Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model

J. Sadlova, V. Seblova, J. Votypka, A. Warburg, P. Volf,

. 2015 ; 8 (-) : 158. [pub] 20150314

Language English Country England, Great Britain

Document type Journal Article, Research Support, Non-U.S. Gov't

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.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc16010326
003      
CZ-PrNML
005      
20160408124135.0
007      
ta
008      
160408s2015 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1186/s13071-015-0765-x $2 doi
024    7_
$a 10.1186/s13071-015-0765-x $2 doi
035    __
$a (PubMed)25881258
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Sadlova, Jovana $u Department of Parasitology, Faculty of Science, Charles University in Prague, Prague 2, Vinicna 7, 128 44, Czech Republic. sadlovaj@natur.cuni.cz.
245    10
$a Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model / $c J. Sadlova, V. Seblova, J. Votypka, A. Warburg, P. Volf,
520    9_
$a 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.
650    _2
$a zvířata $7 D000818
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé $7 D006801
650    _2
$a Leishmania donovani $x izolace a purifikace $7 D007893
650    _2
$a leishmanióza viscerální $x diagnóza $x parazitologie $x přenos $7 D007898
650    _2
$a myši $7 D051379
650    _2
$a myši inbrední BALB C $7 D008807
650    _2
$a Phlebotomus $x parazitologie $7 D010691
650    _2
$a xenodiagnóza $x metody $7 D020525
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Seblova, Veronika $u Department of Parasitology, Faculty of Science, Charles University in Prague, Prague 2, Vinicna 7, 128 44, Czech Republic. vera_vera@seznam.cz.
700    1_
$a Votypka, Jan $u Department of Parasitology, Faculty of Science, Charles University in Prague, Prague 2, Vinicna 7, 128 44, Czech Republic. vapid@natur.cuni.cz.
700    1_
$a Warburg, Alon $u Department 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 Jerusalem, Jerusalem, 91120, Israel. alonw@ekmd.huji.ac.il.
700    1_
$a Volf, Petr $u Department of Parasitology, Faculty of Science, Charles University in Prague, Prague 2, Vinicna 7, 128 44, Czech Republic. volf@cesnet.cz.
773    0_
$w MED00165371 $t Parasites & vectors $x 1756-3305 $g Roč. 8, č. - (2015), s. 158
856    41
$u https://pubmed.ncbi.nlm.nih.gov/25881258 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20160408 $b ABA008
991    __
$a 20160408124213 $b ABA008
999    __
$a ok $b bmc $g 1113755 $s 934694
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 8 $c - $d 158 $e 20150314 $i 1756-3305 $m Parasites & vectors $n Parasit Vectors $x MED00165371
LZP    __
$a Pubmed-20160408

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...