Effects of Eucalyptus Crude Oils Supplementation on Rumen Fermentation, Microorganism and Nutrient Digestibility in Swamp Buffaloes

Article information

Asian-Australas J Anim Sci.. 2014;27(1):46-54
Publication date (electronic) : 2014 January 01
doi : https://doi.org/10.5713/ajas.2013.13301
1Department of Animal Science and Veterinary Medicine, An Giang University, An Giang, Vietnam
2Tropical Feed Resources Research and Development Center, (TROFREC), Department of Animal Science, Faculty of Agriculture, Khon Kaen University, Khon Kaen 40002, Thailand.
*Corresponding Author: M. Wanapat. Tel: +66-4320-2368, Fax: +66-4320-2368, E-mail: metha@kku.ac.th
Received 2013 May 29; Revised 2013 November 01; Accepted 2013 September 26.

Abstract

This study was conducted to investigate the effects of eucalyptus (E. Camaldulensis) crude oils (EuO) supplementation on voluntary feed intake and rumen fermentation characteristics in swamp buffaloes. Four rumen fistulated swamp buffaloes, body weight (BW) of 420±15.0 kg, were randomly assigned according to a 2×2 factorial arrangement in a 4×4 Latin square design. The dietary treatments were untreated rice straw (RS) without EuO (T1) and with EuO (T2) supplementation, and 3% urea-treated rice straw (UTRS) without EuO (T3) and with EuO (T4) supplementation. The EuO was supplemented at 2 mL/h/d in respective treatment. Experimental animals were kept in individual pens and concentrate mixture was offered at 3 g/kg BW while roughage was fed ad libitum. Total dry matter and roughage intake, and apparent digestibilites of organic matter and neutral detergent fiber were improved (p<0.01) by UTRS. There was no effect of EuO supplementation on feed intake and nutrient digestibility. Ruminal pH and temperature were not (p>0.05) affected by either roughage sources or EuO supplementation. However, buffaloes fed UTRS had higher ruminal ammonia nitrogen and blood urea nitrogen as compared with RS. Total volatile fatty acid and butyrate proportion were similar among treatments, whereas acetate was decreased and propionate molar proportion was increased by EuO supplementation. Feeding UTRS resulted in lower acetate and higher propionate concentration compared to RS. Moreover, supplementation of EuO reduced methane production especially in UTRS treatment. Protozoa populations were reduced by EuO supplementation while fungi zoospores remained the same. Total, amylolytic and cellulolytic bacterial populations were increased (p<0.01) by UTRS; However, EuO supplementation did not affect viable bacteria. Nitrogen intake and in feces were found higher in buffaloes fed UTRS. A positive nitrogen balance (absorption and retention) was in buffaloes fed UTRS. Supplementation of EuO did not affect nitrogen utilization. Both allantoin excretion and absorption and microbial nitrogen supply were increased by UTRS whereas efficiency of microbial protein synthesis was similar in all treatments. Findings of present study suggested that EuO could be used as a feed additive to modify the rumen fermentation in reducing methane production both in RS and UTRS. Feeding UTRS could improve feed intake and efficiency of rumen fermentation in swamp buffaloes. However, more research is warranted to determine the effect of EuO supplementation in production animals.

INTRODUCTION

Mitigation of methane (CH4) production in the tropics is important because more than half of the world’s livestock population is raised in this area. Moreover, due to low quantity and quality of feedstuffs the feed requirement in the tropics tends to be higher for similar production than that in the subtropics. Feedstuffs in the tropics, especially rice straw, are characterized by high fiber and lignin, and low digestible fractions (Kebreab et al., 2012). Therefore, the animal needs more feed per unit of production, and emits higher CH4 levels because dry matter intake (DMI) is highly correlated with CH4 production (Shibata et al., 1993). Improving feed quality is one of the proven methods to reduce CH4 production (Leng, 1993). Swamp buffaloes are raised all over Asia and contribute directly to human nutrition and socio-economic welfare and to the productivity of mixed crop-livestock production systems, national resources management and the security of resource-poor farmers. Swamp buffaloes play a very important role in providing draught power, manure as fertilizer and meat for human consumption (Chantalakhana, 2001). Moreover, swamp buffaloes are considered potentially the most efficient ruminant due to their ability to utilize low quality tropical feedstuffs (Devendra, 1992).

Essential oils, which are extracted from plants by steam distillation, are known to have antimicrobial effects due to their ability to modify cell permeability in microbes (Helander et al., 1998). These substances have also been proposed to be modifiers of rumen fermentation due to their toxicity to some unfavorable strains of rumen bacteria, such as methanogens (Wallace, 2004). Eucalyptus oils (EuO) are also well known as a traditional medicine with several biological activities such as bacteriostatic, fungistatic, anti-protozoa, anti-inflammatory and could modify ruminal fermentation characteristic and CH4 mitigation (Sallam et al., 2009; Sallam et al., 2010). However, there is very little experimental evidence of the effects of EuO on rumen microbial fermentation and nutrient digestibility. Therefore, this study was undertaken to investigate the effects of EuO supplementation on feed intake rumen fermentation and nutrients digestibility in swamp buffaloes fed with untreated and urea treated rice straw.

MATERIALS AND METHODS

Animals, diets and experimental design

In brief, EuO extraction procedure was based on a water distillation process. Approximately 100 kg of Eucalyptus leaves were collected and put into 300 L steel barrel with 100 L of water. The barrel was then covered tightly with a lid which was connected with a pipe and cooling coil in a cooling device. At the end of cooling device, a plastic bottle was used for collecting aromatic fluid. The barrel was then boiled for approximately 5 h, and essential oils were then collected by separating the oils floating on the aromatic fluid.

Four, ruminal stulated swamp buffaloes with initial body weight (BW) of 420±15.0 kg, were randomly assigned to four dietary treatments according to a 2×2 factorial arrangement in a 4×4 Latin square design. The dietary treatments were as follow: untreated rice straw (RS) without EuO (T1) and with EuO (T2) supplementation, and 3% urea-treated rice straw (UTRS) without EuO (T3) and with EuO supplementation (T4). The EuO was supplemented at 2 mL/hd/d and both RS and UTRS were fed ad libitum. Concentrate (14.2% CP) was fed daily at 0.3% BW twice daily at 07.00 h and 16.00 h. All experimental animals were kept in individual pens with availability of clean fresh water and mineral blocks at all times. The experiment was conducted for 4 periods, and each period lasted for 21 d. During the first 14 d, DMI was recorded, while during the last 7 d, all animal were moved to metabolism crates for total feces and urine collections.

Data collection and sampling procedures

Feed and fecal samples were collected by total collection from each individual buffalo during the last 7 d of each period at the morning and afternoon feeding, and a 10% sample was composited by buffalo and period, and then stored (−20°C) until analysis. Samples were dried in a forced-air oven at 60°C for 96 h and ground through a 1-mm stainless steel screen (Cyclotec 1093 Sample mill, Tecator, Hoganas, Sweden), then analyzed for dry mater (DM) and organic matter (OM) according to the AOAC (1995). The crude protein (CP) content was determined by using a Kjeltec Auto 1030 Analyzer (Tecator). The method of Van Soest et al. (1991) was used to determine neutral detergent fiber (NDF) (amylase added) and acid detergent fiber (ADF) on an ash-free basis using an Ankom Fiber Analyzer incubator (Ankom Technology, Fairport, NY).

At the end of each period, a rumen fluid sample was collected immediately at 0, 2, 4, 6 h post morning feeding on the last day of each period. Approximate 200 mL of rumen fluid was collected at each time from the different parts of the rumen using a 60 mL hand syringe. The pH and temperature of rumen fluid was measured immediately by a portable pH temperature meter (HANNA Instruments HI 8424 microcomputer, Singapore). Rumen fluid samples were then filtered through 4 layers of cheesecloth and divided into 3 portions. The first 45 mL of rumen fluid sample was collected and kept in a plastic bottle to which 5 mL of 1 M H2SO4 was added to stop the fermentation process due to microbial activity and then centrifuged at 3,000×g for 10 min. About 20 to 30 mL of supernatant was collected and analyzed for NH3-N by Kjeltech Auto 1030 Analyzer (AOAC, 1995) and VFA using High Pressure Liquid Chromatography (HPLC, Instruments by Water and Novapak model 600E; water mode l484 UV detector; column novapak C18; column size 3.9 mm×300 mm; mobile phase10 mM H2PO4 [pH 2.5]) according to Samuel et al. (1997). The second portion of 1 mL rumen fluid was collected and kept in a plastic bottle to which 9 mL of 10 mL/L formalin solution (1:9 v/v, rumen fluid: 10 mL/L formalin) was added and stored at 4°C for measuring protozoal populations by total direction counts using methods of Galyean (1989) by haemacytometer (Boeco, Singapore). The third portion was for the total viable bacteria count (cellulolytic, proteolytic, amylolytic and total viable bacteria) using the Hungate (1969) roll-tube technique.

A blood sample (about 10 mL) was collected from the jugular vein at the same time as rumen fluid sampling into tubes containing 12 mg of EDTA and plasma was separated by centrifugation at 500×g for 10 min at 4°C and stored at −20°C until analysis for blood urea nitrogen (BUN) according to Crocker (1967). Calculation of ruminal methane (CH4) production was based on VFA proportions according to Moss et al. (2000) as follows: CH4 production = 0.45(acetate)−0.275(propionate)+0.4(butyrate).

Total urine excretion was collected and acidified using 10 mL of H2SO4 solution (2 M). Urine samples were analyzed for total N (AOAC, 1995) to calculate for N balance and allantoin in urine was determined by HPLC as described by Chen et al. (1993). The amount of microbial purines derivative absorption was calculated from purine derivative (PD) excretion based on the relationship derived by the equation of Liang et al. (1994): Y = 0.12X+(0.20 BW0.75). The supply of microbial N (MN) was estimated by urinary excretion of PD according to Chen and Gomes (1995): MN (g/d) = 70X/(0.116×0.83×1,000) = 0.727X; where X and Y are, respectively, absorption and excretion of PD in mmol/d. Efficiency of microbial N synthesis (EMNS) was calculated using the following formula: EMNS = microbial N (g/d)/DOMR; where DOMR = digestible OM apparently fermented in the rumen (assuming that rumen digestion was 650 g/kg OM of digestion in total tract, DOMR = DOMI×0.65; DOMI = digestible organic matter intake).

Statistical analysis

All data obtained from the experiment were subjected to ANOVA for a 4×4 Latin square design with 2×2 factorial arrangements of treatments using the General Linear Models (GLM) procedures of the Statistical Analysis System Institute (SAS, 1998). The statistical model included terms for animal, period, roughage sources, EuO and the roughage sources×EuO interactions. Treatment means were compared by Tukey’s Multiple Comparison Test (Crichton, 1999).

RESULTS

Chemical composition of diet

Experimental feeds and their chemical compositions are presented in Table 1. The mixture concentrates consisted of cassava chip, rice bran, coconut meal, palm meal, molasses, sulfur and minerals and had high quality in terms of high CP and low fiber fraction. Rice straw had low CP and high NDF and ADF content; however, the quality of rice straw was improved by urea treatment at 3% in increasing CP and reducing fiber content.

Ingredients and chemical compositions of concentrate, rice straw and urea treated rice straw

Feed intake and nutrient digestibility

Supplementing swamp buffaloes with EuO had no effect on DM intake (Table 2) but urea treatment increased (p<0.01) straw intake. Apparent digestibility of OM and NDF were also found to have increased (p<0.001) in buffaloes fed UTRS diets. However, EuO supplementation did not changed nutrient digestibility.

Effects of roughage source and Eucalyptus crude oil supplementation on voluntary feed intake and nutrients digestibility

Rumen fermentation and blood metabolites

As shown in Table 3, rumen temperature and pH were similar among treatments and values were quite stable. Buffaloes fed with UTRS had higher concentration of ruminal NH3-N and BUN as compared to RS. However, EuO supplementation did not affect on ruminal NH3-N and BUN concentrate. There were no differences in total volatile fatty acid (TVFA) and butyrate (C4) concentration among treatments by roughage source or EuO supplementation. Roughage sources and EuO supplementation influenced acetate (C2) and propionate (C3) concentrations and CH4 production. The treatments with UTRS resulted in lower C2, but higher C3 as compared to RS. EuO supplementation reduced C2 and increased C3 concentration in both RS and UTRS. Production of CH4 was reduced by EuO supplementation especially in buffaloes fed UTRS.

Effect of roughage source and Eucalyptus crude oils on rumen fermentation and blood metabolites

Rumen microorganism population

The pprotozoa population was strongly inhibited by EuO supplementation, but not by roughage source, while the fungal zoospore population was similar in all treatments (Table 4). Total viable, amylolytic and cellulolytic bacteria counts were higher (p<0.001) in treatments with UTRS fed buffaloes whereas the population of proteolytic bacteria did not change by straw treatment or EuO supplementation. EuO supplementation did not affect the bacterial population in swamp buffaloes fed RS or UTRS.

Effects of roughage sources and Eucalyptus oils supplementation on microbial population

Nitrogen utilization, purine derivative and efficiency of microbial protein synthesis

Total nitrogen intake and its excretion in feces and urine was higher in UTRS treatment (Table 5). However, EuO supplementation in diet did not affect nitrogen utilization in swamp buffaloes. Allantoin excretion and absorption, and microbial nitrogen supply (MNS) were increased by roughage treatment but EuO supplementation did not influence these attributes. Neither roughage treatment nor EuO supplementation changed efficiency of microbial nitrogen synthesis (EMNS) in buffaloes.

Effects of roughage source and Eucalyptus crude oils supplementation on nitrogen metabolism and microbial protein synthesis

DISCUSSION

Feed intake and nutrient digestibility

There was no interaction between EuO supplementation and roughage sources on feed intake and nutrient digestibility in the present study. Total DMI and roughage intake were increased by UTRS, but not by EuO supplementation. However, it has been reported that there are variable observations on feed intake depending on the type of essential oil (EO) and dose (Cardozo et al., 2006). Feeding 250 mg/d of oregano plants EO in sheep (Wang et al., 2009), 2 g/d of juniper berry EO in cows (Yang et al., 2007), 0.75 or 2 g of EO mixture in dairy cattle (Benchaar et al., 2006a, 2007) and 0.043 or 0.43 g/kg feed intake in dairy goats (Malecky et al., 2009) did not influence on feed intake. On the other hand, Busquest et al. (2003) reported that high dose of cinnamadehyde (500 mg/d) in dairy cattle adversely affected on feed intake. In contrast, Yang et al. (2010) clearly demonstrated that cinnamaldehyde had a greater feed intake response at low dose (0.4 g/d), whereas a higher dose at 1.6 g/d had no effect on intake of steers. Under the present study, buffaloes fed with UTRS had greater feed intake and digestibility of OM and NDF as compared with those fed with RS. This result agreed with Wanapat et al. (1985) who reported that urea-treatment could increase overall feed intake and nutrient digestibility of straw. It was also reported that urea could provide a source of CP which is deficient in straw (Preston and Leng, 1987). Moreover, in the process of treating rice straw, the concentrated alkaline agents in form of ammonium hydroxide can chemically break the ester bonds between lignin, hemicelluloses and cellulose, and physically make structural fibers swollen. These effects enable rumen microbes to attack the structural carbohydrates more easily, hence higher intake and degradability could be obtained (Fadel Elseed et al., 2003). However, apparent digestibilities of DM, OM, CP, NDF and ADF were not influenced by EuO supplementation, which agreed with the results of Benchaar et al. (2006b, 2007) and Santos et al. (2004), who reported no changes in apparent total tract digestibility in dairy cows fed with 2 g/d of mixture EO.

Rumen fermentation and blood metabolites

There were no effects of EuO supplementation and roughage sources on ruminal pH and temperature (p>0.05). Ruminal pH and temperature in the present study were in normal range at 38.6°C to 39.5°C and 6.0–6.3, respectively, as reported by Wanapat (1990). Yang et al. (2007) who used garlic (5 g/d) and juniper berry (2 g/d) EO in lactating cows found that there was no effect of EO on ruminal pH. In addition, Chaves et al. (2008a) also reported that no change in ruminal pH when growing lambs were supplemented with cinnamaldehyde, garlic and juniper berry EO.

Supplementation of EuO did not affect on ruminal NH3-N and BUN in this study. Buquest et al. (2006), who conducted in vitro studies, reported that addition of anethol (3,000 mg/L), carvacrol and carvone (300 mg/L) had no effect on NH3-N concentration. Indeed, Benchaar et al. (2006b Indeed, Benchaar et al. (2007) observed no change in ruminal NH3-N concentration, when lactating dairy cows were supplemented with EO at doses of 0.75 or 2 g/d. McIntosh et al. (2003) demonstrated that EO inhibited growth of some (i.e., Clostridium sticklandii and Peptostreptococcus anaerobius) hyper-ammonia producing (HAP) bacteria, but other HAP bacteria (e.g., Clostridium aminophilum) were less sensitive. Hyper-ammonia producing bacteria are present in low numbers in the rumen (<0.01 of the rumen bacterial population), but they possess a very high deamination activity (Russell et al., 1988). Wallace (2004) reported that the number of HAP bacteria was reduced by 77% in sheep receiving a low protein diet supplemented with EO at 100 mg/d, but that EO had no effect on HAP bacteria when sheep were fed a high-protein diet. On the other hand, NH3-N and BUN were higher in buffaloes fed with UTRS as compared with RS. This could be a consequent result from having a higher nitrogen intake contributed by UTRS. Similarly, Hess et al. (2000) found that ruminal NH3-N concentration was linearly correlated with the level of dietary CP (p<0.001, r2 = 0.77–0.92). According to numerous reports, the optimal level of ruminal ammonia concentration for efficient digestion ranged from 5.0 to 25.0 mg/dL (Preston and Leng, 1987) and 15 to 30 mg/dL (Perdok and Leng, 1989; Wanapat and Pimpa, 1999). Bunting et al. (1987) reported that BUN levels reflected the protein status of cattle and positively corresponded to the change in NH3-N concentration in rumen fluid.

Under this current study, no effects of both EuO supplementation and type of rice straw were found on total VFA production and C4 concentration. These results agreed with Newbold et al. (2004) and Beauchamin and Mc Ginn (2006) who observed no changes in total VFA production when EO was fed to sheep or cattle. Indeed, Busquest et al. (2006), who studied the effects of various plant extracts and secondary plant metabolites on ruminant fermentation in a 24 h batch culture, where each treatment was supplied at varying dose up to 3 g/L of culture fluid, found that none of the EO or EO compounds could increase total VFA concentration; although they decreased VFA concentration at the highest concentration. The lack of EuO supplement effect on molar proportion of C4 is consistent with the results obtained from dairy cows supplemented with a mixture of EO in the study of Benchaar et al. (2006a, 2007). Meanwhile, Eucalyptus oils addition reduced C2 proportion and increased C3 proportion. This result agreed with Agarwal et al. (2009) who reported that peppermint oils addition to buffaloes rumen liquor resulted in decreasing C2 and increasing C3. Another in vitro study conducted by Buquest et al. (2005), using garlic oils, found results similar to the previous report. In the present results, EuO supplementation caused a reduction of C2:C3 ratio and this was consistent to several works in vivo of Cardozo et al. (2006), Wanapat et al. (2008) and Giannenas et al. (2011). The present study showed that feeding UTRS resulted in reducing C2 and increasing C3 proportions in the rumen as compared to RS. This result was similar with the studies by Wanapat et al. (2009) who reported that urea treatment of straw could alter VFA proportion concentration in the rumen. These results could be due to the treatment of straw with urea that would result in increased availability of carbohydrate for degradation by the rumen microorganisms; hence, lead to the improvement of digestibility rate. Thereby, it could lead to the decrease of molar proportion of C2 and increase that of C3.

The inhibition of CH4 production in the rumen by specifically targeting the methanogens is usually associated with a decrease in C2 to C3 ratio (Patra, 2011). Results in present study showed that CH4 production calculated by the equation of Moss et al. (2000) was approximately 8% lower in EuO treatments compared to non supplemented treatments. This result was in agreement with several previous studies on inhibitory properties of EO both in vitro and in vivo. For instance, juniper berry EO and cinnamol oil (Chaves et al., 2008b) and peppermint oil (Tatsouka et al., 2008; Agarwal et al., 2009) have been reported to have strong inhibitory effect on methanogennesis in vitro study. Furthermore, the in vivo study of Wang et al. (2009) showed that inclusion of EO from oregano plants in the diet could reduce CH4 profusion in sheep. In addition, Mohammed et al. (2004) observed that encapsulated horseradish EO decreased CH4 production by 19% in steers. Moreover, data in the present study showed that the total direct count of protozoa population (Table 4) in treatments with inclusion of EuO was lower than that in treatment without EuO supplementation and this could be the explanation for the decreasing CH4 production since ruminal protozoa provide a habitat for methanogens that live on and within them.

Rumen microorganism population

Total fungal zoospores, total viable, cellulolytic, proteolytic, and amylolytic bacteria populations were not affected by EuO supplementation in the diet. In agreement with this finding, Wallace et al. (2002) and Benchaar et al. (2007) reported that no changes in bacteria count was found when sheep and dairy cows were fed with mixed EO, respectively. However, the protozoa population was reduced by EuO addition in this study. Similarity, Ando et al. (2003) reported that feeding 200 g/d peppermint to Holstein steers decreased the total number of protozoa which was attributed to the present of EO. It also has been observed that clove extract containing EO decreased total number of protozoa (Patra et al., 2010). More recently, Wanapat et al. (2008); Kongmun et al. (2010) Kongmun et al. (2011) reported that supplementation of garlic powder resulted in lower protozoa numbers in beef cattle and buffalo. In contrast, feeding UTRS significantly increased (p<0.01) microbe growth in buffaloes as compared to RS feeding. These results were in agreement with the studies by Wanapat et al. (2009) and Khejornsart et al. (2011) who found that population of cellulolytic bacteria was increased by urea treated rice straw. Goto et al. (1993) reported that alkaline treatment partially damages the lignin polysaccharide bond that solublizes hemicelluloses and lignin in straw, and hence exposes the cellulose to microbial attack. Moreover, Chen et al. (2008) reported that chemical treatment enhanced the nutritive value of rice straw through increasing the number of accessible sites of microbial attachment on the surface of particles, increasing fibrolytic microbe quantity and hence fibrolytic enzyme activities, and improving rumen fermentation characteristics.

Nitrogen utilization and microbial protein synthesis

Inclusion of EuO in the treatments dietary did not affect nitrogen utilization and microbial protein synthesis in the present study. Benchaar et al. (2006a,b; 2007) observed that there was no change in nitrogen retention and duodenal bacteria flow (estimate from urinary purine derivative) when cows were fed with EO. In addition, Tekipper et al. (2010) reported that supplementation of 500 g of origanum vulgare leaves in lactating dairy cows had no effect on urinary and fecal loss as well as urinary purine derivative and microbial protein synthesis. Nitrogen retention and microbial protein synthesis estimated using purine derivative was higher in urea-treated rice straw diet. This result agreed with Pradan et al. (1996) who reported that N retention was increased by urea or ammonia treated rice straw when compared with untreated rice straw. Under this study, allantoin excretion and allantoin absorption were increased (p<0.001) in the buffaloes fed with urea-treated rice straw. In addition, Hoover and Stokes (1991) reported that the rate of digestion of carbohydrates was a major factor controlling the energy available for microbial growth. As discussed above, urea treatment of rice straw could break-down the physical form of rice straw, hence resulted in higher digestibility of OM with the consequence of improving the rate of digestion. Moreover, urea as ammonium or ammonium carbonate in urea-treated rice straw could provide nitrogen source for microbes for a more rapid colonization on the surface of roughage in the rumen.

CONCLUSION

In summary, feeding UTRS could enhance feed intake, nutrient digestibility and efficiency of rumen fermentation of swamp buffaloes. Moreover, supplementation EuO at 2 mL/hd/d did not show any negative effect on feed intake and rumen fermentation; however, it could reduce protozoa population and methane production. Therefore, it could be concluded that EuO could be used to manipulate rumen fermentation in swamp buffaloes as potential feed additive to improve rumen fermentation, mitigation methane production without negative effect on feed intake, nutrient digestibility and rumen fermentation.

ACKNOWLEDGEMENTS

Tropical Feed Resources Research and Development Center (TROFREC), Department of Animal Science, Faculty of Agriculture, Khon Kaen University, Thailand and the Vietnam International Education Development (VIED), Ministry of Education and Training, Vietnam are gratefully acknowledged for the use of research facilities and financial support.

References

Agarwal N, Shekhar C, Kumar R, Chaudhary LC, Kamra DN. 2009;Effect of peppermint (Mentha piperita) oil on in vitro methanogenesis and fermentation of feed with buffalo rumen liquor. Anim Feed Sci Technol 148:321–327.
Ando S, Nishida T, Ishida M, Hosoda K, Bayaru E. 2003;Effect of peppermint feeding on the digestibility, ruminant fermentation and protozoa. Livest Prod Sci 82:245–248.
AOAC. 1995. Official methods of analyses. 16th edth ed. Animal Feeds Association of Official Analytical Chemists. VA, USA:
Beauchemin KA, McGinn SN. 2006;Methane emissions from beef cattle: effects of fumaric acid, essential oil, and canola oil. J Anim Sci 84:1489–1496.
Benchaar C, Petit HV, Berthiaume R, Whyte TD, Chouinard PY. 2006a;Effects of addition of essential oils and monensin premix on digestion, ruminal fermentation, milk production and milk composition in dairy cows. J Dairy Sci 89:4352–4364.
Benchaar C, Duynisveld JL, Charmley E. 2006b;Effects of monensin and increasing dose levels of a mixture of essential oil compounds on intake, digestion and growth performance of beef cattle. Can J Anim Sci 86:91–96.
Bencharr C, Petit HV, Berthiaume R, Ouellet DR, Chiquette J, Chouinard PY. 2007;Effects of essential oils on digestion, ruminal fermentation, rumen microbial populations, milk production, and milk composition in dairy cows fed alfalfa silage or corn silage. J Dairy Sci 90:886–897.
Bunting LD, Boling JA, MacKown CT, Muntifering RB. 1987;Effect of dietary protein level on nitrogen metabolism in lambs: Studies using 15N-nitrogen. J Anim Sci 64:855–867.
Busquet M, Calsamiglia S, Ferret A, Kamel C. 2003;Efecto del extracto de ajo y/o cinnamaldehí do sobre la producción, composición y residuos en vacas de alta producción. ITEA Vol-Extra 24:756–758.
Busquet M, Calsamiglia S, Ferret A, Kamel C. 2006;Plant extracts affect in vitro rumen microbial fermentation. J Dairy Sci 89:761–771.
Busquet M, Calsamiglia S, Ferret A, Carro MD, Kamel C. 2005;Effects of garlic oil and four of its compounds on rumen microbial fermentation. J Dairy Sci 88:4393–4404.
Cardozo PW, Calsamiglia S, Ferret A, Kamel C. 2006;Effects of alfalfa extract, anise, capsicum and a mixture of cinnamaldehyde and eugenol on ruminal fermentation and protein degradation in beef heifers fed a high concentrate diet. J Anim Sci 84:2801–2808.
Chantalakhana C. 2001. Contribution of Water Buffaloes in Rural Development. In : Proceeding Regional Workshop on Water Buffalo Development. Thongtarin Hotel, Surin, Thailand; 8–10 February, 2001;
Chaves AV, Stanford K, Dugan MER, Gibson LL, McAllister TA, Van Herk F, Benchaar C. 2008a;Effects of cinnamaldehyde, garlic and juniper berry essential oils on rumen fermentation, blood metabolites, growth performance, and carcass characteristics of growing lambs. Livest Sci 117:215–224.
Chaves AV, He ML, Yang WZ, Hristov AN, McAllister TA, Benchaar C. 2008b;Effects of essential oils on proteolytic, deaminative and methanogenic activities of mixed ruminal bacteria. Can J Anim Sci 88:117–122.
Chen XB, Gomes MJ. 1995. Estimation of microbial protein supply to sheep and cattle based on urinary excretion of purine derivative – An overview of the technique details. Occasional publication 1992 International Feed Resources Unit, Rowett Research Institute. Aberdeen, UK:
Chen XB, Kyle DJ, Orskov ER. 1993;Measurement of allantoin in urine and plasma by high performance liquid chromatography with pre-column derivatization. J Chromatogr B Biomed Sci Appl 617:241–247.
Chen XL, Wang JK, Wu YM, Liu JX. 2008;Effects of chemical treatments of rice straw on rumen fermentation characteristics, fibrolytic enzyme activities and populations of liquid- and solid-associated ruminal microbes in vitro. Anim Feed Sci Technol 141:1–14.
Crichton N. 1999;Information point: Tukey’s multiple Comparison test. Blackwell Science Ltd. J Clinical Nursing 8:299–304.
Crocker CL. 1967;Rapid determination of urea nitrogen in serum or plasma without deproteinization. Am J Med Technol 33:361–365.
Devendra C. 1992. Nutrition of swamp buffalo. Buffalo Production, World Animal Science C6In : Tulloh NM, Holmes JHG, eds. Elsevier. Tokyo:
Fadel-Elseed AMA, Sekine J, Hishinuma M, Hamana K. 2003;Effects of ammonia, urea plus calcium hydroxide and animal urine treatments on chemical composition and in sacco degradability of rice straw. Asian-Aust J Anim Sci 16:368–373.
Galyean M. 1989. Laboratory procedure in animal nutrition research. Department of animal and range science New Mexico State University. USA:
Giannenas I, Skoufos J, Giannakopoulos C, Wiemann M, Gortzi O, Lalas S, Kyriazakis I. 2011;Effect of essential oils on milk production, milk composition, and rumen microbiota in Chios dairy ewes. J Dairy Sci 94:5569–5577.
Goto M, Yokoe Y, Takabe K, Nishikawa S, Morita O. 1993;Effects of gaseous ammonia on chemical and structural features of cell walls in spring barley straw. Anim Feed Sci Technol 40:207–221.
Helander IM, Alakomi H, Latva-Kala K, Mattila-Sandholm T, Pol I, Smid EJ, Gorris LGM, Wright A. 1998;Characteritzation of the action of selected essential oil components on gram-negative bacteria. J Agric Food Chem 46:3590–3595.
Hess HD, Lascano CE, Flórez H. 2000. Blood and milk urea nitrogen as a tool to monitor the protein nutrition of cattle under tropical conditions Institute of Animal Sciences, Animal Nutrition, ETH. Zurich, Switzerland:
Hoover WH, Stokes SR. 1991;Balancing carbohydrates and proteins for optimum rumen microbial yield. J Dairy Sci 74:3630–3644.
Hungate RE. 1969. A role tube method for cultivation of strict anaerobes. Method in mMicrobiology In : Norris JR, Ribbons DW, eds. New York. Academic NY: p. 313.
Kebreab E, Cruz GD, Hai PH, Anatassok N, Polyorach S, Beelen P, Rosa HD. 2012. Methane emission profile in dairy heifers feed rice straw. In : Proc. The 1st International Conference on Animal Nutrition and Environment. Khon Kaen, Thailand.
Khejornsart P, Wanapat M, Rowlinson P. 2011;Diversity of anaerobic fungi and rumen fermentation characteristic in swamp buffalo and beef cattle fed on different diet. Livest Sci 139:230–236.
Kongmun P, Wanapat M, Pakdee P, Navanukraw C, Yu Z. 2011;Manipulation of rumen fermentation and ecology of swamp buffalo by coconut oil and garlic powder supplementation. Livest Sci 135:84–92.
Kongmun P, Wanapat M, Pakdee P, Navanukraw C. 2010;Effect of coconut oil and garlic powder on in vitro fermentation using gas production technique. Livest Sci 127:38–44.
Leng RA. 1993. The impact of livestock development on environmental change. FAO Corporate Documentary Repository p. 1–14.
Liang JB, Matsumoto M, Young BA. 1994;Purine derivative excretion and rumen microbial yield in Malaysian cattle and swamp buffalo. Anim Feed Sci Technol 47:189–199.
Malecky M, Broudiscou LP, Schmidely P. 2009;Effects of two levels of monoterpene blend on rumen fermentation, terpene and nutrient flows in the duodenum and milk production in dairy goats. Anim Feed Sci Technol 154:24–35.
McInstosh FM, Williams P, Losa R, Wallace RJ, Beever DA, Newbold CJ. 2003;Effect of essential oils on ruminal microorganisms and their protein metabolism. Appl Environ Microbiol 69:5011–5014.
Mohammed N, Ajisaka N, Lila ZA, Mikuni K, Kanda S, Itabashi H. 2004;Effects of Japanese horseradish oil on methane production and ruminal fermentation in vitro and in steers. J Anim Sci 82:1839–1846.
Moss AR, Jouan JP, Newbold J. 2000;Methane production by ruminants: its contribution to global warming. Ann Zootech 49:231–253.
Newbold CJ, McInstosh FM, Williams P, Losa R, Wallace J. 2004;Effects of a specific blend of essential oils compounds on rumen fermentation. Anim Feed Sci Technol 114:105–112.
Patra AK. 2011;Effects of essential oils on rumen fermentation, microbial ecology and ruminant production. Asian J Anim Vet Adv 6:416–428.
Patra AK, Kamra DN, Agarwal N. 2010;Effects of extracts of spices on rumen methanogenesis, enzyme activity and fermentation of feeds in vitro. J Sci Food Agric 90:511–520.
Perdok H, Leng RA. 1989. Rumen ammonia requirements for efficient digestion and intake of straw by cattle. The Roles of Protozoa and Fungi in ruminant Digestion In : Nolan JV, Demeyer RA Leng, eds. Penambul Books. Armidale, Australia:
Preston TP, Leng RA. 1987. Matching ruminant production systems with available resources in the tropics and sub-tropics Penambul Books. Armidale, N.S.W. Australia:
Russell JB, Strobel HJ, Chen G. 1988;Enrichment and isolation of a ruminal bacterium with a very high specific activity of ammonia production. Appl Environ Microbiol 54:872–877.
Sallam SMA, Bueno ICS, Nasser MEA, Abdalla AL. 2010;Effect of eucalyptus (Eucalyptus citriodora) fresh or residue leaves on methane emission in vitro. Ital. J. Anim. Sci. 9:e58.
Sallam SMA, Nasser MEA, Araujo RC, Abdalla AL. 2009. Methane emission in vivo by sheep consuming diet with different levels of eucalyptus essential oil. In : Proc FAO/IAEA Int. Symp. On sustainable improvement of animal production and health. Vienna, Austria.
Samuel M, Sagathewan S, Thomas J, Mathen G. 1997;An HPLC method for estimation of volatile fatty acids of ruminal fluid. Indian J Anim Sci 67:805–807.
Santos MB, Robinson PH, Williams P, Losa R. 2010;Effect of addition of an essential oil complex to the diet of lactating dairy cows on whole tract digestion of nutrients and productive performance. Anim Feed Sci Technol 157:64–71.
SAS. 1998. SAS/STAT User’s Guid 6 12th edth ed. SAS Institue Inc. Cary Nort Carolina:
Shibata M, Terada F, Kurihara M, Nishida T, Iwasaki K. 1993;Estimation of methane production in ruminants. Anim Sci Technol 64:790–796.
Tatsouka N, Hara K, Mikuni K, Hara K, Hashimoto H, Itabashi H. 2008;Effects of the essential oil cyclodextrin complexes on ruminal methane production in vitro. Anim Sci J 79:68–75.
Tekippe JA, Hristov AN, Heyler KS, Cassidy TW, Zheljazkov VD, Ferreira JFS, Karnati SK, Varga GV. 2011;Rumen fermentation and production effects of Origanum vulgare L. leaves in lactating dairy cows. J Dairy Sci 94:5065–5079.
Van Soest PJ, Robertson JB, Lewis BA. 1991;Methods of dietary fiber, neutral detergent fiber and non-starch carbohydrates in relation to animal nutrition. J Dairy Sci 74:3583–3597.
Wallace RJ. 2004;Antimicrobial properties of plant secondary metabolites. Proc Nutr Soc 63:621–629.
Wallace RJ, McEwan NR, McIntosh FM, Teferedegne B, Newbold CJ. 2002;Natural products as manipulators of rumen fermentation. Asian-Aust J Anim Sci 15:1458–1468.
Wanapa M, Khejornsart P, Pakdee P, Wanapat S. 2008;Effect of supplementation of garlic powder on rumen ecology and digestibility of nutrients in ruminants. J Sci Food Agric 88:2231–2237.
Wanapat M, Pimpa O. 1999;Effect of ruminal ammonia nitrogen levels on ruminal fermentation, purine derivatives, digestibility and rice straw intake in swamp buffaloes. Asian-Aus J Anim Sci 12:904–907.
Wanapat M. 1985. Improving rice straw qulity as ruminant feed by urea-treatment in Thailand. p. 147–175. Relevance of crop Residues as Animal Feed in Developing Countries In : Wanapat M, Devendra C, eds. Funny Press. Bangkok:
Wanapat M. 1990. Nutritional aspects of ruminant production in Southeast Asia with special reference to Thailand Funny Press, Ltd.. Bangkok, Thailand:
Wanapat M, Polyorach S, Boonnop K, Mapato C, Cherdthong A. 2009;Effects of treating rice straw with urea or urea and calcium hydroxide upon intake, digestibility, rumen fermentation and milk yield of dairy cows. Livest Sci 125:238–243.
Wang CJ, Wang SP, Zhou H. 2009;Influences of flavomycin, ropadiar and saponin on nutrient digestibility, rumen fermentation and methane emission from sheep. Anim Feed Sci Technol 148:157–166.
Yang WZ, Ametaj BN, Benchaar C, He ML, Beauchemin KA. 2010;Cinnamadehyde in feedlot cattle diets: Intake, growth performance, carcass characteristics and blood metabolites. J Anim Sci 88:1082–1092.
Yang WZ, Benchaar C, Ametaj BN, Chaves AV, He ML, McAllister TA. 2007;Effects of garlic and juniper berry essential oils on ruminal fermentation and on the site and extent of digestion in lactating cows. J Dairy Sci 90:5671–5681.

Article information Continued

Table 1

Ingredients and chemical compositions of concentrate, rice straw and urea treated rice straw

Items Concentrate RS UTRS
Ingredients (% dry matter)
 Cassava chip 65.0
 Rice bran 10.0
 Palm meal 20.2
 Urea 1.5
 Molasses 1.5
 Sulfur 0.3
 Premix minerala 1.0
 Salt 0.5
Chemical composition (%)
 Dry matter 93.2 91.6 53.5
———% dry matter———
 Organic matter 94.7 87.5 88.2
 Ash 5.3 12.5 11.8
 Crude protein 14.2 2.5 5.4
 Neutral detergent fiber 16.0 76.2 74.3
 Acid detergent fiber 8.4 53.8 57.8

RS = Rice straw; UTRS = 3% urea-treated rice straw.

a

Minerals and vitamins (each kg contain): vitamin A 10,000,000 IU; vitamin E 70,000 IU; Vitamin D 1,600,000 IU; Fe 50 g; Zn 40 g; Mn 40 g; Co 0.1 g; Se 0.1 g; I 0.5 g.

Table 2

Effects of roughage source and Eucalyptus crude oil supplementation on voluntary feed intake and nutrients digestibility

Items RS UTRS SEM Contrasts



−EuO +EuO −EuO +EuO R EuO R×EuO
Feed intake (dry mater)
Total
 kg/d 6.1a 5.8a 8.7b 8.5b 0.26 ** ns ns
 % BW 1.5a 1.4a 2.1b 2.0b 0.23 ** ns ns
Roughage
 kg/d 5.1a 4.8a 7.7b 7.6b 0.27 ** ns ns
Concentrate
 kg/d 1.0 1.0 1.0 0.9 0.05 ns ns ns
Apparent digestibility (%)
 DM 59.1 60.0 63.6 65.5 2.45 ns ns ns
 OM 61.5a 63.2ab 66.6b 67.3b 1.74 ** ns ns
 CP 51.0 54.5 56.2 56.6 4.16 ns ns ns
 NDF 55.1a 60.1ab 64.1bc 67.4c 1.94 ** ns 0.07
 ADF 47.5 49.2 52.6 51.6 2.88 ns ns ns

RS = Rice straw; UTRS = 3% urea-treated rice straw; R = Roughage source; EuO = Eucalyptus crude oil supplementation at 2 mL/hd/d.

ns = Non-significant; SEM = Standard error of mean.

DM = Dry matter; OM = Organic matter; CP = Crude protein; NDF = Neutral detergent fiber; ADF = Acid detergent fiber.

a, b, c

Values in the same row with different superscripts differ.

**

p<0.01.

Table 3

Effect of roughage source and Eucalyptus crude oils on rumen fermentation and blood metabolites

Items RS UTRS SEM Contrasts



−EuO +EuO −EuO +EuO R EuO R×EuO
Ruminal temp. (°C) 38.6 38.6 39.5 39.1 0.26 ns ns ns
Ruminal pH 6.3 6.3 6.0 6.2 0.10 ns ns ns
NH3-N (mg/dL) 11.9a 10.7a 16.8b 19.4b 2.43 ** ns ns
BUN (mg/dL) 8.1a 8.4a 13.6b 17.6b 1.64 ** ns ns
Total VFA (mM/L) 133.9 135.8 129.4 134.4 5.07 ns ns ns
———mol/100 mol———
 Acetate 72.4a 69.2b 68.7b 62.7c 1.13 ** ** ns
 Propionate 15.4a 18.9b 19.2b 23.8c 0.04 ** ** ns
 Butyrate 12.2 11.8 12.1 13.4 0.45 ns ns ns
Methane1 (mol/100 mol) 33.2a 30.1b 30.4b 27.0c 0.85 ** ** ns

RS = Rice straw; UTRS = 3% urea-treated rice straw; R = Roughage source; EuO = Eucalyptus crude oil supplementation at 2 mL/hd/d.

NH3-N = Ammonia nitrogen; BUN = Blood urea nitrogen; VFA = Volatile fatty acid.

ns = Non-significant; SEM = Standard error of mean.

a, b, c

Values in the same row with different superscripts differ.

*

p<0.05;

**

p<0.01.

1

Calculated: CH4 = (0.45×acetate)−(0.275×propionate)+(0.40×butyrate) based on Moss et al. (2000).

Table 4

Effects of roughage sources and Eucalyptus oils supplementation on microbial population

Items RS UTRS SEM Contrasts



−EuO +EuO −EuO +EuO R EuO R×EuO
Ruminal microbes (cell/mL)
 Protozoa (×105) 7.3a 5.8b 8.7a 6.9b 0.47 ns ** ns
 Fungi (×105) 3.8 2.9 3.6 3.2 0.35 ns ns ns
Viable bacteria (cfu/mL)
 Total (×109) 1.9a 2.4a 4.0b 2.3a 0.45 0.07 ns *
 Proteolytic (×107) 1.8 2.1 2.3 2.7 0.63 0.09 ns ns
 Amylolytic (×107) 2.9a 1.9a 3.5b 4.7b 0.57 ** ns ns
 Cellulolytic (×108) 1.7a 2.1a 5.4b 4.4b 0.52 ** ns ns

RS = Rice straw; UTRS = 3% urea-treated rice straw; R = Roughage source; EuO = Eucalyptus crude oil supplementation at 2 mL/hd/d.

a, b, c

Values in the same row with different superscripts differ.

*

p<0.05;

**

p<0.01.

Table 5

Effects of roughage source and Eucalyptus crude oils supplementation on nitrogen metabolism and microbial protein synthesis

Items RS UTRS SEM Contrast



−EuO +EuO EuO +EuO R EuO R×EuO
N utilization (g/d)
 Intake 42.1a 43.2a 89.0b 88.8b 0.70 ** ns ns
 Excretion
  Feces 21.2a 20.2a 38.0b 38.6b 0.55 ** ns ns
  Urine 9.1 7.5 11.2 13.1 1.62 0.05 ns ns
 Balance
  Absorption 20.9a 23.0a 51.0b 50.2b 1.53 ** ns ns
  Retention 13.0a 16.4a 38.8b 37.2b 1.55 ** ns ns
Purine derivative (mmol/d)
 Allantoin excretion 22.9a 22.7a 26.2b 28.4b 1.32 ** ns ns
 Allantoin absorption 66.5a 66.9a 94.5b 114.2b 5.18 ** ns ns
 MNS (gN/d) 48.7a 48.7a 68.7b 83.0b 3.78 * ns ns
 EMPS (gN/kg OMDR) 27.3 28.5 24.3 29.4 1.93 ns ns ns

RS = Rice straw; UTRS = 3% urea-treated rice straw; R = Roughage source; EuO = Eucalyptus crude oil supplementation at 2 mL/hd/d.

MNS = Microbial nitrogen supply; EMPS = Efficiency of microbial nitrogen synthesis; OMDR = Digestible organic matter apparently fermented in the rumen.

a, b

Values in the same row with different superscripts differ.

*

p<0.05;

**

p<0.01.