Plasmodium falciparum sexual differentiation in malaria patients is associated with host factors and GDV1-dependent genes.
Miho UsuiSurendra K PrajapatiRuth Ayanful-TorgbyFestus K AcquahElizabeth CudjoeCourage KakaneyJones A AmponsahEvans K ObbohDeepti K ReddyMichelle C BarbeauLacy M SimonsBeata CzesnySorana RaiciulescuCara OlsenBenjamin K AbuakuLinda E AmoahKim C WilliamsonPublished in: Nature communications (2019)
Plasmodium sexual differentiation is required for malaria transmission, yet much remains unknown about its regulation. Here, we quantify early gametocyte-committed ring (gc-ring) stage, P. falciparum parasites in 260 uncomplicated malaria patient blood samples 10 days before maturation to transmissible stage V gametocytes using a gametocyte conversion assay (GCA). Seventy six percent of the samples have gc-rings, but the ratio of gametocyte to asexual-committed rings (GCR) varies widely (0-78%). GCR correlates positively with parasitemia and is negatively influenced by fever, not hematocrit, age or leukocyte counts. Higher expression levels of GDV1-dependent genes, ap2-g, msrp1 and gexp5, as well as a gdv1 allele encoding H217 are associated with high GCR, while high plasma lysophosphatidylcholine levels are associated with low GCR in the second study year. The results provide a view of sexual differentiation in the field and suggest key regulatory roles for clinical factors and gdv1 in gametocytogenesis in vivo.
Keyphrases
- plasmodium falciparum
- end stage renal disease
- mental health
- transcription factor
- genome wide
- ejection fraction
- chronic kidney disease
- newly diagnosed
- poor prognosis
- prognostic factors
- peripheral blood
- high throughput
- peritoneal dialysis
- case report
- genome wide identification
- dna methylation
- high resolution
- long non coding rna