Article | Open | Published:

Rapid changes in Atlantic grey seal milk from birth to weaning – immune factors and indicators of metabolic strain

Scientific Reportsvolume 7, Article number: 16093 (2017) | Download Citation

Abstract

True seals have the shortest lactation periods of any group of placental mammal. Most are capital breeders that undergo short, intense lactations, during which they fast while transferring substantial proportions of their body reserves to their pups, which they then abruptly wean. Milk was collected from Atlantic grey seals (Halichoerus grypus) periodically from birth until near weaning. Milk protein profiles matured within 24 hours or less, indicating the most rapid transition from colostrum to mature phase lactation yet observed. There was an unexpected persistence of immunoglobulin G almost until weaning, potentially indicating prolonged trans-intestinal transfer of IgG. Among components of innate immune protection were found fucosyllactose and siallylactose that are thought to impede colonisation by pathogens and encourage an appropriate milk-digestive and protective gut microbiome. These oligosaccharides decreased from early lactation to almost undetectable levels by weaning. Taurine levels were initially high, then fell, possibly indicative of taurine dependency in seals, and progressive depletion of maternal reserves. Metabolites that signal changes in the mother’s metabolism of fats, such as nicotinamide and derivatives, rose from virtual absence, and acetylcarnitines fell. It is therefore possible that indicators of maternal metabolic strain exist that signal the imminence of weaning.

Introduction

Milk is the sole source of nutrition and passive immune protection for neonatal mammals. Milk changes dramatically in composition in the immediate postpartum period from colostrum to mature phase milk that, in eutherians (‘placental mammals’), then changes little until weaning1,2. That initial transition may take about 48 hours (as in cattle, sheep, camel3,4,89), or it can extend to 30–40 days (as in at least one species of bear5). The composition of colostrum varies among species, particularly in the concentration of immunoglobulins (antibodies) that are a sample of those in circulation in the mother. The class of immunoglobulin that predominates in colostrum is a function of the type of placenta possessed by a given species2.

Immunoglobulins are not the only form of maternally-derived immune protection. Others include several anti-microbial proteins and oligosaccharides. The latter may not be digested for energy provision but instead act against colonisation by potentially pathogenic microorganisms by competitively blocking their mucous and cell surface attachment receptors6,7,12. Importantly, oligosaccharides are also important for the establishment of a gut microbiome appropriate for the neonates of a species (to both aid digestion of milk and compete with incoming pathogens), and can be heterogeneous and polymorphic between individuals7,8,9,10. Like the proteins present during the colostrum to mature milk transition, oligosaccharides may change in composition with time after birth, some appearing early, then disappearing, and others may show the inverse5,11. The diversity and changes in oligosaccharide content during lactation has, however, been investigated in only a few species.

We recently reported on the dramatic changes in the proteins, oligosaccharides, metabolites and lipids in the species of eutherian mammal with the longest colostrum to mature milk transition known, the giant panda5,70,13. This prolonged transition time may be associated with the altriciality of ursid neonates5,96, which is the most extreme known amongst eutherians, though not as pronounced as in marsupials14,15.

We now report on the opposite extreme, in true seals (Phocidae), which give birth to large, precocious pups that are, in many species, nursed without the mother leaving to feed16. The pups are typically deserted after a very short lactation, such that weaning is sudden and there is no period of mixed feeding. As a whole, the true seals are remarkable in these highly abbreviated lactation periods relative to their body masses, the most extreme case being hooded seals that lactate for the shortest time known for any mammal, three to five days16, the longest amongst marine seals being between five and seven weeks in Weddell seals16. The lactation strategies of marine phocids are distinct from other pinnipeds, the otariids (sea lions and fur or eared seals) and odobenids (walrus) despite the fact that they occupy superficially similar marine environments and ecological positions (see summary in Supplementary Figure S1). Otariids lactate for considerably longer (4 to 18 months) during which time some mothers cease lactation for periods while foraging in distant feeding grounds, and, remarkably, re-start lactation on their return14,16,17. Odobenids may nurse for up to two years, and, unusually amongst pinnipeds, nurse their young while at sea16,17.

True seals are considered to be capital breeders, in that maternal body reserves are transferred to their neonates with little or no replenishment until weaning17,18,19. During this period of fasting there is a dramatic loss of maternal body mass to fund a doubling of pup body mass18,20. The adaptive advantage of this intense, abbreviated lactation is under debate but represents a strategy by which a capital breeder can rapidly transfer food with reduced energy expenditure associated with foraging17.

Here we chose a species of true seal with a lactation period before weaning that is in the mid range amongst phocids, and in which females do not forage at sea during lactation. This is the Atlantic grey seal, Halichoerus grypus, that lactate for approximately 16 days, though this varies regionally16,21, and our sampled population lactated for between 17 and 23 days. In this we had two aims. First, to establish the time course of colostrum to mature phase lactation in a true seal, and, secondly, to seek components indicative of changes in maternal metabolism and potential signals of approaching weaning. We found that the colostrum to milk transition is extremely rapid in this species, in terms of establishment of mature protein and oligosaccharide profiles. On the other hand, we found that other micronutrients and metabolites change more gradually through lactation, some of which may be indicative of alterations in maternal metabolism leading to weaning.

Results and Discussion

Proteins

We first compared the protein profiles of milk samples taken at intervals postpartum from several seals, and typical results from single mothers are shown in Fig. 1 and Supplementary Figure S4. These show that the mature, main phase lactation pattern appeared very rapidly after birth, with some major protein bands changing in intensity. Establishing the precise times of birth is difficult in the field, but in a subsequent season we were able to obtain samples from mothers that gave birth between 10 and 19 hours before, and compared the protein profiles with those of two 7-day postpartum samples (Fig. 2). This emphasised the very rapid development of the mature protein profile, which was essentially complete within a day. The protein bands numbered in Fig. 1 were excised from that gel and submitted for proteomics, the results of which are given in Table 1, along with the putative functions of each protein. The identities of the proteins found were provided with additional confidence from a 2-dimensional protein electrophoresis gel (Supplementary Figure S5 and Supplementary Table S1).

Figure 1
Figure 1

Changing protein profiles of grey seal milk with time after birth. Gradient SDS-PAGE of milk samples obtained from a single mother seal on the days indicated, stained with Coomassie Blue. The protein bands indicated by numbers were excised from the gel and subjected to proteomic identification, the results are given in Table 1. See Figure S1 for a similar protein gel analysis of a sample series from a different seal mother that shows closely similar profiles. M, size reference proteins with their molecular masses given in kiloDaltons (kDa). Samples reduced with β-mercaptoethanol where indicated. An electronic image of the stained gel was made as described in Materials and Methods with no subsequent electronic manipulation except for cropping and assembly to improve clarity and conciseness of presentation, and the full-sized, uncropped gel image is presented in the Supplementary.

Figure 2
Figure 2

Protein profiles of grey seal milk soon after birth. Milk samples were collected between 10 and 19 hours after birth (numbered tracks), except for tracks 4 and 8 (underlined) which were instead loaded with comparator samples taken 7 days after birth from different mothers in a previous year. Note the absence of the band indicated by the arrow in track 2 and that this band was of lesser intensity in all tracks relative to that in the day 7 samples. Information on the proteins in the two minor bands appearing in the 30 kDa region of track 2 is given in the Supplementary. The milk sample for track 2 (and, to a lesser extent, track 7) had the smallest fat layer following centrifugation at 4 °C (Supplementary Figure S3). Different mothers sampled on the Isle of May during November 2016, with those of tracks 4 and 8 taken in November 2014. Samples were reduced with β-2-mercaptoethanol where indicated. M, size reference proteins with their molecular masses given in kiloDaltons (kDa). Electronic images of the gels were made as described in Materials and Methods with no subsequent electronic manipulation except for cropping to improve clarity and conciseness of presentation, and the full-sized, uncropped gel images are presented in the Supplementary.

Table 1 Identification of the proteins isolated from bands excised from the protein electrophoresis gel shown in Fig. 1.

The main proteins segregate between those for adaptive and innate immune protection, and those for nutritional support. Among the former were three immunoglobulin classes (IgG, IgM and IgA), as detected by the presence of their eponymous heavy chains, along with their associated light chains. The immunoglobulins generally appeared in greatest amounts early after birth, such as seen in Fig. 1. They were accompanied by the polymeric immunoglobulin receptor that mediates the trans-epithelial transport of immunoglobulins into secretions, predominately IgA, which it then protects against proteolytic cleavage22,23,24. In all species, IgA appears to be continuously present in both colostrum and mature phase milk, presumably to protect the mammary gland and the oral and gastrointestinal tracts of the neonate24,25. IgA tends to be the predominant immunoglobulin in the colostrum of species in which trans-placental transfer of IgG occurs (such as in humans and rodents, which have haemochorial placentae26,27) using the FcRn transporter system28,29. In contrast, IgG tends to be particularly enriched in the colostrum of species in which trans-placental transfer does not occur (e.g. cattle, sheep, horses, camels; epitheliochorial placentae; ref.26). In these species, IgG (along with IgM) crosses the gut epithelia directly into the neonate’s circulation for the short period before the gut cell layer closes (24 hours post-partum or less), it then appears at much lower levels from the time at which the colostrum period ends (~24–36 hours)30.

The zonary discoid endotheliochorial placentae of many Carnivora have peripheral haemophagous zones through which transfer of large plasma proteins such as immunoglobulins may occur, possibly by pinocytosis and phagocytosis of maternal blood rather than mediated by FcRn31,32. Among the Carnivora, trans-placental transfer of IgG occurs to a limited degree in dogs33, but apparently not in cats34, and trans-placental transfer of IgG to only 3% of maternal levels has been reported in harbour seals35. Surprisingly, IgG appears to persist at high levels throughout lactation in grey seal milk (Figs 1, 2 and Supplementary Figure S4). In some mammals, such as rats28, IgG is actively transported across the gut mucosa (using the same FcRn receptor system as for trans-placental transfer28), so it may be that this also applies to seals. If so, then this would be an unusual adaptation in seals that might relate to immune protection of a rapidly growing pup that will soon be deserted and exposed to infections circulating in a breeding colony.

Several proteins of innate immunity were detected. Xanthine dehydrogenase/oxidase is found in most mammal milks and is thought to be defensive, but it also has a role in lipid synthesis and secretion36,37. α-1-acid glycoprotein, ceruloplasmin and haptoglobin were also found and are among a set of proteins that rapidly appear in greatly enhanced amounts in blood at the onset of an acute phase (fever) reaction in mammals38,39,81. They are usually synthesised in the liver, but it is now known that some acute phase proteins can be synthesised in mammary gland tissue in response to infections, and then appear in milk40,41,77. An inflammatory response in mammary gland tissue is observable during phases of the lactation cycle when the gland is undergoing reconstruction and may be in a vulnerable state42. The presence of protective proteins in grey seal milk could therefore be due to microbes colonising an active mammary gland, or as a prophylactic against infection.

The other main proteins found are well-established as being specialised for milk-based nutrition, such as the caseins43,44,45. β-casein was present at lower levels in the earliest samples relative to day 7 (Figs 1, 2 and Supplementary Figure S4), and even missing in one (arrowed in Fig. 2; Fig. 1, band 7). A delayed post-parturient appearance of caseins has also been observed in the giant panda, in which secretion of both β- and κ-caseins may take 30–40 days to reach main phase levels5. β-casein is a highly phosphorylated protein that transports calcium ions and forms micelles that appear to be stabilised by κ-casein46. The delayed appearance of caseins may explain how the soluble, fat-depleted layer of early grey seal milk samples is less turbid (milky) than later ones (Supplementary Figure S2), as is also the case in giant pandas5.

β-lactoglobulin was present at high relative levels in all samples, including those collected soon after birth (Figs 1 and 2; Table 1). It is present in all Carnivoran milks that have been examined, in which it may occur in one to three isoforms5,47. It is thought to be a carrier of long chain fatty acids and retinol (Vitamin A)47,48. Retinol is insoluble and highly sensitive to oxidation but can be protected within an apolar protein binding site47,49,50,51 (and M.W. Kennedy, unpublished). Retinoic acid derivatives of retinol are crucial to a wide range of cell differentiation and developmental processes in vertebrate52,53, so the safe delivery of its precursor to a rapidly growing neonatal seal may be particularly important. Curiously, humans (and camels, elephants) do not produce β-lactoglobulin5,54,92, though some primates do (macaques and baboons)47, so its true role in milk remains mysterious.

Proteinase inhibitors were also found. A specific colostrum trypsin inhibitor is present in many mammal milks, the concentration of which appears to correlate positively with that of IgG55. In bovine milk, for example, this inhibitor is found for only 2–48 hours postpartum, which fits with the idea that it is there to reduce cleavage of immunoglobulins undergoing transfer to the neonate. The encoding gene has been examined in otariids and odobenids in which it appears to be functional, but it is disrupted in one phocid (Weddell seal)55. If this is also true in the grey seal, then its absence in our survey is explicable, but this then begs the question of whether the other proteinase inhibitors we found act to compensate for protection of the unusually prolonged secretion of IgG into the milk of this species.

Two proteins that are more usually associated with blood plasma were present, albumin and apolipoprotein A, both of which are involved in lipid transport in blood, albumin carrying a range of small charged molecules in addition to fatty acids. Whether these two proteins are made in, or actively transported from blood by, the mammary gland, or leak passively into milk from blood plasma, remains to be established, though the high level of albumin present suggests an influence of some kind in milk. A general, non-specific leakage of blood plasma components into the milk is unlikely given that we did not find other major plasma proteins such as complement C3 or transferrin.

α-lactalbumin was found, which is interesting given its absence in otariid and odobenid milks and role in lactose production (see below).

Oligosaccharides

Complex sugars are abundant in the milk of many species, though not all, and are active as free or protein-linked oligosaccharides8,56,57,58,59. In humans, these complex sugars vary dramatically in quantity and types between mothers8,60. They are generally not digested to provide a neonate’s energy metabolism but are instead thought to control colonisation by pathogens through interfering with their sugar-based adhesion mechanisms required for binding to mucus layers or cell surfaces7,61. Milk oligosaccharides also play a crucial role in establishing an appropriate microbiome by, for instance, acting as a selective nutrient supply for species of Bifidobacterium 7,62,63.

We found that both fucosyllactose and sialyllactose were present soon after parturition in grey seal milk but were then rapidly lost with time after birth, until little or none of either was detectable towards the end of lactation (Fig. 3). Sialyllactose (N-acetylneuraminyllactose) occurs in 3′ and 6′ forms, the former being the most common in milks. Our MS analysis indicated that only one form was present in the seal milk, the 3′ form. The amounts of these sugars varied considerably between mothers in the first week, which could indicate intrinsic differences between the mothers in how much they produce, or the rates at which secretion of these oligosaccharides change with time after birth. Levels of these two complex sugars decreased roughly simultaneously, which is the opposite to the trend found in the giant panda5. In that species, fucosyllactose rose with time, but the 3′ form of sialyllactose fell. The rate of change in the concentrations of these oligosaccharides in seal milk was very much greater in seals than in giant pandas, in which it takes 20 to 60 days at least for levels of these oligosaccharides to stabilise5.

Figure 3
Figure 3

Changes in grey seal milk metabolites and micronutrients with time after birth. Selection of compounds exhibiting changing concentrations as lactation progresses. Fucosyllactose and sialyllactose are oligosaccharides that control colonisation by microbes. Taurine is an essential dietary requirement in some species of hyperpredator. The remaining metabolites are associated with fat metabolism, potentially pertinent to nursing seals in terms of mobilisation of their body reserves, and lipids required for rapid growth and maintenance of pups that need to accumulate large fat reserves for the forthcoming starvation period and for subsequent thermal insulation at sea. The data indicated for 18 days after birth are a mixture from samples taken on days 17, 18 and 19. The square symbol in a box is the mean; the band in the box is the median; the box extends to the standard error of the mean; the whiskers indicate the range.

Lactose is the principal energy component of the milk of many species of land mammal (e.g. cow, sheep, horse, dog, camel, human), but is either at very low levels or absent in marine mammals2,17. Lactose is found at very low levels in phocids, but is absent in the milks of otariids and odobenids2,17. This loss is postulated to have evolved because lactose’s role in energy provision is supplanted by milk fats, and that one of lactose’s functions, the osmotic drawing in of water into milk64,65, is not advantageous in marine mammals66. Lactose is synthesised by lactose synthase, which is a two-component enzyme comprising β1,4-galactosyltransferase (which is produced in many tissues) and α-lactalbumin (which is specific to mammary glands). Otariids and odobenids have alterations to their α-lactalbumin–encoding gene that would disable the protein’s enhancement of lactose synthesis - which is not the case in phocids66. Despite finding α-lactalbumin in grey seal milk (see Fig. 1 and Table 1), lactose was present in amounts that are very low relative to those in cow, goat and camels (data not shown), consistent with studies on other phocids64,66. In true seals, therefore, lactose may instead be there to provide a substrate for the synthesis of its fucosylated and sialated forms of lactose that are for management of the gut or mammary gland microbiome, or protection against microbial pathogens, rather than for energy supply67,12.

Taurine

Taurine has a multitude of biological functions, such as involvement in membrane stabilisation and modulation of calcium signalling, and it is essential for cardiovascular function, development and function of skeletal muscle, the retina, and the central nervous system68,69. In addition there is increasing evidence that taurine is essential for supporting the immune system since it is found at very high levels in phagocytes83. Moreover, of potential pertinence to mammalian neonates in general, neonates may have a limited capacity to produce taurine84,85,86,87. One of the primary bile acids of mammals is taurine-conjugated, so a rich supply of it may be crucial for the processing of a fat-rich diet, which particularly applies to the neonates of marine mammals. In that regard, bile salts also activate bile salt-activated lipase that is involved in digestion of lipids5,88,93, and is found in grey seal milk (Supplementary Table S2). Some species of hypercarnivore, such as cats and possibly also polar bears71,72,73, cannot synthesise taurine, and are thereby dependent on dietary sources. As we will report elsewhere, we find that taurine occurs at considerably higher concentrations in seal milk than in milks of many other species. Being piscivorous hypercarnivores that have ready access to plentiful sources of taurine in their diet, seals, like other hypercarnivores, may have foregone synthesising taurine, which would then be an essential requirement in their milks. Here, we found that the concentration of taurine is, like other small molecules, highly variable in milk samples from mother to mother, but is highest soon after birth and then falls as weaning approaches (Fig. 3). If grey seals cannot synthesise and replenish taurine, then that reduction could be due to depletion in the mother during her fast, which should not apply to those phocids in which the females periodically forage during lactation (Supplementary Figure S1 and ref.16).

Micronutrients or indicators of metabolic activity?

We examined changes in metabolites that are involved directly in, or are indicative of, fat-fuelled energy metabolism, and have here selected nicotinamide, acetylcarnitine and N1-methyl-2-pyridone-5-carboxamide for note. As we will report elsewhere, we find that nicotinamide, its derivatives and precursors (such as anthranilic acid) are dramatically higher in concentration in seal milk than in a selection of land mammals (cow, goat, camel), that this also applies to N1-Methyl-2-pyridone-5-carboxamide, and some carnitines.

Nicotinamide is required for the production of NAD+, which is a key co-factor in fatty acid β-oxidation. Since the energy metabolism of both seal mothers and pups is based on large scale oxidation of fats, then a high requirement for NAD+ would be expected, and we found that the concentration of nicotinamide increases with time of lactation (Fig. 3). As with taurine and oligosaccharides, there is substantial diversity in milk nicotinamide levels between mothers at all four sampling times, which could relate to their initial nutritional states, physiological condition, or demand for milk by their pups. As with other small molecule metabolites, the increasing concentrations of nicotinamide could be a reflection of the need for the pups to be supplied. Or that a mother’s own fat metabolism is increasingly drawn upon as she continues her fast, and nicotinamide leaks into her milk from her blood circulation.

Nicotinamide can also be converted to N-methylnicotinamide, which has in the past been viewed as a non-biologically active waste product, but is increasingly attracting interest as a stimulator of peroxisome proliferation74,94,90, which is pertinent to a fasting mother seal - the metabolism of long chain fatty acids takes place in peroxisomes before transfer to the mitochondria. N-methylnicotinamide is metabolised into N1-methyl-2-pyridone-5-carboxamides via the action of aldehyde oxidase and also cytochrome P450 2E1 (CYP2E1), and it has been proposed that its levels give an indication of peroxisome proliferation74,75,76. N1-methyl-2-pyridone-5-carboxamide is only present at very low levels at the beginning of lactation and increases dramatically with time until the end of lactation (Fig. 3). This compound could therefore be an indicator of increasing fat metabolism in the mothers and possibly a potential marker of when a mother may soon depart that may be detectable in both blood and milk.

Carnitine is centrally involved in fatty acid metabolism and fulfils three main functions - it transports fatty acids into mitochondria so that they can undergo β-oxidation to generate NADH; it removes fatty acids from the mitochondria in order to maintain the levels of free CoA within a certain range; and it removes waste fatty acids from the body as water soluble carnitine conjugates75,91,95. As we will report elsewhere, carnitines that are conjugated with long acyl chains (e.g., oleoyl, palmitoyl, and docosahexanoyl in particular) are substantially more abundant in seal milk than in cow, goat or camel milks, whereas those conjugated with short acyl chains (acetyl, propionyl, butyl) were of similar abundances or slightly lower. However, the post-parturition changes in seal milk were similar for all types, and Fig. 3 illustrates the trend for acetylcarnitine, which diminishes to low levels towards the end of lactation.

As for the other small molecules that we found in seal milk, we cannot be sure whether the carnitines are there to supplement a pup’s metabolic activity or whether they are reflecting a mother’s physiology at the time of sampling, or both. Dietary carnitine is an important contributor to the carnitine pool and short chain acyl forms may have improved bioavailability in comparison to free carnitine. Also, acylcarnitines are activated for metabolism by mitochondria since they can be converted directly to acyl CoA with the investment of a molecule of ATP, which is required for the conjugation of free acyl groups to CoA75,95. Long chain fatty acids such as docosahexenoic acid are metabolised in peroxisomes to shorter chain acids before entering the mitochondria for further metabolism. They are required for conversion to acyl CoAs before they can be oxidised in the peroxisomes and, again, it would be advantageous if they were available in their activated form e.g. docosahexanoyl carnitine. Thus, aside from whether or not the acylcarnitines can be efficiently absorbed by seal pups, for every molecule of acyl carnitine assimilated a molecule of ATP is conserved.

Amongst food sources derived from animals, carnitine is most abundant in red meats, followed by fish and milk. Given the extremely high dependence of seal pups on fats, it is perhaps not surprising that they are provided with such high levels of acylcarnitines, and that maternal provision early in lactation would be valuable. It is interesting, though, that, whilst carnitine levels drop overall with time, other metabolites involved in fatty acid metabolism and long chain acyl carnitines increase (e.g. nicotinamide). This perhaps reflects the use of carnitine in the formation of the “ready to go” acyl carnitines and the requirement for nicotinamide for NAD+ formation to support β-oxidation after their conversion to acyl CoAs.

Conclusions

There is no widely accepted definition of what colostrum is. We previously defined the point at which colostrum ends and main phase lactation begins as being when the components of milk stabilise in relative concentrations5. We find that there is no such point in the brief lactation period of grey seals. We have therefore here taken the end of colostrum as being when the protein profiles have stabilised.

The transition from colostrum to main phase lactation in the Atlantic grey seal is the shortest yet recorded for any species of mammal. It is in stark contrast to the longest known for a eutherian, that which occurs in a fellow member of the Carnivora, a bear5. This divergence is all the more impressive given that true seals, along with other pinnipeds, share membership of the Caniformia suborder within the Carnivora78,79. It is conceivable that the transition occurs even more quickly in species of seal in which the lactation period is even shorter, the hooded seal in particular.

Our focus has been on the components involved in immune defence and indicators of metabolic changes. The rapid change in protein profile is particularly impressive, but so too is the persistence of IgG with time after birth. This is unusual and could indicate a particular need to provision a rapidly growing offspring with a sufficient supply of antibody to maintain its defence against pathogens in circulation in breeding colonies, phocine and other morbilliviruses being obvious examples80,82. A question, therefore, is whether this prolonged delivery of IgG is only for protection of the gut, or instead results in a systemically protective build-up of this antibody class in the blood of the pups before weaning. Of innate immune protection, the changes in oligosaccharides are also of note. Those probably involved in antimicrobial activity were present only at the beginning of lactation in our seals, and many fewer types were found in comparison to bears5. The differences between the composition and changes in milk oligosaccharides between two species within the Caniformia suggest stark differences in their adaptations to pathogen defence and the microbiomes they need to establish, despite their close phylogenetic relationship.

We observed changes in compounds central to fat metabolism that could either be reflections of how the mother’s metabolism alters as she mobilises and transfers her own body resources to her pup without replenishment, or donation of compounds to aid the pup’s own fat metabolism, or both. Either way, our findings merit optimism in finding a metabolic signal of when a seal mother reaches the end of her resources and must leave.

Materials and Methods

Milk collection, storage and processing

The seal milk samples were collected from the Isle of May, Scotland, colony of Atlantic grey seals during October and November 2013, and stored frozen until processed. A further collection was made in November 2016 in an attempt to obtain samples as close after birth as possible without risking adverse maternal behaviour or survival of pups; these collection times would have fallen between 10 to 19 hours post parturition. Females were tranquilised with a mass-adjusted dose of ®Zoletil 100 (Virbac, Bury St Edmunds, Suffolk, UK), followed by intravenous oxytocin to stimulate milk let-down, and finally an intramuscular prophylactic dose of tetracycline. Oxytocin was administered as a 1 ml intravenous injection (10 iu ml−1 or 0.18 mg ml−1; Oxytocin-S, Intervet UK). Post-parturition female grey seals in this population weighed about 180 kg, so the dose of oxytocin would have approximated 1 μg kg−1. No deaths or premature desertions of pups following any samplings were observed. Milk samples were centrifuged at 3,000 rpm at 4 °C in a Heraeus 1.0 R centrifuge with swing-out buckets for 15 minutes and the layer between the upper fat layer and the pellet was taken for analysis (see Supplementary Figures S2 and S3).


Ethical approval

Collection of milk samples was approved by the ethical committee of Scottish Oceans Institute, University of St Andrews, and the College of Medical, Veterinary and Life Sciences Ethics Committee of the University of Glasgow. All sampling and animal handling were carried out in strict accordance with relevant guidelines and regulations, and as approved by the above authorities.


Protein electrophoresis

One-dimensional (1-D) vertical sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) was carried out using the Invitrogen (Thermo Scientific, Paisley, UK) NuPAGE system with precast 4–12% gradient acrylamide gels, and β-mercaptoethanol (25 μl added to 1 ml sample buffer) as reducing agent when required. Gels were stained for protein using colloidal Coomassie Blue (InstantBlue; Expedion, Harston, UK) and images of gels were recorded using a Kodak Image Station 440CF imager. Electronic images of stained gels were taken under ambient laboratory light and modified only for slight adjustment of contrast and brightness so as to include all visible bands, and final images were taken using the near-default setting of camera aperture f2.8, and no subsequent electronic modifications were made. The complete, uncropped images are presented in the Supplementary. Pre-stained molecular mass/relative mobility (Mr) standard proteins were obtained from New England Biolabs, Ipswich, MA, USA.


Proteomics

Stained protein bands or spots were excised from preparative 1-D or 2-D gels stained with Coomassie Blue and analysed by liquid chromatography-mass spectrometry (LC-MS). Gel pieces were washed with 100 mM NH4HCO3 for 30 minutes and then for a further hour with 100 mM NH4HCO3 in 50% (v/v) acetonitrile. After each wash, all solvent was discarded. Gel pieces were dehydrated with 100% acetonitrile for 10 minutes prior to solvent being removed and dried by vacuum centrifugation. Dry gel pieces were rehydrated with 10 µl trypsin at a concentration of 20 ng µl−1 in 25 mM NH4HCO3 (Promega, Madison, WI, USA) and proteins digested overnight at 37 °C. This liquid was transferred to a fresh tube, and gel pieces washed for 10 min with 10 µl of 50% acetonitrile. This wash was pooled with the first extract, and the tryptic peptides dried to completion. Tryptic peptides were solubilized in 0.5% (v/v) formic acid and fractionated on a nanoflow UHPLC system (RSLCnano system; ThermoFisher Scientific, Inchinnan, UK) before analysis by electrospray ionisation (ESI) mass spectrometry on an Amazon ion trap MS/MS (Bruker, Coventry, UK). Peptide separation was performed on a PepMap C18 reversed phase column (LC Packings/Dionex/ThermoFisher), using a 5–85% v/v acetonitrile gradient (in 0.5% v/v formic acid) run over 45 min at a flow rate of 0.2 µl min−1. Mass spectrometric (MS) analysis was performed using a continuous duty cycle of survey MS scan followed by up to five MS/MS analyses of the most abundant peptides, choosing the most intense multiply-charged ions with dynamic exclusion for 120 s. MS data were processed using Data Analysis software (Bruker) and the automated Matrix Science Mascot Daemon server (v2.1.06). Protein identifications were assigned using the Mascot search engine to interrogate sequences in the NCBI databases, restricting the search to Caniformiae and allowing a mass tolerance of 0.4 Da for both MS and MS/MS analyses. Cysteine carbamidomethylation and methionine oxidation were set as fixed and variable modifications, respectively. Mascot uses probability based scoring to match MS/MS fragment ion masses to genome and protein sequence datasets. The total score reflects the −10*LOG10(P) probability that the observed match is a random event and, for the searches reported here, a Mascot score >38 reports a P value < 0.05. A commonly accepted threshold is that an event is significant if it would be expected to occur at random with a frequency of less than 5%. This is the default value that is reported on the results summary page. BLAST searches, or searches of genome databases within or beyond the Carnivora, were carried out to check the annotations.


Metabolomics

Ammonium carbonate, HPLC grade acetonitrile, and methanol were purchased from Sigma-Aldrich, UK. HPLC grade water was produced by a Direct-Q 3 Ultrapure Water System from Millipore, UK. The mixtures of metabolite authentic standards were prepared from standards obtained from Sigma-Aldrich, UK. In order to analyse the more polar fraction of the milk samples (0.5 mL) were thawed at room temperature and then centrifuged or 10 minutes at 15,000 rpm at 4 °C (Eppendorf 5424 R, maximum RCF = 21.130 g). An aliquot of the supernatant (200 µl) was mixed with acetonitrile (800 µl). The solution was mixed thoroughly, emulsion was centrifuged for 10 minutes at 15,000 rpm at 4 °C (Eppendorf 5424 R), and the supernatant was transferred to an HPLC vial for Liquid Chromatography-Mass Spectrometry (LC-MS) analysis. The lipids in the milk were analysed by mixing 200 µl of the whole milk with 800 µl of isopropanol. The solution was mixed thoroughly and emulsion centrifuged for 10 minutes at 15,000 rpm at 4 °C (Eppendorf 5424 R). The supernatant was transferred to an HPLC vial for Liquid Chromatography-Mass Spectrometry (LC-MS) analysis.

HILIC–HRMS and multiple tandem HRMS analysis and data processing was carried out on an Accela 600 HPLC system combined with an Exactive (Orbitrap) mass spectrometer (ThermoFisher Scientific). An aliquot of each sample solution (10 μL) was injected onto a ZIC-pHILIC column (150 × 4.6 mm, 5 µm; HiChrom, Reading, UK) with mobile phase A: 20 mM ammonium carbonate in HPLC grade water (pH 9.2), and B: HPLC grade acetonitrile. The gradient programme was as follows: 80% B (0 min) 20% B (30 min) 5% B (36 min) 80% B (37 min) 80% B (45 min). Peak extraction and alignment were calculated by integration of the area under the curve, using MZMine 2.14 software (open source). Resulting data were searched against an in-house metabolite database. Similar procedures were used for the lipids analysis which was carried out on an ACE Silica gel column (150 × 3 mm, 3 µm particle size) with mobile phase A 20 mM ammonium formate in water isopropanol (80:20) and mobile phase B acetonitrile/isopropanol (20:80). The flow rate was 0.3 mL/min and gradient was as follows: 0–1 min 8% B, 5 min 9% B, 10 min 20% B, 16 min 25% B, 23 min 35% B, 26–40 min 8% B.


Data availability

All the proteomics and metabolomics data are available in the figshare data repository with doi: 10.6084/m9.figshare.5570305 and at https://figshare.com/s/3f3bfd7408c1733a2e2d.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  1. 1.

    Langer, P. The phases of maternal investment in eutherian mammals. Zoology 111, 148–162, https://doi.org/10.1016/j.zool.2007.06.007 (2008).

  2. 2.

    Langer, P. Differences in the composition of colostrum and milk in eutherians reflect differences in immunoglobulin transfer. Journal of Mammalogy 90, 332–339, https://doi.org/10.1644/08-mamm-a-071.1 (2009).

  3. 3.

    Ogawa, S. et al. Shotgun proteomic analysis of porcine colostrum and mature milk. Animal Science Journal 85, 440–448, https://doi.org/10.1111/asj.12165 (2014).

  4. 4.

    Zhang, H. et al. Changes in chemical composition of Alxa bactrian camel milk during lactation. Journal of Dairy Science 88, 3402–3410, https://doi.org/10.3168/jds.S0022-0302(05)73024-1 (2005).

  5. 5.

    Griffiths, K. et al. Prolonged transition time between colostrum and mature milk in a bear, the giant panda, Ailuropoda melanoleuca. Royal Society Open Science 2, https://doi.org/10.1098/rsos.150395 (2015).

  6. 6.

    Hinde, K. & Lewis, Z. T. Mother’s littlest helpers. Science 348, 1427–1428, https://doi.org/10.1126/science.aac7436 (2015).

  7. 7.

    Zivkovic, A. M., German, J. B., Lebrilla, C. B. & Mills, D. A. Human milk glycobiome and its impact on the infant gastrointestinal microbiota. Proceedings of the National Academy of Sciences of the United States of America 108, 4653–4658, https://doi.org/10.1073/pnas.1000083107 (2011).

  8. 8.

    McGuire, M. K. et al. What’s normal? Oligosaccharide concentrations and profiles in milk produced by healthy women vary geographically. American Journal of Clinical Nutrition 105, 1086–1100, https://doi.org/10.3945/ajcn.116.139980 (2017).

  9. 9.

    Moon, J. S., Joo, W., Ling, L., Choi, H. S. & Han, N. S. In vitro digestion and fermentation of sialyllactoses by infant gut microflora. Journal of Functional Foods 21, 497–506, https://doi.org/10.1016/j.jff.2015.12.002 (2016).

  10. 10.

    ten Bruggencate, S. J. M., Bovee-Oudenhoven, I. M. J., Feitsma, A. L., van Hoffen, E. & Schoterman, M. H. C. Functional role and mechanisms of sialyllactose and other sialylated milk oligosaccharides. Nutrition Reviews 72, 377–389, https://doi.org/10.1111/Nure.12106 (2014).

  11. 11.

    Gabrielli, O. et al. Preterm milk oligosaccharides during the first month of lactation. Pediatrics 128, E1520–E1531, https://doi.org/10.1542/peds.2011-1206 (2011).

  12. 12.

    Chen, X. Y. & Ganzle, M. G. Lactose and lactose-derived oligosaccharides: More than prebiotics? International Dairy Journal 67, 61–72, https://doi.org/10.1016/j.idairyj.2016.10.001 (2017).

  13. 13.

    Zhang, T. et al. Changes in the milk metabolome of the giant panda (Ailuropoda melanoleuca) with time after birth - three phases in early lactation and progressive individual differences. PLoS ONE 10, e0143417 (2015).

  14. 14.

    Brennan, A. J. et al. The tammar wallaby and fur seal: Models to examine local control of lactation. Journal of Dairy Science 90, E66–E75, https://doi.org/10.3168/jds.2006-483 (2007).

  15. 15.

    Modepalli, V. et al. Differential temporal expression of milk miRNA during the lactation cycle of the marsupial tammar wallaby (Macropus eugenii). BMC Genomics 15, 1012, https://doi.org/10.1186/1471-2164-15-1012 (2014).

  16. 16.

    Schulz, T. M. & Bowen, W. D. Pinniped lactation strategies: Evaluation of data on maternal and offspring life history traits. Marine Mammal Science 20, 86–114, https://doi.org/10.1111/j.1748-7692.2004.tb01142.x (2004).

  17. 17.

    Crocker, D. E. & McDonald, B. I. In Marine Mammal Physiology: Requisites for Ocean Living. Vol. CRCPress (eds Michael A. Castellini & Jo-Ann Mellish) Ch. 10, 219–241 (2016).

  18. 18.

    Berta, A., Sumich, J. L. & Kovacs, K. M. In Marine Mammals - Evolutionary Biology (eds A. Berta, J. L. Sumich, & K. M. Kovacs) Ch. 13, 465–532 (Academic Press, 2015).

  19. 19.

    Oftedal, O. T. Use of maternal reserves as a lactation strategy in large mammals. Proceedings of the Nutrition Society 59, 99–106, https://doi.org/10.1017/s0029665100000124 (2000).

  20. 20.

    Lydersen, C., Hammill, M. O. & Kovacs, K. M. Activity of lactating ice-breeding grey seals, Halichoerus grypus, from the Gulf of St Lawrence, Canada. Animal Behaviour 48, 1417–1425, https://doi.org/10.1006/anbe.1994.1377 (1994).

  21. 21.

    Lydersen, C., Hammill, M. O. & Kovacs, K. M. Milk intake, growth and energy-consumption in pups of ice-breeding grey seals (Halichoerus grypus) from the gulf of St Lawrence, Canada. Journal of Comparative Physiology B-Biochemical Systemic and Environmental Physiology 164, 585–592, https://doi.org/10.1007/bf00389798 (1995).

  22. 22.

    Kaetzel, C. S. The polymeric immunoglobulin receptor: bridging innate and adaptive immune responses at mucosal surfaces. Immunological Reviews 206, 83–99, https://doi.org/10.1111/j.0105-2896.2005.00278.x (2005).

  23. 23.

    Kaetzel, C. S. & Mostov, K. Immunoglobulin Transport and the Polymeric Immunoglobulin Receptor. Mucosal Immunology, 3rd Edition, 211–250, https://doi.org/10.1016/b978-012491543-5/50016-4 (2005).

  24. 24.

    Brandtzaeg, P. Secretory IgA: Designed for anti-microbial defense. Frontiers in Immunology 4, 222–222, https://doi.org/10.3389/fimmu.2013.00222 (2013).

  25. 25.

    Moor, K. et al. High-avidity IgA protects the intestine by enchaining growing bacteria. Nature 544, 498–502, https://doi.org/10.1038/nature22058 (2017).

  26. 26.

    Mess, A. & Carter, A. M. Evolution of the placenta during the early radiation of placental mammals. Comparative Biochemistry and Physiology A -Molecular & Integrative Physiology 148, 769–779, https://doi.org/10.1016/j.cbpa.2007.01.029 (2007).

  27. 27.

    Gundling, W. E. & Wildman, D. E. A review of inter- and intraspecific variation in the eutherian placenta. Philosophical Transactions of the Royal Society B-Biological Sciences 370, https://doi.org/10.1098/rstb.2014.0072 (2015).

  28. 28.

    Roopenian, D. C. & Akilesh, S. FcRn: the neonatal Fc receptor comes of age. Nature Reviews Immunology 7, 715–725, https://doi.org/10.1038/nri2155 (2007).

  29. 29.

    Simister, N. E. Placental transport of immunoglobulin G. Vaccine 21, 3365–3369, https://doi.org/10.1016/s0264-410x(03)00334-7 (2003).

  30. 30.

    Baumrucker, C. R. & Bruckmaier, R. M. Colostrogenesis: IgG(1) transcytosis mechanisms. Journal of Mammary Gland Biology and Neoplasia 19, 103–117, https://doi.org/10.1007/s10911-013-9313-5 (2014).

  31. 31.

    Carter, A. M. & Enders, A. C. Placentation in mammals: Definitive placenta, yolk sac, and paraplacenta. Theriogenology 86, 278–287, https://doi.org/10.1016/j.theriogenology.2016.04.041 (2016).

  32. 32.

    Burton, G. J. Placental uptake of maternal erythrocytes - a comparative-study. Placenta 3, 407–434, https://doi.org/10.1016/s0143-4004(82)80033-7 (1982).

  33. 33.

    Krakowka, S., Long, D. & Koestner, A. Influence of transplacentally acquired antibody on neonatal susceptibility to canine-distemper virus in gnotobiotic dogs. Journal of Infectious Diseases 137, 605–608 (1978).

  34. 34.

    Casal, M. L., Jezyk, P. F. & Giger, U. Transfer of colostral antibodies from queens to their kittens. American Journal of Veterinary Research 57, 1653–1658 (1996).

  35. 35.

    Ross, P. S. et al. Relative immunocompetence of the newborn harbour seal. Phoca vitulina. Veterinary Immunology and Immunopathology 42, 331–348, https://doi.org/10.1016/0165-2427(94)90077-9 (1994).

  36. 36.

    Vorbach, C., Capecchi, M. R. & Penninger, J. M. Evolution of the mammary gland from the innate immune system? Bioessays 28, 606–616, https://doi.org/10.1002/bies.20423 (2006).

  37. 37.

    Vorbach, C., Harrison, R. & Capecchi, M. R. Xanthine oxidoreductase is central to the evolution and function of the innate immune system. Trends in Immunology 24, 512–517, https://doi.org/10.1016/s1471-4906(03)00237-0 (2003).

  38. 38.

    Ceciliani, F., Ceron, J. J., Eckersall, P. D. & Sauerwein, H. Acute phase proteins in ruminants. Journal of Proteomics 75, 4207–4231, https://doi.org/10.1016/j.jprot.2012.04.004 (2012).

  39. 39.

    Ceron, J. J., Eckersall, P. D. & Martinez-Subiela, S. Acute phase proteins in dogs and cats: current knowledge and future perspectives. Veterinary Clinical Pathology 34, 85–99 (2005).

  40. 40.

    Gronlund, U., Hulten, C., Eckersall, P. D., Hogarth, C. & Waller, K. P. Haptoglobin and serum amyloid A in milk and serum during acute and chronic experimentally induced Staphylococcus aureus mastitis. Journal of Dairy Research 70, 379–386, https://doi.org/10.1017/s0022029903226484 (2003).

  41. 41.

    Whelehan, C. J., Meade, K. G., Eckersall, P. D., Young, F. J. & O’Farrelly, C. Experimental Staphylococcus aureus infection of the mammary gland induces region-specific changes in innate immune gene expression. Veterinary Immunology and Immunopathology 140, 181–189, https://doi.org/10.1016/j.vetimm.2010.11.013 (2011).

  42. 42.

    Stein, T. et al. Involution of the mouse mammary gland is associated with an immune cascade and an acute-phase response, involving LBP, CD14 and STAT3. Breast Cancer Research 6, R75–R91, https://doi.org/10.1186/bcr753 (2004).

  43. 43.

    Holt, C. & Carver, J. A. Darwinian transformation of a ‘scarcely nutritious fluid’ into milk. Journal of Evolutionary Biology 25, 1253–1263, https://doi.org/10.1111/j.1420-9101.2012.02509.x (2012).

  44. 44.

    Holt, C., Carver, J. A., Ecroyd, H. & Thorn, D. C. Invited review: Caseins and the casein micelle: Their biological functions, structures, and behavior in foods. Journal of Dairy Science 96, 6127–6146, https://doi.org/10.3168/jds.2013-6831 (2013).

  45. 45.

    Holt, C. & Clegg, R. A. The 500 Myr story of the evolution of phosphoproteins that made milk possible. Journal of Dairy Science 88, 241–242 (2005).

  46. 46.

    Ossowski, S. et al. Aggregation behavior of bovine κ- and β-casein studied with small angle neutron scattering, light scattering, and cryogenic transmission electron microscopy. Langmuir 28, 13577–13589, https://doi.org/10.1021/la302416p.

  47. 47.

    Kontopidis, G., Holt, C. & Sawyer, L. Invited review: β-lactoglobulin: Binding properties, structure, and function. Journal of Dairy Science 87, 785–796 (2004).

  48. 48.

    Le Maux, S., Bouhallab, S., Giblin, L., Brodkorb, A. & Croguennec, T. Bovine β-lactoglobulin/fatty acid complexes: binding, structural, and biological properties. Dairy Science & Technology 94, 409–426, https://doi.org/10.1007/s13594-014-0160-y (2014).

  49. 49.

    Breustedt, D. A., Schonfeld, D. L. & Skerra, A. Comparative ligand-binding analysis of ten human lipocalins. Biochimica et Biophysica Acta-Proteins and Proteomics 1764, 161–173, https://doi.org/10.1016/j.bbapap.2005.12.006 (2006).

  50. 50.

    Kawaguchi, R. et al. A membrane receptor for retinol binding protein mediates cellular uptake of vitamin A. Science 315, 820–825, https://doi.org/10.1126/science.1136244 (2007).

  51. 51.

    Suire, S., Stewart, F., Beauchamp, J. & Kennedy, M. W. Uterocalin, a lipocalin provisioning the preattachment equine conceptus: fatty acid and retinol binding properties, and structural characterization. Biochemical Journal 356, 369–376, https://doi.org/10.1042/0264-6021:3560369 (2001).

  52. 52.

    Cunningham, T. J. & Duester, G. Mechanisms of retinoic acid signalling and its roles in organ and limb development. Nature Reviews Molecular Cell Biology 16, 110–123, https://doi.org/10.1038/nrm3932 (2015).

  53. 53.

    Vilhais-Neto, G. C. et al. Rere controls retinoic acid signalling and somite bilateral symmetry. Nature 463, 953–957, https://doi.org/10.1038/nature08763 (2010).

  54. 54.

    Hinz, K., O’Connor, P. M., Huppertz, T., Ross, R. P. & Kelly, A. L. Comparison of the principal proteins in bovine, caprine, buffalo, equine and camel milk. Journal of Dairy Research 79, 185–191, https://doi.org/10.1017/s0022029912000015 (2012).

  55. 55.

    Pharo, E. A. et al. A colostrum trypsin inhibitor gene expressed in the Cape fur seal mammary gland during lactation. Gene 578, 7–16, https://doi.org/10.1016/j.gene.2015.11.042 (2016).

  56. 56.

    Douellou, T., Montel, M. C. & Sergentet, D. T. Anti-adhesive properties of bovine oligosaccharides and bovine milk fat globule membrane-associated glycoconjugates against bacterial food enteropathogens. Journal of Dairy Science 100, 3348–3359, https://doi.org/10.3168/jds.2016-11611 (2017).

  57. 57.

    Martin-Ortiz, A. et al. Changes in caprine milk oligosaccharides at different lactation stages analyzed by high performance liquid chromatography coupled to mass spectrometry. Journal of Agricultural and Food Chemistry 65, 3523–3531, https://doi.org/10.1021/acs.jafc.6b05104 (2017).

  58. 58.

    Liu, Z., Auldist, M., Wright, M., Cocks, B. & Rochfort, S. Bovine milk oligosaccharide contents show remarkable seasonal variation and intercow variation. Journal of Agricultural and Food Chemistry 65, 1307–1313, https://doi.org/10.1021/acs.jafc.6b04098 (2017).

  59. 59.

    Wang, W.-L. et al. Comparison of anti-pathogenic activities of the human and bovine milk N-glycome: Fucosylation is a key factor. Food Chemistry 235, 167–174, https://doi.org/10.1016/j.foodchem.2017.05.026 (2017).

  60. 60.

    Thurl, S. et al. Variation of human milk oligosaccharides in relation to milk groups and lactational periods. British Journal of Nutrition 104, 1261–1271, https://doi.org/10.1017/s0007114510002072 (2010).

  61. 61.

    Gnoth, M. J., Kunz, C., Kinne-Saffran, E. & Rudloff, S. Human milk oligosaccharides are minimally digested in vitro. Journal of Nutrition 130, 3014–3020 (2000).

  62. 62.

    Ehara, T. et al. Combinational effects of prebiotic oligosaccharides on bifidobacterial growth and host gene expression in a simplified mixed culture model and neonatal mice. British Journal of Nutrition 116, 270–278, https://doi.org/10.1017/s0007114516001987 (2016).

  63. 63.

    Turroni, F. et al. Genome analysis of Bifidobacterium bifidum PRL2010 reveals metabolic pathways for host-derived glycan foraging. Proceedings of the National Academy of Sciences of the United States of America 107, 19514–19519, https://doi.org/10.1073/pnas.1011100107 (2010).

  64. 64.

    Oftedal, O. T. In Encyclopedia of Dairy Sciences Vol. 3 (ed J. W. Fuquay, Fox, P. F. and McSweeney, P. L. H.) 563–580 (Academic Press, 2011).

  65. 65.

    Oftedal, O. T. The evolution of milk secretion and its ancient origins. Animal 6, 355–368, https://doi.org/10.1017/s1751731111001935 (2012).

  66. 66.

    Reich, C. M. & Arnould, J. P. Y. Evolution of Pinnipedia lactation strategies: a potential role for alpha-lactalbumin? Biology Letters 3, 546–549, https://doi.org/10.1098/rsbl.2007.0265 (2007).

  67. 67.

    Messer, M. & Urashima, T. Evolution of milk oligosacharides and lactose. Trends in Glycoscience and Glycotechnology 14, 153–176 (2002).

  68. 68.

    Lambert, I. H., Kristensen, D. M., Holm, J. B. & Mortensen, O. H. Physiological role of taurine - from organism to organelle. Acta Physiologica 213, 191–212, https://doi.org/10.1111/apha.12365 (2015).

  69. 69.

    Menzie, J., Pan, C., Prentice, H. & Wu, J.-Y. Taurine and central nervous system disorders. Amino Acids 46, 31–46, https://doi.org/10.1007/s00726-012-1382-z (2014).

  70. 70.

    Zhang, T. et al. Changeover from signalling to energy-provisioning lipids during transition from colostrum to mature milk in the giant panda (Ailuropoda melanoleuca). Scientific Reports 6, 36141, https://doi.org/10.1038/srep36141 (2016).

  71. 71.

    Chesney, R. W. et al. In Taurine 7 Vol. 643 Advances in Experimental Medicine and Biology (eds J. Azuma, S. W. Schaffer, & T. Ito) 325–331 (2009).

  72. 72.

    Hedberg, G. E. et al. Milk composition in free-ranging polar bears (Ursus maritimus) as a model for captive rearing milk formula. Zoo Biology 30, 550–565, https://doi.org/10.1002/zoo.20375 (2011).

  73. 73.

    Hedberg, G. E., Dierenfeld, E. S. & Rogers, Q. R. Taurine and zoo felids: Considerations of dietary and biological tissue concentrations. Zoo Biology 26, 517–531, https://doi.org/10.1002/zoo.20158 (2007).

  74. 74.

    Delaney, J. et al. Tryptophan-NAD(+) pathway metabolites as putative biomarkers and predictors of peroxisome proliferation. Archives of Toxicology 79, 208–223, https://doi.org/10.1007/s00204-004-0625-5 (2005).

  75. 75.

    Patterson, A. D. et al. Human urinary metabolomic profile of PPAR alpha Induced fatty acid β-oxidation. Journal of Proteome Research 8, 4293–4300, https://doi.org/10.1021/pr9004103 (2009).

  76. 76.

    Ament, Z., Masoodi, M. & Griffin, J. L. Applications of metabolomics for understanding the action of peroxisome proliferator-activated receptors (PPARs) in diabetes, obesity and cancer. Genome Medicine 4, doi:10.1186/gm331 (2012).

  77. 77.

    Thomas, F. C. et al. Mastitomics, the integrated omics of bovine milk in an experimental model of Streptococcus uberis mastitis: 1. High abundance proteins, acute phase proteins and peptidomics. Molecular Biosystems 12, 2735–2747, https://doi.org/10.1039/c6mb00239k (2016).

  78. 78.

    Agnarsson, I., Kuntner, M. & May-Collado, L. J. Dogs, cats, and kin: A molecular species-level phylogeny of Carnivora. Molecular Phylogenetics and Evolution 54, 726–745, https://doi.org/10.1016/j.ympev.2009.10.033 (2010).

  79. 79.

    Eizirik, E. et al. Pattern and timing of diversification of the mammalian order Carnivora inferred from multiple nuclear gene sequences. Molecular Phylogenetics and Evolution 56, 49–63, https://doi.org/10.1016/j.ympev.2010.01.033 (2010).

  80. 80.

    Beineke, A., Baumgartner, W. & Wohlsein, P. Cross-species transmission of canine distemper virus-an update. One health (Amsterdam, Netherlands) 1, 49–59, https://doi.org/10.1016/j.onehlt.2015.09.002 (2015).

  81. 81.

    Schrodl, W. et al. Acute phase proteins as promising biomarkers: Perspectives and limitations for human and veterinary medicine. Proteomics Clinical Applications 10, 1077–1092, https://doi.org/10.1002/prca.201600028 (2016).

  82. 82.

    Garnier, R., Gandon, S., Harding, K. C. & Boulinier, T. Length of intervals between epidemics: evaluating the influence of maternal transfer of immunity. Ecology and Evolution 4, 568–575, https://doi.org/10.1002/ece3.955 (2014).

  83. 83.

    Kim, C., & Cha, Y.-N. Taurine chloramine produced from taurine under inflammation provides anti-inflammatory and cytoprotective effects. Amino Acids 46, 89-100 (2014)

  84. 84.

    Tang, C., Marchand, K., Lam, L., Lux-Lantos, V., Thyssen, S.M, Guo, J., Giacca, A., & Arany, E. Maternal taurine supplementation in rats partially prevents the adverse effects of early-life protein deprivation on β-cell function and insulin sensitivity. Reproduction 145, 609-620 (2013)

  85. 85.

    Sturman, JA. Taurine in development. Physiological Reviews. 73, 119-147 (1993)

  86. 86.

    Mortensen, O.H., Olsen, H.L., Frandsen, L., Nielsen, P.E., Nielsen, F.C., Grunnet, N. & Quistorff, B. Gestational protein restriction in mice has pronounced effects on gene expression in newborn offspring's liver and skeletal muscle; protective effect of taurine. Pediatric Research. 67, 47-53 (2010)

  87. 87.

    Huxtable, R.J. Physiological actions of taurine. Physiological Reviews. 72, 101-163 (1992)

  88. 88.

    Lindquist, S, & Hernell, O. Lipid digestion and absorption in early life: an update. Current Opinion in Clinical Nutrition and Metabolic Care. 13, 314-320 (2010)

  89. 89.

    Thomas, F.C., Waterston, M., Hastie, P., Haining, & H., Eckersall, P.D. Early post parturient changes in milk acute phase proteins. Journal of Dairy Research 83, 352-359 (2016)

  90. 90.

    Xu, Y., Wang, Q., Cook, T.J., & Knipp, G.T. Effect of placental fatty acid metabolism and regulation by peroxisome proliferator activated receptor on pregnancy and fetal outcomes. Journal of Pharmaceutical Sciences 96, 2582-2606 (2007)

  91. 91.

    Daskalaki, E., Blackburn, G., Kalna, G., Zhang, T., Anthony, N., & Watson, D.G. A study of the effects of exercise on the urinary metabolome using normalisation to individual metabolic output. Metabolites 5,119-139 (2015)

  92. 92.

    Sawyer, L. & Kontopidis, G. The core lipocalin, bovine β-lactoglobulin. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 1482, 136-148 (2000)

  93. 93.

    Andersson, E.-L., Hernell, O., Bläckberg, L., Fält, H., Lindquist, S.  BSSL & PLRP2: key enzymes for lipid digestion in the newborn examined using the Caco-2 cell line. Journal of Lipid Research 52,1949-1956 (2011)

  94. 94.

    Ringeissen, S., Connor, S.C., Brown, H.R., Sweatman, B.C., Hodson, M.P., Kenny, S.P., Haworth, R.I., Mcgill, P., Price, M.A., Aylott, M.C., Nunez, D.J., Haselden, J.N., Waterfield, C.J.  Potential urinary and plasma biomarkers of peroxisome proliferation in the rat: identification of N-methylnicotinamide and N-methyl-4-pyridone-3-carboxamide by H-1 nuclear magnetic resonance and high performance liquid chromatography. Biomarkers 8, 240-271 (2008)

  95. 95.

    Ramsay, R. & Zammit, V.A. Carnitine acyltransferases and their influence on CoA pools in health and disease. Molecular Aspects of Medicine 25, 475-493 (2004)

  96. 96.

    Ramsay, M.A. & Dunbrack, R.L. Physiological constraints on life history phenomena: the example of small bear cubs at birth. The American Naturalist 127, 735-743 (1986)

Download references

Acknowledgements

We are grateful to Scottish National Heritage for permitting our time and sampling on the Isle of May. We are also extremely grateful to Alan Scott for his skilled help in performing 2-D protein electrophoresis gels. The work was funded from core support given to the Sea Mammal Research Unit, Scottish Oceans Institute, from the National Environmental Research Council (UK), and separately by the Universities of Glasgow and Strathclyde. The funding of mass spectrometry equipment for metabolomics was provided by the Scottish Life Sciences Alliance. The Glasgow proteomics facility is supported by the Wellcome Trust.

Author information

Affiliations

  1. Institute of Biodiversity, Animal Health & Comparative Medicine, and School of Life Sciences, Graham Kerr Building, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, Scotland, UK

    • Amanda D. Lowe
    •  & Malcolm W. Kennedy
  2. Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161 Cathedral Street, Glasgow, G4 0RE, Scotland, UK

    • Sami Bawazeer
    •  & David G. Watson
  3. Institute of Infection, Immunity and Inflammation, and Glasgow Polyomics, College of Medical, Veterinary and Life Sciences, University of Glasgow, Garscube Campus, Glasgow, G12 1QH, Scotland, UK

    • Suzanne McGill
    •  & Richard J. S. Burchmore
  4. Sea Mammal Research Unit, Scottish Oceans Institute, University of St Andrews, St Andrews, Fife, United Kingdom

    • P. P (Paddy) Pomeroy

Authors

  1. Search for Amanda D. Lowe in:

  2. Search for Sami Bawazeer in:

  3. Search for David G. Watson in:

  4. Search for Suzanne McGill in:

  5. Search for Richard J. S. Burchmore in:

  6. Search for P. P (Paddy) Pomeroy in:

  7. Search for Malcolm W. Kennedy in:

Contributions

Conceived and developed the project – M.W.K., P.P.P. Carried out the analyses – A.D.L., S.B., D.G.W., S.Mc.G., R.J.S.B., M.W.K. Analysed the data – A.D.L., S.B., D.G.W., S.Mc.G., R.J.S.B., M.W.K. Created the figures – M.W.K. Wrote the paper – M.W.K., P.P.P., D.G.W., R.J.S.B. in consultation with all authors.

Competing Interests

The authors declare that they have no competing interests.

Corresponding author

Correspondence to Malcolm W. Kennedy.

Electronic supplementary material

About this article

Publication history

Received

Accepted

Published

DOI

https://doi.org/10.1038/s41598-017-16187-7

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.