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8/14/2019 Effect of eucalyptus leaf meal supplementation on feed intake ruminal ecology and microbial protein synthesis of
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75KHON KAEN AGR. J. 41 SUPPL. 1 : (2013). KHON KAEN AGR. J. 41 SUPPL. 1 : (2013). 41 1 : (2556).
Effect of eucalyptus leaf meal supplementation on feed intake
ruminal ecology and microbial protein synthesis of swamp buffaloes
Nguyen The Thao1and Metha Wanapat1*
ABSTRACT:This study was conducted to investigate the effects of Eucalyptus (E. Camaldulensis) leaf meal
(ELM) supplementation on voluntary feed intake, ruminal ecology and microbial protein synthesis of swamp
buffaloes fed with rice straw. In this, ruminally stulated swamp buffaloes with initial body weight of 321 23 kg
were randomly assigned according to a 4 x 4 Latin square design. The dietary treatments were different levels of ELM
supplementation and were as follows: T1= 0 g ELM/hd/d; T2 = 40 g ELM/hd/d; T3 = 80 g ELM/hd/d; T4 = 120 g
ELM/hd/d. Experimental animals were kept in individual pens, concentrates were offered at 0.3%BW and rice straw
was fed ad libitum. These results revealed that voluntary feed intake were similar among treatments. Ruminal pH,
temperature were not signicantly affected; however, ELM supplementation resulted in signicantly lower concentration
of ruminal ammonia nitrogen. Population of bacteria and fungal zoospores were not different (P>0.05) amongtreatments while population of protozoa was decreased (P
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76 41 1 : (2556).
characteristics, anti-protozoa and methane
mitigration (Sallam et al., 2009). However,
there are few experimental data on effects of the
Eucalyptus leaves were conducted in in vivo
trials, especially in swam buffaloes. Therefore, the
objective of this study was to evaluate the effects
of eucalyptus leaf meal supplementation on feed
intake and rumen ecology and microbial protein
synthesis of swamp buffaloes.
Materials and Methods
Four, ruminal stulated buffaloes with initial
body weight (BW) of 420 15 kg, were randomly
assigned to receive four dietary treatments
according to a 4 4 Latin square design.
The dietary treatments were as follow: T1 =
supplementation at 0 g ELM/day (control);
T2 = supplementation at 40 g ELM/day; T3 =
supplementation at 80 g MUP/day; T4 =
supplementation at 120 g ELM/day, respectively.
Concentrate (14.2% CP) was fed daily to animals
at 0.3% of BW/day, and rice straw was offered
ad libitum. All experimental animals were kept in
individual pens with clean fresh water and mineral
blocks were available at all times.
The experiment was conducted for four periods
and each lasted for 21 days. During the rst
14 days, all animals were fed respective diets,
whereas during the last 7 days, they were moved to
metabolism crates for total urine and fecal
collection.
Feeds and fecal samples were collected by
total collection of each individual buffaloes during
the last 7 days of each period at the morning and
afternoon feeding. Feeds and refusals samples
analyzed for DM, ash and CP content (AOAC,
1995). Urine samples were analyzed for total
N (AOAC, 1995) and allantonin in urine was
determined by HPLC as describes by Chen et al.
(1993). At the end of each period, rumen uid
samples were collected immediately post feeding
at 2, 4 and 6 h. Rumen uid was immediately
measured for pH and temperature by using
a portable pH temperature meter. Ruminal
ammonia nitrogen (NH3-N) analyzed by micro
Kjeldahl methods (AOAC, 1990). Total direct
count of protozoa and fungal zoospores were
determined by using the method of Galyean (1989)
and group of bacteria (total viable, cellulolytic,proteolytic and amylolytic) were measured using
roll-tube technique (Hungate, 1969).
All data from the experiment were analyzed by
using the SAS(1998) GLM procedure according
to the model: Yijk = + Mi + Aj + Pk + ijk; where
Yijk: observation from animal j, receiving diet i,
in period k; : the overall mean; Mi: effect of the
different level of ELM supplementation (i = 1, 2,
3, 4); Aj: the effect of steer (j = 1, 2, 3, 4); Pk: the
effect of period (k = 1, 2, 3, 4); and ijk: the
residual effect. Difference between treatment
means were determined by Duncans New Multiple
Rang Test (DMRT) with P
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77KHON KAEN AGR. J. 41 SUPPL. 1 : (2013).
Supplementation of ELM did not affect on
ruminant pH, temperature (Table 2) and those
values were in normal ranges as reported for
optimal microbial digestion of ber by Wanapat
and Pimpa (1999). However, ruminal ammonia
nitrogen concentration was signicantly
decreased (P
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78 41 1 : (2556).
Table 2 Effects of Eucalyptus leaf meal on rumen fermentation characteristics.
(ELM, g/hd/d)
Items 0 40 80 120 SEM
Ruminal pH 6.6 6.5 6.4 6.5 0.06Ruminal temperature, 0C 38.6 38.6 38.5 38.6 0.05
NH3-N, mg/dL 11.8a 10.3ab 8.5ab 7.8b 0.99
Total direct count, cell/ml
Protozoa, x 105 9.1a 8.6ab 7.6ab 7.1b 0.51
Fungi zoospores, x 105 3.9 3.4 3.2 4.5 0.40
Viable bacteria, CFU/ml
Total, x 108 0.72 0.76 0.8 1.1 1.13
Amylolytic, x107 4.7 3.4 3.1 5.1 0.91
Proteolytic, x 10
7
6.8
a
5.7
ab
5.0
b
3.1
c
0.45Cellulolytic, x108 2.0 1.1 1.2 1.3 0.33
a,bValues on the same row with different superscripts differed (P
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79KHON KAEN AGR. J. 41 SUPPL. 1 : (2013).
Education and Training, Vietnam are gratefully
acknowledged for the use of research facilities and
nancial support, respectively.
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