Register      Login
Animal Production Science Animal Production Science Society
Food, fibre and pharmaceuticals from animals
RESEARCH ARTICLE

Diet composition at weaning affects the rumen microbial population and methane emissions by lambs

D. R. Yáñez-Ruiz A B D , K. J. Hart A , A. I. Martin-Garcia B , S. Ramos C and C. J. Newbold A
+ Author Affiliations
- Author Affiliations

A University of Wales, Aberystwyth, UK.

B Estación Experimental del Zaidín (CSIC), Granada, Spain.

C Universidad de León, León, Spain.

D Corresponding author. Email: david.yanez@eez.csic.es

Australian Journal of Experimental Agriculture 48(2) 186-188 https://doi.org/10.1071/EA07237
Submitted: 3 August 2007  Accepted: 4 November 2007   Published: 2 January 2008

Abstract

The aim of this experiment was to investigate whether different diets at weaning determine the microbial populations established in the rumen, together with its methanogenic capacity, and whether these differences are consistent over a longer time period. Twenty ewes with single lambs were used in two periods. Period I: 10 lambs had access only to grass hay whilst with the dam and for 8 weeks after weaning (group H). The other 10 lambs had free access to concentrate and grass hay whilst with the dam and were fed with a 60 : 40 mix of concentrate and grass hay for 8 weeks after weaning (group C). Eight weeks after weaning, methane emissions were measured in polycarbonate chambers over a 3-day period. After methane emission measurements, five lambs from each group were randomly selected and slaughtered and samples of rumen content collected for measuring rumen fermentation parameters and for microbial enumeration (total and cellulolytic bacteria and methanogenic archeaea) by most probable number. Period II: the remaining 10 lambs were grouped together and fed the same diet (grass and concentrate) for 4 months. After this period, all animals were fed concentrate and grass hay (60 : 40) for 2 weeks and introduced in to the chambers to measure methane emissions over a 3-day period. After measurements, they were slaughtered and rumen samples collected and analysed as in Period I. Lambs from group H produced more (P = 0.04) methane than group C lambs (26.0 v. 22.5 L/kg DM intake) in Period I. Group H lambs also had less total bacteria (10.2 × 1010 v. 61.6 × 1010 cells; P = 0.284) but more cellulolytic bacteria (40.6 × 109 v. 10.0 × 109 cells; P = 0.098) and methanogenic archaea (37.1 × 109 v. 19.0 × 109 cells; P = 0.113) than group C lambs in Period I. The acetate to propionate ratio tended to be higher (P = 0.089) in group H lambs than in group C lambs (3.00 v. 2.35). In Period II, methane produced was not different (P > 0.05) between the groups (26.6. v. 25.7 L/kg DM intake by group C and H lambs, respectively). Microbial numbers and fermentation parameters were also similar in samples collected from both experimental groups in Period II. Our results show that the differences observed as a result of providing different diets at weaning disappear in the long-term. It may be appropriate to study a wider range of dietary treatments to better understand the factors determining the microbial populations establishing in the rumen.


Acknowledgements

D. R. Yáñez-Ruiz gratefully acknowledges the receipt of a research contract from the European Commission (Marie Curie Program RUMENOMICS 010972).


References


Dehority BA, Tirabasso PA, Grifo AP (1989) Most-probable-number procedure for enumerating ruminal bacteria, including simultaneous estimation of total and cellulolytic numbers in one medium. Applied and Environmental Microbiology 55, 2789–2792.
CAS | PubMed |
open url image1

Fonty G, Gouet P, Jouany J-P, Senaud J (1987) Establishment of the microflora and anaerobic fungi in the rumen of lambs. Journal of General Microbiology 133, 1835–1843. open url image1

Hegarty RS (2004) Genotype differences and their impact on digestive tract function of ruminants: a review. Australian Journal of Experimental Agriculture 44, 459–467.
Crossref | GoogleScholarGoogle Scholar | open url image1

Joblin KN (2006) Methanogenic archaea. In ‘Methods in gut microbial ecology for ruminants’. (Eds HPS Makkar, CS McSweeney) pp. 47–53. (Springer)

Joblin KN, Naylor GE, Williams AG (1990) Effect of Methanobrevibacter smithii on xylanolytic activity of anaerobic ruminal fungi. Applied and Environmental Microbiology 56, 2287–2295.
CAS | PubMed |
open url image1

Lovett D, Lovell S, Stack L, Callan J, Finlay M, Conolly J, O’Mara FP (2003) Effect of forage/concentrate ratio and dietary coconut oil level on methane output and performance of finishing beef heifers. Livestock Production Science 84, 135–146.
Crossref | GoogleScholarGoogle Scholar | open url image1

Marvin-Sikkema FD, Richardson AJ, Stewart CS, Gottschal JC, Prins RA (1990) Influence of hydrogen-consuming bacteria on cellulose degradation by anaerobic fungi. Applied and Environmental Microbiology 56, 3793–3797.
CAS | PubMed |
open url image1

Morvan B, Dore J, Rieu-Lesme F, Foucat L, Fonty G, Gouet P (1994) Establishment of hydrogen-utilizing bacteria in the rumen of the newborn lamb. FEMS Microbiology Letters 117, 249–256.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Ohene-Adjei S, Teather RM, Ivan M, Forster RJ (2007) Post-inoculation protozoan establishment and association patterns of methanogenic archaea in the ovine rumen. Applied and Environmental Microbiology 73, 4609–4618.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Skillman LC, Evans PN, Naylor GE, Morvan B, Jarvis GN, Joblin KN (2004) 16S ribosomal DNA-directed PCR primers for ruminal methanogens and identification of methanogens colonising young lambs. Anaerobe 10, 277–285.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Stewart CS, Fonty G, Gouet P (1988) The establishment of rumen microbial communities. Animal Feed Science and Technology 21, 69–97.
Crossref | GoogleScholarGoogle Scholar | open url image1

Stewart CS , Flint HJ , Bryant MP (1997) The rumen bacteria. In ‘The rumen microbial ecosystem’. (Eds PN Hobson, CS Stewart) pp. 10–72. (Chapman and Hall: London, UK)

Vogels GD, Hoppe W, Stumm CK (1980) Association of methanogenic bacteria with rumen ciliates. Applied and Environmental Microbiology 40, 608–612.
CAS | PubMed |
open url image1

Wolin MJ, Miller TL (1987) Bioconversion of organic carbon to CH4 and CO2. Geomicrobiology Journal 5, 239–259.
CAS |
open url image1