Effect of eucalyptus leaf meal supplementation on feed intake ruminal ecology and microbial protein...

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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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