Skip to main content

Advertisement

Log in

Prevalence of antibodies to Anaplasma in cattle and buffaloes of different organized herds in India

  • Original Article
  • Published:
Journal of Parasitic Diseases Aims and scope Submit manuscript

Abstract

Bovine anaplasmosis is one of the most important tick borne disease in ruminants causing huge economic loss to the dairy industry. A cross-sectional study was carried out to detect serum antibodies to Anaplasma infection in cattle and buffaloes housed in 14 organized herds located at various climatic zones spreading over 9 different states in India. A total of 911 serum samples, collected from 667 cattle and 244 buffaloes, were subjected to a competitive enzyme linked immune-sorbent assay detecting an epitope of major surface protein 5 (MSP5) of Anaplasma. The overall true prevalence was 48.72% (95% CI 45.13–52.32%). The prevalence rate was higher in cattle (51.58%) than buffaloes (40.89%) and the difference was statistically significant (p < 0.05). Indigenous cattle (59.30%) showed higher seropositivity than crossbreed (57.16%) and exotic cattle breeds (42.28%). Although statistically not significant, female (52.37%) showed higher seropositivity than male (46.43%). Similarly, significant difference in prevalence (p < 0.05) was observed for animals reared in different climatic zones with highest prevalence recorded in arid zone (90.49%) and lowest in semi-arid zone (29.83%). Very wide variation in prevalence (9.95–100%) was recorded between farms. The present study indicates endemicity of Anaplasma in India, similar to other tropical and sub-tropical countries of the world. Endemic instability was recorded in some of the studied farms suggesting possibility of outbreak of new clinical cases resulting in economic loss. Therefore, suitable policies and procedures for prevention and control of Anaplasma infection should be adopted in these farms.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ait Hamou S, Rahali T, Sahibi H, Belghyti D, Losson B, Goff W, Rhalem A (2012) Molecular and serological prevalence of Anaplasma marginale in cattle of North Central Morocco. Res Vet Sci 93:1318–1323

    CAS  PubMed  Google Scholar 

  • Aubry P, Geale DW (2011) A review of bovine anaplasmosis. Transbound Emerg Dis 58(1):1–30

    CAS  PubMed  Google Scholar 

  • da Silva JB, Vinhote WM, Oliveira CM, André MR, Machado RZ, da Fonseca AH, Barbosa JD (2014) Molecular and serological prevalence of Anaplasma marginale in water buffaloes in northern Brazil. Ticks Tick-Borne Dis 5(2):100–104

    Google Scholar 

  • Dreher UM, de la Fuente J, Hofmann-Lehmann R, Meli ML, Pusterla N, Kocan KM, Woldehiwet Z, Braun U, Regula G, Staerk KDC, Lutz H (2005) Serologic cross-reactivity between Anaplasma marginale and Anaplasma phagocytophilum. Clin Diagn Lab Immunol 12(10):1177–1183

    CAS  PubMed  PubMed Central  Google Scholar 

  • Filia G, Mahajan V, Bal MS, Leishangthem GD, Singh A (2015) Seroprevalence of babesiosis and anaplasmosis in apparently healthy large ruminants of Punjab, India. Proc Natl Acad Sci India Sec B 85:885–888

    Google Scholar 

  • Fosgate GT, Urdaz-Rodríguez JH, Dunbar MD, Rae DO, Donovan GA, Melendez P, Dobek GL, Alleman AR (2010) Diagnostic accuracy of methods for detecting Anaplasma marginale infection in lactating dairy cattle of Puerto Rico. J Vet Diagn Investig 22(2):192–199

    Google Scholar 

  • Ganguly A, Bisla RS, Singh H, Vandna B, Kumar A, Kumari S, Maharana BR, Ganguly I (2017) Prevalence and haemato-biochemical changes of tick-borne haemoparasitic diseases in crossbred cattle of Haryana, India. Indian J Anim Sci 87(5):552–557

    Google Scholar 

  • Ganguly A, Maharana BR, Ganguly I, Kumar A, Potliya S, Arora D, Bisla RS (2018) Molecular diagnosis and hematobiochemical changes in Anaplasmamarginale infected dairy cattle. Indian J Anim Sci 88(9):989–993

    CAS  Google Scholar 

  • Ganguly A, Maharana BR, Ganguly I (2020) Pentaplex PCR assay for rapid differential detection of Babesia bigemina, Theileria annulata, Anaplasma marginale and Trypanosoma evansi in cattle. Biologicals 63:81–88

    CAS  PubMed  Google Scholar 

  • Gioia GV, Vinueza RL, Marsot M, Devillers E, Cruz M, Petit E, Boulouis HJ, Moutailler S, Monroy F, Coello MA, Gondard M, Bournez L, Haddad N, Zanella G (2018) Bovine anaplasmosis and tick-borne pathogens in cattle of the Galapagos Islands. Transbound Emerg Dis 65(5):1262–1271

    CAS  PubMed  Google Scholar 

  • Guglielmone AA (1995) Epidemiology of babesiosis and anaplasmosis in south and central America. Vet Parasitol 57(1–3):109–119

    CAS  PubMed  Google Scholar 

  • Hairgrove TB, Schroeder ME, Budke CM, Rodgersb S, Chungd C, Uetie MW, Bounpheng MA (2015) Molecular and serological in-herd prevalence of Anaplasma marginale infection in Texas cattle. Prev Vet Med 119:1–9

    PubMed  Google Scholar 

  • Hairgrove TB, Craig TM, Budke CM, Rodgers SJ, Gill RJ (2014) Seroprevalence of Anaplasma marginale in Texas cattle. Prev Vet Med 116(1–2):188–192

    PubMed  Google Scholar 

  • Howden KJ, Geale DW, Paré J, Golsteyn-Thomas EJ, Gajadhar AA (2010) An update on bovine anaplasmosis (Anaplasma marginale) in Canada. Can Vet J 51(8):837–840

    PubMed  PubMed Central  Google Scholar 

  • Humphry RW, Cameron A, Gunn GJ (2004) A practical approach to calculate sample size for herd prevalence surveys. Prev Vet Med 65:173–188

    PubMed  Google Scholar 

  • Knowles D, Torioni de Echaide S, Palmer G, McGuire T, Stiller D, McElwain T (1996) Antibody against an Anaplasma marginale MSP5 epitope common to tick and erythrocyte stages identifies persistently infected cattle. J Clin Microbiol 34:2225–2230

    CAS  PubMed  PubMed Central  Google Scholar 

  • Kocan KM, De La Fuente J, Guglielmone AA, Melendéz RD (2003) Antigens and alternatives for control of Anaplasma marginale infection in cattle. Clin Microbiol Rev 16:698–712

    PubMed  PubMed Central  Google Scholar 

  • Kumar PP, Sangwan AK (2010) Comparative prevalence of subclinical bovine anaplasmosis under different cattle management systems in Haryana. Haryana Vet 49:1–5

    Google Scholar 

  • Kumar B, Maharana BR, Prasad A, Joseph JP, Patel B, Patel JS (2015) Seasonal incidence of parasitic diseases in bovines of south western Gujarat (Junagadh), India. J Parasit Dis 40(4):1342–1346

    PubMed  PubMed Central  Google Scholar 

  • Magona JW, Mayende JSP (2002) Occurrence of concurrent trypanosomosis, theileriosis, anaplasmosis and helminthosis in Friesian, Zebu and Sahiwal cattle in Uganda. J Vet Res 69:133–140

    CAS  Google Scholar 

  • Maharana BR, Tewari AK, Saravanan BC, Sudhakar NR (2016a) Important hemoprotozoan diseases of livestock: challenges in current diagnostics and therapeutics: an update. Vet World 9(5):487–495

    CAS  PubMed  PubMed Central  Google Scholar 

  • Maharana BR, Kumar B, Prasad A, Patbandha TK, Sudhakar NR, Joseph JP, Patel BR (2016b) Prevalence and assessment of risk factors for haemoprotozoan infections in cattle and buffaloes of South-West Gujarat, India. Indian J Anim Res 50(5):733–739

    Google Scholar 

  • M’ghirbi Y, Bèji M, Oporto B, Khrouf F, Hurtado A, Bouattour A (2016) Anaplasma marginale and A. phagocytophilum in cattle in Tunisia. Parasites Vectors 9(1):556

    PubMed  PubMed Central  Google Scholar 

  • Morley RS, Hugh-Jones ME (1989) The effect of management and ecological factors on the epidemiology of anaplasmosis in the Red river plains and south-east areas of Louisiana. Vet Res Commun 13:359–369

    CAS  PubMed  Google Scholar 

  • Nair AS, Ravindran R, Lakshmanan B, Sreekumar C, Kumar SS, Raju R, Tresamol PV, Vimalkumar MB, Saseendranath MR (2013) Bovine carriers of Anaplasma marginale and Anaplasma bovis in South India. Trop Biomed. 30(1):105–112

    CAS  PubMed  Google Scholar 

  • OIE (Office international des epizooties) (2015) Bovine anaplasmosis. In: The manual of diagnostic tests and vaccines for terrestrial animals, O.I.E., pp 999–1013

  • Oliveira JB, Montoya J, Romero JJ, Urbina A, Soto-Barrientos N, Melo ES, Ramos CA, Araújo FR (2011) Epidemiology of bovine anaplasmosis in dairy herds from Costa Rica. Vet Parasitol 177(3–4):359–365

    CAS  PubMed  Google Scholar 

  • Paramanandham K, Mohankumar A, Puttahonnappa Suresh K, Susan Jacob S, Roy P (2019) Prevalence of Anaplasma species in India and the World in dairy animals: a systematic review and meta-analysis. Res Vet Sci 123:159–170

    PubMed  Google Scholar 

  • Salih DA, Abdel Rahman MB, Mohammed AS, Ahmed R, Kamal S, El Hussein AM (2009) Seroprevalence of tick-borne diseases among cattle in the Sudan. Parasit Res 104(4):845–850

    CAS  Google Scholar 

  • Seo MG, Ouh IO, Lee SH, Son UH, Geraldino P, Rhee MH, Kwon OD, Kim TH, Kwa D (2018) Serological detection of antibodies against Anaplasma spp. in cattle reared in the Gyeongsangbuk-do, Korea. Korean J Parasitol 56(3):287–290

    PubMed  PubMed Central  Google Scholar 

  • Sergeant ESG (2017) Epitools epidemiological calculators. Retrieved from http://epitools.ausvet.com.au/

  • Sharma A, Singla LD, Kaur P, Bal MS (2015a) PCR and ELISA Vis-à-vis Microscopy for detection of bovine anaplasmosis: a study on associated risk of an upcoming problem in North India. Sci World J 15:1–8

    CAS  Google Scholar 

  • Sharma A, Singla LD, Tuli A, Kaur P, Bal MS (2015b) Detection and assessment of risk factors associated with natural concurrent infection of Trypanosoma evansi and Anaplasma marginale in dairy animals by duplex PCR in eastern Punjab. Trop Anim Health Prod 47:251–257

    PubMed  Google Scholar 

  • Singh NK, Singh H, Jyoti Haque M, Rath SS (2012) Prevalence of parasitic infections in cattle of Ludhiana district, Punjab. J Parasit Dis 36(2):256–259

    CAS  PubMed  PubMed Central  Google Scholar 

  • Somparn P, Gibb MJ, Markvichitr K, Chaiyabutr N, Thummabood S, Vajrabukka C (2004) Analysis of climatic risk for cattle and buffalo production in northeast Thailand. Int J Biometeorol 49:59–64

    CAS  PubMed  Google Scholar 

  • Tembue AA, da Silva JB, da Silva FJ, Pires MS, Baldani CD, Soares CO, Massard CL, da Fonseca AH (2011) Seroprevalence of IgG antibodies against Anaplasma marginale in cattle from south Mozambique. Rev Bras Parasitol Vet 20(4):318–324

    PubMed  Google Scholar 

  • Terkawi MA, Huyen NX, Shinuo C, Inpankaew T, Maklon K, Aboulaila M, Ueno A, Goo YK, Yokoyama N, Jittapalapong S, Xuan X, Igarashi I (2011) Molecular and serological prevalence of Babesia bovis and Babesia bigemina in water buffaloes in the northeast region of Thailand. Vet Parasitol 78:201–207

    Google Scholar 

  • Torioni de Echaide S, Knowles DP, McGuire TC, Palmer GH, Suarez CE, McElwain TF (1998) Detection of cattle naturally infected with Anaplasma marginale in a region of endemicity by nested PCR and a competitive enzymelinked immunosorbent assay using recombinant major surface protein 5. J Clin Microbiol 36:777–782

    CAS  PubMed  PubMed Central  Google Scholar 

  • Tucker TR, Aly SS, Maas J, Davy JS, Foley JE (2016) Investigation of Anaplasma marginale seroprevalence in a traditionally managed large California beef herd. Vet Med Int 16:6186078

    Google Scholar 

  • Uilenberg G (1995) International collaborative research: Significance of tick-borne hemoparasitic diseases to world animal health. Vet Parasitol 57:19–41

    CAS  PubMed  Google Scholar 

  • Urdaz-Rodríguez JH, Fosgate GT, Alleman AR, Rae DO, Donovan GA, Melendez P (2009) Seroprevalence estimation and management factors associated with high herd seropositivity for Anaplasma marginale in commercial dairy farms of Puerto Rico. Trop Anim Health Prod 41:1439–1448

    PubMed  Google Scholar 

  • Vetrivel D, Pandian ASS, Shree JS (2017) A study on predisposing factors for the prevalence of anaplasmosis in dairy cattle. J Entomol Zool Stud 5(6):1228–1230

    Google Scholar 

  • Visser ES, McGuire TC, Palmer GH, Davis WC, Shkap V, Pipano E, Knowles DP Jr (1992) The Anaplasma marginale msp5 gene encodes a 19-kilodalton protein conserved in all recognized Anaplasma species. Infect Immun 60(12):5139–5144

    CAS  PubMed  PubMed Central  Google Scholar 

  • Ybanez AP, Ybanez RHD, Cruz-Flores MJ, Xuenan X, Yokoyama N, Inokuma H (2014) High genetic diversity of Anaplasma marginale detected from Philippine cattle. J Vet Med Sci 76:1009–1014

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

The authors are grateful to the management of the National Dairy Development Board (NDDB), Anand for providing necessary facilities and funding to carry out this work.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Samir Kumar Rana.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

In this study, serum samples submitted as part of routine disease screening program (Brucellosis and IBR) and stored in the repository of NDDB R&D laboratory, Hyderabad were used. These serum samples were collected by the organized herds as per the standard protocol. The present study does not come under the category of experimental research on animals, therefore, formal ethical approval is not required.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sarangi, L.N., Rana, S.K., Prasad, A. et al. Prevalence of antibodies to Anaplasma in cattle and buffaloes of different organized herds in India. J Parasit Dis 45, 359–365 (2021). https://doi.org/10.1007/s12639-020-01312-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12639-020-01312-7

Keywords

Navigation