Open access peer-reviewed chapter

Aflatoxin in Fish Flour from the Amazon Region

By Ariane M. Kluczkovski and Augusto Kluczkovski Junior

Submitted: March 5th 2012Reviewed: July 29th 2012Published: January 23rd 2013

DOI: 10.5772/51948

Downloaded: 1767

1. Introduction

The Amazon region is well-known for biodiversity and nutritious food. The sustainable use of wildlife is considered strategically as an action for the conservation of the natural tropical environments and maintaining biodiversity [1]. The fish trade market, for example, comprises different countries and consumers with different intention of use, and requires a process chain of frozen fish as support. On the other hand, the Fish waste management has been of the problems with the greatest inpect on teh environment. Most of the waste is discarded or used in other fish products. Treated fish waste has found many applications among which the most important are animal feed, biodiesel/biogas, dietic products (chitosan), natural pigments (after extraction), food-packaging applications (chitosan), cosmetics (collagen), enzyme isolation, soil fertilizer and moisture maintenance in foods (hydrolysates)[2]. The muscle of some fish species with low fat, for example, can be useful in the flour production. In Brazil, the fish industries waste provides environmental pollution due to the inadequate disposable ways, in most of the cases. About 50% of the biomass produced by the industries is discarded along the process. Thus, there is an increasing interest for other ways of profitability of those wastes, since a high amount of fish protein has been lost [3]. With the increasing world population, it became necessary to search for alternative foods, to increase the demand and supply. These sources of food should be nutritious, have good sensory characteristics and be low cost, to achieve much of the population [4]. The alternative that has grown tremendously in the market is to concentrate the protein of raw materials. The protein concentrate which has a high nutritional value and has a low cost of raw material used, aims to provide a product with the human element constructor, no fat, avoiding the intake of saturated fats cause high cholesterol, obesity and other consequences negative health [3]. Thus, a more directed waste recovery of slaughtered animals can be used in the form of direct consumption by humans, or indirectly by means of the feeding [4]. This protein concentrate product could be obtained by other sources of animals such as fish [5] and soy or nuts [6, 7]. The fish flour is an alternative protein source for the natives of the Amazon region and came from the Indian culture. Beyond that, the fish flour is used as animal feed in some regions. The flour of the acari-bodó (Liposarcuspardalis) fish, for example, is called “piracui” and it is considered the “classic” fish flour. In the Tupi language, “piracuí” means fish dry fire, pounded in a mortar, grind him to powder, sifted, put into and kept in a smokehouse. The idea was born of conserving food for all the Indian tribes of the Amazon. At the time of low water (drought) had plenty of food (hunting and fishing). And at the time of the great waters (floods), food was difficult because the fish moved around. Thus was born the idea of ​​storing food: game meat (boiling them with herbs that will retain for several days). The native long dominate technique resulting in dehydration of fish product known as piracuí. Only one type of fish derived from fish muscle, dried and shredded, which represents a major source of protein, average of 70% protein of optimum digestibility in the diet of some population especially the poor [8].The production involves an artisanal drying process, with the raw material of the fish waste or the whole meat from the fish. The flour is regularly sailed in a bulk in local markets of the Amazon region at the Amazon environmental conditions with temperature above 25°C and relative humidity (RH) above 70%. In most of the markets it is sailed between other products. The illustration of the fish flour presentation is presented in Figure 1 (a and b).

Figure 1.

Fish Flour (Piracuí) presentation

It is consumed as ingredient in the local cuisine or as a protein source. Some authors reported the final product proximate composition of flour and protein concentrate as described in Table 01.

Proximate Composition of fish products
Peixoto Castro[9] aMurueta [10] bRomanelli&Schmidt [11]c
Moisture g7.311.869.9-82.52.4-3.8

Table 1.

Proximate composition of fish and fish products samples according different authors.

aSamples of piracui from Liposacus pardalis; b Protein concentrate from nine different fish species (range); c Samples of Viscera Flour from Caiman yacare; d Expressed in kcal; e Piracuí done by grilled fish; f Piracuí done by cooked fish; g expressed in g%.

The protein levels around 78% from piracuí seems to be higher than other protein concentrate obtained from other fish ranging from 57.4 to 77.8g% [10]. The fish flour is sailed in common markets and there is no color or granulometry standard, since each artisanal production region has different procedures of process. It can be visible in the product the presence of bones and collagen fibers such as showed in Figure 2.

Figure 2.

Small bones in Fish Flour (Piracuí)

The production of piracuí takes some stages and the flowchart is described in Figure 3. The fish or fish waste are washed and, the fish is eviscerated. They are cooked in an oven (100°C) and Sodium Chloride 2% is added. Then, a stage of drying is applied with temperatures of 60 to 80°C for 50 to 60 min. The material is cooled in room temperature and packaged in polyethylene bags and stored at room temperature.

The low water activity (aw) and moisture content (mc) levels in the product can increase the stability and shelf life, because the flour does not require refrigeration or low temperatures of storage, and can be kept in the environmental conditions. This is an advantage of the fish flour for some Amazon communities, because they are geographically far from the power energy supplies to keep poultry food. On the other hand, some environmental conditions from the Amazon region, such as high temperature (>30°C) and RH >80% associated to the poor safety conditions of the process can favor the contamination, especially by fungi that can be toxigenic, such as the mycotoxin producers [12]. The aflatoxin is one of those metabolic produced by some fungi strains with carcinogenic action to human beings and their level in food supply must be studied [13].

Figure 3.

Flowchart of general Fish Flour Process

They have been reported, not only in nuts and vegetable products, but also in animal feed and meat products. Some aflatoxigenic moulds have been isolated from salted fish samples such as Candidaspp., Rhodotorullaspp. and Aspergillusspp. [14]. Concerning the possibility of aflatoxigenic moulds in animal feed and to prevent contamination in the Amazon region consumers diet, a work was carried out in order to evaluate the presence of aflatoxin in fish flour samples from the Amazon Region a work was carried out concerning the evaluation of water activity (aw), moisture content (mc), aflatoxigenic fungi strains and total aflatoxin.


2. Material and methods

The total of 30 (thirty) samples (500g each) of fish flour from Brazil were collected from public markets at the Amazon region. The samples were sailed in a bulk.

The methods of analysis were:

  1. Aflatoxigenic moulds:the samples were prepared and examined according to the technique recommended by APHA [15]. The identification of isolated mould and yeast genera was carried out according to Pitt & Hocking [16]. For the evaluation of aflatoxigenic strains, we used the method of incubation of strains from coconut agar (5-7 d, 26-28° C) [17]. To the Aspergillusspp. strain, only that identified as A. flavuswere tested. After incubation the colonies were observed in UV light. The fluorescence indicative of the presence of aflatoxins was observed at the reverse of the plate.

  2. Total aflatoxin (B1+B2+G1+G2): the samples were analyzed by HPLC [18]. The Limit of Quantification (LOQ) was 0.95 µg/kg. Five points were used to build an analytical curve, in order to obtain the correlation coefficient (R) values for LOD and LOQ. Each point corresponded to a mean of five injections of each extract. The recoveries for each aflatoxin (B1, B2, G1 and G2) were: 91.0; 75.0; 95.0 and 92.0%, respectively.

Sample preparation:the samples were visually inspected in order to identify the presence of bones. The samples were finely ground in a mill (particle size <100 µm) and homogenized;

Chemicals: aflatoxin standards and trifluoroacetic acid (TFA) were purchased by Sigma-Aldrich while acetonitrile, methanol (HPLC grade) and n-hexane were purchased by Nuclear;

Instrumentation: The HPLC operating conditions were as follows: Colum type and size: C18 Supelco; 25cm x 4.6 mm id; 5 micron particle size; Temperature: room temperature 25C; Mobile phase: deionized water: acetonitrile:methanol:water (8:27:65) and the flow rate was fixed at 1.0 ml min-1; membrane filter and degassed in an ultrasonic bath for 25 min prior to use;

Standards preparation: the aflatoxin B1, B2, G1 and G2 standards (1.0 mg of each aflatoxin) in capped amber bottles) were used to the working solutions were prepared according to the AOAC [19] procedure by injecting 1 ml of acetonitrile into each vial to dissolve the aflatoxins.

Extraction and clean-up: 20 g of sample was extracted with 80 mL acetonitrile:water (9:1) mixture for 30 min by shaking under high speed and then filtered using a N°. 04 Whatman filter paper. A 1 mL portion of the filtrate was loaded on a multifunctional column and passed through at a flow rate of 2 mL/min. Then 1mL of acetonitrile:water (9:1) was applied to the column for 5 times. The filtrates were combined and evaporated to dryness under nitrogen and the residue was used for the derivatisation.

Derivatization:a 100 µl of the TFA solution and 300 µl of n-hexane were added to the residue from the sample extracted or to the aflatoxin work standards, vortexed for 30 s and kept in the dark for 15 minutes in room temperature. Nine hundred microlitres of acetonitrile:water (9:1) was added to the vial and vortexed for 30 s. The mixture was left to stand to allow the two layers to be separated. Twenty microlitres of the derivatized product (bottom layer) was injected into the HPLC column.

  1. Water activity(aw): was determined in triplicate in an Aqualab series 3TE instrument (Decagon, USA) at 25±0.1°C;

(d)Moisture Content (mc):the mclevels were determined by the gravimetric method [19];

3. Results and discussion

3.1. Aflatoxigenic moulds

All the samples (100%) presented fungi growth. The Aspergillus spp.was identified in 85% of the samples and 15 isolated were obtained and tested concerning aflatoxin production as showed in Table 02. According to other authors, Aspergillusspp. was the most frequent strain reported in feed and fish products. Hassan et al. [14] also found levels of the presence of Aspergillusspp. (66.6%). The Penicilliumspp. was found in 43% of the samples and 90% of the isolated tested for aflatoxin production was negative.

Fungi StrainsIncidence in the samples (%)Number of isolated testedaToxigenic Strains
Aspergillus spp.851585%15%
Penicillium spp.431010%90%

Table 2.

Fungi and aflatoxin production in fish four

a Strains identified as Aspergillus flavus

In our work, from the Aspergillusspp strains identified as A. flavus,85% presented aflatoxin production as showed in Figure 4. Alinezhad et al. [20] reported A. flavus(60.66%) isolated from feed ingredients as well as pellet feed. Among 37 A. flavusisolates, 19 (51.35%) were able to produce AFB1 in the range of 10.2 to 612.8 μg/g fungal dry weight. The aflatoxigenic behavior with fluorescence was showed in Figure 4.

Figure 4.

Aflatoxigenic behavior with fluorescence production fromA. flavusfrom fish flour

The presence of aflatoxigenic fungi strains can be explained by the environment contamination, since the product was disposable in room temperatures with no regards of hygienic standards. The Brazilian regulation does not require the fungi analysis in fish or fish products [21]. In the process of fish flour temperatures of > 60-80° C for 60 min are applied with the binomial time-temperature acting on the microbiological control. The fish flour is rich in protein and nutrients to be spoiled by aflatoxigenic fungi strains. Adding NaCl 2%, during the process seems to not affect efficiently as a preservative factor to avoid fungi strains. In cured fish, for example, slight inhibition of mycelial growth and/or sporulation was recorded when isolates were cultured in basal medium containing 5% sodium chloride. On the other hand, the extent of inhibition increased with increasing salt concentrations, at 25% level, all the species had their growth completely inhibited [22].

3.2. Aw, Mc and total aflatoxin

The samples presented the following results with mean (range) described in Table 03. The (a) aw: 0.65 (0.64-0.70); (b)mc: 15.5 (10.0-20.8) % and (c)total aflatoxin (B1+B2+G1+G2): 10.5 (1.5-18.0) µg/kg. The aflatoxin was found in 20% of the samples under the LOQ. All the positive samples were under the limit of the Brazilian regulation for animal feed of 50 µg/kg [23]. The 05 (five) positive samples for aflatoxin belong to the group of samples with A. flavusisolated in the fungi test, and identified as aflatoxin producers. This fact, confirms the association between the presence of aflatoxigenic strains and the aflatoxin production in fish flour samples.

Number of SamplesAwMc %Total Aflatoxin µg/kga
Mean (range)Mean (range)Positive samplesMean (range)
300.65 (0.64-0.70)15.5 (10.0-20.8)05 (20%)10.5 (1.5-18.0)

Table 3.

Aw, Mcand Total Aflatoxin in fish flour from the Amazon region

aTotal aflatoxin= B1+B2+G1+G2

The aflatoxin production in the fish flour could be affected by the levels of awand mc. Those parameters have shown to allow the toxigenic fungi strains into the aflatoxin production, as showed in other dry food, such as nuts [24]. In previous work [25], the awlevels ranged from 0.1-0.90 and the microbiological stability of piracuí was showed at aw< 0.6 if mcwill be below 10g%. The levels of our findings of mcwere higher than 10%, so these levels must be concerned, because in awbelow 0.6, there was reported shortly halophilic bacteria growth. Our results, concerning the mclevels were below 18.6%, reported by Santos & Freitas [26].

4. Conclusions

Despite the levels of aflatoxin in the samples below the limits of the Brazilian regulation for animal feed, the mycotoxin must be avoided. The studies in this matter are necessary, especially in areas such as the Amazon communities where the consumption of fish or fish products occurs 6 d/week, with 6.1 g/capital/d [27]. This data confirms that “piracuí” has an economic relevance [28]. Concerning the levels of aflatoxin found in the samples, it is necessary a work of good manufacture practices and safety storages conditions. The results of awand mcthis research provide data for the study of materials that can be used as packaging for storage of piracuí due the product to be frequently traded in the Amazon region. Concerning the significance of the fish flour for the Amazon region consumers, other studies are necessary to evaluate other toxicological aspects and the risk analysis.

© 2013 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Ariane M. Kluczkovski and Augusto Kluczkovski Junior (January 23rd 2013). Aflatoxin in Fish Flour from the Amazon Region, Aflatoxins - Recent Advances and Future Prospects, Mehdi Razzaghi-Abyaneh, IntechOpen, DOI: 10.5772/51948. Available from:

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