dc.contributor.author |
Dutra, Gisele Ferreira |
|
dc.contributor.author |
Pinto, Nitza Souto França |
|
dc.contributor.author |
Avila, Luciana Farias da Costa de |
|
dc.contributor.author |
Telmo, Paula de Lima |
|
dc.contributor.author |
Hora, Vanusa Pousada da |
|
dc.contributor.author |
Martins, Lourdes Helena Rodrigues |
|
dc.contributor.author |
Berne, Maria Elisabeth Aires |
|
dc.contributor.author |
Scaini, Carlos James |
|
dc.date.accessioned |
2017-03-20T18:36:25Z |
|
dc.date.available |
2017-03-20T18:36:25Z |
|
dc.date.issued |
2013 |
|
dc.identifier.citation |
DUTRA, Gisele Ferreira et al. Evaluation of the initial and chronic phases of toxocariasis after consumption of liver treated by freezing or cooling. Parasitology Research, v. 112, p. 2171-2175, 2013. Disponível em: <https://www.researchgate.net/publication/236048587>. Acesso em: 04 fev. 2017. |
pt_BR |
dc.identifier.issn |
1432-1955 |
|
dc.identifier.uri |
http://repositorio.furg.br/handle/1/7105 |
|
dc.description.abstract |
Human toxocariasis is a neglected parasitic zoonosis
of worldwide distribution. The consumption of raw or
undercooked meat and offal from paratenic hosts of the
Toxocara canis nematode can cause infection in humans, but
there have been a lack of studies examining specific prophylactic
measures to combat this mode of transmission. The aim
of this study was to evaluate the establishment of infection by T.
canis larvae at the initial and chronic phases of visceral
toxocariasis after the consumption of mouse liver subjected to
cold treatment. This study was divided into two stages using
groups (G) of five donor mice inoculated with 2,000 eggs of T.
canis. Two days post-inoculation, the livers of donor mice in
G1 and G2 were kept at −20 °C and between 0 and 4 °C,
respectively, for 10 days. In the first stage of the study, the livers
of mice from G1, G2, and G3 (control) were subjected to a
tissue digestion technique and found to be positive for infection.
In the second stage, which evaluated infection in mice that
had consumed livers from donor mice, receiver mice of G4 and
G7 were fed with livers of donor mice from G1 (freezing),
receiver mice of G5 and G8 were fed with livers of donor mice
from G2 (cooling), and receiver mice of G6 and G9 with livers
from G3 (control). Then, the tissue digestion technique was
performed for recovering larvae from organs and carcasses of
mice, at 2 days (G4, G5, and G6) and 60 days after liver
consumption (G7, G8, and G9). It was observed that freezing
inhibited the viability of 100 % of the larvae, while cooling
promoted 87.7 and 95.7 % reductions in the intensity of infection
at 2 and 60 days after liver consumption, respectively.
Under the studied conditions, cold treatment shows great potential
to help control this parasitosis, both in the initial and
chronic phases of toxocariasis. |
pt_BR |
dc.language.iso |
eng |
pt_BR |
dc.rights |
open access |
pt_BR |
dc.title |
Evaluation of the initial and chronic phases of toxocariasis after consumption of liver treated by freezing or cooling |
pt_BR |
dc.type |
article |
pt_BR |
dc.identifier.doi |
10.1007/s00436-013-3376-5 |
pt_BR |