Livestock Research for Rural Development 15 (1) 2003 | Citation of this paper |
A total of 16 castrate male pigs [Mong Cai (MC) or Large White (LW)] with an average weight of 20 kg were
used in a random two-block design to study N utilization from a high fibre diet consisting
of wheat bran as the major dietary component (68% in dry basis). Daily feed consumption
was 40 g DM/kg body weight and crude protein (Nx6.25) of the diet was 18% in DM.
There was no effect of genotype on total tract digestibility for DM, organic matter, crude fibre and NDF but MC pigs digested less N than LW animals. Faecal pH values were lower and short chain fatty acids and ammonia tended toward a higher output in MC pigs than in LW. N retention was lower in MC than in LW pigs when expressed as a proportion of live weight or of N intake. This trend was not apparent for N retention as proportion of N digested..
The results from the present experiment suggest that the N requirement of Mong Cai pigs
may be lower than what is recommended for "improved" genotypes selected for lean
meat production.
Experimental
evidence has been accumulated suggesting that the scheme of N utilization in Mong Cai pigs is somewhat different from
that observed in improved pig genotypes selected for lean meat traits (Bun Tean 2002; Nguyen Thi Thuy and Ly 2002; Chiv Phiny et al 2002). The Mong Cai breed has probably originated in the
A
somewhat similar trend in N utilization has been observed in another Asian breed, the Meishan pigs from
The
aim of the present experiment was to obtain additional information
about the characteristics of some digestive processes and N balance in Mong Cai as compared to Large
White pigs, kept in a common environment, in terms of feeding management and high air
temperature.
Eight
Mong Cai
and eight Large White castrate male pigs, with an average weight of 20 kg, were
allocated in a random two-block design to study N utilization from a high fibre diet
consisting of wheat bran as the major dietary component. The Mong
Cai pigs were of Vietnamese origin
(from Thu Duc, near
The
diet was composed (% DM basis) of wheat bran 68.0, maize bran 20.0, dried fresh
water fish 10, vitamin and mineral premix 2.0. The vitamin and mineral supplementation was
according to NRC (1998) recommendations. Details of the chemical composition of the
ingredients and the diet are in Table 1. Daily feed intake was adjusted to 40 g/kg of live
body weight, which was close to ad libitum based on previous observations. The daily feed
allowance was given in a meal form twice daily (
Table
1. Characteristics
of the ingredients and the diet (in per cent, dry basis) |
|||||
Wheat bran |
Maize bran |
Dried fresh water fish |
Vitamin, mineral supp. |
Diet |
|
Dry
matter |
85.1 |
84.8 |
86.4 |
89.9 |
85.2 |
Ash |
3.36 |
1.38 |
30.1 |
61.4 |
9.13 |
Organic
matter |
96.6 |
98.6 |
69.9 |
38.3 |
90.9 |
Crude
fibre |
8.79 |
10.02 |
- |
- |
6.98 |
NDF |
45.1 |
37.72 |
- |
- |
38.2 |
Ether
extract |
4.90 |
3.20 |
12.3 |
- |
5.20 |
NFE |
66.8 |
73.9 |
2.32 |
38.1 |
60.6 |
Nx6.25 |
16.12 |
11.44 |
55.25 |
0.20 |
18.1 |
Gross
energy, KJ/g DM1 |
17.70 |
15.96 |
17.36 |
6.11 |
17.8 |
WHC,
g/g DM2 |
8.73 |
7.50 |
- |
- |
7.44 |
1
Estimated according to Nehring and Haenlein
(1973) |
The
animals had a five-day adaptation to the diets. During the adaptation period, feed
consumption was adjusted to a level with no feed refusals. Thereafter, quantitative
collection of faeces, urine and any feed residue were made
during another five days. During the entire 10-day period, the animals were housed
individually in metabolism crates designed for quantitative collection of faeces and urine separately. These crates were in an open stable
without walls. Urine was collected in covered plastic buckets, under enough H2SO4
solution to keep the liquid at pH below 4.
The
DM content of feeds and faeces was determined according to Undersander et al (1993) by microwave radiation until constant
weight, and N in feeds, faeces and urine was as indicated by
the A0AC (1990) the wet oxidation Kjeldahl procedure. The
content of cell walls (NDF) in the samples was determined according to Van Soest et al (1991). The gross energy value of feed ingredients and
the diet was calculated according to the Nehring and Haenlein (1973) formula. Water holding capacity of feed
ingredients was determined by the filtration technique described by Tsaras
et al (1998) as adapted by Ly (2003), by using during five minutes a gentle vacuum
originated from a commercial dust aspirator connected to a vacuum flask.
The
pH value in fresh faeces was determined with a glass electrode
fitted to a digital pH meter. In addition, faecal
concentrations of short chain fatty acids (SCFA) and NH3 were estimated in
fresh faecal material filtered through three sheets of cotton
after suspending the samples in distilled water (1:4 by weight). The samples were mixed in
the ratio of 1:1 (by volume) with a saturated solution of MgSO4 in H2SO4
and the resulting acid product of steam distillation titrated,
following the method outlined by the standard procedure of Pennington (1952; quoted by Ly
1986). In this particular case, an aliquot of the faecal filtered slurry was steam distilled after mixing with NaOH 40% in the ratio 1:5 (by volume) as recommended in the standard
Kjeldahl procedure, and then titrated by the acid-base
method.
The
indicators of daily faecal output were calculated as described
by Ly et al (1998). All analyses were conducted in duplicate.
Means
between treatments were compared by the standard t-test (Steel and Torrie
1980) following ANOVA analysis using the Minitab program software (Ryan et al 1992).
Regression analysis was employed in the required cases.
Average
air temperature during the trial was 35.0 ± 3.5oC as measured every day
at
There
was no effect of genotype on faecal excretion of fresh material and water, the values of
which were high as expected from the high water holding capacity of the diet (Table
2). The Large
White pigs had a higher faecal pH than Mong
Cai animals. On the other hand, faecal concentration and output of metabolites tended to be higher
(a trend for NH3 (P<0.10) and higher for SCFA (P<0.05) in the Mong Cai than in the Large White
pigs.
Table 2. Faecal characteristics in Mong Cai and Large White young pigs |
|||
Genotype |
SE ± |
||
Mong Cai |
Large White |
||
Number of animals |
8 |
8 |
- |
Faecal characteristics |
|||
pH |
6.74 |
7.41 |
0.14*** |
DM, % |
27.9 |
29.3 |
1.54 |
SCFA, mmol/100 g DM |
51.2 |
37.1 |
3.74* |
NH3, mmol/100 g DM |
37.7 |
30.5 |
3.12+ |
Faecal output per kg DM intake |
|||
Fresh material, g |
669 |
664 |
38 |
DM, g |
186 |
178 |
23 |
Water, g |
483 |
466 |
42 |
SCFA, mmol |
94.8 |
72.9 |
18.0+ |
NH3, mmol |
70.5 |
54.5 |
7.3* |
+ P<0.10; * P<0.05; *** P<0.001 |
In
previous experiments, faecal output of SCFA and ammonia
appeared to be inversely proportional to pH values in faeces
from Mong Cai
pigs ((Ly and Pok Samkol 2001; Ly
2003), and this phenomenum appeared to hold true for faecal SCFA and pH (P<0.08) on one hand, and for faecal ammonia and pH (P<0.04) on the other hand. At the same
time a straight, negative relationship has previously been found between faecal output of these types of metabolites and organic matter
digestibility (Ly 2003). A similar significant relationship (Table 3) was observed in the
current study, which appeared to be stronger for ammonia than for SCFA output, and on the
other hand, stronger for Large White than for Mong Cai pigs.
Table 3.
Linear
interdependence between faecal output of SCFA and ammonia (y, mmol/kg DM intake) and organic matter digestibility (x, %) in Mong Cai and Large White pigs |
||||||
n |
a |
b |
Syx |
r |
P |
|
Faecal SCFA output |
||||||
Mong Cai |
8 |
581 |
6.0 |
37.3 |
- 0.362 |
0.378 |
Large White |
8 |
657 |
7.1 |
0.8 |
- 0.999 |
0.001 |
Overall |
16 |
581 |
6.0 |
27.8 |
-0.443 |
0.086 |
Faecal ammonia output |
||||||
Mong Cai |
8 |
655 |
7.0 |
18.9 |
- 0.669 |
0.070 |
Large White |
8 |
480 |
5.1 |
0.7 |
- 0.998 |
0.001 |
Overall |
16 |
530 |
5.6 |
15.9 |
- 0.628 |
0.009 |
Since
it has been revealed that bacterial metabolism in pig's faeces
is similar to that occurring in the terminal part of the gastrointestinal tract in this
species (Williams et al 1998; Bauer et al 2001), it is possible to think that there exists
certain influence, other than the dietary effect, on microbial activity in the large
intestine of the pig due to the nature of the genotype under examination. In fact, Bruininx et al (2002) observed a noticeable influence of piglet
genotype on SCFA and ammonia concentration in large intestinal digesta.
An increase in microbial activity in caecum and colon of Mong Cai
pigs, through a shift of bacterial balance to enhance the cellulolytic
bacteria population (Varel et al 1984; Varel
1987), could support an increase in degradation of the fibrous fractions of the diet, as
data from the present experiment could indicate. As it is well known, the large intestine
of the pig is the main site of the alimentary canal for fibre
degradation (Bach Knudsen and Jorgensen 2001). An
increase in activity of the large intestinal microbiota could
occur too in organs susceptible to be further anatomically adapted to room bulky feeds
(Low 1985, 1993; Kyriazakis and Emmans
1995).
There
was no significant influence of breed on DM and organic matter digestibility (Table 4),
which was relatively high, in spite of a high NDF content in the diet that could in turn
negatively affect digestive indices, as it has been claimed elsewhere (Fernández and Jorgensen 1986; Close 1993; Le Goff et al 2002).
Digestibility of NDF and crude fibre were relatively high too
in both breeds taking into account the highly fibrous nature of the rations, with a very
slight inclination, although not significant (P>0.10) for Mong
Cai pigs to better digest several fibre
fractions as compared to the Large White animals. In this connection, it has been found
that total tract digestibility of hemicellulose and cellulose
is not higher than 45 and 35% respectively for wheat bran in Large White pigs (Chabeauti 1991; Chabeauti et al 1991).
Table 4. Total tract
digestibility in Mong Cai and
Large White young pigs |
|||
Genotype |
SE ± |
||
Mong
Cai |
Large White |
||
Number of animals |
8 |
8 |
- |
Total tract digestibility, % |
|||
DM |
81.4 |
82.2 |
1.2 |
Organic matter |
83.3 |
82.9 |
1.1 |
Crude fibre |
43.5 |
40.0 |
6.8 |
NDF |
55.0 |
50.0 |
7.2 |
There
are conflicting results concerning fibre fraction utilization
by local pigs from the Far East of Asia. Aumaitre et al (1992)
did not find differences between improved European on one hand and Chinese breeds on the
other in digestive capacity for utilization of dietary fibre. In a previous experiment with Mong
Cai pigs (Nguyen Thi Thuy and Ly 2002), it was observed a
non significant improvement of NDF digestibility as compared to Large White animals.
Several
indices of N balance indicated that Mong Cai utilized less dietary N than Large White pigs (Table 5).
There was a similar mean daily N intake in both breeds, but Mong
Cai showed a high variability for this index. Faecal excretion of N was higher (P<0.05) in Mong
Cai animals than in the Large
White, and this phenomenum determined a significantly higher
digestibility (P<0.01) for pigs of the Large White breed. These results are in
accordance with others comparing these two same genotypes (Nguyen Thi
Thuy and Ly 2002).
Table 5. N balance in Mong Cai and Large White young pigs |
|||
Genotype |
SE ± |
||
Mong
Cai |
Large White |
||
Number of animals |
8 |
8 |
- |
N balance, g/day |
|||
Consumption |
14.63 |
14.50 |
1.08 |
Excretion in faeces |
3.23 |
2.24 |
0.51* |
Digestion |
11.40 |
12.26 |
0.68 |
Digestibility, % |
78.6 |
84.6 |
2.0** |
Excretion in urine |
4.69 |
4.44 |
0.61 |
Total excretion |
7.92 |
6.62 |
0.83+ |
Retention |
6.71 |
7.87 |
0.59* |
Retention:consumption |
45.9 |
54.3 |
3.2** |
Retention:digestion |
58.9 |
63.3 |
3.7 |
+ P<0.10; * P<0.05; **
P<0.01 |
It
was found that 40.8% of total N excretion was via faeces in
the Mong Cai
pigs whereas the same index was only 33.8% in the Large White animals (Figure 1). As it
can be clearly deduced, urine was the main route of N elimination in both breeds eating a
highly fibrous diet.
A
trend was found for total excretion of N to be higher in the Mong
Cai animals when this index was
compared to that of Large White pigs. In consequence, animals from the Large White
genotype had a significantly higher N retention in terms of the daily total amount
retained (P<0.05) or related to the N intake in percentage (P<0.01). N retention in Mong Cai pigs
(6.7 g/day) accounted for 83.6% of the same index for Large White pigs (7.9 g/day). This
same trend was not apparent for N retention expressed as percentage of digested N
(P<0.26) between both genotypes studied. However, the efficiency of utilization of
digested N accounted for 93.7% in compared values for Mong Cai and Large White pigs.
Results
concerning the effect of genotype on N balance are in accordance with other previous
studies (Bun Tean 2002; Chiv Phiny et al 2002) indicating a lower N
utilization by Mong Cai pigs as
compared to other improved breeds. The data from the current investigation are in
accordance too with a similar trend previously observed with Meishan
pigs as compared to Large White (Février et al 1990; Kemp et
al 1991), or with Jiaxing pigs if compared to Jiaxing x Landrace animals (Guohai et al
1990; cited by Aumaitre et al 1992).
Results
from the present experiment support the hypothesis that N requirement of Mong Cai pigs
must probably be lower than that recommended for certain improved genotypes for lean meat.
More
research is needed in order to clarify the pattern of microbial digestion of N in the
large intestine of pigs fed high levels of fibrous materials, with emphasis on the nature
of the pig's genotype and the botanical origin of the dietary fibre.
This
publication is an output from a collaborative research work carried out by members of the
staff of the
Thanks
are given to the MEKARN project (supported by SIDA-SAREC of Sweden), for
partial funding of the current investigation. The authors are grateful to Dr. Claude Février, formerly from the Swine Research Station at INRA,
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Received 19 November 2002; Accepted 12 December 2002