Livestock Research for Rural Development 27 (2) 2015 | Guide for preparation of papers | LRRD Newsletter | Citation of this paper |
Twenty three growing bulls about 1-1.5 yrs old and 185±23.6 kg live weight were allocated to 4 treatments (DEF1, DEF2, REF and CTL). The DEF1 treatment was a single drench with 3g of soybean oil per kg live weight; DEF2 animals were drenched twice (the second drench 30 days after the first one), cattle on the REF treatment were refaunated 30 days after the initial oil drench, while the CTL treatment was neither renched nor refaunated.
Dry matter (DM) feed converson (FCR) and live weight gain were better for the cattle given a repeated drench with soybean oil than for the control animals. Between the defaunated treatments, the repeaated defaunation (DEF2) showed better feed utilization and growth rate with lower feed intake than the single defaunation. The higher growth rates were associated with protozoal counts less than 50,000/ml compared with counts of the order of 200,000/ml before oil treatment. It is concluded that oil drenching may be a suitable option for profitable cattle fattening.
Key words: beef production, defaunation, refaunation, rumen protozoa
A sensible livestock development strategy needs to match with the feed resources, type of animals and the animal products with the national requirement. It is obvious from the experience over generations in Bangladesh, that an exclusive diet of rice straw, with little or no supplementation, barely supports the nutritional needs of livestock, resulting in stunted growth, impaired reproduction and lactation and reduced working ability. The feeding value of rice straw can be improved with a number of treatment techniques that have been developed (Trach and Thom 2004). However, neither improved feeding techniques such as urea-treated straw or urea-molasses block supplementation are being used by the farmers in Bangladesh.
In ruminants, protozoa account for 20 to 70% of the ruminal microbial biomass, but their contribution to microbial protein flow at the duodenum is limited to only 20 to 40% (Jouany 1996). Nhan et al (2003) confirmed the advantages of an oil drench in increasing the live weight gain of local Yellow cattle fed on untreated rice straw supplemented with cassava foliage. The oil drench has an anti-protozoal effect which might improve rumen cellulolysis, increase digestibility and intake, and eventually animal growth (Seng et al 2001).
The early procedures used a chemical surfactant for eliminating the protozoa but this was a difficult procedure which often resulted in the death of the animals, and thus had a negative impact at farmer level. Using oil to eliminate the protozoa from the rumen has been shown to improve growth rates, increasing bacterial population and microbial protein flow from the rumen to lower tract (Leng 1990). Lipids are toxic to rumen ciliate protozoa (Newbold and Chamberlain 1988) and the approach for reducing rumen protozoa with oil drenchng has a positive effect on growth rate of cattle (Nguyen Thi Hong Nhan et al 2001). A single dose oral administration of oil at farmer level resulted in better growth performance of cattle (Nguyen Thi Hong Nhan et al 2003, Seng et al 2001).
The Government of Bangladesh has taken beef fattening as an action program to generate income for the rural farmers. Thus this research focused on the effects of defaunation on the growth rate of local cattle.
Several methods are available for eliminating protozoa from the rumen, and they are mostly based on the use of chemicals (e.g., copper sulfate and calcium peroxide) that have toxic effects on ruminal protozoa (Jouany 1996). A major drawback of using chemicals to eliminate ruminal protozoa is that they can be toxic to experimental animals and can also alter other aspects of the ruminal microbial ecosystem (Jouany et al 1998), hence it was decided to use soybean oil as a defaunating agent in this program following the research of Nguyen Thi Hong Nhan et al (2001).
Twenty three native Pabna bulls about 1-1.5 yrs old and 185±23.6 kg live weight were selected from the stock herd of Bangladesh Livestock Research Institute for a trial of 120 days duration. They were allocated to 4 treatments (DEF1, DEF2, REF and CTL). The DEF1 treatment was a single oil drench, DEF2 was drenched twice (the second drench 30 days after the first one), the REF treatment was refaunated following the initial defaunation, while the CTL treatment was neither defaunated not refaunated. Animal on each treatment were housed in different sheds to avoid contamination. All the cattle were fed ad libitum straw supplemented with urea-molasses (3% urea, 20% molasses) plus a concentrate mixture (wheat bran, gram bran 1: 1) at 1% of their live weight. A pre-experimental period of 10 days was considered as an adjustment period to adapt the animals with whole experimental feeding system. The urea-molasses supplemented straw (UMS) and the concentrate were given twice daily, in the morning and evening. Feed offered and feed residues were recorded daily. Samples were taken three times per week for determination of dry matter (DM). Live weights were recorded every 2 weeks.
Removal of protozoa in treatments (DEF1, DEF2 and REF) was performed by drenching the animals with 3g of soybean oil per kg live weight. After 15 days DEF2 cattle were given a second oil drench and at the same time the REF animals were refaunated by feeding 500 ml of fresh rumen liquor collected from rumen-cannulated bulls. Prior to, and after 7 days of oil treatment and at the termination (120th days) of the experiment, rumen liquor was collected through a stomach tube from all animals 1.5-2 hours after the morning feed. Immediately after collection of the rumen sample, the pH was measured and the sample stored at 5ºC for counting of protozoa. For the protozoa counting, the samples were at kept room temperature before diluting (1:1) with formalin and the protozoa then counted under a microscope. For the measurement of NH3, the rumen samples were acidified with 3-4 drops of concentrated sulfuric acid (99% purity) and then stored in a deep freezer until laboratory analysis.
DM intake was reduced, growth rate appeared to be increased (p=0.099), and DM feed conversion was improved, in the cattle given a repeated oil drench (DEF2) as compared with the control (CTL)treatment (Table 1; Figure 1). These effects were less marked for the single oil drench treatment. The growth performance of the refaunated (REF) animals was similar to that on the control treatment.
Table 1: Mean values for feed intake, live weight change and DM feed conversion of cattle fed rice straw supplemented with molasses-urea and wheat bran and subjected to a single (DEF1), or repeated (DEF2) oil drench, or a single drench followed by re-faunation (REF). CTL was the control treatment with no oil drench. |
||||||
CTL |
DEF1 |
DEF2 |
REF |
SEM |
p |
|
DM intake, kg/d |
5.88c |
5.74 bc |
5.02a |
5.53b |
0.094 |
<0.01 |
Live weight, kg | ||||||
Initial | 189 | 187 | 186 | 184 | 10.7 | 0.99 |
Final | 241 | 245 | 258 | 239 | 10.8 | 0.62 |
Growth rate, kg/d |
0.461 |
0.572 |
0.664 | 0.495 |
0.047 |
0.099 |
FCR, kg DMI/kg LW gain |
12.5b |
11.1b |
7.82a |
11.3b |
0.501 |
<0.01 |
abc Means in the same row without common superscript differ at P<0.05 |
Figure 1. Effect of a single or repeated oil drench
on cattle fed rice straw supplemented with molasses-urea and wheat bran |
Before oil treatment, protozoal numbers on all the treatments were similar, but 7 days after the first oil drench, the protozoal population was decreased to levels much lower than in control animals (Table 2). After the second oil drench (DEF2 treatment), protozoal numbers in these animlas remained low, but they tended to increase in those animals drenched only once (DEF1), while in the refaunated animals (REF) numbers of protozoa were almost back to the levels before the oil drench. After 120 days (end of the trial), protozoal numbers in DEF1 and DEF2 had increased but were still lower than in the control and refaunated treatments.
Table 2: Protozoa population in the rumen of cattle given a single (DEF1) or repeated (DEF2) oil drench, were refaunated after a single oil drench (REF) or were not treated (CTL) |
||||||
CTL |
DEF1 |
DEF2 |
REF |
SEM |
p |
|
Before oil drench |
182521 |
173400 |
196320 |
183440 |
2356 |
0.81 |
7 d after 1st oil drench |
191530b |
53580a |
42787a |
38507a |
18389 |
<0.01 |
7 d after 2nd oil drench# |
205373b |
76960a |
46123a |
142950c |
17740 |
<0.01 |
After 112 d |
205800b |
83800a |
69600a |
145100c |
15608 |
<0.01 |
abc Means in the same row without common superscript differ at P<0.05
|
The pH in the rumen was not changed by the oil drench (Table 3).
Table 3: Rumen pH before and after oil drenching |
||||
|
CTL |
DEF1 |
DEF2 |
REF |
Before oil feeding |
6.70 |
6.70 |
6.71 |
6.71 |
7 days after 1st oil drench |
6.71 |
6.67 |
6.68 |
6.67 |
28 days after 1st oil drench# |
6.70 |
6.70 |
6.67 |
6.72 |
# 7 days after the DEF2 treatment received the 2nd oil drench and the REF animals were refaunated |
The increase in growth rate following defaunation is in agreement with many reports in the literature of the positive effects of defaunation in roughage-based diets (eg: Demeyer et al I982; Leng 1982; Trach and Thom 2004; Seng et al 2001; Nguyen Thi Hong Nhan et al 2001, 2003, 2007, 2008). The decrease in the protozoal population as as a result of the oil drench, and the subsequent gradual restoration of protozoal numbers is in accordance with the findings of Seng et al (2001). The better feed conversion, and the tendency for a higher growth rate in DEF2, compared with DEF1 animals, implies that there may be advantages in repeated oil drenching. There appear to be no reports of this method being used in a practical feeding situation. This procedure merits further research.
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Trach N X and Thom M T 2004 Responses of growing beef cattle to a feeding regime combining road side grazing and rice straw feeding supplemented with urea and brewers' grains following an oil drench. Livestock Research for Rural Development. Volume 16, Article # 53 from http://www.lrrd.org/lrrd16/7/trac16053.htm
Received 18 September 2014; Accepted 4 January 2015; Published 4 February 2015