Skip Navigation Links.
Animal welfare issues are becoming increasingly prominent in animal prodution, for both economic and moral reasons. This book presents a clear understanding of the relationship between the welfare of major food animal species and their physiology, and the Presented from the book:
Animal Welfare and Meat Production
(Impacts of Genetic Improvement)

Buy this book
   by Neville G Gregory
Published By:
CABI
Purchase the entire book at the book link above. Sale! Receive 10% off with the promotional code, TPC1126.
Add To Favorites!     Email this page to a friend!
 
<-- Previous Page
Page   of 2   
Next Page -->

 

The halothane gene and the RN gene are two major genes that have a direct effect on meat quality. Both arose as mutations. In the case of the halothane gene ( nn ), the effects are mediated through the rate of post-mortem muscle pH decline. The h 2 of pH 45 min is usually in the range 0.14 to 0.37. It is difficult to predict the likely responses in pH 45 min to genetic improvement in growth and carcass composition in populations with an unknown prevalence of the n / condition. In Large White pigs, which normally have a low prevalence of n/– , it is thought that selection for growth rate and fatness is more likely to raise pH 45 min , whilst selection against fatness will have little effect (Sonesson et al ., 1998). The halothane gene has a large effect on WHC, whereas the effect is smaller for the RN gene.

 

The h 2 of most other pigmeat quality traits is generally low (Verbeke et al ., 1999). The h 2 of pH ult is about 0.21 (0.07 to 0.39), and in NN and Nn pigs it is invariably low. Pigmeat quality is best improved by breed substitution, rather than by selection within breed. For example, insufficient marbling in lean pig genotypes has been controlled by using the Duroc breed in developing meat sire lines. This has been highly successful, and dry meat with insufficient succulence is not such a problem as it was in the past. If this were taken too far, such that very high levels of marbling were present in the ham, there could be negative effects on flavour and the odour of cooked ham slices, but these repercussions are not likely at present (Fernandez et al ., 2000). Breeds like the Belgian Landrace, which have heavily muscled hams and a high lean meat yield, do not necessarily have superior eating quality. They have poorer meat flavour, tenderness and juiciness in comparison with the Large White (Verbeke et al ., 1999).

 

Breast meat has been getting paler in recent years and the reason may be genetic. The h 2 of meat paleness in broilers is high (0.50). It has not reached the stage where it is a consumer complaint, but it is causing processors inconvenience when trying to match breast meat colour in retail display packs. Pale breast meat can indicate other problems such as excessive amounts of purge in the pack and this adds to the negative image. In broilers, genetic selection for growth rate and size of breast meat can lead to paler, less red breast meat and a large abdominal fat pad (Le Bihan-Duval et al ., 1999). Theoretically, this could be from one of three causes. They are:

 

an increase in the PSE condition

lower haem pigment content in the meat, associated with

either a lower capillary density and residual haemoglobin content

or a lower myoglobin content

 

The evidence indicating which of these is most important is conflicting. When pale broiler and turkey breast fillets were selected at a processing plant and compared with normal fillets, it was found that the paler meat had a lower pH ult and cooking yield and produced more drip (Owens et al ., 2000b). This implies circumstantially that paleness is commonly due to the PSE condition. In contrast, when broilers were genetically selected for growth rate and breast meat yield, their pectoralis major pH 15 min and pH ult were higher than normal whilst the meat was paler, less red and had a lower iron content (Berri et al ., 2005). This suggests that genetic selection has increased paleness through some other mechanism, and perhaps it is a lower haem pigmentation in the meat.

 

The situation in turkeys is different. Selection for high growth rate and breast yield is linked to DFD characteristics instead of paleness (Le Bihan- Duval et al ., 2003). Fast-growing turkey genotypes are prone to producing high pH 60 min leg meat. This is not due to pre-slaughter glycogen depletion from their greater weight-bearing (Fernandez et al ., 2001). In fact, faster-growing strains have greater glycogen storage capacity in their ilio tibialis muscles. Breast meat in these lines can be darker than normal, and it is prone to producing more drip during storage, but the difference in breast meat quality from traditional lines is small. A more striking feature in fast-growing turkey lines is the uniformity of their breast meat compared with traditional strains. For example, there was less variation between birds in the pH 20 min for the pectoralis major in a fast-growing line. The implication is that there could be greater uniformity in quality in the modern fast-growing type, and this could be an advantage in retail display packs. A low pH 20 min in turkey breast muscle is associated with a more acceptable paler and slightly redder colour when the meat is cured with nitrite (Fernandez et al ., 2002b), but it also produces more drip and has a lower processing yield. It is likely to be less preferred in terms of flavour and texture.

 

There is limited information on the genetic relationships between stress-related behaviours and meat quality. In broilers, there are strain differences in meat pH 15 min , which are probably due to differences in the severity of wing flapping when they are hung on the shackle line at processing plants (Debut et al ., 2003). Birds from the strain with faster growth rate flapped their wings less. A nervous temperament in subtropical cattle breeds (measured from their shorter flight time when released from a cattle crush) has been linked genetically to tougher meat (see Table 12.7). This could be due to a greater prevalence of intermediate pH meat.

 

Table 12.7. Some examples of genetic correlations between production performance and meat quality traits.

 

Other points worth noting are:

 

in cattle, culling for dystocia could lead to indirect benefits for meat tenderness (Splan et al ., 1998)

in Australian Merino sheep, genetic selection for wool fineness is leading to darker meat ( r g = 0.66; Fogarty et al ., 2003)

selection for fast growth in rabbits could be leading to harder, more chewy and poorer WHC meat (Ramírez et al ., 2004)

selection for growth rate and leanness in ducks has resulted in slightly darker and redder breast meat, but so far the effect on overall acceptability has been negligible

triploid Atlantic salmon produce larger fibres in their muscle. This imparts a softer texture to the meat, but it has a higher proportion of soluble collagen and is more prone to gaping (Bjørnevik et al ., 2004). In addition, the meat may be redder, with a low pH ult

<-- Previous Page
Page   of 2   
Next Page -->
er