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Use of blade tenderization to improve wooden breast meat texture2

G. Tasoniero,∗ B. Bowker,∗,1 A. Stelzleni,† H. Zhuang,∗ M. Rigdon,† and H. Thippareddi‡



USDA, Agricultural Research Service, U.S. National Poultry Research Center, Athens, GA 30605; † Department
of Animal & Dairy Science, University of Georgia, Athens, GA 30605; and ‡ Department of Poultry Science,
University of Georgia, Athens, GA 30605

ABSTRACT The effectiveness of blade tenderiza- by greater compression force (P < 0.0001) in both raw
tion (BT) in improving the texture of wooden breast and cooked fillets. Shear force of raw meat progressively
(WB) meat was evaluated through compression and increased from NORM to WB SEV (P < 0.0001) but
shear analyses. Butterfly fillets (n = 144) were col- there were no shear differences between NORM and
lected during 3 sampling replications and scored as nor- WB MOD after cooking. Blade tenderization decreased
mal (NORM), moderate (WB MOD), or severe wooden compression and shear values in both raw and cooked
breast (WB SEV). One side from each butterfly was WB fillets compared to untreated controls (P < 0.01).
blade tenderized and the other side served as an un- The significance of location effect for compression force
treated control. Fillets were subjected to both com- (P < 0.0001) suggested that WB texture was not uni-
pression and shear analyses in either the raw or cooked form within the same fillet. In raw fillets, an M × T in-
state. At 24 h postmortem, drip loss, pH, and color teraction (P < 0.0001) was found for both compression
traits were assessed on raw fillets. Muscle condition and shear values and indicated that blade-tenderized
(M), treatment (T), measurement location (L), and WB MOD and WB SEV still possessed harder texture
their interaction effects were investigated. WB fillets than NORM meat. However, the cooked shear values of
were heavier (P < 0.0001) and possessed greater pH WB SEV fillets subjected to BT were similar to those of
(P < 0.0001) than NORM fillets. L∗ a∗ b∗ values on the untreated NORM fillets. Therefore, BT improved, but
skin side were increased in WB fillets (P < 0.0001), as did not fully resolve the issues of abnormal tactile and
were drip and cook loss (P < 0.0001). Irrespective of texture characteristics in WB meat in either the raw or
degree of severity, WB meat was harder as evidenced cooked state.
Key words: poultry meat, wooden breast, blade tenderization, meat texture
2019 Poultry Science 98:4204–4211
http://dx.doi.org/10.3382/ps/pez163

INTRODUCTION has been drawn to an emerging defect of chicken pec-


toralis major muscle called “wooden breast” (WB),
During the last several decades, poultry meat which is characterized by remarkably hard consistency
production and consumption have increased rapidly at palpation (Sihvo et al., 2014). In affected fillets,
worldwide, and this trend forced poultry supply chains hardness is accompanied by an unappealing appear-
to improve growth rate, feed efficiency, and breast meat ance (Sihvo et al., 2014), as well as notably impaired
yield of broilers to fulfill the ever-increasing demand functionality and cooked meat texture (Mudalal et al.,
for chicken meat (Petracci et al., 2015; Kuttappan 2015; Sanchez-Brambila et al., 2018).
et al., 2016). Challenging birds to reach high body and The WB condition is of great relevance for the poul-
breast weights within a short rearing period permitted try sector due to the huge economic losses. Affected
the industry to achieve greater production. However, meat is often marketed as a downgraded product
rapidly growing broiler strains exhibit substantial or even diverted from human consumption thereby
breast myopathies that have a profoundly negative causing an estimated loss of $200 million per year (Kut-
impact on meat quality (Petracci and Cavani, 2012; tappan et al., 2016). To limit the economic losses, the
Kuttappan et al., 2016). Only recently, global attention poultry industry can include affected chicken meat into
value-added further processed products. An alternative

C 2019 Poultry Science Association Inc. option could be to enhance the eating quality of intact
Received October 1, 2018.
1
Corresponding author: brian.bowker@ars.usda.gov
WB fillets by improving their texture characteristics
2
The use of trade, firm, or corporation names in this publication is through tenderizing techniques. This could potentially
for the information and convenience of the reader. Such use does not help the industry by allowing WB fillets to be utilized
constitute an official endorsement or approval by the United States as intact whole-muscle products and reducing the
Department of Agriculture or the Agricultural Research Service of any
product or service to the exclusion of others that may be suitable.
necessity of downgrades. Blade tenderization (BT) is

4204
BLADE TENDERIZATION AND WOODEN BREAST 4205
a mechanical method that has been successfully used Table 1. Experimental groups and number of fillets per replica-
to tenderize tough red meat cuts. Blade tenderization tion.1
consists of piercing the meat with a set of blades or nee- Experimental groups
dles spaced at a given interval as the meat passes along RAW COOKED
a conveyor belt. This weakens the meat structure by Treatment CTRL2 (L)3 BT4 (R)5 CTRL (L) BT (R)
severing the myofibrillar protein network and the con-
nective tissue (Jeremiah et al., 1999; Bekhit et al., 2014; NORM 1 (n = 8) 4 (n = 8) 7 (n = 8) 10 (n = 8)
WB MOD 2 (n = 8) 5 (n = 8) 8 (n = 8) 11 (n = 8)
Obuz et al., 2014). It is unknown if BT would have a WB SEV 3 (n = 8) 6 (n = 8) 9 (n = 8) 12 (n = 8)
positive impact on the texture attributes of WB meat.
1
The purpose of this study was to evaluate whether The experiment was replicated 3 times using a total of 288 breast
fillets.
BT is an effective strategy to improve the meat texture 2
CTRL = control, not blade-tenderized.
3
characteristics of WB meat. Despite the obvious L = left fillets.
4
abnormal tactile properties of WB meat in the raw BT = blade-tenderized.
5
R = right fillets.
state, an understanding of how these traits mechanis-
tically influence cooked meat texture is still lacking
(Chatterjee et al., 2016). Thus, instrumental meat tex- of fillet for texture analysis (raw or cooked), and treat-
ture measurements in this study were assessed on both ment (control—CTRL or blade tenderized—BT) (Table
raw and cooked breast fillets using multiple methods. 1). Groups 1 (NORM), 2 (WB MOD), and 3 (WB SEV)
Both compression and shear analyses were utilized to consisted of left halves used as controls, whereas their
determine the effects of BT on the texture and tactile right counterparts (groups 4, 5, and 6, respectively)
traits of WB meat. The effect of measurement location were blade tenderized. Similarly, groups 7 (NORM),
was also considered, as WB lesions are not uniform 8 (WB MOD), and 9 (WB SEV) consisted of left
within the pectoralis major but are localized mainly halves used as controls, whereas their right counterparts
in the cranial portion of the muscle (Sihvo et al., 2014; (groups 10, 11, and 12, respectively) were blade tender-
Clark and Velleman, 2016; Dalle Zotte et al., 2017). ized. Texture analysis was performed on raw fillets for
groups 1 to 6 and after cooking for groups 7 to 12.
MATERIALS AND METHODS
Sample Treatments and Measurements
Sample Collection and Experimental
Groups At 24 h postmortem, all fillets were reweighed
to determine drip loss. Meat pH and color were
A total of 144 butterfly fillets were selected at 3 h measured on fillets belonging to groups 1, 2, and
postmortem from a commercial broiler slaughter plant 3. Meat pH was measured once with a Hach H160
during 3 different sampling sessions. Samples were portable pH meter (Loveland, CO), and a spear-tipped
transported to the U.S. National Poultry Research Cen- probe inserted into the fillet cranial end. Color values
ter (Athens, GA) packed in resealable bags on ice. But- (CIE 1976, L∗ a∗ b∗ ) were measured on the cranial,
terfly fillets were trimmed; left and right halves were medial, and caudal ends of both the skin and bone
separated, individually weighed, tagged, scored for WB, sides of the fillets with a Konica Minolta CM-700d
packed, and stored at 4◦ C until the next day. On each spectrophotometer (Konica Minolta, Ramsey, NJ;
of the 3 sampling days (replications), 48 butterfly fillets settings of illuminant D65, 10◦ observer, no specular
were sorted and scored according to their muscle con- component, and an 8 mm aperture). The L∗ a∗ b∗
dition into normal (NORM; n = 16 butterfly fillets), values reported for each side represent an average
moderate wooden breast (WB MOD; n = 16 butterfly of the 3 measurements. Fillets in treatment groups
fillets), and severe wooden breast (WB SEV; n = 16 4 to 6 and 10 to 12 were blade tenderized using 2
butterfly fillets). Selection criteria were based on the passes through an automatic Ross Tenderizer TC700M
palpation of pectoralis major muscle cranial and cau- (Ross Industries Inc., Midland, VA), with the first
dal ends. According to Sihvo et al. (2014) and Tijare et pass skin-side up and the second pass bone-side up.
al. (2016), breasts exhibiting a normal, soft consistency The tenderizer was equipped with a dual head (224
were classified as normal (NORM); those exhibiting a needles per head; 32 incisions per inch) and a 12-inch
hard consistency only on the cranial end were classi- wide stainless-steel conveyor belt having a speed of
fied as moderate (WB MOD); and fillets having a dif- 5.5 ft/min. Samples designated for cooked texture
fuse hard consistency throughout the entire muscle were analyses were weighed, vacuum packed, and cooked in a
considered severely impacted (WB SEV). Both the left Henny Penny MCS-6 Combi oven (Henny Penny Corp.,
and the right halves of the butterfly fillets were indepen- Eaton, OH) set at 83.9◦ C until a core temperature of
dently scored. Only butterfly fillets having both sides 76◦ C was reached (Zhuang and Savage, 2009). During
with matching WB scores were selected for the trial. cooking, core temperatures were monitored using a
Breasts were assigned to 12 experimental groups (n = copper/constantan thermocouple system (Thermalert
8 fillets/group/rep) created according to different mus- TH-8) with hypodermic needle microprobes (Type
cle conditions (NORM, WB MOD, or WB SEV), status MT-23/5, Physitemp Instruments, Inc., Clifton, NJ)
4206 TASONIERO ET AL.

inserted into the thickest portions of the fillets. Once Table 2. Pectoralis major weight, pHu , L∗ a∗ b∗ values, drip loss,
cooked, samples were placed in a refrigerated room and cook loss according to muscle condition (NORM, WB MOD,
and WB SEV).1
at 4◦ C and allowed to cool, reweighed to determine
cook loss, and kept refrigerated overnight prior to Muscle condition (M)
texture analysis. Compression tests were carried out Traits NORM WB MOD WB SEV SE P-value
on all raw and cooked samples using a TA-XTplus
Texture Analyzer equipped with Texture Exponent Weight, g 415B
495 A
513 A
19 < 0.0001
pHu 5.99B 6.14A,b 6.24A,a 0.03 < 0.0001
Version 4.0.13.0 software (Texture Technologies Corp., Skin side
Scarsdale, NY). Intact fillets were subjected to a single L∗ 63.2B 65.8A 65.6A 0.5 < 0.0001
30% compression strain exerted perpendicular to fiber a∗ –0.83B 0.05A,b 0.51A,a 0.23 < 0.0001
b∗ 8.16B 11.7A,b 12.9A,a 0.6 < 0.0001
orientation using a 50-kg loading cell connected to an Bone side
aluminium cylinder probe of 12-mm diameter (Zhuang L∗ 60.6 61.3 61.1 1.1 NS
and Bowker, 2018). Pre- and post-test speeds were set a∗ –0.89 –0.45 –0.41 0.30 NS
b∗ 10.8B 12.9A 13.1A 0.6 < 0.0001
at 3.00 mm/s, test speed was 1.00 mm/s, and trigger Drip loss, % 1.40B 1.66A 1.77A 0.24 < 0.0001
force was 20 g. Measurements were performed on the Cook Loss, % 24.8C 31.6B 33.3A 1.3 < 0.0001
skin-side surface of each breast at 3 different locations: A,B
Means within the same row followed by different uppercase super-
cranial (location 1), cranial/medial (location 2), and script letters differ P < 0.0001.
medial (location 3). Following compression analysis, a,b
Means within the same row followed by different lowercase super-
the same raw and cooked breast fillets were subjected script letters differ P < 0.05.
1
Fillet weight was included in the model as a covariate for the analysis
to shear force determination utilizing a modified of drip loss and cook loss.
multi-blade shear head (Supplementary Figure). The
multi-blade shear head (Jaccard Supertendermatic
48-Blade Meat Tenderizer, Jaccard Corp., Buffalo, NY) data, muscle condition, treatment, and their interac-
consisted of 3 rows of 16 blades each with pointed ends tion were analyzed as fixed effects, whereas replication
at 45◦ . Each blade was 2 mm wide with a 3-mm spacing represented a random effect. Means were separated
between blades, and blades were aligned in alternating using Bonferroni adjustments with significance set at
directions. The modified shear head ensured that the α = 0.05.
entire length of the fillet would be tested at one time
regardless of WB localization. The shear head was set RESULTS AND DISCUSSION
to come to rest 1 mm above the sample tray so that
the blades would penetrate the entire sample. Fillets Breast fillet weights, ultimate pH, and color traits
were placed on the sample tray in a cranial to caudal are reported in Table 2. WB fillets were heavier than
orientation, with the cranial end of the shear head NORM fillets (P < 0.0001) and exhibited ultimate pH
contacting the fillet 0.5 cm from the cranial crown values above 6.00 (P < 0.0001). Previous metabolomic
of the pectoralis major. The rest of the fillet was findings suggest that reduced muscle glycogen content
centered under the longitudinal axis of the shear head. and altered glucose metabolism may cause higher
The shear head was attached to a Universal Testing ultimate pH in WB meat (Abasht et al., 2016). The
Machine (Instron Dual Column Model 3365, Instron skin-side color values (L∗ a∗ b∗ ) of the breasts were
Corp., Norwood, MA) with a 500 N load cell and was altered by the occurrence of WB, with the change even
operated at 250 mm/min. The peak shear force (N) was detectable in moderate cases. Compared to NORM
recorded for analysis (Bluehill software, Instron Corp). meat, affected fillets were paler (L∗ ; P < 0.0001), more
yellow (b∗ ; P < 0.0001), and redder (a∗ ; P < 0.0001).
Increased L∗ and b∗ may be a consequence of fibrosis
Statistical Analysis and lipidosis occurring in WB meat (Dalle Zotte
et al., 2017). Greater light scattering due to increased
SAS (version 9.4, SAS Institute Inc., Cary, NC) sta- moisture content and redistribution of water molecules
tistical software package was used to perform analysis of toward the extra-myofibrillar compartment (Soglia
variance. A mixed model (PROC MIXED) with muscle et al., 2016a; Tasoniero et al., 2017) may also contribute
condition (NORM, WB MOD, or WB SEV) as a fixed to paleness in WB meat. As for a∗ index, Mutryn et
effect and experimental replication as a random effect al. (2015) reported myoglobin overexpression in WB
was used to determine the influence of muscle condition muscles. Only a minor effect was exerted by WB on
on weight, pH, color traits, and water-holding capacity bone-side color traits, as only b∗ values differed among
(WHC). Drip and cook loss data were analyzed using groups. This observation corroborates the hypothesis
fillet weight as a covariate. A mixed model was used that the myopathic insult primarily impacts the ante-
to analyze texture data. For compression data, muscle rior end of the pectoralis major (Clark and Velleman,
condition, treatment, measurement location (1, 2, 2016) on the skin-side surface and gradually decreases
or 3), and their interactions were evaluated as fixed moving toward the deep layer (Soglia et al., 2016b).
effects, whereas replication represented a random effect An overall reduction in WHC was observed in WB
and measuring depth was used as a covariate. For shear fillets (Table 2). This phenomenon is likely due to
BLADE TENDERIZATION AND WOODEN BREAST 4207
tissue myodegeneration and reparative responses (Si-

M×T×L
Table 3. Raw and cooked pectoralis major muscle compression force values (N) according to muscle condition (NORM, WB MOD, and WB SEV), treatment (control, CTRL
hvo et al., 2014) leading to a reduction in myofibrillar

NS
NS
proteins in lesioned breasts (Bowker and Zhuang,
2016; Soglia et al. 2016a,b). The worsened oxidative
status of WB meat proteins and lipids as well as
protein denaturation could also have contributed to

0.0110
T×L

NS
reduced WHC (Soglia et al. 2016a; Baldi et al., 2019).
Interestingly, WHC impairment in WB fillets appeared
to be independent from pH, as lesioned fillets possessed

0.0003
M×L
higher pH and reduced ability to bind water, as

NS
indicated by greater drip loss values (P < 0.0001). The
significance of the covariate (P = 0.0064) indicates that
drip loss was also strongly influenced by fillet weight.

P-value

< 0.0001
M×T
Cook loss increased with the occurrence and severity

NS
of the WB condition (P < 0.0001). These results are
consistent with previous literature on WB meat quality
traits (Mudalal et al., 2015; Chatterjee et al., 2016;

< 0.0001
< 0.0001
Soglia et al., 2016b; Tasoniero et al., 2016; Tijare et

L
al., 2016; Dalle Zotte et al., 2017; Sanchez-Brambila

and blade tenderized, BT), measurement location (1, 2, 3), and their interactions with compression depth as a covariate.
et al., 2017; Sun et al., 2018). In addition to the

< 0.0001
0.0017
empirical and instrumental hardness measurements,

T
these quality data helped confirm the adequacy of the
WB and NORM fillets used in this study.
Table 3 presents the meat texture data obtained

< 0.0001
< 0.0001
by applying a 30% compression to raw and cooked

M
samples. In raw fillets, meat compression values were
affected by muscle condition, treatment, measurement
location, and by the interaction between muscle

3.9
1.9
SE
condition and treatment (M × T). As for muscle

Means within the same row followed by different uppercase superscript letters differ P < 0.001.
condition, in accordance with published literature

36.8B
15.2
(Chatterjee et al., 2016; Sun et al., 2018), samples af-
fected by both moderate and severe degrees of WB were 3
Location (L)1

harder than unaffected fillets (P < 0.0001). The com-


A

45.0A
pression test objectively reflected the hard consistency 23.2
2

empirically detected at the processing plant. Raw WB


meat stiffness has been previously ascribed to the repar-
A

39.1B
24.4
1

ative fibrosis characterizing lesioned fillets. The WB


myopathy results in an abnormal deposition and re-
modeling of extracellular matrix components, primarily
B

39.1B
Treatment (T)
BT

16.7

of collagen and proteoglycans, in muscle interstitium,


epimysium, and perimysium (Sihvo et al., 2014; Mutryn
Locations: 1 = cranial; 2 = cranial/medial; 3 = medial.

et al., 2015; Abasht et al., 2016). Collagen is a fibrous


CTRL
A

41.5A
25.2

macromolecule conferring tensile strength (Velleman et


al., 1997), whereas proteoglycans play an essential role
in maintaining tissue structures and their mechanical
WB SEV
A

49.3A

function (Eggen et al., 1994; Velleman et al., 1997;


25.1

Serrano and Muñoz-Canoves, 2010). Interestingly,


Muscle condition (M)

Velleman and Clark (2015) reported that WB fibrosis


might vary in composition, severity, and structure,
WB MOD

thereby differently affecting meat toughness. Indeed,


A

41.3B
24.7

affected chicken belonging to different genotypes


may possess variable degrees of collagen cross-
linking due to the differential expression of decorin.
NORM

30.2C
B

Where overexpressed, this proteoglycan may lead


13.1

to more tightly packed fibrils and tougher meat.


Baldi and others (2019) observed that intramus-
cular collagen content was greater in the surface
Cooked
Traits

A,B
Raw

of WB fillets compared to NORM fillets but that


1

collagen cross-linking was not different. These ob-


4208 TASONIERO ET AL.

Figure 1. Effect of the interaction between muscle condition and Figure 2. Effect of the interaction between muscle condition and
treatment (M × T) on raw pectoralis major muscle compression force measurement location (M × L) on cooked pectoralis major muscle com-
values (N). pression force values (N). Locations: 1 = cranial; 2 = cranial/medial;
3 = medial.

servations suggest that connective tissue may be an


important contributor to the altered texture and tactile compression values for WB fillets decreased by half
traits of WB meat. Meat texture can also be related to between 0 and 72 h postmortem. Additionally, Soglia
muscle shortening during rigor and sarcomere length. et al. (2017) reported a progressive softening of the con-
However, previous studies found that WB fillets have nective tissue on the surface of WB fillets through 72 h
longer sarcomeres (Tijare et al., 2016) especially within postmortem. Thus, it is possible that the improvements
the cranial portion of the fillet (Xiao and Owens, 2016). in the tactile properties of WB fillets could have been
Therefore, the muscle stiffness, contracted appearance, further enhanced by combining BT with refrigerated
and increased compression values in WB meat do not storage.
seem to be related to sarcomere shortening. Cooked fillets required higher compression forces
Overall, BT decreased compression force in raw than raw fillets (Table 3) regardless of muscle condition,
breast fillets (P < 0.0001) (Table 3). The softening treatment, and location, similar to Chatterjee et al.
action of BT was likely due to the physical severing (2016). Indeed, whereas average raw fillet compression
of the myofibrillar and connective tissue networks, forces ranged between 13.1 and 25.1 N, cooked fillets
thereby weakening the meat structure (Jeremiah et al., ranged between 30.2 and 49.3 N. Texture evolution
1999; Pietrasik and Shand, 2004). As for compression during cooking is linked to myofibrillar and sarcoplas-
measurement location, the cranial and cranial/medial mic protein denaturation, shrinkage of myofibers and
areas (locations 1 and 2) were harder than the medial intramuscular collagen occurring at different temper-
area (location 3) (P < 0.0001). It is increasingly atures (Tornberg, 2005), cooking loss, and changes
evident that WB lesions are not uniform throughout in collagen solubility (Wattanachant et al., 2004;
the affected muscle. Macroscopically, Dalle Zotte et al. Kong et al., 2008). In cooked fillets, muscle condition,
(2017) noticed that characterizing lesions are mainly treatment, and location affected meat compression
distributed in the cranial end of the fillet. Microscop- values, together with the interactions between muscle
ically, it was discovered that not only pathological condition and location (M × L) and between treatment
fibrosis can be more abundant in the anterior end of the and location (T × L). The instrumental hardness dif-
breast, but also that collagen arrangement could vary ferences observed in raw WB fillets were still apparent
within impacted fillets (Clark and Velleman, 2016). The after cooking. The compression forces of cooked WB
magnitude of the BT effect on raw compression values SEV fillets were greater than NORM fillets, whereas
was dependent upon the WB status of the fillets as WB MOD samples were intermediate (P < 0.0001).
there was a significant muscle condition by treatment These findings suggest that WB meat may possess
(M × T) interaction effect (Figure 1). Blade tender- a greater amount of insoluble collagen stabilized by
ization significantly decreased raw compression force heat-resistant intermolecular bonds. Additionally, the
values in WB MOD and WB SEV fillets but had less im- higher cook loss observed in WB fillets may have led to
pact on NORM fillets. This is consistent with previous greater muscle shrinkage and packing density of fibers
studies on beef (Jeremiah et al., 1999; Schilling et al., (Wattanachant et al., 2004; Huff-Lonergan and Loner-
2003), in which BT was more effective at decreasing the gan, 2005). The beneficial effect of BT on compression
toughness of cuts containing high amounts of collagen. force was small but still distinguishable in cooked fillets
Despite the softening action exerted by BT on WB fil- (CTRL = 41.5 N vs. BT = 39.1 N; P = 0.0017). Dif-
lets (Figure 1), it is worth noting that blade-tenderized ferences in compression values between measurement
WB SEV fillets were still harder than NORM fillets locations within the same fillet were observed in the
(NORM BT = 11.9 N; WB SEV BT = 20.4 N; P < cooked state, with the cranial/medial location being
0.05). This finding could partially be explained con- the hardest (P < 0.0001). The interaction between
sidering that raw samples were analyzed at 24 h post- muscle condition and location showed that cooked meat
mortem. Sun et al. (2018) described the softening effect texture is not homogeneous throughout WB fillets
of refrigerated storage on breast meat by reporting that (Figure 2). The cranial/medial area (location 2)
BLADE TENDERIZATION AND WOODEN BREAST 4209

Figure 3. Effect of the interaction between treatment and mea-


surement location (T × L) on cooked pectoralis major muscle com- Figure 4. Effect of the interaction between muscle condition and
pression force values (N). Locations: 1 = cranial; 2 = cranial/medial; treatment (M × T) on raw pectoralis major muscle shear force values
3 = medial. (N).

350.0 a
exhibited the greatest compression force in both WB b
b b
MOD and WB SEV fillets (P = 0.0003) (Figure 2). 300.0 c c

Compared to NORM and WB MOD fillets, the WB 250.0

Shear force, N
SEV fillets exhibited the highest compression values for 200.0 CTRL
all 3 locations after cooking (P < 0.001). Interestingly, 150.0
BT
from the T × L interaction (Figure 3), it emerged
100.0
that the cranial/medial portion of the cooked fillets
(location 2) was the only location in which compression 50.0
290 254 281 255 312 2 80
force significantly decreased with BT. Nevertheless, 0.0
NORM WB MOD WB SEV
the cranial/medial portion of the cooked fillets had
the highest compression values, both in CTRL and BT Figure 5. Effect of muscle condition and treatment on cooked pec-
treatments (P < 0.0001). toralis major muscle shear force values (N).
Table 4 shows the texture assessment obtained by
shearing raw and cooked fillets with a multi-blade ness in beef (Jeremiah et al., 1999; Kolle et al., 2004;
shear head designed to imitate the “hardness to bite” Pietrasik and Shand, 2004; Pietrasik et al., 2010). Sim-
(Garcı́a-Segovia et al., 2014). The WB SEV fillets ex- ilar to the compression data, the M × T interaction
hibited the greatest shear force in both the raw (P < effect for shear values was significant in raw fillets but
0.0001) and cooked states (P = 0.0318). The results in- not cooked fillets. Blade tenderization decreased shear
dicate that both the shear and compression tests used force (P < 0.0001) in raw WB MOD and WB SEV fil-
in this study were able to discriminate between normal lets but not in NORM fillets (Figure 4). However, blade-
and severe WB meat in both raw and cooked fillets. tenderized WB fillets still possessed greater raw shear
However, the discriminating ability of the tests was not values than NORM fillets (NORM BT = 51.1 N; WB
consistent in terms of the degree of WB severity. With MOD BT = 75.1 N; WB SEV BT = 88.5 N; P < 0.05).
the shear test, WB MOD and WB SEV were different In cooked fillets, blade-tenderized WB SEV samples ex-
in both the raw and cooked fillets. However, the com- hibited greater shear force values than blade-tenderized
pression test only sorted the 2 WB degrees in cooked NORM samples (WB SEV BT = 280 N; NORM BT =
meat. As both compression and shear forces are ap- 254 N; P < 0.05) (Figure 5). However, the cooked shear
plied to the meat during shear testing (Garcı́a-Segovia values of WB SEV fillets subjected to BT were similar
et al., 2014), it might be that breasts experienced dif- to those of untreated NORM fillets (WB SEV BT =
ferent deformation ease and behavior under the 2 anal- 280 N; NORM CTRL = 290 N). The combined action
yses. Blade tenderization decreased shear force values of cooking and BT seemed to have minimized the tex-
in both raw (P < 0.0001) and cooked breast fillets (P < ture differences between the fillets. These data suggest
0.0001). These data are consistent with previous reports that BT has the potential to improve the cooked tex-
in which BT was found to decrease Warner-Bratzler ture of WB meat such that it has similar shear force
shear force values and improve cooked meat tender- values to normal breast meat.

Table 4. Raw and cooked pectoralis major muscle shear force values (N) according to muscle condition (NORM, WB MOD, and
WB SEV), treatment (control, CTRL and BT, blade tenderized), and their interaction.

Muscle condition (M) Treatment (T) P-value


Traits NORM WB MOD WB SEV CTRL BT SE M T M×T

Raw 53.2C 81.9B 97.9A 83.8A 71.6B 4.4 < 0.0001 < 0.0001 < 0.0001
Cooked 272b 268b 296a 294A 263B 10 0.0318 < 0.0001 NS
A,B
Means within the same row followed by different uppercase superscript letters differ P < 0.0001;
a,b
Means within the same row followed by different lowercase superscript letters differ P < 0.05.
4210 TASONIERO ET AL.

Overall, WB fillets exhibited impaired quality traits. Jeremiah, L. E., L. L. Gibson, and B. Cunningham. 1999. The in-
Both compression and shear force values were greater in fluence of mechanical tenderization on the palatability of certain
bovine muscles. Food Res. Int. 32:585–591.
WB fillets when measured in both the raw and cooked Kolle, B. K., D. R. McKenna, and J. W. Savell. 2004. Methods to
states. Blade tenderization significantly decreased com- increase tenderness of individual muscles from beef rounds when
pression and shear force in both raw and cooked fil- cooked with dry or moist heat. Meat Sci. 68:145–154.
lets. The 2 instrumental texture analyses utilized in this Kong, F., J. Tang, M. Lin, and B. Rasco. 2008. Thermal effects on
chicken and salmon muscles: tenderness, cook loss, area shrinkage,
study highlighted differences in the extent to which BT collagen solubility and microstructure. LWT - Food Sci. Technol.
can improve the tactile and texture characteristics of 41:1210–1222.
WB meat. Compression analyses revealed that although Kuttappan, V. A., B. M. Hargis, and C. M. Owens. 2016. White
BT significantly softened WB fillets in both the raw and striping and woody breast myopathies in the modern poultry in-
dustry: a review. Poult. Sci. 95:2724–2733.
cooked states, WB fillets were still harder than normal Mudalal, S., M. Lorenzi, F. Soglia, C. Cavani, and M. Petracci. 2015.
breast meat. On the other hand, shear force analyses Implications of white striping and wooden breast abnormalities
indicated that BT improved the cooked meat texture on quality traits of raw and marinated chicken meat. Animal
of WB meat to the point that shear force values were 9:728–734.
Mutryn, M. F., E. M. Brannick, W. Fu, W. R. Lee, and B. Abasht.
similar to normal non-treated breast meat. These data 2015. Characterization of a novel chicken muscle disorder through
suggest that although BT alone may not be able to differential gene expression and pathway analysis using RNA-
fully resolve the issues of abnormal tactile and texture sequencing. BMC Genomics 16:399.
Obuz, E., L. Akkaya, V. Gök, and M. E. Dikeman. 2014. Effects
characteristics in WB fillets, BT shows potential for im- of blade tenderization, aging method and aging time on meat
proving cooked meat texture in WB fillets and merits quality characteristics of Longissimus lumborum steaks from cull
further investigation. Holstein cows. Meat Sci. 96:1227–1232.
Petracci, M., and C. Cavani. 2012. Muscle growth and poultry meat
quality issues. Nutrients 4:1–12.
SUPPLEMENTARY DATA Petracci, M., S. Mudalal, F. Soglia, and C. Cavani. 2015. Meat qual-
ity in fast-growing broiler chickens. Worlds Poult. Sci. J. 71:363–
374.
Supplementary data are available at Poultry Science Pietrasik, Z., J. L. Aalhus, L. L. Gibson, and P. J. Shand. 2010.
online. Influence of blade tenderization, moisture enhancement and pan-
creatin enzyme treatment on the processing characteristics and
tenderness of beef semitendinosus muscle. Meat Sci. 84:512–517.
REFERENCES Pietrasik, Z., and P. J. Shand. 2004. Effect of blade tenderization and
tumbling time on the processing characteristics and tenderness of
Abasht, B., M. F. Mutryn, R. D. Michalek, and W. R. Lee. 2016. injected cooked roast beef. Meat Sci. 66:871–879.
Oxidative stress and metabolic perturbations in wooden breast Sanchez-Brambila, G., B. C. Bowker, D. Chatterjee, and H. Zhuang.
disorder in chickens. PLoS One 11:e0153750. 2018. Descriptive texture analyses of broiler breast fillets with
Baldi, G., F. Soglia, L. Laghi, S. Tappi, P. Rocculi, S. Ta- the wooden breast condition stored at 4◦ C and -20◦ C. Poult Sci.
vaniello, D. Prioriello, R. Mucci, G. Maiorano, and M. Pe- 97:1762–1767.
tracci. 2019. Comparison of quality traits among breast meat Sanchez-Brambila, G., D. Chatterjee, B. Bowker, and H. Zhuang.
affected by current muscle abnormalities. Food Res. Int. 2017. Descriptive texture analyses of cooked patties made of
115:369–376. chicken breast with the woody breast condition. Poult Sci.
Bekhit, A. E. A., A. Carne, M. Ha, and P. Franks. 2014. Physical 96:3489–3494.
interventions to manipulate texture and tenderness of fresh meat: Schilling, M. W., N. G. Marriott, H. Wang, and M. B. Solomon.
a review. Int. J. Food Prop. 17:433–453. 2003. Characteristics of USDA utility cow beef subjected to blade
Bowker, B. C., and H. Zhuang. 2016. Impact of white striping tenderization and hydrodynamic shock waves. J. Muscle Foods
on functionality attributes of broiler breast meat. Poult. Sci. 14:131–142.
95:1957–1965. Serrano, A. L., and P. Muñoz-Cánoves. 2010. Regulation and dys-
Chatterjee, D., H. Zhuang, B. C. Bowker, A. M. Rincon, and G. regulation of fibrosis in skeletal muscle. Exp. Cell Res. 316:3050–
Sanchez Brambila. 2016. Instrumental texture characteristics of 3058.
broiler pectoralis major with the wooden breast condition. Poult. Sihvo, H. K., K. Immonen, and E. Puolanne. 2014. Myodegeneration
Sci. 95:2449–2454. with fibrosis and regeneration in the pectoralis major muscle of
CIE, Commission Internationale d’Eclairage (1976). Supplement n.2 broilers. Vet. Pathol. 51:619–623.
to CIE publication no. 15 Colorimetry (E-1.3.1) 1971. Soglia, F., G. Jingxian, M. Mazzoni, E. Puolanne, C. Cavani, M.
Clark, D. L., and S. G. Velleman. 2016. Spatial influence on breast Petracci, and P. Ertbjerg. 2017. Superficial and deep changes of
muscle morphological structure, myofiber size, and gene expres- histology, texture and particle size distribution in broiler wooden
sion associated with the wooden breast myopathy in broilers. breast muscle during refrigerated storage. Poult. Sci. 96:3465–
Poult. Sci. 95:2930–2945. 3472.
Dalle Zotte, A., G. Tasoniero, E. Puolanne, H. Remignon, M. Cecchi- Soglia, F., L. Laghi, L. Canonico, C. Cavani, and M. Petracci.
nato, E. Catelli, and M. Cullere. 2017. Effect of “Wooden Breast” 2016a. Functional property issues in broiler breast meat related
appearance on poultry meat quality, histological traits, and le- to emerging muscle abnormalities. Food Res. Int. 89:1071–1076.
sions characterization. Czech J. Anim. Sci. 62:51–57. Soglia, F., S. Mudalal, E. Babini, M. D. Nunzio, M. Mazzoni, F.
Eggen, K. H., A. Malmstrom, and S. O. Kolset. 1994. Decorin and Sirri, C. Cavani, and M. Petracci. 2016b. Histology, composition,
a large dermatan sulfate proteoglycan in bovine striated muscle. and quality traits of chicken pectoralis major muscle affected by
Biochem. Biophys. Acta. 1204:287–297. wooden breast abnormality. Poult. Sci. 95:651–659.
Garcı́a-Segovia, P., M. J. P. Moreno, and J. Martı́nez-Monzó. 2014. Sun, X., D. A. Koltes, C. N. Coon, K. Chen, and C. M. Owens.
Texture in meat and fish products. Pages 76–109 in Methods in 2018. Instrumental compression force and meat attribute changes
Food Analysis. Taylor Francis, CRC Press, LLC, Boca Raton, in woody broiler breast fillets during short-term storage. Poult.
FL. Sci. 97:2600–2606.
Huff-Lonergan, E., and S. M. Lonergan. 2005. Mechanisms of water- Tasoniero, G., H. C. Bertram, J. F. Young, A. Dalle Zotte, and
holding capacity of meat: the role of postmortem biochemical and E. Puolanne. 2017. Relationship between hardness and my-
structural changes. Meat Sci. 71:194–204. owater properties in wooden breast affected chicken meat: a
BLADE TENDERIZATION AND WOODEN BREAST 4211
nuclear magnetic resonance study. LWT-Food Sci. Technol. 86: collagen organization, mitochondrial activity, and protein
20–24. metabolism, in the avian low score normal muscle weakness. Dev.
Tasoniero, G., M. Cullere, M. Cecchinato, E. Puolanne, and A. Dalle Growth Differ. 39:563–570.
Zotte. 2016. Technological quality, mineral profile and sensory Wattanachant, S, S Benjakul, and D. A. Ledward. 2004. Effect of
attributes of broiler chicken breasts affected by white striping heat treatment on changes in texture, structure and properties of
and wooden breast myopathies. Poult. Sci. 95:2707–2714. Thai indigenous chicken muscle. Poult. Sci. 83:123–128.
Tijare, V. V., F. L. Yang, V. A. Kuttapan, C. Z. Alvarado, C. N. Xiao, S., and C. M. Owens. 2016. The relationship between in-
Coon, and C. M. Owens. 2016. Meat quality of broiler breast strumental compression forces and meat quality traits of woody
fillets with white striping and woody breast muscle myopathies. breast fillets during short-term storage. Poult. Sci. 64 (E. Suppl.
Poult. Sci. 95:2167–2173. 1) (Abstr. P214).
Tornberg, E. 2005. Effects of heat on meat proteins—implications Zhuang, H., and B. C. Bowker. 2018. The wooden breast condition
on structure and quality of meat products. Meat Sci. 70:493–508. results in surface discoloration of cooked broiler pectoralis major.
Velleman, S. G., and D. L. Clark. 2015. Histopathological and myo- Poult. Sci. 97:4458–4461.
genic gene expression changes associated with wooden breast in Zhuang, H., and E. M. Savage. 2009. Variation and Pear-
broiler breast muscles. Avian Dis. 59:410–418. son correlation coefficients of Warner-Bratzler shear force
Velleman, S. G., D. C. McFarland, Z. Li, N. H. Ferrin, R. Whit- measurements within broiler breast fillets. Poult. Sci.
moyer, and J. E. Dennis. 1997. Alterations in sarcomere structure, 88:214–220.

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