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Brazilian Journal of Poultry Science

Print version ISSN 1516-635X

Rev. Bras. Cienc. Avic. vol.15 no.1 Campinas Jan./Mar. 2013

http://dx.doi.org/10.1590/S1516-635X2013000100010 

Traceability of animal meals in Japanese quail eggs using the technique of 13C e 15N* stable isotopes

 

 

Mori CI; Ducatti CII; Pizzolante CCIII; Kakimoto SKIV; Denadai JCV

IProfessor at UNESP - Registro Experimental Campus
IIProfessor of the Department of Physics and Biophysics/IBB/UNESP/Botucatu
IIIResearcher of Agência Paulista de Tecnologia dos Agronegócios/Brotas
IVDVM - Granjas Kakimoto
VPh. D. student at the Department of Animal Science /FMVZ/UNESP/Botucatu

Correspondence

 

 


ABSTRACT

The objective of this study was to trace the inclusion of bovine meat and bone meal (BMBM) in the diet of Japanese quails by analyzing eggs and egg fractions (yolk and albumen) by the technique of carbon-13 (13C) and nitrogen-15 (15N) stable isotopes. In the trial, 120 Japanese quails were distributed in six treatments with four replicates of five birds each. The following treatments were applied: feed based on corn and soybean meal, containing graded BMBM inclusions (0, 1, 2, 3, 4 or 5%). After 42 days, 20 eggs per treatment were randomly collected for three consecutive days. Ten eggs were used for yolk and albumen sample collection, and ten for total egg sample collection. It was possible to detect the dietary inclusion of 1% BMBM in the egg and its fractions. Therefore, the technique of isotopes 13C and 15N is able of tracing since 1% inclusion level of BMBM in the diet of Japanese quails in eggs and their fractions.

Keywords: Carbon-13, Coturnix coturnix japonica, bovine meat and bone meal, certification, nitrogen-15.


 

 

INTRODUCTION

The increasing demands for food quality and safety has forced farmers and agribusinesses to change their production systems in order supply to their customers products that are reliably and provenly safe.

Global food incidents, such as BSE (Bovine Spongiform Encefalopathy) or "mad cow disease", dioxin contamination, allergens, genetically modified organisms, pesticide and heavy metal contamination, and avian fly have scared consumers, who now demand safe food supply.

During the last decades, the stable isotope technique has been increasingly applied in agricultural, ecological, and physiological research, and has shown to be a reliable method to study processes related to nutrient digestion, absorption, and metabolism in humans and animals, as well as to identify the origin and quality of animal and vegetable products (González-Martin et al. 2001; Gonzáles-Martin et al., 1999; Piasentier et al., 2003).

Denadai et al. (2005), using the double isotope axis (δ13C and δ15N), analyzed eggs produced in two farms of the region of Bastos, São Paulo, Brazil. One of the farmers informed that layers were fed only vegetable feedstuffs, whereas the other, said animal ingredients were used. The authors indeed found different isotope patterns, and suggested the possibility of tracing the inclusion of animal meals in layer diets in the final product (eggs).

Therefore, methodologies that detect animal by-products in the diet of Japanese quail layers analyzing their eggs should ensure reliable information on this product, as well as allow certification of origin by governmental regulation agencies. This would ensure the safety of Japanese quail eggs, which consumption has significantly increased in the last few years, particularly when consumed as preserved eggs.

Japanese quails are an important sector of the Brazilian poultry industry, as shown by its accelerated growth during the last few years. According to IBGE data (2010), the inventory of Japanese quails housed in Brazil between 2005 and 2010 doubled, going from 6.8 million to 13 million birds, representing an increase of approximately 90%, which is very significant when compared with the 12.96% increase in the numbers of layer chickens during the same period. Egg production increased from 117,638,000 to 232,398,000 dozen or 97.55%.

The objective of this study was to trace the inclusion of bovine meat and bone meal (BMBM) in the diet of Japanese quails by analyzing eggs and egg fractions (yolk and albumen) by the technique of carbon-13 (13C) and nitrogen-15 (15N) stable isotopes.

 

MATERIALS AND METHODS

The field experiment was carried out at the facilities of the Research and Development Unit of Brotas of the Agribusiness Technology Agency (Agência Paulista de Tecnologia dos Agronegócios - APTA) of the Agriculture Department of the State of São Paulo. Feeds and eggs were analyzed at the Center of Environmental Stable Isotope Center of the Biosciences Center of UNESP, Botucatu campus. In this trial, 120 Japanese quail females were reared under the same management conditions, with feed and water offered ad libitum. Birds were housed in a 3.0 m wide and 12.0 m long barn made of bricks, with open sides with 0.50 m high walls and 1.50 m high wire mesh, side curtains, and clay-tile roof. Birds were distributed in 24 100 cm long, 34 cm deep, and 16-cm high cages divided in four 25 cm internal compartments that housed five birds each, totaling 20 birds per cage (170 cm2 per bird). Each cage compartment was equipped with a nipple drinker and a trough feeder placed in front of the cage. Natural and artificial light were provided 16 hours per day at an intensity of 22 lumen m-2, and timer was used to control the light period during the entire experimental period. Maximal and minimal temperatures were daily recorded using a thermometer placed at the center of the barn. A completely randomized experimental design was applied, with six treatments with four replicates each. Each cage, which four divisions contained five birds each, was considered one replicate. The following treatments were applied: T0 - control feed based on corn and soybean meal with no inclusion of bovine meat and bone meal (BMBM); T1 - 1% BMBM inclusion; T2 - 2% BMBM inclusion; T3 - 3% BMBM inclusion; T4 - 4% BMBM inclusion; and T5 - 5% BMBM inclusion.

Protein, calcium, phosphorus, metabolizable energy, and amino acid levels of the feedstuffs used in the experimental diets were estimated according to Rostagno et al. (2005). The chemical analysis showed that the used BMBM contained 93.75% dry matter (DM), 45.75% crude protein (CP), 8.43% ether extract (EE), and 48.17% ash content (A).

The experimental diets (Table 1) were formulated to supply birds' nutritional requirements, as established by Rostagno et al. (2005), and to contain equal energy, protein, calcium, phosphorus, methionine+cystine, and lysine levels.

After egg production peak, birds were fed the experimental diets for 42 days (Table 1) in order to replace carbon and nitrogen in the tissues for those present in the experimental diets.

After 42 days of the beginning of the experiment, 20 eggs per treatment were randomly collected for three consecutive days. Ten eggs were used for yolk and albumen sample collection, and ten for total egg sample collection.

Yolk and albumen were separated and placed in duly identified plastic bags, whereas entire eggs (yolk + albumen) were homogenized in a food processor and also placed in duly identified plastic bags. Samples were then frozen at -20ºC until processing. At processing, samples were thawed and dried in a forced-ventilation oven (Marconi - model MA 035) at 56°C for 24 h (albumen) and for 48 h (egg and yolk). Dried samples were then frozen in a cryogenic mill (Spex-model 6750 freezer/mill) at -190°C. Freeze-milling of the samples were carried out in two steps: pre-freezing for one minute and then freezing and grinding to powder for 5 min. This procedure allowed obtaining particle sizes smaller than 60 mm (Rosa et al., 2002).

After grinding, egg (yolk + albumen) and yolk samples were de-fatted in ethylic ether in a Soxhlet apparatus for 4 h, and ground again to obtain a homogenous mixture. This extraction is necessary, according to Tieszen et al. (1983), because lipid-rich fractions are poorer in 13C relative to those with lower lipid content.

Analyses were conducted at the Stable Isotopes Center of the Biosciences Institute of UNESP, Botucatu campus, SP, Brazil. Samples were weighed and approximately 50-60 µg and 500-600 µg were placed in tin capsules to determine carbon and nitrogen isotope ratios, respectively. For feed analysis, volumes of 60-70 µg and 1600-1700 µg were used, respectively.

Capsules were introduced using an automatic sampler in the element analyzer (EA 1108 - CHN - Fisons Instruments, Rodano, Italy), in which samples were burnt, producing CO2 and N2. These gases were separated in gas chromatography column and analyzed in an isotope ratio mass spectrometer (Delta S - Finnigan MAT, Bremen, Germany).

Sample isotope composition was determined using a mass spectrometer (DELTA-S, Finnigan Mat) coupled to an element analyzer (EA 1108 CHN).

Isotope ratio values were expressed as delta per thousand relative to PeeDee Belemnite (PDB) international standards for 13C, and atmospheric air nitrogen for 15N, according to the following general equation:

d

Where: R represents the ratio between the least and the most abundant isotope, in particular 13C/12C and 15N/14N. Adimensional.

The obtained isotope results were submitted to multivariate analysis of variance (MANOVA) with the aid of the GLM procedure (General Linear Model) of the statistical program SAS (1999).

Data were generated by the error matrix of each tissue, and then graphically distributed into regions (ellipses) at 95% confidence level to detect possible isotope pair differences as a function of experimental treatments. In order to be different from the control treatment, the confidence region of a determined treatment (ellipse) cannot overlap any of the graph axes (control treatment). When an ellipse overlaps one of the axes, the difference between 13C and 15N treatment means is equal to zero, and therefore, there are no differences among the evaluated treatments.

 

RESULTS AND DISCUSSION

Table 2 shows that 13C isotope values increased as the percentage of meat and bone meal (BMBM) dietary inclusion increased. This was probably due to the variations in the percentage composition of the dietary ingredients. As diets were formulated to contain equal energy and protein levels, when BMBM inclusion increased, soybean meal and soybean oil levels were reduced and corn inclusion increased. This 13C and 15N isotope enrichment is consistent with the findings of Oliveira et al. (2010), Carrijo et al. (2006), Gottmann (2007), Mori et al. (2007, 2008) e Denadai et al. (2008), who used animal meal in poultry diets (broilers, meat-type Japanese quails, and commercial layers).

 

 

According to Vogel (1993), carbon-13 dietary enrichment may be due to the isotope enrichment of C4 plants relative to C3 plants, which d13C vary between -9 and -16 and -22 and -34, respectively, considering plant species and analyzed part. DeNiro & Esptein (1978) observed the animal meals used as feedstuffs reflect the isotope signal of the animal from which they derive, and it is around 2 for δ13C.

The d15N to 14N ratio in plants changes according to how plants fix nitrogen. Soybeans have a δ15N value around one unit, which is close to the standard N2 (d15N = 0.0 ± 1.0) because it fixes nitrogen from the air (Handley & Raven, 1992; Werner & Schimidt, 2002). Plants that cannot fix atmospheric N2 depend mostly on nitrogen soil content, which may present significant differences as a function of fertilization (Choi et al. 2002). When nitrogen is absorbed from organic matter, d15N is higher, around 5. Negative d15N values are observed in dry and sandy soils, which organic matter content is very low. When manure is added as natural soil fertilizer, isotope fractioning is high, with d15N around 10 (Shibuya et al., 2006).

Moreover, isotope values of animal meals used as feedstuffs reflect the isotope signal of the animal from which they derive, and are around 2 for δ13C (Deniro & Esptein, 1978) and around 3 (2-5) for d15N, because body nitrogen as a whole is enriched as trophic level increases (Deniro & Esptein, 1981).

There was an increasing enrichment of d13C and d15N in eggs and their fractions (Table 3), similar to diet enrichment due to the inclusion of increasing BMBM levels. Although each egg fraction belonging to a same treatment presented different isotope signature, the obtained values are consistent with those presented by Deniro & Epstein (1976; 1978; 1981), who said that animals are what they isotopically eat, with ± 2 variation for 13C and ± 3 for 15N.

One week before the beginning of the experiment, egg (n=12) and diet (n=2) samples were collected and isotopically analyzed. Egg presented d13C = -20.13± 0.10 and d15N = 4.14 ± 0.15, whereas diets showed d13C = -17.66 ± 0.18 and d15N = 1.10 ± 0.16. When the experimental diets started to be fed, these values changed (Table 3), with complete replacement by the isotopes present in the experimental diets. This finding is in agreement with Denadai et al. (2006), who showed that there is complete carbon replacement in egg tissue in 24.5 to 33.6 as experimental diet changes.

In order to be considered different from the control group, the confidence region of any determined treatment cannot overlap any axis of the graph. The fact of the ellipse overlaps one the axes shows that the d13C and d15 difference between the compared treatments is equal to zero, and therefore, treatments are not different. It was observed that in eggs (yolk + albumen), isotope pair mean for the treatment with 1.0% BMBM inclusion was different from the control treatment, because the confidence region did not overlap the graph axis where the difference was equal to zero for nitrogen-15 (Figure 1). As BMBM dietary levels increased, the distance of the isotope pairs from the graph axes increased, presenting statistical difference from the treatment consisting of the strictly vegetable diet.

 

 

The same trend observed for eggs was detected in the yolk fraction (Figure 2), with difference of the 1.0% BMBM from the strictly vegetable treatment (T0) and the same linear increase in the distance of the confidence ellipses from the axes as animal meal inclusion in the diet increased.

 

 

In the albumen fraction, isotope pair means of the treatment with 1.0% inclusion BMBM were different from the strictly vegetable treatment (T0) (Figure 3). Although the confidence ellipses presented increasing linearity, these overlapped for the treatment with the dietary inclusion of 2.0% and 3.0% BMBM.

 

 

The variations among fractions are not well understood yet. According to Tiezen et al. (1983), different biochemical fractions are isotopically different, and isotope differences in the body may be a reflex of their different biochemical compositions. Fractions are poorer in lipids would possibly have higher d13C values than those with higher lipid content, being relatively poor in 13C. However, in the present study, this was not observed, as the behavior of the entire egg and the yolk fraction was similar to that of the albumen fraction, which lipid content is lower.

The BMBM detection level in the eggs obtained in the present study was lower than that found by Denadai et al. (2008, 2011) in commercial layer chickens. This may have been due to metabolism differences between these two species, as well as between the numbers of replicates between these studies.

The figures above show that any internal egg fraction, i.e., both egg and albumen can be used to detect the inclusion of BMBM in the diet of Japanese quail layers from the level of 1.0%. When birds are fed animal meals since their first day of life, dietary animal meal inclusion can be immediately detected, because quails start lay at 38 days of age. Moreover, it is possible to trace animal meals in Japanese quail feeding also in the albumen, which is faster to process than other egg fractions and meat because it dehydrates faster. For instance, 48 hours are required to dry yolk, whereas 24 hours are necessary when albumen is used. Another advantage is that albumen is poor in fatty acids, reducing the fat-extraction step during sample processing.

 

CONCLUSION

Under the conditions of the present experiment, it may be concluded that the technique of 13C and 15N stable isotopes is capable of tracing the inclusion of 1% or more of bovine meat and bone meal in the diet of Japanese quail layers by analyzing eggs and their fractions.

 

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Correspondence to:
Cleusa Mori
Rodovia Br 116 Km 460 - Caixa Postal 122
CEP: 11900-000 Registro, São Paulo
cleusamori@uol.com.br

Submitted: January/2011
Approved: October/2012

 

 

* Post-doctorate grant given by Fundação de Amparo a Pesquisa do Estado de São Paulo Process n. 2007/06707-8

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