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1.
Zoonoses Public Health ; 61(2): 113-23, 2014 Mar.
Article in English | MEDLINE | ID: mdl-23672285

ABSTRACT

Leptospirosis is the most widespread zoonosis in the world. In northern Botswana, humans live in close proximity to a diversity of wildlife and peridomestic rodents and may be exposed to a variety of zoonotic pathogens. Little is known regarding the occurrence and epidemiology of L. interrogans in Africa despite the recognized global importance of this zoonotic disease and the threat it poses to public health. In Botswana, banded mongooses (Mungos mungo) live in close proximity to humans across protected and unprotected landscapes and may be a useful sentinel species for assessing the occurrence of zoonotic organisms, such as L. interrogans. We utilized PCR to screen banded mongoose kidneys for leptospiral DNA and identified 41.5% prevalence of renal carriage of L. interrogans (exact binomial 95% CI 27.7-56.7%, n = 41). Renal carriage was also detected in one Selous' mongoose (Paracynictis selousi). This is the first published confirmation of carriage of L. interrogans in either species. This is also the first report of L. interrogans occurrence in northern Botswana and the only report of this organism in a wildlife host in the country. Pathogenic Leptospira are usually transmitted indirectly to humans through soil or water contaminated with infected urine. Other avenues, such as direct contact between humans and wildlife, as well as consumption of mongooses and other wildlife as bushmeat, may pose additional exposure risk and must be considered in public health management of this newly identified zoonotic disease threat. There is a critical need to characterize host species involvement and pathogen transmission dynamics, including human-wildlife interactions that may increase human exposure potential and infection risk. We recommend that public health strategy be modified to include sensitization of medical practitioners to the presence of L. interrogans in the region, the potential for human infection, and implementation of clinical screening. This study illustrates the need for increased focus on neglected zoonotic diseases as they present an important threat to public health.


Subject(s)
Communicable Diseases, Emerging/epidemiology , Herpestidae/microbiology , Leptospira interrogans/isolation & purification , Leptospirosis/epidemiology , Meat/microbiology , Animals , Base Sequence , Botswana/epidemiology , Communicable Diseases, Emerging/microbiology , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Female , Geography , Host Specificity , Humans , Leptospira interrogans/genetics , Leptospirosis/microbiology , Leptospirosis/transmission , Male , Molecular Sequence Data , Polymerase Chain Reaction/veterinary , Prevalence , Public Health , Sequence Alignment/veterinary , Sequence Analysis, DNA/veterinary , Zoonoses
2.
Cytogenet Genome Res ; 127(1): 21-5, 2009.
Article in English | MEDLINE | ID: mdl-19940438

ABSTRACT

The tammar wallaby (Macropus eugenii) is a model marsupial that has recently had its genome sequenced to a depth of 2-fold coverage. Although this is a great resource for comparative genomic studies, information on gene location is essential if this resource is to be used to its full potential. In this study, tammar wallaby bacterial artificial chromosomes (BACs) containing key immune genes were isolated from the tammar wallaby BAC library. BACs containing T cell receptor (TCR) and immunoglobulin (Ig) genes were physically mapped using fluorescence in situ hybridisation (FISH) to tammar wallaby chromosomes. Congruence between the locations of these immune genes in the tammar wallaby genome, with those predicted from chromosome painting data, highlights the conservation of genomic context of these important immune genes in marsupials. The isolation and mapping of these key immune genes in the tammar wallaby will aid in the assembly of the recently sequenced light coverage genome and assignment of sequence to chromosomes.


Subject(s)
Chromosomes, Mammalian , Immunoglobulins/genetics , Macropodidae/genetics , Receptors, Antigen, T-Cell/genetics , Animals , Chromosomes, Artificial, Bacterial , Databases, Nucleic Acid , Immunoglobulins/isolation & purification , In Situ Hybridization, Fluorescence , Physical Chromosome Mapping , Receptors, Antigen, T-Cell/isolation & purification
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