Eran Levin
Tel Aviv University
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Featured researches published by Eran Levin.
Aging Cell | 2010
Yariv Kanfi; Victoria Peshti; Reuven Gil; Shoshana Naiman; Liat Nahum; Eran Levin; Noga Kronfeld-Schor; Haim Y. Cohen
The NAD+‐dependent SIRT6 deacetylase is a therapeutic candidate against the emerging metabolic syndrome epidemic. SIRT6, whose deficiency in mice results in premature aging phenotypes and metabolic defects, was implicated in a calorie restriction response that showed an opposite set of phenotypes from the metabolic syndrome. To explore the role of SIRT6 in metabolic stress, wild type and transgenic (TG) mice overexpressing SIRT6 were fed a high fat diet. In comparison to their wild‐type littermates, SIRT6 TG mice accumulated significantly less visceral fat, LDL‐cholesterol, and triglycerides. TG mice displayed enhanced glucose tolerance along with increased glucose‐stimulated insulin secretion. Gene expression analysis of adipose tissue revealed that the positive effect of SIRT6 overexpression is associated with down regulation of a selective set of peroxisome proliferator‐activated receptor‐responsive genes, and genes associated with lipid storage, such as angiopoietin‐like protein 4, adipocyte fatty acid‐binding protein, and diacylglycerol acyltransferase 1, which were suggested as potential targets for drugs to control metabolic syndrome. These results demonstrate a protective role for SIRT6 against the metabolic consequences of diet‐induced obesity and suggest a potentially beneficial effect of SIRT6 activation on age‐related metabolic diseases.
Proceedings of the Royal Society of London B: Biological Sciences | 2014
Noam Cvikel; Eran Levin; Edward Hurme; Ivailo M. Borissov; Arjan Boonman; Eran Amichai; Yossi Yovel
Animals often deal with situations in which vast sensory input is received simultaneously. They therefore must possess sophisticated mechanisms to select important input and ignore the rest. In bat echolocation, this problem is at its extreme. Echolocating bats emit sound signals and analyse the returning echoes to sense their environment. Bats from the same species use signals with similar frequencies. Nearby bats therefore face the difficulty of distinguishing their own echoes from the signals of other bats, a problem often referred to as jamming. Because bats commonly fly in large groups, jamming might simultaneously occur from numerous directions and at many frequencies. Jamming is a special case of the general phenomenon of sensory segregation. Another well-known example is the human problem of following conversation within a crowd. In both situations, a flood of auditory incoming signals must be parsed into important versus irrelevant information. Here, we present a novel method, fitting wild bats with a miniature microphone, which allows studying jamming from the bats ‘point of view’. Previous studies suggested that bats deal with jamming by shifting their echolocation frequency. On-board recordings suggest otherwise. Bats shifted their frequencies, but they did so because they were responding to the conspecifics as though they were nearby objects rather than avoiding being jammed by them. We show how bats could use alternative measures to deal with jamming instead of shifting their frequency. Despite its intuitive appeal, a spectral jamming avoidance response might not be the prime mechanism to avoid sensory interference from conspecifics.
Naturwissenschaften | 2009
Eran Levin; Yoram Yom-Tov; Anat Barnea
In many ant species, nuptial flight tends to be short in time and assumed to be synchronous across a large area. Here, we report that, in the upper Jordan Valley, northern Israel, massive nuptial flights of Carpenter ants (Camponotus sp.) occur frequently throughout the summer, and their alates form up to 90% of the diet of the greater mouse-tailed bat (Rhinopoma microphyllum) during this period. This fat and protein-rich diet enables female bats to lactate during summer, and the large amount of fat that both sexes accumulate may serve as an energy source for their following winter hibernation and posthibernation mating in early spring (March–April). We suggest that the annual movement of these bats to the Mediterranean region of Israel may have evolved in order to enable them to exploit the extremely nutritious forms of ant alates when the bats’ energetic demands are highest.
PLOS ONE | 2013
Eran Levin; Uri Roll; Amit Dolev; Yoram Yom-Tov; Noga Kronfeld-Shcor
Competition has long been assumed to be a major driver in regulating ecological communities. Intra-specific competition is considered to be maximal as members of the same species use the same ecological niches in a similar way. Many species of animals exhibit great physiological, behavioral, and morphological differences between sexes (sexual dimorphism). Here we report an extreme geographical segregation between the sexes in the greater mouse-tailed bat (Rhinopoma microphyllum). To gain insight into the driving mechanisms of sexual segregation outside the mating season, we collected and integrated environmental, behavioral, physiological, and spatial information. We found that both sexes choose roosts with similar characteristics and the same food type, but use different habitats for different durations. Males forage around cliffs at higher and cooler elevations while females forage in lowlands around a river delta. We suggest that it is their different physiological and social needs, and not competition, that drives sexual segregation in this species.
Science | 2017
Eran Levin; G. Lopez-Martinez; Bentley A. Fane; Goggy Davidowitz
Sugar rush Flying requires high levels of energy production, which causes muscular oxidative damage. Food-derived antioxidants can protect against such damage; however, nectar is devoid of these compounds. Levin et al. found that nectar-feeding hawkmoths fed high concentrations of sugar had lower levels of damage than unfed moths. Sugar-fed moths generated antioxidant compounds by shunting glucose through a pentose phosphate pathway. This mechanism may have allowed for the evolution of energy-intensive flying nectarivores. Science, this issue p. 733 Nectar-derived sugars protect nectar-eating insects from flight muscle oxidative damage. Nectar-feeding animals have among the highest recorded metabolic rates. High aerobic performance is linked to oxidative damage in muscles. Antioxidants in nectar are scarce to nonexistent. We propose that nectarivores use nectar sugar to mitigate the oxidative damage caused by the muscular demands of flight. We found that sugar-fed moths had lower oxidative damage to their flight muscle membranes than unfed moths. Using respirometry coupled with δ13C analyses, we showed that moths generate antioxidant potential by shunting nectar glucose to the pentose phosphate pathway (PPP), resulting in a reduction in oxidative damage to the flight muscles. We suggest that nectar feeding, the use of PPP, and intense exercise are causally linked and have allowed the evolution of powerful fliers that feed on nectar.
Proceedings of the Royal Society B: Biological Sciences | 2017
Eran Levin; Marshall D. McCue; Goggy Davidowitz
The ability to allocate resources, even when limited, is essential for survival and fitness. We examine how nutrients that occur in minute amounts are allocated among reproductive, somatic, and metabolic demands. In addition to sugar, flower nectars contain two macronutrients—amino acids and fatty acids. We created artificial nectars spiked with 13C-labelled amino acids and fatty acids and fed these to adult moths (Manduca sexta: Sphingidae) to understand how they allocate these nutrients among competing sinks (reproduction, somatic tissue, and metabolic fuel). We found that both essential and non-essential amino acids were allocated to eggs and flight muscles and were still detectable in early-instar larvae. Parental-derived essential amino acids were more conserved in the early-instars than non-essential amino acids. All amino acids were used as metabolic fuel, but the non-essential amino acids were oxidized at higher rates than essential amino acids. Surprisingly, the nectar fatty acids were not vertically transferred to offspring, but were readily used as a metabolic fuel by the moth, minimizing losses of endogenous nutrient stores. We conclude that the non-carbohydrate components of nectar may play important roles in both reproductive success and survival of these nectar-feeding animals.
Animal Behaviour | 2016
Eran Levin; Chandreyee Mitra; Goggy Davidowitz
Direct benefits provided by males have large effects on the fitness of females and their offspring in many species. Here, we examined whether mating or feeding experience of male Carolina sphinx moths, Manduca sexta (Sphingidae), affects the quality of direct benefits that males provide to their mates. We mated virgin females with fed and unfed, virgin and previously mated males. Feeding experience affected male mating success, spermatophore size and flight muscle size. In addition, females mated to fed males laid more eggs than females mated to unfed males, and females mated to virgin males laid more eggs than females mated to previously mated males. Using 13C-enriched glucose in the nectar of the fed males, we found that the second and third spermatophores of males were strongly labelled, but this labelled glucose was not present either in the females fat body or in her eggs. Therefore, although fed males provided females direct benefits from the sugar in the nectar, the sugar was not used as a nutrient by females. We suggest that in short-lived species, where females mate singly and males mate multiply, and where nectar availability is highly variable, males may be selected to conserve their resources to maintain flight capability and to invest in sperm performance and, thus, provide only limited (non-nutritive) direct fitness benefits to their mates.
Proceedings of the Royal Society of London B: Biological Sciences | 2015
Eran Levin; Brit Plotnik; Eran Amichai; Luzie J. Braulke; Shmulik Landau; Yoram Yom-Tov; Noga Kronfeld-Schor
We report that two species of mouse-tailed bats (Rhinopoma microphyllum and R. cystops) hibernate for five months during winter in geothermally heated caves with stable high temperature (20°C). While hibernating, these bats do not feed or drink, even on warm nights when other bat species are active. We used thermo-sensitive transmitters to measure the bats’ skin temperature in the natural hibernacula and open flow respirometry to measure torpid metabolic rate at different ambient temperatures (Ta, 16–35°C) and evaporative water loss (EWL) in the laboratory. Bats average skin temperature at the natural hibernacula was 21.7 ± 0.8°C, and no arousals were recorded. Both species reached the lowest metabolic rates around natural hibernacula temperatures (20°C, average of 0.14 ± 0.01 and 0.16 ± 0.04 ml O2 g−1 h−1 for R. microphyllum and R. cystops, respectively) and aroused from torpor when Ta fell below 16°C. During torpor the bats performed long apnoeas (14 ± 1.6 and 16 ± 1.5 min, respectively) and had a very low EWL. We hypothesize that the particular diet of these bats is an adaptation to hibernation at high temperatures and that caves featuring high temperature and humidity during winter enable these species to survive this season on the northern edge of their world distribution.
The Journal of Experimental Biology | 2017
Eran Levin; Marshall D. McCue; Goggy Davidowitz
ABSTRACT The different reproductive strategies of males and females underlie differences in behavior that may also lead to differences in nutrient use between the two sexes. We studied sex differences in the utilization of two essential amino acids (EAAs) and one non-essential amino acid (NEAA) by the Carolina sphinx moth (Manduca sexta). On day one post-eclosion from the pupae, adult male moths oxidized greater amounts of larva-derived AAs than females, and more nectar-derived AAs after feeding. After 4 days of starvation, the opposite pattern was observed: adult females oxidized more larva-derived AAs than males. Adult males allocated comparatively small amounts of nectar-derived AAs to their first spermatophore, but this allocation increased substantially in the second and third spermatophores. Males allocated significantly more adult-derived AAs to their flight muscle than females. These outcomes indicate that adult male and female moths employ different strategies for allocation and oxidation of dietary AAs. Summary: Young adult male moths oxidize greater amounts of larva-derived amino acids than females, and more nectar-derived amino acids after feeding. Under starvation conditions, adult females exhibit the opposite pattern.
Biochemical Genetics | 2010
Lihong Yuan; Xueguo Zuo; Lingjiang He; Paul A. Racey; Eran Levin; Shuyi Zhang
Spermatogenesis is a complex physiological process controlled by many genes. The BOULE gene, a new member of the Deleted in Azoospermia (DAZ) family (which consists of BOULE, DAZ, and DAZ-like DAZl), is regarded as the ancestor of the DAZ family and a key factor in controlling the meiosis of male germ cells, which can regulate the expression of the twine gene and promote progression through meiosis (Eberhart et al. 1996; Karashima et al. 2000; Maines and Wasserman 1999; Xu et al. 2001). Bats account for about 20% of mammals and, during evolution, have evolved many reproductive strategies, including sperm storage, delayed fertilization, delayed implantation, and delayed development (Nowak et al. 1994; Racey and Entwistle 2000). The strategies of sperm storage and delayed fertilization allow many bat species, especially hibernating bats, to achieve synchrony between birth peaks and food availability (Racey 1979). As little is known about the cell biology of bat spermatogenesis, in this study, we obtained BOULE gene sequences from four bat species (Rhinolophus ferrumequinum, Myotis ricketti, Eonycteris spelaea, and Rousettus leschenaultii) to test the role of the BOULE gene in bat