SDS-PAGE-Based Quantitative Assay of Hemolymph Proteins in Honeybees: Progress and Prospects for Field Application

In human and veterinary medicine, serum proteins are considered to be useful biomarkers for assessing the health and nutritional status of the organism. Honeybee hemolymph has a unique proteome that could represent a source of valuable biomarkers. Therefore, the aims of this study were to separate and identify the most abundant proteins in the hemolymph of worker honeybees to suggest a panel of these proteins that could represent useful biomarkers for assessing the nutritional and health status of the colonies and, finally, to analyze them in different periods of the year. Four apiaries were selected in the province of Bologna, and the bees were analyzed in April, May, July, and November. Thirty specimens from three hives of each apiary were sampled and their hemolymph was collected. The most represented bands obtained after 1D sodium-dodecyl-sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) were cut from the gel, and the proteins were identified using an LC-ESI-Q-MS/MS System. A total of twelve proteins were unmistakably identified; the two most abundant proteins were apolipophorin and vitellogenin, which are known biomarkers of bee trophic and health status. The two other proteins identified were transferrin and hexamerin 70a, the first being involved in iron homeostasis and the second being a storage protein. Most of these proteins showed an increase from April to November, mirroring the physiological changes of honeybees during the productive season. The current study suggests a panel of biomarkers from honeybee hemolymph worth testing under different physiological and pathological field conditions.

[1]  G. Amdam,et al.  How Honey Bee Vitellogenin Holds Lipid Cargo: A Role for the C-Terminal , 2022, Frontiers in Molecular Biosciences.

[2]  G. DeGrandi-Hoffman,et al.  Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera , 2021, PLoS pathogens.

[3]  E. Bellei,et al.  Essential (Mg, Fe, Zn and Cu) and Non-Essential (Cd and Pb) Elements in Predatory Insects (Vespa crabro and Vespa velutina): A Molecular Perspective , 2020, International journal of molecular sciences.

[4]  F. Dondi,et al.  Urinary proteome and metabolome in dogs (Canis lupus familiaris): The effect of chronic kidney disease. , 2020, Journal of proteomics.

[5]  B. Lemaître,et al.  Iron sequestration by transferrin 1 mediates nutritional immunity in Drosophila melanogaster , 2020, Proceedings of the National Academy of Sciences.

[6]  A. Imdorf,et al.  A scientific note on the ‘Liebefeld Method’ to estimate honey bee colony strength: its history, use, and translation , 2020, Apidologie.

[7]  P. Hyršl,et al.  Winter honeybee (Apis mellifera) populations show greater potential to induce immune responses than summer populations after immune stimuli , 2020, Journal of Experimental Biology.

[8]  J. Lundgren,et al.  Nutritional status of honey bee (Apis mellifera L.) workers across an agricultural land-use gradient , 2019, Scientific Reports.

[9]  V. Beneš,et al.  Expansion of Imaginal Disc Growth Factor Gene Family in Diptera Reflects the Evolution of Novel Functions , 2019, Insects.

[10]  L. Vojtek,et al.  The Year of the Honey Bee (Apis mellifera L.) with Respect to Its Physiology and Immunity: A Search for Biochemical Markers of Longevity , 2019, Insects.

[11]  Vincent A. Ricigliano,et al.  Honey bee colony performance and health are enhanced by apiary proximity to US Conservation Reserve Program (CRP) lands , 2019, Scientific Reports.

[12]  J. Carlson,et al.  The diverse small proteins called odorant-binding proteins , 2018, Royal Society Open Biology.

[13]  G. Cowin,et al.  Multi-modal imaging and analysis in the search for iron-based magnetoreceptors in the honeybee Apis mellifera , 2018, Royal Society Open Science.

[14]  R. Galuppi,et al.  Biomarkers of nutritional status in honeybee haemolymph: effects of different biotechnical approaches for Varroa destructor treatment and wintering phase , 2018, Apidologie.

[15]  Chuan Ma,et al.  Proteome Comparisons between Hemolymph of Two Honeybee Strains (Apis mellifera ligustica) Reveal Divergent Molecular Basis in Driving Hemolymph Function and High Royal Jelly Secretion. , 2018, Journal of proteome research.

[16]  P. Kryger,et al.  Differential proteomics reveals novel insights into Nosema-honey bee interactions. , 2016, Insect biochemistry and molecular biology.

[17]  M. Kamler,et al.  Detailed proteome mapping of newly emerged honeybee worker hemolymph and comparison with the red-eye pupal stage , 2016, Apidologie.

[18]  F. Dondi,et al.  The effect of chronic kidney disease on the urine proteome in the domestic cat (Felis catus). , 2015, Veterinary journal.

[19]  J. V. D. van der Steen,et al.  The fraction haemolymph vitellogenin of a honey bee colony, derived from a pooled haemolymph sample, a colony vitality parameter , 2015 .

[20]  K. Antúnez,et al.  Bee bread increases honeybee haemolymph protein and promote better survival despite of causing higher Nosema ceranae abundance in honeybees. , 2014, Environmental microbiology reports.

[21]  Bin Han,et al.  Hemolymph proteome changes during worker brood development match the biological divergences between western honey bees (Apis mellifera) and eastern honey bees (Apis cerana) , 2014, BMC Genomics.

[22]  C. Aurori,et al.  What is the main driver of ageing in long-lived winter honeybees: antioxidant enzymes, innate immunity, or vitellogenin? , 2014, The journals of gerontology. Series A, Biological sciences and medical sciences.

[23]  R. Moritz,et al.  Origin and function of the major royal jelly proteins of the honeybee (Apis mellifera) as members of the yellow gene family , 2014, Biological reviews of the Cambridge Philosophical Society.

[24]  L. Vanagas,et al.  Conversion of High and Low Pollen Protein Diets Into Protein in Worker Honey Bees (Hymenoptera: Apidae) , 2013, Journal of economic entomology.

[25]  G. Amdam,et al.  Aging and its modulation in a long-lived worker caste of the honey bee , 2013, Journal of Experimental Biology.

[26]  Eric P. Skaar,et al.  Nutritional immunity: transition metals at the pathogen–host interface , 2012, Nature Reviews Microbiology.

[27]  D. Geiser,et al.  Insect transferrins: multifunctional proteins. , 2012, Biochimica et biophysica acta.

[28]  G. Amdam,et al.  Deconstructing honeybee vitellogenin: novel 40 kDa fragment assigned to its N terminus , 2011, Journal of Experimental Biology.

[29]  K. Rodenburg,et al.  Lipoprotein assembly and function in an evolutionary perspective , 2010, Biomolecular concepts.

[30]  A. Cristino,et al.  The four hexamerin genes in the honey bee: structure, molecular evolution and function deduced from expression patterns in queens, workers and drones , 2010, BMC Molecular Biology.

[31]  Leonard J Foster,et al.  Quantitative Comparison of Caste Differences in Honeybee Hemolymph*S , 2006, Molecular & Cellular Proteomics.

[32]  P. Pelosi,et al.  Soluble proteins in insect chemical communication , 2006, Cellular and Molecular Life Sciences CMLS.

[33]  G. Amdam,et al.  Social reversal of immunosenescence in honey bee workers , 2005, Experimental Gerontology.

[34]  G. Amdam,et al.  Hormonal control of the yolk precursor vitellogenin regulates immune function and longevity in honeybees , 2004, Experimental Gerontology.

[35]  L. Cerenius,et al.  The prophenoloxidase‐activating system in invertebrates , 2004, Immunological reviews.

[36]  G. Amdam,et al.  Social exploitation of vitellogenin , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[37]  T. Burmester Origin and evolution of arthropod hemocyanins and related proteins , 2002, Journal of Comparative Physiology B.

[38]  Z. Simões,et al.  Inhibition of vitellogenin synthesis in Apis mellifera workers by a juvenile hormone analogue, pyriproxyfen. , 2000, Journal of insect physiology.

[39]  D. Jong,et al.  Quantification of Hemolymph Proteins as a Fast Method for Testing Protein Diets for Honey Bees (Hymenoptera: Apidae) , 1998 .

[40]  C. Masson,et al.  Identification and developmental profiles of hexamerins in antenna and hemolymph of the honeybee, Apis mellifera. , 1998, Insect biochemistry and molecular biology.

[41]  J. H. Law,et al.  Lipophorin of the larval honeybee, Apis mellifera L. , 1985, Journal of lipid research.

[42]  Morton B. Brown,et al.  Robust Tests for the Equality of Variances , 1974 .

[43]  S. Shapiro,et al.  An Analysis of Variance Test for Normality (Complete Samples) , 1965 .

[44]  W. Kruskal,et al.  Use of Ranks in One-Criterion Variance Analysis , 1952 .

[45]  J. Tukey Comparing individual means in the analysis of variance. , 1949, Biometrics.

[46]  J. Mauchly Significance Test for Sphericity of a Normal $n$-Variate Distribution , 1940 .

[47]  M. Friedman A Comparison of Alternative Tests of Significance for the Problem of $m$ Rankings , 1940 .

[48]  J. Nally,et al.  Proteomic Research in Urine and Other Fluids , 2018 .

[49]  A. M. Almeida Proteomics in Domestic Animals: from Farm to Systems Biology , 2018, Springer International Publishing.

[50]  R. Green,et al.  One-dimensional SDS-polyacrylamide gel electrophoresis (1D SDS-PAGE). , 2014, Methods in enzymology.

[51]  E. L. Arrese,et al.  Insect fat body: energy, metabolism, and regulation. , 2010, Annual review of entomology.

[52]  Z. Simões,et al.  The relationship between level of pollen in the diet, vitellogenin and juvenile hormone titres in Africanized Apis mellifera workers , 1996 .

[53]  M. Haydak Honey Bee Nutrition , 1970 .