|
REFERENCES
- 1. Mirabella N., Castellani V., Sala S. Current options for the valorization of
food manufacturing waste: a review. J. o f Cleaner Production. 2014. Vol. 65. P. 28-41.
doi: 10.1016/j.jclepro.2013.10.051
- 2. Yadav D., Negi P. S. Bioactive components of mushrooms: Processing
effects and health benefits. Food Research Intern. (Ottawa, Ont.). 2021. Vol. 148.
110599. doi: 10.1016/j.foodres.2021.110599
- 3. Venturella G., Ferraro V., Cirlincione F., Gargano M. L. Medicinal
Mushrooms: Bioactive Compounds, Use, and Clinical Trials. Intern. J. o f Molecular Sci.
2021. Vol. 22(2). 634. doi: 10.3390/ijms22020634
- 4. de Frutos P. Changes in world patterns o f wild edible mushrooms use
measured through international trade flows. Forest Policy and Economics. 2020.
Vol. 112. 102093. doi: 10.1016/j.forpol.2020.102093
- 5. Kaushal L. A., Prashar A. Agricultural crop residue burning and its
environmental impacts and potential causes - case o f northwest India. J. o f
Environmental Planning and Management. 2021. Vol. 64(3). P. 464-484. doi:
10.1080/09640568.2020.1767044
- 6. Martin C. Pretreatment of crop residues for bioconversion. Agronomy.
2021. Vol. 11(5). 924. doi: 10.3390/agronomy11050924
- 7. Brunetti G., Soler-Rovira P., Matarrese F., Senesi N. Composition and
structural characteristics o f humified fractions during the co-composting process o f spent
mushroom substrate and wheat straw. J. o f Agricultural and Food Chemistry. 2009.
Vol. 57(22). P. 10859-10865. doi: 10.1021/jf903014f
- 8. Huang J., Liu J., Chen J., Xie W., Kuo J., Lu X., Chang K., Wen S., Sun G.,
Cai H., Buyukada M., Evrendilek F. Combustion behaviors of spent mushroom substrate
using TG-MS and TG-FTIR: Thermal conversion, kinetic, thermodynamic and emission
analyses. Bioresource Technology. 2018. Vol. 266. P. 389-397. doi:
10.1016/j.biortech.2018.06.106
- 9. Hu T., Wang X., Zhen L., Gu J., Zhang K., Wang Q., Ma J., Peng H.,
Lei L., Zhao W. Effects of inoculating with lignocellulose-degrading consortium on
cellulose-degrading genes and fungal community during co-composting o f spent
mushroom substrate with swine manure. Bioresource Technology. 2019. Vol. 291.
121876. doi: 10.1016/j.biortech.2019.121876
- 10. Singh U. B., Malviya D., Khan W., Singh S., Karthikeyan N., Imran M.,
Rai J. P., Sarma B. K., Manna M. C., Chaurasia R., Sharma A. K., Paul D., Oh J. W.
Earthworm Grazed-Trichoderma harzianum Biofortified Spent Mushroom Substrates
Modulate Accumulation of Natural Antioxidants and Bio-Fortification of Mineral
Nutrients in Tomato. Frontiers in Plant Sci. 2018. Vol. 9. 1017. doi:
10.3389/fpls.2018.01017
- 11. Wei Y., Jin Z., Zhang M., Li, Y., Huang S., Liu X., Jin Y., Wang H., Qu J.
Impact of spent mushroom substrate on Cd immobilization and soil property.
Environmental Scie. and Pollution Research International. 2020. Vol. 27(3). P. 3007
3022. doi: 10.1007/s11356-019-07138-y
- 12. Lou Z., Sun Y., Bian S., Ali Baig S., Hu B., Xu X. Nutrient conservation
during spent mushroom compost application using spent mushroom substrate derived
biochar. Chemosphere. 2017. Vol. 169. P. 23-31. doi:
10.1016/j.chemosphere .2016.11.044
- 13. Sewu D. D., Jung H., Kim S. S., Lee D. S., Woo S. H. Decolorization of
cationic and anionic dye-laden wastewater by steam-activated biochar produced at an
industrial-scale from spent mushroom substrate. Bioresource technology. 2019. Vol. 277.
P. 77-86. doi: 10.1016/j.biortech.2019.01.034
- 14. Phan C. W., Sabaratnam V. Potential uses of spent mushroom substrate
and its associated lignocellulosic enzymes. Applied microbiology and biotechnology.
2012. Vol. 96(4). P. 863-873. doi: 10.1007/s00253-012-4446-9
- 15. Zhu H., Sheng K., Yan E., Qiao J., Lv F. Extraction, purification and
antibacterial activities of a polysaccharide from spent mushroom substrate. International
J. o f Biological Macromolecules. 2012. Vol. 50(3). P. 840-843. doi:
10.1016/j.ijbiomac.2011.11.016
- 16. Medina E., Paredes C., Perez-Murcia M. D., Bustamante M. A., Moral R.
Spent mushroom substrates as component of growing media for germination and growth
of horticultural plants. Bioresource Technology. 2009. Vol. 100(18). P. 4227-4232. doi:
10.1016/j.biortech.2009.03.055
- 17. Liu Y., Zhao C., Lin D., Lin H., Lin Z. Effect of water extract from spent
mushroom substrate after Ganoderma balabacense cultivation by using JUNCAO
technique on production performance and hematology parameters of dairy cows. Animal
Scie. J. = Nihon Chikusan Gakkaiho. 2015. Vol. 86(9). P. 855-862. doi:
10.1111/asj.12371
- 18. Seok, J. S., Kim, Y. I., Lee, Y. H., Choi, D. Y., & Kwak, W. S. Effect of
feeding a by-product feed-based silage on nutrients intake, apparent digestibility, and
nitrogen balance in sheep. J. o f Animal Sci. and Technology. 2016. Vol. 58. 9. doi:
10.1186/s40781-016-0091-7
- 19. Aida F. M. N. A., Shuhaimi M., Yazid M., Maaruf A. G. Mushroom as a
Potential Source of Prebiotics : A Review. Trends in Food Sci. and Technology. 2009.
Vol. 20. P. 567-575. doi: 10.1016/j.tifs.2009.07.007
- 20. Friedman M. Mushroom Polysaccharides: Chemistry and Antiobesity,
Antidiabetes, Anticancer, and Antibiotic Properties in Cells, Rodents, and Humans.
Foods (Basel, Switzerland). 2016. Vol. 5(4). 80. doi: 10.3390/foods5040080
- 21. Chuang W. Y., Hsieh Y. C., Lee T. T. The Effects of Fungal Feed
Additives in Animals: A Review. Animals: an open access journal from M DPI. 2020.
Vol. 10(5). 805. doi: 10.3390/ani10050805
- 22. Atallah, E., Zeaiter, J., Ahmad, M.N., Leahy, J.J., Kwapinski, W.
Hydrothermal Carbonization of Spent Mushroom Compost Waste Compared against
Torrefaction and Pyrolysis. Fuel Processing Technology. 2021. Vol. 216. 106795. doi:
10.1016/J.FUPROC.2021.106795
- 23. Leong Y. K., Ma T. W., Chang J. S., Yang F. C. Recent advances and
future directions on the valorization of spent mushroom substrate (SMS) : A review.
Bioresource Technology. 2022. Vol. 344(Pt. A). 126157. doi:
10.1016/j.biortech.2021.126157
- 24. Martin C., Zervakis G. I., Xiong S., Koutrotsios G., Stratkvern K. O. Spent
substrate from mushroom cultivation: exploitation potential toward various applications
and value-added products. Bioengineered. 2023. Vol. 14(1). 2252138. doi:
10.1080/21655979.2023.2252138
- 25. Zisopoulos F. K., Becerra Ramirez H. A., van der Goot A. J., Boom R. M.
A resource efficiency assessment of the industrial mushroom production chain : The
influence of data variability. J. o f Cleaner Production. 2016. Vol. 126. P. 394-408. doi:
10.1016/j.jclepro.2016.03.066
- 26. Beckers S. J., Dallo I. A., Del Campo I., Rosenauer C., Klein K.,
Wurm F. R. From Compost to Colloids - Valorization of Spent Mushroom Substrate.
ACS Sustainable Chemistry & Engineering. 2019. Vol. 7. P. 6991-6998. doi:
10.1021/acssuschemeng.8b06710
- 27. Elsakhawy T., Tawfik W. Evaluation of Spent Mushroom Substrate
Extract as Biofertilizer for Growth Improvement of Rice (Oriza Sativa). Egyptian J. o f
Soil Sci. 2019. Vol. 60. P. 31-42. doi: 10.21608/EJSS.2019.18835.1320
- 28. Beyer D. M. Impact of the mushroom industry on the environment. Penn
State Extension. Pennsylvania State University. 2011. URL:
https://extension.psu.edu/impact-of-the-mushroom-industry-on-the-environment (date of
access: 20.05.24).
- 29. Council directive 1999/31/EC on the landfill of waste [Internet]. 1999.
URL: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=celex%3A31999L0031
(date of access: 31.05.24).
- 30. Chen L., Qian L., Zhang X., Li J. Z., Zhang Z. J., Chen X. M. Research
progress on indoor environment of mushroom factory. International J. of Agricultural and
Biological Engineering. 2022. Vol. 15(1). P. 25-32. doi: 10.25165/j.ijabe.20221501.6872
- 31. Picornell-Buendia R., Pardo-Gimenez A., de Juan-Valero J.A. Agronomic
assessment of spent substrates for mushroom cultivation. Biotechnologie, Agronomie,
Societe et Environnement. Biotechnology, Agronomy, Society and Environment. 2016.
Vol. 20(3). P. 263-374. doi: 10.25518/1780-4507.13138
- 32. Economou C. N., Philippoussis A. N., Diamantopoulou P. A. Spent
mushroom substrate for a second cultivation cycle of Pleurotus mushrooms and
dephenolization of agro-industrial wastewaters. FEMS Microbiology Letters. 2020.
Vol. 367(8). fnaa060. doi: 10.1093/femsle/fnaa060
- 33. Wu C.Y., Liang C. H., Liang Z. C. Evaluation of using spent mushroom
sawdust wastes for cultivation of Auricularia Polytricha. Agronomy. 2020. Vol. 10(12).
1892. doi: 10.3390/agronomy10121892
- 34. Qi Q., Peng Q., Tang M., Chen D., Zhang H. Microbiome Analysis
Investigating the Impacts of Fermented Spent Mushroom Substrates on the Composition
of Microbiota in Weaned Piglets Hindgut. Frontiers in Veterinary Sci. 2020. Vol. 7.
584243. doi: 10.3389/fvets.2020.584243
- 35. Fazaeli H., Shafyee-Varzeneh H., Farahpoor A., Moayyer А. Recycling of
mushroom compost wheat straw in the diet of feedlot calves with two physical forms.
Inter. J. o f Recycling o f Organic Waste in Agriculture. 2014. Vol. 3(3). 3. doi:
10.1007/s40093 -014-0065-z
- 36. Aldoori Z. T., Al-Obaidi A. S. A., Abdulkareem A. H., Abdullah M. K.
Effect of dietary replacement of barley with mushroom cultivation on carcass
characteristics of Awassi lambs. J. o f Animal Health and Production, 2015. Vol. 3(4).
P. 94-98. doi: 10.14737/journal.jahp/2015/3.4.94.98
- 37. Herrero-Hernandez E., Andrades M. S., Villalba Eguren G., SanchezMartrn M. J., Rodriguez-Cruz S. M., Marin-Benito J. M. Organic amendment for the
recovery of vineyard soils: effects of a single application on soil properties over two
years. Processes. 2022. Vol. 10(2). 317. doi: 10.3390/pr10020317
- 38. Meng X., Liu B., Zhang H., Wu J., Yuan X., Cui Z. Co-composting of the
biogas residues and spent mushroom substrate: Physicochemical properties and maturity
assessment. Bioresource Technology. 2019. Vol. 276. P. 281-287. doi:
10.1016/j.biortech.2018.12.097
- 39. Wang H. W., Xu M., Cai X. Y., Tian F. (Evaluation of soil microbial
communities and enzyme activities in cucumber continuous cropping soil treated with
spent mushroom (Flammulina velutipes) substrate. J. o f Soils and Sediments. 2021.
Vol. 21(8). P. 2938-2951. doi: 10.1007/s11368-021-02989-w
- 40. Li H., Yoshida S., Mitani N., Egusa M., Takagi M., Izawa H.,
Matsumoto T., Kaminaka H., Ifuku S. Disease resistance and growth promotion activities
of chitin/cellulose nanofiber from spent mushroom substrate to plant. Carbohydrate
Polymers. 2022. Vol. 284. 119233. doi: 10.1016/j.carbpol.2022.119233
- 41. Singh G., Tiwari A., Gupta A., Kumar A., Hariprasad P., Sharma S.
Bioformulation development via valorizing silica-rich spent mushroom substrate with
Trichoderma asperellum for plant nutrient and disease management. J. o f Environmental
Management. 2021. Vol. 297. 113278. doi: 10.1016/j.jenvman.2021.113278
- 42. Ntougias S., Papadopoulou K. K., Zervakis G. I., Kavroulakis N.,
Ehaliotis C. Suppression of soil-borne pathogens of tomato by composts derived from
agro-industrial wastes abundant in Mediterranean regions. Biology and Fertility o f Soils.
2008. Vol. 44. P. 1081-1090.
- 43. Lin H., Sun M., Li J., Xu Q., Yang B., Wang Q., Xie W., Sun S., Hu K.,
Zhang L. Purification and characterization of xylanase from spent mushroom compost
and its application in saccharification of biomass wastes. BioResources. 2018. Vol. 13(1).
P. 220-230. doi: 10.15376/biores.13.1.220-230
- 44. Ball A. S., Jackson A. M. The recovery of lignocellulose-degrading
enzymes from spent mushroom compost. Bioresource Technology. 1995. Vol. 54(3).
P. 311-314. doi: 10.1016/0960-8524(95)00153-0
- 45. Ko H. G., Park S. H., Kim S. H., Park H. G., Park W. M. Detection and
recovery of hydrolytic enzymes from spent compost of four mushroom species. Folia
Microbiologica. 2005. Vol. 50(2). P. 103-106. doi: 10.1007/BF02931456
- 46. Zhang J., Meng G., Zhai G., Yang Y., Zhao H., Jia L. Extraction,
characterization and antioxidant activity of polysaccharides of spent mushroom compost
of Ganoderma lucidum. Intern. J. o f Biological Macromolecules. 2016. Vol. 82. P. 432
439. doi: 10.1016/j.ijbiomac.2015.10.016
- 47. Aguiar T., Luiz C., Neto A., Di Piero R. M. Residual polysaccharides from
fungi reduce the bacterial spot in tomato plants. Bragantia. 2018. Vol. 77(2). P. 299-313.
doi: 10.1590/1678-4499.2016514
- 48. Park J. H., Kim S. W., Do Y. J., Kim H., Ko Y. G., Yang B. S., Shin D.,
Cho Y. M. Spent mushroom substrate influences elk (Cervus elaphus canadensis)
hematological and serum biochemical parameters. Asian-Australasian J. o f Animal Sci.
2012. Vol. 25(3). P. 320-324. doi: 10.5713/ajas.2011.11329
- 49. Vaz J. A., Barros L., Martins A., Santos-Buelga C., Vasconcelos H.,
Ferreira I. C. F. R. Chemical composition of wild edible mushrooms and antioxidant
properties of their water soluble polysaccharidic and ethanolic fractions. Food Chemistry.
2011. Vol. 126(2). P. 610-616. doi: 10.1016/j.foodchem.2010.11.063
- 50. Skapa S., Vochozka M. Waste energy recovery improves price
competitiveness of artificial forage from rapeseed straw. Clean Technologies and
Environmental Policy. 2019. Vol. 5. P. 1165-1171. doi: 10.1007/s10098-019-01697-x
- 51. Correddu F., Lunesu M. F., Buffa G., Atzori A. S., Nudda A.,
Battacone G., Pulina G. Can Agro-Industrial By-Products Rich in Polyphenols be
Advantageously Used in the Feeding and Nutrition of Dairy Small Ruminants?. Animals:
an Open Access J. from MDPI. 2020. Vol. 10(1). P. 131. doi: 10.3390/ani10010131
- 52. Wilkinson J. M., Lee M. R. F. Review: Use of human-edible animal feeds
by ruminant livestock. Animal: an Intern. J. o f Animal Bioscience, 2018. Vol. 12(8).
P. 1735-1743. doi: 10.1017/S175173111700218X
- 53. Bath D. L. Feed by-products and their utilization by ruminants. Upgrading
Residues and By-Products fo r Animals; CRC Press: Boca Raton, FL, USA, 2018. P. 116.
- 54. Rahman M. M., Mat K., Ishigaki G., Akashi R. A review of okara (soybean
curd residue) utilization as animal feed: Nutritive value and animal performance aspects.
Animal Scie. J. = Nihon Chikusan Gakkaiho. 2021. Vol. 92(1). e13594. doi:
10.1111/asj.13594
- 55. Kalvandi S., Zaboli K., Malecky M. Effect of spent mushroom compost
(Agaricus bisporus) silage processing on its chemical composition, digestibility and
ruminal fermentation kinetic in Mehraban sheep. Animal Production Research. 2018.
Vol. 7(2). P. 69-82. doi: 10.22124/AR.2018.9256.1270
- 56. Motta F., GershwinM. E., Selmi C. Mushrooms and immunity. J. o f
Autoimmunity. 2021. Vol. 117. 102576. doi: 10.1016/j.jaut.2020.102576
- 57. Mohd Hanafi F. H., Rezania S., Mat Taib S., Md Din M.F., Yamauchi M.,
Sakamoto M., Hara H., Park J., Ebrahimi S.S. Environmentally sustainable applications
of agro-based spent mushroom substrate (SMS): an overview. J. o f Material Cycles and
Waste Management. 2018. Vol. 20. P. 1383-1396. doi: 10.1007/s10163-018-0739-0
- 58. Iannaccone F., Alborino V., Dini I., Balestrieri A., Marra R., Davino R.,
Di Francia A., Masucci F., Serrapica F., Vinale F. In Vitro Application of Exogenous
Fibrolytic Enzymes from Trichoderma Spp. to Improve Feed Utilization by Ruminants.
Agriculture. 2022. Vol. 12(5). 573. doi: 10.3390/agriculture12050573
- 59. Niego A. G., Rapior S., Thongklang N., Raspe O., Jaidee W., Lumyong S.,
Hyde K. D. Macrofungi as a Nutraceutical Source: Promising Bioactive Compounds and
Market Value. J. o f fungi (Basel, Switzerland). 2021. Vol. 7(5). 397. doi:
10.3390/jof7050397
- 60. Mhlongo G., Mnisi C. M., Mlambo V. Cultivating oyster mushrooms on
red grape pomace waste enhances potential nutritional value of the spent substrate for
ruminants. PloS One. 2021. Vol. 16(2). e0246992. doi: 10.1371/journal.pone.0246992
- 61. Ahmed Z., Faisal S., Jamal A. O. Upgrading of Raw Wheat Straw
Applying Fungal Treatment. Open J. o f Animal Sci. 2021. Vol. 11. P. 376-383. doi:
10.4236/ojas.2021.113027
- 62. Kwak W. S., Kim Y. I., Seok J. S., Oh Y. K., Lee S. M. Molasses and
microbial inoculants improve fermentability and silage quality of cotton waste-based
spent mushroom substrate. Bioresource Technology. 2009 Vol. 100(3). P. 1471-1473.
doi: 10.1016/j.biortech.2008.07.066
- 63. Kwak W. S., Jung S. H., Kim Y. I. Broiler litter supplementation improves
storage and feed-nutritional value of sawdust-based spent mushroom substrate.
Bioresource Technology. 2008. Vol. 99(8). P. 2947-2955. doi:
10.1016/j.biortech.2007.06.021
- 64. Xu C., Cai Y., Zhang J., Matsuyama H. Feeding value of total mixed ration
silage with spent mushroom substrate. Animal Scie. J. = Nihon Chikusan Gakkaiho. 2010.
Vol. 81(2). P. 194-198. doi: 10.1111/j.1740-0929.2009.00728.x
- 65. Katya K., Yun Y. H., Park G., Lee J. Y., Yoo G., Bai S. C. Evaluation of
the Efficacy of Fermented By-product of Mushroom, Pleurotus ostreatus, as a Fish Meal
Replacer in Juvenile Amur Catfish, Silurus asotus: Effects on Growth, Serological
Characteristics and Immune Responses. Asian-Australasian J. o f Animal Sci. 2014.
Vol. 27(10). P. 1478-1486. doi: 10.5713/ajas.2014.14038
- 66. Liebl M., Gierus M., Rocchi E., Potthast C., Schedle K. Effects of energy
reduced diets including alternative protein sources and a phytogenic supplement on
performance, carcass traits and digestibility in broiler chickens. J. o f Applied Poultry
Research. 2022. Vol. 31(3). 100265. doi: 10.1016/j.japr.2022.100265
- 67. Research and Market. Global Poultry (Broiler) Market with Focus on US,
Brazil & Mexico: Insights, Trends and Forecast (2019-2023) (Research and Market,
Issue). 2019. URL:
https://www.businesswire.com/news/home/20190801005884/en/Global-PoultryBroiler-Market-Insights-Trends-and-Forecast-2019-2023-with-Focus-on-US-BrazilMexico—ResearchAndMarkets.com (date of access: 10.05.2024).
- 68. Henchion M., Hayes M., Mullen A. M., Fenelon M., Tiwari B. Future
Protein Supply and Demand : Strategies and Factors Influencing a Sustainable
Equilibrium. Foods (Basel, Switzerland). 2017. Vol. 6(7). 53. doi: 10.3390/foods6070053
- 69. Hejdysz M., Kaczmarek S. A., Kubis M., Adamski M., Perz K.,
Rutkowski A. The effect of faba bean extrusion on the growth performance, nutrient
utilization, metabolizable energy, excretion of sialic acids and meat quality of broiler
chickens. Animal: an Inter. J. e f Animal Bioscie. 2019. Vol. 13(8). P. 1583-1590. doi:
10.1017/S175173111800366X
- 70. Shi S., Lu J., Tong H., Zou J., Wang K. Effects of graded replacement of
soybean meal by sunflower seed meal in laying hen diets on hen performance, egg quality,
egg fatty acid composition, and cholesterol content. J. o f Applied Poultry Research. 2012.
Vol. 21(2). P. 367-374. doi: 10.3382/japr.2011-00437
- 71. Pimentel D., Marklein A., Toth M. A., Karpoff M., Paul G. S.,
McCormack R., Kyriazis J., Krueger T. Biofuel impacts on world food supply: use of
fossil fuel, land and water resources. Energies. 2008. Vol. 1(2). P. 41-78. doi:
10.3390/en1010041
72. Attia Y. A., El-Tahawy W. S., Abd El-Hamid A. E. H. E., Nizza A.,
Al-Harthi M. A., El-Kelway M. I., Bovera F. Effect of feed form, pellet diameter and
enzymes supplementation on carcass characteristics, meat quality, blood plasma
constituents and stress indicators of broilers. Archives Animal Breeding. 2014. Vol. 57(1).
34. doi: 10.7482/0003-9438-57-034
- 73. Al-Sagan A. A., Al-Yemni A. H., Al-Abdullatif A. A., Attia Y. A.,
Hussein E. O. S. Effects of Different Dietary Levels of Blue Lupine (Lupinus
angustifolius) Seed Meal With or Without Probiotics on the Performance, Carcass
Criteria, Immune Organs, and Gut Morphology of Broiler Chickens. Frontiers in
Veterinary Sci. 2020. Vol. 7. P. 124. doi: 10.3389/fvets.2020.00124
- 74. de Maria M., Robinson E. J., Kangile J. R., Kadigi R., Dreoni I., Couto M.,
Howai N., Peci J. Global soybean trade-the geopolitics of a bean. Global Soybean Trade:
The Geopolitics of a Bean Ukri Gcrf Trade Hub., 2020. doi: 10.34892/7yn1-k494).
- 75. Panda A., Zaidi P., Rama Rao S., Raju M. Efficacy of quality protein
maize in meeting energy and essential amino acid requirements in broiler chicken
production. J. o f Applied Animal Research. 2014. Vol. 42. P. 133-139.
- 76. Mallick P., Muduli K., Biswal J. N., Pumwa J. Broiler poultry feed cost
optimization using linear programming technique. J. o f Operations and Strategic
Planning. 2020. Vol. 3. P. 31-57. doi: 10.1177/2516600X19896910
-
- 77. Sauer S. Soy expansion into the agricultural frontiers of the Brazilian
Amazon: The agribusiness economy and its social and environmental conflicts. Land Use
Policy. 2018. Vol. 79. P. 326-338.
- 78. Mthana M. S., Mthiyane D. M. N. Low dietary oyster mushroom spent
substrate limitedly ameliorates detrimental effects of feeding combined marula seed cake
and mucuna seed meal as soya bean replacements in broiler chickens. Tropical Animal
Health and Production. 2024. Vol. 56(1). 37. doi: 10.1007/s11250-023-03878-9
- 79. Elkhateeb W. A., EL-Ghwas D. E., Daba G. M. Mushrooms as efficient
enzymatic machinery. J. o f Biomededical Research and Environmental Sci. 2022. Vol. 3.
P. 423-428. doi: 10.37871/jbres1460
- 80. Chuang W. Y., Liu C. L., Tsai C. F., Lin W. C., Chang S. C., Shih H.,
Shy Y. M., Lee T. T. Evaluation of Waste Mushroom Compost as a Feed Supplement and
Its Effects on the Fat Metabolism and Antioxidant Capacity of Broilers. Animals: an open
access J. from MDPI. 2020. Vol. 10(3). 445. doi: 10.3390/ani10030445
- 81. Lee T. T., Ciou J. Y., Chiang C. J., Chao Y. P., Yu B. Effect of Pleurotus
eryngii stalk residue on the oxidative status and meat quality of broiler chickens. J. o f
Agricultural and Food Chemistry. 2012. Vol. 60(44). P. 11157-11163. doi:
10.1021/jf302740h
- 82. Laudadio V., Tufarelli V. Dehulled-micronised lupin (Lupinus albus L. cv.
Multitalia) as the main protein source for broilers : influence on growth performance,
carcass traits and meat fatty acid composition. J. o f the Sci. o f Food and Agriculture.
2011. Vol. 91(11). P. 2081-2087. doi: 10.1002/jsfa.4426
- 83. Khan S., Chand N., Naz S., Alrefaei A. F., Albeshr M. F., Losacco C.,
Khan R. U. Response to dietary methionine and organic zinc in broilers against coccidia
under Eimeria tenella-challenged condition. Livestock Sci. 2023. Vol. 276. 105317. doi:
10.1016/j .livsci.2023.105317
- 84. Chand N., Ali P., Alhidary I. A., Abdelrahman M. A., Albadani H.,
Khan M. A., Seidavi A., Laudadio V., Tufarelli V., Khan R. U. Protective Effect of Grape
(Vitis vinifera) Seed Powder and Zinc-Glycine Complex on Growth Traits and Gut
Health of Broilers Following Eimeria tenella Challenge. Antibiotics (Basel, Switzerland).
2021. Vol. 10(2). 186. doi: 10.3390/antibiotics10020186
- 85. Ishaq R., Chand N., Khan R. U., Saeed M., Laudadio V., Tufarelli V.
Methanolic extract of neem (Azadirachta indica) leaves mitigates experimentally induced
coccidiosis challenge in Japanese quails. J. o f Applied Animal Research, 2022. Vol. 50.
P. 498-503. doi: 10.1080/09712119.2022.2096037
- 86. Hafeez A., Ullah Z., Khan R. U., Ullah Q., Naz S. Effect of diet
supplemented with coconut essential oil on performance and villus histomorphology in
broiler exposed to avian coccidiosis. Tropical Animal Health and Production. 2020.
Vol. 52(5). P. 2499-2504. doi: 10.1007/s11250-020-02279-
- 87. Ali M., Chand N., Khan R. U., Naz S., Gul S. Anticoccidial effect of garlic
(Allium sativum) and ginger (Zingiber officinale) against experimentally induced
coccidiosis in broiler chickens. J. o f Applied Animal Research, 2019. Vol. 47. P. 79-84.
doi: 10.1080/09712119.2019.1573731
- 88. Chand N., Faheem H., Khan R. U., Qureshi M. S., Alhidary I. A.,
Abudabos A. M. Anticoccidial effect of mananoligosacharide against experimentally
induced coccidiosis in broiler. Environmental Sci. and Pollution Research International.
2016. Vol. 23(14). P. 14414-14421. doi: 10.1007/s11356-016-6600-x
- 89. Nasir J. A., Chand N., Naz S., Alhidary I. A., Khan R. U., Batool S.,
Zelai N. T., Pugliese G., Tufarelli V., Losacco C. Dietary Oyster Mushroom (Pleurotus
ostreatus) Waste Inhibits Experimentally Induced Eimeria tenella Challenge in Japanese
Quails Model. Animals: an Open Access J. from MDPI. 2023. Vol. 13(21). 3421. doi:
10.3390/ani13213421
- 90. Lloyd-Price J., Abu-Ali G., Huttenhower C. The healthy human
microbiome. Genome Medicine. 2016. Vol. 8(1). 51. doi: 10.1186/s13073-016-0307-y
- 91. Byndloss M. X., Pernitzsch S. R., Baumler A. J. Healthy hosts rule within:
ecological forces shaping the gut microbiota. Mucosal Immunology. 2018. Vol. 11(5).
P. 1299-1305. doi: 10.1038/s41385-018-0010-y
- 92. Plata G., Baxter N. T., Susanti D., Volland-Munson A., Gangaiah D.,
Nagireddy A., Mane S. P., Balakuntla J., Hawkins T. B., Kumar Mahajan A. Growth
promotion and antibiotic induced metabolic shifts in the chicken gut microbiome.
Communications biology. 2022. Vol. 5(1). 293. doi: 10.1038/s42003-022-03239-6
- 93. Hossain M. D., Bulbul S. M., Nishibori M., Islam M. A. Effect of different
growth promoters on growth and meat yield of broilers. J. o f Poultry Sci. 2008. Vol. 45.
P. 287-291. doi: 10.2141/jpsa.45.287
- 94. Barros R., Vieira S. L., Favero A., Taschetto D., Mascarello N. C.,
Cemin H. Reassessing flavophospholipol effects on broiler performance. Revista
Brasileira de Zootecnia. 2012. Vol. 41. P. 2458-2462. doi: 10.1590/S1516-
35982012001200011
- 95. Castanon J. I. History of the use of antibiotic as growth promoters in
European poultry feeds. Poultry Sci. 2007. Vol. 86(11). P. 2466-2471. doi:
10.3382/ps.2007-00249
- 96. Jha R., Mishra P. Dietary fiber in poultry nutrition and their effects on
nutrient utilization, performance, gut health, and on the environment: a review. J. o f
Animal Sci. and Biotechnology. 2021. Vol. 12(1). 51. doi 10.1186/s40104-021-00576-0
- 97. Cui Y., Diao Z. P., Fan W. T., Wei J. L., Zhou J. S., Zhu H. Y., Li D. S.,
Guo L. W., Tian Y. M., Song H., Su Y. H. Effects of dietary inclusion of alfalfa meal on
laying performance, egg quality, intestinal morphology, caecal microbiota and
metabolites in Zhuanghe Dagu chickens. Italian J. o f Animal Sci. 2022. Vol. 21(1).
P. 831-846. doi: 10.1080/1828051X.2022.2067009
- 98. Rohe I., Zentek J. Lignocellulose as an insoluble fiber source in poultry
nutrition: a review. J. o f Animal Sci. and Biotechnology. 2021. Vol. 12(1). 82. doi:
10.1186/s40104-021 -00594-y
- 99. Zhang T., Ye J., Xue C., Wang Y., Liao W., Mao L., Yuan M., Lian S.
Structural characteristics and bioactive properties of a novel polysaccharide from
Flammulina velutipes. Carbohydrate Polymers. 2018. Vol. 197. P. 147-156. doi:
10.1016/j.carbpol.2018.05.069
- 100. Hao Y., Wang X., Yuan S., Wang Y., Liao X., Zhong M., He, Q., Shen H.,
Liao W., Shen J. Flammulina velutipes polysaccharide improves C57BL/6 mice gut
health through regulation of intestine microbial metabolic activity. Intern. J. o f Biological
Macromolecules. 2021. Vol. 167. P. 1308-1318. doi: 10.1016/j.ijbiomac.2020.11.085
- 101. Wei J., Xiao H., Wei Y., Nguepi Tsopmejio I. S., Sun C., Wu H., Jin Z.,
Song H. Longitudinal Study of the Effects of Flammulina velutipes Stipe Wastes on the
Cecal Microbiota of Laying Hens. mSystems. 2023. Vol. 8(1). e0083522. doi:
10.1128/msystems.00835-22
- 102. Ko S. H., Kim H. S. Menopause-Associated Lipid Metabolic Disorders
and Foods Beneficial for Postmenopausal Women. Nutrients. 2020. Vol. 12(1). 202. doi:
10.3390/nu12010202
- 103. Wang L., Tang J., Wang L., Tan F., Song H., Zhou J., Li F. Oxidative
stress in oocyte aging and female reproduction. J. e f Cellular Physiology. 2021.
Vol. 236(12). P. 7966-7983. doi: 10.1002/jcp.30468
- 104. Yoshimura Y., Tamura T. Effects of gonadotrophins, steroid hormones,
and epidermal growth factor on the in vitro proliferation of chicken granulosa cells.
Poultry Sci. 1988. Vol. 67(5). P. 814-818. doi: 10.3382/ps.0670814
- 105. Zhu M., Miao S., Zhou W., Elnesr S. S., Dong X., Zou X. MAPK,
AKT/FoxO3a and mTOR pathways are involved in cadmium regulating the cell cycle,
proliferation and apoptosis of chicken follicular granulosa cells. Ecotoxicology and
Environmental Safety. 2021. Vol. 214. 112091. doi: 10.1016/j.ecoenv.2021.112091
- 106. Liu X., Lin X., Zhang S., Guo C., Li J., Mi Y., Zhang C. Lycopene
ameliorates oxidative stress in the aging chicken ovary via activation of Nrf2/HO-1
pathway. Aging. 2018. Vol. 10(8). P. 2016-2036. doi: 10.18632/aging.101526
- 107. Ciccone N. A., Sharp P. J., Wilson P. W., Dunn I. C. Changes in
reproductive neuroendocrine mRNAs with decreasing ovarian function in ageing hens.
General and Comparative Endocrinology. 2005. Vol. 144(1). P. 20-27. doi:
10.1016/j.ygcen.2005.04.009
- 108. Meng X. T., Hou N. N., Wang X. J., Jiao H. C., Zhao J. P., Song Z. G.,
Lin H. Increased hepatic yolk precursor synthesis, secretion and facilitated uptake by
follicles are involved in the rejuvenation of reproductive performance of molted hens
(Gallus gallus domesticus). General and Comparative Endocrinology. 2013. Vol. 194,
198-207. doi: 10.1016/j.ygcen.2013.09.007
- 109. Gu Y. F., Chen Y. P., Jin R., Wang C., Wen C., Zhou Y. M. Age-related
changes in liver metabolism and antioxidant capacity of laying hens. Poultry Sci. 2021.
Vol. 100(12). 101478. doi: 10.1016/j.psj.2021.101478
- 110. Schneider W. J. Lipoprotein receptors in oocyte growth. The Clinical
Investigator. 1992. Vol. 70(5). P. 385-390. doi: 10.1007/BF00235517
- 111. Walzem R. L., Hansen R. J., Williams D. L., Hamilton R. L. Estrogen
induction of VLDLy assembly in egg-laying hens. The J. o f Nutrition, 129(2S Suppl.).
1999. P. 467S-472S. doi: 10.1093/jn/129.2.467S
- 112. Barber D. L., Sanders E. J., Aebersold R., Schneider W. J. The receptor
for yolk lipoprotein deposition in the chicken oocyte. The J. o f Biological Chemistry.
1991. Vol. 266(28). P. 18761-18770.
- 113. Li J., Leghar, I. H., H, B., Zen, W., M, Y., Zhang C. Estrogen stimulates
expression of chicken hepatic vitellogenin II and very low-density apolipoprotein
II through ER-a. Theriogenology. 2014. Vol. 82(3). P. 517-524. doi:
10.1016/j.theriogenology.2014.05.003
- 114. Bujo H., Hermann M., Kaderli M. O., Jacobsen L., Sugawara S., Nimpf J.,
Yamamoto T., Schneider W. J. Chicken oocyte growth is mediated by an eight ligand
binding repeat member of the LDL receptor family. The EMBO J. 1994. Vol. 13(21).
P. 5165-5175. doi: 10.1002/j.1460-2075.1994.tb06847.x
- 115. Liu X. T., Lin X., Mi Y. L., Zeng W. D., Zhang C. Q. Age-related changes
of yolk precursor formation in the liver of laying hens. J. o f Zhejiang University. Sci. B.
2018. Vol. 19(5). P. 390-399. doi: 10.1631/jzus.B1700054
- 116. Omer N. A., Hu Ya., Hu Yu., Idriss A. A., Abobaker H., Hou Z., Dong H.,
Zhao R. Dietary betaine activates hepatic VTGII expression in laying hens associated
with hypomethylation of GR gene promoter and enhanced GR expression. J. o f Animal
Sci. cmdBiotechnology. 2018. Vol. 9. 2. doi: 10.1186/s40104-017-0218-9
117. Yang J. X., Chaudhry M. T., Yao J. Y., Wang S. N., Zhou B., Wang M.,
Han C. Y., You Y., Li Y. Effects of phyto-oestrogen quercetin on productive
performance, hormones, reproductive organs and apoptotic genes in laying hens. J. o f
Animal Physiology and Animal Nutrition. 2018. Vol. 102(2). P. 505-513. doi:
10.1111/jpn.12778
- 118. Xing C., Wang Y., Dai X., Yang F., Luo J., Liu P., Zhang C., Cao H.,
Hu G. The protective effects of resveratrol on antioxidant function and the mRNA
expression of inflammatory cytokines in the ovaries of hens with fatty liver hemorrhagic
syndrome. Poultry Sci. 2020. Vol. 99(2). P. 1019-1027. doi: 10.1016/j.psj.2019.10.009
- 119. Yeh M. Y., Ko W. C., Lin L. Y. Hypolipidemic and antioxidant activity of
enoki mushrooms (Flammulina velutipes). BioMed Research International. 2014.
352385. doi: 10.1155/2014/352385
- 120. Rahman M. A., Abdullah N., Aminudin N. Antioxidative Effects and
Inhibition of Human Low Density Lipoprotein Oxidation In Vitro of Polyphenolic
Compounds in Flammulina velutipes (Golden Needle Mushroom). Oxidative Medicine
and Cellular Longevity, 2015. 403023. doi: 10.1155/2015/403023
- 121. Hu Q., Yu J., Yang W., Kimatu B. M., Fang Y., Ma N., Pei F.
Identification of flavonoids from Flammulina velutipes and its neuroprotective effect on
pheochromocytoma-12 cells. Food Chemistry. 2016. Vol. 204. P. 274-282. doi:
10.1016/j.foodchem.2016.02.138
- 122. Sirtori C. R., Arnoldi A., Johnson S. K. Phytoestrogens: end of a tale?
Annals o f Medicine. 2005. Vol. 37(6). P. 423-438. doi: 10.1080/07853890510044586
- 123. Mahfuz S., He T., Liu S., Wu D., Long S., Piao X. Dietary Inclusion of
Mushroom (Flammulina velutipes) Stem Waste on Growth Performance, Antibody
Response, Immune Status, and Serum Cholesterol in Broiler Chickens. Animals: an Open
Access J. from MDPI. 2019. Vol. 9(9). 692. doi: 10.3390/ani9090692
- 124. Liu X., Zhao J., Zhang G., Hu J., Liu L., Piao X., Zhang S., Li Y. Dietary
Supplementation with Flammulina velutipes Stem Waste on Growth Performance, Fecal
Short Chain Fatty Acids and Serum Profile in Weaned Piglets. Animals: an open access
J. from MDPI. 2020. Vol. 10(1). 82. doi: 10.3390/ani10010082
- 125. Nguepi Tsopmejio I. S., Ding M., Wei J. L., Zhao C., Jiang Y., Li Y. T.,
Song H. Auricularia polytricha and Flammulina velutipes ameliorate inflammation and
modulate the gut microbiota via regulation of NF-kB and Keap1/Nrf2 signaling pathways
on DSS-induced inflammatory bowel disease. Food Bioscience. 2022. Vol. 47. 101426.
doi: 10.1016/j .fbio.2021.101426
- 126. Wu H., Yuan J., Yin H., Jing B., Sun C., Nguepi Tsopmejio I. S., Jin Z.,
Song, H. Flammulina velutipes stem regulates oxidative damage and synthesis of yolk
precursors in aging laying hens by regulating the liver-blood-ovary axis. Poultry Sci.
2023. Vol. 102(1). 102261. doi: 10.1016/j.psj.2022.102261
- 127. Malmuthuge N., Guan L. L. Understanding the gut microbiome of dairy
calves: Opportunities to improve early-life gut health. J. o f Dairy Sci. 2017. Vol. 100(7).
P. 5996-6005. doi: 10.3168/jds.2016-12239
- 128. Szacawa E., Dudek K., Wasiak M., Bednarek D., Bederska-Lojewska D.,
Muszynska B., Pieszka M. Effect of Supplementation with the Combination of SeEnriched Lentinula edodes Mycelium, Exogenous Enzymes, Acidifiers, Sodium Butyrate
and Silicon Dioxide Nanoparticle Feed Additives on Selected Parameters in Calves.
Molecules (Basel, Switzerland). 2022. Vol. 27(16). 5163. doi:
10.3390/molecules27165163
- 129. El-Nour H. H., Whba T. M., Ibrahim M. A., Anwer A. M. Impact of
supplementation with carboxylic acid salts on growth rate and some blood biochemical
values in male lambs. Global Veterinaria. 2010. Vol. 4. P. 90-96.
- 130. Pearlin B. V., Muthuvel S., Govidasamy P., Villavan M., Alagawany M.,
Ragab Farag M., Dhama K., Gopi M. Role of acidifiers in livestock nutrition and health:
A review. J. o f Animal Physiology and Animal Nutrition. 2020. Vol. 104(2). P. 558-569.
doi: 10.1111/jpn.13282
- 131. Mroczek I., Frankiewicz A., Selwet M. The effect of acidifying additives
on the microbiological stability of feed mixtures. J. o f Animal and Feed Sci. 2005.
Vol. 14. 385. doi: 10.22358/jafs/70586/2005
- 132. Carro M. D., Ungerfeld E. M. Utilization of organic acids to manipulate
ruminal fermentation and improve ruminant productivity. In: Rumen Microbiology :
From Evolution to Revolution; Springer: New Delhi, India, 2015. P. 177-197.
- 133. Quigley J. D., Drewry J. J., Murray L. M., Ivey S. J. Body weight gain,
feed efficiency, and fecal scores of dairy calves in response to galactosyl-lactose or
antibiotics in milk replacers. J. o f Dairy Sci. 1997. Vol. 80(8). P. 1751-1754. doi:
10.3168/j ds.S0022-0302(97)76108-3
- 134. Sarker M., Ko S., Lee S., Kim G., Choi J., Yang C. Effect of Different
Feed Additives on Growth Performance and Blood Profiles of Korean Hanwoo Calves.
Asian-Australasian J. o f Animal Sci. 2010. Vol. 23(1). P. 52-60. doi:
10.5713/ajas.2010.90280
- 135. Ribeiro M. D., Pereira J. C., Queiroz A. C. D., Cecon P. R., Detmann E.,
Azevedo J. A. G. Performance of dairy calves fed milk, milk replacer or post-weaning
concentrate with acidifiers. Revista Brasileira de Zootecnia. 2009. Vol. 38(5). P. 956
963. doi: 10.1590/S1516-35982009000500024
- 136. Placzek A., St^pien P., Zarczynski P., Patorczyk-Pytlik B. Methods for
enrichment of animal diets with selenium. J. o f Elementology. 2019. Vol. 24(3). P. 1159
1172. doi: 0.5601/jelem.2018.23.3.1703
- 137. Muller A., Bertram A., Freude B. Saisonale und uberregionale
Unterschiede im Selenversorgungsstatus von Rindern [Differences in the selenium supply
of cattle across Europe]. Tierarztliche Praxis. Ausgabe G, Grosstiere. Nutztiere. 2014.
Vol. 42(3). P. 131-144.
- 138. Kiremidjian-Schumacher L., Stotzky G. Selenium and immune responses.
Environmental Research. 1987. Vol. 42(2). P. 277-303. doi: 10.1016/s0013-
9351(87)80194-9
- 139. Hidiroglou M., Proulx J., Jolette J. Intraruminal selenium pellet for control
of nutritional muscular dystrophy in cattle. J. o f Dairy Sci. 1985. Vol. 68(1). P. 57-66.
doi: 10.3168/jds.S0022-0302(85)80797-9
- 140. Pecoraro B. M., Leal D. F., Frias-De-Diego A., Browning M., Odle J.,
Crisci E. The health benefits of selenium in food animals: a review. J. o f Animal Sci. and
Biotechnology. 2022. Vol. 13(1). 58. doi: 10.1186/s40104-022-00706-2
- 141. Pehrson B., Ortman K., Madjid N., Trafikowska U. The influence of
dietary selenium as selenium yeast or sodium selenite on the concentration of selenium
in the milk of Suckler cows and on the selenium status of their calves. J. o f Animal Sci.
1999. Vol. 77(12). P. 3371-3376. doi: 10.2527/1999.77123371x
- 142. Ran L., Wu X., Shen X., Zhang K., Ren F., Huang K. Effects of selenium
form on blood and milk selenium concentrations, milk component and milk fatty acid
composition in dairy cows. J. o f the Sci. o f Food and Agriculture. 2010. Vol. 90(13).
P. 2214-2219. doi: 10.1002/jsfa.4073
- 143. Suchocki P., Misiewicz-Krzeminska I., Skupinska K., Niedzwiecka K.,
Lubelska K., Fijalek Z., Kasprzycka-Guttman T. Selenitetriglicerydes affect CYP1A1
and QR activity by involvement of reactive oxygen species and Nrf2 transcription factor.
Pharmacological reports: PR. 2010. Vol. 62(2). P. 352-361. doi: 10.1016/s1734-
1140(10)70275-9
- 144. Guo F. C., Williams B. A., Kwakkel R. P., Li H. S., Li X. P., Luo J. Y.,
Li W. K., Verstegen M. W. Effects of mushroom and herb polysaccharides, as
alternatives for an antibiotic, on the cecal microbial ecosystem in broiler chickens.
Poultry Sci. 2004. Vol. 83(2). P. 175-182. doi: 10.1093/ps/83.2.175
- 145. Turlo J., Gutkowska B., Herold F., Dawidowski M., Slowinski T.,
Zobel A. Relationship between selenium accumulation and mycelial cell composition in
Lentinula edodes (Berk.) cultures. J. o f Toxicology and Environmental Health. Part A.
2010. Vol. 73(17-18). P. 1211-1219. doi: 10.1080/15287394.2010.492005
- 146. Drori A., Shabat Y., Ben Ya'acov A., Danay O., Levanon D., Zolotarov L.,
Ilan Y. Extracts from Lentinula edodes (Shiitake) Edible Mushrooms Enriched with
Vitamin D Exert an Anti-Inflammatory Hepatoprotective Effect. J. o f Medicinal Food.
2016. Vol. 19(4). P. 383-389. doi: 10.1089/jmf.2015.0111
- 147. Kieliszek M., Blazejak S. Current Knowledge on the Importance of
Selenium in Food for Living Organisms : A Review. Molecules (Basel, Switzerland).
2016. Vol. 21(5). 609. doi: 10.3390/molecules21050609
- 148. Murphy E. A., DavisJ. M., Carmichael M. D. Immune modulating effects
of P-glucan. Current Opinion in Clinical Nutrition andMetabolic Care. 2010. Vol. 13(6).
P. 656-661. doi: 10.1097/MCO.0b013e32833f1afb
- 149. Rop O., Mlcek J., Jurikova T. Beta-glucans in higher fungi and their health
effects. Nutrition Reviews. 2009. Vol. 67(11). P. 624-631. doi: 10.1111/j.1753-
4887.2009.00230.x
- 150. Mizuno M., Nishitani Y. Immunomodulating compounds in
Basidiomycetes. J. o f Clinical Biochemistry and Nutrition. 2013. Vol. 52(3). P. 202-207.
doi: 10.3164/jcbn.13-3
- 151. Mizuno M., Minato K. I. Anti-inflammatory and immunomodulatory
properties of polysaccharides in mushrooms. Current Opinion in Biotechnology. 2024.
Vol. 86. 103076. doi: 10.1016/j.copbio.2024.103076
- 152. Rangel-Vargas E., Rodriguez J. A., Dominguez R., Lorenzo J. M.,
Sosa M. E., Andres S. C., Rosmini M., Perez-Alvarez J. A., Teixeira A., Santos E. M.
Edible Mushrooms as a Natural Source of Food Ingredient. Additive Replacer. Foods
(Basel, Switzerland). 2021. Vol. 10(11). 2687. doi: 10.3390/foods10112687
- 153. Elhusseiny S. M., El-Mahdy T. S., Awad M. F., Elleboudy N. S.,
Farag M. M. S., Yassein M. A., Aboshanab K. M. Proteome Analysis and In Vitro
Antiviral, Anticancer and Antioxidant Capacities of the Aqueous Extracts of Lentinula
edodes and Pleurotus ostreatus Edible Mushrooms. Molecules (Basel, Switzerland). 2021.
Vol. 26(15). 4623. doi: 10.3390/molecules26154623
- 154. Roszczyk A., Turlo J., Zagozdzon R., Kaleta B. Immunomodulatory
Properties of Polysaccharides from Lentinula edodes. Intern. J. o f Molecular Sci. 2022.
Vol. 23(16). 8980. doi: 10.3390/ijms23168980
- 155. Lysakowska P., Sobota A., Wirkijowska A. Medicinal Mushrooms : Their
Bioactive Components, Nutritional Value and Application in Functional Food
Production-A Review. Molecules (Basel, Switzerland). 2023. Vol. 28(14). 5393. doi:
10.3390/molecules28145393
- 156. Gariboldi M. B., Marras E., Ferrario N., Vivona V., Prini P., Vignati F.,
Perletti G. Anti-Cancer Potential of Edible/Medicinal Mushrooms in Breast Cancer.
International J. o f Molecular Sci. 2023. Vol. 24(12). P. 10120. doi:
10.3390/ijms241210120
- 157. Muszynska B., Kala K., Wlodarczyk A., Krakowska A., Ostachowicz B.,
Gdula-Argasinska J., Suchocki P. Lentinula edodes as a Source of Bioelements Released
into Artificial Digestive Juices and Potential Anti-inflammatory Material. Biological
Trace Element Research. 2020. Vol. 194(2). P. 603-613. doi: 10.1007/s12011-019-
01782-8
- 158. Spim S. R. V., Castanho N. R. C. M., Pistila A. M. H., Jozala A. F.,
Oliveira Junior J. M., Grotto D. Lentinula edodes mushroom as an ingredient to enhance
the nutritional and functional properties of cereal bars. J. o f Food Sci. and Technology.
2021. Vol. 58(4). P. 1349-1357. doi: 10.1007/s13197-020-04646-5
- 159. Szacawa E., Dudek K., Bednarek D., Pieszka M., BederskaLojewska D. A Pilot Study on The Effect of a Novel Feed Additive Containing
Exogenous Enzymes, Acidifiers, Sodium Butyrate and Silicon Dioxide Nanoparticles on
Selected Cellular Immune Indices and Body Weight Gains of Calves. J. o f Vet. Research.
2021. Vol. 65(4). P. 497-504. doi: 10.2478/jvetres-2021-000068
- 160. Bederska-Lojewska D., Muszynska B., Orczewska-Dudek S.,
Kamyczek M., Kmiecik E., Lazur J., Pieszka M. Effect of Two Feed Additives-One
Multicomponent Based on Nanosilica and the Second Containing Mycelium of Lentinula
edodes Fortified with Selenium-On Production Parameters and Histological Analysis of
Calves' Duodenum and Abdominal Rumen. Animals: an Open Access J. from MDPI.
2022. Vol. 12(10). 1246. doi: 10.3390/ani12101246
- 161. Bintsis T. Foodborne pathogens. AIMS Microbiology, 2017. Vol. 3(3).
P. 529-563. doi: 10.3934/microbiol.2017.3.529
- 162. Litt P. K., Kelly A., Omar A., Johnson G., Vinyard B. T., Kniel K. E.,
Sharma M. Temporal and Agricultural Factors Influence Escherichia coli Survival in Soil
and Transfer to Cucumbers. Applied and Environmental Microbiology. 2021. Vol. 87(7).
e02418-20. doi: 10.1128/AEM.02418-20
- 163. Parmar S., Shrivastav S., Bhattacharya S. Insights on broad spectrum
applications and pertinence of biofiltration in various fields (1st ed.), An Innovative Role
of Biofiltration in Wastewater Treatment Plants (WWTPs). 2020. Chapter 10.
- 164. Couto S. R., Toca-Herrera J. L. Laccase production at reactor scale by
filamentous fungi. Biotechnology Advances. 2007. Vol. 25(6). P. 558-569. doi:
10.1016/j.biotechadv.2007.07.002
- 165. Chirnside A. E. M., Harris J. P., Gregory N. Degradation of harmful
bacteria in simulated wastewater by the white rot fungus P. ostreatus. World
Environmental and Water Resources Congress. 2013. doi: 10.1061/9780784412947.149
- 166. Omar A. N., Chirnside A., Kniel K. E. Evaluation of White Rot Fungus to
Control Growth of Escherichia coli in Cattle Manure. J. o f Food Protection. 2024.
Vol. 87(1). 100206. doi: 10.1016/j.jfp.2023.100206
- 167. Pointing S. B. Feasibility of bioremediation by white-rot fungi. Applied
microbiology and biotechnology. 2001. Vol. 57(1-2). P. 20-33. doi:
10.1007/s002530100745
- 168. Wu F., Ozaki H., Terashima Y., Imada T., Ohkouchi Y. Activities of
ligninolytic enzymes of the white rot fungus, Phanerochaete chrysosporium and its
recalcitrant substance degradability. Water Sci. and Technology. 1996. Vol. 34(7-8).
P. 69-78.
- 169. Verma P., Madamwar D. Production of ligninolytic enzymes for dye
decolorization by cocultivation of white-rot fungi Pleurotus ostreatus and phanerochaete
chrysosporium under solid-state fermentation. Applied Biochemistry and Biotechnology.
2002. Vol. 102-103(1-6). P. 109-118. doi: 10.1385/abab:102-103:1-6:109
- 170. Barron G. L., Thorn R. G. Destruction of nematodes by species of
Pleurotus. Canadian J. of Botany. 1987. Vol. 65(4). P. 774-778. doi: 10.1139/b87-103
- 171. Carroll G. C., Wicklow D.T. The Fungal Community; Its organization and
role in the ecosystem (4th ed.), The CRC Press, 1992. P. 535-539.
- 172. Palani S. Determination of the efficacy of fungal bioreactors to remove E.
coli from aqueous dairy manure. A thesis submitted to the Faculty of the University of
Delaware in partial fulfillment of the requirements for the degree of Master of Civil
Engineering (Order No. 28085953). 2020.
- 173. Barron G. L. Predatory fungi, wood decay, and the carbon cycle.
Biodiversity. 2003. Vol. 4(1). P. 3-9. doi: 10.1080/14888386.2003.9712621
- 174. Adeb O. A., Njobe P. B., Gbashi S., Nwinyi O. C., Mavumengwana V.
Review on microbial degradation of aflatoxins. Critical Reviews in Food Sci. and
Nutrition. 2017. Vol. 57(15). P. 3208-3217. doi: 10.1080/10408398.2015.1106440
- 175. Pitta D. W., Indugu N., Kumar S., Vecchiarelli B., Sinha R., Baker L. D.,
Bhukya B., Ferguson J. D. Metagenomic assessment of the functional potential of the
rumen microbiome in Holstein dairy cows. Anaerobe. 2016. Vol. 38. P. 50-60. doi:
10.1016/j.anaerobe.2015.12.003
- 176. Matthews C., Crispie F., Lewis E., Reid M., O'Toole P. W., Cotter P. D.
The rumen microbiome: a crucial consideration when optimising milk and meat
production and nitrogen utilisation efficiency. Gut Microbes. 2019. Vol. 10(2). P. 115
132. doi: 10.1080/19490976.2018.1505176
- 177. Henderson G., Cox F., Ganesh S., Jonker A., Young W., Global Rumen
Census Collaborators, Janssen P. H. Rumen microbial community composition varies
with diet and host, but a core microbiome is found across a wide geographical range.
Scientific reports. 2015. Vol. 5. 14567. doi: 10.1038/srep14567
- 178. Maga E. A., Weimer B. C., Murray J. D. Dissecting the role of milk
components on gut microbiota composition. Gut Microbes. 2013. Vol. 4(2). P. 136-139.
doi: 10.4161/gmic.23188
- 179. Chu G. M., Yang J. M., Kim H. Y., Kim C. H., Song Y. M. Effects of
fermented mushroom (Flammulina velutipes) by-product diets on growth performance
and carcass traits in growing-fattening Berkshire pigs. Animal Sci. J. = Nihon Chikusan
Gakkaiho. 2012. Vol. 83(1). P. 55-62. doi: 10.1111/j.1740-0929.2011.00924.x
- 180. Gao X. H., Dou L. M., Li J. T., Chen L., Zhang E. P. Fermentation
condition of Pleurotus eryngii waste sticks feed and its feed effects on goats. Chinese J.
o f Animal Nutrition. 2018. Vol. 30. P. 1973-1980.
- 181. Gao X. H., Qu X. M., Zhou Y. T., Zhang E. P. Isolation and identification
of forage microbial community and its effect on the fermentation quality of Pleurotus
eryngii substrate. Acta Microbiologica Sinica. 2018. Vol 58. P. 2110-2122. doi:
10.13343/j.cnki.wsxb.20170626
- 182. Rabelo C. H. S., Basso F. C., Lara E. C., Jorge L. G. O., Harter C. J.,
Mesquita L. G., Silva L. F. P., Reis R. A. Effects of Lactobacillus buchneri as a silage
inoculant and as a probiotic on feed intake, apparent digestibility and ruminal
fermentation and microbiology in wethers fed low-dry-matter whole-crop maize silage.
Grass and Forage Sci. 2018. Vol. 73(1). P. 67-77. doi: 10.1111/gfs.12303
- 183. Yang C. X., Wang T., Gao L. N., Yin H. J., Lu X. Isolation, identification
and characterization of lignin-degrading bacteria from Qinling, China. J. o f Applied
Microbiology. 2017. Vol. 123(6). P. 1447-1460. doi: 10.1111/jam.13562
- 184. Zhang B., Li Y., Zhang F., Linhardt R. J., Zeng G., Zhang A. Extraction,
structure and bioactivities of the polysaccharides from Pleurotus eryngii: A review.
Intern. J. o f Biological Macromolecules. 2020. Vol. 150. P. 1342-1347. doi:
10.1016/j.ijbiomac.2019.10.144
- 185. Guo Y., Chen X., Gong P., Wang R., Qi Z., Deng Z., Han A., Long H.,
Wang J., Yao W., Yang W., Wang J., Li N. Advances in Postharvest Storage and
Preservation Strategies for Pleurotus Eryngii. Foods (Basel, Switzerland). 2023.
Vol. 12(5). 1046. doi: 10.3390/foods12051046
- 186. Amerikanou C., Tagkouli D., Tsiaka T., Lantzouraki D. Z., Karavoltsos S.,
Sakellari A., Kleftaki S. A., Koutrotsios G., Giannou V., Zervakis G. I., Zoumpoulakis
P., Kalogeropoulos N., Kaliora A. C. Pleurotus eryngii Chips-Chemical Characterization
and Nutritional Value of an Innovative Healthy Snack. Foods (Basel, Switzerland). 2023.
Vol. 12(2). P. 353. doi: 10.3390/foods12020353
- 187. Huang X., Zhou L., You X., Han H., Chen X., Huang X. Production
performance and rumen bacterial community structure of Hu sheep fed fermented spent
mushroom substrate from Pleurotus eryngii. Sci. Reports. 2023. Vol. 13(1). 8696. doi:
10.1038/s41598-023 -35828-8
- 188. Bisen P. S., Baghel R. K., Sanodiya B. S., Thakur G. S., Prasad G. B.
Lentinus edodes : a macrofungus with pharmacological activities. Current Medicinal
Chemistry. 2010. Vol. 17(22). P. 2419-2430. doi: 10.2174/092986710791698495
- 189. Li X., Zhang H., Xu H. Analysis of chemical components of shiitake
polysaccharides and its anti-fatigue effect under vibration. Inter. J. o f Biological
Macromolecules. 2009. Vol. 45(4). P. 377-380. doi: 10.1016/j.ijbiomac.2009.07.005
- 190. Hobbs C. R. Medicinal value of Lentinus edodes (Berk.) Sing.
(Agaricomycetidae). A literature review. Intern J. o f Med. Mushrooms. 2000. Vol. 2.
P. 287-302. doi: 10.1615/IntJMedMushr.v2.i4.90
- 191. Regula J., Siwulski M. Dried shiitake (Lentinulla edodes) and oyster
(Pleurotus ostreatus) mushrooms as a good source of nutrient. Acta Scientiarum
Polonorum-TechnologiaAlimentaria. 2007. Vol. 6. P. 135-142.
- 192. Reis F. S., Barros L., Martins A., Ferreira I. C. Chemical composition and
nutritional value of the most widely appreciated cultivated mushrooms: an inter-species
comparative study. Food and Chemical Toxicology 2012. Vol. 50(2). P. 191-197. doi:
10.1016/j .fct.2011.10.056
- 193. Singh R. S., Kaur H. P., Kanwar J. R. Mushroom Lectins as Promising
Anticancer Substances. Current Protein & Peptide Sci. 2016. Vol. 17(8). P. 797-807.
doi: 10.2174/1389203717666160226144741
- 194. Fukushima M., Ohashi T., Fujiwara Y., Sonoyama K., Nakano M.
Cholesterol-lowering effects of maitake (Grifola frondosa) fiber, shiitake (Lentinus
edodes) fiber, and enokitake (Flammulina velutipes) fiber in rats. Experimental Biology
and Medicine (Maywood, N. J.). 2001. Vol. 226(8). P. 758-765. doi:
10.1177/153537020222600808
- 195. Anwar H., Suchodolski J. S., Ullah M. I., Hussain G., Shabbir M. Z.,
Mustafa I., Sohail M. U. Shiitake Culinary-Medicinal Mushroom, Lentinus edodes
(Agaricomycetes), Supplementation Alters Gut Microbiome and Corrects Dyslipidemia
in Rats. Inter. J. o f Med. Mushrooms. 2019. Vol. 21(1). P. 79-88. doi:
10.1615/IntJMedMushrooms.2018029348
- 196. Yang H., Hwang I., Kim S., Hong E. J., Jeung E. B. Lentinus edodes
promotes fat removal in hypercholesterolemic mice. Experimental and Therapeutic
Medicine. 2013. Vol. 6(6). P. 1409-1413. doi: 10.3892/etm.2013.1333
- 197. Pang F. H., Xie M. Q., Ling H. H. The investigation of immunodulator
tested for the results on the control of a coccidial infection. Chinese J. o f Vet.
Parasitology. 2000. Vol. 8. P. 1-3.
- 198. Yu J. G., Zhu L.Y. The use of Astragalus polysaccharide against infectious
bursa disease in chickens. American J. o f Traditional Chinese Vet. Medicine. 2000.
Vol. 6. P. 3-4.
- 199. Hearst R., Nelson D., McCollum G., Millar B. C., Maeda Y.,
Goldsmith C. E., Rooney P. J., Loughrey A., Rao J. R., Moore J. E. An examination of
antibacterial and antifungal properties of constituents of Shiitake (Lentinula edodes) and
oyster (Pleurotus ostreatus) mushrooms. Complementary Therapies in Clinical Practice.
2009. Vol. 15(1). P. 5-7. doi: 10.1016/j.ctcp.2008.10.002
- 200. Lee S. H., Lillehoj H. S., Jang S. I., Kim D. K., Ionescu C., Bravo D. Effect
of dietary curcuma, capsicum, and lentinus, on enhancing local immunity against Eimeria
acervulina infection. J. o f Poultry Sci. 2010. Vol. 47. P. 89-95. doi: 10.2141/jpsa.009025
- 201. Kusaba A., Okada Y., Ueno H., Yamamoto I., Mori Y., Tanaka N., Arai T.,
Kawasumi K. Effects of supplementation with Shiitake powder, Lentinula edodes, on
anti-oxidative activities and energy/lipid metabolism in healthy dogs. Research Square.
2022. doi: 10.21203/rs.3.rs-1199968/v1
- 202. Soroko M., Gorniak W., Zielinska P., Gorniak A., Sniegucka K.,
Nawrot K., Korczynski M. Effect of Lentinula edodes on Morphological and
Biochemical Blood Parameters of Horses. Animals: an Open Access J. from MDPI. 2022.
Vol. 12(9). 1106. doi: 10.3390/ani12091106
- 203. Soroko-Dubrovina M., Gorniak W., Zielinska P., Gorniak A.,
Cebulj-Kadunc N., Korczynski M. Evaluation of Shiitake Mushroom (Lentinula edodes)
Supplementation on the Blood Parameters of Young Thoroughbred Racehorses. Animals:
an Open Access J. from MDPI. 2022. Vol. 12(22). 3212. doi: 10.3390/ani12223212
- 204. Oh Y. K., Lee W. M., Choi C. W., Kim K. H., Hong S. K., Lee S. C.,
Seol Y. J., Kwak W. S., Choi N. J. Effects of spent mushroom substrates supplementation
on rumen fermentation and blood metabolites in Hanwoo steers. Asian-Australasian J. o f
Animal Sci. 2010. Vol. 23(12). P. 1608-1613. doi: 10.5713/ajas.2010.10200
- 205. Lee S. M., Hwang J. H., Yoon Y. B., Kwak W. S., Kim Y. I., Moo S. H.,
Jeon B. T. Effects of spent mushroom substrates addition on eating behavior of growing
Hanwoo. J. o f The Korean Society o f Grassland and Forage Sci. 2008. Vol. 28. P. 107
117. doi: 10.5333/KGFS.2008.28.2.107
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