Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatments

<p>Abstract</p> <p>Background</p> <p>In Europe most dogs with clinical leishmaniosis are treated with leishmanicides, typically antimonials combined with allopurinol and good clinical recovery is observed in a high number of these dogs. Through xenodiagnosis, the capaci...

Full description

Bibliographic Details
Main Authors: Descalzo Miguel A, Fraile Cristeta, Gálvez Rosa, Miró Guadalupe, Molina Ricardo
Format: Article
Language:English
Published: BMC 2011-04-01
Series:Parasites & Vectors
Online Access:http://www.parasitesandvectors.com/content/4/1/52
id doaj-84038a6e9a4a4b898cbbc17301eeeb6b
record_format Article
spelling doaj-84038a6e9a4a4b898cbbc17301eeeb6b2020-11-24T22:12:44ZengBMCParasites & Vectors1756-33052011-04-01415210.1186/1756-3305-4-52Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatmentsDescalzo Miguel AFraile CristetaGálvez RosaMiró GuadalupeMolina Ricardo<p>Abstract</p> <p>Background</p> <p>In Europe most dogs with clinical leishmaniosis are treated with leishmanicides, typically antimonials combined with allopurinol and good clinical recovery is observed in a high number of these dogs. Through xenodiagnosis, the capacity of a treated animal to infect the vector of the disease under treatment is assessed as a measure of the chemotherapeutic efficacy of the drug used. The objective of the present study was to evaluate through direct xenodiagnosis the infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after treatment, and to follow the clinical and parasite course of disease. Thirty two dogs with clinical leishmaniosis were assigned to one of three treatment groups: meglumine antimoniate plus allopurinol (Group A), meglumine antimoniate (Group B) or allopurinol (Group C). During the study, the dogs were examined before treatment (Day 0) and bimonthly thereafter until Day 180 (six months post-treatment onset).</p> <p>Results</p> <p>The three groups were scored over time according to the effects of treatment on clinical signs and clinical-pathological variables. Significant differences in clinical scores were observed between Group A and the other two groups, indicating the combined treatment was the most effective. After treatment, bone marrow cultures were positive for the parasite in 30.8% of dogs in some of the check ups (3 or 25% in Group A, 1 or 11.1% in Group B, and 4 or 80% in Group C). Our xenodiagnosis experiments revealed that 15.4% of treated dogs were still able to infect sand flies at some point after treatment (2 dogs or 16.6% in Group A, 2 or 22.2% in Group B and none in Group C). Only 7.7% of the entire study population could infect sand flies as from the second month post-treatment onset.</p> <p>Conclusion</p> <p>The three treatment regimens tested significantly reduced the infectivity of dogs towards sand flies, thus diminishing the epidemiological risks of treated dogs both for human beings and other healthy dogs. Despite its low cure rate, the use of allopurinol after a course of leishmanicide treatment is proposed to keep dogs non-infectious during the disease transmission season (4-6 months in southern Europe).</p> http://www.parasitesandvectors.com/content/4/1/52
collection DOAJ
language English
format Article
sources DOAJ
author Descalzo Miguel A
Fraile Cristeta
Gálvez Rosa
Miró Guadalupe
Molina Ricardo
spellingShingle Descalzo Miguel A
Fraile Cristeta
Gálvez Rosa
Miró Guadalupe
Molina Ricardo
Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatments
Parasites & Vectors
author_facet Descalzo Miguel A
Fraile Cristeta
Gálvez Rosa
Miró Guadalupe
Molina Ricardo
author_sort Descalzo Miguel A
title Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatments
title_short Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatments
title_full Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatments
title_fullStr Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatments
title_full_unstemmed Infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after different treatments
title_sort infectivity to <it>phlebotomus perniciosus </it>of dogs naturally parasitized with <it>leishmania infantum </it>after different treatments
publisher BMC
series Parasites & Vectors
issn 1756-3305
publishDate 2011-04-01
description <p>Abstract</p> <p>Background</p> <p>In Europe most dogs with clinical leishmaniosis are treated with leishmanicides, typically antimonials combined with allopurinol and good clinical recovery is observed in a high number of these dogs. Through xenodiagnosis, the capacity of a treated animal to infect the vector of the disease under treatment is assessed as a measure of the chemotherapeutic efficacy of the drug used. The objective of the present study was to evaluate through direct xenodiagnosis the infectivity to <it>Phlebotomus perniciosus </it>of dogs naturally parasitized with <it>Leishmania infantum </it>after treatment, and to follow the clinical and parasite course of disease. Thirty two dogs with clinical leishmaniosis were assigned to one of three treatment groups: meglumine antimoniate plus allopurinol (Group A), meglumine antimoniate (Group B) or allopurinol (Group C). During the study, the dogs were examined before treatment (Day 0) and bimonthly thereafter until Day 180 (six months post-treatment onset).</p> <p>Results</p> <p>The three groups were scored over time according to the effects of treatment on clinical signs and clinical-pathological variables. Significant differences in clinical scores were observed between Group A and the other two groups, indicating the combined treatment was the most effective. After treatment, bone marrow cultures were positive for the parasite in 30.8% of dogs in some of the check ups (3 or 25% in Group A, 1 or 11.1% in Group B, and 4 or 80% in Group C). Our xenodiagnosis experiments revealed that 15.4% of treated dogs were still able to infect sand flies at some point after treatment (2 dogs or 16.6% in Group A, 2 or 22.2% in Group B and none in Group C). Only 7.7% of the entire study population could infect sand flies as from the second month post-treatment onset.</p> <p>Conclusion</p> <p>The three treatment regimens tested significantly reduced the infectivity of dogs towards sand flies, thus diminishing the epidemiological risks of treated dogs both for human beings and other healthy dogs. Despite its low cure rate, the use of allopurinol after a course of leishmanicide treatment is proposed to keep dogs non-infectious during the disease transmission season (4-6 months in southern Europe).</p>
url http://www.parasitesandvectors.com/content/4/1/52
work_keys_str_mv AT descalzomiguela infectivitytoitphlebotomusperniciosusitofdogsnaturallyparasitizedwithitleishmaniainfantumitafterdifferenttreatments
AT frailecristeta infectivitytoitphlebotomusperniciosusitofdogsnaturallyparasitizedwithitleishmaniainfantumitafterdifferenttreatments
AT galvezrosa infectivitytoitphlebotomusperniciosusitofdogsnaturallyparasitizedwithitleishmaniainfantumitafterdifferenttreatments
AT miroguadalupe infectivitytoitphlebotomusperniciosusitofdogsnaturallyparasitizedwithitleishmaniainfantumitafterdifferenttreatments
AT molinaricardo infectivitytoitphlebotomusperniciosusitofdogsnaturallyparasitizedwithitleishmaniainfantumitafterdifferenttreatments
_version_ 1725802536871395328