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Effect of a mixture of Galla rhois and Cinnamomum cassia extracts on susceptibility to the colonization of Campylobacter jejuni in broiler chickens

  • Cho, Byung-Wook (Department of Animal Science, College of Life Sciences, Pusan National University) ;
  • Lee, Soo-Mi (Department of Environmental Health, Graduate School of Public Health, Gyeongsang National University) ;
  • Cha, Chun-Nam (Engineering Research Institute and Department of Industrial Systems Engineering, Gyeongsang National University) ;
  • Yoo, Chang-Yeol (Department of Smart Information Convergence, Gyeongnam Provincial Namhae College) ;
  • Son, Song-Ee (Research Institute of Life Sciences and College of Veterinary Medicine, Gyeongsang National University) ;
  • Kim, Suk (Research Institute of Life Sciences and College of Veterinary Medicine, Gyeongsang National University) ;
  • Lee, Hu-Jang (Department of Environmental Health, Graduate School of Public Health, Gyeongsang National University)
  • 투고 : 2015.11.12
  • 심사 : 2016.02.15
  • 발행 : 2016.03.31

초록

The present study evaluated the effects of a mixture of Galla rhois and Cinnamomum cassia extracts (GCE) (1 : 1, w/w) on susceptibility to the colonization of Campylobacter (C.) jejuni in broilers. Eighty two-week-old broilers (n = 20 per group) were used to estimate the efficacy of GCE against C. jejuni infection via drinking water. Antibacterial activity testing revealed that the minimum bactericidal concentration of GCE against C. jejuni was 2.5 mg/mL. Broilers challenged with C. jejuni were administered 0.0 (Non-GCE), 2.5 (GCE-2.5), 5.0 (GCE-5.0) and 10.0 g/L (GCE-10) GCE for 7 days, and the cecal contents were collected from five broilers per group on the 1st, 3rd, 5th, and 7th day post-treatment. On day 3 post-administration, the number of C. jejuni in GCE-5.0 (p < 0.05) and GCE-10 (p < 0.01) was significantly decreased relative to Non-GCE, while on day 7 those in all GCE-treated groups were significantly decreased compared to the Non-GCE group (p < 0.001). Hematological and blood biochemical analysis revealed no significant differences in parameters between the Non-GCE and GCE-treated groups. Based on the results of the present study, GCE was identified as a safe and alternative candidate to suppress C. jejuni colonization in broilers.

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참고문헌

  1. Adedayo O, Kirkpatrick BD. Campylobacter jejuni infections: update on presentation, diagnosis, and management. Hosp Physician 2008, 44, 9-15.
  2. Cha CN, Yu EA, Park EK, Kim S, Lee HJ. Effects of dietary supplementation with Galla Rhois on growth performance and diarrhea incidence in postweaning piglets. J Vet Clin 2013, 30, 353-358.
  3. Cwikla C, Schmidt K, Matthias A, Bone KM, Lehmann R, Tiralongo E. Investigations into the antibacterial activities of phytotherapeutics against Helicobacter pylori and Campylobacter jejuni. Phytother Res 2010, 24, 649-656.
  4. European Food Safety Authority, European Centre for Disease Prevention and Control. The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2011. EFSA J 2013, 11, 3196. https://doi.org/10.2903/j.efsa.2013.3196
  5. Friedman M, Henika PR, Mandrell RE. Bactericidal activities of plant essential oils and some of their isolated constituents against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica. J Food Prot 2002, 65, 1545-1560. https://doi.org/10.4315/0362-028X-65.10.1545
  6. Ghareeb K, Awad WA, Mohnl M, Porta R, Biarnes M, Bohm J, Schatzmayr G. Evaluating the efficacy of an avian-specific probiotic to reduce the colonization of Campylobacter jejuni in broiler chickens. Poult Sci 2012, 91, 1825-1832. https://doi.org/10.3382/ps.2012-02168
  7. Griekspoor P, Colles FM, McCarthy ND, Hansbro PM, Ashhurst-Smith C, Olsen B, Hasselquist D, Maiden MC, Waldenstrom J. Marked host specificity and lack of phylogeographic population structure of Campylobacter jejuni in wild birds. Mol Ecol 2013, 22, 1463-1472. https://doi.org/10.1111/mec.12144
  8. Hao H, Cheng G, Iqbal Z, Ai X, Hussain HI, Huang L, Dai M, Wang Y, Liu Z, Yuan Z. Benefits and risks of antimicrobial use in food-producing animals. Front Microbiol 2014, 5, 288.
  9. Hermans D, Van Steendam K, Verbrugghe E, Verlinden M, Martel A, Seliwiorstow T, Heyndrickx M, Haesebrouck F, De Zutter L, Deforce D, Pasmans F. Passive immunization to reduce Campylobacter jejuni colonization and transmission in broiler chickens. Vet Res 2014, 45, 27. https://doi.org/10.1186/1297-9716-45-27
  10. Ho HW, Dong HJ, Kim W, Bang K, An JU, Kim C, Chon JW, Seo KH, Hahn TW, Ku BK, Cho S. Genetic relationship of Campylobacter jejuni isolates from different sources by PFGE and flaA typing. J Prev Vet Med 2015, 39, 23-26. https://doi.org/10.13041/jpvm.2015.39.1.23
  11. Hwa JS, Jin YS, Lee YS, Ko YS, Kim YM, Shi LY, Kim HJ, Lee JH, Ngoc TM, Bae KH, Kim YS, Chang KC. 2-Methoxycinnamaldehyde from Cinnamomum cassia reduces rat myocardial ischemia and reperfusion injury in vivo due to HO-1 induction. J Ethnopharmacol 2012, 139, 605-615. https://doi.org/10.1016/j.jep.2011.12.001
  12. Karmegam N, Karuppusamy S, Prakash M, Jayakumar M, Rajasekar K. Antibacterial potency and synergistic effect of certain plant extracts against food-borne diarrheagenic bacteria. Int J Biomed Pharm Sci 2008, 2, 88-93.
  13. Kittler S, Fischer S, Abdulmawjood A, Glunder G, Klein G. Effect of bacteriophage application on Campylobacter jejuni loads in commercial broiler flocks. Appl Environ Microbiol 2013, 79, 7525-7533. https://doi.org/10.1128/AEM.02703-13
  14. Kurekci C, Al Jassim R, Hassan E, Bishop-Hurley SL, Padmanabha J, McSweeney CS. Effects of feeding plant-derived agents on the colonization of Campylobacter jejuni in broiler chickens. Poult Sci 2014, 93, 2337-2346. https://doi.org/10.3382/ps.2014-03950
  15. Lee CF, Han CK, Tsau JL. In vitro inhibitory activity of Chinese leek extract against Campylobacter species. Int J Food Microbiol 2004, 94, 169-174. https://doi.org/10.1016/j.ijfoodmicro.2004.01.009
  16. Lee HA, Hong S, Chung YH, Song KD, Kim O. Anticoccidial effects of Galla rhois extract on Eimeria tenella-infected chicken. Lab Anim Res 2012, 28, 193-197. https://doi.org/10.5625/lar.2012.28.3.193
  17. Lee JJ, Cho WK, Kwon H, Gu M, Ma JY. Galla rhois exerts its antiplatelet effect by suppressing ERK1/2 and $PLC\hat{a}$ phosphorylation. Food Chem Toxicol 2014, 69, 94-101. https://doi.org/10.1016/j.fct.2014.03.032
  18. Luo N, Pereira S, Sahin O, Lin J, Huang S, Michel L, Zhang Q. Enhanced in vivo fitness of fluoroquinolone-resistant Campylobacter jejuni in the absence of antibiotic selection pressure. Proc Natl Acad Sci U S A 2005, 102, 541-546. https://doi.org/10.1073/pnas.0408966102
  19. Naseri KG, Rahimi S, Khak P. Comparison of the effects of probiotic, organic acid and medicinal plant on Campylobacter jejuni challenged broiler chickens. J Agr Sci Tech 2012, 14 (Suppl), 1485-1496.
  20. O'Loughlin JL, Samuelson DR, Braundmeier-Fleming AG, White BA, Haldorson GJ, Stone JB, Lessmann JJ, Eucker TP, Konkel ME. The intestinal microbiota influences Campylobacter jejuni colonization and extraintestinal dissemination in mice. Appl Environ Microbiol 2015, 81, 4642-4650. https://doi.org/10.1128/AEM.00281-15
  21. Park MS, Kim YS, Lee SH, Kim SH, Park KH, Bahk GJ. Estimating the burden of foodborne disease, South Korea, 2008-2012. Foodborne Pathog Dis 2015, 12, 207-213. https://doi.org/10.1089/fpd.2014.1858
  22. Phillips I, Casewell M, Cox T, De Groot B, Friis C, Jones R, Nightingale C, Preston R, Waddell J. Antibiotic use in animals. J Antimicrob Chemother 2004, 53, 885. https://doi.org/10.1093/jac/dkh149
  23. Salehi E, Shafaei E, Bameri Z, Shareki zahedani S, Bokaeian M, Mirzaee B, Mirfakhraee S, Rigi TB, Akbari M. Prevalence and antimicrobial resistance of Campylobacter jejuni. Int J Infect 2014, 1, e19229.
  24. Schielke A, Rosner BM, Stark K. Epidemiology of campylobacteriosis in Germany - insights from 10 years of surveillance. BMC Infect Dis 2014, 14, 30. https://doi.org/10.1186/1471-2334-14-30
  25. Sirirak T, Voravuthikunchai SP. Eleutherine americana: a candidate for the control of Campylobacter species. Poult Sci 2011, 90, 791-796. https://doi.org/10.3382/ps.2010-01166
  26. Smith JL, Fratamico PM. Fluoroquinolone resistance in Campylobacter. J Food Prot 2010, 73, 1141-1152. https://doi.org/10.4315/0362-028X-73.6.1141
  27. Solis de los Santos F, Donoghue AM, Venkitanarayanan K, Metcalf JH, Reyes-Herrera I, Dirain ML, Aguiar VF, Blore PJ, Donoghue DJ. The natural feed additive caprylic acid decreases Campylobacter jejuni colonization in market-aged broiler chickens. Poult Sci 2009, 88, 61-64. https://doi.org/10.3382/ps.2008-00228
  28. Toghyani M, Toghyani M, Gheisari A, Ghalamkari G, Eghbalsaied S. Evaluation of cinnamon and garlic as antibiotic growth promoter substitutions on performance, immune responses, serum biochemical and haematological parameters in broiler chicks. Livest Sci 2011, 138, 167-173. https://doi.org/10.1016/j.livsci.2010.12.018
  29. Wagenaar JA, French NP, Havelaar AH. Preventing Campylobacter at the source: why is it so difficult? Clin Infect Dis 2013, 57, 1600-1606. https://doi.org/10.1093/cid/cit555