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PROCESSING, PRODUCTS, AND FOOD SAFETY |


* Department of Animal Science, Faculty of Agriculture, Chiang Mai University, Chiang Mai, Thailand 50200;
ETH Zurich, Institute of Animal Science, Universitaetstrasse 2, 8092 Zurich, Switzerland; and
Institute of Animal Breeding and Husbandry, Georg-August University of Göttingen, Albrecht-Thaer-Weg 3, 37075 Göttingen, Germany
2 Corresponding author: agisjtrs{at}chiangmai.ac.th
| ABSTRACT |
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Key Words: indigenous chicken muscle carcass meat fatty acid
| INTRODUCTION |
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A group of Thai consumers have acquired a preference for the taste of meat from native chicken, still having a small market but with a rapidly growing popularity (Wattanachant et al., 2005). Chicken strains indigenous to Thailand also have traits important for cock fighting (Ausungnern, 1999). This behavioral trait is suspected to result, for instance via a high collagen content, in the development of tough meat when compared with the very tender meat of broilers. Some Thai consumers even prefer meat that is not too tender (chewy) and low in fat at the same time (Jaturasitha et al., 2002). Black-boned chickens and Thai native chickens are such indigenous strains of Thailand, where they are currently reared in the rural and mountainous areas. The dark bones in the Black-boned chickens are another special property searched for by certain consumers, and also the meat is known to be darker (Siriwan et al., 2004). Both indigenous strains are suitable for extensive low-cost scavenging-type production systems. Previous investigations on these strains have aimed at obtaining fundamental data to improve growth performance and carcass traits (Siriwan et al., 2004). However, other imported breeds suitable for extensive fattening have been introduced to Thailand. Bresse chickens, originating from the south of Burgundy County (France), have been imported to Thailand because of their described intensively red meat. Rhode Island Red is a layer breed but is occasionally fattened in Thailand to complement indigenous chickens in times of high demand for meat of indigenous origin such as New Years celebrations (DLD, 2002).
The objective of the present study was to compare carcass and meat quality traits as well as muscle fiber characteristics in Blacked-boned and Thai chickens as opposed to Bresse and Rhode Island Red chickens to confirm or disprove the hypothesis that the indigenous strains have developed unique features. The results could give indications as to which genotypes should be used for which situation, eventually resulting in an upscaling of the production of meat from such extensive fattening systems based on either native or imported genotypes. Because breast and thigh meat are the major valuable cuts, both meat types were followed in the present study.
| MATERIALS AND METHODS |
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Analyses
After chilling for 24 h, all carcasses were dressed by both the international (Henrickson, 1978) and Thai (boneless) cutting style (Jaturasitha, 2004). In all carcasses, pH (model 191, Knick, Berlin, Germany) and electrical conductivity (model LF 196, WTW, Weilheim, Germany) were measured at 45 min and 24 h postmortem (p.m.) in the breast muscle at a 2-cm depth. Skin and meat (breast and thigh) color were evaluated at 48 h p.m. with the Chroma Meter (model CR-300, Minolta Camera Co. Ltd., Osaka, Japan) to record lightness, redness, and yellowness (L*, a*, and b*, respectively). From 40 birds per genotype, randomly selected out of the 60 slaughtered animals each, breast (pectoralis major) and thigh muscles (biceps femoris) were harvested during dressing and refrigerated at –20°C until being analyzed.
In the 2 muscles, water-holding capacity was determined as drip loss (according to Honikel, 1987; using half of the slaughtered birds), thawing, and cooking losses (either boiled in a water bath in sealed bags or grilled in a convection oven until an internal temperature of 80°C was reached).
Samples of breast and thigh muscle were taken from a quarter of the samples from the center of the ventral side of these muscles for histological analyses. Serial cross-sections (10-µm thick) were cut and stained for combined ATPase-nicotinamide A dinucleotide diaphorase treatment (modified after Horak, 1983). The density of the histochemical reaction product in the ATPase-nicotinamide A dinucleotide diaphorase staining was determined for each fiber. By using 3 density classes for ATPase, different fiber types could be identified using an image analyzer (LUCIA E600, Nikon, Tokyo, Japan). Muscle fibers are commonly classified into 3 groups according to their biochemical and functional properties (Brooke and Kaiser, 1970; Peter et al., 1972): type I, slow-twitch oxidative (red); type IIA, fast-twitch oxidative-glycolytic (intermediate); and type IIB, fast-twitch glycolytic (white). Because the number of type I fibers is typically very small in poultry muscles (von Lengerken et al., 2002), we decided to combine type I and IIA fibers. The proportion of each fiber type in muscle was determined, and the cross-sectional area (µm2) of individual myofibers was measured by a microscope at a magnification of 1:10 (Klont et al., 1998). At that occasion, photographs were taken.
Homogenized, uncooked breast and thigh muscles were analyzed for contents of moisture, protein, and fat as outlined by AOAC (1995). Triglyceride and cholesterol concentrations were determined in both muscles after extraction of the fat from the tissue according to Folch et al. (1957). In this extract, triglyceride contents were measured as outlined by Biggs et al. (1975). The extract was further saponified as described by Abell et al. (1951) to eliminate triglycerides. In the remainder, total cholesterol was determined according to Jung et al. (1975). Collagen determinations were performed by a 3-step procedure allowing the separation of soluble and insoluble collagen as described by Hill (1966). Separation was performed by centrifugation (Polytron PT 1200B, Kinematic AG, Littau, Switzerland) for 1 min at 3,540 x g. This was followed by hydrolysis and ultraviolet detection in the 2 fractions of hydroxyproline at a 558-nm wavelength with a spectrophotometer (Gynesys, Spectronic Instruments Inc., New York, NY) as suggested by Bergman and Loxley (1963).
Shear values of the boiled breast and thigh muscles were determined in six 1.27-cm diameter cores cut perpendicular to the muscle fibers using a Warner-Bratzler shear device attached to a universal testing machine (model 5565, Instron Ltd., Buckinghamshire, UK). A crosshead speed of 200 mm/min and a 5-kN load cell calibrated to read over range of 0 to 100°N were applied.
The fatty acid profile of breast and thigh muscle lipids was analyzed in the lipids extracted by chloroform and methanol (2:1 vol/vol; Folch et al., 1957). Fatty acid methyl esters were prepared by the method of Morrison and Smith (1964) and quantified by a gas chromatograph (model GC-2010, Shimadzu, Tokyo, Japan) equipped with a 0.25 mm x 30 m x 0.25 µm wall-coated fused wax capillary column. The temperature of the oven was programmed with an initial temperature of 160°C, held for 2 min, and a final temperature of 230°C, held for 5 min. The temperature was increased at a rate of 5°C/ min. Injector and detector temperatures were 230 and 280°C, respectively. Helium was used as a carrier gas, and flow rate was 1 mL/min when measured at the outlet terminal. Split ratio of injector was approximately 1:50. Eluting peaks were identified by comparison with retention time of known mixed standards (Supelco 37, Bellefonte, PA).
Statistical Analyses
Data were subjected to ANOVA by the GLM procedure considering genotype as effect and animal within genotype (replicate) as random effect using SAS (2001; version 8.2 for Windows). Comparisons among treatment means were carried out by Tukeys method. The tables give the least square mean values for the genotypes, the corresponding SEM, and the probabilities of error (P-value).
| RESULTS AND DISCUSSION |
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The indicators of water-holding capacity of breast and thigh meat mostly were not significantly different among genotypes. Joseph et al. (1997) reported that fat loss from high temperature (85°C) caused increasing fluid loss in meat, but the internal temperatures of the samples investigated in the current study did not exceed 80°C. One exception for genotype differences in water-holding capacity was that the thigh meat of Black-boned chickens had higher (P < 0.05) grilling losses than that of Bresse chickens, with the other genotypes ranging in between. This may have been the result of the small size of the muscles of the Black-boned chickens (grilling loss was numerically highest also in breast muscle), making it easier to lose water compared with larger pieces of meat (Jaturasitha et al., 2004a).
Histological Properties
There was no significant difference in the proportions of fiber types in breast muscle among genotypes, with the white fibers accounting for 93 to 96% of the total (Table 3
). The dominance of this fiber type is also obvious from Figure 1
. Von Lengerken et al. (2002) even found 99.5 and 99.8% of white fibers in the pectoralis muscle of broilers and turkeys, respectively. In the thigh muscle, the indigenous strains, especially when compared with Rhode chickens, had more (P < 0.05) red and intermediate fibers at the cost of white fibers (with the latter being much lower in percentage compared with the breast muscle in all groups; Figure 1
). In the imported breeds, this probably reflects breeding for higher muscle accretion, which is often associated with a shift from oxidative to glycolytic muscle metabolism (Jurie et al., 1995) and, at very high selection intensity (which is probably not yet the case for Bresse and Rhode), a higher frequency of meat-quality problems. The cross-sectional areas of the breast muscle fibers, independent of their type, were smallest in Thai chickens, intermediate in Black-boned chickens, and highest in the imported breeds (P < 0.05). In thigh muscle, no such difference was found between the indigenous strains, but the difference to the imported breeds persisted. These results are in a certain contrast to Wattanachant et al. (2005), who found a larger fiber diameter in breast and thigh muscles in Thai indigenous chicken than in that of broilers.
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Fatty Acid Composition
Various fatty acids were different in proportion among genotypes, but not all differences were similar in both muscles (Table 5
). Nevertheless, some differences were characteristic for certain genotypes. Meat of Black- boned chickens had relatively low contents of saturated fatty acids and, in breast muscle, high contents of poly- unsaturated fatty acids compared with the other genotypes (P < 0.05 relative to several other genotypes, each). In previous studies (Qiao et al., 2002; Jaturasitha et al., 2004b; Wattanachant et al., 2004), lipids from indigenous chickens other than Black-boned chicken were found to be similarly different from that of layer breeds. Thai chicken meat was characterized by relatively low C18:1trans fatty acids and high proportions of individual and total n-3 fatty acids and had a favorable n-6/n-3 fatty acid ratio (P < 0.05 in thigh meat). Differences in fatty acid profile were mostly less pronounced between the 2 imported breeds.
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| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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Received for publication November 19, 2006. Accepted for publication October 3, 2007.
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