Karsten Neumann

Golden hamsters are nocturnal in captivity but diurnal in nature

Daily activity rhythms are nearly universal among animals and their specific pattern is an adaptation of each species to its ecological niche. Owing to the extremely consistent nocturnal patterns of activity shown by golden hamsters (Mesocricetus auratus) in the laboratory, this species is a prime model for studying the mechanisms controlling circadian rhythms. In contrast to laboratory data, we discovered that female hamsters in the wild were almost exclusively diurnal. These results raise many questions about the ecological variables that shape the activity patterns in golden hamsters and the differences between laboratory and field results.

Notes on the current distribution and the ecology of wild golden hamsters (Mesocricetus auratus)

Two expeditions were carried out during September 1997 and March 1999 to confirm the current existence of Mesocricetus auratus in northern Syria. Six females and seven males were caught at different sites near Aleppo. One female was pregnant and gave birth to six pups. Altogether, 30 burrows were mapped and the structures of 23 golden hamster burrows investigated. None of the inhabited burrows contained more than one adult. Burrow depths ranged from 36 to 106 cm (mean 65 cm). Their structure was simple, consisting of a single vertical entrance (gravity pipe) that proceeded to a nesting chamber and at least one additional food chamber. The mean length of the entire gallery system measured 200 cm and could extend up to 900 cm. Most burrows were found on agricultural fields preferentially on leguminous cultures. The distribution of golden hamsters is discussed in association with historical data, soil types, geography, climate and human activities. All 19 golden hamsters were transferred to Germany and, together with three wild individuals supplied by the University of Aleppo, form a new breeding stock.

Genetic spatial structure of European common hamsters (Cricetus cricetus) — a result of repeated range expansion and demographic bottlenecks

The spatial genetic structure of common hamsters (Cricetus cricetus) was investigated using three partial mitochondrial (mt) genes and 11 nuclear microsatellite loci. All marker systems revealed significant population differentiation across Europe. Hamsters in central and western Europe belong largely to two allopatric mitochondrial lineages south and northwest of the Carpathian and Sudetes. The southern group, ‘Pannonia’, comprises populations inside the Carpathian basin (Czech Republic, Hungary) while the second group, ‘North’, includes hamsters from Belgium, the Netherlands, France, and Germany. Isolation of the lineages is maintained by a combination of geographical and ecological barriers. Both main phylogeographical groups show signs of further subdivision. North is separated into highly polymorphic central German and less polymorphic western populations, which most likely split during late glacial expansion (15 000–10 000 bp). Clock estimates based on haplotype distributions predict a divergence of the two major lineages 85 000–147 000 bp. Expansion times fall during the last glaciation (115 000–10 000 bp) corroborating fossil data, which identify Cricetus cricetus as characteristic of colder climatic phases. Despite the allopatry of mt haplotypes, there is an overlap of nuclear microsatellite alleles between phylogeographical units. Although there are strong evidence that Pannonian hamsters have persisted inside the Carpathian basin over the last 50 000 years, genetic differentiation among European hamsters has mainly been caused by immigration from different eastern refugia. Possible source populations are likely to be found in the Ukrainian and the southern Russian plains — core areas of hamster distribution. From there, hamsters have repeatedly expanded during the Quaternary.

Comparative studies of body mass, body measurements and organ weights of wild-derived and laboratory golden hamsters (Mesocricetus auratus)

All laboratory golden hamsters originate from a sibling pairing back in 1930. To investigate possible differences between domesticated and wild conspecifics, descendants of both strains were maintained under standardized laboratory conditions individually and in unisexual groups. Body mass and food consumption were monitored from birth to 22 weeks of age. The animals were subsequently sacrificed, and body measurements and body composition were analysed. In addition, the absolute and relative masses of different organs were measured. Laboratory hamsters gained more body mass through higher food consumption. However, they did not get fatter, since relative fat values were the same for both strains. Body measurements revealed only minor differences (in body and ear lengths). As deducible from the body mass, the organs (spleen, kidneys, adrenal glands, testes, epididymis and ovaries) were seen to be heavier in laboratory hamsters. Furthermore, with the exception of the kidneys, the same went for the relative values. There were distinct sexual specific differences in both strains only for body fat (♂♂↑) and adrenal glands (♂♂↑). In females, group housing induced an elevated level of aggression. In general, these housing conditions led to social stress symptoms, such as heavier adrenal glands. Additionally, spleen, kidneys, ovaries, body length and mass, body water and body fat were increased in group-housed hamsters. In conclusion, no major differences between laboratory and wild-derived hamsters were observed.

Molecular and immunohistochemical p53 Status in Liposarcoma and Malignant Fibrous Histiocytoma Identification of Seven New Mutations for Soft Tissue Sarcomas

Background. p53 mutations are the most frequently observed tumor‐related genetic changes. Mutational analysis concerns mostly carcinomas and is not comprehensive for soft tissue sarcomas. Among soft tissue sarcomas, malignant fibrous histiocytoma (MFH) and liposarcoma represent the most frequent tumor types. Most of the few identified mutations for soft tissue sarcomas are localized in the core domain of p53. A correlation between p53 positive immunoreactivity, missense mutations, and a poor prognosis is generally assumed. However, the character of p53 mutations and their functional importance for the clinical process is still unknown.

Multiple bottlenecks in threatened western European populations of the common hamster Cricetus cricetus (L.)

Common hamsters Cricetus cricetus (L.)show a highly fragmented distributionpattern across Europe. Over the last decades,human influence caused significant populationdeclines in particular at the western rangeboundary. Despite the initiation of breedingand release programs the genetic structure anddiversity of European common hamsterpopulations is largely unknown. In this study,hamsters from ten localities in five Europeancountries were investigated. Mitochondrialcontrol region was sequenced from 145 animalsrepresenting all sampled populations. 385hamster were screened for polymorphisms at 11microsatellite loci. Both marker systemsrevealed extensive genetic differentiationamong European common hamsters. Westernpopulations displayed very low levels of mtDNAdiversity (H = 0 − 0.2, Alsace, Limburg,Flanders, Baden-Wuerttemberg) compared toeastern populations from Saxony-Anhalt,Thuringia and Southern Moravia (H = 0.663− 0.816). Microsatellite analyses revealed asimilar pattern with low to moderate diversityvalues in western hamsters (A = 1.636 −5.364; He = 0.111 − 0.504) and highlevels of polymorphism in eastern hamsters(A = 8.909 − 9.818; He = 0.712− 0.786). High microsatellite based FSTmeasures (up to 0.635) suggest a typical islandmodel of distribution with no current gene flowbetween most areas. Western hamster populationsexhibit obvious similarities in mitochondrialhaplotype and microsatellite alleledistributions. Gene trees group westernhamsters consistently together on the samebranch but bootstrap values never reachedsignificance. There are strong indications thatlow diversity in western populations ispartially caused by a joint historic founderevent and not only by recent population breakdowns. Overlapping mitochondrial haplotypesprove a close association between westernhamsters and animals from the east German rangein the recent past which does not support theexistence of a separate subspecies C. c.canescens in Europe. Hamsters from southernMoravia emerged as the genetically mostdistinguished population and could be part of a different genetic lineage in Europe.

Differences in reproductive success between laboratory and wild-derived golden hamsters (Mesocricetus auratus) as a consequence of inbreeding

All laboratory golden hamsters (Mesocricetus auratus) originated from a sibling pairing back in 1930. Due to this extreme founder event, domestic golden hamsters are presumed to be one of the most bottlenecked animal populations. Nevertheless, domestic hamsters show no obvious signs of inbreeding depression in commonly used breeding stocks. To explore the existence of potentially masked inbreeding effects, we compared the reproductive success of laboratory (lab) and wild-derived (wild) golden hamsters. We allowed oestrus females to mate consecutively with lab and wild males. The resulting offspring was genotyped using microsatellites to assess paternity. Finally, we compared male reproductive success to genetic variability, sexual behaviour and different sperm characteristics. Both hamster strains exhibited the expected large difference in genetic diversity (Hwild=0.712±0.062 vs Hlab=0.007±0.007. The reproductive success of wild males dramatically exceeded that of lab males (87% of pups were sired by wild males). Sexual behaviour of wild and lab males only varied in the number of long intromissions (intromissions without ejaculation at the end of the mating). No significant differences were observed in relation to mounting, ejaculation and intromission. There were also no apparent differences in sperm motility, velocity and density or testis histology between wild and lab hamsters. We conclude that the reduced reproductive success of lab males represents a hidden inbreeding effect, although its precise physiological cause remains unclear. These results provide first evidence for a major fitness disadvantage in captive golden hamsters.

Characterization of the porcine CDKN3 gene as a potential candidate for congenital splay leg in piglets

Congenital splay leg is a hereditary disease observed in newborn piglets. The etiology and pathogenetic mechanism of the disorder are still unknown. The gene for cyclin-dependent protein kinase inhibitor 3 (CDKN3) was identified as a potential candidate gene in a differential display experiment. We analyzed the gene on sequence variations and compared its expression in M. biceps femoris between healthy and affected piglets. Comparative sequencing of the coding region of three healthy and four splay leg piglets revealed twelve single nucleotide polymorphisms (SNP) resulting in six amino acid exchanges in the deduced sequences. However, all polymorphisms were observed in healthy as well as in splay leg piglets thus excluding structural differences of the gene as a cause of the disease. Besides full length transcripts, we found a variety of aberrantly transcribed cDNA in clones derived from M. biceps femoris of healthy as well as of splay leg piglets. All alternative transcripts coexist with normal cDNA. Expression analysis revealed a trend towards higher values in M. biceps femoris of splay leg piglets supporting the results obtained from a differential display.

BIOMETRIC AND GENETIC EVALUATION OF SPERMOPHILUS (MAMMALIA: RODENTIA) POPULATIONS IN WESTERN TURKEY

Three Spermophilus populations in western Turkey with two different karyotypic forms were analyzed biometrically (NTSYS) and genetically from their 16S rRNA sequence data. Two of these populations, from Turkish Thrace and southwest Anatolia, share the same chromosomal number of 2n = 40 but were previously considered to represent two closely related species, Spermophilus citellus and Spermophilus xanthoprymnus. Our study revealed a high degree of biometric and genetic similarity between these two populations, concluding that both belong to the same species, S. citellus. In contrast, the population from central Anatolia was identified as S. xanthoprymnus, which shows the diploid chromosomal number of 2n = 42 and distinct biometric and genetic differences. UPGMA cluster analysis established the close relationship between S. citellus (Turkish Thrace) and S. citellus (southwest Anatolia) with a distance of 0.84, and S. xanthoprymnus connected to this cluster with a distance of 0.93. The similar cluster was als...