ABSTRACT
The abundance and affordability of cassava root, a carbohydrate‐dense tuber, in tropical regions have drawn attention to it as a possible substitute of conventional energy source in poultry ration. This study investigated the impact of substituting maize meal with varying amounts of cassava root meal on the growth performance, carcass characteristics, hemato‐biochemical parameters, meat composition and sensory properties of broiler chickens. In this study, 400 broiler chicks (Arbor Acres) were assigned to four treatment groups: T1 (0%, diet without cassava root meal; CRM) and T2, T3 and T4 containing 10%, 20%, and 30% cassava root meal, respectively. Each group had five replicates consisting of 20 birds each, and trial ran for 35 days. The results indicated that broilers in the T2 group had significantly higher body weight, feed intake and feed efficiency ratio, with a lower feed conversion ratio (FCR). T2 also showed exceptional carcass characteristics without adversely affecting meat quality and blood parameters of broilers. The proximate composition of breast and thigh muscles showed significant changes (p < 0.05). In breast muscle, crude protein (CP), ash, and metabolizable energy (ME) increased with higher cassava root meal (CRM) inclusion, peaking in T4. In thigh muscle, crude protein (CP) significantly improved in all CRM‐based diets compared to the control (15.30%), reaching a maximum in T3 (20.28%). The diet having 10% cassava root meal (CRM) had the highest amount of total phenolic content, total flavonoid content and DPPH scavenging activity along with the best overall acceptability. The results indicate that cassava root meal can be used as a substitute for maize grains in broiler diets, without any adverse effects on the broiler's growth performance and general health status. It is suggested that maize can be replaced by 10% cassava root meal (CRM) for promoting the growth, meat quality and healthy blood profile of broilers.
Keywords: antioxidant properties, broiler, cassava root meal, feed cost, meat quality, poultry nutrition
Partial replacement of maize with cassava root meal (CRM) improved growth performance, carcass traits, antioxidant activity, meat quality, and sensory acceptability in broiler chickens. Among all treatments, 10% CRM supplementation showed optimal feed efficiency, water‐holding capacity, and antioxidant status without adverse health effects, indicating that moderate CRM inclusion is a sustainable and cost‐effective alternative energy source in poultry diets.

1. Introduction
Poultry production is one of the fastest‐growing sectors in the livestock industry worldwide, driven by the increasing demand for high‐quality protein sources such as chicken meat (Choi et al. 2023; Raquib et al. 2022). However, the high and variable cost of conventional feedstuffs (especially maize) present major constraints to sustainable broiler production (Siddik et al. 2026). As the main source of energy in poultry feed, maize represents a large proportion of feed costs and must also contend with human consumption and industrial use (Erenstein et al. 2022). Now‐a‐days it is an alarming issue for the inadequate supply of maize as main energy source feed ingredient for livestock feeding (Ahiwe et al. 2018).
The increasing growth of the animal food production sector and the continuous increase of the global population have caused growing concerns about the challenge for food supplies between humans and animals. This issue holds significant impact, particularly in developing countries like Bangladesh. Therefore, it is vital to evaluate feed alternatives to energy that have the ability to substitute grain (Ahmed et al. 2026). Cassava ( Manihot esculenta ) has superior land productivity, with yields ranging from 25 to 60 metric tons per hectare, surpassing those of maize (Erenstein et al. 2022). Furthermore, cassava meal has resulted in reduced manufacturing expenses and has a greater starch content that spans a wider range from 70% to 80% (Chang'a et al. 2020). A study recommended the potentials of using cassava root as a viable substitute for maize in chicken feed (Chang'a et al. 2020). Crude protein and carbohydrates are the main constituents of the cassava root (Abdul Kuddus et al. 2020; Alam et al. 2024; Stupak et al. 2006). Cassava root is rich in carbohydrates, ash, crude protein, and minerals (Ahmed et al. 2024). Moreover, it exhibited 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) free radical activity (Yi et al. 2011). Because of its elevated starch content, cassava root meal has the capacity to function as a viable substitute for maize and other cereal grains. The application of suitable processing techniques, such as boiling, sun‐drying, marinating, and fermenting, can lower the amounts of cyanogenic glycosides in cassava (Omede et al. 2017).
Numerous research studies of the effects of using pre‐treated or cassava instead of maize meal as an energy source in chicken feed (Alade et al. 2020; Chukwukaelo et al. 2018; Okrathok et al. 2023). They have also looked at how to increase the availability of glucose and improve the efficiency of its absorption (Alade et al. 2020; Chukwukaelo et al. 2018; Okrathok et al. 2023). Previous study has displayed that including cassava root concentrate into broiler meals might yield positive outcomes when the nutrients are appropriately harmonized (Diarra et al. 2015), including potential improvements in the systemic antioxidant status of the broilers due to the presence of bioactive phenolic compounds.
However, there is a lack of comprehensive data regarding the physiological safety of high‐level CRM inclusion and its direct effect on meat oxidative stability. The impact of alternating fed maize to cassava root on growth performance, carcass features, and meat quality of broiler chickens, however, was not extensively investigated. We hypothesize that the partial replacement of maize with CRM will support optimal growth while enhancing the nutritional profile and antioxidant capacity of the meat without compromising the hemato‐biochemical health of the broilers. The purpose of this study was to investigate the effects of replacing maize with cassava root on broiler chicken diets on growth performance, carcass features, hemato‐biochemical profile, breast and thigh meat composition, and sensory attributes. Additionally, this study aimed to quantify the antioxidant potential of CRM‐fed broiler meat using DPPH assays to determine its value as a functional feed ingredient.
2. Materials and Methods
2.1. Ethics Statement
The Ethical Review Committee of the Jashore University of Science and Technology, Jashore, Bangladesh, provided permission for the animal‐based research methods used in this study (ERC/FBST/JUST/2023‐152).
2.2. Preparation of the Cassava Root Meal
Freshly harvested cassava roots from Boda upazilla, Panchagarh District, Bangladesh were cleaned, peeled, and chopped (7–8 cm) into smaller segments (Ahmed et al. 2026). Peeling significantly reduced cyanide content, particularly in sweet cassava varieties where hydrogen cyanide (HCN) is primarily concentrated in the peel. Chopped segments were sun‐dried on protected concrete surfaces for 7 days, reducing soluble cyanide compounds. Sun drying on slanted trays preserved linamarase enzyme activity, facilitating cyanogenic glycoside neutralization (Hassan et al. 2012). To ensure the safety of the ingredient, the processing was conducted until the residual HCN reached safe levels for broiler consumption. Dried cassava chips were ground into a fine powder and stored in polythene bags (Aerni 2006). According to Ahmed et al. (2024) the nutrient values of cassava root meal were as follows: ash 2.96%, crude protein 2.55%, crude fat 0.98%, crude fiber 3.44%, nitrogen free extract (NFE) 82.55% and metabolizable energy (ME) 3061.8 kcal kg−1.
2.3. Experimental Design, Rations, Treatments and Management of Broiler
In the feeding study, 400‐day‐old commercial broiler chicks (Arbor Acres, AA marketed by Nourish Poultry Hatchery Limited, Dhaka, Bangladesh) of either sex were weighed and randomly allocated to four dietary treatments (T1–T4) in a Completely Randomized Design (CRD). Each treatment consisted of five replicates with 20 birds per replicate (100 birds per treatment). The treatments included a control diet (T1) and diets containing 10% (T2), 20% (T3), and 30% (T4) cassava root meal (CRM) as a partial replacement for maize. The stated inclusion levels of 10%, 20%, and 30% refer specifically to the proportion of maize replaced by cassava root meal (CRM), rather than total dietary inclusion. All experimental diets were formulated on an isocaloric and isonitrogenous basis, where CRM was used as a partial substitute for maize at the respective replacement levels. Growth performance was evaluated weekly, while carcass, hematological, biochemical, meat quality, antioxidant, and sensory analyses were performed at Day 35 using randomly selected birds from each replicate. NRC (1994) standards were followed for creating the broiler ration, which consisted of a starter mash feed for the first 21 days and a grower mash feed for the next 22–35 days. The nutrient contents and trial feed ingredients utilized in this trial are all listed in Table 1. The formulation was performed using (Microsoft Excel Solver) software to ensure a balanced least‐cost ration. The study was conducted in an open‐system chicken house‐oriented east‐to‐west to minimize direct solar radiation. Temperature and relative humidity (RH) were regulated through natural ventilation and manual curtain management, maintaining a brooding temperature of 33°C–35°C in the first week, which was gradually reduced to 24°C by the end of the trial. An appropriate lighting system providing a 23 L: 1 D (23 h light, 1 h dark) photoperiod was implemented to support broiler growth. The broiler chickens were housed in pens on a deep litter floor using rice husks rather than cage systems or individual housing. All birds had ad libitum access to clean drinking water and experimental diets throughout the study period. In accordance with the manufacturer's guidelines (Ceva‐phylaxia Veterinary Biologicals Co. Ltd., Hungary) and recommendations by (Akter et al. 2023), the chicks were immunized against Infectious Bronchitis (IB) using CEVAC BIL, against Infectious Bursal Disease (IBD) using CEVAC IBDL, and Newcastle Disease (ND) using CEVAC NEW L on days (Day, 3, 12, and 21) respectively. Each of the management techniques has been carried out for rearing AA broiler.
TABLE 1.
Proportion of ingredients used in formulating the experimental diets (as fresh basis).
| Treatments: starter (d 0–21); grower (d 21–35) | ||||||||
|---|---|---|---|---|---|---|---|---|
| Item (%) | T1 | T2 | T3 | T4 | ||||
| Starter | Grower | Starter | Grower | Starter | Grower | Starter | Grower | |
| Corn | 57.00 | 60.00 | 51.30 | 54.00 | 45.60 | 48.00 | 39.90 | 42.00 |
| Cassava root | — | — | 5.70 | 6.00 | 11.40 | 12.00 | 17.10 | 18.00 |
| Rice polish | 5.00 | 4.00 | 5.00 | 4.00 | 5.00 | 4.00 | 5.00 | 4.00 |
| Choline chloride | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 |
| Soybean meal | 26.00 | 24.00 | 26.00 | 24.00 | 26.00 | 24.00 | 26.00 | 24.00 |
| Probiozyme | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 |
| Esel dry | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 |
| Fishlog | 6.00 | 6.00 | 6.00 | 6.00 | 6.00 | 6.00 | 6.00 | 6.00 |
| Turbotox | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 |
| Salt | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 |
| NaHCO3 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 |
| Methionine | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 |
| Lysine | 0.15 | 0.15 | 0.15 | 0.15 | 0.15 | 0.15 | 0.15 | 0.15 |
| Vitamin premix | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 |
| Sqzyme SME | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 |
| Soybean oil | 2.25 | 2.00 | 2.25 | 2.00 | 2.25 | 2.00 | 2.25 | 2.00 |
| Hamecosaldry | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 |
| Hamecomoltox | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 | 0.20 |
| Lime stone | 1.00 | 1.00 | 1.00 | 1.00 | 1.00 | 1.00 | 1.00 | 1.00 |
| DCP | 0.80 | 1.00 | 0.80 | 1.00 | 0.80 | 1.00 | 0.80 | 1.00 |
| Coccidiostat | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 | 0.05 |
| DB vitamin | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 |
| Toxol powder | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 | 0.10 |
| Total | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 |
| Analyzed values | ||||||||
| Crude protein % | 21.07 | 20.34 | 20.70 | 19.95 | 20.33 | 19.57 | 19.97 | 19.18 |
| Crude fat % | 3.85 | 3.80 | 3.83 | 3.79 | 3.81 | 3.77 | 3.78 | 3.74 |
| Crude fiber % | 3.46 | 3.37 | 3.31 | 3.22 | 3.17 | 3.07 | 3.03 | 2.92 |
| Calcium % | 0.89 | 0.94 | 0.91 | 0.95 | 0.92 | 0.96 | 0.93 | 0.97 |
| Phosphorus % | 0.44 | 0.47 | 0.44 | 0.48 | 0.45 | 0.48 | 0.45 | 0.49 |
| Methionine % | 0.57 | 0.61 | 0.56 | 0.59 | 0.55 | 0.59 | 0.54 | 0.58 |
| Lysine % | 1.24 | 1.18 | 1.23 | 1.17 | 1.22 | 1.16 | 1.22 | 1.16 |
| Calculated values | ||||||||
| ME kcal/kg | 3038 | 3037 | 3038 | 3037 | 3034 | 3033 | 3030 | 3031 |
| Digestible protein % | 18.12 | 17.50 | 17.68 | 17.03 | 17.23 | 16.56 | 16.79 | 16.09 |
Note: Supplied per kilogram of diet—Vitamin A: 12500 IU; vitamin D3: 1250 IU; vitamin E: 18 IU; vitamin K3: 3.7 mg; thiamine: 1.8 mg; riboflavin: 6.6 mg; calcium pantothenate: 10 mg; niacin: 37.5 mg; pyridoxine: 32.5 mg; vitamin B12: 2.5 mg; Mn (manganese sulfate): 50 mg; Zn (zinc sulfate): 37.5 mg; Fe (ferrous sulfate): 25 mg; Cu (tribasic copper chloride): 7.5 mg.
Abbreviations: CRM = cassava root meal, DCP = dicalcium phosphate, Esel Dry = A combination of Vitamin E and Selenium for antioxidant support, Fishlog = A high‐quality fish protein concentrate, Hamecosaldry = A commercial gut acidifier/salinity regulator, ME = metabolizable energy, Rice Polish = A conventional energy and fiber‐rich byproduct of rice milling, Sqzyme SME = A multi‐enzyme complex (Xylanase, Protease, Amylase), T1 = control, T2 = 10% CRM, T3 = 20% CRM, T4 = 30% CRM as a partial replacement for maize, Turbotox & Hamecomoltox = multi‐component mycotoxin binders.
2.4. Data Collection and Experimental Procedure
2.4.1. Determination of Growth Performance
The initial live weights of the chicks were recorded at the commencement of the investigation using an electronic weighing scale (Model: HESA 3303). Data collection was performed on a weekly basis throughout the experimental period. To determine growth performance, body weights were recorded individually for all birds within each pen, while feed intake was monitored on a per‐pen basis. These primary data points were used to calculate the following parameters following the protocols of Imranuzzaman et al. (2025) and Rahman et al. (2025):
Body weight gain (BWG): BWG = final body weight − Initial body weight
Total feed intake (TFI): TFI = total feed supplied − Feed refusal
2.4.2. Measurement of Carcass Characteristics
At 35 days of age, two broilers (10 from each diet group) were randomly chosen from each replicate, and they were euthanized by cervical disarticulation in order to assess the carcass characteristics, determine the weight of the internal organs, and get the necessary samples. The percentage of the chicken's dressed weight that was made up of its thigh, drumstick, shank, breast muscle, wing, and internal organs (spleen, gizzard, liver, heart, and small intestine) was measured. The organ weights of each bird were measured immediately after slaughtering, and the results were expressed as a percentage of the bird's live weight. Each sample was tested three times, and the mean value was utilized to ascertain the result (Nkukwana et al. 2016). The organs' relative weight was subsequently estimated by utilizing the body weight at the time of slaughter (Martínez et al. 2021).
Yield percentage was calculated as the proportion of dressed carcass weight relative to live body weight.
2.4.3. Hematological and Serum Biochemical Evaluation
Two broilers from each replicate (10 from each diet group) were randomly selected at the age of 35 days. Hematological characteristics were assessed by collecting blood from the wing veins and placing it in labeled containers that contained ethylene diamine tetra acetic acid (EDTA). In order to quantify serum metabolites, an additional set of blood samples was collected in simple vials. The serum was separated after the blood samples were allowed to coagulate following centrifugation. The method reported by Ogbuewu and Mbajiorgu (2023) and Hossain et al. (2025) was used to measure the hematological parameters, which include PCV, RBC, hemoglobin, WBC, lymphocytes, neutrophils, monocytes, eosinophils, basophils, MCH, MCV, and MCHC. AGAPPE Diagnostics Switzerland GmbH devised the AGGAPE test kits, which were used to quantify a variety of blood biochemical markers (total protein, albumin, globulin, glucose, urea, creatinine, cholesterol, AST, ALT, and ALP). A BA‐88A type semi‐automatic chemistry analyzer from Mindray, Nansha, Shenzhen, China was used to evaluate the biochemical parameters of blood.
2.4.4. Meat Quality Analysis
After the required data on carcass characteristics had been recorded, samples of thigh and breast meat were taken from the same birds used for carcass cut evaluation. The breast and thigh meat samples were processed and placed in hermetically sealed plastic bags, then kept in a sub‐zero freezer at a temperature of −4°C for duration of 5 days. The proximate compositions (Moisture, CP, CF, EE, Ash, NFE, and metabolizable energy) of meat was conducted using the AOAC technique (AOAC 2003). The proximate composition was expressed on a dry matter basis without any adjustments or modifications. The physical meat quality attributes were estimated by following the methods of (Ashim and Prabhat 2020).
Accordingly, a method outlined by Cheng et al. (2017) was used to calculate the drip loss and water holding capacity of flesh from the breast and thigh. The following equation was used to calculate drip loss:
The interior temperature of the meat was measured using a digital needle‐tipped thermometer (H 1145, Hanna Instruments, Padova, Italy). The following formula (Vargas‐Ramella et al. 2022) was used to determine the cooking loss:
A portable pH meter (Orion model 301; Orion, Beverly, MA, US) with an electrode was used to measure the pH levels of the breast and thigh muscles after the animals were slaughtered.
The DPPH radical scavenging activity of the aqueous supernatant obtained from raw breast and thigh meat was evaluated using the Blois method, as described by Alam et al. 2024, with some modifications. Using an SP‐870 TURNER Barnstead US analyzer, the absorbance of the solution was determined at a wavelength of 517 nm. An equation was used to quantify the DPPH radical scavenging activity, and it is as follows:
The total phenolics were determined by calorimetry using the Folin–Ciocalteu reagent and, with somewhat modified methods, the methods described by Alam et al. (2024). The measurement of flavonoid contents in the breast and thigh meat extracts was conducted using an updated colorimetric approach described by Sakanaka et al. (2005), with quercetin being used as the reference compound. Each sample was tested three times to make determinations.
2.4.5. Sensory Evaluation
The sensory evaluation protocol for poultry meat was reviewed and institutionally approved by the Ethical Review Committee of Jashore University of Science and Technology, Jashore, Bangladesh (ERC/FBST/JUST/2023‐152). A team of 10 trained panelists was recruited through internal university advertisements. To be eligible, participants had to be self‐reported poultry meat consumers within the age range of 18–65 years. Exclusion criteria included individuals with known food allergies (particularly to poultry or specific seasonings), non‐consumers of poultry, or those under the age of 18. Following the study (Radikara et al. 2016), poultry meat samples (breast and thigh muscles) were collected immediately after slaughter. Following strict food safety protocols, samples were individually vacuum‐packed in food‐grade polyethylene bags and stored at −20°C to prevent microbial growth. For preparation, samples were transported to the sensory laboratory in insulated cold boxes (at 4°C) and boiled without salt or spices until an internal core temperature of 75°Cwas reached, as verified by a digital meat thermometer. Each panelist consumed one sample per treatment in a randomized order. Panelists evaluated color, taste, texture, and flavor using a 9‐point hedonic scale (1 = dislike extremely; 9 = like extremely). To prevent sensory fatigue, water and unsalted crackers were provided as palate cleansers between samples. The collected sensory data were analyzed using STAR (Statistical Tool for Agricultural Research) software (version 2.0.1, 2014) via One‐way Analysis of Variance (ANOVA), with mean separations performed using Tukey's Honestly Significant Difference (HSD) test at a significance level of p < 0.05.
2.5. Statistical Analysis
Data were subjected to a one‐way Analysis of Variance (ANOVA) using the Statistical Tool for Agricultural Research (STAR, version 2.0.1, 2014) software, developed by the International Rice Research Institute (IRRI). To evaluate the dose–response relationship, orthogonal polynomial contrasts were employed to test for linear and quadratic effects of increasing levels of cassava root meal in the diet. Treatment means were compared using the Least Significant Difference (LSD) test at a 5% significance level (p < 0.05). All graphical representations were generated using the ggplot2 package in R Studio (version 4.3.3).
3. Results
The analyzed nutrient composition of the experimental diets is presented in Table 1, showing slight variation in CP and ME values among treatments. The rising percentage of CRM correlates with a marginal decline in metabolizable energy. The analyzed nutrient composition of the experimental diets is presented in Table 1. The analyzed CP values ranged from 19.97% to 21.07% in starter diets and 19.18%–20.34% in grower diets, while the calculated ME remained consistent across treatments at approximately 3030–3038 kcal/kg.
3.1. Growth Performance
The growth performance of broilers fed diets containing different levels of cassava root meal is presented in Table 2. Initial body weights were similar among all treatments (p > 0.05), indicating uniformity at the start. However, significant differences (p < 0.05) were observed in final body weight, with the highest weight recorded in T2 (2087.94 g), followed by T3 (1988.28 g), T4 (1957.26 g), and the lowest in control group T1 (1901.70 g). A similar trend was noted in average daily gain (ADG), where T2 birds showed superior growth (58.37 g/day). Weekly body weights and feed intake were significantly influenced by treatments across all weeks (p < 0.05), with T2 showing higher values. FCR was the best in T2 during Week 5 (1.49), while T1 showed the poorest FCR (1.66). FER followed a similar pattern, being highest in T2 across all weeks, particularly Week 1 (140.80%) and Week 5 (67.19%). Mortality rates remained low across all groups but showed slight variations, with T2 consistently exhibiting lower mortality throughout the trial (p < 0.05). Overall, inclusion of cassava root meal at appropriate levels (T2) enhanced broiler growth performance, feed efficiency, and survivability compared to other treatments (Table 2).
TABLE 2.
Growth performance of experimental broilers diets on graded levels of cassava root meal.
| Growth parameters | Treatments | ||||
|---|---|---|---|---|---|
| T1 | T2 | T3 | T4 | Significance level | |
| Initial body weight (g) | 44.86 ± 0.92 | 44.76 ± 1.06 | 44.58 ± 0.89 | 45.30 ± 1.13 | ns |
| Final body weight (g) | 1901.70 ± 0.73d | 2087.94 ± 0.66a | 1988.28 ± 0.64b | 1957.26 ± 0.61c | *** |
| Final body weight gain (g) | 1856.84 | 2043.18 | 1943.70 | 1911.96 | |
| ADG (g) | 53.05 | 58.37 | 55.53 | 54.62 | |
| Body weight gain (g) | |||||
| 1st week | 132.26 ± 1.03d | 164.60 ± 1.43a | 152.08 ± 0.93b | 145.34 ± 1.84c | *** |
| 2nd week | 379.08 ± 9.65d | 454.48 ± 1.17a | 432.54 ± 0.95bc | 427.22 ± 2.08c | *** |
| 3rd week | 733.56 ± 3.86d | 775.88 ± 2.20a | 760.54 ± 1.61bc | 750.40 ± 1.90c | *** |
| 4th week | 1304.68 ± 0.47d | 1397.70 ± 0.70a | 1376.52 ± 0.85b | 1361.40 ± 0.65c | *** |
| 5th week | 1901.70 ± 0.73d | 2087.94 ± 0.66a | 1988.28 ± 0.64b | 1957.26 ± 0.61c | *** |
| Total feed intake (g) | |||||
| 1st week | 106.04 ± 1.24c | 117.04 ± 1.83b | 130.64 ± 1.27a | 130.76 ± 1.47a | * |
| 2nd week | 420.82 ± 2.25b | 475.48 ± 1.27a | 473.02 ± 0.66a | 471.82 ± 0.91a | ** |
| 3rd week | 930.54 ± 5.29d | 975.46 ± 1.71a | 967.40 ± 6.22bc | 951.10 ± 1.65c | ** |
| 4th week | 1840.02 ± 0.15d | 1957.52 ± 0.38b | 1921.38 ± 0.71c | 1988.14 ± 0.96a | *** |
| 5th week | 3083.30 ± 0.68d | 3107.64 ± 0.25a | 3085.72 ± 1.08b | 3037.18 ± 1.49c | *** |
| Feed conversion ratio (FCR) | |||||
| 1st week | 0.80 ± 0.004c | 0.71 ± 0.01d | 0.86 ± 0.003b | 0.90 ± 0.01a | * |
| 2nd week | 1.11 ± 0.003 | 1.04 ± 0.003 | 1.09 ± 0.002 | 1.10 ± 0.006 | ns |
| 3rd week | 1.26 ± 0.002 | 1.26 ± 0.003 | 1.27 ± 0.007 | 1.26 ± 0.005 | ns |
| 4th week | 1.41 ± 0.002b | 1.40 ± 0.003bc | 1.39 ± 0.004c | 1.46 ± 0.005a | * |
| 5th week | 1.62 ± 0.12a | 1.49 ± 0.005c | 1.55 ± 0.007b | 1.55 ± 0.003b | * |
| Feed efficiency ratio (%) | |||||
| 1st week | 124.73 ± 0.42b | 140.63 ± 2.91a | 116.42 ± 1.36c | 111.15 ± 0.62c | ** |
| 2nd week | 90.08 ± 0.31b | 95.58 ± 0.32a | 91.44 ± 0.20b | 90.55 ± 0.56b | * |
| 3rd week | 78.83 ± 0.15 | 79.54 ± 0.21 | 78.62 ± 0.42 | 78.89 ± 0.27 | ns |
| 4th week | 70.90 ± 0.21b | 71.40 ± 0.32a | 71.64 ± 0.45a | 68.47 ± 0.03c | * |
| 5th week | 61.67 ± 0.24b | 67.19 ± 0.53a | 64.43 ± 0.45b | 64.43 ± 0.26b | * |
| Mortality (%) | |||||
| 1st week | 0.61 ± 0.32b | 0.56 ± 0.02ab | 0.54 ± 0.34a | 0.52 ± 0.23a | * |
| 2nd week | 0.50 ± 0.01c | 0.34 ± 0.23b | 0.36 ± 0.07a | 0.42 ± 0.09a | * |
| 3rd week | 0.31 ± 0.05 | 0.28 ± 0.087 | 0.28 ± 0.085 | 0.28 ± 0.34 | ns |
| 4th week | 0.26 ± 0.03 | 0.26 ± 0.07 | 0.24 ± 0.028 | 0.25 ± 0.05 | ns |
| 5th week | 0.24 ± 0.04d | 0.16 ± 0.023c | 0.19 ± 0.09b | 0.22 ± 0.078a | * |
Note: 400 broiler hatchlings were randomly assigned to 4 treatments (5 reps/trmt) and fed ad libitum for 35 days varying inclusion levels of CRM. Body weights and feed weights were collected weekly, a,b,c,dMeans (± Standard error mean) with different superscript letters in the same rows are significantly different (*p < 0.05, **p < 0.01, ***p < 0.001). The mean values represent 15 birds per treatment group.
Abbreviations: ADG = average daily gain, CRM = cassava root meal, FCR = feed conversion ratio, total feed intake (g)/body weight gain (g), FER = feed efficiency ratio, body weight gain (g)/total feed intake (g) × 100, ns = non‐significant (p > 0.05), T1 = control, T2 = 10% CRM, T3 = 20% CRM, T4 = 30% CRM as a partial replacement for maize.
3.2. Carcass Characteristics
The inclusion of cassava root meal in broiler diets significantly influenced carcass traits and internal organ development (p < 0.05) as shown in Table 3. The highest dressing percentage was observed in T2 (75.50%), followed by T3 (73.12%), with T1 and T4 showing lower values. Head, neck, thigh, drumstick, breast, abdominal fat, shank, crop, kidney, lung, spleen, liver, heart, and gizzard weights all differed significantly among treatments. Notably, broilers in T2 consistently showed superior carcass yields, including highest values for breast (28.21%), drumstick (16.51%), and thigh (15.18%) weights. Internal organ weights such as kidney (1.54%), spleen (0.46%), liver (3.92%), and heart (1.49%) were also highest in T2, indicating enhanced physiological development. The lowest values for most parameters were observed in T1 and T4, suggesting suboptimal utilization at those cassava inclusion levels. Proventriculus weight showed minor variation but remained statistically significant (p = 0.031).
TABLE 3.
Carcass yield characteristics of experimental broilers diets on graded levels of cassava root meal at the age of 35 days.
| Parameters | Treatments | ||||
|---|---|---|---|---|---|
| T1 | T2 | T3 | T4 | p | |
| Dressing weight (%) | 72.68 ± 0.52b | 75.50 ± 0.44a | 73.12 ± 0.47b | 72.64 ± 0.41b | * |
| Head weight (%) | 2.38 ± 0.02d | 2.65 ± 0.01a | 2.58 ± 0.01b | 2.50 ± 0.01c | * |
| Neck weight (%) | 4.35 ± 0.01c | 4.59 ± 0.04a | 4.53 ± 0.01ab | 4.44 ± 0.01bc | * |
| Thigh weight (%) | 13.42 ± 0.009d | 15.18 ± 0.02a | 14.28 ± 0.02b | 13.61 ± 0.007c | * |
| Drumstick weight (%) | 12.87 ± 0.01d | 16.51 ± 0.02a | 14.16 ± 0.02b | 13.84 ± 0.03c | * |
| Wing weight (%) | 11.34 ± 0.009 | 11.74 ± 0.73 | 12.33 ± 0.01 | 11.88 ± 0.02 | ns |
| Breast weight (%) | 23.31 ± 0.05c | 28.21 ± 0.02a | 25.32 ± 0.06b | 21.49 ± 0.03d | ** |
| Abdominal fat (%) | 1.93 ± 0.01c | 2.37 ± 0.01a | 2.01 ± 0.007c | 2.13 ± 0.04b | * |
| Shank weight (%) | 3.74 ± 0.01d | 4.12 ± 0.009a | 3.95 ± 0.01b | 3.82 ± 0.008c | * |
| Crop weight (%) | 1.15 ± 0.01d | 1.82 ± 0.02a | 1.60 ± 0.02b | 1.23 ± 0.007c | ** |
| Kidney weight (%) | 1.15 ± 0.01d | 1.54 ± 0.01a | 1.33 ± 0.01b | 1.24 ± 0.01c | * |
| Lung weight (%) | 1.33 ± 0.01d | 1.50 ± 0.02a | 1.43 ± 0.01bc | 1.38 ± 0.01cd | * |
| Spleen weight (%) | 0.19 ± 0.008c | 0.46 ± 0.01a | 0.34 ± 0.01b | 0.21 ± 0.02c | ** |
| Proventriculus weight (%) | 0.55 ± 0.01d | 0.59 ± 0.008cd | 0.62 ± 0.01abc | 0.60 ± 0.01bcd | * |
| Liver weight (%) | 3.58 ± 0.01d | 3.92 ± 0.02a | 3.78 ± 0.01b | 3.69 ± 0.02c | * |
| Heart weight (%) | 1.26 ± 0.008d | 1.49 ± 0.02a | 1.41 ± 0.03ab | 1.35 ± 0.01cd | * |
| Gizzard weight (%) | 5.16 ± 0.01b | 5.60 ± 0.01a | 5.34 ± 0.01b | 5.19 ± 0.11b | * |
Note: The data represent the mean value of 10 samples per treatment; All parameters (except dressing weight) are expressed as relative weights calculated as (Weight of organ or part/live body weight)×100; a,b,c,dMeans (± standard error mean) with different superscript letters in the same rows are significantly different (*p < 0.05, **p < 0.01). The mean values represent 15 samples per treatment group.
Abbreviations: CRM = cassava root meal, ns = non‐significant (p > 0.05), T1 = control, T2 = 10% CRM, T3 = 20% CRM, T4 = 30% CRM as a partial replacement for maize.
3.3. Hematological and Biochemical Parameters
Feeding different levels of cassava root meal significantly influenced the hematological and biochemical profiles of broilers at 35 days (p < 0.05). Hemoglobin, RBC, PCV, MCH, and MCHC levels were highest in T1 and T2 but declined significantly in T4. WBC count peaked in T4 (19,700 × 109/L), indicating a possible stress or immune response. Lymphocyte percentages were highest in T2 (73.00%) and lowest in T3. Neutrophils were significantly elevated in T1 and T3. Basophils appeared only in T4. Among biochemical parameters, random blood sugar (RBS), uric acid, and BUN levels increased progressively with higher cassava inclusion, with maximum values in T4. Cholesterol was lowest in T2 and highest in T4, while triglycerides were significantly reduced in T2. HDL was highest in T4 (68.58 mg/dL), and LDL peaked in T2. Liver enzymes (AST, ALT, ALP) showed marked variation; ALT and AST were significantly elevated in T2, indicating potential hepatic stress. ALP was highest in T3 as shown in Table 4.
TABLE 4.
Hematological and biochemical parameters of broiler on graded levels of experimental diets of cassava root meal at the age of 35 days.
| Treatments | |||||||
|---|---|---|---|---|---|---|---|
| Parameters | T1 | T2 | T3 | T4 | SEM | Linear | Quadratic |
| Hematological parameters | |||||||
| Hb g/dl | 10.02a | 9.12b | 9.26b | 8.20c | 0.37 | 4.24** | 0.02 |
| RBC ×106/μL | 2.53a | 2.32b | 2.23b | 2.18c | 0.08 | 0.19** | 0.02 |
| WBC ×109/L | 17240c | 18280b | 15540d | 19700a | 876.22 | 3229440** | 7300800** |
| PCV % | 28.64a | 27.68b | 27.70b | 25.30c | 0.71 | 15.00** | 1.55** |
| MCV fL | 128.76b | 130.60b | 128.80b | 120.10a | 2.36 | 116.04** | 82.79** |
| MCH pg | 45.40a | 43.32ab | 43.06b | 39.22c | 1.29 | 53.02** | 2.32** |
| MCHC g/dl | 35.60a | 33.34ab | 34.20b | 32.72b | 0.62 | 9.10** | 0.45** |
| Neutrophil % | 32.60a | 22.80b | 32.40a | 25.40b | 2.48 | 1310.44** | 5.88** |
| Lymphocytes % | 65.00c | 73.00a | 62.80b | 64.40c | 2.28 | 21.60** | 30.72** |
| Monocytes % | 2.00 | 2.60 | 2.60 | 2.40 | 0.14 | 0.22** | 0.48** |
| Eosinophils % | 1.60 | 3.40 | 2.40 | 2.60 | 0.37 | 0.60** | 1.92** |
| Basophils % | 00 | 00 | 00 | 1.08 | 0.27 | 1.57** | 0.87** |
| Biochemical parameters | |||||||
| RBS mg/dL | 158.62d | 180.66c | 203.60b | 213.44a | 12.26 | 5267.81** | 111.63** |
| Uric Acid mg/dL | 3.83d | 4.55c | 4.86b | 4.94a | 0.25 | 1.99** | 0.31** |
| Total Protein g/dL | 2.73c | 2.95a | 2.91a | 2.77b | 0.05 | 0.00 | 0.09** |
| BUN mg/dl | 6.64c | 7.52b | 6.67c | 7.77a | 0.29 | 0.94** | 0.03** |
| Cholesterol mg/dL | 110.62b | 100.78a | 111.56c | 117.42d | 3.45 | 145.73** | 184.79** |
| Triglyceride mg/dL | 108.62a | 80.60d | 89.64c | 96.40b | 5.90 | 114.42** | 907.24** |
| HDL mg/dL | 59.48c | 45.54d | 63.58b | 68.58a | 4.95 | 308.35** | 269.04** |
| LDL mg/dL | 29.34c | 39.32a | 29.92b | 29.34c | 2.45 | 14.12** | 78.89** |
| AST U/I | 187.72b | 208.84a | 167.18d | 183.44c | 8.58 | 445.54** | 17.71** |
| ALT U/I | 9.32c | 16.30a | 7.65d | 9.90b | 1.90 | 7.31** | 16.85** |
| ALP U/I | 8034b | 5288d | 8466a | 7282c | 703.71 | 127512** | 1829883** |
Note: The data represent the mean value of 10 samples per treatment; a,b,c,dMeans with different superscript letters in the same rows are significantly different. The mean values represent 15 samples per treatment group.
Abbreviations: ALP U/I = alkaline phosphatase (units per liter), ALT U/I = alanine aminotransferase (units per liter), AST U/I = aspartate aminotransferase (units per liter), BUN mg/dl = blood urea nitrogen (milligrams per deciliter), CRM = cassava root meal, Hb = hemoglobin, HDL mg/dl = high‐density lipoprotein (milligrams per deciliter), LDL mg/dl = law density lipoprotein (milligrams per deciliter), MCH pg. = mean corpuscular hemoglobin (picograms), MCHC g/dl = mean corpuscular hemoglobin concentration (grams per deciliter), MCV fL = mean corpuscular volume (femtoliters), PCV = packed cell volume, RBC = red blood cell, RBS mg/dl = random blood sugar (milligrams per deciliter), SEM = standard error mean, T1 = control, T2 = 10% CRM, T3 = 20% CRM, T4 = 30% CRM as a partial replacement for maize, WBC = white blood cell.
p < 0.01.
3.4. Proximate Composition of Meat
3.4.1. Breast Muscle Proximate Composition
The proximate composition of breast muscle among the treatment groups is presented in Table 5. Moisture, crude protein (CP), ether extract (EE), crude fiber (CF), and ash contents did not differ significantly among the dietary treatments (p > 0.05). However, nitrogen‐free extract (NFE) and metabolizable energy (ME) were significantly affected by cassava root meal (CRM) inclusion (p < 0.05). The highest NFE value was observed in T2 (1.27%), which differed significantly from the other treatment groups, whereas the lowest value was recorded in T1. Similarly, ME content was significantly higher in T4 (972.04 kcal/kg) compared to the remaining treatments. Although statistically non‐significant, EE content tended to increase with higher CRM inclusion levels, with the highest value in T4 (2.00%) and the lowest in T2 (1.03%).
TABLE 5.
Proximate composition of breast and thigh muscle of broiler on graded levels of experimental diets of cassava root meal at the age of 35 days.
| Treatments | ||||||||
|---|---|---|---|---|---|---|---|---|
| Meat cuts | Parameters | T1 | T2 | T3 | T4 | SEM | Linear | Quadratic |
| Breast muscle | Moisture % | 75.32 | 72.78 | 73.96 | 72.37 | 0.66 | 8.82** | 0.68* |
| CP % | 21.27 | 22.65 | 22.98 | 22.52 | 0.37 | 2.49** | 2.54** | |
| EE % | 1.80ab | 1.03c | 1.60bc | 2.00a | 0.21 | 0.21** | 1.03** | |
| CF% | 0.85 | 0.81 | 0.50 | 1.06 | 0.12 | 0.02* | 0.27** | |
| Ash % | 1.23 | 1.30 | 1.30 | 1.82 | 0.14 | 0.47** | 0.15** | |
| NFE % | 0.39ab | 1.27a | 0.30b | 0.29 | 0.24 | 0.24** | 0.59** | |
| ME (kcal/kg) | 894.57c | 955.67b | 935.29ab | 972.04a | 16.72 | 6732.91** | 438.63** | |
| Thigh muscle | Moisture % | 74.05 | 70.32 | 72.59 | 73.21 | 0.80 | 0.03 | 13.69** |
| CP % | 15.30c | 18.40ab | 20.28a | 18.33bc | 1.03 | 18.05** | 19.13** | |
| EE % | 1.2 | 1.7 | 1.8 | 1.5 | 0.13 | 0.15** | 0.48** | |
| CF% | 0.55d | 1.00bc | 0.70c | 1.03a | 0.12 | 0.19** | 0.01* | |
| Ash % | 0.90d | 1.01cd | 2.46a | 2.04b | 0.38 | 3.56** | 0.21** | |
| NFE % | 7.99a | 7.61b | 4.25c | 2.07d | 1.41 | 67.27** | 2.59** | |
| ME (kcal/kg) | 917.18b | 1055.63a | 928.02b | 920.38b | 33.52 | 2084.00** | 16016.94** | |
Note: The data represent the mean value of 10 samples per treatment; a,b,c,dMeans with different superscript letters in the same rows are significantly different. The mean values represent 15 samples per treatment group.
Abbreviations: CF = crude fiber, CP = crude protein, CRM = cassava root meal, EE = ether extract, kcal/kg = kilo calorie/kg, ME = metabolizable energy, NFE = nitrogen free extract, SEM = standard error mean, T1 = control, T2 = 10% CRM, T3 = 20% CRM, T4 = 30% CRM as a partial replacement for maize.
p ≤ 0.05.
p ≤ 0.01.
3.4.2. Thigh Muscle Proximate Composition
The proximate composition of thigh muscle showed significant variation in several parameters among the treatments (Table 5). Crude protein (CP) content differed significantly (p = 0.027), with the highest value observed in T3 (20.28%), followed by T4 and T2, while the lowest value was recorded in T1 (15.30%). Crude fiber (CF) content was significantly higher in T4 (1.03%) compared to the other groups (p < 0.05). Ash content also varied significantly, with the highest value in T3 (2.46%). Nitrogen‐free extract (NFE) decreased significantly with increasing CRM inclusion levels, declining from 7.99% in T1 to 2.07% in T4% (p < 0.05). Metabolizable energy (ME) was significantly higher in T2 (1055.63 kcal/kg) than in the other treatment groups.
3.5. Meat Quality Attributes
3.5.1. Breast Muscle Quality Attributes
The effects of dietary CRM inclusion on breast muscle quality traits are shown in Table 6. Drip loss (DL) did not differ significantly among the treatments (p > 0.05). However, cooking loss (CL) was significantly lower in T2 (27.58%) compared to the control group T1 (35.95%) (p = 0.016). Water‐holding capacity (WHC) was significantly improved in T2 (78.22%) relative to all other treatments (p = 0.0001). Muscle pH was also significantly affected, with the lowest pH recorded in T4 (5.65), differing significantly from the remaining groups (p = 0.002).
TABLE 6.
Quality attributes of breast and thigh muscle of broiler on graded levels of experimental diets of cassava root meal at the age of 35 days.
| Meat cuts | Parameters | Treatments | Linear | Quadratic | ||||
|---|---|---|---|---|---|---|---|---|
| T1 | T2 | T3 | T4 | SEM | ||||
| Breast muscle | DL % | 10.51 | 9.19 | 9.41 | 9.73 | 0.29 | 0.67 | 2.02 |
| CL % | 35.95a | 27.58c | 33.39ab | 31.68bc | 1.76 | 7.35* | 33.27** | |
| WHC % | 71.50c | 78.22a | 73.16b | 74.21ab | 1.43 | 1.41 | 24.11** | |
| pH | 6.21b | 6.12b | 6.11b | 5.65a | 0.13 | 0.43* | 0.10 | |
| DPPH scavenging activity (mg TE/100 g) | 44.98c | 60.62a | 51.94b | 51.76b | 3.20 | 20.39** | 187.70** | |
| TPC (mg GAE/100 g sample) | 32.17c | 36.40a | 33.44ab | 33.19bc | 0.91 | 0.00 | 15.05** | |
| TFC (mg QE/100 g sample) | 27.94c | 35.49a | 35.34ab | 31.31bc | 1.81 | 14.88** | 100.57** | |
| L* | 63.71ab | 55.60bc | 46.50c | 65.21a | 4.30 | 3.17 | 539.48** | |
| a* | 0.65b | 0.36b | 3.80a | 0.57b | 0.82 | 1.54** | 6.48** | |
| b* | 10.48ab | 9.65bc | 11.39a | 11.39a | 0.42 | 2.99** | 0.52 | |
| Thigh muscle | DL % | 7.15a | 4.15d | 5.24c | 5.73b | 0.62 | 1.51** | 9.14** |
| CL % | 36.25a | 33.44bc | 32.55c | 35.36ab | 0.85 | 1.90 | 23.69** | |
| WHC % | 71.55c | 74.81a | 72.21bc | 73.21ab | 0.71 | 0.85 | 3.83 | |
| pH | 6.45 | 6.39 | 6.33 | 6.10 | 0.08 | 0.18* | 0.02 | |
| DPPH scavenging activity (mg TE/100 g) | 57.80b | 73.38a | 72.29a | 57.39b | 4.41 | 0.79 | 696.32** | |
| TPC (mg GAE/100 g sample) | 42.17b | 66.17a | 41.30b | 44.08b | 5.94 | 54.95** | 337.72** | |
| TFC (mg QE/100 g sample) | 44.43b | 72.35a | 44.55b | 48.52b | 6.70 | 36.18** | 430.20** | |
| L* | 55.24a | 54.30a | 48.23b | 56.38a | 1.82 | 1.49** | 59.72** | |
| a* | 2.49a | 2.35a | 0.98b | 2.35b | 0.36 | 0.48** | 1.71** | |
| b* | 9.32ab | 9.53a | 4.80c | 8.24b | 1.09 | 9.53** | 7.82** | |
Note: The data represent the mean value of 10 samples per treatment. a,b,cMeans with different superscript letters in the same rows are significantly different. The mean values represent 15 samples per treatment group.
Abbreviations: a* = greenness to redness, b* = blueness to yellowness, CL = cooking loss, CRM = cassava root meal, DL = drip loss, L* = darkness to lightness, mg GAE/100 g sample = milligram of gallic acid equivalent per 100 g sample, mg QE/100 g sample = milligram of quercetin equivalent per 100 g sample, mg TE/100 g sample = milligram of trolox equivalent per 100 g sample, SEM = standard error mean, T1 = control, T2 = 10% CRM, T3 = 20% CRM, T4 = 30% CRM as a partial replacement for maize, TFC = total flavonoid content, TPC = total phenolic content, WHC = water holding capacity.
p ≤ 0.05.
p ≤ 0.01.
Antioxidant‐related parameters were significantly enhanced by CRM supplementation. The highest DPPH scavenging activity, total phenolic content (TPC), and total flavonoid content (TFC) were observed in T2, with values of 60.62 mg TE/100 g, 36.40 mg GAE/100 g, and 35.49 mg QE/100 g, respectively, which were significantly higher than those of the other treatment groups (p < 0.05).
Regarding meat color attributes, significant differences were observed in L*, a*, and b* values (p < 0.05). The highest lightness (L*) and yellowness (b*) values were recorded in T4 (65.21 and 11.39, respectively), whereas redness (a*) was significantly higher in T3 (3.80) compared to the other treatments.
3.5.2. Thigh Muscle Quality Attributes
The quality traits of thigh muscle were significantly influenced by CRM inclusion levels (Table 6). Drip loss (DL) significantly decreased with increasing CRM supplementation, with the lowest value observed in T2 (4.15%) and the highest in the control group T1 (7.15%) (p = 0.0001). Water‐holding capacity (WHC) was significantly higher in T2 (74.81%) compared to the other groups (p = 0.039). Cooking loss (CL) was significantly reduced in T3 (32.55%) relative to the other treatments (p = 0.017). In contrast, pH values did not differ significantly among the treatment groups (p = 0.283).
The antioxidant profile of thigh muscle showed marked improvement with CRM supplementation. T2 exhibited significantly higher DPPH scavenging activity (73.38 mg TE/100 g), TPC (66.17 mg GAE/100 g), and TFC (72.35 mg QE/100 g) than all other treatment groups (p < 0.0001).
Color characteristics also varied significantly among treatments. The highest L* value was recorded in T4 (56.38), whereas the lowest was observed in T3 (48.23) (p = 0.002). Redness (a*) was significantly lower in T3 (0.98) compared to the other groups, while yellowness (b*) was also significantly reduced in T3 (4.80) (p = 0.0001).
3.6. Sensory Evaluation of Meat
3.6.1. Breast Muscle Sensory Attributes
The sensory evaluation results of breast muscle are presented in Figure 1. No significant differences were observed among the treatment groups for color, flavor, texture, juiciness, and taste (p > 0.05). However, overall acceptability differed significantly among the treatments, with birds fed diets containing up to 10% CRM showing significantly higher overall acceptability scores compared to the control group.
FIGURE 1.

Sensory evaluation of meat/muscle; (A) (breast muscle) and (B) (thigh muscle). (T1–T4) represents dietary treatments with different inclusion levels of cassava root meal (CRM). T1 = control, T2 = 10% CRM, T3 = 20% CRM, T4 = 30% CRM as a partial replacement for maize. Sensory attributes of breast and thigh muscles were evaluated by 10 trained panelists using a 9‐point hedonic scale (1 = dislike extremely, 9 = like extremely). Error bars indicate variability among panelists (± standard deviation/standard error, as applicable). Samples were evaluated for color, flavor, texture, juiciness, taste, and overall acceptability.
3.6.2. Thigh Muscle Sensory Attributes
In thigh muscle, sensory parameters such as color and juiciness did not vary significantly among the treatments (p > 0.05). In contrast, flavor, texture, and overall acceptability showed significant differences (p < 0.05), with the control group (T1) demonstrating superior scores compared to the CRM‐fed groups. Taste scores did not differ significantly among the treatments, and no CRM treatment group significantly outperformed the control (Figure 1).
4. Discussion
The use of cassava root meal (CRM) as an alternative to the conventional energy source maize has demonstrated ameliorative effects on growth performance, biochemical parameters, and meat quality attributes. The cassava root is a popular food source in many African regions and South America for human consumption. It is prepared into various foods, including cassava flour, tapioca, gari, fufu, cassava chips, cassava bread, cassava noodles, and alcoholic beverages (Fathima et al. 2023). It is widely used as an industrial product, similar to bioethanol, biodegradable plastics, textile and paper binders, adhesives, and glues (Fathima et al. 2023; Otekunrin 2024). Unfortunately, its use in livestock or poultry feed is infrequent due to a lack of knowledge on its beneficial effect on poultry as a substitute for maize.
The utilization of innovative feed additives and ingredients to promote broiler chicken production is being investigated on number of trails and the present study specifically focused on including cassava root meal into the diet. When compared to the other treatment groups, birds reared as control group showed a lower body weight and diet having 10% CRM showed higher body weights. The current finding was similar as that of Akapo et al. (2014), who noted that broilers' body weight and feed intake significantly improved when supplementing peeled CRM. A number of studies have shown that giving diets containing between 30 and 35 g kg−1 of seaweed meal to chickens has no effect on their ability to get weight (Abudabos et al. 2013; Nhlane et al. 2021). In case of feed intake, the supplementing 10% CRM significantly influence to more feed intake than the other groups. The trend in feed intake similarity across various diets aligns with the findings of Hassan et al. (2012), who documented a notable decrease in feed intake in birds that were fed with more than 25% sun‐dried CRM. Considering FCR, T2 group had the lowest FCR throughout the experiment, indicating the most efficient feed utilization. The supplementation of CRM improves FER, suggesting a potential trade‐off between feed intake and feed efficiency at higher levels of cassava root meal. Moderate CRM inclusion may improve growth performance due to its highly digestible starch and readily available energy, which enhance nutrient utilization and protein deposition. However, excessive CRM inclusion may reduce feed efficiency because of lower protein content and residual anti‐nutritional factors.
Nonetheless, this study agrees with the results of Yang et al. (2024), who noted a significant increase in feed consumption in response to a diet's increased cassava meal content during the finisher phase. The findings of other studies reported no significant effects on broiler chickens align with the insignificant results obtained for daily feed intake, FCR, FER, and mortality in broiler chickens fed sun‐dried CRM (Agunbiade et al. 2004; Autónoma De Yucatán et al. 2011; Okpara et al. 2022; Wumnokol et al. 2023).
In broilers, cassava root meal enhances growth performance due to its high carbohydrate content, which serves as a readily available source of energy, contributing to metabolic and body weight gain. Its readily digestible starch helps improve nutrient utilization and feed productivity (Wumnokol et al. 2023). Good nutrient utilization from cassava can be achieved if it is processed correctly, as it contains low levels of anti‐nutritional factors. Additionally, its presence could play a role in maintaining a healthy gut microbiome balance, helping beneficial bacteria and hindering the colonization of pathogens (Akapo et al. 2014). These effects collectively result in a better feed conversion ratio, improved protein synthesis, and increased growth performance in broilers compared to control broilers fed the standard maize diet.
Chukwukaelo et al. (2018) discovered that including cassava meal in the diet resulted in a higher dressing percentage in terms of carcass composition. In this study, we observed that, diet having 10% CRM had the highest dressing percentage. Similarly, Sultana et al. (2012) found that head and thigh weights increased when subjects were fed diets containing 15% and 30% CRM. A study conducted by Abera et al. (2016) revealed an increased proportion of liver in broilers that were fed a diet containing 15% cassava root and leaf meals. Conversely, Morgan and Choct (2016) reported that no notable alterations in yield weight while including 25% cassava meal in the diet. In addition, Abera et al. (2016) and Adeyemo and Longe (2008) observed that broilers fed with 12% cassava meals had higher levels of lungs and kidneys, with the exception of the liver, which showed a more substantial increase when the cassava meal inclusion was at 25%. The high lung weight in broilers is linked to enhanced metabolic activity, which enables sufficient oxygen supply to meet the body's metabolic requirements (Aladi et al. 2021; Namakparvar et al. 2014). Elnour et al. (2020) reported that there were no significant alterations in the weights of breast, abdomen fat, or drumstick but substantial variations in spleen size when cassava root was included in the diet, with an inclusion rate of up to 40%. Abera et al. (2016) confirmed that including 15% cassava in the diet resulted in a higher liver percentage. According to Ukachukwu (2008), liver enlargement and weight gain are associated with detoxifying processes caused by anti‐nutrients. In addition, Alahmari (2024) and Adedokun (2023) linked intestinal expansion to higher levels of indigestible fiber, whereas (Alahmari 2024) attributed the increased weights of the kidneys and heart to the metabolic impact of anti‐nutritional chemicals.
The inclusion of 10% CRM to broiler diets promotes an increase in carcass characteristics, as it enhances the supply of available energy, improves nutrient digestibility, and increases metabolic efficiency, ultimately leading to greater weight and muscle accretion.
Improved carcass yield in T2 may be associated with better energy utilization and muscle accretion. Higher CRM inclusion levels may dilute essential amino acids, potentially limiting optimal carcass development. In addition, improved nutrient digestibility may have enhanced protein retention and tissue growth in broilers receiving moderate CRM supplementation.
Differences among studies are attributable to the processing of cassava, levels of inclusion, broiler lines, feeding diets, and ambient conditions (Amos et al. 2021). The existence or depletion of anti‐nutritional factors, such as cyanogenic glycosides and indigestible fiber, also affects organ development and carcass yield, thereby leading to the limited results achieved by different research reports (Adedokun 2023).
Blood indices are essential diagnostic tools for determining the metabolic, health, and nutritional status of an animal. They are employed for the evaluation of the nutritive quality of non‐conventional feedstuffs (Ogbuewu et al. 2017). The inclusion of cassava root in broiler diets resulted in decreased blood hemoglobin (Hb), packed cell volume (PCV), and red blood cell (RBC) values. However, all blood parameters were within the normal range (Hb: 7.0–13.0 g/dL, PCV: 22%–35%, RBC: 2.5–3.5 × 106/μL) (Okafor et al. 2015). The higher MCV in the broilers on a 10% CRM diet implied larger RBCs with normal Hb content. The numbers of WBCs and CKCs, which are important for immunity, were not significantly different, and lymphocytes were within the normal range (51.17%–75.33%) (Kongpechr et al. 2020). Higher root cassava content resulted in decreased MCV and MCH, a sign of both modified RBC size and set‐up, which may increase the risk of anemia. The reduction in erythrocytic indices at higher CRM levels may be linked to residual anti‐nutritional compounds affecting nutrient utilization. Lower cholesterol and triglyceride levels in T2 suggest improved lipid metabolism and reduced fat deposition. The maintenance of most hematological values within normal physiological ranges further indicates that moderate CRM inclusion did not adversely affect bird health.
Increased MCH may be suggestive of regeneration anemia (Coles et al. 2008). The concentration of total protein levels, ranging from 3.32 to 4.57 g/dL for birds (Adeyemo and Longe 2008), was unremarkably maintained, denoting that dietary protein was not affected in quality. The broilers fed a diet with 10% CRM (T2) showed lower total cholesterol and triglycerides (p < 0.05) compared to the control. The activities of AST and ALT were also significantly different between diets and fell within normal reference levels (167.18–208.84 and 7.65–16.30 U/L, respectively), as reported by Coles et al. (2008). Because increased levels of AST, ALT, and ALP can be a sign of liver disease, monitoring these values is essential. Results corroborate Ogbuewu et al. (2017), who associated serum protein status with dietary intake and noted that cassava root meal had no effect on serum proteins and preserved protein quality.
Proximate compositions of broiler breast and thigh muscles showed significant variation due to inclusion of cassava root mix in the diets fed to broilers. According to Chukwukaelo et al. (2018), the highest levels of cassava root mix were reflected in an increase in CP and ME content while decreasing moisture as well as NFE. The CF, EE, and ash content decreased in breast muscle. On the other hand, the CF, EE, and ash percentage in thigh muscle were increased. In this study, we found 10% of CRM improved ME rather than 20% or 30% inclusion of CRM in broiler diet. Furthermore, the present study reveals that the introduction of cassava root mix in broiler diets could cause an evident effect on nutritional attributes and energy content among multiple muscle tissues. Broiler production could be transformed, as crude protein and energy content are improved together with managing other nutritional factors such as moisture and fiber levels according to diet modifications, which will lead to increased broiler meat quality by meeting consumer demand (Chukwukaelo et al. 2018). According to Bogosavljević‐Bošković et al. (2010), the primary elements influencing the chemical composition and quality of poultry meat are the kind of raw materials used and their chemical composition, as well as the ration's protein and energy values. Differences in the nutritional content of meats were seen in the quantities of protein and energy across treatment diets in the current study, and these differences were strongly correlated with the degree of replacement of cassava root meal. Variations in meat composition may reflect altered nutrient partitioning and muscle metabolism due to CRM inclusion. Moderate CRM supplementation improved protein and energy deposition without negatively affecting overall meat quality. Dietary energy balance and nutrient availability may also influence muscle biochemical composition and meat nutritional value.
Meat quality characteristics have a significant impact on consumers' purchasing behavior of products (Mir et al. 2017). Characteristic parameters, such as color, pH, water‐holding capacity (WHC), cooking loss, and juiciness, are important to the meat industry, enabling the production of high‐quality value‐added products (Hussein et al. 2019). Different treatments had a significant influence on the quality characteristics of breast and thigh muscles in this study. Drip loss was significantly decreased in the thigh muscles among the treatment groups, with the T1 group demonstrating the lowest value. Cooking loss, however, was significantly (p < 0.05) higher in broilers fed the control diet (T1). As meat pH has an effect on cooking loss, this is in line with Navid et al. (2010) and Barbut (2015), who stated that pre‐ and post‐slaughter treatments influence the pH of meat. A smaller value in cooking loss represents a more desirable meat quality because it loses less protein during cooking (Abubakar et al. 2021). T2 showed the highest levels of total phenolic content (TPC) and total flavonoid content (TFC), as well as the highest antioxidant activity.
Higher antioxidant activity in T2 may be associated with phenolic and flavonoid compounds present in cassava, which could improve oxidative stability, water‐holding capacity, and overall meat quality.
The T4, T1, and T2 had the highest L, a, and b* values, respectively, as measured by color. These results are corroborated by the studies of Bakare et al. (2021), who proposed that cassava leaf products (CLP) enhance the stability of meat color and antioxidant capacity. In conclusion, T2 (10% CRM) consistently performed the best across all quality parameters.
The results of the study indicated that the sensory attributes of broiler meat were not reduced as a result of the dietary treatments. Abubakar et al. (2021) reported that meat color is affected by muscle composition, structure, condition, and myoglobin type. Organoleptic tests did not reveal differences in meat color among treatments, contrary to (Fofana et al. 2023), who observed that snail meal did not affect the color of meat in broiler. Overall, flavor, which is related to both chemical composition and cooking‐induced changes, was not affected. Texture, with tenderness being a major consumer preference (Warner et al. 2021), was scored as ranging from 7.02 to 8.14 in all groups. Juiciness, a characteristic associated with water‐holding capacity and muscle protein structure (Lorenzo et al. 2019), was also not negatively impacted. The unchanged sensory scores indicate that moderate CRM inclusion did not adversely affect meat palatability, texture, or consumer acceptability. Improved antioxidant stability and water‐holding capacity may also have contributed to maintaining desirable sensory characteristics in CRM‐fed broilers.
Panel differences might indicate variations in dietary habits (Howie et al. 2009). The outcome is similar to that of (Mayulu et al. 2019), who observed that dietary treatments resulted in tastier and consumer‐preferred broiled.
From a poultry nutrition perspective, CRM can serve as a cost‐effective partial substitute for maize when properly processed and nutritionally balanced with adequate protein and amino acid supplementation. However, this study was limited to a single strain and short‐term feeding trial, which may not reflect long‐term health impacts or applicability to other poultry breeds. The present study did not evaluate cyanogenic compounds, nutrient digestibility, gut health, or intestinal morphology, which may provide deeper insight into the nutritional effects of CRM in broilers.
5. Conclusion
The dietary inclusion of cassava root meal (CRM) significantly influenced growth performance, carcass traits, hematological and biochemical indices, meat composition, and meat quality attributes of broiler chickens. Among the treatment groups, 10% CRM inclusion (T2) produced the most favorable outcomes, including improved body weight gain, feed efficiency, dressing percentage, antioxidant status, water‐holding capacity, and overall meat acceptability without causing detrimental health effects. However, higher inclusion levels negatively affected some hematological and biochemical parameters, indicating possible nutritional imbalance or residual anti‐nutritional effects. Therefore, CRM can be considered a suitable partial substitute for maize in broiler diets at moderate inclusion levels, particularly at 10%, when properly processed and nutritionally balanced. Further studies are recommended to evaluate long‐term effects, nutrient digestibility, and strategies to reduce anti‐nutritional compounds in cassava‐based poultry diets.
Author Contributions
Shahabuddin Ahmed: data curation, investigation, methodology, software, formal analysis, writing – original draft, writing – review and editing. Hemayet Hossain: data curation, methodology, software, formal analysis, writing – original draft, writing – review and editing. Khadiza Akter Brishty: data curation, methodology, software, formal analysis, writing – original draft, writing – review and editing. Aminul Islam: data curation, writing – review and editing. M. Shalim Uddin: data curation, writing – review and editing. Md. Mahfujur Rahman: data curation, formal analysis, methodology, software, validation, visualization, writing – original draft, writing – review and editing. Mrityunjoy Biswas: conceptualization, data curation, investigation, validation, formal analysis, supervision, visualization, resources, writing – original draft, writing – review and editing.
Funding
The authors have nothing to report.
Conflicts of Interest
The authors declare no conflicts of interest.
Acknowledgments
The authors are grateful to the Laboratory of Agro Product Processing Technology and Nutrition and Food Technology Department of Jashore University of Science and Technology, Jashore, Bangladesh for their assistance and facilities which were invaluable in this study. Also, the authors would like to thank the Poultry Research Center of Bangladesh Livestock Research Institute (BLRI), Dhaka, Bangladesh for their kind support.
Contributor Information
Md. Mahfujur Rahman, Email: mahfuj.vetmed@sau.ac.bd.
Mrityunjoy Biswas, Email: mrityunjoy_appt@just.edu.bd.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.
References
- Abdul Kuddus, M. , Chandra Datta G., Mahbubul Alam Miah M., et al. 2020. “Performance Study of Selected Orange Fleshed Sweet Potato Varieties in North Eastern Bangladesh.” International Journal of Environment, Agriculture and Biotechnology 5: 673–680. 10.22161/ijeab.53.21. [DOI] [Google Scholar]
- Abera, A. , Negasi A., and Mengistu U.. 2016. “Evaluation of the Carcass Parameters of Growers Fed on Cassava ( Manihot esculenta Crantz) Leaf and Root Mixture.” Journal of Biology, Agriculture and Healthcare 6, no. 7: 129–136. [Google Scholar]
- Abubakar, A. , Fitri C. A., and Koesmara H.. 2021. “Analysis of pH and Cooking Losses of Chicken Meat due to the Use of Different Percentages of Turmeric Flour.” IOP Conference Series: Earth and Environmental Science 667, no. 1: 012042. 10.1088/1755-1315/667/1/012042. [DOI] [Google Scholar]
- Abudabos, A. M. , Okab A. B., Aljumaah R. S., Samara E. M., Abdoun K. A., and Al‐Haidary A. A.. 2013. “Nutritional Value of Green Seaweed ( Ulva lactuca ) for Broiler Chickens.” Italian Journal of Animal Science 12, no. 2: 177–181. 10.4081/IJAS.2013.E28. [DOI] [Google Scholar]
- Adedokun, O. O. 2023. “Carcass Characteristics, Organ Proportion, Haematology, Serum Chemistry and Digestibility of Broiler Chickens Fed Umucass 36 Cassava Root Meal.” Fudma Journal of Sciences 7, no. 3: 87–92. 10.33003/FJS-2023-0703-1825. [DOI] [Google Scholar]
- Adeyemo, G. O. , and Longe O. G.. 2008. “Effects of Cottonseed Cake‐Based Diets on Performance and Egg Quality Characteristics of Layers.” Pakistan Journal of Nutrition 7, no. 4: 597–602. 10.3923/PJN.2008.597.602. [DOI] [Google Scholar]
- Aerni, P. 2006. “Mobilizing Science and Technology for Development: The Case of the Cassava Biotechnology Network (CBN).” AgBioforum 9, no. 1: 1–14. [Google Scholar]
- Agunbiade, J. A. , Tolorunji B. O., and Awojobi H. A.. 2004. “Shrimp Waste Meal Supplementation of Cassava Products‐Based Diet Fed to Broiler Chickens.” Nigerian Journal of Animal Production 31, no. 2: 182–188. 10.51791/NJAP.V31I2.1796. [DOI] [Google Scholar]
- Ahiwe, E. U. , Omede A. A., Abdallh M. B., and Iji P. A.. 2018. “Managing Dietary Energy Intake by Broiler Chickens to Reduce Production Costs and Improve Product Quality.” Animal Husbandry and Nutrition. InTech. 10.5772/INTECHOPEN.76972. [DOI]
- Ahmed, S. , Biswas M., Sunny A. R., et al. 2024. “Nutritional Evaluation of Cassava Meal Components and Maize in Securing Feed and Food.” Integrative Biomedical Research (Former Journal of Angiotherapy) 8, no. 3: 1–7. 10.25163/angiotherapy.839572. [DOI] [Google Scholar]
- Ahmed, S. , Hossain H., Hossain M. T., et al. 2026. “Cassava Root and Leaf Meal as Alternatives to Energy and Protein Sources in Broiler Diets: Impacts on Growth, Carcass Traits, Blood Biochemistry, Meat Quality.” Open Veterinary Journal 16, no. 1: 560–576. 10.5455/OVJ.2026.v16.i1.53. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Akapo, A. O. , Oso A. O., Bamgbose A. M., et al. 2014. “Effect of Feeding Cassava ( Manihot esculenta Crantz) Root Meal on Growth Performance, Hydrocyanide Intake and Haematological Parameters of Broiler Chicks.” Tropical Animal Health and Production 46, no. 7: 1167–1172. 10.1007/S11250-014-0622-5. [DOI] [PubMed] [Google Scholar]
- Akter, M. S. , Uddin M. T., and Dhar A. R.. 2023. “Advancing Safe Broiler Farming in Bangladesh: An Investigation of Management Practices, Financial Profitability, and Consumer Perceptions.” Commodities 2, no. 3: 312–328. 10.3390/COMMODITIES2030018. [DOI] [Google Scholar]
- Alade, A. A. , Bamgbose A. M., Oso A. O., et al. 2020. “Effects of Dietary Inclusion of Zymomonas mobilis Degraded Cassava Sifting on Growth Performance, Apparent Nutrient Digestibility, Ileal Digesta Viscosity, and Economy of Feed Conversion of Broiler Chickens.” Tropical Animal Health and Production 52, no. 3: 1413–1423. 10.1007/S11250-019-02146-Z/METRICS. [DOI] [PubMed] [Google Scholar]
- Aladi, N. O. , Nwafor E. J., Odoemelam V. U., Emenalom O. O., Okoli I. C., and Okeudo N. J.. 2021. “Performance, Carcass, and Organoleptic Scores of Broiler Chickens Fed Diets Containing Wet or Sun‐Dried Fermented Mixture of Grated Cassava Roots and Palm Kernel Cake as Replacements for Maize.” Tropical Animal Health and Production 53, no. 2: 255. 10.1007/S11250-021-02687-2. [DOI] [PubMed] [Google Scholar]
- Alahmari, L. A. 2024. “Dietary Fiber Influence on Overall Health, With an Emphasis on CVD, Diabetes, Obesity, Colon Cancer, and Inflammation.” Frontiers in Nutrition 11: 1510564. 10.3389/FNUT.2024.1510564/BIBTEX. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Alam, M. , Jannat M., Datta N., et al. 2024. “The Influence of Microwave‐Assisted Osmotic Dehydration in Coconut Meat Preservation Technique.” Applied Food Research 4, no. 2: 100448. 10.1016/J.AFRES.2024.100448. [DOI] [Google Scholar]
- Amos, A. T. , Kareem D. U., Amos A. O., and Idowu O. M. O.. 2021. “Nutritional Evaluation of Differently Processed Cassava‐Soya Blends in the Diets of Broiler Chickens.” Nigerian Journal of Animal Production 48, no. 2: 111–127. 10.51791/NJAP.V48I2.2929. [DOI] [Google Scholar]
- AOAC International . 2003. Official Methods of Analysis of AOAC International. 17th ed. Association of Official Analytical Chemists (AOAC). [Google Scholar]
- Ashim, K. B. , and Prabhat K. M.. 2020. “Meat Quality Analysis.” ScienceDirect. 10.1016/C2018-0-01364-X. [DOI]
- Autónoma De Yucatán, U. , Uchegbu M., Etuk M. C., et al. 2011. “Effect of Replacing Maize With Cassava Root Meal and Maize/Sorghum Brewers' Dried Grains on the Performance of Starter Broilers.” Tropical and Subtropical Agroecosystems 14, no. 1: 363–367. [Google Scholar]
- Bakare, A. G. , Cawaki P., Ledua I., et al. 2021. “Quality Evaluation of Breast Meat From Chickens Fed Cassava Leaf Meal‐Based Diets.” Animal Production Science 61, no. 6: 613–619. 10.1071/AN20031. [DOI] [Google Scholar]
- Barbut, S. 2015. “Meat Processing, Cooling and Preservation Methods.” In The Science of Poultry and Meat Processing, 313–372. University of Guelph. [Google Scholar]
- Bogosavljević‐Bošković, S. , Pavlovski Z., Petrović M. D., Dosković V., and Rakonjac S.. 2010. “Broiler Meat Quality: Proteins and Lipids of Muscle Tissue.” African Journal of Biotechnology 9, no. 54: 9177–9182. [Google Scholar]
- Chang'a, E. P. , Abdallh M. E., Ahiwe E. U., et al. 2020. “Replacement Value of Cassava for Maize in Broiler Chicken Diets Supplemented With Enzymes.” Asian‐Australasian Journal of Animal Sciences 33, no. 7: 1126–1137. 10.5713/AJAS.19.0263. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheng, Y. , Chen Y., Li X., et al. 2017. “Effects of Synbiotic Supplementation on Growth Performance, Carcass Characteristics, Meat Quality and Muscular Antioxidant Capacity and Mineral Contents in Broilers.” Journal of the Science of Food and Agriculture 97, no. 11: 3699–3705. 10.1002/JSFA.8230. [DOI] [PubMed] [Google Scholar]
- Choi, J. , Kong B., Bowker B. C., Zhuang H., and Kim W. K.. 2023. “Nutritional Strategies to Improve Meat Quality and Composition in the Challenging Conditions of Broiler Production: A Review.” Animals 13, no. 8: 1386. 10.3390/ANI13081386. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chukwukaelo, A. K. , Aladi N. O., Okeudo N. J., Obikaonu H. O., Ogbuewu I. P., and Okoli I. C.. 2018. “Performance and Meat Quality Characteristics of Broilers Fed Fermented Mixture of Grated Cassava Roots and Palm Kernel Cake as Replacement for Maize.” Tropical Animal Health and Production 50, no. 3: 485–493. 10.1007/S11250-017-1457-7/METRICS. [DOI] [PubMed] [Google Scholar]
- Coles, B. H. , Krautwald‐Junghanns M., Orosz S. E., and Tully T. N.. 2008. “Essentials of Avian Medicine and Surgery.” In Essentials of Avian Medicine and Surgery, 3rd ed., 1–397. Wiley. 10.1002/9780470692349. [DOI] [Google Scholar]
- Diarra, S. S. , Sandakabatu D., Perera D., Tabuaciri P., and Mohammed U.. 2015. “Growth Performance and Carcass Yield of Broiler Chickens Fed Commercial Finisher and Cassava Copra Meal‐Based Diets.” Journal of Applied Animal Research 43, no. 3: 352–356. 10.1080/09712119.2014.978774. [DOI] [Google Scholar]
- Elnour, Z. , Babiker M., and Habib A.. 2020. “Effect of Different Levels of Cassava Roots on Growth Performance, Carcass Traits and Meat Quality of Broiler Chickens.” International Journal of Livestock Research 10, no. 12: 20–28. 10.5455/IJLR.20200627105321. [DOI] [Google Scholar]
- Erenstein, O. , Jaleta M., Sonder K., Mottaleb K., and Prasanna B. M.. 2022. “Global Maize Production, Consumption and Trade: Trends and R&D Implications.” Food Security 14, no. 5: 1295–1319. 10.1007/S12571-022-01288-7. [DOI] [Google Scholar]
- Fathima, A. A. , Sanitha M., Tripathi L., and Muiruri S.. 2023. “Cassava ( Manihot esculenta ) Dual Use for Food and Bioenergy: A Review.” Food and Energy Security 12, no. 1: e380. 10.1002/FES3.380. [DOI] [Google Scholar]
- Fofana, D. , Ouattara A., and Diomande M.. 2023. “Effect of Cashew Meal (Anacardium Occidental) on Organ Yields and Organoleptic Characteristics of Broiler Meat in Côte D'ivoire.” International Journal of Science and Technology Research Archive 4, no. 1: 244–254. 10.53771/IJSTRA.2023.4.1.0045. [DOI] [Google Scholar]
- Hassan, A. , Tamburawa M., Alponsus C., and Yusuf J.. 2012. “Studies on Growth, Organs Weight and Haematological Parameters of Broiler Chicken Fed Graded Level of Sun‐Dried Cassava Root Meal.” Bayero Journal of Pure and Applied Sciences 5, no. 1: 98–102. 10.4314/BAJOPAS.V5I1.18. [DOI] [Google Scholar]
- Hossain, H. , Nuradji H., Miah M. Y., Islam M. N., and Siddiqui M. S. I.. 2025. “Impact of Synbiotic on Growth Performance, Histo‐Architectural Modulation of Lymphoid Organ, Hematology, Blood Biochemistry and Humoral Immune Response in Naked Neck Chicken.” Tropical Animal Health and Production 57, no. 1: 4. 10.1007/S11250-024-04254-X. [DOI] [PubMed] [Google Scholar]
- Howie, J. A. , Tolkamp B. J., Avendano S., and Kyriazakis I.. 2009. “The Structure of Feeding Behavior in Commercial Broiler Lines Selected for Different Growth Rates.” Poultry Science 88, no. 6: 1143–1150. 10.3382/PS.2008-00441. [DOI] [PubMed] [Google Scholar]
- Hussein, E. O. S. , Suliman G. M., Al‐Owaimer A. N., et al. 2019. “Effects of Stock, Sex, and Muscle Type on Carcass Characteristics and Meat Quality Attributes of Parent Broiler Breeders and Broiler Chickens.” Poultry Science 98, no. 12: 6586–6592. 10.3382/ps/pez464. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Imranuzzaman, M. , Hossain H., Pory F. S., et al. 2025. “Phytase Supplementation in Broilers: Influence on Growth Performance and Physiological Health.” Journal of Advanced Biotechnology and Experimental Therapeutics 8, no. 2: 342–352. 10.5455/JABET.2025.28. [DOI] [Google Scholar]
- Kongpechr, S. , Sukon P., and Sohsuebngarm D.. 2020. “The Study of Hematology in Commercial Broiler Chickens of Cobb 500, Ross 308, and Arbor Acres Plus.” Journal of Mahanakorn Veterinary Medicine 15, no. 2: 209–221. [Google Scholar]
- Lorenzo, I. , Serra‐Prat M., and Yébenes J. C.. 2019. “The Role of Water Homeostasis in Muscle Function and Frailty: A Review.” Nutrients 11, no. 8: 1857. 10.3390/NU11081857. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Martínez, Y. , Altamirano E., Ortega V., Paz P., and Valdivié M.. 2021. “Effect of Age on the Immune and Visceral Organ Weights and Cecal Traits in Modern Broilers.” Animals 11, no. 3: 845. 10.3390/ANI11030845. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mayulu, H. , Rahman A., and Yusuf R.. 2019. “Consumer Preference of Broiler Meat Attributes in Traditional Markets.” Hasanuddin Journal of Animal Science (HAJAS) 1, no. 2: 28–36. 10.20956/HAJAS.V1I2.9877. [DOI] [Google Scholar]
- Mir, N. A. , Rafiq A., Kumar F., Singh V., and Shukla V.. 2017. “Determinants of Broiler Chicken Meat Quality and Factors Affecting Them: A Review.” Journal of Food Science and Technology 54, no. 10: 2997–3009. 10.1007/S13197-017-2789-Z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morgan, N. K. , and Choct M.. 2016. “Cassava: Nutrient Composition and Nutritive Value in Poultry Diets.” Animal Nutrition 2, no. 4: 253–261. 10.1016/J.ANINU.2016.08.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Namakparvar, R. , Shariatmadari F., and Hossieni S. H.. 2014. “Strain and Sex Effects on Ascites Development in Commercial Broiler Chickens.” Iranian Journal of Veterinary Research 15, no. 2: 116–121. 10.22099/IJVR.2014.2349. [DOI] [Google Scholar]
- National Research Council . 1994. Nutrient Requirements of Poultry: Ninth Revised Edition. National Academies Press. [Google Scholar]
- Navid, S. , Hilmi M., Sazili A. Q., and Sheikhlar A.. 2010. “Effects of Papaya Leaf Meal, Pineapple Skin Meal and Vitamin D3 Supplementation on Meat Quality of Spent Layer Chicken.” Journal of Animal and Veterinary Advances 9, no. 22: 2873–2876. 10.3923/JAVAA.2010.2873.2876. [DOI] [Google Scholar]
- Nhlane, L. T. , Mnisi C. M., Mlambo V., and Madibana M. J.. 2021. “Effect of Seaweed‐Containing Diets on Visceral Organ Sizes, Carcass Characteristics, and Meat Quality and Stability of Boschveld Indigenous Hens.” Poultry Science 100, no. 2: 949–956. 10.1016/j.psj.2020.11.038. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nkukwana, T. T. , Muchenje V., Masika P. J., Pieterse E., Hoffman L. C., and Dzama K.. 2016. “Proximate Composition and Variation in Colour, Drip Loss and pH of Breast Meat From Broilers Supplemented With Moringa oleifera Leaf Meal Over Time.” Animal Production Science 56, no. 7: 1208–1216. 10.1071/AN14055. [DOI] [Google Scholar]
- Ogbuewu, I. P. , Emenalom O. O., and Okoli I. C.. 2017. “Alternative Feedstuffs and Their Effects on Blood Chemistry and Haematology of Rabbits and Chickens: A Review.” Comparative Clinical Pathology 26, no. 2: 277–286. 10.1007/S00580-015-2210-0/METRICS. [DOI] [Google Scholar]
- Ogbuewu, I. P. , and Mbajiorgu C. A.. 2023. “Dietary Dialium guineense Stem‐Bark Supplementation Improves Growth Performance and Haemato‐Biochemical Characteristics of Broiler Chickens.” Heliyon 9, no. 6: e17341. 10.1016/j.heliyon.2023.e17341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Okafor, B. , Kalio G., Manilla H., and Wariboko O.. 2015. “Haematology and Carcass Visual Appraisal of Broiler Chickens Fed Supplemental Diets of Aspilia Africana, Azadirachta Indica and Centrosema Pubescence Leaf Meals in Humid Tropical Nigeria.” American Journal of Experimental Agriculture 7, no. 6: 389–394. 10.9734/AJEA/2015/16152. [DOI] [Google Scholar]
- Okpara, O. , Obakanurhe O., Onowhakpor C. N., Sorhue U. G., and Gbayisomore O. S.. 2022. “Effect of Replacing Maize With Processed Cassava on the Growth Performance and Haematological Characteristics of Broiler Chickens.” Animal Nutrition and Feed Technology 22, no. 1: 155–166. 10.5958/0974-181X.2022.00013.0. [DOI] [Google Scholar]
- Okrathok, S. , Sirisopapong M., Mermillod P., and Khempaka S.. 2023. “Modified Dietary Fiber From Cassava Pulp Affects the Cecal Microbial Population, Short‐Chain Fatty Acid, and Ammonia Production in Broiler Chickens.” Poultry Science 102, no. 1: 102265. 10.1016/J.PSJ.2022.102265. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Omede, A. A. , Ahiwe E. U., Zhu Z. Y., et al. 2017. “Improving Cassava Quality for Poultry Feeding Through Application of Biotechnology. InTech.” 10.5772/INTECHOPEN.72236. [DOI]
- Otekunrin, O. A. 2024. “Cassava ( Manihot esculenta Crantz): A Global Scientific Footprint—Production, Trade, and Bibliometric Insights.” Discover Agriculture 2, no. 1: 1–20. 10.1007/S44279-024-00121-3. [DOI] [Google Scholar]
- Radikara, M. V. , Moreki J. C., Kgwatalala P. M., Mareko M. H. D., and Machete J. B.. 2016. “Meat Quality and Sensory Attributes of Orpington and Indigenous Tswana Chickens Reared Under Intensive System From Day Old to 18 Weeks of Age.” Journal of Animal Science and Veterinary Medicine 1, no. 3: 60–66. 10.31248/JASVM2016.016. [DOI] [Google Scholar]
- Rahman, M. , Hossain H., Mia M., et al. 2025. “Selection of Efficient Broiler Strain for Productive Performances and Immunity Under Local Farming System in Bangladesh.” Journal of Advanced Biotechnology and Experimental Therapeutics 8, no. 2: 218–231. 10.5455/JABET.2025.18. [DOI] [Google Scholar]
- Raquib, A. , Uddin A., Nurozzaman S. M., et al. 2022. “Seroprevalence of Mycoplasma Gallisepticum Infection in Layer Chickens of Bangladesh.” Iraqi Journal of Veterinary Sciences 36, no. 1: 9–13. 10.33899/ijvs.2020.127511.1506. [DOI] [Google Scholar]
- Sakanaka, S. , Tachibana Y., and Okada Y.. 2005. “Preparation and Antioxidant Properties of Extracts of Japanese Persimmon Leaf Tea (Kakinoha‐Cha).” Food Chemistry 89, no. 4: 569–575. 10.1016/J.FOODCHEM.2004.03.013. [DOI] [Google Scholar]
- Siddik, M. A. , Khatun M. A., Mondal S. R., et al. 2026. “Impact of Soybean Meal, Mustard Meal, Rapeseed Meal and Black Cumin on Production Performance, Egg Quality and Gut Microflora of Laying Hens.” Veterinary Medicine and Science 12, no. 2: e70863. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stupak, M. , Vanderschuren H., Gruissem W., and Zhang P.. 2006. “Biotechnological Approaches to Cassava Protein Improvement.” Trends in Food Science & Technology 17, no. 12: 634–641. 10.1016/J.TIFS.2006.06.004. [DOI] [Google Scholar]
- Sultana, F. , Ali M., and Jahan I.. 2012. “Growth Performance Meat Yield and Profitability of Broiler Chickens Fed Diets Incorporating Cassava Tuber Meal.” Journal of Environmental Science and Natural Resources 5, no. 1: 47–53. 10.3329/JESNR.V5I1.11552. [DOI] [Google Scholar]
- Ukachukwu, S. 2008. “Chemical Evaluation of Mucuna cochinchinensis as Alternative Protein Feeds Stuff.” Journal of Applied Chemistry and Agricultural Research 2, no. 1: 37–41. 10.4314/JACAR.V2I1.41106. [DOI] [Google Scholar]
- Vargas‐Ramella, M. , Pateiro M., Rois D., et al. 2022. “Effect of Breed and Diet on Carcass Parameters and Meat Quality of Spent Hens.” Annals of Animal Science 22, no. 1: 477–500. 10.2478/AOAS-2021-0036. [DOI] [Google Scholar]
- Warner, R. , Miller R., Ha M., et al. 2021. “Meat Tenderness: Underlying Mechanisms, Instrumental Measurement, and Sensory Assessment.” Meat and Muscle Biology 4, no. 2: 17–18. 10.22175/MMB.10489. [DOI] [Google Scholar]
- Wumnokol, D. P. , Magaji S. T., Magaji S. T., et al. 2023. “Performance of Broiler Chickens Fed Graded Level of Sun‐Dried Cassava Root Meal (SDCRM) Based Diets at Starter Phase.” BW Academic Journal 10, no. 1: 5. [Google Scholar]
- Yang, Y. , Lei F., Zhang Z., Liu L., Li Q., and Guo A.. 2024. “Effects of Cassava Root Meal on the Growth Performance, Apparent Nutrient Digestibility, Organ and Intestinal Indices, and Slaughter Performance of Yellow‐Feathered Broilers.” Tropical Animal Health and Production 56, no. 8: 274. 10.21203/RS.3.RS-3984805/V1. [DOI] [PubMed] [Google Scholar]
- Yi, B. , Hu L., Mei W., et al. 2011. “Antioxidant Phenolic Compounds of Cassava ( Manihot esculenta ) From Hainan.” Molecules 16, no. 12: 10157–10167. 10.3390/MOLECULES161210157. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.
