Abstract

Variation in the intensity and duration of infections is often driven by variation in the network and strength of host immune responses. While many of the immune mechanisms and components are known for parasitic helminths, how these relationships change from single to multiple infections and impact helminth dynamics remains largely unclear. Here, we used laboratory data from a rabbit-helminth system and developed a within-host model of infection to investigate different scenarios of immune regulation in rabbits infected with one or two helminth species. Model selection suggests that the immunological pathways activated against Trichostrongylus retortaeformis and Graphidium strigosum are similar. However, differences in the strength of these immune signals lead to the contrasting dynamics of infections, where the first parasite is rapidly cleared and the latter persists with high intensities. In addition to the reactions identified in single infections, rabbits with both helminths also activate new pathways that asymmetrically affect the dynamics of the two species. These new signals alter the intensities but not the general trend of the infections. The type of interactions described can be expected in many other host-helminth systems. Our immune framework is flexible enough to capture different mechanisms and their complexity, and provides essential insights to the understanding of multi-helminth infections.

Highlights

  • Population-level processes of infection are strongly affected by the way parasites interact with the host immune response

  • We examine the immune reactions of hosts infected with one or two gastrointestinal parasites, using a rabbit-helminth system and a modeling approach to laboratory experiments

  • We found that similar immune interactions operate for the two parasites, changes in the strength of the relationships lead to contrasting dynamics

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Summary

Introduction

Population-level processes of infection are strongly affected by the way parasites interact with the host immune response. These responses are complex, and involve components and functions that are time and space dependent, whilst targeting specific attributes and phases of the infecting parasite (both macro- and micro-parasites). The network of interactions could be altered, such that new immune functions could be activated or suppressed, with consequences that are not fully predictable from basic knowledge on single infections [2]. Disentangling the critical mechanisms and their impact on each parasite species is challenging because of the often limited information on the immune network and the interactions with the co-infecting parasites

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