Type A Allatostatin III

The genome of Tribolium castaneum encodes two allatostatin [AS type B; W(X)(6)Wamide and AS type C; PISCF-OH] and one allatotropin (AT) precursor, but no AS type A (FGLamide) (Tribolium Genome Sequencing Consortium, 2008: Nature 452:949-955). Here we studied the activity (in vitro) of peptides derived from these precursors on the synthesis/release of juvenile hormone (JH) III. The corpora cardiaca-corpora allata (CC-CA) complexes of adult females of another tenebrionid beetle, the mealworm Tenebrio molitor, were used. Incubating the gland complexes in a medium containing Trica-AS B3 peptide, we showed that the peptide has allatostatic function in T. molitor. The activity of the type C AS depended on the age of the test animals and their intrinsic rate of JH III biosynthesis. The Trica-AS C peptide inhibited the JH release from CA of 3-day-old females with a high intrinsic rate of JH synthesis, but activated JH release from the CA of 7-day-old females with a lower intrinsic rate of JH production. The allatotropin peptide (Trica-AT) also activated the JH release from the CA of 7-day-old females in a dose-dependent and reversible manner. Unexpectedly, a type A AS derived from the precursor of the American cockroach Periplaneta americana (Peram-AS A2b) inhibited the JH release from the CA of younger and older females in the concentration range of 10(-8) to 10(-4) M, and the effects were fully reversible in the absence of peptide. These data suggest a complex role of allatoactive neuropeptides in the regulation of JH III biosynthesis in beetles.

The juvenile hormone (JH) titer was measured by liquid chromatography-mass spectrometry (LC-MS) with electrospray ionization (ESI). Three JH homologs, the JH I-III were detected in various amounts in larvae, prepupae and virgin adult females of Spodoptera frugiperda. In penultimate larvae, the JH II and III titers were relatively high, but decreased continuously during the 3 days of that stage, whereas JH I was detectable at low amounts only on the first 2 days. At the beginning of the last larval stage almost no JH could be detected but thereafter, a consistent low amount of JH III was present until the prepupal stage. In adult virgins, the JH titer peaked on the 2nd and 6th day after the imaginal molt. The measured hormone titers well agree with general lepidopteran physiology, because in larvae the JH titer should be high to prevent premature metamorphosis, but decrease in last instar larvae before pupation, whereas in adults JH returns to control various aspects of reproduction. JH biosynthesis is thought to be the main factor influencing the JH titer in the hemolymph and there is evidence that neuropeptides either act stimulatory (allatotropins) or inhibitory (allatostatins) on this process. After silencing of either the allatostatin AS-C-type (Spofr/Manse-AS) or the allatotropin AT 2 (Spofr-AT 2) gene the transcript level was reduced in brain and gut of last instar larvae as well as of adult S. frugiperda. This suppression led to an increased JH titer in larvae, suggesting an allatostatic activity of both the peptides in this stage. As a result of the elevated hormone titer, the last larval stage was prolonged. In prepupae, the JH titer was decreased, but the animals pupated and molted normally. In adult female virgin moths the effect on the JH titer was inversely dependent on the age of the moths and varied among the JH homologs, indicating that the peptides act either allatostatic or allatotropic. For both peptides, gene silencing clearly reduced the oviposition rates of adult females.

The antennal lobe (AL) of the sphinx moth Manduca sexta is a well-established model system for studying mechanisms of neuronal development. To understand whether neuropeptides are suited to playing a role during AL development, we have studied the cellular localization and temporal expression pattern of neuropeptides of the A-type allatostatin family. Based on morphology and developmental appearance, we distinguished four types of AST-A-immunoreactive cell types. The majority of the cells were local interneurons of the AL (type Ia) which acquired AST-A immunostaining in a complex pattern consisting of three rising (RI-RIII) and two declining phases (DI, DII). Type Ib neurons consisted of two local neurons with large cell bodies not appearing before 7/8 days after pupal ecdysis (P7/P8). Types II and III neurons accounted for single centrifugal neurons, with type II neurons present in the larva and disappearing in the early pupa. The type III neuron did not appear before P7/P8. RI and RII coincided with the rises of the ecdysteroid hemolymph titer. Artificially shifting the pupal 20-hydroxyecdysone (20E) peak to an earlier developmental time point resulted in the precocious appearance of AST-A immunostaining in types Ia, Ib, and III neurons. This result supports the hypothesis that the pupal rise in 20E plays a role in AST-A expression during AL development. Because of their early appearance in newly forming glomeruli, AST-A-immunoreactive fibers could be involved in glomerulus formation. Diffuse AST-A labeling during early AL development is discussed as a possible signal providing information for ingrowing olfactory receptor neurons.