Effect of Production Systems on Carcass Traits, Visceral Development and Meat Quality in Fattening Rabbits
Research Article
Effect of Production Systems on Carcass Traits, Visceral Development and Meat Quality in Fattening Rabbits
Divanildo Outor-Monteiro1,2,3*, José António Silva2,3,4, José Luís Mourão1,2,3, Victor Pinheiro1,2,3
1Department of Animal Science, Universidade de Trás-os-Montes e Alto Douro (UTAD), Quinta dos Prados, 5001-801, Vila Real, Portugal; 2Centro de Estudos em Ciência Animal e Veterinária (CECAV), Universidade de Trás-os-Montes e Alto Douro (UTAD), Quinta dos Prados, 5001-801, Vila Real, Portugal; 3Associate Laboratory for Veterinary and Animal Science (AL4AnimalS-UTAD), Universidade de Trás-os-Montes e Alto Douro (UTAD), Quinta dos Prados, 5001-801, Vila Real, Portugal; 4Department of Veterinary Science, Universidade de Trás-os-Montes e Alto Douro (UTAD), Quinta dos Prados, 5001-801, Vila Real, Portugal.
Abstract | Actually, some consumers have displayed a growing preference for rabbit meat sourced from alternative rearing systems as opposed to intensive cage-based systems. This trial was designed to explore the influence of production systems (cages - Cg; 13.3 rabbits/m2, closed parks - CP; 7.7 rabbits/m2, and open-air systems - Oa; 0.25 rabbits/m2) and slaughter age (70 and 84 days) on the growth, carcass traits and meat quality of growing rabbits. 120 animals were randomly allocated to three different production systems. At both slaughter ages, the M. biceps femoris of Oa and CP rabbits exhibited higher cooking losses (5.50 vs. 3.83%) and total pigments (0.37 vs. 0.28 mg/g) compared to Cg rabbits. The production system did not significantly impact dressing out, visceral development, Warner-Bratzler Shear Force – WBSF and meat pH. In contrast, 84-day-old rabbits reared in cages displayed reduced digestive organ development, decreased caecal acetic acid and increased butyric acid concentration, compared to their counterparts. When comparing slaughter ages, the 84-day-old rabbits exhibited higher dressing out percentages, lower relative organ weights (liver, kidney, lung and heart), decreased hind part proportions and lower cooking loss values. Furthermore, the hind legs of these rabbits had a greater proportion of muscle and less bone, along with increased luminosity and reduced redness. In conclusion, production systems exert influence on specific carcass and meat characteristics.
Keywords | Rabbit, Housing system, Slaughter-age, Carcass, Meat
Received | May 26, 2023; Accepted | October 27, 2023; Published | January 10, 2024
*Correspondence | Divanildo Outor-Monteiro, Department of Animal Science, Universidade de Trás-os-Montes e Alto Douro (UTAD), Quinta dos Prados, 5001-801, Vila Real, Portugal; Email: divanildo@utad.pt
Citation | Monteiro DO, Silva JA, Mourão JL, Pinheiro V (2024). Effect of production systems on carcass traits, visceral development and meat quality in fattening rabbits. Adv. Anim. Vet. Sci., 12(1):165-172.
DOI | https://dx.doi.org/10.17582/journal.aavs/2024/12.1.165.172
ISSN (Online) | 2307-8316
Copyright: 2024 by the authors. Licensee ResearchersLinks Ltd, England, UK.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Introduction
Presently, consumers exhibit a clear preference for rabbit meat derived from alternative farming systems over intensive cage-based systems, with a focus on preserving environmental sustainability, animal welfare, economic viability, and food safety (Matics et al., 2019; Krunt et al., 2022). Carcass quality must meet economic objectives and saleable meat yield, while also appealing to consumer preferences. Significant alterations in carcass traits and meat quality have been observed when animals are reared in alternative systems (Dalle Zotte, 2002; Combes and Lebas, 2003). Some studies have examined alternative housing systems for growing rabbits (Orova et al., 2004; Jekkel et al., 2010; Krunt et al., 2020).
Housing systems have a substantial impact on rabbit performance (Dal Bosco et al., 2000; Dalle Zotte et al., 2009) as well as carcass and meat quality (Xicatto et al., 2013). Factors such as stocking density, group size, and floor type have been identified as crucial (Matics et al., 2019). The European Food Safety Authority (EFSA) established a housing systems committee to provide recommendations, recognizing the importance of this aspect (EFSA, 2020). Confined housing systems have historically yielded optimal productive performance (Maertens and De Groote, 1984) and superior meat quality (Xiccato et al., 2013). Collective housing systems with environmental enrichment have gained popularity due to their welfare benefits (Buijs et al., 2011). However, it should be noted that larger group sizes, exceeding 10 rabbits, can lead to reduced performance and compromised carcass and meat quality (Dal Bosco et al., 2000; Xiccato et al., 2013).
In response to the End the Cage Age European Citizens’ Initiative (ECI), the European Commission has outlined plans to phase out the use of cages for rabbits and other farmed animals by 2027, necessitating comprehensive research into alternative housing systems. Consequently, our study aimed to investigate the effects of different productio/housing systems (cages, closed pens, and open-air pens) on visceral development, carcass characteristics and meat traits in growing rabbits.
Materials and Methods
Housing, animals and experimental design
The research was conducted at the Rabbit Experimental Unit within the Animal Science Department at the University of Trás-os-Montes e Alto Douro in Portugal. This experiment adhered to the guidelines set forth by Portuguese legislation governing animal welfare in scientific research, as stipulated in Government Order No. 113/2013 dated August 7th.
A total of 120 rabbits (New Zealand x Californian) of both genders were monitored throughout their growth period, spanning from 35 to 84 days of age. These rabbits were randomly assigned to three distinct housing groups: cages, closed pens, and open-air pens. The caged rabbits (Cg; n=40) were accommodated in 10 wire cages, each with a total area of 0.03 m2 (0.5m×0.6m; housing 4 animals per cage). Another 40 rabbits were situated in 10 pens within a closed building (CP), offering an area of 0.525 m2 per pen (1.05m×0.5m; housing 4 animals per pen), featuring a bedding of wood shavings with a depth of 10cm. All animals, whether in cages or pens, were housed within a climate-controlled facility, maintaining an air temperature ranging between 20 and 25°C, with a daily light exposure of 12 hours. The third group (Oa), consisting of 40 rabbits, was accommodated in two outdoor pens, each spanning 80 m2 (10 m×8 m), housing 20 animals per pen, and providing access to pasture.
All rabbits were provided with ad libitum access to a pellet diet, which consisted of 91.6% organic matter, 24.7% starch, 17.2% acid detergent fiber, 16.2% crude protein and 3.7% crude fat. Additionally, rabbits housed in the outdoor pens were afforded access to natural pasture. Importantly, all rabbits had continuous access to drinking water throughout the duration of the study.
Slaughter traits and sample collections
When the rabbits reached the ages of 70 and 84 days, 30 animals per age group (10 per treatment) were selected for slaughter to conduct carcass and meat studies. Carcass preparation and dissection followed the guidelines established by the World Rabbit Science Association (WRSA) as outlined in Blasco and Ouhayoun (1996). Following the slaughtering process, the hot carcasses, which included the head, kidneys, liver, and thoracic viscera, were weighed and then suspended in a well-ventilated area for 60 minutes. Subsequently, they were cooled in a chamber maintained at 3°C for 24 hours to obtain the weight of the chilled carcass and calculate the drip loss and dressing out percentage.
The weight of the hind part was recordedin accordance with Blasco and Ouhayoun (1996), and the right hind legs were dissected into bone and meat, with their respective weights documented. Measurements of the femur length and diameter were also taken. The weights of the head, liver, and reference carcass were expressed as a percentage of the chilled carcass weight, while the hind part weights and dissectible fat were expressed as a percentage of the reference carcass weight. The meat-to-bone ratio of the hind leg was calculated as the ratio between the dissected meat weight and bone weight.
For rabbits slaughtered at 84 days of age, additional measurements were conducted to gain further insight into digestive characteristics, organ development, and volatile fatty acid (VFA) concentrations. After slaughter, the pH levels of the cecal and stomach contents were measured, and the weights and lengths of both full and empty gastrointestinal tracts were recorded. Samples of cecal content were collected and frozen for subsequent determination of VFA concentrations. The analysis of VFA followed the procedures outlined by Costa-Silva et al. (2022).
Rheological and analytical measurements
Measures of color in the CIELAB color space (lightness, L*; redness, a*; yellowness, b*) were conducted following the method outlined by Ouhayoun and Dalle Zotte (1996). These measurements were taken at 24 hours post-mortem using a Minolta CR-300 Minolta Chromameter (Osaka, Japan). The color of the carcass was assessed on the surface of the M. biceps femoris muscle (left), while the meat color was evaluated in the transverse section of the same muscle.
The pH of the chilled carcass at 24 hours post-mortem (pH24h) was determined using a pH glass electrode (pH 91, WTW, Weilheim, Germany), which was inserted to a depth of 5 mm into the right M. biceps femoris muscle.
Cooking loss (CL, %), tenderness (WBSF), and pigment concentration were assessed following the methodology described by Pinheiro et al. (2011).
Statistical analysis
The results obtained for visceral development, carcass traits, and meat characteristics were subjected to a two-factorial analysis, considering the housing system and age as factors, along with their interaction. In the analysis pertaining to gut development and cecal volatile fatty acids (VFA), the influence of age was not taken into consideration. All statistical analyses were conducted using JMP-SAS software (v.13; JMP-SAS Institute Inc., Cary, NC).
Results and Discussion
Carcass characteristics
The housing system exhibited a significant effect (P < 0.05) on carcass, chilled carcass, and reference carcass weights, as well as the percentage of lean meat (Table 1). The rabbits housed in cages or closed pens displayed higher average slaughter and chilled carcass weights, approximately 12.5% and 12.8% greater, respectively, compared to rabbits housed in open-air systems. Caged rabbits also showed a higher percentage of excreta (P < 0.05) than those in closed pens and open-air systems (60.1 vs. 58.4 and 58.9%, respectively). Reference carcass weight, expressed both in grams and as a percentage of chilled carcass weight, was significantly greater (P < 0.05) for Cg and CP in comparison to Oa. No differences were observed in the relative weights of the liver, kidneys, heart, and lungs concerning the chilled carcass among the various housing systems (Table 1). However, the head weight of rabbits kept outdoors was 8.9% higher (P < 0.05) than that of rabbits in other housing groups (Table 1). Viscera weight, which includes the liver, kidneys, heart, and lungs, remained similar to values previously reported by Pinheiro et al. (2011) and was not influenced by the housing system.
Hind leg weight also exhibited differences (P < 0.001) among the three housing systems, with open-air rabbits having the highest weight, closed-park rabbits intermediate, and caged rabbits the lowest. In relation to the reference carcass weight, the proportion of the hind part in open-air housed rabbits was 11.7% and 6.5% higher compared to caged or closed-park rabbits, respectively (Table 1).
Table 1: Carcass characteristics of rabbits housed in cages, closed pens or in open air systems at 70 or 84 days of age.
Housing System (HS) |
Slaughter Age (SA) |
SEM1 |
P value |
|||||||
Cages |
Closed Pen |
Open |
70d |
84d |
HS |
SA |
HSxSA |
|||
No. of rabbits |
20 |
20 |
20 |
30 |
30 |
|||||
Slaughter weight (g) |
2645 a |
2635 a |
2309 b |
2161 |
2899 |
56.9 |
<0.001 |
<0.001 |
0.226 |
|
Chilled carcass weight (g) |
1594 a |
1542 a |
1368 b |
1251 |
1750 |
38.1 |
<0.001 |
<0.001 |
0.375 |
|
Dressing Out Percentage (DP) |
60.1 a |
58.4 b |
58.9 b |
57.8 |
60.4 |
0.333 |
0.044 |
<0.001 |
0.821 |
|
Drip Loss Percentage (DLP) |
1.53 |
2.63 |
1.59 |
1.81 |
2.02 |
0.250 |
0.124 |
0.670 |
0.147 |
|
Reference carcass |
||||||||||
Weight (g) |
1321 a |
1271 a |
1112 b |
1011 |
1458 |
34.3 |
<0.001 |
<0.001 |
0.457 |
|
Percentage of chilled carcass |
82.6 a |
82.3 a |
81.1 b |
80.6 |
83.3 |
0.28 |
0.010 |
<0.001 |
0.470 |
|
Head (% chilled carcass) |
8.14 b |
8.18 b |
8.96 a |
9.04 |
7.80 |
0.147 |
0.012 |
<0.001 |
0.267 |
|
Liver (% chilled carcass) |
6.08 |
6.52 |
6.68 |
6.87 |
5.98 |
0.154 |
0.224 |
0.003 |
0.767 |
|
Kidneys (% chilled carcass) |
1.06 |
1.05 |
1.14 |
1.18 |
0.98 |
0.022 |
0.087 |
<0.001 |
0.585 |
|
Heart and Lungs (% chilled carcass) |
2.07 |
2.10 |
2.19 |
2.30 |
1.94 |
0.051 |
0.540 |
<0.001 |
0.316 |
|
Dissectible fat (% reference carcass) |
3.74 |
2.75 |
1.90 |
2.32 |
3.27 |
0.183 |
<0.001 |
<0.001 |
0.002 2 |
|
Hind part (% reference carcass) |
32.5 c |
34.4 b |
36.8 a |
35.3 |
33.8 |
0.39 |
<0.0001 |
0.016 |
0.06 |
1SEM: Stand error of mean. 2At 70 days of age, differences are observed between the values of cages and pens. At 84 days the values of closed pens do not differ from cages and open pens. a, b, c: Means having a common letter did not differ significantly at level P>0.05. No. of rabbits were 10 per treatment.
Table 2: Hind leg characteristics of rabbits housed in cages, closed pens or in open air systems at 70 or 84 days of age.
Housing system (HS) |
Slaughter age (SA) |
SEM1 |
P value |
||||||
Cages |
Closed pen |
Open air |
70d |
84d |
HS |
SA |
HSxSA |
||
No. of rabbits |
20 |
20 |
20 |
30 |
30 |
||||
Hind leg |
|||||||||
Weight (g) |
189 a |
189 a |
174 b |
161 |
207 |
3.80 |
0.007 |
<0.001 |
0.174 |
Meat (% hind leg) |
80.6 a |
80.6 a |
78.8 b |
78.6 |
81.4 |
0.35 |
0.023 |
<0.001 |
0.115 |
Bone (% hind leg) |
19.4 b |
19.4 b |
21.2 a |
21.3 |
18.6 |
0.34 |
0.023 |
<0.001 |
0.115 |
Meat/bone |
4.22 a |
4.20 a |
3.81 b |
3.76 |
4.41 |
0.081 |
0.033 |
<0.001 |
0.131 |
Femur |
|||||||||
Weight (g) |
15.3 |
15.0 |
14.6 |
14.8 |
15.2 |
0.22 |
0.341 |
0.372 |
0.007 |
Length (mm) |
84.7 a |
84.3ab |
82.7 b |
80.6 |
87.2 |
0.53 |
0.019 |
<0.001 |
0.352 |
Diameter (mm) |
9.11 |
9.34 |
8.95 |
8.71 |
9.60 |
0.095 |
0.062 |
<0.001 |
0.073 |
1SEM: Stand error of mean. a, b: Means having a common letter did not differ significantly at level P>0.05. No. of rabbits were 10 per treatment.
The proportion of the hind part was influenced by the housing system, consistent with observations made by Matics et al. (2019) and Pinheiro et al. (2011). Available space significantly influences animal movement and hind leg development, as previously noted (Combes et al., 2003).
An interaction effect (HSxSA) was observed between the housing system and slaughter age for dissectible fat content (Table 1). At 70 days of age, rabbits in closed-park or open-air systems had dissectible fat content approximately one-third (35%) that of cage-housed animals. At 84 days, rabbits reared in open-air systems displayed dissectible fat content 62% lower (P<0.01) than rabbits reared in cages (1.7 vs. 4.5%). Closed-park rabbits had intermediate values (3.7%) and did not differ significantly from the other treatments.
Generally, slaughter age had a significant impact (P<0.05) on all carcass traits (Table 1), except for drip loss percentage. Slaughter weight, dressing out percentage, chilled carcass weight and reference carcass weight of rabbits increased significantly with age, reflecting greater overall development. The reference carcass weight and carcass yield also increased due to earlier viscera development, a phenomenon noted by others (Ouhayoun, 1998; Dalle Zotte, 2002). The percentage of the hind part and dissected fat also increased with age, indicating differential tissue development, consistent with findings by other authors (Dalle Zotte, 2002; Metzger et al., 2011).
Hind leg characteristics in relation to housing system and slaughter age are presented in Table 2. Caged and closed-park housed rabbits had heavier hind legs and higher meat content (80.6 vs. 78.8%) compared to open-air housed rabbits. However, open-air housed rabbits displayed a higher bone content (% hind leg). The meat-to-bone ratio of the hind leg in open-air housed rabbits was 37.4% lower (P<0.05) than that of cage-housed rabbits and 35.2% lower than that of closed-park rabbits (Table 2). These effects are attributed to the increased exercise afforded to rabbits in the larger available space of the open-air system. The results of this study are consistent with those of Dal Bosco et al. (2000) and Chodová et al. (2014), although Loponte et al. (2018) did not observe differences in rabbits housed in pens or cages.
Femur weight was not influenced by housing system or slaughter age. However, femur length was longer in caged rabbits and shorter in open-air animals, while femur diameter remained unaffected by the housing system. Outdoor rabbits experienced less growth and, consequently, had shorter femur lengths.
Drip loss was not affected by slaughter age (P>0.05). The relative weights of the head, liver, kidneys, and heart/lungs concerning the chilled carcass decreased with age. The hind part content also decreased (P<0.05) with slaughter age and was 4.2% lower at 84 days (Table 2).
Slaughter age influenced the hind leg characteristics of rabbits (Table 2). Rabbits slaughtered at 84 days had heavier hind legs (207 vs. 161g), higher meat content (81.4 vs. 78.6%), a higher meat-to-bone ratio (4.41 vs. 3.76), and lower bone content (18.6 vs. 21.3%). Furthermore, at 84 days, rabbits had longer femurs (87.2 vs. 80.6 mm) and larger femur diameters (9.6 vs. 8.71 mm) (Table 2).
The dissectible fat content of caged rabbits at 84 days of age was higher than that observed in open-air housed rabbits. This effect can be attributed to the lower energy available for growth and fat deposition (Dal Bosco et al., 2000).
Cooking loss was lower at 84 days, likely due to the higher maturity of the animals, which alters the meat composition and decreases water content (Dal Bosco et al., 2001; Dalle Zotte, 2002).
Table 3: Meat quality of carcass (M. biceps femoris) of rabbits housed in cages, closed pens or in open air systems at 70 or 84 days of age.
Housing system (HS) |
Slaughter age (SA) |
SEM1 |
P value |
||||||
Cages |
Closed pen |
Open air |
70d |
84d |
HS |
SA |
HSxSA |
||
No. of rabbits |
20 |
20 |
20 |
30 |
30 |
||||
pH |
|||||||||
Slaughter |
6.62 |
6.59 |
6.60 |
6.56 |
6.63 |
0.023 |
0.863 |
0.139 |
0.167 |
24 h post mortem |
6.03 |
5.93 |
5.97 |
6.01 |
5.95 |
0.022 |
0.188 |
0.191 |
0.07 |
Carcass color of biceps femoris |
|||||||||
L* |
53.5 |
52.6 |
52.9 |
50.4 |
55.6 |
0.58 |
0.753 |
<0.001 |
0.523 |
a* |
4.24 |
5.83 |
4.57 |
6.57 |
3.19 |
0.505 |
0.320 |
0.005 |
0.221 |
b* |
5.96 |
6.42 |
5.80 |
6.07 |
6.05 |
0.299 |
0.698 |
0.962 |
0.518 |
Meat color of M.biceps femoris |
|||||||||
L* |
59.7 |
59.1 |
58.8 |
59.0 |
59.4 |
0.38 |
0.617 |
0.615 |
0.412 |
a* |
-1.24 |
-0.92 |
-1.21 |
-1.38 |
-0.87 |
0.109 |
0.386 |
0.018 |
0.142 |
b* |
3.82 |
4.55 |
4.57 |
5.56 |
4.06 |
0.199 |
0.189 |
0.192 |
0.070 |
Cooking loss (%) |
3.83 b |
5.46a |
5.55a |
6.28 |
3.61 |
0.304 |
0.005 |
<0.001 |
0.217 |
WBSF (N) |
50.90 |
54.92 |
54.03 |
50.80 |
55.70 |
1.569 |
0.527 |
0.118 |
0.304 |
Total pigments (mg/g) |
0.28 b |
0.38a |
0.36a |
0.33 |
0.35 |
0.014 |
0.002 |
0.250 |
0.432 |
1SEM: Stand error of mean. a, b: Means having a common letter did not differ significantly at level P>0.05. L*, lightness; a*, redness; b*, yellowness; WBSF: Warner-Bratzler Shear Force. No. of rabbits were 10 per treatment.
Meat physical characteristics
The effects of housing system and age on meat quality are presented in Table 3. Color characteristics, pH values, and tenderness were not influenced by the housing system. However, cooking loss and the total pigment content of the M. biceps femoris (BF) muscle were affected (P<0.01). Cooking loss and total pigment content in the BF muscle of cage-housed rabbits were 30.5% and 24.3% lower, respectively, than those of the BF muscle in rabbits housed in closed pens or open-air systems.
The pH of the meat at slaughter and the pH at 24 hours post-mortem were not influenced by the housing system, which aligns with observations made by other authors (Pla et al., 1996; Pascual and Pla, 2007; Dalle Zotte et al., 2009). The housing system did not impact the color of the carcass and meat. These results were unexpected, given that the meat of open-air (Oa) rabbits had a higher pigment content, which could confer a reddish color. Therefore, a positive correlation between the two factors, as observed by Pinheiro et al. (2011), could have been anticipated. In similar studies, some authors reported an effect of rabbit housing on color (Pla, 2008; DalleZotte et al., 2009), while others, like us, did not observe housing system effects on color (Dal Bosco et al., 2001; Metzger et al., 2003).
Cooking loss was lower in cage (Cg) rabbits compared to other systems. This result could possibly be explained by differences in maturity, growth rate, and higher fat content (Lukefahr et al., 1983) among the treatments. The treatments did not affect the Warner-Bratzler Shear Force (WBSF) of the meat, which is in line with findings from other studies (Combes and Lebas, 2003; Metzger et al., 2003).
The increase in total pigments in the meat of Oa rabbits can be attributed to the fact that exercise enhances the oxidative capacity of muscle, resulting in a higher proportion of oxidative myofibers and the transition from type IIB to type IA fibers (Monin and Ouali, 1991; Volek et al., 2012), along with increased metabolism (Krunt et al., 2020).
The development of bone occurs earlier than that of muscular tissue (Picard et al., 2002), which may explain the higher proportion of muscle mass, lower bone mass, and a higher meat-to-bone ratio in older rabbits. In this study, slaughter age had a significant effect on carcass color defined by the L* and a* indices. L* increased with age, whereas a* decreased, but the a* color increased with age. Changes in carcass and meat color are not universally consistent, and results in the literature differ, as noted by Dalle Zotte (2002). These color changes may be associated with alterations in the predominant fiber types and modifications in oxidative muscular metabolism (Hernández et al., 2004), although in our study, pigment concentrations did not differ with age.
The reduction in pHu (ultimate pH) in the meat of older animals, observed in some studies, may correspond to a
Table 4: Gut characteristics of rabbits housed in cages, closed pens or in open air systems at 84 days of age.
Housing system |
SEM1 |
P level |
|||
Cages |
Closed pen |
Open air |
|||
No. of rabbits |
10 |
10 |
10 |
||
Live weight (LW) |
3036 a |
3068 a |
2619 b |
61.0 |
<0.001 |
Stomach pH |
1.60 b |
2.20 a |
1.95 a |
0.163 |
0.047 |
Caecal pH |
5.51 |
5.62 |
5.63 |
0.054 |
0.143 |
Organ weight g by g of LW |
|||||
Full stomach |
29.8 b |
42.8 a |
44.6 a |
2.326 |
<0.001 |
Empty stomach |
7.71 b |
9.04 a |
10.09 a |
0.364 |
<0.001 |
Stomach content |
22. 0 b |
33.7 a |
34.5 a |
2.12 |
<0.001 |
Full small intestine |
35.3 b |
42.6 a |
39.3 a |
1.28 |
0.002 |
Full caeco |
44.1 b |
52.6 a |
49.5 a |
2.23 |
0.045 |
Empty caeco |
13.72 |
14.13 |
12.25 |
0.557 |
0.062 |
Caecal content |
30.4 b |
38.4 a |
36.3 a |
2.03 |
0.020 |
Full colon |
21.8 |
24.2 |
25.4 |
1.39 |
0.184 |
Total digestive tract |
129.6 b |
154.9 a |
156.9 a |
3.74 |
0.001 |
Organ length cm by LW |
|||||
Small intestine |
1.14 b |
1.16 a |
1.36 a |
0.035 |
<0.001 |
Caeco |
16.6 b |
17.2 ab |
18.5 a |
0.49 |
0.030 |
Colon |
46.8 b |
45.0 b |
54.2 a |
1.82 |
0.004 |
1SEM: Stand error of mean; a, b, c: Means having a common letter did not differ significantly at level P>0.05.
decrease in water holding capacity in meat. However, this alteration was not observed in other studies (Dalle Zotte, 2002). Contradictory results may arise from differences in breeding conditions and breeds used by different authors, which may overlap with age.
Gut characteristics
The effects of the production system on gut traits at 84 days of age are summarized in Table 4. Rabbits housed in cages exhibited less development in various organs of the digestive tract compared to other housing conditions (P < 0.05), relative to their live weight. These findings align with results reported by other authors (Lambertini et al., 2001; Loponte et al., 2018). It is likely that animals with access to pasture or straw have higher fiber intake, leading to increased gut development. Additionally, the earlier development of digestive organs (as indicated by an allometry coefficient greater than 1) results in their relative proportion being smaller in animals of the same age but heavier. However, some other studies did not observe such differences (Maertens and van Oeckel, 2001; Dalle Zotte et al., 2009; Roy et al., 2017; Matics et al., 2019), possibly due to variations in genotypes, feed composition, or stocking density.
Housing conditions also had a significant effect (P < 0.05) on the proportion of volatile fatty acids (VFAs) in the cecum (Table 5), even though the total concentration and dry matter content were not different. In rabbits housed in cages, the concentration of acetic acid decreased while that of butyric acid increased. Rabbits housed in pens or outdoor systems have access to bedding or forage, which alters the composition of their diet, making it more fibrous. The fiber content of the diet impacts the VFA profile, leading to an increase in the proportion of acetic acid and a decrease in butyric and propionic acid levels (Gidenne et al., 2000).
Table 5: Caecal VFA concentration of rabbits housed in cages, closed pens or in open air systems at 84 days of age.
Housing system |
SEM1 |
P level |
|||
Cages |
Closed pen |
Open air |
|||
No. of rabbits |
10 |
10 |
10 |
||
Total (mmol/100ml) |
9.89 |
9.73 |
10.38 |
0.686 |
0.789 |
Acetic ( %) |
69.1 b |
73.2 a |
74.4a |
0.86 |
<0.001 |
Propionic (%) |
5.59 a |
5.13 ab |
4.44b |
0.304 |
0.040 |
Butyric (%) |
25.3 a |
21.7 b |
21.1b |
0.84 |
0.003 |
Propionic/Butyric |
0.22 |
0.24 |
0.21 |
0.016 |
0.617 |
Caecal VFA pool(mmol) |
6.98 |
8.05 |
7.90 |
0.312 |
0.305 |
Caecal dry mater (%) |
23.3 |
22.2 |
22.0 |
0.39 |
0.332 |
1SEM: Stand error of mean. a, b, c -Means having a common letter did not differ significantly at level P>0.05.
Conclusions and Recommendations
The carcasses of rabbits housed in cages displayed a higher fat content, whereas the hind legs exhibited a higher proportion of muscle and lower cooking loss. Furthermore, in older rabbits (84 days of age compared to 70 days), the hind legs contained more meat with reduced cooking loss, while maintaining similar Warner-Bratzler Shear Force (WBSF) and total pigment content. In future research, it will be valuable to work with a larger sample size to gain a more comprehensive understanding of the impact of the housing system on growth, carcass characteristics, and meat quality.
Acknowledgments
The authors integrated in the CECAV, recognize the support of the Foundation for Science and Technology (FCT) of Portugal, project number UIDB/CVT/00772/2020 and LA/P/0059/2020.
Novelty Statement
Provide information on the influence of the production system on meat quality.
Author’s contribution
All authors contributed equally.
Conflict of interest
The authors have decalred no conflict of interest.
REFERENCES
Blasco A, Ouhayoun J (1996). Harmonization of criteria and terminology in rabbit meat research. Revised proposal. World Rabbit Sci., 4: 93-99. https://doi.org/10.4995/wrs.1996.278
Buijs S, Keeling LJ, Tuytens FAM (2011). Behaviour and use of space in fattening rabbits as influenced by cage size and enrichment. Appl. Anim. Behav. Sci., 134: 229-238. https://doi.org/10.1016/j.applanim.2011.06.008
Chodová D, Tůmová E, Martinec M, Blízková Z, Skřivanová V, Volek Z, Zita L (2014). Effect of housing system and genotype on rabbit meat quality. Czech J. Anim. Sci., 59(4): 190-199. https://doi.org/10.17221/7343-CJAS
Combes S, Lebas F (2003). Les modes de logement du lapin en engraissement: Influence sur les qualités des carcasses et des viands. 10 èmes Journées de la Recherche Cunicole, pp. 186-200.
Combes S, Lebas F, Juin H, Lebreton L, Martin T, Jehl N, Cauquil L, Darche B, Corboeuf MA (2003). Comparaison lapin bio lapin standard: Analyse sensorielle, tendreté mécanique de la viande. In Proceedings 10èmes Journ. Rech. Cunicole Fr. 19–20 Novembre, Paris, France, pp. 137-141.
Costa-Silva V, Pinheiro V, Alves A, Silva J, Marques G, Lorenzo J, Rodrigues M, Ferreira L (2022). Effects of dietary incorporation of grape stalks untreated and fungi-treated in growing rabbits: A preliminary study. Animals, 12: 112. https://doi.org/10.3390/ani12010112
Dal Bosco A, Castellini C, Bernardini M (2000). Productive performance and carcass and meat characteristics of cage or pen-raised rabbits. World Rabbit Sci., 8: 579-583.
Dal Bosco A, Castellini C, Mugnai C (2001). Rearing rabbits on a wire net floor or straw litter: Behaviour, growth and meat qualitative traits. Livest. Prod. Sci., 75: 149-153. https://doi.org/10.1016/S0301-6226(01)00307-4
Dalle Zotte A (2002). Perception of rabbit meat quality and major factors influencing the rabbit carcass and meat quality. Livest. Prod. Sci., 75: 11-32. https://doi.org/10.1016/S0301-6226(01)00308-6
Dalle Zotte A, Princz Z, Metzger S, Szabó A, Radnai I, Biró-Németh É, Orova Z, Szendrö Z (2009). Response of fattening rabbits reared under different housing conditions. 2. Carcass and meat quality. Livest. Sci., 122: 39-47. https://doi.org/10.1016/j.livsci.2008.07.021
EFSA (European Food safety Authority). (2020). Health and welfare of rabbits farmed in different production systems. EFSA J., pp. 96.
Gidenne T, Pinheiro V, Falcão e Cunha L (2000). A comprehensive approach of the rabbit digestion: Consequences of a reduction in dietary fibre supply. Livest. Prod. Sci., 64: 225-237. https://doi.org/10.1016/S0301-6226(99)00141-4
Hernández P, Aliaga S, Pla M, Blasco A (2004). The effect of selection for growth rate and slaughter age on carcass composition and meat quality traits in rabbits 1. J. Anim. Sci., 82: 3138-3143. https://doi.org/10.2527/2004.82113138x
Jekkel G, Milisits G, Nagy I (2010). Effect of alternative rearing methods on the behavior and on the growth and slaughter traits of growing rabbits. Arch. Anim. Breed., 53: 205-215. https://doi.org/10.5194/aab-53-205-2010
Krunt O, Zita L, Kraus A (2020). A review of the effects of housing system on production and welfare in growing rabbits. Anim. Sci. Pap. Rep., 38(4): 321-332.
Krunt O, Zita L, Kraus A, Bures D, Needham T, Volek Z (2022). The effect of housing system on rabbit growth performance, carcass traits, and meat quality characteristics of different muscles. Meat Sci., 193: 108953. https://doi.org/10.1016/j.meatsci.2022.108953
Lambertini L, Vignola G, Zaghini G (2001). Alternative pen housing system for fattening rabbits: Effects of group density and litter. World Rabbit Sci., 9: 141-147. https://doi.org/10.4995/wrs.2001.457
Loponte R, Secci G, Mancini S, Bovera F, Panettieri V, Nizza A, Di Meo C, Piccolo G, Parisi G (2018). Effect of the housing system (free-range vs. open air cages) on growth performance, carcass and meat quality and antioxidant capacity of rabbits. Meat Sci., 145: 137-143. https://doi.org/10.1016/j.meatsci.2018.06.017
Lukefahr S, Hohenboken WD, Cheeke PR, Patton NM (1983). Appraisal of nine genetic groups of rabbits for carcass and lean yield traits. J. Anim. Sci., 57: 899-907. https://doi.org/10.2527/jas1983.574899x
Maertens L, De Groot (1984). Influence of the number of fryer rabbits per cage on their performance. J. Appl. Rabbit Res., 7: 151-155.
Maertens L, van Oeckel MJ (2001). Effect of housing rabbits in cages or in parks and its enrichment on performances and meat colour. In: Proccedings 9eme Journnés Recherche Cunicole, 200, November, Paris, France, pp. 31-34.
Matics Z, Cullere M, Dalle Zotte A, Szendrő K, Szendrő K, Odermatt M, Atkári T, Radnai I, Nagy I, Gerencsér Z (2019). Effect of cage and pen housing on the live performance, carcase, and meat quality traits of growing rabbits. Ital. J. Anim. Sci., 18(1): 441-449. https://doi.org/10.1080/1828051X.2018.1532329
Metzger S, Odermatt M, Szabo A, Radnai I, Biro-Nemeth E, Nagy I, Szendro Z (2011). Effect of age and body weight on carcass traits and meat composition of rabbits. Arch. Tierzucht, 54(4): 406-418. https://doi.org/10.5194/aab-54-406-2011
Metzger S, Kustos K, Szendrõ Z, Szabó A, Eiben C, Nagy I (2003). The effect of housing system on carcass traits and meat quality of rabbit. World Rabbit Sci., 11: 1-11. https://doi.org/10.4995/wrs.2003.492
Monin G, Ouali A (1991). Muscle differentiation and meat quality. In: Developments in meat science (ed. R. Lawrie). Elsevier Appl. Sci. Lon. N. Y., 5: 89-157.
Orova Z, Szendrő Z, Matic Z, Radnai I, Biró-Németh E (2004). Free choice of growing rabbits between deep litter and wire net floor in pens. In: Proccedings of the 8th World Rabbit Congress, 2000 September, Puebla, Mexico, pp. 1263–1265.
Ouhayoun J (1998). Influence of the diet on rabbit meat quality. In: (eds. De Blas C. and Wiseman, J.,), CAB International, Wallingford, UK. The nutrition of the rabbit. pp. 177-195.
Ouhayoun J, Dalle Zotte A (1996). Harmonization of muscle and meat criteria in rabbit meat research. World Rabbit Sci., 4: 211-218. https://doi.org/10.4995/wrs.1996.297
Pascual M, Pla M (2007). Changes in carcass composition and meat quality when selecting rabbits for growth rate. Meat Sci., 77: 474-481. https://doi.org/10.1016/j.meatsci.2007.04.009
Picard B, Lefaucheur L, Berri C, Duclos MJ (2002). Muscle fibre ontogenesis in farm animal species. Reprod. Nutr. Dev., 42: 415-431. https://doi.org/10.1051/rnd:2002035
Pinheiro V, Outor-Monteiro D, Silva S, Silva JA, Mourão JL (2011). Growth performance, carcass characteristics, and meat quality of growing rabbits housed in cages or open-air park. Arch. Anim. Breed., 54: 625-635. https://doi.org/10.5194/aab-54-625-2011
Pla M (2008). A comparison of the carcass traits and meat quality of conventionally and organically produced rabbits. Livest. Sci., 115: 1-12. https://doi.org/10.1016/j.livsci.2007.06.001
Pla M, Hernández P, Blasco A (1996). Carcass composition and meat characteristics of two rabbit breeds of different degrees of maturity. Meat Sci., 44: 85-92. https://doi.org/10.1016/S0309-1740(96)00079-4
Roy P, Fonteniaud J, Charrier JF, Lebas F (2017). Performances de croissance et d’abattage de lapins engraissés en cages ou en parcs avec une alimentation rationnée. Effect de la distribution de foin. 17èmes Journées de la Recherche Cunicole, Le Mans, pp. 47-50.
Volek Z, Chodová D, Tůmová E, Volková L, Kudrnová E, Marounek M (2012). Effect of stocking density on growth performance, meat quality and fibre properties of biceps femoris muscle of slow-growing rabbits. In: Proc. 10th world rabbit congress, editor Sharm El-Sheikh, Egypt, pp. 891-895.
Xiccato G, Trocino A, Filiou E, Majolini D, Tazzoli M, Zuffellato A (2013). Bicellular cage vs. collective pen housing for rabbits: Growth performance, carcass and meat quality. Livest. Sci., 155: 407-414. https://doi.org/10.1016/j.livsci.2013.05.013
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