Prevalence and Risk Factors of Theileriosis in Goat and Sheep in Lahore
In Pakistan, theileriosis is a common hemoparasitic disease in small ruminants. In order to establish the prevalence of theileriosis in Lahore, Pakistan, a total of n=730 animals were chosen. n = 103 (14.11%) of the samples tested positive for theileria under a microscope. Theileria spp. was found to be present in 10.73% of goats (44/410) and 18.44% of sheep (59/320), respectively. Theileria infection in goats was unaffected by age, sex, or season (P > 0.05). Age and season had an effect on the prevalence of theileriosis in sheep (P < 0.05), with a gender trend. To determine the effect of the risk variables on sheep and goats, more prevalence studies are needed.
Introduction
Theileria lestoquardi (hirci), T. ovis (recondita), and T. separate cause ovine theileriosis, an economically important illness of small ruminants in the tropics and subtropics [1, 2, 3]. Malignant theileriosis in sheep and goats is caused by Theileria lestoquardi, a severe lymphoproliferative disease with substantial mortality and morbidity [4, 5]. T. lestoquardi causes fever, lymphadenopathy, wasting, anaemia, and jaundice when transmitted by ticks of the Ixodidae family. The acute type of the condition is the most common, although there are also subacute and chronic forms. The illness is enzootic from North Africa to India via the Middle East [3, 6, 7]. In Pakistan, the primary tickborne haemoparasitic illnesses of cattle and small ruminants are babesiosis and theileriosis [8]. Theileriosis (T. annulata) in cattle has been thoroughly investigated; however, little is known about ovine theileriosis in small ruminants in Pakistan. Clinical signs and microscopic inspection of blood smears are the most common ways to diagnose theileriosis. As a result, the purpose of this study was to establish the prevalence of Theileria in goats and sheep in and around Lahore, as well as the many risk factors that contribute to disease occurrence.
Materials and Methods
A total of n= 730 animals (n=410 goats and n=320 sheep) were chosen from herds in and around Lahore and transported to the UVAS Lahore Veterinary Hospital, for treatment. The research took place between August 2020 and July 2021. The animals were checked clinically, and blood samples were examined microscopically to detect the prevalence of theileria in stained smears. Ticks were meticulously searched throughout each animal’s body. A
blood sample was taken from each animal’s ear vein. A thin blood smear was made on a grease-free glass slide, air- dried, fixed in methanol for 2–3 minutes, and stained for 30 minutes with Giemsa at a dilution of 5% in PBS. Based on morphology, the stained smears were examined using an oil- immersion lens (100x) for the presence of theileria [9, 10, 11]. Age, gender, season, and clinical symptoms were used to sort the data. The data was divided into two categories based on age (less than 6 months and more than 6 months), sex (male and female), species (sheep and goat), and tick infestation (less than 6 months and more than 6 months) (presence or absence). Seasonal data was separated into four categories: dry hot, wet hot, winter, and spring). The Chi square test was used to investigate the relationship between the presence of theileria (positive and negative blood samples) and other risk factors (SPSS, Inc, USA). At P>0.05, the likelihood of significance was predetermined.
Results and Discussion
The presence of Theileria spp. was tested in a total of n=730 blood samples (n=410 from goats and n=320 from sheep). Blood smears were obtained and stained with Giemsa, and the existence of piroplasms in the infected animals’ erythrocytes was investigated under light microscopy. Theileria spp. was found to be present in 10.73 % of goats and 18.44 % of sheep, respectively (Table 1).
| Species | Total Sample | No of Positive | Prevalence (%) |
|---|---|---|---|
| Goat | 410 | 44 | 10.73 |
| Sheep | 320 | 59 | 18.44 |
| Total | 730 | 103 | 14.11 |
Table 1: Prevalence of Theileria in goat and sheep.
The parasite prevalence was higher in sheep than in goats, which could be attributed to the nature of their skin. Sheep were shown to be more vulnerable to T. ovis than goats [12]. Because of the nature of sheep’s skin, this parasite has a greater prevalence rate. In comparison to sheep, goats have thin skin that appears to be more resistant to ticks. Ticks can easily become entangled in sheep’s wool, resulting in an infestation. The fact that no theileria was identified in animals that were devoid of ticks also supports this notion (Table 2).
| Species | Category | Total Sample | No of Positive | Prevalence (%) |
|---|---|---|---|---|
| Goat | Positive | 381 | 44 | 11.55 |
| Negative | 29 | 0 | 0 | |
| Sheep | Positive | 276 | 59 | 21.38 |
| Negative | 44 | 0 | 0 |
Table 2: Prevalence of Theileria based on Tick infestation.
The prevalence of theileriosis in sheep was higher (18.44%) in this study than in a previous study by Rehman, et al. [13], who found a 16.5% prevalence of theileriosis in the District Okara. This disparity could be attributed to the fact that the two districts are located in different parts of the country. Durrani, et al. [11] also discovered that the incidence of theileria in sheep was affected by the geographical distribution of animals. In the current investigation, a link between gender (Table 3) and age (Table 4) was discovered.
| Species | Sex | Total Sample | No of Positive | Prevalence (%) |
|---|---|---|---|---|
| Goat | Male | 170 | 15 | 8.82 |
| Female | 240 | 29 | 12.08 | |
| Sheep | Male | 170 | 37 | 21.76 |
| Female | 150 | 22 | 14.67 | |
| Species | Season | Total Sample | No of Positive | Prevalence (%) |
| Goat | Dry Hot | 120 | 12 | 10 |
| Wet Hot | 102 | 14 | 13.73 | |
| Winter | 78 | 7 | 8.97 | |
| Spring | 110 | 11 | 10 | |
| Sheep | Dry Hot | 81 | 18 | 22.22 |
| Wet Hot | 102 | 25 | 24.51 | |
| Winter | 64 | 5 | 7.81 | |
| Spring | 73 | 11 | 15.07 |
Table 3: Prevalence of Theileria based on sex.
On the other hand, found no correlation between gender and age and the prevalence of theileria in sheep and goats Table. In the current study, the overall prevalence rate in both sheep and goats was found to be 14.11% (Table 1). In the same geographical area, Durrani, et al. [14] found 22% and 35% prevalence by microscopic examination and PCR, respectively. Season has been identified as one of the major risk factors influencing the parasite’s prevalence. Summer and spring seasons are key risk factors for the incidence of Theileria spp. in sheep and goats, according to our findings (Table 4). During different seasons of the year, the prevalence of Theileria spp. varied. During the winter season, the prevalence was low in goats 8.97% and sheep 7.81% (Table 4). Tick infestation rate is impacted by temperature, rainfall, and relative humidity, thus the rise in prevalence during hot seasons could be due to this Gosh, et al. [15, 16, 17]. The incidence of theileria in sheep was found to be influenced by age and sex in the current investigation. Tick infestation was revealed to be a risk factor for the emergence of this parasite solely in goats. It’s possible that the lack of ticks as a risk factor is due to a low number of positive samples. In goats, the parasite was distributed similarly (p > 0.05) in kids and adults, although it was greater (p > 0.05) in youngsters than adult sheep. In sheep, the prevalence of parasites was higher in males than females, whereas gender was not determined to be a risk factor in goats. Rehman, et al. [13] found a prevalence of 15.8 % and 16.6 % of Theileria spp. in male and female sheep, respectively. Transfer of maternal immunity to lambs could explain the low incidence of these parasites in lambs under six months of age. In goats, this impact was not detected (Table 5).
| Species | Age | Total Sample | No of Positive | Prevalence (%) |
|---|---|---|---|---|
| Goat | < 6 months | 183 | 16 | 8.74 |
| > 6 Months | 227 | 28 | 12.33 | |
| Sheep | < 6 months | 135 | 18 | 13.33 |
| > 6 Months | 185 | 41 | 22.16 |
Table 4: Prevalence of Theileria based on Age.
In comparison to humans Jianxung and Hong [1] found a greater prevalence rate (78-85 %) in lambs. Pyrexia, emaciation, dyspnea, and swelling of the superficial lymph nodes were detected in the animals in the current investigation.
References
-
Jianxung L, Hong Y (1997) Theileriosis in sheep and goats in China. Tropical Animal Health and Production 29: 8- 10.
-
Guo S, Yuan Z, Wu G, Wang W, Ma D, et al. (2002) Epidemiology of ovine theileriosis in Ganan region, Gansu Province, China. Parasitology Research 88(13): 36-37.
-
May AA, Hasso SA (2002) Laboratory diagnosis of novel species of Theileria hirci, Eimeria caprovina and Eimeria pallida in goats in Iraq. Small Ruminant Res 44(2): 163- 166.
-
Maitra DN (1982) Incidence of Theileria hirci infection of sheep in India. Indian Journal of Animal Health 21: 78.
-
Yin H, Liu G, Luo J, Guan G, Ma M, et al. (2003) Observation on the schizont stage of an unidentified Theileria sp. in experimentally infected sheep. Parasitology Research 91(1): 34-39.
-
Rao VNA, Palaniswami KS, Ghellappa DJ, Joseph SA, Gnanabaranam JF (1991) A report of concurrent haemoprotozoan and rickettsial infection in sheep. Indian Veterinary Journal 68(5): 487-488.
-
Sasmal NK, Biswas SS, Bhattacharyya B, Banerjee CD, Uilenberg G (1981) Theilerial species of domestic livestock. In: Advances in the Control of Theileriosis. Irvin AD, et al. (Eds.), Martinus Nijhoff, the Haue, pp: 4-37.
-
(1994-95) Pakistan Agricultural Research Council (PARC), Epidemiology of Major Livestock Diseases in Pakistan.
-
Soulsby EJL (1982) In: Helminthes, Arthropods and Protozoa of Domesticated Animals. Bailiere Tindall and Cassell Ltd., London, UK.
-
Urquhart GM, Armour J, Duncan JL, Dunn AM, Jennings FW (1996) In: Veterinary Parasitology, 2nd (Edn.), Black Well Science Ltd., London, UK, pp: 307.
-
William JF (2001) In: Veterinary Parasitology Reference Manual. 5th (Edn.), Blackwell, New York, pp: 105- 108.
-
Durrani SZK., Khattak RM, Andleeb M, Ali M, Hameed H, et al. (2012) A comparison of the presence of Theileria ovis by PCR amplification of their SSU rRNA gene in small ruminants from two provinces of Pakistan. Asian Pacific Journal of Tropical Disease 2(1): 43-47.
-
Rehman ZU, Khan MS, Avais M, Aleem M, Shabbir Z, et al (2010) Prevalence of Theileriosis in Sheep in Okara District, Pakistan. Pakistan Journal of Zoology 42(5): 639- 643.
-
Durrani AZ, Younus M, Kamal N, Mehmood N, Shakoori AR (2011) Prevalence of ovine Theileria species in District Lahore, Pakistan. Pakistan Journal of Zoology 43(1): 57-60.
-
Gosh S, Bansal GC, Gupta SC, Ray D, Khan MQ, et al. (2007) Status of tick distribution in Bangladesh, India and Pakistan. Parasitology Research 101: 207-216.
-
Radostits OM, Gay CC, Hinchcliff KW, Constable PD (2007) Veterinary medicine. 10th (Edn.), Elsevier’s Health Department Phildelphia, USA, pp: 1527-1531.
-
Zahid IA, Latif M, Baloch KB (2005) Incidence and treatment of theileriasis and babesiasis. Pakistan Veterinary Journal 25(3): 137-139.
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