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Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season
BACKGROUND: Transmission stemming from asymptomatic infections is increasingly being recognized as a threat to malaria elimination. In many regions, malaria transmission is seasonal. It is not well understood whether Plasmodium falciparum modulates its investment in transmission to coincide with sea...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797145/ https://www.ncbi.nlm.nih.gov/pubmed/33422001 http://dx.doi.org/10.1186/s12879-020-05761-6 |
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author | Oduma, Colins O. Ogolla, Sidney Atieli, Harrysone Ondigo, Bartholomew N. Lee, Ming-Chieh Githeko, Andrew K. Dent, Arlene E. Kazura, James W. Yan, Guiyun Koepfli, Cristian |
author_facet | Oduma, Colins O. Ogolla, Sidney Atieli, Harrysone Ondigo, Bartholomew N. Lee, Ming-Chieh Githeko, Andrew K. Dent, Arlene E. Kazura, James W. Yan, Guiyun Koepfli, Cristian |
author_sort | Oduma, Colins O. |
collection | PubMed |
description | BACKGROUND: Transmission stemming from asymptomatic infections is increasingly being recognized as a threat to malaria elimination. In many regions, malaria transmission is seasonal. It is not well understood whether Plasmodium falciparum modulates its investment in transmission to coincide with seasonal vector abundance. METHODS: We sampled 1116 asymptomatic individuals in the wet season, when vectors are abundant, and 1743 in the dry season, in two sites in western Kenya, representing different transmission intensities (Chulaimbo, moderate transmission, and Homa Bay, low transmission). Blood samples were screened for P. falciparum by qPCR, and gametocytes by pfs25 RT-qPCR. RESULTS: Parasite prevalence by qPCR was 27.1% (Chulaimbo, dry), 48.2% (Chulaimbo, wet), 9.4% (Homabay, dry), and 7.8% (Homabay, wet). Mean parasite densities did not differ between seasons (P = 0.562). pfs25 transcripts were detected in 119/456 (26.1%) of infections. In the wet season, fewer infections harbored detectable gametocytes (22.3% vs. 33.8%, P = 0.009), but densities were 3-fold higher (wet: 3.46 transcripts/uL, dry: 1.05 transcripts/uL, P < 0.001). In the dry season, 4.0% of infections carried gametocytes at moderate-to-high densities likely infective (> 1 gametocyte per 2 uL blood), compared to 7.9% in the wet season. Children aged 5–15 years harbored 76.7% of infections with gametocytes at moderate-to-high densities. CONCLUSIONS: Parasites increase their investment in transmission in the wet season, reflected by higher gametocyte densities. Despite increased gametocyte densities, parasite density remained similar across seasons and were often below the limit of detection of microscopy or rapid diagnostic test, thus a large proportion of infective infections would escape population screening in the wet season. Seasonal changes of gametocytemia in asymptomatic infections need to be considered when designing malaria control measures. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-020-05761-6. |
format | Online Article Text |
id | pubmed-7797145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77971452021-01-11 Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season Oduma, Colins O. Ogolla, Sidney Atieli, Harrysone Ondigo, Bartholomew N. Lee, Ming-Chieh Githeko, Andrew K. Dent, Arlene E. Kazura, James W. Yan, Guiyun Koepfli, Cristian BMC Infect Dis Research Article BACKGROUND: Transmission stemming from asymptomatic infections is increasingly being recognized as a threat to malaria elimination. In many regions, malaria transmission is seasonal. It is not well understood whether Plasmodium falciparum modulates its investment in transmission to coincide with seasonal vector abundance. METHODS: We sampled 1116 asymptomatic individuals in the wet season, when vectors are abundant, and 1743 in the dry season, in two sites in western Kenya, representing different transmission intensities (Chulaimbo, moderate transmission, and Homa Bay, low transmission). Blood samples were screened for P. falciparum by qPCR, and gametocytes by pfs25 RT-qPCR. RESULTS: Parasite prevalence by qPCR was 27.1% (Chulaimbo, dry), 48.2% (Chulaimbo, wet), 9.4% (Homabay, dry), and 7.8% (Homabay, wet). Mean parasite densities did not differ between seasons (P = 0.562). pfs25 transcripts were detected in 119/456 (26.1%) of infections. In the wet season, fewer infections harbored detectable gametocytes (22.3% vs. 33.8%, P = 0.009), but densities were 3-fold higher (wet: 3.46 transcripts/uL, dry: 1.05 transcripts/uL, P < 0.001). In the dry season, 4.0% of infections carried gametocytes at moderate-to-high densities likely infective (> 1 gametocyte per 2 uL blood), compared to 7.9% in the wet season. Children aged 5–15 years harbored 76.7% of infections with gametocytes at moderate-to-high densities. CONCLUSIONS: Parasites increase their investment in transmission in the wet season, reflected by higher gametocyte densities. Despite increased gametocyte densities, parasite density remained similar across seasons and were often below the limit of detection of microscopy or rapid diagnostic test, thus a large proportion of infective infections would escape population screening in the wet season. Seasonal changes of gametocytemia in asymptomatic infections need to be considered when designing malaria control measures. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-020-05761-6. BioMed Central 2021-01-09 /pmc/articles/PMC7797145/ /pubmed/33422001 http://dx.doi.org/10.1186/s12879-020-05761-6 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Oduma, Colins O. Ogolla, Sidney Atieli, Harrysone Ondigo, Bartholomew N. Lee, Ming-Chieh Githeko, Andrew K. Dent, Arlene E. Kazura, James W. Yan, Guiyun Koepfli, Cristian Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season |
title | Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season |
title_full | Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season |
title_fullStr | Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season |
title_full_unstemmed | Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season |
title_short | Increased investment in gametocytes in asymptomatic Plasmodium falciparum infections in the wet season |
title_sort | increased investment in gametocytes in asymptomatic plasmodium falciparum infections in the wet season |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797145/ https://www.ncbi.nlm.nih.gov/pubmed/33422001 http://dx.doi.org/10.1186/s12879-020-05761-6 |
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