Experimental infection with Rangelia vitalii in dogs: Acute phase, parasitemia, biological cycle, clinical-pathological aspects and treatment

[Display omitted] ► Rangelia vitalli is a member of the protozoan phylum Apicomplexa. ► It is a disease that commonly affects dogs from rural and suburban areas in Brazil. ► The parasite erythrocyte cycle presents an acute phase of the disease. ► After the peak of parasitemia, the protozoan invades...

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Veröffentlicht in:Experimental parasitology 2011-08, Vol.128 (4), p.347-352
Hauptverfasser: Da Silva, Aleksandro S., França, Raqueli T., Costa, Marcio M., Paim, Carlos B., Paim, Francine C., Dornelles, Guilherme L., Soares, João F., Labruna, Marcelo B., Mazzanti, Cinthia M., Monteiro, Silvia G., Lopes, Sonia T.A.
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container_end_page 352
container_issue 4
container_start_page 347
container_title Experimental parasitology
container_volume 128
creator Da Silva, Aleksandro S.
França, Raqueli T.
Costa, Marcio M.
Paim, Carlos B.
Paim, Francine C.
Dornelles, Guilherme L.
Soares, João F.
Labruna, Marcelo B.
Mazzanti, Cinthia M.
Monteiro, Silvia G.
Lopes, Sonia T.A.
description [Display omitted] ► Rangelia vitalli is a member of the protozoan phylum Apicomplexa. ► It is a disease that commonly affects dogs from rural and suburban areas in Brazil. ► The parasite erythrocyte cycle presents an acute phase of the disease. ► After the peak of parasitemia, the protozoan invades and multiplies in vascular endothelial cells and leukocytes. ► The therapeutic protocol based on diminazene aceturate has 100% efficacy. Recently we conducted the molecular characterization of Rangelia vitalii, a protozoan with high pathogenicity for young dogs in southern Brazil. To date, the descriptions of the disease have been restricted to natural infection cases. Therefore, this study aimed to evaluate the parasitemia, biological cycles and clinical-pathological findings in dogs experimentally infected with R. vitalii in the acute phase of disease, and also aimed to test a therapeutic protocol based on the diminazene aceturate. For this study, we used 12 young dogs (females), separated into two groups. Group A was composed of healthy dogs, not-infected (n=5), and Group B consisted of animals infected with R. vitalii (n=7). After infection, the animals were monitored by blood smear examinations, which showed intra-erythrocytic forms of the parasite 5 days post-infection (PI). Parasitemia increased progressively in these animals and had the highest peak of circulating parasites between 9 and 11days PI. Subsequently, the parasitemia reduced and the protozoan was seen inside the leukocytes in days 17, 19 and 21 PI. The most prominent clinical signs observed at the 20day PI of experiment were lethargy, fever and anorexia. We observed a decrease of hematocrit of infected animals compared with not-infected dogs, featuring a moderate anemia. Pathological evaluation of one dog in Group B at day 21 PI revealed splenomegaly, hepatomegaly, lymphadenopathy, and hemorrhages at necropsy. Histological examination showed only follicular hyperplasia in the spleen and lymph nodes, and the etiologic agent in the vascular endothelium. At 21days PI, it was performed the treatment of dogs in Group B (n=6) with a single dose of diminazene aceturate, which showed a curative efficacy of 100% in cleaning R. vitalii from blood of infected dogs.
doi_str_mv 10.1016/j.exppara.2011.04.010
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Recently we conducted the molecular characterization of Rangelia vitalii, a protozoan with high pathogenicity for young dogs in southern Brazil. To date, the descriptions of the disease have been restricted to natural infection cases. Therefore, this study aimed to evaluate the parasitemia, biological cycles and clinical-pathological findings in dogs experimentally infected with R. vitalii in the acute phase of disease, and also aimed to test a therapeutic protocol based on the diminazene aceturate. For this study, we used 12 young dogs (females), separated into two groups. Group A was composed of healthy dogs, not-infected (n=5), and Group B consisted of animals infected with R. vitalii (n=7). After infection, the animals were monitored by blood smear examinations, which showed intra-erythrocytic forms of the parasite 5 days post-infection (PI). Parasitemia increased progressively in these animals and had the highest peak of circulating parasites between 9 and 11days PI. Subsequently, the parasitemia reduced and the protozoan was seen inside the leukocytes in days 17, 19 and 21 PI. The most prominent clinical signs observed at the 20day PI of experiment were lethargy, fever and anorexia. We observed a decrease of hematocrit of infected animals compared with not-infected dogs, featuring a moderate anemia. Pathological evaluation of one dog in Group B at day 21 PI revealed splenomegaly, hepatomegaly, lymphadenopathy, and hemorrhages at necropsy. Histological examination showed only follicular hyperplasia in the spleen and lymph nodes, and the etiologic agent in the vascular endothelium. 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Psychology ; hematocrit ; Hematocrit - veterinary ; hyperplasia ; leukocytes ; Leukocytes - parasitology ; Life cycle. Host-agent relationship. Pathogenesis ; lymph nodes ; Male ; necropsy ; parasitemia ; Parasitemia - parasitology ; Parasitemia - veterinary ; parasites ; parasitology ; pathogenicity ; Protozoa ; Protozoan Infections, Animal - drug therapy ; Protozoan Infections, Animal - parasitology ; Protozoan Infections, Animal - pathology ; Rangeliosis ; spleen ; splenomegaly ; Treatment</subject><ispartof>Experimental parasitology, 2011-08, Vol.128 (4), p.347-352</ispartof><rights>2011 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Inc. 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Recently we conducted the molecular characterization of Rangelia vitalii, a protozoan with high pathogenicity for young dogs in southern Brazil. To date, the descriptions of the disease have been restricted to natural infection cases. Therefore, this study aimed to evaluate the parasitemia, biological cycles and clinical-pathological findings in dogs experimentally infected with R. vitalii in the acute phase of disease, and also aimed to test a therapeutic protocol based on the diminazene aceturate. For this study, we used 12 young dogs (females), separated into two groups. Group A was composed of healthy dogs, not-infected (n=5), and Group B consisted of animals infected with R. vitalii (n=7). After infection, the animals were monitored by blood smear examinations, which showed intra-erythrocytic forms of the parasite 5 days post-infection (PI). Parasitemia increased progressively in these animals and had the highest peak of circulating parasites between 9 and 11days PI. Subsequently, the parasitemia reduced and the protozoan was seen inside the leukocytes in days 17, 19 and 21 PI. The most prominent clinical signs observed at the 20day PI of experiment were lethargy, fever and anorexia. We observed a decrease of hematocrit of infected animals compared with not-infected dogs, featuring a moderate anemia. Pathological evaluation of one dog in Group B at day 21 PI revealed splenomegaly, hepatomegaly, lymphadenopathy, and hemorrhages at necropsy. Histological examination showed only follicular hyperplasia in the spleen and lymph nodes, and the etiologic agent in the vascular endothelium. At 21days PI, it was performed the treatment of dogs in Group B (n=6) with a single dose of diminazene aceturate, which showed a curative efficacy of 100% in cleaning R. vitalii from blood of infected dogs.</description><subject>Acute Disease</subject><subject>anemia</subject><subject>Animals</subject><subject>anorexia</subject><subject>Antiprotozoal Agents - pharmacology</subject><subject>Antiprotozoal Agents - therapeutic use</subject><subject>Apicomplexa - drug effects</subject><subject>Apicomplexa - physiology</subject><subject>Biological and medical sciences</subject><subject>Biological cycle</subject><subject>Canine</subject><subject>Case-Control Studies</subject><subject>diminazene</subject><subject>Diminazene - analogs &amp; derivatives</subject><subject>Diminazene - pharmacology</subject><subject>Diminazene - therapeutic use</subject><subject>dog diseases</subject><subject>Dog Diseases - drug therapy</subject><subject>Dog Diseases - parasitology</subject><subject>Dog Diseases - pathology</subject><subject>Dogs</subject><subject>endothelium</subject><subject>Endothelium, Vascular - parasitology</subject><subject>Endothelium, Vascular - pathology</subject><subject>Erythrocytes - parasitology</subject><subject>Female</subject><subject>females</subject><subject>fever</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hematocrit</subject><subject>Hematocrit - veterinary</subject><subject>hyperplasia</subject><subject>leukocytes</subject><subject>Leukocytes - parasitology</subject><subject>Life cycle. Host-agent relationship. Pathogenesis</subject><subject>lymph nodes</subject><subject>Male</subject><subject>necropsy</subject><subject>parasitemia</subject><subject>Parasitemia - parasitology</subject><subject>Parasitemia - veterinary</subject><subject>parasites</subject><subject>parasitology</subject><subject>pathogenicity</subject><subject>Protozoa</subject><subject>Protozoan Infections, Animal - drug therapy</subject><subject>Protozoan Infections, Animal - parasitology</subject><subject>Protozoan Infections, Animal - pathology</subject><subject>Rangeliosis</subject><subject>spleen</subject><subject>splenomegaly</subject><subject>Treatment</subject><issn>0014-4894</issn><issn>1090-2449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks9u1DAQxi0EokvhEQBfEByaZZzY2ZgLqqryR6qEBPRsTZzJrlfZJNjZ0j4E78xEu5QbnCxrfp755vssxHMFSwWqfLtd0u04YsRlDkotQS9BwQOxUGAhy7W2D8UCQOlMV1afiCcpbQGgUrl-LE5yZVZgy3Ihfl3ejhTDjvoJOxn6lvwUhl7-DNNGfsV-TV1AeRO4GgLXZTOs0zt57vcTyXGDic7krCKFiXYBz2Qdhm5YB8_d_J3vuOy70M_3bMRpc1_ENPKoJLFv5BQJp1nCU_GoxS7Rs-N5Kq4_XH6_-JRdffn4-eL8KvPaqClTqNFUZHhxrywpsjVZgpw3LWrAoqW8rY3XpFsLtS2ryoBpqALD1hVlUZyK14e-Yxx-7ClNbheSp67DnoZ9ctXKKiiNBSbf_JNUuqwKU6zs3NQcUB-HlCK1bmRjMd45BW7OzG3dMTM3Z-ZAO86M3704jtjXO2ruX_0JiYFXRwATW9dG7H1IfzmtQSs1C3h54FocHK4jM9ffeJLhf7AqtKmYeH8giM29CRRd8oF6T02InIZrhvAfsb8BVL7CDw</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Da Silva, Aleksandro S.</creator><creator>França, Raqueli T.</creator><creator>Costa, Marcio M.</creator><creator>Paim, Carlos B.</creator><creator>Paim, Francine C.</creator><creator>Dornelles, Guilherme L.</creator><creator>Soares, João F.</creator><creator>Labruna, Marcelo B.</creator><creator>Mazzanti, Cinthia M.</creator><creator>Monteiro, Silvia G.</creator><creator>Lopes, Sonia T.A.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>20110801</creationdate><title>Experimental infection with Rangelia vitalii in dogs: Acute phase, parasitemia, biological cycle, clinical-pathological aspects and treatment</title><author>Da Silva, Aleksandro S. ; França, Raqueli T. ; Costa, Marcio M. ; Paim, Carlos B. ; Paim, Francine C. ; Dornelles, Guilherme L. ; Soares, João F. ; Labruna, Marcelo B. ; Mazzanti, Cinthia M. ; Monteiro, Silvia G. ; Lopes, Sonia T.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-1a4a58e5011c19e1e9be9e028943b0a3fe2fb5c4e4f90b9688505de8051013633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acute Disease</topic><topic>anemia</topic><topic>Animals</topic><topic>anorexia</topic><topic>Antiprotozoal Agents - pharmacology</topic><topic>Antiprotozoal Agents - therapeutic use</topic><topic>Apicomplexa - drug effects</topic><topic>Apicomplexa - physiology</topic><topic>Biological and medical sciences</topic><topic>Biological cycle</topic><topic>Canine</topic><topic>Case-Control Studies</topic><topic>diminazene</topic><topic>Diminazene - analogs &amp; derivatives</topic><topic>Diminazene - pharmacology</topic><topic>Diminazene - therapeutic use</topic><topic>dog diseases</topic><topic>Dog Diseases - drug therapy</topic><topic>Dog Diseases - parasitology</topic><topic>Dog Diseases - pathology</topic><topic>Dogs</topic><topic>endothelium</topic><topic>Endothelium, Vascular - parasitology</topic><topic>Endothelium, Vascular - pathology</topic><topic>Erythrocytes - parasitology</topic><topic>Female</topic><topic>females</topic><topic>fever</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hematocrit</topic><topic>Hematocrit - veterinary</topic><topic>hyperplasia</topic><topic>leukocytes</topic><topic>Leukocytes - parasitology</topic><topic>Life cycle. Host-agent relationship. 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Recently we conducted the molecular characterization of Rangelia vitalii, a protozoan with high pathogenicity for young dogs in southern Brazil. To date, the descriptions of the disease have been restricted to natural infection cases. Therefore, this study aimed to evaluate the parasitemia, biological cycles and clinical-pathological findings in dogs experimentally infected with R. vitalii in the acute phase of disease, and also aimed to test a therapeutic protocol based on the diminazene aceturate. For this study, we used 12 young dogs (females), separated into two groups. Group A was composed of healthy dogs, not-infected (n=5), and Group B consisted of animals infected with R. vitalii (n=7). After infection, the animals were monitored by blood smear examinations, which showed intra-erythrocytic forms of the parasite 5 days post-infection (PI). Parasitemia increased progressively in these animals and had the highest peak of circulating parasites between 9 and 11days PI. Subsequently, the parasitemia reduced and the protozoan was seen inside the leukocytes in days 17, 19 and 21 PI. The most prominent clinical signs observed at the 20day PI of experiment were lethargy, fever and anorexia. We observed a decrease of hematocrit of infected animals compared with not-infected dogs, featuring a moderate anemia. Pathological evaluation of one dog in Group B at day 21 PI revealed splenomegaly, hepatomegaly, lymphadenopathy, and hemorrhages at necropsy. Histological examination showed only follicular hyperplasia in the spleen and lymph nodes, and the etiologic agent in the vascular endothelium. At 21days PI, it was performed the treatment of dogs in Group B (n=6) with a single dose of diminazene aceturate, which showed a curative efficacy of 100% in cleaning R. vitalii from blood of infected dogs.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>21570966</pmid><doi>10.1016/j.exppara.2011.04.010</doi><tpages>6</tpages></addata></record>
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identifier ISSN: 0014-4894
ispartof Experimental parasitology, 2011-08, Vol.128 (4), p.347-352
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1090-2449
language eng
recordid cdi_proquest_miscellaneous_879106590
source Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE
subjects Acute Disease
anemia
Animals
anorexia
Antiprotozoal Agents - pharmacology
Antiprotozoal Agents - therapeutic use
Apicomplexa - drug effects
Apicomplexa - physiology
Biological and medical sciences
Biological cycle
Canine
Case-Control Studies
diminazene
Diminazene - analogs & derivatives
Diminazene - pharmacology
Diminazene - therapeutic use
dog diseases
Dog Diseases - drug therapy
Dog Diseases - parasitology
Dog Diseases - pathology
Dogs
endothelium
Endothelium, Vascular - parasitology
Endothelium, Vascular - pathology
Erythrocytes - parasitology
Female
females
fever
Fundamental and applied biological sciences. Psychology
hematocrit
Hematocrit - veterinary
hyperplasia
leukocytes
Leukocytes - parasitology
Life cycle. Host-agent relationship. Pathogenesis
lymph nodes
Male
necropsy
parasitemia
Parasitemia - parasitology
Parasitemia - veterinary
parasites
parasitology
pathogenicity
Protozoa
Protozoan Infections, Animal - drug therapy
Protozoan Infections, Animal - parasitology
Protozoan Infections, Animal - pathology
Rangeliosis
spleen
splenomegaly
Treatment
title Experimental infection with Rangelia vitalii in dogs: Acute phase, parasitemia, biological cycle, clinical-pathological aspects and treatment
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