Schistosomiasis mansoni: evidence for a milder response in germfree mice

Detalhes bibliográficos
Autor(a) principal: Viera, Leda Q.
Data de Publicação: 1987
Outros Autores: Moraes-santos, Tasso
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista do Instituto de Medicina Tropical de São Paulo
Texto Completo: https://www.revistas.usp.br/rimtsp/article/view/28488
Resumo: Germfree (GF and conventional (CV) mice were infected intraperitoneally with GF cercariae of Schistosoma mansoni and kept for six weeks. Twenty four hours before killing, they were injected with [³H]-thymidine. Schistosoma worms, harvested after perfusion of portal system, were counted as well as eggs from liver and intestines. Liver was also used for DNA, protein, and collagen determinations. [³H] -Thymidine incorporation and collagen determinations were used to establish the indices given by the difference between their contents in infected and control animals and expressed per thousand eggs in liver. The recovery of worms in GF mice was around twice as much as in CV ones, and the total number of eggs was higher in the liver of GF animals. No hypertrophy of liver cells was observed by the ratio protein/DNA, but [³H]-thymidine incorporation into DNA was higher than in controls in both GF and CV infected animals. The [³H]-thymidine and collagen indices were lower in GF animals which indicate a more discrete cellular replication and smaller collagen content in relation to the number of eggs present in livers of these mice. It was concluded that the disease seems to be less severe in GF animals.
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spelling Schistosomiasis mansoni: evidence for a milder response in germfree mice Esquistossomose mansônica: evidência de menor resposta nos camundongos isentos de germes Schistosomiasis mansoniAxenic cercariae Germfree (GF and conventional (CV) mice were infected intraperitoneally with GF cercariae of Schistosoma mansoni and kept for six weeks. Twenty four hours before killing, they were injected with [³H]-thymidine. Schistosoma worms, harvested after perfusion of portal system, were counted as well as eggs from liver and intestines. Liver was also used for DNA, protein, and collagen determinations. [³H] -Thymidine incorporation and collagen determinations were used to establish the indices given by the difference between their contents in infected and control animals and expressed per thousand eggs in liver. The recovery of worms in GF mice was around twice as much as in CV ones, and the total number of eggs was higher in the liver of GF animals. No hypertrophy of liver cells was observed by the ratio protein/DNA, but [³H]-thymidine incorporation into DNA was higher than in controls in both GF and CV infected animals. The [³H]-thymidine and collagen indices were lower in GF animals which indicate a more discrete cellular replication and smaller collagen content in relation to the number of eggs present in livers of these mice. It was concluded that the disease seems to be less severe in GF animals. Camundongos isentos de germes (GF) e convencionais (CV) foram infectados intraperito-nealmente com cercárias GF de Schistosoma mansoni e mantidos por seis semanas. Vinte e quatro horas antes do sacrifício, eles foram injetados com [³H]-timidina. Vermes de Schistosoma, recolhidos através de perfusão do sistema porta, foram contados, assim como os ovos no fígado e intestino delgado. O fígado foi também usado para determinações de DNA, proteínas e colágeno. A incorporação de [³H]-timidina e as determinações de colágeno foram usadas para calcular os índices dados pela diferença entre seus conteúdos nos animais infectados e controles e expressos por mil ovos no fígado. A recuperação de vermes nos camundongos GF foi cerca de duas vezes aquela dos CV. O número total de ovos foi maior no fígado dos animais GF. Nenhuma hipertrofia das células hepáticas foi observada pela relação proteína/DNA mas a incorporação de [³H]-timidina em DNA foi maior que nos controles em ambos animais infectados (GF e CV). Os índices de [³H]-timidina e colágeno foram menores nos animais GF indicando uma replicação celular mais discreta e um conteúdo de colágeno menor em relação ao número de ovos presentes nos fígados destes camundongos. Concluiu-se que a doença parece ser menos se vera em animais GF. Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo1987-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/rimtsp/article/view/28488Revista do Instituto de Medicina Tropical de São Paulo; Vol. 29 No. 1 (1987); 37-42 Revista do Instituto de Medicina Tropical de São Paulo; Vol. 29 Núm. 1 (1987); 37-42 Revista do Instituto de Medicina Tropical de São Paulo; v. 29 n. 1 (1987); 37-42 1678-99460036-4665reponame:Revista do Instituto de Medicina Tropical de São Pauloinstname:Instituto de Medicina Tropical (IMT)instacron:IMTenghttps://www.revistas.usp.br/rimtsp/article/view/28488/30341Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Pauloinfo:eu-repo/semantics/openAccessViera, Leda Q.Moraes-santos, Tasso2012-07-02T00:56:47Zoai:revistas.usp.br:article/28488Revistahttp://www.revistas.usp.br/rimtsp/indexPUBhttps://www.revistas.usp.br/rimtsp/oai||revimtsp@usp.br1678-99460036-4665opendoar:2022-12-13T16:50:12.989445Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)true
dc.title.none.fl_str_mv Schistosomiasis mansoni: evidence for a milder response in germfree mice
Esquistossomose mansônica: evidência de menor resposta nos camundongos isentos de germes
title Schistosomiasis mansoni: evidence for a milder response in germfree mice
spellingShingle Schistosomiasis mansoni: evidence for a milder response in germfree mice
Viera, Leda Q.
Schistosomiasis mansoni
Axenic cercariae
title_short Schistosomiasis mansoni: evidence for a milder response in germfree mice
title_full Schistosomiasis mansoni: evidence for a milder response in germfree mice
title_fullStr Schistosomiasis mansoni: evidence for a milder response in germfree mice
title_full_unstemmed Schistosomiasis mansoni: evidence for a milder response in germfree mice
title_sort Schistosomiasis mansoni: evidence for a milder response in germfree mice
author Viera, Leda Q.
author_facet Viera, Leda Q.
Moraes-santos, Tasso
author_role author
author2 Moraes-santos, Tasso
author2_role author
dc.contributor.author.fl_str_mv Viera, Leda Q.
Moraes-santos, Tasso
dc.subject.por.fl_str_mv Schistosomiasis mansoni
Axenic cercariae
topic Schistosomiasis mansoni
Axenic cercariae
description Germfree (GF and conventional (CV) mice were infected intraperitoneally with GF cercariae of Schistosoma mansoni and kept for six weeks. Twenty four hours before killing, they were injected with [³H]-thymidine. Schistosoma worms, harvested after perfusion of portal system, were counted as well as eggs from liver and intestines. Liver was also used for DNA, protein, and collagen determinations. [³H] -Thymidine incorporation and collagen determinations were used to establish the indices given by the difference between their contents in infected and control animals and expressed per thousand eggs in liver. The recovery of worms in GF mice was around twice as much as in CV ones, and the total number of eggs was higher in the liver of GF animals. No hypertrophy of liver cells was observed by the ratio protein/DNA, but [³H]-thymidine incorporation into DNA was higher than in controls in both GF and CV infected animals. The [³H]-thymidine and collagen indices were lower in GF animals which indicate a more discrete cellular replication and smaller collagen content in relation to the number of eggs present in livers of these mice. It was concluded that the disease seems to be less severe in GF animals.
publishDate 1987
dc.date.none.fl_str_mv 1987-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/rimtsp/article/view/28488
url https://www.revistas.usp.br/rimtsp/article/view/28488
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/rimtsp/article/view/28488/30341
dc.rights.driver.fl_str_mv Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Paulo
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Paulo
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
publisher.none.fl_str_mv Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
dc.source.none.fl_str_mv Revista do Instituto de Medicina Tropical de São Paulo; Vol. 29 No. 1 (1987); 37-42
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 29 Núm. 1 (1987); 37-42
Revista do Instituto de Medicina Tropical de São Paulo; v. 29 n. 1 (1987); 37-42
1678-9946
0036-4665
reponame:Revista do Instituto de Medicina Tropical de São Paulo
instname:Instituto de Medicina Tropical (IMT)
instacron:IMT
instname_str Instituto de Medicina Tropical (IMT)
instacron_str IMT
institution IMT
reponame_str Revista do Instituto de Medicina Tropical de São Paulo
collection Revista do Instituto de Medicina Tropical de São Paulo
repository.name.fl_str_mv Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)
repository.mail.fl_str_mv ||revimtsp@usp.br
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