Ceratothoa oestroides

Ceratothoa oestroides is a crustacean isopod,[1] obligate ectoparasite of marine fish that dwells in the buccal cavity. It is the causative agent of various pathologies including tissue damage at the parasitisation site (tongue), growth defects, decrease in mean host weight and size and increases mortalities in farmed and wild fish populations.[2]  It has been recorded in six different fish families: Sparidae (Boops boops, Diplodus annularis, Pagelus erythrinus, Spicara smaris, Sparus aurata), Carangidae (Trachurus mediterraneus), Clupeidae (Sardina pilchardus), Maenidae, Scorpenidae (Scorpaena notata, Scorpaena porcus), and Mugilidae (Liza aurata).[3][4]

Fig 1: Adult female Ceratothoa oestroides settled in the buccal cavity of the juvenile European sea bass (Dicentrarchus labrax).

Ceratothoa oestroides
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Malacostraca
Superorder: Peracarida
Order: Isopoda
Family: Cymothoidae
Genus: Ceratothoa
Species:
C. oestroides
Binomial name
Ceratothoa oestroides
(Risso, 1826)
Synonyms[1]
  • Canolira oestroides Risso, 1826
  • Ceratothoa sargorum Gourret, 1891

Adult male and female mate in the host buccal cavity (Fig. 1). Embryos develop in the female marsupium, where offspring pass through different pullus stages until they are released from the marsupium as free swimming manca, ready for infecting fish hosts. C. oestroides is one of the most devastating ectoparasites in Mediterranean aquaculture, with an unequal distribution along different geographical areas[5][6][7][8]

Life cycle
Fig 2: Infective stages (pulli) extracted from the marsupium of the adult female Ceratothoa oestroides.

The life cycle of Cymothoidae, which are protandric hermaphrodites,[9] encompasses mating of adult male and female in the host buccal cavity, development of embryos in the female marsupium followed by moulting through pullus stages (I–IV stages). The first pullus (I stage) can be found only in the marsupium where it moults into second pullus (II stage). Although most Cymothoidae have pullus stages I–IV, only pullus stages I and II seem to exist in Ceratothoa oestroides (Fig. 2).

Fig 3: Ventral view of the head of the adult female Ceratothoa oestroides.
Fig 4: Dorsal view of the head of the adult female Ceratothoa oestroides.

Sexual differentiation occurs only after young leave the brood pouch.[10] As free swimming manca (infective stage), the parasite will seek and attach to an appropriate host, and will then moult, losing the swimming setae and becoming immotile. The parasite attaches on the host body (flanks, fins), and then crawls towards the operculum, where it enters the buccal cavity and settles on the base of the tongue. After permanent attachment is completed, another moult follows. A seventh segment and pair of pereopods appears, typical for the isopod pre-adult form. An isopod in this pre-adult form will function as male until conditions require it to transform in to female. Sexual transformation is a complex process and depends on many factors. After transformation into female (Figs. 3 and 4), the isopod is known as an adult.[11] Alternatively, individuals that are first to reach the buccal cavity may undergo sexual differentiation (male puberty, mature male, transitory male stage, female puberty, mature female). Females block sexual differentiation of a second individual parasite within a host. This second individual remains in the mature male stage as long as the female is alive. All the life stages of C. oestroides are found on the fish host, if we also include the pulli that are situated in the female pouch.

Pathology and clinical signs

This parasite causes various pathologies, including tissue damage of the tongue, growth defects, anaemia, decrease in mean host weight and size and increased mortalities in farmed and wild fish populations.[2] It has not been observed to impair feed intake in pre- and harvest-sized fish. Instead, the decrease in fingerlings’ weight is likely attributed to the suspected hematophagous nature of the parasite. Athanassopoulou et al. (1999)[12] noticed that Ceratothoa-infected fish are also infected with Rickettsia-like organisms (RLO), and related the latter pathogen to transmission by the isopod. Apparently, infection of RLO is higher in Ceratothoa-highly infected farms[7] (Vagianou et al. 2006). Vagianou et al. (2006)[7] observed that larval stages of C. oestroides (pulli II) that attack small fish induce the most damage, causing severe ulcers and extensive granulomatous lesions in the eyes that lead to blindness or the total loss of the eyeball. However, this was not reported in other geographic area where the isopod has been found in reared fish. Fish infected with adult parasites did not show serious pathology. Lesions were localized at the upper and lower jaws and the tongue.

Impact

Growth of farmed fish can be depressed and fish can suffer from post-haemorrhagic anaemia.[13] Growth of market size caged fish infected with the parasite can be reduced by up to 20% compared to market size, uninfected caged fish.[14] For example, parasitised sea bass (Dicentrarchus labrax) in the age group of 291–293 days had reduced growth by 20.1% (14 g) and reduced length of 7.1% (12.63 mm) compared to non-parasitised fish.[5]

Diagnosis

C. oestroides infection is easily diagnosed by examining the buccal cavity and determining the presence of the parasite.

Treatments

Treatment of isopod infestations on young fish has been attempted with success by means of hourly formalin baths and manual removing from the buccal cavity during the vaccination for other diseases.

Other control strategies

Within a fish farm, it is common practice to decrease the number of wild fish population by fish net, as well as periodically clean the floating cages nets, depending on the season. Horton and Okamura (2001) suggest grading of smaller and larger fish and their separation, mooring the cages in deeper sites with sufficient currents to disperse the juvenile parasites in a direction away from the cages.[5] Often, in cases of heavy parasitism and mortality, reducing the fish density is enough to remedy the situation.

References
  1. Schotte M, Boyko CB, Bruce NL, Poore GC, Taiti S, Wilson GD, eds. (2021). "Ceratothoa oestroides (Risso, 1826)". World Marine, Freshwater and Terrestrial Isopod Crustaceans database. World Register of Marine Species. Retrieved 2 September 2021.
  2. Adlard, R. D.; Lester, R. J. G. (September 1994). "Dynamics of the interaction between the parasitic isopod, Anilocra pomacentri, and the coral reef fish, Chromis nitida". Parasitology. 109 (3): 311–324. doi:10.1017/S0031182000078343. PMID 7970888.
  3. Charfi-Cheikhrouha, F.; Zghidi, W.; Yarba, L. O.; Trilles, J. P. (2000). "Le Cymothoidae (Isopods parasites de poissons) des cotes tunisiennes: ecologie et indices parasitologiques". Systematic Parasitology. 46 (2): 143–150. doi:10.1023/A:1006336516776. PMID 10830837. S2CID 35895535.
  4. Trilles, J.P.; Radujkovic, B.M. & Romestand, B. (1989). "Parasites des Poissons marins du Montenegro: isopods". Acta Adriatica. 30 (1/2): 279–306.
  5. Horton, T; Okamura, B (2001). "Cymothoid isopod parasites in aquaculture: a review and case study of a Turkish sea bass (Dicentrarchus labrax) and sea bream (Sparus auratus) farm". Diseases of Aquatic Organisms. 46 (3): 181–188. doi:10.3354/dao046181. PMID 11710552.
  6. Mladineo, I. (2002). "Prevalance of Ceratothoa oestroides (Risso, 1826), a cymothoid isopode parasite, in cultured sea bass Dicentrarchus labrax L. on two farms in middle Adriatic Sea". Acta Adriatica. 43: 97–102.
  7. Vagianou, S.; Athanassopoulou, F.; Ragias, V.; Di Cave, D.; Leontides, L.; Golomazou, E. (2006). "Prevalence and pathology of ectoparasites of Mediterranean sea bream and sea bass reared under different environmental and aquaculture conditions". Israeli Journal of Aquaculture. 60: 128–133. hdl:10524/19164.
  8. Čolak, Slavica; Kolega, Matko; Mejdandžić, Danijel; Župan, Ivan; Šarić, Tomislav; Piplović, Edi; Mustać, Bosiljka (February 2018). "Prevalence and effects of the cymothoid isopod (Ceratothoa oestroides, Risso 1816) on cultured meagre (Argyrosomus regius, Asso 1801) in the Eastern Adriatic Sea". Aquaculture Research. 49 (2): 1001–1007. doi:10.1111/are.13547.
  9. Mladineo, Ivona (December 2003). "Life cycle of Ceratothoa oestroides, a cymothoid isopod parasite from sea bass Dicentrarchus labrax and sea bream Sparus aurata". Diseases of Aquatic Organisms. 57: 57(1-2):97-101. doi:10.3354/dao057097.
  10. Brusca, R.C. (1978). "Studies on the cymothoid fish symbionts of the eastern Pacific (Crustacea: Isopoda: Cymothoidae) I. Biology of Nerocila californica". Crustaceana. 34: 141–154. doi:10.1163/156854078X00718.
  11. Lincoln, R. J. (1971). "Isopod fish parasites". Marine Observer. 41 (234): 184–186.
  12. Athanassopoulou F.; Sabatakou O.; Groman D. & A. Prapas (1999). First indices of Rickettsia-like infections in cultured sea bass (D. labrax). 9th Int. Conference, Eur. Assoc. Fish Pathologists. Rhodes, Greece.
  13. Horton, T.; Okamura, B. (2003). "Post-haemorrhagic anaemia in sea bass, Dicentrarchus labrax (L.), caused by blood feeding of Ceratothoa oestroides (Isopoda: Cymothoidae)". Journal of Fish Diseases. 26 (7): 401–406. doi:10.1046/j.1365-2761.2003.00476.x. PMID 12946009.
  14. Šarušić, G. (1999). "Preliminary report of infestation by isopod Ceratothoa oestroides (Risso, 1926), in marine cultured fish". Bulletin of the European Association of Fish Pathologists. 19: 110–113.

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