Food availability and secondary sex ratio variation in wild and laboratory house mice (Mus musculus)

Female house mice deprived of food intermittently for 1 week before mating gave birth to fewer male young, but litters of females deprived of food for 2 weeks did not differ from control litters. Since mean weights of females did not differ between the two treatments, our results suggest that females were initially stressed by food deprivation, but recovered in the second week.     

Cryptosporidium tyzzeri and Cryptosporidium muris originated from wild West-European house mice (Mus musculus domesticus) and East-European house mice (Mus musculus musculus) are non-infectious for pigs

Three and 8 week old pigs were inoculated with Cryptosporidium muris HZ206 (Mus musculus musculus isolate), Cryptosporidium tyzerri CR2090 (M. m. musculus isolate) or C. tyzzeri CR4293 (isolate from a hybrid between Mus musculus domesticus and M. m. musculus) at a dose of 1 × 10(7) oocysts per animal. Inoculated pigs showed no detectable infection and no clinical symptoms of cryptosporidiosis during 30 days post infection (DPI), and no macroscopic changes were detected in the digestive tract following necropsy. Developmental stages were not detected in gastrointestinal tract tissue by histology or PCR throughout the duration of the experiment. The infectivity of isolates was verified on SCID mice, in which oocysts shedding started from 4 to 8 DPI. Based on our findings, it can be concluded that pigs are not susceptible to C. muris or C. tyzzeri infection.     

Norwegian house mice (Mus musculus musculus/domesticus): distributions, routes of colonization and patterns of hybridization

We investigated the distributions and routes of colonization of two commensal subspecies of house mouse in Norway: Mus musculus domesticus and M. m. musculus. Five nuclear markers (Abpa, D11 cenB2, Btk, SMCY and Zfy2) and a morphological feature (tail length) were used to differentiate the two subspecies and assess their distributions, and mitochondrial (mt) D‐loop sequences helped to elucidate their colonization history. M. m. domesticus is the more widespread of the two subspecies, occupying the western and southern coast of Norway, while M. m. musculus is found along Norway’s southeastern coast and east from there to Sweden. Two sections of the hybrid zone between the two subspecies were localized in Norway. However, hybrid forms also occur well away from that hybrid zone, the most prevalent of which are mice with a M. m. musculus‐type Y chromosome and an otherwise M. m. domesticus genome. MtDNA D‐loop sequences of the mice revealed a complex phylogeography within M. m. domesticus, reflecting passive human transport to Norway, probably during the Viking period. M. m. musculus may have colonized earlier. If so, that leaves open the possibility that M. m. domesticus replaced M. m. musculus from much of Norway, with the widely distributed hybrids a relict of this process. Overall, the effects of hybridization are evident in house mice throughout Norway.     

Social domination and reproductive success in male laboratory mice (Mus musculus)

The task of the present study was to evaluate effect of social status and of genotype on success of reproduction of male laboratory mice with use of ethological model of social hierarchy of “minimal socium”. The model represents the paired maintenance of two male mice of different genotypes (PT and CBA/Lac). The mice resided for 30 days in one experimental cage and established between them the dominant-subordinant relations. After this, each pair of males was supplemented by two DD/He females. Regardless of their genotype, the dominants became fathers more often than the subordinants and left more offspring. It has been established that the complete suppression of fertility did not occur. It is suggested that this allows them to make genetic contribution to the next generation and to remain in the genetic pool of population.     

Chromosomes and speciation in Mus musculus domesticus

Thirty years after its identification, the model of chromosomal speciation in Mus musculus domesticus is reevaluated using the methods of population biology, molecular cytogenetics and functional genomics. Three main points are considered: (1) the structural predisposition of M. m. domesticus chromosomes to Robertsonian fusion; (2) the impediment of structural heterozygosity to gene flow between populations of mice with karyotypes rearranged by Robertsonian fusion and between them and populations with the standard all-acrocentric 40-chromosome karyotype; (3) the selective advantage of chromosomal novelty, essential for the attainment of homozygosis and the rapid fixation of the new karyotype in the population.     

Solitary and social play in wild Mus musculus (Mammalia)

Play behaviour was observed in wild caught Mus musculus housed in a semi-natural environment. The behaviour of interest (1) is very exaggerated and jerky in appearance. (2) occurs almost exclusively in highly enriched areas of the observation room, (3) disappears under stressful conditions and (4) occurs primarily in juveniles. Solitary and social play were observed. Aggressive and pouncing play were the two major types of social play seen. Juveniles were found to play with littermates significantly more often than with non-littermates but did not show a significant preference with respect to the sex of their play partners.     

Intermittent stimulation and acceleration of puberty by urinary chemosignals in female mice (Mus musculus domesticus)

A sequence of 17 experiments was used to test the effects of intermittent stimulation with urinary chemosignals on the age of puberty in young female mice. The three chemosignals tested all accelerate the age of sexual maturation: urine from adult males, urine from females in estrus, and urine from females that are pregnant or lactating. The basic technique involved presenting the prepubertal females with 'Nestlets' on which the urine was placed. The 'Nestlets' were placed in the cages of the test females for a 15-min period, removed for a variable period, and then replaced in the cage for 15 min. In this manner it was possible to vary the number of exposures, the total length of exposure, and the total time period over which the exposures occurred. Control procedures, involving exposures of young females to cotton squares with water rather than urine placed upon them, resulted in no alterations in puberty relative to untreated females. For mice exposed to the urine-treated cotton squares, acceleration of puberty occurred with less total stimulus-exposure time when the stimulus was presented in short exposures over a number of hours than in previous investigations when the exposure to the urinary chemosignal occurred in a single block of time of one or two hours. For each of the three acceleratory chemosignals, there was a diminution of acceleratory effect when the ratio of total stimulus-exposure time to total exposure time grew smaller. This diminution was more pronounced for urine from pregnant or lactating females than for urine from males or from females in estrus.(ABSTRACT TRUNCATED AT 250 WORDS)     

Seasonal variation in fertility, fecundity and litter sex ratio in laboratory and wild stocks of house mice (Mus domesticus)

Data compilations were made for three parameters pertaining to reproduction in a domestic strain (14 years) and a wild stock (4 years) of commensal house mice: (a) the percentage of females mated that produced litters; (b) the average number of pups per litter; and (c) the sex ratio of the pups in the litters. Fecundity and fertility varied seasonally in both domestic and wild mice. More females become pregnant and litter sizes were larger in the spring, summer, and fall months than during the winter season. Sex ratios also varied seasonally with more male biased litters produced during the 4 winter months. There appear to be seasonal shifts in productivity for both stocks of mice and these seasonal trends have not been altered by domestication under laboratory conditions. In spite of the fact that house mice are generally opportunistic, it is possible that there has been selection in the mice for shifting rates of production in relation to the best seasons of the year in terms of climate and resource availability. The higher production of males during summer months may be geared toward greater success in dispersal at that season and a higher probability that the males can find a territory and mate successfully in summer rather than winter. These results have potential implications for animal breeders and for those who maintain mouse colonies to produce animals for scientific investigations.     

Use of the MHC for mate choice in wild house mice (Mus domesticus)

The mechanisms maintaining natural diversity at the major histocompatibility complex (MHC) are not well understood. To increase knowledge of one potential mechanism, I examined the use of MHC genes for mate choice by wild house mice in a controlled laboratory setting. Three rearing groups of wild test mice were produced: non‐fostered control mice, mice fostered into families of an inbred laboratory mouse strain, and mice fostered into families of a second, MHC‐congenic mouse strain. Mature test mice were given a choice of two opposite‐sex stimulus mice from the two MHC‐congenic strains used for fostering, and were scored for several measures of preference. The results were non‐significant in general, but females of two rearing groups spent significantly more time with mice of one MHC‐type, and in most rearing groups, mice tended to spend more time with this same MHC‐type. Other results showed that male test mice ejaculated indiscriminantly and that female wild mice mated to ejaculation more often in longer length trials, but showed no significant preferences. In this study, fostering seemed to have little or no effect on MHC‐based mate preferences of wild house mice, and wild mice did not appear to be using the MHC to avoid inbreeding. However, some wild female mice used the MHC to choose potential mates. This revised version was published online in July 2006 with corrections to the Cover Date.     

Aggressive behaviour in related and unrelated wild house mice (Mus musculus L.)

Aggressive behaviour was observed to be rare in small family groups of confined wild house mice, Mus musculus L. Unrelated mice were attacked when they were introduced to a family group and in their presence intra-family aggressive behaviour increased. When two family groups of mice were allowed to meet there were frequent aggressive encounters between unrelated animals and the two groups remained separate. Resident mice were found to be aggressive towards males and females individually isolated and returned to their own family after 2 or 3 weeks absence but not after 1 week. The possibility is discussed that in wild mice odour discrimination influences the dispersal and build-up of free-living populations.     

A tail length modifier gene discovered in the Japanese wild mice (Mus musculus molossinus)

The presence of the t haplotypes in strains derived from the Japanese wild mice (Mus musculus molossinus) was investigated. Crosses between the T/+ heterozygous short tailed mice and five normal tailed molossinus strains (MOL-ANJ, MOA, MOL-NEM, MOM and Mns) produced no tailless mice, indicating that these strains possess no t haplotype. In contrast, tailless mice were produced by a cross between the T/+ heterozygotes and a MOL-NIS strain. Mating experiments showed that the tailless character was due to an interaction between the T gene and an autosomal recessive gene carried by the MOL-NIS strain that expresses the short tail character under the homozygous condition. We have tentatively named this gene brachyury-interacting tail length modifier (btm). It remains to be investigated whether the btm gene is located in the t complex region or in the other locus.     

Measures of immune function of wild mice, Mus musculus

The immune function of wild animals has been rather little studied. Wild animals' immune function may differ from that of laboratory bred animals because of their different environments. This idea follows from the concept of resource partitioning in which animals distribute scarce resources to all aspects of life, including to costly immune responses. A logical extension of this idea is that there may be substantial interindividual variation in the immune function of wild animals. To begin to investigate this, we compared the immune function of a laboratory bred mouse strain (C57BL/6, a widely used mouse strain that makes potent immune responses) and wild caught Mus musculus. We found that by most measures of immune function, the wild caught mice had greater immune function. Specifically, wild mice had greater concentrations and more avid antigen-specific IgG responses, as well as higher concentrations of total IgG and IgE, compared with those laboratory bred mice. Moreover, flow cytometric analysis showed a comparatively greater overall level of activation of the cells of the immune system in wild mice. Lastly, we observed that immune function was substantially more variable among wild caught mice than among the laboratory bred mice. The next research challenge is to understand which aspects of an individual animal's life determine its immune function.     

Town Mouse, Country Mouse: adaptation and adaptability in Mus domesticus (M. musculus domesticus)

The generally accepted idea that the house mouse is a single, world-wide species which owes its success largely to commensalism with man is wrong. There are at least five European and two Asian species lumped together under the name Mus musculus, plus another fourteen Asian species in the same genus. The house mouse of western Europe is the one that has been introduced to the Americas and Australasia, as well as being domesticated in the laboratory and ‘fancy’ strains; it is properly described as Mus domesticus. A complication of this particular species is the existence of chromosomal races involving the fusion of pairs of chromosomes, apparently at random. These races seem to be reproductively isolated from normal (2n = 40) mice. They have been described in southern Europe and northern Britain. Genetical studies of wild-living mice have shown the operation of powerful natural selection, contrary to earlier assumptions that most of the polymorphic variation in the species (especially that revealed by electrophoresis) was neutral. The effects of such selection are reduced (but not eliminated) by the deme structure of established mouse populations; this social structure is much less rigid than some laboratory experiments have suggested, because of opportunism by individual mice in replacing dead or debilitated animals, and filling new niches as these become available. Virtually every mouse population is unique, since a population tends to be founded by a small group of animals drawn from a genetically variable ancestral population. This differentiation has allowed laboratory workers to develop inbred strains with characteristic properties; it has also resulted in over 130 sub-species being described from wild caught animals. A substantial proportion of these latter have probably arisen by instant sub-speciation through the founder effect. This is well illustrated by the mice of the Faroe islands, which are often quoted as standard examples of extremely rapid evolution. The adaptive properties of the house mouse that have made it such an effective pest and such a good laboratory animal have enabled it to colonize habitats as different as Antarctic tundra and tropical atolls. The species is an ideal one for the general biological task of dissecting the traits that contribute to this adaptability; the material is largely available for this task in the diversity of local forms established in different habitats and characterized genetical varieties maintained in the laboratory. More is known about M. domesticus than any other mammal, except possibly man; the time is ripe for fusing laboratory work on reproduction, mortality, and behaviour with the information increasingly coming from field studies of wild-living animals.     

Serological survey of virus infection among wild house mice (Mus domesticus) in the UK

The serological prevalence of 13 murine viruses was surveyed among 103 wild-caught and 51 captive-bred house mice (Mus domesticus), originating from several trapping locations in northwest England, using blood samples obtained during routine health screening of an established wild mouse colony. A high proportion of recently caught wild mice were seropositive for mouse hepatitis virus (86%), mouse cytomegalovirus (79%), mouse thymic virus (78%), mouse adenovirus (68%), mouse parvovirus (59%) and minute virus of mice (41%). Seroprevalences of lymphocytic choriomeningitis virus (LCMV), orthopoxvirus, reovirus-3 and murid herpesvirus 4 (MuHV-4, also called murine gamma-herpesvirus [MHV-68]) were low (3-13%), and no animals were seropositive to Sendai virus, pneumonia virus or polyomavirus. Seroprevalence in wild-caught animals that had been in captivity for over six months was generally consistent with the range found in recently caught wild animals, while seroprevalence was generally much lower in captive-bred mice despite no attempt to prevent viral spread. A notable exception to this was LCMV, which appeared to have spread efficiently through the captive population (both captive-bred and wild-caught animals). Given the known viral life cycles in laboratory mice, it appears that viral persistence in the host was an important contributing factor in the spread of infection in captivity.