Cats are obligate carnivores and under most circumstances eat only animal products. Owing to the pseudogenization of one of two subunits of the sweet receptor gene, they are indifferent to sweeteners, presumably having no need to detect plant-based sugars in their diet. Following this reasoning and a recent report of a positive correlation between the proportion of dietary plants and the number of Tas2r (bitter receptor) genes in vertebrate species, we tested the hypothesis that if bitter perception exists primarily to protect animals from poisonous plant compounds, the genome of the domestic cat (Felis catus) should have lost functional bitter receptors and they should also have reduced bitter receptor function. To test functionality of cat bitter receptors, we expressed cat Tas2R receptors in cell-based assays. We found that they have at least 7 functional receptors with distinct receptive ranges, showing many similarities, along with some differences, with human bitter receptors. To provide a comparative perspective, we compared the cat repertoire of intact receptors with those of a restricted number of members of the order Carnivora, with a range of dietary habits as reported in the literature. The numbers of functional bitter receptors in the terrestrial Carnivora we examined, including omnivorous and herbivorous species, were roughly comparable to that of cats thereby providing no strong support for the hypothesis that a strict meat diet influences bitter receptor number or function. Maintenance of bitter receptor function in terrestrial obligate carnivores may be due to the presence of bitter compounds in vertebrate and invertebrate prey, to the necessary role these receptors play in non-oral perception, or to other unknown factors. We also found that the two aquatic Carnivora species examined had fewer intact bitter receptors. Further comparative studies of factors driving numbers and functions of bitter taste receptors will aid in understanding the forces shaping their repertoire.
Citation: Lei W, Ravoninjohary A, Li X, Margolskee RF, Reed DR, Beauchamp GK, et al. (2015) Functional Analyses of Bitter Taste Receptors in Domestic Cats (Felis catus). PLoS ONE 10(10): e0139670. doi:10.1371/journal.pone.0139670
Editor: Maik Behrens, German Institute of Human Nutrition Potsdam-Rehbruecke, GERMANY
Received: April 30, 2015; Accepted: September 15, 2015; Published: October 21, 2015
Copyright: © 2015 Lei et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported in part by the National Institute on Deafness and other communication disorders at the National Institutes of Health (R01DC010842 to PJ) and institutional funds from the Monell Chemical Senses Center; DNA analysis and calcium mobilization assays were performed at the Monell Genotyping and DNA/RNA Analysis Core and the Chemosensory Receptor Signaling Core, respectively, which was supported in part by funding from the National Institute on Deafness and Other Communication Disorders at the National Institutes of Health (1P30DC011735 to RFM). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The so-called basic tastes (e.g., sweet and bitter) have traditionally been presumed to have evolved to ensure that animals consume an appropriate source of calories while avoiding toxic compounds [1, 2]. Although most mammals avidly consume sugars, obligate carnivores such as meat-eating cats are indifferent to them, and one component of their sweet taste receptor gene repertoire (Tas1r2) is a pseudogene. This loss has happened independently in several obligate carnivore species in the order Carnivora , presumably because there is no need to detect sweet sugars from plants. It appears that all birds have lost the Tas1r2 taste receptor gene after birds and non-avian reptiles diverged but some birds (e.g., hummingbirds) consume foods that consist primarily of sugars . It was recently discovered that the nectar-eating hummingbirds have repurposed their amino acid Tas1r1/Tas1r3 receptor to detect sugars .
Bitter taste may provide another source of comparative evidence for an intimate relationship between diet and taste sensitivity (e.g., number of compounds and range of concentrations). Compounds that taste bitter to humans (hereafter “bitter compounds”) are widely rejected throughout the animal kingdom. It is thought that rejection is based on a mutual interaction between plants that do not “want” to be eaten and animals that do not “want” to be poisoned. A similar logic may pertain to avoidance of bitter-tasting invertebrates, reptiles and amphibians although the evidence for the extent to which cats may be exposed to such bitterness in prey as compared with exposure to plant-based bitter compounds for species that consume plants is unclear. Glendinning has argued that the relative occurrence of bitter and potentially toxic foods is lower for carnivores than for omnivores and herbivores .
Li and Zhang  have recently described a relationship between diet and the number of Tas2r genes from 54 diverse vertebrate species. Based on correlational analyses, they reported that species that tend to eat more plant food have more intact bitter receptors than species that eat little or no plant food. However, the number of functional bitter receptors may not be the only factor determining the importance of bitter taste in a species diet. For example, a species could be highly responsive to bitterness if it had a few bitter receptors that were responsive to many different bitter compounds (broadly “tuned”) as has recently been reported for the chicken . Nevertheless, given the vast potential array of bitter and toxic compounds, it is hard to imagine that a few receptors could detect many or all of them. And indeed, species differ greatly in bitter receptor number. There must be a selective reason for the existence of multiple bitter receptors, particularly in light of the relative paucity of taste receptors for other modalities such as sweet, umami and probably salty and sour [1, 2].
As an initial approach to the study of bitter receptor number and function in obligate carnivores, we evaluated bitter taste receptor function in a single meat-eating obligate carnivore, the domestic cat (Felis catus), by expressing the receptors in cell-based assays to test their function. This strategy ensures that genes that appear to be intact by computational methods are actually functional. It also allows us to test the breadth of tuning which cannot currently be predicted with in silico methods. We chose the domestic cat for this study since much work has been done on sweet taste receptors in cats [8, 9] and because of the inherent interest in factors influencing feeding in this companion animal. We also sought to provide a comparative perspective by examining the broader pattern of bitter receptor number in a single order, Carnivora, in light of the question concerning the functional significance of bitter receptors in obligate carnivores.
Domestic cats have at least seven functional bitter taste receptors
The results of nucleotide sequence searches of the feline genome indicate a total of 12 intact Tas2r receptor genes. Using cat Tas2r-specific primers, we amplified the entire coding regions of 10 of the 12 cat Tas2r receptors and inserted these receptor sequences into an expression cloning vector pCDNA3.1 (S1 Table). Two of the 12 receptors could not be amplified from feline DNA using primer sets designed to amplify the entire coding regions (Tas2r1 and Tas2r43). We expressed the 10 bitter taste receptors with a coupling chimeric G protein (Gα16-gust44) in a heterologous system. For bitter taste stimuli, we chose 25 commercially available compounds, eight derived from plants, that activate human bitter taste receptors . For each compound, mock-transfected cells were used as negative controls (see Methods).
Bitter receptors differed in the number of compounds that elicited a response. Some receptors appeared to be broadly tuned, such as Tas2r2 and Tas2r46 (Figs 1A, 1F, 2A and 2F), some appeared to have an intermediate range of tuning (e.g., Tas2r4, Figs 1B and 2B; Tas2r7; Figs 1C and 2C; Tas2r67, Figs 1G and 2G), and some seemed to be narrowly tuned (e.g., Tas2r12; Figs 1D and 2D; Tas2r38; Figs 1E and 2E). Three of the bitter receptors (Tas2r3, Tas2r9, and Tas2r42) showed no responses to any of 25 compounds tested (S2 Table) although this is not evidence that they are not functional; it is likely that in our small repertoire of bitter compounds tested we did not include those that activate these receptors.
HEK293 cells transiently transfected with one of the feline Tas2r bitter receptors (Tas2r2, Tas2r4, Tas2r7, Tas2r12, Tas2r38, Tas2r46, or Tas2r67), with Gα16-gust44, were assayed for their responses to 25 bitter compounds. Black traces, calcium mobilization of seven feline bitter receptors to bitter compounds; grey traces, those of mock transfected cells used as control.
HEK293 cells were transiently transfected with a feline bitter receptor (Tas2r2, Tas2r4, Tas2r7, Tas2r12, Tas2r38, Tas2r46, or Tas2r67), with Gα16-gust44, and assayed for their responses to bitter compounds. Data are expressed as mean ± SE percent change in fluorescence (ΔF, peak fluorescence–baseline fluorescence) compared with baseline fluorescence (F) from three independent wells. Two-tailed Student’s t-tests were performed to determine when responses from Tas2r-transfected cells were significantly different from that of mock-transfect cells. Only bitter compounds that elicited significant responses above mock-transfected cell baseline are shown in the Figure.
To confirm the validity of receptor responses, dose-dependent curves were obtained for a subset of Tas2r receptors and compounds. The Tas2r38 receptor responded to its ligand phenylthiocarbamide (PTC) in a dose-dependent manner (EC50 = 7.6 × 10−5). Dose-responsive curves were also obtained for a few additional receptors and compounds with similar results (Fig 3).
HEK293 cells transiently transfected with feline Tas2rs with Gα16-gust44 showed dose-dependent responses to bitter compounds. Mock-transfected cells were used as controls. The data were fit by a sigmoidal function using GraphPad Prism 5.
A comparative perspective: Bitter receptor genes in other Carnivora
Bitter receptor gene numbers for several species were available from public sources (dog, ferret, giant panda, and polar bear; see Materials and Methods). We also extracted bitter receptor gene information from the genome of two recently sequenced species from the order Carnivora (walrus and seal) using amino acid sequences of intact bitter receptors from dogs and ferrets as queries (N = 15 sequences from dog, N = 14 sequences from ferret). We found 5 and 4 intact bitter receptor genes from walrus and seal, respectively, as well as 17 (walrus) and 11 (seal) presumably non-functional bitter receptor genes (Tables 1 & 2; S1 & S2 Datasets). This result is consistent with our previous report  of reduced taste receptor function in other aquatic mammals. A phylogenetic tree constructed with all predicted intact Tas2rs from seven Carnivora species (Fig 4, Table 2; see also below) shows a nearly one-to-one orthologous relationship among Tas2rs. One exclusive plant-eating Carnivora species (Giant Panda, 16 intact Tas2rs) has 1–4 more intact bitter receptors than does meat-eating species (cat, 12; polar bear, 13; ferret, 14; dog 15).
Only the predicted intact Tas2r receptors are included. Sequences were either taken from Li and Zhang or obtained from reBLASTing genomes of these seven species. The tree was constructed by using the maximum-likelihood method based on the matrix-based model of  implemented in Mega 6 . The tree is drawn to scale, with branch lengths measured in the number of substitutions per site.
The goal of this study was to determine whether domestic cats, which are obligate carnivores, have multiple fully functional bitter receptors based on their activity in cell-based assays. The results confirmed that they do. Bitter receptor function in the cat exhibited similarities and some differences with that in humans. For instance, the human TAS2R38 receptor responds to a few thiourea compounds , including PTC and 6-propyl-2-thiouracil (PROP). The cat Tas2r38 only responds to PTC but not PROP, at the concentrations tested. A similar observation was reported recently . Likewise, human TAS2R46 is a broadly tuned receptor that responds to a wide range of structurally diverse bitter compounds (e.g., angrographolide, chloramphenicol, chloropheniramine, denatonium benzoate, Diphenidol, Picrotoxinin, yohimbine, etc) , and the cat receptor was also similarly broadly tuned and responded to an overlapping set of compounds (e.g., angrographolide, chloramphenicol, chloropheniramine, diphenidol, limonin, phenanthroline). Moreover, the Tas2r2 gene is intact in cats (and all species within Carnivora we surveyed), but it is a pseudogene in humans [27, 28].
The breadth of tuning properties of cat bitter receptors as described here are based on responses to a small set of both naturally occurring and synthetic compounds. Also, some compounds tested at higher concentration than we used may activate the receptor but were untested in this study due to non-specific responses and solubility issues. Additional work with a wider range of “bitter” compounds, especially those derived from animal products consumed by cats, will surely reveal more interesting properties of these receptors. Moreover, we note that the responses of the cat Tas2r2-transfected cells to bitter compounds appeared to have a higher baseline than that of mock-transfected cells. Although we don’t know the reason, potential constitutive activity of Tas2r2 may contribute to a higher baseline in Tas2r2-transfected cells.
To provide a comparative perspective on bitter taste receptors, we examined the number of intact bitter receptor genes in species of the order Carnivora (Tables 1 and 2). This order contains species that eat foods derived virtually exclusively from animals (obligate carnivores), eat foods derived predominantly from animals (carnivores), eat foods derived from animals and plants (omnivores), or only eat plant-based foods (herbivores). All species in this order apparently arose from a meat-eating common ancestor about 60 million years ago . If bitter receptor function is strongly influenced by whether a species consumes plants, we would expect that obligate carnivores should have fewer functional bitter receptors than do herbivores perhaps through pseudogenization as happened for the sweet receptor. We found that the numbers among terrestrial Carnivora were roughly the same regardless of the amount of meat in the species’ diets although the herbivorous giant panda did have 1–4 more intact bitter receptors than meat eating carnivores (Table 1). Thus these comparative data do not provide strong support for the hypothesis that an all-meat diet would result in reduced bitter receptor number or function , However, due to the small number of species examined, they also do not refute this hypothesis. More comparative data are needed to critically test it.
Consistent with our previous report of major taste loss in some aquatic mammals (; see also Tables 1 and 2) the two mainly water-dwelling Carnivora we examined, walrus and seal, both of which are obligate carnivores, did have a smaller number of bitter receptors (5 and 4 respectively) than the terrestrial Carnivora we examined. However, due to the small set of species available for our comparative analysis, we cannot conclude with confidence that mammals that have become sea living consistently or universally loose bitter receptor number and/or function. Nevertheless the consistency is striking. For example, in three separate lineages of mammals that have returned to aquatic life (Cetacea [dolphin, whale]; Tethytheria [manatee] and Pinnipedimorpha [walrus, seal]), all appear to have very low numbers of functional bitter receptors ( and Table 1). Future work with more species is warranted to further clarify the role of ecological niches (e.g., water-dwelling vs land-dwelling) in taste receptor evolution.
What factors could maintain bitter taste receptor function in terrestrial obligate carnivores? First, it could be that even obligate carnivores such as cats are actually exposed to plant material through consumption of prey viscera that contains plant material consumed by the prey. There are two arguments against this having an important role. First, plants eaten by prey may not be bitter and highly toxic since the prey species consumed them themselves. However, some species have evolved detoxification mechanisms enabling them to consume potentially toxic plants (e.g., the koala [Phascolarctos cinereus] feeding on the foliage of eucalyptus species, which are typically rather poisonous to most animal species) . Second, the frequency that carnivores actually consume plant material in prey viscera is unclear and it has been reported, at least for wolves, that this plant-material is avoided .
Another possible reason for maintenance of bitter receptor number and function in cats and perhaps other carnivores is that there are also bitter compounds in many non-plant prey items in the carnivore diets (but see reference ). For example, domestic cats are known to feed on animal products that are also potentially bitter and toxic such as bile acids, venom and skin secretions from arthropods, reptiles and amphibians . Thus our observations that bitter receptors in cats and most likely other land-dwelling Carnivora are functional could be due to selection to insure that consumption of these toxic substances is minimized.
A third reason why the number of bitter taste receptors may not be strongly influenced by the amount of dietary plant material relates to the possible non-oral functions of these receptors. Bitter receptors are found in cell types other than taste on the tongue. Neither the natural ligands nor the functions of these receptors are fully known, but we suggest they may be important in maintaining bitter receptor functionality in species that might not otherwise “need” them to avoid plant-based or animal-based toxins. For instance, respiratory-expressed bitter receptors are important for innate defense against bacterial infections [33–35].
Domestic cats have a reputation as picky eaters. Perhaps their apparently intact bitter system provides some explanation for their dietary habits. While the cell-based assays used here may not exactly recapitulate the native taste system, it allows investigators to gauge the response of the cat to bitter chemicals, including items that are poisonous, without risk to the animal. Commercial cat foods and veterinary medicines may contain bitter compounds that at least some cats find off-putting, and one way to predict their response in advance is through use of these cell-based systems.
Materials and Methods
Feline Tas2r receptor constructs
The coding sequences of feline Tas2r receptors were amplified from feline genome DNA using gene-specific primers (S1 Table). The coding sequences were inserted into an expression cassette with the first 45 amino acid residues of rat somatostatin receptor 3 as the signal peptide at the N-terminal and the herpes simplex virus glycoprotein D epitope at the C-terminal, following previously established methods . All constructs were verified by direct sequencing.
With the exception of acetylthiourea (Acros Organics), diphenidol hydrochloride (Reagent World), and limonin (LKT Laboratories), all chemicals were purchased from Sigma-Aldrich. For the catalog numbers and concentrations used in the assays, see S2 Table. Concentrations were chosen according to Meyerhof et al  to ensure that there were no or little unspecific responses distinguishable from that of Tas2r-transfected cells. As stated in Meyerhof et al., higher concentrations of bitter compounds could not be used because bitter compounds generated artificial calcium responses in the absence of transfected Tas2rs at high concentrations.
Functional assays of feline bitter taste receptors
Human embryonic kidney 293 (Peakrapid) cells were obtained from ATCC and cultured in Opti-MEM supplemented with 5% fetal bovine serum. Cells were seeded in 96-well plate at a density of 50,000 per well. The next day, cells were transiently transfected with a Tas2r construct (0.1 μg/well) with a coupling chimeric G protein Gα16-gust44 (0.1 μg/well) using Lipofectamine 2000 (0.5 μl/well). After 24 h, cells were washed once with Hanks’ balanced salt solution (HBSS) and loaded with Fluo–4 for 1 h. After three washes with HBSS, cells were assayed for their responses to bitter compounds using a FlexStation III. Relative fluorescence units (excitation at 488 nm, emission at 525 nm, and cutoff at 515 nm) were read every 2 s after addition of HBSS supplemented with 2× tastants. Calcium mobilization traces were recorded.
Calcium mobilization was quantified as described previously . In short, changes in fluorescence (ΔF) were quantified as peak fluorescence minus the baseline level (F) and are expressed as percent ΔF relative to F, averaged from triplicate studies. Calcium mobilization traces were drawn using Excel, and bar graphs were generated using GraphPad Prism 5. Two-tailed Student’s t-tests were performed for statistical analysis.
Genetic analysis of bitter taste receptor genes from selected species in Carnivora
The protein sequences of dog and ferret Tas2rs obtained from Li and Zhang  were used to query the domestic cat, seal, and walrus genomes. The retrieved sequences were analyzed for open reading frame mutations. For the intact genes, the predicted protein sequences were further examined for the presence of the seven-transmembrane helices using TMHMM methods (www.cbs.dtu.dk/services/TMHMM) . The deduced amino acid sequences from cat, seal, walrus, dog, ferret, giant panda and polar bear(S1 Dataset) were aligned using Clustal X implemented in Mega 6 . A phylogenetic tree among these receptors was then inferred using maximum likelihood implemented in Mega 6 . All DNA sequences were provided in S2 Dataset.
S1 Dataset. The predicted amino acid sequences of intact polar bear, feline, dog, ferret, giant panda, walrus, and seal Tas2r genes.
S2 Dataset. DNA sequences of Tas2rs from the polar bear, cat, dog, ferret, giant panda, walrus, and Weddell seal were presented in FASTA format.
S1 Table. Primer sequences used to amplify cat Tas2rs for cloning.
S2 Table. Responses of cat bitter taste receptors to 25 bitter compounds
Conceived and designed the experiments: WL RFM DRR GKB PJ. Performed the experiments: WL AR. Analyzed the data: WL AR XL RFM DRR GKB PJ. Wrote the paper: DRR GKB PJ.
- 1. Bachmanov AA, Beauchamp GK. Taste receptor genes. Annu Rev Nutr. 2007;27:389–414. Epub 2007/04/21. doi: 10.1146/annurev.nutr.26.061505.111329 pmid:17444812; PubMed Central PMCID: PMC2721271.
- 2. Liman ER, Zhang YV, Montell C. Peripheral coding of taste. Neuron. 2014;81(5):984–1000. Epub 2014/03/13. doi: 10.1016/j.neuron.2014.02.022 S0896-6273(14)00153-6 [pii]. pmid:24607224; PubMed Central PMCID: PMC3994536.
- 3. Jiang P, Josue J, Li X, Glaser D, Li W, Brand JG, et al. Major taste loss in carnivorous mammals. Proc Natl Acad Sci U S A. 2012;109(13):4956–61. Epub 2012/03/14. doi: 10.1073/pnas.1118360109 [pii]. pmid:22411809; PubMed Central PMCID: PMC3324019.
- 4. Baldwin MW, Toda Y, Nakagita T, O'Connell MJ, Klasing KC, Misaka T, et al. Sensory biology. Evolution of sweet taste perception in hummingbirds by transformation of the ancestral umami receptor. Science. 2014;345(6199):929–33. Epub 2014/08/26. doi: 10.1126/science.1255097 345/6199/929 [pii]. pmid:25146290; PubMed Central PMCID: PMC4302410.
- 5. Glendinning JI. Is the bitter rejection response always adaptive? Physiol Behav. 1994;56(6):1217–27. Epub 1994/12/01. pmid:7878094. doi: 10.1016/0031-9384(94)90369-7
- 6. Li D, Zhang J. Diet shapes the evolution of the vertebrate bitter taste receptor gene repertoire. Mol Biol Evol. 2014;31(2):303–9. Epub 2013/11/10. doi: 10.1093/molbev/mst219 [pii]. pmid:24202612; PubMed Central PMCID: PMC3907052.
- 7. Behrens M, Korsching SI, Meyerhof W. Tuning Properties of Avian and Frog Bitter Taste Receptors Dynamically Fit Gene Repertoire sizes. Mol Biol Evol. 2014;31(12):3216–27. Epub 2014/09/03. doi: 10.1093/molbev/msu254 msu254 [pii]. pmid:25180257.
- 8. Li X, Li W, Wang H, Cao J, Maehashi K, Huang L, et al. Pseudogenization of a sweet-receptor gene accounts for cats' indifference toward sugar. PLoS Genet. 2005;1(1):27–35. Epub 2005/08/17. doi: 10.1371/journal.pgen.0010003 pmid:16103917; PubMed Central PMCID: PMC1183522.
- 9. Sandau MM, Goodman JR, Thomas A, Rucker JB, Rawson NE. A functional comparison of the domestic cat bitter receptors Tas2r38 and Tas2r43 with their human orthologs. BMC Neurosci. 2015;16:33. Epub 2015/06/04. doi: 10.1186/s12868-015-0170-610.1186/s12868-015-0170-6 [pii]. pmid:26037485; PubMed Central PMCID: PMC4453034.
- 10. Meyerhof W, Batram C, Kuhn C, Brockhoff A, Chudoba E, Bufe B, et al. The molecular receptive ranges of human TAS2R bitter taste receptors. Chem Senses. 2010;35(2):157–70. Epub 2009/12/22. doi: 10.1093/chemse/bjp092 [pii]. pmid:20022913.
- 11. Bradshaw JW, Goodwin D, Legrand-Defretin V, Nott HM. Food selection by the domestic cat, an obligate carnivore. Comp Biochem Physiol A Physiol. 1996;114(3):205–9. Epub 1996/07/01. pmid:8759144. doi: 10.1016/0300-9629(95)02133-7
- 12. Legrand-Defretin V. Differences between cats and dogs: a nutritional view. Proc Nutr Soc. 1994;53(1):15–24. Epub 1994/03/01. doi: S0029665194000066 [pii]. pmid:8029223. doi: 10.1079/pns19940004
- 13. Johnson-Delaney CA. Ferret nutrition. Vet Clin North Am Exot Anim Pract. 2014;17(3):449–70. Epub 2014/08/27. doi: 10.1016/j.cvex.2014.05.008 S1094-9194(14)00039-5 [pii]. pmid:25155665.
- 14. Schaller GB, Hu J, Pan W, Zhu J. The Giant Pandas of Wolong: University of Chicago Press; 1985.
- 15. Thiemann GW, Iverson SJ, Stirling I. Polar bear diets and arctic marine food webs: Insights from fatty acid analysis Ecological Monographs. 2008;78(4):591–613. doi: 10.1890/07-1050.1.
- 16. Fay FH. Ecology and Biology of the Pacific Walrus, Odobenus rosmarus divergens Illiger. North American Fauna. 1982:1–279. doi: 10.3996/nafa.74.0001.
- 17. Riedman M. The Pinnipeds: Seals, Sea Lions, and Walruses: University of California Press; 1991.
- 18. Santos MB, Fernández R, López A, Martínez JA, Pierce GJ. Variability in the diet of bottlenose dolphin, Tursiops truncatus, in Galician waters, north-western Spain, 1990–2005. Journal of the Marine Biological Association of the United Kingdom. 2007;87(01):231–41. doi: 10.1017/S0025315407055233.
- 19. Lydersen C, Weslawski JM, øritsland NA. Stomach content analysis of minke whales Balaenoptera acutorostrata from the Lofoten and Vesterålen areas, Norway. Ecography. 1991;14(3):219–22. doi: 10.1111/j.1600-0587.1991.tb00655.x.
- 20. Burn DM. The digestive strategy and efficiency of the West Indian manatee, Trichechus manatus. Comp Biochem Physiol A Comp Physiol. 1986;85(1):139–42. Epub 1986/01/01. pmid:2876808. doi: 10.1016/0300-9629(86)90475-5
- 21. Feng P, Zheng J, Rossiter SJ, Wang D, Zhao H. Massive losses of taste receptor genes in toothed and baleen whales. Genome Biol Evol. 2014;6(6):1254–65. Epub 2014/05/08. doi: 10.1093/gbe/evu095 evu095 [pii]. pmid:24803572; PubMed Central PMCID: PMC4079202.
- 22. Zhu K, Zhou X, Xu S, Sun D, Zhou K, Yang G. The loss of taste genes in cetaceans. BMC Evol Biol. 2014;14(1):218. Epub 2014/10/13. doi: s12862-014-0218-8 [pii] doi: 10.1186/s12862-014-0218-8 pmid:25305673; PubMed Central PMCID: PMC4232718.
- 23. Krogh A, Larsson B, von Heijne G, Sonnhammer EL. Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol. 2001;305(3):567–80. Epub 2001/01/12. doi: 10.1006/jmbi.2000.4315 S0022-2836(00)94315-8 [pii]. pmid:11152613.
- 24. Jones DT, Taylor WR, Thornton JM. The rapid generation of mutation data matrices from protein sequences. Comput Appl Biosci. 1992;8(3):275–82. Epub 1992/06/01. pmid:1633570. doi: 10.1093/bioinformatics/8.3.275
- 25. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol. 2013;30(12):2725–9. Epub 2013/10/18. doi: 10.1093/molbev/mst197 mst197 [pii]. pmid:24132122; PubMed Central PMCID: PMC3840312.
- 26. Bufe B, Breslin PA, Kuhn C, Reed DR, Tharp CD, Slack JP, et al. The molecular basis of individual differences in phenylthiocarbamide and propylthiouracil bitterness perception. Curr Biol. 2005;15(4):322–7. Epub 2005/02/23. doi: S0960982205001090 [pii] doi: 10.1016/j.cub.2005.01.047 pmid:15723792; PubMed Central PMCID: PMC1400547.
- 27. Conte C, Ebeling M, Marcuz A, Nef P, Andres-Barquin PJ. Identification and characterization of human taste receptor genes belonging to the TAS2R family. Cytogenet Genome Res. 2002;98(1):45–53. Epub 2003/02/14. doi: 68546 [pii]. pmid:12584440. doi: 10.1159/000068546
- 28. Go Y, Satta Y, Takenaka O, Takahata N. Lineage-specific loss of function of bitter taste receptor genes in humans and nonhuman primates. Genetics. 2005;170(1):313–26. Epub 2005/03/04. doi: genetics.104.037523 [pii] doi: 10.1534/genetics.104.037523 pmid:15744053; PubMed Central PMCID: PMC1449719.
- 29. Eizirik E, Murphy WJ, Koepfli KP, Johnson WE, Dragoo JW, Wayne RK, et al. Pattern and timing of diversification of the mammalian order Carnivora inferred from multiple nuclear gene sequences. Mol Phylogenet Evol. 2010;56(1):49–63. Epub 2010/02/09. doi: 10.1016/j.ympev.2010.01.033 S1055-7903(10)00044-8 [pii]. pmid:20138220.
- 30. Stupans I, Jones B, McKinnon RA. Xenobiotic metabolism in Australian marsupials. Comp Biochem Physiol C Toxicol Pharmacol. 2001;128(3):367–76. Epub 2001/03/20. doi: S1532-0456(00)00211-8 [pii]. pmid:11255110. doi: 10.1016/s1532-0456(00)00211-8
- 31. Mech LD, Boitani L. Wolves: behavior, ecology, and conservation. Chicago: University of Chicago Press; 2003. xvii, 448 p. p.
- 32. Doherty TS, Davis RA, van Etten EJB, Algar D, Collier N, Dickman CR, et al. A continental-scale analysis of feral cat diet in Australia. Journal of Biogeography. 2015;42(5):964–75. doi: 10.1111/jbi.12469.
- 33. Lee RJ, Xiong G, Kofonow JM, Chen B, Lysenko A, Jiang P, et al. T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection. J Clin Invest. 2012;122(11):4145–59. Epub 2012/10/09. doi: 10.1172/JCI64240 [pii]. pmid:23041624; PubMed Central PMCID: PMC3484455.
- 34. Shah AS, Ben-Shahar Y, Moninger TO, Kline JN, Welsh MJ. Motile cilia of human airway epithelia are chemosensory. Science. 2009;325(5944):1131–4. Epub 2009/07/25. doi: 10.1126/science.1173869 [pii]. pmid:19628819; PubMed Central PMCID: PMC2894709.
- 35. Tizzano M, Gulbransen BD, Vandenbeuch A, Clapp TR, Herman JP, Sibhatu HM, et al. Nasal chemosensory cells use bitter taste signaling to detect irritants and bacterial signals. Proc Natl Acad Sci U S A. 2010;107(7):3210–5. Epub 2010/02/06. doi: 10.1073/pnas.0911934107 [pii]. pmid:20133764; PubMed Central PMCID: PMC2840287.
- 36. Bufe B, Hofmann T, Krautwurst D, Raguse JD, Meyerhof W. The human TAS2R16 receptor mediates bitter taste in response to beta-glucopyranosides. Nat Genet. 2002;32(3):397–401. Epub 2002/10/16. doi: 10.1038/ng1014 [pii]. pmid:12379855.
- 37. Jiang P, Cui M, Zhao B, Liu Z, Snyder LA, Benard LM, et al. Lactisole interacts with the transmembrane domains of human T1R3 to inhibit sweet taste. J Biol Chem. 2005;280(15):15238–46. Epub 2005/01/26. doi: M414287200 [pii] doi: 10.1074/jbc.M414287200 pmid:15668251.