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Compared with the Mock group, FGF8+10 treatment mature the differentiated LPM-like cells to form LM-like cells [RNA-seq]

ABSTRACT: Compared with the Mock group, FGF8+10 treatment mature the differentiated LPM-like cells to form LM-like cells [RNA-seq]

PROVIDER: PRJNA972759 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR24575412_1.fastq.gz	Fastqsanger.gz
	SRR24575412_2.fastq.gz	Fastqsanger.gz
	SRR24575413_1.fastq.gz	Fastqsanger.gz
	SRR24575413_2.fastq.gz	Fastqsanger.gz
	SRR24575414_1.fastq.gz	Fastqsanger.gz

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Compared with the Mock group, FGF8+10 treatment mature the differentiated LPM-like cells to form LM-like cells [RNA-seq]

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Compared with the Mock group, FGF8+10 treatment mature the differentiated LPM-like cells to form LM-like cells, and gene expression profile at single cell level of Msx1+ mesenchymal progenitors from mouse E10.5 embryos

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Project description:The combination therapy of the Artemisinin-derivative Artemether (ART) with Lumefantrine (LM) (Coartem®) is an important malaria treatment regimen in many endemic countries. Resistance to Artemisinin has already been reported, and it is feared that LM resistance (LMR) could also evolve quickly. Therefore molecular markers which can be used to track Coartem®efficacy are urgently needed. Often, stable resistance arises from initial, unstable phenotypes that can be identified in vitro. Here we have used the Plasmodium falciparum multidrug resistant reference strain V1S to induce LMR in vitro by culturing the parasite under continuous drug pressure for 16 months. The initial IC50 (inhibitory concentration that kills 50% of the parasite population) was 24 nM. The resulting resistant strain V1SLM, obtained after culture for an estimated 166 cycles under LM pressure, grew steadily in 378 nM of LM; this corresponds to 15 times the IC50 of the parental strain. However, after two weeks of culturing V1SLM in drug-free medium, the IC50 returned to that of the initial, parental strain V1S. This transient drug tolerance was associated with major changes in gene expression profiles: when we explored V1SLM using the PFSANGER Affymetrix custom array, we identified 184 differentially expressed (DE) genes; amongst those 18 putative transporters including the multidrug resistance gene (pfmdr1), the multidrug resistance associated protein (pfmrp1) and the V-type H+ pumping pyrophosphatase 2 (pfvp2). Moreover, our results showed significant enrichment of genes associated with fatty acid metabolism and a clear selective advantage for two genomic loci in parasites grown under LM drug pressure, suggesting these genes may contribute to LM response in P. falciparum and could prove useful as molecular markers to monitor LM susceptibility.

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Project description:Following infection with LCMV, CD4+ SMARTA TCR transgenic cells (specific for the gp61-80 epitope of the LCMV glycoprotein) rapidly expand, become effector cells, and go on to form a long-lived memory population. Following infection with a recombinant Listeria monocytogenes expressing the LCMV epitope gp61-80, SMARTA cells also expand but display defective effector differentiation and fail to form memory. In an attempt to understand the signals required for CD4 T cell memory differentiation, we compared gene expression by SMARTA cells at the peak of the primary response following either Lm-gp61 or LCMV infection. Keywords: response to LCMV or Lm-gp61 infection

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Salmonella enterica subsp. enterica serovar Infantis strain:LPM-ST01

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Salmonella enterica subsp. enterica serovar Infantis strain:LPM-ST02

Project description:Salmonella enterica LPM-ST02