Hostname: page-component-8448b6f56d-t5pn6 Total loading time: 0 Render date: 2024-04-16T23:44:24.531Z Has data issue: false hasContentIssue false

Persistence of Toxoplasma gondii tissue stages in poultry over a conventional fattening cycle

Published online by Cambridge University Press:  16 June 2014

A.-C. GEUTHNER
Affiliation:
Institute of Parasitology, Centre for Infectious Diseases, University Leipzig, An den Tierkliniken 35, D-04103 Leipzig, Germany
M. KOETHE
Affiliation:
Institute of Food Hygiene, Centre for Veterinary Public Health, University Leipzig, An den Tierkliniken 1, D-04103 Leipzig, Germany
M. LUDEWIG
Affiliation:
Institute of Food Hygiene, Centre for Veterinary Public Health, University Leipzig, An den Tierkliniken 1, D-04103 Leipzig, Germany
S. POTT
Affiliation:
Institute of Food Hygiene, Centre for Veterinary Public Health, University Leipzig, An den Tierkliniken 1, D-04103 Leipzig, Germany
G. SCHARES
Affiliation:
Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Epidemiology, Südufer 10, D-17493 Greifswald–Insel Riems, Germany
A. DAUGSCHIES
Affiliation:
Institute of Parasitology, Centre for Infectious Diseases, University Leipzig, An den Tierkliniken 35, D-04103 Leipzig, Germany
B. BANGOURA*
Affiliation:
Institute of Parasitology, Centre for Infectious Diseases, University Leipzig, An den Tierkliniken 35, D-04103 Leipzig, Germany
*
*Corresponding author: Institute of Parasitology, Centre for Infectious Diseases, University Leipzig, An den Tierkliniken 35, D-04103 Leipzig, Germany. E-mail: bangoura@vetmed.uni-leipzig.de

Summary

Toxoplasma gondii is a widely spread protozoon in humans, mammals and poultry. Regarding the latter, nothing is known yet about the duration of T. gondii persistence and distribution over a conventional fattening cycle of turkeys and chickens. Twenty-four turkeys and 12 broiler chickens were infected intravenously with 1×106T. gondii tachyzoites (strain NED). Serum antibody levels were determined weekly by ELISA (turkeys) or immunofluorescent antibody test (chickens). Turkeys were slaughtered at 4, 8, 12 and 16 weeks post-infection (p.i.), and chickens 5 or 10 weeks p.i. (n = 6 per group). Sixteen different tissue samples per bird were analysed for T. gondii by PCR. All infected animals showed seroconversion. In turkeys, 15·9% of all samples were tested positive for T.-gondii-DNA. Among the edible tissues (drumstick, thigh, breast muscle, heart, liver and gizzard) 7·8% tested positive. Among poultry slaughtered after different periods of time after infection no significant differences (P>0·05) regarding the number of positive samples were observed. Only 4 out of 192 samples (2·1%) from infected chickens contained detectable T. gondii DNA.The PCR findings suggested that T. gondii may persist in poultry. Particularly in turkey it was shown that edible tissues stay infected for at least 16 weeks p.i. which indicates a potential risk for consumers of undercooked turkey meat whereas chickens appear less susceptible to T. gondii infection.

Type
Special Issue Article
Copyright
Copyright © Cambridge University Press 2014 

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

Bangoura, B., Zöller, B., Koethe, M., Ludewig, M., Pott, S., Fehlhaber, K., Straubinger, R. K. and Daugschies, A. (2013). Experimental Toxoplasma gondii oocyst infections in turkeys (Meleagris gallopavo). Veterinary Parasitology 196, 272277.Google Scholar
Beverley, J. K., Henry, L., Hunter, D. and Brown, M. E. (1977). Experimental toxoplasmosis in calves. Research in Veterinary Sciences 23, 3337.Google Scholar
Biancifiori, F., Rondini, C., Grelloni, V. and Frescura, T. (1986). Avian toxoplasmosis: experimental infection of chicken and pigeon. Comparative Immunology, Microbiology and Infectious Diseases 9, 337346.Google Scholar
Bickford, A. A. and Saunders, J. R. (1966). Experimental toxoplasmosis in chickens. American Journal of Veterinary Research 27, 308318.Google Scholar
Chumpolbanchorn, K., Anankeatikul, P., Ratanasak, W., Wiengcharoen, J., Thompson, R. C. A. and Sukthana, Y. (2009). Prevalence of Toxoplasma gondii indirect fluorescent antibodies in naturally- and experimentally-infected chickens (Gallus domesticus) in Thailand. Acta Parasitologica 54, 194196.Google Scholar
Cook, A. J., Gilbert, R. E., Buffolano, W., Zufferey, J., Petersen, E., Jenum, P. A., Foulon, W., Semprini, A. E. and Dunn, D. T. (2000). Sources of toxoplasma infection in pregnant women: European multicentre case-control study. European Research Network on Congenital Toxoplasmosis. British Medical Journal 321, 142147.Google Scholar
Drobeck, H. P., Manwell, R. D., Bernstein, E. and Dillon, R. D. (1953). Further studies of toxoplasmosis in birds. American Journal of Hygiene 58, 329339.Google Scholar
Dubey, J. P. (1988). Long-term persistence of Toxoplasma gondii in tissues of pigs inoculated with T. gondii oocysts and effect of freezing on viability of tissue cysts in pork. American Journal of Veterinary Research 49, 910913.Google Scholar
Dubey, J. P. (1997). Survival of Toxoplasma gondii tissue cysts in 0·85–6% NaCl solutions at 4–20 °C. Journal of Parasitology 83, 946949.Google Scholar
Dubey, J. P. (2010 a). Toxoplasmosis of Animals and Humans, 2nd Edn, p. 235. CRC Press, Boca Raton, FL, USA.Google Scholar
Dubey, J. P. (2010 b). Toxoplasma gondii infections in chickens (Gallus domesticus): prevalence, clinical disease, diagnosis and public health significance. Zoonoses and Public Health 57, 6073.CrossRefGoogle ScholarPubMed
Dubey, J. P. and Thulliez, P. (1993). Persistence of tissue cysts in edible tissues of cattle fed Toxoplasma gondii oocysts. American Journal of Veterinary Research 54, 270273.CrossRefGoogle ScholarPubMed
Dubey, J. P., Murrell, K. D. and Fayer, R. (1984). Persistence of encysted Toxoplasma gondii in tissues of pigs fed oocysts. American Journal of Veterinary Research 45, 19411943.Google Scholar
Dubey, J. P., Camargo, M. E., Ruff, M. D., Wilkins, G. C., Shen, S. K., Kwok, O. C. and Thulliez, P. (1993 a). Experimental toxoplasmosis in turkeys. Journal of Parasitology 79, 949952.Google Scholar
Dubey, J. P., Ruff, M. D., Camargo, M. E., Shen, S. K., Wilkins, G. L., Kwok, O. C. and Thulliez, P. (1993 b). Serologic and parasitologic responses of domestic chickens after oral inoculation with Toxoplasma gondii oocysts. American Journal of Veterinary Research 54, 16681672.Google Scholar
Howe, D. K. and Sibley, L. D. (1995). Toxoplasma gondii comprises three clonal lineages: correlation of parasite genotype with human disease. Journal of Infectious Diseases 172, 15611566.Google Scholar
Howerth, E. W. and Rodenroth, N. (1985). Fatal systemic Toxoplasmosis in a wild turkey. Journal of Wildlife Diseases 21, 446449.Google Scholar
Kaneto, C. N., Costa, A. J., Paulillo, A. C., Moraes, F. R., Murakami, T. O. and Meireles, M. V. (1997). Experimental toxoplasmosis in broiler chicks. Veterinary Parasitology 69, 203210.CrossRefGoogle ScholarPubMed
Kijlstra, A., Meerburg, B. G. and Mul, M. F. (2004). Animal-friendly production systems may cause re-emergence of Toxoplasma gondii . Njas-Wageningen Journal of Life Sciences 52, 119132.CrossRefGoogle Scholar
Koethe, M., Pott, S., Ludewig, M., Bangoura, B., Zöller, B., Daugschies, A., Tenter, A. M., Spekker, K., Bittame, A., Mercier, C., Fehlhaber, K. and Straubinger, R. K. (2011). Prevalence of specific IgG-antibodies against Toxoplasma gondii in domestic turkeys determined by kinetic ELISA based on recombinant GRA7 and GRA8. Veterinary Parasitology 180, 179190.CrossRefGoogle ScholarPubMed
Krautwald-Junghanns, M. E., Ellerich, R., Bohme, J., Cramer, K., DellaVolpe, A., Mitterer-Istyagin, H., Ludewig, M., Fehlhaber, K., Schuster, E., Berk, J., Aldehoff, D., Fulhorst, D., Kruse, W., Dressel, A., Noack, U. and Bartels, T. (2009). Examination of rearing standards and health status in turkeys in Germany. Berliner und Munchener Tierarztliche Wochenschrift 122, 271283.Google ScholarPubMed
Maksimov, P., Buschtons, S., Herrmann, D. C., Conraths, F. J., Gorlich, K., Tenter, A. M., Dubey, J. P., Nagel-Kohl, U., Thoms, B., Bötcher, L., Kühne, M. and Schares, G. (2011). Serological survey and risk factors for Toxoplasma gondii in domestic ducks and geese in Lower Saxony, Germany. Veterinary Parasitology 182, 140149.Google Scholar
Martinez-Carrasco, C., Ortiz, J. M., Bernabe, A., Ruiz De Ybanez, M. R., Garijo, M. and Alonso, F. D. (2004). Serologic response of red-legged partridges (Alectoris rufa) after oral inoculation with Toxoplasma gondii oocysts. Veterinary Parasitology 121, 143149.Google Scholar
Opsteegh, M., Langelaar, M., Sprong, H., den Hartog, L., De Craeye, S., Bokken, G., Ajzenberg, D., Kijlstra, A. and van der Giessen, J. (2010). Direct detection and genotyping of Toxoplasma gondii in meat samples using magnetic capture and PCR. International Journal of Food Microbiology 139, 193201.CrossRefGoogle ScholarPubMed
Pott, S., Koethe, M., Bangoura, B., Zöller, B., Daugschies, A., Straubinger, R. K., Fehlhaber, K. and Ludewig, M. (2012). Tenacity of T. gondii tissue cysts in fermented sausages – literature survey and own studies. Journal of Food Safety and Food Quality 63, 147154.Google Scholar
Quist, C. F., Dubey, J. P., Luttrell, M. P. and Davidson, W. R. (1995). Toxoplasmosis in wild Turkeys - a case-report and serologic survey. Journal of Wildlife Diseases 31, 255258.Google Scholar
Sedlak, K., Literak, I., Vitula, F. and Benaak, J. (2000). High susceptibility of partridges (Perdix perdix) to toxoplasmosis compared with other gallinaceous birds. Avian Pathology 29, 563569.CrossRefGoogle ScholarPubMed
Tenter, A. M., Heckeroth, A. R. and Weiss, L. M. (2000). Toxoplasma gondii: from animals to humans. International Journal for Parasitology 30, 12171258.Google Scholar
Vitaliano, S. N., Mineo, T. W. P., Andre, M. R., Machado, R. Z., Mineo, J. R. and Werther, K. (2010). Experimental infection of Crested Caracara (Caracara plancus) with Toxoplasma gondii simulating natural conditions. Veterinary Parasitology 172, 7175.CrossRefGoogle ScholarPubMed
Zintl, A., Halova, D., Mulcahy, G., O'Donovan, J., Markey, B. and DeWaal, T. (2009). In vitro culture combined with quantitative TaqMan PCR for the assessment of Toxoplasma gondii tissue cyst viability. Veterinary Parasitology 164, 167172.Google Scholar
Zöller, B., Koethe, M., Ludewig, M., Pott, S., Daugschies, A., Straubinger, R. K., Fehlhaber, K. and Bangoura, B. (2013). Tissue tropism of Toxoplasma gondii in turkeys (Meleagris gallopavo) after parenteral infection. Parasitology Research 112, 18411847.Google Scholar
Supplementary material: File

Geuthner Supplementary Material

Tables S1-S2

Download Geuthner Supplementary Material(File)
File 23.2 KB