Prevalence of amphistomes of cattle in Thailand

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Hungarian Natural History Museum Hungarian Society of Parasitologists Parasit, hung., 29-30: 27-32, 1996-1997 Prevalence of amphistomes of cattle in Thailand p. PRASITIRAT 1, T. CHOMPOOCHAN 1, S.

1 Hungarian Natural History Museum Hungarian Society of Parasitologists Parasit, hung., 29-30: 27-32, Prevalence of amphistomes of cattle in Thailand p. PRASITIRAT 1, T. CHOMPOOCHAN 1, S. NITHIUTHAI 2, s. WONGKASEMJIT 1, T. PUNMAMOAMG 1, P. PONGRUT 1, S. CHINONE 3 and H. ITAGAKI NIAH, Käset Klang, Jatujuk, Bankok, Thailand Faculty of Veterinary Science, Chulalongkorn University Bankok, Thailand 3 Department of Parasitology, Azabu University, Kanagawa Ken, Japan (Received 23 March, 1997) Abstract: An epidemiological investigation of amphistome flukes of cattle was carried out in Thailand from 1991 to 1995 by examination of faecal samples and the presence of flukes in the forestomachs. During the period of 1992 to 1995, 4,122 and 3,087 faecal samples were collected from dairy and beef cattle in 17 and 2 provinces, respectively. Faecal examinations were performed by the beads technique and flotation method. The results revealed that the prevalence of amphistomes was obviously higher in beef cattle than in dairy cattle. The prevalence of infection in dairy cattle was 35.8, 14.0, 17.4 and 21.1% in 1992, 1993, 1994 and 1995, respectively. Eggs per gram of faeces (EPG) count ranged from 1 to 1,896. Other concurrent parasitic infections were caused by Fasciola spp. (2.9, 0.3, 3.8 and 4.1% in the years of study, respectively), Moniezia spp.(0.4, 0.1, 0.1, 0.9%), gastrointestinal strongyles (4.7, 2.8, 3.0, 5.7%), coccidia (0.6, 1.3, 0.4,0.4%) and other parasites. The prevalence of amphistomes in beef cattle was 74.4, 72.7, 63.3 and and 80% in 1992, 1993, 1994 and 1995, respectively, with EPG counts ranging from 1 to 2,152. Other current parasitic infections were due to Fasciola spp. (21.2, 14.6, 13.1, 3%), Moniezia (0.5, 2.4, 2, 1%), gastrointestinal strongyles (16.3, 7.3, 16.6, 42%), coccidia (1.5, 0, 3.8, 2.3%), and other parasites. Adult amphistome flukes were looked for at the abattoir in Nonthaburi Province from 1991 to 1995, and the prevalence of was found to be 46, 41, 39, 30 and 50% in those years, respectively. Key words: Amphistomes, cattle, prevalence, Thailand INTRODUCTION The occurrence of infections caused by adult flukes of the superfamily Paramphistomoidea has been investigated in sheep, goats, cattle and buffaloes in many countries of the world. The disease, amphistomosis, caused by massive infection of the small intestine by immature amphistomes, and no information is available on the association of adult flukes with the clinical signs. Amphistomosis causes sporadic outbreaks characterised by acute

gastroenteritis with high morbidity and mortality rates, particularly in young animals, and is mainly confined to Africa, Asia, Australia, Eastern Europe and Russia (Boray 1959, Horak 1962, Boray

2 gastroenteritis with high morbidity and mortality rates, particularly in young animals, and is mainly confined to Africa, Asia, Australia, Eastern Europe and Russia (Boray 1959, Horak 1962, Boray 1969, Horak 1971, Gupta et al. 1978, Nikitin 1979, Hanna et al. 1988). It has been considered that all cases of amphistomosis are caused by certain species of the parasite. In Australia and New Zealand the species of amphistomes affecting cattle and sheep are Calicophoron calicophorum and Paramphistomum ichikawai (Brotowidjoyu and Copeman 1979). In Asia, according to information available from India and Ceylon, intestinal amphistomosis in cattle, buffalo, sheep and goat has been identified. The flukes most frequently responsible for the disease are Gastrothylax crumenifer, Cotylophoron cotylophorum, Paramphistomum cervi, Fishoederius elongatus and Explanatum explanatum (Boray 1959, Katiyar and Garg 1965, Rolfe and Boray 1987, Hanna et al. 1988, Sey 1989). Brotowidjoyu and Copeman (1979) assessed the prevalence and intensity of immature and mature flukes in cattle at abattoirs in North Queensland, using high, moderate and low intensity categories of > 20, and < 10, respectively. The species of amphistomes obtained was Calicophoron calicophorum. In Thailand, the occurrence of amphistome infections has been reported (Chethanon et al. 1985). The objective of this study is to describe the general trend in the prevalence rates of amphistome infections in beef and dairy cattle in Thailand between 1991 and MATERIALS AND METHODS Identification of amphistome infections by detection of eggs in the faeces In the period from April 1992 to August 1995, faecal samples were obtained from 4,122 dairy cattle and 3,087 beef cattle in 17 (Bankok, Chaing mai, Nonthaburi, Prachin buri, Nakhorn ratchasima, Saraburi, Ratchaburi, Nakhorn nayok, Phetchaburi, Ayuthaya, Suphanburi, Chonburi, Nakhonpathom, Samuttsakhon, Chanthaburi, Srakaeo, Singhburi) and 2 (Singhburi, Chaînât) provinces of Thailand as illustrated in Fig. 1. Faecal examination was performed by the beads technique (Taira 1985) to determine the prevalence rate of amphistome infections and by simple flotation method to detect concurrent infections. Determination of amphistome infections by detection of adult flukes in the rumen A total of 3,000 beef cattle were examined for rumen flukes from June 1991 to November 1995 at local abattoirs from 7 provinces (Sukhothai, Nakhonpathom, Prachuapkhirikhan, Lopburi, Chonburi, Phetchaburi, Rayong) as illustrated in Fig. 1. to determine the prevalence of adult amphistome infections. Fig. 1. Map of Thailand and study areas of amphistome infections in dairy and beef cattle

RESULTS The prevalence of parasitic infections in examination in the period between 1992 and obviously higher in beef cattle than in dairy animals comprised protozoan oocysts and eggs of nematodes,

3 RESULTS The prevalence of parasitic infections in examination in the period between 1992 and obviously higher in beef cattle than in dairy animals comprised protozoan oocysts and eggs of nematodes, cestodes and trematodes including amphistomes. A higher percentage of beef cattle was found to be infected by amphistomes as compared to dairy cattle (Figs 3 and 4). The prevalence of amphistome infection ranged from 14.0 to 35.8% in dairy cattle while it was as high as 63.3 to 80.0% in beef cattle, and the eggs per gram of faeces (EPG) ranged from 1-1,896 and 1-2,152, respectively. The amphistome-infected animals were concurrently infected with other parasites such as Fasciola spp., strongyles, Moniezia sp. and coccidia (Figs 5 and 6). Of these parasites, liver flukes and strongyles showed a high prevalence throughout the years of study. In dairy and beef cattle without amphistome infection the prevalence of strongyles was rather high (Figs 7 and 8). Concurrent parasites except Strongyloides sp. and Trichuris spp. found in these groups of cattle were similar to those found in the animals infected by amphistomes. The prevalence of adult amphistomes in beef cattle examined at an abattoir from 1991 to 1995 was 46, 41, 39, 30 and 50%, respectively (Fig. 9). dairy and beef cattle, as determined by faecal 1995, is shown in Fig. 2. The prevalence was cattle. Parasites found in the faeces of those % Dairy cattle S Beef cattle Fig. 2. Prevalence of parasitic infections in dairy and beef cattle between 1992 and 1995 amphistomes other parasites amph. + other parasites Fig. 3. Prevalence of amphistome and other concurrent parasitic infections in dairy cattle between 1992 and 1995 DISCUSSION Muangyai (1989) reviewed the parasites of cattle and buffaloes and listed economically important parasites wich included amphistomes. Intestinal amphistomosis has been described as an important disease of young stock in endemic areas (Boray 1959, Horak 1962, Boray 1969, Hanna et al. 1988, Sey 1989). Clinical disease usually develops only when there are massive numbers of immature amphistomes parasitic in the duodenum, causing acute enteritis. The diagnosis may be easily missed because the immature flukes, which cause the clinical signs, do not yet lay eggs. The adult egg-laying flukes appear to exert very little effect on the host animals, and eggs can be usually detected by the faecal sedimentation method.

4 Fig. 4. Prevalence of amphistome and other parasitic infections in beef cattle from 1992 to 1995 Fig. 5. Prevalence of concurrent parasitic infections found in amphistomeinfected dairy cattle from 1992 to 1995 Fig. 6. Prevalence of concurrent parasitic infections found in amphistomeinfected beef cattle from 1992 to 1995 Fig. 7. Prevalence of other parasitic infections found in dairy cattle not infected by amphistomes between 1992 and 1995 Fig. 8. Prevalence of other parasitic infections found in beef cattle not infected by amphistomes between 1992 and 1995 Fig. 9. Prevalence of adult amphistome infection in beef cattle examined at abattoirs between 1991 and 1995 A = Amphistomes, Lf = Liver fluke, S = Strongyles, C = Coccidia, M = Moniezia, T = Trichuris, St = Strongyloides

The results presented here show that the prevalence of amphistome infection was rather high throughout the experiment. The maximum EPG was 2,152.

5 The results presented here show that the prevalence of amphistome infection was rather high throughout the experiment. The maximum EPG was 2,152. The maximum prevalence was clearly higher in beef than in dairy cattle. The difference in prevalence may be due to ingestion of amphistome metacercariae by dairy cattle during grazing on less contaminated pastures. Contrarily, the high prevalence of amphistomes in beef cattle indicates that the animals may be kept on heavily infected pastures where the intensity of egg contamination is high and snail intermediate hosts occcur in large numbers. Attempts to prevent grazing cattle from becoming infected by amphistomes are economically unfeasible, as almost all beef cattle were found to be infected and since an unusual combination of environmental conditions may lead to an outbreak of the disease. Since the disease is not often diagnosed, economic losses associated with amphistomosis are still unrecognised and underestimated in Thailand. In many fatal cases the immature flukes could not be found and identified due to their very small size. Young animals originating from endemic areas should be inspected carefully at postmortem examination. Also, the detection of intermediate host snails from pastures or water sources may be a useful aid to diagnosis. ACKNOWLEDGEMENT The authors would like to thank the farmers and the members of NIAM for their help in sample collection. Thanks are due to R. Inthararuksa, P. Tanajalearnwat and L. Sukteenthai for assistance and to Dr. S. Soonthornchad for his technical help with the figures. Prasitirat, P.,Chompoochan, T., Nithiuthai, S., Wongkasemjit, S., Punmamoamg, T., Pongrut, P., Chinone, S. and Itagaki, IL: Thaiföldi szarvasmarhák amphsstoma fertőzöttsége Thaiföldi szarvasmarhák amphistoma fertőzöttségét vizsgálták a szerzők 1991 és 1995 között bélsárminták és előgyomortartalom adatok alapján. A hízómarhák amphistomákkal való fertőzöttsége erőteljesebb volt, mint a tejelő állományoké. További parazitás fertőzöttségét okoztak Fasciola és Moniezia fajok, strongilidák ill. coccidiumok. REFERENCES Boray, J.C. (1959): Studies on intestinal amphistomosis in cattle. Aust. Vet. J. 35: Boray, J.C. (1969): Studies on intestinal paramphistomosis in sheep due to Paramphistomum ichikawai Fukui, Vet. Med. Rev. 4: Brotowidjoyu, M.D. and Copeman, D.B. (1979): Abattoir survey of bovine paramphistomiasis in North Queensland. Aust. Vet. J. 55: 402. Chethanon, U., Ausavamatha, P. and Piriyayon, S. (1985): Parasitological survey of cattle in the south of Thailand. Proceedings of the 4th Annual Livestock Conference, 3-5 July Department Livestock Development, p Gupta, P.P., Singh, B. and Dutt, S.C. (1978): A note on amphistomiasis in an adult buffalo. Indian Vet. J. 55: 491^192.

6 Hanna, R.E.B., Williamson, D.S., Mattison, R.G. andnizami, W.A. (1988): Seasonal reproduction in Paramphistomum epiclitum and Gastrothylax crumenifer, rumen paramphistomes of the Indian water buffalo and comparison with the biliary paramphistome G. explanatum. Int. J. Parasitol. 18: Horak, I.G. (1962): Studies on paramphistomiasis. Part IV. Modified critical and controlled anthelmitic tests on the conical fluke Paramphistomum microbothrium - J. S. Afr. Vet. Med. Ass. 33: Horak, I.G. (1971): Paramphistomiasis of domestic ruminants Adv. Parasitol. 9: Katiyar, R.D. and Grag, R.K. (1965): Comparative efficacy of various chemoterapeutic agents in amphistomiasis. Indian Vet. J. 42: Muangyai, M. (1989): Parasitic diseases of buffalo calves and the control in Thailand. Buffalo J. 5: Nikitin, V.F. ( 1979) : The course of acute enzootic amphistomiasis in calves in the lower Volga region. Helminthol. Abst. Ser. A. 48: 463. Rolfe, P.F. and Boray, J.C. (1987): Chemotherapy of paramphistomosis in cattle. Aust. Vet. J. 64: Sey, O. (1989): A review of chemotherapy of paramphistomosis of domestic ruminants in Europe. Parasit, hung. 22: Taira, N. (1985): Sieving technique with the glass bead layer for detection and quantitation of Fasciola eggs in cattle feces. Jpn. Agric. Res. Quart. 18:

Detection of Gastrointestinal Helminthic and Protozoan Infections in Diarrhoeic Goats

Detection of Gastrointestinal Helminthic and Protozoan Infections in Diarrhoeic Goats International Journal of Current Microbiology and Applied Sciences ISSN: 2319-7706 Volume 6 Number 4 (2017) pp. 801-805 Journal homepage: http://www.ijcmas.com Original Research Article https://doi.org/10.20546/ijcmas.2017.604.100