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Increased Toxoplasma gondii positivity relative to age in 125 Scottish sheep flocks; evidence of frequent acquired infection
© Katzer et al; licensee BioMed Central Ltd. 2011
- Received: 11 August 2011
- Accepted: 21 December 2011
- Published: 21 December 2011
Toxoplasma gondii seroprevalence was determined in 3333 sheep sera from 125 distinct sheep flocks in Scotland, with the majority of flocks being represented by 27 samples, which were collected between July 2006 and August 2008. The selected farms give a representative sample of 14 400 sheep holdings identified in the Scottish Government census data from 2004. Overall T. gondii seroprevalence, at individual sheep level, was determined to be 56.6%; each flock tested, had at least a single positive animal and in four flocks all ewes tested positive. The seroprevalence of sheep increased from 37.7% in one year old stock to 73.8% in ewes that were older than six years, showing that acquired infections during the life of the animals is frequent and that environmental contamination by T. gondii oocysts must be significant. The median within-flock seroprevalence varied significantly across Scotland, with the lowest seroprevalence of 42.3% in the South and the highest seroprevalence of 69.2% in the far North of Scotland and the Scottish Islands, while the central part of Scotland had a seroprevalence of 57.7%. This distribution disequilibrium may be due to the spread and survival of oocysts on pasture and lambing areas. A questionnaire accompanying sampling of flocks identified farms that used Toxovax®, a commercial vaccine that protects sheep from abortion due to T. gondii infection. Only 24.7% of farmers used the vaccine and the vaccine did not significantly affect the within flock seroprevalence for T. gondii. The implications for food safety and human infection are discussed.
- Infected Animal
- Sheep Breed
- Percentage Positivity
- Tissue Cyst
Toxoplasma gondii is the most successful parasitic pathogen world-wide, infecting all warm blooded animals including humans . This protozoan parasite is of great economic importance to the sheep industry. In the UK, T. gondii was shown to be the second most commonly diagnosed cause of abortions in sheep (25.4%), after Chlamydophila abortus (45.6%), based on data from Veterinary Investigation Diagnosis Analysis (VIDA) for 2009 . The scope for clinical toxoplasmosis is great; in the UK alone there are 14.2 million sheep, of which 6.5 million are breeding ewes . Using average annual incidence rates of clinical toxoplasmosis of between 1% and 2% , this would mean that between 65 000 and 130 000 pregnancies are lost annually due to T. gondii infection in the UK alone, while in European Union, with a total number of 68.1 million breeding ewes  the loss would be between 680 000 and 1 360 000 pregnancies annually.
Most T. gondii infections in sheep occur through the ingestion of oocysts, a stage of the parasite, which is very stable and can survive in favourable conditions in the environment for over 12 months, contaminating pasture, feeds and drinking water . Oocysts are produced in the definitive hosts of T. gondii, cats, which shed the parasite in their faeces after eating meat, infected with tissue cysts . Intermediate hosts, including sheep and humans, that ingest oocysts are thought to become infected for life, with detectable and persistent IgG antibody levels specific for T. gondii and this has aided the assessment of infection levels in many host species .
Abortions in sheep due to T. gondii are associated with a primary infection during the first or second trimester of gestation, while primary infection in the later stages of pregnancy leads to the birth of congenitally infected lambs, which are relatively rare [9, 10]. Infected animals develop an effective immune response, which will protect against disease in subsequent pregnancies . These studies and others showed that vaccination may be a feasible option to control disease and lead to the development of a live vaccine preparation. Toxovax® was licensed in 1988 in New Zealand and was launched in 1992 in UK and Ireland . Toxovax® consists of a live attenuated T. gondii strain (S48) that will not cause a persistent infection [13, 14]. The efficacy and safety of this vaccine were tested by Intervet B.V. in collaboration with the Moredun Research Institute in Scotland, where it was shown that a single vaccine dose will induce an effective immune response that will persist for at least 18 months without further challenge .
Human congenital infections with T. gondii are very similar to those seen in pregnant sheep but there are no licensed vaccines for humans that protect against toxoplasmosis. Another difference is the main transmission route by which humans may become infected . A multicentre epidemiologic study among pregnant women in Europe identified ingestion of raw or undercooked meat/meat-products, containing tissue cysts, as the major source of T. gondii infection, while infection through oocysts, from environmental contamination, plays only a minor part .
In 2007, 1851 cases of T. gondii infection in humans were clinically diagnosed and reported by 18 European Union member states, 149 of which originated from the United Kingdom , giving an incidence rate of 0.83 reported clinical cases per 100 000 people within Europe. Although this incidence seems low, this does not express the severity of the potential consequence of infection, which could be abortion or the birth of congenitally infected babies, which may suffer from learning disabilities, requiring assistance throughout life; these congenitally infected children are likely to develop ocular toxoplasmosis later in life. Therefore the resulting disease burden, due to T. gondii infection, was rated higher than that of any other food borne pathogens in Europe, by the National Institute of Public Health and the Environment (RIVM) of The Netherlands [19, 20]. In another recent report by the RIVM, based on calculations of the long-term socio-economic impact of emerging zoonotic pathogens relevant for The Netherlands, T. gondii was ranked as the second most important pathogen due to its high disease burden .
The European food safety authority recommended in 2007, that there is a need to improve data collection on surveillance and monitoring of T. gondii in animals and food products for human consumption, in order to better evaluate the disease risk of toxoplasmosis in member states . There is no current data on the prevalence of T. gondii in food animals in the UK and very little is known about environmental contamination levels of T. gondii oocysts. Existing prevalence figures are only regional and predate the licensing of Toxovax® in the UK. In this study we set out to ascertain how frequent T. gondii infections are within a representative section of Scottish sheep flocks, when sheep become infected and how widely Toxovax® is used.
Study design and serum collection
The serum samples for the T. gondii prevalence study stem from a national study, aimed to assess the prevalence of different endemic sheep diseases in Scotland, conducted between July 2006 and August 2008 . The sample frame comprising 825 sheep holdings was generated on the basis of Scottish Government census data from June 2004 and was stratified by three separate regions (South (i.e. south of Glasgow and Edinburgh), Central (i.e. Aberdeenshire, Perthshire and Argyll) and North (i.e. Highlands and Islands) consisting of 40, 35 and 50 farms, respectively) to take account of the distribution of sheep of different Scottish regions. Flocks with at least 50 breeding ewes were eligible to take part in the study; on farms that had multiple flocks, information was gathered only for one flock. Study farms were initially contacted by mail and then by telephone to identify farmers willing to participate in the study. On 125 farms information was gathered on general farm characteristics, management practices and animal health during a face-to-face interview; the standardised questionnaire had been designed with the help of sheep specialists and was pre-tested on 5 sheep owners. At the end of the interview farmers were given a printout of the questionnaire for a crosscheck to ensure optimal data quality. A postal follow-up questionnaire including specific questions on the use of Toxovax®, a commercially available vaccine against toxoplasmosis, was also conducted. Age and breed were recorded for typically 27 sheep per flock from which serum samples were taken. The samples were sent to the laboratory by next day delivery at ambient temperature and serum was separated from clotted blood and stored at -20 C until tested.
An ELISA was used to detect IgG antibodies to T. gondii in sheep sera as described by Buxton and colleagues . This ELISA used a water-soluble antigen fraction of T. gondii tachyzoites of the S48 strain . Data was expressed as percentage positivity in comparison to a standard, high titre, positive control serum obtained from an experimentally infected animal. Optical density (OD) readings, resulting in a percentage positivity under 25% were considered to be negative; percentage positivity values of 25% and under 30% were classified as borderline and percentage positivity values of 30% and above were interpreted as positive . Sera were tested in duplicate and results that did not match or borderline results were repeated.
Data were described using graphs and boxplots produced in MS Office Excel (version 2007) and R (version 2.12.0). Univariate tests of equality were performed at animal level (age) and flock level (geographic region, management practices). Individual animals were treated as independent. Differences between strata of varied management practices and geographic regions were assessed by Wilcoxon-Mann-Whitney test; confidence bands were calculated using bootstrapping methods . Linear regression models were used to assess the association of age with serostatus of individual animals as well as geographic latitude with within-flock seroprevalence. Variables identified at the univariate stage of analysis were included in multivariate regression models and non-significant variables were removed in a stepwise fashion. For variables with multiple categories, all categories were maintained in model if one category proved significant. The final model selection was based on the Akaike information criterion (AIC), as well as the plausibility to affect seroprevalence of explanatory variables.
T. gondii seroprevalence
Effect of vaccination on T. gondii seroprevalence
The follow-up questionnaire data were analysed in order to evaluate if the use of Toxovax®, a commercially available vaccine against toxoplasmosis, had a significant impact on the seroprevalence shown above. Questionnaires were returned by 93 of the 125 farmers, with an equal response rate across the different regions. The vaccine was used by 22 of the 93 farmers that responded (24.7%). In most cases the farmers used the vaccine on a yearly basis (n = 16) to vaccinate their replacement stock, while the remaining farmers used the vaccine less frequently. The vaccine uptake was about equal across the country, when divided into three regions: South 8/32 (25.0%), Central 6/26 (23.1%) and North/Islands 8/35 (22.9%). The median within flock seroprevalence for T. gondii on farms without vaccination was 55.5% (95% CI: 50.0, 65.2%) and on farms with vaccination 59.2% (95% CI: 53.8, 82.7%). Statistical comparison revealed no significant difference of median within-flock prevalence between flocks with and without vaccination (p-value = 0.29). Consequently the full data set (n = 125) was used for further analysis.
Age effect on T. gondii seroprevalence
Seropositivity for Toxoplasma gondii in sheep according to animal age.
Age of Sheep
Numbers of Animals
Percentage of Animals
> 6 years
Regional variation in T. gondii prevalence
Multivariate analysis with region, common pasture, mean sheep age, farm boundary and lambing location as explanatory variables identified mean sheep age and boundary consistently as significant risk factors for within-flock T. gondii seroprevalence. The best fitting model included region as an explanatory variable; however, deemed a proxy for geographic differences in flock management, further models were run without region. Common pasture consequently was identified as significant factor, whilst lambing location made no significant additional contribution to explain the variability observed in seroprevalence. Sheep breed was not found to be a significant factor for T. gondii seroprevalence.
The results from this Scotland wide study showed an overall seroprevalence for T. gondii in sheep of 56.6%. Previous seroprevalence studies in Scotland, conducted 20 years ago, only examined animals from specific regions where the prevalence of T. gondii in sheep from locations around Glasgow was found to be 26.2% .
Results from our study showed an increase in T. gondii seroprevalence with age confirming that a major source of infection for sheep is likely to be through the consumption of sporulated oocysts from the environment. This trend has also been reported by other authors where seroprevalence to T. gondii in market weight lambs was found to be only about half that of adult ewes , reflecting an increase in seropositivity with animal age. Further studies looking at development of specific antibodies in sheep, as an indicator of exposure to T. gondii, have shown that there is an increase in seroprevalence associated with age indicating that there is extensive environmental contamination with T. gondii oocysts and that most infections in sheep occur following birth [28–30]. These studies taken together with the extensive study reported in this paper do not support the hypothesis, based on a more limited data set, that vertical transmission of T. gondii is significant in sheep flocks . This direct correlation of increasing age and sero-prevalence has also been described in humans [32–34].
During T. gondii infection animals mount a humoral immune response which can be detected by measuring immunoglobulin G (IgG) antibody levels. Following an initial infection, antibody levels are expected to stay elevated for the lifetime of the animal, because the immune response of infected animals does not completely clear the parasite and animals stay persistently infected. However, recent longitudinal serology based studies have shown that T. gondii IgG antibody levels may drop in some infected animals leading to false negative results [35, 36]. One of these studies followed 524 sheep for one year and T. gondii antibody levels were measured at 4 different time points. Around 10% of the animals had negative test results following a previously positive result which raises issues about the sensitivity of some of the serological assays used to measure T. gondii antibodies and also the persistence of the elevated antibody titres following infection.
This study revealed a significant positive correlation of increasing T. gondii prevalence and age of animals tested, reflecting an accumulation of T. gondii infection throughout life. This study confirms that sheep in Scotland are frequently exposed to T. gondii oocysts and that horizontal transmission is a significant route of infection. This observation provides further support to previous papers stating that horizontal rather than vertical transmission is the main cause of ovine abortion [6, 9, 10, 12, 37]. Smaller increases in T. gondii prevalence, observed between the older age groups are likely to represent a decreasing number of naïve animals, in these groups, that are still able to become infected. This may yet be further confounded by some persistently infected animals, without recent T. gondii challenge becoming antibody negative as seen in longitudinal seroprevalence studies [35, 36]. This effect will result in a reduction of detection of infected animals, which will particularly affect the older age groups. A reason, why the higher rate of T. gondii seroconversion is seen in the younger age groups, maybe due to the use of Toxovax®. Analysis of the questionnaire data revealed that most farmers tend to vaccinate replacement ewes, i.e. young animals. The vaccine consists of a live attenuated strain that does not cause persistent infection . It induces humoral and cell mediated immune responses that will protect sheep very effectively for more than 18 month against T. gondii induced abortions without the need for booster vaccination or field challenge . However, detectable antibody levels may not persist for more than six month without subsequent challenge . Therefore, an increased rate of seroconversion is likely to be seen in the younger age groups. However, this effect is not long lived, without field challenge, and did not result in a significant difference in mean within flock difference for vaccinated and non-vaccinated sheep due to mixed ages of animals tested on each farm.
The results of this study show that there is a gradient of T. gondii seroprevalence across Scotland, where the South has a significantly lower mean within-flock seroprevalence (36.8%) than the North/Islands (60.5%), with the Central part of Scotland having an intermediate seroprevalence (54.8%). This result is independent of sheep breed, which was not significantly associated with T. gondii infection. The observed infection gradient is different to trends seen in other European studies, in France  and Finland , where studies have shown higher seroprevalence figures for the south of the countries and lower figures for the north. The French study observed an increasing prevalence gradient from north-western to southern France in sheep and explained this due to more favourable conditions to oocyst survival . The Finnish study reported a geographical gradient in T. gondii prevalence for sheep and moose, where the seroprevalence in both host species was lower in the North and higher in the South-Western part of Finland. The authors suggested that this observation may reflect areas of habitation and therefore cat density because T. gondii oocysts are very unlikely to survive the severe Finnish winters. It is unlikely that the figures obtained for Scotland reflect cat density or areas of habitation alone but are also likely to involve minimum temperatures during winter, which for the UK does not only depend on a North-South gradient but may depend on altitude and closeness to the coast and other large bodies of water, which do not freeze during winter and may aid oocyst survival during winter. In the absence of severe winters in the UK, Ireland and New Zealand, it has been speculated that oocyst may survive in the environment for up to 18 month due to the mild and humid climates in these countries . Climate change predictions of increasing temperatures, drier summers, and wetter winters have lead to the speculation that sporulated oocyst survival is likely to increase, leading to an increase in T. gondii prevalence in intermediate and final hosts . The latter study focused on the effect climate change on T. gondii prevalence in Europe and predicted an increase in human toxoplasmosis cases that will be higher in the South of England with only modest increases in the North of England and Scotland. However, T. gondii prevalence figures in this survey would indicate that sheep in the North of Scotland and the Scottish Islands are either more susceptible hosts for T. gondii, which seems unlikely, since no breed effect was identified. An alternative reason is that there is more environmental contamination by viable oocysts, which may reflect more favourable conditions for oocysts survival or alternatively higher cat densities.
The analysis of the questionnaire has shown that the practice of lambing in paddocks is a potential risk factor leading to increased seropositivity in sheep flocks, which could be explained by the proximity of these paddocks to farm buildings and access by cats, which in turn may lead to elevated levels of oocysts present in the paddocks as a source of infection for the sheep flock. A previous study identified grazing by lambs in close proximity to farms as potential risk factor for T. gondii infection and the authors recommended that lambs should not be grazed near farms to lower exposure to oocysts shed by cats . Paddocks, in this study, are likely to represent a similar risk factor. Variation in lambing practices and cat densities may explain differences in T. gondii flock prevalence figures for farms are geographically very close.
The questionnaire results also highlighted that there is a relatively low (24.7%) uptake of the Toxovax® vaccine, which protects ewes very effectively against T. gondii associated abortion. All farms had sheep that were seropositive indicating that all flocks had exposure to T. gondii and the potential of experiencing abortions induced by this parasite. Analysis of the questionnaire data did not allow identification of reasons for the low vaccine uptake by farmers but it could be speculated that only farmers that had previous abortion problems that were caused by T. gondii used the vaccine. The low uptake of this vaccine may also explain why T. gondii is still the second most frequently detected abortifacient in ovine abortions, according to current VIDA reports .
The high T. gondii seroprevalence in Scottish sheep flocks indicate that a significant number of persistently infected animals will enter the food chain. A recent survey identified that eating undercooked meat is not commonly seen as a risk factor for T. gondii infection by people, only 30% of people asked, were aware of this risk, while the majority recognised cats as risk . In Europe it has been well documented that a major source of T. gondii infection for humans is ingestion of meat or meat products containing T. gondii tissue cysts that have not been inactivated, either by cooking or freezing [16, 17, 22]. Vaccines that would have great potential beneficial to both animal and public health would be those that reduce or stop shedding of oocysts by cats [44, 45] or reduce T. gondii cyst formation in food animal species [11, 46, 47], particular targets would be sheep and pigs [12, 43, 46–48], while cattle seem to pose a lower risk for transmission of T. gondii via infected meat .
The prevalence figures described in this study demonstrate that T. gondii is widely distributed across sheep flocks in Scotland, and that the within-flock prevalence is not the same across Scotland but that it is higher in the North and the Islands and significantly lower in Southern Scotland. An increase in seroprevalence was associated with increasing animal age, indicating that acquired infection in life due to oocyst consumption is a major route of transmission. The seroprevalence data also indicates that contamination of the environment with oocysts is high in Scotland and that sheep meat if undercooked may pose a significant risk of T. gondii transmission to people.
The authors would like to acknowledge the Scottish Government, Rural and Environment Research and Analysis Directorate, for funding this study. Franz Brülisauer, George Gunn and Chris Cousens were supported by Flexible Fund Project No. MRI/843/04. Esther Collantes-Fernández was supported by a postdoctoral fellowship from the Spanish Government (n. 2007-1055).
- Ferguson DJP: Toxoplasma gondii: 1908-2008, homage to Nicolle, Manceaux and Splendore. Mem Inst Oswaldo Cruz. 2009, 104: 133-148. 10.1590/S0074-02762009000200003.View ArticlePubMedGoogle Scholar
- VIDA, Yearly trends 2002-2009 for sheep. [http://vla.defra.gov.uk/reports/docs/rep_vida_sheep02_09.pdf]
- DEFRA 2010 survey for agriculture and horticulture (UK crop areas/livestock numbers 2010). [http://archive.defra.gov.uk/evidence/statistics/foodfarm/landuselivestock/junesurvey/documents/Jun2010-Eng.pdf]
- Blewett DA, Trees AJ: The epidemiology of ovine toxoplasmosis with especial respect to control. Br Vet J. 1987, 143: 128-135.View ArticlePubMedGoogle Scholar
- Hybu Cig Cymru- Meat Promotion Wales: The Current trends in breeding ewe numbers and meat production within the EU. [http://www.hccmpw.org.uk/medialibrary/publications/Sheep%20industry%20in%20the%20EU%5B1%5D.pdf]
- Innes EA, Bartley PM, Buxton D, Katzer F: Ovine toxoplasmosis. Parasitology. 2009, 136: 1887-1894. 10.1017/S0031182009991636.View ArticlePubMedGoogle Scholar
- Dubey JP: History of the discovery of the life cycle of Toxoplasma gondii. Int J Parasitol. 2009, 39: 877-882. 10.1016/j.ijpara.2009.01.005.View ArticlePubMedGoogle Scholar
- Dubey JP, Jones JL: Toxoplasma gondii infection in humans and animals in the United States. Int J Parasitol. 2008, 38: 1257-1278. 10.1016/j.ijpara.2008.03.007.View ArticlePubMedGoogle Scholar
- Buxton D, Rodger SM, Maley SW, Wright SE: Toxoplasmosis: The possibility of vertical transmission. Small Rumin Res. 2006, 62: 43-46. 10.1016/j.smallrumres.2005.07.037.View ArticleGoogle Scholar
- Rodger SM, Maley SW, Wright SE, Mackellar A, Wesley F, Sales J, Buxton D: Ovine toxoplasmosis; the role of endogenous transmission. Vet Rec. 2006, 159: 768-772.PubMedGoogle Scholar
- Innes EA, Bartley PM, Maley S, Katzer F, Buxton D: Veterinary vaccines against Toxoplasma gondii. Mem Inst Oswaldo Cruz. 2009, 104: 246-251.View ArticlePubMedGoogle Scholar
- Dubey JP: Toxoplasmosis in sheep--the last 20 years. Vet Parasitol. 2009, 163: 1-14. 10.1016/j.vetpar.2009.02.026.View ArticlePubMedGoogle Scholar
- O'Connell E, Wilkins MF, Te Punga WA: Toxoplasmosis in sheep. II. The ability of a live vaccine to prevent lamb losses after an intravenous challenge with Toxoplasma gondii. N Z Vet J. 1988, 36: 1-4. 10.1080/00480169.1988.35461.View ArticlePubMedGoogle Scholar
- Buxton D: Toxoplasmosis: the first commercial vaccine. Parasitol Today. 1993, 9: 335-337. 10.1016/0169-4758(93)90236-9.View ArticlePubMedGoogle Scholar
- Buxton D, Thomson KM, Maley S, Wright S, Bos H: Experimental challenge of sheep 18 months after vaccination with a live (S48) Toxoplasma gondii vaccine. Vet Rec. 1993, 133: 310-312. 10.1136/vr.133.13.310.View ArticlePubMedGoogle Scholar
- Tenter AM, Heckeroth AR, Weiss LM: Toxoplasma gondii: from animals to humans. Int J Parasitol. 2000, 30: 1217-1258. 10.1016/S0020-7519(00)00124-7.PubMed CentralView ArticlePubMedGoogle Scholar
- Cook AJC, Gilbert RE, Buffolano W, Zufferey J, Petersen E, Jenum PA, Foulon W, Semprini AE, Dunn DT: Sources of Toxoplasma infection in pregnant women: European multicentre case control study. Br Med J. 2000, 321: 142-147. 10.1136/bmj.321.7254.142.View ArticleGoogle Scholar
- Annual epidemiological report on communicable diseases in Europe 2009. [http://ecdc.europa.eu/en/publications/Publications/0910_SUR_Annual_Epidemiological_Report_on_Communicable_Diseases_in_Europe.pdf]
- Kemmeren JM, Mangen M.-JJ, van Duynhoven YTHP, Havelaar AH: Priority setting of foodborne pathogens. RIVM-rapport 330080001. 2006, [http://www.rivm.nl/bibliotheek/rapporten/330080001.pdf]Google Scholar
- Havelaar AH, Kemmeren JM, Kortbeek LM: Disease burden of congenital toxoplasmosis. Clin Infect Dis. 2007, 44: 1467-1474. 10.1086/517511.View ArticlePubMedGoogle Scholar
- Van der Giessen JWB, van de Giessen AW, Braks MAH: Emerging zoonoses: early warning and surveillance in the Netherlands. RIVM-rapport 330214002. 2010, [http://www.rivm.nl/bibliotheek/rapporten/330214002.pdf]Google Scholar
- Scientific opinion of the panel on Biological Hazards and Animal Health Animal Welfare on a request from the European Food Safety Authority (self mandate) to issue a scientific opinion on the review of the Community Summary Report on Trends and Sources of Zoonoses, Zoonotic Agents and Antimicrobial Resistance in the European Union in 2005. EFSA J. 2007, 600: 1-32. [http://www.efsa.europa.eu/en/scdocs/doc/600.pdf]
- Lewis FI, Brülisauer F, Cousens C, McKendrick IJ, Gunn GJ: Diagnostic accuracy of PCR for Jaagsiekte sheep retrovirus using field data from 125 Scottish sheep flocks. Vet J. 2011, 187: 104-108. 10.1016/j.tvjl.2009.10.024.View ArticlePubMedGoogle Scholar
- Buxton D, Blewett DA, Trees AJ, McColgan C, Finlayson J: Further studies in the use of monensin in the control of experimental ovine toxoplasmosis. J Comp Pathol. 1988, 98: 225-236. 10.1016/0021-9975(88)90021-7.View ArticlePubMedGoogle Scholar
- Wastling JM, Harkins D, Maley S, Innes E, Panton W, Thomson K, Buxton D: Kinetics of the local and systemic antibody response to primary and secondary infection with S48 Toxoplasma gondii in sheep. J Comp Pathol. 1995, 112: 53-62. 10.1016/S0021-9975(05)80089-1.View ArticlePubMedGoogle Scholar
- Efron BTR: Bootstrap methods for standard errors, confidence intervals, and other measures of statistical accuracy. Stat Sci. 1986, 1: 54-77. 10.1214/ss/1177013815.View ArticleGoogle Scholar
- Johnston WS: An investigation into toxoplasmosis as a cause of barrenness in ewes. Vet Rec. 1988, 122: 283-284. 10.1136/vr.122.12.283.View ArticlePubMedGoogle Scholar
- Dubey JP, Kirkbride CA: Enzootic toxoplasmosis in sheep in North-Central United-States. J Parasitol. 1989, 75: 673-676. 10.2307/3283047.View ArticlePubMedGoogle Scholar
- Waldeland H: Toxoplasmosis in sheep. Influence of various factors on the antibody contents. Acta Vet Scand. 1977, 18: 237-247.PubMedGoogle Scholar
- Lundén A, Näsholm A, Uggla A: Long-term study of Toxoplasma gondii infection in a Swedish sheep flock. Acta Vet Scand. 1994, 35: 273-281.PubMedGoogle Scholar
- Morley EK, Williams RH, Hughes JM, Thomasson D, Terry RS, Duncanson P, Smith JE, Hide G: Evidence that primary infection of Charollais sheep with Toxoplasma gondii may not prevent foetal infection and abortion in subsequent lambings. Parasitology. 2008, 135: 169-173.View ArticlePubMedGoogle Scholar
- Walker J, Nokes DJ, Jennings R: Longitudinal study of Toxoplasma seroprevalence in South Yorkshire. Epidemiol Infect. 1992, 108: 99-106. 10.1017/S0950268800049542.PubMed CentralView ArticlePubMedGoogle Scholar
- Nash JQ, Chissel S, Jones J, Warburton F, Verlander NQ: Risk factors for toxoplasmosis in pregnant women in Kent, United Kingdom. Epidemiol Infect. 2005, 133: 475-483. 10.1017/S0950268804003620.PubMed CentralView ArticlePubMedGoogle Scholar
- Allain JP, Palmer CR, Pearson G: Epidemiological study of latent and recent infection by Toxoplasma gondii in pregnant women from a regional population in the UK. J Infect. 1998, 36: 189-196. 10.1016/S0163-4453(98)80012-1.View ArticlePubMedGoogle Scholar
- Caballero-Ortega H, Quiroz-Romero H, Olazarán-Jenkins S, Correa D: Frequency of Toxoplasma gondii infection in sheep from a tropical zone of Mexico and temporal analysis of the humoral response changes. Parasitology. 2008, 135: 897-902.PubMedGoogle Scholar
- Zedda MT, Rolesu S, Pau S, Rosati I, Ledda S, Satta G, Patta C, Masala G: Epidemiological study of Toxoplasma gondii infection in ovine breeding. Zoonoses Public Health. 2010, 57: 7-8.View ArticleGoogle Scholar
- Buxton D, Rodger SM: Toxoplasmosis and neosporosis. Diseases of sheep. Edited by: Aitken ID. 2008, Wiley-Blackwell, Hoboken, 112-118. 4Google Scholar
- Maley SW, Thomson KM, Bos HJ, Buxton D: Serological diagnosis of toxoplasmosis in sheep following vaccination and challenge. Vet Rec. 1997, 140: 558-559. 10.1136/vr.140.21.558.View ArticlePubMedGoogle Scholar
- Halos L, Thébault A, Aubert D, Thomas M, Perret C, Geers R, Alliot A, Escotte-Binet S, Ajzenberg D, Dardé ML, Durand B, Boireau P, Villena I: An innovative survey underlining the significant level of contamination by Toxoplasma gondii of ovine meat consumed in France. Int J Parasitol. 2010, 40: 193-200. 10.1016/j.ijpara.2009.06.009.View ArticlePubMedGoogle Scholar
- Jokelainen P, Näreaho A, Knaapi S, Oksanen A, Rikula U, Sukura A: Toxoplasma gondii in wild cervids and sheep in Finland: north-south gradient in seroprevalence. Vet Parasitol. 2010, 171: 331-336. 10.1016/j.vetpar.2010.04.008.View ArticlePubMedGoogle Scholar
- Meerburg BG, Kijlstra A: Changing climate-changing pathogens: Toxoplasma gondii in North-Western Europe. Parasitol Res. 2009, 105: 17-24.PubMed CentralView ArticlePubMedGoogle Scholar
- Skjerve E, Waldeland H, Nesbakken T, Kapperud G: Risk factors for the presence of antibodies to Toxoplasma gondii in Norwegian slaughter lambs. Prev Vet Med. 1998, 35: 219-227. 10.1016/S0167-5877(98)00057-9.View ArticlePubMedGoogle Scholar
- Pappas G, Roussos N, Falagas ME: Toxoplasmosis snapshots: global status of Toxoplasma gondii seroprevalence and implications for pregnancy and congenital toxoplasmosis. Int J Parasitol. 2009, 39: 1385-1394. 10.1016/j.ijpara.2009.04.003.View ArticlePubMedGoogle Scholar
- Frenkel JK, Smith DD: Immunization of cats against shedding of Toxoplasma oocysts. J Parasitol. 1982, 68: 744-748. 10.2307/3280978.View ArticlePubMedGoogle Scholar
- Mateus-Pinilla NE, Dubey JP, Choromanski L, Weigel RM: A field trial of the effectiveness of a feline Toxoplasma gondii vaccine in reducing T. gondii exposure for swine. J Parasitol. 1999, 85: 855-860.View ArticlePubMedGoogle Scholar
- Falcón J, Freyre A: Toxoplasma gondii: prototype immunization of lambs against formation of muscle and brain cysts. Vet Parasitol. 2009, 166: 15-20. 10.1016/j.vetpar.2009.08.012.View ArticlePubMedGoogle Scholar
- Dubey JP: Toxoplasmosis in pigs--the last 20 years. Vet Parasitol. 2009, 164: 89-103. 10.1016/j.vetpar.2009.05.018.View ArticlePubMedGoogle Scholar
- Innes EA, Bartley PM, Rocchi M, Benavides-Silvan J, Burrells A, Hotchkiss E, Chianini F, Canton G, Katzer F: Developing vaccines to control protozoan parasites in ruminants: Dead or alive?. Vet Parasitol. 2011, 180: 155-163. 10.1016/j.vetpar.2011.05.036.View ArticlePubMedGoogle Scholar
- Esteban-Redondo I, Maley SW, Thomson K, Nicoll S, Wright S, Buxton D, Innes EA: Detection of T. gondii in tissues of sheep and cattle following oral infection. Vet Parasitol. 1999, 86: 155-171. 10.1016/S0304-4017(99)00138-7.View ArticlePubMedGoogle Scholar
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