Alterations in Taenia crassiceps cysticerci cytoskeleton induced by nitazoxanide and flubendazole

Acta Tropica ◽  
2021 ◽  
pp. 106027
Author(s):  
Nayana Ferreira de Lima ◽  
Guaraciara de Andrade Picanço ◽  
Diana Gabriela Ríos Valencia ◽  
Edgar Oliver López Villegas ◽  
María Del Rosário Espinoza Mellado ◽  
...  
Keyword(s):  
2019 ◽  
Vol 15 (01) ◽  
pp. 83-84
Author(s):  
B J Thakre ◽  
Joice P Joseph ◽  
Binod Kumar ◽  
Nilima Brahmbhatt ◽  
Krishna Gamit

Taenia spp. are long, segmented, parasitic tapeworms and are relatively uncommon in canine gastrointestinal diseases compared to other tapeworms like Dipylidium caninum. These parasites have an indirect life cycle, cycling between definitive and intermediate hosts. Dogs act as definitive hosts of different species of Taenia including Taenia multiceps, Taenia serialis, Taenia crassiceps, Taenia hydatigena, Taenia pisiformis, etc. Taenia multiceps is of greatest zoonotic relevance in human. In the definitive host, it causes only mild infection. Larvae are more likely to cause disease than adult tapeworms. Taeniasis in pets should be cautiously handled because of its zoonotic importance. This communication reports a case of 3 months old pup suffering from Taenia infection that was successfully managed with a combination of praziquantel and fenbendazole.


1962 ◽  
Vol 40 (6) ◽  
pp. 969-990 ◽  
Author(s):  
Reino S. Freeman

Taenia crassiceps was common in Vulpes fulva examined from southern Ontario. Metacestodes occurred naturally in Microtus pennsylvanicus, Marmota monax, Tamias striatus, and Ondatra zibethicus, and Peromyscus maniculatus, Tamiasciurus hudsonicus, and Sciurus carolinensis were infected experimentally; all rodents are new host records. Cysticerci developed into adults in dogs or foxes within 5 to 6 weeks; five coyote pups resisted infection. Development of the metacestode was followed mainly in white mice. Infections were most common subcutaneously, but also occurred in both body cavities. Mice approximately 4 weeks of age were most susceptible. Asexual reproduction occurred by exogenous, and rarely endogenous, budding from the abscolex pole beginning approximately 3 weeks after infection. Metacestodes in various stages of development were injected into mice subcutaneously, intrapleurally, but mainly intraperitoneally. Subsequent development and reproduction were similar to that following infection with eggs. Apparently all metacestodes are capable of budding. The initial rate of reproduction was higher subcutaneously and intrapleurally than intraperitoneally, but within approximately 100 days the rate became higher and continued higher intraperitoneally than elsewhere. Reproduction never reached a logarithmic rate. Metacestodes inoculated serially up to 21 times at 50-day intervals increased greatly in size and continued budding. Four other series were maintained by serial subinoculation at 50-day intervals through 23 generations without a significant change in the rate of reproduction.


1999 ◽  
Vol 77 (9) ◽  
pp. 1367-1372 ◽  
Author(s):  
I Corbin ◽  
B J Blackburn ◽  
M Novak

Carbon-13-decoupled proton spin-echo nuclear magnetic resonance (NMR) spectroscopy, with and without 13C population inversion, was used to study carbon flow between the host and the parasite in the mouse - Taenia crassiceps system. This NMR analysis revealed that 2 h after intraduodenal injection of [3-13C]alanine, livers from both uninfected mice and those infected with cysticerci of T. crassiceps contained 13C label in glycogen, glucose, succinate, glutamate, alanine, and lactate. Livers of infected animals had a lower percentage of 13C in alanine, indicating increased utilization of the substrate. In addition, infected mice had a lower concentration of total hepatic glucose and glutamate. The data are consistent with an increased rate of gluconeogenesis in the liver of infected animals. Cysticerci possessed 13C label in glucose, acetate, alanine, and lactate. Since these metacestodes are unable to make glucose de novo from pyruvate, labelled glucose found in cysticerci had to be newly synthesized via the host gluconeogenic pathway and then siphoned off by the parasite.


2020 ◽  
Vol 14 (12) ◽  
pp. e0008966
Author(s):  
Anja de Lange ◽  
Ulrich Fabien Prodjinotho ◽  
Hayley Tomes ◽  
Jana Hagen ◽  
Brittany-Amber Jacobs ◽  
...  

Larvae of the cestodes Taenia solium and Taenia crassiceps infect the central nervous system of humans. Taenia solium larvae in the brain cause neurocysticercosis, the leading cause of adult-acquired epilepsy worldwide. Relatively little is understood about how cestode-derived products modulate host neural and immune signalling. Acetylcholinesterases, a class of enzyme that breaks down acetylcholine, are produced by a host of parasitic worms to aid their survival in the host. Acetylcholine is an important signalling molecule in both the human nervous and immune systems, with powerful modulatory effects on the excitability of cortical networks. Therefore, it is important to establish whether cestode derived acetylcholinesterases may alter host neuronal cholinergic signalling. Here we make use of multiple techniques to profile acetylcholinesterase activity in different extracts of both Taenia crassiceps and Taenia solium larvae. We find that the larvae of both species contain substantial acetylcholinesterase activity. However, acetylcholinesterase activity is lower in Taenia solium as compared to Taenia crassiceps larvae. Further, whilst we observed acetylcholinesterase activity in all fractions of Taenia crassiceps larvae, including on the membrane surface and in the excreted/secreted extracts, we could not identify acetylcholinesterases on the membrane surface or in the excreted/secreted extracts of Taenia solium larvae. Bioinformatic analysis revealed conservation of the functional protein domains in the Taenia solium acetylcholinesterases, when compared to the homologous human sequence. Finally, using whole-cell patch clamp recordings in rat hippocampal brain slice cultures, we demonstrate that Taenia larval derived acetylcholinesterases can break down acetylcholine at a concentration which induces changes in neuronal signalling. Together, these findings highlight the possibility that Taenia larval acetylcholinesterases can interfere with cholinergic signalling in the host, potentially contributing to pathogenesis in neurocysticercosis.


2004 ◽  
Vol 93 (4) ◽  
Author(s):  
Kaethe Willms ◽  
Lilia Robert ◽  
Jos�Agust�n Jim�nez ◽  
Mary Everhart ◽  
RaymondE. Kuhn

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