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Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)

Detalhes bibliográficos
Ano de defesa: 2015
Autor(a) principal: Jordanna Luíza de Lima Celeste
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Minas Gerais
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://hdl.handle.net/1843/34762
Resumo: In Brazil, there are two clinical forms of leishmaniasis: Visceral Leishmaniasis (VL) and Tegumentary Leishmaniasis (LT). The VL has the etiologic agent Leishmania (L.) infantum (= L. (L.) chagasi) affecting mainly organs such as the spleen and liver, and TL has several clinical manifestations and has as etiological agents several species, including L. (L.) amazonensis, causing skin lesions. It is known that in country there are overlapping areas of these two species, which may facilitate the occurrence of coinfection. Although it is more common VL caused by L. infantum and TL caused by L. amazonensis, in Brazil there are reports of visceralization caused by L. amazonensis in humans and dogs from urban areas. Hamsters are considered good experimental models in Leishmania spp infections and were used in this study to a better understanding of this type of infection. Thus, the species L. (L.) infantum (MCAN/BR/2002/BH401) and L. (L.) amazonensis (IFLA/BR/1967/PH8) were inoculated separately and simultaneously in these animals by intraperitoneal and subcutaneous routes, and they were followed for 90 days. The route of inoculation had no influence on the clinical changes of infection by L. infantum or L. amazonesis, however, L. infantum has more typical establishment intraperitoneally while L. amazonensis subcutaneously. L. amazonensis has the capacity to invade the spleen and liver earlier than L. infantum in all situations evaluated, but L. infantum can prevail over time. The coinfection was more severe, with L. amazonensis causing early splenomegaly and skin lesions in the inoculum site and disseminated.
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spelling 2021-01-18T18:19:19Z2025-09-09T01:11:11Z2021-01-18T18:19:19Z2015-02-25https://hdl.handle.net/1843/34762In Brazil, there are two clinical forms of leishmaniasis: Visceral Leishmaniasis (VL) and Tegumentary Leishmaniasis (LT). The VL has the etiologic agent Leishmania (L.) infantum (= L. (L.) chagasi) affecting mainly organs such as the spleen and liver, and TL has several clinical manifestations and has as etiological agents several species, including L. (L.) amazonensis, causing skin lesions. It is known that in country there are overlapping areas of these two species, which may facilitate the occurrence of coinfection. Although it is more common VL caused by L. infantum and TL caused by L. amazonensis, in Brazil there are reports of visceralization caused by L. amazonensis in humans and dogs from urban areas. Hamsters are considered good experimental models in Leishmania spp infections and were used in this study to a better understanding of this type of infection. Thus, the species L. (L.) infantum (MCAN/BR/2002/BH401) and L. (L.) amazonensis (IFLA/BR/1967/PH8) were inoculated separately and simultaneously in these animals by intraperitoneal and subcutaneous routes, and they were followed for 90 days. The route of inoculation had no influence on the clinical changes of infection by L. infantum or L. amazonesis, however, L. infantum has more typical establishment intraperitoneally while L. amazonensis subcutaneously. L. amazonensis has the capacity to invade the spleen and liver earlier than L. infantum in all situations evaluated, but L. infantum can prevail over time. The coinfection was more severe, with L. amazonensis causing early splenomegaly and skin lesions in the inoculum site and disseminated.CNPq - Conselho Nacional de Desenvolvimento Científico e TecnológicoFAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas GeraisCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorporUniversidade Federal de Minas Geraishttp://creativecommons.org/licenses/by-nc-nd/3.0/pt/info:eu-repo/semantics/openAccessLeishmaniose visceralLeishmaniose cutâneaParasitologiaLeishmaniose cutâneaLeishmaniose visceralLeishmania infantumAvaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisJordanna Luíza de Lima Celestereponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGhttp://lattes.cnpq.br/0956543496382057Hélida Monteiro de Andradehttp://lattes.cnpq.br/9446050242071321Wagner Luiz TafuriNelder de Figueiredo GontijoNo Brasil, encontram-se duas formas clínicas das leishmanioses: Leishmaniose Visceral (LV) e a Leishmaniose Tegumentar (LT). A LV tem como agente etiológico Leishmania (L.) infantum (=L. (L.) chagasi) atingindo principalmente órgãos como o baço e fígado, e a LT apresenta diversas manifestações clínicas e tem como agentes etiológicos várias espécies, incluindo L. (L.) amazonensis, causando lesões cutâneas. Sabe-se que no país existem áreas de sobreposição dessas duas espécies, o que pode possibilitar a ocorrência de coinfecção. Embora seja mais comum o relato de LV causada por L. infantum e de LT causada por L. amazonensis, no Brasil há relatos de casos de visceralização causada por L. amazonensis em humanos e cães de área urbana. Por serem considerados bons modelos experimentais em infecções por Leishmania spp, hamsters foram utilizados nesse estudo para um melhor entendimento desse tipo de infecção. Assim, as espécies L. (L.) infantum (MCAN/BR/2002/BH401) e L. (L.) amazonensis (IFLA/BR/1967/PH8) foram inoculadas separadamente e simultaneamente nesses animais, pelas vias intraperitoneal e subcutânea, e estes foram acompanhados durante 90 dias. A via de inoculação não teve influência nas alterações clínicas das infecções por L. infantum ou L. amazonesis, porém, L. infantum tem estabelecimento mais típico por via IP enquanto L. amazonensis por via SC. L. amazonensis possui capacidade de invadir baço e fígado mais precocemente que L. infantum em todas as situações avaliadas, mas L. infantum pode prevalecer com o passar do tempo. A coinfecção foi mais grave, com L. amazonensis provocando esplenomegalia precoce e lesões de pele no local do inóculo e disseminadas.BrasilICB - INSTITUTO DE CIÊNCIAS BIOLOGICASPrograma de Pós-Graduação em ParasitologiaUFMGORIGINALDISSERTAÇÃO VERSÃO FINAL.pdfapplication/pdf3644419https://repositorio.ufmg.br//bitstreams/cf7a4a83-c312-435f-8510-650570aa4d49/downloadbe5f8698e98026a81915e8b3a5441c56MD51trueAnonymousREADCC-LICENSElicense_rdfapplication/octet-stream811https://repositorio.ufmg.br//bitstreams/ffac5f84-6c92-491b-a52e-1ffdc17c06e6/downloadcfd6801dba008cb6adbd9838b81582abMD52falseAnonymousREADLICENSElicense.txttext/plain2119https://repositorio.ufmg.br//bitstreams/90f02cde-e358-4d89-a1fe-0112947789da/download34badce4be7e31e3adb4575ae96af679MD53falseAnonymousREAD1843/347622025-09-08 22:11:11.14http://creativecommons.org/licenses/by-nc-nd/3.0/pt/Acesso Abertoopen.accessoai:repositorio.ufmg.br:1843/34762https://repositorio.ufmg.br/Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2025-09-09T01:11:11Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)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
dc.title.none.fl_str_mv Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
title Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
spellingShingle Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
Jordanna Luíza de Lima Celeste
Parasitologia
Leishmaniose cutânea
Leishmaniose visceral
Leishmania infantum
Leishmaniose visceral
Leishmaniose cutânea
title_short Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
title_full Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
title_fullStr Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
title_full_unstemmed Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
title_sort Avaliação clínica e parasitológica da coinfecção experimental por Leishmania (Leishmania) amazonensis e Leishmania (L.) infantum em hamster (Mesocricetus auratus)
author Jordanna Luíza de Lima Celeste
author_facet Jordanna Luíza de Lima Celeste
author_role author
dc.contributor.author.fl_str_mv Jordanna Luíza de Lima Celeste
dc.subject.por.fl_str_mv Parasitologia
Leishmaniose cutânea
Leishmaniose visceral
Leishmania infantum
topic Parasitologia
Leishmaniose cutânea
Leishmaniose visceral
Leishmania infantum
Leishmaniose visceral
Leishmaniose cutânea
dc.subject.other.none.fl_str_mv Leishmaniose visceral
Leishmaniose cutânea
description In Brazil, there are two clinical forms of leishmaniasis: Visceral Leishmaniasis (VL) and Tegumentary Leishmaniasis (LT). The VL has the etiologic agent Leishmania (L.) infantum (= L. (L.) chagasi) affecting mainly organs such as the spleen and liver, and TL has several clinical manifestations and has as etiological agents several species, including L. (L.) amazonensis, causing skin lesions. It is known that in country there are overlapping areas of these two species, which may facilitate the occurrence of coinfection. Although it is more common VL caused by L. infantum and TL caused by L. amazonensis, in Brazil there are reports of visceralization caused by L. amazonensis in humans and dogs from urban areas. Hamsters are considered good experimental models in Leishmania spp infections and were used in this study to a better understanding of this type of infection. Thus, the species L. (L.) infantum (MCAN/BR/2002/BH401) and L. (L.) amazonensis (IFLA/BR/1967/PH8) were inoculated separately and simultaneously in these animals by intraperitoneal and subcutaneous routes, and they were followed for 90 days. The route of inoculation had no influence on the clinical changes of infection by L. infantum or L. amazonesis, however, L. infantum has more typical establishment intraperitoneally while L. amazonensis subcutaneously. L. amazonensis has the capacity to invade the spleen and liver earlier than L. infantum in all situations evaluated, but L. infantum can prevail over time. The coinfection was more severe, with L. amazonensis causing early splenomegaly and skin lesions in the inoculum site and disseminated.
publishDate 2015
dc.date.issued.fl_str_mv 2015-02-25
dc.date.accessioned.fl_str_mv 2021-01-18T18:19:19Z
2025-09-09T01:11:11Z
dc.date.available.fl_str_mv 2021-01-18T18:19:19Z
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url https://hdl.handle.net/1843/34762
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dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
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