Jaculus Orientalis Research Articles

Cranial differences in three-toed jerboas (Dipodinae, Dipodidae, Rodentia) according to recent taxonomic revisions.

Recent phylogenetic studies amended the taxonomy of three-toed jerboas (subfamily Dipodinae), including raising subspecies to full species. Here, we use geometric morphometrics to compare scaled-shape differences in dipodine crania while considering their revised taxonomy. We sampled Dipus deasyi, D. sagitta halli, D. s. sowerbyi, Jaculus blanfordi blanfordi, J. hirtipes, J. jaculus, J. loftusi, J. orientalis gerboa, J. o. mauritanicus, and Stylodipus andrewsi. Crania were not sexually dimorphic. Common allometry explained some of the shape variation, for example, reduced braincases in larger specimens. Most operational taxonomic unit pairs differed in both size and shape. Dipus and Stylodipus clustered together based on their cranial shape. Jaculus differed from the aforementioned genera by its larger tympanic bulla, broader braincase, larger infraorbital foramen, along with reduced molars and rostra. Jaculus orientalis differed from other Jaculus by its broader face versus reduced cranial vault. Jaculus blanfordi (subgenus Haltomys) resembles members of the subgenus Jaculus more than its consubgener (J. orientalis). Jaculus loftusi, previously considered a synonym of J. jaculus, clearly differed from the latter by its shorter rostrum, smaller infraorbital foramen, and more caudolaterally expanded tympanic bulla. Jaculus hirtipes, another recent synonym of J. jaculus, resembled J. blanfordi more in scaled cranial shape than it did J. jaculus. Dipus sagitta halli and D. s. sowerbyi were indistinguishable, but they clearly differed from D. deasyi (recently raised to full species) with the latter having a larger molar row, more inflated tympanic bulla, and shorter, slenderer rostrum. Ecological explanations for detected cranial shape differences are considered, including diet and habitat (particularly substrate).

Purification and characterization of aldose reductase from jerboa (Jaculus orientalis) and evaluation of its inhibitory activity by Euphorbia regis-jubae (Webb & Berth) extracts

This study aimed, for the first time, to assess the purification of aldose reductase (AR) in Jaculus orientalis (Dipodidae family) kidney and to evaluate the in vitro aldose reductase inhibitory (ARI) effects of Euphorbia regis-jubae (Euphorbiaceae family) aqueous and hydroethanolic extracts. Initial screening assay of the enzymatic AR activity in different jerboa states (euthermic, prehibernating and hibernating) and tissues (brain, brown adipose tissue, liver and kidneys) was assessed. Then, AR has been purified to homogeneity from the kidneys of prehibernating jerboas by a series of chromatographic technics. Furthermore, the in vitro and in silico ARI effects of E. regis-jubae (Webb & Berth) extracts, characterized by hight performance liquid chromatography (HPLC) on the purified enzyme were evaluated. Our results showed that the highest enzyme activity was detected in the kidneys, followed by white adipose tissue and the lungs of pre-hibernating jerboa. The enzyme was purified to homogeneity from jerboa kidneys during prehibernating state with a purification factor of 53.4-fold and a yield of about 6%. AR is monomeric, active in D(+)-glyceraldehyde substrate and in disodium phosphate buffer. The pH and temperature for AR were determined to be 6.5–7.5 and 35 °C, respectively. Results of the in vitro ARI activity was strongest with both the hydroethanolic extract (IC50 = 96.45 μg/mL) and aqueous extract (IC50 = 140 μg/mL). Molecular docking study indicated that catechin might be the main component in both aqueous and hydroethanolic extracts to inhibited AR. This study provides new evidence on the ARI effect of E. regis-jubae (Webb & Berth), which may be related to its phenolic constituents.

NEW RECORD OF TWO RODENT SPECIES FROM KHENCHELA REGION (EAST OF ALGERIA)

Mus spretus is endemic to the Mediterranean region and Jaculus orientalis is only found in North Africa and Saudi Arabia. Their presence in Algeria was previously evidenced in other studies, the present paper focuses on the recent discovery of the Jaculus orientalis Erxleben, 1777 and Mus spretus Lataste, 1883 in a new locality of the East of Algeria, in Khenchela region (Aurès Mountain), based on weight and external measurements. The sampling period took four months between April and July 2019. This observation will enrich the knowledge of Algerian Rodents fauna in general and of Khenchela in particular.

Geographic patterns of genetic variation in the greater Egyptian jerboa Jaculus orientalis (Dipodidae, Rodentia) from Tunisia

The biogeographic area of Tunisia is characterized by several geographic and climatic zones that shaped the spatial distribution and genetic differentiation in many species. Despite the merit studies carried out on different species in this region, yet the distribution patterns of genetic diversity and taxonomy of many taxa remain unresolved. This study aimed to elucidate the geographic patterns of genetic variation in one of the endemic species of Tunisia, the greater Egyptian jerboa, Jaculus orientalis. The extent of phylogeographic patterns and molecular genetic diversity (mitochondrial cytochrome b gene) were addressed in a survey of 65 specimens from 11 localities. Twenty-four haplotypes were identified among populations which organized them into two well-supported clades separated by a higher genetic divergence (K2P = 1%; Фct = 0.65; P < 0.05). The first, clade I, included populations from the northern and central parts of Tunisia, while the second, clade II, comprised only populations from the southern part. Divergence between populations of the two clades would have occurred by Middle Pleistocene (ca. 0.71 Mya). Barrier Software showed that the populations of the two clades were separated by a geographical barrier, namely Chott El Jerid, located in the middle zone. Additionally, the clear distinction between the northern and central populations from those of the southern part was probably due to a Libyan origin of the latter.

Coordinated seasonal regulation of metabolic and reproductive hypothalamic peptides in the desert jerboa.

Jerboa (Jaculus orientalis) is a semi-desert rodent displaying strong seasonal variations in biological functions in order to survive harsh conditions. When environmental conditions become unfavorable in early autumn, it shuts down its reproductive axis, increases its body weight, and finally hibernates. In spring, the jerboa displays opposite regulations, with a reactivation of reproduction and reduction in body weight. This study investigated how genes coding for different hypothalamic peptides involved in the central control of reproduction (Rfrp and Kiss1) and energy homeostasis (Pomc, Npy, and Somatostatin) are regulated according to seasons in male jerboas captured in the wild in spring or autumn. Remarkably, a coordinated increase in the mRNA level of Rfrp in the dorso/ventromedial hypothalamus and Kiss1, Pomc, and Somatostatin in the arcuate nucleus was observed in jerboas captured in spring as compared to autumn animals. Only Npy gene expression in the arcuate nucleus displayed no significant variations between the two seasons. These variations appear in line with the jerboa's seasonal physiology, since the spring increase in Rfrp and Kiss1 expression might be related to sexual reactivation, while the spring increase in genes encoding anorexigenic peptides, POMC, and somatostatin may account for the reduced body weight reported at this time of the year. J. Comp. Neurol. 524:3717-3728, 2016. © 2016 Wiley Periodicals, Inc.

Patterns of skull variation in relation to some geoclimatic conditions inthe greater jerboa Jaculus orientalis (Rodentia, Dipodidae) from Tunisia

Patterns of skull variation in relation to some geoclimatic conditions inthe greater jerboa Jaculus orientalis (Rodentia, Dipodidae) from Tunisia

Molecular assessment of Hepatozoon (Apicomplexa: Adeleorina) infections in wild canids and rodents from north Africa, with implications for transmission dynamics across taxonomic groups.

Parasites play a major role in ecosystems, and understanding of host-parasite interactions is important for predicting parasite transmission dynamics and epidemiology. However, there is still a lack of knowledge about the distribution, diversity, and impact of parasites in wildlife, especially from remote areas. Hepatozoon is a genus of apicomplexan parasites that is transmitted by ingestion of infected arthropod vectors. However, alternative modes of transmission have been identified such as trophic transmission. Using the 18S rRNA gene as a marker, we provide an assessment of Hepatozoon prevalence in six wild canid and two rodent species collected between 2003 and 2012 from remote areas in North Africa. By combining this with other predator-prey systems in a phylogenetic framework, we investigate Hepatozoon transmission dynamics in distinct host taxa. Prevalence was high overall among host species (African jerboa Jaculus jaculus [17/47, 36%], greater Egyptian jerboa Jaculus orientalis [5/7, 71%], side-striped jackal Canis adustus [1/2, 50%], golden jackal Canis aureus [6/32, 18%], pale fox Vulpes pallida [14/28, 50%], Rüppell's fox Vulpes rueppellii [6/11, 55%], red fox Vulpes vulpes [8/16, 50%], and fennec fox Vulpes zerda [7/11, 42%]). Phylogenetic analysis showed further evidence of occasional transmission of Hepatozoon lineages from prey to canid predators, which seems to occur less frequently than in other predator-prey systems such as between snakes and lizards. Due to the complex nature of the Hepatozoon lifecycle (heteroxenous and vector-borne), future studies on these wild host species need to clarify the dynamics of alternative modes of Hepatozoon transmission and identify reservoir and definitive hosts in natural populations. We also detected putative Babesia spp. (Apicomplexa: Piroplasmida) infections in two canid species from this region, V. pallida (1/28) and V. zerda (1/11).

Geographic range, morphometric variation and niche differentiation in greater Egyptian jerboa, Jaculus orientalis 1)

Abstract Geographic range, morphometric skull variation and niche differentiation were analyzed in the greater Egyptian jerboa, Jaculus orientalis, and compared with published data on the species’ phylogeographic structure. The species occurs in 15 separate areas, which are grouped into two main blocks and divided by a wide gap. The first block goes from Morocco to western Libya and the second from eastern Libya to Israel; the second block is subdivided into two sub-blocks, eastern Libya and Egypt and Israel and Sinai. Analysis of niche similarity indicated niche convergence within the eastern and western parts of the species’ geographic range and niche divergence between these two major parts of the geographic range. There was a strong congruence among distributional, genetic and ecological patterns. Morphological variation in J. orientalis did not completely coincide with the distribution, genetic and ecological patterns. Three morphologically well-differentiated population groups were found within the geographic range of the species. The same level of morphological differentiation was demonstrated between highly isolated geographically and deeply diverged genetically and ecologically western and eastern groups of populations and between the weakly geographically isolated and ecologically similar populations of Egypt/Libya and Israel/Sinai. A taxonomic revision of the sub-specific division of J. orientalis is proposed.

The arcuate nucleus and RF-amide neuropeptides in the seasonal adaptation of mammals

The arcuate nucleus and RF-amide neuropeptides in the seasonal adaptation of mammals

Bartonella jaculi sp. nov., Bartonella callosciuri sp. nov., Bartonella pachyuromydis sp. nov. and Bartonella acomydis sp. nov., isolated from wild Rodentia

Four novel strains of members of the genus Bartonella, OY2-1(T), BR11-1(T), FN15-2(T) and KS2-1(T), were isolated from the blood of wild-captured greater Egyptian jerboa (Jaculus orientalis), plantain squirrel (Callosciurus notatus), fat-tailed gerbil (Pachyuromys duprasi) and golden spiny mouse (Acomys russatus). All the animals were imported to Japan as pets from Egypt, Thailand and the Netherlands. The phenotypic characterization (growth conditions, incubation periods, biochemical properties and cell morphologies), DNA G+C contents (37.4 mol% for strain OY2-1(T), 35.5 mol% for strain BR11-1(T), 35.7 mol% for strain FN15-2(T) and 37.2 mol% for strain KS2-1(T)), and sequence analyses of the 16S rRNA genes indicated that those strains belong to the genus Bartonella. Sequence comparisons of gltA and rpoB genes suggested that all of the strains should be classified as novel species of the genus Bartonella. In phylogenetic trees based on the concatenated sequences of five loci, including the 16S rRNA, ftsZ, gltA and rpoB genes and the ITS region, and on the concatenated deduced amino acid sequences of three housekeeping genes (ftsZ, gltA and rpoB), all strains formed distinct clades and had unique mammalian hosts that could be discriminated from other known species of the genus Bartonella. These data strongly support the hypothesis that strains OY2-1(T), BR11-1(T), FN15-2(T) and KS2-1(T) should be classified as representing novel species of the genus Bartonella. The names Bartonella jaculi sp. nov., Bartonella callosciuri sp. nov., Bartonella pachyuromydis sp. nov. and Bartonella acomydis sp. nov. are proposed for these novel species. Type strains of Bartonella jaculi sp. nov., Bartonella callosciuri sp. nov., Bartonella pachyuromydis sp. nov. and Bartonella acomydis sp. nov. are OY2-1(T) ( = JCM 17712(T) = KCTC 23655(T)), BR11-1(T) ( = JCM 17709(T) = KCTC 23909(T)), FN15-2(T) ( = JCM 17714(T) = KCTC 23657(T)) and KS2-1(T) ( = JCM 17706(T) = KCTC 23907(T)), respectively.

Phylogeography of the Greater Egyptian Jerboa (Jaculus orientalis) (Rodentia: Dipodidae) in Mediterranean North Africa

AbstractThe Mediterranean Basin is an acknowledged hotspot for biodiversity, yet historical processes that shaped this biodiversity in North Africa remain poorly understood. This study aimed to elucidate the phylogeographic pattern of an endemic species of Mediterranean areas of North Africa, the Greater Egyptian Jerboa, Jaculus orientalis. The extent of phylogeographic patterns and molecular genetic diversity (mitochondrial cytochrome b gene) were addressed in a survey of 45 jerboas from 24 localities. Our phylogeographical analyses show a strong genetic subdivision into three areas along a west‐east axis, corresponding to (1) Morocco and western Algeria; (2) eastern Algeria, Tunisia and western Libya; (3) eastern Libya and Egypt. Demographic analyses revealed different modalities of population expansion since the last glacial age depending on geographic areas. The dating using relaxed molecular clock analyses revealed that most splits occurred during the Quaternary (&lt;1 million of years ago). Finally, we discussed the relative roles of geological and climatic change in generating this pattern of genetic structure observed for the Greater Egyptian Jerboa and other vegetal and animal species in North Africa.

Overwinter body temperature patterns in captive jerboas (Jaculus orientalis): influence of sex and group

The jerboa (Jaculus orientalis) has been described in the past as a hibernator, but no reliable data exist on the daily and seasonal rhythmicity of body temperature (T (b)). In this study, T (b) patterns were determined in different groups of jerboas (isolated males and females, castrated males and grouped animals) maintained in captivity during autumn and winter, and submitted to natural variations of light and ambient temperature (T (a)). T (b) and T (a) variations were recorded with surgically implanted iButton temperature loggers at 30-min intervals for two consecutive years. About half (6/13) of isolated female jerboas hibernated with a T (b)<33°C, with hibernation bouts interspersed with short periods of normothermy from November to February. Hibernation bout durations were longer (4-5days) than those of normothermia phases (1-4days). During hibernation, the minimum T (b) was low (T (b)min ~10.7°C). In contrast, one of the 12 isolated males showed short hibernation bouts of ca. 2days late in the hibernation season, February-March. The males had T (b)min values of 15.1°C. In contrast to predictions, no castrated males hibernated. When jerboas were grouped, females and males exhibited concomitant torpor bouts. In males, the longest bouts were observed during the late hibernation season. These data suggest complex regulation of hibernation in jerboas.

Karyotypic Variation in Two Species of Jerboas Jaculus jaculus and Jaculus orientalis (Rodentia, Dipodidae) from Tunisia

The karyotypes of the lesser Egyptian jerboa Jaculus jaculus and the greater Egyptian jerboa Jaculus orientalis from Tunisia are described and compared with available data particularly from Egypt. The species examined have a similar karyotype consisting of 2n = 48 chromosomes and a fundamental number of autosomes (NFa) varying from 88 to 90 in J. jaculus and from 84 to 88 in J. orientalis. The X chromosome is submetacentric in both species, while the Y is submetacentric in J. orientalis and acrocentric in J. jaculus. Most of the autosomes are meta/submetacentric but the small pairs 22 - 23 in J. jaculus and 20-23 in J. orientalis are frequently acrocentric, yielding considerable differences in the NFa within and among species. Morphological variation in these small pairs of autosomes and/or in the Y chromosome in J. orientalis may distinguish populations of the two species from Egypt and Tunisia. The differences observed either between Egypt and Tunisia or between the Tunisian Jaculus species are probably associated with chromosomal rearrangements such as pericentric inversions or heterochromatin variation. They appear of lesser magnitude than other changes (especially molecular) that have occurred during the evolution of this genus.

Kisspeptin in the hypothalamus of the jerboa (Jaculus orientalis): sexual dimorphism and seasonal variation

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Sensitivity of liver metabolism in jerboa (Jaculus orientalis) to ciprofibrate, a peroxisome proliferator

Ciprofibrate is a well-known drug used to normalize lipid parameters and fibrinogen in atherosclerosis patients. In laboratory rodents such as rats or mice, ciprofibrate exhibits peroxisome proliferator activity. However, to date, no clear alterations or side effects caused by ciprofibrate have been noted in humans. In order to further investigate such possible relationships, we studied the effects of sustained ciprofibrate treatment in jerboas (Jaculus orientalis). In these rodents, ciprofibrate does not induce hepatomegaly or promote liver cell DNA replication, confirming that this species more closely resembles humans than do rats or mice. The jerboas were treated daily with ciprofibrate at 3 mg/kg body weight for 4 weeks. Subcellular markers, clinical enzymes and enzymatic antioxidant defenses were then assessed. The results showed a strong decrease in peroxisomal catalase activity and an increase in the level of malondialdehyde (a stress biomarker). Moreover, ciprofibrate in vivo and in vitro inhibited D-3-hydroxybutyrate dehydrogenase, a mitochondrial enzyme of the ketone body interconversion that is important in redox balance (NAD+/NADH+H+ ratio). In conclusion, under these conditions, ciprofibrate induced alterations in the liver oxidative metabolism.

Differential Regulation of Peroxisome Proliferator-Activated Receptor (PPAR)-α1 and Truncated PPARα2 as an Adaptive Response to Fasting in the Control of Hepatic Peroxisomal Fatty Acid β-Oxidation in the Hibernating Mammal

Seasonal obesity and fasting-associated hibernation are the two major metabolic events governing hepatic lipid metabolism in hibernating mammals. In this process, however, the role of the nuclear receptor known as peroxisome proliferator-activated receptor (PPAR)-alpha has not been elucidated yet. Here we show, as in human, that jerboa (Jaculus orientalis) liver expresses both active wild-type PPARalpha (PPARalpha1wt) and truncated PPARalpha forms and that the PPARalpha1wt to truncated PPARalpha2 ratio, which indicates the availability of active PPARalpha1wt, is differentially regulated during fasting-associated hibernation. Functional activation of hepatic jerboa PPARalpha, during prehibernating and hibernating states, was demonstrated by the induction of its target genes, which encode peroxisomal proteins such as acyl-CoA oxidase 1, peroxisomal membrane protein 70, and catalase, accompanied by a concomitant induction of PPARalpha thermogenic coactivator PPARgamma coactivator-1alpha. Interestingly, sustained activation of PPARalpha by its hypolipidemic ligand, ciprofibrate, abrogates the adaptive fasting response of PPARalpha during prehibernation and overinduces its target genes, disrupting the prehibernation fattening process. In striking contrast, during fasting-associated hibernation, jerboas exhibit preferential up-regulation of hepatic peroxisomal fatty acid oxidation instead of the mitochondrial pathway, which is down-regulated. Taken together, our results strongly suggest that PPARalpha is subject to a hibernation-dependent splicing regulation in response to feeding-fasting conditions, which defines the activity of PPARalpha and the activation of its target genes during hibernation bouts of jerboas.

Immunoaffinity purification and characterization of mitochondrial membrane-bound D-3-hydroxybutyrate dehydrogenase from Jaculus orientalis.

BackgroundThe interconversion of two important energy metabolites, 3-hydroxybutyrate and acetoacetate (the major ketone bodies), is catalyzed by D-3-hydroxybutyrate dehydrogenase (BDH1: EC 1.1.1.30), a NAD+-dependent enzyme. The eukaryotic enzyme is bound to the mitochondrial inner membrane and harbors a unique lecithin-dependent activity. Here, we report an advanced purification method of the mammalian BDH applied to the liver enzyme from jerboa (Jaculus orientalis), a hibernating rodent adapted to extreme diet and environmental conditions.ResultsPurifying BDH from jerboa liver overcomes its low specific activity in mitochondria for further biochemical characterization of the enzyme. This new procedure is based on the use of polyclonal antibodies raised against BDH from bacterial Pseudomonas aeruginosa. This study improves the procedure for purification of both soluble microbial and mammalian membrane-bound BDH. Even though the Jaculus orientalis genome has not yet been sequenced, for the first time a D-3-hydroxybutyrate dehydrogenase cDNA from jerboa was cloned and sequenced.ConclusionThis study applies immunoaffinity chromatography to purify BDH, the membrane-bound and lipid-dependent enzyme, as a 31 kDa single polypeptide chain. In addition, bacterial BDH isolation was achieved in a two-step purification procedure, improving the knowledge of an enzyme involved in the lipid metabolism of a unique hibernating mammal. Sequence alignment revealed conserved putative amino acids for possible NAD+ interaction.

Biochemical and histological alterations of cellular metabolism from jerboa ( Jaculus orientalis) by 2,4-dichlorophenoxyacetic acid: Effects on d-3-hydroxybutyrate dehydrogenase

2,4-Dichlorophenoxyacetic acid (2,4D) is one of the widely used herbicide of the phenoxy family with possible startling number of adverse effects on species other than the weeds which is designed to kill. The effects of 2,4D were investigated in jerboa ( Jaculus orientalis), a wild animal of subdesert highlands. The jerboas have been daily treated intraperitonally with 2,4D 3 mg/kg body weight for 4 weeks. Plasmatic markers, and antioxidants defences systems were assessed and histological alterations were evaluated. The in vivo and in vitro effects of 2,4D on the mitochondrial d-3-hydroxybutyrate dehydrogenase (BDH) were also determined. Our results showed a strong decrease of triglycerides level and HDL cholesterol and an increase in GOT level and LDL cholesterol. The microscopic evaluation showed that 2,4D induced necrosis of seminiferous tubules cells in testis, hyperplasia of hepatocytes in liver and presence of multinucleated giant cells in brain. The results show also an inhibitory effect on BDH in terms of activity and kinetic parameters. All of these results show that 2,4D induces toxicity which affects energy metabolism, morphological perturbation and oxidative stress.

Prehibernation and hibernation effects on the d-3-hydroxybutyrate dehydrogenase of the heavy and light mitochondria from liver jerboa ( Jaculus orientalis) and related metabolism

The d-3-hydroxybutyrate dehydrogenase (BDH) (EC 1.1.1.30) from liver jerboa ( Jaculus orientalis), a ketone body converting enzyme in mitochondria, in two populations of mitochondria (heavy and light) has been studied in different jerboa states (euthermic, prehibernating and hibernating). The results reveal: (1) important variations between states in terms of ketones bodies, glucose and lipid levels; (2) significant differences between the BDH of the two mitochondrial populations in term of protein expression and kinetic properties. These results suggest that BDH leads an important conformational change depending on the physiological state of jerboa. This BDH structural change could be the consequence of the lipid composition modifications in inner mitochondrial membrane leading to changes in BDH catalytic properties.

Prehibernation and hibernation effects on D-3-hydroxybutyrate dehydrogenase of heavy and light mitochondria from liver of jerboa (Jaculus orientalis) and related metabolism

Prehibernation and hibernation effects on D-3-hydroxybutyrate dehydrogenase of heavy and light mitochondria from liver of jerboa (Jaculus orientalis) and related metabolism