Genetic susceptibility to infectious disease: lessons from mouse models of leishmaniasis
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
16543933
DOI
10.1038/nrg1832
PII: nrg1832
Knihovny.cz E-resources
- MeSH
- Genetic Predisposition to Disease genetics MeSH
- Communicable Diseases genetics MeSH
- Leishmania pathogenicity MeSH
- Leishmaniasis genetics immunology parasitology MeSH
- Humans MeSH
- Quantitative Trait Loci * MeSH
- Disease Models, Animal MeSH
- Mice MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
Susceptibility to infectious disease is influenced by multiple host genes, most of which are low penetrance QTLs that are difficult to map in humans. Leishmaniasis is a well-studied infectious disease with a variety of symptoms and well-defined immunological features. Mouse models of this disease have revealed more than 20 QTLs as being susceptibility genes, studies of which have made important contributions to our understanding of the host response to infection. The functional effects of individual QTLs differ widely, indicating a networked regulation of these effects. Several of these QTLs probably also influence susceptibility to other infections, indicating that their characterization will contribute to our understanding of susceptibility to infectious disease in general.
References provided by Crossref.org
Effects of Leishmania major infection on the gut microbiome of resistant and susceptible mice
Gene-Specific Sex Effects on Susceptibility to Infectious Diseases
Genetic Regulation of Guanylate-Binding Proteins 2b and 5 during Leishmaniasis in Mice
Gene-specific sex effects on eosinophil infiltration in leishmaniasis
Mapping the genes for susceptibility and response to Leishmania tropica in mouse
Genetic control of resistance to Trypanosoma brucei brucei infection in mice
Leishmania parasite detection and quantification using PCR-ELISA
Mouse to human comparative genetics reveals a novel immunoglobulin E-controlling locus on Hsa8q12