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Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus

BACKGROUND: Polyparasitism is the rule in all animal species, including humans, and has an important role in pathogenicity, diagnosis and control measures. Among them, co-infections by gastrointestinal helminths and protists are very prevalent under natural conditions but experimental infections are...

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Autores principales: González-Sánchez, M. E., Cuquerella, M., Alunda, J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042253/
https://www.ncbi.nlm.nih.gov/pubmed/29996937
http://dx.doi.org/10.1186/s13071-018-2987-1
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author González-Sánchez, M. E.
Cuquerella, M.
Alunda, J. M.
author_facet González-Sánchez, M. E.
Cuquerella, M.
Alunda, J. M.
author_sort González-Sánchez, M. E.
collection PubMed
description BACKGROUND: Polyparasitism is the rule in all animal species, including humans, and has an important role in pathogenicity, diagnosis and control measures. Among them, co-infections by gastrointestinal helminths and protists are very prevalent under natural conditions but experimental infections are relatively scarce. Thus, despite the frequent association of visceral Leishmania infections and intestinal helminth parasitism the experimental co-infection has not been addressed. Heligmosomoides polygyrus, an intestinal nematode of mice, is related to other helminths causing important pathologies and is a model species for immunological studies. Mice are valuable experimental model for visceral leishmaniasis. METHODS: BALB/c mice infected with H. polygyrus (200 third-stage larvae, L3) were subsequently infected seven days later with Leishmania infantum (10(7) promastigotes) with the aim of determining the effect of the overinfection on the host response to the primary infection with the helminth. RESULTS: Overinfection with the protist did not affect the establishment rate of the nematode but induced a higher fecal egg output. Helminth burdens in co-infected animals were significant at the end of the experiment. Early unspecific immune suppression induced by the nematode in mesenteric lymph nodes was not switched by L. infantum infection. Co-infection elicited a higher serum antibody (IgG(1)) response against the helminth. CONCLUSIONS: Visceral leishmanial overinfection aggravated the early host response against primary infections with the intestinal helminth. This effect was evidenced by an increased longevity and higher production of non-protective antibodies.
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spelling pubmed-60422532018-07-13 Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus González-Sánchez, M. E. Cuquerella, M. Alunda, J. M. Parasit Vectors Research BACKGROUND: Polyparasitism is the rule in all animal species, including humans, and has an important role in pathogenicity, diagnosis and control measures. Among them, co-infections by gastrointestinal helminths and protists are very prevalent under natural conditions but experimental infections are relatively scarce. Thus, despite the frequent association of visceral Leishmania infections and intestinal helminth parasitism the experimental co-infection has not been addressed. Heligmosomoides polygyrus, an intestinal nematode of mice, is related to other helminths causing important pathologies and is a model species for immunological studies. Mice are valuable experimental model for visceral leishmaniasis. METHODS: BALB/c mice infected with H. polygyrus (200 third-stage larvae, L3) were subsequently infected seven days later with Leishmania infantum (10(7) promastigotes) with the aim of determining the effect of the overinfection on the host response to the primary infection with the helminth. RESULTS: Overinfection with the protist did not affect the establishment rate of the nematode but induced a higher fecal egg output. Helminth burdens in co-infected animals were significant at the end of the experiment. Early unspecific immune suppression induced by the nematode in mesenteric lymph nodes was not switched by L. infantum infection. Co-infection elicited a higher serum antibody (IgG(1)) response against the helminth. CONCLUSIONS: Visceral leishmanial overinfection aggravated the early host response against primary infections with the intestinal helminth. This effect was evidenced by an increased longevity and higher production of non-protective antibodies. BioMed Central 2018-07-11 /pmc/articles/PMC6042253/ /pubmed/29996937 http://dx.doi.org/10.1186/s13071-018-2987-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
González-Sánchez, M. E.
Cuquerella, M.
Alunda, J. M.
Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus
title Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus
title_full Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus
title_fullStr Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus
title_full_unstemmed Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus
title_short Superimposed visceral leishmanial infection aggravates response to Heligmosomoides polygyrus
title_sort superimposed visceral leishmanial infection aggravates response to heligmosomoides polygyrus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042253/
https://www.ncbi.nlm.nih.gov/pubmed/29996937
http://dx.doi.org/10.1186/s13071-018-2987-1
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