Enteromyxum spp are a myxosporidian parasite that causes a wasting disease in more than 40 marine fishes.
Affected fish include tiger puffer (Takifugu rubripes), Japanese flounder (Paralichthys olivaceus), red seabream (Pagrus major), spotted knifejaw (Oplegnathus punctatus), gilthead seabream (Sparus aurata), Mediterranean rainbow wrasse (Coris julis), blenids and ocean sunfish (Mola mola).
Outbreaks of this disease usually occur in summer to late autumn and cease by the end of winter. This may be because the development of E. leei is suppressed by low water temperature (< 15 C.).
Enteromyxum leei infects the digestive tract of fish, leading to severe emaciation including sunken eyes and bony ridges on the head. Mucous liquid in the digestive tract and a flimsy intestinal wall are evident.
Many parasites are observed in the intestinal epithelia and lumen. Most of them are multinucleate developmental stages (10-20 μmin diameter). In particular, the parasite hardly sporulates in tiger puffer. A spore is equipped with 2 obliquely arranged polar capsules (length 15.9-19.1 (average 17.5) μm; width 7.9-11.0 (9.2)) μm whose size is different between host species. The parasite has a broad host range (over 40 marine fishes around the world). Since this parasite transmits from fish to fish, its infection spreads rapidly in fish farms.
Proliferation and sloughing of the intestinal epithelia are observed. As a result, the osmoregulatory and nutrition system may be impaired, causing the emaciation of a host.
Since this parasite is not infectious to human, it is harmless in food hygiene.
Technical expertise is required to diagnose based on the morphology of development stages. Leptotheca fugu and Enteromyxum fugu also parasitize to the intestine of tiger puffer. The former is highly pathogenic and the causative agent of the emaciation disease like E. leei, but does not transmit from fish to fish. The latter causes no diseases because its pathogenicity is low. Considering these things, it is practically important to identify the parasite species. These two parasites can be differentiated in the presence of the spherical polar capsules for L. fugu and the 2 vegetative nuclei in a primary cell for E. fugu. The sensitive PCR method was developed to detect these parasites. Moreover, non-lethal diagnosis can be performed by samples obtained using a sterile swab inserting into the anal orifice of fish.
There are no effective methods to treat this disease. It is recommended to remove infected fish before introduction of fish by detecting the parasite using the PCR.
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