Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2

Detalhes bibliográficos
Autor(a) principal: Amaral, Bruna Portolan
Data de Publicação: 2020
Tipo de documento: Tese
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/001300000260q
Texto Completo: http://repositorio.ufsm.br/handle/1/21588
Resumo: Bovine alphaherpesvirus 2 (BoHV-2) - the agent of bovine herpetic mamillitis (BHM) – is related to Human alphaherpesviruses 1 and 2 (HHV-1, HHV-2) and has been proposed as a model for vaccine and drug testing. In addition, very little is known about the pathogenesis of BoHV-2 infection. Herein we studied the pathogenesis of BoHV-2 in calves after inoculation through different routes and investigated the activity of candidate anti-viral drugs in vitro and in vivo against BoHV-2. In the first study, 3 to 4-months-old calves were inoculated with BoHV-2 (107TCID50.mL-1) intramuscularly (IM, n=4), intravenously (IV, n=4) or transdermally (TD) after mild scarification (n=4) and monitored thereafter. Calves inoculated by the IV route presented as light increase in body temperature between days 6 to 9 post-inoculation (pi). Virus inoculation by the TD route resulted in mild inflammatory lesions at the sites of inoculation, characterized by hyperemia, small vesicles, mild exudation and scab formation, between days 2 and 8pi.Virus or viral DNA was detected by PCR in the crusts/swabs collected from lesions of 3 out of 4 animals inoculated TD from day 2 to 8pi. Viremia was detected in 3/4 animals of the IM group (from day 4 to 8pi); in 2/4 animals of the IV group (days 6 and 8pi) but not in the TD group. Administration of dexamethasone (Dex) to the inoculated calves at day 48pi, did not result in virus reactivation. In the second study, we investigated the anti-viral activity in vitro against BoHV-2 of three anti-herpetic drugs: Cidofovir (CDV), Fanciclovir (FAM), Foscarnet (PFA), and diphenyl disselenide (PhSe)2 by plaque reduction assays (PRA). A significant reduction in the number of viral plaques was observed by treating the monolayers with (PhSe)2 (79.7% reduction, p<0.05) or CDV (62.8%, p<0.05). FAM treatment resulted in a slight decrease in plaque number (22.9%, p<0.05) and PFA showed no anti-viral activity. Next, we investigated the effects of (PhSe)2 and CDV, alone or in combination, in the infection and disease produced by BoHV-2 in ewes inoculated transdermally and submitted to topic treatment with a vehicle gel containing (PhSe)2, CDV, and combined (PhSe)2 + CDV. Thirteen out of 14 (92.8%) inoculated ewes developed local lesions that typically progressed through the stages of hyperemia (days 2 – 6pi), large papules or depressed/flat dark areas (day 4 to 12pi), accompanied/followed by scab/crust formation that lasted beyond day 15pi in untreated ewes. Treatment with (PhSe)2 resulted in an important reduction in clinical score from day 8 pi onwards (p<0.05), shortening of clinical course and reduction in duration of virus shedding (p<0.05) compared to untreated controls. Combined ((PhSe)2+CDV) treatment and CDV alone, also led to clinical improvement (p<0.05), yet less pronounced and delayed (after day 11 pi and 13 pi, respectively), but no significant reduction in virus shedding. Taken together, these findings contribute to the knowledge of BoHV-2 pathogenesis and are promising towards the use of diphenyl disselenide (PhSe)2, alone or in combination with anti-herpetic drugs, in the treatment of lesions induced by BoHV-2 in the udder and teats of dairy cows.
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spelling Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2Experimental pathogenesis and therapy of bovine alphaherpesvirus 2 infectionAlfaherpesvírus bovino 2BovinosPatogêneseMamiliteTratamentoOvelhasBovine alphaherpesvirus 2CattlePathogenesisMammillitisTherapyEwesCNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIABovine alphaherpesvirus 2 (BoHV-2) - the agent of bovine herpetic mamillitis (BHM) – is related to Human alphaherpesviruses 1 and 2 (HHV-1, HHV-2) and has been proposed as a model for vaccine and drug testing. In addition, very little is known about the pathogenesis of BoHV-2 infection. Herein we studied the pathogenesis of BoHV-2 in calves after inoculation through different routes and investigated the activity of candidate anti-viral drugs in vitro and in vivo against BoHV-2. In the first study, 3 to 4-months-old calves were inoculated with BoHV-2 (107TCID50.mL-1) intramuscularly (IM, n=4), intravenously (IV, n=4) or transdermally (TD) after mild scarification (n=4) and monitored thereafter. Calves inoculated by the IV route presented as light increase in body temperature between days 6 to 9 post-inoculation (pi). Virus inoculation by the TD route resulted in mild inflammatory lesions at the sites of inoculation, characterized by hyperemia, small vesicles, mild exudation and scab formation, between days 2 and 8pi.Virus or viral DNA was detected by PCR in the crusts/swabs collected from lesions of 3 out of 4 animals inoculated TD from day 2 to 8pi. Viremia was detected in 3/4 animals of the IM group (from day 4 to 8pi); in 2/4 animals of the IV group (days 6 and 8pi) but not in the TD group. Administration of dexamethasone (Dex) to the inoculated calves at day 48pi, did not result in virus reactivation. In the second study, we investigated the anti-viral activity in vitro against BoHV-2 of three anti-herpetic drugs: Cidofovir (CDV), Fanciclovir (FAM), Foscarnet (PFA), and diphenyl disselenide (PhSe)2 by plaque reduction assays (PRA). A significant reduction in the number of viral plaques was observed by treating the monolayers with (PhSe)2 (79.7% reduction, p<0.05) or CDV (62.8%, p<0.05). FAM treatment resulted in a slight decrease in plaque number (22.9%, p<0.05) and PFA showed no anti-viral activity. Next, we investigated the effects of (PhSe)2 and CDV, alone or in combination, in the infection and disease produced by BoHV-2 in ewes inoculated transdermally and submitted to topic treatment with a vehicle gel containing (PhSe)2, CDV, and combined (PhSe)2 + CDV. Thirteen out of 14 (92.8%) inoculated ewes developed local lesions that typically progressed through the stages of hyperemia (days 2 – 6pi), large papules or depressed/flat dark areas (day 4 to 12pi), accompanied/followed by scab/crust formation that lasted beyond day 15pi in untreated ewes. Treatment with (PhSe)2 resulted in an important reduction in clinical score from day 8 pi onwards (p<0.05), shortening of clinical course and reduction in duration of virus shedding (p<0.05) compared to untreated controls. Combined ((PhSe)2+CDV) treatment and CDV alone, also led to clinical improvement (p<0.05), yet less pronounced and delayed (after day 11 pi and 13 pi, respectively), but no significant reduction in virus shedding. Taken together, these findings contribute to the knowledge of BoHV-2 pathogenesis and are promising towards the use of diphenyl disselenide (PhSe)2, alone or in combination with anti-herpetic drugs, in the treatment of lesions induced by BoHV-2 in the udder and teats of dairy cows.Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqCoordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESO Alfaherpesvírus bovino 2 – agente da mamilite herpética bovina (BHM) – é relacionado aos Alfaherpesvírus humanos 1 e 2 (HHV-1, HHV-2) e, como tal, tem sido sugerido como modelo para testes de vacinas e drogas antivirais. Além disso, pouco é conhecido sobre a patogenia do BoHV-2. Neste trabalho foi estudada a patogenia da infecção pelo BoHV-2 em bezerros, após diferentes rotas de inoculação e investigada a atividade de diferentes fármacos antivirais in vitro e in vivo contra o BoHV-2. No primeiro estudo, bezerros soronegativos de três a quatro meses foram inoculados com BoHV-2 (107TCID50.mL-1) por via intramuscular (IM, n=4), por via intravenosa (IV, n=4) ou transdérmica (TD, n=4) após escarificação leve e submetidos a monitoramento. Os bezerros inoculados pela via IV apresentaram aumento leve da temperatura corporal entre os dias 6 a 9 pós-inoculação (pi). A inoculação do vírus pela via TD resultou em lesões inflamatórias leves nos locais de inoculação, caracterizadas por hiperemia, pequenas vesículas, exsudação leve e formação de crostas, entre os dias 2 e 8pi. O vírus ou DNA viral foi detectado por PCR nas crostas/swabs coletados de lesões de 3 de 4 animais inoculados TD do dia 2 ao 8pi. Viremia foi detectada em 3/4 dos animais do grupo IM (do dia 4 ao 8pi); em 2/4 animais do grupo IV (dias 6 e 8pi), mas não no grupo TD. Administração de dexametasona (Dex) nos bezerros inoculados no dia 48pi, não resultou em reativação do vírus. No segundo estudo, investigou-se a atividade anti-viral in vitro contra o BoHV-2 de três drogas anti-herpéticas: Cidofovir (CDV), Famciclovir (FAM), Foscarnet (PFA), e do disseleneto de difenila (PhSe)2 pelo teste de redução de placas (PRA). Redução significativa do número de placas virais foi observada pelo tratamento dos tapetes celulares com (PhSe)2 (redução de 79.7%, p<0.05) ou com CDV (62.8%, p<0.05). Tratamento com FAM resultou em redução menor (22.9%, p<0.05) e o PFA não demonstrou atividade antiviral. A seguir, investigou-se o efeito do (PhSe)2 e CDV, isoladamente ou combinados, sobre a infecção e doença produzida pelo BoHV-2 em ovelhas inoculadas pela via transdérmica e submetidas a tratamento tópico com um veículo cremoso contendo (PhSe)2, CDV, e (PhSe)2 + CDV associados. Treze de 14 ovelhas (92.8%) inoculadas desenvolveram lesões locais que progrediram pelas fases de hiperemia (dias 2 – 6pi), grandes pápulas ou áreas planas achatadas/escuras (dias 4 a 12pi), acompanhadas pela formação de crostas que duraram além do dia 15pi nos animais não-tratados. Tratamento com (PhSe)2 resultou em redução importante no escore clínico a partir do dia 8 pi (p<0.05), em redução do período clínico e na duração da excreção viral (p<0.05) comparado aos controles. Tratamento combinado ((PhSe)2+CDV) e CDV sozinho, também resultaram em melhoria clínica (p<0.05), mas menos pronunciada e mais tardia (após dias 11 pi e 13 pi, respectivamente), mas não reduziram significativamente o tempo de excreção viral. Em conjunto, esses resultados contribuem para o conhecimento da patogenia da infecção pelo BoHV-2 e são promissores no sentido do uso disseleneto de difenila (PhSe)2, isolado ou em combinação com drogas anti-herpéticas, no tratamento de lesões ocasionadas pelo BoHV-2 no úbere de vacas leiteiras.Universidade Federal de Santa MariaBrasilMedicina VeterináriaUFSMPrograma de Pós-Graduação em Medicina VeterináriaCentro de Ciências RuraisFlores, Eduardo Furtadohttp://lattes.cnpq.br/0446078331070694Anziliero, DenizCargnelutti, Juliana FelipettoSlhessarenko, Renata DezengriniWeiblen, RudiAmaral, Bruna Portolan2021-07-23T14:37:57Z2021-07-23T14:37:57Z2020-08-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/21588ark:/26339/001300000260qporAn error occurred on the license name.An error occurred getting the license - uri.info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2021-07-24T06:03:38Zoai:repositorio.ufsm.br:1/21588Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2021-07-24T06:03:38Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
Experimental pathogenesis and therapy of bovine alphaherpesvirus 2 infection
title Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
spellingShingle Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
Amaral, Bruna Portolan
Alfaherpesvírus bovino 2
Bovinos
Patogênese
Mamilite
Tratamento
Ovelhas
Bovine alphaherpesvirus 2
Cattle
Pathogenesis
Mammillitis
Therapy
Ewes
CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA
title_short Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
title_full Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
title_fullStr Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
title_full_unstemmed Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
title_sort Patogênese e terapia experimental da infecção pelo alfaherpesvírus bovino 2
author Amaral, Bruna Portolan
author_facet Amaral, Bruna Portolan
author_role author
dc.contributor.none.fl_str_mv Flores, Eduardo Furtado
http://lattes.cnpq.br/0446078331070694
Anziliero, Deniz
Cargnelutti, Juliana Felipetto
Slhessarenko, Renata Dezengrini
Weiblen, Rudi
dc.contributor.author.fl_str_mv Amaral, Bruna Portolan
dc.subject.por.fl_str_mv Alfaherpesvírus bovino 2
Bovinos
Patogênese
Mamilite
Tratamento
Ovelhas
Bovine alphaherpesvirus 2
Cattle
Pathogenesis
Mammillitis
Therapy
Ewes
CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA
topic Alfaherpesvírus bovino 2
Bovinos
Patogênese
Mamilite
Tratamento
Ovelhas
Bovine alphaherpesvirus 2
Cattle
Pathogenesis
Mammillitis
Therapy
Ewes
CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA
description Bovine alphaherpesvirus 2 (BoHV-2) - the agent of bovine herpetic mamillitis (BHM) – is related to Human alphaherpesviruses 1 and 2 (HHV-1, HHV-2) and has been proposed as a model for vaccine and drug testing. In addition, very little is known about the pathogenesis of BoHV-2 infection. Herein we studied the pathogenesis of BoHV-2 in calves after inoculation through different routes and investigated the activity of candidate anti-viral drugs in vitro and in vivo against BoHV-2. In the first study, 3 to 4-months-old calves were inoculated with BoHV-2 (107TCID50.mL-1) intramuscularly (IM, n=4), intravenously (IV, n=4) or transdermally (TD) after mild scarification (n=4) and monitored thereafter. Calves inoculated by the IV route presented as light increase in body temperature between days 6 to 9 post-inoculation (pi). Virus inoculation by the TD route resulted in mild inflammatory lesions at the sites of inoculation, characterized by hyperemia, small vesicles, mild exudation and scab formation, between days 2 and 8pi.Virus or viral DNA was detected by PCR in the crusts/swabs collected from lesions of 3 out of 4 animals inoculated TD from day 2 to 8pi. Viremia was detected in 3/4 animals of the IM group (from day 4 to 8pi); in 2/4 animals of the IV group (days 6 and 8pi) but not in the TD group. Administration of dexamethasone (Dex) to the inoculated calves at day 48pi, did not result in virus reactivation. In the second study, we investigated the anti-viral activity in vitro against BoHV-2 of three anti-herpetic drugs: Cidofovir (CDV), Fanciclovir (FAM), Foscarnet (PFA), and diphenyl disselenide (PhSe)2 by plaque reduction assays (PRA). A significant reduction in the number of viral plaques was observed by treating the monolayers with (PhSe)2 (79.7% reduction, p<0.05) or CDV (62.8%, p<0.05). FAM treatment resulted in a slight decrease in plaque number (22.9%, p<0.05) and PFA showed no anti-viral activity. Next, we investigated the effects of (PhSe)2 and CDV, alone or in combination, in the infection and disease produced by BoHV-2 in ewes inoculated transdermally and submitted to topic treatment with a vehicle gel containing (PhSe)2, CDV, and combined (PhSe)2 + CDV. Thirteen out of 14 (92.8%) inoculated ewes developed local lesions that typically progressed through the stages of hyperemia (days 2 – 6pi), large papules or depressed/flat dark areas (day 4 to 12pi), accompanied/followed by scab/crust formation that lasted beyond day 15pi in untreated ewes. Treatment with (PhSe)2 resulted in an important reduction in clinical score from day 8 pi onwards (p<0.05), shortening of clinical course and reduction in duration of virus shedding (p<0.05) compared to untreated controls. Combined ((PhSe)2+CDV) treatment and CDV alone, also led to clinical improvement (p<0.05), yet less pronounced and delayed (after day 11 pi and 13 pi, respectively), but no significant reduction in virus shedding. Taken together, these findings contribute to the knowledge of BoHV-2 pathogenesis and are promising towards the use of diphenyl disselenide (PhSe)2, alone or in combination with anti-herpetic drugs, in the treatment of lesions induced by BoHV-2 in the udder and teats of dairy cows.
publishDate 2020
dc.date.none.fl_str_mv 2020-08-25
2021-07-23T14:37:57Z
2021-07-23T14:37:57Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
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dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/21588
dc.identifier.dark.fl_str_mv ark:/26339/001300000260q
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identifier_str_mv ark:/26339/001300000260q
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv An error occurred on the license name.
An error occurred getting the license - uri.
info:eu-repo/semantics/openAccess
rights_invalid_str_mv An error occurred on the license name.
An error occurred getting the license - uri.
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Medicina Veterinária
UFSM
Programa de Pós-Graduação em Medicina Veterinária
Centro de Ciências Rurais
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Medicina Veterinária
UFSM
Programa de Pós-Graduação em Medicina Veterinária
Centro de Ciências Rurais
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
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