Clinically immune hosts as a refuge for drug-sensitive malaria parasites
Abstract Background Mutations in Plasmodium falciparum that confer resistance to first-line antimalarial drugs have spread throughout the world from a few independent foci, all located in areas that were likely characterized by low or unstable malaria transmission. One of the striking differences be...
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ftdoajarticles:oai:doaj.org/article:c84468b160754601bf48eea64ddef371 2023-05-15T15:16:41+02:00 Clinically immune hosts as a refuge for drug-sensitive malaria parasites Smith David L Klein Eili Y Boni Maciej F Laxminarayan Ramanan 2008-04-01T00:00:00Z https://doi.org/10.1186/1475-2875-7-67 https://doaj.org/article/c84468b160754601bf48eea64ddef371 EN eng BMC http://www.malariajournal.com/content/7/1/67 https://doaj.org/toc/1475-2875 doi:10.1186/1475-2875-7-67 1475-2875 https://doaj.org/article/c84468b160754601bf48eea64ddef371 Malaria Journal, Vol 7, Iss 1, p 67 (2008) Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 article 2008 ftdoajarticles https://doi.org/10.1186/1475-2875-7-67 2022-12-31T08:35:07Z Abstract Background Mutations in Plasmodium falciparum that confer resistance to first-line antimalarial drugs have spread throughout the world from a few independent foci, all located in areas that were likely characterized by low or unstable malaria transmission. One of the striking differences between areas of low or unstable malaria transmission and hyperendemic areas is the difference in the size of the population of immune individuals. However, epidemiological models of malaria transmission have generally ignored the role of immune individuals in transmission, assuming that they do not affect the fitness of the parasite. This model reconsiders the role of immunity in the dynamics of malaria transmission and its impact on the evolution of antimalarial drug resistance under the assumption that immune individuals are infectious. Methods The model is constructed as a two-stage susceptible-infected-susceptible (SIS) model of malaria transmission that assumes that individuals build up clinical immunity over a period of years. This immunity reduces the frequency and severity of clinical symptoms, and thus their use of drugs. It also reduces an individual's level of infectiousness, but does not impact the likelihood of becoming infected. Results Simulations found that with the introduction of resistance into a population, clinical immunity can significantly alter the fitness of the resistant parasite, and thereby impact the ability of the resistant parasite to spread from an initial host by reducing the effective reproductive number of the resistant parasite as transmission intensity increases. At high transmission levels, despite a higher basic reproductive number, R 0 , the effective reproductive number of the resistant parasite may fall below the reproductive number of the sensitive parasite. Conclusion These results suggest that high-levels of clinical immunity create a natural ecological refuge for drug-sensitive parasites. This provides an epidemiological rationale for historical patterns of resistance ... Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Malaria Journal 7 1 67 |
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Directory of Open Access Journals: DOAJ Articles |
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English |
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Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 |
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Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 Smith David L Klein Eili Y Boni Maciej F Laxminarayan Ramanan Clinically immune hosts as a refuge for drug-sensitive malaria parasites |
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Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 |
description |
Abstract Background Mutations in Plasmodium falciparum that confer resistance to first-line antimalarial drugs have spread throughout the world from a few independent foci, all located in areas that were likely characterized by low or unstable malaria transmission. One of the striking differences between areas of low or unstable malaria transmission and hyperendemic areas is the difference in the size of the population of immune individuals. However, epidemiological models of malaria transmission have generally ignored the role of immune individuals in transmission, assuming that they do not affect the fitness of the parasite. This model reconsiders the role of immunity in the dynamics of malaria transmission and its impact on the evolution of antimalarial drug resistance under the assumption that immune individuals are infectious. Methods The model is constructed as a two-stage susceptible-infected-susceptible (SIS) model of malaria transmission that assumes that individuals build up clinical immunity over a period of years. This immunity reduces the frequency and severity of clinical symptoms, and thus their use of drugs. It also reduces an individual's level of infectiousness, but does not impact the likelihood of becoming infected. Results Simulations found that with the introduction of resistance into a population, clinical immunity can significantly alter the fitness of the resistant parasite, and thereby impact the ability of the resistant parasite to spread from an initial host by reducing the effective reproductive number of the resistant parasite as transmission intensity increases. At high transmission levels, despite a higher basic reproductive number, R 0 , the effective reproductive number of the resistant parasite may fall below the reproductive number of the sensitive parasite. Conclusion These results suggest that high-levels of clinical immunity create a natural ecological refuge for drug-sensitive parasites. This provides an epidemiological rationale for historical patterns of resistance ... |
format |
Article in Journal/Newspaper |
author |
Smith David L Klein Eili Y Boni Maciej F Laxminarayan Ramanan |
author_facet |
Smith David L Klein Eili Y Boni Maciej F Laxminarayan Ramanan |
author_sort |
Smith David L |
title |
Clinically immune hosts as a refuge for drug-sensitive malaria parasites |
title_short |
Clinically immune hosts as a refuge for drug-sensitive malaria parasites |
title_full |
Clinically immune hosts as a refuge for drug-sensitive malaria parasites |
title_fullStr |
Clinically immune hosts as a refuge for drug-sensitive malaria parasites |
title_full_unstemmed |
Clinically immune hosts as a refuge for drug-sensitive malaria parasites |
title_sort |
clinically immune hosts as a refuge for drug-sensitive malaria parasites |
publisher |
BMC |
publishDate |
2008 |
url |
https://doi.org/10.1186/1475-2875-7-67 https://doaj.org/article/c84468b160754601bf48eea64ddef371 |
geographic |
Arctic |
geographic_facet |
Arctic |
genre |
Arctic |
genre_facet |
Arctic |
op_source |
Malaria Journal, Vol 7, Iss 1, p 67 (2008) |
op_relation |
http://www.malariajournal.com/content/7/1/67 https://doaj.org/toc/1475-2875 doi:10.1186/1475-2875-7-67 1475-2875 https://doaj.org/article/c84468b160754601bf48eea64ddef371 |
op_doi |
https://doi.org/10.1186/1475-2875-7-67 |
container_title |
Malaria Journal |
container_volume |
7 |
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1 |
container_start_page |
67 |
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1766346985081667584 |