Livestock Research for Rural Development 22 (12) 2010 | Notes to Authors | LRRD Newsletter | Citation of this paper |
A study was conducted in three selected districts of Central Shoa, Ethiopia, from November 2007 to April 2008 to determine the prevalence and burden of strongyle and parascaris population in working donkeys in Adaa, Bereh and Boset districts. A total of 246 fecal samples were collected randomly from Bereh (n=56), Boset (n=85) and Ada (n=105) for qualitative and quantitative faecal analysis.
The overall prevalence of strongyles and Parascaris equorum was 92% and 32.5%, respectively. The prevalence of strongyle was 92.5% in Bereh, 87% in Boset and 95% in Adaa. The prevalence of Parascaris equorum was 43%, 26% and 32% in Bereh, Boset and Ada, respectively. Overall, 33% of the donkeys were positive for both strongyle and Parascaris equorum. There was no statistically significant difference (P>0.05) in prevalence rate of strongyle and parascaris across the study districts. The overall mean egg per gram of feces (epg) for strongyle and Parascaris equorum was 2893 and 120, respectively. Body condition score was not found to be a good indicator of level of parasitism in working donkeys. There was statistically significance difference (P<0.05) between age groups for the prevalence and mean egg per gram of feces of parascaris infection. As donkeys get access to deworming program increases, prevalence of parasitic burden decreases. Cultural identification of larvae revealed Strongylus vulgaris (67.5%), Strongylus edentatus (46%), Strongylus equines (8%), Trichostronglus axei (58.5%), cyathostomes (35.8%), Strongylus westeri (35.8%) and Triodontophorus (15.8%). Strongyle and parascaris were extensively prevalent in the study districts. Regular dewormining by Donkey Health and Welfare Project of Faculty of Veterinary Medicine of Addis Ababa university had an impact on the prevalence of strongyle and parascaris parasites.
Key words: Donkey, Ethiopia, Parascaris equorum, prevalence, strongyles
Ethiopia, located in Eastern Africa, is predominantly an agricultural nation. The country has diverse agro-ecological zones, which contributed to the evolution of different agricultural production systems. Animal production is practiced in all ecological zones of the country (Tegegne and Crawford 2000).
The domestic donkey (Equus asinus) belongs to the genus Equus and the family Equidae, which includes the wild asses of Africa and Asia as well as all the species of the horse and zebra. It is believed that all the domestic donkeys in the world are descended from Africa wild ass (Fielding and Krauser 1998). There are about 115.2 million domestic equids (horses, donkeys and mules) in the world of which 44.3 million are donkeys and 57.6 million are horses. With 5.2 million donkeys Ethiopia has second largest donkey population in the world and nearly 40% of Africa donkey population (FAO 2003).
Donkeys play an important role in socio-economic development by providing transportation in areas that are inaccessible by motorized vehicles or unaffordable modern form of transportation. In Ethiopia, the unsuitability of the area for motorized transportation, cost of road construction and high donkey population allow the use of these animals for transportation (Abayneh et al 2002). Donkeys have also been used in land tillage in areas where the soil is loose and assist in threshing and trampling (Abayneh et al 2002, Getachew et al 1991)
Although donkeys are often described as hardy and resistant animals, they do suffer a number of health problems (Svendsen 1986). Parasitic diseases have an economic impact on donkey as they cause loss through lowered fertility, reduced work capacity and increased treatment cost (Krecek et al 2002). These diseases are also serious to donkey welfare, causing pain in affected animals (Fikru et al 2005). Infections of working donkeys with gastro- intestinal parasites are recorded from most countries of Africa and a few parts of Ethiopia. In Ethiopia, few studies were done in central and eastern parts of the country (Gebreab 1998, Mohammed and Teketel 1991).
The donkey health and welfare project has launched a deworming program since 1994 in selected districts of central Oromia. The project intended to know the current status of worm population in these intervention sites. Therefore, the objectives of this study were
To determine the prevalence and worm burden of strongyle and parascaris population in working donkeys of central Shoa.
To assess the effect of frequency of deworming on strongyle and parascaris population of working donkeys
The study was conducted in three different agro-ecological zones, namely Adaa (mid-land), Bereh (high-land), and Boset (low-land) from November 2007 to April 2008.
It is located at 80 7' N latitude and 390E (EMPDA 1984), 45km South East of Addis Ababa. The geography of the area is marked by a number of crater lakes. The altitude rages from 1500-1800m asl and mean annual rainfall is 1115.6mm. The mean annual maximum and minimum temperatures are 30.50C and 8.50C, respectively with a relative humidity of 61.3% (NMSA 1986). The total land area of the district is 161,056 hectares. The donkey population is 46,222 (MOA 2004).
It located 44-66 km North of Addis Ababa and at an altitude range of 2300-3000m asl. The mean annual rainfall is 3000mm. The average daily maximum and minimum temperature are 280C and 150C, respectively (NMSA 2004). The total land coverage is 138,900 hectares. The donkey population is 24, 395 (MOA 2004).
It is located in the East Africa Rift Valley, 100 km East of Addis Ababa with an altitude of 1500 m asl. Its total land coverage is 124,160 hectares. It has annual rain fall from 400mm to 800mm and temperature of 13.60 to 27.70c (NMSA 2004). The donkey population is 37,181(MOA 2004).
The study animals were donkeys in three districts of Oromia Regional State, Central Shoa, maintained under traditional small holder extensive management production system. The total number of donkeys in donkey health and welfare project sites was 107,798. All working donkeys in the donkey health and welfare project study areas were considered irrespective of age, sex, body condition score and color. Donkeys were grouped in to three age categories. Donkeys under two years of age were classed as young, those in range of two to ten years were classed as adult and those beyond ten years were classed as old. These age classes were based on age of first work, productive age and the life span of Ethiopian donkeys (Yoseph et al 2001; Svendsen 1997). Donkeys were also grouped in to different body condition score according to Svendsen 1997.
A sample size was calculated with expected 80% prevalence and 95% confidence interval with an absolute precision of 5% according to (Thrusfield 1995). Thus,
P exp = expected prevalence
d = desired absolute precision
1.96 = constant from normal distribution at a given confidence level
Consequently, a total of 246 working donkeys were sampled, 56, 85 and 105 from Bereh, Boset and Ada, respectively.
A purposive sampling method was employed to select the three study districts (Adaa, Bereh and Boset) for logistic reasons. These districts consist of peasant associations (PAs). The study PAs were selected from each study district based on simple random sampling based on the sampling frame obtained from the districts' Agricultural Department. Systematic random sampling was employed to select donkeys for faecal sampling.
Faecal samples were collected directly from the rectum by using rectal gloves. Each sample was labeled with animal identification, owner’s name, date and area of collection with indelible pen. Samples were kept in refrigerator at 40C to be examined for coproscopy and coproculture. Zinc sulfate solution was used as flotation fluid for this study.
This quantitative technique was used to determine the number of eggs or larvae per gram of feces as described by Urquhart et al 1996 and MAFF, 1979.
Those samples positive to McMaster technique were subjected to fecal culture to see the strongyle larvae profile in study districts. The samples were cultured according to (MAFF 1979).
Approximately 20gm moist and crumbly feces were broken up finely using spatula. Wide mounted plastic jars were filled with the feces, closed with the lid and left at room temperature for 10-20days stirring the feces each day to prevent the growth of fungi in the culture and L3 (Third stage) larvae were recovered using the Baerman technique. A drop of lugol's iodine was added to the sediment which stains the free living nematode yellow, while parasitic 3rd stage larvae remain unstained. The larvae was then identified under low power microscopy (10x objective), based on the shape and number of gut cells, relative size of sheath tail and shape of larvae’s tail (MAFF 1979, Kaufmann 1996).
The collected data were entered in to the computer using Excel software. The data were in a list format, i.e., a single row for each donkey, with columns for parasites recovered, EPG and animal identifications. Data were cleared and STATA 9.2 for windows was used to analyze. In the analysis, confidence level was held at 95% and p<0.05 was set for significance.
Prevalence of concurrent infection to both strongyle and Parascaris was 33%.The over all prevalence and mean egg per gram of feces of strongyle and parascaris were 92% and 32.5%, respectively. There was no statistically significance difference (P>0.05) in the prevalence of strongyles and parascaris among districts. District level prevalence determined for parascaris and strongyles are indicated in table1.
Table 1. Prevalence and the over all mean (se) eggs per gram of feces (epg) of strongyles and parascaris in donkeys in three districts of central Ethiopia |
|||||||
Districts |
No. examined |
Prevalence, % |
Mean (se) epg |
Ranges |
|||
Strongyles |
Parascaris |
Strongyles |
Parascaris |
Strongyles |
Parascaris |
||
Bereh |
56 |
93 |
43 |
2447 (303) |
94.7(11.7) |
100-9000 |
50-1150 |
Boset |
85 |
87 |
26 |
2576 (266) |
93.2 (11.5) |
100-10000 |
50-3300 |
Ada |
105 |
95 |
32 |
3656(315) |
87.5(10.8) |
100-11850 |
50-3300 |
Total |
246 |
92 |
32.5 |
3008 (180) |
121.5(14.9) |
- |
- |
There was no statistically significance difference between age groups for the prevalence and mean egg per gram of feces of strongyles infection (Table 2).
Table 2. Age based prevalence and mean EPG of strongyles and parascaris |
|||||
Age, years |
No examined |
Prevalence, % |
Mean (se) epg |
||
Strongyles |
Parascaris |
Strongyles |
Parascaris |
||
<2.5yrs |
19 |
97.8 |
43 |
94.7(0.5) |
447(231) |
2.5-4.5yrs |
73 |
93.2 |
63 |
93.2(0.03) |
207(32.63) |
4.5-8yrs |
64 |
87.5 |
19 |
87.5(0.04) |
40.6(12.93) |
>8yrs |
90 |
93.3 |
10 |
93.33(0.03) |
41.1(20.94) |
There was statistically significance difference (P< 0.05) ) between age groups for the prevalence and mean egg per gram of feces of parascaris infection (Table 2). Body condition score is poorly associated with the mean egg per gram of feces for both strongyle (r=0.05) and parascaris (r=0.05) infection. The overall mean egg per gram of feces (epg) for strongyle and Parascaris equorum was 2893 and 120, respectively.
Deworming frequency with ivermectin had statistically significant association with prevalence of strongyle (p=0.001) and parascaris equorum (p=0.016). The prevalence decreased as the frequency of deworming increases (strongyle: OR=0.33; parascaris equorum: OR= 0.53) (Table 3).
Table 3. Proportion of strongyles and parascaris recovered against rate of deworming. |
|||
No examined |
Frequency of deworming |
Strongyles, % |
Parascaris, % |
78 |
Once |
100 |
44.9 |
119 |
Two times |
91.6 |
29.4 |
28 |
Three times |
82 |
14.3 |
21 |
Four times |
76.2 |
28.6 |
Larvae were recognized and identified by their specific morphology traits according to MAFF (1979). Seven types of helminth parasitic larvae were identified namely Strongylus vulgaris, Strongylus edentatus, Strongylus equinus,T richostrongylus axei, Cyathostomes, Strongylus westeri, Triodontophoros species (Table 4).
Table 4. Relative occurrence of the different parasites recovered from coproculture. |
||||||||
Districts |
No |
Prevalence, % |
||||||
S. vulgaris |
S. edentatus |
S. equinus |
T. axei |
Cyathomes |
S. westeri |
Triodontophoros |
||
Bereh |
56 |
58.9 |
32 |
0 |
67.8 |
51.8 |
17.8 |
14 |
Boset |
85 |
56.5 |
32.9 |
11.7 |
28 |
30.6 |
48.2 |
14 |
Ada |
105 |
81 |
63.8 |
9.5 |
78 |
69.5 |
35 |
18 |
Total |
246 |
67.5 |
45.9 |
8 |
58.5 |
35.7 |
35.7 |
15.8 |
P-value |
P<0.001 |
P<0.001 |
P=0.035 |
P<0.001 |
P<0.001 |
P=0.001 |
P<0.001 |
There was statistically significant difference (P=0.05) in the recovery rate between districts (Table 4). Strongylus vulgaris, which is known for its high pathogenic effect, was 58.9%, 56.5% and 81% prevalence in Bereh, Boset and Ada respectively.
The prevalence of strongyle was 93% in Bereh, 87% in Boset and 95% in Adaa. This study was comparable with results of Yoseph et al 2001, Mulate 2005, Ayele et al 2006 and Fikru et al 2005 who reported 100%, 100%, 100% and 98.2% in donkeys of Wonchi, highland of Wollo province, Dugda Bora and western high land of Oromia, respectively. Age group had no statistically significant association with the prevalence and mean egg per gram of feces of strongyles. A similar finding was reported by Ayele et al 2006. This might be attributed to increase of land cultivation which restricts donkeys on small communal grazing land allowing the animals for continuous larvae exposure to infected pasture.
Parascaris equorum was detected in 43%, 26% and 32% of the donkeys of Bereh, Boset and Ada, respectively. This finding is also similar to the findings of Feseha 1998, Mulate 2005 and Ayele et al 2006 who reported 40%, 44 % and 50% in donkeys of Debre Zeit, South and North Wollo provinces and Dugda Bora.
Cultural identification of larvae indicated 58.9%, 56.5% and 81% recovery rate of strongyle vulgaris in Bereh, Boset and Ada, respectively. There was significance difference (P<0.05) among the three districts. Donkeys in Ada have the highest prevalence than the other two districts. Recovery rate of Strongylus vulgaris in the present study was lower than results reported by Yoseph et al 2001 and Ayele et al 2006. This may be due to the seasonal variation between these studies where the current study included only the dry season of the year. Strongylus vulgaris is the most pathogenic parasite in equine, causing unthriftness, weakness, and increased susceptibility to other infections and even death and fatal colic could also have arisen from strongylid overload (Khallaayoune 1991).
The prevalence of Strongylus edentates was is higher in Ada (63.8%) than Bereh (32%) and Boset (32.9%).This result is in agreement with the work of Yoseph (1996). The prevalence of Cyathostomes was lower than the report of Ayele et al 2006 and Yoseph et al 2001 who reported 100% in donkeys of Dugda Bora and central Oromia. This lower recovery rate in the current study might be due to the intervention of Donkey Health and Welfare Project of Addis Ababa University Faculty of Veterinary Medicine, through regular deworming programme.
The prevalence of Trichostrongylus axei, as determined from different ova culture was 68%, 28% and 78% in Bereh, Boset and Ada, respectively and this was statistically different(P<0.05). The larvae recovery rate of Trichostrongylus axei in Bereh and Ada was higher than the report of Yoseph et al. 2001. The prevalence of T.axei in Boset (28%) was in agreement with the study of Yoseph et al. 2001 and Desalegne 2005. Frequency of deworming had an association with the prevalence of both strongyles and parascaris equarum. Donkeys which had higher access to ivermectin had relatively lower prevalence. This reduced prevalence might be because of decreased pasture contamination among the dewormed donkeys.
Abayneh T, Gebreab F, Zekarias B and Tadesse G 2002 The potential role of donkeys in land tillage in central Ethiopia. Bulletin of Animal Health and Production in Africa 50: 172-178.
Ayele G, Feseha G, Bojia E and Joe A 2006 Prevalence of gastro-intestinal parasites of donkeys in Dugda Bora District, Ethiopia. Livestock Research for Rural Development. Volume 18, Article #136. Retrieved December 23, 2009, from http://www.lrrd.org/lrrd18/10/ayel18136.htm
Desalegne A 2005 Status of Parasitism in Donkeys of intervention and non-intervention Areas: A comparative study DVM thesis, Faculty of veterinary medicine, Addis Ababa, Debre-zeit, Ethiopia.
EMPDA 1984 Educational Material Production and Distribution Agency. Atlas for secondary high school of Ethiopia, kindergarten and formal Curriculum division, Social Science panel. Ministry of education, Macmillan.
FAO 2003 Economic and Social Department. The statistics division, online Data base FAO STAT 2003 http://faostat.fao.org/site/377/default.aspx#ancor
Fesseha G 1998 Maximization and use of donkeys in the dry lands of Ethiopian. Proceeding of the National Workshop on Challenges and Opportunities for Research and Development in Pastoral and Agro-pastoral Areas of Ethiopia, Mekelle, Ethiopia
Fielding D and Krauser P 1998 Donkeys: The Tropical Agriculturist series, Macmillan, CTA, Pp: 2-87
Fikru R, Reta D and Bizunesh M 2005 Prevalence of equine gastrointestinal parasites in western high lands of Oromia, Ethiopia. Bulletin of Animal Health and Production in Africa. Pp. 161-166.
Gebreab F 1998 Proceedings of the international conference on equine infectious diseases held in Dubai, United Arab Emirate
Getachew A, Ercole Z and Abate T 1991 Proceedings of forth national livestock implementation conference. 13-15 November 1991, Addis Ababa, Ethiopia, Pp: 29-35
Kaufmann J 1996 Parasitic Infections of Domestic Animals, a Diagnostic Manual. Birhavsen verleg, Germany, Pp: 224-227
Khallaayoune K 1991 Benefit of a strategic deworming program in working donkeys in Morocco. In: Fielding D and Pearson RA (editors) Donkeys mules and horses in Tropical Agricultural Development. Pp. 174-180, CTVM Edinburgh.
Krecek R.C, Mathee S, Pearson R.A, Fieldings D and Tabba D 2002 Forth international colloquium on working equines 20-26th April 2002, Hama, Syria, Pp: 249
MAFF 1979 Manual of Veterinary Laboratory Techniques, Technical Bulletin, No. 18, Ministry of Agricultural Fisheries and Food, London, Pp: 14
MOA 2004 Ministry of Agriculture Addis Ababa, Ethiopia.
Mohammed A and Teketel F 1991 In proceedings of forth national livestock improvement conference, Addis Ababa, Ethiopia Pp: 176-179
Mulate B 2005 Preliminary study on helminthosis of equines in south and north Wollo Zone, Ethiopian Journal of Veterinary Association, Pp: 25-37
NMSA 2004 National Metrological service Agency Addis Ababa, Ethiopia
Svendsen E D 1986 The Professional Handbook of the Donkey, sovereign printing group, England, Pp: 77-78
Svendsen E D 1997 Parasites abroad. The professional hand book of the donkey, 3rd edition. Pp.166-182, Whittet Books Limited, 18 Anley Road, London W14 OBY, Pp.166-182.
Tegegne A and Crawford T W 2000 Draft animal power use in Ethiopia. In: Draft animal news, No. 33, December 2000. Center for Tropical Veterinary Medicine, University Edinburgh
Thrusfield M 1995 Veterinary Epidemiology, 2nd edition. UK, Blackwell Science Ltd, Pp: 182-183
Urquhart G M, Armour J, Duncan J L, Dunn A M, Jennings F W 1996 Veterinary parasitology, 2nd edition, Blackwell science, limited, Scotland Pp: 276-277
Yoseph L.W 1996 Preliminary survey on management aspects and health problems of donkeys in Dire Dawa and east Oromia, Ethiopia. DVM thesis, FVM, Addis Ababa, Debre Zeit, Ethiopia.
Yoseph S, Feseha G and Abebe W 2001. Survey on helminthosis of equines in Wonchi, Ethiopia. Journal of the Ethiopian Veterinary Association 5: 47-61. -182.
Received 23 December 2009; Accepted 15 March 2010; Published 9 December 2010