Zoonotic bacterial populations, gut fermentation characteristics and methane production in feedlot steers during oral nitroethane treatment and after the feeding of an experimental chlorate product

Anaerobe

Volumn 13, Issue 1, 2007, Pages 21-31

  Gutierrez Bañuelos, Hector ^a   Anderson, Robin C ^b   Carstens, Gordon E ^a   Slay, Lisa J ^a   Ramlachan, Nicole ^b   Horrocks, Shane M ^b   Callaway, Todd R ^b   Edrington, Thomas S ^b   Nisbet, David J ^b  

^a TEXAS A AND M UNIVERSITY   (United States)

^b SOUTHERN PLAINS AGRICULTURAL RESEARCH CENTER   (United States)

Author keywords

Chlorate; Feces; Methane; Nitroethane; Pre harvest food safety; Rumen

Indexed keywords

CHLORATE; METHANE; NITROETHANE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL FOOD; ANIMAL MODEL; ARTICLE; BULLOCK; CALORIC INTAKE; CAMPYLOBACTER; CONTROLLED STUDY; ESCHERICHIA COLI; GREENHOUSE EFFECT; NONHUMAN; OZONE LAYER; PRIORITY JOURNAL; RUMEN MICROORGANISM; SALMONELLA; ZOONOSIS;

ADMINISTRATION, ORAL; ANIMALS; CAMPYLOBACTER; CAMPYLOBACTER INFECTIONS; CATTLE; CATTLE DISEASES; CHLORATES; ESCHERICHIA COLI INFECTIONS; ESCHERICHIA COLI O157; ETHANE; FERMENTATION; GRAM-NEGATIVE BACTERIAL INFECTIONS; MALE; METHANE; NITROPARAFFINS; RUMEN; SALMONELLA; SALMONELLA INFECTIONS, ANIMAL; ZOONOSES;

ANIMALIA; BACTERIA (MICROORGANISMS); CAMPYLOBACTER; ESCHERICHIA COLI; SALMONELLA;

EID: 33847033628     PISSN: 10759964     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.anaerobe.2006.11.002     Document Type: Article

References (46)

1. Mead P.S., Slutsker L., Dietz V., McCaig L.F., Bresee J.S., Shapiro C., et al. Food-related illness and death in the United States. Emerg Inf Dis 5 (1999) 607-625
2. USDA/ERS. US Department of Agriculture. Economic Research Service. ERS estimates foodborne disease costs at $6.9 billion per year. 2004. Available at: 〈http://www.ers.usda.gov/briefing/FoodborneDisease/features.htm〉.
3. Hynes NA, Wachsmuth IK. Escherichia coli O157:H7 risk assessment in ground beef: a public health tool. In: Abstracts of the 4th international symposium and workshop on Shiga toxin (Verocytotoxin)-producing Escherichia coli infections, Kyoto, Japan, 2000. p. 46.
4. Vugia D., Hadler J., Chaves S., Blythe D., Smith K., Morse D., et al. Preliminary FoodNet data on the incidence of foodborne illness-selected sites, United States, 2002. MMWR 52 (2003) 340-343
5. Potter A.A., Klashinsky S., Li Y., Frey E., Townsend H., Rogan D., et al. Decreased shedding of Escherichia coli O157:H7 by cattle following vaccination with type III secreted proteins. Vaccine 22 (2004) 362-369
6. Schamberger G.P., Phillips R.L., Jacobs J.L., and Diez-Gonzalez F. Reduction of Escherichia coli O157:H7 populations in cattle by addition of colicin E7-producing Escherichia coli to feed. Appl Environ Microbiol 70 (2004) 6053-6060
7. Zhoa T., Doyle M.P., Harmon B.G., Brown C.A., Mueller P.O.E., and Parks A.H. Reduction of carriage of enterohemorrhagic Escherichia coli O157:H7 in cattle by inoculation with probiotic bacteria. J Clin Microbiol 36 (1998) 641-647
8. Zhoa T., Tkalcic S., Doyle M.P., Harmon B.G., Brown C.A., and Zhoa P. Pathogenicity of enterohemorrhagic Escherichia coli in neonatal calves and evaluation of fecal shedding by treatment with probiotic Escherichia coli. J Food Prot 66 (2003) 924-930
9. Brashears M.M., Galyean M.L., Loneragan G.H., Mann J.E., and Killinger-Mann K. Prevalence of Escherichia coli O157:H7 and performance by beef feedlot cattle given lactobacillus direct-fed microbials. J Food Prot 66 (2003) 748-754
10. Brashears M.M., Jaroni D., and Trimble J. Isolation, selection and characterization of lactic acid bacteria for a competitive exclusion product to reduce shedding of Escherichia coli O157:H7 in cattle. J Food Prot 66 (2003) 355-363
11. Elder RO, Keen JE, Edrington T, Callaway T, Anderson R, Nisbet D. Intervention to reduce fecal shedding of enterohemmorrhagic Escherichia coli O157:H7 in fed beef cattle. In: Abstracts of the 5th international symposium on Shiga toxin (Verocytotoxin)- producing Escherichia coli infections. Edinburgh, Scotland, 2003. p. 94.
12. Anderson R.C., Callaway T.R., Anderson T.J., Kubena L.F., Keith N.K., and Nisbet D.J. Bactericidal effect of sodium chlorate on Escherichia coli concentrations in bovine ruminal and fecal concentrations in vivo. Microb Ecol Health Dis 14 (2002) 24-29
13. Anderson R.C., Carr M.A., Miller R.K., King D.A., Carstens G.E., Genovese K.J., et al. Effects of experimental chlorate preparations as feed and water supplements on Escherichia coli colonization and contamination of beef cattle and carcasses. Food Microbiol 22 (2005) 439-447
14. Callaway T.R., Anderson R.C., Genovese K.J., Poole T.L., Anderson T.J., Byrd J.A., et al. Sodium chlorate supplementation reduces Escherichia coli 0157:H7 populations in cattle. J Anim Sci 80 (2002) 1683-1689
15. Fox J.T., Anderson R.C., Carstens G.E., Miller R.K., Jung Y.S., McReynolds J.L., et al. Effect of nitrate adaption on the bactericidal activity of an experimental chlorate product against Escherichia coli in cattle. Int J Appl Res Vet Med 3 (2005) 76-80
16. ® and the Hawaiian marine algae, Chaetoceros, on ruminal methane production and some zoonotic pathogens in vitro. In: Second international conference of greenhouse gases and animal agriculture GGAA, vol. 27. Publication series, Institute of Animal Science, Zurich, Switzerland, 2005. p. 440-3.
17. Anderson R.C., Jung Y.S., Genovese K.J., McReynolds J.L., Callaway T.R., Edrington T.S., et al. Low level nitrate or nitroethane preconditioning enhances the bactericidal effect of suboptimal experimental chlorate treatment against Escherichia coli and Salmonella typhimurium but not Campylobacter in swine. Foodborne Path Dis 3 (2006) 461-465
18. Jung YS, Anderson RC, Genovese KJ, Edrington TS, Callaway TR, Byrd JA, et al. Reduction of Campylobacter and Salmonella in pigs treated with a select nitrocompound. In: Proceedings of the 5th international symposium on the epidemiology and control of foodborne pathogens in pork, Hersonissos, Crete, 2003. p. 205-7.
19. Anderson RC, Jung YS, Oliver CE, Horrocks SM, Genovese KJ, Harvey RB, et al. Effects of nitrate or nitro-supplementation, with or without added chlorate, on Salmonella enterica serovar Typhimurium and Escherichia coli in swine feces. J Food Prot, in press.
20. Miller T.L. The ecology of methane production and hydrogen sinks in the rumen. In: Englehardt W.V., Leonhard-Marek S., Breves G., and Giesecke D. (Eds). Ruminant physiology: digestion, metabolism, growth and reproduction (1995), Ferdinand Enke Verlag, Berlin 317-331
21. Johnson K.A., and Johnson D.E. Methane emissions from cattle. J Anim Sci 73 (1995) 2483-2492
22. Van Nevel C., and Demeyer D. Control of rumen methanogenesis. Environ Monitor Assess 42 (1996) 73-97
23. Moss A.R., Jouany J., and Newbold J. Methane production by ruminants: its contribution to global warming. Ann Zoot 49 (2000) 231-253
24. Van Nevel C.J., and Demeyer D.I. Feed additives and other interventions for decreasing methane emissions. In: Wallace R.J., and Chesson A. (Eds). Biotechnology in animal feeds & animal feeding (1995), VCH, Weinheim 329-349
25. Anderson R.C., Callaway T.R., Van Kessel J.S., Jung Y.S., Edrington T.S., and Nisbet D.J. Effect of select nitrocompounds on ruminal fermentation; an initial look at their potential to reduce economic and environmental costs associated with ruminal methanogenesis. Bioresour Technol 90 (2003) 59-63
26. Anderson R.C., Carstens G.E., Miller R.K., Callaway T.R., Schultz C.L., Edrington T.S., et al. Effect of oral nitroethane and 2-nitropropanol administration on methane-producing activity and volatile fatty acid production in the ovine rumen. Bioresour Technol 97 (2006) 2421-2426
27. Majak W., Cheng K.J., and Hall J.W. Enhanced degradation of 3-nitropropanol by ruminal microorganisms. J Anim Sci 62 (1986) 1072-1080
28. 6 tracer technique. Environ Sci Technol 28 (1994) 359-362
29. Hinton A., Corrier D.E., Spates G.E., Norman J.O., Ziprin R.L., Beier R.C., et al. Biological control of Salmonella typhimurium in young chickens. Avian Dis 34 (1990) 626-633
30. Wolin M.J. A theoretical rumen fermentation balance. J Dairy Sci 43 (1960) 1452-1459
31. Bryant M.P., and Burkey L.A. Cultural methods and some characteristics of the more numerous groups of bacteria in the bovine rumen. J Dairy Sci 36 (1953) 205-217
32. Allison M.J., Mayberry W.R., McSweeney C.S., and Stahl D.A. Synergistes jonessi, gen. nov., sp. nov.: a ruminal bacterium that degrades toxic pyridinediols. Syst Appl Microbiol 15 (1992) 522-529
33. Stern N.J., Wojton B., and Kwiater K. A differential selective medium, and dry-ice generated atmosphere for recovery of Campylobacter jejuni. J Food Prot 55 (1992) 514-517
34. Anderson R.C., Genovese K.J., Harvey R.B., Stanker L.H., DeLoach J.R., and Nisbet D.J. Assessment of the long term shedding pattern of Salmonella serovar choleraesuis following experimental infection of neonatal piglets. J Vet Diagn Invest 12 (2000) 257-260
35. Elder R.O., Keen J.E., Siragusa G.R., Barkocy-Gallagher G.A., Koohmaraire M., and Laegreid W.W. Correlation of enterohemorrhagic Escherichia coli O157 prevalence in feces, hides, and carcasses of beef cattle during processing. Proc Natl Acad Sci 97 (2000) 2999-3003
36. Moreno-Vivián C., Cabello P., Martínez-Luque M., Blasco R., and Castillo F. Prokaryotic nitrate reduction: molecular properties and functional distinction among bacterial nitrate reducases. J Bacteriol 181 (1999) 6573-6584
37. Edrington T.S., Callaway T.R., Anderson R.C., Genovese K.J., Jung Y.S., McReynolds J.L., et al. Reduction of Escherichia coli O157:H7 populations in sheep by supplementation of an experimental sodium chlorate product. Small Rumin Res 49 (2003) 173-181
38. Horrocks SM, Jung YS, Ricke SC, Callaway TR, Edrington TS, Harvey RB, et al. Effects of nitroethane and 2-nitropropanol against Campylobacter jejuni, In: Proceedings 6th international symposium on the epidemiology and control of foodborne pathogens in pork, Rohnert Park, CA, USA, 2005. p. 194-6.
39. Anderson R.C., Rasmussen M.A., Jensen N.S., and Allison M.J. Denitrobacterium detoxificans gen. nov., sp. nov., a ruminal bacterium that respires on nitrocompounds. Int J Syst Evol Microbiol 50 (2000) 633-638
40. Brown E.G., Carstens G.E., Slay L.J., Woods S.A., Quinn M.J., McReynolds J.L., et al. Effects of nitroethane administration on methane production in growing steers. J Anim Sci Suppl. 2 (2005) 34
41. Wright A.D.G., Kennedy P., O'Neill C.J., Toovey A.F., Popovski S., Rea S.M., et al. Reducing methane emissions in sheep by immunization against rumen methanogens. Vaccine 22 (2004) 3976-3985
42. Anderson R.C., Rasmussen M.A., and Allison M.J. Enrichment and isolation of a nitropropanol metabolizing bacterium from the rumen. Appl Environ Microbiol 62 (1996) 3885-3886
43. Majak W. Further enhancement of nitropropanol detoxification by ruminal bacteria in cattle. Can J Anim Sci 72 (1992) 863-870
44. Anderson R.C., and Rasmussen M.A. Use of a novel nitrotoxin-metabolizing bacterium to reduce ruminal methane production. Bioresour Technol 64 (1998) 89-95
45. Saengkerdsub S., Kim W.K., Anderson R.C., Nisbet D.J., and Nisbet S.C. Effects on nitrocompounds and feedstuffs on in vitro methane production in chicken cecal contents and rumen fluid. Anaerobe 12 (2006) 85-92
46. Chhour K., Nadkarni M.A., Byun R., Martin F.E., Jacques N.A., and Hunter N. Molecular analysis of microbial diversity in advanced caries. J Clin Microbiol 43 (2005) 843-849