Pathological and molecular characterization of Mycobacterium tuberculosis complex in necropsied tissues of Sambar deer (Rusa unicolor) and Nilgai (Boselaphus tragocamelus) from Assam, India

Document Type : Original Article

Authors

1 Research Associate, ADMaC, Department of Veterinary Microbiology, College of Veterinary Science, Assam Agricultural University, Khanapara, Ghy-22

2 HOD, Department of Vety. Microbiology, CVSc,AAU, Ghy-22, India

3 3.Asstt.professor, Department of Vety. Microbiology, CVSc,AAU, Ghy-22, India

4 Associate professor, Department of Vety. Microbiology, CVSc,AAU, Ghy-22, India

5 Asstt.professor, Department of Animal Biotechnology, CVSc,AAU, Ghy-22, India

6 Asstt.professor, Department of Vety. Microbiology, CVSc,AAU, Ghy-22, India

7 PhD, Research Associate, ADMaC, CVSc,AAU, Ghy-22, India

8 pathologist, Assam State Zoo, Guwahati, India

9 Asstt.professor, Department of Vety. Pathology, CVSc,AAU, Ghy-22, India

10 Senior Scientist, ICAR research complex for NEH region, Meghalaya, India

10.30466/vrf.2025.2059566.4747
Abstract
Bovine tuberculosis (bTB) is a chronic bacterial disease primarily caused by Mycobacterium bovis, a member of the Mycobacterium tuberculosis complex (MTBC), with significant zoonotic implications. This study aimed to detect MTBC in wildlife species, specifically Nilgai (Boselaphus tragocamelus) and Sambar deer (Rusa unicolor), using gross pathology, histopathology, acid-fast staining and molecular confirmation. Necropsied tissue samples were collected during post-mortem examination of a Nilgai and a Sambar deer from Assam State Zoo, India. Macroscopically, multiple granulomatous tubercles of varying sizes were observed in the lungs and liver, with creamy white caseous material marked upon sectioning. Ziehl-Neelsen staining of tissue smears from granulomatous lesions confirmed the presence of acid-fast bacilli. Microscopic examination of TB granulomas revealed a central necrotic mass surrounded by inflammatory cell infiltration, including Langerhans-type giant cells. Molecular confirmation of MTBC infection was achieved by amplifying hsp65 and IS1081 in tissue samples, further validated by nBLAST analysis following Sanger dideoxynucleotide sequencing. In conclusion, this study confirmed the presence of tuberculosis in these wildlife species through an integrated approach combining pathology, microbiology and molecular diagnostics, highlighting the need to understand pathogen entry into the herd and prevent potential spillover.

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Articles in Press, Accepted Manuscript
Available Online from 18 May 2026

  • Receive Date 21 May 2025
  • Revise Date 18 August 2025
  • Accept Date 11 October 2025