Effects of high temperature and disinfectants on the viability of Sarcocystis neurona sporocysts.
Abstract: The effect of moist heat and several disinfectants on Sarcocystis neurona sporocysts was investigated. Sporocysts (4 million) were suspended in water and heated to 50, 55, 60, 65, and 70 C for various times and were then bioassayed in interferon gamma gene knockout (KO) mice. Sporocysts heated to 50 C for 60 min and 55 C for 5 min were infective to KO mice, whereas sporocysts heated to 55 C for 15 min and 60 C or more for 1 min were rendered noninfective to mice. Treatment with bleach (10, 20, and 100%), 2% chlorhexidine, 1% betadine, 5% o-benzyl-p-chlorophenol, 12.56% phenol, 6% benzyl ammonium chloride, and 10% formalin was not effective in killing sporocysts. Treatment with undiluted ammonium hydroxide (29.5% ammonia) for 1 hr killed sporocysts, but treatment with a 10-fold dilution (2.95% ammonia) for 6 hr did not kill sporocysts. These data indicate that heat treatment is the most effective means of killing S. neurona sporocysts in the horse feed or in the environment.
Publication Date: 2003-01-23 PubMed ID: 12537123DOI: 10.1645/0022-3395(2002)088[1252:EOHTAD]2.0.CO;2Google Scholar: Lookup
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Summary
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This research investigates the effects of high temperature and several disinfectants on a dangerous parasite called Sarcocystis neurona. The findings suggest that heat treatment is the most effective method of killing this parasite in horse feed or the environment.
Understanding Sarcocystis neurona
- Sarcocystis neurona is a protozoan parasite that can infect horses and other animals, causing a severe neurological disease known as equine protozoal myeloencephalitis (EPM).
- Poorly understood and difficult to control, researchers are keen to devise methods to reduce the threat of S. neurona in the environment, particularly where horses are kept.
Research Methodology and Findings
- The scientists exposed Sarcocystis neurona sporocysts (the infective stage of the parasite) to various temperatures, ranging from 50 – 70 degrees Celsius for different time durations. They then tested the viability of these sporocysts by bioassaying them in special interferon gamma gene knockout (KO) mice. This type of mice is deficient in specific immune responses and is commonly used in such bioassays.
- They found that sporocysts heated to 50 C for 60 min and 55 C for 5 min were still infective to KO mice. However, sporocysts exposed to temperatures of 55 C for 15 min and 60 C or above for at least 1 min lost their ability to infect mice, indicating that they had been rendered nonviable.
Disinfectant Evaluation
- Next, the researchers exposed the sporocysts to a variety of disinfectants including bleach, chlorhexidine, betadine, o-benzyl-p-chlorophenol, phenol, benzyl ammonium chloride, formalin, and ammonium hydroxide.
- Surprisingly, most did not kill the sporocysts. Undiluted ammonium hydroxide (29.5% ammonia) was the only exception, killing off the sporocysts after 1 hour of exposure. In contrast, a 10x dilution of this solution (2.95% ammonia) failed to kill the sporocysts after 6 hours of exposure.
Conclusion
- These findings demonstrate that high temperature (55 C for 15 min or 60 C and above for at least 1 min) is effective in killing S. neurona sporocysts.
- Of the tested disinfectants, only undiluted ammonium hydroxide proved effective. Consequently, heat appears to be the most promising method for reducing the prevalence of this parasite in horse feed or the environment.
Cite This Article
APA
Dubey JP, Saville WJ, Sreekumar C, Shen SK, Lindsay OS, Pena HF, Vianna MC, Gennari SM, Reed SM.
(2003).
Effects of high temperature and disinfectants on the viability of Sarcocystis neurona sporocysts.
J Parasitol, 88(6), 1252-1254.
https://doi.org/10.1645/0022-3395(2002)088[1252:EOHTAD]2.0.CO;2 Publication
Researcher Affiliations
- Parasite Biology, Epidemiology and Systematics Laboratory, Building 1001, Animal and Natural Resources Institute, Agricultural Research Service, United States Department of Agriculture, Beltsville, Maryland 20705-2350, USA. jdubey@anri.barc.usda.gov
MeSH Terms
- Animal Feed / parasitology
- Animals
- Disinfectants / pharmacology
- Disinfection / methods
- Food Contamination / prevention & control
- Horse Diseases / prevention & control
- Horses
- Hot Temperature
- Mice
- Mice, Knockout
- Opossums
- Raccoons
- Sarcocystis / drug effects
- Sarcocystis / physiology
- Sarcocystosis / prevention & control
- Sarcocystosis / veterinary
Citations
This article has been cited 5 times.- Honda M, Sawaya M, Taira K, Yamazaki A, Kamata Y, Shimizu H, Kobayashi N, Sakata R, Asakura H, Sugita-Konishi Y. Effects of temperature, pH and curing on the viability of Sarcocystis, a Japanese sika deer (Cervus Nippon centralis) parasite, and the inactivation of their diarrheal toxin.. J Vet Med Sci 2018 Aug 30;80(8):1337-1344.
- Verma SK, Lindsay DS, Grigg ME, Dubey JP. Isolation, Culture and Cryopreservation of Sarcocystis species.. Curr Protoc Microbiol 2017 May 16;45:20D.1.1-20D.1.27.
- Dubey JP, Howe DK, Furr M, Saville WJ, Marsh AE, Reed SM, Grigg ME. An update on Sarcocystis neurona infections in animals and equine protozoal myeloencephalitis (EPM).. Vet Parasitol 2015 Apr 15;209(1-2):1-42.
- Fayer R, Esposito DH, Dubey JP. Human infections with Sarcocystis species.. Clin Microbiol Rev 2015 Apr;28(2):295-311.
- Rejmanek D, Miller MA, Grigg ME, Crosbie PR, Conrad PA. Molecular characterization of Sarcocystis neurona strains from opossums (Didelphis virginiana) and intermediate hosts from Central California.. Vet Parasitol 2010 May 28;170(1-2):20-9.
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