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Prevalence of Gastrointestinal Parasites of Goats in Aeolian Plains of Haryana, India

Priyanka Sukhdeep Vohra Satyavir Singh Arun K. Sangwan
Vol 9(12), 28-33

A total of 1080 goat faecal samples were examined from six villages of three districts (Charkhi dadri, Bhiwani and Mahindergarh) in aeolian plains of Haryana, of which 988 (91.50%) were positive for helminthic infections. The various helminth parasites observed were strongyles (89.81%), Strongyloides spp. (37.04%), Trichuris spp. (11.67%) and Moniezia spp. (3.15 %). Infection was significantly higher in adults (92.90%) as compared to young animals (80.8%). Significantly higher (p<0.05) infection rate was observed in monsoon (98.9%) as compared to winter (86.7%), spring (87.8%) and summer (92.6%) season. A non-significant difference was observed between male and female for gastrointestinal parasites in the study area. Coproculture studies revealed Haemonchus contortus (86-94%) as predominant parasite during all the seasons, followed by Strongyloides spp. (1-8%), Trichostrongylus spp. (2-5%) and Oesophagostomum spp (1%).

Keywords : Aeolian Plains Goats Prevalence Risk Factors

Goats are considered as an important livestock species all over the globe, especially in tropical and subtropical regions. Goat has a pivotal role in small scale farming and rural economy of developing societies because goat farming generates employment and supplement house hold income. Furthermore, goats can survive under limited fodder and are also capable to withstand water scarcity (Upadhyay, 2003). Goats are primarily raised for milk, meat, hair and leather production (Hassan et al., 2011). These small ruminants suffer from various diseases among which helminth parasitism is globally considered to be the most important (Sanyal, 1996). Among helminth parasitism, gastrointestinal (GI) nematodosis, is a major parasitic disease and is widely spreading in the world (Men et al., 2016) causing huge economic losses in a wide range of agro-climatic zones (Waller, 1997). These infections are responsible for a number of economic losses in a variety of ways like losses through lower fertility, reduced work capacity, involuntary culling, reduction in feed intake, lower weight gains, reduction in milk and meat production, increased treatment costs and mortality in heavily parasitized animals (Fikru et al., 2006). It has always been a major impediment in small ruminant production and this problem is severe in tropical and sub-tropical climates due to favourable ecological factors available for transmission of helminth parasites (Gupta et al., 2013). Hence, a proper understanding about the epidemiology of GI parasitism is a prerequisite for the rational designing of the effective preventive and control measures against these diseases. In Haryana, limited studies have been undertaken to provide information on the epidemiology of GI infections in small ruminants of Haryana (Gupta et al., 1987). Keeping the same in view, the present study was taken into consideration in order to explore the prevalence of various GI parasites infecting the goats in aeolian plains of Haryana and various associated risk factors for an effective management.

Materials and Methods

Study Area

The prevalence of GI parasites was studied in goats of six villages belonging to three districts i.e. Satnali and Dalanwas village of Mahendergarh district, Loharu and Kairu village of Bhiwani district and Badhra and Kadma village of Charkhi Dadri district in aeolian plains of Haryana.

Sample Collection and Processing

Fifteen faecal samples per month, from the same flock of each village were collected throughout the year from March, 2018 to February, 2019. Faecal samples were collected at random along with relevant epidemiological data according to the age, sex, month and season. The faecal samples were collected appropriately from rectum using protective disposable gloves. All the samples were subjected to floatation and sedimentation techniques to enumerate the prevalence of GI parasitism in goats. Positive samples were subjected to quantitative examination using McMaster coprological diagnostic technique to assess the intensity of GI parasitism (EPG) (Soulsby, 1982). Coproculture techniques were employed to differentiate the third stage larvae (L3) for species identification of GI parasites based on morphological and morphometric characteristics (Keith, 1953). Results of these techniques were analyzed and interpreted. Seasons were categorized as spring (February-March), summer (April to June), monsoon (July to September) and winter (October to January). Animal’s factors like age i.e. young (< 6 months) or adult (>6 months) and sex (male or female) were also incorporated in study. The data was statistically analysed using chi square and z-test.



Results and Discussion

The coprological examination of 1080 faecal samples in aeolian plains of Haryana revealed the presence of strongyle, Strongyloides spp., Trichuris spp. and Moniezia spp. eggs (Table 1). A total of 988 (91.50%) animals were positive for single or mixed infection. The infection of strongyle, Strongyloides spp., Trichuris spp. and Moniezia spp. was 89.81%, 37.04%, 11.67% and 3.15%, respectively. Almost similar findings have been reported by Singh et al. (2015) in goats of Madhya Pradesh; Varadharajan and Vijayalakshmi (2015) in small ruminants of Tamil Nadu; Vohra et al. (2018) in small ruminants in Hisar, Haryana and Zvinorovae et al. (2016) in goats in Zimbabwe.

Table 1: Prevalence of various gastrointestinal (G.I) parasites in aeolian plains of Haryana

GI Parasites Number of examined goats (n= 1080)
No. of goats infected Prevalence (%)
Strongyle 970 89.81
Strongyloides spp. 400 37.04
 Trichuris spp. 126 11.67
Moniezia spp. 34 3.15
Overall positive 988 91.5

The number of goats positive for different GI parasites and their prevalence in relation to age, sex and season is depicted in Table 2. The results in relation to age showed a significantly higher infection of strongyle (p<0.01) and Strongyloides spp. (p<0.05) in adults as compared to young animals.

Table 2: Prevalence of various gastrointestinal parasites in relation to age, sex and season

Risk factors No.


Number positive (%)
Strongyle Strongyloides spp. Trichuris spp. Moniezia spp. Overall
Age Young 125 93 (74.40) 35 (28.00) 21 (16.80) 7 (5.60) 101 (80.8a)
Adult 955 877 (91.83) 365(38.22) 105 (10.99) 27 (2.83) 887 (92.9b)
Chi-square 36.719** 4.951* 3.615NS 2.787 NS
Sex Male 111 96 (86.49) 49 (44.14) 13 (11.71) 5 (4.50) 99 (89.2a)
Female 969 874 (90.20) 351 (36.22) 113 (11.66) 29 (2.99) 889 (91.8a)
Chi-square 1.498NS 2.68 NS .000NS 0.746NS
Season Spring 180 153 (85.00a) 70 (38.89b) 39 (21.67b) 11 (6.11a) 158 (87.8ab)
Summer 270 250 (92.59b) 91 (33.70b) 74 (27.41b) 8 (2.96a) 250 (92.6b)
Monsoon 270 265 (98.15c) 149 (55.19c) 9 (3.33a) 6 (2.22a) 267 (98.9c)
Winter 360 302 (83.89a) 90 (25.00a) 4 (1.11a) 9 (2.50a) 312 (86.7a)
Chi-square   41.155** 62.052** 139.497** 6.468NS  

** Significant at 1% level, * Significant at 5% level, NS- Non-Significant

The infection of Trichuris spp. and Moniezia spp. did not reveal any statistical difference. Our findings were in concordance with Yadav et al. (2006), Emiru et al. (2013) and Singh et al. (2017) at Jammu, South west Ethiopia and Punjab, respectively. The possible reason may be consumption of higher amount of vegetation and grazing on larger area of pastures being contaminated with various flocks and different stress conditions on animals like climate, long daily traveling and gestation in adults. On the other hand, young animals are less affected by parasites due to consumption of lesser amount of vegetation and less exposure for grazing as they mainly depend upon milk feeding. The coprological results revealed a non-significant difference between males and females. Almost similar percentage of infection in both male and female animals in our study might be due to similar management practices and same area visited during grazing activity.

The results in goats showed maximum infection of strongyle and Strongyloides during monsoon season. The infection of strongyle, Strongyloides spp. and Trichuris spp. was significantly (p<0.01) associated between seasons. Similar were the observation of Gupta et al. (1987) in eastern region of Haryana and Gaherwal et al. (2016) in Madhya Pradesh. The higher prevalence in monsoon could be attributed to the favourable climatic conditions, viz., humidity and temperature which support parasitic growth and development leading to increased availability of infective larvae during monsoon. It is well documented that GI parasitism in grazing animals is directly related to the availability of larvae on pasture and seasonal pasture contamination (Gaherwal et al., 2016). Climatic factors also influence larval dispersion on the herbage which increases the chance of contact between host and larvae. Higher rate of infection in monsoon may also be attributed to suitable molarities of salt present in soil which is an important factor for ecdysis (Soulsby, 1966). Such climatic conditions also help in bacterial multiplication which provides nutrition to free-living larvae.

The monthly examination of faeces revealed maximum (100%) animals were infected with one or other type of infection during August and September months. A minimum of 82.22% infections in goats was observed during October. There was a significant difference (P < 0.05) between prevalence of various GI parasites during July (96.7%), August (100%) and September (100%) with other months. This may be due to the seasonal dynamics influencing ecological and environmental conditions for the development and survival of preparasitic stages in the study area. The month wise mean egg per gram (EPG) counts of strongyles in goats belonging to aeolian plains of Haryana revealed that the mean EPG of animals was maximum (2081.11) during the month of August and minimum (262.78) during the month of February. The present result varied with the report of Khajuria et al. (2013) from Jammu who reported two peaks of EPG i.e. August and May months. This might be due to variation in the geographical location and environmental conditions of the study areas.

The results of coproculture studies of GI nematodes in sheep are presented in Table 3. The faecal culture showed that the larvae of Haemonchus contortus, Trichostrongylus spp., Oesophagostomum spp.  and Strongyloides sp.  were present. The larvae of H. contortus (86-94%) were the main contributor throughout the study period among all the four species identified in coproculture. Gupta et al. (1987) also demonstrated infective larvae of Haemonchus spp. and Trichostrongylus spp. throughout the year in goats and sheep of eastern Haryana. Other workers who reported the predominance of Haemonchus were Tariq et al. (2010) in goats of Kashmir valley; Lone et al. (2012) in small ruminants at Ganderbal district, Kashmir; Gaherwal et al. (2016) in Barwani district, Madhya Pradesh; Zvinorovae et al. (2016) in Zimbabwe and Sivajothi and Reddy (2018) in Andhra Pradesh.

Table 3: Larval composition (%) in coproculture studies in aeolian plains of Haryana

Season Haemonchus  contortus (%) Trichostrongylus spp. (%) Oesophagostomum spp. (%) Strongyloides  spp. (%)
Spring 91 2 1 6
Summer 94 4 1 1
Monsoon 86 5 1 8
Winter 93 2 1 3


The prevalence of GI parasites in goats of aeolian plains in Haryana was 91.50%. The highest prevalence of strongyle, followed by Strongyloides, Trichuris and Moniezia was observed. Maximum prevalence was recorded in monsoon season during August and September months and highest epg of strongyles was observed during August. The coproculture study revealed the predominance of Haemoncus contortus throughout the study period.


  1. Emiru, B., Amede, Y., Tigre, W., Feyera, T. and Deressa, B. (2013). Epidemiology of gastrointestinal parasites of small ruminants in Gechi district, Southwest Ethiopia. Advances in Biological Research. 7(5): 169-174.
  2. Fikru, R., Teshale, S., Reta, D. and Yosef, K. (2006). Epidemiology of gastrointestinal parasites of ruminants in Western Oromia, Ethiopia. International Journal of AppliedResearch in Veterinary Medicine. 4(1): 51- 57.
  3. Gaherwal, S., Prakash, M.M. and Dudwe, J. (2016). Prevalence and incidence of nematodes in goats at five different villages of Barwani district (M.P.). International Journal of Advance Research. 4(3): 1126-1137.
  4. Gupta, A., Dixit, A.K., Dixit, P. and Mahajan, C. (2013). Prevalence of gastrointestinal parasites in small ruminants in and around Jabalpur, India. Journal of Veterinary Parasitology. 27(1): 59-60.
  5. Gupta, R.P., Yadav, C.L. and Chaudhri, S.S. (1987). Epidemiology of gastrointestinal nematodes of sheep and goats in Haryana, India. Veterinary Parasitology. 24(1–2): 117-127.
  6. Hassan, M. M., Hoque, M. A., Islam, S. K. M. A., Khan, S. A., Roy, K., Banu, Q. (2011). A prevalence of parasites in black Bengal goats in Chittagong, Bangladesh. International Journal of Livestock Production. 2(4): 40-44.
  7. Keith, R.K. (1953). The differentiation of the infective larvae of some common nematode of cattle. Australian Journal of Zoology. 1: 233-235.
  8. Khajuria, J. K.,  Katoch, R.,  Yadav, A.,  Godara, R., Gupta, S.K. and Singh, A. (2013). Seasonal prevalence of gastrointestinal helminths in sheep and goats of middle agro-climatic zone of Jammu province. Journal of Parasitic Disease. 37(1): 21–25.
  9. Lone, B.A., Chishti, M.Z., Ahmad, F. and Tak, H. (2012). A survey of gastrointestinal helminth parasites of slaughtered sheep and goats in Ganderbal, Kashmir. Global Veterinaria. 8(4): 338-341.
  10. Men, Q., Han, H., Zhao, Q., Xia, W., Dong, H. and Zhu, S. (2016). The prevalence of helminth parasites in Pelophylax nigromaculatus (annura: ranidae) from Shanghai, China. Acta Parasitologica. 61: 802-807.
  11. Sanyal, P.K. (1996). Gastrointestinal parasites and small ruminant production in India. In: Sustainable parasite control in small ruminants. L.F. LeJambre and M.R. Knox Eds. ACIAR Proceedings series. 74: 109-112.
  12. Singh, A.K., Das, G., Roy, B., Nath, S., Naresh, R. and Kumar, S. (2015). Prevalence of gastrointestinal parasitic infections in goat of Madhya Pradesh, India. Journal of Parasitic Disease. 39(4): 716–719.
  13. Singh, E., Kaur, P., Singla, L.D. and Bal, M.S. (2017). Prevalence of gastrointestinal parasitism in small ruminants in western zone of Punjab, India. Veterinary World. 10(1): 61-66.
  14. Sivajothi, S. and Reddy, B.S. (2018). Seasonal prevalence of gastrointestinal parasites of small ruminants in YSR Kadapa district of Andhra Pradesh, India. International Journal of Livestock Research. 8(1): 184-189
  15. Soulsby, E.J.L. (1966). Biology of Parasites. Academic Press, New York and London. Pp. 185-196.
  16. Soulsby E. J. L. (1982). Helminths, arthropods and protozoa of domesticated animals (7th edition). London: Baillière Tindall, 809 pp., illus. ISBN 0-7020-0820-6.
  17. Tariq, K.A., Chishti,Z. and Ahmad, F. (2010).  Gastrointestinal nematode infections in goats relative to season, host sex and age from the Kashmir valley, India. Journal of Helminthology. 84(1): 93-97.
  18. Upadhyay, B. A., (2003). Goat breeding strategy with reference to commercial goat production. Deptt. of Animal Science & Dairy Science, Mahatma phule Krishi Vidhyapeeth, Rabtri, Maharastra. State level workshop on recent advance in goat rearing, 29-30 Dec.
  19. Varadharajan, A. and Vijayalakshmi, R., (2015). Prevalence and seasonal occurrence of gastrointestinal parasites in small ruminants of coastal areas of Tamil Nadu. International Journalof Science and Research. 5(2): 1-4.
  20. Vohra, S., Singh, S., Kumar, P. and Patil, C.S. (2018). Incidence and severity of gastrointestinal parasites in small ruminants at Hisar, Haryana. Journal of Animal Research. 8(6): 1021-1025.
  21. Waller, P.J. (1997). Anthelmintic resistance. Veterinary Parasitology. 72: 391-412.
  22. Yadav, A., Khajuria, J.K. and Raina, A.K. (2006). Seasonal prevalence of gastrointestinal parasites in sheep and goats of Jammu. Journal of Veterinary Parasitology. 20(1): 65-68.
  23. Zvinorovae, P.I., Halimanic, T.E., Muchadeyid, F.C., Matikae, O., Riggioe, V. and Dzama, K. (2016). Prevalence and risk factors of gastrointestinal parasitic infections in goats in low-input low-output farming systems in Zimbabwe. Small Ruminants Research. 143: 75–83.


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