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Parasitol Res (1989) 75: 503-511

Parasitnlngy
Research
9 Springer-Verlag 1989

Review article

Chemotherapy of fish parasites


Giinter Schmahl, Horst Taraschewski, and Heinz Mehlhorn
Lehrstuhl fiir Spezielle Zoologie und Parasitologie, Ruhr-Universit/it Bochum, D-4630 Bochum, Federal Republic of Germany

Abstract. There are few agents on the market that Flagellata


control fish parasites. These are substances that
Flagellata (e.g., Hexamita salmonis, Oodinium pil-
are mainly used in other hosts; due to the different
metabolism of fish, they often have only moderate
lularis, Cryptobia spp.) are mainly ectoparasites of
the skin and gills. Only in cases of general weak-
effects on fish parasites. Therefore, the research
ness do these parasitic species cause severe impacts
and development of fish-specific antiparasitic com-
on their hosts (Table 1).
pounds is needed to avoid the high losses suffered
by commercial fish hatcheries. Drugs similar to tol-
trazuril would perhaps be promising, due to their Sporozoa, Coccidia
broad spectrum of efficacy. Specimens of the genera Eimeria, Goussia, and
Haemogregarina intracellularly parasitize the intes-
Key words: Chemotherapy - Fish parasites tinal tract and kidneys of fish. Their pathological
effects are not yet well understood (Table 1).

Ciliates
Fish, commonly thought to be tight as a trivet Among motile (Trichodina spp.) or sessile (Apio-
or sound as a bell, are among the most heavily soma spp.) skin- and gill-parasitizing ciliates, Ich-
infected animals in the world. The future looks thyophthirius multifiliis is the most important, since
black for fry - due not to polluted water but it has an extremely wide host range (Table 1).
mainly to parasite infection, which kills about 50% Especially in salmonids, carp and catfish, the losses
of the fry, especially in crowded hatchery ponds. due to ichthyophthiriosis (commonly known as
Unfortunately, only a few chemotherapeutical " I c h " or "white spot disease") are calculated in
agents are available. These drugs and recent devel- millions of dollars (Hines and Spira 1973). This
opments in controlling fish parasites are reviewed. parasite inhabits the skin without being intracellu-
lar; low-grade infections destroy the natural shield
against other pathogens, whereas high parasitae-
Commercially important fish parasites
mia leads to death in a short time. These parasites
In commercial farming of food and ornamental have an enormous potential for infection, since the
fish all over the world, many parasites (Table 1), cysts have a high propagation rate at the bottom
belonging to nearly all systematical groups (Proto- of ponds.
zoa, Helminthes and Arthropoda), are encoun-
tered. These parasites find optimal conditions in Microsporidia
crowded ponds with rising water temperatures and,
thus, lead to enormous losses. In this review, the Most stages of Microsporidia parasitize intracellu-
most important examples are chosen to represent larly in a variety of host cells (Table 1). Some spe-
their systematical groups. cies may cause high mortality in fish, i.e. Glugea
plecoglossi in cultured Japanese ayu (Plecoglossus
Reprint requests to: G. Schmabl altivelis). In heavy infestations, the xenomas are
504 G. Schmahl eta!. : Chemotherapy of fish parasites

Table 1. Selection of commercially important fish parasites

Parasites Size Host Infection site in fish Mode of infection

Flagellata:
Hexamita salmonis 7.4-12.3 x 3-6 grn Trouts Gut, gall bladder, Oral uptake
(e.g. Salmo trutta) blood
Oodinium pillularis 70 x 45 gm Freshwater Gills, skin Invasion of the skin
fish by swimming stages
Trypanoplasma spp. 6-25 x t .2-4 gm Common carp Blood Transmission by
( Cyprinus carpio), leeches
Tench ( Tinca tinea),
Crucian carp
(Carassius carassius)
Sporozoa/Coccidia:
Eimeria 14-17 gm Common carp Midgut, hindgut Oral uptake of spores
subepithelialis (oocysts) ( C. carpio)
Haemogregarina spp. i0 gm Freshwater and Erythrocytes Transmission by
marine fish leeches (?)
Ciliates:
Iehthyophthirius 50-1000 gm Freshwater fish Inside tissues Invasion by swimming
multifiliis (trophozoites) of epithelia theronts (swarmers)
Trichodina spp. 35-60 gm Freshwater and Motile on Invasion of gills,
marine fish gills, skin skin by swimming stages
Apiosoma spp. 80 x 38 gm Freshwater fish Sessile on Invasion of gills,
gills, skin skin by swimming stages
Microsporidia:
Glugea plecoglossi 5.8 • 2.1 gm Japanese ayu Body cavity, ovaries, Oral uptake of spores
(spores) (Plecoglossus testis, digestive tract,
altivelis) spleen, liver
Pleistophora 6 x 4 ~tm Members of four Skeletal muscles Oral uptake of spores
hyphessobryconis (spores) families of
freshwater fish
Myxozoa:
Myxobolus (syn. 4 x 7-10 gm Trouts Cartilaginous parts, Oral uptake of spores
Myxosoma) cerebralis (spores) (e.g., S. trutta), especially regio otica
Rainbow trout
(S. gairdneri)
Myxidium giardi 7 x 15 gm European eel Gills, kidney Oral uptake of spores
(spores) (Anguilla anguilla)
Sphaerospora renicola 10 • 10 ~m Common carp Swim bladder, Oral uptake of spores
(spores) ( C. carpio) kidney
Monogenea:
Gyrodactylus salaris 0.4 • 0.15 mm Atlantic salmon Ectoparasites on Body contact
(S. salar) skin, fins
Pseudodactylogyrus 0.58-1.16 x 0.15-0.24 mm European, Japanese Gills Invasion of
anguillae eel (A. anguilla, swimming oncomiracidia
A. japonica)
P. bini 0.54-1.6x0.12~.31mm European, Japanese Gills Invasion of
eel (A. anguilla, swimming oncomiraeidia
A. japonica)
Digenea:
Diplostomum 0.1x0.08mm Freshwater fish Endoparasites in Penetration of
spathaceum eyes cereariae
(metacercariae)
P osthodiplostomum 0.9x0.9mm Freshwater fish Skin, musculature Penetration of
cuticola cercariae
(metacercariae)
Sanguinicola inermis 1.5x0.3mm Common carp Blood vessels Penetration of
(adults) (C. carpio) cercariae

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