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Journal of Parasitic Diseases: Official Organ of the Indian Society for Parasitology logoLink to Journal of Parasitic Diseases: Official Organ of the Indian Society for Parasitology
. 2015 May 8;40(4):1342–1346. doi: 10.1007/s12639-015-0686-9

Seasonal incidence of parasitic diseases in bovines of south western Gujarat (Junagadh), India

Binod Kumar 1,, B R Maharana 1, Amit Prasad 2,3, Joice P Joseph 2,3, Bhavika Patel 2,3, J S Patel 2,3
PMCID: PMC5118312  PMID: 27876944

Abstract

The current study was conducted to investigate the incidence of parasitic diseases in bovines which were sick and brought at veterinary hospital for treatment. A total of 366 samples were investigated from cattle (n = 175) and buffaloes (n = 191) presented at Teaching Veterinary Clinical Complex (TVCC), Veterinary College, Junagadh, Gujarat during January to December 2014. Examination of Giemsa-stained peripheral blood smears exhibited that 58.6 % of cattle and 41.2 % of buffaloes were infected with haemoparasites comprising Babesia bigemina, Theileria annulata, and Anaplasma marginale @ of 54.0, 3.4 and 1.1 in cattle and 38.8, 1.2 and 1.2 percent in buffaloes, respectively. The incidence of total haemoparasites and B. bigemina infections was significantly higher (p < 0.05) in cattle whereas, incidence of haemoparasites were recorded significantly higher in the month of July to November (i.e., rainy and autumn) in both cattle and buffaloes, respectively (p < 0.01 and p < 0.001). Coprological examination revealed that the overall incidence of gastrointestinal (GI) parasitic infection was 45.5 % in cattle and 43.4 % in buffaloes. The incidence of individual parasite was 11.4, 1.1, 2.3, 4.5, 1.1, 3.4, 2.3 and 19.3 in cattle and 4.7, 0.9, 0.0, 2.8, 0.9, 5.7, 0.0 and 28.3 % in buffaloes for Eimeria spp., Trichuris spp., Toxocara vitulorum, Strongyle, Fasciola spp., amphistomes, Schistosoma indicum and Buxtonella sulcata, respectively which differ insignificantly (p > 0.05). Seasonal prevalence of GI parasites was highest in summer in both cattle and buffaloes, the data being statistically non-significant (p > 0.05). However, the incidence of B. sulcata in both cattle (19.3 %) and buffaloes (28.3 %) was higher in comparisons to other GI parasites. The present investigation emphasized that B. bigemina and B. sulcata are the most important parasites of bovines of this region.

Keywords: Incidence, Cattle, Buffalo, Junagadh, TVCC, Gujarat

Introduction

Parasitic infection is a serious constrain to health and productivity of the livestock in tropical and sub-tropical parts of the world including India. Among the various economically important bovine diseases, vector-borne haemoparasites infections such as babesiosis, theileriosis and anaplasmosis are recognized as a cause of severe clinical illness in cattle. Similarly, in buffaloes though considered as refractory host to various parasitic infections, frequently produce productivity loss and occasionally turn out as severe clinical disease. In the recent years, various epidemiological surveys of haemoprotozoan and gastrointestinal (GI) parasitic infections in domesticated animals have been carried out in different parts of India (Samanta and Santra 2007; Jyoti et al. 2011; Singh et al. 2012a; Rahman et al. 2012; Krishnamurthy and D’souza 2014, Krishnamurthy et al. 2014). The epidemiology of GI parasites and haemoparasite infections in livestock varies depending on the prevailing climatic conditions and managemental practices followed locally. Therefore, the parasitic fauna of each and every species, when mapped out accurately in different agro-climatic zones, elucidates fundamental information, depending upon which further control measures can be followed.

In this regard, scanty information is available on the prevalence of haemoparasites and GI parasitic infections in bovines of Junagadh (Gujarat), India (Maharana et al. 2015). As this district has rich source of livestock with breeds like Gir cattle, Jaffrabadi buffaloes, it is the need of the hour, to conduct a thorough study regarding the occurrence of various haemoparasites and GI parasitic infections and its co-relation with climatic conditions. Therefore, the present study was conducted to investigate the incidence of haemoparasites and GI parasitic infections in bovines presented at Teaching Veterinary Clinical Complex (TVCC) with various ailments with an objective of determining their incidence and evolving the strategic and tactical methods of control.

Materials and methods

Sample collection and processing

The clinical samples of cattle and buffaloes were collected after accessing the clinical status of the animals by the clinician at TVCC. In general, faecal samples were collected from the rectum of animals having digestive disturbance and blood samples from Jugular vein and/ear vein of animals having general health problems like fever, anaemia, prolonged anorexia etc.

A total of 175 samples were collected from cattle (87 blood and 88 faecal) and 191 from buffaloes (85 blood and 106 faecal) during January–December 2014. Faecal and blood samples were processed using standard technique (Coles 1986, Soulsby 1982). In brief, faecal sample were subjected to floatation and sedimentation techniques and blood samples were screened through thin smeared Giemsa-stain method. Seasonal prevalence was studied throughout the year dividing into five seasons, winter (December–February), spring (March–April), summer (May–June), rainy (July–September) and autumn (October–November).

Statistical analysis

Data thus obtained were compiled and formulated for frequency and finally converted into percentage to draw interpretations. Statistical analysis was performed on data by SPSS 13.0 software by applying χ2 test and statistical differences being considered significant when p < 0.05.

Results

The incidence of parasitic infections in cattle and buffaloes was recorded as 52 % (91/175) and 42.4 % (81/191), respectively whereas overall incidence of parasitic infections in bovines was 47 % (172/366).

Prevalence of haemoparasitic infections

Examination of Giemsa-stained thin blood smears revealed that 58.6 % (51/87) of cattle and 41.2 % (35/85) of buffaloes were infected with haemoparasites involving Babesia bigemina, Theileria annulata, and Anaplasma marginale @ of 54.0, 3.4 and 1.1 % in cattle and 38.8, 1.2 and 1.2 % in buffaloes, respectively (Table 1). The incidence of total haemoparasites and B. bigemina infections was significantly higher (p < 0.05) in cattle compare to buffaloes. Seasonal incidence of parasitic infection showed considerable increase from winter (December–February) to autumn (October–November). Data showed that infections of haemoparasites in month of July–November (i.e., rainy and autumn) were significantly higher (p < 0.01 and p < 0.001), in comparison of other season, in both cattle and buffaloes, respectively (Table 3).

Table 1.

Incidence of haemoparasite infections in bovines of south western Gujarat (Junagadh)

Animal Total sample Positive (%) Parasite (%)
Babesia bigemina Theileria annulata Anaplasma marginale
Cattle 87 51 (58.6) 47 (54.0) 3 (3.4) 1 (1.1)
Buffalo 85 35 (41.2) 33 (38.8) 1 (1.2) 1 (1.2)
χ2 value 5.233* 3.993* 0.977 0.000
Over all 172 86 (50.0) 80 (46.5) 4 (2.3) 2 (1.2)

* p < 0.05

Table 3.

Seasonal incidence of parasitic infections in bovines of south western Gujarat (Junagadh)

Season Gastrointestinal parasitic infections Haemoprotozoan infections
Cattle Buffalo Cattle Buffalo
Name Months Total sample Positive (%) Total sample Positive (%) Total sample Positive (%) Total sample Positive (%)
Winter Dec–Feb 12 7 (8.0) 15 5 (4.7) 10 2 (20.0) 11 0 (0.0)
Spring March–April 7 2 (2.3) 10 3 (2.8) 8 2 (25.0) 8 0 (0.0)
Summer May–June 27 12 (13.6) 30 18 (17.0) 19 11 (57.9) 7 1 (14.3)
Rainy July–Sept 20 9 (10.2) 21 11 (10.4) 35 25 (71.4) 31 16 (51.6)
Autumn Oct–Nov 22 10 (11.4) 30 9 (8.5) 15 11 (73.3) 28 18 (64.3)
χ2 value 1.620 7.598 13.587* 22.957**
Over all 88 40 (45.5) 106 46 (43.4) 87 51 (58.6) 85 35 (41.2)

* p < 0.01

** p < 0.001

Prevalence of GI parasitic infections

Coprological examination revealed that the overall incidence of GI parasitic infection was 45.5 % (40/88) in cattle and 43.4 % (46/106) in buffaloes. The incidence of individual parasite was 11.4, 1.1, 2.3, 4.5, 1.1, 3.4, 2.3 and 19.3 % in cattle and 4.7, 0.9, 0.0, 2.8, 0.9, 5.7, 0.0 and 28.3 % in buffaloes for Eimeria spp., Trichuris spp., Toxocara vitulorum, Strongyle, Fasciola spp., Amphistomes, Schistosoma indicum and Buxtonella sulcata, respectively with none significant difference (p > 0.05) (Table 2). Similarly, the incidence of GI parasite within season and between two animal species was not significant. However, the incidence of B. sulcata in both cattle (19.3 %) and buffaloes (28.3 %) was higher in comparisons to other GI parasites (Table 3).

Table 2.

Incidence of gastrointestinal parasitic infections in bovines of south western Gujarat (Junagadh)

Animal Total sample Positive (%) Parasite (%)
Eimeria spp. Trichuris spp. Toxocara vitulorum Strongyle Fasciola spp. Amphistomes Schistosoma indicum Buxtonella sulcata
Cattle 88 40 (45.5) 10 (11.4) 1 (1.1) 2 (2.3) 4 (4.5) 1 (1.1) 3 (3.4) 2 (2.3) 17 (19.3)
Buffalo 106 46 (43.4) 5 (4.7) 1 (0.9) 0 (0.0) 3 (2.8) 1 (0.9) 6 (5.7) 0 (0.0) 30 (28.3)
χ2 value 0.083 2.978 0.018 2.243 0.407 0.018 0.551 2.434 2.114
Over all 194 86 (44.3) 15 (7.7) 2 (1.0) 2 (1.0) 7 (3.6) 2 (1.0) 9 (4.6) 2 (1.0) 47 (24.2)

Discussion

Haemoprotozoan diseases like babesiosis, theileriosis and anaplasmosis are the important tick-borne diseases of bovines caused by B. bigemina, T. annulata and A. marginale, respectively (Krishnamurthy et al. 2014). In the present study, the very high incidence of B. bigemina infections (46.5 %) were recorded mainly because of abundance of vector population i.e., Rhipicephalus microplus in Junagadh, Gujarat (unpublished data). Though, this is the first report of B. bigemina infections in bovines of Saurastra region of Junagadh district of Gujarat, a variable prevalence of bovine babesiosis were recorded from different parts of India viz. 1.56 and 3.84 % in Punjab (Singh et al. 2012b, c), 2.7 and 6.9 % in Karnataka (Muraleedharan et al. 2005; Krishnamurthy et al. 2014), and 0.76–18.50 % from various parts of the country (Yadav et al. 1985; Mallick et al. 1987; Sharma et al. 2000). One of the important reason for the higher incidence of the Babesia infections in bovines may be due to the collection of samples specifically from sick animals presented at hospital.

A very low incidence of T. annulata and A. marginale infections were recorded in both cattle and buffaloes. The reasons for the low incidence of T. annulata infections may be due to the low prevalence of vector i.e., Hyalomma anatolicum anatolicum (unpublished data) or less number of exotic breeds or cross breed animals in this geographical region of the country. A higher prevalence of T. annulata infections in bovines was recorded as 14.65 % Singh et al. (2012c) and 15.38 % (Haque et al. 2012) in Punjab where H. a. anatolicum is the major tick species and most of the dairy animals are either exotic breed or cross breed. Bovine anaplasmosis, caused by A. marginale, is an important rickettsial disease, transmitted to cattle biologically by ticks and mechanically by biting flies and blood contaminated fomites causing significant economic losses in tropical and subtropical areas of world (Ruybal et al. 2009). However, the prevalence depends largely on the distribution and density of the reservoir hosts and tick vectors (Ogden et al. 2002). In the present study, examination of Giemsa stained peripheral thin blood smears revealed 1.2 % animals positive for the inclusion bodies of A. marginale. In similar studies from different states, variable incidence rates of bovine anaplasmosis ranging from 0.45 to 9.09 % had been reported (Singh and Gill 1977; Yadav et al. 1985; Mallick et al. 1987).

It was well established that incidence of vector borne diseases increases as population of vectors increases which depends upon the climatic conditions like temperature and humidity (Haque et al. 2011). In the present study, similar findings are once again established. The data shows that the infections are very high in summer, rainy and autumn when the temperature and humidity were very high and very low to nil during winter and spring when temperature and humidity both are very low.

Coprological examination of faecal samples revealed that incidence of GI parasitic infections is more in cattle than buffaloes. Results revealed that in cattle, strongyles (4.5 %) were the most prevalent helminths followed by amphistomes (3.4 %), T. vitulorum,(2.3 %), S. indicum (2.3 %), and Fasciola spp. (1.1 %) and in buffaloes, the amphistomes (5.7 %) were the most prevalent ones followed by strongyles (2.8 %), Fasciola spp. (0.9 %) and Trichuris spp. (0.9 %) whereas infection of T. vitulorum and S. indicum were not detected. B. sulcata and Eimeria spp. were the most prevalent GI protozoa recorded in cattle (19.3 and 11.4 %) and buffaloes (28.3 and 4.7 %), respectively. Both cattle and buffaloes had the highest incidence of infection of ciliated protozoa, B. sulcata which is closely related to Balantidium coli (particularly found in swine and man) differentiated on the basis of morphometry of trophozoites, cysts and managemental history. Though, B. sulcata is considered as a non-pathogenic protozoa, in recent times many researchers have reported its pathogenicity leading to diarrhoea (AI-Saffar et al. 2010). In the present study, 24.2 % of diarrhoeic animals had infection of B. sulcata. which is in conformity with the reports of earlier workers.

Our observations of 45.5 and 43.4 % GI parasitic infections in cattle and buffaloes, respectively is relatively similar to the earlier reports from Andhra Pradesh, Rajasthan, Meghalaya and Punjab (Sreedhar et al. 2009; Godara and Sharma 2010, Wadhwa et al. 2011; Bandyopadhyay et al. 2010; Singh et al. 2012b). Hirani et al. (2006) reported 44.2 % prevalence of GI parasites in adult cattle in central Gujarat, which is in array with present study conducted in south western part of Gujarat. However, more than 50 % incidence of parasitic infections in cattle and buffaloes has also been recorded from Gujarat (Pethkar and Hiregoudar 1972), Karnataka (Krishnamurthy and D’ Souza 2014) and Rajasthan (Choubisa and Jaroli 2013). In this study, the most prevalent GI parasites in cattle and buffaloes were B. sulcata and Eimeria spp. and B. sulcata and amphistomes, respectively.

A highest incidence of GI parasites was observed in cattle in summer (13.6 %) followed by autumn (11.4 %) and rainy (10.2 %) and in case of buffaloes, the incidence was recorded highest in summer (17.0 %) followed by rainy (10.4 %) and autumn (8.5 %), but the data being statistically non-significant (p > 0.05). High moisture content along with temperature prevailed during rainy season favours the growth and development of larvae is the reason behind highest prevalence of GI parasitic infections during these season as also observed in earlier studies carried by various workers (Laha et al. 2013; Chattopadhyay and Bandyopadhyay 2013). Devoid of optimum moisture and temperature for development of larvae in the pasture during hot and cold season, could be the reason of lower and lowest prevalence during spring and winter seasons, respectively.

The knowledge of pathogens in a particular regions is very much essential for the formulation of effective control strategies to prevalent these type of infections which is possible only by carrying out surveys as conducted in the present study. The current work emphasized that B. bigemina and B. sulcata were the most prevalent haemoprotozoa and GI parasite, respectively. Therefore, strategic control and management programme should be adopted to combat these GI parasites and haemoparasites.

Acknowledgments

The authors are highly thankful to Director of Research and Dean P.G. studies, JAU, Junagadh for approval of the project in 20th ZEARC (Item No. ZREAC Meeting-20.4.9.15) to carry out this study on parasitic infections in animals presented at TVCC, Veterinary College, Junagadh, Gujarat. Authors are highly thankful to Principal and Dean, College of Veterinary Science & A.H., Junagadh for providing the necessary facilities. The facilities provided by TVCC, Veterinary College, Junagadh are thankfully acknowledged.

References

  1. AI-Saffar TM, Suliman EG, AI-Bakri HS. Prevalence of intestinal ciliate Buxtonella sulcata in cattle Mosul. Iraqui J Vet Sci. 2010;24(1):27–30. [Google Scholar]
  2. Bandyopadhyay S, Devi P, Nasker S, Bera A, Dandapat P, Bandyopadhyay S, Bhattacharya D. Incidence of strongyle infection in cattle and pig with relevance to rainfall in Meghalaya. Webmed Cent Epidemiol. 2010;1(10):1–15. [Google Scholar]
  3. Chattopadhyay AK, Bandyopadhyay S. Seasonal variations of EPG Levels in gastro-intestinal parasitic infection in a southeast asian controlled locale: a statistical analysis. Springer Plus. 2013;2:205. doi: 10.1186/2193-1801-2-205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Choubisa SL, Jaroli VJ. Gastrointestinal parasitic infection in diverse species of domestic ruminants inhabiting tribal rural areas of southern Rajasthan, India. J Parasit Dis. 2013;37(2):271–275. doi: 10.1007/s12639-012-0178-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Coles EH. Veterinary clinical pathology. Philadelphia: WB Saunder’s Company; 1986. [Google Scholar]
  6. Godara R, Sharma RL. Parasitic infections in livestock at Jaipur. J Vet Parasitol. 2010;24:193–195. [Google Scholar]
  7. Haque M, Jyoti Singh NK, Rath SS, Ghosh S. Epidemiology and seasonal dynamics of ixodid ticks of dairy animals of Punjab state, India. Indian J Anim Sci. 2011;81:661–664. [Google Scholar]
  8. Haque M, Singh H, Jyoti Singh NK, Singh R, Rath SS. Detection of latent Theileria annulata infection in cattle of Punjab using PCR. Indian Vet J. 2012;89:19–21. [Google Scholar]
  9. Hirani ND, Solanki JB, Patel AI, Hasanani JJ, Joshi RS, Savaliya FP. Prevalence of gastro-intestinal parasites in cows of Panjarapols in middle Gujarat. Indian J Field Vet. 2006;1:15–18. [Google Scholar]
  10. Jyoti Haque M, Singh NK, Juyal PD, Kaur A, Rath SS. Prevalence of gastrointestinal parasites in organized dairy farms. Indian Vet J. 2011;88:77–78. [Google Scholar]
  11. Krishnamurthy CM, D’souza PE. Prevalence of gastrointestinal parasites in bovines in Bangalore district. Karnataka: J Parasit Dis; 2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Krishnamurthy CM, Anand KJ, Adeppa J. Prevalence of Haemoprotozoan infections in bovines of Shimoga region of Karnataka state. J Parasit Dis. 2014 doi: 10.1007/s12639-014-0599-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Laha R, Das M, Goswami A. Gastrointestinal parasitic infections in organized cattle farms of Meghalaya. Vet World. 2013;6(2):109–112. doi: 10.5455/vetworld.2013.109-112. [DOI] [Google Scholar]
  14. Maharana BR, Binod Kumar, Sudhakar NR, Behera SK, Patbandha TK (2015) Prevalence of gastrointestinal parasites in bovines in and around Junagadh (Gujarat). J Parasit Dis (in press) [DOI] [PMC free article] [PubMed]
  15. Mallick KP, Dwivedi SK, Srivastava NK, Kumar S. A report on the occurrence of haemoprotozoan infection in rural livestock. Indian J Parasitol. 1987;11:25–26. [Google Scholar]
  16. Muraleedharan K, Syed ZK, Margoob HP, Pattabyatappa B, Mallikarjun GB, Seshadri SJ. Incidence of Anaplasma sp., Babesia sp. and Trypanosoma sp. in cattle of Karnataka. J Vet Parasitol. 2005;19:135–137. [Google Scholar]
  17. Ogden NH, Casey ANJ, French NP, Adams JDW, Woldehiwet Z. Field evidence for density-dependent facilitation amongst Ixodes ricinus ticks feeding on sheep. Parasitology. 2002;124:117–125. doi: 10.1017/s0031182001001081. [DOI] [PubMed] [Google Scholar]
  18. Pethkar DK, Hiregoudar LS. Helminthic infections of cattle and buffaloes in Gujarat state. Gujarat Vet. 1972;6:30–31. [Google Scholar]
  19. Rahman H, Pal P, Bandyopadhyay S, Chatlod LR. Epidemiology of gastrointestinal parasitism in cattle in Sikkim. Indian J Anim Sci. 2012;82(2):355–358. [Google Scholar]
  20. Ruybal P, Moretta R, Perez A, Petrigh R, Zimmer P, Alcaraz E, Echaide I, Echaide TS, Kocan KM, Fuente J, Farber M. Genetic diversity of Anaplasma marginale in Argentina. Vet Parasitol. 2009;162:176–180. doi: 10.1016/j.vetpar.2009.02.006. [DOI] [PubMed] [Google Scholar]
  21. Samanta A, Santra PK. Prevalence of gastrointestinal helminths in hot and humid zone of West Bengal. J Vet Parasitol. 2007;21:145–148. [Google Scholar]
  22. Sharma AK, Katoch RC, Nagal KB, Kishtwaria RS, Sharma SK. Bovine babesiosis in Palam valley of Himachal Pradesh. Indian Vet J. 2000;77:731–732. [Google Scholar]
  23. Singh A, Gill BS. A note of the prevalence of subclinical anaplasmosis in three herds of cattle and buffaloes in Punjab state. Indian J Anim Sci. 1977;47:224–226. [Google Scholar]
  24. Singh NK, Singh H, Jyoti Haque M, Rath SS. Prevalence of parasitic infections in buffaloes in and around Ludhiana district, Punjab, India: a preliminary study. J Buffalo Sci. 2012;1:1–3. [Google Scholar]
  25. Singh NK, Singh H, Jyoti Haque M, Rath SS. Prevalence of parasitic infections in cattle of Ludhiana district, Punjab. J Parasit Dis. 2012;36(2):256–259. doi: 10.1007/s12639-012-0119-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Singh NK, Singh H, Jyoti, Haque M, Rath SS. Prevalence of parasitic infections in cattle of Ludhiana district, Punjab. J Parasit Dis. 2012;36(2):256–259. doi: 10.1007/s12639-012-0119-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Soulsby EJL. Helminthes, arthropod and protozoa of domestic animals. 7. London: The English Language Book Soc. & Bailliere Tindal; 1982. [Google Scholar]
  28. Sreedhar S, Mohan EM, Babu DS. Prevalence of parasitic infections in cattle and buffaloes of Anantapur district of Andhra Pradesh. Indian J Anim Res. 2009;43(3):230–231. [Google Scholar]
  29. Wadhwa A, Tanwar RK, Singla LD, Eda S, Kumar N, Kumar Y. Prevalence of gastrointestinal helminths in cattle and buffaloes in Bikaner, Rajasthan, India. Vet World. 2011;4(9):417–419. doi: 10.5455/vetworld.2011.417-419. [DOI] [Google Scholar]
  30. Yadav CL, Gupta RP, Ruprah NS. Studies on protozoan infections in cattle and buffaloes. Indian Vet Med J. 1985;9:205–209. [Google Scholar]

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