Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model
Abstract Background In areas endemic for visceral leishmaniasis (VL), the majority of infected hosts remain asymptomatic but potentially infectious to biting sand flies. Their infectiousness for sand fly vectors is crucial for the transmission of the disease and can be quantified only by xenodiagnos...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2015-03-01
|
Series: | Parasites & Vectors |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13071-015-0765-x |
_version_ | 1797811806114152448 |
---|---|
author | Jovana Sadlova Veronika Seblova Jan Votypka Alon Warburg Petr Volf |
author_facet | Jovana Sadlova Veronika Seblova Jan Votypka Alon Warburg Petr Volf |
author_sort | Jovana Sadlova |
collection | DOAJ |
description | Abstract Background In areas endemic for visceral leishmaniasis (VL), the majority of infected hosts remain asymptomatic but potentially infectious to biting sand flies. Their infectiousness for sand fly vectors is crucial for the transmission of the disease and can be quantified only by xenodiagnosis. However, in the case of human hosts, xenodiagnosis can be problematic for ethical and logistic reasons. The BALB/c mouse model described in this paper was designed to enable xenodiagnostic studies on VL hosts circumventing the need for human volunteers, it permits xenodiagnosis using the same individual host repeatedly, over several months. Methods BALB/c mice were intradermally inoculated in the ear pinnae with Leishmania donovani, primarily metacyclic stages isolated from the thoracic midguts of experimentally-infected Phlebotomus orientalis females. Naïve sand flies were allowed to feed on anaesthetized mice in 1-3-weeks- interval, firstly on the site of inoculation of L. donovani (weeks 2–8 post infection, p.i.), later on the whole body of mice (weeks 9 – 15 p.i.). Infections of sand flies were evaluated microscopically or by PCR analysis. Results Although infected mice did not show any signs of disease, 19% (N = 876) of the P. orientalis females that fed at the site of inoculation, became infected. The majority of L. donovani-positive females (76%) had heavy infections with their stomodeal valves colonized by attached parasites. Inoculated mouse ears remained infective for sand flies until week 15 p.i. Females feeding on other parts of the body remained negative with exception of two groups feeding on contralateral ears by week 12 p.i. On week 15, however, these two mice returned negative at xenodiagnosis of the contralateral ears. In sacrificed mice, the highest parasite numbers were found in inoculated ears and their draining lymph nodes. Infections were detected also in the spleen, liver, blood and rarely in the contralateral ear. Conclusions The study showed that BALB/c mice harbored parasites in sufficient numbers to promote heavy infections in P. orientalis and thus comprised a suitable laboratory model for xenodiagnoses of L. donovani. Parasites persisted in the inoculation site and were found transmissible for months to sand flies biting on the same site. |
first_indexed | 2024-03-13T07:29:13Z |
format | Article |
id | doaj.art-36db8d65efac4aba898108df27d638ef |
institution | Directory Open Access Journal |
issn | 1756-3305 |
language | English |
last_indexed | 2024-03-13T07:29:13Z |
publishDate | 2015-03-01 |
publisher | BMC |
record_format | Article |
series | Parasites & Vectors |
spelling | doaj.art-36db8d65efac4aba898108df27d638ef2023-06-04T11:12:58ZengBMCParasites & Vectors1756-33052015-03-01811810.1186/s13071-015-0765-xXenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory modelJovana Sadlova0Veronika Seblova1Jan Votypka2Alon Warburg3Petr Volf4Department of Parasitology, Faculty of Science, Charles University in PragueDepartment of Parasitology, Faculty of Science, Charles University in PragueDepartment of Parasitology, Faculty of Science, Charles University in PragueDepartment of Microbiology & Molecular Genetics, The Institute for Medical Research Israel-Canada, The Kuvin Centre for the Study of Infectious & Tropical Diseases, The Hebrew University - Hadassah Medical School, The Hebrew University of JerusalemDepartment of Parasitology, Faculty of Science, Charles University in PragueAbstract Background In areas endemic for visceral leishmaniasis (VL), the majority of infected hosts remain asymptomatic but potentially infectious to biting sand flies. Their infectiousness for sand fly vectors is crucial for the transmission of the disease and can be quantified only by xenodiagnosis. However, in the case of human hosts, xenodiagnosis can be problematic for ethical and logistic reasons. The BALB/c mouse model described in this paper was designed to enable xenodiagnostic studies on VL hosts circumventing the need for human volunteers, it permits xenodiagnosis using the same individual host repeatedly, over several months. Methods BALB/c mice were intradermally inoculated in the ear pinnae with Leishmania donovani, primarily metacyclic stages isolated from the thoracic midguts of experimentally-infected Phlebotomus orientalis females. Naïve sand flies were allowed to feed on anaesthetized mice in 1-3-weeks- interval, firstly on the site of inoculation of L. donovani (weeks 2–8 post infection, p.i.), later on the whole body of mice (weeks 9 – 15 p.i.). Infections of sand flies were evaluated microscopically or by PCR analysis. Results Although infected mice did not show any signs of disease, 19% (N = 876) of the P. orientalis females that fed at the site of inoculation, became infected. The majority of L. donovani-positive females (76%) had heavy infections with their stomodeal valves colonized by attached parasites. Inoculated mouse ears remained infective for sand flies until week 15 p.i. Females feeding on other parts of the body remained negative with exception of two groups feeding on contralateral ears by week 12 p.i. On week 15, however, these two mice returned negative at xenodiagnosis of the contralateral ears. In sacrificed mice, the highest parasite numbers were found in inoculated ears and their draining lymph nodes. Infections were detected also in the spleen, liver, blood and rarely in the contralateral ear. Conclusions The study showed that BALB/c mice harbored parasites in sufficient numbers to promote heavy infections in P. orientalis and thus comprised a suitable laboratory model for xenodiagnoses of L. donovani. Parasites persisted in the inoculation site and were found transmissible for months to sand flies biting on the same site.https://doi.org/10.1186/s13071-015-0765-xXenodiagnosisVisceral leishmaniasisPhlebotomine sand fliesAsymptomatic reservoir hostsVector-borne diseasesLeishmania donovani |
spellingShingle | Jovana Sadlova Veronika Seblova Jan Votypka Alon Warburg Petr Volf Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model Parasites & Vectors Xenodiagnosis Visceral leishmaniasis Phlebotomine sand flies Asymptomatic reservoir hosts Vector-borne diseases Leishmania donovani |
title | Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model |
title_full | Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model |
title_fullStr | Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model |
title_full_unstemmed | Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model |
title_short | Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model |
title_sort | xenodiagnosis of leishmania donovani in balb c mice using phlebotomus orientalis a new laboratory model |
topic | Xenodiagnosis Visceral leishmaniasis Phlebotomine sand flies Asymptomatic reservoir hosts Vector-borne diseases Leishmania donovani |
url | https://doi.org/10.1186/s13071-015-0765-x |
work_keys_str_mv | AT jovanasadlova xenodiagnosisofleishmaniadonovaniinbalbcmiceusingphlebotomusorientalisanewlaboratorymodel AT veronikaseblova xenodiagnosisofleishmaniadonovaniinbalbcmiceusingphlebotomusorientalisanewlaboratorymodel AT janvotypka xenodiagnosisofleishmaniadonovaniinbalbcmiceusingphlebotomusorientalisanewlaboratorymodel AT alonwarburg xenodiagnosisofleishmaniadonovaniinbalbcmiceusingphlebotomusorientalisanewlaboratorymodel AT petrvolf xenodiagnosisofleishmaniadonovaniinbalbcmiceusingphlebotomusorientalisanewlaboratorymodel |