M. E. Afkhami and J. A. Rudgers, Symbiosis lost: imperfect vertical transmission of fungal endophytes in grasses, Am. Nat, vol.172, pp.405-416, 2008.

E. Arias-cordero, L. Ping, K. Reichwald, H. Delb, M. Platzer et al., Comparative evaluation of the gut microbiota associated with the below-and above-ground life stages (larvae and beetles) of the forest cockchafer, Melolontha hippocastani, PLoS One, vol.7, p.51557, 2012.

S. Bahrndorff, T. Alemu, T. Alemneh, and J. L. Nielsen, The microbiome of animals: implications for conservation biology, Int. J. Genomics, p.5304028, 2016.

T. Becker, G. Loch, M. Beyer, I. Zinke, A. C. Aschenbrenner et al., FOXOdependent regulation of innate immune homeostasis, Nature, vol.463, pp.369-373, 2010.

C. L. Bevins and N. H. Salzman, The potter's wheel: the host's role in sculpting its microbiota, Cell. Mol. Life Sci, vol.68, pp.3675-3685, 2011.

C. Bozzuto and S. Canessa, Impact of seasonal cycles on hostpathogen dynamics and disease mitigation for Batrachochytrium salamandrivorans, Glob. Ecol. Conserv, vol.17, p.551, 2019.

R. L. Brandenburg and G. G. Kennedy, Overwintering of the pathogen Entomophthora floridana and its host, the twospotted spider mite, J. Econ. Entomol, vol.74, pp.428-431, 1981.

J. Breton, N. Tennoune, N. Lucas, M. Francois, R. Legrand et al., Gut commensal E. coli proteins activate host satiety pathways following nutrient-induced bacterial growth, Cell Metab, vol.23, pp.324-334, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01397996

N. A. Broderick, A common origin for immunity and digestion, Front. Immunol, vol.6, p.72, 2015.

M. Brumin, S. Kontsedalov, and M. Ghanim, Rickettsia influences thermotolerance in the whitefly Bemisia tabaci B biotype: Rickettsia influence on thermotolerance, Insect Sci, vol.18, pp.57-66, 2011.

T. D. Bruns, M. I. Bidartondo, and D. L. Taylor, Host specificity in ectomycorrhizal communities: What do the exceptions tell us?, Integr. Comp. Biol, vol.42, pp.352-359, 2002.

H. V. Carey and K. N. Duddleston, Animal-microbial symbioses in changing environments, J. Therm. Biol, vol.44, pp.78-84, 2014.

H. V. Carey, W. A. Walters, and R. Knight, Seasonal restructuring of the ground squirrel gut microbiota over the annual hibernation cycle, Am. J. Physiol. Regul. Integr. Comp. Physiol, vol.304, pp.33-42, 2013.

J. Chuche and D. Thiéry, Cold winter temperatures condition the egg-hatching dynamics of a grape disease vector, Naturwissenschaften, vol.96, pp.827-834, 2009.
URL : https://hal.archives-ouvertes.fr/hal-02667027

C. M. Cirimotich, J. L. Ramirez, and G. Dimopoulos, Native microbiota shape insect vector competence for human pathogens, Cell Host Microbe, vol.10, pp.307-310, 2011.

C. Corbin, E. R. Heyworth, J. Ferrari, and G. D. Hurst, Heritable symbionts in a world of varying temperature, Heredity, vol.118, pp.10-20, 2017.

E. K. Costello, K. Stagaman, L. Dethlefsen, B. J. Bohannan, and D. A. Relman, The application of ecological theory toward an understanding of the human microbiome, Science, vol.336, pp.1255-1262, 2012.

H. V. Danks, Insect Dormancy: An Ecological Perspective. Biological Survey of Canada, 1987.

M. S. Datta, A. A. Almada, M. F. Baumgartner, T. J. Mincer, A. M. Tarrant et al., Inter-individual variability in copepod microbiomes reveals bacterial networks linked to host physiology, ISME J, vol.12, p.2103, 2018.

B. J. Davis, R. D. Phillips, M. Wright, C. C. Linde, and K. W. Dixon, Continent-wide distribution in mycorrhizal fungi: implications for the biogeography of specialized orchids, Ann. Bot, vol.116, pp.413-421, 2015.

D. L. Denlinger, Why study diapause?, Entomol. Res, vol.38, pp.1-9, 2008.

L. Dethlefsen, M. Mcfall-ngai, and D. A. Relman, An ecological and evolutionary perspective on human-microbe mutualism and disease, Nature, vol.449, pp.811-818, 2007.

K. A. Dill-mcfarland, K. L. Neil, A. Zeng, R. J. Sprenger, C. C. Kurtz et al., Hibernation alters the diversity and composition of mucosa-associated bacteria while enhancing antimicrobial defence in the gut of 13-lined ground squirrels, Mol. Ecol, vol.23, pp.4658-4669, 2014.

M. S. Dionne, L. N. Pham, M. Shirasu-hiza, and D. S. Schneider, Akt and FOXO dysregulation contribute to infection-induced wasting in Drosophila, Curr. Biol, vol.16, pp.1977-1985, 2006.

P. Dirksen, S. A. Marsh, I. Braker, N. Heitland, S. Wagner et al., The native microbiome of the nematode Caenorhabditis elegans: gateway to a new host-microbiome model, BMC Biol, vol.14, p.38, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02332386

A. J. Dobson, J. M. Chaston, P. D. Newell, L. Donahue, S. L. Hermann et al., Host genetic determinants of microbiota-dependent nutrition revealed by genome-wide analysis of Drosophila melanogaster, Nat. Commun, vol.6, p.6312, 2015.

A. E. Douglas, Reproductive diapause and the bacterial symbiosis in the sycamore aphid Drepanosiphum platanoidis, Ecol. Entomol, vol.25, pp.256-261, 2000.

A. E. Douglas, Multiorganismal insects: diversity and function of resident microorganisms, Annu. Rev. Entomol, vol.60, pp.1-18, 2014.

A. E. Douglas, Symbiosis as a general principle in eukaryotic evolution. Cold Spring Harbor Perspect, Biol, vol.6, p.16113, 2014.

H. E. Dunbar, A. C. Wilson, N. R. Ferguson, and N. A. Moran, Aphid thermal tolerance is governed by a point mutation in bacterial symbionts, PLoS Biol, vol.5, p.96, 2007.

D. Ebert, The epidemiology and evolution of symbionts with mixed-mode transmission, Annu. Rev. Ecol. Evol. Syst, vol.44, pp.623-643, 2013.

L. V. Ferguson, P. Dhakal, J. E. Lebenzon, D. E. Heinrichs, C. Bucking et al., Seasonal shifts in the insect gut microbiome are concurrent with changes in cold tolerance and immunity, Funct. Ecol, vol.32, pp.2357-2368, 2018.

M. A. Fischbach and J. A. Segre, Signaling in host-associated microbial communities, Cell, vol.164, pp.1288-1300, 2016.

T. Flatt, M. Tu, and M. Tatar, Hormonal pleiotropy and the juvenile hormone regulation of Drosophila development and life history, BioEssays, vol.27, pp.999-1010, 2005.

L. J. Funkhouser and S. R. Bordenstein, Mom knows best: the universality of maternal microbial transmission, PLoS Biol, vol.11, p.1001631, 2013.

A. I. Furness, D. N. Reznick, M. S. Springer, and R. W. Meredith, Convergent evolution of alternative developmental trajectories associated with diapause in African and South American killifish, Proc. R. Soc. B Biol. Sci, vol.282, 2015.

J. A. Gilbert, J. A. Steele, J. G. Caporaso, L. Steinbrück, J. Reeder et al., Defining seasonal marine microbial community dynamics, ISME J, vol.6, pp.298-308, 2012.

S. F. Gilbert, T. C. Bosch, and C. Ledón-rettig, Eco-evodevo: developmental symbiosis and developmental plasticity as evolutionary agents, Nature, vol.16, pp.1-12, 2015.

D. A. Hahn and D. L. Denlinger, Energetics of insect diapause, Annu. Rev. Entomol, vol.56, pp.103-121, 2011.

N. G. Hairston, Zooplankton egg banks as biotic reservoirs in changing environments, Limnol. Oceanogr, vol.41, pp.1087-1092, 1996.

S. C. Hand, D. L. Denlinger, J. E. Podrabsky, and R. Roy, Mechanisms of animal diapause: recent developments from nematodes, 2016.

A. A. Mushegian-and-k and . Tougeron, This content downloaded from 130.104.214.125 on, 2019.

, Am. J. Physiol. Regul. Integr. Comp. Physiol, vol.310, pp.1193-1211

E. A. Heath-heckman, The metronome of symbiosis: interactions between microbes and the host circadian clock, Integr. Comp. Biol, vol.56, pp.776-783, 2016.

Y. Henry and H. Colinet, Microbiota disruption leads to reduced cold tolerance in Drosophila flies, Naturwissenschaften, vol.105, p.59, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01900715

M. Hodkova and I. Hodek, Photoperiod, diapause and coldhardiness, Eur. J. Entomol, vol.101, pp.445-458, 2004.

G. E. Hofmann and A. E. Todgham, Living in the now: physiological mechanisms to tolerate a rapidly changing environment, Annu. Rev. Physiol, vol.72, pp.127-145, 2010.

T. Ikeno, H. Numata, and S. G. Goto, Circadian clock genes period and cycle regulate photoperiodic diapause in the bean bug Riptortus pedestris males, J. Insect Physiol, vol.57, pp.935-938, 2011.

R. M. Jones, C. Desai, T. M. Darby, L. Luo, A. A. Wolfarth et al., Lactobacilli modulate epithelial cytoprotection through the Nrf2 pathway, Cell Rep, vol.12, pp.1217-1225, 2015.

M. Kaltenpoth, W. Göttler, G. Herzner, and E. Strohm, Symbiotic bacteria protect wasp larvae from fungal infestation, Curr. Biol, vol.15, pp.475-479, 2005.

T. Kashima, T. Nakamura, and S. Tojo, Uric acid recycling in the shield bug, Parastrachia japonensis (Hemiptera: Parastrachiidae), during diapause, J. Insect Physiol, vol.52, pp.816-825, 2006.

T. K. Kaul, P. R. Rodrigues, I. V. Ogungbe, P. Kapahi, and M. S. Gill, Bacterial fatty acids enhance recovery from the dauer larva in Caenorhabditis elegans, PLoS One, vol.9, p.86979, 2014.

A. Khanna, J. Kumar, M. A. Vargas, L. Barrett, S. Katewa et al., A genome-wide screen of bacterial mutants that enhance dauer formation in C, elegans. Sci. Rep, vol.6, p.38764, 2016.

Y. Kikuchi, T. Hosokawa, and T. Fukatsu, An ancient but promiscuous host-symbiont association between Burkholderia gut symbionts and their heteropteran hosts, ISME J, vol.5, pp.446-460, 2011.

Y. Kikuchi, M. Hayatsu, T. Hosokawa, A. Nagayama, K. Tago et al., Symbiont-mediated insecticide resistance, Proc. Natl. Acad. Sci. U.S.A, vol.109, pp.8618-8622, 2012.

R. J. Knell and K. M. Webberley, Sexually transmitted diseases of insects: distribution, evolution, ecology and host behaviour, Biol. Rev. Camb. Philos. Soc, vol.79, pp.557-581, 2004.

S. Koehler, J. Doubsk?, and M. Kaltenpoth, Dynamics of symbiont-mediated antibiotic production reveal efficient long-term protection for beewolf offspring, Front. Zool, vol.10, p.3, 2013.

A. D. Kostic, M. R. Howitt, and W. S. Garrett, Exploring hostmicrobiota interactions in animal models and humans, Genes Dev, vol.27, pp.701-718, 2013.

D. S. Koveos and M. E. Tzanakakis, Diapause aversion in the adult olive fruit fly through effects of the host fruit, bacteria, and adult diet, Ann. Entomol. Soc. Am, vol.86, pp.668-673, 1993.

P. Kriesner, W. R. Conner, A. R. Weeks, M. Turelli, and A. A. Hoffmann, Persistence of a Wolbachia infection frequency cline in Drosophila melanogaster and the possible role of reproductive dormancy, Evolution, vol.70, pp.979-997, 2016.

A. Kroon, R. L. Veenendaal, J. Bruin, M. Egas, and M. W. Sabelis, Sleeping with the enemy": predator-induced diapause in a mite, Naturwissenschaften, vol.95, pp.1195-1198, 2008.

O. I. Kubrak, L. Ku?erová, U. Theopold, and D. R. Nässel, The sleeping beauty: how reproductive diapause affects hormone signaling, metabolism, immune response and somatic maintenance in Drosophila melanogaster, PLoS One, vol.9, p.113051, 2014.

L. A. Lacey and R. L. Chauvin, Entomopathogenic nematodes for control of diapausing codling moth (Lepidoptera: Tortricidae) in fruit bins, J. Econ. Entomol, vol.92, pp.104-109, 1999.

J. Lee, C. Kim, H. A. Jang, J. K. Kim, T. Kotaki et al., Burkholderia gut symbiont modulates titer of specific juvenile hormone in the bean bug Riptortus pedestris, Dev. Comp. Immunol, vol.99, p.103399, 2019.

J. E. Lendrum, B. Seebach, B. Klein, and S. Liu, Sleep and the gut microbiome: Antibiotic-induced depletion of the gut microbiota reduces nocturnal sleep in mice, 2017.

J. T. Lennon and S. E. Jones, Microbial seed banks: the ecological and evolutionary implications of dormancy, Nat. Rev. Microbiol, vol.9, pp.119-130, 2011.

N. Lindquist, Chemical defense of early life stages of benthic marine invertebrates, J. Chem. Ecol, vol.28, 1987.

W. Liu, Y. Li, S. Guo, H. Yin, C. Lei et al., Association between gut microbiota and diapause preparation in the cabbage beetle: a new perspective for studying insect diapause, Sci. Rep, vol.6, p.38900, 2016.

J. Ludvigsen, A. Rangberg, E. Avershina, M. Sekelja, C. Kreibich et al., Shifts in the midgut/pyloric microbiota composition within a honey bee apiary throughout a season, Microbes Environ, vol.30, pp.235-244, 2015.

C. F. Maurice, S. C. Knowles, J. Ladau, K. S. Pollard, A. Fenton et al., Marked seasonal variation in the wild mouse gut microbiota, ISME J, vol.9, pp.2423-2434, 2015.

M. Mcfall-ngai, M. G. Hadfield, T. C. Bosch, H. V. Carey, T. Domazet-lo?o et al., Animals in a bacterial world, a new imperative for the life sciences, Proc. Natl. Acad. Sci. U.S.A, vol.110, pp.3229-3236, 2013.
URL : https://hal.archives-ouvertes.fr/hal-00972300

V. Medina, P. M. Sardoy, M. Soria, C. A. Vay, G. O. Gutkind et al., Characterized non-transient microbiota from stinkbug (Nezara viridula) midgut deactivates soybean chemical defenses, PLoS One, vol.13, p.200161, 2018.

N. A. Moran and H. E. Dunbar, Sexual acquisition of beneficial symbionts in aphids, Proc. Natl. Acad. Sci. U.S.A, vol.103, pp.12803-12806, 2006.

A. A. Mushegian, Sources of variation: animal microbiota, Sci. Signal, vol.10, p.9011, 2017.

A. A. Mushegian, J. Walser, K. E. Sullam, and D. Ebert, The microbiota of diapause: how host-microbe associations are formed after dormancy in an aquatic crustacean, J. Anim. Ecol, vol.87, pp.400-413, 2018.

A. Nakamura, K. Miyado, Y. Takezawa, N. Ohnami, M. Sato et al., Innate immune system still works at diapause, a physiological state of dormancy in insects, Biochem. Biophys. Res. Commun, vol.410, pp.351-357, 2011.

R. S. Nasci, H. M. Savage, D. J. White, J. R. Miller, B. C. Cropp et al., West Nile virus in overwintering Culex mosquitoes, Emerg. Infect. Dis, vol.7, p.3, 2000.

G. Neelakanta, H. Sultana, D. Fish, J. F. Anderson, and E. Fikrig, Anaplasma phagocytophilum induces Ixodes scapularis ticks to express an antifreeze glycoprotein gene that enhances their survival in the cold, J. Clin. Investig, vol.120, pp.3179-3190, 2010.

B. M. Nelms, E. Fechter-leggett, B. D. Carroll, P. Macedo, S. Kluh et al., Experimental and natural vertical transmission of West Nile virus by California Culex (Diptera: Culicidae) mosquitoes, J. Med. Entomol, vol.50, pp.371-378, 2013.

H. Neuman, J. W. Debelius, R. Knight, and O. Koren, Microbial endocrinology: the interplay between the microbiota and the endocrine system, FEMS Microbiol. Rev, vol.39, pp.509-521, 2015.

O. Nougué, R. Gallet, L. Chevin, and T. Lenormand, Niche limits of symbiotic gut microbiota constrain the salinity tolerance of brine shrimp, Am. Nat, vol.186, pp.390-403, 2015.

M. F. Palominos, L. Verdugo, C. Gabaldon, B. Pollak, J. Ortíz-severín et al., Transgenerational diapause as an avoidance strategy against bacterial pathogens in Caenorhabditis elegans, vol.8, pp.1234-1251, 2017.

A. Diapause,

V. E. Panov, P. I. Krylov, and N. Riccardi, Role of diapause in dispersal and invasion success by aquatic invertebrates, J. Limnol, vol.63, pp.56-69, 2004.

J. Peccoud, J. Bonhomme, F. Mahéo, M. Huerta, O. Cosson et al., Inheritance patterns of secondary symbionts during sexual reproduction of pea aphid biotypes, Insect Sci, vol.21, pp.291-300, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01208708

M. J. Perrot-minnot, L. R. Guo, and J. H. Werren, Single and double infections with Wolbachia in the parasitic wasp Nasonia vitripennis: effects on compatibility, Genetics, vol.143, pp.961-972, 1996.

A. Pringle, J. D. Bever, M. Gardes, J. L. Parrent, M. C. Rillig et al., Mycorrhizal symbioses and plant invasions, Annu. Rev. Ecol. Evol. Syst, vol.40, pp.699-715, 2009.

G. J. Ragland and E. Keep, Comparative transcriptomics support evolutionary convergence of diapause responses across Insecta, Physiol. Entomol, vol.42, pp.246-256, 2017.

S. Rahimi-kaldeh, A. Ashouri, and A. Bandani, Does Wolbachia infection change the overwintering ability of Trichogramma brassicae (Hymenoptera: Trichogrammatidae)?, Neotrop. Entomol, vol.47, pp.583-590, 2017.

S. Rahimi-kaldeh, A. Ashouri, A. Bandani, and K. Tomioka, The effect of Wolbachia on diapause, fecundity, and clock gene expression in Trichogramma brassicae (Hymenoptera: Trichogrammatidae), 2017.

, Dev. Genes Evol, vol.227, pp.401-410

K. H. Redford, J. A. Segre, N. Salafsky, C. M. Del-rio, and D. Mcaloose, Conservation and the microbiome, Conserv. Biol, vol.26, pp.195-197, 2012.

B. S. Samuel, H. Rowedder, C. Braendle, M. Félix, and G. Ruvkun, Caenorhabditis elegans responses to bacteria from its natural habitats, Proc. Natl. Acad. Sci. U.S.A, vol.113, pp.3941-3949, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02332365

J. G. Sanders, S. Powell, D. J. Kronauer, H. L. Vasconcelos, M. E. Frederickson et al., Stability and phylogenetic correlation in gut microbiota: lessons from ants and apes, Mol. Ecol, vol.23, pp.1268-1283, 2014.

C. L. Sansone, J. Cohen, A. Yasunaga, J. Xu, G. Osborn et al., Microbiotadependent priming of antiviral intestinal immunity in Drosophila, Cell Host Microbe, vol.18, pp.571-581, 2015.

A. Shade, M. Jacques, and M. Barret, Ecological patterns of seed microbiome diversity, transmission, and assembly, Curr. Opin. Microbiol, vol.37, pp.15-22, 2017.
URL : https://hal.archives-ouvertes.fr/hal-02516692

E. Sheikh-jabbari, M. D. Hall, F. Ben-ami, and D. Ebert, The expression of virulence for a mixed-mode transmitted parasite in a diapausing host, Parasitology, vol.141, pp.1097-1107, 2014.

N. J. Shikuma, M. Pilhofer, G. L. Weiss, M. G. Hadfield, G. J. Jensen et al., Marine tubeworm metamorphosis induced by arrays of bacterial phage tail-like structures, Science, vol.343, pp.529-533, 2014.

S. C. Shin, S. Kim, H. You, B. Kim, A. C. Kim et al., Drosophila microbiome modulates host developmental and metabolic homeostasis via insulin signaling, Science, vol.334, pp.670-674, 2011.

C. Sim and D. L. Denlinger, Insulin signaling and the regulation of insect diapause, Front. Physiol, vol.4, p.189, 2013.

J. Simon, S. Boutin, T. Tsuchida, R. Koga, J. L. Gallic et al., Facultative symbiont infections affect aphid reproduction, PLoS One, vol.6, p.21831, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00729321

M. P. Sison-mangus, A. A. Mushegian, and D. Ebert, Water fleas require microbiota for survival, growth and reproduction, ISME J, vol.9, pp.59-67, 2015.

P. Smith, D. Willemsen, M. Popkes, F. Metge, E. Gandiwa et al., Regulation of life span by the gut microbiota in the short-lived African turquoise killifish, vol.6, pp.1-26, 2017.

F. Sommer, M. Ståhlman, O. Ilkayeva, J. M. Arnemo, J. Kindberg et al., The gut microbiota modulates energy metabolism in the hibernating brown bear Ursus arctos, Cell Rep, vol.14, pp.1655-1661, 2016.

J. L. Sonnenburg, J. Xu, D. D. Leip, C. Chen, B. P. Westover et al., Glycan foraging in vivo by an intestine-adapted bacterial symbiont, Science, vol.307, pp.1955-1959, 2005.

T. J. Stevenson, K. N. Duddleston, and C. L. Buck, Effects of season and host physiological state on the diversity, density, and activity of the arctic ground squirrel cecal microbiota, Appl. Environ. Microbiol, vol.80, pp.5611-5622, 2014.

M. J. Tauber, C. A. Tauber, and S. Masaki, Seasonal Adaptations of Insects, 1986.

K. Tougeron, G. Hraoui, C. L. Lann, J. Van-baaren, and J. Brodeur, Intraspecific maternal competition induces summer diapause in insect parasitoids, Insect Sci, vol.25, pp.1080-1088, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01810996

B. K. Trevelline, S. S. Fontaine, B. K. Hartup, and K. D. Kohl, Conservation biology needs a microbial renaissance: a call for the consideration of host-associated microbiota in wildlife management practices, Proc. R. Soc. B Biol. Sci, vol.286, 2019.

D. E. Ullman and D. L. Mclean, Feeding behavior of the winterform pear psylla, Psylla pyricola (Homoptera: Psyllidae), on reproductive and transitory host plants, Environ. Entomol, vol.17, pp.675-678, 1988.

D. B. Vizoso and D. Ebert, Phenotypic plasticity of host-parasite interactions in response to the route of infection, J. Evol. Biol, vol.18, pp.911-921, 2005.

M. P. Waldrop and M. K. Firestone, Seasonal dynamics of microbial community composition and function in oak canopy and open grassland soils, Microb. Ecol, vol.52, pp.470-479, 2006.

L. Warnecke, J. M. Turner, T. K. Bollinger, J. M. Lorch, V. Misra et al., Inoculation of bats with European Geomyces destructans supports the novel pathogen hypothesis for the origin of white-nose syndrome, Proc. Natl. Acad. Sci, vol.109, pp.6999-7003, 2012.

K. M. Webberley and G. D. Hurst, The effect of aggregative overwintering on an insect sexually transmitted parasite system, J. Parasitol, vol.88, p.707, 2002.

N. S. Webster, R. E. Cobb, and A. P. Negri, Temperature thresholds for bacterial symbiosis with a sponge, ISME J, vol.2, p.830, 2008.

J. J. Wernegreen, Mutualism meltdown in insects: Bacteria constrain thermal adaptation, Curr. Opin. Microbiol, vol.15, pp.255-262, 2012.

D. W. Whitman and A. A. , What is phenotypic plasticity and why is it important?, Pp. 1-63 in Phenotypic Plasticity of Insects: Mechanisms and Consequences, 2009.

J. M. Wiebler, K. D. Kohl, R. E. Lee, and J. P. Costanzo, Urea hydrolysis by gut bacteria in a hibernating frog: evidence for ureanitrogen recycling in Amphibia, Proc. R. Soc. B Biol. Sci, vol.285, 2018.

A. M. Wier, S. V. Nyholm, M. J. Mandel, R. P. Massengo-tiassé, A. L. Schaefer et al., Transcriptional patterns in both host and bacterium underlie a daily rhythm of anatomical and metabolic change in a beneficial symbiosis, Proc. Natl. Acad. Sci. U.S.A, vol.107, p.2259, 2010.

S. C. Woll and J. E. Podrabsky, Insulin-like growth factor signaling regulates developmental trajectory associated with diapause in embryos of the annual killifish Austrofundulus limnaeus, J. Exp. Biol, vol.220, pp.2777-2786, 2017.

X. Zhang, X. Wu, and J. Wu, Critical contact rate for vector-hostpathogen oscillation involving co-feeding and diapause, J. Biol. Syst, vol.25, pp.657-675, 2017.

H. Zheng, J. E. Powell, M. I. Steele, C. Dietrich, and N. A. Moran, Honeybee gut microbiota promotes host weight gain via bacterial metabolism and hormonal signaling, Proc. Natl. Acad. Sci. U.S.A, vol.114, pp.4775-4780, 2017.

A. A. Mushegian-and-k and . Tougeron, This content downloaded from 130.104.214.125 on, 2019.