Dose-response effects of multiple Ascaris suum exposures and their impact on lung protection during larval ascariasis

PLoS Negl Trop Dis. 2024 Dec 2;18(12):e0012678. doi: 10.1371/journal.pntd.0012678. eCollection 2024 Dec.

Abstract

Background: Human ascariasis is the most prevalent geohelminthiasis worldwide, affecting approximately 446 million individuals. In regions with endemic prevalence, the majority of infected adults are frequently exposed to the parasite and tend to have a low parasite load. Further studies are necessary to provide more evidence on the dynamics of infection and to elucidate the possible mechanisms involved in regulating protection, especially during the acute phase, also known as larval ascariasis. The aim of this study is to compare the impact of lung function between single and multiple infections in a murine model.

Methods: We infected BALB/c mice considering the frequency of exposures: single-exposure-SI; twice-exposures-RE 2x and thrice-exposures-RE 3x, and considering the doses of infection: 25 eggs-RE 25; 250 eggs-RE 250 and 2,500 eggs-RE 2500, followed by infection challenge with 2,500 eggs. From this, we evaluated: parasite burden in lungs, cellular and humoral response, histopathological and physiological alterations in lungs.

Results: The main results showed a reduction of parasite burden in the reinfected groups compared to the single-infected group, with protection increasing with higher exposure and dose. Furthermore, the RE 250 group exhibited a decrease of parasite burden close to RE 2500, but with less tissue damage, displaying the most favorable prognosis among the reinfected groups.

Conclusion: Our research indicates a dose-dependent relationship between antibody production and the intensity of the immune response required to regulate the parasite burden.

MeSH terms

  • Animals
  • Antibodies, Helminth / blood
  • Ascariasis* / immunology
  • Ascariasis* / parasitology
  • Ascariasis* / prevention & control
  • Ascaris suum* / physiology
  • Disease Models, Animal
  • Female
  • Larva
  • Lung* / parasitology
  • Lung* / pathology
  • Mice
  • Mice, Inbred BALB C*
  • Parasite Load

Substances

  • Antibodies, Helminth

Grants and funding

This study was supported by the following grants: RTF received financial support from Fundação de Amparo a Pesquisa do Estado de Minas Gerais/FAPEMIG, Brazil (http://www. fapemig.br) (Grant# APQ-02592-17; RED-0067-23); Conselho Nacional de Desenvolvimento Científico e Tecnológico/CNPq, Brazil (http://www. cnpq.br) (Grant# 403278/2023-6, 442994/2019-2, 305514/2022-9); and Pró-Reitoria de Pesquisa of Universidade Federal de Minas Gerais (https://www.ufmg.br/prpq). RCR, LLB and RTF are Research Fellows (Bolsa de Produtividade em Pesquisa) from CNPq. CCOA was supported by a master’s degree fellowship from the CNPq and a PhD fellowship from CAPES (Coordenação Aperfeiçoamento de Pessoal de Nível Superior). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.