Skip to main content
Log in

Antibiotic resistance and probiotic properties of dominant lactic microflora from Tungrymbai, an ethnic fermented soybean food of India

  • Note
  • Published:
Journal of Microbiology Aims and scope Submit manuscript

Abstract

The present investigation was conducted to assess lactic acid bacteria present in traditionally fermented food of ethnic tribes in India for probiotic properties, antibacterial activity, and antibiotic tolerance behavior. Enterococcus sp., Lactobacillus sp., and Lactococcus sp. showed antibacterial activity against Bacillus cereus MTCC 430, Staphylococcus aureus subsp. aureus MTCC 740, and Salmonella enterica ser. paratyphi A MTCC 735. Lactococcus sp. and Lactobacillus sp. could tolerate acidic conditions (pH 2) and high bile salt concentration (4000 ppm). The lactic microflora were found to be sensitive to most common antibiotics, except for cloxacillin (5 μg), cephalexin (30 μg), and cephalothin (30 μg).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ampe, F., Omar, N.B., Moizan, C., Wacher, C., and Guyot, J.P. 1999. Polyphasic study of the spatial distribution of microorganisms in Mexican Pozol, a fermented maize dough, demonstrates the need for cultivation-independent methods to investigate traditional fermentations. Appl. Environ. Microbiol. 65, 5464–5473.

    PubMed  CAS  Google Scholar 

  • Arihara, K., Ota, H., Itoh, M., Kondo, Y., Sameshima, T., Yamanaka, H., Akimoto, M., Kanai, S., and Miki, T. 1998. Lactobacillus acidophilus group lactic acid bacteria applied to meat fermentation. J. Food Sci. 63, 544–547.

    Article  CAS  Google Scholar 

  • Batish, V.K. and Ranganathan, B. 1986. Antibiotic susceptibility of deoxyribonuclease positive enterococci isolated from milk and milk products and their epidemiological significance. Int. J. Food Microbiol. 16, 203–206.

    Google Scholar 

  • Bauer, A.W., Kirby, W.M.M., Sherris, J.C., and Turck, M. 1966. Antibiotic susceptibility testing by a standardized single disk method. Am. J. Clin. Pathol. 45, 493–496.

    PubMed  CAS  Google Scholar 

  • Davies, R. and Roberts, T.A. 1999. Antimicrobial susceptibility of enterococci recovered from commercial swine carcasses: effect of feed additives. Lett. Appl. Microbiol. 29, 327–333.

    Article  PubMed  CAS  Google Scholar 

  • Erkkila, S. and Petaja, E. 2000. Screening of commercial meat starter cultures at low pH in the presence of bile salts for potential probiotic use. J. Meat Sci. 55, 297–300.

    Article  CAS  Google Scholar 

  • Franz, C.M., Muscholl-Silberhorn, A.B., Yousif, N.M.K., Vancanneyt, M., Swings, J., and Holzapfel, W.H. 2001. Incidence of virulence factors and antibiotic resistance among Enterococci isolated from food. Appl. Environ. Microbiol. 67, 4385–4389.

    Article  PubMed  CAS  Google Scholar 

  • Gilliland, S., Staley, T., and Bush, L. 1984. Importance of bile tolerance of Lactobacillus acidophilus used as dietary adjunct. J. Dairy Sci. 67, 3045–3051.

    Article  PubMed  CAS  Google Scholar 

  • Giraffa, G. 2002. Enterococci from foods. FEMS Microbiol. Rev. 26, 163–171.

    Article  PubMed  CAS  Google Scholar 

  • Goldin, B. and Gorbach, S. 1992. Probiotics for humans, pp. 355–376. In Fuller, R. (ed.), Probiotics-the scientific basis, Chapman and Hall, London, UK.

    Google Scholar 

  • Gonzalez, C.F. and Kunka, B.S. 1987. Plasmid-associated bacteriocin production and sucrose fermentation in Pediococcus acidilactici. Appl. Environ. Microbiol. 53, 2534–2538.

    PubMed  CAS  Google Scholar 

  • Holt, J.G., Krieg, N.R., Sneath, P.H.A., Staley, J.T., and Williams, S.T. 2000. Bergey’s Manual of Determinative Bacteriology. 9th edition, Lippincott Williams & Wilkins, USA.

    Google Scholar 

  • Jeyaram, K., Mohendro, S.W., Premarani, T., Ranjita, D.A., Selina, C.K., Talukdar, N.C., and Rohinikumar, S.M. 2008. Molecular identification of dominant microflora associated with ‘Hawaijar’ — A traditional fermented soybean (Glycine max (L.)) food of Manipur, India. Int. J. Food. Microbiol. 122, 259–268.

    Article  PubMed  CAS  Google Scholar 

  • Klaenhammer, T., Altermann, E., Arigoni, F., Bolotin, A., Breidt, F., Broadbent, J., Cano, R., Chaillou, S., Deutscher, J., Gasson, M., and et al. 2002. Discovering lactic acid bacteria by genomics. Antonie van Leeuwenhoek 82, 29–58.

    Article  PubMed  CAS  Google Scholar 

  • Klein, G., Pack, A., and Reuter, G. 1998. Antibiotic resistance patterns of enterococci and occurrence of vancomycin-resistant enterococci in raw minced beef and pork in Germany. Appl. Environ. Microbiol. 64, 1825–1830.

    PubMed  CAS  Google Scholar 

  • Lim, S.M. and Im, D.S. 2009. Screening and characterization of probiotic lactic acid bacteria isolated from Korean fermented foods. J. Microbiol. Biotechnol. 19, 178–186.

    Article  PubMed  CAS  Google Scholar 

  • Paludan-Muller, C., Huss, H.H., and Gram, L. 1999. Characterization of lactic acid bacteria isolated from a Thai low-salt fermented fish product and the role of garlic as substrate for fermentation. Int. J. Food Microbiol. 46, 219–229.

    Article  PubMed  CAS  Google Scholar 

  • Pennacchia, C., Ercolini, D., Blaiotta, G., Pepe, O., Mauriello, F., and Villani, F. 2004. Selection of Lactobacillus strains from fermented sausages for their potential use as probiotics. J. Meat Sci. 67, 309–317.

    Article  CAS  Google Scholar 

  • Robrido, B., Singh, K.V., Baquero, F., Murray, B.E., and Torres, C. 2000. Vancomycin-resistant enterococci isolated from animals and food. Int. J. Food Microbiol. 54, 197–204.

    Article  Google Scholar 

  • Singh, N.I. and Umabati, D.A. 1995. Fermentation prospects of two phylloplane bacteria in traditional Hawaijar made from boiled soybean (Glycine max L.). J. Food Sci. Technol. 32, 219–220.

    Google Scholar 

  • Sohliya, I., Joshi, S.R., Bhagobaty, R.K., and Kumar, R. 2009. Tungrymbai-traditional fermented soybean food of the ethnic tribes of Meghalaya. Ind. J. Trad. Knowle. 8, 559–561.

    Google Scholar 

  • Tamang, J.P. 2003. Native microorganisms in the fermentation of Kinema. Int. J. Food Microbiol. 43, 127–130.

    Google Scholar 

  • Teuber, M. and Perreten, V. 2000. Role of milk and meat products as vehicles for antibiotic-resistant bacteria. Acta Vet. Scand. 93, 75–87.

    CAS  Google Scholar 

  • Vlková, E., Rada, V., Popelářová, P., Trojanová, I., and Killer, J. 2006. Antimicrobial susceptibility of bifidobacteria isolated from gastrointestinal tract of calves. Livestock Sci. 105, 253–259.

    Article  Google Scholar 

  • Yang, R., Chen, Y., and Ray, B. 1999. Enhanced bacteriocin production by lactic acid bacteria in a diary based medium, supplemented with β-galactosidase. Ind. J. Microbiol. 39, 235–240.

    CAS  Google Scholar 

  • Zamudio-Maya, M., Narva ez-Zapata, J., and Rojas-Herrera, R. 2008. Isolation and identification of lactic acid bacteria from sediments of a coastal marsh using a differential selective medium. Lett. Appl. Microbiol. 46, 402–407.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Santa Ram Joshi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Thokchom, S., Joshi, S.R. Antibiotic resistance and probiotic properties of dominant lactic microflora from Tungrymbai, an ethnic fermented soybean food of India. J Microbiol. 50, 535–539 (2012). https://doi.org/10.1007/s12275-012-1409-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12275-012-1409-x

Keywords

Navigation