Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-22T21:16:34.553Z Has data issue: false hasContentIssue false

Detection of high levels of congenital transmission of Toxoplasma gondii in natural urban populations of Mus domesticus

Published online by Cambridge University Press:  19 January 2004

P. A. MARSHALL
Affiliation:
Built and Human Environment Research Institute, School of Environment and Life Sciences, University of Salford, Salford M5 4WT, UK
J. M. HUGHES
Affiliation:
Centre for Parasite Biology, Molecular Epidemiology and Ecology, Biosciences Research Institute, School of Environment and Life Sciences, University of Salford, Salford M5 4WT, UK
R. H. WILLIAMS
Affiliation:
Centre for Parasite Biology, Molecular Epidemiology and Ecology, Biosciences Research Institute, School of Environment and Life Sciences, University of Salford, Salford M5 4WT, UK
J. E. SMITH
Affiliation:
School of Biology, University of Leeds, Leeds LS2 9JT, UK
R. G. MURPHY
Affiliation:
Built and Human Environment Research Institute, School of Environment and Life Sciences, University of Salford, Salford M5 4WT, UK
G. HIDE
Affiliation:
Centre for Parasite Biology, Molecular Epidemiology and Ecology, Biosciences Research Institute, School of Environment and Life Sciences, University of Salford, Salford M5 4WT, UK

Abstract

The relative importance of different transmission routes of Toxoplasma gondii has been a matter for debate. This ubiquitous parasite is generally thought to be transmitted by infective oocysts excreted by the definitive host, the cat. Ingestion of undercooked meat has also been considered an important route of transmission in many mammals while congenital transmission has generally been considered relatively rare. Experimental studies demonstrate the ability of T. gondii to be transmitted congenitally, but few studies have investigated the frequency of this transmission route in natural populations. We use PCR amplification of the SAG1 gene to investigate the frequency of congenital transmission in a wild population of mice (Mus domesticus) and show that congenital transmission is occurring in 75% of pregnancies in this population. Furthermore, for infected pregnant mice, transmission occurs to at least one foetus in 100% of cases while variable penetrance of congenital infection is observed. These high levels of congenital transmission in this wild population of mice, taken together with other recent data on congenital transmission in sheep, suggests that this phenomenon might be more widespread than previously thought.

Type
Research Article
Copyright
2004 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

BARBER, J. S. & TREES, A. J. (1998). Naturally occurring vertical transmission of Neospora caninum in dogs. International Journal for Parasitology 28, 5764.CrossRefGoogle Scholar
BJORKMAN, C., JOHANSSON, O., STENLUND, S., HOLMDAHL, O. J. & UGGLA, A. (1996). Neospora species infection in a herd of dairy cattle. Journal of the American Veterinary Medical Association 208, 14411444.Google Scholar
BLEWETT, D. A. & TREES, A. J. (1987). The epidemiology of ovine toxoplasmosis with especial respect to control. British Veterinary Journal 143, 128135.CrossRefGoogle Scholar
BUXTON, D. (1998). Protozoan infections (Toxoplasma gondii, Neospora caninum and Sarcocystis spp.) in sheep and goats: recent advances. Veterinary Research 29, 289310.Google Scholar
COLE, R. A., LINDSAY, D. S., BLAGBURN, B. L. & DUBEY, J. P. (1995). Vertical transmission of Neospora caninum in mice. Journal of Parasitology 81, 730732.CrossRefGoogle Scholar
DUBEY, J. P. & BEATTIE, C. P. (1988). Toxoplasmosis of Animals and Man. CRC Press, Boca Raton, Fl, USA.
DUNCANSON, P., TERRY, R. S., SMITH, J. E. & HIDE, G. (2001). High levels of congenital transmission of Toxoplasma gondii in a commercial sheep flock. International Journal for Parasitology 31, 16991703.CrossRefGoogle Scholar
ELSAID, M. M. A., MARTINS, M. S., FREZARD, F., BRAGA, E. M., & VITOR, R. W. A. (2001). Vertical toxoplasmosis in a murine model, protection after immunization with antigens of Toxoplasma gondii incorporated into liposomes. Memorias do Instituto Oswaldo Cruz 96, 99104.CrossRefGoogle Scholar
HENDERSON, D. C. (1990). The Veterinary Book for Sheep Farmers. Farming Press, Ipswich.
JOHNSON, A. M. (1997). Speculation on possible life cycles for the clonal lineages in the genus Toxoplasma. Parasitology Today 13, 393397.CrossRefGoogle Scholar
OWEN, M. R. & TREES, A. J. (1998). Vertical transmission of Toxoplasma gondii from chronically infected house (Mus musculus) and field (Apodemus sylvaticus) mice determined by polymerase chain reaction. Parasitology 116, 299304.CrossRefGoogle Scholar
SAVVA, D., MORRIS, J. C., JOHNSON, J. D. & HOLLIMAN, R. E. (1990). Polymerase chain reaction for detection of Toxoplasma gondii. Journal of Medical Microbiology 32, 2531.CrossRefGoogle Scholar
SCHARES, G., WENZEL, U., MULLER, T. & CONRATHS, F. J. (2001). Serological evidence for naturally occurring transmission of Neospora caninum among foxes (Vulpes vulpes). International Journal for Parasitology 31, 418423.CrossRefGoogle Scholar
STAHL, W., SEKIGUCHI, M. & KANEDA, Y. (2002). Cerebellar anomalies in congenital murine toxoplasmosis. Parasitology Research 88, 507512.CrossRefGoogle Scholar
TENTER, A. M., HECKEROTH, A. R. & WEISS, L. M. (2000). Toxoplasma gondii: from animals to humans. International Journal for Parasitology 30, 12171258.CrossRefGoogle Scholar
TERRY, R. S., SMITH, J. E., DUNCANSON, P. & HIDE, G. (2001). MGE-PCR: a novel approach to the analysis of Toxoplasma gondii strain differentiation using mobile genetic elements. International Journal for Parasitology 31, 155161.CrossRefGoogle Scholar