Ichthyophthirius multifiliis as a potential vector of Edwardsiella ictaluri in channel catfish.

There is limited information on whether parasites act as vectors to transmit bacteria in fish. In this trial, we used Ichthyophthirius multifiliis and fluorescent Edwardsiella ictaluri as a model to study the interaction between parasite, bacterium, and fish. The percentage (23-39%) of theronts fluorescing after exposure to E. ictaluri was significantly higher than control theronts (~ 6%) using flow cytometry. Theronts exposed to E. ictaluri at 4 × 10(7)  CFU mL(-1) showed a higher percentage (~ 60%) of fluorescent theronts compared to those (42%) exposed to 4 × 10(3)  CFU mL(-1) at 4 h. All tomonts (100%) carried the bacterium after exposure to E. ictaluri. Edwardsiella ictaluri survived and replicated during tomont division. Confocal microscopy demonstrated that E. ictaluri was associated with the tomont surface. Among theronts released from tomonts exposed to E. ictaluri, 31-66% were observed with attached E. ictaluri. Sixty percent of fish exposed to theronts treated with 5 × 10(7) E. ictaluri mL(-1) were positive for E. ictaluri at 4 h as determined by qPCR or fluorescent microscopy. Fluorescent E. ictaluri were observed on trophonts in skin and gill wet mounts of dead fish. This study demonstrated that Ich could vector E. ictaluri to channel catfish.

Ichthyophthirius multifiliis infection induces apoptosis in different species of Tilapia.

The parasitic ciliate Ichthyophthirius multifiliis (Ich) is one of the most important protozoan pathogens of freshwater fish worldwide. Examination of 4 species of Tilapia from the River Nile recorded highest rate infection in Oreochromis niloticus, followed by Oreochromis aureus, Sarotherodon galilaeus and Tilapia zilli. By electron microscopy, apoptotic cells collected from Tilapia species infected with "Ich" showed an aggregation on the apical and basal parts of the ciliated and non-ciliated endothelial lining the gill epithelium. Ultrastructural analysis showed that the chromatin in the liver of Ich-infected O. niloticus was highly condensed and massed at the center of the nucleus. UItrastructural analysis of "Ich" infected O. aureus showed that the nuclear membrane of hepatocytes was also shrunken. In S. galilaeus, chromatin was highly condensed, fragmented and massed at the nuclear center, occasionally forming crescent-shaped masses. Ultrastructural of O. niloticus spleen showed that the macrophage number was comparatively high as compared to control. In O. aureus, damaged splenic cell number did not change, and phagocytic capacity of macrophages was not very high. In Ich-infected S. galilaeus, a marked decrease in splenic cells number was seen. Analysis of DNA by agarose gel electrophoresis on gill, liver and spleen cells showed a ladder of DNA fragments in multiple of 180bp in length, pointing to an internucleosomal DNA cleavage.

The occurrence and ape-to-ape transmission of the entodiniomorphid ciliate Troglodytella abrassarti in captive gorillas.

Entodiniomorphid ciliates are often present in the colons of wild apes. In captive apes the infection tends to gradually disappear, with the exception of Troglodytella abrassarti. We used fecal examinations to screen the gorillas (Gorilla gorilla gorilla) in European (Czech Republic, UK) and Australian Zoos to explore the ape-to-ape transmission pattern of T. abrassarti. Gorillas from two out of three European Zoos were positive for T. abrassarti, while gorillas from the Australian Zoo were negative. We documented a horizontal transmission of T. abrassarti to a non-infected adult gorilla introduced into a Troglodytella-positive group in the Prague Zoo and traced the origin of the ciliate infection to the Paignton Zoo (UK) using serial fecal examinations. During this study, two infant gorillas born in the Prague Zoo (CZ) first became positive for T. abrassarti at the age of 9 mo. Ciliate morphology and the sequencing of the small subunit rRNA gene and the internal transcribed spacer rDNA spacer region revealed that T. abrassarti affects both captive gorillas and chimpanzees. We conclude that zoo transport plays a major role in the distribution of T. abrassarti among captive gorillas.

Evaluation of a cohabitation challenge model in immunization trials for channel catfish Ictalurus punctatus against Ichthyophthirius multifiliis.

Calcein marking and cohabitation challenges have not been investigated in fish parasite research. This study evaluated a cohabitation challenge method in immunization trials against Ichthyophthirius multifiliis (Ich) using calcein, a fluorescent dye, to mark channel catfish Ictalurus punctatus (Rafinesque). Fish were marked by calcein immersion at 0, 500, and 1500 mg l(-1), and then challenged with 15 000 theronts fish(-1). No difference was noted in fish infection levels, mortality, and mean days to death (MDD) caused by Ich between unmarked and marked fish or between fish marked with high (1500 mg l(-1)) and low (500 mg l(-1)) concentrations of calcein. After ensuring that calcein marking had no effect on the susceptibility of fish to Ich theronts, 2 immunization trials were conducted to evaluate the cohabitation challenge model using calcein-marked catfish. Fish mortality, relative percent survival (RPS), and MDD were compared between cohabitation-challenged fish and fish challenged by non-cohabitation. No significant difference was observed in RPS for cohabitation-challenged fish and fish challenged by non-cohabitation. A cohabitation challenge can be used as an alternative challenge method in parasite studies, since it closely mimics natural exposure.