Protein profiles of hatchery egg shell membrane
© The Author(s). 2017
Received: 22 November 2016
Accepted: 21 February 2017
Published: 3 March 2017
Eggshells which consist largely of calcareous outer shell and shell membranes, constitute a significant part of poultry hatchery waste. The shell membranes (ESM) not only contain proteins that originate from egg whites but also from the developing embryos and different contaminants of microbial and environmental origins. As feed supplements, during post hatch growth, the hatchery egg shell membranes (HESM) have shown potential for imparting resistance of chickens to endotoxin stress and exert positive health effects. Considering that these effects are mediated by the bioactive proteins and peptides present in the membrane, the objective of the study was to identify the protein profiles of hatchery eggshell membranes (HESM).
Hatchery egg shell membranes were extracted with acidified methanol and a guanidine hydrochloride buffer then subjected to reduction/alkylation, and trypsin digestion. The methanol extract was additionally analyzed by matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF-MS). The tryptic digests were analyzed by liquid chromatography and tandem mass spectrometry (LC-MS-MS) to identify the proteins.
Our results showed the presence of several proteins that are inherent and abundant in egg white such as, ovalbumin, ovotransferrin, ovocleidin-116, and lysozyme, and several proteins associated with cytoskeletal, cell signaling, antimicrobial, and catalytic functions involving carbohydrate, nucleic acid, and protein metabolisms. There were some blood derived proteins most likely originating from the embryos and several other proteins identified with different aerobic, anaerobic, gram positive, gram negative, soil, and marine bacterial species some commensals and others zoonotic.
The variety of bioactive proteins, particularly the cell signaling and enzymatic proteins along with the diverse microbial proteins, make the HESM suitable for nutritional and biological application to improve post hatch immunity of poultry.
KeywordsHatchery egg shell membrane Proteins Mass spectrometry
Egg shells that constitute a significant part of poultry hatchery waste, comprise largely of calcium carbonate crusts and underlying shell membranes laced with proteins originating from egg whites as well as contaminants of microbial and environmental origins . The shell membranes have been considered for various engineering, agricultural, and biomedical applications, spurring many studies of their biochemical compositions [2–9]. Most such studies however, have used membranes harvested from fresh eggs and shown to contain proteins and peptides of structural, antimicrobial, cell regulatory, and stress protective categories which likely contribute to their some of their health beneficial and therapeutic effects [2, 10–19]. Recently, we reported that the hatchery shell membranes (HESM), used as nutritional supplement, in post hatch chicks, promote growth, show protection against bacterial lipopolysaccharide (LPS) induced inflammatory response and diminish stress markers such as plasma levels of corticosterone . Presuming that these effects could be mediated through the bioactive proteins present in the HESM, we were interested to analyze the proteomic composition of HESM that has never been investigated. Besides, the protein population of HESM can be qualitatively different from the fresh egg shell membrane because the embryo development not only induce dynamic changes in egg proteome [21, 22] but also, alter the membrane structure to facilitate the hatching process. Hence, the current study was conducted utilizing the HESM that were dried at room temperature in a chemical hood without additional cleanup for 2 month period in the room temperature.
Chemicals and reagents
The reagents and devices such as C18 Nu tips (Glysci.com), Spectra/Por membranes (Spectrumlabs.com), bicinchoninic acid (BCA) protein assay kit, Pierce C18 spin columns, MS grade trypsin (Fisher Scientific.com), peptide and protein calibration standards (m/z 500–16000, Bruker Daltonics, Bremen, Germany), and 2-iodoacetamide (IAA) (MP Biomedical, OH) were purchased from their respective vendors. Most other chemicals and supplies including 1, 4-dithiothreitol (DTT), 2, 5-dihydroxybenzoic acid (DHB), were purchased from Sigma Aldrich (St. Louis, MO).
Empty eggshells were obtained from the University of Arkansas poultry hatcheries, dried at room temperature under the hood for 2 months, the membranes separated manually then ground to coarse powder using an IKA mill (Cole Palmer). Duplicate samples of membrane powder from two separate preparations, each made from >50 eggs, were extracted (a) with 0.1% acetic acidified 70% methanol for soluble proteins, peptides, and their degradation products, and (b) with 4 M guanidine hydrochloride (GuHCl) containing 20 mM EDTA, and 50 mM Na-acetate, pH 5.8 for all soluble proteins [17, 23]. The membrane powder were extracted with 20 volumes of respective solutions overnight at 4 °C by constant stirring then centrifuged at 20,000 g for 15 min and the supernatants containing all soluble factors were dialyzed against excess volumes of 50 mM ammonium bicarbonate with three successive changes using 1000 Da Spectra/Por dialysis membranes. The solutions containing approximately 20 μg of protein from each extract, measured by BCA protein assay, were reduced with 10 mM dithiothreitol (DTT) for 1 h at 60 °C and alkylated with 40 mM iodoacetamide (IAA) then digested with 0.4 μg trypsin for 48 h at 37 °C [23, 24]. The tryptic digests were desalted using Pierce C18 spin columns according to the manufacturer suggested protocol prior to liquid chromatography-tandem mass spectrometry (LC-MS/MS).
Following desalting with C18 columns, the peptides were eluted, dried and re-suspended in 0.1% formic acid (FA) then subjected to LC-MS/MS using an Agilent 1200 series micro flow HPLC coupled to a Bruker Amazon-SL quadrupole ion trap mass spectrometer, and a captive spray ionization source. Tryptic peptides were separated at a solvent flow rate of 1.6 μL/min with 0 to 40% gradients of 0.1% FA (solvent A) and acetonitrile (ACN) in 0.1% FA (solvent B) over a period of 300 min each using a C18 (150 × 0.1 mm, 3.5 μm particle size, 300 Å pore size, Zorbax SB) capillary column. The captive electrospray source was operated in a positive ion mode with a dry gas temperature of 150 °C, dry nitrogen flow 3 L/minute, and capillary voltage of 1500 V. The data were acquired in the auto MS (n) mode with optimized trapping condition for the ions at m/z 1000. MS scans were performed in the enhanced scanning mode (8100 m/z/second), while the collision-induced dissociation or the MS/MS fragmentation scans performed automatically for top ten precursor ions for 1 min each in the UltraScan mode (32,500 m/z/second). The samples were run three times as technical repeats.
For direct matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF-MS), aliquots of methanol extracts were subjected to reduction/ alkylation using DTT and iodoacetamide (IAA) as described previously  or mock treated omitting DTT from the reaction for respective controls then spotted on a MALDI target plate mixing at 1:1 ratio with two dihydroxybenzoic acid. In all cases, samples were first subjected C18 nu tip cleaning up process using manufacturer recommended protocol before spotting on the MALDI target plate. The mass spectra were acquired with a Bruker Ultraflex II MALDI-TOF mass spectrometer (Bruker Daltonics GMBH, Bremen, Germany) operated in the positive-ion reflectron mode with the TOF analyzer calibrated with Bruker peptide standard II. Accurate mono isotopic protonated, intact peptide, masses were determined by MALDI-TOF-MS using combinations of external and internal calibration procedures, spotting the samples with equal volumes of α-cyano-4-hydroxycinnamic acid matrix, prepared in 0.1% FA, and 50:50 water/ACN. The MALDI-TOF-MS data were processed and some selective peaks were fragmented using LIFT-TOF/TOF MS to obtain their identities .
Peaks were picked from the LC-MS/MS chromatogram using instrument’s default settings and the mzML files created using Bruker Data Analysis 4.0 software. The mzML files created as such were used in Bruker ProteinScape 3.1 server with MASCOT data base search tool to perform MS/MS data search against the UniProt Gallus and NCBI bacterial data bases to identify the proteins. All proteins were identified with a 95% confidence limit and <1% false discovery rate with at least one unique peptide. The parent ion mass- and fragment ion mass tolerance were both, set at 0.6 Da with cysteine carbamidomethylation and methionine oxidation as fixed and variable modifications. MASCOT.dat data base search files and.mzML raw data files were then exported into Skyline v3.1 software (http://proteome.gs.washington.edu/software/Skyline) [26, 27] to further refine the tryptic peptide identification based on their relative hydrophobicity and retention time correlations. Protein identities were also refined based on the uniqueness of the identified tryptic peptides by comparing them against respective background proteomes (either UniProt Gallus or the NCBI Bacteria data bases). The MALDI-TOF-MS data were processed using Bruker Flex Analysis 3.3 and Bruker BioTools 3.1 software. Peptides were identified by MASCOT MS/MS ion search tool with a peptide mass tolerance of 200 ppm and MS/MS ion tolerance of 0.6 Da. Functional annotation and classification of the proteins identified by LC-MS/MS with two or more unique peptides were performed using gene ontology (GO) based PANTHER classification system (http://www.pantherdb.org)  and proteins refined by Skyline from both guanidine and methanol extracts. Also, the same proteins were used in STRING functional protein association networks, version 10 (http://string-db.org) , under a high confidence setting to identify protein co-occurrence and possible functional relations.
Proteins identified in methanol extract by LC-MS/MS. Proteins with a single peptide are considered “tentatively identified”
Orosomucoid 1 (ovoglycoprotein) precursor
peptidyl-prolyl cis-trans isomerase FKBP1A
keratin 8, type II
SH3 domain binding glutamic acid-rich protein like (SH3BGRL), mRNA
Ubiquitin-fold modifier 1
Diazepam binding inhibitor (GABA receptor modulator, acyl-CoA binding protein) (DBI), mRNA.
Keratin, type I cytoskeletal 19
Usher syndrome 1C
Thymosin, beta 4
Collagen, type XVI, alpha 1
Signal peptidase complex subunit 1 homolog
Zinc finger BED domain-containing protein 4
Alpha-D-globin (HBAD), mRNA.
Fatty acid-binding protein, heart
Polycystic kidney and hepatic disease 1 (autosomal recessive)
Serine peptidase inhibitor, Kazal type 2 (acrosin-trypsin inhibitor)
Probable arginyl-tRNA synthetase, mitochondrial
Transforming, acidic coiled-coil containing protein 1
elaC ribonuclease Z 2
Fibroblast growth factor 2
Nuclear receptor coactivator 2
WD repeat-containing protein 36
High mobility group protein B1
tRNA (adenine-N(1)-)-methyltransferase non-catalytic subunit TRM6
Fibrinogen silencer binding protein
SH3 domain binding glutamate-rich protein like 3
UPF3 regulator of nonsense transcripts homolog B (yeast)
Mutated in colorectal cancers
As expected the HESM contained many proteins such as ovalbumin, ovomucoid, ovocleidin-116, and lysozyme that are inherent to egg proteome [8, 30–32]. Structural proteins such as keratins, collagens, decorin, lumican, and tropomyosin, and cytoskeletal proteins, such as actin, tubulin, vimentin, and their interacting proteins, were present along with several blood (hemoglobin, α-D-globin, annexin, fibronectin) and embryo associated proteins (vitellogenin, zona pellucida sperm-binding proteins, and vitelline membrane outer layer protein). These results are consistent with the reports of Cordeiro and Hincke  who showed the occurrence of fibronectin, vitellogenin, and apolipoproteins in the shell membranes of fertilized eggs. The HESM also contained many different enzymes, protease inhibitors, and signaling proteins similar to fresh ESM. However, the HESM seemed to be differentially populated with several proteins associated with glycolysis, carbohydrate, protein, and nucleic acid metabolisms. Many ribosomal, histone, and ribonuclear proteins, and enzymes, associated with protein folding and translocations, were also identified in the HESM extract. However, there was a conspicuous absence of clusterin, a glycoprotein which we and others have found present in the fresh ESM and has been reported as a major component of egg proteome [17, 19, 21, 33–36]. Clusterin is implicated in the maintenance of cellular homeostasis, developmental remodeling, and in the egg, it is correlated with the changes in viscosity of egg white [36–39]. In our previous study with fresh ESM we identified several clusterin peptide fragments in the methanol extract of ESM. However, the absence of any clusterin peptide in HESM under similar extraction condition was intriguing. It is possible that clusterin, in shell membrane, is involved in early embryo development and utilized completely, as the development reaches to its termination. Similarly, there was also a conspicuous absence of gallin, an antimicrobial peptide that occurs uniquely in egg proteome of fresh eggs [17, 33, 40] whereas two other avian defensins, gallinacin 9 and 10, were identified along with several other antimicrobial proteins including ovotransferrin, lysozyme, keratin, and ovomucoid. Because the protein profiles of egg undergo qualitative and quantitative changes both, during incubation and passive storage [21, 22, 32, 38, 41, 42], the differences in protein profiles of membranes between fresh and hatchery shells appear logical and consistent.
A functional association bioinformatics showed co-occurrence of proteins associated with ubiquitination and apoptosis activities, indicative of large scale protein degradation, expected, with the embryo development and hatching. The other notable protein clusters were carbohydrate and energy metabolizing enzymes (glyceraldehyde phosphate dehydrogenase, α-enolase, isocitrate dehydrogenase, aldolase, triose phosphate isomerase) as well as the proteins associated to nucleic acid metabolism, and stress protection functions such as heat shock and heat shock cognate proteins (HSP). Besides the endogenous proteins and peptides, the HESM also contained several proteins identified with multi species of both gram positive and gram negative bacteria some belonging to families of phytobacteria, soil bacteria even, marine bacteria. Proteins identified with bacteria such as Candidatus, Enterococci, Yersinia, Butyrivibrio Pseudomonas, Clostridium, and Vibrio are zoonotic that are implicated in human gastrointestinal and respiratory illness including one peptide that belonged to a Eimeria, a protozoa, that causes coccidiosis and enteritis in poultry.
The objective of the study was to gain a better understanding of the potential of egg membrane as an adjuvant that likely provides epigenetic conditioning influencing the post hatch immunity through its proteomic constituents . Based on the above results, it appears that the HESM with its plethora of bioactive proteins, peptides, enzymes, and multi species microbial protein factors, may be a suitable modulator of immunity of post hatch chickens with its muco-adhesive properties and action on gastrointestinal mucosa. Besides, the HESM protein profile also provides a reference to compare and identify similar other allogeneic and xenogeneic sources of material that can improve immunity of post hatch poultry reducing the dependence on antibiotics growth promoters. The identification of diverse bacterial proteins in the HESM makes it appealing since numerous body of evidence has shown that the immunity and disease resistance is greatly influenced by biodiverse factors that include various bacterial and viral antigens [43–45].
The HESM is a rich source of a variety of bioactive proteins particularly belonging to signaling enzymatic, and regulatory varieties that along with many microbial proteins make it uniquely suitable for use as a modulator to improve post hatch immunity of poultry.
Egg shell membrane
Hatchery egg shell membrane
Liquid chromatography-tandem mass spectrometry
Matrix assisted laser desorption ionization time of flight
We thank Sonia Tsai and Scott Zornes for assistance.
This work was carried out as in house project and partly conducted in the State wide Mass spectrometry Facility supported by a grant P30 GM103450 to the University of Arkansas.
Availability of data and materials
MS data available.
NCR and RL conceived and designed the experiments; experiments performed by SKM, RL and NCR; NCR, RL, SKM wrote the manuscript, discussed and approved by NCR, RL, and JL.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
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