Does Mealworm (Tenebrio molitor) Can be Considered as a Functional Additive in Japanese Quails̓ Diets?
محورهای موضوعی : Camel
1 - Department of Animal Science, East Azerbaijan Agricultural and Natural Resources Research and Education Center, Agricultural Research Education and Extension Organization (AREEO), Tabriz, Iran
2 - Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Science, Sari, Iran
کلید واژه: humoral immunity, Japanese quails, mealworm,
چکیده مقاله :
This study was conducted to evaluate the effects of mealworm (Tenebrio molitor) dietary supplementation on egg production, egg traits, humoral immunity and ileal microbiota in Japanese quails. A hundred and twenty female Japanese quails (Coturnix coturnix japonica) were used in a completely randomized design with three treatments, five replicates, and eight birds in each replicate. Experimental diets included: basal diet (without any additives), basal diet + 0.1% full-fat mealworm powder, basal diet + 0.2% mealworm powder. The experiment lasted five weeks, and the quails had free access to the feed and water. The results showed that mealworm supplementation did not have any significant effect on feed conversion ratio of the quails during the whole period of the experiment. At the 5th week of the experiment, egg weight and egg mass of the quails fed with mealworm increased linearly, and the feed intake of the birds fed with 0.1% mealworm was different quadratically. Different levels of mealworm powder supplementation increased egg albumen weight and yolk height linearly during the whole period of the experiment. Adding mealworm powder increased antibody titer against sheep red blood cell in laying quails on 89 and 96 d of age. It is concluded that mealworm supplementation at the level of 0.1% improved egg weight, egg production, albumen weight, yolk height, and humoral immunity of Japanese laying quails, so it has the potential to be considered as an organic functional additive in quails' diet.
Agunbiade J.A., Adeyemi O.A., Ashiru O.M., Awojobi H.A., Taiwo A.A., Oke D.B. and Adekunmisi A.A. (2007). Replacement of fish meal with maggot meal in cassava-based layers' diets. J. Poul. Sci. 44, 278-282.
Al-Qazzaz M.F.A., Ismail D., Akit H. and Idris L.H. (2016). Effect of using insect larvae meal as a complete protein source on quality and productivity characteristics of laying hens. Rev. Bras. Zootec. 45, 518-523.
Amao O.A., Oladunjoye I.O., Togun V.A., Olubajo K. and Oyaniyi O. (2010). Effect of westwood (Cirina forda) larva meal on the laying performance and egg characteristics of laying hen in a tropical environment. Int. J. Poult. Sci. 9, 450-454.
AOAC. (2005). Official Methods of Analysis. Vol. I. 18th Ed. Association of Official Analytical Chemists, Arlington, VA, USA.
Bava L., Jucker C., Gislon G., Lupi D., Savoldelli S., Zucali M. and Colombini S. (2019). Rearing of hermetia illucens on different organic by-products: Influence on growth, waste reduction, and environmental impact. Animals. 9, 289-295.
Benzertiha A., Kierończyk B., Kołodziejski P., Pruszyńska–Oszmałek E., Rawski M., Józefiak D. and Józefiak A. (2020). Tenebrio molitor and Zophobas morio full-fat meals as functional feed additives affect broiler chickens' growth performance and immune system traits. Poult. Sci. 99, 196-206.
Borrelli L., Coretti L., Dipineto L., Bovera F., Menna F., Chiariotti L., Nizza A., Lembo F. and Fioretti A. (2017). Insect-based diet, a promising nutritional source, modulates gut microbiota composition and SCFAs production in laying hens. Sci. Rep. 7, 1-11.
Bovera F., Loponte R., Marono S., Piccolo G., Parisi G., Iaconisi V., Gasco L. and Nizza A. (2016). Use of Tenebrio molitor larvae meal as protein source in broiler diet: Effect on growth performance, nutrient digestibility, and carcass and meat traits. J. Anim. Sci. 94, 639-647.
Bovera F., Piccolo G., Gasco L., Marono S., Loponte R., Vassalotti G., Mastellone V., Lombardi P., Attia Y.A. and Nizza A. (2015). Yellow mealworm larvae (Tenebrio molitor) as a possible alternative to soybean meal in broiler diets. British Poult. Sci. 56, 569-575.
Care ICoA. (1995). Guide to the Care and Use of Experimental Animals. University of Technology Isfahan, Isfahan, Iran.
Dalle Zotte A., Singh Y., Michiels J. and Cullere M. (2019). Black soldier fly (Hermetia illucens) as dietary source for laying quails: live performance, and egg physico-chemical quality, sensory profile and storage stability. Animals. 9, 115-123.
Dankwa D., Nelson F.S., Oddoye E.O.K. and Duncan J.L. (2002). Housefly larvae as a feed supplement for rural poultry. Ghana J. Agric. Sci. 35, 185-187.
Dillak S.Y.F.G., Suryatni N.P.F., Handayani H.T., Temu S.T., Nastiti H.P., Osa D.B., Ginting R. and Henuk Y.L. (2019). The effect of fed maggot meal as a supplement in the commercial diets on the performance of finisher broiler chickens. Pp. 25-33 in IOP Conf. Ser.: Earth Environ. Sci., Bristol, England, United Kingdom.
Duncan D.B. (1955). Multiple ranges and multiple F-test. Biometrics. 11, 1-42.
Esteban M.A., Cuesta A., Ortuno J. and Meseguer J. (2001). Immunomodulatory effects of dietary intake of chitin on gilthead seabream (Sparus aurata) innate immune system. Fish Shellfish Immunol. 11, 303-315.
FAO. (2010). Promoting the Contribution of Edible Forest Insects in Assuring Food Security. FAO Forestry Department Programme. Forest Economy, Policy and Product Divisions. Food and Agriculture Organization of the United Nations (FAO), Rome, Italy.
Gadde U., Kim W.H., Oh S.T. and Lillehoj H.S. (2017). Alternatives to antibiotics for maximizing growth performance and feed efficiency in poultry: a review. Anim. Health Res. Rev. 18, 26-45.
Grasman K.A. (2010). In vivo functional tests for assessing immunotoxicity in birds. Pp. 387-398 in Immunotoxicity Testing. R.R. Dietert, Ed. Humana Press, Totowa, New Jersey.
Hesami Y., Esmaielzadeh L., Karimi-Torshizi M.A., Seidavi A., and Vlčková R. (2020). Effect of diets containing earthworm powder and vermihumus on egg production, hatchability, blood parameters and immunity of Japanese breeder quails. J. Anim. Physiol. Anim. Nutr. 205(2), 316-325.
Hu C.H., Gu L.Y., Luan Z., Song J. and Zhu K. (2012). Effects of montmorillonite-zinc oxide hybrid on performance, diarrhea, intestinal permeability and morphology of weanling pigs. Anim. Feed Sci. Technol. 177, 108-115.
Islam M.M. and Yang C.J. (2016). Efficacy of mealworm and super mealworm larvae probiotics as an alternative to antibiotics challenged orally with Salmonella and E. coli infection in broiler chicks. Poult. Sci. 96, 27-34.
Józefiak A., Kierończyk B., Rawski M., Mazurkiewicz J., Benzertiha A., Gobbi P., Nogales-Mérida S., Świątkiewicz S. and Józefiak D. (2018). Full-fat insect meals as feed additive–the effect on broiler chicken growth performance and gastrointestinal tract microbiota. J. Anim. Feed Sci. 27, 131-139.
Józefiak D., Józefiak A., Kierończyk B., Rawski M., Świątkiewicz S., Długosz J. and Engberg R.M. (2016a). Insects–a natural nutrient source for poultry–a review. Ann. Anim. Sci. 16, 297-313.
Józefiak D., Świątkiewicz S., Kierończyk B., Rawski M., Długosz J., Engberg R.M. and Højberg O. (2016b). Clostridium perfringens challenge and dietary fat type modifies performance, microbiota composition and histomorphology of the broiler chicken gastrointestinal tract. European Poult. Sci. 80, 130-140.
Khan M., Chand N., Khan S., Khan R.U. and Sultan A. (2018). Utilizing the house fly (Musca domestica) larva as an alternative to soybean meal in broiler ration during the starter phase. Brazilian J. Poult. Sci. 20, 9-14.
Khempaka S., Chitsatchapong C. and Molee W. (2011). Effect of chitin and protein constituents in shrimp head meal on growth performance, nutrient digestibility, intestinal microbial populations, volatile fatty acids, and ammonia production in broilers. J. Appl. Poult. Res. 20, 1-11.
Khusro M., Andrew N.R. and Nicholas A. (2012). Insects as poultry feed: A scoping study for poultry production systems in Australia. World's Poult. Sci. J. 68, 435-446.
Kierończyk B., Rawski M., Józefiak A., Mazurkiewicz J., Świątkiewicz S., Siwek M., Bednarczyk M., Szumacher-Strabel M., Cieślak A., Benzertiha A. and Józefiak D. (2018). Effects of replacing soybean oil with selected insect fats on broilers. Anim. Feed Sci. Technol. 240, 170-183.
Kul S. and Seker I. (2004). Phenotypic correlations between some external and internal egg quality traits in the Japanese quail (Coturnix coturnix japonica). Int. J. Poult. Sci. 3, 400-405.
Lee C.G., Da Silva C.A., Lee J.Y., Hartl D. and Elias J.A. (2008). Chitin regulation of immune responses: An old molecule with new roles. Curr. Opin. Immunol. 2, 684-689.
Lee J.A., Kim Y.M., Park Y.K., Yang Y.C., Jung B.G. and Lee B.J. (2018). Black soldier fly (Hermetia illucens) larvae enhances immune activities and increases survivability of broiler chicks against experimental infection of Salmonella Gallinarum. J. Vet. Med. Sci. 80(5), 736-740.
Manniello M.D., Moretta A., Salvia R., Scieuzo C., Lucchetti D., Vogel H., Sgambato A. and Falabella P. (2021). Insect antimicrobial peptides: Potential weapons to counteract the antibiotic resistance. Cell. Mol. Life Sci. 78, 4259-4282.
Marareni M. and Mnisi C.M. (2020). Growth performance, serum biochemistry and meat quality traits of Jumbo quails fed with mopane worm (Imbrasia belina) meal-containing diets. Vet. Anim. Sci. 10, 100141-100147.
Maurer V., Holinger M., Amsler Z., Früh B., Wohlfahrt J., Stamer A. and Leiber F. (2016). Replacement of soybean cake by Hermetia illucens meal in diets for layers. J. Insects Food Feed. 2, 83-90.
Nogales-Mérida S., Gobbi P., Józefiak D., Mazurkiewicz J., Dudek K., Rawski M., Kierończyk B. and Józefiak A. (2019). Insect meals in fish nutrition. Rev. Aquac. 11, 1080-1103.
North M.O. and Bell D.D. (1990). Commercial chicken production manual. Van Nostrand Reinhold, New York.
NRC. (1994). Nutrient Requirements of Poultry, 9th Rev. Ed. National Academy Press, Washington, DC., USA.
Park S.I., Chang B.S. and Yoe S.M. (2014). Detection of antimicrobial substances from larvae of the black soldier fly, Hermetia illucens (Diptera: Stratiomyidae). Entomol. Res. 44, 58-64.
Park S.I., Kim J.W. and Yoe S.M. (2015). Purification and characterization of a novel antibacterial peptide from black soldier fly (Hermetia illucens) larvae. Dev. Compar. Immunol. 52, 98-106.
Rumpold B.A. and Schlüter O.K. (2013). Potential and challenges of insects as an innovative source for food and feed production. Innov. Food Sci. Emerg. Technol. 17, 1-11.
SAS Institute. (2001). SAS®/STAT Software, Release 9.4. SAS Institute, Inc., Cary, NC. USA.
Sayed W.A., Ibrahim N.S., Hatab M.H., Zhu F. and Rumpold B.A. (2019). Comparative study of the use of insect meal from Spodoptera littoralis and Bactrocera zonata for feeding Japanese quail chicks. Animals. 9, 136-145.
Stoops J., Crauwels S., Waud M., Claes J., Lievens B. and Van Campenhout L. (2016). Microbial community assessment of mealworm larvae (Tenebrio molitor) and grasshoppers (Locusta migratoria migratorioides) sold for human consumption. Food Microbiol. 53, 122-127.
Swiatkiewicz S., Swiatkiewicz M., Arczewska Wlosek A. and Jozefiak D. (2015). Chitosan and its oligosaccharide derivatives (chito oligosaccharides) as feed supplements in poultry and swine nutrition. J. Anim. Physiol. Anim. Nutr. 99, 1-12.
Tabata E., Kashimura A., Wakita S., Ohno M., Sakaguchi M., Sugahara Y., Kino Y., Matoska V., Bauer P.O. and Oyama F. (2017). Gastric and intestinal proteases resistance of chicken acidic chitinase nominates chitin-containing organisms for alternative whole edible diets for poultry. Sci. Rep. 7, 1-11.
Ullah R., Khan S., Khan N.A., Mobashar M., Sultan A., Ahmad N. and Lohakare J. (2017). Replacement of soybean meal with silkworm meal in the diets of white leghorn layers and effects on performance, apparent total tract digestibility, blood profile and egg quality. Int. J. Vet. Health Sci. Res. 5, 200-207.
Van Huis A. (2013). Potential of insects as food and feed in assuring food security. Ann. Rev. Entomol. 58, 563-583.
Veldkamp T., Van Duinkerken G., van Huis A., Lakemond C.M.M., Ottevanger E., Bosch G. and Van Boekel T. (2012). Insects as a Sustainable Feed Ingredient in Pig and Poultry Diets: A Feasibility Study. Wageningen UR Livestock Research, Wageningen, The Netherlands.
Velten S., Neumann C., Schäfer J. and Liebert F. (2018). Effects of the partial replacement of soybean meal by insect or algae meal in chicken diets with graded amino acid supply on parameters of gut microbiology and dietary protein quality. Open J. Anim. Sci. 8, 259-279.
Xu Y., Shi B., Yan S., Li T., Guo Y. and Li J. (2013). Effects of chitosan on body weight gain, growth hormone and intestinal morphology in weaned pigs. Asian-Australasian J. Anim. Sci. 26, 1484-493.
Zadeh Z.S., Kheiri F. and Faghani M. (2019). Use of yellow mealworm (Tenebrio molitor) as a protein source on growth performance, carcass traits, meat quality and intestinal morphology of Japanese quails (Coturnix japonica). Vet. Anim. Sci. 8, 1-5.