The burden of leptospirosis in humans and animals in Africa is higher than that reported from other parts of the world. However, the disease is not routinely diagnosed in the continent. One of major factors limiting diagnosis is the poor availability of live isolates of locally circulating Leptospira serovars for inclusion in the antigen panel of the gold standard microscopic agglutination test (MAT) for detecting antibodies against leptospirosis. To gain insight in Leptospira serovars and their natural hosts occurring in Tanzania, concomitantly enabling the improvement of the MAT by inclusion of fresh local isolates, a total of 52 Leptospira isolates were obtained from fresh urine and kidney homogenates, collected between 1996 and 2006 from small mammals, cattle and pigs. Isolates were identified by serogrouping, cross agglutination absorption test (CAAT), and molecular typing. Common Leptospira serovars with their respective animal hosts were: Sokoine (cattle and rodents); Kenya (rodents and shrews); Mwogolo (rodents); Lora (rodents); Qunjian (rodent); serogroup Grippotyphosa (cattle); and an unknown serogroup from pigs. Inclusion of local serovars particularly serovar Sokoine in MAT revealed a 10-fold increase in leptospirosis prevalence in Tanzania from 1.9% to 16.9% in rodents and 0.26% to 10.75% in humans. This indicates that local serovars are useful for diagnosis of human and animal leptospirosis in Tanzania and other African countries.
The availability of resources, their effect on population density and territoriality, and the ways in which these factors are interwoven with mating systems are important determinants of small mammal space use. It is often difficult to study these patterns in an integrated way, however, especially because long‐term data are needed but not readily available. In this paper, we investigate effects of population density, season and breeding status on home range patterns of the promiscuous rodent Mastomys natalensis using monthly capture‐mark‐recapture data collected over 17 years in a 3‐ha grid. Home ranges were estimated using minimum convex polygons bounded by trap locations, and home range overlap and visitation rates were calculated as a measure of territoriality. As higher population densities coincide with increased resource availability, we predicted that home range sizes would correlate negatively with density. Furthermore, as M. natalensis is promiscuous and population densities are generally high, we predicted that territoriality would be low, and home range overlap would therefore be high. Contrary to expectations the home ranges of female adults increased with population density, although those of male adults and subadults followed the expected decrease. Home range overlap and visitation rates were generally high, and increased significantly with population density. More importantly, they were never lower than those of simulated datasets consisting of randomly moved home ranges. These results therefore suggest that M. natalensis displays a complete lack of territoriality that is rarely seen in small mammals but still meets predictions based on knowledge of density and mating system.
With the rising number of patients with human immunodeficiency virus (HIV)/AIDS in developing countries, the control of mycobacteria is of growing importance. Previous studies have shown that rodents and insectivores are carriers of mycobacteria. However, it is not clear how widespread mycobacteria are in these animals and what their role is in spreading them. Therefore, the prevalence of mycobacteria in rodents and insectivores was studied in and around Morogoro, Tanzania. Live rodents were trapped, with three types of live traps, in three habitats. Pieces of organs were pooled per habitat, species, and organ type (stratified pooling); these sample pools were examined for the presence of mycobacteria by PCR, microscopy, and culture methods. The mycobacterial isolates were identified using phenotypic techniques and sequencing. In total, 708 small mammals were collected, 31 of which were shrews. By pool prevalence estimation, 2.65% of the animals were carriers of mycobacteria, with a higher prevalence in the urban areas and in Cricetomys gambianus and the insectivore Crocidura hirta. Nontuberculous mycobacteria (Mycobacterium chimaera, M. intracellulare, M. arupense, M. parascrofulaceum, and Mycobacterium spp.) were isolated from C. gambianus, Mastomys natalensis, and C. hirta. This study is the first to report findings of mycobacteria in African rodents and insectivores and the first in mycobacterial ecology to estimate the prevalence of mycobacteria after stratified pool screening. The fact that small mammals in urban areas carry more mycobacteria than those in the fields and that potentially pathogenic mycobacteria were isolated identifies a risk for other animals and humans, especially HIV/AIDS patients, that have a weakened immune system.
A serosurvey involving 2,520 small mammals from Tanzania identified a hot spot of arenavirus circulation in Morogoro. Molecular screening detected a new arenavirus in Natal multimammate mice (Mastomys natalensis), Morogoro virus, related to Mopeia virus. Only a small percentage of mice carry Morogoro virus, although a large proportion shows specific antibodies.
This study investigated mammalian involvement in an outbreak of bubonic plague in Mbulu District, northern Tanzania, in March 2007. Plague is a rodent-borne zoonotic disease that spreads to humans through fleas infected with Yersinia pestis. Live trapping of rodents and shrews was conducted in fallow and crop fields, peridomestic areas, houses and the neighboring forest reserve. Serum was separated from blood of captured animals. A rapid diagnostic test (RDT) was used for diagnosis of plague infection. An ELISA technique was used to detect antibodies against Yersinia pestis fraction 1 antigen. Wild and commensal rodents tested positive by RDT, indicating current infection in clinically healthy animals. The ELISA showed that wild rodents (Lophuromys flavopunctatus, Praomys delectorum, Graphiurus murinus, Lemniscomys striatus) and commensal rats (Rattus rattus, Mastomys natalensis, Mus minutoides) were Y. pestis-positive. Two potential vectors, Xenopsylla brasiliensis and Dinopsyllus lypusus, were found on wild and commensal rodents with a flea index of 1.8. We conclude that diverse potential mammalian reservoirs and efficient vectors of Y. pestis are present in abundance in Dongobesh and could lead to persistence and future plague outbreaks.
Rodent population dynamics during the study periods in all habitats indicated that high birth rates accounted for the rapid population growth and turnover. Regular control and sustainable operations are thus essential if rodent pest populations are to be kept within tolerable limits.
This study did not indicate that transmission of antibiotic resistant bacteria is a frequent event following co-grazing of wild life and cattle.
A Capture‐Mark‐Recapture study was undertaken in Central Tanzania to compare variations in community structure and population dynamics of rodents in two types of habitats. The study was conducted in fallow field mosaic habitat dominated by perennial and annual grasses (grid BEA) and a more heterogeneous habitat (grid BEB) which was previously woodland cleared of most trees with vegetation dominated by shrubs, bushes, scattered trees and perennial grass. The relative abundance of rodents in BEA was: Mastomys natalensis (73.5%) > Aethomys chrysophilus (8.9%) > Gerbilliscus vicina (7.3%) > Arvicanthis neumanni (6.1%) > Acomys spinosissimus (4.1%) and for grid BEB: M. natalensis (67.6%) > G. vicina (11.2%) > A. neumanni (10.3%) > A. chrysophilus (7.6%) > A. spinosissimus (2.9%). Graphiurus sp., Mus minutoides, Saccostomus mearnsi, Lemniscomys striatus and L. griselda were rare and only occasionally trapped in BEB. Spatial variations in population density were non‐significant except for A. chrysophilus. Significant temporal variations within grids were observed, with synchrony of population peaks for some species. The rare species boosted species richness of grid BEB rather artificially, without significantly contributing to higher species diversity. Temporal variations in Simpson’s Diversity indices between grids were non‐significant except for three out of twenty‐one trapping sessions.
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