Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.

Malaria is caused by parasite of the genus Plasmodium and is still one of the most important infectious diseases in the world. Several biological characteristics of Plasmodium vivax contribute to the resilience of this species, including early gametocyte production, both of which lead to efficient m...

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Main Authors: Alice O Andrade, Najara A C Santos, Alessandra S Bastos, José D C Pontual, Jéssica E Araújo, Alexia M V Silva, Leandro N Martinez, Alzemar A Lima, Anna Caroline C Aguiar, Carolina B G Teles, Jansen F Medeiros, Dhelio B Pereira, Joseph M Vinetz, Ricardo T Gazzinelli, Maisa S Araújo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-06-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://doi.org/10.1371/journal.pntd.0011425
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author Alice O Andrade
Najara A C Santos
Alessandra S Bastos
José D C Pontual
Jéssica E Araújo
Alexia M V Silva
Leandro N Martinez
Alzemar A Lima
Anna Caroline C Aguiar
Carolina B G Teles
Jansen F Medeiros
Dhelio B Pereira
Joseph M Vinetz
Ricardo T Gazzinelli
Maisa S Araújo
author_facet Alice O Andrade
Najara A C Santos
Alessandra S Bastos
José D C Pontual
Jéssica E Araújo
Alexia M V Silva
Leandro N Martinez
Alzemar A Lima
Anna Caroline C Aguiar
Carolina B G Teles
Jansen F Medeiros
Dhelio B Pereira
Joseph M Vinetz
Ricardo T Gazzinelli
Maisa S Araújo
author_sort Alice O Andrade
collection DOAJ
description Malaria is caused by parasite of the genus Plasmodium and is still one of the most important infectious diseases in the world. Several biological characteristics of Plasmodium vivax contribute to the resilience of this species, including early gametocyte production, both of which lead to efficient malaria transmission to mosquitoes. This study evaluated the impact of currently used drugs on the transmission of P. vivax. Participants received one of the following treatments for malaria: i) chloroquine [10 mg/kg on day 1 and 7.5 mg/kg on day 2 and 3] co-administered with Primaquine [0.5 mg/kg/day for 7 days]; ii) Chloroquine [10 mg/kg on day 1 and 7.5 mg/kg on day 2 and 3] co-administered with one-dose of Tafenoquine [300 mg on day 1]; and iii) Artesunate and Mefloquine [100 mg and 200 mg on day 1, 2 and 3] co-administered with Primaquine [0.5 mg/kg/day for 14 days]. Patient blood was collected before treatment and 4 h, 24 h, 48 h and 72 h after treatment. The blood was used to perform a direct membrane feeding assay (DMFA) using Anopheles darlingi mosquitoes. The results showed 100% inhibition of the mosquito infection after 4 h using ASMQ+PQ, after 24 h for the combination of CQ+PQ and 48 h using CQ+TQ. The density of gametocytes declined over time in all treatment groups, although the decline was more rapid in the ASMQ+PQ group. In conclusion, it was possible to demonstrate the transmission-blocking efficacy of the malaria vivax treatment and that ASMQ+PQ acts faster than the two other treatments.
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spelling doaj.art-d4d92659f6bf43899bc4120b0ea5fb3b2024-12-11T05:32:08ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352023-06-01176e001142510.1371/journal.pntd.0011425Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.Alice O AndradeNajara A C SantosAlessandra S BastosJosé D C PontualJéssica E AraújoAlexia M V SilvaLeandro N MartinezAlzemar A LimaAnna Caroline C AguiarCarolina B G TelesJansen F MedeirosDhelio B PereiraJoseph M VinetzRicardo T GazzinelliMaisa S AraújoMalaria is caused by parasite of the genus Plasmodium and is still one of the most important infectious diseases in the world. Several biological characteristics of Plasmodium vivax contribute to the resilience of this species, including early gametocyte production, both of which lead to efficient malaria transmission to mosquitoes. This study evaluated the impact of currently used drugs on the transmission of P. vivax. Participants received one of the following treatments for malaria: i) chloroquine [10 mg/kg on day 1 and 7.5 mg/kg on day 2 and 3] co-administered with Primaquine [0.5 mg/kg/day for 7 days]; ii) Chloroquine [10 mg/kg on day 1 and 7.5 mg/kg on day 2 and 3] co-administered with one-dose of Tafenoquine [300 mg on day 1]; and iii) Artesunate and Mefloquine [100 mg and 200 mg on day 1, 2 and 3] co-administered with Primaquine [0.5 mg/kg/day for 14 days]. Patient blood was collected before treatment and 4 h, 24 h, 48 h and 72 h after treatment. The blood was used to perform a direct membrane feeding assay (DMFA) using Anopheles darlingi mosquitoes. The results showed 100% inhibition of the mosquito infection after 4 h using ASMQ+PQ, after 24 h for the combination of CQ+PQ and 48 h using CQ+TQ. The density of gametocytes declined over time in all treatment groups, although the decline was more rapid in the ASMQ+PQ group. In conclusion, it was possible to demonstrate the transmission-blocking efficacy of the malaria vivax treatment and that ASMQ+PQ acts faster than the two other treatments.https://doi.org/10.1371/journal.pntd.0011425
spellingShingle Alice O Andrade
Najara A C Santos
Alessandra S Bastos
José D C Pontual
Jéssica E Araújo
Alexia M V Silva
Leandro N Martinez
Alzemar A Lima
Anna Caroline C Aguiar
Carolina B G Teles
Jansen F Medeiros
Dhelio B Pereira
Joseph M Vinetz
Ricardo T Gazzinelli
Maisa S Araújo
Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.
PLoS Neglected Tropical Diseases
title Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.
title_full Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.
title_fullStr Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.
title_full_unstemmed Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.
title_short Transmission-blocking activity of antimalarials for Plasmodium vivax malaria in Anopheles darlingi.
title_sort transmission blocking activity of antimalarials for plasmodium vivax malaria in anopheles darlingi
url https://doi.org/10.1371/journal.pntd.0011425
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