Peninsular Malaysia has historically supported large nesting populations of green turtles (Chelonia mydas), predominantly found in the east-coast state of Terengganu (Redang and Perhentian Islands, Kemaman and Kerteh) and surrounding islands. Green turtles recorded the highest nesting density, with between 2,000 and 2,500 nests annually in that state. The species can also be found in Melaka and some parts of Pahang (Chendor and Cherating) and Perak (Pantai Remis), as well as the states of Sabah and Sarawak in East Malaysia Borneo (Chan, 2006). The green turtle was added to the IUCN (International Union for Conservation of Nature) Red List of threatened species in 1982 and it is also listed in Appendix I of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES). This program basically prevents any marine turtle parts or products from being misused or traded for commercial purposes, as their population faces a high risk of extinction.

In Malaysia, one of the most significant threats contributing to the decline of green turtle nesting is the commercial harvest for food and excessive collection of eggs for local consumption (Aguirre et al., 2006; TRAFFIC Southeast Asia for WWF-Malaysia, 2009; Jolis et al., 2015; Brei et al., 2016; Azlina et al., 2019). The long-standing problem of local demand for turtle eggs in the states of Sabah and Terengganu remains active. In Terengganu, other species of marine turtle eggs are allowed to be marketed except the eggs of leatherback turtle (Abd Mutalib et al., 2013). Furthermore, state laws of different states differ with regard to the sale and consumption of turtle eggs (TRAFFIC Southeast Asia for WWF-Malaysia, 2009). Only Sabah and Sarawak have total protection for these endangered marine animals because they are totally prohibited from any trade in marine turtles, parts and products due to the implementation of the Sabah Wildlife Conservation Enactment 1997 and Sarawak Wildlife Protection Ordinance 1998, respectively. Yet, illegal collection and consumption of turtle eggs are still uncontrollable due to insufficient man-power to monitor the areas.

Consumption of turtle products (eggs, meat, adipose tissue, organs and blood) is typical in some regions. Therefore, green turtles are harvested and exploited for their parts, such as their meat, eggs and organs, which are consumed as an important source of protein for coastal communities, for religious and cultural reasons as well as for traditional medicine purposes (TRAFFIC Southeast Asia for WWF-Malaysia, 2009). The consumption is believed to be related to fertility that works as a natural aphrodisiac, although there is no scientific evidence to prove it. Thus, turtles (meat and eggs) are among the many species of reptiles that are most intensely abused worldwide (Magnino et al., 2009; Hochberg and Bhadelia, 2016). Human perceptions might be one of the challenges to extensively publicizing the idea of marine turtle conservation. According to a survey, majority of the respondents consume marine turtle eggs due to its delicacy and the belief of nutritious and rare diet (TRAFFIC Southeast Asia for WWF-Malaysia, 2009). Some of them consume the egg just out of curiosity, especially the first-timers. In addition, some older generation consumers are unaware that marine turtle populations are declining as they believe that marine turtles produce a large number of eggs in each season (Abd Mutalib et al., 2013).

There are relatively few studies conducted on the quality of these products, raising concerns about public health risks due to pathogenic and environmental contaminants. Marine turtles are known as an excellent biological indicators of heavy metals because they can accumulate contaminants in the ecosystems they live in (Al-Rawahy et al., 2007; Yipel et al., 2017). Some factors that influence the toxicity of heavy metals, whether essential or not, include dosage, type of chemical, route of exposure, along with gender, genetics, age and nutritional status of the exposed individuals. According to a previous study, persistent organic pollutants (POPs) were found deposited in the turtle egg during vitellogenesis or development of follicles, which later become eggs (Stewart et al., 2011). It shows that pollutants can be transferred to the egg through maternal transfer and contaminate the reproductive organs where eggs are developed (Sinaei and Bolouki, 2017). Lots of studies have been done and suggested that consumption of sea turtle products (tissues, eggs, and blood) might pose a number of public health concerns because of their high lipid content and the presence of bacteria, parasites, and environmental contaminants (Aguirre et al., 2006; Van de Merwe et al., 2009; Warwick et al., 2013; Al-Musharafi et al., 2015). Nursing women and children are most likely to be affected following consumption of turtle eggs (Aguirre et al., 2006). It is unacceptable to assume that consumption of these products carries zero risk to health, even if well cooked, and possibly creates potential health hazards if consumed raw. It is vital to analyse the quality of green turtle eggs as a food source. Apparently, egg consumption may pose a health threat to the consumer and lead a population decline of green turtles. Therefore, the present study was conducted to determine the nutritional composition, pathogenic bacteria and heavy metal contaminations of green turtle eggs from Terengganu and Sabah, Malaysia.

Typically, green turtle egg is a soft-shelled egg with the size of a ping-pong ball. However, the size of turtle eggs varies amongst marine turtle species, with the Hawksbill turtle having the smallest egg size of 3.8 cm in diameter and weighing approximately 28 g, while the largest egg size belongs to the Leatherback turtle at 5.3 cm in diameter and weighing 90 g. The development of green turtle eggs can be influenced by both biotic and abiotic factors (Wallace et al., 2006). For example, the dietary intake of female green turtles is essential for the production of eggs, especially the egg yolk that contains proteins, fatty acids, fat-soluble antioxidants (vitamins A, E and carotenoids) and lipids. In fact, fatty acids and carotenoids are vital for the development of embryonic tissues of the green turtle egg. Other than seagrass, some green turtle populations in certain habitats depend on marine algae, invertebrates, and fish for their diets. Apparently, green turtle egg is an amniotic egg, which consists of membranes that protect the embryo while the eggshell allows for gas, heat and moisture exchanges with the external environment (Ackerman, 1997; Robinson and Paladino, 2013). Therefore, any microbial or heavy metal contamination will probably affect the composition of the eggs.

Green turtle eggs are not commercially used for human consumption as chicken eggs are. Chicken eggs are more suitable as primary food for humans and are more preferred to consume than turtle eggs due to the high nutritional quality (Réhault-Godbert et al., 2019). Meanwhile, green turtle eggs have to be protected solely for the continuity of the species. However, this endangered species is getting popular for consumption, especially the eggs. This raised a concern that the phenomenon might trigger a public health risk due to insufficient data on its nutritional properties. The present study revealed that there was not much difference in the overall turtle egg parameters collected from different sampling sites of Terengganu and Sabah, although the average weight of the green turtle egg was higher in Terengganu but lower in height and diameter of the eggs.

Protein and fat contents were slightly higher in Terengganu, while moisture content was the lowest composition recorded in the turtle eggs. This shows that protein is a major component of the nutritional composition in green turtle eggs, likely due to the consumption of seagrass as the main diet of female green turtles (Wyneken et al., 2013). In fact, seagrass contains high protein, especially during summer (Pradheeba et al., 2011) and contributes to the nutritional composition of its consumers. A previous study revealed similar protein and fat contents but different moisture content in Hermann’s tortoise egg (Stvarnik et al., 2017). On the other hand, moisture and protein contents are the highest components in Olive ridley (Lepidochelys olivacea) eggs (Castro-González and Romo, 2011). The differences in nutritional compositions between different species of turtle could be due to species variations in dietary intake (Kabir et al., 2015). In fact, almost 95% of the mean gut content biomass of green turtle male and non-breeding females and 58% of gravid females were dominated by seagrass (Stokes et al., 2019). However, diets of green turtles are different between the Western South Atlantic and the tropical Pacific since there are tropical reefs that become habitats for macroalgae and turf algae (Goatley et al., 2012; Santos et al., 2015). Therefore, nutritional compositions of green turtle eggs coming from different regions might be different from the present study due to disparities in food sources consumed by the gravid females. Furthermore, the olive ridley turtle is a carnivorous species that mainly feeds on shellfish and small crabs, and this may influence the findings. Thus, the differences in nutritional values of these reptiles depend on the diet, genetics, age, management and feeding of the source animal (Yang et al., 2020). In this study, the energy content of turtle eggs was around 25 - 29 MJ/kg, which is similar to a previous study (Booth, 2003). The lipid and protein contents in egg yolk act as sources of energy for the development of the embryo (Thompson and Speake, 2002). Nevertheless, the relatively low energy content found in these samples was probably influenced by the low protein intake by female green turtles.

In this study, 12 genera of Gram-negative bacteria consisted of 12 species were identified. They are mainly represented by the phylum of proteobacteria, and the most prevalent bacteria were Salmonella and Proteus. Green turtle eggs can be contaminated by potentially pathogenic microorganisms prior to oviposition or even before the eggshell construction (Al-Bahry et al., 2009). They are prone to being exposed to pathogenic microorganisms due to the fact that their marine environment is subjected to a variety of contaminants, including oil spills, chemical waste and other debris. Furthermore, green turtles undergo dietary changes throughout the ontogenetic shift. During their juvenile stage, they are mostly omnivorous that commonly found in surface-pelagic habitats, feeding on algae, seagrass, invertebrates and terrestrial plants (Nagaoka et al., 2012). However, they eventually become herbivorous once they grow into adulthood and move to neritic habitats that consist of huge sources of seagrass that become the major component of green turtles diets (Howell et al., 2016; Price et al., 2017). This long-term exposure to contaminated feed leads to an accumulation of poisons in the blood and organs of green turtles. Similarly, pathogenic microorganisms like Salmonella are ingested with contaminated feed or water, infecting the digestive system that subsequently contaminate the eggs (Alkindi et al., 2006). Other than that, the gut microbiome of green turtles and other marine mammals can also be influenced by age, diet, habitat and health status (Nelson et al., 2013). Since green turtles have high mobility and their movement patterns vary during migration between breeding and foraging habitats, this facilitates long-term exposure to environmental toxicants along their migratory routes.

Proteus is commonly found in nature, particularly in soil, stagnant water and sewage, and in the gastrointestinal tract. This study revealed that Proteus vulgaris and Proteus mirabilis dominated the turtle egg contents collected from Terengganu and Sabah, respectively. Keene (2012) suggested that the bacterial contamination could affect the reproductive organs, mainly the ovary and uterus (Keene, 2012). Therefore, it is also possible that harmful microorganisms are transmitted to the egg through maternal transmission and through cloacal passage during oviposition (Gantois et al., 2009). However, a low percentage of Proteus sp was isolated from oral and cloacal samples of healthy loggerhead sea turtles (Gantois et al., 2009), since cloacal microbial community is commonly dominated by Citrobacter freundii, Edwardsiella tarda and Serratia odorifer (Keene et al., 2014; Ahasan et al., 2017). More studies should be conducted to understand the relationship between a female’s infection status and the infection status of her eggs.

This study revealed that both Salmonella enterica spp arizonae and Salmonella enterica dominated the turtle egg surface. Green turtle eggs can be contaminated by a wide spectrum of bacterial species while being incubated in the sand since the nest chamber is also a potential source of microbial infection of eggs. In fact, proteobacteria is the predominant bacterial phylum commonly found in nesting sea turtles (Scheelings et al., 2020), which includes Bacillus sp., Salmonella sp., Citrobacter freundii and Mucor sp. (Estika, 2013). It should be noted that the condition of the sand in the nest chamber, such as high humidity, nutrients and warm temperature influence bacterial growth in the sand that subsequently contaminate the green turtle eggs. These environmental factors promote the filtration of microorganisms into the eggs (Al-Bahry et al., 2009). It is easier for the microorganisms to penetrate the egg when there are damages on the eggshells (Al-Bahry et al., 2004). Furthermore, the longer an egg remains in direct contact with contaminated sand, the more likely bacteria penetrate the egg. Similarly, other environmental variables such as rain and runoff, wave action and the presence of organics provide significantly impact on the prevalence of microorganisms in sand. A recent study showed that the diversity of eggshell bacterial communities was correlated with the bacteria found in the egg content. In this study, Aeromonas, Citrobacter sp, Citrobacter freundii, Enterobacter spp, Klebsiella pneumonia, Proteus vulgaris and Salmonella enterica were found in both egg content and eggshell. This indicates that microorganisms on the outer shells had succeeded in penetrating the eggs through the eggshell pores (Al-Bahry et al., 2011). Originally, the function of eggshell pores is to modulate the movement of water and gases into and out of the egg. However, certain conditions such as low temperatures and high humidity promote the filtration of microorganisms into the eggs (Al-Bahry et al., 2011).

Some proteobacteria have been associated poor percentage of hatching success (Santoro et al., 2006; Elshafie et al., 2007; Sarmiento-Ramirez et al., 2017). However, a recent study found that microbiomes that are vertically transmitted to the eggs of oviparous animals can decrease egg failure and inhibit fungal growth on the eggshells (Bunker et al., 2021). Nevertheless, this does not change the fact that being associated with the animal and consuming green turtle products on a regular basis can endanger human health (Aguirre et al., 2006). Coastal communities of Mexico prefer sea turtles as a source of food, medicine and decoration (Delgado, 2005). They usually consume the entire animal, including blood and eggs as a remedy for anaemia and asthma. Subsequently, there is an issue related to sea turtle and chelonitoxin that leads to chelonitoxism to the consumers who consume contaminated sea turtles. It is harmful to infants and fetuses following maternal poisoning through breast milk and transplacental transfer (Fussy et al., 2007). In fact, a total of sixty-eight cases were reported, with four deaths in association with the illness due to consumption turtle meat and turtle meat soup (Ventura et al., 2015). Therefore, marine turtles are one of the sources of foodborne toxicity in humans.

Salmonella sp., Proteus sp., Aeromonas, Escherichia coli, Citrobacter sp., Enterobacter sp., Klebsiella sp., Morganella morganii, Pseudomonas aeruginosa, Salmonella sp. and Shigella sp. are some of the pathogenic microorganisms found in this study. Some of these microorganisms are common bacterial flora of nesting green turtles (Santoro et al., 2006). In this study, Salmonella sp. and Proteus sp. were the most common Gram-negative microbes, but Salmonella infection in green turtles can cause symptoms ranging from mild disruption of the gastrointestinal tract to death. According to a group of researchers, Salmonella is commonly isolated from poultry (De Freitas et al., 2010). However, a study reported cases of human salmonellosis in Japan that occurred due to the consumption of raw meat, blood and cooked meat of snapping turtles (Fukushima et al., 2008). Meanwhile, Proteus species are parts of human intestinal flora. However, it can cause severe infections in humans along with Escherichia coli and Klebsiella sp. such as urinary tract infections and gastrointestinal disease. Marine turtle products are one of the typical routes of human contamination either through consumption or contact. Numerous studies have reported them as a significant reservoir of potential pathogenic microbes and toxin contaminations (Fussy et al., 2007; Soslau et al., 2011; Domiciano et al., 2017; Mashkour et al., 2018). In lined with this, this study was able to identify the potential pathogenic microorganisms in the green turtle eggs that might be harmful to consumers. The high demand for green turtle eggs for human consumption has inhibited the growth of turtle population for the past few years. Although conservation efforts have been conducted thoroughly by responsible people, it is not enough due to limited human resources and infrastructure.

There were no significant differences in fatty acid composition between the two sampling sites except for linoleic acid, C18:2 n-6. The current study revealed that among the polyunsaturated fatty acids, (PUFAs), α-linolenic acid (ALA; C18:3 n-3) was the dominant fatty acid of omega-3 (n-3) PUFAs in Terengganu, while linoleic acid (LA; C18:2 n-6) of omega-6 (n-6) PUFAs in Sabah. This might be the outcomes of consumptions of seagrass and algae, which are known sources of ALA and LA. In fact, studies have shown that the sources of ALA and LA are principally plant-based essential fatty acids, and algae have proven as a good source of n-3 PUFAs (Peltomaa et al., 2018; Harwood, 2019). Due to its nutritional value, algae has been described as a “functional food” that benefits human health (Wells et al., 2017). Sources of n-3 fatty acids include water plants of algae, fish oil, vegetable oil and marine animals (Rajaram, 2014). Alpha-linolenic acid acts as a precursor in the human and animal body by converting into EPA and DHA through desaturation and elongation reactions (Barcelo´-Coblijn and Murphy, 2009). However, synthesis of these long-chain n-3 PUFA is inefficient. This explains the low levels of EPA and DHA detected in the current study. Besides, the sources of EPA and DHA mostly come from marine animals. On the contrary, a previous study exhibited different fatty acid results where α-linolenic acid was not detected in the eggs of green turtles caught from the wild but showed a low value of LA (Craven et al., 2008). Both n-3 and n-6 PUFAs are known as essential fatty acids, which are required only in small amounts in the human diet. However, an imbalance of n-6 and n-3 PUFAs (n-6/n-3) in the diet can influence human health (Ristic-Medic et al., 2013). Consequently, excessive dietary intake of PUFAs contributes to the development of a variety of chronic diseases. Therefore, the balanced ratio concept of n-6/n-3 was developed as a nutritional indicator in food (Simopoulos, 2008). It is recommended to reduce the ratio of n-6/n-3 PUFAs to as close to a 1:1 ratio, which is ideal for a healthy balanced diet (Bhardwaj et al., 2016). However, this study has revealed contradicting results for n-6/n-3 PUFAs when samples from Terengganu recorded three times higher ratio than Sabah, and exceeded the recommended ratios. The imbalanced n-6/n-3 PUFAs can trigger cholesterol levels in humans, increase the tendency for blood clotting and lead to the potential risk of having coronary heart disease (Swanson et al., 2012; Sokoła-Wysoczańska et al., 2018). Saturated fatty acid (SFA) has been known to have the potential of causing cardiovascular disease (CVD) (DiNicolantonio et al., 2016; Ruiz-Núñez et al., 2016). However, there is not much debate about SFA of marine turtle eggs, especially when the total saturated fatty acids reported in this study was low compared to unsaturated fatty acid, similar to the eggs of snail-eating turtle (Malayemys macrocephala) and quail (Coturnic coturnix japonica) (Tunsaringkarn et al., 2013a; Tunsaringkarn et al., 2013b). The current finding has reported that both myristic acids (C14:0) and palmitic acids (C16:0) are the major components of SFA, which apparently could lead to the increase of low-density lipoprotein (LDL) cholesterol as one of the risk factors for cardiovascular disease (Grundy, 2012; Mensink, 2016). Therefore, saturated fatty acid should be consumed in low quantities as it is not an essential fatty acid and replacing SFA with PUFA and proteins, especially plant proteins could probably reduce risks of CVD (Siri-tarino et al., 2010; Briggs et al., 2017).

The amino acid profiles of green turtle eggs from Terengganu and Sabah revealed that lysine was the most abundant essential amino acids, which is in agreement with the eggs of Hermann’s tortoise and snail-eating turtle (Tunsaringkarn et al., 2013b). In fact, lysine was among the highest amino acid found in chicken eggs (Attia et al., 2020). The highest essential amino acid composition in an egg would be the combination of phenylalanine and tyrosine (Sakanaka et al., 2000), with tryptophan at the lowest value (Attia et al., 2020). The main functions of lysine are to support the immune system, prevent osteoporosis through involvement in calcium absorption, and enhance the release of growth hormone that increases muscle mass. Meat, poultry, soy-based and dairy-based products are some of the food sources that are rich in lysine. A study has shown that valine is the highest amino acid in beef meat, followed by lysine and leucine, which are higher than lamb and pork (Ahmad et al., 2018). Meanwhile, among the ten non-essential amino acids measured in this study, glutamic acid was the dominant amino acid recorded in both sampling sites, followed by serine and aspartic acid, similar to previous studies (Tunsaringkarn et al., 2013b; Stvarnik et al., 2017). These could be due to the dietary intake of female green turtles that affect the composition of eggs (Craven et al., 2008; Weber, 2010). Glutamic acid or its ionic form, glutamate has some important roles in amino acid metabolism and physiological processes in humans, mainly within the intestines and the nervous system of the brain (Brosnan and Brosnan, 2013). In general, this study revealed that the total non-essential amino acids were more dominant that essential amino acids in turtle eggs of both sites, which is similar to other consumable eggs like Hermanns tortoise and snail-eating turtle. Since relatively low levels of amino acids were recorded in turtle eggs, it is perhaps not worth to consume turtle eggs on daily basis. Insufficient or excessive intake of certain foods is not recommended on a daily basis because it may cause certain dysfunctional processes in the body and probably lead to some diseases. The public is advised to have a moderate consumption of nutrient intake and follow the guidelines of the food pyramid in order to maintain good health.

The present study revealed that accumulations of heavy metals do happen in turtle eggs other than the blood and tissue of the animals. However, a study reported that there were relatively low levels of trace elements and organic contaminants in the tissues and blood samples of green turtles than in vertebrates (D’ilio et al., 2011). Additionally, different heavy metals were acquired in different samples obtained from different locations (Hostetler et al., 2003). Toxic contaminants in marine green turtles are most probably dependent on the availability of food resources, particularly from the polluted foraging grounds and through trophic transfer (Van de Merwe, 2008). Trace elements normally accumulate in water and sediment as well as algae and seagrass that become the main diet of marine turtles (Wyneken et al., 2013). Therefore, they are unintendedly more exposed to pollutions. In other words, they are susceptible to any contamination coming from their surroundings.

Numerous studies have suggested that female marine turtles have the potential to excrete their toxic contaminants through reproductive tract and is transferred to the egg (Guirlet et al., 2008; Páez-Osuna et al., 2010; Stewart et al., 2011; Ehsanpour et al., 2014; De Andrés et al., 2016). This process is called vitellogenesis that takes place during the development of follicles in female marine turtles where ingested nutrients from the foraging ground as well as the contaminants that are present in the lipid store of the animals are deposited into the follicles to form the yolk of an individual egg (Van de Merwe, 2008). Therefore, vitellogenesis usually occurs during breeding seasons and is completed before the first nesting (Hamann et al., 2002). However, it also depends on the species of turtle, for example, Dermochelys coriacea has the highest reproduction output among reptiles, so they transfer more energy, nutrients and trace elements to the egg. Furthermore, their longevity gives them the ability to accumulate diverse contaminants in a wide range of migration areas.

The comparison of heavy metal concentration in eggs of marine turtles of previous studies from different location is presented in Table 5 . The current findings revealed a high lead concentration in samples from Terengganu but lower than green turtle eggs collected from the Northern Coast of the Sea of Oman (Sinaei and Bolouki, 2017), moderately higher than Hong Kong, Peninsular Malaysia and the Pacific Coast of Panama (Fussy et al., 2007; Warwick et al., 2013; Rajaram, 2014). The concentrations of Pb vary in different places and could be influenced by the environment, especially those close to anthropogenic sources like urban areas (Burger and Gochfeld, 2000). Zinc (Zn) was the highest level of heavy metal found in this study, but the concentrations were similar to the green turtle eggs collected from West Papua, Indonesia (Tapilatu et al., 2020) and from other places in Peninsular Malaysia (Joseph et al., 2014). However, some studies reported lower Zinc levels (Van de Merwe et al., 2009; Ross et al., 2016), including in hawksbill turtle eggs (Ehsanpour et al., 2014) and olive ridley turtle eggs (Ross et al., 2016). Nevertheless, Zn is an essential heavy metal other than magnesium (Mn) and copper (Cu) that is needed in an adequate amount for the growth and metabolism of cells as well as the development of foetus (Hostetler et al., 2003). Besides, the differences might be caused by the different amounts of heavy metals being discharged into the foraging ground by natural or anthropogenic sources (Richir and Gobert, 2016). Moreover, the chemical levels may vary depending on the geographical area and the natural enrichment of trace elements in that area (Ahmadi and Rahimi, 2011).

Mercury (Hg) and cadmium (Cd) are non-essential heavy metals that are toxic, even at low concentration. Any foodstuff containing Hg concentration higher than the permissible limit of 0.01 mg/kg could initiate potential toxicity in humans and animals. In this study revealed low Hg concentration, well below the detection limit of 0.02 mg/kg fresh weight of mercury in food (World Health Organization. Regional Office for Europe, 2000). Generally, the concentration of Hg tends to be low in marine turtle eggs (Kaska and Furness, 2001; Lam et al., 2006; Guirlet et al., 2008; Ehsanpour et al., 2014; Sinaei and Bolouki, 2017) and a similar pattern was detected in current studies. On the other hand, some of the previous reports contradict this observation (Ross et al., 2016; Tapilatu et al., 2020). They investigated selected heavy metals in green turtle eggs and found Hg levels exceeded the maximum permissible limit. This toxicant element is also hazardous for fish when exposed to considerable amounts and might easily enter the nervous system of humans in the form of methyl mercury present in food (Tchounwou et al., 2012). Meanwhile, slightly low levels of Cd were measured, well within the 0.01 to 0.05 mg/kg acceptable levels and are comparable with previous studies (Van de Merwe et al., 2009; Ehsanpour et al., 2014; Sinaei and Bolouki, 2017). Besides, kidney and liver are the target organs for Cd (D’ilio et al., 2011; Yipel et al. (2017). In fact, highest bio-concentration of Cd was found in kidney of green turtles collected from Australia, Brazil, Hawaii, Japan and the Gulf of Mexico (Fraga et al., 2018). Similarly, kidney and liver tissues are also the target tissues for heavy metals in humans as they consume contaminated food products, which are then distributed through the blood (Gall et al., 2015; Engwa et al., 2019).

Many studies have been conducted on sea turtles in relation to the concentration of heavy metals in muscles, kidneys, and liver (Barbieri, 2009; Ross et al., 2017; Yipel et al., 2017). Once a contaminant enters the body, it is difficult to dissipate it from the body, but it was concluded that excretion of contaminants via eggs is not the main pathway for removing trace elements. However, during the nesting season, concentrations of heavy metals in the blood of female green turtles increased and to reduce the amount of contaminants, parts of the contaminant are transferred to the eggs (Van De Merwe et al., 2010). Usually, essential metals are passed on into the yolk and available for development of embryo. On the other hand, transfer of non-essential metals is limited, hence they persistently accumulate in the muscle, kidney, liver and pancreas of the mother (Kaska and Furness, 2001). Indeed, heavy metals are harmful to mammals, reptiles, fish and birds by disrupting the growth, immune systems and reproduction (Gall et al., 2015).

The metal concentrations in the present study were considerably different as there were low concentrations compared to previous study on green turtle eggs in Peninsular Malaysia (Joseph et al., 2014). It is probably due to the short period of time spent by those female marine turtles in polluted places and the different diets in the habitats. Besides, the green turtles are freely on the move to different foraging grounds that are often remote, expansive and inaccessible. Thus, it is quite challenging to trace the source of contamination. Their potential traits of having high mobility and their movement patterns during migration between breeding and foraging habitats facilitate long-term exposure to environmental toxicants along their migratory route. In fact, marine turtles have a long lifespan of up to several decades. Consequently, it poses a health risk to these animals due to their life pattern. Aside from that, contamination by trace elements in their blood and tissues has raised concern about public health risk, particularly for the consumer of green turtle. Nevertheless, this made them an excellent organism for contaminant biomonitoring of overall health status of marine ecosystem. Further study on this topic should be considered because the knowledge on this issue is applicable to the management and conservation of endangered species.

This study reveals the minor nutritional differences between green turtle eggs collected from Terengganu and Sabah. Nutrient contents including fatty acid and amino acid compositions varied slightly. However, the heavy metal concentrations might raise a concern about the public health risks. Furthermore, pathogenic bacteria of human concern were also isolated from turtle eggs, particularly Salmonella spp. The data contribute to public awareness of consuming green turtle eggs. Instead of purchasing green turtle eggs, the public has many options for healthier, more nutritious foods that are readily available. Further research is required on how the consumption of green turtle eggs affects the health of consumers. Perhaps this study is also helpful as a guideline for the future conservation of the green turtle population.

The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.

HH contributed to the original idea of manuscript writing. NK performed the data collection, analyses and wrote the first draft of manuscript. All authors contributed to the article and approved the submitted version.

The authors were thankful to Prof Zainudin bin Bachok from INOS, UMT for his invaluable support in providing some of the lab equipment. The authors would like to acknowledge the laboratory Centre of Research and Field Service - CRAFS, UMT and Nutrition’s laboratory, UPM in providing the facilities for conducting the experiments. The authors would like to acknowledge all person involved in this study.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.