Taeniasis

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This article is about the infection. For the organism, see Taenia (genus).
Taeniasis
Taenia saginata LifeCycle.gif
The life cycle of Taenia saginata, the beef tapeworm
Classification and external resources
Specialty infectious disease
ICD-10 B68
ICD-9-CM 123.3
DiseasesDB 12875
MedlinePlus 001391
eMedicine ped/2201
MeSH D013622

Taeniasis is a parasitic disease due to infection with tapeworms belonging to the genus Taenia. The two most important human pathogens in the genus are Taenia solium (the pork tapeworm) and Taenia saginata (the beef tapeworm). The third species Taenia asiatica is found only in East Asia. Taeniasis is generally asymptomatic, but severe infection causes weight loss, dizziness, abdominal pain, diarrhea, headaches, nausea, constipation, chronic indigestion, and loss of appetite.

A type of taeniasis called cysticercosis is caused by accidental infection with the eggs of T. solium from contaminated food and water. It is known as the most pathogenic form caused by tapeworms.[1] A specific form of cysticercosis called neurocysticercosis is said to be the most common infection of the central nervous system.

Signs and symptoms[edit]

Taeniasis is generally asymptomatic and is diagnosed when a portion of the worm is passed in the stool. It is not fatal, although cysticercosis can cause epilepsy and neurocystocercosis can be fatal.[2][3][4]

Taenia solium[edit]

Infection by T. solium is normally asymptomatic. Heavy infection is indicated by intestinal irritation, anaemia, and indigestion.

Cysticercosis[edit]

Main article: Cysticercosis

There are accidental consumptions of eggs of T. solium from contaminated vegetables or water. The eggs enter the intestine where they develop into larvae. The larvae enter bloodstream and invade host tissues. This clinical condition, called cysticercosis, is the most frequent and severe disease caused by any tapeworm. It can lead to severe headaches, dizziness, occasional seizures, dementia, hypertension, lesions in the brain, blindness, tumor-like growths, and low eosinophil levels. It is the cause of major neurological problems, such as hydrocephalus, paraplegy, meningitis, convulsions, and even death.[5]

Taenia saginata[edit]

Taenia saginata infection is asymptomatic, but heavy infection causes weight loss, dizziness, abdominal pain, diarrhea, headaches, nausea, constipation, chronic indigestion, and loss of appetite. It can cause antigen reaction that induce allergic reaction.[6] It is an also rare cause of ileus, pancreatitis, cholecystitis, and cholangitis.[7]

Taenia asiatica[edit]

Taenia asiatica is also usually asymptomatic. The only severe case was in a 60-year-old woman at the Mackay Memorial Hospital in Taiwan. Her stomach and intestine were severely damaged with active bleeding from ulcers caused by a single tapeworm.[8][9]

In pigs, the cysticercus can produce cysticercosis. Cysts develop in liver and lungs. (T. saginata does not cause cysticercosis.)[10] Due to its biological similarity to T. solium, which is the major cause of neurocysticercosis, T. asiatica may also cause cysticercosis.[11][12][13]

Transmission[edit]

Taeniasis is contracted after eating undercooked or raw pork and beef that contain the larvae. Cysticercosis occurs after ingestion of contaminated food, water, or soil that contain T. solium eggs.[14][15] Infection is acquired by eating undercooked beef and pork that contain the fluid-filled cysticerci of the tapeworms. The adult worms live in the lumen of the intestine where they cause the symptoms. They acquire nutrients from the intestine, leading to malnutrition of the host. The gravid proglottids, body segments containing fertilised eggs, are released in the faeces of the host. Then they are consumed by an intermediate host such as a cow or pig, where they hatch within the duodenum to become larvae, penetrate through the intestinal wall into nearby blood vessels, and enter the bloodstream. Once they reach organs such as the skeletal muscles, liver or lungs, the larvae then develop into a cyst, which then becomes a fluid-filled cysticercus. These contaminated tissues are then consumed through raw or undercooked meat.[2]

Diagnosis[edit]

Diagnosis of taeniasis is mainly using stool sample, particularly by identifying the eggs. However, this has limitation at the species level because tapeworms basically have similar eggs. Examination of the scolex or the gravid proglottids can resolve the exact species.[16] But body segments are not often available, therefore, laborious histological observation of the uterine branches and PCR detection of ribosomal 5.8S gene are sometimes necessary.[17][18] Ziehl–Neelsen stain is also used for T. saginata and T. solium, in most cases only the former will stain, but the method is not entirely reliable.[19] Loop-mediated isothermal amplification (LAMP) is highly sensitive (~2.5 times that of multiplex PCR), without false positives, for differentiating the taenid species from faecal samples.[20]

To date the most relevant test for T. asiatica is by enzyme-linked immunoelectrotransfer blot (EITB). EITB can effectively identify asiatica from other taenid infections since the serological test indicates an immunoblot band of 21.5 kDa exhibited specifically by T. asiatica.[21] Even though it gives 100% sensitivity, it has not been tested with human sera for cross-reactivity, and it may show a high false positive result.

Prevention[edit]

The fundamental prevention strategy is hygiene and sanitation. Secondary measures include stricter meat-inspection standards, livestock confinement, health education, safe meat preparation, mass drug therapy, and identifying and treating human and pig carriers.[22] Moreover, a high level of sanitation and prevention of human faecal contamination of pig feeds also plays a major role in prevention. Infection can be prevented with proper disposal of human faeces around pigs, cooking meat thoroughly and/or freezing the meat at −10 °C for 5 days. For human cysticercosis, dirty hands are attributed to be the primary cause, and especially common among food handlers.[2]

Proper cooking of meat is an effective prevention. For example, cooking (56 °C for 5 minutes) of beef viscera destroys cysticerci. Refrigeration, freezing (-10 °C for 9 days) or long periods of salting is also lethal to cysticerci. Inspection of beef and proper disposal of human excreta are also important measures.[6]

Treatment[edit]

Oral anti-parasitic drugs such as praziquantel are the treatment of choice. Treatment with praziquantel has been approved by the U.S. Food and Drug Administration and is quite effective against these parasites.[23] Usual treatments are with praziquantel (5–10 mg/kg, single-administration) or niclosamide (adults and children over 6 years: 2 g, single-administration after a light breakfast, followed after 2 hours by a laxative; children aged 2–6 years: 1 g; children under 2 years: 500 mg).[6] Albendazole is also highly effective.[24] Atrabine is quite effective but has adverse effects in humans.[25]

Epidemiology[edit]

Regions[edit]

Taeniasis is predominatly found in Asia, Africa, Latin America, particularly on farms in which pigs are exposed to human excrement. It occurs everywhere though where beef and pork are eaten, even in countries such as the United States, with strict federal sanitation policies. Taenia saginata is relatively common in Africa, some parts of Eastern Europe, the Philippines, and Latin America.[26] It is most prevalent in Sub-Saharan Africa and the Middle East.[27] Taenia asiatica is retricted to East Asia, including Taiwan, Korea, Indonesia, Nepal, Thailand and China.[28][29]

Infection estimates[edit]

The total global infection is estimated to be between 40 and 60 million people.[30] In the US, the incidence of infection is low, but 25% of cattle sold are still infected.[16]

See also[edit]

Tapeworm infection

References[edit]

  1. ^ "Neglected Tropical Diseases". cdc.gov. June 6, 2011. Retrieved 28 November 2014. 
  2. ^ a b c Garcia, Oscar H. Del Brutto, Hector H. (2014). "Taenia solium: Biological Characteristics and Life Cycle". Cysticercosis of the Human Nervous System. (1., 2014 ed.). Berlin: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG. pp. 11–21. ISBN 978-3-642-39021-0. 
  3. ^ "About Taeniasis/cysticercosis". Retrieved 13 March 2014. 
  4. ^ "Signs, symptoms and treatment of taeniasis/cysticercosis". Retrieved 13 March 2014. 
  5. ^ Flisser, A.; Avila G; Maravilla P; Mendlovic F; León-Cabrera S; Cruz-Rivera M; Garza A; Gómez B; Aguilar L; Terán N; Velasco S; Benítez M; Jimenez-Gonzalez DE (2010). "Taenia solium: current understanding of laboratory animal models of taeniosis". Parasitology 137 (03): 347–57. doi:10.1017/S0031182010000272. PMID 20188011. 
  6. ^ a b c "Taeniasis/Cysticercosis". WHO Fact sheet N°376. World Health Organization. 2013. Retrieved 7 February 2014. 
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  8. ^ Liao, Wen-Shen; Bair, Ming Jong (2007). "Taenia in the Gastrointestinal Tract". New England Journal of Medicine 357 (10): 1028–1028. doi:10.1056/NEJMicm067761. PMID 17804847. 
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  10. ^ Galán-Puchades, M.T.; Fuentes, M.V. (2008). "Taenia asiatica and pig cysticercosis". Veterinary Parasitology 157 (1-2): 160–161. doi:10.1016/j.vetpar.2008.07.008. PMID 18752896. 
  11. ^ Galán-Puchades, M. Teresa; Fuentes, Mario V. (2013). "Taenia asiatica : the most neglected human Taenia and the possibility of cysticercosis". The Korean Journal of Parasitology 51 (1): 51–4. doi:10.3347/kjp.2013.51.1.51. PMC 3587749. PMID 23467406. 
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  17. ^ González LM, Montero E, Harrison LJ, Parkhouse RM, Garate T. (2000). "Differential diagnosis of Taenia saginata and Taenia solium infection by PCR.". J Clin Microbiol. 38 (2): 737–744. PMC 86191. PMID 10655377. 
  18. ^ Zarlenga DS. (1991). "The differentiation of a newly described Asian taeniid from Taenia saginata using enzymatically amplified non-transcribed ribosomal DNA repeat sequences.". Southeast Asian J Trop Med Public Health. 22 (suppl): 251–255. PMID 1822899. 
  19. ^ Juan A. Jimenez, Silvia Rodriguez, Luz M. Moyano, Yesenia Castillo, Héctor H. García (2010). "Differentiating Taenia eggs found in human stools - Does Ziehl Neelsen staining help?". Tropical Medicine & International Health 15 (9): 1077–1081. doi:10.1111/j.1365-3156.2010.02579.x. 
  20. ^ Nkouawa, A; Sako, Y; Li, T; Chen, X; Wandra, T; Swastika, IK; Nakao, M; Yanagida, T; Nakaya, K; Qiu, D; Ito, A (2010). "Evaluation of a loop-mediated isothermal amplification method using fecal specimens for differential detection of Taenia species from humans". Journal of Clinical Microbiology 48 (9): 3350–2. doi:10.1128/JCM.00697-10. PMC 2937673. PMID 20631114. 
  21. ^ Jeon, Hyeong-Kyu; Eom, Keeseon S. (2009). "Immunoblot Patterns of Taenia asiatica Taeniasis". The Korean Journal of Parasitology 47 (1): 73–7. doi:10.3347/kjp.2009.47.1.73. PMC 2655338. PMID 19290097. 
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  23. ^ http://www.dpd.cdc.gov/DPDx/
  24. ^ Lopes, Welber Daniel Zanetti; Cruz, Breno Cayeiro; Soares, Vando Edésio; Nunes, Jorge Luis N.; Teixeira, Weslen Fabricio Pires; Maciel, Willian Giquelin; Buzzulini, Carolina; Pereira, João Carlos Melo; Felippelli, Gustavo; Soccol, Vanette Thomaz; de Oliveira, Gilson Pereira; da Costa, Alvimar José (2014). "Historic of therapeutic efficacy of albendazol sulphoxide administered in different routes, dosages and treatment schemes, against Taenia saginata cysticercus in cattle experimentally infected". Experimental Parasitology 137 (1): 14–20. doi:10.1016/j.exppara.2013.11.007. PMID 24309372. 
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  29. ^ Ale, Anita; Victor, Bjorn; Praet, Nicolas; Gabriël, Sarah; Speybroeck, Niko; Dorny, Pierre; Devleesschauwer, Brecht (2014). "Epidemiology and genetic diversity of Taenia asiatica: a systematic review". Parasites & Vectors 7 (1): 45. doi:10.1186/1756-3305-7-45. PMC 3900737. PMID 24450957. 
  30. ^ Eckert, J. (2005). "Helminths". In Kayser, F.H., Bienz, K.A., Eckert, J., Zinkernagel, R.M. Medical Microbiology. Stuttgart: Thieme. pp. 560–562. ISBN 9781588902450.