Metabolomic evidence of independent biotransformation pathways for terpenes in two specialist mammalian herbivores (genus Neotoma)

Katharina SCHRAMM, Michele SKOPEC, Denise DEARING

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Integrative Zoology ›› 2024, Vol. 19 ›› Issue (1) : 143-155. DOI: 10.1111/1749-4877.12734
ORIGINAL ARTICLE

Metabolomic evidence of independent biotransformation pathways for terpenes in two specialist mammalian herbivores (genus Neotoma)

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Abstract

Herbivory is common in mammals, yet our understanding of detoxification processes used by mammals to biotransform plant secondary compounds (PSCs) is limited. Specialist herbivores are thought to have evolved detoxification mechanisms that rely more heavily on energetically cheap Phase I biotransformation reactions to process high levels of PSCs in their diets. We explored this hypothesis by comparing the urinary metabolite patterns of two specialist herbivores (genus Neotoma). Neotoma stephensi is an obligate specialist on one-seeded juniper (Juniperus monosperma). Neotoma lepida is a generalist forager across its range, yet populations in the Great Basin specialize on Utah juniper (J. osteosperma). While both juniper species have high levels of terpenes, the terpene profiles and quantities differ between the two. Individuals from both woodrat species were fed diets of each juniper in a cross-over design. Urine, collected over a 24-h period, was extracted and analyzed in an untargeted metabolomics approach using both GC-MS and HPLC-MS/MS. The obligate specialist N. stephensi excreted a unique pattern of Phase I metabolites when fed its native juniper, while N. lepida excreted a unique pattern of Phase II metabolites when fed its native juniper. Both woodrat species utilized the Phase II metabolic pathway of glucuronidation more heavily when consuming the more chemically diverse J. osteosperma, and N. stephensi utilized less glucuronidation than N. lepida when consuming J. monosperma. These results are consistent with the hypothesis that obligate specialists may have evolved unique and efficient biotransformation mechanisms for dealing with PSCs in their diet.

Keywords

dietary specialization / herbivory / juniper / metabolomics / Neotoma

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Katharina SCHRAMM, Michele SKOPEC, Denise DEARING. Metabolomic evidence of independent biotransformation pathways for terpenes in two specialist mammalian herbivores (genus Neotoma). Integrative Zoology, 2024, 19(1): 143‒155 https://doi.org/10.1111/1749-4877.12734

References

[1]
AdamsRP (1994). Geographic variation in the volatile terpenoids of Juniperus monosperma and J. osteosperma. Biochemical Systematics and Ecology 22, 65–71.
[2]
AdamsRP (2014). Junipers of the World: The Genus Juniperus, 4th edn. Trafford Publishing, Bloomington, IN.
[3]
AdamsRP, SkopecMM, KohlKD,Dearing MD (2014). Comparison of volatile leaf terpenoids from Juniperus monosperma and J. osteosperma leaves: Intact, ground and exposed to ambient temperature. Phytologia 96, 207–17.
[4]
AyalaA,CutlerRG (1997). Preferential use of less toxic detoxification pathways by long-lived species. Archives of Gerontology and Geriatrics 24, 87–102.
[5]
BoyleR, McLeanS, FoleyWJ, Davies NW (1999). Comparative metabolism of dietary terpene, p-cymene, in generalist and specialist folivorous marsupials. Journal of Chemical Ecology 25, 2109–26.
[6]
BoyleR, McLeanS, FoleyWJ, Davies NW, PeacockEJ, MooreB (2001). Metabolites of dietary 1, 8-cineole in the male koala (Phascolarctos cinereus). Comparative Biochemistry and Physiology C 129, 385–95.
[7]
BrownJH, Lieberman GA, DenglerWF (1972). Woodrats and cholla : dependence of a small mammal population on the density of cacti. Ecology 53, 310–3.
[8]
CameronGN, RaineyDG (1972). Habitat utilization by Neotoma lepida in the Mohave Desert. Journal of Mammalogy 53, 251–66.
[9]
ChengXY, TianXL, WangYS et al. (2013). Metagenomic analysis of the pinewood nematode microbiome reveals a symbiotic relationship critical for xenobiotics degradation. Scientific Reports 3, 1869.
[10]
DearingMD, McLister JD, SorensenJS (2005). Woodrat (Neotoma) herbivores maintain nitrogen balance on a low-nitrogen, high-phenolic forage, Juniperus monosperma. Journal of Comparative Physiology B 175, 349–55.
[11]
DialKP (1988). Three sympatric species of Neotoma: Dietary specialization and coexistence. Oecologia 76, 531–7.
[12]
FoleyW, McArthur C (1994). The effects and costs of allelochemicals for mammalian herbivores: an ecological perspective. In: ChiversDJ, LangerP, eds. The Digestive System in Mammals: Food, Form and Function. Cambridge University Press, Cambridge, pp. 370–91.
[13]
FreelandWJ (1991). Plant secondary metabolites: biochemical coevolution with herbivores. In: PaloRT, Robbins CT, eds. Plant Defenses against Mammalian Herbivory. CRC Press, Boca Raton, FL, pp. 61–81.
[14]
FreelandWJ, JanzenDH (1974). Strategies in herbivory by mammals: The role of plant secondary compounds. American Naturalist 108, 269–89.
[15]
HaleySL, LambJG, FranklinMR, Constance JE, DearingMD (2007). Xenobiotic metabolism of plant secondary compounds in juniper (Juniperus monosperma) by specialist and generalist woodrat herbivores, genus Neotoma. Comparative Biochemisty and Physiology C 146, 552–60.
[16]
IlliusAW, JessopNS (1995). Modeling metabolic costs of allelochemical ingestion by foraging herbivores. Journal of Chemical Ecology 21, 693–719.
[17]
IshidaT, Asakawa Y, TakemotoT, ArataniT (1981). Terpenoids biotransformation in mammals III: Biotransformation of alpha-pinene, beta-pinene, pinane, 3-carene, carane, myrcene, and p-cymene in rabbits. Journal of Pharmaceutical Sciences 4, 406–15.
[18]
KesslerA, KalskeA (2018). Plant secondary metabolite diversity and species interactions. Annual Review of Ecology, Evolution, and Systematics 49, 115–38.
[19]
KitonovicS, OrrTJ, SpalinkD et al. (2018). Role of cytochrome P450 2B sequence variation and gene copy number in facilitating dietary specialization in mammalian herbivores. Molecular Ecology 27, 723–36.
[20]
KlaassenCD (2019). Casarett and Doull's Toxicology: The Basic Science of Poisons, 9th edn. McGraw-Hill, New York.
[21]
KohlKD, WeissRB, CoxJ, DaleC, DearingMD (2014). Gut microbes of mammalian herbivores facilitate intake of plant toxins. Ecology Letters 17, 1238–46.
[22]
KoppelC, Tenczer J, TonnesmannU, SchiropT, IbeK (1981). Acute poisoning with pine oil - metabolism of monoterpenes. Archives of Toxicology 49, 73–8.
[23]
MacMillenRE (1964). Population ecology, water relations, and social behavior of a southern California desert rodent fauna. University of California Publications in Zoology 71, 1–66.
[24]
MangioneAM, Dearing MD, KarasovW (2001). Detoxification in relation to toxin tolerance in desert woodrats eating creosote bush. Journal of Chemical Ecology 27, 2559–79.
[25]
MarshKJ, WallisIR, AndrewRL, Foley WJ (2006). The detoxification limitation hypothesis: Where did it come from and where is it going? Journal of Chemical Ecology 32, 1247–66.
[26]
McLeanS, FoleyW, DavisN (1993). Metabolic fate of dietary terpenes from Eucalyptus radiata in common ringtail possum (Pseudocheirus peregrinus). Journal of Chemical Ecology 19, 1625–43.
[27]
McLeanS, FoleyWJ (1997). Metabolism of Eucalyptus terpenes by herbivorous marsupials. Drug Metabolism Reviews 29, 213–8.
[28]
McLeanS, PassG, FoleyW, Brandon S, DaviesN (2001). Does excretion of secondary metabolites always involve a measurable metabolic cost? Fate of plant antifeedant salicin in common brushtail possum, Trichosurus vulpecula. Journal of Chemical Ecology 27, 1077–89.
[29]
MorseMA, StonerGD (1993). Cancer chemoprevention: Principles and prospects. Carcinogenesis 14, 1737–46.
[30]
NishiyamaT, OguraK, NakanoH et al. (2002). Reverse geometrical selectivity in glucuronidation and sulfation of cis- and trans-4-hydroxytamoxifens by human liver UDP-glucuronosyltransferases and sulfotransferases. Biochemical Pharmacology 63, 1817–30.
[31]
PattonJL, Huckaby DG, Alvarez-CastanedaST (2014). The Evolutionary History and a Systematic Revision of Woodrats of the Neotoma lepida Group. UC Publications in Zoology, Oakland, CA.
[32]
SchmidtL, GoenT (2017). Human metabolism of a-pinene and metabolite kinetics after oral administration. Archives of Toxicology 91, 677–87.
[33]
ShipleyLA, ForbeyJS, MooreBD (2009). Revisiting the dietary niche: When is a mammalian herbivore a specialist. Integrative and Comparative Biology 49, 274–90.
[34]
SkopecMM, AdamsRP, MuirJP (2019). Terpenes may serve as feeding deterrents and foraging cues for mammalian herbivores. Journal of Chemical Ecology 45, 993–1003.
[35]
SkopecMM, Dearing MD (2011). Differential expression and activity of catechol-O-methyl tranferase (COMT) in a generalist (Neotoma albigula) and juniper specialist (Neotoma stephensi) woodrat. Comparative Biochemistry and Physiology C 154, 383–90.
[36]
SkopecMM, HaleyS, DearingMD (2007). Differential hepatic gene expression of a dietary specialist (Neotoma stephensi) and generalist (Neotoma albigula) in response to juniper (Juniperus monosperma) ingestion. Comparative Biochemistry and Physiology D 2, 34–43.
[37]
SkopecMM, KohlKD, SchrammK, Halpert JR, DearingMD (2015). Using the specialization framework to determine degree of dietary specialization in a herbivorous woodrat. Journal of Chemical Ecology 41, 1059–68.
[38]
SmithFA, MurrayIW, HardingLE, Lease HM, MartinJ (2014). Life in an extreme environment: a historical perspective on the influence of temperature on the ecology and evolution of woodrats. Journal of Mammalogy 95, 1128–43.
[39]
SorensenJS, McLister JD, DearingMD (2005). Novel plant secondary metabolites impact dietary specialists more than generalists (Neotoma spp.). Ecology 86, 140–54.
[40]
SorensenJS, Turnbull CA, DearingMD (2004). A specialist herbivore (Neotoma stephensi) absorbs fewer plant toxins that does a generalist (Neotoma albigula). Physiological Biochemistry and Zoology 77, 139–48.
[41]
StoneAN, Mackenzie PI, GaletinA, HoustonJB, MinersJO (2003). Isoform selectivity and kinetics of morphine 3- and 6-glucuronidation by human UDP-glucuronosyltransferases: Evidence for atypical glucuronidation kinetics by UGT2B7. Drug Metabolism and Disposition 31, 1086–9.
[42]
StonesRC, Hayward CL (1968). Natural history of the desert woodrat, Neotoma lepida. American Midland Naturalist 80, 458–76.
[43]
TorregrossaA-M, AzzaraAV, DearingMD (2012). Testing the diet-breadth trade-off hypothesis: Differential regulation of a novel plant secondary compounds by a specialist and a generalist herbivore. Oecologia 168, 711–8.
[44]
VaughanTA (1982). Stephens' woodrat, a dietary specialist. Journal of Mammalogy 63, 53–62.
[45]
VertsBJ, Carraway LN (2002). Neotoma lepida. Mammalian Species 699, 1–12.
[46]
WhiteRA, Franklin RT, AgosinM (1979). Conversion of α-pinene to α-pinene oxide by rat liver and the bark beetle Dendroctonus terebrans microsomal fractions. Pesticide Biochemistry and Physiology 10, 233–42.
[47]
WuB, BasuS, MengS, Wang X, HuM (2011). Regioselective sulfation and glucuronidation of phenolics: Insights into the structural basis of conjugation. Current Drug Metabolism 12, 900–16.
[48]
XiaJ, MandalR, SinelnikovIV, BroadhurstD, Wishart DS (2012). MetaboAnalyst 2.0—A comprehensive server for metabolomic data analysis. Nucleic Acids Research 40, W127–33.
[49]
XiaJ, Sinelnikov IV, HanB, WishartDS (2015). Metabo-Analyst 3.0—Making metabolomics more meaningful. Nucleic Acids Research 43, W251–7.

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2023 2023 The Authors. Integrative Zoology published by International Society of Zoological Sciences, Institute of Zoology/Chinese Academy of Sciences and John Wiley & Sons Australia, Ltd.
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