of the soybean cultivars and related to biological development of C. virescens. Resistance levels in soybean cultivars in antibiosis assays were best differentiated using one larva per 150‐ml confinement container, fed only on soybean leaves. Higher contents of condensed tannins in the leaves of IAC‐100 cultivar may be one of the main chemical mechanisms of resistance to C. virescens. Our study is the first to determine the optimal combination of larval density, confinement container size, and plant structure for antibiosis assays in soybean cultivars to C. virescens. The developed protocol will benefit high‐throughput phenotyping in genetic breeding programs to obtain cultivars resistant to lepidopterans for use in integrated pest management. [ABSTRACT FROM AUTHOR]

Analysis of orthology is important for understanding protein conservation, function, and phylogenomics. In this study, we performed a comprehensive analysis of gene orthology in the family Ascoviridae based on identification of 366 protein homologue groups and phylogenetic analysis of 34 non-single-copy proteins. Our findings revealed 90 newly annotated proteins, five newly identified core proteins for the family Ascoviridae, and 14 core proteins for the genus Ascovirus. A phylogenomic tree of 11 Ascoviridae members was constructed based on a concatenation of 35 of the 45 ortholog groups. In combination with phosphoproteomic results and conservation estimations, 30 conserved phosphorylation sites on 17 phosphoproteins were identified from a total of 176 phosphosites on 57 phosphoproteins from Heliothis virescens ascovirus 3h (HvAV-3h), providing potential research targets for investigating the role of these protein in the regulation of viral infection. This study will facilitate genome annotation and comparison of further Ascoviridae members as well as functional genomic investigations. [ABSTRACT FROM AUTHOR]

Sexual selection in animals has been mostly studied in species in which males are signalers and females are choosers. However, in many species, females are (also) signalers. In species with non‐signaling females, virgin females are hypothesized to be less choosy than mated females, as virgins must mate to realize fitness and the number of available males is generally limited. Yet, when females signal to attract males, mate limitation can be overcome. We tested how virgin and mated females differ in their calling behavior, mating latency, and in mate choice, using the tobacco budworm Chloridea (Heliothis) virescens as an example for a species in which females are not only choosers but also signalers. We found that virgin females signaled longer than mated females, but virgin and mated signaling females were equally ready to mate, in contrast to non‐signaling females. However, we found that virgin signaling females showed weaker mate preference than mated females, which can be explained by the fact that females increase their fitness with multiple matings. Mated females may thus further increase their fitness by more stringent mate selection. We conclude that signaling is a crucial aspect to consider when studying female mate choice because signaling may affect the number of available mates to choose from. [ABSTRACT FROM AUTHOR]

Bacillus thuringiensis (Bt) has been used as sprayable pesticides for many decades. Bt strains utilized in these products produce multiple insecticidal proteins to complement a narrow insect specificity of each protein. In the late 1990s, genes encoding Bt insecticidal proteins were expressed in crop plants such as cotton and corn to protect these crops from insect damage. The first Bt protein used in transgenic cotton was Cry1Ac to control Heliothis virescens (tobacco budworm). Cry1Ab was applied to corn to control Ostrinia nubilalis (European corn borer). Since these insects have developed resistance to Cry1Ac and Cry1Ab, new Bt proteins are required to overcome the resistance. In order to protect corn furthermore, it is desired to control Diabrotica virgifera (Western corn rootworm), Helicoverpa zea (corn earworm) and Spodoptera frugiperda (fall armyworm). Recently, many new Bt insecticidal proteins have been discovered, but most of them require protein engineering to meet the high activity standard for commercialization. The engineering process for higher activity necessary for Bt crops is called optimization. The seed industry has been optimizing Bt insecticidal proteins to improve their insecticidal activity. In this review, several optimization projects, which have led to substantial activity increases of Bt insecticidal proteins, are described. [ABSTRACT FROM AUTHOR]

Ascoviruses are double‐stranded DNA viruses that are pathogenic to noctuid larvae. In vitro infection causes the cells to fail to replicate and proliferate normally. However, the molecular mechanisms are unclear. In this study, the transmission electron microscopy data of infected‐Spodoptera exigua (Hübner) fat body cells (SeFB, IOZCAS‐SpexII‐A cells) showed that virions were internalized in phagocytic vesicles, but not in the nucleus. FACS of cell‐cycle progression was performed in SeFB cells infected with Heliothis virescens ascovirus 3h (HvAV‐3h). The cell cycle phase distributions of the SeFB cells were G1 = 29.52 ± 1.10%, S = 30.33 ± 1.19%, and G2/M = 40.06 ± 0.75%. The cell culture doubling time was approximately 24 h. The G1, S, and G2/M phases were each approximately 8 h. The unsynchronized or synchronized cells were arrested at G2/M phase after infection with HvAV‐3h. Our data also showed that cells with more than 4N DNA content appeared in the HvAV‐3h‐treated group. While the mRNA levels of cyclin B1, cyclin H, and cyclin‐dependent kinase 1 (CDK1) were downregulated after HvAV‐3h infection, the mRNA expression levels of cyclin A, cyclin D, and cyclin B2 were not significantly changed. Western blotting results showed that the expression of cyclin B1 and CDK1 in infected SeFB cells within 24 h postinfection (hpi), and HvAV‐3h infection inhibited the expression of cyclin B1 and CDK1 at 12–24 hpi. Overall, these data implied that HvAV‐3h infection leads to an accumulation of cells in the G2/M phases by downregulating the expression of cyclin B1 and CDK1. [ABSTRACT FROM AUTHOR]

Chickpea is a legume with nutrient-rich grains important for human feeding. Tobacco budworm, Chloridea virescens (Lepidoptera: Noctuidae), is one of the most major pests of chickpea (Cicer arietinum) in Brazil. This pest damages leaves, flowers, pods, and grains. Plant resistance to insects is an important tactic of pest management, which usually facilitates and reduce costs of implementing an Integrated Pest Management for farmers. Thus, this study aimed to evaluate the resistance in chickpea cultivars to C. virescens. Six chickpea cultivars were evaluated for antixenosis, initial antibiotic parameters, and behavior under field conditions. The cultivars BRS Kalifa and BRS Cícero were less attractive in a freechoice test, while Jamu 96 and BRS Kalifa were less attractive in a no-choice test. BRS Kalifa and BRS Toro leaves had a higher trichome density. Jamu 96 and BRS Toro had higher contents of oxalic and malic acids. C. virescens larvae in BRS Cícero, BRS Toro, and BRS Kalifa showed the lowest weights. Jamu 96 pods were the least damaged, and BRS Aleppo and Jamu 96 had the highest yields. The chickpea cultivars Jamu 96 and BRS Aleppo, which had resistance levels and mechanisms, can be used in integrated pest management programs to control C. virescens. [ABSTRACT FROM AUTHOR]

It is increasingly clear that pest species vary widely in their propensities to develop insecticide resistance. This review uses a comparative approach to analyze the key pest management practices and ecological and biochemical or genetic characteristics of the target that contribute to this variation. We focus on six heliothine species, three of which, Helicoverpa armigera, Heliothis virescens, and Helicoverpa zea, have developed resistances to many pesticide classes. The three others, Helicoverpa punctigera, Helicoverpa assulta, and Helicoverpa gelotopoeon, also significant pests, have developed resistance to very few pesticide classes. We find that host range and movement between alternate hosts are key ecological traits that influence effective selection intensities for resistance. Operational issues are also critical; area-wide, cross-pesticide management practices that account for these ecological factors are key to reducing selection intensity. Without such management, treatment using broad-spectrum chemicals serves to multiply the effects of host plant preference, preadaptive detoxification ability, and high genetic diversity to create a pesticide treadmill for the three high-propensity species.Without rigorous ongoing management, such a treadmill could still develop for newer, more selective chemistries and insecticidal transgenic crops. [ABSTRACT FROM AUTHOR]

Insects acquire cold hardiness for survival during the winter by increasing cryoprotectants concentration such as glycerol and trehalose after induction of rapid cold hardening (RCH). The oriental tobacco budworm, Helicoverpa assulta, is a freeze‐tolerant species which increases glycerol level in the hemolymph after RCH induction. In this study, we identified two glycerol biosynthesis‐related genes, glycerol‐3‐phosphate dehydrogenase (Has‐GPDH) and glycerol kinase (Has‐GK) in the fat body of H. assulta larvae. Has‐GPDH harbored a conserved NAD+‐dependent glycerol‐3‐phosphate dehydrogenase signature sequence, and Has‐GK harbored two conserved FGGY carbohydrate kinase signature sequences. Phylogenetic analysis revealed both Has‐GPDH and Has‐GK were relatively close to those of Helicoverpa armigera. The expression levels of Has‐GPDH and Has‐GK were increased after RCH induction at 4°C for 6 h. After suppression of Has‐GPDH and Has‐GK by RNA interference, the survival rate of H. assulta at −10°C was much lower than the control after RCH induction. These results suggest that glycerol biosynthesized by Has‐GPDH and Has‐GK plays a crucial role in RCH‐induced cold tolerance in H. assulta. [ABSTRACT FROM AUTHOR]

Copyright of Agricultural Research in the Tropics / Pesquisa Agropecuária Tropical is the property of Pesquisa Agropecuaria Tropical and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

A high-quality genome is of significant value when seeking to control forest pests such as Dendrolimus kikuchii , a destructive member of the order Lepidoptera that is widespread in China. Herein, a high quality, chromosome-level reference genome for D. kikuchii based on Nanopore, Pacbio HiFi sequencing and the Hi-C capture system is presented. Overall, a final genome assembly of 705.51 Mb with contig and scaffold N50 values of 20.89 and 24.73 Mb, respectively, was obtained. Of these contigs, 95.89% had unique locations on 29 chromosomes. In silico analysis revealed that the genome contained 15,323 protein-coding genes and 63.44% repetitive sequences. Phylogenetic analyses indicated that D. kikuchii may diverged from the common ancestor of Thaumetopoea. Pityocampa , Thaumetopoea ni, Heliothis virescens , Hyphantria armigera , Spodoptera frugiperda , and Spodoptera litura approximately 122.05 million years ago. Many gene families were expanded in the D. kikuchii genome, particularly those of the Toll and IMD signaling pathway, which included 10 genes in peptidoglycan recognition protein , 19 genes in MODSP , and 11 genes in Toll. The findings from this study will help to elucidate the mechanisms involved in protection of D. kikuchii against foreign substances and pathogens, and may highlight a potential channel to control this pest. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

The use of insect-resistant transgenic crops producing Bacillus thuringiensis protein Cry toxins (Bt) to control caterpillars is wide-spread. Development of a mechanism to prevent Bt from reaching its target site in the digestive system could result in Bt resistance and resistance to other insecticides active per os. Increased feeding rates by increasing temperature in tobacco budworms, Chloridea virescens, and bollworms, Helicoverpa zea, decreased Bt Cry1Ac susceptibility and mortality. The same was found in C. virescens for Bollgard II plant extract containing Bt Cry1Ac and Cry2Ab2 toxins. Furthermore, H. zea from the same inbred laboratory colony that fed faster independent of temperature manipulation were less susceptible to Bt intoxication. A laboratory derived C. virescens Bt resistant strain demonstrated a higher feeding rate on non-Bt artificial diet than the parental, Bt susceptible strain. A laboratory-reared Bt resistant fall armyworm, Spodoptera frugiperda, strain also fed faster on non-Bt diet compared to Bt susceptible caterpillars of the same species, both originally collected from corn. The studies in toto and the literature reviewed support the hypothesis that increased feeding rate is a behavioral mechanism for reducing caterpillar susceptibility to Bt. Its possible role in resistance needs further study.

The objective of this work was to evaluate oil formulations of Beauveria bassiana and Metarhizium anisopliae against larvae of Chloridea virescens, the tobacco budworm that causes significant economic losses to tomato crops in Sinaloa. Each fungal formulation was done at a concentration of 1 × 108 conidia/ml, mixing mineral oil, corn oil, and soybean oil, adding an algal extract and an ultraviolet lightprotective dye as adjuvants. In the laboratory the two fungi formulations in mineral oil HF2-Ma and HF1-Bb killed 93.3 and 96.6% of third-instar larvae with a mean lethal time (LT50) of 3 days, whereas those with corn oil (HF4-Ma y HF3-Bb), and soybean oil (HF6-Ma and HF5-Bb) had mortality of 63.3, 63.3, 50.0, and 53.3% with a LT50 of 3.5 days. The formulation with only mineral oil killed 36.6% with LT50 of 4 days, while the check with water had no mortality. This indicated that all formulations had biological activity to kill tobacco budworm larvae, killing most with conidia in mineral oil. The lethal time was shorter with the fungi in mineral oil than in vegetable oil and longer with only mineral oil. The HF2-Ma and HF1-Bb formulations were tested in a greenhouse sprayed at 3.0 × 108 conidia/ml over ‘Saladette’ variety of tomato plants artificially infested with second and third instar larvae, killing 64.5% (HF2-Ma) and 50.5% (HF1-Bb), with LT50 of 4 and 4.5 days. Larvae avoided direct contact with the formulations by moving away from the treated surface. However, 64.5 and 50.5% were killed, which were high compared with only 3.5% in the check. The persistence of conidia on the leaves was 14 days, showing the effectiveness of the formulations to kill larvae in 4 and 4.5 days. These results are considered promising to control C. virescens with the mixture of these fungi in mineral oil and evaluating mortality of younger larvae on tomatoes in the greenhouse. [ABSTRACT FROM AUTHOR]

The tobacco budworm, Chloridea (Heliothis) virescens (F.), has evolved resistance to numerous insecticides in the field. In tobacco, chlorantraniliprole can be applied as either a preventative systemic soil application at or near transplant, or a foliar application timed to current treatment thresholds. With a novel mode of action chlorantraniliprole provides an option for rotation with other insecticides to reduce the probability of insecticide resistance development. However, specific usage patterns in tobacco have the potential to increase the risk of resistance development to this insecticide. In particular, soil applied treatments may expose C. virescens to sublethal concentrations of the insecticide. We studied chlorantraniliprole susceptibility in nine field populations and one laboratory strain of C. virescens using a diet incorporation bioassay. Mortality was measured at 7, 10, and 14 d after exposure. Our results demonstrated that bioassays should be evaluated at 14 d after exposure to optimize interpretation of the dose–response due to the antifeeding properties of chlorantraniliprole. We observed low variation within field-collected populations. Field populations were as susceptible as the laboratory strain; the resistance ratio at the 14-d evaluation for field-collected populations ranged from 1.01 to 1.05. A discriminating dose of 0.117, 0.080, and 0.070 μg a.i./g diet could be used at 7, 10, and 14 d, respectively. Larval growth varied between field populations. Two field populations continued growing on diet containing chlorantraniliprole and differed in size from the laboratory and other populations. Further evaluation of growth inhibition will be necessary. [ABSTRACT FROM AUTHOR]

The oriental tobacco budworm Helicoverpa assulta (Lepidoptera: Noctuidae) is a specialist pest that may cause serious damages to important crops such as chili pepper and tobacco. Various man-made insecticides have been applied to control the infestation of this pest. To understand how this pest copes with insecticides, it is required to identify key players involved in insecticide transformation. In this study, a P450 gene of CYP6B subfamily was identified in the oriental tobacco budworm, and its expression pattern was revealed. Moreover, the activities of HassCYP6B6 against 12 insecticides were explored using recombinant enzymes produced in the facile Escherichia coli. Data from metabolic experiments showed that HassCYP6B6 was able to metabolize conventional insecticides including organophosporates (diazinon, malathion, phoxim), carbamate propoxur, and pyrethroid esfenvalerate, while no significant metabolism was observed towards new-type pesticides such as neonicotinoids (acetamiprid, imidacloprid), diamides (chlorantraniliprole, cyantraniliprole), macrocyclic lactone (emamectin benzoate, ivermectin), and metaflumizone. Structures of metabolites were proposed based on mass spectrometry analyses. The results demonstrate that HassCYP6B6 plays important roles in the transformation of multiple insecticides via substrate-dependent catalytic mechanisms including dehydrogenation, hydroxylation and oxidative desulfurization. The findings have important applied implications for the usage of insecticides. [Display omitted] • A new P450 gene (HassCYP6B6) is identified in Helicoverpa assulta. • The recombinant HassCYP6B6 protein is successfully produced in Escherichia coli. • HassCYP6B6 enzyme is able to metabolize multiple insecticides. • Hydroxylation and desulfuration are common pathways in HassCYP6B6 catalyzed insecticide metabolism. • A unique alkyl dehydrogenated metabolite of propoxur is firstly discovered. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Heliothine species (Lepidoptera: Noctuidae, Heliothinae) include some of the world's most devastating pest species, such as Heliothis virescens (Fabricius) in the Americas and Helicoverpa armigera (Hübner) in the Old World. Sex pheromone communication of these agricultural pest species has been investigated from pheromone receptors (PRs) to brains and behavior in detail. In recent years, great progress has been made in the mechanistic dissection of pheromone reception, demonstrating that PRs play a key role in determining the response characteristics of pheromone‐sensitive olfactory receptor neurons. In this review, we focus on the functional characterization of PRs in heliothine species, and summarize recent progress in the identification of receptors tuned to principal sex pheromone components including Z11‐16:Ald, Z9‐16:Ald, Z9‐14:Ald, and other related alcohols and acetates. Evolution of PRs in ligand selectivity is also discussed. The efficiency and faithfulness of three frequently used heterologous expression systems – Xenopus laevis Daudin oocytes, modified HEK 293 cells, and Drosophila 'empty neuron' mutants – are compared, and the research strategies, skills, and perspectives in the studies are envisioned. Finally, we propose future research topics on PRs in heliothine species. [ABSTRACT FROM AUTHOR]

The ecdysone receptor (EcR) possesses the remarkable capacity to adapt structurally to different types of ligands. EcR binds ecdysteroids, including 20-hydroxyecdysone (20E), as well as nonsteroidal synthetic agonists such as insecticidal dibenzoylhydrazines (DBHs). Here, we report the crystal structures of the ligand-binding domains of Heliothis virescens EcR/USP bound to the DBH agonist BYI09181 and to the imidazole-type compound BYI08346. The region delineated by helices H7 and H10 opens up to tightly fit a phenyl ring of the ligands to an extent that depends on the bulkiness of ring substituent. In the structure of 20E-bound EcR, this part of the ligand-binding pocket (LBP) contains a channel filled by water molecules that form an intricate hydrogen bond network between 20E and LBP. The water channel present in the nuclear receptor bound to its natural hormone acts as a critical molecular adaptation spring used to accommodate synthetic agonists inside its binding cavity. [ABSTRACT FROM AUTHOR]

The discovery of juvenile hormones (JH) and their synthetic analogs (JHA) generated excitement and hope that these compounds will replace first- and second-generation insecticides that have not so desirable environmental and human safety profiles. However, JHAs used commercially during the past four decades did not meet these expectations. The recent availability of advanced molecular and histological methods and the discovery of key players involved in JH action provided some insights into the functioning of JHA in a stage and species-specific manner. In this review, we will summarize recent findings and stage-specific action of JHA, focusing on three commercially used JHA, methoprene, hydroprene and pyriproxyfen and economically important pests, the red flour beetle, Tribolium castaneum, and the tobacco budworm, Heliothis virescens, and disease vector, the yellow fever mosquito, Aedes aegypti. [ABSTRACT FROM AUTHOR]

Larvae of Heliothis virescens (Fabricius) (Lepidoptera: Noctuidae) often infest soybean crops, Glycine max (L.) (Fabaceae), causing significant yield losses in important soybean‐producing regions. The use of soybean varieties resistant to lepidopteran larvae is a major approach in soybean integrated pest management. However, standardization and optimization of bioassays that are used to screen genotypes for insect resistance are essential for high‐throughput phenotyping. Methodologies for screening were assessed to determine the most effective method for discriminating levels of antixenosis to H. virescens in soybean plants. Feeding and oviposition preference assays were performed to determine optimal densities of larvae and adults, and optimal plant structures and growth stages for conducting assays. In addition, trichome densities, and fiber and lignin contents were quantified in plant structures of soybean cultivars differing in resistance. Resistance levels of cultivars were best differentiated using nine neonate larvae and two 6‐day‐old larvae, and by using young leaves of plants at the vegetative stage. This was likely due to the more pronounced differences in lignin and fiber contents in young leaves of vegetative‐stage plants. Density of adult pairs, plant structure, and growth stage did not affect ability to distinguish differences in oviposition preference by H. virescens. Higher numbers of eggs were found on the leaves, which were the plant structures that exhibited the lowest trichome densities. The protocol developed in this work will benefit future evaluations of soybean genotypes for antixenosis against H. virescens. [ABSTRACT FROM AUTHOR]

A meridic diet overlay bioassay using empty, positively charged zein nanoparticles ((+)ZNP) was performed on soybean looper (Chrysodeixis includens (Walker)), tobacco budworm (Heliothis virescens (F.)), and velvetbean caterpillar (Anticarsia gemmatalis Hübner) (Lepidoptera: Noctuidae). Assessment of effects on mortality and development weights 7 d after ingestion of (+)ZNP were evaluated on larvae of each species. Treatments involved different concentrations, with H. virescens and A. gemmatalis offered 0 and 3,800 ppm (+)ZNP, whereas C. includens colonies were offered 0, 630, 1,260, and 2,520 ppm (+)ZNP. Mortality of A. gemmatalis and C. includens increased after ingestion of the highest (+)ZNP concentrations, while H. virescens neonate mortality was unaffected. Neonate and third-instar weights of A. gemmatalis and C. includens , and neonate H. virescens , decreased with high (+)ZNP concentrations. Following mortality results from A. gemmatalis neonates, a concentration response test was performed using a range of (+)ZNP concentrations. The LC50 for A. gemmatalis was 1,478 ppm. The potential of (+)ZNP as a pest management tactic is discussed. [ABSTRACT FROM AUTHOR]

In solitary endoparasitoids, oviposition in a host previously parasitized by a conspecific (superparasitism) leads to intraspecific competition, resulting in the elimination of all but one parasitoid offspring. Therefore, avoidance of parasitized hosts presents a strong selective advantage for such parasitoid species. Parasitoids use herbivore-induced plant volatiles (HIPVs) to find their hosts. In this study, we evaluated the ability of Microplitis croceipes (Hymenoptera: Braconidae) to discriminate between unparasitized and parasitized Heliothis virescens (Lepidoptera: Noctuidae) larvae using cotton plant odors as cues. A combination of behavioral and analytical techniques were used to test two hypotheses: (i) parasitoids will show preference for plant odors induced by unparasitized hosts over odors induced by parasitized hosts, and (ii) the parasitism status of herbivores affects HIPV emission in plants. Heliothis virescens larvae were parasitized for varying durations (0, 2 and 6-days after parasitism (DAP)). In four-choice olfactometer bioassays, female M. croceipes showed greater attraction to plant odors induced by unparasitized hosts compared to plant odors induced by parasitized hosts (2 and 6-DAP). Comparative gas chromatography-mass spectrometry analyses of cotton volatiles indicated reduced emission of 10 out of 21 identified compounds from plants infested by parasitized hosts compared with plants infested by unparasitized hosts. The results suggest that changes in plant volatile emission due to the parasitism status of infesting herbivores affect recruitment of parasitoids. Avoidance of superparasitism using plant odors optimizes host foraging in M. croceipes, and this strategy may be widespread in solitary parasitoid species. [ABSTRACT FROM AUTHOR]

BACKGROUND The insect olfactory system can recognize odorants for feeding, courtship, oviposition and avoiding natural enemies. Odorant cues from host plants play important roles in insect behaviours. Tobacco (Nicotiana tabacum) is the main cultivated host of the oriental tobacco budworm Helicoverpa assult. Volatiles of tobacco plants attract and stimulate oviposition in female moths. However, it is still not known how female H. assulta recognize tobacco volatiles and which odorant compounds are used as oviposition cues. RESULTS: We detected 14 volatile compounds emitted from a tobacco plant during vegetative growth, using gas chromatography–mass spectrometry. Electroantennogram tests indicated that eight of the 14 compounds induced responses in female H. assulta. Among these eight volatiles, nonanal greatly increased oviposition preference. Single‐sensillum recording (SSR) results showed that many neurons housed in three types of short basiconic sensilla and four types of long basiconic sensilla responded to nonanal and heptanal as its structural analogue. The responses to nonanal were significantly stronger than those to the other compounds. Nonanal was the main ligand of OR67, an odorant receptor from H. assulta. This was demonstrated using an in vitro Xenopus oocytes expression system that supported the SSR results. CONCLUSION: Nonanal is a key signal volatile of tobacco plants that attracts female H. assulta moths to oviposit. © 2020 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Most species of moths use a female-produced sex pheromone to bring mates together. Typically, sex pheromone is synthesized in a specialized gland and released during the behavior of "calling", in which the ovipositor and gland are extruded, allowing pheromone to evaporate. Although there has been much study on how a gland makes specific pheromone components, we know relatively little about how it actually functions with regard to synthesis, storage and release. In this paper, we investigated three aspects of gland function in the noctuid moth Chloridea virescens (Fabricius): (i) whether translocation of pheromone from site of synthesis to release is dependent on calling or ovipositor movement, (ii) whether pheromone synthesis rate limits release and (iii) how intermittent calling (observed in this and other species) might affect the dynamics of release rate. Firstly, by manipulating the gland to simulate calling (extruded) or non-calling (retracted), we showed that pheromone translocation occurred regardless of whether the gland was retracted or extruded. Secondly, by manipulating pheromone production, we found that females that produced more pheromone had higher release rates. It was especially noticeable that females had a higher release rate at the start of calling, which dropped rapidly and leveled off over time. Together, these data suggest that intermittent calling in C. virescens (and other species) may function to allow females to replenish pheromone stores on the gland surface between calling bouts, so that brief, high release rates occur at the start of a calling bout; thus, potentially increasing a female's chances of attracting a mate. [ABSTRACT FROM AUTHOR]

Despite the fact that temperatures fluctuate on a daily basis in the field, the effect of fluctuating temperature on the susceptibility of pest insects to agricultural management tactics are lacking. We thus tested how the development of Spodoptera littoralis and Heliothis virescens (Lepidoptera: Noctuidae) is influenced by exposure to an insecticidal genetically engineered pulverized powder of, Bollgard II cotton producing the Bt proteins Cry1Ac and Cry2Ab, or an entomopathogenic fungus (Beauveria bassiana) under fluctuating temperatures in comparison with constant temperature. When temperature fluctuated symmetrically around 25 °C either in small range (± 5 °C) or in a large range (± 10 °C) on daily basis, development of both lepidopteran species was positively or not influenced in absence of additional stressors. Both species were affected by Bt-cotton when added at low concentrations to the artificial diet, but their reaction to Bt-cotton did not differ between fluctuating temperatures compared to a constant 25 °C. When H. virescens larvae were dipped into spore suspension of B. bassiana, all larvae reared at constant 25 °C died before pupation, while no detrimental effect of the fungus was visible in the fluctuating temperature regimes. In contrast, S. littoralis was not affected by the fungus in any treatment. Since fungal growth was reduced at fluctuating temperatures, this might have affected the infection rate in H. virescens. The results of this study indicate that fluctuating, compared to constant temperatures, can influence the susceptibility of pest insects to biological control agents, while temperature regimes seem to be less important for the efficacy of insecticidal genetically engineered crops. [ABSTRACT FROM AUTHOR]

Insect chitinases play essential roles in the molting and metamorphosis of insects. The virus Heliothis virescens ascovirus 3h (HvAV-3h) can prolong the total duration of the larval stage in its host larvae. In this study, the molecular character and function of chitinase and chitin-binding domain (CBD) were analyzed in larvae of Spodoptera exigua (Hübner) (Lepidoptera: Noctuidae). In detecting the chitinase activity of mock-infected and HvAV-3h-infected larval whole bodies and four different larval tissues, the results showed that larval chitinase activity was significantly decreased at 48 h post infection (hpi) and that the chitinase activity of HvAV-3h-infected larval fat body and cuticle was notably decreased at 144 and 168 hpi. The transcription level of S. exigua chitinase 7 (SeCHIT7) was down-regulated at the 6, 9, 12, 48, 72, and 96 hpi sample times, the S. exigua chitinase 11 (SeCHIT11) was down-regulated at 3–96 hpi, while both S. exigua chitinases (SeCHIT s) were up-regulated at 120–168 hpi. Further tissue-specific detection of SeCHIT7 and SeCHIT11 transcription showed that SeCHIT7 was down-regulated at 144 and 168 hpi in the fat body and cuticle. SeCHIT11 was down-regulated at 168 hpi in the fat body, midgut, and cuticle. Additionally, the transcription and expression of S. exigua chitin-binding domain (SeCBD) could not be detected in HvAV-3h-infected larvae. The in vitro analyses of SeCHIT7N, SeCHIT11, and SeCBD showed that SeCHIT7N and SeCHIT11 were typical chitinases. Conversely, no chitinase activity was detected with SeCBD. SeCBD, however, could significantly increase the activity of SeCHIT7N and SeCHIT11. In conclusion, HvAV-3h not only interfered with the transcription and expression of SeCHIT s but also affected the normal transcription and expression of SeCBD and, in doing so, influenced the host larval chitinase activity. These results will aid in providing a foundation for further studies on the pathogenesis of HvAV-3h. [ABSTRACT FROM AUTHOR]

Although the cotton bollworm Helicoverpa armigera has traditionally been controlled by application of chemical pesticides, chemical control selects for resistance, pollutes the environment, and endangers human health. New methods for controlling H. armigera are therefore needed. Heliothis virescens ascovirus 3i (HvAV-3i) is a recently identified virus of the lepidopteran larvae. We tested the effects of HvAV-3i on H. armigera larvae following oral ingestion of HvAV-3i-containing hemolymph (about 1.0 × 1010 virus genome copies per larvae) and following injection of HvAV-3i-containing hemolymph by insertion of a needle. Following oral ingestion, first-instar to fifth-instar larvae grew and developed normally. Following needle injection, in contrast, the corrected mortality of third and fourth instars was 88.9 ± 2.1 and 93.7 ± 3.4%, respectively. Food intake was significantly lower for larvae injected with virus-containing hemolymph than with virus-free hemolymph. Larvae injected with virus-containing hemolymph had extended survival times and could not complete the pre-pupal stage. These results indicate that inoculation of HvAV-3i via needle injection, but not via oral ingestion, significantly reduced the growth and development of H. armigera larvae. [ABSTRACT FROM AUTHOR]

Plants produce species‐specific herbivore‐induced plant volatiles (HIPVs) after damage. We tested the hypothesis that herbivore‐specific HIPVs prime neighboring plants to induce defenses specific to the priming herbivore. Since Manduca sexta (specialist) and Heliothis virescens (generalist) herbivory induced unique HIPV profiles in Nicotiana benthamiana, we used these HIPVs to prime receiver plants for defense responses to simulated herbivory (mechanical wounding and herbivore regurgitant application). Jasmonic acid (JA) accumulations and emitted volatile profiles were monitored as representative defense responses since JA is the major plant hormone involved in wound and defense signaling and HIPVs have been implicated as signals in tritrophic interactions. Herbivore species‐specific HIPVs primed neighboring plants, which produced 2 to 4 times more volatiles and JA after simulated herbivory when compared to similarly treated constitutive volatile‐exposed plants. However, HIPV‐exposed plants accumulated similar amounts of volatiles and JA independent of the combination of priming or challenging herbivore. Furthermore, volatile profiles emitted by primed plants depended only on the challenging herbivore species but not on the species‐specific HIPV profile of damaged emitter plants. This suggests that feeding by either herbivore species primed neighboring plants for increased HIPV emissions specific to the subsequently attacking herbivore and is probably controlled by JA. Both Heliothis virescens and Manduca sexta feeding induces Nicotiana benthamiana to emit species‐specific herbivore‐induced plant volatiles (HIPVs), which prime neighboring N. benthamiana plants for higher jasmonic acid and HIPVs emissions specific to the attacking herbivore independent of the priming herbivore. [ABSTRACT FROM AUTHOR]

In insects, male and female pheromone signals are detected by olfactory sensory neurons (OSNs) expressing the "sensory neuron membrane protein type 1". SNMP1 is supposed to function as a co-receptor involved in the transfer of pheromones to adjacent pheromone receptors. In the moth Heliothis virescens, we previously found OSNs that project their dendrites into pheromone-responsive trichoid sensilla and are associated with cells containing transcripts for the HvirSNMP1-related protein HvirSNMP2. Like HvirSNMP1, HvirSNMP2 belongs to the CD36-family of two-transmembrane domain receptors and transporters for lipophilic compounds, but its role in the olfactory system is unknown. Here, we generated polyclonal anti-peptide antibodies against HvirSNMP2 as well as HvirSNMP1 and conducted an in-depth immunohistochemical analysis of their subcellular localization in the antenna of both sexes. In line with a function in pheromone detection, HvirSNMP1 was immunodetected in the somata and the dendrites of distinct OSNs in subsets of trichoid sensilla. These trichoid sensilla contained only one α-SNMP1-positive OSN in males and clusters of 2–3 labeled cells in females. In contrast, experiments with α-SNMP2-antibodies revealed a broad labeling of non-neuronal support cells (SCs) that are associated with OSNs in likely all trichoid and basiconic sensilla of the antenna with no differences between sexes. Detailed confocal microscope examinations of olfactory sensilla revealed SNMP2-like immunoreactivity close to the apical membrane of SCs and interestingly inside the sensillum. Together, these findings indicate a potential function of SNMP2 in pheromone- as well as general odorant-responsive sensilla and a role fundamentally different from SNMP1. [ABSTRACT FROM AUTHOR]

The tobacco budworm, Chloridea virescens (F.) (Lepidoptera: Noctuidae), once a major insect pest of tobacco, Nicotiana sp., and cotton, Gossypium hirsutum L., in the Americas, has decreased in abundance, especially in cotton fields, during the past 2 decades. Little is known of the biological factors, crop management techniques, and effect that ample planting of cultivars of cotton expressing Bacillus thuringiensis Berliner (Bt-cotton) might have had on their reduction, nor of changes in the conditions of the 'source' areas that produce migrant populations of tobacco budworm. Detailed knowledge of its population dynamics is lacking. This work proposed a mathematical model considering only seasonal changes in temperature as the driving factor to explain variations of tobacco budworm during a 20-year collection of males in pheromone traps in Washington County, MS. Tobacco budworm dynamics according to the model suggested the stability of the population of the geographical area did not depend on immigration and that larvae of the last generation of the year that survive winter temperatures better explain the dynamics, contrary to what was commonly assumed that larvae in the area could not survive prolonged wet and cold winter weather. The Mississippi Delta has planted Bt-cotton in high proportions, however, this might be a more reasonable force behind reduction in abundance of tobacco budworms. [ABSTRACT FROM AUTHOR]

Microplitis croceipes is a solitary parasitoid that specializes on noctuid larvae of Helicoverpa zea and Heliothis virescens. Both the parasitoid and its hosts are naturally distributed across a large part of North America. When parasitoids deposit their eggs into hosts, venom and polydnaviruses (PDVs) are also injected into the caterpillars, which can suppress host immune responses, thus allowing parasitoid larvae to develop. In addition, PDVs can regulate host oral cues, such as glucose oxidase (GOX). The purpose of this study was to determine if parasitized caterpillars differentially induce plant defenses compared to non-parasitized caterpillars using two different caterpillar host/plant systems. Heliothis virescens caterpillars parasitized by M. croceipes had significantly lower salivary GOX activity than non-parasitized caterpillars, resulting in lower levels of tomato defense responses, which benefited parasitoid performance by increasing the growth rate of parasitized caterpillars. In tobacco plants, parasitized Helicoverpa zea caterpillars had lower GOX activity but induced higher plant defense responses. The higher tobacco defense responses negatively affected parasitoid performance by reducing the growth rate of parasitized caterpillars, causing longer developmental periods, and reduced cocoon mass and survival of parasitoids. These studies demonstrate a species-specific effect in different plant-insect systems. Based on these results, plant perception of insect herbivores can be affected by parasitoids and lead to positive or negative consequences to higher trophic levels depending upon the particular host-plant system. [ABSTRACT FROM AUTHOR]

In insect antenna, following the activation of olfactory sensory neurons, odorant molecules are inactivated by enzymes in the sensillum lymph. How the inactivation products are cleared from the sensillum lymph is presently unknown. Here we studied the role of support cells (SCs) and the so-called sensory neuron membrane protein 2 (SNMP2), a member of the CD36 family of lipid transporters abundantly expressed in SCs, in sensillum lymph clearance processes in the moths Heliothis virescens and Bombyx mori. In these species, the sex pheromone components are inactivated to long-chain fatty acids. To approach a role of SNMP2 in the removal of such inactivation products, we analyzed the uptake of a fluorescent long-chain fatty acid analog into a newly generated HvirSNMP2-expressing cell line. We found an increased uptake of the analog into SNMP2-cells compared to control cells, which could be blocked by the CD36 protein inhibitor, SSO. Furthermore, analyses of sensilla from antenna treated with the fatty acid analog indicated that SNMP2-expressing SCs are able to take up fatty acids from the sensillum lymph. In addition, sensilla from SSO-pretreated antenna of B. mori showed reduced removal of the fluorescent analog from the sensillum lymph. Finally, we revealed that SSO pretreatment of male silkmoth antenna significantly prolonged the duration of the female pheromone-induced wing-fluttering behavior, possibly as a result of impaired lymph clearance processes. Together our findings in H. virescens and B. mori support a pivotal role of olfactory SCs in sensillum lymph maintenance processes and suggest an integral role of SNMP2 in the removal of lipophilic "waste products" such as fatty acids resulting from sex pheromone inactivation. [Display omitted] • SNMP2 mediates the uptake of long-chain fatty acids in cell culture. • Support cells take up fatty acids from the sensillum lymph. • Olfactory support cells abundantly express SNMP2. • Both SNMP2 and support cells are implicated sensillum lymph clearance processes. [ABSTRACT FROM AUTHOR]

Huitlacoche or corn smut, Ustilago maydis (DC.) Corda, is a biotrophic fungal pathogenic. The scales that grow in ears of maize, Zea mays L., are used as fresh or raw vegetables. In some regions of Mexico, maize is planted to harvest "huitlacoche", a crop also susceptible to attack by insect pests that affect its quality. The purpose of this study was to recognize entomofauna in maize ears infected with huitlacoche (corn smut) and identify pest species that attack huitlacoche in five maize hybrids. We collected a total of 515 specimens in four orders, seven families, and 11 species. The orders Coleoptera and Lepidoptera comprised 71.4% of the total number of families, 81.8% of the species, and 99.6% of individuals. The percentage of damaged ears ranged from 47.5 to 65.0%. Species best represented were Cotinis mutabilis (Gory and Percheron), Spodoptera frugiperda (J.E. Smith), Heliothis virescens (Fabricius), and Carpophilus lugubris Murray considered primary pest of huitlacoche because they were present in all maize studied. Shannon-Wiener diversity (0.592 bits per individual) and Simpson (0.302 bits per individual) indices showed less diversity of individuals and moderate species dominance. Greatest richness of species was in hybrids 'AN388' and 'H-318', each with seven. [ABSTRACT FROM AUTHOR]