Long-lasting infectivity of Plasmodium vivax present in malarial patient blood to Anopheles aquasalis

Experimental studies for understanding the relationship between Plasmodium vivax and its vector hosts are difficult, because of to the lack of a long-term, in vitro continuous culture system unavailability of infected blood samples, seasonality of the disease, and the concentration of most cases in...

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Veröffentlicht in:Experimental parasitology 2021-03, Vol.222, p.108064-108064, Article 108064
Hauptverfasser: Pereira-Silva, Jordam William, Martins-Campos, Keillen Monick, Sabrina dos Reis Martins, Elen, de Souza Menezes, Alexandre, Guimarães Lacerda, Marcus Vinicius, Costa Pessoa, Felipe Arley, Ríos-Velásquez, Claudia Maria
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container_title Experimental parasitology
container_volume 222
creator Pereira-Silva, Jordam William
Martins-Campos, Keillen Monick
Sabrina dos Reis Martins, Elen
de Souza Menezes, Alexandre
Guimarães Lacerda, Marcus Vinicius
Costa Pessoa, Felipe Arley
Ríos-Velásquez, Claudia Maria
description Experimental studies for understanding the relationship between Plasmodium vivax and its vector hosts are difficult, because of to the lack of a long-term, in vitro continuous culture system unavailability of infected blood samples, seasonality of the disease, and the concentration of most cases in remote areas. This study evaluates the duration of the infectivity of P. vivax to Anopheles aquasalis after collecting blood from malaria-infected patients. Blood was collected from patients and stored at 4 °C and 37 °C. Every day, for 4 days, the blood was fed to An. aquasalis adult females, and a Giemsa-stained thick blood smear was mounted to account for sexual (gametocytes) and asexual (trophozoites and schizonts) stages and calculate parasitemia. Oocysts in the midgut of the mosquitoes were counted on the seventh day after feeding. Kruskal-Wallis test was used to compare the mean number of oocysts (MO) and the parasite density (PD) in each storage condition and post-infection time-points. The Mann-Whitney test was used to compare the number of oocysts for each day between temperatures. The results show that P. vivax stored at 4 °C and at 37 °C has its infectivity to An. aquasalis preserved for 2 days and 3 days, respectively. Infection rate (IR), PD and MO were higher on the day of blood collection and decreased gradually over time. The parasite density (number of parasites/μL) diminished faster at 4 °C than at 37 °C. In this study, a preservation protocol is shown for long-lasting infectivity of P. vivax in a blood sample taken from malaria-infected patients. These results show that infectivity of P. vivax stored at 4 °C and at 37 °C to An. aquasalis persist until 3 days after blood collection, but parasite density, infection rate, and mean of oocysts decreased 24h after blood collection. Since the malaria cases are increasingly far from the urban areas these results indicate that is possible, losing some infectivity, to realize experimental infections several dozen hours after the blood collection. However, it is necessary to improve the procedures for preserving P. vivax gametocytes for mosquito infection in the laboratory. [Display omitted] •We present a preservation protocol for long-lasting infectivity of P. vivax parasites in blood samples collected from malaria-infected patients.•The blood sample infected by P. vivax, stored at 4 °C and 37 °C, preserves the parasite for 2 or 3 days after blood collection.•37 °C seems to be the most suitable temperat
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This study evaluates the duration of the infectivity of P. vivax to Anopheles aquasalis after collecting blood from malaria-infected patients. Blood was collected from patients and stored at 4 °C and 37 °C. Every day, for 4 days, the blood was fed to An. aquasalis adult females, and a Giemsa-stained thick blood smear was mounted to account for sexual (gametocytes) and asexual (trophozoites and schizonts) stages and calculate parasitemia. Oocysts in the midgut of the mosquitoes were counted on the seventh day after feeding. Kruskal-Wallis test was used to compare the mean number of oocysts (MO) and the parasite density (PD) in each storage condition and post-infection time-points. The Mann-Whitney test was used to compare the number of oocysts for each day between temperatures. The results show that P. vivax stored at 4 °C and at 37 °C has its infectivity to An. aquasalis preserved for 2 days and 3 days, respectively. Infection rate (IR), PD and MO were higher on the day of blood collection and decreased gradually over time. The parasite density (number of parasites/μL) diminished faster at 4 °C than at 37 °C. In this study, a preservation protocol is shown for long-lasting infectivity of P. vivax in a blood sample taken from malaria-infected patients. These results show that infectivity of P. vivax stored at 4 °C and at 37 °C to An. aquasalis persist until 3 days after blood collection, but parasite density, infection rate, and mean of oocysts decreased 24h after blood collection. Since the malaria cases are increasingly far from the urban areas these results indicate that is possible, losing some infectivity, to realize experimental infections several dozen hours after the blood collection. However, it is necessary to improve the procedures for preserving P. vivax gametocytes for mosquito infection in the laboratory. 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Infection rate (IR), PD and MO were higher on the day of blood collection and decreased gradually over time. The parasite density (number of parasites/μL) diminished faster at 4 °C than at 37 °C. In this study, a preservation protocol is shown for long-lasting infectivity of P. vivax in a blood sample taken from malaria-infected patients. These results show that infectivity of P. vivax stored at 4 °C and at 37 °C to An. aquasalis persist until 3 days after blood collection, but parasite density, infection rate, and mean of oocysts decreased 24h after blood collection. Since the malaria cases are increasingly far from the urban areas these results indicate that is possible, losing some infectivity, to realize experimental infections several dozen hours after the blood collection. However, it is necessary to improve the procedures for preserving P. vivax gametocytes for mosquito infection in the laboratory. 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This study evaluates the duration of the infectivity of P. vivax to Anopheles aquasalis after collecting blood from malaria-infected patients. Blood was collected from patients and stored at 4 °C and 37 °C. Every day, for 4 days, the blood was fed to An. aquasalis adult females, and a Giemsa-stained thick blood smear was mounted to account for sexual (gametocytes) and asexual (trophozoites and schizonts) stages and calculate parasitemia. Oocysts in the midgut of the mosquitoes were counted on the seventh day after feeding. Kruskal-Wallis test was used to compare the mean number of oocysts (MO) and the parasite density (PD) in each storage condition and post-infection time-points. The Mann-Whitney test was used to compare the number of oocysts for each day between temperatures. The results show that P. vivax stored at 4 °C and at 37 °C has its infectivity to An. aquasalis preserved for 2 days and 3 days, respectively. Infection rate (IR), PD and MO were higher on the day of blood collection and decreased gradually over time. The parasite density (number of parasites/μL) diminished faster at 4 °C than at 37 °C. In this study, a preservation protocol is shown for long-lasting infectivity of P. vivax in a blood sample taken from malaria-infected patients. These results show that infectivity of P. vivax stored at 4 °C and at 37 °C to An. aquasalis persist until 3 days after blood collection, but parasite density, infection rate, and mean of oocysts decreased 24h after blood collection. Since the malaria cases are increasingly far from the urban areas these results indicate that is possible, losing some infectivity, to realize experimental infections several dozen hours after the blood collection. However, it is necessary to improve the procedures for preserving P. vivax gametocytes for mosquito infection in the laboratory. [Display omitted] •We present a preservation protocol for long-lasting infectivity of P. vivax parasites in blood samples collected from malaria-infected patients.•The blood sample infected by P. vivax, stored at 4 °C and 37 °C, preserves the parasite for 2 or 3 days after blood collection.•37 °C seems to be the most suitable temperature to maintain the viability of P. vivax, in field and laboratory.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33421382</pmid><doi>10.1016/j.exppara.2021.108064</doi><tpages>1</tpages></addata></record>
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ispartof Experimental parasitology, 2021-03, Vol.222, p.108064-108064, Article 108064
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Adult
Aged
Animals
Anopheles - parasitology
Anopheles aquasalis
Brazil
Female
Humans
Infectivity
Malaria
Malaria, Vivax - blood
Malaria, Vivax - parasitology
Malaria, Vivax - transmission
Male
Membrane Feeding Assay
Middle Aged
Mosquito Vectors - parasitology
Plasmodium vivax
Plasmodium vivax - pathogenicity
Plasmodium vivax - physiology
Rural Population
Temperature
Time Factors
Young Adult
title Long-lasting infectivity of Plasmodium vivax present in malarial patient blood to Anopheles aquasalis
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