Cardiocephaloides longicollis (Rudolphi, 1819) Dubois, 1982

Born-Torrijos, Ana, van Beest, Gabrielle S., Merella, Paolo, Garippa, Giovanni, Raga, Juan Antonio & Montero, Francisco E., 2023, Mapping a brain parasite: occurrence and spatial distribution in fish encephalon, International Journal for Parasitology: Parasites and Wildlife 21, pp. 22-32 : 26-29

publication ID

https://doi.org/ 10.1016/j.ijppaw.2023.03.004

persistent identifier

https://treatment.plazi.org/id/03C787DA-0B40-FFFC-FCBC-4E3123C50293

treatment provided by

Felipe

scientific name

Cardiocephaloides longicollis
status

 

3.3. Mono- and multicysts of Cardiocephaloides longicollis View in CoL

Cercariae of C. longicollis were found in the brain by 6 dpi with a similar morphology to that of free-swimming cercariae ( Fig. 3 View Fig ). However, by 21 dpi the parasite increased considerably in size and the tegumental structures changed to resemble metacercariae rather than free-

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living cercariae, but lacking a visible cyst. Larvae found at 8 and 15 mpi had the normal morphology of encysted metacercariae that had developed a cyst in the brain. These were surrounded by a wall, and filled with a viscous glycocalyx-like material that maintained the position of the parasite within the cyst. Nevertheless, the host surface showed little disruption in response to the parasite.

Two types of cyst of C. longicollis metacercariae were observed in the brain of captured and experimentally-infected fish: (i) monocyst in which a single metacercaria was wrapped by a capsule ( Fig. 4 B View Fig ), or (ii) multicyst in which 2 to 25 metacercariae were encapsulated together ( Fig. 4 I View Fig ). Whereas the first type had a single wall in direct contact with the host, the multicyst may have a common capsule surrounding all metacercariae, or each metacercariae may produce its own capsule as a single parasite, likely resulting in metacercariae with more than one capsule. The composition of the capsule walls, both inner and outer, was identified by TEM and was composed mostly of host cells in necrosis and filamentous material possibly originated from the glycocalyx between the tegument of the parasite and the capsule ( Fig. 4 C, G View Fig ). The capsule was produced by the parasite so that the material accumulated in the inner layers of the capsule wall ( Fig. 4 C–D View Fig ), where the necrotic cells were probably produced by the host tissue when it came into contact with the parasite. Thus, the necrotic cells appeared to accumulate on the

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outer layers of the capsule of monocysts and also in the outermost capsule of a multicyst ( Fig. 4 A–E View Fig ). However, the composition of the wall in each individual capsule within a multicyst was different, showing cells in necrosis on both sides of the wall ( Fig. 4 F–M View Fig ). In this case, the degraded material was not only in the outer, but also in the inner layers of the capsule wall, resulting in a thick but loose capsule wall ( Fig. 4 L, M View Fig ) that likely merged with other inner wall capsules close to it ( Fig. 4 K View Fig ). Although the immune response was likely to be very low, TEM revealed

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that the capsule wall was characterised by the presence of fibrocytes that were flattened in the inner layers of the wall. In addition, the host tissue in contact with the cyst showed the occasional presence of macrophages ( Fig. 4 E View Fig ).

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