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Revisiting the initial steps of sexual development in the malaria parasite Plasmodium falciparum.
Bancells, Cristina; Llorà-Batlle, Oriol; Poran, Asaf; Nötzel, Christopher; Rovira-Graells, Núria; Elemento, Olivier; Kafsack, Björn F C; Cortés, Alfred.
Afiliación
  • Bancells C; ISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
  • Llorà-Batlle O; ISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
  • Poran A; Institute for Computational Biomedicine, Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
  • Nötzel C; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Rovira-Graells N; Physiology, Biophysics and Systems Biology Graduate Program, Weill Cornell Medicine, New York, NY, USA.
  • Elemento O; Biochemistry, Cell & Molecular Biology Graduate Program, Weill Cornell Medicine, New York, NY, USA.
  • Kafsack BFC; Department of Microbiology & Immunology, Weill Cornell Medicine, New York, NY, USA.
  • Cortés A; ISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Nat Microbiol ; 4(1): 144-154, 2019 01.
Article en En | MEDLINE | ID: mdl-30478286
ABSTRACT
Human to vector transmission of malaria requires that some blood-stage parasites abandon asexual growth and convert into non-replicating sexual forms called gametocytes. The initial steps of gametocytogenesis remain largely uncharacterized. Here, we study this part of the malaria life cycle in Plasmodium falciparum using PfAP2-G, the master regulator of sexual conversion, as a marker of commitment. We demonstrate the existence of PfAP2-G-positive sexually committed parasite stages that precede the previously known committed schizont stage. We also found that sexual conversion can occur by two different routes the previously described route in which PfAP2-G-expressing parasites complete a replicative cycle as committed forms before converting into gametocytes upon re-invasion, or a direct route with conversion within the same cycle as initial PfAP2-G expression. The latter route is linked to early PfAP2-G expression in ring stages. Reanalysis of published single-cell RNA-sequencing (RNA-seq) data confirmed the presence of both routes. Consistent with these results, using plaque assays we observed that, in contrast to the prevailing model, many schizonts produced mixed plaques containing both asexual parasites and gametocytes. Altogether, our results reveal unexpected features of the initial steps of sexual development and extend the current view of this part of the malaria life cycle.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Plasmodium falciparum / Desarrollo Sexual / Estadios del Ciclo de Vida Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Microbiol Año: 2019 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Plasmodium falciparum / Desarrollo Sexual / Estadios del Ciclo de Vida Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Microbiol Año: 2019 Tipo del documento: Article País de afiliación: España