Literature DB >> 2052590

Periodic and chaotic host-parasite interactions in human malaria.

D Kwiatkowski1, M Nowak.   

Abstract

It has been recognized since ancient times that malaria fever is highly periodic but the mechanism has been poorly understood. Malaria fever is related to the parasite growth cycle in erythrocytes. After a fixed period of replication, a mature parasite (schizont) causes the infected erythrocyte to rupture, releasing progeny that quickly invade other erythrocytes. Simultaneous rupture of a large number of schizonts stimulates a host fever response. Febrile temperatures are damaging to Plasmodium falciparum, particularly in the second half of its 48-hr replicative cycle. Using a mathematical model, we show that these interactions naturally tend to generate periodic fever. The model predicts chaotic parasite population dynamics at high multiplication rates, consistent with the classical observation that P. falciparum causes less regular fever than other species of parasite.

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Year:  1991        PMID: 2052590      PMCID: PMC51821          DOI: 10.1073/pnas.88.12.5111

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  10 in total

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Authors:  R M Anderson; R M May; S Gupta
Journal:  Parasitology       Date:  1989       Impact factor: 3.234

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Authors:  R M May
Journal:  Nature       Date:  1976-06-10       Impact factor: 49.962

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Journal:  Sci Am       Date:  1970-06       Impact factor: 2.142

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Authors:  F Hawking; M J Worms; K Gammage
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Review 5.  Anti-parasite effects of cytokines in malaria.

Authors:  K N Mendis; T D Naotunne; N D Karunaweera; G Del Giudice; G E Grau; R Carter
Journal:  Immunol Lett       Date:  1990-08       Impact factor: 3.685

6.  Cell-mediated immunity in protection and pathology of malaria.

Authors:  I A Clark
Journal:  Parasitol Today       Date:  1987-10

7.  Why is malaria fever periodic? A hypothesis.

Authors:  D Kwiatkowski; B M Greenwood
Journal:  Parasitol Today       Date:  1989-08

8.  TNF concentration in fatal cerebral, non-fatal cerebral, and uncomplicated Plasmodium falciparum malaria.

Authors:  D Kwiatkowski; A V Hill; I Sambou; P Twumasi; J Castracane; K R Manogue; A Cerami; D R Brewster; B M Greenwood
Journal:  Lancet       Date:  1990-11-17       Impact factor: 79.321

9.  Tumour necrosis factor production in Falciparum malaria and its association with schizont rupture.

Authors:  D Kwiatkowski; J G Cannon; K R Manogue; A Cerami; C A Dinarello; B M Greenwood
Journal:  Clin Exp Immunol       Date:  1989-09       Impact factor: 4.330

10.  Febrile temperatures can synchronize the growth of Plasmodium falciparum in vitro.

Authors:  D Kwiatkowski
Journal:  J Exp Med       Date:  1989-01-01       Impact factor: 14.307

  10 in total
  31 in total

1.  Selection for high and low virulence in the malaria parasite Plasmodium chabaudi.

Authors:  M J Mackinnon; A F Read
Journal:  Proc Biol Sci       Date:  1999-04-07       Impact factor: 5.349

2.  Link between immune response and parasite synchronization in malaria.

Authors:  Igor M Rouzine; F Ellis McKenzie
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-05       Impact factor: 11.205

3.  Population robustness arising from cellular heterogeneity.

Authors:  Pawel Paszek; Sheila Ryan; Louise Ashall; Kate Sillitoe; Claire V Harper; David G Spiller; David A Rand; Michael R H White
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-07       Impact factor: 11.205

4.  Cross-reactive immune responses as primary drivers of malaria chronicity.

Authors:  Eili Y Klein; Andrea L Graham; Manuel Llinás; Simon Levin
Journal:  Infect Immun       Date:  2013-10-14       Impact factor: 3.441

5.  Plasmodium falciparum: differential merozoite dose requirements for maximal production of various inflammatory cytokines.

Authors:  Xianzhu Wu; Nagaraj M Gowda; D Channe Gowda
Journal:  Exp Parasitol       Date:  2010-08-03       Impact factor: 2.011

6.  Serum levels of the proinflammatory cytokines interleukin-1 beta (IL-1beta), IL-6, IL-8, IL-10, tumor necrosis factor alpha, and IL-12(p70) in Malian children with severe Plasmodium falciparum malaria and matched uncomplicated malaria or healthy controls.

Authors:  K E Lyke; R Burges; Y Cissoko; L Sangare; M Dao; I Diarra; A Kone; R Harley; C V Plowe; O K Doumbo; M B Sztein
Journal:  Infect Immun       Date:  2004-10       Impact factor: 3.441

7.  Synchrony in malaria infections: how intensifying within-host competition can be adaptive.

Authors:  Megan A Greischar; Andrew F Read; Ottar N Bjørnstad
Journal:  Am Nat       Date:  2013-12-16       Impact factor: 3.926

8.  Factors contributing to delay in parasite clearance in uncomplicated falciparum malaria in children.

Authors:  Akintunde Sowunmi; Elsie O Adewoye; Grace O Gbotsho; Christian T Happi; Abayomi Sijuade; Onikepe A Folarin; Titilope M Okuboyejo; Obaro S Michael
Journal:  Malar J       Date:  2010-02-15       Impact factor: 2.979

9.  Detectability of Plasmodium falciparum clones.

Authors:  Michael T Bretscher; Francesca Valsangiacomo; Seth Owusu-Agyei; Melissa A Penny; Ingrid Felger; Tom Smith
Journal:  Malar J       Date:  2010-08-18       Impact factor: 2.979

10.  Malarial hemozoin activates the NLRP3 inflammasome through Lyn and Syk kinases.

Authors:  Marina Tiemi Shio; Marina Tiemi Shio; Stephanie C Eisenbarth; Myriam Savaria; Adrien F Vinet; Marie-Josée Bellemare; Kenneth W Harder; Fayyaz S Sutterwala; D Scott Bohle; Albert Descoteaux; Richard A Flavell; Martin Olivier
Journal:  PLoS Pathog       Date:  2009-08-21       Impact factor: 6.823

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