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Nano-Se Assimilation and Action in Poultry and Other Monogastric Animals: Is Gut Microbiota an Answer?
Nanoscale Research Letters volume 12, Article number: 612 (2017)
Recently, a comprehensive review paper devoted to roles of nano-Se in livestock and fish nutrition has been published in the Nanoscale Research Letters. The authors described in great details an issue related to nano-Se production and its possible applications in animal industry and medicine. However, molecular mechanisms of nano-Se action were not described and the question of how nano-Se is converted into active selenoproteins is not resolved. It seems likely that the gut microbiota can convert nano-Se into selenite, H2Se or Se-phosphate with the following synthesis of selenoproteins. This possibility needs to be further studied in detail, and advantages and disadvantages of nano-Se as a source of Se in animal/poultry/fish nutrition await critical evaluations.
Recently, a comprehensive review paper devoted to roles of nano-Se in livestock and fish nutrition has been published in the Nanoscale Research Letters . The authors described in great detail an issue related to nano-Se production and its possible applications in animal industry and medicine. Indeed, it is well established that many molecules presented as nanoparticles have unusual behaviour due to the new properties of such particles. In fact, in most of the published work relevant to animal nutrition, nanoparticles have size less than 100 nm. In such a state, the ultra-small size of the particles allows them to penetrate many biological barriers and be used as a delivery system for various elements including Ag, titanium, Se and others.
In this respect, Se is especially interesting, since it is proven that most areas worldwide are deficient in this element . The deficiency in many cases is a human creation, since Se content in soils greatly varies, and what is more important, Se availability from soils is even more variable. In fact, soil acidification as a result of agricultural practices as well as usage of sulfur-containing fertilizers substantially decreased Se availability for plants and leads to low Se consumption by livestock, where grains (wheat, corn, barley) and oil seeds (soybean) comprise a major part of the diet. Therefore, Se supplementation of the commercial diets of poultry, farm animals and fish became a common practice and is used since the 1970s. Indeed, vitamin-mineral premixes are a major source of Se for the commercial production of eggs, meat/fish and milk.
What is relevant to the nano-Se story is the source of Se in the supplements. Indeed, the main supplemental form of Se is sodium selenite which is a by-product of copper production. With over more than 40 years of usage, sodium selenite has clearly demonstrated its advantages and disadvantages. In fact, due to the commercial feed Se supplementation, Se deficiency in livestock with clinical signs of deficiency practically disappeared. The exception is in ruminants, where sodium selenite can precipitate in acidic rumen environment, as well as due to technical limitations of the usage of feed supplements; Se deficiency is still seen worldwide and such applications as selenium injections and boluses are used. However, as it is rightly mentioned in the aforementioned review, Se is extremely important in commercially relevant stress conditions, especially for modern genetics of highly productive farm animals and poultry.
Today, the animal industry is moving from prevention of nutrient deficiencies to meeting the exact requirements of animals in important nutrients, including Se. Indeed, “precise nutrition” is a term describing this concept. In such conditions, it has become apparent that sodium selenite (as well as selenate) has a range of disadvantages as a feed supplement. First of all, it is quite a reactive compound and can be reduced in feed/premix to an unavailable metallic form by various nutrients, including ascorbic acid, and some feed ingredients. It can also be dissolved in feed moisture and converted into volatile compounds to be lost. Secondly, sodium selenite possesses pro-oxidant properties in a dose-dependent manner, which could have a negative effect on the animal/chick gut. Finally, selenium in the form of sodium selenite is poorly transferred to eggs, via placenta to foetuses, which is not able to build Se reserves in the body which can be used in stress conditions when Se requirement increases but feed consumption usually decreases. Sodium selenite is also toxic for animals and humans in excess. However, we do not agree with a conclusion in the aforementioned review  that Se toxicity is a problem for the animal industry. It is only related to human error in calculation or in mixing feeds. The safe window for selenium is quite narrow (the usual dose of Se supplementation for poultry and pigs is about 0.3 ppm, while a negative effect would be observed at doses of sodium selenite exceeding 1–2 ppm), but modern feed mill equipment gives an opportunity of good feed mixing avoiding problems of toxicity.
Advances in analytical sciences were a driving force in discovery that the main form of Se in major feed ingredients is SeMet, comprising more than 50% of total Se in corn, soybean, wheat, barley, etc. . Therefore, during evolution, the digestive system of animals was adapted to this form of selenium, and as a result, SeMet is more efficiently assimilated from the diet and non-specific incorporation into body proteins builds Se reserves. Indeed, a range of organic Se sources appeared in the market including Se-Yeast, pure SeMet and OH-SeMet (2-hydroxy-4-(methylthio)butanoic acid-Se), with OH-SeMet to show maximum efficacy.
The main lack of knowledge in the nano-Se issue is related to its metabolism and particularly its conversion to H2Se with the following SeCys synthesis and incorporation into selenoproteins. In the review , only very few selenoproteins, including glutathione peroxidase, are mentioned, while at least 25 selenoproteins are identified in humans and animals. It is generally accepted that the major role of Se in human/animal nutrition is related to the synthesis of selenoproteins possessing unique catalytic properties and more than half of them are involved in redox balance maintenance and antioxidant defences . In the aforementioned review , the direct antioxidant properties (reduction of ROS) of nano-Se are mentioned as a possible mechanism of its action. However, Se concentration in major animal/poultry tissues including the liver and muscles usually does not exceed 800–900 ng/g fresh tissue which is in the range of 10 μM, and in plasma, the Se level is about 0.2–0.3 μg/ml or 2–3 μM, while in the most cited work devoted to antioxidant properties of nano-Se in vitro, the Se concentrations were tested and showed antioxidant effects 5–10-folds higher . Furthermore, for an antioxidant compound to be an effective free-radical scavenger, it is important to have the right concentration of the antioxidant in the right place at the right time. This would complicate the issue further, and therefore, it seems unlikely that nano-Se could have a direct AO effect in the biological systems.
Therefore, similar to other forms of selenium used in animal diets, an antioxidant effect of nano-Se is related to selenoprotein gene expression and protein synthesis. Indeed, in the review , there are several references confirming a positive effect of nano-Se on the GSH-Px activity. Now the question is how nano-Se is converted into active selenoproteins. In the review , there is a suggestion (without a reference) that nano-Se can be converted to selenophosphate with the following Se-protein synthesis. This suggestion should be experimentally proven. The second suggestion that nano-Se can be converted to SeMet is fundamentally wrong, since SeMet cannot be synthesized in the human/animal body; only plants and bacteria can produce it .
There are very attractive suggestions that gut microbiota can oxidize nano-Se into selenite/selenate or reduce it into H2Se with the following synthesis of selenoproteins [6, 7]. Recently, some experimental evidence have been provided to prove that nano-Se particles can be dissolved and oxidized to inorganic oxoanions of Se in the gut in the presence of microbiota before their absorption . Furthermore, a hypothetical schematic diagram showing an intracellular dynamic cycle of endogenous selenium nanoparticles (SeNPs) was proposed . In fact, it was suggested that elemental selenium could be re-oxidized by superoxide radicals into selenite. There is also a possibility that gut microbiota can perform/accelerate this process. Indeed, four major biological transformations of Se are proven to occur in nature including reduction, oxidation, methylation, and demethylation . Data accumulated for the last three decades clearly indicate that microorganisms play a major role in the selenium cycle in the environment by participating in both oxidation and reduction reactions . Interestingly, the microbial oxidation of Se0 to Se4+ by a group of unidentified autotrophic bacteria was discovered more than 90 years ago . Furthermore, oxidation of elemental selenium to selenite by a heterotrophic bacterium, Bacillus megaterium, isolated from soil was reported much later . Indeed, Se0 oxidation in soils was shown to occur at a relatively slow rate and to be largely biotic in nature and yields both SeO3 2− and SeO4 2− . Furthermore, the microbial oxidation of elemental selenium (Se0) by chemoheterotrophs and chemoautotrophic thiobacilli was confirmed by using 75Se0 as a tracer . The authors showed that soil slurries were able to oxidize Se0 with SeO3 2− and SeO4 2− formation. Interestingly, microbial inactivation in soil by autoclaving or chemical treatments inhibited the process. Furthermore, cultures of sulfur-oxidizing bacterium Thiobacillus ASN-1 are shown to perform the oxidation of Se(0) with enzymes that are used for generating energy from reduced sulfur compounds . Furthermore, heterotrophic bacterium which can oxidize Mn(II) or Fe(II) (Leptothrix MnB1) was shown to oxidize Se0 with the formation of SeO3 2− as the major product of reaction. Interestingly, the reaction was shown to depend on an electron donor such as acetate or glucose . The oxidation of Se0 by various bacteria has not been fully addressed and is an area of important research opportunities. In fact, a great variety of microbes residing in the gut provides necessary conditions for various Se conversions. For example, when nano-Se particles were incubated with lactic acid bacteria (Lactobacillus delbrueckii subsp. bulgaricus LB-12), organic Se compounds (mainly SeCys and SeMet) were produced and also nano-Se particles were partially dissolved and non-metabolically transformed into inorganic selenium, probably with the assistance of substances excreted by the bacteria cell wall .
Alternatively, elemental selenium can be reduced/converted into selenide by a selenite-respiring bacterium (for example, Bacillus selenitireducens). The aforementioned reaction conducted by the bacteria with the incomplete oxidation of the electron donor lactate to acetate as follows was presented as follows :
Therefore, the free energies for the reaction (∆GI) is shown to be − 2.8 kcal/mol e−. This shows that in Bacillus selenitireducens, the reduction mechanism involves energy conservation by using Se-specific dissimilatory enzymes . Indeed, a selenite-respiring bacterium, Bacillus selenitireducens, could produce significant levels of Se− 2 (as aqueous HSe−) using Se0 as a substrate . Earlier it was demonstrated that red selenium was reduced by obligate acidophile Thiobacillus ferrooxidans under acidic (pH 3), anaerobic conditions with H2Se production at a rate of 0.03 μmol/mg protein/h . Furthermore, another anaerobic bacterium Veillonella atypica was shown to be able to reduce selenium oxyanions to form elemental selenium with its further reduction by the bacterium to form reactive selenide . Interestingly, more than 45 years earlier, it was described that extracts of Micrococcus lactilyticus (Veillonella alcalescens) were able to quantitatively reduce colloidal selenium into H2Se . Recently, genes encoding YedE and YedF proteins have been considered as new candidate genes involved in Se metabolism in prokaryotes including bacteria . Indeed, both YedE, a predicted Se transporter, and YedF, a redox protein, could be involved in the metabolic transformation of selenium in bacterial cells. Therefore, the principal ability of various microbes to oxidize or reduce elemental selenium was proven (Table 1); however, there is a need for further investigations to answer a question if such reactions take place in the animal gut. Interestingly, from all bacterial species mentioned in Table 1, anaerobic, gram-negative bacteria of the genus Veillonella deserve special attention. Indeed, Veillonellae are found in the alimentary canal of warm-blooded animals . In fact, in food animals, Veillonella strains are detected regularly as indigenous inhabitants of all sections of the gastrointestinal tract ( and references there), including the upper gastrointestinal tract  and caeca  of chickens. Indeed, an additional research is needed to elucidate the fate and mechanisms of the possible conversions of nano-Se in the gastrointestinal tract of animals. The nano-Se metabolism depends on the nanoparticle composition, including the nanoparticle coating agent. A proposed scheme of nano-Se participation in selenoprotein synthesis is shown in Fig. 1, and a basic understanding of the nano-Se metabolism including absorption, distribution, and clearance is of great importance in animal/poultry sciences .
The mammalian/avian gastrointestinal tract harbours trillions of commensal microorganisms, collectively known as the microbiota . For example, chicken intestinal tract is composed of duodenum, jejunum, ileum, cecum, and colon, and there are significant differences in microbiota concentration and composition between the aforementioned gut sections . Interestingly, the cecum is characterized by the most complex microbial community dominated by the phyla Firmicutes, Bacteroidetes, Actinobacteria and Proteobacteria . On the other hand, at the genus level, the major microbial genera across all gut sections were shown to be Lactobacillus, Enterococcus, Bacteroides, and Corynebacterium . Furthermore, Bacteroides was shown to be the dominant group in the cecum, while Lactobacillus was predominant in the small intestine sections (duodenum, jejunum and ileum; ). In this complex intestinal ecosystem, there could be a range of microbes able to facilitate oxidation/reduction of nano-Se particles, and this assumption awaits further investigation.
From one side, some microbes would use Se for their own needs to synthesize microbial selenoproteins and compete with the host for this element. It is well known that Se is an important element for a variety of organisms in almost all bacterial phyla; however, it seems likely that only one third of characterized bacteria use this element in their metabolism . Indeed, in Se deficiency, there is a competition between bacteria and the host for the available selenium, and germ-free animals have a lower selenium requirement than conventionally colonized animals . Recent results indicate that dietary Se supplementation can affect both the composition and diversity of the existing microbiota and establishment of gastrointestinal microflora . For example, weaned beef calves fed selenium-enriched alfalfa hay were shown to have an enriched nasal microbiota compared with control animals . Possible effects of Se in various forms and concentrations on gut microbiota await further investigation.
On the other hand, it seems likely that there is an active uptake of Se by microbiota, and this process depends on the Se form used. In fact, the uptake of SeMet by colon microbiota was shown to be much more efficient compared to the uptake of selenate . However, whether bacteria composition and concentration affect the absorption of selenium compounds in the gut has not been investigated. It is generally accepted that the gut microbiota is responsible for the excretion of excess selenium by its methylation and elemental Se formation . Interestingly, in rats fed SeMet, this form of Se was found in all segments of the gut. However, the level of Se in the ileum, cecum and colon were significantly higher than that in the corresponding sections of rats after probiotic treatment . This could mean that Streptococcus Salivarius, Lactobacillus rhamnosus, Lactobacillus acidophilus and Bifidobacterium lactis were delivered to the gut with probiotic effected Se metabolism mainly in the distant gut. Indeed, the effect of different bacteria in the conversion of Se should be identified to understand the roles of each segment of the gut in Se metabolism and assimilation. Furthermore, reflux of the fluid from the upper part from the large intestine back to the small intestine may be responsible for the absorption of H2Se and other forms of Se from the intestine. In fact, recently, it has been shown that chickens are characterized by reverse peristaltic contractions which could move the marker from the cloaca to the gizzard .
Direct involvement of nano-Se into selenoprotein synthesis could be expected, since in cell culture nano-Se increased selenoproteins (GSH-Px and TR activity). However, the recent understanding of the selenoprotein expression priority could complicate this issue. In fact, many selenoproteins are oxidative stress-regulated. In particular, GSH-Px1, GSH-Px4 and TR1 were shown to be upregulated in response to oxidative stress , and such a response was more pronounced when Se supply was limiting. It should be mentioned that the aforementioned response depends also on the level of oxidative stress, because it is true in mild oxidative stress, but at an extremely high level, some other mechanisms are activated .
It could well be that in cell culture, increased expression/activities of such selenoproteins are a response to an oxidative stress created by nano-Se, but not a reflection of improved Se supply. Therefore, there should be some caution in interpretation of the results based on cell-culture studies. An additional confirmation of the stress-related changes in biological systems due to nano-Se supplementation came from the recent study showing that biogenic nano-Se could activate the nuclear factor (erythroid-derived-2)-like 2 (Nrf2) and increase the expression of its downstream genes, responsible for antioxidant synthesis in dose- and time-dependent manners . Furthermore, the authors found that the knockdown of Nrf2 significantly blocked the antioxidative effect of such nano-Se particles.
When critically analysing positive effects of nano-Se supplementation on productive and reproductive performance of poultry, farm animals and fish, it is necessary to take into account that in most cases, Se did not improve the performance but rather prevented performance deterioration due to environmental or nutritional constraints. In many cases, animal experiments were conducted at extremely low Se background level, and therefore, adding Se in any available form can have positive effects.
The challenges of nano-Se commercialization to be used as a feed additive could be as follows:
It is necessary to understand molecular mechanisms of nano-Se absorption, assimilation and action at the cellular, subcellular and gene levels. Without such data, it would be difficult to have reproducible results and find proper explanations of the observed effects. For example, in a recently published paper, only few genes (18 proteins and none of them are directly related to Se metabolism) were affected in the liver due to overdose of nano-Se in chickens , while it is known that other forms of dietary Se, including SeMet, can affect few hundred genes.
It is important to understand if nano-Se can build any Se reserves in the body, like SeMet, and if those reserves are available in stress conditions.
It is necessary to design a technology able to provide nano-Se particles of the same size, stability and reasonably good (at least 6–12 months) storability .
It is likely that microbial probiotics can be useful in the conversion of nano-selenium used as feed additive. From the one hand, such probiotics can contain specific microorganisms helping nano-Se assimilation in the gut (e.g. Veillonella species). On the other hand, probiotics enriched with Se could be another possibility [34, 39]
Side effects, risks and environmental concerns should be addressed in full. Indeed, further research is required in order to inform policy makers and regulatory bodies about the nanotoxicological potential of nano-Se . In particular, a very small size of particles in dry form makes the product very dusty, and unusual nano-Se particle behaviour, once in the body, gives a warning with the main concern for feed mill workers’ protection. Since the gut microbiota is responsible for the excretion of excess selenium by its methylation and elemental Se formation , the enhancement/modulation of the microbiota could open a new horizon to deal with possible nano-Se toxicity.
Positive effects of nano-Se in animal nutrition should not overshadow possible detrimental consequences of its usage. Indeed, nanoparticle behaviour in various conditions could differ substantially, and before we understand how to control that behaviour, nano-Se usage on a wide industrial scale should not be possible. For example, when considering nano-Se absorption, it is necessary to mention the so-called Trojan horse effect, when nanoparticles may have permeation-enhancing properties for other substances in the gut . This could create some problems, since there is a range of “unwanted” compounds in the feed and the gut is protective against their absorption. Indeed, nano-Se behaviour in the gut warrants further investigation.
In the aforementioned review , substantial attention is given to antimicrobial and anti-cancer properties of nano-Se, and it seems likely that the unique properties of nanoparticles could help in fighting various disease conditions. Indeed, nano-Se can be considered as a new drug to be used in various medical conditions, including cancer therapy, while its usage as an effective feed additive is rather questionable. Future research has to answer those important questions and concerns.
For the last few years, a range of papers were published devoted to nano-Se and the topic is quickly developing. However, before this form of Se can find a way to commercial poultry/animal production, it is necessary to understand and explain how nano-Se is converted into active selenoproteins. One of the possible mechanisms/pathways of nano-Se action could be mediated by the gut microbiota which could convert nano-Se into selenite, H2Se or Se-phosphate with the following synthesis of selenoproteins (Fig. 1). There is some evidence that in nature, bacteria could reduce or oxidize metallic Se (Se0) with the production of Se−2 or Se+4 and Se+6 respectively. Among microorganisms involved in Se redox changes, the genus Veillonella deserves special attention because of the presence of such bacteria in the gut of food animals, including chicken. The possibility of participation of gut microbiota in nano-Se assimilation and metabolism needs to be further investigated in detail, and advantages and disadvantages of nano-Se as a source of Se in animal/poultry nutrition await further critical evaluations.
Sarkar B, Bhattacharjee S, Daware A, Tribedi P, Krishnani KK, Minhas PS (2015) Selenium nanoparticles for stress-resilient fish and livestock. Nanoscale Res Lett 10:371
Surai PF (2006) Selenium in nutrition and health. Nottingham University Press, Nottingham
Surai PF, Fisinin VI (2016) Selenium in livestock and other domestic animals. In: Hatfield DL, Schweizer U, Tsuji PA, Gladyshev VN (eds) Selenium. Its molecular biology and role in human health. Springer International Publishing, pp 595–606
Huang B, Zhang J, Hou J, Chen C (2003) Free radical scavenging efficiency of nano-Se in vitro. Free Radic Biol Med 35:805–813
Schrauzer GN, Surai PF (2009) Selenium in human and animal nutrition: resolved and unresolved issues. A partly historical treatise in commemoration of the fiftieth anniversary of the discovery of the biological essentiality of selenium, dedicated to the memory of Klaus Schwarz (1914–1978) on the occasion of the thirtieth anniversary of his death. Crit Rev Biotechnol 29:2–9
Loeschner K, Hadrup N, Hansen M, Pereira SA, Gammelgaard B, Møller LH, Mortensen A, Lam HR, Larsen EH (2014) Absorption, distribution, metabolism and excretion of selenium following oral administration of elemental selenium nanoparticles or selenite in rats. Metallomics 6:330–337
Bao P, Chen SC, Xiao KQ (2015) Dynamic equilibrium of endogenous selenium nanoparticles in selenite-exposed cancer cells: a deep insight into the interaction between endogenous SeNPs and proteins. Mol BioSyst 11:3355–3361
Dungan RS, Frankenberger WT (1999) Microbial transformations of selenium and the bioremediation of seleniferous environments. Bioremediation Journal 3:171–188
Nancharaiah YV, Lens PN (2015) Ecology and biotechnology of selenium-respiring bacteria. Microbiol Mol Biol Rev 79:61–80
Lipman JG, Waksman SA (1923) The oxidation of elemental selenium by a new group of autotrophic microorganisms. Science 1463:60
Sarathchandra SU, Watkinson JH (1981) Oxidation of elemental selenium to selenite by Bacillus megaterium. Science 211:600–601
Losi ME, Frankenberger WT (1998) Microbial oxidation and solubilization of precipitated elemental selenium in soil. J Environ Qual 27:836–843
Dowdle PR, Oremland RS (1998) Microbial oxidation of elemental selenium in soil slurries and bacterial cultures. Environ Sci Technol 32:3749–3755
Palomo-Siguero M, Madrid Y (2017) Exploring the behavior and metabolic transformations of SeNPs in exposed lactic acid bacteria. Effect of nanoparticles coating agent. Int J Mol Sci 18:8. doi:10.3390/ijms18081712
Blum JS, Bindi AB, Buzzelli J, Stolz JF, Oremland RS (1998) Bacillus arsenicoselenatis, sp. nov., and Bacillus selenitireducens, sp. nov.: two haloalkaliphiles from Mono Lake, California that respire oxyanions of selenium and arsenic. Arch Microbiol 171:19–30
Herbel MJ, Blum JS, Oremland RS (2003) Reduction of elemental selenium to selenide: experiments with anoxic sediments and bacteria that respire Se-oxyanions. Geomicrobiol J 20:587–602
Bacon M, Ingledew WJ (1989) The reductive reactions of Thiobacillus ferrooxidans on sulphur and selenium. FEMS Microbiol Lett 58:189–194
Pearce CI, Coker VS, Charnock JM, Pattrick RA, Mosselmans JFW, Law N, Lloyd JR (2008) Microbial manufacture of chalcogenide-based nanoparticles via the reduction of selenite using Veillonella atypica: an in situ EXAFS study. Nanotechnology 19:155603
Woolfolk CA, Whiteley HR (1962) Reduction of inorganic compounds with molecular hydrogen by Micrococcus lactilyticus. I. Stoichiometry with compounds of arsenic, selenium, tellurium, transition and other elements. J Bacteriol 84:647–658
Lin J, Peng T, Jiang L, Ni JZ, Liu Q, Chen L, Zhang Y (2015) Comparative genomics reveals new candidate genes involved in selenium metabolism in prokaryotes. Genome Biol Evol 7:664–676
Kolenbrander P (2006) The genus Veillonella. The Prokaryotes 4:1022–1040
Kraatz M, Taras D (2008) Veillonella magna sp. nov., isolated from the jejunalmucosa of a healthy pig, and emended description of Veillonella ratti. Int J Syst Evol Microbiol 58:2755–2761
Gong J, Si W, Forster RJ, Huang R, Yu H, Yin Y, Han Y (2006) 16S rRNA gene-based analysis of mucosa-associated bacterial community and phylogeny in the chicken gastrointestinal tracts: from crops to ceca. FEMS Microbiol Ecol 59:147–157
Wise MG, Siragusa GR (2007) Quantitative analysis of the intestinal bacterial community in one-to three-week-old commercially reared broiler chickens fed conventional or antibiotic-free vegetable-based diets. J Appl Microbiol 102:1138–1149
Pelyhe C, Mézes M (2013) Myths and facts about the effects of nano selenium in farm animals—mini-review. Eur Chem Bulletin 2:1049–1052
Bhat MI, Kapila R (2017) Dietary metabolites derived from gut microbiota: critical modulators of epigenetic changes in mammals. Nutr Rev 75:374–389
Xiao Y, Xiang Y, Zhou W, Chen J, Li K, Yang H (2017) Microbial community mapping in intestinal tract of broiler chicken. Poult Sci 96:1387–1393
Sergeant MJ, Constantinidou C, Cogan TA, Bedford MR, Penn CW, Pallen MJ (2014) Extensive microbial and functional diversity within the chicken cecal microbiome. PLoS One 9:e91941
Peng T, Lin J, Xu YZ, Zhang Y (2016) Comparative genomics reveals new evolutionary and ecological patterns of selenium utilization in bacteria. ISME J 10:2048–2059
Hrdina J, Banning A, Kipp A, Loh G, Blaut M, Brigelius-Flohé R (2009) The gastrointestinal microbiota affects the selenium status and selenoprotein expression in mice. J Nutr Biochem 20:638–648
Kasaikina MV, Kravtsova MA, Lee BC, Seravalli J, Peterson DA, Walter J, Gladyshev VN (2011) Dietary selenium affects host selenoproteome expression by influencing the gut microbiota. FASEB J 25:2492–2499
Hall JA, Isaiah A, Estill CT, Pirelli GJ, Suchodolski JS (2017) Weaned beef calves fed selenium-biofortified alfalfa hay have an enriched nasal microbiota compared with healthy controls. PLoS One 12:e0179215
Lavu RVS, Van De Wiele T, Pratti VL, Tack F, Du Laing G (2016) Selenium bioaccessibility in stomach, small intestine and colon: comparison between pure Se compounds, Se-enriched food crops and food supplements. Food Chem 197:382–387
Krittaphol W, McDowell A, Thomson CD, Mikov M, Fawcett JP (2011) Biotransformation of L-selenomethionine and selenite in rat gut contents. Biol Trace Elem Res 139:188–196
Sacranie A, Svihus B, Denstadli V, Moen B, Iji PA, Choct M (2012) The effect of insoluble fiber and intermittent feeding on gizzard development, gut motility, and performance of broiler chickens. Poult Sci 91:693–700
Touat-Hamici Z, Legrain Y, Bulteau AL, Chavatte L (2014) Selective up-regulation of human selenoproteins in response to oxidative stress. J Biol Chem 289:14750–14761
Song D, Cheng Y, Li X, Wang F, Lu Z, Xiao X, Wang Y (2017) Biogenic nanoselenium particles effectively attenuate oxidative stress-induced intestinal epithelial barrier injury by activating the Nrf2 antioxidant pathway. ACS Appl Mater Interfaces 9:14724–14740
Gulyas G, Csosz E, Prokisch J, Javor A, Mezes M, Erdelyi M, Balogh K, Janaky T, Szabo Z, Simon A, Czegledi L (2017) Effect of nano-sized, elemental selenium supplement on the proteome of chicken liver. J Anim Physiol Anim Nutr (Berl) 101:502–510
Lv CH, Wang T, Regmi N, Chen X, Huang K, Liao SF (2015) Effects of dietary supplementation of selenium-enriched probiotics on production performance and intestinal microbiota of weanling piglets raised under high ambient temperature. J Anim Physiol Anim Nutr 99:1161–1171
Elsaesser A, Howard CV (2012) Toxicology of nanoparticles. Adv Drug Deliv Rev 64:129–137
Fröhlich E, Roblegg E (2012) Models for oral uptake of nanoparticles in consumer products. Toxicology 291:10–17
Peter F. Surai and Ivan I. Kochish are supported by a grant of the Government of Russian Federation (Contract No. 14.W03.31.0013).
The authors declare that they have no competing interests.
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Surai, P.F., Kochish, I.I. & Velichko, O.A. Nano-Se Assimilation and Action in Poultry and Other Monogastric Animals: Is Gut Microbiota an Answer?. Nanoscale Res Lett 12, 612 (2017). https://doi.org/10.1186/s11671-017-2383-3
- Selenoprotein Activity
- Nanoscale Research Letters
- Bacillus Selenitireducens
- Aforementioned Review