Quality of the Seafood in Southern Nigeria with References to Microbial Loads and Trace Metals in Citharidium ansorgii, An Endemic Fish Species
Received 28 May, 2021 |
Accepted 01 Aug, 2021 |
Published 01 Jan, 2022 |
Background and Objective: Trace metals may contaminate food sources and accumulate the agricultural product and seafood through water, air soil pollution, contamination of soil may further pose risks to human health through direct ingestion with the food chain. Hence, the microbial loads and heavy metals concentrations in Citharidium ansorgii, one of the most common fish species in Southern Nigeria were investigated to ascertain its health status. Materials and Methods: Sampling was done monthly and a total of 36 fish samples were randomly purchased from fishmongers in six major markets in the region. Bacteriological isolates were analyzed using standard bacteriological procedures, while standard identification keys and atlas were used in identifying fungal isolates. The trace metals were analyzed using the atomic absorption spectrophotometer (G105 UV-VIS). Results: The total bacteria population of C. asorgii from the markets varied from 8.40-43.10 CFU g–1. The fungi count ranged from 3.80-18.20 CFU g–1. The bacteria isolates were, Micrococcus species, Klebsiella pneumonia, Enterococcus species, Bacillus cereus, Staphylococcus albus, Actinomycetes species, Enterobacter aerogenes, Pseudomonas species, Salmonella species, Listeria monocytogenes, Yersinia species, Proteus species, Shigella species, Chromatium species. Klebsiella pneumonia, Staphylococcus albus, Shigella species and Salmonella species had the highest frequency of occurrence. The fungi isolated were Aspergillus flavus, Fusarium species, Rhizopus stolonifera, Mucor species and Trichophyton species. A. flavus, Fusarium species and Trichophyton species had the highest frequency of occurrence. The concentration ranges of the metals were, Cu, 1120-3540 μg g–1 dw, Zn, 2250-7420 μg g–1 dw, Cd, 1.60-600 μg g–1 dw and Pb, 7.80-7.20 μg g–1 dw and were above the standard limits prescribed by regulatory bodies. Conclusion: The pathogenic microorganism and heavy metals detected in the endemic fish in this region can pose serious health hazards to consumers as they are not safe for human consumption, an observation that calls for regular monitoring of the kinds of seafood in this region.
Copyright © 2022 Thomas Ohwofasa and Bosede. This is an open-access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
INTRODUCTION
Nigeria is a maritime state where nine of the thirty-six federal states have a coastline in the Atlantic Ocean. The coastal federal states of Nigeria are Ogun, Lagos, Ondo, Edo, Delta, Bayelsa, Rivers, Akwa-Ibom and Cross rivers states and are located in the southern part of the country.
It is well documented that fish is one of the major sources of food and income globally1 and the importance of the fisheries sector to individuals and the economy of many developing countries cannot be over-emphasized.
It is a major source of animal protein and contains most of the important essential amino acids, particularly lysine, methionine and tryptophan that are lacking in plant proteins2,3. Also, important essential amino acids, particularly lysine, methionine and tryptophan that are lacking in plant proteins are abundant in fishes4. They have wider acceptability in most parts of Nigeria due to their unique taste, flavor and good texture. Species such as bonga fish (Ethmalosa fimbriata) and catfish (Clarias gariepinus) are highly accepted and consumed in their smoke-dried form in Nigeria, particularly in Akwa Ibom state due to their affordability and highly delicious flesh5.
Anthropogenic activities have been a source of contamination in the aquatic environment and aquatic organisms are susceptible to contamination, especially microbial and heavy metals. The microbial organisms, which are either naturally present in the aquatic environment or from terrestrial sources often find the surface or organs of aquatic organisms for colonization6. The number and type of microorganisms found in freshly caught seafood are influenced by location, season and rate of environmental pollution.
Aquatic organisms accumulate metals in their different organs and tissues7. The accumulation of heavy metals in fish mainly depends on their concentration in food and water. Heavy metal concentration in water, sediment and aquatic animal, such as fish, could indicate the level and tendency of the population. This is important not only for the protection of the environment but for the evaluation of the quality of fish meat either captured from natural water or cultured in fishponds8. The mechanism of accumulation and storage of trace metals in aquatic organisms are diverse, varying with the chemical form of metal, mode of uptake and animal species9. Many aquatic organisms can excrete the excess proportion of their metal intake under contaminated conditions and thus maintain trace metal concentration in the body at normal levels of the essential elements10.
Microbial contamination leads to spoilage in fish and makes fishery products to be sources of various foodborne diseases and may affect not only the health of fish but also raise safety concerns with regard to human consumption. Similarly, heavy metals are potentially harmful to most organisms at some levels of exposure and absorption. The ingestion of heavy metals by fish via food and water may affect not only the productivity and reproductive capacities of such fish but also affect the health of man that depends on these organisms as a major source of protein. Heavy metals are natural components of the Earth’s crust, they cannot be degraded or destroyed. To a small extent, they enter the body via food, drinking water and air. As trace elements, some heavy metals (e.g., copper, selenium, zinc) are essential to maintain the metabolism of the human body, however, at a higher concentration they can lead to poisoning.
The poor condition in our local markets, fish handlers and fish smoking facilities may contribute to the presence of micro-organisms in smoked fish. These have led to the persistence of food poisoning which is an alarming healthy problem in developing countries where sanitation is low. Trace metals may contaminate food sources and accumulate the agricultural product and seafood through water, air soil pollution, contamination of soil may further pose risks to human health through direct ingestion with the food chain. Hence, the microbial loads and heavy metals concentrations in C. ansorgii, one of the most common fish species in Southern Nigeria was investigated to ascertain its health status.
MATERIALS AND METHODS
Study Area: The experiment was carried out in Southern Nigeria, where seafood is prevalent. From January through February 2022, the investigation was conducted.
Equipment/reagents: Sterile stomacher laboratory blender, Durham tube, McCartney bottles, Culture plates, Gallenkamp digital colony counter, Triplicate plates, Microscope, Test tubes, A sterile cotton swab, Oven, Weighing beaker and Mueller-Hinton agar plate, Peptone water, Nutrient Agar (NA), MacConkey Agar (MA), Potato Dextrose Agar (PDA), Eosin Methylene Blue (EMB), Methylene blue dye, lead, copper, cadmium, zinc, nickel, manganese and magnesium.
Collection of samples: A total of 27 samples of smoked C. ansorgii were randomly purchased from fishmongers in six major markets in Southern Nigeria (Opolo, Igbogene, Swali, Tombia, Zarama and Kpansia). The samples were collected monthly and transported to the Department of Biological Sciences laboratories of Federal University Otuoke Bayelsa State for analysis.
Microbiological analysis: The fish sample that was initially pulverized in a sterile Stomacher laboratory blender, was homogenized in 225 mL distilled water in the ratio of 1:10 dilution. Further, tenfold dilutions of the sample homogenate to 10-6 were accomplished. Aliquot 0.1 mL of appropriate dilutions were spread plated in triplicate onto Nutrient Agar (NA), for total plate count, MacConkey Agar (MA) for a coliform count and Potato Dextrose Agar (PDA) for the fungal count. One-gram samples were inoculated into Eosin Methylene Blue (EMB) broth with an inverted Durham tube in McCartney bottles and subsequent plating out on Eosin Methylene blue agar after incubation for the coliform test. Cultures on NA, MA and EMB broth were incubated for 24-48 hrs at 37°C. PDA was incubated at 28±2°C laboratory room temperature for 3-7 days.
Enumeration and identification of microbial isolates: Culture plates were examined at the expiration of the incubation period and colonies were enumerated using the Gallenkamp digital colony counter (Gallenkamp, England). Means of the total and specific microbial population from the triplicate plates were expressed as colony-forming units per mL (CFU mL–1). Colonial morphology and other cultural characteristics were observed and recorded and pure cultures of microbial isolates were obtained by repeated sub-culturing on appropriate media. Preliminary identification of bacterial isolates was based on cultural, morphological and basic biochemical characteristics, Gram staining, catalase activity, indole, methyl red, Voges Proskauer test, motility, citrate utilization, urease production, oxidase, starch hydrolysis, gelatin liquefaction, coagulase and fermentation of sugars. Further identification of bacterial isolates was based on standard bacteriological procedures and employing the Biomerieux sa API system. Confirmation for coliform organisms was based on presumptive, confirmatory and completed tests following the description of Speck11.
Fungal isolates were identified based on cultural and morphological characteristics, pigmentation on media, microscopic characteristics, sporulation, mycelia arrangement and sugar assimilation tests, concerning standard identification key and atlas12.
Sensitivity test of isolates to commonly used antibiotics and antifungal agents: Disc diffusion technique13,14 was used to carry out the susceptibility testing of the isolates. Three to five colonies of pure isolates were transferred into test tubes containing 5 mL of peptone water and incubated for 6 hrs. The turbidity of the broth culture was adjusted to that of the 0.5 McFarland standards-approximately 1-2×108 CFU mL–1 (for bacteria). Turbidity for fungal cultures was adjusted to 1-5×106 cells mL–1. A sterile cotton swab was dipped into the adjusted suspension, rotated several times and pressed firmly on the inside wall of the tube above the fluid level to remove excess inoculum from the swab. The entire dried surface of the Mueller-Hinton agar plate (Oxoid) prepared based on the manufacturer’s instruction, was evenly streak inoculated. Mueller-Hinton agar for fungal sensitivity was, however, supplemented with 2% glucose+0.5 μg mL–1 Methylene Blue Dye. The plates were allowed to stand for 5 min to allow for any excess inoculum to diffuse before introducing the discs. The following antimicrobial agents were employed, Cefuroxime (30 μg), Ceftriaxone (30 μg), Erythromycin (5 μg), Amoxycillin (25 μg), Co-trimoxazole(25 μg), Nitrofurantoin (50 μg), Gentamycin (10 μg), Nalidixic acid (15 μg), Ofloxacin (5 μg), Tetracycline (10 μg), Streptomycin (10 μg), Chloramphenicol (30 μg) and Amphotericin B (20 μg), Ketoconazole (15 μg), Fluconazole (25 μg), Griseofulvin (10 μg) and Nystatin(100 unit). The plates were incubated at 37°C for 18-24 hrs for bacteria and the fungi culture was kept at room temperature for 5 days after which the zones of inhibition were measured.
Determination of heavy metals: The fish samples collected from the markets were further dried in the laboratory at 60°C to maintain a constant dried weight (1.0 g). Digestion of the samples was done by heating the dried weight in a Teflon beaker with mixed concentrated hydrochloric acid (HCl), hydrogen tetraoxosulphate six acid (H2SO4), trioxonitrate acid (HNO3) and hydrogen peroxide (H2O2) in the ration 1:115. Immediately after the digestion process, a hundred times dilution was performed using Mili-Q water and analyzed by the atomic absorption spectrophotometer (G105 UV-VIS, Thermo Fisher Scientific, GeneSys, Madison, USA).
Data analysis: Data of the fish species from the six markets were subjected to Statistical analysis of the t-test and ANOVA two factor without replication. Additionally, data from the heavy metal assessment was compared to the acceptable standard of World Health Organization and Federal Environmental Protection Agency safety levels in regulation and guidance for fish and fisheries products16.
RESULTS
The analysis of the health status of dried C. ansorgii from major markets in Southern Nigeria revealed that the endemic fish harbours microbes and is contaminated with heavy metals in Table 1-3. The level of microbial loads depends on the market’s location, with the Igbogene market having the highest TBC 43.10×107 CFU g–1 and the Zarma market having the least 8.40×107 CFU g–1. The magnitude of contamination revealed that Igbogene> Opolo>Tombia>Kpansia>Swali>Zarama markets. The bacteria counts vary significantly among the markets (p<0.05) except for, Swali and Tombia markets, Swali and Kpansia and Swali and Zarama markets in Table 1.
The bacteria isolated from the fish shows that the fish was highly contaminated in Table 2. Micrococcus species are found in the fish from Opolo, Igbogene, Swali and Tombia markets but absent in Zarama and Kpansia markets. K. pneumonia was present in all six markets. Enterococcus species were present in Opolo and Tombia markets but absent in Igbogene, Swali, Zarama and Kpansia markets. B. cereus was present in Igbogene, Kpansia and Tombia but absent in Opolo, Swali and Zarama markets. S. albus was present in the six markets. Actinomycetes species were present in Opolo, Igbogene and Kpansia but absent in Swali, Tombia and Zarama markets. E. aerogenes was present in Opolo, Igbogene, Swali and Tombia but absent in Zarama and Kpansia markets. Pseudomonas species were present in Opolo and Kpansia but absent in Igbogene, Swali, Tombia and Zarama markets. Salmonella species were present in all six markets. L. monocytogenes were present in Opolo, Swali, Tombia and Kpansia but absent in Igbogene and Zarama markets. Yersinia species was present in Igbogene, Tombia and Kpansia but absent in Opolo, Swali and Zarama. Proteus species were present in Opolo, Igbogene, Tombia and Kpansia markets but absent in Swali and Zarama. Shigella species were present in all the markets. Chromatium species were present in Opolo, Igbogene, Tombia and Kpansia but absent in Swali and Zarama markets.
The total fungal counts of the investigated fish disclosed that Igbogene has the highest TFC (18.20×107 CFU g–1), with the least (1.10×107 CFU g–1) reported in the Zarma market. The TFCs of the endemic fish in the region shows that Igbogene>Opolo>Tombia>Kpansia>Swali>Zarama market (Table 1). Similarly, the TFCs vary significantly among the markets excepting Opolo and Igbogene markets, Swali and Zarama, Tombia and Kpansa markets (p>0.05) (Table 1).
Table 1: | Microbial load (CFU g–1) in C. ansorgii from major markets in Niger Delta, Nigeria |
Markets | Cu |
Zn |
Cd |
Pb |
Opolo | 3540±1.60a |
5120±1.50a |
2.50±0.10a |
15.20±0.60a |
Igbogene | 1120±5.30b |
5960±12.20b |
3.80±0.50b |
12.10±0.20ab |
Swali | 3840±12.10c |
7420±2.20c |
6.00±0.10c |
17.20±0.50a |
Tombia | 3420±1.40c |
2250±2.10d |
3.20±0.41b |
11.30±1.50b |
Zarama | 1360±2.20b |
2730±3.10d |
1.60±0.10d |
7.80±2.10b |
Kpansia | 3250±2.80c |
3110±5.20e |
4.00±0.50b |
12.80±1.900ab |
Recommendation limit | ||||
FEPA | 1000 |
3000 |
3 |
10 |
WHO | 2000 |
- |
3 |
10 |
Means with the same superscript and subscript within the column are not significant (p>0.05) |
Table 2: | Microbials isolated from smoked C. ansorgii from major markets in Yenagoa Metropolis, Nigeria |
Isolates | Opolo |
Igbogene |
Swali |
Tombia |
Zarama |
Kpansia |
Bacteria | ||||||
Micrococcus species | + |
+ |
+ |
+ |
- |
- |
Klebsiella pneumoniae | + |
+ |
+ |
+ |
+ |
+ |
Enterococcus species | + |
- |
- |
+ |
- |
- |
Bacillus cereus | - |
+ |
- |
+ |
- |
+ |
Staphylococcus albus | + |
+ |
+ |
+ |
+ |
+ |
Actinomycetes species | + |
+ |
- |
- |
- |
+ |
Enterobacter aerogenes | + |
+ |
+ |
+ |
- |
- |
Pseudomonas species | + |
- |
- |
- |
- |
+ |
Salmonella species | + |
+ |
+ |
+ |
+ |
+ |
Listeria monocytogenes | + |
- |
+ |
+ |
- |
+ |
Yersinia species | - |
+ |
- |
+ |
- |
+ |
Proteus species | + |
+ |
- |
+ |
- |
+ |
Shigella species | + |
+ |
+ |
+ |
+ |
+ |
Chromatium species | + |
+ |
- |
+ |
- |
+ |
Fungi | ||||||
Aspergillus flavus | + |
+ |
+ |
+ |
+ |
+ |
Fusarium species | + |
+ |
+ |
+ |
+ |
+ |
Rhizopus stolonifer | + |
- |
- |
+ |
+ |
+ |
Mucor species | - |
+ |
- |
- |
- |
+ |
Trichophyton species | + |
+ |
+ |
+ |
+ |
+ |
Aspergillus niger | + |
+ |
- |
- |
- |
+ |
Candida tropicalis | + |
+ |
+ |
+ |
- |
+ |
+: Present and -: Absent |
Table 3: | Heavy metal concentrations (μg g–1 dw) in C. ansorgii from major markets in Yenagoa Metropolis, Nigeria |
Markets | TBC (×107) |
TFC (×107) |
Opolo | 34.60a |
12.50a |
Igbogene | 43.10b |
18.20a |
Swali | 11.40cd |
1.70b |
Tombia | 17.80c |
3.80c |
Zarama | 8.40d |
1.10b |
Kpansia | 15.90c |
3.30c |
Mean with different superscripts within the column varies significantly (p<0.05), TBC: Total bacteria count and TFC: Total fungi count |
Fungal isolated from the fish shows that A. flavus and Fusarium species were present in all the markets. R. stolonifera was found in Opolo, Tombia, Zarama and Kpansia but not found in Igbogene and Swali markets (Table 2).
The heavy metals concentrations in C. ansorgii from major markets in southern Nigeria are shown in Table 3. The findings revealed that C. ansorgii sampled from the six major markets in the region was contaminated with heavy metals.
Swali had the highest level of copper concentrations (3840±12.10 μg g–1 dw) among the six major markets, while Igbogene had the least of copper concentrations (1120±5.30 μg g–1 dw). The magnitude of the copper concentration shows that Swali>Opolo>Tombia>Kpansia>Zarama> Igbogene. Statistical analysis revealed that Cu concentrations in Opolo vary significantly (p<0.05) with Igbogene and Swali markets and Igbogene varies significantly (p<0.05) with Opolo and Swali. Zarama, Kpansia and Opolo vary significantly (p<0.05). In contrast, Cu concentration in Swali, Tombia and Kpansia does not vary significantly (p<0.05). The Cu concentration in the fish from Opolo, Swali, Kpansia and Tombia markets was higher than the recommended limit set by FEPA and WHO. Also, the metal in the fish from Igbogene and Zarama markets was higher compared to that of the recommended limit of FEPA but lesser than the WHO recommendation limit. The copper concentration in Zarama is higher than the recommended limit of FEPA but lesser than that of the WHO recommendation limit (Table 3).
The Zinc concentration from the six markets shows that Swali had the highest level (7420±2.20 μg g–1 dw), while Tombia had the least (2250±2.10 μg g–1 dw). The concentration of Zn shows that Sawali>Igbogene>Opolo> Kpansia>Zarama>Tombia. Statistically, the metal concentration in Opolo varies significantly (p<0.05) with Igbogene, Swali, Tombia and Zarama, also in Igbogene, it varies significantly (p<0.05) with Opolo, Swali, Tombia and Kpansia markest. The Zn concentration in Swali varies significantly (p>0.05) with Zarama and Kpansia markets. Similarly, the Zn in Zarama, Kpansia and Opolo vary significantly (p<0.05). However, this metal concentration in Tombia does not vary significantly (p>0.05) with Zarama). The Zn concentration and their recommendation limit set by regulatory bodies are shown in Table 3.
The fish sampled from all the investigated markets had cadmium with Swali having the highest level of cadmium concentration (6.00±0.10 μg g–1 dw), while Zarama had the least (1.60±0.10 μg g–1 dw). The magnitude level of Cd concentration revealed that Swali>Kpansia> Igbigene>Tombia>Opolo>Zarama. The Cd concentration in Opolo, Igbogene, Swali and Zarama vary significantly (p<0.05). Equally, Cd in Swali varies significantly (p<0.05) with Tombia, Zarama and Opolo. Also, the metal in the fish from in Kpansia market varies significantly (p<0.05) with Opolo, Swali and Zarama. No significant difference (p>0.05) in the metal concentrations in Igbogene with Opolo Swali and Zarama. Similarly, Cd concentration in Tombia does not vary significantly (p<0.05) with Kpansia and Igbogene. The cadmium concentration in all the six major markets is greater than the recommended limit of FEPA and WHO.
Lead concentration in the fish sample also showed that Swali had the highest level (17.20±0.50 μg g–1 dw), while Zarama had the least (7.80±2.10 μg g–1 dw). The magnitude of Pb the fish shows that Swali>Opolo>Kpansia> Igbogene>Tombia>Zarama markets. The Pb concentration in opolo varies significantly (p>0.05) with Zarama only, with no significant difference (p<0.05) from other markets. Conversely, in the Igbogene market, the Pb concentration in the fish does not vary significantly (p<0.05) with Opolo, Swali, Tombia, Zarama and Kpansia. The lead concentration in Opolo, Igbogene, Swali, Tombia and Kpansia is greater than the recommended limit by FEPA and WHO.
DISCUSSION
The microbial loads of C .ansorgii, an endemic fish in major markets in Southern Nigeria revealed that all the markets in this region are highly contaminated with microbial load, with the Igbogene market, the most affected. The high level of microbial loads in this region could be attributed to the human activities in the rivers where the smoked fish was harvested. These activities include, bathing, washing of clothes or other materials, disposal of fecal matters and sewage discharges by municipal authorities and independent outfits, another possible explanation could be the unhygienic environment of the fish source and the open markets. This finding corroborated the proposition of another study17,18 that aquatic organisms, in general, accumulate contaminants from the environment and, therefore, have been extensively used in marine pollution monitoring programs.
The few microbial loads observed in the Zarama market showed that close contact with fish (handlings) enhance the distribution of microbes. Zarama is a weekly market, there is not much contact between the fishmongers and the buyers and that made the microorganism unable to grow and it also reduces the number of bacteria from the fish sample C. ansorgii unlike Igbogene, which is a daily market. This is in agreement with the submission that microbes are normally associated with the individual hygiene of the people who handle them in marketplaces19.
The bacteria isolated from all the six major markets, Micrococcus species, K. pneumonia, Enterococcus species B. cereus, S. albus, Actinomycetes species, E. aerogenes Pseudomonas species, Salmonella species, L. monocytogenes, Yersinia species, Proteus species, Shigella species, Chromatium species. K. pneumonia, S. albus, Salmonella species and Shigella species had the highest frequency of occurrence, their occurrence was following the assertion of20 when he stated that these organisms were the commonest microorganisms associated with smoked fish and were also reported by the researcher21 in his investigation on microbial load of smoke-dried fishes (Ethmalosa fimbriata and pseudotolithus elongatus) sold in Oba and Koko markets in Edo and Delta States, Nigeria at different seasons. Similarly, this investigation is in agreement with the report22 that isolated E. coli, P. aeruginosa, Salmonella paratyphi and B. cereus from freshly harvested Trypanosoma species and Crassostrea species from two different creeks in Nigeria.
All the organisms isolated from the smoked C. asorgii samples have health implications for man. For instance, Salmonella species have been reported to survive and persist in the aquatic environment and have been detected in the gut of tilapia and crabs23,24 and cause newborn meningitis and infantile diarrhea. It is one of the most important food-borne pathogens and an indication of sewage contamination and it is found to be associated with some non-human hosts, for example, reptiles25. Shigella species and Salmonella species are causative agents of illnesses like shigellosis and salmonellosis in the human who are the only reservoir of these organisms26, Some Bacillus species are known to be accountable for food poisoning and their presence as a biological hazard in smoked fish products that are consumed raw have raised many concerns with fish products27.
The fungi isolates include A. flavus, Fusarium species, R. stolonifera, Mucor species, Trichophyton species, A. niger, C. tropicalis, Trichophyton species, A. flavus, Fusarium species and Trichophyton species had the highest occurrence, the occurrence of A. flavus, Fusarium species and Trichophyton species could be because, during storage, the fish sample reabsorb moisture from the environment which then supported the growth of the microorganisms in addition to the contamination during processing, handling and display in the market stalls28. Some of the isolated fungi were identified to be spoilage inducing on smoked fish during storage29. A. niger and A. flavus have also been implicated in causing mycetoma in humans30. A. flavus is involved in allergic aspergillosis (Pulmonary aspergillosis) and also produces aflatoxin that is highly carcinogenic31.
Different metals at high concentrations were detected in the fish sample. The concentration of copper was above the limit32 of 10 μg g–1 dw. Cu is present in most aquatic environments, however, it is also toxic for fish and this is because Copper is an essential part of several enzymes and it is necessary for the synthesis of hemoglobin. Shellfish are the richest sources of Cu especially oysters and Crustaceans33. Underwood33 reported that deficiencies of Cu in infants can lead to anemia and hypoproteinemia and no deficiency of copper in adult have been reported.
The Zinc concentration in the fish from the investigation markets was higher than the recommended limit excepting Tomia and Zarama markets. Zn toxicity is characterized by symptoms of irritability, muscular stiffness and pain, loss of appetite and nausea28. However, zinc is an essential element for both animals and humans, the recommended daily allowance is 10 mg/day in growing children and 15 mg/day for adults11. It has a protective effect against the toxicities of both cadmium and lead 8. A deficiency of zinc is marked by retarded growth, loss of taste and hypogonadism, leading to decrease fertility. Zn toxicity is rare, but at concentrations in water up to 40 mg kg–1, may induce toxicity, characterized by symptoms of irritability, muscular stiffness and pain, loss of appetite and nausea32.
Cadmium was also detected in all the samples, the concentration of Cd in this fish was above the standard limit of FEPA (1000) and WHO (2000). Severe symptoms have been reported to occur with ingestions of 10-326 mg, while ingestions exceeding 350 mg can result in shock and acute renal failure (Calabrese, 1985). Humans are exposed to cadmium through food and the average daily intake for adults has been estimated to be approximately 50 mg25. The standard threshold for acute Cd toxicity would appear to be total ingestion of 3-15 mg33.
Lead was detected in all samples at a very high concentration. The highest was found in Swali and has been implicated in renal failure and liver damage in humans34.
CONCLUSION
This study has established the microbiological quality and trace metal concentration in C. asorgii in southern Nigeria. This revealed that smoked C. asorgii sold in southern Nigeria markets are highly contaminated with microorganisms and heavy metals. These revealed that samples of the C. ansorgii from the six major markets contain an unacceptable level of microorganisms and the presence of organisms such as Staphylococcus species, Shigella species and Salmonella species implies a poor sanitary condition of the water bodies from where the sample was harvested. Caution should be exercised in consuming smoked fish shaded openly because such fish could contain microbial cells and reheating may be necessary to destroy or inactive such cells. Therefore, there is a need to prevent these fish from contaminants especially the biological hazards from the air and during the processing stages. The seller should wear gloves during production and sales.
SIGNIFICANCE STATEMENT
Heavy metals are important environmental contaminants and their toxicity poses a substantial threat to ecological, evolutionary, nutritional and environmental balances. The presence of heavy metals in C. ansorgii, one of the most important seafood in Southern Nigeria, is of great concern because their toxicity can cause a variety of disorders and excessive damage due to oxidative stress caused by free radical formation. Regardless of metal, they all serve important biological activities, in plants and animals. These metals link to protein sites instead of their particular metals by displacing the original metals from their native binding sites, causing cell dysfunction and, eventually, poisoning. Heavy metals that are not digested by the body become harmful and accumulate in soft tissues after entering the human body through diet. Heavy metal exposure might lead to serious issues in the future due to their negative impact on living beings and the environment. However, their chemical coordination and oxidation-reduction characteristics have occasionally provided an added benefit to life.
REFERENCES
- Gram, L. and P. Dalgaard, 2002. Fish spoilage bacteria-problems and solutions. Curr. Opin. Biotechnol., 13: 262-266
- Amuneke, K.E., G.C. Igbodiegwu, P.A. Okeke and A.C. Adibe, 2020. Bacteriological profile of selected fish species and water sample from Otuocha River Anambra State. J. Agric. Food Sci., 18: 11-26
- Svanevik, C.S., I.S. Roiha, A. Levsen and T.L. Bjørn, 2015. Microbiological assessment along the fish production chain of the Norwegian pelagic fisheries sector-results from a spot sampling programme. Food Microbiol., 51: 144-153
- Olaleye, O.N. and T.A. Abegunde, 2015. Microbiological safety assessment of selected smoked fish in Lagos metropolis. Microbiol. Res. J. Int.
- Okon, U.C. Umana, S. Idorenyin, O.K. Fatunla, N.O.A. Essien and J. Peter, 2017. Bacterial contaminants and heavy metal accumulating potentials of fin-fishes (Synodontis obesus and Marcusenius senegalensis) from humic freshwater. J. Adv. Microbiol.
- Ibanga, I.J., E.A. Moses, E.J. Edet and A.E. Moses, 2019. Microbial and some heavy metals analysis of smoked fishes sold in urban and rural markets in Akwa Ibom State, Nigeria. Calabar J. Health Sci., 3: 73-79
- Wuana, R.A. and F.E. Okieimen, 2011. Heavy metals in contaminated soils: A review of sources, chemistry, risks and best available strategies for remediation. Int. Scholarly Res. Not.
- Ogundiran, M.A., S.O. Adewoye, T.A. Ayandiran, and S.O. Dahunsi, 2014. Heavy metal, proximate and microbial profile of some selected commercial marine fish collected from two markets in South Western Nigeria. Afr. J. Biotechnol., 13: 1147-1153
- Ali, M.M., D. Hossain, A. Al-Imran, M.S. Khan, M. Begum and M.H. Osman, 2021. Environmental Pollution with Heavy Metals: A Public Health Concern. In: Heavy Metals-Their Environmental Impacts and Mitigation. Nazal, M.K. and H. Zhao (Eds.), Intech Open, London, United Kingdom, ISBN: 978-1-83968-121-9, pp: 143-152.
- Vromman, V., N. Waegeneers, C. Cornelis, I. de Boosere and M. van Holderbeke et al., 2010. Dietary cadmium intake by the Belgian adult population. Food Addit. Contam.: Part A, 27: 1665-1673
- Djedjibegovic, J., A. Marjanovic, D. Tahirovic, K. Caklovica and A. Turalic et al., 2020. Heavy metals in commercial fish and seafood products and risk assessment in adult population in Bosnia and Herzegovina. Sci. Rep.
- Sfakianakis, D.G., E. Renieri, M. Kentouri and A.M. Tsatsakis, 2015. Effect of heavy metals on fish larvae deformities: A review. Environ. Res., 137: 246-255
- Bawuro, A.A., R.B. Voegborlo and A.A. Adimado, 2018. Bioaccumulation of heavy metals in some tissues of fish in lake Geriyo, Adamawa state, Nigeria. J. Environ. Public Health.
- Zhu, B., Z.F. Wu, J. Li and G.X. Wang, 2011. Single and joint action toxicity of heavy metals on early developmental stages of Chinese rare minnow (Gobiocypris rarus). Ecotoxicol. Environ. Saf., 74: 2193-2202
- Fan, X., L. Wu, T. Hou, J. He, C. Wang, Y. Liu and Z. Wang, 2018. Maternal bisphenol a exposure impaired endochondral ossification in craniofacial cartilage of rare minnow (Gobiocypris rarus) offspring. Ecotoxicol. Environ. Saf., 163: 514-520
- Kamaruzzaman, B.Y., K. Zaleha, M.C. Ong and K.Y.S. Wilson, 2007. Copper and zinc in three dominant brackish water fish species from Paka Estuary, Terengganu, Malaysia. Malaysian J. Sci., 26: 65-70
- Yap, C.K., A. Ismail and S.G. Tan, 2004. Heavy metal (Cd Cu Pb and Zn) concentrations in the green-lipped mussel Perna viridis (Linnaeus) collected from some wild and aquacultural sites in the west coast of Peninsular Malaysia. Food Chem., 84: 569-575
- Usero, J., C. Izquierdo, J. Morillo and I. Gracia, 2004. Heavy metals in fish (Solea vulgaris, Anguilla anguilla and Liza aurata) from salt marshes on the Southern atlantic coast of Spain. Environ. Int., 29: 949-956
- Begum, A., M.N. Amin, S. Kaneco and K. Ohta, 2005. Selected elemental composition of the muscle tissue of three species of fish, Tilapia nilotica, Cirrhina mrigala and Clarius batrachus, from the fresh water Dhanmondi Lake in Bangladesh. Food Chem., 93: 439-443
- Mansour, S.A. and M.M. Sidky, 2002. Ecotoxicology studies. 3. Heavy metals contaminating water and fish from Fayoum Governorate, Egypt. Food Chem., 78: 15-22
- Jeyasekaran, G., P. Ganesan, R. Anandaraj, R.J. Shakila and D. Sukumar, 2006. Quantitative and qualitative studies on the bacteriological quality of Indian white shrimp (Penaeus indicus) stored in dry ice. Food Microbiol., 23: 526-533
- Alderees, F. and Y.H.P. Hsieh, 2012. Real-time assessment of the microbial quality of retail shrimp using CO2 evolution rate. J. Food Prot., 75: 2190-2196
- Magan, N. and D. Aldred, 2007. Post-harvest control strategies: Minimizing mycotoxins in the food chain. Int. J. Food Microbiol., 119: 131-139
- Tayo, A., C. Bukola and A.A. Ogunjobi, 2008. Comparative effects of oven dried and sun dried on the microbiological, proximate nutrient and mineral composition of Trypanotous spp. (Periwinkle) and Crassostrea spp. (Oyster). Electronic Journal of Environment and Agricultural Food Chemistry, 7 (4), 2856-2867.
- Kiin-Kabari, D.B., A.D. Hart and P.T. Nyeche, 2017. Nutritional composition of selected shellfish consumed in Rivers State, Nigeria. Am. J. Food Nutr., 5: 142-146
- Windfield, M.D. and E.A. Groisman, 2003. Role of nonhost environments in the lifestyle of salmonella and Escherichia coli. Appl. Environ. Microbiol., 69: 3687-3694
- Sharma, M. and R. Reynnells, 2016. Importance of soil amendments: Survival of bacterial pathogens in manure and compost used as organic fertilizers. Microbiol. Spectr.
- Akinwumi, F.O. and K.T. Adegbehingbe, 2015. Microbiological analysis of three of smoked fish obtained from the Ondo State, Nigeria. Food Public Health, 5: 122-126
- Hwang, C.A., S. Sheen and V.K. Juneja, 2009. Effect of salt, smoke compound, and temperature on the survival of Listeria monocytogenes in salmon during simulated smoking processes. J. Food Sci., 74: 522-529
- Anihouvi, D.G.H., Y.E. Kpoclou, M.A. Massih, O.H.I. Afé and M.F. Assogba et al., 2019. Microbiological characteristics of smoked and smoked-dried fish processed in Benin. Food Sci. Nutr., 7: 1821-1827
- Yassin, M.F. and S. Almouqatea, 2010. Assessment of airborne bacteria and fungi in an indoor and outdoor environment. Int. J. Environ. Sci. Technol., 7: 535-544
- Agwaranze, D.I., A.C. Ogodo, C.S. Ezeonu, S.T.C. Brow, C.B. Nwaneri, L.M. Husie, 2020. Microbiological assessment of indoor and outdoor air quality in a General Hospital in North-East Nigeria. Res. J. Microbiol., 15: 9-14
- Kim, K.Y., Y.S. Kim and D. Kim, 2010. Distribution characteristics of airborne bacteria and fungi in the general hospitals of Korea. Ind. Health, 48: 236-243
- Lateef, A., 2004. The microbiology of a pharmaceutical effluent and its public health implications. World J. Microbiol. Biotechnol., 20: 167-171
How to Cite this paper?
APA-7 Style
Thomas Ohwofasa,
I., Bosede,
A.A. (2022). Quality of the Seafood in Southern Nigeria with References to Microbial Loads and Trace Metals in Citharidium ansorgii, An Endemic Fish Species. Science International, 10(1), 1-10. https://doi.org/10.17311/sciintl.2022.1.10
ACS Style
Thomas Ohwofasa,
I.; Bosede,
A.A. Quality of the Seafood in Southern Nigeria with References to Microbial Loads and Trace Metals in Citharidium ansorgii, An Endemic Fish Species. Sci. Int 2022, 10, 1-10. https://doi.org/10.17311/sciintl.2022.1.10
AMA Style
Thomas Ohwofasa
I, Bosede
AA. Quality of the Seafood in Southern Nigeria with References to Microbial Loads and Trace Metals in Citharidium ansorgii, An Endemic Fish Species. Science International. 2022; 10(1): 1-10. https://doi.org/10.17311/sciintl.2022.1.10
Chicago/Turabian Style
Thomas Ohwofasa, Ikpesu , and Ariyo Adenike Bosede.
2022. "Quality of the Seafood in Southern Nigeria with References to Microbial Loads and Trace Metals in Citharidium ansorgii, An Endemic Fish Species" Science International 10, no. 1: 1-10. https://doi.org/10.17311/sciintl.2022.1.10
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