Literature DB >> 18538633

Plasmodium falciparum shows transcriptional versatility within the human host.

Fiona E Lovegrove1, Lourdes Peña-Castillo, W Conrad Liles, Timothy R Hughes, Kevin C Kain.   

Abstract

In a recent study published in Nature, Daily et al. profiled parasite gene expression in Plasmodium falciparum infections and identified three in vivo 'states' based on parasite transcription patterns. Despite similar host clinical features, two states displayed highly divergent gene expression, whereas the third was found in individuals with increased inflammatory markers. These findings suggest that parasites exist in different physiological states in vivo, providing an important foundation for future studies investigating how these states might contribute to malaria pathogenesis and outcome.

Entities:  

Mesh:

Year:  2008        PMID: 18538633     DOI: 10.1016/j.pt.2008.04.004

Source DB:  PubMed          Journal:  Trends Parasitol        ISSN: 1471-4922


  3 in total

1.  Antimalarial iron chelator FBS0701 blocks transmission by Plasmodium falciparum gametocyte activation inhibition.

Authors:  Patricia Ferrer; Joel Vega-Rodriguez; Abhai K Tripathi; Marcelo Jacobs-Lorena; David J Sullivan
Journal:  Antimicrob Agents Chemother       Date:  2014-12-15       Impact factor: 5.191

2.  The antimalarial drug quinine disrupts Tat2p-mediated tryptophan transport and causes tryptophan starvation.

Authors:  Combiz Khozoie; Richard J Pleass; Simon V Avery
Journal:  J Biol Chem       Date:  2009-05-05       Impact factor: 5.157

3.  Mitochondrial metabolism of sexual and asexual blood stages of the malaria parasite Plasmodium falciparum.

Authors:  James I MacRae; Matthew Wa Dixon; Megan K Dearnley; Hwa H Chua; Jennifer M Chambers; Shannon Kenny; Iveta Bottova; Leann Tilley; Malcolm J McConville
Journal:  BMC Biol       Date:  2013-06-13       Impact factor: 7.431

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.