Serological and molecular coverage of brucellosis in high-risk human population ofdistrict Swabi, Khyber Pakhtunkhwa, Pakistan

Authors

  • Siraj Ahmad Livestock and Dairy Development Department (Research Wing), Khyber Pakhtunkhwa, Pakistan Author
  • Muhammad Shahid Livestock and Dairy Development Department (Research Wing), Khyber Pakhtunkhwa, Pakistan Author
  • Muhammad Daud Livestock and Dairy Development Department (Research Wing), Khyber Pakhtunkhwa, Pakistan Author
  • Farman Ullah Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction, Education Mini Author
  • Nasrullah Livestock and Dairy Development Department (Extension Wing), Khyber Pakhtunkhwa, Pakistan Author
  • Ziauddin CASVAB University of Balochistan Quetta Author
  • Shahzada Khurram Adrian Shah Department of Animal Health, The university of Agriculture Peshawar, KP, Pakistan Author
  • Sami Ullah Khan Department of Veterinary Microbiology, Faculty of Veterinary Medicine, Universitas Gadjah Mad Author
  • Farman Ullah Faculty of Veterinary and Animal Sciences, National Center for Livestock Breeding Genetics a Author
  • Muhammad Rizwan Center for Biotechnology and Microbiology University of Swat Khyber Pakhtunkhwa, Pakistan Author
  • Nakash Smark Livestock and Dairy Development Department (Research Wing), Khyber Pakhtunkhwa, Pakistan Author

DOI:

https://doi.org/10.63163/jpehss.v3i2.338

Keywords:

Bovine brucellosis, SPAT, RPBT, ELISA, PCR, Human, Swabi

Abstract

Brucellosis is a contagious and zoonotic disease, affecting human and animals equivocally. It is a seriously neglected disease in underdeveloped countries, causing heavy financial losses in the livestock sector in terms of abortion, and a decrease in milk production. To better cope with socioeconomic impact of brucellosis, this study was conducted in district Swabi with the aim to detect brucellosis in high-risk human population through serological Rose Bengal plate test, Serum plate agglutination test, EnzymeLinked Immunosorbent Assay, and molecular Polymerase chain rection techniques with respect to different risk factors and clinical history. A total of 250 blood samples (n=250 each from Human) were collected through predesigned questionnaire and were processed for detection of brucellosis through different techniques in Veterinary Research Institute, Peshawar. Detection of brucellosis frequency was performed through SPAT, RBPT, Indirect ELISA (IgM, IgG) and PCR as 12.4, 10.4, 11.6, 12 and 9.6% respectively. A numerical difference was observed through detection of different tools, but the difference was statistically non-significant (p>0.05). The present research contributes to the existing prevalence data concerning brucella infection in humans and emphasizes the benefits and effectiveness of the molecular technique of PCR compared to serological tests..

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Published

2025-06-30