Chukwuka, Adesida, and Alimba: Carcinogenic and non-carcinogenic risk assessment of consuming metal-laden wild mushrooms in Nigeria: Analyses from field based and systematic review studies
Abstract
This study investigated the potential health risk associated with the consumption of metal-laden mushrooms in Nigeria. Concentrations of Pb, Cd, Cr, Cu, Ni, Zn and Al in wild mushrooms collected from the Nigerian environment were measured using atomic absorption spectrometer. Also, systematic analysis of articles on metal accumulation in mushrooms from Nigeria were obtained from scientific databases. Using hazard model indices, the metal concentration in mushrooms were evaluated for their potential carcinogenic and non-carcinogenic health risk when consumed by adults and children. Zn and Cd, respectively, had the highest and lowest mean concentrations (mg kg-1) in the analysed mushrooms from the field study, while Fe and Co, respectively, had the highest and lowest mean concentrations (mg kg-1) in the systematically reviewed articles. In the field study, the percentage distribution of THQ of the heavy metals greater than 1 was 0% and 42.85% for adults and children respectively. While for the systematic study, 30% and 50% of the heavy metals for adults and children respectively exceeded the limit of 1. The hazard indices obtained from both the systematic and field studies for both age groups were all >1, indicating significant health risk. The findings from both the systematic and field studies revealed that consuming metal-laden mushrooms by adults and children increases the carcinogenic risk to Cd, Cr, and Ni since they exceeded the acceptable limit of 1E-04 stated by USEPA guideline. Based on the findings from the systematic and field studies, it suggests that consuming mushrooms collected from metal polluted substrates increases carcinogenic and non-carcinogenic health risk among Nigerians.
Keywords: Carcinogenic health risk, metal pollution, mushrooms, non-carcinogenic health risk, Nigeria, risk assessment
Introduction
Edible mushrooms are globally acknowledged as potent sources of proteins, vitamins, fibre, minerals and low cholesterol [ 1]. In addition to the nutritional value of mushrooms, they possess various therapeutic properties. Some of the bioactivities they exhibit include anti-inflammatory, antioxidant, antiviral, antibacterial, antifungal, anticancer, immuneregulatory, anti-diabetic and cholesterol-lowering activities [ 2, 3, 4, 5]. Over ten (10) different species of mushroom, with high nutritional and medicinal importance, are commonly consumed in Nigeria [ 6, 7]. However, despite the nutritional and health benefits derived from mushrooms, their ability to readily accumulate pollutants, most importantly metals, from contaminated environment and subsequently bio-concentrate these pollutants in tertiary consumers including humans, is increasingly being reported around the world [ 5, 6, 8- 12]. Human exposure to toxic chemicals through the consumption of mushrooms has been suggested a potential source of direct metal accumulation, and this poses great risk to human and wildlife (herbivores) health and survival [ 9- 11, 13]. It is important to increase research output to enable unraveling the paucity of information which exist on the plausible health effects associated with consuming mushroom laden with heavy metals by organisms at the higher trophic levels.
Mushrooms possess effective mechanisms that enhance adequate absorption and translocation of toxic chemicals from contaminated sites when compared with many other plants growing in the same or similar environment [ 14- 16]. Through the mycelium, mushrooms absorb toxic metals from the substrates into the fruiting bodies [ 11, 12, 17]. Colak et al. [ 18] reported that patients who consumed poisoned mushrooms collected from the wild expressed nausea and alteration in aspartate aminotransferase and alanine aminotransferase. Furthermore, in 2010, an incidence of lead poisoning in Zamfara State, Nigeria which claimed the lives of over 400 children within seven months [ 19], was associated with the consumption of lead-laden food crops harvested from metal contaminated soil between 2010 and 2013 [ 20]. Moszynski [ 21] had earlier reported that the Zamfara State lead poisoning epidemic may be connected with exposure to soil Pb level which exceeded 100,000 mg kg -1. Considering that the consumption of metal-laden mushroom is one of the many ways via which heavy metals gain entry into the human body system [ 22], it becomes imperative to conduct health risk assessment of consuming metal laden mushrooms. Olatunji-ojo et al. [ 11] cultivated Pleurotus ostreatus (mushroom) in Pb-contaminated rice straw and observed high accumulation of Pb in the mushroom fruit bodies. Aqueous extract of the harvested Pb laden mushroom was fed to mice and it resulted in Pb accumulation in the testes with subsequent expression of abnormal sperm morphology, abnormal testes pathology and bone marrow cell micronucleus formation. These are biomarkers of somatic and germline genetic and cellular damage, and may invariably suggest pathophysiological disorders including cancer initiation and progression [ 23].
According to the Nigeria Cancer Statistics, about 102,100 new cancer cases were diagnosed annually, while at least 71,600 mortalities occur annually, due to various stages of cancer progressions [ 6]. Due to increase in hunger (high cost of food and feeding) in Nigeria and many other countries (especially developing countries) of the world, many populations readily depend on mushrooms harvesting from the wild to avert hunger and nutritional deficiencies [ 24]. It is hypothesized that the act of ignorantly consuming wild mushrooms due to intense hunger or its uninformed use in ethnomedicine can increase exposure to heavy metals and subsequently pathophysiological disorders. Therefore, this study aimed at increasing knowledge on the possible carcinogenic and non-carcinogenic risks associated with human consumption of metal-laden mushrooms in Nigeria. The specific objectives include:
I. Heavy metal analysis of mushrooms collected from the wild,
II. Using Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) to collect data of studies on metal accumulation in mushroom from the Nigerian environment.
III. Estimation of carcinogenic and non-carcinogenic health risk associated with the consumption of mushrooms using data generated for different metals in the field and systematic review studies.
Risk assessment models that defined the tolerable intake dose and carcinogenic and non-carcinogenic risk as posited by universal standards [ 25- 28] are employed in the assessment of carcinogenic and non-carcinogenic risk herein reported.
Materials and Methods
Mushroom collection and identification
Six wild mushroom species were collected between July and September, 2021 from two local governments in Ibadan, Southwestern Nigeria ( Fig. 1). Studies in this part of the country have revealed the ethnomycological use of wild edible and medicinal mushrooms by majority (about 87.2%) of the population [ 7, 24, 29]. The mushrooms were mainly collected from decaying logs which served as substratum for their growth. The mushrooms were identified with their morphological characteristics in accordance with taxonomic classifications by Hall et al. [ 30], Loyd et al. [ 31], Mcknight and Mcknight [ 32] and Schwab [ 33]. Details of the mushroom collections are presented in Table 1.
Digestion of the collected mushroom samples and metal analysis
The mushrooms were air dried in the laboratory for 14 days and ground into powdered form using Cutting Boll Mill. The nitric-perchloric acid digestion method was employed in accordance with AOAC recommendation [ 34]. Blanks were prepared as quality control samples by applying 5 mL of concentrated nitric acid into empty digestion flasks and processed through the entire analytical method to ensure accuracy of data [ 34]. Afterwards, 0.5 grams of each air-dried sample was transferred into a 100 mL beaker and 5 mL of an acid mixture containing nitric (HNO 3) and perchloric (HClO 4) acids in the ratio 2:1 was added. The sample was heated at 120 – 150℃ for 45 minutes under a fume-hood in order to initiate the reaction process. The digestion process was completed when a clear solution was obtained. The solution was allowed to cool before further filtering through Whatman No. 42 filter paper and diluting with distilled water to 25 mL. The digested mushroom samples were then measured in triplicates to determine Pb, Cd, Cr, Cu, Ni, Al, and Zn concentrations using atomic absorption spectrophotometer (AAS; Buck Scientific model 210/211 VGP, East Norwalk, USA).
Systematic review analysis of metal accumulation in mushrooms from the Nigerian environment
Search strategy
Published scientific articles that reported toxic metals in mushrooms from the Nigeria environment were searched and selected from scientific databases: Google Scholar, PubMed, Scopus, Directory of Open Access Journals (DOAJ) Web of Science, in accordance with PRISMA (preferred reporting items for systematic reviews and meta-analysis) guidelines ( Fig. 2). Articles published between the year 1980 and 2022 were retrieved. The following keywords, phrases and clauses: “heavy metals in mushrooms from Nigeria”, AND “metal in mushrooms from Nigeria”, AND “metal contamination of mushroom from Nigeria”, AND “names of the individual metals (Pb, Cr, Cd, As, Cu etc.) contaminated mushrooms from Nigerian environment”, AND “Mushrooms collected from contaminated Nigerian environment” were used for article search. At the end, the papers were screened and re-checked in order to eliminate duplicate and unrelated papers.
Inclusion and exclusion criteria
The inclusive criteria include:
1. articles reporting concentration of heavy metals in mushrooms collected from Nigeria,
2. articles published in English language and in peer-reviewed journals,
3. articles must clearly present data of metal concentrations as mean or range.
Papers not included in this study were screened out based on the following criteria:
1. articles reporting heavy metal concentrations in non-mushroom consumables,
2. articles reporting heavy metal concentrations in mushrooms but not collected from Nigeria,
3. articles with duplicate content,
4 articles written in other languages other than English,
5. articles with only abstract available (Book of abstract from conferences).
Statistical analysis
The concentration of metals obtained from the mushroom collected from the field and the systematic review data were analyzed using GraphPad prism version 8.0™ and the results presented as Mean ± SD. These data were used to calculate the carcinogenic and non-carcinogenic health risk using the various human health risk standard models.
Health Risks Assessment
The consumption of metal laden mushrooms suggests that humans are exposed to metals via oral exposure route. Hence, the carcinogenic and non-carcinogenic health risks calculated for Nigerians that consume mushrooms containing metals were based on the estimated daily intake (EDI) of the toxic metals via ingestion of mushroom (oral route) in accordance with the United States Environmental Protection Agency [ 35] model using the threshold values. Target hazard quotients and Hazard index were calculated and the values used to evaluate the potential non-carcinogenic health risk for adult and children who may be consuming metal laden mushroom.
Estimated Daily Intake (EDI)
Daily intake of metals depends on both the metal concentration in food and the daily food consumption. Also, the body weight of exposed person can affect ability to tolerate the metal. EDI is a model that estimates or evaluates the rate of transfer of metals from consumed food substance into the human body [ 4]. EDI values for each metal is calculated using the equation below:
According to Joint FAO/WHO Expert Committee on Food Additives [ 36], average body weight for adult is considered as 70 kg, while that for children is 24 kg. Also, the average daily intake of mushroom is accepted as 0.03 kg per person [ 4]. The concentration of metals obtained from the analyses of mushrooms collected from the field and systematic review (see Tables 2 and 3 respectively) were used for the EDI evaluation and other related estimations where necessary.
Target Hazard Quotient (THQ)
Target Hazard Quotient describes the ratio of exposure to toxic substance and the reference dose which is the highest concentration at which no adverse health effects are possible or envisaged [ 6]. THQ estimated value explains the probability of non-carcinogenic health risk of consuming the mushrooms. It is estimated from calculating the ratio of the determined dose of a pollutant to a reference level considered toxic [ 4]. When the estimated value of THQ is < 1, then non-carcinogenic health effects are not expected. When THQ is >1, there is tendency that adverse health effects may occur [ 4, 8]. THQ of the heavy metals were estimated using the formula:
RfD ingestion represents oral reference dose for each specific metal: Pb = 0.004, Cd = 0.001, Cr = 0.003, Ni = 0.02, Zn = 0.3, Cu = 0.04, Al = 1, Co = 0.0003, Mn = 0.14, Fe = 0.7 [ 26, 37].
Hazard Index (HI)
Hazard Index is calculated from estimating the sum of individual values of the THQ of the studied elements in each mushroom sample. When HI value is higher than 1, it is considered a substantial risk and danger to health [ 6, 38]. The HI index is calculated as follows:
Where; THQ is the target hazard quotient estimated for each toxic element (n)
Carcinogenic Risk (CR)
Carcinogenic Risk is a measure of the likelihood of expressing or developing cancer during a lifetime as a result of exposure to carcinogens [ 26, 38]. The CR value below 1x10-4 is considered an acceptable risk, while values higher than 1x10-4 imply an increased risk of carcinogenic effect associated with exposure to the carcinogens [ 26]. The CR is calculated from the equation below:
Csf represents the oral slope factor of specific carcinogen: Pb = 0.0085, Cd = 6.3, Cr = 0.5, Ni = 0.84 [ 4, 26].
Results
Concentration of heavy metals
Table 2 presents the mean concentrations of the analysed metals observed in the collected mushroom samples. All the collected mushrooms accumulated varying concentrations of the various heavy metals. L. betulina accumulated the highest mean concentration for most of the studied metals including; Cd, Cu, Ni, Zn, and Al while P. ostreatus recorded the lowest mean concentration for Pb, Cu, Ni and Zn. The concentrations of Zn and Cd were the highest and lowest respectively in all analysed mushrooms. Fig. 3 presents morphology of the representatives of analysed mushrooms.
Estimated daily intake
Human health risk assessment of heavy metal contamination of wild mushrooms revealed that Zn and Cd had the highest and lowest mean concentrations in mushrooms obtained from the field study. While Fe and Co had the highest and lowest mean concentration according to the data generated from the analysis of the systematic review. Table 3 presents the estimated daily intake (EDI; µg/kg/day) of metals in mushrooms collected from the field study and calculated for both children and adults. The EDI (µg/kg/day) for Pb range in adult is 2.71 – 3.57 and 7.91 – 10.41 in children. Also, for Cd is 0.46 – 0.69 and 1.35 – 2.03 for adult and children respectively. Cr is 1.26 – 2.06 and 3.66 – 6.01 for adult and children respectively, Cu is 1.83 – 7.69 and 5.33 – 22.44 for adult and children respectively, Ni is 0.72 – 2.48 and 2.10 – 7.23 for adult and children respectively, Zn is 9.27 – 57.60 and 27.03 – 168.00 for adult and children respectively, and Al is 1.59 – 3.47 and 4.65 – 10.13 for adult and children respectively. For the children group, the EDI of Cd in all the studied mushrooms exceeded the Permissible Tolerable Daily Intake (PTDI) set by Joint FAO/WHO Expert Committee on Food Additives [ 36] ( Table 3).
Target hazard quotient
Table 4 presents the target hazard quotient (THQ) of the analysed metals for adult and children. The THQ for Pb is in the range 0.68 – 0.89 and 1.98 – 2.60 for adults and children respectively, Cd in the range 0.46 – 0.69 and 1.35 – 2.03 for adults and children respectively, Cr in the range 0.42 – 0.69 and 1.22 – 2.00 for adults and children respectively, Cu in the range 0.05 – 0.19 and 0.13 – 0.56 for adults and children respectively, Ni in the range 0.04 – 0.12 and 0.11 – 0.36 for adults and children respectively, Zn in the range 0.03 – 0.19 and 0.09 – 0.56 for adults and children respectively, Al in the range 0.0016 - 0.0035 and 0.0047 – 0.01 for adults and children respectively. Lenzites betulina recorded the highest THQ for most of the heavy metals for adults (Pb, Cd, Cu, Ni, Zn, Al) and children (Cd, Cu, Ni, Zn, Al) while the lowest THQ for most of the analyzed heavy metals for adults and children (Pb, Cu, Ni, Zn) was recorded in Pleurotus ostreatus ( Table 4).
Hazard Index
The Hazard indices of the analysed mushrooms collected from the filed study ranged from 1.96 – 2.69 in adults and 5.71 – 7.85 in children ( Table 4). The highest and lowest values for both of these groups were recorded in L. betulina and P. ostreatus respectively ( Fig. 4). The HI of all the mushrooms for both adult and children exceeded the threshold limit of 1. Furthermore, HI estimated for children is higher than that of the adults in all the analysed mushroom samples ( Fig. 4).
Carcinogenic risk.
The Carcinogenic Risk (CR) of the analysed heavy metals in the mushrooms collected from the field is presented in Table 5. The carcinogenic risk of Al [ 39], Cu [ 40] and Zn [ 41] was not estimated in this study since there is no evidence of their classification as carcinogens yet. According to the analysed data on Table 5, the CR for the heavy metals in adults and children respectively ranged as follows: Pb (2.30–3.04E-05 and 6.72–8.85E-05), Cd (2.92–4.37E-03 and 8.51E-03–1.27E-02), Cr (6.3E-04–1.03E-03 and 1.83–3.01E-03), and Ni (6.05E-04–2.08E-03 and 1.76–6.07E-03). The highest values for Cd and Ni for both adults and children were estimated in L. betulina. On the other hand, the lowest values for Pb and Ni in both adult and children were estimated for P. ostreatus while the lowest value for Cd in both adults and children was estimated for P. pulmonarius.
Systematic review
Inclusion of studies
A total of 48 articles were retrieved from the scientific databases. 4 of them were excluded due to duplication (Fi g. 2). The papers were screened for eligibility and 23 papers were further considered unsuitable. 21 articles fulfilled the req uired criteria for selection and were eventually included in the study ( Fig. 2).
Concentration of heavy metals
The mean concentration (mg kg -1) of heavy metals in the reviewed selected articles are in the order: Fe (255.98)>Cu (50.39)>Zn (37.72)>Mn (19.89)>Cr (10.25)>Al (9.15)>Cd (8.45)>Pb (6.49)>Ni (5.16)>Co (3.29) ( Table 6).
Health risk assessment
Analyses of EDI, THQ, HI and CR in adults and children estimated using the generated mean of the respective heavy metals in the reviewed articles were presented in Table 7. Estimated Daily Intake (EDI) analysis of heavy metals from the systematic reviewed articles ranged from 1.41–109.70 µg/kg/day for adults and 4.11–319.98 µg/kg/day for children. The lowest and highest values were respectively recorded for Co and Fe for both adults and children. The THQ analysis for heavy metals in the selected reviewed articles ranged from 0.00392–4.7 for adults and 0.011-13.66 for children. Al and Co respectively recorded the lowest and highest values for both groups. In the adult group, the THQs for Cd, Cr and Co exceeded the safe limit of 1 while the THQs for Pb, Cu, Ni, Zn, Al, Mn and Fe were within the safe limit. Albeit for the children group, the THQs for Pb, Cd, Cr, Cu and Co exceeded the safe limit of 1, while THQs for Ni, Zn, Al, Mn and Fe were within the safe limit. The HI for the adult (11.4) and children (33.2), which described the sum of all THQs for the analysed heavy metals, exceeded the acceptable limit of 1 for both the adults and children categories. The carcinogenic risk (CR) of the metals ranged from 2.36E-05 – 2.28E-02 for adults and 6.89E-05 - 6.65E-02 for children ( Table 7). The CR for Cd, Cr and Ni exceeded the acceptable limit of 1E-06 – 1E-04 while CR for Pb was within the limit for both groups.
Discussion
Heavy metal accumulation in mushrooms
Heavy metals are the oldest ubiquitous chemicals globally studied for their high levels of deleterious effects on public health [ 60- 62]. In the scientific publication “A silent epidemic of environmental metal poisoning”, Nriagu [ 63] stated that “it is incontestable that each environmental compartment has a limited carrying capacity for metal pollution and with enough time, the current rates of metal inputs will become stressful to many ecosystems”. After 30 years of the position, numerous studies abound in literature that reported high metal contamination of most aquatic and terrestrial environments of the world. Also, many other scientific reports showed that biota (both plants and animals) inhabiting these ecosystems were highly laden with different metals [ 64- 68]. Macromycetes (mushrooms) are hyper-accumulators of heavy metals. This informs its use in the cleaning up of contaminated environment [ 69]. However, the health risk associated with the possibility of consuming such mushrooms had gained little attention. According to Oyetayo [ 7], Nigerian traditional herbalists and rural dwellers exploit wild mushrooms for two main reasons: as source of nutrition (food) and biological active molecules which contains pharmaceuticals that can aid specific body functions (medicine). Some of the mushrooms used for medicinal purposes are consumed according to prescriptions to aid the treatment of various ailments. In other instance, the extracts of the fruiting bodies and mycelia of the mushrooms are utilized in the ethnomedicinal practices. The ethnomedicinal use of the wild mushrooms examined in this study has been documented by a number of Nigerian scientists [ 7, 70- 72]. According to reports, the Igbo population residing in the Southeastern Nigeria utilize G. applanatum for anti-oxidative, antihypertensive, and anti-diabetic purposes, while G. sessile is used to treat neoplasia and arthritis [ 70]. Also, the ethnomedicinal use of wild mushrooms was reported to be prevalent among the Igalas of the Northcentral Nigeria [ 71]. Considering that consuming metal laden mushrooms for ethnomedicinal purpose may increase metal accumulation in humans, this justifies the evaluation of both the edible and ethnomedicinal mushrooms collected from the wild for their carcinogenic and non-carcinogenic health risks in the study herein presented.
All the mushrooms collected from the wild had varying concentrations of heavy metals ranking in the order: Zn > Cu > Pb > Al > Cr > Ni > Cd ( Table 6). Also, data generated from the systematic review studies on metal accumulation in mushroom collected from the Nigerian environment using PRISMA ( Fig. 2) presented the mean concentrations of the metals in the order: Fe > Cu > Zn > Mn > Cr > Al > Cd > Pb > Ni > Co ( Table 3). Fe, Cu, Mn, Zn, and Cr are essential micronutrient that forms components of many important enzymes and cofactors required for adequate functioning of the body system both in plants and animals. These metals are important actors in DNA replication (synthesis), protein synthesis, improving and fostering healthy immune systems and repair and healing of damaged tissues [ 73, 74]. Howbeit, they are required in trace quantities by animals and plants, but when accumulated in the body of organisms above the permissible limit, they may induce abnormal pathophysiological processes in the body.
Metal accumulation in mushrooms had been linked to chitin, chitosan, glucan and amino polysaccharide present in the cell wall. These molecules readily absorb metals from the substrates of the mushroom and pass them to the fruiting bodies. Metals may bind to the amine-N group of the chitin which acts as the nucleation site for the absorption of metals into the mushrooms [ 69, 75]. This assertion is supported by the report that Cd accumulation in Neurospora crassa was through the N-acetylglucosamine polymer and chitin present in the fungal cell wall [ 76]. Also, these molecules were isolated from the cell wall of white rot fungus ( Coriolopsis polyzona) in an attempt to understand their role in bioaccumulation [ 77]. In the laboratory settings, the isolated molecules when used as biocatalyst successfully removed endocrine disrupting chemicals, nonylphenol, bisphenol A and personal care product ingredient, triclosan, from contaminated substrates [ 77]. Furthermore, there are some plasma membrane transporters which are similarly involved in metal ion uptake from the soil or substratum into the cytosol of the root cells. For instance, the OsNRAMP6 transporter, which is localized to the plasma membrane and expressed in the shoot system, serves as both Fe and Mn transporter in yeast [ 78]. These evolutionary acquired mechanisms that enables the absorption of essential metals by mushrooms aims at enhancing proper growth and development of mushrooms [ 73]. However, owing to the valence of non-essential metals like Pb and Cd being similar to the essential metals, most of these mushrooms rarely discriminate between absorbing essential and non-essential metals [ 73].
Differences in the rate of absorption of metals by the mushroom species (in morphological part of fruiting body and age of mycelium) and the composition of the metals in the substrates, rate of metal accumulation in mushrooms show variations [ 6, 14, 59], may possibly explain why Lenzites betulina ( Fig. 3a) accumulated the highest concentrations for most of the studied metals; Cd, Cu, Ni, Zn, Al, while Pleurotus ostreatus ( Fig. 3b) accumulated least concentrations for most of the analysed heavy metals; Pb, Cu, Ni, and Zn among the harvested mushrooms ( Table 2). Metal accumulation in mushrooms is a global menace that poses danger to public health. For instance, Świsłowski et al. [ 79] conducted a bibliometric analysis of 200 publications on metal accumulation in mushrooms from the European countries, between 2001 and 2016. The authors observed that 492 species of mushrooms (wild-growing and cultured) common in 26 European countries accumulated majorly Cd, Cu, Fe, Pb, and Zn. More than 50% of the reviewed mushrooms are edible and the studies were primarily from Turkey, Poland, Spain, and the Czech Republic [ 79]. Since it is now well established that toxic metals and other chemical elements accumulates in mushrooms, it is imperative to conduct the risk assessment to human health that may occur when metal-laden (importantly Cd, Hg and Pb) mushrooms are consumed.
Risk assessment to human health from the consumption of metal-laden mushrooms
Collection and consumption of wild mushrooms are cultural and social activities in most countries in Europe, Asia, and in the United States [ 80]. Meanwhile, mushroom consumption is a major source of food and raw material for ethnomedicine in Africa [ 81]. Therefore, exposure to heavy metals and other contaminant through mushroom consumption is imminent. Furthermore, long time consumption of metal-laden mushrooms may be detrimental to human health. Standardize models including Estimated Daily Intakes (EDI), Target Hazard Quotient (THQ), Hazard Index (HI) and Cancer Risk (CR) were used to assess the potential risk associated with the consumption of metal-laden mushroom among Nigerians. The EDI of Pb, Cd, Cr, Cu, Zn, Ni and Al by a 70kg adult and 24kg child who consume 30g of mushrooms daily as calculated from the study herein were below the permissible tolerable daily intake (PTDI) [ 36], except for EDI of Cd in all the analyzed mushroom samples by children which exceeded the PTDI limit. This observation has been similarly observed by Igbiri et al. [ 6] and Nnorom et al. [ 14] from Nigeria, except that Igbiri et al. [ 6] observed safe levels for Cd for children. The estimated THQ of all the heavy metals in the mushrooms consumed by adults were below 1 while that of Pb, Cd and Cr were above 1 in the children group suggesting a high risk of toxicity from oral exposure to these heavy metals by children. The THQ for Cd, Cr and Co exceeded the limit of 1 in the systematic analysis, hence, suggesting adverse health impact of these metals in mushrooms from Nigeria.
The HI, an index that sums up the individual values of THQ of the analyzed metals in a mushroom sample, is used to investigate the human health risk linked with exposure to multiple elements in a mushroom sample [ 5]. The HI observed for both the field and systematic analyses exceeded the acceptable limit of 1. This suggests a significant threat to the health of humans who frequently consume mushrooms in Nigeria. This finding had similarly been observed by Igbiri et al. [ 6] among Southern Nigerians. CR estimation in one per million (1 × 10 -6) suggests that in any population of 1 x 10 6 exposed people, there is possibility that at least a cancer case may be expected [ 6]. CR higher than 10 -4 indicates an increased risk of the carcinogenic effect caused by the contaminant [ 4]. The CR estimated for Cd, Cr, and Ni, in both the field study and data generated from the systematic review, exceeded the tolerable limit of 1x10-4 while the CR of Pb was within the satisfactory range of 1x10 -6 – 1x10 -4. The distinctly high value of CR for Cd, Cr and Ni may suggest they pose significant carcinogenic risk to mushroom consumers in Nigeria.
Metal accumulation in the mushrooms collected from the field and those from the systematic review is mostly due to high metal concentrations in contaminated soils/substrates. In Nigeria, solid wastes which usually serve as substrates for wild mushroom growth, contain mixtures of electronic wastes, hospital wastes, municipal wastes, industrial wastes and agricultural wastes [ 82, 83]. These wastes which are metal-laden are indiscriminately co-disposed in the Nigerian environment [ 84, 85, 86]. Since the spores from mushrooms (fungi) are airborne, the solid wastes provide good environment for their germination and growth. Although, the analyzed metals in most of the collected mushrooms were below standard permissible limits [ 36] ( Table 2), however, it is important to emphasize that heavy metals readily accumulate in both soft and hard tissue part of the body once they gain entry into the body [ 87]. It is possible they reach threshold concentrations in the body and induce deleterious health effects. Furthermore, in vitro cytotoxicity and genotoxicity study using WIL-2 NS cells [ 82], and in vivo genotoxicity study using Clarias gariepinus [ 88, 89], have confirmed that metals are capable of interacting additively, synergistically and/or antagonistically to elicit greater toxicological effects even when present in low concentrations [ 90]. The THQ, HI and CR estimated in the study herein suggest threat to quality health of humans who ignorantly may consume metal-laden mushrooms in Nigeria and other part of the world. This is expected to send signal to environmental and health organizations in Nigeria and other part of the globe to avert unforeseen severe health outbreak due to metal poisoning. This suggestion was supported by some laboratory-based research findings wherein male mice fed with aqueous extracts of Pb-laden Pleurotus ostreatus for 35 days accumulated Pb in the testes. The accumulated Pb induced decreased testicular weight, increased congestion of the blood vessels, necrosis, and disorganization of the seminiferous tubules [ 11]. Also, significant increase in abnormal sperm morphology was observed in the caudal epididymis of the exposed mice [ 11]. Furthermore, the accumulated Pb also increased micronucleated polychromatic (PCE) and normochromatic (NCE) erythrocytes and decrease PCE-NCE ratio in the bone marrow of the exposed mice compared to the control [ 11, 12].
This observation suggests abnormal reproductive toxicity and increase genome instability [ 11]. Genome instability is the hallmark of cancer development. Pb, Cd, Al, Hg, and Co observed in the mushrooms from Nigeria ( Tables 2 and 3), are among the top metals in the priority list of hazardous substances recommended for their toxicological assessment [ 91]. In fact, there has not been any known biological relevance of some of the metals in both plants and animals. For instance, considering their ability to cause chromosomal damage and subsequently tumor formation, Cd was classified as group A human carcinogen while Pb was classified as probable human carcinogen (Group 2B) [ 92]. This further suggests caution and carefulness to avoid any form of ignorance in consuming wild mushrooms and crop plants harvested from soils or substrates laden with metals. It is noteworthy to indicate that all the estimated health risk models in this study were higher for children compared to adults, suggesting that children are more susceptible to carcinogenic and non-carcinogenic health risks from oral exposure to heavy metals. Children are particularly more exposed and susceptible to toxic effects, according to recent WHO [ 28] report, because they drink more water, consume more food, and breathe more air in relation to their body weight [ 93]. The anatomic, immunologic, cognitive, and psychologic differences of children in comparison with adults account for their increased vulnerability to health risks [ 94].
Conclusions
This study filled some knowledge gaps on the possible health risks associated with consuming metal-laden mushrooms in Nigeria, as it combined both an experimental analysis and systematic review of the heavy metal contents in mushrooms from the Nigerian environment. Although, the THQ of some of the heavy metals in the experimental based analysis of mushrooms and systematic analysis were < 1, the HI revealed a significant health risk as values in both experimental and systematic analyses for adults and children age groups were > 1. The Carcinogenic Risk of Cd, Cr and Ni in adults and children exceeded the tolerable limit set by USEPA with Cadmium posing the greatest threat of cancer in both experimental and systematic analyses in the study herein presented. Based on the alignment in the findings from both the systematic and field analyses, it is suggested that consuming mushrooms collected from polluted substrates increases carcinogenic and non-carcinogenic health risk induced by metals. The deleterious effects may be higher among children than adults. Based on the findings from this study, it is recommended that the National Agency for Food and Drug Administration and Control (NAFDAC) in Nigeria promulgate guidelines for consuming mushrooms in Nigeria. These guidelines will encourage the cultivation of mushrooms in heavy metal and other pollutants free substrates. It will also educate ignorant Nigerians on the hazardousness/health impacts of consuming wild mushrooms harvested from contaminated substrates.
List of Abbreviations
AAS
Atomic absorption spectrophotometer
EDI
Estimated daily intake
FAO
Food and Agriculture Organisation
HNO3
Hydrogen trioxonitrate (v) acid
PRISMA
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
PTDI
Permissible Tolerable Daily Intake
RfDingestion
Reference dose for each specific metal
THQ
Target Hazard Quotient
WHO
World Health Organisation
Conflict of interest
The authors declare that they have no competing interests.
This study strictly adhered to guide for plant sample collection from the field stipulated in the Department of Botany, University of Ibadan, Nigeria.
Notes
CRediT author statement
CGA: Conceptualization, Supervision, Resources, Validation, Writing-Reviewing & Editing, Writing-Original draft preparation, Investigation; KSC: Supervision, Resources, Validation, Writing-Reviewing and Editing, Investigation; SOA: Investigation, Resources, Formal analysis, Writing-Reviewing and Editing, Writing-Original draft preparation
References
1. Nakalembe I, Kabasa JD, Olila D. Comparative nutrient composition of selected wild edible mushrooms from two agroecological zones, Uganda. Springerplus 2015;4: 433 https://doi.org/10.1186/s40064-015-1188-z.
2. Kosanić M, Ranković B, Rančić A, Stanojković T. Evaluation of metal concentration and antioxidant, antimicrobial, and anticancer potentials of two edible mushrooms Lactarius deliciosus and Macrolepiota procera. J Food Drug Anal 2016;24(3):477-484 https://doi.org/10.1016/j.jfda.2016.01.008.
3. Moro C, Palacios I, Lozano M, D’Arrigo M, Guillamón E, Villares A, et al. Anti-inflammatory activity of methanolic extracts from edible mushrooms in LPS activated RAW 264.7 macrophages. Food Chemistry 2012;130(2):350-355 https://doi.org/10.1016/j.foodchem.2011.07.049.
4. Nowakowski P, Markiewicz-Żukowska R, Soroczyńska J, Puścion-Jakubik A, Mielcarek K, Borawska MH, et al. Evaluation of toxic element content and health risk assessment of edible wild mushrooms. Journal of Food Composition and Analysis 2020;96: 103698 https://doi.org/10.1016/j.jfca.2020.103698.
5. Nowakowski P, Naliwajko SK, Markiewicz-Żukowska R, Borawska M, Socha K. The two faces of Coprinus comatus – Functional properties and potential hazards. Phytother Res 2020;34(11):2932-2944 https://doi.org/10.1002/ptr.6741.
6. Igbiri S, Udowelle NA, Ekhator OC, Asomugha RN, Igweze ZN, Orisakwe OE. Edible mushrooms from Niger Delta, Nigeria with heavy metal levels of public health concern: A human health risk assessment. Recent Pat Food Nutr Agric 2018;9(1):31-41 https://doi.org/10.2174/2212798409666171129173802.
8. Alsafran M, Usman K, Rizwan M, Ahmed T, Al Jabri H. The carcinogenic and non-carcinogenic health risks of metal(oid)s bioaccumulation in leafy vegetables: a consumption advisory. Front Environ Sci 2021;9: 742269 https://doi.org/10.3389/fenvs.2021.742269.
9. Anyakorah CI, Nwude D, Jinadu T. Lead accumulation in oyster mushroom, Pleurotus tuber-regium (Sing) from a continuously lead contaminated soil. Mycosphere 2015;6(2):145-149 https://doi.org/10.5943/mycosphere/6/2/4.
11. Olatunji-Ojo AM, Alimba CG, Adenipekun CO, Bakare AA. Experimental simulation of somatic and germ cell genotoxicity in male Mus musculus fed extracts of lead contaminated Pleurotus ostreatus (white rot fungi). Environ Sci Pollut Res Int 2020;27(16):19754-19763 https://doi.org/10.1007/s11356-020-08494-w.
12. Onifade RS, Alimba CG, Adenipekun CO, Bakare AA. White rot fungus (Pleurotus pulmonarius) cultivated on lead contaminated rice straw induced haematotoxicity and lead accumulation in liver and kidney of Wistar rats. Journal of Drug Metabolism & Toxicology 2016;7(2):1000210 https://doi.org/10.4172/2157-7609.1000210.
14. Nnorom IC, Eze SO, Ukaogo PO. Mineral contents of three wild-grown mushrooms collected from forests of South Eastern Nigeria: an evaluation of bioaccumulation potentials and dietary intake risks. Scientific African 2020;8: e00163. https://doi.org/10.1016/j.sciaf.2019.e00163.
15. Svoboda L, Zimmermannová K, Kalac P. Concentrations of mercury, cadmium, lead and copper in fruiting bodies of edible mushrooms in an emission area of a copper smelter and a mercury smelter. Sci Total Environ 2000;246(1):61-67 https://doi.org/10.1016/s0048-9697(99)00411-8.
17. Širić I, Humar M, Kasap A, Kos I, Mioč B, Pohleven F. Heavy metal bioaccumulation by wild edible saprophytic and ectomycorrhizal mushrooms. Environ Sci Pollut Res Int 2016;23(18):18239-18252 https://doi.org/10.1007/s11356-016-7027-0.
18. Colak S, Kandis H, Afacan MA, Erdogan MO, Gunes H, Kaya E, et al. Assessment of patients who presented to the emergency department with mushroom poisoning. Hum Exp Toxicol 2015;37(7):725-731 https://doi.org/10.1177/0960327114557902.
19. Galadima A, Garba ZN. Heavy metals pollution in Nigeria: Causes and consequences. Elixir Pollution 2012;45: 7917-7922.
20. Tirima S, Bartrem C, von Lindern I, von Braun M, Lind D, Anka SM, et al. Food contamination as a pathway for lead exposure in children during the 2010–2013 lead poisoning epidemic in Zamfara, Nigeria. J Environ Sci 2018;67: 260-272 https://doi.org/10.1016/j.jes.2017.09.007.
24. Oguntoye AO, Eades NT, Ezenwa MO, Krieger J, Jenerette C, Adegbola M, et al. Factors associated with young adult engagement with a web-based sickle cell reproductive health intervention. PEC Innovat 2022;1: 100063 https://doi.org/10.1016/j.pecinn.2022.100063.
30. Hall IR, Stephenson SL, Buchanan PK, Yun W, Cole ALT. Edible and poisonous mushrooms of the world. Timber Press; 2003. p. 349.
32. Mcknight KH, Mcknight VB. A field guide to mushrooms of North America (Peterson field guides). Houghton Mifflin Company; 1998. p. 409.
33. Schwab A. Mushrooming with confidence; a guide to collecting edible and tasty mushrooms. Skyhorse; 2012. p. 172.
38. Antoine JMR, Hoo Fung LA, Grant CN. Assessment of the potential health risks associated with the aluminium, arsenic, cadmium and lead content in selected fruits and vegetables grown in Jamaica. Toxicol Rep 2017;4: 181-187 https://doi.org/10.1016/j.toxrep.2017.03.006.
43. Adebiyi AO, Adeyemi FP. Bioaccumulation of heavy metals in the fruiting bodies of four edible mushrooms collected from polluted areas in Akure, Ondo State, Nigeria. EAS Journal of Nutrition and Food Sciences 2020;2(2):19-23 https://doi.org/10.36349/easjnfs.2020.v02i01.004.
45. Alofe FV, Odeyemi O, Oke OL. Three edible wild mushrooms from Nigeria: Their proximate and mineral composition. Plant Foods Hum Nutr 1996;49(1):63-73 https://doi.org/10.1007/BF01092523.
46. Ayodele S, Odogbili OD. Metal impurities in three edible mushrooms collected in Abraka, Delta State. Micología Aplicada Internacional 2010;22(1):27-30.
47. Edosomwan EU, Akpaja EO, Iyoha D. Analysis of bacteria, helminths eggs and heavy metals in tropical mushrooms sold in selected markets in Benin City. Botany Research International 2013;6(1):17-22 https://doi.org/10.5829/idosi.bri.2013.6.1.506.
48. Eze CS, Amadi JE, Emeka AN. Survey and proximate analysis of edible mushrooms in Enugu State, Nigeria. Annals of Experimental Biology 2014;2(3):52-57.
49. Ihugba UA, Nwoko CO, Tony-Njoku FR, Ojiaku AA, Izunobi L. Heavy metal determination and health risk assessment of Oyster mushroom Pleurotus tuberregium (Fr.) Singer, collected from selected markets in Imo State, Nigeria. American Journal of Environmental Protection 2018;6(1):22-27 https://doi.org/10.12691/env-6-1-4.
50. Ijioma BC, Ihediohanma NC, Onuegbu NC, Okafor DC. Nutritional composition and some anti-nutritional factors of three edible mushroom species in southeastern Nigeria. European Journal of Food Science and Technology 2015;3(2):57-63.
51. Ita BN, Essien JP, Ebong GA. Heavy metal levels in fruiting bodies of edible and non-edible mushrooms from the NigerDelta region of Nigeria. Journal of Agriculture & Social Sciences 2006;2: 84-87.
52. Ita BN, Ebong GA, Essien JP, Echnok SI. Bioaccumulation potential of heavy metals incredible fungal sporocarps from the Niger Delta region of Nigeria. Pakistan Journal of Nutrition 2008;7(1):93-97 https://doi.org/10.3923/pjn.2008.93.97.
53. Jonathan SG, Okon CB, Oyelakin AO, Oluranti OO. Nutritional value of oyster mushroom (Pleurotus ostreatus) (Jacq. Fr) Kumm. cultivated on different agricultural wastes. Nature and Science 2012;10(9):186-191 Available from: https://ir.bowen.edu.ng:8443/handle/123456789/1441.
54. Nnorom IC, Jarzyńska G, Drewnowska M, Dryżałowska A, Kojta A, Pankavec S, et al. Major and trace elements in sclerotium of Pleurotus tuber-regium (Ósū) mushroom- Dietary intake and risk in southeastern Nigeria. Journal of Food Composition and Analysis 2013;29(1):73-81 https://doi.org/10.1016/j.jfca.2012.10.001.
55. Nwokeke UG, Enyoh CE. Contamination and dietary intake risks assessment of heavy metals in some species of wild edible mushrooms grown in southern Nigeria. World News of Natural Sciences 2021;39: 1-10.
56. Okwulehie IC, Ogoke JA. Bioactive, nutritional and heavy metal constituents of some edible mushrooms found in Abia State of Nigeria. International Journal of Applied Microbiology and Biotechnololgy Research 2013;1: 7-15.
57. Omaka N, Offor IF, Ehiri RC. Fe, Pb, Mn, and Cd concentrations in edible mushrooms (Agaricus campestris) grown in Abakaliki, Ebonyi State, Nigeria. World Academy of Science, Engineering and Technology 2014;8(11):84-88.
58. Onyedinma UP, Nwaru EC, Chukwu PO, Ajong AB, Dehmchi F. Evaluation of risk caused by intake of trace metal through consumption of Pleurotus tuber-regium collected around automobile village in Abia State. Bulletin of the Chemical Society of Ethiopia 2021;35(2):229-241 https://doi.org/10.4314/bcse.v35i2.2.
59. Udochukwu U, Nekpen BO, Udinyiwe OC, Omeje FI. Bioaccumulation of heavy metals and pollutants by edible mushroom from Iselu market, Benin City. International Journal of Current Microbiology and Applied Sciences 2014;3(10):52-57.
64. Lambertucci SA, Donázar JA, Huertas AD, Jiménez B, Sáez M, Sanchez-Zapata JA, et al. Widening the problem of lead poisoning to a South-American top scavenger: lead concentrations in feathers of wild Andean condors. Biological Conservation 2011;144(5):1464-1471 https://doi.org/10.1016/j.biocon.2011.01.015.
65. Li Y, Qin J, Wei X, Li C, Wang J, Jiang M, et al. The risk factors of child lead poisoning in China: a meta-analysis. Int J Environ Res Public Health 2016;13(3):296-309 https://doi.org/10.3390/ijerph13030296.
66. Liu W, Zhou Q, An J, Sun Y, Liu R. Variations in cadmium accumulation among Chinese cabbage cultivars and screening for Cd safe cultivars. J Hazard Mater 2010;173(1-3):737-743 https://10.1016/j.jhazmat.2009.08.147.
67. Lo YC, Dooyema CA, Neri A, Durant J, Jefferies T, Medina Marino A, et al. Childhood lead poisoning associated with gold ore processing: a village-level investigation-Zamfara State, Nigeria, October–November 2010. Environ Health Perspect 2012;120(10):1450-1455 https://doi.org/10.1289/ehp.1104793.
68. Slaninova A, Machova J, Svobodova Z. Fish kill caused by aluminium and iron contamination in a natural pond used for fish rearing: a case report. Vet Med-Czech 2014;59(11):573-581 https://doi.org/10.17221/7821-VETMED.
70. Akpaja EO, Isikhuemhen OS, Okhuoya JA. Ethnomycology and usage of edible and medicinal mushrooms among the Igbo people of Nigeria. International Journal of Medicinal Mushrooms 2003;5(3):313-319 https://doi.org/10.1615/InterJMedicMush.v5.i3.100.
71. Ayodele SM, Akpaja EO, Adamu Y. Some edible and medicinal mushrooms found in Igala land in Nigeria and their sociocultural and ethnomycological uses. In: 5th International Medicinal Mushroom Conference. Nantong, China; 2009, 526–531.
72. Ogidi OC, Oyetayo OV, Akinyele JB. Wild medicinal mushrooms: potential applications in phytomedicine and functional foods. IntechOpen; 2020 [cited Mar 23, 2023] Available from: https://doi.org/10.5772/intechopen.90291.
74. Brown KH, Wuehler SE, Peerson JM. The importance of zinc in human nutrition and estimation of the global prevalence of zinc deficiency. Food and Nutrition Bulletin 2001;22(2):113-125 https://doi.org/10.1177/156482650102200201.
77. Cabana H, Jiwan JH, Rozenberg R, Elisashvili V, Penninckxe M, Agathos SN, et al. Elimination of endocrine disrupting chemicals nonylphenol and bisphenol A and personal care product ingredient triclosan using enzyme preparation from the white rot fungus, Coriolopsis polyzona. Chemosphere 2007;67(4):770-778 https://doi.org/10.1016/j.chemosphere.2006.10.037.
78. Peris-Peris C, Serra-Cardona A, Sánchez-Sanuy F, Campo S, Ariño J, San-Segundo B. Two NRAMP6 isoforms function as iron and manganese transporters and contribute to disease resistance in rice. Mol Plant Microbe Interact 2017;30(5):385-398 https://doi.org/10.1094/MPMI-01-17-0005-R.
79. Świsłowski P, Dołhańczuk-Śródka A, Rajfur M. Bibliometric analysis of European publications between 2001 and 2016 on concentrations of selected elements in mushrooms. Environ Sci Pollut Res 2020;27: 22235-22250 https://doi.org/10.1007/s11356-020-08693-5.
81. Alemu F. Cultivation of Pleurotus ostreatus on Grevillea robusta leaves at Dilla University, Ethiopia. Journal of Yeast and Fungal Research 2014;5(6):74-83 https://doi.org/10.5897/JYFR2014.0139.
82. Alimba CG, Dhillon V, Bakare AA, Fenech M. Genotoxicity and cytotoxicity of chromium, copper, manganese and lead, and their mixture in WIL2-NS human B lymphoblastoid cells is enhanced by folate depletion. Mutat Res Genet Toxicol Environ Mutagen 2016;798-799: 35-47 https://doi.org/10.1016/j.mrgentox.2016.02.002.
83. Alimba CG, Gandhi D, Sivanesan S, Bhanarkar MD, Naoghare PK, Bakare AA, et al. Chemical characterization of simulated landfill soil leachates from Nigeria and India and their cytotoxicity and DNA damage inductions on three human cell lines. Chemosphere 2016;164: 469-479 https://doi.org/10.1016/j.chemosphere.2016.08.093.
84. Alimba CG, Laide AW. Genotoxic and cytotoxic assessment of individual and composite mixture of cadmium, lead and manganese in Clarias gariepinus (Burchell 1822) using micronucleus assay. Nucleus 2019;62: 191-202 https://doi.org/10.1007/s13237-019-00289-w.
85. Alimba CG, Adewumi OO, Binuyo OM, Odeigah PGC. Wild black rats (Rattus rattus Linnaeus, 1758) as zoomonitor of genotoxicity and systemic toxicity induced by hazardous emissions from Abule Egba unsanitary landfill, Lagos, Nigeria. Environ Sci Pollut Res Int 2021;28(9):10603-10621 https://doi.org/10.1007/s11356-020-11325-7.
86. Alimba CG. DNA and systemic damage induced by landfill leachates and health impacts of human exposure to landfills in Lagos and Ibadan, Nigeria [dissertation]. Nigeria: University of Ibadan; 2013.
88. Alimba CG, Bakare AA, Latunji CA. Municipal landfill leachates induced chromosome aberrations in rat bone marrow cells. African Journal of Biotechnology 2006;5(22):2053-2057.
89. Fagbenro OS, Alimba CG, Bakare AA. Experimental modelling of the acute toxicity and cytogenotoxic fate of composite mixtures of chromate, copper and arsenate oxides associated with CCA preservative using Clarias gariepinus (Burchell 1822). Environ Anal Health Toxicol 2019;34(3):e2019010. https://doi.org/10.5620/eaht.e2019010.
90. Bae DS, Gennings C, Carter Jr. WH, Yang RS, Campain JA. Toxicological interactions among arsenic, cadmium, chromium and lead in human keratinocytes. Toxicol Sci 2001;63(1):132-142 https://doi.org/10.1093/toxsci/63.1.132.
93. Alidadi H, Sany SBT, Oftadeh BZG, Mohamad T, Shamszade H, Fakhari M. Health risk assessments of arsenic and toxic heavy metal exposure in drinking water in northeast Iran. Environ Health Prev Med 2019;24(1):59 https://doi.org/10.1186/s12199-019-0812-x.
Figure 1.
Map of study area showing the sampling site
Figure 2.
PRISMA flow chart for the systematic review report on heavy metal concentrations of mushrooms in Nigeria
Figure 3.
presents the harvested mushrooms evaluated for heavy metal accumulation: (a) Lenzites betulina; (b) Pleurotus ostreatus; (c) Calocybe indica; (d) Pleurotus pulmonarius; (e) Ganoderma sessile; (f) Ganoderma applanatum
Figure 4.
showing the hazard indices of the analysed mushroom sampled from the southwest region of Nigeria
Table 1.
Collected mushrooms, sample locations, common names, and the ethnomycological use among Nigerians.
Mushroom samples |
Sampling site |
Sampling coordinates
|
Common name |
Use |
Latitude |
Longitude |
Lenzites betulina
|
Amina way, University of Ibadan |
70 26’54.6’’N |
30 54’2.7’’E |
Birch maze-gill, Gilled polypore |
Medicine |
Pleurotus ostreatus
|
Eketa Omo Street, Oki, Ibadan |
70 25’13.4’’N |
30 59’57’’E |
Oyster |
Edible |
Calocybe indica
|
Obong Road, University of Ibadan |
70 27’0.8’’N |
30 54’11.3’’E |
Milky white mushroom |
Edible |
Pleurotus pulmonarius
|
Eketa Omo Street, Oki, Ibadan |
70 25’13.4’’N |
30 59’57’’E |
Lung Oyster |
Edible |
Ganoderma sessile
|
Amina way, University of Ibadan |
70 26’54.6’’N |
30 54’2.7’’E |
NA |
Medicine |
Ganoderma applanatum
|
Ijoma Road, University of Ibadan |
70 26’58.9’’N |
30 54’13.1’’E |
Artist’s conk |
Medicine |
Table 2.
Mean heavy metal concentrations (mg kg-1) in mushrooms collected from the field in southwest Nigeria
Mushroom samples |
Pb |
Cd |
Cr |
Cu |
Ni |
Zn |
Al |
Lenzites betulina
|
8.26±0.25 (8.0–8.5) |
1.62±0.06 (1.56–1.68) |
4.21±0.13 (4.06–4.30) |
17.95±0.22 (17.7–18.1) |
5.78±0.18 (5.60–5.95) |
134.4±2.35 (132.0–136.7) |
8.1±0.2 (7.90–8.30) |
Pleurotus ostreatus
|
6.33±0.29 (6.0–6.5) |
1.13±0.07 (1.08–1.21) |
4.81±0.31 (4.50–5.11) |
4.26±0.05 (4.2–4.30) |
1.68±0.03 (1.64–1.70) |
21.63±0.15 (21.5–21.8) |
4.28±0.25 (4.01–4.50) |
Calocybe indica
|
8.07±0.21 (7.9–8.3) |
1.24±0.06 (1.19–1.31) |
3.14±0.22 (2.96–3.38) |
6.38±0.08 (6.3–6.45) |
2.18±0.11 (2.08–2.30) |
28.7±0.52 (28.1–29.0) |
3.72±0.19 (3.51–3.89) |
Pleurotus pulmonarius
|
8.33±0.42 (8.0–8.8) |
1.08±0.06 (1.01–1.13) |
2.94±0.10 (2.85–3.05) |
6.83±0.06 (6.8–6.9) |
2.32±0.15 (2.14–2.41) |
38.5±0.87 (38.0–39.5) |
5.37±0.38 (5.1–5.8) |
Ganoderma sessile
|
7.83±0.83 (6.9–8.5) |
1.31±0.03 (1.29–1.34) |
2.93±0.05 (2.90–2.98) |
13.37±0.25 (13.1–13.6) |
3.28±0.11 (2.97–3.22) |
36.3±0.44 (36.0–36.8) |
7.27±0.21 (7.1–7.5) |
Ganoderma applanatum
|
6.57±0.40 (6.1–6.8) |
1.52±0.04 (1.48–1.56) |
3.14±0.11 (3.02–3.22) |
11.29±0.46 (10.9–11.8) |
2.96±0.11 (2.84–3.06) |
37.1±0.96 (36.0–37.8) |
4.47±0.29 (4.3–4.8) |
Table 3.
Estimated daily intake of heavy metals (μg/kg/day) analysed in mushrooms collected during the field study.
Mushrooms |
Lead
|
Cadmium
|
Chromium
|
Copper
|
Nickel
|
Zinc
|
Aluminum
|
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
Lenzites betulina
|
3.54 |
10.33 |
0.69 |
2.03 |
1.80 |
5.26 |
7.69 |
22.44 |
2.48 |
7.23 |
57.60 |
168.00 |
3.47 |
10.13 |
Pleurotus ostreatus
|
2.71 |
7.91 |
0.48 |
1.41 |
2.06 |
6.01 |
1.83 |
5.33 |
0.72 |
2.10 |
9.27 |
27.03 |
1.83 |
5.35 |
Calocybe indica
|
3.46 |
10.08 |
0.53 |
1.55 |
1.35 |
3.93 |
2.73 |
7.98 |
0.93 |
2.73 |
12.30 |
35.87 |
1.59 |
4.65 |
Pleurotus pulmonarius
|
3.57 |
10.41 |
0.46 |
1.35 |
1.26 |
3.68 |
2.93 |
8.54 |
0.99 |
2.90 |
16.50 |
48.13 |
2.30 |
6.71 |
Ganoderma sessile
|
3.36 |
9.79 |
0.56 |
1.64 |
1.26 |
3.66 |
5.73 |
16.71 |
1.41 |
4.10 |
15.60 |
45.38 |
3.12 |
9.09 |
Ganoderma applanatum
|
2.82 |
8.21 |
0.65 |
1.90 |
1.35 |
3.93 |
4.84 |
14.11 |
1.27 |
3.70 |
15.90 |
46.38 |
1.92 |
5.59 |
PTDI [36] |
NA |
0.83 |
NA |
500 |
NA |
300 – 1000 |
140 |
Table 4.
Target hazard quotient and hazard index of heavy metals in mushrooms
Mushrooms |
Lead
|
Cadmium
|
Chromium
|
Copper
|
Nickel
|
Zinc
|
Aluminum
|
Hazard Index (∑THQ)
|
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
Lenzites betulina
|
0.89 |
2.58 |
0.69 |
2.03 |
0.60 |
1.75 |
0.19 |
0.56 |
0.12 |
0.36 |
0.19 |
0.56 |
0.0035 |
0.01 |
2.69 |
7.85 |
Pleurotus ostreatus
|
0.68 |
1.98 |
0.48 |
1.41 |
0.69 |
2.00 |
0.05 |
0.13 |
0.04 |
0.11 |
0.03 |
0.09 |
0.0018 |
0.0054 |
1.96 |
5.73 |
Calocybe indica
|
0.87 |
2.52 |
0.53 |
1.55 |
0.45 |
1.31 |
0.07 |
0.19 |
0.05 |
0.14 |
0.04 |
0.12 |
0.0016 |
0.0047 |
2.00 |
5.84 |
Pleurotus pulmonarius
|
0.89 |
2.60 |
0.46 |
1.35 |
0.42 |
1.23 |
0.07 |
0.21 |
0.05 |
0.15 |
0.06 |
0.16 |
0.0023 |
0.0067 |
1.96 |
5.71 |
Ganoderma sessile
|
0.84 |
2.45 |
0.56 |
1.64 |
0.42 |
1.22 |
0.14 |
0.42 |
0.07 |
0.21 |
0.05 |
0.15 |
0.0031 |
0.0091 |
2.09 |
6.09 |
Ganoderma applanatum
|
0.71 |
2.05 |
0.65 |
1.90 |
0.45 |
1.31 |
0.12 |
0.35 |
0.06 |
0.19 |
0.05 |
0.16 |
0.0019 |
0.0056 |
2.05 |
5.96 |
Table 5.
Carcinogenic risk of heavy metals in analyzed mushroom sample
Mushroom Sample |
Pb
|
Cd
|
Cr
|
Ni
|
Tolerable limit |
AD |
CHL |
AD |
CHL |
AD |
CHL |
AD |
CHL |
L. betulina
|
3.01E-05 |
8.78E-05 |
4.37E-03 |
1.27E-02 |
9.00E-04 |
2.63E-03 |
2.08E-03 |
6.07E-03 |
1E-06 - 1E-04 |
P. ostreatus
|
2.30E-05 |
6.72E-05 |
3.05E-03 |
8.88E-03 |
1.03E-03 |
3.01E-03 |
6.05E-04 |
1.76E-03 |
C. indica
|
2.94E-05 |
8.57E-05 |
3.35E-03 |
9.76E-03 |
6.75E-04 |
1.97E-03 |
7.85E-04 |
2.29E-03 |
P. pulmonarius
|
3.04E-05 |
8.85E-05 |
2.92E-03 |
8.51E-03 |
6.30E-04 |
1.84E-03 |
8.35E-04 |
2.44E-03 |
G. sessile
|
2.86E-05 |
8.32E-05 |
3.53E-03 |
1.03E-02 |
6.30E-04 |
1.83E-03 |
1.18E-03 |
3.44E-03 |
G. applanatum
|
2.40E-05 |
6.98E-05 |
4.10E-03 |
1.20E-02 |
6.75E-04 |
1.97E-03 |
1.07E-03 |
3.11E-03 |
Table 6.
Data of metal concentrations (mg kg-1) in mushroom collected from Nigeria obtained from systematic review of published articles
References |
Study location |
Pb |
Cd |
Cr |
Cu |
Ni |
Zn |
Al |
Co |
Mn |
Fe |
[42] |
Akure, Ondo |
12.10 |
ND |
ND |
7.43 |
ND |
15.31 |
ND |
17.53 |
34.90 |
ND |
[43] |
Akure, Ondo |
10.61 |
25.11 |
66.59 |
649.03 |
36.48 |
ND |
ND |
ND |
ND |
1051.19 |
[44] |
Ife, Osun |
ND |
ND |
0.62 |
ND |
0.53 |
18.07 |
ND |
0.23 |
ND |
ND |
[45] |
Ife, Osun |
ND |
ND |
0.44 |
0.54 |
0.35 |
34.86 |
ND |
0.86 |
2.85 |
ND |
[46] |
Delta |
ND |
ND |
0.70 |
5.07 |
3.95 |
ND |
ND |
ND |
33.47 |
8.02 |
[47] |
Edo State |
ND |
ND |
ND |
ND |
ND |
51.00 |
ND |
ND |
ND |
442.00 |
[48] |
Enugu |
ND |
ND |
ND |
7.00 |
ND |
5.20 |
ND |
ND |
17.7 |
16.80 |
[6] |
Rivers |
0.51 |
0.22 |
ND |
8.72 |
2.22 |
33.78 |
0.29 |
ND |
ND |
ND |
[49] |
Imo |
0.13 |
ND |
ND |
0.164 |
0.0001 |
1.26 |
ND |
ND |
ND |
ND |
[50] |
Imo |
ND |
ND |
ND |
1.86 |
ND |
9.41 |
ND |
ND |
4.77 |
412.69 |
[51] |
Akwa Ibom |
0.86 |
0.25 |
ND |
39.52 |
ND |
90.81 |
ND |
ND |
27.77 |
505.07 |
[52] |
Akwa Ibom |
0.82 |
0.41 |
ND |
29.92 |
0.97 |
47.27 |
ND |
ND |
29.09 |
ND |
[53] |
Bayelsa |
3.75 |
0.20 |
0.60 |
5.43 |
ND |
180.00 |
ND |
0.81 |
28.5 |
584.75 |
[10] |
Ibadan, Oyo |
55.41 |
77.68 |
ND |
75.04 |
ND |
ND |
ND |
ND |
ND |
ND |
[54] |
Abia & Imo |
0.74 |
0.048 |
0.26 |
6.20 |
0.43 |
23.00 |
18.00 |
0.049 |
18.00 |
52.00 |
[14] |
Abia & Imo |
1.35 |
0.79 |
2.55 |
3.51 |
2.14 |
25.56 |
ND |
0.29 |
18.59 |
106.69 |
[55] |
Rivers & Imo |
ND |
0.001 |
ND |
0.07 |
ND |
0.583 |
ND |
ND |
ND |
1.82 |
[56] |
Abia |
1.88 |
0.83 |
ND |
15.49 |
ND |
51.02 |
ND |
ND |
ND |
ND |
[57] |
Ebonyi |
0.52 |
0.69 |
ND |
ND |
ND |
ND |
ND |
ND |
3.05 |
50.79 |
[58] |
Abia |
0.76 |
0.14 |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
74.50 |
[59] |
Benin, Edo |
1.49 |
3.47 |
ND |
1.71 |
4.56 |
16.66 |
ND |
ND |
ND |
21.44 |
Mean ± S.D |
6.49±14.58 |
8.45±21.89 |
10.25±24.85 |
50.39±155.96 |
5.16±11.11 |
37.72±44.57 |
9.15±12.52 |
3.29±6.98 |
19.89±12.01 |
255.98±321.31 |
Table 7.
Estimated Daily Intake, Target Hazard Quotient, Hazard Index and Carcinogenic Risk of heavy metals in mushroom samples from various states in Nigeria.
Heavy metals |
EDI (μg/kg/day)
|
THQ = EDI/RfDingestion
|
CR = EDI*SF
|
AD |
CHL |
AD |
CHL |
AD |
CHL |
Pb |
2.78 |
8.11 |
0.695 |
2.03 |
2.36E-05 |
6.89E-05 |
Cd |
3.62 |
10.56 |
3.62 |
10.56 |
2.28E-02 |
6.65E-02 |
Cr |
4.39 |
12.81 |
1.46 |
4.27 |
2.19E-03 |
6.41E-03 |
Cu |
21.59 |
62.99 |
0.54 |
1.57 |
ND |
Ni |
2.21 |
6.45 |
0.11 |
0.32 |
1.85E-03 |
5.42E-03 |
Zn |
16.17 |
47.15 |
0.054 |
0.16 |
ND |
Al |
3.92 |
11.44 |
0.00392 |
0.011 |
ND |
Co |
1.41 |
4.11 |
4.7 |
13.66 |
ND |
Mn |
8.52 |
24.86 |
0.061 |
0.18 |
ND |
Fe |
109.70 |
319.98 |
0.157 |
0.46 |
ND |
∑THQ (HI) |
|
|
11.4 |
33.2 |
|
|
|