4.5 Article

Clonal and atypical Toxoplasma strain differences in virulence vary with mouse sub-species

期刊

INTERNATIONAL JOURNAL FOR PARASITOLOGY
卷 49, 期 1, 页码 63-70

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ijpara.2018.08.007

关键词

Toxoplasma gondii; Mouse sub-species; Wild-derived mice; Host-parasite interactions; ROP5; ROP18

资金

  1. University of Edinburgh Chancellor's Fellowship
  2. Bill and Melinda Gates Foundation [OPP1127286]
  3. Biotechnology and Biological Sciences Research Council
  4. National Institute of Health [NIH R01AI080621]
  5. Cancer Research UK [FC001076]
  6. UK Medical Research Council [FC001076]
  7. Wellcome Trust [FC001076]
  8. BBSRC [BBS/E/D/20002173] Funding Source: UKRI
  9. MRC [MC_UP_1202/12] Funding Source: UKRI
  10. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI080621] Funding Source: NIH RePORTER

向作者/读者索取更多资源

The severe virulence of Toxoplasma gondii in classical laboratory inbred mouse strains contradicts the hypothesis that house mice (Mus musculus) are the most important intermediate hosts for its transmission and evolution because death of the mouse before parasite transmission equals death of the parasite. However, the classical laboratory inbred mouse strains (Mus musculus domesticus), commonly used to test Toxoplasma strain differences in virulence, do not capture the genetic diversity within Mus musculus. Thus, it is possible that Toxoplasma strains that are severely virulent in laboratory inbred mice are avirulent in some other mouse sub-species. Here, we present insight into the responses of individual mouse strains, representing strains of the genetically divergent Mus musculus musculus, Mus musculus castaneus and Mus musculus domesticus, to infection with individual clonal and atypical Toxoplasma strains. We observed that, unlike M. m. domesticus, M. m. musculus and M. m. castaneus are resistant to the clonal Toxoplasma strains. For M. m. musculus, we show that this is due to a locus on chromosome 11 that includes the genes that encode the interferon gamma (IFNG)-inducible immunity-related GTPases (Irgs) that can kill the parasite by localising and subsequently vesiculating the parasitophorous vacuole membrane. However, despite the localization of known effector Irgs to the Toxoplasma parasitophorous vacuole membrane, we observed that some atypical Toxoplasma strains are virulent in all the mouse strains tested. The virulence of these atypical strains in M. m. musculus could not be attributed to individual rhoptry protein 5 (ROP5) alleles, a secreted parasite pseudokinase that antagonises the canonical effector Irgs and is indispensable for parasite virulence in laboratory inbred mice (M. m. domesticus). We conclude that murine resistance to Toxoplasma is modulated by complex interactions between host and parasite genotypes and may be independent of known effector Irgs on murine chromosome 11. (C) 2018 The Authors. Published by Elsevier Ltd on behalf of Australian Society for Parasitology.

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