A Laboratory Breeding Colony of the Lesser Mouse Lemur

2015 ◽  
pp. 161-171 ◽  
Author(s):  
R. D. Martin
1979 ◽  
Vol 27 (6) ◽  
pp. 945 ◽  
Author(s):  
BJ Fox

A laboratory breeding colony of R. l. lutreolus was used to obtain data on the growth in the length of head, hind foot, tail, head and body, and body weight during the first 130 days of life. The development of external body features was compared to that known for other Australian Rattus. The young are blind and naked at birth and are not fully furred until 13 days. Incisors are visible at day 8 (5-11) and erupt about day 12 (8-15) with the eyes opening at 17 days (15-18). Independence was achieved at about 25 days (23-30) with the first signs of reproductive maturity at about 60-70 days. Five stages of growth can be related to developmental features from teeth eruption to puberty and reproductive maturity. The onset of hearing (14-15) days appear to be as important in development as does the opening of the eyes. Body measurements show sigmoid relationships to a linear equivalence of weight (W*0.33), except for head and body length which is linear. R. l. lutreolus belongs to the fast-growing group in Australian murids. Measurements from laboratory-bred animals are in agreement with those for field animals, with head and body length the best single parameter for obtaining approximate ages.


Viruses ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 590
Author(s):  
David Safronetz ◽  
Kyle Rosenke ◽  
Robert J. Fischer ◽  
Rachel A. LaCasse ◽  
Dana P. Scott ◽  
...  

Mastomys natalensis are a ubiquitous and often dominant rodent across sub-Saharan Africa. Importantly, they are a natural reservoir for microbial pathogens including Lassa virus (LASV), the etiological agent of Lassa fever in humans. Lassa-infected rodents have been documented across West Africa and coincide with regions where annual outbreaks occur. Zoonotic transmission to humans most often occurs directly from infected rodents. Little is known about LASV infection kinetics and transmissibility in M.natalensis, primarily due to available animals. Here, we describe the establishment of a laboratory breeding colony of genetically confirmed M.natalensis from wild-captured rodents. This colony will provide a convenient source of animals to study LASV and other emerging pathogens that utilize M. natalensis in their enzootic lifecycles.


2001 ◽  
Vol 35 (2) ◽  
pp. 140-146 ◽  
Author(s):  
R. H. Foote ◽  
E. Hare

Rabbit seminal plasma catalase is much higher than in the semen of other mammals, and differences appear to be inherited. Because of the scarcity of information on rabbit blood catalase and haematocrit in Dutch-belted rabbits, an investigation of possible effects of gender, age and genetics on these variables was undertaken. There were 191 rabbits sampled at 2-3 months, 130 at 12 months and 61 at 18-24 months of age. There was no age effect on the haematocrit values and on blood catalase activity. At 12 months of age males had an average haematocrit value of 44% compared with 40% for females ( P < 0.05). Corresponding average catalase values were 431 and 356 units/ml of blood ( P < 0.05). Also catalase was measured in the semen and blood of 34 males, and males differed in both their blood and semen catalase activity ( P < 0.05). The correlation between the two traits was r = 0.44. Heritability ( h2) estimates, based on 231 rabbits were 0.40 for blood catalase activity, and 0.26 for haematocrit. The genetic correlation between the two variables was 0.83 ( P < 0.05). These studies are consistent with the literature in that female rabbits have a slightly lower haematocrit value than males, and this is associated with a lower catalase activity. This appears to be the first report of a study that compares rabbit blood catalase in males and females of different ages. Preliminary evidence that differences may have a heritable basis is consistent with previous studies on rabbit semen catalase.


2021 ◽  
Author(s):  
David A. Ehlers Smith ◽  
Brent Coverdale ◽  
Ben Hoffman ◽  
Christopher Kelly ◽  
Yvette C. Ehlers Smith ◽  
...  

BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Umit Akkose ◽  
Veysel Ogulcan Kaya ◽  
Laura Lindsey-Boltz ◽  
Zeynep Karagoz ◽  
Adam D. Brown ◽  
...  

Abstract Background Nucleotide excision repair is the primary DNA repair mechanism that removes bulky DNA adducts such as UV-induced pyrimidine dimers. Correspondingly, genome-wide mapping of nucleotide excision repair with eXcision Repair sequencing (XR-seq), provides comprehensive profiling of DNA damage repair. A number of XR-seq experiments at a variety of conditions for different damage types revealed heterogenous repair in the human genome. Although human repair profiles were extensively studied, how repair maps vary between primates is yet to be investigated. Here, we characterized the genome-wide UV-induced damage repair in gray mouse lemur, Microcebus murinus, in comparison to human. Results We derived fibroblast cell lines from mouse lemur, exposed them to UV irradiation, and analyzed the repair events genome-wide using the XR-seq protocol. Mouse lemur repair profiles were analyzed in comparison to the equivalent human fibroblast datasets. We found that overall UV sensitivity, repair efficiency, and transcription-coupled repair levels differ between the two primates. Despite this, comparative analysis of human and mouse lemur fibroblasts revealed that genome-wide repair profiles of the homologous regions are highly correlated, and this correlation is stronger for highly expressed genes. With the inclusion of an additional XR-seq sample derived from another human cell line in the analysis, we found that fibroblasts of the two primates repair UV-induced DNA lesions in a more similar pattern than two distinct human cell lines do. Conclusion Our results suggest that mouse lemurs and humans, and possibly primates in general, share a homologous repair mechanism as well as genomic variance distribution, albeit with their variable repair efficiency. This result also emphasizes the deep homologies of individual tissue types across the eukaryotic phylogeny.


NeuroImage ◽  
2021 ◽  
Vol 226 ◽  
pp. 117589
Author(s):  
Clément M. Garin ◽  
Nachiket A. Nadkarni ◽  
Brigitte Landeau ◽  
Gaël Chételat ◽  
Jean-Luc Picq ◽  
...  
Keyword(s):  

1972 ◽  
Vol 1 (1) ◽  
pp. 3-28 ◽  
Author(s):  
G. Van Wagenen

2016 ◽  
Vol 27 (1) ◽  
pp. 140-152 ◽  
Author(s):  
DANA G. SCHABO ◽  
SONJA HEUNER ◽  
MICHAEL V. NEETHLING ◽  
SASCHA RÖSNER ◽  
ROGER UYS ◽  
...  

SummaryThe number of vultures is declining in many parts of the world due to numerous threats, such as poisoning and collisions with power-lines as well as the lack of adequate food sources. Vulture restaurants, i.e. supplementary feeding stations, have become a widespread conservation tool aimed at supporting vulture colonies. However, it is poorly understood how vulture restaurants influence population dynamics and whether they affect breeding success of vulture populations. We used a 12-year dataset from a breeding colony of the Cape Vulture Gyps coprotheres and a nearby vulture restaurant in South Africa to investigate the effect of supplementary food on population dynamics and breeding success. We found a significantly positive effect of supplementary food during the nest-building stage on the number of breeding pairs. However, breeding success, i.e. the proportion of successful nests, did not depend on supplementary food during the incubation and rearing stage. Especially during the critical rearing stage, the amount of food supplied might not have been sufficient to meet food demands of the colony. Still, our results indicate that carefully managed vulture restaurants might stabilise vulture colonies and can therefore aid vulture conservation.


2010 ◽  
Vol 139 (2) ◽  
pp. 362-381 ◽  
Author(s):  
Christina J. Maranto ◽  
Thomas P. Good ◽  
Francis K. Wiese ◽  
Julia K. Parrish

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