Indian Journal of Animal Research

  • Chief EditorK.M.L. Pathak

  • Print ISSN 0367-6722

  • Online ISSN 0976-0555

  • NAAS Rating 6.50

  • SJR 0.263

  • Impact Factor 0.4 (2024)

Frequency :
Monthly (January, February, March, April, May, June, July, August, September, October, November and December)
Indexing Services :
Science Citation Index Expanded, BIOSIS Preview, ISI Citation Index, Biological Abstracts, Scopus, AGRICOLA, Google Scholar, CrossRef, CAB Abstracting Journals, Chemical Abstracts, Indian Science Abstracts, EBSCO Indexing Services, Index Copernicus
Indian Journal of Animal Research, volume 52 issue 1 (january 2018) : 131-135

Prevalence of Bacillus anthracis spores in wool, hairs and habitat of small ruminants

Maryam Rajput, Asghar Ali Kamboh, Parkash Dewani, Aslam Parvez Umrani, Shahid Hussian Abro, Muhammad Ammar Khan
1<p>Department of Veterinary Microbiology, Faculty of Animal Husbandry and Veterinary Sciences, Sindh Agriculture University, Tandojam 70060, Pakistan.&nbsp;</p>
Cite article:- Rajput Maryam, Kamboh Ali Asghar, Dewani Parkash, Umrani Parvez Aslam, Abro Hussian Shahid, Khan Ammar Muhammad (2017). Prevalence of Bacillus anthracis spores in wool, hairs and habitat of small ruminants . Indian Journal of Animal Research. 52(1): 131-135. doi: 10.18805/ijar.v0iOF.8496.

The present study investigated the level of Bacillus anthracis (B. anthracis) spores contamination in the soil, as well as in small ruminant’s wool/hair in Tharparkar, Pakistan. A total of 160 samples, including soil (n= 80), sheep wool (n= 40) and goat hair (n= 40) were collected from different areas of Tharparkar. Results showed that almost 33.75% samples were found positive for B. anthracis spores from soil, wool and hair; among those 66.25% were from outbreak area, having significantly higher (P < 0.001) incidence than normal areas. Moreover, the soil samples exhibited higher positive prevalence (P < 0.001) than  wool, which also had significantly higher (P < 0.001) than hair samples. The samples taken from Mithi area exhibited higher (P< 0.001) prevalence of B. anthracis, followed by Chachro, Diplo and Nangar Parkar (60.00, 30.00, 25.00 and 20.00%, respectively). The differences in area-wise prevalence were also significant ((P < 0.05). The highest prevalence of B. anthracis spores was recorded in open area, followed by in earthen boundaries, and in confined houses (46.42, 30.76 and 23.00%, respectively). These results indicated that soil is a main source of B. anthracis spores, moreover, sheep wool harbor more spores than goat hair. 


  1. Banerjee, D. and Ashutosh (2011). Effect of thermal exposure on diurnal rhythms of physiological parameters and feed water intake in Tharparkar and Karan Fries heifers. Biological Rhythm Research 42: 39-51.

  2. Chikerema, S.M., Pfukenyi, D.M., Hang’ombe, B.M., L’Abee-Lund, T.M. and Matope, G. (2012). Isolation of Bacillus anthracis from soil in selected high-risk areas of Zimbabwe. Journal of Applied Microbiology 113:1389-95.

  3. Coffin, J.L., Monje, F., Asiimwe-Karimu, G., Amuguni, H.J. and Odoch, T. (2015). A one health, participatory epidemiology assessment of anthrax (Bacillus anthracis) management in western uganda. Social Science and Medicine 129: 44-50.

  4. Dragon, D.C., Rennie, R.P. and Elkin, B.T. (2001). Detection of anthrax spores in endemic regions of northern Canada. Journal of Applied Microbiology 91:435– 441.

  5. Hammerstrom, T.G., Roh, J.H., Nikonowicz, E.P. and Koehler, T.M. (2011). Bacillus anthracis virulence regulator AtxA: oligomeric state, function and CO2-signalling. Molecular Microbiology 82: 634–647.

  6. Hendricks, K.A., Wright, M.E., Shadomy, S.V., Bradley, J.S., Morrow, M.G., Pavia, A.T., Rubinstein, E., Holty, J.E., Messonnier, N.E. and Smith, T.L. (2014). Centers for Disease Control and Prevention expert panel meetings on prevention and treatment of anthrax in adults. Emerging Infectious Diseases 20: e130687.

  7. Jula, M.G.R., Jabbari, A.R. and Malek, B. (2004). Isolation of Anthrax spores from soil in endemic region of Isfahan, Iran. Applied Journal of Microbiology 58: 29-38.

  8. Kissling, E., Wattiau, P., China, B., Poncin, M. and Fretin, D. (2012). B. anthracis in a wool-processing factory: seroprevalence and occupational risk. Epidemiology and Infection 140: 879–886.

  9. Kracalik, I.T., Malania, L., Tsertsvadze, N., Manvelyan, J., Bakanidze, L., Imnadze, P., Tsanava, S. and Blackburn, J.K. (2013). Evidence of local persistence of human anthrax in the country of Georgia associated with environmental and anthropogenic factors. PLoS Neglected Tropical Diseases 7: e2388.

  10. Kumar, M. (2015). Buffalo healthcare management practices followed by the farmers of Ferozepur district of Punjab, India. Indian Journal of Animal Research 49(3): 413-415.

  11. Mangi, M.H., Kamboh, A.A., Rind, R., Dewani, P., Nizamani, Z.A., Mangi, A.R., Nizamani, A.R. and Vistro, W.A. (2015). Seroprevalence of brucellosis in Holstein-Friesian and indigenous cattle breeds of Sindh Province, Pakistan. Journal of Animal Health and Production 3(4): 82-87.

  12. Mondal, S.P. and Yamage, M. (2014). A retrospective study on the epidemiology of anthrax, foot and mouth disease, haemorrhagic septicaemia, peste des petits ruminants and rabies in Bangladesh, (2010-2012). PLOS One 9: e104435.

  13. Mshelia, I.T., Atsanda, N.N., Bitrus, A.A., Adam, B.M., Fika, I.I., Balami, S.B., Jauro, S. and Malgwi, S.A. (2016). Retrospective study of selected endemic viral diseases of poultry diagnosed in Maiduguri North-Eastern Nigeria. Journal of Animal Health and Production 4(2): 60-64.

  14. OIE (2000). Manual of Standards for Diagnostic Tests and Vaccines. 4th ed. OIE, Paris.

  15. Perry, B.D., Gleeson, L.J., Khounsey, S., Bounma, P. and Blacksell, S.D. (2002). The dynamics and impact of foot and mouth disease in smallholder farming systems in South-East Asia: a case study in Laos. Revue Scientifique et Technique 21: 663–673.

  16. Pirzada, M., Malhi, K.K., Kamboh, A.A., Rind, R., Abro, S.H., Lakho, S.A., Bhutto, K.R. and Huda, N. (2016). Prevalence of subclinical mastitis in dairy goats caused by bacterial species. Journal of Animal Health and Production 4(2): 55-59.

  17. Pyne, S. K. and Samanta, G. (2009). Livestock management at different levels of disaster strategy and execution. Indian Journal of Animal Research 43(2): 99-102.

  18. Rajput, M., Kamboh, A.A., Dewani, P., Umrani, A.P. and Rind, R. (2017). Occurrence of Anthrax spores in small ruminants hair/wool in district Tharparkar, Sindh. Journal of Animal Health and Production 5(1): 5-9.

  19. Rakib, T.M., Hassan, M.M., Al-Faruq, A., Erfan, R., Barua, S.R., Faruk, M.A., Hasanuzzaman, M., Chowdhury, S. and Alam, M. (2016). Effect of transport on physical and haematological status of cattle in Bangladesh. Journal of Animal Health and Production 4(3): 78-86.

  20. Rana, R.S. and Naim, H. (2014). Tharparkar: a forgotten disaster. Lancet Global Health 2: e508.

  21. Shabbir, M.Z., Jamil, T., Ali, A.A., Ahmad, A., Naeem, M., Chaudhary, M.H. and Rabbani, M. (2015). Prevalence and distribution of soil-borne zoonotic pathogens in Lahore district of Pakistan. Frontiers in Microbiology 6: 917.

  22. Sharma, P., Sihag, R.C. and Bhradwaj, A. (2013). Isolation and identification of pathogenic bacteria and fungi isolated from skin ulcers of Cirrhinus mrigala. Indian Journal of Animal Research 47 (4): 283-291.

  23. Sjostedt, A., Eriksoon, U., Ramisse, V. and Garrigue, H. (1997). Detection of Bacillus anthracis spores in soil by PCR. FEMS Microbiology Ecology 23:159-168.

  24. Zaidan, N.K., Mohamed, W.M. and Hamad, A.S. (2015). Activity of phosphatase enzymes, concentration of protein and divalent ions in sheep sera during different physiological status. Journal of Animal Health and Production 3(4): 78-81.

     

Editorial Board

View all (0)