Buffalo- calf gut origin Pediococcus shows superior probiotic potential than Lactobacillus under in vitro system


202 / 158

Authors

  • ANJU KALA ICAR-Indian Veterinary Research Institute, Izatnagar 243 122 (UP), India image/svg+xml
  • KAVIPRIYA JAYSWAL ICAR-Indian Veterinary Research Institute, Izatnagar 243 122 (UP), India image/svg+xml
  • L C CHAUDHARY ICAR-Indian Veterinary Research Institute, Izatnagar 243 122 (UP), India image/svg+xml
  • PAYAL AGARWAL ICAR-Indian Veterinary Research Institute, Izatnagar 243 122 (UP), India image/svg+xml
  • NEETA AGARWAL ICAR-Indian Veterinary Research Institute, Izatnagar 243 122 (UP), India image/svg+xml
  • ZB DUBAL ICAR-Indian Veterinary Research Institute, Izatnagar 243 122 (UP), India image/svg+xml

https://doi.org/10.56093/ijans.v95i10.150307

Keywords:

Lactobacillus, Murrah Buffalo calf, Pediococcus, Probiotic

Abstract

Autochthonous probiotics are preferred over allochthonous probiotics. Therefore, this research was aimed to isolate and characterize lactic acid bacteria (LAB) from buffalo-calves faeces and evaluate their probiotic potential to develop an autochthonous probiotic for buffalo. Thirty two LABs were isolated from Murrah buffalo-calves faeces out of which eight isolates exhibiting maximum hydrophobicity and minimum auto-aggregation, were subjected to further characterization. Out of 8 two isolates, RM119 and RM122, exhibited highest cell surface hydrophobicity, minimum aggregation time, highest lactic acid production, resistance to various temperatures low pH and bile salts. However, antagonism against Escherichia coli ATCC 25922, Klebsiella pneumoniae ATCC 70063, and Staphylococcus aureus was higher with RM119 as compared to RM122. Phylogenetic analysis revealed that the isolates RM103, RM104, RM106, RM107 and RM113 (NCBI Genbank accession no MN880194, MT180734, MN880195, MN880196 and MT907286, respectively), belonged to Lactiplantibacillus fermentum, isolate RM 102 belonged to Lactobacillus plantarum and RM119 and RM122 belonged to Pediococcus pentosaceus. The results revealed that the two strains of P. pentosaceus (RM112 and RM119) were superior over Lactobacillus isolates in terms of probiotic potential.

Downloads

Download data is not yet available.

References

Abbasiliasi S, Tan J S, Ibrahim T A T, Ramanan R N, Vakhshiteh F, Mustafa S, Ling T C, Rahim R A and Ariff A B. 2012. Isolation of Pediococcus acidilactici Kp10 with ability to secrete bacteriocin-like inhibitory substance from milk products for applications in food industry. BMC Microbiology 12: 260. DOI: https://doi.org/10.1186/1471-2180-12-260

Abdulla A A. 2014. Antimicrobial activity of Lactobacillus acidophilus that carry the bacteriocin gene. International Journal of Current Microbiology and Applied 3: 269–76.

Adetoye A, Pinloche E, Adeniyi B A. and Ayeni F A. 2018. Characterization and anti-salmonella activities of lactic acid bacteria isolated from cattle faeces. BMC Microbiology 18: 96. DOI: https://doi.org/10.1186/s12866-018-1248-y

Agarwal Neeta, Kamra D N, Chaudhary L C, Sahoo A and Pathak N N. 2000. Selection of Saccharomyces cerevisiae strains for use as microbial feed additives. Letters Applied Microbiology 31: 270–73. DOI: https://doi.org/10.1046/j.1472-765x.2000.00826.x

Ashmaig A, Hasan A. and El Gaali E. 2009. Identification of lactic acid bacteria isolated from traditional Sudanese fermented camel milk (Gariss). African Journal of Microbiology Research 3: 451–57.

Baker S B and Summerson W H. 1941 The colorimetric determination of lactic acid in biological material. Journal of Biological Chemistry 138: 535–54. DOI: https://doi.org/10.1016/S0021-9258(18)51379-X

Bernardeau M. and Vernoux J P. 2013. Overview of differences between microbial feed additives and probiotics for food regarding regulation, growth promotion effects and health properties and consequences for extrapolation of farm animal results to humans. Clinical Microbiology and Infection 19: 321–30. DOI: https://doi.org/10.1111/1469-0691.12130

Bhat B, Vaid S, Habib B and Bajaj B K. 2020. Design of experiments for enhanced production of bioactive exopolysaccharides from indigenous probiotic lactic acid bacteria. Indian Journal of Biochemistry and Biophysics 57: 539–51.

Cottyn B G and Boucque C V. 1968. Rapid method for the gas chromatographic determination of volatile fatty acids in rumen fluid. Journal of Agricultural and Food Chemistry 16: 105–7. DOI: https://doi.org/10.1021/jf60155a002

De Vugst L and Vandamme E.J. (1994) Bacteriocins of Lactic Acid Bacteria. Microbiology 539. DOI: https://doi.org/10.1007/978-1-4615-2668-1

Dowarah R, Verma A K, Agarwal N, Singh P and Singh B R. 2018. Characterization and selection of probiotic lactic acid bacteria from the feces of weaning piglets. h, https://doi.org/10.1371/ journal.pone.0192978. DOI: https://doi.org/10.1371/journal.pone.0192978

Dowarah R, Verma A K, Agrawal N, Patel B H M and Singh P. 2017. Effect of swine based probiotic on performance, diarrhoea scores, intestinal microbiota and gut health of grower-finisher crossbred pigs. Livestock Science 195: 74–79 DOI: https://doi.org/10.1016/j.livsci.2016.11.006

Du Toit M, Franz CMAP, Dicks L M T, Schillinger U, Haberer P, Warlies B, Ahrens F and Holzapfel W H. 1998. Characterisation and selection of probiotic lactobacilli for a preliminary minipig feeding trial and their effect on serum cholesterol levels, faeces pH and faeces moisture content. International Journal of Food Microbiology 40: 93–104. DOI: https://doi.org/10.1016/S0168-1605(98)00024-5

Fuller R. ed. (2012) Probiotics: the scientific basis. Springer Science & Business Media.

Garriga M, Pascual M, Monfort J M and Hugas M. (1998). Selection of Lactobacilli for chicken probiotic adjuncts. Journal of Applied Microbiology 84: 125–32. DOI: https://doi.org/10.1046/j.1365-2672.1997.00329.x

Gonzalez-Perez C J, Vargas-Arispuro I, Aispuro-Hernández E, Aguilar-Gil C L, Aguirre-Guzmán Y E, Castillo A, Hernández-Mendoza A, Ayala-Zavala J F and Martínez-Téllez M A. 2019. Potential control of foodborne pathogenic bacteria by Pediococcus pentosaceus and Lactobacillus graminis isolated from fresh vegetables. Microbiology Biotechnology Lett 47: 183–94. DOI: https://doi.org/10.4014/mbl.1808.08014

Gotcheva V, Hristozova E, Hristozova T, Guo M, Roshkova Z and Angelov A. 2002. Assessment of potential probiotic properties of lactic acid bacteria and yeast strains. Food Biotechnology 16: 211–25. DOI: https://doi.org/10.1081/FBT-120016668

Huang Y. and Adams M C. 2004. In vitro assessment of the upper gastrointestinal tolerance of potential probiotic dairy Propionibacteria. International Journal of Food Microbiology 91: 253–60. DOI: https://doi.org/10.1016/j.ijfoodmicro.2003.07.001

Jeyanathan J, Martin C and Morgavi D. 2014. The use of direct-fed microbials for mitigation of ruminant methane emissions: a review. Animal 8: 250–61 DOI: https://doi.org/10.1017/S1751731113002085

Kumar S, Dagar S S and Puniya A K. 2014. Prospective use of bacteriocinogenic Pediococcus pentosaceus as direct-fed microbial having methane reducing potential. Journal of Integrative Agriculture doi: 10.1016/S2095-3119(14)60832-7 DOI: https://doi.org/10.1016/S2095-3119(14)60832-7

Liao S F. and Nyachoti M. 2017. Using probiotics to improve swine gut health and nutrient utilization. Animal Nutrition 3: 331–43. DOI: https://doi.org/10.1016/j.aninu.2017.06.007

Neut C, Mahieux S and Dubreuil L J. 2017. Antibiotic susceptibility of probiotic strains: Is it reasonable to combine probiotics with antibiotics? Med Mal Infect 47: 477–83 DOI: https://doi.org/10.1016/j.medmal.2017.07.001

Palomares C, Pérez-Morales R and Acedo-Félix E. 2007. Evaluation of probiotic properties in Lactobacillus isolated from small intestine of piglets. Rev Latinoam Microbiology 49: 46–54.

Patel A K, Ahire J J, Pawar S P, Chaudhari B L and Chincholkar S B. 2009. Comparative accounts of probiotic characteristics of Bacillus spp. isolated from food wastes. International Food Research Journal 42: 505–10. DOI: https://doi.org/10.1016/j.foodres.2009.01.013

Reniero R, Cocconcelli P S, Bottazzi V and Morelli L. 1992. High frequency of conjugation in Lactobacillus mediated by an aggregation-promoting factor. Journal of General Microbiology 138: 763–68. DOI: https://doi.org/10.1099/00221287-138-4-763

Rodriguez Palacios A, Staempfli H R, Duffield T and Weese J S. 2009. Isolation of bovine intestinal Lactobacillus plantarum and Pediococcus acidilactiti with inhibitory activity against Escherichia coli O157 and F5. Journal of Applied Microbiology 106: 393–401. DOI: https://doi.org/10.1111/j.1365-2672.2008.03959.x

Saxelin M. 2008. Probiotic formulations and applications, the current probiotics market, and changes in the marketplace: a European perspective. Clinical Infectious Diseases 46: S76–S79. DOI: https://doi.org/10.1086/523337

Schillinger U, Lücke F K. 1989. Antibacterial activity of Lactobacillus sake isolated from meat. Applied and Environmental Microbiology 55: 1901–6. DOI: https://doi.org/10.1128/aem.55.8.1901-1906.1989

Silva B C, Sandes S H C, Alvim L B, Bomfim M R Q, Nicoli J R, Neumann E and Nunes A C. 2017. Selection of a candidate probiotic strain of Pediococcus pentosaceus from the faecal microbiota of Horses by in vitro testing and health claims in a mouse model of Salmonella infection. Journal of Applied Microbiology 122: 225–38. DOI: https://doi.org/10.1111/jam.13339

Singla V, Mandal S, Sharma P, Anand S and Tomar S K. 2018. Antibiotic susceptibility profile of Pediococcus spp. from diverse sources. Biotechnology 8: 489. DOI: https://doi.org/10.1007/s13205-018-1514-6

SPSS. 2010. Statistical packages for Social Sciences, Version 20, SPSS Inc., Illinois, USA.

Sukumar G and Ghosh A R. 2010. Pediococcus spp. a potential probiotic isolated from Khadi (an Indian fermented food) and identified by 16S rDNA sequence analysis. African Journal of Food Science 4: 597–602.

Taheri H R, Moravej H, Tabandeh F, Zaghari M and Shivazad M. 2009. Screening of lactic acid bacteria toward their selection as a source of chicken probiotic. Poultry Science 88: 1586–93. DOI: https://doi.org/10.3382/ps.2009-00041

Tokatli M, Gulgor G, Bagder Elmaci S, Arslankoz Isleyen N. and Ozcelik F. 2015. In vitro properties of potential probiotic indigenous lactic acid bacteria originating from traditional pickles. BioMed Research International 8: 315819. DOI: https://doi.org/10.1155/2015/315819

Vlkova E, Rada V, Popelarova P, Trojanova I and Killer J. 2006. Antimicrobial susceptibility of bifidobacteria isolated from gastrointestinal tract of calves. Livestock Science 105: 253–59. DOI: https://doi.org/10.1016/j.livsci.2006.04.011

Downloads

Submitted

2024-04-09

Published

2026-02-12

Issue

Section

Articles

How to Cite

KALA, A. ., JAYSWAL, K. ., CHAUDHARY, L. C. ., AGARWAL, P. ., AGARWAL, N. ., & DUBAL, Z. . (2026). Buffalo- calf gut origin Pediococcus shows superior probiotic potential than Lactobacillus under in vitro system. The Indian Journal of Animal Sciences, 95(10), 926–932. https://doi.org/10.56093/ijans.v95i10.150307
Citation