Immune response of fish to parasitic protozoa

Epizootic outbreaks of fish diseases are increasingly common as a result of intensive aquaculture, fish farming and sea ranching. Very few drugs are available for treatment or prophylaxis against fish diseases, and development of such compounds is inhibited by different national regulations governing the use of chemicals in fish for human or animal consumption. Alternative approaches are urgently needed. But although the taxonomy and biology of fish parasites have been extensively studied, relatively little is known about protective immunity in fish and the effects of parasites on the piscine immune system. In this article, Patrick Woo discusses the immune responses of fish to parasitic protozoa, showing that vaccination is a viable control strategy, and stressing the need for a coordinated global research programme on fish diseases.     

Fish introduction and parasites in marine ecosystems: a need for information

Invasive species provide unique and useful systems by which to examine various ecological and evolutionary issues, both in terms of the effects on native environments and the subsequent evolutionary impacts. While biological invasions are an increasing agent of change in aquatic systems, alien species also act as vectors for new parasites and diseases. To date, colonizations by hosts and parasites have not been treated and reviewed together, although both are usually interwoven in various ways and may have unpredictable negative consequences. Fish are widely introduced worldwide and are convenient organisms to study parasites and diseases. We report a global overview of fish invasions with associated parasitological data. Data available on marine and freshwater are in sharp contrast. While parasites and diseases of inland freshwater fish, ornamental, reared and anadromous fish species are well documented, leading to the emergence of several evolutionary hypotheses in freshwater ecosystems during the last decade, the transfer of such organisms are virtually unexplored in marine ecosystems. The paucity of information available on the parasites of introduced marine fish reflects the paucity of information currently available on parasites of non-indigenous species in marine ecosystems. However, such information is crucial as it can allow estimations of the extent to which freshwater epidemiology/evolution can be directly transferred to marine systems, providing guidelines for adapting freshwater control to the marine environment.     

Parasitic diseases in marine cage culture--an example of experimental evolution of parasites?

Rapid development of fish culture in marine cages has been associated with an emergence of parasitic diseases. There is a general trend to an increase in infections with ectoparasites with direct life cycles and a reduced diversity of parasites in aquaculture. Some mariculture creates conditions that are similar to serial passage experiments, which are used to study adaptation during experimental evolution of pathogens. In particular, increased density of fish, repeated introduction of naive hosts, homogenous host populations, fast growth and a potential decrease in genetic diversity are attributes of both aquaculture and serial passage experiments. Some free-living organisms, for example Neoparamoeba spp. and Uronema spp. parasitise fish in culture, but have not been reported from wild populations. Farming fish in marine cages can increase the risk of outbreaks of parasitic diseases, including those caused by opportunistic parasites. However, aquaculture has the potential to control parasitic diseases through selective breeding, vaccination and general fish health management.     

Solving parasite-related problems in cultured freshwater fish

The importance of parasitoses in freshwater fish culture grows parallel with the development of fishbreeding. Especially in intensively cultured fish populations one has to reckon with outbreaks of parasitoses. Although parasite-related problems are different in cultures of salmonids, carp, tilapias, catfishes, eels and ornamental fish protozoan parasites are in general of greatest importance. Among protozoans, myxozoan parasites deserve attention as recent research on this group has brought several new results. Regarding the control of parasitic fish diseases, biological methods might be successful together with prevention and a broader scale of effective medicines.     

Parasitic anomalies observed in snow trout due to anthropogenic stress in water bodies

There is interrelationship of the environmental conditions and fish health. Decrease or increase of pollution in aquatic ecosystem have direct impact on presence or absence of parasites. Fish living under optimum environmental, well-nourished conditions are more resistant to diseases than fish weakened by malnutrition caused by parasite infestation or due to deterioration of environmental conditions because ofpollution. Fish encounters common parasites in wild and in culture systems. Parasites attach to the host through suckers and hooks and make their way inside the host through different means, which include skin, through mouth along with food, by means of gills. The hosts were collected during Jan 2019 to Jan 2020 from river Veshaw. During this study it was observed that presence of parasites causes some changes in fish which can serve as indicators of deterioration in aquatic habitat. Clinical signs were noticed in fish hosts collected from sites which received waste due to anthropogenic activities. Parasitic anomalies in the host collected from polluted site was observed to include body deformaties, gastric distention, lesions in gut, increased mucus production, damage in gill filaments etc.     

Parasites of recruiting coral reef fish larvae in New Caledonia

Recruiting coral reef fish larvae from 38 species and 19 families from New Caledonia were examined for parasites. We found 13 parasite species (Platyhelminthes: Monogenea, Cestoda and Trematoda) but no acanthocephalan, crustacean or nematode parasites. Over 23% of individual fish were infected. Didymozoid metacercariae were the most abundant parasites. We conclude that most of the parasites are pelagic species that become ‘lost’ once the fish larvae have recruited to the reef. Larval coral reef fish probably contribute little to the dispersal of the parasites of the adult fish so that parasite dispersal is more difficult than that of the fish themselves.     

Diseases caused by parasites in the aquaculture of warm water fish

Parasitic infections of fish cultured in fresh and marine waters of subtropical and tropical geographic regions are reviewed. The following parasites are discussed: Ectoparasitic protozoa, Coccidia, Myxosporea, Monogenea, Metacercariae of trematodes, the Asian tapeworm, nematodes, ergasilids, lernaeids, and argulids. Criteria for selection were their impact on farmed fish and the availability of data beyond case reports and surveys. Epizootic ectoparasitic infections are usually the outcome of adverse growth conditions, either climatic or resulting from management practices. Epizootiology of infections by internal parasites, heteroxenous in particular, is more complex, particularly in man-made systems, as it is determined by a wider range of interacting ecological parameters. Exotic species, particularly cyprinids, comprise the bulk of freshwater fish farmed in warm water systems. Most important diseases affecting fishes in such systems are caused by introduced pathogens. Only a few of the autochthonous parasites become involved in epizootic infections, also where indigenous species are farmed. Marine farming is usually based on indigenous species. The relatively short history of piscine mariculture has already recorded epizootic infections and mortalities both by parasites contracted from the local environment and by specific parasites associated with the cultured species. As in freshwater systems, culture practices often create an environment favorable to epizootic infection.     

Solving parasite-related problems in cultured marine fish

• 1.1. Our knowledge of parasite born e diseases of cultured marine fish is restricted by the limited extent of practiced mariculture.
• 2.2. Several parasites, pathogenic to fish including capsaloid, microcotylid and diclidophoran monogeneans and caligid copepods are ubiquitous in mariculture systems in diverse species of fish and geographical regions.
• 3.3. The alga Amyloodinium ocellatum and the ciliated protozoan Cryptocaryon irritons are not as ubiquitous, but nevertheless present the most serious risk to farmed fish of most species due to their high pathogenicity, fecundity and resistance to conventional means of control.
• 4.4. Infections in maricultured fish are dominated by monoxenous parasites. Occurence of heteroxenous parasites is restricted by their requirement for additional hosts to maintain transmission.
• 5.5. Cage culture allows free exchange of infection between caged and native fishes; in inshore systems infections have to be introduced primarily from external sources.
• 6.6. Water supply does not appear to be an efficient route of entry of infection into culture systems; parasites are introduced either by wild fry or wild breeders collected into the system, or with wild fish infiltrating via water supply or drainage.
• 7.7. Adverse growth conditions are the most common circumstances in outbreak of epizooites. Over-crowding does not appear to promote primarily epizooites, its impact is indirect by contributing to the deterioration of the growth conditions.
• 8.8. Epizooites are likely to occur also in juvenile, immunologically naive fish as well as following introduction of parasites into unexperienced fish population.
• 9.9. Control has been implemented thus far through an empirical approach. Recent research is geared towards the development of methodology specifically designed to the needs of mariculture.

     

Vertebrate diets derived from trophically transmitted fish parasites in the Bothnian Bay

Parasites that are transmitted through predator–prey interactions may be used as indicators of trophic relationships between organisms. Yet, they are rarely used as such in the construction of topological (predator–prey) food webs. We constructed food webs of vertebrate trophic interactions using observed diet alone, trophically transmitted parasites alone, and the combination of the two based on data from 31 species of fish from the Bothnian Bay, Finland. The fish food web contained 530 links derived from observed diet, 724 links inferred from parasitism, and 1,058 links calculated from a combination of both stomach contents and parasites. This sub-web constructed from stomach contents had a mean of 17.1 links per fish species, while that using parasites had 23.4 links per fish. Combining the two diet indicators yielded 34.1 links per fish species, illustrating the complementarity of the two methods. Mean number of prey species per fish species was 12.5 using observed diet items, 15.8 using parasites, and 24.5 using both measures together. Mean number of predators per fish species was 7.4 using observed diet, 11.7 using parasites and 15.0 using both. A positive correlation was found between the mean number of parasites and the number of prey taxa in the diet among the fishes. Omnivorous fish had the highest diversity of both parasite species and prey items, while benthophagous fish had among the lowest. Mean total abundance and mean total prevalence of parasites correlated positively with fish size, with piscivores being the largest with the highest abundance and prevalence, while planktivores and benthivores had the lowest. Trophically transmitted parasites may be used to help construct vertebrate sub-webs and derive information about food web processes. Parasites alone provided equivalent if not more information than observed diet. However, resolution is improved by using parasites and observed diet together.     

Defense behavior of fish against predators and parasites

This paper is a review of empirical and theoretical studies of the behavioral mechanisms and ecological consequences of the anti-predator and anti-parasite activities of teleost fishes. While the individual and cooperative behaviors used by fish to protect themselves from predators have received marked attention from researchers in the fields of ecology, ethology and applied fish biology, the behaviors by which fish protect themselves from parasites have been poorly investigated. Generally, free-swimming parasites, which are difficult to distinguish, do not elicit any marked behavioral response from fish prior to contact. We hypothesize that the behaviors by which fish avoid parasites are much more efficient for fish in groups than they are for solitary fish. Early avoidance of predators and parasites is compared with the behavioral tactics fish use when such enemies are in close proximity. Individual versus cooperative tactics, as well as the role of learning, are also analyzed. Learning is more important for behaviors which protect fish from predators than those which they use against parasites, especially at the level of individual fish. Finally, we briefly discuss the importance of coordination of anti-predator and anti-parasite activities, which present the most complicated tasks for fish and intriguing problems for researchers.     

Do parasites affect the behavior of the Hawaiian white-spotted toby, Canthigaster jactator (Pisces)?

This study observed differences in behavior associated with parasites in the fish Canthigaster jactator. These fish were observed both within Kaneohe Bay, Oahu, Hawaii, and just outside the bay. Normal (unparasitized) fish behaved similarly to their congeners. Behavior varied by size class and presumed sex. Larger fish (males) patrolled territories and courted medium-sized fish (females), which freely crossed male territories. Smaller fish appeared to be immature and remained in limited home ranges on the edge of male territories. All fish parasitized with a philometrid nematode acted most like immature ”normal” fish, with limited home ranges and few social interactions. However, parasitized fish ate at twice the rate of unparasitized fish. All fish collected from the bay contained some parasites, and none were sexually mature, whereas no parasites were found in fish from outside the bay. These data suggest that parasites affect the behavior of C. jactator. Moreover, parasites may limit the sexual maturation of their hosts.     

An annotated list of fish parasites (Isopoda, Copepoda, Monogenea, Digenea, Cestoda, Nematoda) collected from Snappers and Bream (Lutjanidae, Nemipteridae, Caesionidae) in New Caledonia confirms high parasite biodiversity on coral reef fish

ABSTRACT: BACKGROUND: Coral reefs are areas of maximum biodiversity, but the parasites of coral reef fishes, and especially their species richness, are not well known. Over an 8-year period, parasites were collected from 24 species of Lutjanidae, Nemipteridae and Caesionidae off New Caledonia, South Pacific. RESULTS: Host-parasite and parasite-host lists are provided, with a total of 207 host-parasite combinations and 58 parasite species identified at the species level, with 27 new host records. Results are presented for isopods, copepods, monogeneans, digeneans, cestodes and nematodes. When results are restricted to well-sampled reef fish species (sample size[THIN SPACE]>[THIN SPACE]30), the number of host-parasite combinations is 20[EN DASH]25 per fish species, and the number of parasites identified at the species level is 9[EN DASH]13 per fish species. Lutjanids include reef-associated fish and deeper sea fish from the outer slopes of the coral reef: fish from both milieus were compared. Surprisingly, parasite biodiversity was higher in deeper sea fish than in reef fish (host-parasite combinations: 12.50 vs 10.13, number of species per fish 3.75 vs 3.00); however, we identified four biases which diminish the validity of this comparison. Finally, these results and previously published results allow us to propose a generalization of parasite biodiversity for four major families of reef-associated fishes (Lutjanidae, Nemipteridae, Serranidae and Lethrinidae): well-sampled fish have a mean of 20 host-parasite combinations per fish species, and the number of parasites identified at the species level is 10 per fish species. CONCLUSIONS: Since all precautions have been taken to minimize taxon numbers, it is safe to affirm than the number of fish parasites is at least ten times the number of fish species in coral reefs, for species of similar size or larger than the species in the four families studied; this is a major improvement to our estimate of biodiversity in coral reefs. Our results suggest that extinction of a coral reef fish species would eventually result in the coextinction of at least ten species of parasites.     

Monoxenous and heteroxenous parasites of fish manipulate behavior of their hosts in different ways

Adaptive host manipulation hypothesis is usually supported by case studies on trophically transmitted heteroxenous endoparasites. Trematodes and cestodes are among efficient manipulators of fish, their common intermediate hosts. In this review paper, new data on modifications of host fish behavior caused by monoxenous ectoparasitic crustaceans are provided together with a review of effects caused by heteroxenous parasites. Differences in modifications of host behavior caused by heteroxenous and monoxenous parasites are discussed. Manipulation by heteroxenous parasites enhances availability of infected fish to predators--definitive hosts of the parasites. Fine-tuned synchronization of modified anti-predator behavior with a certain phase of the trematode Diplostomum spathaceum development in the eyes of fish, their second intermediate host, was shown. Modifications of behavior are habitat specific. When juvenile salmonids are in the open water, parasites impair their cooperative anti-predator behavior; in territorial bottom-dwelling salmonids, individual defense behavior such as sheltering is the main target of manipulation. It was shown that monoxenous ectoparasitic crustaceans Argulus spp. decreased motor activity, aggressiveness and increased shoal cohesiveness of infected fish. Such a behavior facilitates host and mate searching in these parasites, which often change their hosts, especially during reproduction. Reviewed experimental data suggest that heteroxenous parasites manipulate their host mainly through impaired defense behavior, e.g. impairing shoaling in fish. Alternatively, monoxenous parasites facilitate shoaling that is profitable for both parasites and hosts. Coordination of modified host behavior with the parasite life cycle, both temporal and spatial, is the most convincing criterion of the adaptive value of host manipulation.     

Accumulation of plerocercoids of Triaenophorus crassus in the second intermediate host Coregonus lavaretus and their effect on growth of the host

Patterns of accumulation of Triaenophorus crassus in its second intermediate host whitefish Coregonus lavaretus s.l. were studied between 1991 and 1996 from two host populations in two separate areas of Lake Saimaa, Finland. Whitefish were infected commonly with several T. crassus plerocercoids and the parasites were aggregated into the oldest hosts. In one host population the annual parasite accumulation was 0·9 parasites in all host age groups between 3 and 8 years. In the other host population the annual accumulation was 1·6 parasites in 3–5-year-old fish, but increased up to 3 to 4 parasites per year in fish over 5 years old. The increase did not coincide with the period of maturation or any increase in whitefish growth, both of which could alter the food intake of the fish. The sharp increase in the annual accumulation suggests a threshold intensity above which the probability of acquiring further parasites increases. In spite of a heavy aggregation of parasites there was no evidence of parasite-induced host mortality. The annual increase in mean abundance was not correlated with the mean annual weight increase in 2–4-year-old fish within cohorts. However, evidence of a negative effect of parasites on whitefish growth was revealed by back-calculation of lengths of uninfected and infected whitefish and correlations between length or weight of fish and intensity of infection with fish age. Both analyses suggested that larger young fish harboured more parasites than the smaller ones while in older fish the reverse was true, a pattern that has not been shown earlier for parasitized fish.     

Focus: Zoonotic Disease: Biology,Epidemiology, Clinical Features,Diagnosis, and Treatment of Selected Fish-borne Parasitic Zoonoses

Fish-borne parasites have been part of the global landscape of food-borne zoonotic diseases for many decades and are often endemic in certain regions of the world. The past 20 years or so have seen the expansion of the range of fish-borne parasitic zoonoses to new geographic regions leading to a substantial public health burden. In this article, we summarize current knowledge about the biology, epidemiology, clinical characteristics, diagnosis, treatment and control of selected fish-borne helminthic diseases caused by parasitic roundworm (Anisakis), tapeworm (Dibothriocephalus), and fluke (Metagonimus). Humans acquire infection via consumption of raw or improperly cooked fish or fish products. The burden from these diseases is caused by morbidity rather than mortality. Infected patients may present with mild to severe gastrointestinal (eg, abdominal pain, diarrhea, and indigestion) or allergic manifestations. Patients are often admitted to the hospital or clinic with acute symptoms and no prior health problems and no travel history. Diagnosis is often established based on the detection of the diagnostic parasite stages (eg, eggs or tapeworm segments) in the patient’s feces. Sometimes imaging is required to exclude other causes and avoid unnecessary surgery. Dibothriocephalus and Metagonimus are mainly treated with praziquantel. Extraction of adult Dibothriocephalus or Anisakis larvae from the bowel ensures complete elimination of the parasites and prevents a relapse of infection. The development and implementation of more efficient food safety and public health strategies to reduce the burden of zoonotic diseases attributable to fish-borne parasites is highly desirable.     

Parasitic diseases of marine fish: epidemiological and sanitary considerations

Over recent decades, parasitic diseases have been increasingly considered a sanitary and economic threat to Mediterranean aquaculture. In order to monitor the distribution of parasites in cultured marine fish from Italy and study their pathogenic effects on the host, a three-year survey based on parasitological and histopathological exams was carried out on 2141 subjects from eleven fish species and coming from different farming systems (extensive, intensive inland farms, inshore floating cages, offshore floating cages and submersible cages). A number of parasitic species was detected, mostly in European sea bass (Dicentrarchus labrax), gilthead sea bream (Sparus aurata), mullets (Chelon labrosus, Mugil cephalus, Liza ramada) and sharpsnout sea bream (Diplodus puntazzo), with distribution patterns and prevalence values varying in relation to the farming system, in-season period and size category. The epidemiology and pathological effects of the parasites found during the survey are discussed.     

南极鱼类后生动物寄生虫研究进展: 线虫、绦虫与桡足类

极端的环境造就了南极独特的生物群体, 其中鱼类是南大洋生态系统中最具多样性的脊椎动物, 也是许多寄生虫的中间或终末宿主。南极鱼类寄生虫种类丰富, 是南大洋海洋生物多样性的重要组成部分。探究南极鱼类及其寄生虫的营养关系可为阐释南极海洋生态系统功能及其变动提供重要的生态数据。虽然关于南极鱼类寄生虫的研究已有一百多年的历史, 但这些研究主要集中在寄生虫的种类鉴定、区系调查和组织病理等方面。由于南极鱼类寄生虫研究跨度时间长、地域范围广, 相关研究较为零散。文章综述了南极鱼类寄生线虫、绦虫以及桡足类的种类组成、宿主范围和地理分布等方面的研究, 并对今后开展南极鱼类寄生虫研究工作提出了展望。     

Ichthyophthiriasis in the mirror carp Cyprinus carpio (L.) V. Acquired immunity*

Mirror carp (Cyprinus carpio L.) infected with sublethal doses of Ichthyophthirius multifiliis, were free of parasites 21 days after infection. Fish remained free of parasites for at least 8 months when maintained in an infective environment. Such fish were refractory to reinfection with numbers of parasites that killed all normal, previously unexposed fish. Serum from fish recovered from previous infections with sublethal doses of parasites, immobilized free-swimming stages of I. multifiliis to a dilution of up to 1: 1024. The rise in serum-immobilization titre occurred between the 10th and 22nd days of infection, the period during which parasites disappeared from the body surface of the fish. Infective stages of the parasite were unable to penetrate the mucus body covering of resistant fish.     

Toxic pollution and parasitism in freshwater fish

As aquatic habitats throughout the world are increasingly contaminated with toxic chemicals, toxicologist strive to determine what impact these substances will have an biological systems. So far, the effects of this type of pollution on fish parasites has received little attention, despite their important status as determinants of fish health. Robert Poulin discusses the many ways in which toxic pollution may affect infections of metazoan parasites in freshwater fish. Effects on fish immunity, parasites survival and intermediate host populations are not independent, and currently the outcome of toxic pollution and parasitism in fish is impossible to predict. Future research will have to answer several questions if we are to understand and forecast pollution-mediated changes in parasitism, an urgent challenge for ecotoxicologists and fish parasitologists alike.     

Influence of collection methods on the occurrence of alimentary canal helminth parasites in fish.

The effect of collecting trauma on the metazoan parasites in the alimentary canal of French grunts, Haemulon flavolineatum (Desmarest) (Perciformes: Haemulidae), was evaluated by comparing the number and species of parasites in 10-fish lots that were identical except for collecting technique. Collecting techniques included speared (dead), speared through the caudal peduncle (live), trapped, dipnetted at night, and ostracitoxin exposed. Dead, trapped, and toxin-stressed fish had no alimentary canal parasites, whereas speared-live and night-dipnetted fish had comparable numbers of parasites. Fish collected by using apparently traumatic techniques quickly expelled their alimentary canal metazoan parasites. Our results cast doubt on the reliability of traditional fish parasite surveys, studies on population dynamics of fish parasites, and experiments that employ these traumatic collecting methods.