Concomitant experimental coinfection by Plasmodium berghei NK65-NY and Ascaris suum downregulates the Ascaris-specific immune response and potentiates Ascaris-associated lung pathology
Autor: | Fabrício Marcus Silva Oliveira, Remo Castro Russo, Denise Silva Nogueira, Thaís Leal-Silva, Ricardo Toshio Fujiwara, Luiza de Lima Silva Padrão, Marcelo Vidigal Caliari, Lilian Lacerda Bueno, Lucas Kraemer, Ana Cristina Loiola Ruas, Flaviane Vieira-Santos |
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Rok vydání: | 2021 |
Předmět: |
Male
0301 basic medicine Lung inflammation Plasmodium berghei Plasmodium berghei NK65-NY RC955-962 030231 tropical medicine Down-Regulation Infectious and parasitic diseases RC109-216 Lung injury Mice 03 medical and health sciences 0302 clinical medicine Immune system Arctic medicine. Tropical medicine parasitic diseases medicine Animals Respiratory function Helminth infection Lung Ascaris suum Ascariasis medicine.diagnostic_test biology Coinfection business.industry Ascaris Research Pulmonary mechanics biology.organism_classification medicine.disease Immunity Innate Malaria Mice Inbred C57BL 030104 developmental biology Infectious Diseases Bronchoalveolar lavage Gene Expression Regulation Immunology Parasitology business |
Zdroj: | Malaria Journal, Vol 20, Iss 1, Pp 1-15 (2021) Malaria Journal |
ISSN: | 1475-2875 |
DOI: | 10.1186/s12936-021-03824-w |
Popis: | Background Ascariasis and malaria are highly prevalent parasitic diseases in tropical regions and often have overlapping endemic areas, contributing to high morbidity and mortality rates in areas with poor sanitary conditions. Several studies have previously aimed to correlate the effects of Ascaris-Plasmodium coinfections but have obtained contradictory and inconclusive results. Therefore, the present study aimed to investigate parasitological and immunopathological aspects of the lung during murine experimental concomitant coinfection by Plasmodium berghei and Ascaris suum during larvae ascariasis. Methods C57BL/6J mice were inoculated with 1 × 104P. berghei strain NK65-NY-infected red blood cells (iRBCs) intraperitoneally and/or 2500 embryonated eggs of A. suum by oral gavage. P. berghei parasitaemia, morbidity and the survival rate were assessed. On the seventh day postinfection (dpi), A. suum lung burden analysis; bronchoalveolar lavage (BAL); histopathology; NAG, MPO and EPO activity measurements; haematological analysis; and respiratory mechanics analysis were performed. The concentrations of interleukin (IL)-1β, IL-12/IL-23p40, IL-6, IL-4, IL-33, IL-13, IL-5, IL-10, IL-17A, IFN-γ, TNF and TGF-β were assayed by sandwich ELISA. Results Animals coinfected with P. berghei and A. suum show decreased production of type 1, 2, and 17 and regulatory cytokines; low leukocyte recruitment in the tissue; increased cellularity in the circulation; and low levels of NAG, MPO and EPO activity that lead to an increase in larvae migration, as shown by the decrease in larvae recovered in the lung parenchyma and increase in larvae recovered in the airway. This situation leads to severe airway haemorrhage and, consequently, an impairment respiratory function that leads to high morbidity and early mortality. Conclusions This study demonstrates that the Ascaris-Plasmodium interaction is harmful to the host and suggests that this coinfection may potentiate Ascaris-associated pathology by dampening the Ascaris-specific immune response, resulting in the early death of affected animals. |
Databáze: | OpenAIRE |
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