s. MUKARATIRWA 1, K. MAGWEDERE1, E. MATENGA 1 and C.M. FOGGIN2

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Onderstepoort Journal of Veterinary Research, 68:21-25 (2001) Transmission studies on Trichinella species isolated from Crocody/us niloticus and efficacy of fenbendazole and levamisole against muscle L 1 stages in Balb C mice s. MUKARATIRWA 1, K. MAGWEDERE1, E. MATENGA 1 and C.M. FOGGIN2 ABSTRACT MUKARATIRWA, S., MAGWEDERE, K., MATENGA, E. & FOGGIN, C.M. 2001.Transmission studies on Trichinella species isolated from Crocodylus niloticus and efficacy of fenbendazole and levamisole against muscle L 1 stages. Onderstepoort Journal of Veterinary Research, 68:21-25 Forty-four Balb C mice, aged 18 weeks were infected with crocodile (Crocodylus niloticus)-derived Trichinella species. Of the infected mice, 32 were randomly divided into two groups each containing equal numbers of males and females; levamisole treated group and fenbendazole treated group. Each group was randomly subdivided into two subgroups as follows: levamisole group (subgroup 1: treated with levamisole on day 35 post infection, and subgroup 2: treated with levamisole on days 35 and 42 post infection) and fenbendazole group (subgroup 1: treated with fenbendazole on day 35 post infection and subgroup 2: treated with fenbendazole on days 35 and 42 post infection). The first subgroups treated on day 35 post infection were slaughtered on day 42 post infection and the second subgroups were treated on day 35 and day 42 post infection and slaughtered on day 49 post infection. Two female mice were infected a day after mating and were slaughtered together with the offspring on day 64 post-infection. Ten infected control mice were given 1 m ~ distilled water orally as placebo, and five of these were slaughtered on day 42 post infection. The results showed that the mean reproductive capacity index of this strain (RCI) in Balb C mice was 110. There was a significant reduction (P < 0.01) in larval counts in the single treatment groups (day 35) and in the double treatment groups (days 35 and 42) for both anthelmintics when compared the number of parasites in the control groups. After a single treatmeni, levamisole reduced the infection by 79.9 % and fenbendazole by 76.7 %. Following double treatments, levamisole reduced the infection by 95.5 % and fenbendazole by 99.1 %.There was evidence that the infected pregnant mice transmitted the parasite to their offspring. It is not certain whether the parasite was transmitted congenitally or transmammary. Alternative ways of controlling the parasite in crocodile farms in Zimbabwe are discussed. Keywords: Balb C mice, crocodile, fenbedazole, levamisole, transmission, Trichinella sp. INTRODUCTION Recently, the crocodile (Crocodylus niloticus) has been found to be a host of a Trichinella species (Foggin, Vassilev & Widdowson 1997) which has yet to be identified. It is postulated that the feeding of offal and the recycling of crocodile meat enhances the 1 Department of Paraclinical Veterinary Studies, Faculty of Veterinary SCience, University of Zimbabwe, PO Box MP 167, Mt Pleasant, Harare, Zimbabwe 2 Central Veterinary Research Laboratory, PO Box CY 551, Causeway, Harare, Zimbabwe Accepted for publication 7 November 2000-Editor transmission of this parasite (Foggin et al. 1997). Studies on the transmission and infectivity of this parasite to the indigenous Zimbabwean pig (Sus scrota) and rat (Rattus norvegicus) have been reported by Mukaratirwa & Foggin (1999). The Trichinella/mouse model has been widely used to assay the efficacy of benzimidazole-carbamate and imidazothiazole anthelmintic activity (Campbell & Denham 1983; McCracken 1978). This model makes it possible within a short time to test the efficacy of drugs against different parasite stages in various locations within the host. Levamisole is an imidazothiazole that acts by interfering with the parasites nerve transmission causing 21

Trichinella species isolated from Crocodylus niloticus muscular paralysis and its rapid expulsion (Van Nuten 1972). The therapeutic index of levamisole is low in animals. Fenbendazole is a benzimidazole compound which disrupts parasite energy metabolism by binding to tubulin, a protein required for the uptake of nutrients and other functions (Abo-Shehada & Herbert 1984). Its activity is related to the duration of therapeutic blood concentration. The efficacy of levamisole and fenbendazole to the crocodile-derived Trichinella strain has not been tested, although Boczon, Olba & Olaszek (1984) have reported on the efficacy of the two anthelmintics against the adult and larval stages of T. spira lis and T. pseudospiralis. Under natural conditions it is difficult to detect infection in its early stages, hence the need to search for a better drug which is effective on the muscle stage (first stage larvae-l 1) of the parasite. The objective of this study was to evaluate the efficacy of fenbendazole and levamisole against the larval stages of the crocodile-derived Trichinella sp. in muscle and to determine if vertical transmission of the Trichinella sp. strain occurs in Balb C mice. MATERIALS AND METHODS Experimental animals Forty-four Balb C mice were bred at the Faculty of Veterinary Science, University of Zimbabwe animal unit. Equal numbers of females and males aged 18 weeks were randomly selected into groups and subgroups according to the experimental design (cf. Table 1). The mice in two of these groups served as untreated controls. Parasite The crocodile-derived strain of Trichinella sp. used, has been maintained under laboratory conditions by periodical passages through crocodiles. The methods followed for infecting mice and for counting larvae were those described by Kapel, Webster, Bj0rn, Murrell & Nansen (1998). Each mouse was infected with ten Trichinella first stage larvae. Anthelmintic experiments To evaluate the anthelmintic activity of levamisole and fenbendazole, the mice were orally infected with ten first stage (L 1) muscle larvae. Information on the anthelmintics and administration are shown in Table 2. Different groups of mice were anaesthetized by ether and then slaughtered on day 42 and day 49 and the other comprising two females and their offspring on day 49 (vide infra). The slaughtered mice were eviscerated and their carcasses processed to free the muscle larvae according to method described by Kaufmann (1996). The procedure to estimate the effectiveness of the anthelmintic drugs was done according to that described by Martinez-Fernandez (1978). Transmission experiments Two female mice were mated on the 19/01/00 and were infected on the following day (Table 5). The offspring born on 08/02/2000 together with the adult females were slaughtered on 24/03/00, and carcasses were processed and the larvae counted as described above. Statistical analysis The number of L 1 recorded in each treated group was expressed as a percentage of the mean value TABLE 1 Summary of anthelmintics used, number of animals per group, and day of treatment and slaughter post-infection Group No. of mice Subgroup Treatment post-infection Slaughter Trial 1 Levamisole 16 1 (n = 8) Day 35 Day 42 2 (n = 8) Days 35,42 Day 49 Fenbendazole 16 1 (n = 8) Day 35 Day 42 2 (n = 8) Days 35,42 Day 49 Placebo 10 - - Day 42 Trial 2 (Pregnant mice) 2 - - Day 64 22

S. MUKARATIRWA et al. for the control group, and the anthelmintic effect of the various treatment groups were compared by the 1-way ANOVA. RESULTS Both single (day 35, Table 3) and double (days 35 and 42, Table 4) treatments with each compound significantly reduced the numbers of L 1 in the muscles of the mice (P<0.01). While the difference in efficacy of the two anthelmintics was not significant after a single treatment, fenbendazole was significantly more effective than levamisole after double treatments (P< 0.01). Double treatments eliminated 95.5 % of the larvae in levamisole and 99.1 % in fenbendazole-treated animals (Table 4).There was a significant reduction (P < 0.01) in the worm counts of double treated groups (days 35 and 42) (ct. Table 4). Fenbendazole was more effective than levamisole at double treatments (P < 0.01). TABLE 2 Information on the anthelmintics used for treatment Anthelmintic Fenbendazole Levamisole Trade name Zerofen Tramisol Manufacturer Caps Zimbabwe Milborrow Date of manufacture 11/1998 10/1999 Date of expiry 11 /2001 10/2002 Batch number 900010 9981 Concentration 10% 2.5% Dosage 7.5 mg/kg, orally 7.5 mg/kg, orally All the young mice looked healthy and there were no indications of changes in their tissues and organs examined at necropsy. Mother 1 gave birth to four offspring of which three were infected with the parasite and mother 2 gave birth to eight offspring of which five were infected (Table 5). Thus, the mice had apparently transmitted the parasite to their offspring but it is not certain whether this occurred congenitally or transmammary route. DISCUSSION Our observations showed that the crocodile isolate of Trichinella sp. is highly infective to Balb C mice, as also shown previously for pigs (Mukota breed) (Sus scrota) and rats (Rattus norvegicus) (Mukaratirwa & Foggin 1999). The parasite was also found to be noninfective to birds (S. Mukaratirwa, unpublished data 2000). Pozio, La Rosa, Murrell & Lichtenfels (1992a) reported that host species seem unimportant for distinguishing Trichinella species, excepting that Trichinella spiralis is the only species that has a high reproductive capacity index (RCI) for pigs, rats and mice and that Trichinella pseudospira/is is the only species infective to birds. The inability of the present isolate to infect birds makes it highly unlikely to be T. pseudospiralis, but our results are in agreement with work by Foggin et a/. (1997), who tentatively identified the parasite as a subspecies of T. spira/is. The Rei from the untreated group was 110, which is classified as a high index, in agreement with a corresponding value of 145 for T. spira/is in NIH mice (Wakelin & Goyal 1996). The RCI for Trichinella nativa in these mice was found to be low (14). Bolas-Fer- TABLE 3 Summary of mean larval count(lc), mean RCI and mean % larval reduction following on a single treatment at day 35 after infection Group No. Dosage Mean LC Reduction (%) Mean RCI Levamisole 8 7.5 mg/kg 220.9" ± 72.8 79.9 - Fenbendazole 8 7.5 mg/kg 255.8" ± 123.0 76.7 - Control 5-1107.4 b ± 538.3-110 ± 53.8 Values with different superscript within a column are significantly different P < 0.01 RCI number of larvae recovered/number of larvae given % larval reduction = 100 - (mean larval count for treated group/mean larval count for control group)/100 TABLE 4 Summary of mean larval count (LC), mean RCI and mean % larval reduction control group and treatment groups at days 35 and 42 Group No. Dosage Mean LC Reduction (%) Mean RCI Levamisole 8 7.5 mg/kg 49.5" ± 27.3 95.5 - Fenbendazole 8 7.5 mg/kg 9.9 b ± 4.7 99.1 - Control 5-1107.4 c ± 538.3-110 ± 53.8 Values with a different superscript within a column are significantly different P < 0.01 RCI = number of larvae recovered/number of larvae given % larval reduction = 100 - (mean larval count for treated group/mean larval count for control group)/100 23

Trichinella species isolated from Crocodylus niloticus TABLE 5 Data on the two mice that were infected a day after having been mated, and on their offspring Identification Mass (g) No. of L 1 Mother 1 19.6 449.0 Offspring 1 7.1 0.0 Offspring 2 6.7 7.0 Offspring 3 10.2 12.0 Offspring 4 9.4 4.0 Mean larvae/offspring - 5.8 Mother 2 20.1 414.0 Offspring 1 9.2 6.0 Offspring 2 10.2 273.0 Offspring 3 9.6 0.0 Offspring 4 8.9 5.0 Offspring 5 8.3 0.0 Offspring 6 9.5 3.0 Offspring 7 10.1 0.0 Offspring 8 9.7 9.0 Mean larvae/offspring - 37.0 nandez & Wakelin (1989) also reported RCI values to be high for T spiralis, low for T nativa and intermediate for T pseudospiralis, while the values for Trichinella nelsoni and Trichinella britovi were low in pigs and rats (Murrell, Lichtenfels & Rausch 1991). From tissue sections of the muscles of the mice, the parasite was found to be cyst forming. This eliminates T pseudospiralis, which lacks the ability to form a nurse cell and remains unencysted in the muscle (Pozio, La Rosa, Rossi, Murrell & Lichtenfels 1992). In female mice that were first mated and then infected with the Trichinella parasite strain, the infection passed to their offspring, but it is not known whether this occurred vertically (transplacental) or transmammary. While both anthelmintics used considerably reduced the muscle larval stages in all four treatment groups, none of the treatments were fully effective after a single and double treatments. For a drug to be recommended for use against Trichinella parasites, it has to clear the infection completely. We suggest that a serological test for diagnosis of this parasite in crocodiles be developed for the detection of reservoirs or carrier animals. Once detected, these can be culled and the meat disposed of by incineration and so that the meat is not recycled. The present results with levamisole and fen bendazole were similar to those reported for related anthelmintics, which failed to completely eliminate muscle L 1 stages. Flubendazole in Swiss albino mice reduced muscle L 1 stages by 61-64 %, and th e intestinal phase 3 days post-infection by 89. 9 % (EI- Temsahi & EI-Mansoury 1995). Thiabendazole and mebendazole treatment resulted in complete elimination of Trichinella spiralis adult worms in the small intestine and marked reduction of larval infection of muscle larval stages in albino rats (EI-Ridi, Abou Ragab, Ishmail, Shehata, Ramadan & Etewa 1990). Albendazole is ranked as one of the most effective anthelmintics against muscle L 1 stages of Trichinella, but displays a low solubility in aqueous solutions (Hrckova, Velebny & Horak 1993). An increased number of dosages in a liposomised form to improve solubility, resulted in an increased reduction in the number of larvae (Hrckova et al. 1993). Although some anthelmintics have been found to clear the intestinal stage, this is of little practical use because under natural conditions it is difficult or impossible to detect this stage. In view that this parasite is infective to pigs, public health education and economic implications of this parasite has to be reemphasised. Introduction of legislative measures may be required to control this parasite. Although a number of biological characteristics of this parasite have been documented, more studies need to be done to identify this strain of Trichinella to species level. ACKNOWLEDGEMENTS This work was funded by the research Board of the University of Zimbabwe. The authors thank Ms Happiness Chikwaya and Mr Manuel Taruvinga for their assistance. REFERENCES ABO-SHEHADA, M.N. & HERBERT, IV 1984. Anthelmintic effects of levamisole, ivermectin, albendazole, and fenbendazole on larval Toxocara canis infection in mice. Research in Veterinary Science, 36:87-91. BOCZON, K., OLBA, W. & OLASZEK, M. 1984. The influence of some anthelmintics on the bioenergetic metabolism of Trichinella spira lis and Trichinella pseudospiralis. Biochemical Pharmacology, 33:2523-2525. BOLAS-FERNANDEZ, F. & WAKELlN, D. 1989. Infectivity of Trichinella isolates in mice is determined by host immune responsiveness. Parasitology, 99:83-88. CAMPBELL, W.C. & DENHAM, D.A. 1983. Chemotherapy in Trichinella and trichinosis. New York : Plenum Press: 335-366. EL-RIDI, A.M., ABOU-RAGAB, H.A., ISHMAIL, M.M., SHEHATA, M.M., RAMADAN, M.E. & ETEWA, S.E. 1990. Effect of some drugs on some histopathological and immunological aspects of experimental trichinosis in Albino rats. Journal of the Egyptian Society of Parasitology, 20:99-103. EL-TEMSAHI, M.M. & EL-MANSOURY, S.T. 1995. The effect of flubendazole on the course of Trichinella spiralis infection in mice. Journal of the Egytptian Society of Parasitology, 25:453-459. FOGGIN, C.M., VASSILEV, G.D. & WIDDOWSON, M.A. 1997. Infection with Trichinella in farmed crocodiles (Crocodylus 24

S. MUKARATIRWA et a/. niloticus) in Zimbabwe. Abstract book on Proceedings of the 16 th International Conference of the World Association for the Advancement of Veterinary Parasitology, Sun City, South Africa. (Abstract no. 110). HRcKOVA, VELEBNY, S. & HORAK, J. 1993. A morphological study of liposomized albendazole on the muscle phase of Trichinella spiralis in mice. Journal of Helminthology, 67:24-30. KAPEL, C.M.O., WEBSTER, P. BJ0RN, H., MURRELL, K.D. & NANSEN, P 1998. Evaluation of the infectivity of Trichinella spp. for reptiles (Caiman sclerops). International Journal for Parasitology, 28: 1935-1937. KAUFMANN, J. 1996. Parasitic infections of domestic animals. Basel: Birkhauser Verlag. McCRACKEN, R.O. 1978. Efficacy of mebendazole and albendazole against Trichinella spiralis in mice. Journal of Parasitology, 64:214-219. MARTINEZ-FERNANDEZ, A.R. 1978. Algunos efectos de los corticosteroides sobre el cicio endogeno de Trichinella spiralis. Trabajos Compostelanos de 8iologia 7:181-219. MUKARATIRWA, S. & FOGGIN, C.M. 1999. Infectivity of Trichinella sp. isolated from Crocodylus niloticus to the indigenous Zimbabwean pig (Mukota). International Journal for Parasitology, 29:1129-1131. MURRELL, K.D., LICHTENFELS, J.R. & RAUSCH, R.L. 1991. Genetics and systematics of Trichinella. Annales de Parasitologie Humaine et Comparee, 66 (Suppl. 1): 23. POZIO, E., LA ROSA, G., MURRELL, K.D. & LICHTENFELS, J.R., 1992a. Taxonomic revision of the genus Trichinella. Journal of Parasitology, 78:654-655. POZIO, E., LA ROSA, G., ROSSI, P & MURRELL, K.D. 1992b. Biological characterization of Trichinella isolates from various host species and geographical regions. Journal of Parasitology, 78:647-653. VAN NUTEN, J.M. 1972. Comparative biochemistry of parasites, edited by H. van den Bossche. Academic Press, New York. WAKELlN, D. & GOYAL PK. 1996. Trichinella isolates: Parasites variability and host responses. International Journal for Parasitology, 26:471-481. 25