Fatty acid profiles associated with microbial colonization of freshly ingested grass and rumen biohydrogenation.

Two in situ studies were conducted to examine the use of odd-chain fatty acid profiles to study microbial colonization of freshly ingested herbage in the rumen as well as fatty acid biohydrogenation. In the first study, fresh perennial ryegrass was subjected to a range of sample preparation methods before incubation in the rumen for 2 or 7 h. In the second study, fresh perennial ryegrass was chopped into 1-cm lengths and incubated in polyester bags in the rumen for 2, 8, and 24 h. After removal of bags from the rumen, 4 different washing methods, ranging from manual squeezing to machine washing, were applied. Fatty acids were extracted from washed residues and determined, as methyl esters, by gas chromatography. The main odd-chain fatty acids (with the exception of anteiso C(15:0)) were not found in fresh grass and were useful markers of the effects of incubation time, sample preparation method, and washing method on microbial colonization/contamination. The concentration of these and other odd-chain fatty acids increased with incubation time in both studies. The results indicate rapid and continued microbial colonization of freshly ingested forages, although patterns of odd-chain fatty acids did not reveal any further information about the types of bacteria-colonizing herbage. Principal component, biplot analysis provided a useful overall description of the processes of microbial colonization and degradation of plant fatty acids on fresh herbage incubated in the rumen. Bolus formation during mastication and ingestion results in extensive damage to herbage; none of the techniques (cutting, crushing, and drying/grinding) investigated in this work was able to replicate the effects of bolus formation in the animal. The study provided further evidence of loss of unfermented feed particles through polyester bag pores, especially when feeds are dried and ground. Biohydrogenation of the polyunsaturated fatty acids of fresh herbage was used principally by solid-associated bacteria to enable them to take up high levels of trans-11 C(18:1) and C(18:0) fatty acids. Although trans-11 C(18:1) was strongly associated with bacterial markers (odd- and branched-chain fatty acids), its precursor (cis-9, trans-11 C(18:2)) was not associated with bacterial variation, suggesting that its production in the rumen under these conditions was mainly extracellular.

[1]  P. Moreau Lipids , 2007 .

[2]  D. Oh,et al.  Production of conjugated linoleic acid by isolated Bifidobacterium strains , 2003 .

[3]  R. Dewhurst,et al.  Use of principal component analysis to investigate the origin of heptadecenoic and conjugated linoleic acids in milk. , 2003, Journal of dairy science.

[4]  R. Dewhurst,et al.  Nitrogen supplementation of corn silages. 2. Assessing rumen function using fatty acid profiles of bovine milk. , 2003, Journal of dairy science.

[5]  R. Dewhurst,et al.  Comparison of grass and legume silages for milk production. 2. In vivo and in sacco evaluations of rumen function. , 2003, Journal of dairy science.

[6]  L. Jackson,et al.  Erratum to “Soil community composition and land use history in cultivated and grassland ecosystems of coastal California” [Soil Biology & Biochemistry 34(11) 1599–1611] , 2003 .

[7]  J. Peyraud,et al.  The release of intracellular constituents from fresh ryegrass (Lolium perenne L.) during ingestive mastication in dairy cows: effect of intracellular constituent, season and stage of maturity , 2001 .

[8]  B. White,et al.  Analysis of the rumen bacterial diversity under two different diet conditions using denaturing gradient gel electrophoresis, random sequencing, and statistical ecology approaches , 2001 .

[9]  S. Kishino,et al.  Conjugated Linoleic Acid Accumulation via 10-Hydroxy-12-Octadecaenoic Acid during Microaerobic Transformation of Linoleic Acid by Lactobacillus acidophilus , 2001, Applied and Environmental Microbiology.

[10]  M. Theodorou,et al.  Tansley Review No. 118: Post-ingestion metabolism of fresh forage. , 2000, The New phytologist.

[11]  R. Merry,et al.  Evidence of a role for plant proteases in the degradation of herbage proteins in the rumen of grazing cattle. , 1999, Journal of dairy science.

[12]  A. Ibekwe,et al.  Fatty acid methyl ester (FAME) profiles as a tool to investigate community structure of two agricultural soils , 1999, Plant and Soil.

[13]  E. Titgemeyer,et al.  Standardization of in situ techniques for ruminant feedstuff evaluation. , 1998, Journal of animal science.

[14]  Björck,et al.  Production of conjugated linoleic acid by dairy starter cultures , 1998, Journal of applied microbiology.

[15]  L. Zelles Phospholipid fatty acid profiles in selected members of soil microbial communities. , 1997, Chemosphere.

[16]  E. Chodurek,et al.  Intraspecies variability of cellular fatty acids among soil and intestinal strains of Desulfovibrio desulfuricans , 1996, Applied and environmental microbiology.

[17]  R. Dewhurst,et al.  Comparison of in sacco and in vitro techniques for estimating the rate and extent of rumen fermentation of a range of dietary ingredients , 1995 .

[18]  M. Doreau,et al.  Lipid metabolism of liquid-associated and solid-adherent bacteria gin rumen contents of dairy cows offered lipid-supplemented diets , 1990, British Journal of Nutrition.

[19]  J. Patterson,et al.  Influence of in Situ Bag Rinsing Technique on Determination of Dry Matter Disappearance , 1990 .

[20]  D. Palmquist,et al.  Rapid method for determination of total fatty acid content and composition of feedstuffs and feces , 1988 .

[21]  J. Meyer,et al.  Microbiological evaluation of the intraruminal in sacculus digestion technique , 1986, Applied and environmental microbiology.

[22]  R. Merry,et al.  A comparison of the chemical composition of mixed bacteria harvested from the liquid and solid fractions of rumen digesta , 1983, British Journal of Nutrition.

[23]  D. Beever,et al.  A comparison of methods for the estimation of microbial nitrogen in duodenal digesta of sheep , 1982, British Journal of Nutrition.

[24]  D L Massart,et al.  The use of clustering techniques in the elucidation or confirmation of metabolic pathways. Application to the branched-chain fatty acids present in the milk fat of lactating goats. , 1981, The Biochemical journal.

[25]  G. Hazlewood,et al.  Characteristics of a lipolytic and fatty acid-requiring Butyrivibrio sp. isolated from the ovine rumen. , 1979, Journal of general microbiology.

[26]  R. Bailey,et al.  Chemistry and Biochemistry of Herbage , 1973 .

[27]  K. Gabriel,et al.  The biplot graphic display of matrices with application to principal component analysis , 1971 .

[28]  R. Dewhurst,et al.  Alternative strategies for manipulating milk fat in dairy cows , 2004 .

[29]  J. O'kelly,et al.  Influence of host diet on the concentrations of fatty acids in rumen bacteria from cattle , 1991 .

[30]  M. Diedrich,et al.  The natural occurrence of unusual fatty acids. Part 2. Even numbered fatty acids with unusual position of the double bond , 1991 .

[31]  M. Diedrich,et al.  The natural occurrence of unusual fatty acids. Part 1. Odd numbered fatty acids , 1990 .

[32]  J. Abrams Recent Advances in Animal Nutrition , 1982 .