Diel oxygen uptake in Chaoborus punctipennis (diptera : culicidae)

Oxygen consumption (µl/ mg dry wt. · hr^–1 corrected to STP) in Chaoborus punctipennis was measured in a Gilson differential respirometer at two-hour intervals during 24-hour periods. Animals were held at controlled conditions similar to those at the time of collection. Respiration was measured under controlled temperatures and natural photoperiod. Measurements were begun about 36 hours after collection.Winter-collected animals showed a lower and more stable respiration than summer and fall-collected animals which did not differ from one another. Respiration increased with temperature becoming quite variable at 30°C where mortality was highest. Animals collected at different seasons and subjected to a variety of temperatures did not show a predictable pattern of respiration during the daily cycle under any condition tested.Since the 36-hour delay in respiration measurements could have dampened a diel cycle, oxygen consumption was determined within an hour of collection and followed for 24 hours. For this experiment animals were collected at six-hour intervals over a 24-hour period. Respiration did not show a predictable pattern of variation during the day-night cycle.This work was supported in part by a grant from Department of Interior, Office of Water Resources Research. All correspondence should be addressed to A.S. Tombes.     

Effects of vasoactive intestinal peptide on steroid secretion and plasminogen activator activity in granulosa cells of the hen

Studies were conducted to evaluate the effects of vasoactive intestinal peptide (VIP) on steroidogenesis and plasminogen-activator (PA) activity in isolated granulosa cells of the largest preovulatory (F1) follicle of the hen. Vasoactive intestinal peptide, but not avian pancreatic polypeptide, the chicken VIP fragment (16-28) or the VIP congener, PHM-27, induced a dose-related increase in progesterone and androgen secretion, with an apparent median effective dose (ED50) of 5.9 X 10(-7) and 5.7 X 10(-7) M, respectively. The effects of VIP were, at least in part, mediated by the adenylyl cyclase system in that cotreatment of cells with VIP and the phosphodiesterase inhibitor, 3-isobutyl-1-methylxanthine (IBMX), potentiated the steroidogenic effects. However, the time course of action for VIP on steroidogenesis was considerably slower than that for the gonadotropin, luteinizing hormone (LH), and this was attributed to a slower induction of cyclic adenosine 3',5'-monophosphate (cAMP) formation within granulosa cells. Finally, VIP was found to be a potent inhibitor of PA activity, and this inhibition was potentiated by coincubation of VIP with IBMX. We suggest that, in the hen, VIP has a direct and specific action on both steroidogenesis and PA activity, and that these actions are mediated, at least in part, by the adenylyl cyclase system. The comparatively slow induction of cAMP formation by VIP suggests that this peptide is involved in the control of cell differentiation and development rather than the ovulatory process.     

Role of basic residues in the subgroup-determining region of the subgroup A avian sarcoma and leukosis virus envelope in receptor binding and infection.

Receptor specificity in avian sarcoma and leukosis viruses (ASLV) maps to the central region of the envelope surface protein, SU. Two hypervariable regions, hr1 and hr2, within this region of SU are the principal determinants of receptor specificity. The cellular receptor for subgroup A ASLV, Tva, utilizes a 40-residue, acidic, cysteine-rich sequence for viral binding and entry. This domain in Tva is closely related to the ligand-binding domain of the low-density lipoprotein receptor (LDLR). Ligands bind to LDLR via the interaction of clustered basic residues in the ligand with the acidic cysteine-rich domains of the receptor. Analysis of the ASLV envelope sequences revealed a cluster of basic residues within hr2 that is unique to the subgroup A viruses, suggesting a possible role for these residues in receptor recognition. Therefore, the effects of altering these basic residues on subgroup A envelope expression, receptor binding, and infectivity were examined. Most of the mutant proteins were transported to the cell surface and processed normally. Receptor binding was diminished approximately 50% by alanine substitution at amino acid R213 or K227, whereas substitution by alanine at R210, R223, or R224 had no effect. However, when coupled with mutations at R213 or K227, changes at R223,R224 reduced envelope binding by 90%. Mutation of all five basic residues abrogated receptor binding. The effect of the hr2 mutations on ASLV envelope-mediated infection did not parallel the effect on receptor binding. Residues 210, 213, 223, and 224 were important for efficient infection, while mutations at residue 227 had little effect on infectivity. These results demonstrate that the basic residues in the ASLV envelope have roles in both receptor recognition and post-receptor binding events during viral entry.     

Bioerosion in Acropora across the continental shelf of the Great Barrier Reef

The degree of internal bioerosion was examined in the dead basal portions of live branches of the scleractinian coral Acropora formosa collected from six reefs across the continental shelf in the central region of the Great Barrier Reef, Australia. The bioeroders included the sponges Cliona spp. and Cliothosa spp., the boring bivalve Lithophaga sp., and sipunculid and polychaete worms. Total internal bioerosion exhibited higher means and variances inshore and at the mid-shelf than the outer shelf specimens, which were characterized by low means and low variances. Bioerosion by Cliothosa and all sponges combined declined slightly across the shelf. Bivalves accounted for a small proportion of the internal bioerosion in A. formosa. The bioerosion pattern exhibited by worms (polychaetes and sipunculids) was similar in pattern to that of the sponges. All groups exhibited lowest levels of bioerosion at the outer shelf. Highest variance in the data was observed at the intra-branch/intra-colony and the intercolony levels. Inter-site variance was high in worms and vivalves. Boring sponges generally dominated the bioeroder community. The relative abundance of Cliona declined on the outer shelf while the relative abundance of worms increased. Percent bioerosion in Acropora formosa was 2–3 times higher than in Porites lobata in this region. The low level of bioerosion at the outer shelf versus the inner- and mid-shelf areas may be partially due to lower levels of productivity and lower concentrations of terrestrially derived organic matter. Other potential factors may include higher fish grazing/predation activity on the outer shelf.