The role of the veterinary staff in mouse breeding colony management

The rapid increase in the production and use of transgenic mice has been a boon for biomedical research and a challenge for the animal care and use programs responsible for providing housing and medical care to these animals. The authors suggest ways in which the veterinary staff can successfully organize and manage transgenic mouse breeding programs to reduce uncontrolled breeding and the problems associated with it.     

An attempt for eradication of Sendai virus from a mouse breeding colony

Eradication of Sendai virus from an infected mouse breeding colony was successfully made by sacrificing all offspring younger than 5 weeks of age at a time and then newborns as well as severely affected breeder mice for successive 2 weeks. By this method, number of breeders decreased of two third of those in the original colony but recovered again about 2 months later.     

A visual display board used for efficient breeding and utilization of an athymic (nude) mouse colony.

A visual display board was designed to aid in the management of a barrier sustained athymic (nude) mouse colony. The board displayed pertinent information for breeding and weaning, including phenotype and age for each animal in the colony. In addition, the board showed the availability and current status of experimental groups. This system provided an efficient means of organizing production and planning utilization of animals in the colony.     

Reproduction and survival of Glaucous Gulls breeding in an Arctic seabird colony

ABSTRACT.   Despite being widespread and easily observed, little is known about the life history of Glaucous Gulls ( Larus hyperboreus ). From 1984 to 2007, we examined their breeding biology and demography at Coats Island, Nunavut, Canada, where they nest alongside a colony of 30,000 pairs of Thick-billed Murres ( Uria lomvia ). The gulls fed mainly on murre eggs and chicks and by scavenging adult carcasses. The median age at first breeding was 5 yr, and the mean age was 4.8 ± 0.9 yr. Adult survival was estimated as 0.84 ± 0.03 (SE). The mean clutch size was 2.56 eggs and the mean number of young reared per year was 1.6 (range = 0.9–2.2). Birds reared at the colony provided 40% of recruits. Assuming that survival of locally reared chicks that emigrated was similar to that of chicks that returned to the colony, about 22% of the young gulls survived to breeding age. The timing of breeding by Glaucous Gulls appeared related to the timing of laying by murres. Although the demographic characteristics of Glaucous Gulls in our study were similar to those of populations of other large gulls, adult survival was at the lower end of the range for populations of large Larus gulls. There is some evidence that Glaucous Gulls exhibit lower survival than large gulls breeding in temperate areas, possibly because of contaminant burdens. In general, however, the demographic characteristics of large gulls show little variation and are probably a product of their common phylogeny.     

Immunogenetic aspects of a canine breeding colony

A colony of dogs was expanded by selective breeding to study the immunogenetic determinants coded for by the major histocompatibility complex (DLA). Polymorphic determinants were identified by alloantisera specific for DLA-A and B loci antigens and by the mixed lymphocyte culture (MLC) which defined alleles at the D locus. Thirteen families totaling 58 offspring were produced and typed for allelic determinants coded for by each of the three gene loci. Allelic segregation in a codominant manner occurred as expected and a recombinant between the A and B loci was detected. A number of animals were homozygous at one or more loci, thus providing genetically standardized animals as a source of typing cells, antigens, and sera to further study the immunogenetic details of DLA and for in vivo studies in transplantation biology.     

Establishment of a Chinese hamster breeding colony

A colony of outbred Chinese hamsters, Cricetulus griseus, was established. Attempts to use previously published methods of physically protecting the males were unsatisfactory. Rather, females were selected for nonaggressive behavior. Breeding was among pairs allowed to cohabit for 5 1/2 days. Production was typically in excess of 180 offspring per month, with an average breeder population of 44 females and 30 males. Litters were weaned at 3 weeks of age. At that time, appropriate numbers of offspring of female parents with a history including nonaggressive behavior, fecundity and freedom from seizures were retained for use as future breeders. Females were first bred at 8-12 weeks of age and males at 8-12 months. The remaining animals were maintained in groups of like-sex littermates until used. With these methods, mortality among breeder males due to overly aggressive female behavior was reduced to 3%. Animal husbandry procedures and record keeping requirements were relatively simple, not labor intensive and would be easily adaptable to most facilities.     

Successful cryopreservation of mouse ovaries by vitrification

We developed a new method of cryopreservation of whole ovaries by vitrification using DAP213 (2 M dimethyl sulfoxide, 1 M acetamide, and M propylene glycol) as a cryoprotectant. Four-week-old C57BL/6 mice that underwent partial ovariectomy were orthotopically transplanted with cryopreserved or fresh ovaries (experimental or control group) isolated from 10-day-old green fluorescent protein (GFP)-transgenic mice (+/+). GFP-positive pups were similarly obtained from both groups by natural mating or in vitro fertilization (IVF) followed by embryo transfer, indicating that the cryopreserved ovaries by vitrification retain their fecundity. However, a statistically significant difference (P < 0.05) was found between both groups with respect to the following parameters: the number of GFP-positive pups born by natural mating/grafted ovary (0.8 +/- 0.3 for the experimental group versus 2.0 +/- 0.7 for the control group, mean +/- SEM), the number of collected oocytes by superovulation per mouse (7.0 +/- 1.7 for the experimental group versus 22.7 +/- 3.2 for the control group), the percentage of two-cell embryos obtained from GFP-positive oocytes by IVF (38.5% for the experimental group versus 90.0% for the control group). Histologically, normal development of follicles and formation of corpora lutea were observed in frozen-thawed grafts. However, estimated number of follicles decreased in frozen-thawed ovaries compared with fresh ovaries. Taken together, cryopreservation of the ovary by vitrification seems a promising method to preserve ovarian function, but further studies are required to overcome the possible inhibitory effects of this method on the growth of the ovarian graft.     

Establishment of small breeding colony of rhesus monkeys.

A breeding colony of 22 female and 4 male rhesus monkeys (Macaca mulatta) was established in a controlled-environment building with an outdoor run. The animals were quarantined for 2 years prior to their release into the unit. The housing, release and management of the colony are described. During the first year 19 young were born of which 17 have survived to 6 months of age. The cost of production and maintenance of the colony when compared with the cost of importing rhesus monkeys would appear to be acceptable.     

Frequency of prenatal loss in a macaque breeding colony

An accurate knowledge of the historical incidence of prenatal loss is essential for management of breeding colonies and for performing developmental toxicity studies in nonhuman primates. Data from the California Regional Primate Research Center indoor (timed-mated) and outdoor (random-mated) colonies of rhesus, cynomolgus, and bonnet macaques (Macaca mulatta, M. fascicularis, and M. radiata) were evaluated for a 10 year breeding period from 1984 to 1993. Pregnancy outcome data for the three species of macaques summarized in this report indicate that early pregnancy as well as term are vulnerable periods of gestation in terms of prenatal loss. Prematurity as well as twinning were additionally associated with elevated rates of loss during the prenatal or neonatal period. The incidence of pregnancy failure did not appear to be related to different housing/management conditions (i.e., indoor timed-mated vs. outdoor random-mated), parity, animal handling, shipping, or relocation. Some of the annual fluctuations in abortions could be related to disease outbreaks (e.g., measles, pneumonia) in the colony. These data will be invaluable in planning for research needs which focus on developmental biology and perinatology, and in interpreting the significance of abortions following exposure to experimental agents in small numbers of animals. © 1996 Wiley-Liss, Inc.     

Stimulation by normal and leukemic mouse sera of colony formation in vitro by mouse bone marrow cells

Using a modification of the agar gel method for bone marrow culture, serum from various strains of mice has been tested for colony stimulating activity. Ninety percent of sera from AKR mice with spontaneous or transplanted lymphoid leukemia and 40–50% of sera from normal or preleukemic AKR mice stimulated colony formation by C57B1 bone marrow cells. Sera from 6% of C3H and 30% of C57B1 mice stimulated similar colony formation. The incidence of sera with colony stimulating activity rose with increasing age. All colonies were initially mainly granulocytic in nature but later became pure populations of mononuclear cells. Bone marrow cells exhibited considerable variation in their responsiveness to stimulation by mouse serum. Increasing the serum dose increased the number and size of bone marrow cell colonies and with optimal serum doses, 1 in 1000 bone marrow cells formed a cell colony. Preincubation of cells with active serum did not stimulate colony formation by washed bone marrow cells. The active factor in serum was filterable, non-dialysable and heat and ether labile.