Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia

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VETERINARSKI ARHIV 76 (Suppl.), S9-S18, 2006 Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia Alen Slavica 1 *, Tihomir Florijančić 2, Zdravko Janicki 1, Dean Konjević 1, Krešimir Severin 1, Albert Marinculić 3, and Krunoslav Pintur 4 1 Department for Game Biology, Pathology and Breeding, Faculty of Veterinary Medicine, University of Zagreb, Zagreb, Croatia 2 Department of Zootechnics, Faculty of Agriculture, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia 3 Department of Parasitology and Parasitic Diseases, Faculty of Veterinary Medicine, University of Zagreb, Zagreb, Croatia 4 Department of game keeping and environmental protection, Polytechnic of Karlovac, Karlovac, Croatia SLAVICA, A., T. FLORIJANČIĆ, Z. JANICKI, D. KONJEVIĆ, K. SEVERIN, A. MARINCULIĆ, K. PINTUR: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free-ranging and captive red deer (Cervus elaphus L.) at eastern Croatia. Vet. arhiv 76, S9-S18, 2006. ABSTRACT After the large American liver fluke (Fascioloides magna) was detected in Croatia for the first time in 2000, treatment of fascioloidosis was conducted in the free-ranging population over a period of three years (from 2001 to 2003) and in captive red deer during the winter seson of 2002. The free-ranging red deer population was treated with a mixture of triclabendazole and standard deer salt brick components at a dose of 60 mg/kg body weight per deer, twice in seven days. Captive deer were treated individually by intra-ruminal application of triclabendazole using a needle or oesophageal tube. Coprological control was made 30 days after administration of antiparasitic preparation. Positive results (findings of F. magna eggs in faeces) in the free ranging deer population varied from 20% to 80% respectively. In captive deer we recorded almost ideal efficiency of triclabendazole (after treatment 95.5% of all faecal samples was free of F. magna eggs). Key words: red deer, large American liver fluke, Fascioloides magna, antiparasitic treatment, triclabendazole * Contact address: Dr. Alen Slavica, Department for Game Biology, Pathology and Breeding, Faculty of Veterinary Medicine, University of Zagreb, Heinzelova; 55 10 000 Zagreb, Croatia, Phone: + 385 1 2390 156; Fax:+ 385 1 2390 156; E-mail: slavica@vef.hr ISSN 0372-5480 Printed in Croatia S9

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia Introduction The large American liver fluke (Fascioloides magna) is a well-known parasite (STILES and HASSALL, 1894) of primarily North American wild and domestic ruminants (FRANCIS, 1891). At the end of the nineteenth century autochthonous deer species from northern part of American continent were imported into Europe (HALL, 1912). These species, primarily white-tailed deer (Odocoileus virginianus) and wapiti (Cervus elaphus canadiensis) spread the Large American liver fluke through Europe and infected autochthonous red deer (Cervus elaphus). Fascioloides magna was detected for the first time in Italy (BASSI, 1875) and after that in other European countries Germany (SALOMON, 1932), Poland (SLUSARSKI, 1955), the former Czechoslovakia (ERHARDOVA-KOTRLA, 1971), Austria (PFEIFFER, 1983), Slovakia (RAJSKY et al., 1994) and Hungary (SZTOJKOV et al., 1995). In Croatia the first case of fascioloidosis was described by MARINCULIĆ et al. (2002), who reported that infected red deer originated from the Čiprašat area (45 46 N; 18 52 E) in the eastern part of country - the Baranja region. Parasites entered Croatia following the Danube downstream, a river which flows through most countries with persisting problems of F. magna occurrence. Horizontal migrations of European red deer are well known (ERHARDOVA, 1961), and deer usually migrate along riversides from one habitat to another. MARINCULIĆ et al. (2002) presumed that F. magna was carried into eastern Croatia by the infected red deer population from neighboring Hungary. Another possibility is migration of different stages of parasite life cycle (eggs, intermediate host or metacercaria) flooded by water from the Danube. Local conditions of wetland habitats with shallow, medium temperate and slightly alkaline water are very suitable for the F. magna and its intermediate hosts (snails Lymnea spp.). These same conditions of such areas are also very attractive for cervids, so MULVEY et al. (1991) found that prevalence of F. magna in the free-ranging red deer population showed a tendency to be higher in swamp habitats than in dry uplands. In the Baranja region, which is a typical lowland habitat, the free-ranging population of red deer is relatively abundant (around 800 specimens) and the risk of parasite dissemination through the region is reasonably high. That was the main reason why scientists and veterinary practitioners gathered together to prevent potential transmission of F. magna to other game species and domestic livestock. Immediately after detection of the parasite in 2000 an initial plan for monitoring and control of large American liver fluke was prepared and realized in practice over a three year period (2001-2003). The obtained results and field experience are presented in this paper. S10

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia Materials and methods In the lowland area investigated, systematic collecting of red deer faecal samples was organized at 17 different positions in the Baranja region. During the winters of 2000/2001, 01/02 and 02/03 in habitats along the Danube River a total of 755 fecal samples were collected from the deer feeding spots (total deer population in researched area was estimated at 1500 individuals). All fecal samples were examined by the standard fecal analysis procedure at the Department of Parasitology and Parasitic Diseases, of the Faculty of Veterinary Medicine, University of Zagreb. The sedimentation method (VARADY, 1993) was used and the EPG (eggs per gram of faeces) of large American liver fluke eggs was calculated for every sample. Due to the fact that adult mature flukes may release up to four thousand thick-walled operculate eggs per day (SWALES, 1935), preventive therapy of fascioloidosis in the endangered Baranja region had to been done as soon as possible. Prophylactic treatment of infected deer could be carried out in two ways - group therapy, as well as an individual therapy. For the free-ranging red deer population we applied group therapy per os application of anthelminthic agents incorporated in suitable bait. While most researchers used only corn as bait (QURESHI et al., 1989; PYBUS et al., 1991; QURESHI et al., 1994) in our experimental treatment we used a mixture of salt and flukecides. One kilogram of salt mixture was composed of: 2.5% plaster (CaSO 4 ); 60% salt (NaCl); 10% chalk (CaCO 3 ); 17.8% lime (Ca (OH) 2 ); 9.7% Benal - Boehringer Ingelheim Vetmedica GmbH (inert powder); 720 ml Fasinex - Novartis AHC Inc. 10% (100 mg/ml triclabendazole) suspension. After the mixing of all components, the preparation was finished by drying for 24 hours at a maximum temperature of 40 o C. Finally one kg of this mixture contained 72 g triclabendazole, with 6 g representing a single dose for red deer with average weight of 100 kg (a quantity of 60 mg/kg body weight per deer was calculated as an efficient dose). This means that one kilogram of salt mixture was sufficient to feed approximately 10 to 12 adult deer. During the winter months January and February (three yrs in total), the mixture was exposed to the free-ranging deer on 17 feeding tables, with some corn grain on top to increase attractiveness (JANICKI et al., 2005). Consumption was mostly finished in 48 hours from exposure. After seven days second treatment/exposure was made and coprological control was done 30 days after the last treatment. Individual therapy was carried out on 17 animals (1 stag and 16 hinds) during February 2002, in the fenced area Zlatna Greda. All captive deer specimens were weighed preciously (tension helical balance Titan ) and body mass was determined. According to the body weight (b.w.), the effective dose of triclabendazole at 60 mg/kg b.w. was defined repeatedly for each specimen. To those animals the drug was delivered directly by S11

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia intraruminal administration, in two different methods of application by long needle and by oesophageal tube. Both methods of application required chemical immobilization of animal and we used a tiletamine-zolazepam and xylazine hydrochloride mixture (JANICKI et al., 2006). After the treatment, all deer were kept in a fenced enclosure for 30 days and then re-examined for the presence of F. magna eggs by faeces examination control. Results and discussion During the three years of the monitoring period (2001 2003) coprological analysis of the free-ranging deer population showed a remarkable percentage of positive faecal samples (Table 1). Table 1. Percentage of positive faecal samples of free-ranging deer population during three years period (2001-2003) of coprological monitoring in Baranja region Location Year 2001 Year 2002 Year 2003 No. Name Positive Samples Positive Samples Positive Samples 1. Aleksina 33% 31% 29% 2. Hranilište 43% 40% 37% 3. Dvorac I. 77% 67% 58% 4. Dvorac Ii. 80% 57% 44% 5. Zlatna Greda 30% 30% 27% 6. Oldobreda 53% 50% 47% 7. Čakanjska 61% 60% 55% 8. Ludoš I. 57% 53% 50% 9. Ludoš II. 41% 40% 38% 10. Bat Siget 57% 55% 51% 11. Vratić 35% 30% 29% 12. Ludoš II. 50% 48% 46% 13. Siget 26% 22% 20% 14. Bat I. 39% 37% 31% 15. Bat II. 58% 57% 52% 16. Bat III. 56% 54% 50% 17. Bat IV. 59% 58% 54% S12

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia On most collecting positions the percentage of positive samples was similar, while at position three (Dvorac I Gabrijela) and four (Dvorac II - Livada) we recorded a significant decline in the number of positive faecal samples over three years. The distribution of positive faecal samples presented in Fig. 1 showed a slightly decreasing tendency at all collecting spots, with a standard decrease in EPG (eggs per gram of faeces). 90% YEAR 2001 80% 70% YEAR 2002 YEAR 2003 60% 50% 40% 30% 20% 10% 0% 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Fig. 1. Distribution of positive faecal samples on 17 collecting spots during the monitoring period (2001-2003) in Baranja region Before group therapy in 2001 we recorded 143 positive samples (54.1%) from the total number of 264 examined faecal samples. In all positive samples 88 of them (61.5%) had EPG > 5, and in 55 samples (38.5%) we found EPG < 5. After the group therapy in 2003 we recorded 98 positive samples (41.0%) from total number of 239 faecal samples examined. In all positive samples 24 of them (24.5%) had EPG > 5, and in 74 samples (75.5%) we found EPG < 5. The same effect of triclabendazole therapy is reported by other authors (BALBO et al., 1989; QURESHI et al., 1989; PYBUS et al., 1991; QURESHI et al., 1994). Moreover, BALBO et al. (1987) reported a temporary reduction of EPG in red deer after treatment with rafoxanide (15 mg/kg) and 45% reduction of EPG after treatment with triclabendazole. All group therapies have to solve the same problem how to reach the proper dosage of antiparasitic preparation without occurrence of over-dosing in the dominant deer specimens. Another problem is the fact that F. magna infections are difficult to treat (PYBUS, 2001) because in the hosts organism flukes are not directly within the bile ducts, they are encapsulated in the S13

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia liver parenchyma and sufficient amounts of anthelminthics hardly get into the capsules. Triclabendazole was proved as the most effective drug, with equal efficiency on the mature and juvenile stages of large American fluke, but efficacy and dosage also depend of the method of drug administration. The method of offering triclabendazole in feed (per/oral application) as a group therapy, could be useful only for prophylactic purposes. In fenced area collective droppings were analyzed before and after the treatment with flukecides (Table 2). Table 2. Results of group coprological monitoring before and after therapy Examined Samples Positive Samp. Negative Samp. Before Therapy 22 (17 + 5 ) 15 + 3 (81.8%) 2 + 2 (18.2%) After Therapy 22 (17 + 5 ) 1 + 0 (4.5%) 16 + 5 (95.5%) Table 3. Values of EPG (eggs per gram) in hinds faeces before and after the therapy Number of F. magna eggs in faeces (EPG) No. Before treatment After treatment 1. 30 0 2. 9 0 3. 5 0 4. 250 0 5. 3 0 6. 8 0 7. 0 0 8. 10 0 9. 160 0 10. 120 0 11. 7 0 12. 0 0 13. 6 0 14. 4 0 15. 2 0 16. 30 0 17. 300 3 S14

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia Before the therapy F. magna eggs were detected in 14 samples (87.5%) from hinds. After therapy only one sample of hinds contained F. magna eggs (6.25%) in very low concentration (EPG < 2). Individual coprological tests showed that six hinds have numerous eggs of F. magna (EPG > 10) in faecal samples (Table 3). These hinds were treated one by one and results of individual therapy show that Triclabendazole at dosage of 60 mg/kg b.w. is very effective in European red deer against reproductive active F. magna specimens (Table 3). The efficacy of Triclabendazole in individually treated hinds was high (94.75% samples were free of F. magna eggs) and reduction of EPG was significant. Conclusions Health management of autochthonic red deer in Croatia has to implement System of integrated control for large American fluke. This system includes five main points: 1. Up-to-date coprological monitoring and permanent, complete health monitoring 2. Group preventive therapy 3. Individual therapy 4. Quarantine measures (considering prepatent period of min. 30 days) 5. Interrupting the parasite s life cycle Due to numerous limitations which affect the natural biotope with interventions on the intermediate hosts (snails Lymnea spp.) the last point of the protocol had to be skipped, so first four points had to achieve successful control of fascioloidosis. Strategically the most important task is to prompt coprological monitoring in lowland wet habitats where F. magna persists. In the Croatia group preventive therapy achieved success in restricting the F. magna infection exclusively to red deer, despite increased contacts with other wild and domestic ruminants (fallow deer, cattle, and sheep) and the population explosion of wild boar in the Baranja region. In other endangered countries F. magna has spread to other domestic (HALL, 1912; PRICE, 1953; CAMPBELL and TODD, 1954; FOREYT and TODD, 1976; STROMBERG et al., 1985) and wild ruminants (KOTRLA and KOTRLY, 1977; KOTRLY and KOTRLA, 1980). While treatment of the free-ranging deer population has to be resumed as preventive therapy, individual treatment is the only reliable method for suppressing F. magna infection (JANICKI et al., 2005). Of course, this therapy includes handling and chemical immobilisation of treated animals, so it cannot be used in every day practice. Due to these limiting factors of individual treatment, such therapy has to be restricted to animals subjected to transport or translocation. S15

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia References BASSI, R. (1875): Sulla cachessia ittero-verminosa, o marciaia dei cervi, causata dal Distoma magnum. Med. Vet. 4, 497-515. BALBO, T., P. LANFRANCHI, L. ROSSI, P. G. MENEGUZ (1987): Health management of a red deer population infected by Fascioloides magna. Atti Fac. Med. Vet. Torino 33, 1-13. BALBO, T., L. ROSSI, P. G. MENEGUZ (1989): Integrated control of Fascioloides magna infection in northern Italy. Parassitologia 31, 137-144. CAMPBELL, W. C., A. C. TODD (1954): Natural infections of Fascioloides magna in Wisconsin sheep. J. Parasitol. 40, 100. ERHARDOVA, B. (1961): Fascioloides magna in Europe. Helminthologia 3, 91-106. ERHARDOVA-KOTRLA, B. (1971): The occurrence of Fascioloides magna (Bassi, 1875) in Czechoslovakia. Czechoslovak Academy of Science, Prague, Czechoslovakia, pp 155. FOREYT, W. Y., A. C. TODD (1976): Development of the large American fluke, Fascioloides magna in white-tailed deer, cattle, and sheep. J. Parasitol. 62, 26-32. FRANCIS, M. (1891): Liver flukes. Tex. Agricul. Exper. Stat. Bull. 18, 123-136. HALL, M. C. (1912): Our present knowledge of the distribution and importance of some parasitic diseases of sheep and cattle in the United States. United States Department of Agriculture, Bureau of Animal Industry, Circular 193. JANICKI, Z., D. KONJEVIĆ, K. SEVERIN (2005): Monitoring and treatment of Fascioloides magna in semi-farm red deer husbandry in Croatia. Vet. Res. Comm. 29 (Suppl. 2), 83-88. JANICKI, Z., D. KONJEVIĆ, A. SLAVICA, K. SEVERIN (2006): Reversible chemical immobilization of wild red deer (Cervus elaphus L.) using tiletamine zolazepam xylazine hydrochloride mixture. Vet. arhiv 76, 237-244. KOTRLÁ, B., A. KOTRLY (1977): Helminths of wild ruminants introduced into Czechoslovakia. Folia Parasitol. 24, 35-40. KOTRLY, A., B. KOTRLÁ (1980): Der Einfluss der Lebensbedingungen des Schalenwildes auf das Parasitenvorkommen. Angew. Parasitol. 21, 70-78. MARINCULIĆ, A., N. DŽAKULA, Z. JANICKI, Z. HARDY, S. LUČINGER, T. ŽIVIČNJAK (2002): Appearance of American liver fluke (Fascioloides magna, Bassi, 1875) in Croatia a case report. Vet. arhiv 72, 319-325. MULVEY, M., J. M. AHO, C. LYDEARD, P. L. LEBERG, M. H. SMITH (1991): Comparative population genetic structure of a parasite (Fascioloides magna) and its definitive host. Evolution 45, 1628-1640. PFEIFFER, H. (1983): Fascioloides magna: erster Fund in Österreich. Wien. Tierärztl. Monatschr. 70, 168-170. PRICE, E. W. (1953): The fluke situation in American ruminants. J. Parasitol. 39, 119-134. PYBUS, M. J., D. K. ONDERKA, N. COOL (1991): Efficacy of triclabendazole against natural infections of Fascioloides magna in wapiti. J. Wildl. Dis. 27, 599-605. PYBUS, M. J. (2001): Liver flukes. In: Parasitic Diseases of Wild Mammals. (Samuel, W. M., M. J. Pybus, A. A. Kocan, Eds.). Manson Publishing/The Veterinary Press, London, pp. 121-149. S16

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia QURESHI, T., T. M. CRAIG, D. L. DRAWE, D. S. DAVIS (1989): Efficacy of triclabendazole against fascioloidasis (Fascioloides magna) in naturaly infected white-tailed deer (Odocoileus virginianus). J. Wildl. Dis. 25, 378-383. QURESHI, T., D. L. DRAWE, D. S. DAVIS, T. M. CRAIG (1994): Use of bait containing triclabendazole to treat Fascioloides magna infections in free ranging white-tailed deer. J. Wildl. Dis. 30, 346-350. RAJSKY, D., A. PATUS, K. BUKOVJAN (1994): The first finding of Fascioloides magna (Bassi, 1875) in Slovakia. Slov. Vet. Čas. 19, 29-30. SALOMON, S. (1932): Fascioloides magna, bei deutschem Rotwild. Berl. Tierärztl. Wochenschr. 48, 627-628. SLUSARSKI, W. (1955): Studia nad europejskim przedstawicielami przywry Fascioloides magna (Bassi, 1875) I. Ponowne wykrycie inwazji u jeleni na Slacsku. Acta Parasitol. Pol. 3, 1-59. STILES, C. W., A. HASSALL (1894): The anatomy of the large American fluke (Fascioloides magna) and a comparison with other species of the genus Fasciola. J. Comp. Med. Vet. Arch. 15, 161-178, 225-243. STROMBERG, B. E., G. A. CONBOY, D. W. HAYDEN, J. C. SCHLOTTHAUER (1985): Pathophysiologic effects of experimentally induced Fascioloides magna infection in sheep. Am. J. Vet. Res. 46, 1637-1641. SZTOJKOV, V., G. MAJOROS, K. KAMAN (1995): Szarvasokban ebo nagy amerikai majmetely (Fascioloides magna) megjelenese Magyarorszagon. Mag. Allat. Lap. 50, 157-159. SWALES, W. E. (1935): The life cycle of Fascioloides magna (Bassi, 1875) the large liver fluke of ruminants in Canada. Can. J. Res., Series D, Zoological Sciences 12, 177-215. VARADY, M. (1993): Comparison of two methods for counting nematode eggs. Veterinàřstvi 43, 342-343. Received: 15 August 2005 Accepted: 4 April 2006 SLAVICA, A., T. FLORIJANČIĆ, Z. JANICKI, D. KONJEVIĆ, K. SEVERIN, A. MARINCULIĆ, K. PINTUR: Liječenje fascioloidoze (Fascioloides magna, Bassi, 1875) u jelena običnog (Cervus elaphus L.) u otvorenom i ograđenom prostoru na području istočne Hrvatske. Vet. arhiv 76, S9-S18, 2006. SAŽETAK Nakon što je pojava velikoga američkoga metilja (Fascioloides magna) prvi puta potvrđena na tlu Republike Hrvatske tijekom 2000. godine, poduzete su prve mjere za suzbijanje fascioloidoze. Skupno liječenje slobodno živućih jelena antitrematodnim sredstvima provođeno je tijekom tri godine (2001. 2003.), dok je pojedinačno liječenje u ograđenom prostoru izvedeno tijekom zimskih mjeseci 2002. godine. Jelenima koji slobodno žive u prirodnim uvjetima ponuđena je tijekom zime kombinacija triklabendazola i mineralne soli, u dozi od 60 mg djelatne tvari po kilogramu tjelesne mase jelena. Peletirana hrana izlagana je na hranilištima S17

A. Slavica et al.: Treatment of fascioloidosis (Fascioloides magna, Bassi, 1875) in free ranging and captive red deer (Cervus elaphus L.) at eastern Croatia jelenske divljači dvokratno, s razmakom od sedam dana. Jeleni u ograđenom prostoru liječeni su pojedinačno na način da im je triklabendazol apliciran izravno u burag pomoću sonde ili specifične dugačke igle. Koprološka pretraga napravljena je trideset dana nakon posljednjega liječenja jelenske divljači. Pozitivne rezultate pretrage, odnosno pronalazak jajašaca velikoga američkoga metilja u izmetu slobodno živućih jelena utvrdili smo u relativno visokom postotku (20 do 80 %). U jelena s ograničenom slobodom kretanja (ograđeni uzgoj) zabilježili smo vrlo visoku učinkovitost triklabendazola, tako da je nakon terapije 95,5 % pregledanih uzoraka jelenskog izmeta bilo negativno na prisutnost jajašaca velikoga američkoga metilja. Ključne riječi: jelen obični, veliki američki metilj, Fascioloides magna, antiparazitska terapija, triklabendazol S18