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Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung

Filarial infections are tropical diseases caused by nematodes of the Onchocercidae family such as Mansonella perstans. The infective larvae (L3) are transmitted into the skin of vertebrate hosts by blood-feeding vectors. Many filarial species settle in the serous cavities including M. perstans in hu...

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Autores principales: Karadjian, Gregory, Fercoq, Frédéric, Pionnier, Nicolas, Vallarino-Lhermitte, Nathaly, Lefoulon, Emilie, Nieguitsila, Adélaïde, Specht, Sabine, Carlin, Leo M., Martin, Coralie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438187/
https://www.ncbi.nlm.nih.gov/pubmed/28486498
http://dx.doi.org/10.1371/journal.pntd.0005596
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author Karadjian, Gregory
Fercoq, Frédéric
Pionnier, Nicolas
Vallarino-Lhermitte, Nathaly
Lefoulon, Emilie
Nieguitsila, Adélaïde
Specht, Sabine
Carlin, Leo M.
Martin, Coralie
author_facet Karadjian, Gregory
Fercoq, Frédéric
Pionnier, Nicolas
Vallarino-Lhermitte, Nathaly
Lefoulon, Emilie
Nieguitsila, Adélaïde
Specht, Sabine
Carlin, Leo M.
Martin, Coralie
author_sort Karadjian, Gregory
collection PubMed
description Filarial infections are tropical diseases caused by nematodes of the Onchocercidae family such as Mansonella perstans. The infective larvae (L3) are transmitted into the skin of vertebrate hosts by blood-feeding vectors. Many filarial species settle in the serous cavities including M. perstans in humans and L. sigmodontis, a well-established model of filariasis in mice. L. sigmodontis L3 migrate to the pleural cavity where they moult into L4 around day 9 and into male and female adult worms around day 30. Little is known of the early phase of the parasite life cycle, after the L3 is inoculated in the dermis by the vector and enters the afferent lymphatic vessels and before the moulting processes in the pleural cavity. Here we reveal a pulmonary phase associated with lung damage characterized by haemorrhages and granulomas suggesting L3 reach the lung via pulmonary capillaries and damage the endothelium and parenchyma by crossing them to enter the pleural cavity. This study also provides evidence for a transient inflammation in the lung characterized by a very early recruitment of neutrophils associated with high expression levels of S100A8 and S100A9 proteins.
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spelling pubmed-54381872017-05-26 Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung Karadjian, Gregory Fercoq, Frédéric Pionnier, Nicolas Vallarino-Lhermitte, Nathaly Lefoulon, Emilie Nieguitsila, Adélaïde Specht, Sabine Carlin, Leo M. Martin, Coralie PLoS Negl Trop Dis Research Article Filarial infections are tropical diseases caused by nematodes of the Onchocercidae family such as Mansonella perstans. The infective larvae (L3) are transmitted into the skin of vertebrate hosts by blood-feeding vectors. Many filarial species settle in the serous cavities including M. perstans in humans and L. sigmodontis, a well-established model of filariasis in mice. L. sigmodontis L3 migrate to the pleural cavity where they moult into L4 around day 9 and into male and female adult worms around day 30. Little is known of the early phase of the parasite life cycle, after the L3 is inoculated in the dermis by the vector and enters the afferent lymphatic vessels and before the moulting processes in the pleural cavity. Here we reveal a pulmonary phase associated with lung damage characterized by haemorrhages and granulomas suggesting L3 reach the lung via pulmonary capillaries and damage the endothelium and parenchyma by crossing them to enter the pleural cavity. This study also provides evidence for a transient inflammation in the lung characterized by a very early recruitment of neutrophils associated with high expression levels of S100A8 and S100A9 proteins. Public Library of Science 2017-05-09 /pmc/articles/PMC5438187/ /pubmed/28486498 http://dx.doi.org/10.1371/journal.pntd.0005596 Text en © 2017 Karadjian et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Karadjian, Gregory
Fercoq, Frédéric
Pionnier, Nicolas
Vallarino-Lhermitte, Nathaly
Lefoulon, Emilie
Nieguitsila, Adélaïde
Specht, Sabine
Carlin, Leo M.
Martin, Coralie
Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung
title Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung
title_full Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung
title_fullStr Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung
title_full_unstemmed Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung
title_short Migratory phase of Litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of S100A9 expressing neutrophils in the lung
title_sort migratory phase of litomosoides sigmodontis filarial infective larvae is associated with pathology and transient increase of s100a9 expressing neutrophils in the lung
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438187/
https://www.ncbi.nlm.nih.gov/pubmed/28486498
http://dx.doi.org/10.1371/journal.pntd.0005596
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