ABSTRACT
This study aimed to evaluate the expression of calpastatin (CAST) isoforms and their potential associations with fiber type composition (%RA), calpastatin activity (CA) and myofibril fragmentation index (MFI) in three muscles with known differences in tenderness (infraspinatus, triceps brachii and semitendinosus) of Angus steers. Expression of total CAST (CAST-T) and CAST isoforms I, II, III (2-3) and III (2-4) (including or not exon 3) was evaluated by qRT-PCR. CAST expression and CA were significantly higher and MFI was lower in semitendinosus, the muscle with the highest %RA of IIX fibers. Differential expression of isoforms defined the variability in CAST-T among muscles. Semitendinosus had a higher expression of isoforms II and III (2-3), but lower expression of III (2-4) compared to the other two muscles. Relative expression of isoforms II and III that were defined by promoter preference linked to alternative splicing, seem to be the main factors explaining differences in CAST expression and ultimately in MFI among muscles.
Subject(s)
Calcium-Binding Proteins/metabolism , Muscle, Skeletal/metabolism , Myofibrils/metabolism , Red Meat/analysis , Animals , Calcium-Binding Proteins/chemistry , Calcium-Binding Proteins/genetics , Cattle , Gene Expression , Male , Protein Isoforms , Proteolysis , Real-Time Polymerase Chain Reaction/veterinaryABSTRACT
Brangus steers (n=247) finished on pasture were used to evaluate the effects of post-mortem ageing and polymorphism CAPN1 316 and CAPN1 4751 markers on meat tenderness and objective colour measurements (CIEL*a*b*) of m. Longissimus dorsi. Ageing meat for 7 days decreased shear force (SF) by 13.7% and improved a* (8.4%) and b* (10%) compared to ageing for 1 day. No difference between 7 and 14 days of ageing was found for SF, a* and b*. However, L* increased markedly with ageing. Fitting both markers simultaneously, CAPN1 316 showed association with SF and L* and CAPN1 4751 with a* and b*. Fitting the markers individually, CAPN1 4751 affected all traits and CAPN1 316 showed association with SF and L*. Post-mortem ageing and the use of markers represent two independent and alternative tools that could be used for improving quality of meat from Brangus cattle.
Subject(s)
Calpain/genetics , Cattle/genetics , Diet , Food Handling/methods , Meat/standards , Polymorphism, Genetic , Age Factors , Animal Feed , Animals , Color , Genetic Markers , Male , Meat/analysis , Muscle Proteins/genetics , Muscle, Skeletal , Poaceae , Postmortem Changes , Stress, Mechanical , Time FactorsABSTRACT
We describe the isolation and characterization of Shiga toxin (Stx)-producing Escherichia coli (STEC) O157:H7 from cooked and uncooked beef and chicken burgers and from chicken carcasses collected during sampling procedures in 2001 and 2002 in Buenos Aires City, Argentina. Of the 24 STEC O157:H7 strains isolated, 20 were recovered from 19 (6.8%) out of 279 samples of beef and chicken burgers, and 4 strains from 4 (10.3%) out of 39 chicken carcasses. The samples were analyzed following the USDA/FSIS 2002 method. The prevalent stx genotype was stx(2) and stx(2c) (12 strains, 50%). All strains were characterized as eae and ehxA-positive. By XbaI-PFGE, the strains yielded 10 different patterns. Eighteen out of 24 strains were grouped in four clusters: #1 (4 strains, AREXHX01.0043), #2 (4 strains, AREXHX01.0022), #3 (8 strains, AREXHX01.0139), and #4 (2 strains, AREXHX01.0200). Identical strains by phage typing, stx genotyping and PFGE were detected in uncooked and cooked beef and chicken burgers in different restaurants, which had been collected on the same or different sampling dates. These findings help to underline the importance of STEC O157 detection in meat products, to improve active surveillance, and to define control strategies in order to prevent new cases of STEC infection.
