Cargando…

Temporal evaluation of commitment to sexual development in Plasmodium falciparum

BACKGROUND: The production of gametocytes is essential for transmission of malaria parasites from the mammalian host to the mosquito vector. However the process by which the asexual blood-stage parasite undergoes commitment to sexual development is not well understood. This process is known to be se...

Descripción completa

Detalles Bibliográficos
Autores principales: Peatey, Christopher L, Dixon, Matthew WA, Gardiner, Donald L, Trenholme, Katharine R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659030/
https://www.ncbi.nlm.nih.gov/pubmed/23607486
http://dx.doi.org/10.1186/1475-2875-12-134
_version_ 1782270385319837696
author Peatey, Christopher L
Dixon, Matthew WA
Gardiner, Donald L
Trenholme, Katharine R
author_facet Peatey, Christopher L
Dixon, Matthew WA
Gardiner, Donald L
Trenholme, Katharine R
author_sort Peatey, Christopher L
collection PubMed
description BACKGROUND: The production of gametocytes is essential for transmission of malaria parasites from the mammalian host to the mosquito vector. However the process by which the asexual blood-stage parasite undergoes commitment to sexual development is not well understood. This process is known to be sensitive to environmental stimuli and it has been suggested that a G protein dependent system may mediate the switch, but there is little evidence that the Plasmodium falciparum genome encodes heterotrimeric G proteins. Previous studies have indicated that the malaria parasite can interact with endogenous erythrocyte G proteins, and other components of the cyclic nucleotide pathway have been identified in P. falciparum. Also, the polypeptide cholera toxin, which induces commitment to gametocytogenesis is known to catalyze the ADP-ribosylation of the α(s) class of heterotrimeric G protein α subunits in mammalian systems has been reported to detect a number of G(α) subunits in P. falciparum-infected red cells. METHODS: Cholera toxin and Mas 7 (a structural analogue of Mastoparan) were used to assess the role played by putative G protein signalling in the commitment process, both are reported to interact with different components of classical Gαs and Gαi/o signalling pathways. Their ability to induce gametocyte production in the transgenic P. falciparum line Pfs16-GFP was determined and downstream effects on the secondary messenger cAMP measured. RESULTS: Treatment of parasite cultures with either cholera toxin or MAS 7 resulted in increased gametocyte production, but only treatment with MAS 7 resulted in a significant increase in cAMP levels. This indicates that MAS 7 acts either directly or indirectly on the P. falciparum adenylyl cyclase. CONCLUSION: The observation that cholera toxin treatment did not affect cAMP levels indicates that while addition of cholera toxin does increase gametocytogenesis the method by which it induces increased commitment is not immediately obvious, except that is unlikely to be via heterotrimeric G proteins.
format Online
Article
Text
id pubmed-3659030
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-36590302013-05-21 Temporal evaluation of commitment to sexual development in Plasmodium falciparum Peatey, Christopher L Dixon, Matthew WA Gardiner, Donald L Trenholme, Katharine R Malar J Research BACKGROUND: The production of gametocytes is essential for transmission of malaria parasites from the mammalian host to the mosquito vector. However the process by which the asexual blood-stage parasite undergoes commitment to sexual development is not well understood. This process is known to be sensitive to environmental stimuli and it has been suggested that a G protein dependent system may mediate the switch, but there is little evidence that the Plasmodium falciparum genome encodes heterotrimeric G proteins. Previous studies have indicated that the malaria parasite can interact with endogenous erythrocyte G proteins, and other components of the cyclic nucleotide pathway have been identified in P. falciparum. Also, the polypeptide cholera toxin, which induces commitment to gametocytogenesis is known to catalyze the ADP-ribosylation of the α(s) class of heterotrimeric G protein α subunits in mammalian systems has been reported to detect a number of G(α) subunits in P. falciparum-infected red cells. METHODS: Cholera toxin and Mas 7 (a structural analogue of Mastoparan) were used to assess the role played by putative G protein signalling in the commitment process, both are reported to interact with different components of classical Gαs and Gαi/o signalling pathways. Their ability to induce gametocyte production in the transgenic P. falciparum line Pfs16-GFP was determined and downstream effects on the secondary messenger cAMP measured. RESULTS: Treatment of parasite cultures with either cholera toxin or MAS 7 resulted in increased gametocyte production, but only treatment with MAS 7 resulted in a significant increase in cAMP levels. This indicates that MAS 7 acts either directly or indirectly on the P. falciparum adenylyl cyclase. CONCLUSION: The observation that cholera toxin treatment did not affect cAMP levels indicates that while addition of cholera toxin does increase gametocytogenesis the method by which it induces increased commitment is not immediately obvious, except that is unlikely to be via heterotrimeric G proteins. BioMed Central 2013-04-22 /pmc/articles/PMC3659030/ /pubmed/23607486 http://dx.doi.org/10.1186/1475-2875-12-134 Text en Copyright © 2013 Peatey et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Peatey, Christopher L
Dixon, Matthew WA
Gardiner, Donald L
Trenholme, Katharine R
Temporal evaluation of commitment to sexual development in Plasmodium falciparum
title Temporal evaluation of commitment to sexual development in Plasmodium falciparum
title_full Temporal evaluation of commitment to sexual development in Plasmodium falciparum
title_fullStr Temporal evaluation of commitment to sexual development in Plasmodium falciparum
title_full_unstemmed Temporal evaluation of commitment to sexual development in Plasmodium falciparum
title_short Temporal evaluation of commitment to sexual development in Plasmodium falciparum
title_sort temporal evaluation of commitment to sexual development in plasmodium falciparum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659030/
https://www.ncbi.nlm.nih.gov/pubmed/23607486
http://dx.doi.org/10.1186/1475-2875-12-134
work_keys_str_mv AT peateychristopherl temporalevaluationofcommitmenttosexualdevelopmentinplasmodiumfalciparum
AT dixonmatthewwa temporalevaluationofcommitmenttosexualdevelopmentinplasmodiumfalciparum
AT gardinerdonaldl temporalevaluationofcommitmenttosexualdevelopmentinplasmodiumfalciparum
AT trenholmekathariner temporalevaluationofcommitmenttosexualdevelopmentinplasmodiumfalciparum