Prevalance of Ovine Lungworm Infection in and Around Kombolcha, Ethiopia

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1 Acta Parasitologica Globalis 9 (1): 7-3, 018 ISSN IDOSI Publications, 018 DOI: /idosi.apg Prevalance of Ovine Lungworm Infection in and Around Kombolcha, Ethiopia Etsegenet Fentaw, Misgana Duguma and Dereje Abera Wollega University, School of Veterinary Medicine, Nekemte, Ethiopia Abstract: A cross-sectional study was carried out in and around Kombolcha district of north eastern Ethiopia, from November, 015 to April, 016 to determine the prevalence and the predominant species of lungworms infection in sheep and to relate lungworm infection with different risk factors in the study area. Fecal samples were randomly collected from 407 sheep in and around Kombolcha town and laboratory examination was done using Modified Baerman technique. The overall prevalence of lungworm infection in the study area for this current study was 40% (163/407). The lungworm parasite species identified by the fecal sample examination were Muelleries capillaries, Dictyocaulus filaria and Protostrogylus rufescens, with prevalence rate of 44.8% (73/163), 30.1% (49/163), 9.8% (16/163), respectively and also mixed infection 15.3% (5/163) was present. Among those, M. capillaries were more prevalent in study area than D. fillaria and P. rufescens. The sex of animals in study area did not show significant association with the prevalence of lungworm infection (P= 0.68). The prevalence rate of lungworm parasite was higher in adult 46.7% (107/9) and lower in young animals 31.46% (56/178). This indicates there is a significant association between the prevalence of lungworm infection and age of sheep (P = 0.00). The body condition of animals was also found to be significantly associated to the prevalence of lungworm infection (P<0.001) and highest in animals which have poor body conditions 7.% (65/90) than medium and good scores. Management system was another factor found to be significantly associated (P= 0.001) with high prevalence rate under extensive management system 46.7% (114/44) than semi-intensive Management system 30.06% (49/163) with lungworm parasite infection. The present study shows that lungworm infection was one problem of sheep in the study area. Thus, control and prevention of lungworm infection in the study area need due attention. Key words: Ethiopia Kombolcha Lung warm Prevalence Sheep INTRODUCTION short generation cycles and high reproductive rates which lead to high production efficiency and significant role in Africa hosts 05 and 174 million sheep and goats provision of food and generation of cash income. They representing 17 and 13 percent of the world total small serve as a living bank for many farmers, closely linked to ruminant population, respectively. The population of the social and cultural life of resource poor farmers and small ruminants in sub-saharan Africa is estimated to be provide security in bad crop years [3]. 74 million [1]. Currently, the population of livestock Although sheep represent a great resource for the found in Ethiopia is estimated to be 53.4 million cattle, 5.5 nation, the productivity per animal is low and therefore million sheep and.78 million goats. Livestock are an the rich potential from the sector is not efficiently important component of nearly all farming systems in exploited. Sheep diseases, poor management and lesser Ethiopia and provide draught power, milk, meat, manure, efforts provided to improve the performance of the hides, skins and other products []. animals are to be responsible for the reduced productivity Sheep has many purposes as major sources of [4]. In this regard, diseases due to parasites take the lion's livelihood and contribute to the sustenance of landless, share in limiting the productivity of these animals all over smallholder and marginal farmers especially to the poor in the World. This is especially true in many tropical and the rural areas throughout the developing countries and subtropical regions. Small ruminants under intensive and also they are very important for resource poor smallholder extensive production systems are susceptible to the systems of rural Ethiopia due to their ease of management, effects of wide range of helminthes [5]. Corresponding Author: Misgana Duguma, Wollega University, School Of Veterinary Medicine, P.O. Box: 395, Nekemte, Ethiopia. 7

2 Acta Parasitologica Globalis 9 (1): 7-3, 018 The occurrence of lungworms is associated with Ababa with '49'' N latitude and ' 46''0E different nutritional status, level of immunity, rain fall, longitude at an altitude of 1840 meter above sea level humidity, altitude, temperature, feeding habit of small (m.a.s.l). The kombolcha town experiences a bi-modal ruminants, the type of plants used for animal feed, the use rainfall, the short rainy season occurs usually from March of marshy area for grazing, animal management system, 15 to May. The minimum and maximum mean annual the presence of longer time wet or rainy warmer seasons rainfall in and around kombolcha ranges from 750 to and the presence of suitable intermediate hosts in the area 900mm. The average minimum and maximum daily are the preconditions for the development of lungworm temperature during short and long rains are11.7oc and infection [6]. Respiratory diseases resulting from 3.9oc respectively and the relative humidity of the area helminthes parasites are of a great economic concern in varies from 3.9% to 79%. The topography of zone sheep production in the highlands of Ethiopia where generally is marked by the presence of numerous sheep are important livestock units. Dictyocaulidae and mountains, plateaus, hilly and sloppy area and river were certain Metastrongylidae are known to exist in East Africa present, the farming system in the area is mixed farming (Ethiopia, Kenya and Tanzania) and the South Africa [7]. and sheep are the dominant animal species kept by In highland area of Ethiopia respiratory lungworm farmers. The grazing land comprises water logged areas, parasites are the most common cause of high morbidity forest margins, hill tops, mountain sides, stony land and and mortality rates of sheep [8, 9]. Lung worm infection is road sides [1]. infection of lower respiratory tract, resulting in bronchitis or pneumonia or both. These lungworms particularly Study Animals: The study animals were sheep of all age Dictyocaulus filarial can suppress the immunity of the and sex group which come to Kombolcha veterinary clinic respiratory tract and causes death, poor weight gain or for treatment and vaccination purpose during the study loss of body weight as well as greatly affects the potential period and also sheep found at different farms in the town productivity of sheep in the areas where it is prevalent and rural households. [10]. Control of these parasites is therefore essential for releasing the potential of sheep production. For proper Sampling Method and Sample Size: The sample was control to be carried out knowledge of parasitic diseases selected by using simple random sampling based up on and their dynamics must be understood to lay down rigid the different categories like age, sex, body condition and rules for their control which are applicable to all regions. management system to take the required sample. The For this reason, a study of epidemiology of each parasitic sample size was decided based on formula described by disease should be limited to small areas [11]. To increase Thrusfiled [13]. Sample size was calculated using 50% the potential of sheep production and to get the maximum expected prevalence, 5% absolute precision and 95% benefit from sheep, prevention and control of lungworm confidence interval and the calculated total sample size is very important. Although cases of lungworm parasites was 384. have a great impact on livestock productivity, there is lack of relevant information on the magnitude, distribution and n = [1.96 pexp (1-pexp)]/d risk factors of lungworm infection of sheep in and around = [(1.96) 0.5(1-0.5)] (0.05) South Wollo, Kombolcha. Therefore the objectives of this = 384 but the total sample collected was increased to 407 study were: to increase precision and accuracy To estimate the prevalence of lungworm parasites and identify the species of the lungworm infection circulating in study area. To determine risk factors of lungworm infection in sheep in the study area. MATERIALS AND METHODS Study Area: The study was conducted at Kombolcha Town, which in found in South Wollo Administrative Zone of Amhara National Regional State in North Eastern Ethiopia. The study area is located 376 km north of Addis where, n= sample size required 1.96 =the value of Z at 95% confidence interval Pexp =e xpected prevalence d = desired absolute precision Study Methodology Collection and Transportation of Fecal Sample: Individual animals were selected randomly from Kombolcha veterinary clinic and different farms. Accordingly age, sex, management system and body conditions of the animals were recorded during sampling. 8

3 Acta Parasitologica Globalis 9 (1): 7-3, 018 Fecal samples were collected directly from the rectum of <1 year) as described by Dar et al. [17] (Annex 4). all selected animals using disposable gloves and stored in Management system of the animals was classified as semi plastic bag under the ice box and then taken to intensive and extensive as described by Terefe et al. [18]. Kombolcha Regional Veterinary Laboratory for processing. Each plastic bag was properly labeled Data Management and Analysis: The data was entered corresponding to the animal [14]. and manage in Microsoft Excel. All the data analysis was done by Statistical Package for Social Science (SPSS) soft Fecal (Coprological) Examination: Using Barman ware version 0. Descriptive statistics such as technique 5 g of fresh feces was weighed from each percentages and frequency distributions were used to sample. The larvae and enclosed gauze fixed on to describe the data. The association of different risk astringe rode were submerse in a clean glass tube which factors with the prevalence disease was computed by was filed with warm water left for 4 h and the sediment using Chi - square ( ) test. were transferred to the Petri dish for examination of first stage larvae (L1) under lower power of microscope after RESULTS siphoning off the supernatant. Finally if a larvae was identified a drop of 1% iodine solution was added to the From a total of 407 sheep examined for lungworm slide to immobilized the larvae as soon as the larvae are infection 40.0% (163/407) were positive for one or more of detect under microscope to identify the species of the the lungworm parasites. Mullerus capillaries, larvae by morphological feature of the larvae and if not Dyctyocaulus fillaria, Protostrongylus refuse were identified under microscopes, the examined samples was identified. Among those, M. capillaries 44.8% (73/163) registered as negative for lung worm infection. In both were more prevalent in study area than D. fillaria 30.1% cases, the result that was obtained for each sample was (49/163) and P. refuse 9.8% (16/163) and also mixed recorded to their corresponding specific animals [15]. infection 15.3% (5/163) was observed. The higher prevalence rate was encountered in sheep with poor body Definition of Variables condition 7.% (65/90) than those have medium 33.6% Body Condition Scoring (BCS): Three scores of body (41/1) and good 9.3% (57/195) body condition and condition was used (Poor, medium and good) as with statistically significant association ( =51.05, P described by Gatenby [16] and it was indicated in Annex <0.001). The prevalence rate of lungworm infection was 5. Age was grouped in to two (Adult >1 year and Young found to be higher under extensive management system Table : Prevalence of lung warm infection on the basis of lung warm species identified Lungworm species No examined Prevalence (%) Mullerus capillaries Dyctyocaulus fillaria Protostrongylus refuse Mixed infection Total Table 3: Prevalence of Lungworm infection in sheep and associated risk factors in the study area Risk factor No. of tested animal Positive animal Prevalence (%) p. value Sex Female Male Age Young Adult Body condition Poor <0.001 Medium % Good % Management Extensive % Semi-Intensive % 9

4 Acta Parasitologica Globalis 9 (1): 7-3, % (114/4) than in semi-intensive management contamination of pasture and restrict mobility of the system 30.06% (49/163) and showed statically significant young animal, so the adult animals have the heaviest association (x = 11., P <0.001). The prevalence rate of infection and the highest prevalence [1]. lungworm infection did not show statistically significant With regard to the species of lungworms, it was association with sex of the animals (x = 0., P = 0.068). In observed that M. capillaries were the highest prevalent comparison of age groups the prevalence rate of species in the study area followed by D. filaria and lungworm infection shows high prevalence rate in adult P. rufescens. This finding is supported by NMSA [1] in 46.7% (107/9) than young 31.46% (56/178) with Dessie Zuria District, Sissay [8] in and around Bahir Dar significant association (x = 9.7, P = 0.00) (Table ). and Mezgebu [9] in Addis Ababa. In contrast to this As indicated following table, the three species of finding, others [30] in Tabriz, Mekonnen [31] in Gonder, ovine lungworm infection (M. capillaries, D. fillaria and Mihreteab and Aman P. refuse) and mixed infection were identified. [0] Tiyo Ditrict, Dawit [3] in Jimma zone and Nuraddis and Yared [33] in Mekelle who reported DISCUSSION D. filaria to be the highest prevalence in their survey. The reason for this high prevalence of M. capillaries In this study, the overall prevalence rate of lung warm compared with Dictyocaulus could be partly attributable infection identified by using coporological examination to its wide range of intermediate host and the ability of was found to be 40% (163/407). This finding was lower larvae to over winter in the Mollusks. Additional factors than the previous report by Hasen et al. [19] in Assela, which play a part in ensuring the endemicity of the worm Mihreteab and Aman [0] in Tiyo district, Netsanet [1] are, first, the ability of L1 (First larval stage) to survive for in Debre Birhan and Basaznew et al. [] in Dessie Zuria months in fecal pellets and secondly, the persistence of district with the prevalence rate of 55.1%, 57.1 %, 73.75% the L3 (Third larval stage) in the intermediate host for the and 43.33% respectively. But the current prevalence was life time of the Mollusks [34]. higher than 8.6% prevalence in Mekedella [3].7% There was a significant difference in lungworm prevalence in and around Bahirdar [4] and 1.7% infection (P =0.001) between the two management prevalance in Tigray [5] and 18.16% prevalence in Bahir systems. That is, the prevalence was significantly higher Dar [6]. lungworm under extensive management system 46.7% The variation may be due to the difference in agro (114/44) than those kept under semi-intensive ecological zones of the study areas which may favors or management system 30.06% (49/163) this finding is in suppress the survival of the larvae of the lungworms. It consistent with the report of Thru filed [13] in North might be also due to the nutritional status of the animals Gondar. In this study, sheep under extensive management in the respective study areas which can influence level of system had more infection than those kept under immunity to be infested by lung worms. The topography semi-intensive management system. The reason for this of the area might also highly influence the prevalence by could be increased cultivation of land which restricts harboring the intermediate host [6]. animals on communal grazing land so that large numbers In this study, there was no significant difference of the animals are kept together. This could increase the ( = 0., P = 0.68) in the prevalence of lungworm degree of pasture contamination leading to higher infection between male 41.3% (74/179) and female 39.03% prevalence rate. Management practice such as provision (89/8) animals, but the prevalence of male animal of ample nutrition increases the resistance of the host slightly greater than female animal. This finding was under the semi-intensive system, contrary to this different from previous findings by Tewdrose [4] in and mal-nutrition which reduces the host-parasite response around Bahirdar and Gebreyohannes [3] in Mekedella. and favors the fecundity of the parasites that allows the This might be due to sample size and study methodology animals for continuous larvae exposure under extensive difference. system [35]. The prevalence of lungworm infection in adult sheep The prevalence was significantly highest in animals 46.7% (107/9) was significantly greater than ( =9.7, which have poor body conditions 7.% (65/90) than in P = 0.00) in young sheep 31.46% (56/178), this finding those have medium 33.3% (41/1) and good 9.3% agree with Basaznew et al. [] and Bekeleand Abu [7]. (57/195) body conditions. The findings of the present This might be the adult animal highly exposure to the studies was in line with Mihreteab and Aman [0] who 30

5 Acta Parasitologica Globalis 9 (1): 7-3, 018 reported that the prevalence was significantly highest in animals which have poor body conditions than in those with medium or good body conditions. The achievable explanation for this observation could be due to immunesuppression of animal and infection by other parasites including GIT helminthes and/or malnutrition. Poorly nourished sheep appear to be less competent in getting rid of lungworm infection. Evidently, the infection with a parasite by itself might results in progressive emaciation of the animals [11]. CONCLUSION AND RECOMMENDATIONS The result of the present study showed that lungworm infection is one of the problems of sheep production in and around Kombolcha. The different species of lungworm identified by the current investigation were Mullerius capillaries, Dictyocaulus fillaria and Protostrongylus rufescens. The more prevalent species of lungworm identified was M. Capillaries. Adult sheep were found to be more affected by the infection of lungworms than young. Body condition and management system were found to affect the prevalence of lungworm in sheep in the study area. Thus, it needs intervention of responsible bodies to control and prevent the infection of sheep lungworm to get the intended benefit from it in the area. Therefore, based on the above conclusion the following recommendations were forwarded: Animal health workers should give attention to animal health extension to practice the control and prevention of lungworm infection. It is better to the animal owners to practice the improved animal husbandry to keep their animals healthy. More detail epidemiological study should be conducted to get full documentation on the distribution and magnitude of lungworm infection in the area. ACKNOWLEDGEMENTS I would like to thank all the staff members of Wollega University, School of Veterinary Medicine and special thanks goes to all Kombolcha Regional Veterinary Laboratory technicians and workers for their great support with basic guidance and well equipped laboratory facilities. REFERENCES 1. Samson, L. and M. Frehiwot, 010. Prevalence of Small Ruminant Trypanosomosis and Tsetse Fly Challenge in Upper Didessa Vally, Ethiopia. Adami- Tullu Agriculture Research Center, Ziway, Ethiopia, pp: 15.. Kefyalew, A. and F. Tegegne, 01. The effect of climate change on ruminant livestock population dynamics in Ethiopia. Bahir Dar University, college of agriculture and environmental scinces, department of animal production and technology, Bahir Dar, Ethiopia, Livestock Research for Rural Development, 10: Tsedeke, K., 007. Production and Marketing systems of sheep and goats in Alaba, Southern Ethiopia, Msc thesis. Department of animal and range Sciences, Awassa College of Agriculture, school of graduate studies AwassaUniversity Awassa, Ethiopia, pp: Ademosun, A., 199. Constraints and prospects for small ruminant s research and development in Africa. Small Ruminant Development Africa, 1: Abebe, W. and G. Eseyas, 001. Survey of ovine and caprine gastrointestinal helminthosis in eastern part of Ethiopia during the dry season of the year. Revue of Veterinary Medicine, 15: Bradford, P., 00. Large Animal Internal Medicine: nd disease of horses, cattle, sheep and goats, 3 edition. Mosby Inc., pp: , Tony, M., 006. The Vet. Epidemiology and economic research unit, shool of agriculture, policy and development: in diseases of small ruminants in Ethiopia, Netherlands/ UK, pp: FAO, 006. Food and Agricultural Organizations of the United States (FAOSTAT) data. 9. Alemu, S., G. Egigu, A. Gebeyehu and Z. Ageze, 006. Study on Small Ruminants Lungworm in Northeastern Ethiopia. Vet. Parasitol., 14: Gelagay, A., Y. Leakemariam, G. Esayas, T. Selam and A. Kassahun, 005. The Ethiopian Veterinary Journal, 9: Radostitis, O., C. Gay and W. Hinchcriff, 007. Veterinary Medicine: A text book of the disease of cattle, horses, sheep, pigs and goats. Saunders Elsevier, USA, pp: NMSA, 013. National meteorology service agency. 13. Thrusfiled, M., 005. Sampling in veterinary nd Epidemiology, edition. Blackwell Science Ltd. London, pp:

6 Acta Parasitologica Globalis 9 (1): 7-3, Urquhart, G., J. Aremour, L. Dunchan, A. Dunn and 5. Mengestom, G., 008. Preliminary study on nd M. Jeninis, Veterinary parasitology, edition, prevalence of ovine lungworm infection in Atsbi The University of Glasgow, Blackwell sciences, (Tigray). DVM Thesis, Jimma University, Jimma, Scotland, pp: Ethiopia. 15. Anne, M. and A. Gray, 006. Veterinary Clinical 6. Muluken, B., 009. Prevalence of ovine lung warm in. Parasitology, th 7 Edition, Australia Blackwell and around Bahir Dar. DVM Thesis, Jimma Publishing, pp: University, Jimma, Ethiopia. 16. Gatenby, M., Sheep R. Coste and J.A. Smith, 7. Bekele, M. and A. Abu, 011. Ovine lungworms in (eds.), the Tropical Agriculturalist, Macmillan Tiyo District, South-East Ethiopia: Prevalence, effect (London) and CTA (Wageningen), pp: of altitude and major host related risk factors. Global 17. Dar, L., M. Darzi, M. Mir, S. Kamil, A. Rashid, Veterinaria, 7: S. Abdullah and P. Reshi, 01. Prevalence and 8. Sissay, A., Preliminary study on the prevalence Pathology of Lung Worm Infection in Sheep in of ovine lungworm infection in and around Bahir Dar Kashmir Valley, India, J. Anim. Sci. Adv., : DVM thesis, Addis Ababa University, Faculty of 18. Terefe, Y., K. Tafess, G. Fekadie and N. Kebede, 013. Veterinary Medicine, Debre-Zeit, Ethiopia. Prevalence of lungworm infection in small ruminants 9. Mezgebu, M., A survey on ovine fascioliasis in North Gondar zone, Amhara National Regional and lungworm infection in Addis Ababa and the State, Ethiopia. Journal of Parasitology andvector surrounding highland areas. DVM Thesis, Faculty of Biology, 5: Veterinary Medicine, Addis Ababa University, 19. Hasen, A., S. Takele and K. Simenew, 013. Ovine Debre-Zeit, Ethiopia. Lungworm Infestation Rate on Fecal Larvae 30. Nemat, E. and G. Moghadam, 010. A Survey on Recovery Basis, Acta Parasitologica Globalis, Annual Infestation of Sheep with Lung Worms based 1: on Fecal Test and Slaughter House Study in Tabriz. 0. Mihreteab, B. and A. Aman, 011. Ovine Lungworms Journal of Veterinary Research, 64: in Tiyo District, South-East Ethiopia: Prevalence, 31. Mekonnen, A., 011. Study on the Prevalence of Effect of Altitude and Major Host Related Risk Lungworm Infection in Small Ruminants in Gondar Factors, Global Veterinaria, 3: Town, Ethiopia, Journal of Animal and Veterinary 1. Netsanet, B., 199. Study on the Prevalence and Advance, 10: Control of Lung Worms (Dictycaulus and Meullerius) 3. Dawit, W., 01. Prevalence of Small Ruminant Lung in local Ethiopian Highland sheep in and around Worm Infection in Jimma Town.DVM Thesis, Jimma Debre Birhan. DVMThesis, Addis Ababa University, University College of Agriculture and Veterinary Debrezeit, Ethiopia. Medicine, pp: Basaznew, B., E. Ayalew and M. Achenef, Nuraddis, I. and D. Yared, 01. Prevalence of Ovine Ovine Lungworm Infection: Prevalence, Species Lung Worm Infection in Mekelle Town, North Composition and Associated Risk Factors in Dessie Ethiopia. The Internet Journal of Veterinary Zuria District, Northeastern Ethiopia. African Medicine, 9: 1. Journal.of Basic & Applied Sciences, 4: Taylor, M., R. Coop and R. Hall, 007. Veterinary 3. Gebreyohannes, M., T. Alemu and E. Kebede, 013. rd parasitology. 3 edition, USA Blackwell Publishing, Prevalence of Ovine Lungworms in Mekedella pp: 87. Woreda, Ethiopia, pp: Soulsby, E., Helminthes, arthropods and 4. Tewdrose, A., 010. Prevalence of lungworm th protozoa of domestic animals.7 Edition, Lea and infection of small ruminants in and around Bahir dar. Fediger, Philadelphia, pp: DVM Thesis, Gondar university, Gondar, Ethiopia. 3

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