infection as Coelho et al. (1997) showed that
preventing Ascocotyle sp. can be effective by
cooking fish at 100°C and freezing at -20°C.
The significantly greater density of Ascocotyle sp.
metacercariae in the M. curema viscera caught in
river can be explained by known the access to the
river for this species, showing potential proximity
to intermediate hosts and infective parasite forms.
Despite significant correlation between
metacercariae density and M. liza biometric
parameters, the coefficient values were very low,
indicating that the metacercariae presence is not
dependent of fish species length and weight. It is
worth mentioning Almeida Dias & Woiciechovski
(1994) and Oliveira et al., (2007), which had
infected fish from specimens with four cm
fingerlings, not observing infection in juvenile
smaller. Although the metacercariae density in M.
liza viscera and muscles had been greater than in
M. curema, the study results showed no clear
biometrics and density correlation of biometric
and density of M. liza metacercariae. However,
other authors found a greater number of
metacercariae in larger fish (Coelho et al., 1997).
Vianna et al. (2005) studied metacercariae of
Clinostomum complanatum (Rudolphi, 1819) and
Rhamdia quelen (Quoy & Gaimard, 1824) showed
that fish parasites density is greater than 30 cm.
Literature data suggest gradual metacercariae
acquisition, which minor variations, all in
accordance with the size set by IBAMA (Instituto
Brasileiro do Meio Ambiente e dos Recursos
Naturais Renováeis) extractive fishing.
Ascocotyle sp. metacercariae were found in 100%
fish mullets obtained in the fish trade of the Iguape
city, Sao Paulo, Brazil, between January 2009 and
February 2010. The M. liza and M. curema
consumption generates a zoonotic risk potential to
population for high infection prevalence and large
metacercariae numbers in their tissues.
We thank to Unicamp Procad Program NF
69/2010. The authors were also grateful to Naércio
Aquino Menezes (Museu de Zoologia - USP), for
the fishes identification support.
ACKNOWLEDGMENTS
REFERENCES
Almeida Dias, ER & Woiciechovski, E. 1994.
Antunes, AS & Almeida Dias, ER. 1994.
Barros, LA & Amato, SB. 1996.
Bush, AO, Lafferty, KD, Lotz, JM & Shostak, AW.
1997.
Castro, JM. 1994.
Cavalcanti, ETS, Pavanelli, GC, Chellappa, S &
Takemoto, RM. 2005.
Chieffi, PP, Gorla, MCO, Torres, DMAGV, Dias,
RMDS, Mangini, ACS, Monteiro, AV &
Woiciechovski, E. 1992.
Chieffi, PP, Leite, OH, Dias, RMDS, Torres,
DMAGV & Mangini, ACS. 1990.
Ocorrência da Phagicola longa
(Trematoda: Heterophyidae) em mugilídeos
e no homem, em Registro e Cananéia, SP.
Higiene Alimentar, vol. 31, pp. 43-46.
Phagicola
longa (Trematoda: Heterophyidae) em
mugilídeos estocados resfriados e seu
consumo cru em São Paulo, SP. Higiene
Alimentar, vol. 31, pp. 41-42. Infecções
experimentais de cães com metacercárias
de Phagicola longus (Ransom, 1920) Price,
1932. Revista Brasileira de Parasitologia
Veterinária, vol. 5, pp. 61-64.
Parasitology meets ecology on its
own terms: Margolis et al. revisited. The
Journal of Parasitology, vol. 83, pp. 575-
583. Extração de cistos de
metacercárias de Phagicola Faust, 1920
(Trematoda: Heterophyidae) dos tecidos de
tainha Mugil Linnaeus, 1758 (Pisces:
Mugilidae) mediante emprego das técnicas
de digestão enzimática e homogeneização.
Dissertação de Mestrado, Faculdade de
Medicina Veterinária e Zootecnia,
Universidade de São Paulo, São Paulo.
Ocorrência de
Ergasilus versicolor e E. lizae (Copepoda:
Ergasilidae) na tainha, Mugil curema
(Osteichthyes: Mugilidae) em Ponta Negra,
Natal, Rio Grande do Norte. Arquivos de
Ciências do Mar, vol. 38, pp. 131-134.
Human infection
b y P ha gi c o l a sp . ( Tre m a t o d a,
Heterophyidae) in the municipality of
Registro, São Paulo State, Brazil. Journal of
Tropical Medicine and Hygiene, vol. 95, pp.
346-348.
Human
parasitism by Phagicola sp. (Trematoda,
Heterophyidae) in Cananéia, São Paulo
State, Brazil. Revista do Instituto de
Medicina Tropical, vol. 32, pp. 285-288.
Namba et al.
Ascocotyle in tissues of mullets Mugil
274