Robert H. Devlin

Sex determination and sex differentiation in fish: an overview of genetic, physiological, and environmental influences

Abstract A great deal of information is known regarding the process of sex differentiation in fish, and the mechanisms involved in primary sex determination are now beginning to be defined. A range of gonadal differentiation types have been described for fish, including gonochoristic species possessing purely ovarian or testicular tissues, as well as hermaphroditic species that can initially mature either as males (protandrous) or females (protogynous). Sex determination in fish is a very flexible process with respect to evolutionary patterns observed among genera and families, and within individuals is subject to modification by external factors. These influences can affect the fate of both somatic and germ cells within the primordial gonad, and include the action of genetic, environmental (e.g. temperature), behavioural, and physiological factors. Exogenous sex steroids administered at the time of sex determination can strongly influence the course of sex differentiation in fish, suggesting that they play a critical role in assignment of gonad determination as well as subsequent differentiation. Detailed information is available from fish systems describing the production of sex steroids, as well as the enzymes involved in steroid production. Both estradiol and the maturation hormone 17α, 20β-dihydroxy-4-pregnen-3-one (17α, 20β-DP) are produced by a two-step process involving different cell layers in the gonad, and have effects on the differentiation of gonadal and nongonadal tissues. Gonadal development and differentiation in some fish is also controlled by hormones from the pituitary gland (gonadotropins) that are regulated by release hormones (GnRH) and other neuroendocrine and gonadal factors. Genetic determination of sex in fish can involve monogenic or polygenic systems, with factors located on the autosomes or on sex chromosomes. In the latter case, both male (XY) and female (ZW) heterogametic systems have been described, as well as many subtle variations on these themes. Sex chromosomes are found in approximately 10% of fish species examined, and sex-linked phenotypic traits, and protein and molecular genetic markers have been identified in several fish systems. Some species of fish reproduce gynogenetically, producing all-female populations. Several gene families known to be involved in sex determination in other vertebrates have recently been shown to be similarly involved in fish, suggesting conservation of sex determination pathways. The lability of sex-determination systems in fish makes some species sensitive to environmental pollutants capable of mimicking or disrupting sex hormone actions. Such observations provide important insight into potential impacts from endocrine disruptors, and can provide useful monitoring tools for impacts on aquatic environments.

Recent advances in our knowledge of the Myxozoa

Abstract In the last few years two factors have helped to significantly advance our understanding of the Myxozoa. First, the phenomenal increase in fin fish aquaculture in the 1990s has lead to the increased importance of these parasites; in turn this has lead to intensified research efforts, which have increased knowledge of the development, diagnosis, and pathogenesis of myxozoans. The hallmark discovery in the 1980s that the life cycle of Myxobolus cerebralis requires development of an actinosporean stage in the oligochaete, Tubifex tubifex, led to the elucidation of the life cycles of several other myxozoans. Also, the life cycle and taxonomy of the enigmatic PKX myxozoan has been resolved: it is the alternate stage of the unusual myxozoan, Tetracapsula bryosalmonae, from bryozoans. The 18S rDNA gene of many species has been sequenced, and here we add 22 new sequences to the data set. Phylogenetic analyses using all these sequences indicate that:1) the Myxozoa are closely related to Cnidaria (also supported by morphological data); 2) marine taxa at the genus level branch separately from genera that usually infect freshwater fishes; 3) taxa cluster more by development and tissue location than by spore morphology; 4) the tetracapsulids branched off early in myxozoan evolution, perhaps reflected by their having bryozoan, rather than annelid hosts; 5) the morphology of actinosporeans offers little information for determining their myxosporean counterparts (assuming that they exist); and 6) the marine actinosporeans from Australia appear to form a clade within the platysporinid myxosporeans. Ribosomal DNA sequences have also enabled development of diagnostic tests for myxozoans. PCR and in situ hybridisation tests based on rDNA sequences have been developed for Myxobolus cerebralis, Ceratomyxa shasta, Kudoa spp., and Tetracapsula bryosalmonae (PKX). Lectin-based and antibody tests have also been developed for certain myxozoans, such as PKX and C. shasta. We also review important diseases caused by myxozoans, which are emerging or re-emerging. Epizootics of whirling disease in wild rainbow trout (Oncorhynchus mykiss) have recently been reported throughout the Rocky Mountain states of the USA. With a dramatic increase in aquaculture of fishes using marine netpens, several marine myxozoans have been recognized or elevated in status as pathological agents. Kudoa thyrsites infections have caused severe post-harvest myoliquefaction in pen-reared Atlantic salmon (Salmo salar), and Ceratomyxa spp., Sphaerospora spp., and Myxidium leei cause disease in pen-reared sea bass (Dicentrarchus labrax) and sea bream species (family Sparidae) in Mediterranean countries.

Status and opportunities for genomics research with rainbow trout

The rainbow trout (Oncorhynchus mykiss) is one of the most widely studied of model fish species. Extensive basic biological information has been collected for this species, which because of their large size relative to other model fish species are particularly suitable for studies requiring ample quantities of specific cells and tissue types. Rainbow trout have been widely utilized for research in carcinogenesis, toxicology, comparative immunology, disease ecology, physiology and nutrition. They are distinctive in having evolved from a relatively recent tetraploid event, resulting in a high incidence of duplicated genes. Natural populations are available and have been well characterized for chromosomal, protein, molecular and quantitative genetic variation. Their ease of culture, and experimental and aquacultural significance has led to the development of clonal lines and the widespread application of transgenic technology to this species. Numerous microsatellites have been isolated and two relatively detailed genetic maps have been developed. Extensive sequencing of expressed sequence tags has begun and four BAC libraries have been developed. The development and analysis of additional genomic sequence data will provide distinctive opportunities to address problems in areas such as evolution of the immune system and duplicate genes.

Growth of domesticated transgenic fish

A growth-hormone transgene boosts the size of wild but not domesticated trout.

Growth hormone transgenic salmon pay for growth potential with increased predation mortality

Recent advances in gene technology have been applied to create fast–growing transgenic fish, which are of great commercial interest owing to their potential to shorten production cycles and increase food production. However, there is growing concern and speculation over the impact that escaped growth hormone (GH)–transgenic fish may have on the natural environment. To predict these risks it is crucial to obtain empirical data on the relative fitness of transgenic and non–transgenic fish under nature–like conditions. Using landscaped stream aquaria with live food and predators, we show that the predation mortality of newly hatched GH-transgenic coho salmon fry (Oncorhynchus kisutch) is much higher than in non–transgenic conspecifics, and that this difference is amplified when food abundance decreases. The growth rate of transgenic and non–transgenic fish is similar at high food levels, whereas transgenic fish grow more slowly than non-transgenic fish when food abundance is reduced. Our results suggest that the fitness of young GH–transgenic coho salmon in the wild will be determined by both predation pressure and food availability.

TETRACAPSULA RENICOLA N. SP. (MYXOZOA:SACCOSPORIDAE); THE PKX MYXOZOAN—THE CAUSE OF PROLIFERATIVE KIDNEY DISEASE OF SALMONID FISHES

Proliferative kidney disease (PKD) of salmonid fishes is caused by the extrasporogonic stage of an enigmatic myxozoan, referred to as PKX. Sporogenesis occurs in the renal tubules, resulting in monosporous pseudoplasmodia. The spores are ovoid with indistinguishable valves and measure 12 µm in length and 7 µm in width. Two spherical polar capsules (2 µm diameter) with 4 coils occur at the anterior end of the spore. Prominent capsulogenic cell nuclei posterior to the polar capsules are evident in histological sections stained with hematoxylin and eosin. Regardless of the true nature of the valves (indistinguishable or absent), this myxozoan is morphologically distinct from all other described members of the phylum Myxozoa. Comparisons of small subunit rDNA sequences of PKX with other myxozoans demonstrated that it branches from all other members of the myxosporeans from fish examined thus far, including representatives of the phenotypically most closely related genera, Sphaerospora and Parvicapsula. Recent reports, based on rDNA comparisons, indicate that the alternate stage of PKX occurs in bryozoans, and that PKX clusters in a clade with Tetracapsula bryozoides. Our analyses and those of others, along with phenotypic observations, indicate that salmonids are the primary myxosporean hosts for PKX, that the cryptic spores of PKX in salmonids are the fully formed myxospores as they occur in the fish host, and that PKX represents distinct species that we previously place in the genus Tetracapsula in the family Saccosporidae. The latter 2 taxa were described based on stages from bryozoans, and the myxosporean stage in fish of the type species, T. bryozoides, has not been identified (if it exists). Thus, more complete resolution of the life cycle of both PKX and T. bryozoides, as well as more genetic data, are required to determine the precise relationship of these organisms.

Transgene and host growth hormone gene expression in pituitary and nonpituitary tissues of normal and growth hormone transgenic salmon

Growth hormone (GH) gene expression has been examined in control and transgenic coho salmon containing a transgene comprised of the sockeye salmon GH1 gene under the control of the MT-B promoter from the same species. This transgene dramatically enhances the growth of salmonids, and raises serum GH levels some forty-fold. Transcript levels from this transgene were detected by RT-PCR using construct-specific GH primers in all tissues examined (liver, kidney, skin, intestine, stomach, muscle, spleen, pyloric caeca), and ranged from 0.1 - 9.4 pg/50 microg total RNA in different tissues as estimated by dot blot analysis. Interestingly, GH gene expression was also observed in intestine of control coho salmon by RT-PCR capable of detecting host and transgene transcripts using general primers. Sequence analysis of the intestinal GH mRNA from controls indicated it was derived from the coho GH2 gene. GH mRNA abundance analyzed by northern analysis indicates lower levels are found in large (400-500 g) than small transgenic salmon (20-21 g). No molecular evidence for transgene expression was obtained in tissues from transgenic fry, despite an obvious increase in size relative to control siblings, suggesting very low levels of transgene expression early in development. GH mRNA levels (per microg RNA) were also examined in the pituitary gland, and were found to be significantly lower (P < 0.01) in transgenic coho compared to nontransgenic animals of the same size. Pituitary glands of transgenic animals were also smaller than control animals of the same size, and pituitary size, expressed as a proportion of body weight, decreased with body size in transgenic but not control animals. These results imply that pituitary GH expression is regulated by negative feed-back controls as occurs in other vertebrate systems. GH mRNA was examined in pituitary glands by whole-mount in situ hybridization, and, whereas overall levels appeared reduced in transgenic animals, the site of hybridization did not differ between transgenic and control glands.

TRANSMISSION AND PHENOTYPIC EFFECTS OF AN ANTIFREEZE/GH GENE CONSTRUCT IN COHO SALMON (ONCORHYNCHUS KISUTCH)

Abstract Transmission of the opAFPGHc gene construct from parental transgenic coho salmon to F 1 progeny has been observed. Just prior to first feeding, these offspring were found to fall into two distinct phenotypic classes on the basis of morphology and external colouration. One group possessed the normal brown colouration typical of coho salmon alevins, whereas the other had a distinct green colouration and showed signs of cranial deformities and opercular overgrowth. Polymerase chain reaction analysis revealed that green phenotype was correlated with the presence of the opAFPGHc gene construct, and thus colouration could be used to identify transgenic progeny. On this basis, frequencies of transgene transmission to F 1 progeny from four individuals ranged from 2.2 to 18.9%, while a fifth male produced no transgenic progeny. Prior to first feeding, the transgenic progeny were found to be 21.2% heavier and 11.9% longer than their non-transgenic siblings, suggesting that the expression of GH in early development can influence the rate or efficiency of conversion of yolk energy reserves. After 1 year of development of F 1 progeny, the atypical phenotype associated with overgrowth of cartilage in the cranial and opercular regions became progressively more severe and resulted in reduced viability.

Genetic mapping of Y-chromosomal DNA markers in Pacific salmon

Sex chromosomes in fish provide an intriguing view of how sex-determination mechanisms evolve in vertebrates. Many fish species with single-factor sex-determination systems do not have cytogenetically-distinguishable sex chromosomes, suggesting that few sex-specific sequences or chromosomal rearrangements are present and that sex-chromosome evolution is thus at an early stage. We describe experiments examining the linkage arrangement of a Y-chromosomal GH pseudogene (GH-Y) sequence in four species of salmon (chum, Oncorhynchus keta; pink, O. gorbuscha; coho, O. kisutch; chinook, O. tshawytscha). Phylogenetic analysis indicates that GH-Y arose early in Oncorhynchus evolution, after this genus had diverged from Salmo and Salvelinus. However, GH-Y has not been detected in some Oncorhynchus species (O. nerka, O. mykiss and O. clarki), consistent with this locus being deleted in some lineages. GH-Y is tightly linked genetically to the sex-determination locus on the Y chromosome and, in chinook salmon, to another Y-linked DNA marker OtY1. GH-Y is derived from an ancestral GH2 gene, but this latter functional GH locus is autosomal or pseudoautosomal. YY chinook salmon are viable and fertile, indicating the Y chromosome is not deficient of vital genetic functions present on the X chromosome, consistent with sex chromosomes that are in an early stage of divergence.

Genetic, environmental and interaction effects on the incidence of jacking in Oncorhynchus tshawytscha (chinook salmon)

Jacking in chinook salmon, Oncorhynchus tshawytscha, is defined as sexual maturation of males after at least 1 year in sea water, occurring 1 year prior to any of the females of the same cohort. A breeding experiment was carried out with jack and non-jack sires nested within six dams. The resulting 12 families were reared under two different temperatures for the first part of their lives to test for the effect of early developmental acceleration on jacking rates. Significant sire age (jack vs. non-jack), dam and environment (water temperature) effects were found for the incidence of jacking. Significant genotype-by-environment interactions were also found, indicating that accelerated early development does not increase jacking rates uniformly across all genotypes. There were no significant correlations between mean family growth- and size-related variables and the observed jacking rates. Heritability estimates based on intra-dam sire-offspring regressions were 0.48 (±0.24) and 0.32 (±0.14) for the accelerated and non-accelerated family groups, respectively. The results of sib-analysis heritability calculations indicated large dominance effects or sex linkage. The genetic component to jacking found in this study for chinook salmon was greater than has been generally reported for age of first maturation in salmonids.