研究论文 RESEARCHPAPER

饲粮中添加精氨酸对意大利蜜蜂工蜂幼虫生理机能的影响

  • 孙桂云 ,
  • 胡希怡 ,
  • 于静 ,
  • 王红芳 ,
  • 刘振国 ,
  • 胥保华
展开
  • 山东农业大学动物科技学院, 泰安 271000
孙桂云(1996—),女,山东安丘人,硕士研究生,从事动物营养与饲料科学研究。E-mail:3350634378@qq.com

收稿日期: 2021-11-04

  网络出版日期: 2022-06-14

基金资助

泰山产业领军人才高效生态农业创新类项目(LJNY202003);财政部和农业农村部国家现代农业产业技术体系(CARS-44)

Effects of Dietary Arginine on Physiological Function of Apis mellifera ligustica Worker Bee Larvae

  • SUN Guiyun ,
  • HU Xiyi ,
  • YU Jing ,
  • WANG Hongfang ,
  • LIU Zhenguo ,
  • XU Baohua
Expand
  • College of Animal Science and Technology, Shandong Agricultural University, Tai'an 271000, China

Received date: 2021-11-04

  Online published: 2022-06-14

摘要

本试验旨在研究饲粮中添加不同水平精氨酸对意大利蜜蜂(Apis mellifera ligustica)工蜂幼虫化蛹率、羽化率、抗氧化能力、免疫力和中肠形态的影响。选取意大利蜜蜂工蜂幼虫1 200只,随机分成5组,每组5个重复,每个重复48只。5组工蜂幼虫分别饲喂精氨酸添加水平为0(对照组)、0.2%、0.4%、0.6%、0.8%的试验饲粮,在室内饲养幼虫直至成虫羽化出房,观察幼虫的化蛹率和羽化率;测4、6日龄工蜂幼虫抗氧化、免疫等指标;测6日龄工蜂幼虫中肠形态、血淋巴生化指标。结果显示:1)与对照组相比,饲粮中添加0.6%和0.8%精氨酸显著降低了工蜂幼虫的化蛹率和羽化率(P<0.05)。2)与对照组相比,饲粮中添加0.2%~0.8%精氨酸显著提高了工蜂幼虫血淋巴中尿素含量(P<0.05),添加0.2%精氨酸显著提高了工蜂幼虫血淋巴中白蛋白含量(P<0.05)。3)与对照组相比,饲粮中添加0.2%精氨酸显著提高了4日龄工蜂幼虫鸟氨酸脱羧酶的活性(P<0.05),添加0.6%精氨酸显著提高了6日龄工蜂幼虫精氨酸酶的活性(P<0.05),添加0.2%、0.4%和0.8%精氨酸显著提高了6日龄工蜂幼虫鸟氨酸脱羧酶基因的相对表达量(P<0.05)。4)与对照组相比,饲粮中添加0.4%精氨酸显著提高了4、6日龄工蜂幼虫的过氧化氢酶活性和过氧化氢酶基因相对表达量(P<0.05),添加0.8%精氨酸显著提高了4、6日龄工蜂幼虫的总抗氧化能力(P<0.05)。5)与对照组相比,饲粮中添加0.2%精氨酸显著提高了4日龄工蜂幼虫的溶菌酶基因相对表达量和6日龄工蜂幼虫的溶菌酶活性(P<0.05)。6)精氨酸添加水平为0.8%时对6日龄工蜂幼虫的中肠重建有抑制作用。由此可知,饲粮中添加精氨酸对意大利蜜蜂工蜂幼虫化蛹率和羽化率、抗氧化能力以及免疫力均有一定的影响,适量添加可以提高意大利蜜蜂工蜂幼虫的抗氧化能力,而高剂量添加则会降低意大利蜜蜂工蜂幼虫的化蛹率和羽化率。

本文引用格式

孙桂云 , 胡希怡 , 于静 , 王红芳 , 刘振国 , 胥保华 . 饲粮中添加精氨酸对意大利蜜蜂工蜂幼虫生理机能的影响[J]. 动物营养学报, 2022 , 34(6) : 3918 -3929 . DOI: 10.3969/j.issn.1006-267x.2022.06.051

Abstract

This experiment was conducted to investigate the effects of dietary arginine supplemental level on pupation rate, emergence rate, antioxidant capacity, immunity and midgut morphology of Apis mellifera ligustica worker bee larvae. A total of 1 200 Apis mellifera ligustica worker bee larvae were randomly divided into 5 groups with 5 replicates per group and 48 larvae per replicate. The larvae in the 5 groups were fed experimental diets supplemented with 0 (control group), 0.2%, 0.4%, 0.6% and 0.8% arginine, respectively. The larvae were reared in lab condition until emergence, and the pupation rate and emergence rate of the larvae were measured. The antioxidant and immune indexes of 4- and 6-day-old worker bee larvae in each group were measured; midgut morphology and hemolymph biochemical indexes of 6-day-old worker bee larvae were measured. The results showed as follows:1) dietary supplemented with 0.6% and 0.8% arginine significantly decreased the pupation rate and emergence rate of worker bee larvae compared with the control group (P<0.05). 2) Compared with the control group, dietary supplemented with 0.2% to 0.8% arginine significantly increased the hemolymph urea content of worker bee larvae (P<0.05); meanwhile, dietary supplemented with 0.2% arginine supplementation significantly increased the hemolymph albumin content of worker bee larvae (P<0.05). 3) Compared with the control group, dietary supplemented with 0.2% arginine significantly increased ornithine decarboxylic enzyme activity of 4-day-old worker bee larvae (P<0.05); the arginase activity of 6-day-old worker bee larvae was significantly increased when supplemented with 0.6% arginine (P<0.05); when dietary supplemented with 0.2%, 0.4% and 0.8% arginine, the relative expression level of ornithine decarboxylase gene of 6-day-old worker bee larvae was significantly increased (P<0.05). 4) Compared with the control group, dietary supplemented with 0.4% arginine significantly increased the catalase activity and the relative expression level of catalase gene of 4- and 6-day-old worker bee larvae (P<0.05); dietary supplemented with 0.8% arginine significantly increased the total antioxidant capacity of 4- and 6-day-old worker bee larvae (P<0.05). 5) Compared with the control group, dietary supplemented with 0.2% arginine significantly increased the relative expression level of lysozyme gene of 4-day-old worker bee larvae and the lysozyme activity of 6-day-old worker bee larvae (P<0.05). 6) Supplementation of 0.8% arginine significantly inhibited midgut remodeling in 6-day-old worker bee larvae. Thus, it can be seen that dietary arginine supplementation has certain effects on the pupation rate and emergence rate, antioxidant capacity and immunity of Apis mellifera ligustica worker bee larvae. The antioxidant capacity of Apis mellifera ligustica worker bee larvae can be improved at the appropriate dosage of arginine, but the pupation rate and emergence rate of Apis mellifera ligustica worker bee larvae can be reduced at the high dosage of arginine.

参考文献

[1] GURBUZ A T, KUNZELMAN J, RATZER E E.Supplemental dietary arginine accelerates intestinal mucosal regeneration and enhances bacterial clearance following radiation enteritis in rats[J].Journal of Surgical Research, 1998, 74(2):149-154.  
[2] NIEVES C, Jr, LANGKAMP-HENKEN B.Arginine and immunity:a unique perspective[J].Biomedicine & Pharmacotherapy, 2002, 56(10):471-482.  
[3] 周凡.饲料赖氨酸和精氨酸对黑鲷幼鱼生长影响及其拮抗作用机理研究[D].博士学位论文.杭州:浙江大学, 2011. ZHOU F.Study on effects of dietary lysine and arginine on growth performance, and the arginine/lysine antagonism mechanism in juvenile black sea bream, Acanthopagrus schlegelii[D].Ph.D.Thesis.Hangzhou:Zhejiang University, 2011.(in Chinese)
[4] 姚康, 褚武英, 邓敦, 等.不同精氨酸添加水平对哺乳仔猪生长性能的影响[J].天然产物研究与开发, 2008(1):121-124. YAO K, CHU W Y, DENG D, et al.Effects of different dietary arginine supplementation on sucking piglets' growth performance[J].Natural Product Research and Development, 2008(1):121-124.(in Chinese)
[5] 陈思琦, 程镇燕, 安贸麟, 等.豆粕替代鱼粉并添加精氨酸对点带石斑鱼消化酶活性和肠道组织结构的影响[J].中国饲料, 2019(1):57-64. CHEN S Q, CHENG Z Y, AN M L, et al.Effect of dietary soybean meal replacing fish meal and supplemented with arginine on digestion and intestinal structure of grouper in Epinephelus malabaricus[J].China Feed, 2019(1):57-64.(in Chinese)
[6] BAYLIAK M M, LYLYK M P, MANIUKH O V, et al.Dietary L-arginine accelerates pupation and promotes high protein levels but induces oxidative stress and reduces fecundity and life span in Drosophila melanogaster[J].Journal of Comparative Physiology B, 2018, 188(1):37-55.  
[7] LUCKHART S, VODOVOTZ Y, CUI L, et al.The mosquito Anopheles stephensi limits malaria parasite development with inducible synthesis of nitric oxide[J].Proceedings of the National Academy of Sciences of the United States of America, 1998, 95(10):5700-5705.  
[8] KRAAIJEVELD A R, ELRAYES N P, SCHUPPE H, et al.L-arginine enhances immunity to parasitoids in Drosophila melanogaster and increases NO production in lamellocytes[J].Developmental & Comparative Immunology, 2011, 35(8):857-864.  
[9] DE GROOT A P.Amino acid requirements for growth of the honeybee (Apis mellifica L.)[J].Experientia, 1952, 8(5):192-194.  
[10] NEGRI P, RAMIREZ L, QUINTANA S, et al.Dietary supplementation of honey bee larvae with arginine and abscisic acid enhances nitric oxide and granulocyte immune responses after trauma[J].Insects, 2017, 8(3):85.
[11] 封福鲜.精氨酸、赖氨酸和苏氨酸对瓦氏黄颡鱼幼鱼生长、代谢及免疫力的影响[D].硕士学位论文.青岛:中国海洋大学, 2011. FENG F X.Effects of dietary arginine, lysine and threonine on growth, metabolism and immune responses of juvenile darkbarbel catfish (Pelteobagrus vachelli)[D].Master's Thesis.Qingdao:Ocean University of China, 2011.(in Chinese)
[12] VIERSTRAETE E, CERSTIAENS A, BAGGERMAN G, et al.Proteomics in Drosophila melanogaster:first 2D database of larval hemolymph proteins[J].Biochemical and Biophysical Research Communications, 2003, 304(4):831-838.  
[13] CHAN Q W T, HOWES C G, FOSTER L J.Quantitative comparison of caste differences in honeybee hemolymph[J].Molecular & Cellular Proteomics, 2006, 5(12):2252-2262.  
[14] IGARASHI F, OGIHARA M H, IGA M, et al.Cholesterol internalization and metabolism in insect prothoracic gland, a steroidogenic organ, via lipoproteins[J].Steroids, 2018, 134:110-116.
[15] 刘军, 仲召鑫, 彭众, 等.哺乳期补饲精氨酸对断奶仔猪肝脏脂代谢功能的影响[J].动物营养学报, 2020, 32(2):674-681. LIU J, ZHONG Z X, PENG Z, et al.Effects of arginine supplementation during lactation period on liver lipid metabolism function of weaned piglets[J].Chinese Journal of Animal Nutrition, 2020, 32(2):674-681.(in Chinese)
[16] SAMSON M L.Drosophila arginase is produced from a nonvital gene that contains the elav locus within its third intron[J].Journal of Biological Chemistry, 2000, 275(40):31107-31114.  
[17] 曾雯娉.凡纳滨对虾幼虾对赖氨酸、蛋氨酸、精氨酸和苯丙氨酸需要量的研究[D].硕士学位论文.湛江:广东海洋大学, 2012. ZENG W P.Study on the requirements of lysine, methionine, arginine and phenylalanine for juvenile pacific white shrimp, Litopenaeus vannamei[D].Master's Thesis.Zhanjiang:Guangdong Ocean University, 2012.(in Chinese)
[18] EREL O.A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation[J].Clinical Biochemistry, 2004, 37(4):277-285.  
[19] VASYLKOVSKA R, PETRIV N, SEMCHYSHYN H.Carbon sources for yeast growth as a precondition of hydrogen peroxide induced hormetic phenotype[J].International Journal of Microbiology, 2015, 2015:697813.
[20] 王世昌, 张文杰, 韩明, 等.补喂瘤胃保护性精氨酸对绵羊血浆中氨基酸浓度、激素水平和抗氧化能力的影响[J].中国饲料, 2020(17):20-28. WANG S C, ZHANG W J, HAN M, et al.The supplemental effects of rumen-protected arginine on plasma amino acids concentrations, hormone levels and antioxidant status in sheep[J].China Feed, 2020(17):20-28.(in Chinese)
[21] CAO W, XIAO L, LIU G M, et al.Dietary arginine and N-carbamylglutamate supplementation enhances the antioxidant statuses of the liver and plasma against oxidative stress in rats[J].Food & Function, 2016, 7(5):2303-2311.  
[22] 贾建英, 李成贤.精氨酸对人工饲养仔猪生长性能及机体抗氧化功能的影响[J].饲料研究, 2020, 43(5):52-54. JIA J Y, LI C X.Effect of arginine on growth performance and body antioxidation function of artificial feeding piglets[J].Feed Research, 2020, 43(5):52-54.(in Chinese)
[23] CASTELLI L, BRANCHICCELA B, GARRIDO M, et al.Impact of nutritional stress on honeybee gut microbiota, immunity, and Nosema ceranae infection[J].Microbial Ecology, 2020, 80(4):908-919.  
[24] GILLESPIE J P, KANOST M R, TRENCZEK T.Biological mediators of insect immunity[J].Annual Review of Entomology, 1997, 42:611-643.
[25] IMLER J L, BULET P.Antimicrobial peptides in Drosophila:structures, activities and gene regulation[J].Chemical Immunology and Allergy, 2005, 86:1-21.
[26] 武文一.吉富罗非鱼对饲料精氨酸、苯丙氨酸和缬氨酸的需要量研究[D].硕士学位论文.上海:上海海洋大学, 2016. WU W Y.Studies on the requirements of arginine, phenylalanine and valine in the diet to GIFT tilapia (Oreochromis niloticus)[D].Master's Thesis.Shanghai:Shanghai Ocean University, 2016.(in Chinese)
[27] DA CRUZ-LANDIM C, CAVALCANTE V M.Ultrastructural and cytochemical aspects of metamorphosis in the midgut of Apis mellifera L. (Hymenoptera:Apidae:Apinae)[J].Zoological Science, 2003, 20(9):1099-1107.  
[28] MARTINS G F, NEVES C A, CAMPOS L A O, et al.The regenerative cells during the metamorphosis in the midgut of bees[J].Micron, 2006, 37(2):161-168.  
[29] GREGORC A, BOWEN I D.Programmed cell death in the honey-bee (Apis mellifera L.) larvae midgut[J].Cell Biology International, 1997, 21(3):151-158.  
[30] GONCU E, URANLI R, SELEK G, et al.Developmental expression of ecdysone-related genes associated with metamorphic changes during midgut remodeling of silkworm Bombyx mori (Lepidoptera:Bombycidae)[J].Journal of Insect Science, 2016, 16(1):86.
文章导航

/