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A simple model for the within-host dynamics of a protozoan parasite.

ABSTRACT: The dynamics of parasite-host systems can be complicated if the parasite life cycle contains an obligatory environmental stage and if the hosts' immunity increases upon re-infection. The dynamics then greatly depend on the relation between infection history and parasite uptake and excretion of individual hosts. In an effort to better understand such systems, we study Eimeria spp. in chickens as our model. In this paper we take a first step and study the within-host dynamics of Eimeria spp. transmitted through oocysts in the environment, with a mathematical model for the parasite life cycle in discrete time, interacting with a single variable describing the immune response. The model can explain various types of oocyst input-output behaviour as described in previous experiments, in particular the characteristic crowding effect, which causes a decreasing oocyst production with increasing single dose oocyst uptake. Oocyst excretion during constant oocyst uptake (trickle infection) and the immunizing effect of single and trickle infections also appears in accordance with published experiments. The model seems a good description of oocyst input-output behaviour in individual hosts; it provides a solid basis for the study of between-host dynamics, where individuals interact in a common environment, thereby affecting their own and each other's infection pattern.

SUBMITTER: Klinkenberg D

PROVIDER: S-EPMC1564076 | biostudies-literature | 2005 Mar

REPOSITORIES: biostudies-literature

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A simple model for the within-host dynamics of a protozoan parasite.

Klinkenberg D D Heesterbeek J A P JA

Proceedings. Biological sciences 20050301 1563

The dynamics of parasite-host systems can be complicated if the parasite life cycle contains an obligatory environmental stage and if the hosts' immunity increases upon re-infection. The dynamics then greatly depend on the relation between infection history and parasite uptake and excretion of individual hosts. In an effort to better understand such systems, we study Eimeria spp. in chickens as our model. In this paper we take a first step and study the within-host dynamics of Eimeria spp. trans ...[more]

PMID: 15817433

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Project description:The protozoan parasite Trichomonas vaginalis (TV), exclusively adapted to the human genital tract, is one of the most common sexually transmitted pathogens. Adding to the complexity of the host-pathogen interactions, the parasite harbors TV-specific endosymbiont viruses (Trichomonasvirus, TVV). It was reported that small extracellular vesicles (sEVs) released by TV play a role in host immunity; however, the role of the viral endosymbiosis in this process remained unknown. We hypothesized that the virus may offer evolutionary benefit to its protozoan host at least in part by altering the immunomodulatory properties of sEVs spreading from the site of infection to non-infected immune effector cells. We infected human vaginal epithelial cells, the natural host of the parasite, with TV natively harboring TVV and an isogenic derivative of the parasite cured from the viral infection. sEVs were isolated from vaginal cell culture 24 h post TV infection and from medium where the isogenic TV strains were cultured in the absence of the human host. sEVs from TVV-negative but not TVV-positive parasites cultured alone caused NF-κB activation and increase of IL-8 and RANTES expression by uterine endocervical cells, which provide innate immune defense at the gate to the upper reproductive tract. Similarly, mononuclear leukocytes increased their IL-8, IL-6 and TNF-α output in response to sEVs from virus-negative, but not isogenic virus-positive parasites, the latter exosomes being immunosuppressive in comparison to TV medium control. The same phenomenon of suppressed immunity induced by the TVV-positive compared to TVV-negative phenotype was seen when stimulating the leukocytes with sEVs originating from infected vaginal cultures. In addition, the sEVs from the TVV-positive infection phenotype suppressed immune signaling of a toll-like receptor ligand derived from mycoplasma, another frequent TV symbiont. Quantitative comparative proteome analysis of the secreted sEVs from virus-positive versus virus-negative TV revealed differential expression of two functionally uncharacterized proteins and five proteins involved in Zn binding, protein binding, electron transfer, transferase and catalytic activities. These data support the concept that symbiosis with viruses may provide benefit to the protozoan parasite by exploiting sEVs as a vehicle for inter-cellular communications and modifying their protein cargo to suppress host immune activation.

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A simple model for the within-host dynamics of a protozoan parasite.

Publications

A simple model for the within-host dynamics of a protozoan parasite.

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