Comparative Evaluation of Different Test Combinations for Diagnosis ofMycobacterium aviumSubspeciesparatuberculosisInfecting Dairy Herds in India

Author:

Garg Rajni1,Patil Prasanna Kumar2,Singh Shoor Vir3ORCID,Sharma Shukriti4,Gandham Ravi Kumar5,Singh Ajay Vir6,Filia Gurusimiran1,Singh Pravin Kumar7,Jayaraman Sujata8,Gupta Saurabh3,Chaubey Kundan Kumar3,Tiwari Ruchi9ORCID,Saminathan Mani10,Dhama Kuldeep10ORCID,Sohal Jagdip Singh8ORCID

Affiliation:

1. Animal Disease Research Centre, Guru Angad Dev Veterinary and Animal Sciences University (GADVASU), Ludhiana, Punjab 141004, India

2. Aquatic Animal Health Division, Central Institute of Brackishwater Aquaculture (CIBA), 75 Santhome High Road, R.A. Puram, Chennai 600028, India

3. Microbiology Laboratory, Animal Health Division, Central Institute for Research on Goats, Makhdoom, P.O. Farah, Mathura, Uttar Pradesh 281122, India

4. Department of Veterinary Medicine, Guru Angad Dev Veterinary and Animal Sciences University (GADVASU), Ludhiana, Punjab 141004, India

5. Division of Animal Biotechnology, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh 243122, India

6. National JALMA Institute for Leprosy and Other Mycobacterial Diseases (NJIL & OMD), Tajganj, Agra, Uttar Pradesh 282001, India

7. Department of Microbiology, King George’s Medical University, Lucknow, Uttar Pradesh 226003, India

8. Amity Institute of Microbial Technology, Amity University Rajasthan, Kant Kalwar, NH-11C Delhi-Jaipur Highway, Jaipur 303 002, India

9. Department of Veterinary Microbiology and Immunology, Uttar Pradesh Pandit Deen Dayal Upadhayay Pashu Chikitsa Vigyan Vishwa Vidyalaya Evam Go-Anusandhan Sansthan (DUVASU), Mathura, Uttar Pradesh 281001, India

10. Division of Pathology, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh 243122, India

Abstract

A total of 355 cows were sampled (serum,n=315; faeces,n=355; milk,n=209) from dairy farms located in the Punjab state of India. Faeces and serum/milk samples were screened by acid fast staining and “indigenous ELISA,” respectively. IS900PCR was used to screen faeces and milk samples. Bio-load of MAP in dairy cows was 36.9, 15.6, 16.3, and 14.4%, using microscopy, serum ELISA, milk ELISA and milk PCR, respectively. Estimated kappa values between different test combinations: serum and milk ELISA, faecal microscopy and faecal PCR, milk ELISA and milk PCR, faecal PCR and serum ELISA were 0.325, 0.241, 0.682, and 0.677, respectively. Estimation of the relative sensitivity and specificity of different tests in the present study indicated that “serum ELISA” and “milk ELISA” were good screening tests, add “milk PCR” was “confirmatory test” for MAP infection. Combination of milk ELISA with milk PCR may be adopted as a model strategy for screening and diagnosis of JD in lactating/dairy cattle herds in Indian conditions.

Funder

Animal Disease Monitoring and Surveillance (PD ADMAS)

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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