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

Authors

  • Siraj Ahmad Livestock Research and Dairy Development Department Khyber Pakhtunkhwa, Pakistan
  • Muhammad Rizwan Center for Biotechnology and Microbiology University of Swat Khyber Pakhtunkhwa, Pakistan
  • Farman Ullah Faculty of Veterinary and Animal Sciences, National Center for Livestock Breeding Genetics and Genomics LUAWMS, Pakistan
  • Sami Ullah Khan Department of Veterinary Microbiology, Faculty of Veterinary Medicine, University of Gadjah Mada, Yogyakarta, Indonesia
  • Ziauddin CASVAB University of Balochistan Quetta
  • Muhammad Shahid Veterinary Research Institute Peshawar Khyber Pakhtunkhwa, Pakistan
  • Nasrullah Livestock Research and Dairy Development Department Khyber Pakhtunkhwa, Pakistan
  • Nakash Smark Veterinary Research Institute Peshawar Khyber Pakhtunkhwa, Pakistan
  • Shahzada Adrian Shah Department of Animal Health, The university of Agriculture Peshawar, KP, Pakistan
  • Farman Ullah Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction, Education Ministry of China, College of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan 430070, Peoples Republic of China

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, Enzyme-Linked 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

2025-05-12

How to Cite

Siraj Ahmad, Muhammad Rizwan, Farman Ullah, Sami Ullah Khan, Ziauddin, Muhammad Shahid, Nasrullah, Nakash Smark, Shahzada Adrian Shah, & Farman Ullah. (2025). Serological and molecular coverage of brucellosis in high-risk human population of district Swabi, Khyber Pakhtunkhwa, Pakistan. Physical Education, Health and Social Sciences, 3(2), 222–245. https://doi.org/10.63163/jpehss.v3i2.338