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Parasite load significantly impacts host health and fitness and may vary substantially among individuals within a population. The immunocompetence handicap hypothesis posits that sexual signals are honest indicators of male quality because they are maintained by testosterone, an immunosuppressant that yields higher parasite loads. Additionally, testosterone may influence parasite load by increasing activity levels. We examined these two hypotheses in a wild population of Yarrow’s Spiny Lizards (Sceloporus jarrovii Cope, 1875) in Arizona. We (i) compared fecal testosterone levels to ectoparasite and haemoparasite loads, (ii) tested if sexual signals (total coloured area, aggression, and head size), locomotor activity, and body size correlated with testosterone levels, and (iii) compared sexual signals, locomotor activity, and body size to parasite load. Ectoparasite loads increased with total coloured area and tended to increase with testosterone, but this latter relationship was only nearly significant. Parasite loads increased with body size. Thus, we found some support for the immunocompetence handicap hypothesis and none for the activity hypothesis. Our results are consistent with an alternative hypothesis that larger individuals have more parasites because they have more surface area and (or) have had longer to accumulate parasites. Future studies should examine the relative contributions of testosterone and glucocorticoids in driving variation in parasite loads.

Sexual dimorphism in fishes may be obvious during the reproductive period and less clear during the nonreproductive periods. Despite being difficult to discern during the nonreproductive period, sex-related differences in body condition and shape can yield important insights into a species’ behaviour and ecology. The purpose of this study was to test hypotheses about body condition and shape variation related to sex and season (nonreproductive and reproductive periods) in a population of adult adfluvial bull trout (Salvelinus confluentus (Suckley, 1859)), which is a poorly understood and imperiled species across much of its range. Geometric morphometric samples were collected by angling in the spring and late summer in a reservoir in British Columbia. Principal components analysis identified two principal components (PC) that were related to body condition and that varied according to season and sex. Spring-caught females were in better body condition than spring-caught males. There was a significant sex × season interaction on body condition such that late-summer males were not different from late-summer females. Spawning bull trout exhibited a decline in body condition during the summer season. An additional PC that described head size was found to vary significantly between sexes; however, an assignment test showed that it failed to reliably distinguish between the sexes. We hypothesized that the ecology of these animals, including sex-specific behaviour, is responsible for sexual and seasonal differences in bull trout body condition and morphology. This study offers new insight into the ecology of bull trout and shows that shape data for fishes can be obtained nonlethally, which is particularly important for species that are imperiled.

Knowledge of the reproductive biology of wild sturgeon populations is critical to ensure the survival of this unique group of animals. We combined gill-netting surveys, nonlethal blood sampling, radiotelemetry, and egg collection to examine the reproductive biology of lake sturgeon (Acipenser fulvescens Rafinesque, 1817) at a suspected spawning ground below a dam on the Richelieu River, Quebec. Lake sturgeon were present at the beginning of sampling in early May, and spawning took place from 26 May to 5 June when water temperature averaged 13.4 ± 0.1 °C (range 11.5–15.5 °C). Daily spawning population estimates ranged from 285 to 1282 individuals and the sex ratio of spawners was estimated at 2.1 males per female. The presence of radio-tagged individuals on the spawning grounds peaked from 20 to 28 May, corresponding with known spawning bouts. Residence time of spawners on the spawning ground ranged from 1 to 27 days (median = 5 days) and there were no differences in residence time between sexes. Nonlethal blood sampling enabled the quantification of steroid levels to determine the spawning population sex ratio, and steroid levels were highest before spawning was known to occur and decreased concurrently with, and after, known spawning events.

We evaluate the utility of an inexpensive, portable recovery bag designed to facilitate recovery of fish from capture stress by combining physiological assays, biotelemetry, and social science surveys. Adult migrating Pacific salmon (Oncorhynchus spp.) were used as a model, since some of their populations are threatened. While catch-and-release is common, there is a need to ensure that it is sustainable. A social science survey revealed that anglers generally have positive attitudes towards recovery bag use, particularly if research identifies that such techniques could be effective. Physiological assays on pink salmon (Oncorhynchus gorbuscha) revealed benefits of both high- and low-velocity recovery, but high velocity was most effective with reduced plasma cortisol concentrations and similar plasma sodium and chloride concentrations as those found in controls at all recovery durations. A biotelemetry study on sockeye salmon (Oncorhynchus nerka) captured by anglers and stressed by air exposure then placed in recovery bags had 20% higher, but not significantly different, survival than no-recovery salmon. The integration of natural science and social science provides an important step forward in developing methods for promoting recovery of fish from capture. Resume : Nous evaluons l'utilite d'un sac de recuperation portable et peu dispendieux pour ce qui est de favoriser la recuperation de poissons apres un stress de capture, en combinant des essais physiologiques, des donnees de biotelemetrie et des etudes sociologiques. Des saumons du Pacifique (Oncorhynchus spp.) adultes en migration ont ete utilises comme modele etant donne que certaines de leurs populations sont menacees et que, bien que la peche avec remise al'eau soit repandue, il importe de verifier qu'il s'agit d'une pratique durable. Une etude sociologique a revele que les pecheurs ala ligne voient generalement d'un bon œil l'utilisation d'un sac de recuperation, en particulier si la recherche etablit l'efficacite de telles methodes. Des essais physi- ologiques sur des saumons roses (Oncorhynchus gorbuscha) ont revele que la recuperation tant ahaute vitesse qu'abasse vitesse presentait des avantages, mais que la recuperation ahaute vitesse etait plus efficace, se traduisant par une reduction des concentrations de cortisol plasmatique et des concentrations semblables de sodium et de chlorure, utilisees comme temoins, pour toutes les durees de recuperation. Dans une etude biotelemetrique, des saumons sockeye (Oncorhynchus nerka) captures par des pecheurs ala ligne et soumis au stress de l'exposition al'air, puis places dans des sacs de recuperation presentaient un taux de survie de 20 % superieur acelui des saumons n'ayant pas recupere, bien que cette difference ne soit pas significative. L'integration des sciences naturelles et de la sociologie a donc permis une importante avancee dans la mise au point de methodes favorisant la recuperation de poissons suite aleur capture. (Traduit par la Redaction)

Human immunodeficiency virus type 1 (HIV-1) Nef is important for viral infectivity and pathogenicity. HIV-1 infection is associated with inappropriate activation and defects in the function of monocytes/macrophages. We have studied the effects of HIV-1 Nef in the murine (RAW264.7) and human (THP-1) monocyte-macrophage cell lines. Investigation of the activator protein-1 (AP-1) transcription factor showed that Nef expression induced both its DNA binding and transcriptional activities. Increased AP-1 DNA binding activity in RAW264.7 cells was associated with raised levels of c-Fos expression and induction of mRNA for the AP-1 responsive tissue inhibitor of metalloproteinases-1 (TIMP-1) gene. Mutagenesis and kinase inhibition studies were employed to determine signaling pathways used by Nef to induce AP-1. Data from these studies indicated that induction of AP-1 by Nef is likely to be mediated through the MAPK (ERK1 and 2) signaling pathway and requires the proline-rich PxxP motif of Nef, suggesting the involvement of upstream protein kinases belonging to the Src family. Effects of Nef on AP-1 induction were cell lineage-specific, being stimulatory in macrophages, inhibitory in T cells and without effect in HeLa cells. These latter two observations led us to test the possibility that cell-specific interactions of Nef with Src family proteins may modulate AP-1 activity. To this end we demonstrated that a dominant-negative Hck mutant caused inhibition of Nef-mediated AP-1 DNA binding activity in RAW cells. In conclusion, induction of AP-1 by Nef is a specific feature of human and murine macrophage cell lines that requires signal transduction events involving Hck and MAPKs.

The gene coding for the major inner capsid protein VP6 of human group C rotavirus was cloned into baculovirus using the pBlueBac2 vector and expressed in insect cells. When cultured in High Five cells, VP6 was expressed at a high level and exported to the cell culture medium. Purified VP6 was used to immunise rabbits. Hyperimmune rabbit serum, which reacted with native human group C rotavirus in infected cells, was used to develop and optimise an EIA for the detection of antibodies to group C rotavirus using the recombinant VP6 as a source of antigen. In a local epidemiological survey of 1000 sera grouped by age, an average of 43% of samples were found to have antibodies to human group C rotavirus with the highest proportion (66%) in the 71-75 year age group. In comparison, 97% of adults and 85% of children had antibodies to recombinant VP6 from the bovine RF strain of group A rotavirus. These results suggest that infection with human group C rotavirus is a common occurrence despite the apparent rarity of reports of human group C rotavirus in clinical samples from patients with gastroenteritis.

A novel, sequence-independent strategy has been developed for the amplification of full-length cDNA copies of the genes of double-stranded RNA (dsRNA) viruses. Using human (Bristol) group C rotavirus as an example, a single amino-linked modified oligonucleotide (primer 1) was ligated to either end of each dsRNA genome segment by using T4 RNA ligase. Following reverse transcription, annealing, and repair of cDNA strands, amplification of the viral dsRNA genome was accomplished by polymerase chain reaction using a single complementary oligonucleotide (primer 2). Northern (RNA) hybridization of cDNA to virus dsRNA indicated that it was possible to generate cDNA representing the complete genome from very small clinical samples. This technique was used to determine the complete nucleotide sequence (728 bp) and coding assignment of gene 10, which revealed an open reading frame of 212 amino acids with limited homology to NS26 from human group A rotavirus. In contrast to previous tailing methods, the addition of one defined primer allowed unequivocal identification of terminal nucleotides and should be generally applicable to viruses with segmented dsRNA genomes and especially for analysis of clinical samples, for which very limited quantities of biological material are available.

The VP6 gene of human group C rotavirus was cloned and sequenced. Hybridization to the human group C and the porcine group C/Cowden dsRNA genomes assigned this coding sequence to segment 5. The complete human VP6 sequence contained an open reading frame of 1185 nucleotides (395 amino acids; deduced Mr 44,669 Da). The protein sequence demonstrated low homology with the group A VP6 sequences (41.7 to 42.7%) and high homology (88.9%) with the porcine group C VP6 sequence. However, the protein sequence alignments revealed a region of 10 amino acids that were significantly different between the human and the porcine group C viruses.

Amino acid sequence alignments between the human group C/Bristol and the published porcine group C/Cowden VP6 proteins have revealed a region of extreme sequence divergence. We have been unable to confirm the nucleotide sequence of the Cowden VP6 gene corresponding to this region of divergence. Direct sequencing of a PCR-amplified cDNA pool has revealed a frame shift, and three nucleotide changes, within the published sequence of the porcine (Cowden) VP6 gene. The corrected sequence of the porcine protein revealed a closer homology with VP6 from the Bristol strain and two new human group C rotavirus isolates. Atypical rotaviruses have been detected in the feces of children living in Belem, Brazil, and Preston, U.K. Direct sequencing of PCR-amplified cDNA corresponding to the VP6 gene of one isolate from each location confirmed the presence of a group C rotavirus. The complete nucleotide sequences of the VP6 genes from the group C/Belem and C/Preston rotaviruses contained an open reading frame of 1185 nucleotides (395 amino acids; deduced M(r) 44,669 Da). The Belem VP6 gene demonstrated 97.9% nucleotide homology with the human group C/Bristol VP6 gene and 83.4% nucleotide homology (91.6% deduced amino acid homology) with the corrected porcine group C/Cowden sequence. The Preston VP6 gene demonstrated 99.6% nucleotide homology with the human group C/Bristol VP6 gene and 84.0% nucleotide homology (91.6% deduced amino acid homology) with the corrected porcine group C/Cowden sequence. Remarkably, the deduced amino acid sequence of the Brazilian strain was identical to that of the U.K. isolates.