Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection

Filariases are caused by onchocercid nematodes that are transmitted by arthropod vectors. More than 180 million people are infected worldwide. Mass drug administration has been set up in many endemic areas to control the parasite burden. Although very successful in limiting microfilarial load, trans...

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Main Authors: Bouchery T., Ehrhardt K., Lefoulon E., Hoffmann W., Bain O., Martin C.
Format: Article
Language:English
Published: EDP Sciences 2012-11-01
Series:Parasite
Subjects:
Online Access:http://dx.doi.org/10.1051/parasite/2012194351
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spelling doaj-a0f6547f129149048b27702e43bd98122021-02-02T00:49:05ZengEDP SciencesParasite1252-607X1776-10422012-11-0119435135810.1051/parasite/2012194351parasite2012194p351Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infectionBouchery T.Ehrhardt K.Lefoulon E.Hoffmann W.Bain O.Martin C.Filariases are caused by onchocercid nematodes that are transmitted by arthropod vectors. More than 180 million people are infected worldwide. Mass drug administration has been set up in many endemic areas to control the parasite burden. Although very successful in limiting microfilarial load, transmission has not been completely interrupted in such areas. A proportion of infected patients with lymphatic filariasis or loiasis are known to be amicrofilaremic, as they do not present microfilariae in their bloodstream despite the presence of adult worms. A mirror status also exists in CBA/Ca mice infected with Litomosoides sigmodontis, the well-established model of filariasis. Using this model, the goal of this study was to determine if the kinetics of blood clearance of microfilariae differed between amicrofilaremic CBA/Ca mice and microfilaremic BALB/c mice. For this purpose, a qPCR approach was devised to detect microfilariae in different tissues, after a controlled inoculation of microfilariae. We showed that the rapid clearance of microfilariae from the pleural cavity or from the bloodstream of CBA/Ca mice was associated with a massive accumulation of first stage larvae in the lungs, liver and spleen.http://dx.doi.org/10.1051/parasite/2012194351filariasisLitomosoides sigmodontismicrofilariaeamicrofilaremicreal-time PCRlungsliverspleen
collection DOAJ
language English
format Article
sources DOAJ
author Bouchery T.
Ehrhardt K.
Lefoulon E.
Hoffmann W.
Bain O.
Martin C.
spellingShingle Bouchery T.
Ehrhardt K.
Lefoulon E.
Hoffmann W.
Bain O.
Martin C.
Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection
Parasite
filariasis
Litomosoides sigmodontis
microfilariae
amicrofilaremic
real-time PCR
lungs
liver
spleen
author_facet Bouchery T.
Ehrhardt K.
Lefoulon E.
Hoffmann W.
Bain O.
Martin C.
author_sort Bouchery T.
title Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection
title_short Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection
title_full Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection
title_fullStr Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection
title_full_unstemmed Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection
title_sort differential tissular distribution of litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection
publisher EDP Sciences
series Parasite
issn 1252-607X
1776-1042
publishDate 2012-11-01
description Filariases are caused by onchocercid nematodes that are transmitted by arthropod vectors. More than 180 million people are infected worldwide. Mass drug administration has been set up in many endemic areas to control the parasite burden. Although very successful in limiting microfilarial load, transmission has not been completely interrupted in such areas. A proportion of infected patients with lymphatic filariasis or loiasis are known to be amicrofilaremic, as they do not present microfilariae in their bloodstream despite the presence of adult worms. A mirror status also exists in CBA/Ca mice infected with Litomosoides sigmodontis, the well-established model of filariasis. Using this model, the goal of this study was to determine if the kinetics of blood clearance of microfilariae differed between amicrofilaremic CBA/Ca mice and microfilaremic BALB/c mice. For this purpose, a qPCR approach was devised to detect microfilariae in different tissues, after a controlled inoculation of microfilariae. We showed that the rapid clearance of microfilariae from the pleural cavity or from the bloodstream of CBA/Ca mice was associated with a massive accumulation of first stage larvae in the lungs, liver and spleen.
topic filariasis
Litomosoides sigmodontis
microfilariae
amicrofilaremic
real-time PCR
lungs
liver
spleen
url http://dx.doi.org/10.1051/parasite/2012194351
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