Literature DB >> 24433262

From stillness to motion: 80 years after the first description of Taenia solium oncosphere hatching.

Fela Mendlovic, Adriana Garza-Rodríguez, Joaquin Carrillo-Farga, Fernando González-Domínguez, Pablo Maravilla, Ana Flisser1.   

Abstract

BACKGROUND: Human neurocysticercosis (NCC) is a considered public health problem in many underdeveloped and developing countries. Because of the enormous increase in international tourism and migration, NCC nowadays is also found in some developed countries. Our group was the first to demonstrate that tapeworm carriers in the household are the main risk factor for acquiring cysticercosis in humans and pigs, since the disease results from the ingestion of microscopic tapeworm eggs.
FINDINGS: We had the opportunity to film the liberation of the embryo from the oncospheral membrane after the hatching of the egg, which is the activation process required for intestinal wall invasion by the onchosphere. Yoshino (J Formosa Med Ass 32:139-142, 1933) described with great detail in diagrams and photographs this process eighty years ago after he infected himself with three living cysticerci in order to study the life cycle of Taenia solium. Other authors further described this process. Nevertheless it has never been filmed before. The purpose of this paper is to shift from stillness to motion since we can now show for the first time a movie of an activated oncosphere and its release from the oncospheral membrane.
CONCLUSION: Oncospheral activation is the requisite for T. solium embryos to invade the intestinal mucosa and develop into cysticerci. This process has been amply described but here it is shown for the first time in motion; thus it may be of interest for readers of the journal and useful for educational purposes towards the control of NCC.

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Year:  2014        PMID: 24433262      PMCID: PMC3896852          DOI: 10.1186/1756-3305-7-12

Source DB:  PubMed          Journal:  Parasit Vectors        ISSN: 1756-3305            Impact factor:   3.876


Findings

The life cycle of T. solium includes the human being as the definitive host that harbors the intestinal tapeworm and the pig as the intermediate host in which the larval stage or cysticercus develops. Definitive hosts acquire the disease after ingesting undercooked infected pork meat, while cysticercosis is produced after swine consume infected human feces that contain tapeworm gravid proglottids full of eggs. In addition, accidental ingestion of these eggs can cause human neurocysticercosis (NCC), a public health problem in many developing countries and an emerging infectious disease in some developed ones [1-3]. NCC is a neglected tropical disease that is underfinanced and caused 25,341 disability adjusted life years (DALYs) in Mexico during 2005 due to epilepsy (90%) and severe chronic headaches (10%) associated to NCC [4]. Improvements in research, diagnosis, treatment and control have been achieved in Mexico, suggesting that NCC may no longer be a public health problem in this country [5]. This approach should be taken into consideration for the control of zoonoses and marginalized infectious diseases of poverty recently reviewed [6]. Our group was the first to demonstrate that patients with NCC are found mainly where a tapeworm carrier is part of the household [7], thus the egg is one of the main targets for the control of NCC. The morphology of tapeworm eggs has been described and illustrated in photographs and diagrams as early as 1933 by Yoshino [8], and afterwards by other authors [9-13]. Eggs measure between 26 and 34 μm and have a radial appearance because of the embryophore that surrounds and protects the oncosphere that is covered by the oncospheral membrane. After ingesting eggs, hexacanths must be released from their envelopes and penetrate the intestinal mucosa. Yoshino described the conditions for the hatching and activation of T. solium eggs after he infected himself with three live cysticerci to study the life cycle of Taenia solium. Disaggregation of the embryophore is known as hatching, while liberation from the oncospheral membrane is the activation process that take place in the presence of bile salts. Now, 80 years later, we had the opportunity to film the liberation of the hexacanth from the oncospheral membrane (film enclosed). By shifting from stillness to motion we show, for the first time, a movie filmed under an optic microscope (AX70 Olympus microscope with a Carl Zeiss camera attachment) of an oncosphere in the process of activation, as it liberates itself from the oncospheral membrane. Eggs were treated as described by Kyngdon et al.[13]. At the beginning of the film the oncosphere is seen after hatching, still surrounded by the oncospheral membrane, body movements are slow and increase in frequency as time elapses. Hooks also start moving and the structure of the hook described by Yoshino [8], as a stem with a terminal sickle-shaped portion, can be seen (Additional file 1: Movie S1 and Figure  1A and B). One minute after the beginning of the movie, a hook in the center of the embryo is seen seemingly scratching the inside of the oncospheral membrane. The oncosphere contracts and expands escaping from the membrane, probably through a hole, since a constriction around the embryo is evident. The hexacanth emerges towards the left side of the movie leaving the membrane behind (Additional file 1: Movie S1 and Figure  1C). The overall process of filming was speeded-up 5 times.
Figure 1

Activation process of a oncosphere. At the beginning of the activation process, an oncosphere completely surrounded by the oncospheral membrane is seen (A). With time, the oncospheral membrane is detached and seen above and below the oncosphere (B). At the end, the hexacanth is seen almost completely out of the oncospheral membrane, which remains, at the right side (C). Hooks are evident in (A) and (B).

Activation process of a oncosphere. At the beginning of the activation process, an oncosphere completely surrounded by the oncospheral membrane is seen (A). With time, the oncospheral membrane is detached and seen above and below the oncosphere (B). At the end, the hexacanth is seen almost completely out of the oncospheral membrane, which remains, at the right side (C). Hooks are evident in (A) and (B). Oncospheral activation is the requisite for T. solium embryos to invade the intestinal mucosa and develop into cysticerci. This process has been amply described but here it is shown for the first time in motion, thus it may be of interest for readers of the journal and useful for educational purposes towards the control of NCC.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

AGR and PM obtained and activated onchospheres. JCF, FGD, FM and AF participated in the filming process. FM and AF wrote the manuscript. All authors read and approved the final version of the manuscript.

Additional file 1: Movie S1

The movie was filmed under an optic microscope and speeded-up 5 times. It shows the activation of a Taenia solium oncosphere. Click here for file
  8 in total

1.  In vitro oncosphere-killing assays to determine immunity to the larvae of Taenia pisiformis, Taenia ovis, Taenia saginata, and Taenia solium.

Authors:  Craig T Kyngdon; Charles G Gauci; Rick A Rolfe; Jeanette C Velásquez Guzmán; Marilú J Farfán Salazar; Manuela R Verástegui Pimentel; Armando E Gonzalez; Hector H Garcia; Robert H Gilmanl; Richard A Strugnell; Marshall W Lightowlers
Journal:  J Parasitol       Date:  2006-04       Impact factor: 1.276

2.  A comparative study on egg hatching methods and oncosphere viability determination for Taenia solium eggs.

Authors:  I C Wang; Y X Ma; C H Kuo; P C Fan
Journal:  Int J Parasitol       Date:  1997-11       Impact factor: 3.981

3.  Taenia solium taeniasis and cysticercosis in a Mexican village.

Authors:  E J Sarti-Gutierrez; P M Schantz; R Lara-Aguilera; H Gomez Dandoy; A Flisser
Journal:  Trop Med Parasitol       Date:  1988-09

4.  Neurocysticercosis may no longer be a public health problem in Mexico.

Authors:  Ana Flisser; Dolores Correa
Journal:  PLoS Negl Trop Dis       Date:  2010-12-21

5.  Zoonoses and marginalised infectious diseases of poverty: where do we stand?

Authors:  David Molyneux; Zuhair Hallaj; Gerald T Keusch; Donald P McManus; Helena Ngowi; Sarah Cleaveland; Pilar Ramos-Jimenez; Eduardo Gotuzzo; Kamal Kar; Ana Sanchez; Amadou Garba; Helene Carabin; Amal Bassili; Claire L Chaignat; Francois-Xavier Meslin; Hind M Abushama; Arve L Willingham; Deborah Kioy
Journal:  Parasit Vectors       Date:  2011-06-14       Impact factor: 3.876

6.  Estimating the non-monetary burden of neurocysticercosis in Mexico.

Authors:  Rachana Bhattarai; Christine M Budke; Hélène Carabin; Jefferson V Proaño; Jose Flores-Rivera; Teresa Corona; Renata Ivanek; Karen F Snowden; Ana Flisser
Journal:  PLoS Negl Trop Dis       Date:  2012-02-21

Review 7.  Neurocysticercosis: neglected but not forgotten.

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Journal:  PLoS Negl Trop Dis       Date:  2012-05-29

Review 8.  Taeniasis and cysticercosis due to Taenia solium in Japan.

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Journal:  Parasit Vectors       Date:  2012-01-17       Impact factor: 3.876

  8 in total
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1.  Freiburg neuropathology case conference: multiple small ring-enhancing lesions in a 75-year-old patient.

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Journal:  Clin Neuroradiol       Date:  2014-05-14       Impact factor: 3.649

Review 2.  Taenia solium Cysticercosis and Its Impact in Neurological Disease.

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Journal:  Clin Microbiol Rev       Date:  2020-05-27       Impact factor: 26.132

  2 in total

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