Print ISSN: 2476-535X, Online ISSN: 2717-2910

Document Type : Short Commu‌nication

Authors

1 Department of pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad

2 The Health Department , Veterinary Head Office of Khorasan Razavi Province

3 Department of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran

4 Food Hygiene Department, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad

Abstract

C
Cysticercus bovis, the larval stage of the beef tapeworm Taenia saginata, occurs mainly in young calves via ingestion of the worms’ eggs excreted in the feces of infected persons. The most heavily infected muscles include heart, masseters, shoulder, and tongue. In February 2021, during abattoir meat inspection at Mashhad abattoir, Cysticercus bovis cysts ranging from 0.5 to 1 cm were detected in striated muscles of 22 / 33 (66.66%) of Holstein bulls of 1-2 years old originating from one farm that located in Qom province. This is the first report of bovine cysticercosis in slaughtered cattle in Mashhad abattoir. However, this case report shows zoonotic importance of C.bovis infection and meat inspection. Improving personal and environmental hygiene are the most important measures to decrease bovine cysticercosis.

Keywords

Main Subjects

Introduction

Cysticercus bovis, as T. saginata larve, is formed in the striated muscles of cattle as intermediated host after ingestion of T. saginata eggs. The size of C. bovis with invaginated scolex reaches 5-10 mm in diameter. It remains alive and active for one year, and then it gradually becomes calcified (Arfaa, 1989; Eslami, 1997). Human is the definitive host and is infected with adult T. saginata after ingestion of infected raw or undercooked meat to C. bovis. The scolex of cysticercus is released and attached to the small intestine mucosa of human. It grows and changes to T. saginata, which reaches up to ten meters in the small intestine. The T. saginata infection causes diarrhea, abdominal pain, weight loss, chronic hunger, sensitivity, nausea, and dizziness in humans (Afraa, 1989). Routine meat inspection is generally the only diagnostic tool that is used for cysticercus bovis infection (Eslami, 1990). In Iran, the frequency of C. bovis infection was detected at 0.3 - 7.7% in Fars province (Oryan et al.,1995; Oryan et al., 2012), 3% of cattle in Ardabil (Garadaghi et al., 2012); 0.95% of cattle in Isfahan province (Hosseinzadeh et al., 2013), 0.03-0.07% of cattle in Kermansh province (Faraji et al., 2015; Hashemnia et al., 2015), and 1.7% of cattle in Tabriz province (Mirzaei et al., 2016). Here in, we report the occurrence of C. bovis infection in slaughtered cattle in Mashhad abettor.

 

Material and Methods

In February 2021, a batch of Holstein bulls, approximately 1-2 years old, was slaughtered in Mashhad slaughterhouse. During post-mortem examination, many carcasses were suspected to be infected with C. bovis. Many cysts with a diameter of 0.5 to 1 cm were found in the heart and the surface and depth of skeletal muscles in many care cases. Muscle samples of each carcass were submitted to the laboratory for parasitology examination. The viable cysts of muscles were dissected from muscle tissue using forceps and scissors and transferred into a petri dish containing saline solution. After slitting the cysts with a scalpel, the contents of the cysts were carefully observed under the stereo microscope. The scolex of each sample was placed in a drop of lactophenol on the slide and covered with a coverslip. The slide was incubated at 37 °C for 60-90 minutes. The cleared temporary mounts were examined under a light microscope.

Results

Of the 33 slaughtered cattle, 22 (66.6%) were suspected to be infected with cysticerci. Gross examination of the muscle samples showed the presence of white-colored cysts at 5-10 mm diameter on the surface and depth of the muscles (Figures 1 and 2). Some of the cysts were degenerated or mineralized. Cysts of all muscle samples were microscopically identified as C. bovis based on having a scolex with four suckers and a short neck without rostellar hooks (Figures 3 and 4).

Discussion

Despite post- mortem examination of carcasses at slaughtered houses, bovine cysticercosis remains an important zoonotic disease in Iran (Moazeni et al., 2019). In this report, we found that 66.6% (22/33) of bull carcasses were infected with C.bovis. In Iran, the range of bovine cysticercosis prevalence was usually reported to be between 0.5 to 7.7% in cattle (Moazeni et al., 2019). However, the highest prevalence of bovine cysticercosis was reported in slaughtered cattle in Caspian area (52%; Thornton, 1952) and 23% in slaughtered cattle in Arak area (Gholami et al., 2020). Two epidemiological patterns have been reported in developing and developed countries (Taylor et al., 2007). In developed countries such as Europe, North America, Australia, and New Zealand, the prevalence of cysticercosis is low as the standard sanitation is high and meat is carefully inspected. The prevalence of bovine cysticercosis was below 6.2% in many European countries (Laranjo-González et al., 2016). Despite the remarkable progress made in the control of bovine cysticercosis in these countries, several outbreaks were reported with an infection rate of 42.8-50.9% in Canada (McAninch, 1974; Bundza et al., 1988), 58% in Australia (Jenkins et al., 2013), and 65% in New Zealand (McFadden et al., 2012). The occurrence of cysticercosis storms can be associated with to use of human sewage on pasture as a fertilizer in the form of sludge and the use of migrant labor from a country with a high prevalence of infection. In contrast to the epidemiology of developing countries, cattle of any age are susceptible to infection (Taylor et al., 2007). In developing countries including many parts of Africa, Asia, and Latin America, cattle are reared on an extensive scale, whereas human sanitation is poorly developed and the incidence of human infection with T. saginata is high and calves are usually infected in early life (Taylor et al., 2007). The moderate prevalence of C. bovis infection has been reported in Latin America (0.1–19%; Braae et al., 2018) and in the Middle East and North Africa (0.2-20%; Saratsis et al., 2020). The high prevalence of C. bovis ranged has been reported in East, South and South East Asia (i.e., 0.76–46.7%; Eichenberger et al., 2020) and in South and East Africa (i.e., 6.1-34.9%; Dermauw et al., 2018). In the present study, the breeding place of the slaughtered cattle was not determined, but they were shipped to Mashhad slaughterhouse from Qom province. Recently, a similar outbreak with a high prevalence has been reported in slaughtered cattle in Arak area, Markazi province (Gholami et al., 2020), where T. saginata eggs were detected in the fecal sample of a former worker, who was working during the outbreak of bovine cysticercosis.

Conclusion

Despite post- mortem examination of carcasses at slaughtered houses, bovine cysticercosis remains an important zoonotic disease in Iran. It seems that infected human feces are also as a source of this outbreak. However, the health of the workers should be approved by the health departments through clinical and paraclinical examinations. In addition, basic health training about personal hygiene and proper disposal of excreta should be given to the farm workers.

Acknowledgments

We sincerely thank Mr. Hamid Eshrati for his help with the research work.

Conflict of interest statement

The authors declare no conflict of interest.

Ethical approval

Not applicable.

 

 

References
Arfaa F. 1989, Medical helminthology, Vol.2. Daneshpajouh publication, Mashhad,104-110.
Braae U.C., Thomas L.F., Robertson L.J., Dermauw V., Dorny P., Willingham A.L., Saratsis A. & Devleesschauwer B. Epidemiology of Taenia saginata taeniosis/cysticercosis: a systematic review of the distribution in the Americas. Parasites & vectors, 2018 1, 1(1):1-2.
Bundza A., Finley G.G. & Easton K.L. An outbreak of cysticercosis in feedlot cattle. The Canadian Veterinary Journal, 1988, 29(12), 993
Dermauw V., Dorny P., Braae U.C., Devleesschauwer B., Robertson L.J., Saratsis A. & Thomas L.F. Epidemiology of Taenia saginata taeniosis/cysticercosis: a systematic review of the distribution in southern and eastern Africa. Parasites & vectors, 2018, 11(1), 1-2.
Eichenberger R.M., Thomas L.F., Gabriël S., Bobić B., Devleesschauwer B., Robertson L.J., Saratsis A., Torgerson P.R., Braae U.C, Dermauw V. & Dorny P. Epidemiology of Taenia saginata taeniosis/cysticercosis: a systematic review of the distribution in East, Southeast and South Asia. Parasites & Vectors, 2020, 13(1), 1-11.
Eslami A. 1997, Veterinary Helminthology: Cestoda, Vol.2, 2nd edition, Tehran University Publication, 78-100.
Faraji R., Nazari N. & Negahdary M. Prevalence of cysticercus of Taenia saginata in cattle slaughtered. International Journal of Research in Medical Sciences, 2015, 3(7), 1662-5.
Gholami N., Mosayebi M., Dehghan Rahim Abadi P., Rasmi Atigh H., Sedaghat R., Naji Zadeh M.H. & Farahani M. Bovine cysticercosis in feedlot cattle in central region of Iran. Journal of Parasitic Diseases, 2020, 44(1), 25-30.
Hosseinzadeh S., Setayesh A., Shekarforoush S.S. & Fariman S.H. An epidemiological survey on the determination of Taenia saginata cysticercosis in Iran, using a PCR assay. Veterinary Record, 2013, 172(17), 451.
Jahed Khaniki G.R., Raei M., Kia E.B., Motevalli Haghi A., Selseleh M. Prevalence of bovine cysticercosis in slaughtered cattle in Iran. Tropical Animal Health and Production, 2010; 42(2):141-3
Jenkins D.J., Brown G.K. & Traub R.J. ‘Cysticercosis storm’in feedlot cattle in north‐west New South Wales. Australian Veterinary Journal, 2013, 91(3), 89-93.
Oryan A., Goorgipour, S., Moazeni, M, & Shirian S. Abattoir prevalence, organ distribution, public health and economic importance of major metacestodes in sheep, goats and cattle in Fars, southern Iran. Tropical Biomedicine, 2012, 29(3), 349–359
Oryan A., Moghaddar N. & Gaur S.N. Taenia saginata cysticercosis in cattle with special reference to its prevalence, pathogenesis and economic implications in Fars Province of Iran. Veterinary Parasitology, 1995, 57(4), 319-27.
Laranjo-González M., Devleesschauwer B., Gabriël S., Dorny P. & Allepuz A. Epidemiology, impact and control of bovine cysticercosis in Europe: a systematic review. Parasites & Vectors, 2016, 9(1), 1-2.
McAninch N.H. An outbreak of cysticercosis in feedlot cattle. The Canadian Veterinary Journal, 1974, 15(4), 120.
McFadden A.M., Heath D.D., Morley C.M. & Dorny P. Investigation of an outbreak of Taenia saginata cysts (cysticercus bovis) in dairy cattle from two farms. Veterinary Parasitology, 2011, 176(2-3), 177-84.
McCool C.J. Distribution of cysticercus bovis in lightly infected young cattle. Australian Veterinary Journal, 1979, 55(5), 214-6.
Mirzaei M., Nematolahi A., Ashrafihelan J., Rezaei H. Prevalence of infection with the larval form of the cestode parasite Taenia saginata in cattle in northwest Iran and its zoonotic importance. Türkiye Parazitolojii Dergisi, 2016, 40(4), 190-3.
Moazeni M., Khamesipour F., Anyona D.N. & Dida G.O. Epidemiology of taeniosis, cysticercosis and trichinellosis in Iran: A systematic review. Zoonoses and Public Health, 2019, 66(1), 140-54.
Saratsis A., Sotiraki S., Braae U.C., Devleesschauwer B., Dermauw V., Eichenberger R.M., Thomas L.F., Bobić B., Dorny P., Gabriël S. & Robertson L.J. Epidemiology of Taenia saginata taeniosis/cysticercosis: a systematic review of the distribution in the Middle East and North Africa. Parasites & Vectors, 2019, 12(1), 1-5.
Thornton H. The incidence of cysticercus bovis in Persia. Veterinary Record, 1957, 69(5), 102
Taylor M.A., Coop R.L. & Wall R.L. 2007, Veterinary Parasitology. Blackwell publishing, Oxford, UK, 121-123.