Comparative Proteome Analysis Reveals that Cuticular Proteins Analogous to Peritrophin‐Motif Proteins are Involved in the Regeneration of Chitin Layer in the Silk Gland of Bombyx mori at the Molting Stage

The silk gland of silkworm produces silk proteins during larval development. Many studies have long focused on the silk gland of the fifth instar larvae, but few have investigated this gland at other larval stages. In the present study, the silk gland proteomes of the fourth instar and fourth molt are analyzed using liquid chromatography–tandem mass spectrometry. In total, 2654 proteins are identified from the silk gland. A high abundance of ribosomal proteins and RR‐motif chitin‐binding proteins is identified during day 2 of the fourth instar (IV‐2) larval developmental stage, and the expression of cuticular proteins analogous to peritrophin (CPAP)‐motif chitin‐binding proteins is higher during the fourth molt (IV‐M). In all, nine enzymes are found to be involved in the chitin regeneration pathway in the silk gland. Among them, two chitinase and two chitin deacetylases are identified as CPAP‐motif proteins. Furthermore, the expression of CPAP3‐G, the most abundant CPAP‐motif cuticular protein in the silk gland during the IV‐M stage, is investigated using western blot and immunofluorescence analyses; CPAP3‐G shows a reverse changing trend with chitin in the silk gland. The findings of this study suggest that CPAP‐motif chitin‐binding proteins are involved in the degradation of the chitin layer in the silk gland. The data have been deposited to the ProteomeXchange with identifier PXD008677.     

Effects of parental care on resource allocation into immune defense and buccal microbiota in mouthbrooding cichlid fishes*

Sexual dimorphism is founded upon a resource allocation trade‐off between investments in reproduction versus other life‐history traits including the immune system. In species with conventional parental care roles, theory predicts that males maximize their lifetime reproductive success by allocating resources toward sexual selection, while females achieve this through prolonging their lifespan. Here, we examine the interrelation between sexual dimorphism and parental care strategies in closely related maternal and biparental mouthbrooding cichlid fishes from East African Lake Tanganyika. We measured cellular immune parameters, examined the relative expression of 28 immune system and life history‐related candidate genes and analyzed the microbiota composition in the buccal cavity. According to our predictions, maternal mouthbrooders are more sexually dimorphic in immune parameters than biparental mouthbrooders, which has possibly arisen through a differential resource allocation into parental care versus secondary sexual traits. Biparental mouthbrooders, on the other hand, which share the costs of parental care, feature an upregulated adaptive immune response and stronger antiviral properties, while their inflammation response is reduced. Overall, our results suggest a differential resource allocation trade‐off between the two modes of parental investment.     

Morphology of the foveal glands and foveae dorsales in male Hyalomma truncatum and Rhipicephalus evertsi mimeticus ticks (Acari; Ixodidae) before and during feeding

The ultrastructure of the foveae dorsales and foveal glands in unfed and attached male Hyalomma truncatum and Rhipicephalus evertsi mimeticus ticks was studied. Both species are provided with a paired foveal gland system, which is similar in unfed as well as in attached ticks. This gland system consists of the fovea dorsalis with pores and pore tubes as the external part, the foveal neck zone as a link between the fovea dorsalis and the lobes of the gland and the bulbous lobes as the innermost part. The fovea dorsalis is located on either side of the dorsal midline in the midsection of the body and appears as a roundish plate containing 15±6.5 and 21±7 slit-like pores in R. evertsi mimeticus (n=210) and H. truncatum (n=210), respectively. Each pore leads into a cuticular lined channel containing a pore tube. Below each fovea, the foveal neck zone is located within a groove of the cuticle and consists of the termini of the pore tubes which enlarge basally to form a cup-shaped ampulla each. Furthermore, secretory lobes are located below the foveal neck zone. Each lobe consists of secretory cells and a central excretory duct which leads into the ampulla. The ducts are lined with microvilli. The secretory cells contain numerous vesicles of varying size with one or more granules. In male ticks of both species the secretory lobe cells remained unchanged in size, structure and granule content irrespective of whether they were unfed or attached for up to 30 days. Axons occur in the fascicles between the secretory lobe cells containing numerous neurosecretory vesicles. A possible role of the foveal glands in the production of pheromones is hypothesized.     

Cytochemical localization of cellulase in glandular trichomes ofcannabis (cannabaceae)

Cellulase reaction product was localized cytochemically at the ultrastructural level in the cell wall of disc cells, the secretory cavity and in the subcuticular wall of glands inCannabis. Cellulase reaction product was evident in the less dense region of the disc cell wall prior to secretory cavity formation. Reactivity in this region was associated with separation of an outer zone, forming the subcuticular wall, from the inner wall zone adjacent to the plasma membrane of the disc cells. Reaction product was associated with the disc cell wall and fibrillar matrix extending from it into the secretory cavity. Reactivity remained evident over the subcuticular wall throughout enlargement of the secretory cavity. Reaction product also was present over fibrillar matrix in the secretory cavity associated with both the inner wall and the subcuticular wall. The distribution of cellulase reaction product supports an interpretation that cellulase is involved in formation of the secretory cavity and subsequent redistribution of wall products to form the subcuticular wall during development of the secretory cavity.     

High frequency plant regeneration from Eucalyptus globulus Labill. hypocotyls: Ontogenesis and ploidy level of the regenerants

Up to 70% regenerating hypocotyls provided with 5 to 20 buds were obtained on MS medium containing 0.01 or 1 mg l^-1 NAA and 0.2 mg l^-1 BA or 0.2 mg l^-1 BA and 0.2 mg l^-1 TDZ. The ability to regenerate buds was correlated with the presence of oil glands at a stage in germination when oil secretion was not yet occurring. The regeneration of shoot meristems took place from the cells involved in the differentiation of these glands. Such glands could also appear during callus redifferentiation, giving rise to indirect regeneration. Rooting of the regenerants was efficient using a two-step procedure of induction under darkness in the presence of 3 mg l^-1 IBA, followed by root development on medium devoid of growth regulators under a 16-h photoperiod, the medium being solidified with Gelrite. Regenerated plants showed no phenotypic alterations. Nuclear DNA contents in mother-plant material and regenerants were analysed using flow cytometry. There was no evidence of polyploidy in any of the samples, indicating the absence of polyploidisation during cell differentiation and under in vitro conditions. No regeneration was obtained from leaf or stem explants from micropropagated plantlets. This revised version was published online in June 2006 with corrections to the Cover Date.     

Source of alate excitant pheromones in the red imported fire antSolenopsis invicta (Hymenoptera: Formicidae)

At the onset of mating flights inSolenopsis invicta, workers swarm excitedly over the mound as alates prepare to fly. Previous studies demonstrated that this excitement is stimulated by the male and female alates. We investigated the glandular source(s) of pheromones produced by the alates that cause excitement. The only common female and male alate body part that elicited excitement when crushed was the head. Within the head, excised mandibular glands were found to be responsible for worker excitement. Fire ant workers are very sensitive to external stimuli and some excitement was elicited by crushed female gasters and male thoraces, but the response was never as significant as with crushed heads. Tests with summer and winter alates revealed similar results, except that gasters of winter female alates had a greater excitant effect than did gasters of summer female alates. This may be due to the production of attractant pheromones by the poison glands of overwintering female alates. We conclude that the mandibular gland is the source of alate excitant pheromones.     

NPY-, galanin-, VIP/PHI-, CGRP- and substance P-immunoreactive neuronal subpopulations in cat autonomic and sensory ganglia and their projections

Summary The neuronal subpopulations in the cat stellate, lower lumbar and sacral sympathetic ganglia were studied with regard to the cellular distribution of immunoreactivity to tyrosine hydroxylase (TH), acetylcholinesterase (AChE) and various neuronal peptides. Coexistence of neuropeptide Y (NPY)- and galanin (GAL)-like immunoreactivity (LI) was found in a high proportion of the neuronal cell bodies; these cells also contained immunoreactivity to TH, confirming their presumably noradrenergic nature. Some TH- and GAL-immunoreactive principal ganglion cells lacked NPY-LI. Two populations (scattered and clustered) of vasoactive intestinal polypeptide (VIP)- and peptide histidine isoleucine (PHI)-positive cell bodies were found in the sympathetic ganglia studied. The scattered VIP/PHI neurons also contained AChE-LI, calcitonin gene-related peptide (CGRP)-and, following culture, substance P (SP)-LI. The clustered type only contained AChE-LI. In the submandibular and sphenopalatine ganglia, neurons were AChE- and VIP/ PHI-immunoreactive but lacked CGRP- and SP-LI. Many GAL- and occasional TH-positive neurons were found in these ganglia. In the spinal ganglia, single NPY-immunoreactive sensory neuronal cells were observed, in addition to CGRP- and SP-positive neurons. The present results show that there are at least two populations of sympathetic cholinergic neurons in the cat. Retrograde tracing experiments indicate that the scattered type of cholinergic neurons contains four vasodilator peptides (VIP, PHI, CGRP, SP) and provides an important input to sweat glands, whereas the clustered type (containing VIP and PHI) mainly innervates blood vessels in muscles.     

Calcitonin gene-related peptide-like immunoreactive cells in the secretory portions of rat sweat glands

Summary We found cells with calcitonin gene-related peptide-like immunoreactivity and with many cored vesicles in the secretory portions of sweat glands of rat foot pads. About 10% of sweat glands contained single immunoreactive cells. The immunoreactive cells were flaskshaped, with a narrow apex facing the glandular lumen and the bulk of the cell body in the basal half of the glandular wall. In the cytoplasm, there were many vesicles, 100–250 nm in diameter, with cores of various electron densities. These cytochemical and cytological characteristics suggest that the immunoreactive cells are homologous to gastrointestinal basal granulated cells.     

Effects of female wasp accessory secretions, host fat body, and host hemolymph on protein synthesis and egg viability in Microplitis croceipes (Braconidae)

Effects of female wasp reproductive gland secretions, host fat body and hemolymph, and mechanical constriction of the parasitoid egg on protein synthesis were studied in eggs of Microplitis croceipes (Braconidae) dissected from the wasp ovary. Protein synthesis was measured by 35S-methionine incorporation in eggs held in tissue culture medium for 16 h after treatment. Synthesis was stimulated in oocytes obtained from three regions of the ovary (egg tube, reservoir, and calyx) by fat body and venom gland but not by calyx fluid. A combination of fat body, venom gland, and calyx fluid did not enhance the level of synthesis relative to that of fat body or venom gland alone. Host hemolymph inhibited protein synthesis when incubated directly with the dissected eggs but not when the eggs were collected from an artificial oviposition substrate (AOS) containing hemolymph. The inhibitory effect of the hemolymph is thought to be due to the occurrence of melanization. Mechanical constriction did not alter the rate of synthesis, confirming an earlier report that synthesis in newly deposited eggs in ongoing and is not dependent on mechanical activation during the act of oviposition. Mechanisms responsible for sustaining protein synthesis in eggs for 16 h in vitro after their exposure to host hemolymph in the AOSs or fat body and venom gland are not known. Only a small percentage (less than 2%) of dissected ovarial reservoir oocytes that were mechanically constricted and exposed to the venom gland, calyx fluid, and host fat body hatched in vitro. In contrast, an earlier study demonstrated that 38% of eggs oviposited by female wasps into AOSs developed and hatched.