Molecular studies on HSV: replication rate, infection capacity and progeny
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Tipo de documento: | Dissertação |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.18/8320 |
Resumo: | Dissertação de mestrado em Genética molecular e Biomedicina, apresentada à Faculdade de Ciências e Tecnologias da Universidade Nova de Lisboa, 2016. |
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Molecular studies on HSV: replication rate, infection capacity and progenySexually Transmitted DiseasesHSV1HSV2Herpes Simplex VirusReplication RateInfection CapacityProgenyCell CultureInfecções Sexualmente TransmissíveisHerpes GenitalCapacidade de InfeçãoProgeniaCultura CelularDissertação de mestrado em Genética molecular e Biomedicina, apresentada à Faculdade de Ciências e Tecnologias da Universidade Nova de Lisboa, 2016.Herpes simplex viruses (HSV) are ubiquitous host-adapted pathogens that cause a variety of different disorders. There are two sub-types: HSV-1, which is traditionally associated with oro-facial infections, and HSV-2 that is mostly associated with genital ulcers. This distinction, however, is becoming less evident since HSV-1 frequency in genital infections is increasing due to social, demographic and migratory tendencies, making genital herpes one of the most prevalent sexually transmitted infections worldwide. A better understanding on genital HSV-1 and HSV-2 infections is mandatory to the pathogenesis of human herpes disease. The scope of this thesis was to evaluate the life cycle of various HSV-1 and HSV-2 genital clinical isolates with different viral loads in three distinct host cell lines, giving special focus on both capacity and efficiency of viral infection, in terms of replication rate and progeny. Our results showed that: i) both HSV-1 and HSV-2 isolates exhibited similar infection patterns regardless MOI, with DNA starting to be synthesized nearly at 6-12h post-infection; ii) regardless HSV subtype, initial viral concentrations do not apparently affect adherence to any host cell line nor the generated progeny; iii) Vero E6 cells seemed the most appropriated cell line for HSV-2 infection; iv) HeLa229 cells appeared to be the most suitable for HSV-1 infection for smaller inoculums; and v) Vero cell line had the worst viral growth results for both HSV subtypes. In general, HSV-2 displayed always lower both attachment capacities and growth rates than HSV-1, although higher progenies were seen in Vero E6 cell line. Overall, the findings presented in this MSc thesis will certainly constitute a step forward for the understanding of the pathogenesis of the human herpes genital infections.Herpes simplex viruses (HSV) are ubiquitous host-adapted pathogens that cause a variety of different disorders. There are two sub-types: HSV-1, which is traditionally associated with oro-facial infections, and HSV-2 that is mostly associated with genital ulcers. This distinction, however, is becoming less evident since HSV-1 frequency in genital infections is increasing due to social, demographic and migratory tendencies, making genital herpes one of the most prevalent sexually transmitted infections worldwide. A better understanding on genital HSV-1 and HSV-2 infections is mandatory to the pathogenesis of human herpes disease. The scope of this thesis was to evaluate the life cycle of various HSV-1 and HSV-2 genital clinical isolates with different viral loads in three distinct host cell lines, giving special focus on both capacity and efficiency of viral infection, in terms of replication rate and progeny. Our results showed that: i) both HSV-1 and HSV-2 isolates exhibited similar infection patterns regardless MOI, with DNA starting to be synthesized nearly at 6-12h post-infection; ii) regardless HSV subtype, initial viral concentrations do not apparently affect adherence to any host cell line nor the generated progeny; iii) Vero E6 cells seemed the most appropriated cell line for HSV-2 infection; iv) HeLa229 cells appeared to be the most suitable for HSV-1 infection for smaller inoculums; and v) Vero cell line had the worst viral growth results for both HSV subtypes. In general, HSV-2 displayed always lower both attachment capacities and growth rates than HSV-1, although higher progenies were seen in Vero E6 cell line. Overall, the findings presented in this MSc thesis will certainly constitute a step forward for the understanding of the pathogenesis of the human herpes genital infections.Lopo, SílviaNunes, AlexandraRepositório Científico do Instituto Nacional de SaúdeAzevedo, Aleksandra2022-11-18T14:35:51Z20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10400.18/8320enginfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-20T15:40:27Zoai:repositorio.insa.pt:10400.18/8320Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:39:26.089950Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Molecular studies on HSV: replication rate, infection capacity and progeny |
title |
Molecular studies on HSV: replication rate, infection capacity and progeny |
spellingShingle |
Molecular studies on HSV: replication rate, infection capacity and progeny Azevedo, Aleksandra Sexually Transmitted Diseases HSV1 HSV2 Herpes Simplex Virus Replication Rate Infection Capacity Progeny Cell Culture Infecções Sexualmente Transmissíveis Herpes Genital Capacidade de Infeção Progenia Cultura Celular |
title_short |
Molecular studies on HSV: replication rate, infection capacity and progeny |
title_full |
Molecular studies on HSV: replication rate, infection capacity and progeny |
title_fullStr |
Molecular studies on HSV: replication rate, infection capacity and progeny |
title_full_unstemmed |
Molecular studies on HSV: replication rate, infection capacity and progeny |
title_sort |
Molecular studies on HSV: replication rate, infection capacity and progeny |
author |
Azevedo, Aleksandra |
author_facet |
Azevedo, Aleksandra |
author_role |
author |
dc.contributor.none.fl_str_mv |
Lopo, Sílvia Nunes, Alexandra Repositório Científico do Instituto Nacional de Saúde |
dc.contributor.author.fl_str_mv |
Azevedo, Aleksandra |
dc.subject.por.fl_str_mv |
Sexually Transmitted Diseases HSV1 HSV2 Herpes Simplex Virus Replication Rate Infection Capacity Progeny Cell Culture Infecções Sexualmente Transmissíveis Herpes Genital Capacidade de Infeção Progenia Cultura Celular |
topic |
Sexually Transmitted Diseases HSV1 HSV2 Herpes Simplex Virus Replication Rate Infection Capacity Progeny Cell Culture Infecções Sexualmente Transmissíveis Herpes Genital Capacidade de Infeção Progenia Cultura Celular |
description |
Dissertação de mestrado em Genética molecular e Biomedicina, apresentada à Faculdade de Ciências e Tecnologias da Universidade Nova de Lisboa, 2016. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2016-01-01T00:00:00Z 2022-11-18T14:35:51Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.18/8320 |
url |
http://hdl.handle.net/10400.18/8320 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
dc.format.none.fl_str_mv |
application/pdf |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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