The strontium content of roe collected from spawning brown trout Salmo trutta L. reflects recent otolith microchemistry

The relationship between the strontium content of the outer layers of otoliths (an indication of recent marine, estuarine or riverine habitat use) and the strontium content of roe in ripe female brown trout Salmo trutta was examined in fish collected from the Pomahaka River and the lower reaches of the Clutha River, South Island, New Zealand. A close relationship was found between the strontium content of roe and the outer layers of otoliths. This finding suggests that spawned eggs collected from redds could potentially be used to track the extent of upstream spawning migrations by anadromous brown trout.     

Does foraging mode influence life history traits? A comparative study of growth,maturation and survival of two species of sympatric snakes from south‐eastern Australia

Abstract Theory predicts that compared with active searchers, ambush foragers should have lower rates of energy intake, slower growth, and higher survival rates. We tested these predictions with data on two species of sympatric, saurophagous, small‐bodied, viviparous elapid snakes: the broad‐headed snake, Hoplocephalus bungaroides, and the small‐eyed snake, Rhinoplocephalus nigrescens. Demographic parameters and growth curves for both species were estimated from a long‐term (9 years) mark‐recapture study in Morton National Park, south‐eastern Australia. The ambush predator (H. bungaroides) displayed slower juvenile growth and later maturation (5 years for males, 6 years for females) than did the active forager (R. nigrescens, 3 years). Litter sizes were similar in both species, but reproductive frequency was higher in R. nigrescens (90–100%) than in H. bungaroides (50%). Juvenile survival was lower in the active searcher (31%) than in the ambush forager (55%), but adult survivorship was similar (74% vs 82%). Our results support the hypothesis that ambush foragers display ‘slow’ life history traits, but additional phylogenetically independent comparisons are needed to evaluate the generality of this pattern.     

Heart rate deceleration is not an orienting reflex; heart rate acceleration is not a defensive reflex

Graham and Clifton (1966) proposed an integration of Sokolov's theory of orienting and defensive reflexes with the stimulus intake/rejection dichotomy of the Laceys. This integration consisted of hypothesizing that heart rate deceleration is a measure of the orienting reflex, and that cardiac acceleration is a measure of the defensive reflex. This article demonstrates that Graham and Clifton failed to establish a valid integration of these two theories. This failure is a consequence of 1) their misconstruing Sokolov's theory, and 2) an inaccurate and selective review of the research literature then available. Consideration of more recent research would seem to rule out the possibility that their thesis was correct in spite of these flaws in its derivation. Cardiac responding in the OR context thus remains open to further investigation and interpretation.     

Topology of the disulfide bonds in the antiviral lectin scytovirin

The antiviral lectin scytovirin (SVN) contains a total of five disulfide bonds in two structurally similar domains. Previous reports provided contradictory results on the disulfide pairing in each individual domain, and we have now re‐examined the disulfide topology. N‐terminal sequencing and mass spectrometry were used to analyze proteolytic fragments of native SVN obtained at acidic pH, yielding the assignment as Cys7–Cys55, Cys20–Cys32, Cys26–Cys38, Cys68–Cys80, and Cys74–Cys86. We also analyzed the N‐terminal domain of SVN (SD1, residues 1–48) prepared by expression/oxidative folding of the recombinant protein and by chemical synthesis. The disulfide pairing in the chemically synthesized SD1 was forced into predetermined topologies: SD1A (Cys20–Cys26, Cys32–Cys38) or SD1B (Cys20–Cys32, Cys26–Cys38). The topology of native SVN was found to be in agreement with the SD1B and the one determined for the recombinant SD1 domain. Although the two synthetic forms of SD1 were distinct when subjected to chromatography, their antiviral properties were indistinguishable, having low nM activity against HIV. Tryptic fragments, the “cystine clusters” [Cys20–Cys32/Cys26–Cys38; SD1] and [Cys68–Cys80/Cys74–C‐86; SD2], were found to undergo rapid disulfide interchange at pH 8. This interchange resulted in accumulation of artifactual fragments in alkaline pH digests that are structurally unrelated to the original topology, providing a rational explanation for the differences between the topology reported herein and the one reported earlier (Bokesh et al., Biochemistry 2003;42:2578–2584). Our observations emphasize the fact that proteins such as SVN, with disulfide bonds in close proximity, require considerable precautions when being fragmented for the purpose of disulfide assignment.     

Effect of calcium removal on monoamine-elicited depressions of cultured tuberal neurons

The role of extracellular calcium in monoamine responses of central neurons was investigated using explant cultures of tuberal hypothalamus. The spontaneous activity of neurons in cultures was recorded in balanced salt and calcium-deficient salt solutions. The firing rate was reversibly augmented during perfusion with calcium-free salt solutions. This increased firing rate was counteracted by the addition of magnesium. Addition of magnesium also regularized the pattern of firing. Iontophoretic application of putative monoamine neurotransmitters reversibly decreased the rate of firing in both normal and calcium-deficient salt solutions. These results suggest that monoamine inhibitions are not primarily mediated by transmembrane calcium fluxes.     

Membrane-associated reactions in ubiquinone biosynthesis: 2-octaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone methyltransferase

The O-methylation of 2-octaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone, which has been previously postulated to be the final reaction in the biosynthesis of ubiquinone was demonstrated in vitro using cell extracts of Escherichia coli. $\text{S-}\text{Adenosyl}\text{-}\text{l}\text{-}\text{methionine}$ was active as the methyl donor for the reaction. The enzyme concerned, S-adenosyl-l-methionine: 2-octaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone-O- methyltransferase, was partially purified and shown to have a molecular weight of about 50 000 and to require a divalent metal and dithiothreitol for optimal acitivity in vitro. The methyltransferase was absent from extracts from ubiG^? mutants suggesting that the ubiG gene is the structural gene coding for the methyltransferase. The enzyme, although not firmly membrane-bound, showed some affinity for the cell membrane in broken cell preparations and could utilize the benzoquinone substrate when the latter was free or bound to the cell membrane, with about equal efficiency. It is concluded that in vivo, the methyltransferase reaction probably occurs at the internal surface of the cytoplasmic membrane.     

Hepatitis C Virus Phylogenetic Clustering Is Associated with the Social-Injecting Network in a Cohort of People Who Inject Drugs

It is hypothesized that social networks facilitate transmission of the hepatitis C virus (HCV). We tested for association between HCV phylogeny and reported injecting relationships using longitudinal data from a social network design study. People who inject drugs were recruited from street drug markets in Melbourne, Australia. Interviews and blood tests took place three monthly (during 2005–2008), with participants asked to nominate up to five injecting partners at each interview. The HCV core region of individual isolates was then sequenced and phylogenetic trees were constructed. Genetic clusters were identified using bootstrapping (cut-off: 70%). An adjusted Jaccard similarity coefficient was used to measure the association between the reported injecting relationships and relationships defined by clustering in the phylogenetic analysis (statistical significance assessed using the quadratic assignment procedure). 402 participants consented to participate; 244 HCV infections were observed in 238 individuals. 26 genetic clusters were identified, with 2–7 infections per cluster. Newly acquired infection (AOR = 2.03, 95% CI: 1.04–3.96, p = 0.037, and HCV genotype 3 (vs. genotype 1, AOR = 2.72, 95% CI: 1.48–4.99) were independent predictors of being in a cluster. 54% of participants whose infections were part of a cluster in the phylogenetic analysis reported injecting with at least one other participant in that cluster during the study. Overall, 16% of participants who were infected at study entry and 40% of participants with newly acquired infections had molecular evidence of related infections with at least one injecting partner. Likely transmission clusters identified in phylogenetic analysis correlated with reported injecting relationships (adjusted Jaccard coefficient: 0.300; p<0.001). This is the first study to show that HCV phylogeny is associated with the injecting network, highlighting the importance of the injecting network in HCV transmission.