Xenorhabdus innexi is a bacterial symbiont of Steinernema scapterisci nematodes, which is a cricket-specialist parasite and together the nematode and bacteria infect and kill crickets. Curiously, X. innexi expresses a potent extracellular mosquitocidal toxin activity in culture supernatants. We sequenced a draft genome of X. innexi and compared it to the genomes of related pathogens to elucidate the nature of specialization.

Insects provide an excellent model for examining concepts in endocrinology in the classroom. They are relatively inexpensive to rear, short-lived, and free from animal welfare regulations. Using the tobacco hornworm (Manduca sexta) as a model, we have developed a simple laboratory experiment to demonstrate the role of hormones in development. In this experiment, students will use a readily available agonist to disrupt insect development, preventing metamorphosis. This exercise fits well into the AP lab curriculum and the NGSS LSB. 1 objectives.

Reduction of mosquito-borne diseases relies, in part, on the use of synthetic pesticides to control pest mosquitoes. This reliance has led to genetic resistance, environmental contamination and the nondiscriminatory elimination of both pest and non-pest species. To expand our options for control, we screened entomopathogenic bacteria for potential larvicidal activity. A lipopeptide from the bacterium, Xenorhabdus innexi, was discovered that displayed potent larvicidal activity. The LC50s of the lipopeptide towards Aedes aegypti, Culex pipiens and Anopheles gambiae larvae were 1.81, 1.25 and 1.86 parts-per-million, respectively. No mortality was observed in other insect species tested. The putative mode of action of the lipopeptide suggested that after orally ingestion, it bound to the apical membrane of anterior midgut cells and created pores in the cellular membranes. The rapid neutralization of midgut pH suggested the pores disabled the H+-V-ATPase on the basal membrane and led to epithelial cell death. Specificity and toxicity towards mosquito larvae and the unique mode of action makes this lipopeptide a potentially attractive bacterial insecticide for control of mosquitoes.

Juvenile hormone (JH) is a key regulator of insect development and reproduction. In adult mosquitoes, it is essential for maturation of the ovary and normal male reproductive behavior, but how JH distribution and activity is regulated after secretion is unclear. Here, we report a new type of specific JH-binding protein, given the name mosquito juvenile hormone-binding protein (mJHBP), which circulates in the hemolymph of pupal and adult Aedes aegypti males and females. mJHBP is a member of the odorant-binding protein (OBP) family, and orthologs are present in the genomes of Aedes, Culex, and Anopheles mosquito species. Using isothermal titration calorimetry, we show that mJHBP specifically binds JH II and JH III but not eicosanoids or JH derivatives. mJHBP was crystallized in the presence of JH III and found to have a double OBP domain structure reminiscent of salivary "long" D7 proteins of mosquitoes. We observed that a single JH III molecule is contained in the N-terminal domain binding pocket that is closed in an apparent conformational change by a C-terminal domain-derived α-helix. The electron density for the ligand indicated a high occupancy of the natural 10R enantiomer of JH III. Of note, mJHBP is structurally unrelated to hemolymph JHBP from lepidopteran insects. A low level of expression of mJHBP in Ae. aegypti larvae suggests that it is primarily active during the adult stage where it could potentially influence the effects of JH on egg development, mating behavior, feeding, or other processes.

Non-invasive 3D magnetic resonance imaging techniques were used to investigate metamorphosis of the alimentary tract of Manduca sexta from the larval to the adult stage. The larval midgut contracts in volume immediately following cessation of feeding and then greatly enlarges during the late pharate pupal period. Magnetic resonance imaging revealed that the foregut and hindgut of the pharate pupa undergo ecdysis considerably earlier than the external exoskeleton. Expansion of air sacs in the early pupa and development of flight muscles several days later appear to orient the midgut into its adult position in the abdomen. The crop, an adult auxiliary storage organ, begins development as a dorsal outgrowth of the foregut. This coincides with a reported increase in pupal ecdysteroid titers. An outgrowth of the hindgut, the rectal sac, appears several days later and continues to expand until it nearly fills the dorsal half of the abdominal cavity. This development correlates with a second rise in pupal ecdysteroid titers. In the pharate pupa, the presence of paramagnetic species renders the silk glands hyperintense.

Sesamia nonagrioides (Lepidoptera: Noctuidae) larvae reared under long day (LD; 16L:8D) conditions pupate after 5 or 6 larval instars, whereas under short day (SD; 12L:12D) conditions they undergo up to 12 additional molts before pupating. This extended period of repeated molting is maintained by high levels of juvenile hormone (JH). Previous work demonstrated that both LD and SD larvae decapitated in the 6th instar pupate but further development is halted. By contrast, about one-third of SD larvae from which only the brain has been removed, undergo first a larval molt, then pupate and subsequently developed to the adult stage. Debrained LD larvae molt to larvae exceptionally but regularly pupate and produce adults. Implanted brains may induce several larval molts in debrained recipient larvae irrespectively of the photoperiodic conditions. The results of present work demonstrate that the prothoracic glands (PGs) and the corpora allata (CA) of debrained larvae continue to produce ecdysteroids and JHs, respectively. PGs are active also in the decapitated larvae that lack JH, consistent with the paradigm that CA, which are absent in the decapitated larvae, are the only source of this hormone. Completion of the pupal-adult transformation in both LD and SD debrained insects demonstrates that brain is not crucial for the development of S. nonagrioides but is required for diapause maintenance. Application of JH to headless pupae induces molting, presumably by activating their PGs. It is likely that JH plays this role also in the induction of pupal-adult transformation in debrained insects. Application of the ecdysteroid agonist RH 2485 (methoxyfenozide) to headless pupae also elicits molting: newly secreted cuticle is in some cases thin and indifferent, in other cases it bears distinct pupal or adult features.

A microchip array encompassing probes for 14,010 genes of Drosophila melanogaster was used to analyze the effect of juvenile hormone (JH) on genome-wide gene expression. JH is a member of a group of insect hormones involved in regulating larval development and adult reproductive processes. Total RNA was isolated from Drosophila S2 cells after 4 hours treatment with 250 ng/ml (10R) JH III or 250 ng/ml methyl linoleate. A collection of 32 known or putative genes demonstrated a significant change with JH III treatment (r > 2.0, P <or= 0.005). Of these, the abundance of 13 transcripts was significantly increased and 19 decreased. The expression of a subset of these loci was analyzed by real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR). Three loci that exhibited constant expression in the presence and absence of JH III (RP49 [FBgn0002626], FBgn0023529, and FBgn0034354) were evaluated and found to be reliable invariant reference transcripts for real-time RT-qPCR analysis using BestKeeper and geNorm software. Increased expression in presence of JH III was confirmed by real-time RTqPCR analysis. However, only one of five loci that exhibited reduced expression on microarrays could be confirmed as significantly reduced (P <or= 0.05). Among the confirmed JH III up-regulated genes were two loci of unknown function (FBgn0040887 and FBgn0037057) and Epac, an exchange protein directly activated by cyclic AMP, a guanine nucleotide exchange factor for Rap1 small GTPase.

Real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to characterize the effects of juvenile hormone (JH) on Epac (Exchange Protein directly Activated by Cyclic AMP; NM_001103732), a guanine nucleotide exchange factor for Rap1 in Drosophila S2 cells. JH treatment led to a rapid, dose-dependent increase in Epac relative expression ratio (RER) when compared to treatment with methyl linoleate (MLA) that lacks biological activity. The minimal level of hormone needed to elicit a response was 100 ng/ml. Time-course studies indicated a significant rise in the RER 1h after treatment. S2 cells were challenged with 20-hydroxyecdysone and a series of compounds similar in structure to JH to determine the specificity of the response. Methoprene and JH III displayed the greatest increases in RER. Late third instar (96 h) Drosophila were exposed to diet containing methoprene (500 ng/g diet); significantly higher RERs for Epac were observed 12h after exposure. JH had no effect on Epac RERs in the human cell line HEK-293.

External stressors disrupt physiological homeostasis; in insects, the response to stress may result in delayed development as the animal attempts to restore homeostasis before proceeding with its complex life cycle. Previous studies have demonstrated that exposure to stress leads to increased levels of the juvenile hormone (JH), a hormone responsible for maintaining the insect larval state. In Manduca sexta, JH is transported to target tissue by a high-affinity binding protein, hemolymph JH binding protein (hJHBP). Since JH titers are elevated in stressed Manduca, we examined levels of hJHBP to better understand (1) the role of JH in regulating hJHBP levels and (2) the hJHBP-regulated bioavailability of hormone at the target site. Fourth stadium Manduca (48 h post-ecdysis) were exposed for 24 h to various stressors including nutritional deprivation, microbial infection, cutaneous injury, episodic movement, and temperature elevation. Insects raised on diets lacking nutritional content exhibited mean hJHBP levels that were less than half (45%) those of control insects. Similarly, insects injected with Escherichia coli demonstrated a 47% reduction in hJHBP titers. Cutaneous injury, episodic movement, and temperature elevation lowered hJHBP levels by 47%, 43%, and 38%, respectively. Total hemolymph protein concentration was not affected. After a stress event (injury), a 50% reduction in abundance of fat body hJHBP mRNA was observed within 4 h; hJHBP levels did not drop until 24 h after injury. Stress in the fourth stadium was manifest in fifth instars, with 100% of the injured insects displaying an extended larval stadium or failing to pupate. Computational modeling of the JH–hJHBP interaction indicates that unbound JH doubles in stressed insects. These results indicate that in response to stress larval hJHBP titers are significantly reduced, increasing JH bioavailability at the target site and thereby impacting development and survival of the insect. Treatment of unstressed insects with physiological doses of JH I did not affect hJHBP levels, suggesting that elevated JH levels were not solely responsible for the observed down-regulation in stressed insects.

A simple immunological assay was developed as an alternative to the dissection/visualization method for detecting the presence of the parasitoid, Microctonus aethiopoides Loan, in the alfalfa weevil, Hypera postica (Gyllenhal). The dot-blot assay was validated using laboratory-reared and field-collected adult weevils of known parasitization status. The dot-blot assay was also used to estimate the developmental stage of the parasitoid within parasitized adult hosts. The assay results can be used to forecast parasitoid emergence dates and estimate the parasitism rate of M. aethiopoides in alfalfa weevil populations.

The hemolymph juvenile hormone binding protein (hJHBP) gene of Manduca sexta is a key target of its specific ligand, juvenile hormone (JH). While the cDNA for hJHBP has been partially characterized, little is known about the hJHBP gene structure or its promoter(s) and enhancers(s). Previous studies have demonstrated that JH stimulates a rapid accumulation of hJHBP mRNA in the fat body. To better understand the underlying molecular events affecting regulation, we sequenced the M. sexta hJHBP gene and its mRNA transcript, characterized its genomic organization, and determined the spatial and temporal expression patterns of the hJHBP gene. The gene is composed of 5 exons spanning 6.7 kb. Southern blot analysis indicates that the gene is present as a single copy. The earliest expression of hJHBP occurs 24 to 48 h after fertilization. Distribution studies indicate that fat body is the only site for hJHBP expression. Elements displaying similarity with sequences of other lepidopteran genes were discovered outside the open reading frame and may represent mobile insertion elements.

The juvenile hormones (JHs) regulate a diverse array of insect developmental and reproductive processes. One molecular target of JH action is its transporter, hemolymph JH binding protein (hJHBP); in the larva of the tobacco hornworm, Manduca sexta, low doses of JH can immediately increase hJHBP gene expression. Less explored are the effects of JH on embryological development, where early hormonal treatment has been shown to affect embryonic development and pupation. This study examines the egg form of JHBP and its gene expression during embryogenesis of M. sexta, as well as the phenotypic effect JH treatment has on embryos and on JHBP gene expression. We here demonstrate that the preponderance of JHBP found in the egg is maternally derived and that the embryonic gene and protein appear identical to those found in the larva. Expression of the JHBP gene begins in both the embryo itself and extra-embryonic tissues 15 h after fertilization, long before emergence of a functional fat body and circulatory system. Topical application of low JH doses to early embryos resulted in larval abnormalities while high doses of the hormone induced embryonic mortality. These effects are not mediated through regulation of the JHBP gene, since embryonic expression appears invariant in response to JH challenge. The toxicity of JH is tightly correlated with the concentration of unbound hormone.

A simple immunological assay was developed as an alternative to the dissection/visualization method for detecting the presence of the parasitoid, Microctonus aethiopoides Loan, in the alfalfa weevil, Hypera postica (Gyllenhal). The dot-blot assay was validated using laboratory-reared and field-collected adult weevils of known parasitization status. The dot-blot assay was also used to estimate the developmental stage of the parasitoid within parasitized adult hosts. The assay results can be used to forecast parasitoid emergence dates and estimate the parasitism rate of M. aethiopoides in alfalfa weevil populations. Keywords: Dot-blot AssayPolyclonal AntibodyAdult ParasitoidMonitoringBiological Control

In most insect species, juvenile hormones regulate critical physiological processes such as metamorphosis and reproduction. In insects, these sesquiterpenoids are synthesized by retrocerebral endocrine organs, the corpora allata, via the classical mevalonate (MVA) pathway. One of these compounds, juvenile hormone III (JH III), has also been identified in the sedge Cyperus iria. In higher plants, biosynthesis of the sesquiterpenoid backbone may proceed through two distinct pathways: the MVA pathway or the 2C-methyl erythritol 4-phosphate pathway or through a combination of both pathways. Cell suspension cultures of C. iria were used to elucidate the biosynthetic pathway of JH III in the plant. Enzyme inhibition and labeling studies conclusively demonstrated that the biosynthesis of the sesquiterpenoid backbone of JH III proceeds via the MVA pathway. Inhibitor and precursor feeding studies also suggest that later steps of JH III biosynthesis inC. iria are similar to the insect pathway and that the final enzymatic reaction in JH III biosynthesis is catalyzed by a cytochrome P450 monooxygenase.

Overcrowding of a species is often its undoing. Competition for limited resources, spread of disease, and behavioral changes lead to death or severe stress that ultimately reduces the population. This important biological principle is not easily demonstrated in the classroom since a reasonably large population of easily viewed organisms must be maintained. In our work with the tobacco hornworm, Manduca s exta, we noted c urious behavioral changes in overcrowded larvae that may be used to demonstrate both the intermediate as well as the long-term effects of overpopulation. These r esponses include i ncreased mobility and aggressiveness that delay development and reduce fecundity. From a classroom standpoint, the behavioral changes can easily be monitored in a few minutes and, importantly, offer the student a chance to observe, develop hypotheses and make systematic observations to better understand basic principles of behavior. The relatively large size of the larva, its surface-feeding behavior, and its sessile nature make student observations simple.

Pablo Picasso is well known as one of the most eminent artists in the history of Western civilization, and certainly the most famous artistic creator of the twentieth century. This entry begins by narrating his life and works in order to give an overview of his personal and artistic development. The article then turns to empirical studies, which may be divided into those that deal with his life and those that deal with his work. In the former case, Picasso has been a subject of psychobiographical, comparative, and historiometric research, albeit in the latter case this usage is more covert. In the case of works, a number of researchers have examined specific paintings, with the vast bulk of the studies concentrated on the extensive sketches that Picasso drew for his 1937 Guernica. These studies provide insight into Picasso's creative process.

Transcription of the early trypsin gene occurs in the midgut after adult emergence under control of juvenile hormone (JH). We tested the hypothesis that factors that affect the steady-state levels of early trypsin mRNA do so by influencing the levels of JH. We investigated the effect of ingesting different meals on early trypsin mRNA levels as well as on JH levels. We also studied how early trypsin mRNA levels changed when the midgut was isolated from different components of the neuroendocrine system by abdominal ligation and decapitation. Early trypsin transcripts levels are high in unfed females; feeding different meals had three distinct effects on the changes of steady-state levels of early trypsin mRNA: (1) blood and protein meals caused the level to decrease drastically and remained low for at least 24 h; (2) amino acid meals caused a transient decrease in the mRNA level, but it returned to high levels after 12-18 h; and (3) sugar, latex and saline meals had no effect on the early trypsin mRNA steady-state levels. The changes in JH levels after ingesting blood and amino acid meals show profiles resembling the changes in early trypsin mRNA levels for the corresponding meal. Decapitation at 1, 2 and 3 days after emergence does not affect the steady-state levels of early trypsin in unfed females. In contrast, 24 h after feeding, transcript levels were significantly higher in decapitated females when compared with non-decapitated fed females. We propose that the changes in the steady-state levels of early trypsin mRNA observed after the ingestion of different meals, ligations and decapitations are generated by changes in the levels of juvenile hormone.

Juvenile hormone III (JH III), a sesquiterpenoid involved in the regulation of insect development and reproduction, appears to be ubiquitous in insects and has also been isolated from some species of sedge. The quantification of JH III extracted from the sedge Cyperus iria by HPLC and by radioimmunoassay (RIA) has been compared. The RIA, developed originally to determine insect haemolymph titres, was optimized for the analysis of plant tissues. The antiserum 31867 displayed minimal cross-reactivity with precursors of JH III from the insect biosynthetic pathway or with extracts from related plant species. Analysis of standards and plant extracts by HPLC and RIA confirmed that there was no significant difference between the ability of these two techniques to quantify JH III (paired t-test). Therefore, RIA was subsequently used to determine the distribution of JH III in mature plants of C. iria. Substantial concentrations were detected in the above-ground plant tissues (0.2–1.2 µg/g fresh weight), but the majority of JH III was found in the roots (43.5 µg/g fresh weight). Copyright © 2000 John Wiley & Sons, Ltd.

Insect hemolymph juvenile hormone binding protein (hJHBP) regulates peripheral titers of its ligands, the juvenile hormones. In larvae of the black (bl) strain of the tobacco hornworm, Manduca sexta, treatment with small doses of juvenile hormone I (JH I) can also regulate titers of hJHBP. To further investigate this regulation, responsiveness of hJHBP mRNA expression to JH I was characterized in vivo. RNA analyzes revealed that transcript levels in fat body, the site of hJHBP synthesis, increased fivefold within several hours of treatment with physiological doses of hormone and remained elevated for approximately 16 h. Sensitivity to JH treatment was found to vary temporally. To ensure transcript identity, a wild-type cDNA clone and a bl RT-PCR fragment were sequenced and found to be 99% homologous. Together, these results suggest that JH participates in regulating expression of its transport protein in bl larvae by modifying the in vivo abundance of hJHBP's mRNA transcript.