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Recent Development In 
The Culturing OF 
Cestodes 
By M.Abdullah M.phil Scholar (mail 
abdullahjan135@yahoo.com)
A numbed of issues are involved in 
culturing of cestode parasite, 
which make these procedure 
highly complex and subjected to 
many variable some of which are 
known and some are still 
undefined.
 As we know that cestode parasite 
have complex life cycle because 
having a differ morphological state, 
definitive host, intermediate host, 
host temperature, host immune 
responses and parasitic strain. 
 All these are a number of variable 
which we can be control difficulty in 
culture system.
Despite of these difficulties 
researchers try to maintain all 
these parameter for culturing 
cestode parasites for a number 
of purposes including
VACCINATION AGAINST CESTODE 
INFECTIONS 
 Vaccines for prevention of infection with 
cestode parasites would be valuable in 
reducing the economic losses due to 
infections with these parasites in livestock 
and also in breaking the life cycle of the 
medically important species.
Cestode Antigen vaccine 
 Substantial progress has been made towards 
developing a practical vaccine for the prevention 
of T. ovis infection in sheep. An antigen derived 
from the parasite egg has been identified and 
produced in E . coli using recombinant DNA 
techniques. The vaccine, which protects sheep 
against challenge infection with T. ovis, is the 
first highly effective defined antigen vaccine 
against any parasite infection of man or animals.
Cestode Vaccine 
 Vaccine have been developed, by using 
antigens of onchospheral larvae which is 
derived from adult tape worm (Taenia solium) 
having definitve host man and intermediate 
host sheep. These vaccine produced 
antibodies to prevent infection in some 
intermediate host of larval cestode. This 
immunity of the host can be transferred to 
neonates through clostral antibody.
Cysticercus antigen 
diagnosis 
 Immunochemical analysis of Cysticercus 
antigens is providing valuable information and 
may identify specific diagnostic components This 
approach has been applied with outstanding 
success to the diagnosis of T. solium cysticercosis 
in man . The immunoblotting technique used is 
not applicable to large-scale use for diagnosis of 
animal cysticercosis, but the information gained 
provides the basis for research towards the 
production of these particular diagnostic 
components using recombinant DNA 
techniques.
Screening Of Drug 
 In Vitro culture of parasitic helminths provide 
an important tool to study cell regeneration 
and physiology as well as molecular biology 
and genetic engineering study. 
 We establish a cell line from the Echinococcus 
granulosus germinal layer and we propose it 
as important tool for practical purposes 
including the screening of new drugs and for 
obtaining parasite material.
Cestode in cancer cells 
 Hydatid cyst is the larval stage of the 
tapeworm Echinococcus granulosus ,it is 
collected from sheep or cattle. When fluid of 
hydatid cyst protoscolices is added to Hella 
cell in the culture medium, its antigen inhibit 
the growth of cancer cell. This is one of the 
major development in cestode culture.
Differentiation of cell 
 Kanan and Chain explored the effect of 
hydatid cyst fluid on differentiation of human 
monocyte to dendritic cell in the culture 
medium. Their results showed that hydatid 
cyst fluid modulated differentiation of 
dendritic cells.
Eosinophil in cestode 
culturing 
 By continuous culturing of cestodes it was 
found that , eosinophils have been shown to 
be strong effectors killing cestode parasites in 
vitro, especially the larval stages. However, 
this function in vivo was established only for 
the very small number of parasites. The 
highly toxic basic proteins in eosinophil 
granules exert a range of biological effects 
against cestode parasites.
Cultured cestodes showing 
phylogenitic relationship 
 Three hymenolepidid tapeworms, H. diminuta, H 
nana and H. microstoma, are commonly maintained laboratory rodents and used in experimental model 
systems of tapeworm infections. Authers examined 
partial sequences from the mitochondrial cytochrome 
c oxidase subunit 1 (CO1) gene and nuclear ribosomal 
internal transcribed spacer 2 sequences infer(conclude) phylogenetic relationships. Genes 
were amplied by PCR and sequenced directly. The 
CO1 gene sequence obtained was the same in length 
(391 bp) among specimens. (M. Okamoto et al.1997)
Culture improve diagnosis by 
antigen preparation 
 Controlled study on lambs experimentally with 
E. granulosus have provide no doubt that sheep 
do respond to hydated infection by producing 
specific antibodies. This infected sheep shown a 
specific antibody response to E. granulosus does 
occur in sheep, even though of low titer ( 
antibody concentration) have encouraged 
attempts to improve the specificity of diagnosis 
by comparative analysis of result with different 
antigen preparation.
Culture broadness 
 In addition to the economically and medically 
important culturing, other naturally occurring 
(taeniid) have been used extensively in 
experimental investigation of the 
immunobioogy of the host parasite 
relationship in cestode parasites.. 
 Also cultured as a bioindecator for the 
purpose of identification.
Culture aid in oncosphere gene 
cloning,sequencing and stored in 
cDNA library 
 Genes are cloned in vectors and stodred in data 
bank (cDNA library). 
 A cDNA library was constructed from 
oncosphere mRNA and screened with 
antibodies from vaccinated and immune 
sheep. One particular cloned antigen, 
designated EG95, induced high levels of 
protection (96% and 97%) in 2 independent 
vaccination trials (Heath et al. 1981)
 Morphology , ultra structure, life cycle, mode 
of transmission, optimum temperature and all 
other information are mostly available by the 
blessing of culture biologist. This 
investigation aid in controlling of zoonotic 
infection.

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recent development in culture od Cestode

  • 1. Recent Development In The Culturing OF Cestodes By M.Abdullah M.phil Scholar (mail abdullahjan135@yahoo.com)
  • 2. A numbed of issues are involved in culturing of cestode parasite, which make these procedure highly complex and subjected to many variable some of which are known and some are still undefined.
  • 3.  As we know that cestode parasite have complex life cycle because having a differ morphological state, definitive host, intermediate host, host temperature, host immune responses and parasitic strain.  All these are a number of variable which we can be control difficulty in culture system.
  • 4. Despite of these difficulties researchers try to maintain all these parameter for culturing cestode parasites for a number of purposes including
  • 5. VACCINATION AGAINST CESTODE INFECTIONS  Vaccines for prevention of infection with cestode parasites would be valuable in reducing the economic losses due to infections with these parasites in livestock and also in breaking the life cycle of the medically important species.
  • 6. Cestode Antigen vaccine  Substantial progress has been made towards developing a practical vaccine for the prevention of T. ovis infection in sheep. An antigen derived from the parasite egg has been identified and produced in E . coli using recombinant DNA techniques. The vaccine, which protects sheep against challenge infection with T. ovis, is the first highly effective defined antigen vaccine against any parasite infection of man or animals.
  • 7. Cestode Vaccine  Vaccine have been developed, by using antigens of onchospheral larvae which is derived from adult tape worm (Taenia solium) having definitve host man and intermediate host sheep. These vaccine produced antibodies to prevent infection in some intermediate host of larval cestode. This immunity of the host can be transferred to neonates through clostral antibody.
  • 8. Cysticercus antigen diagnosis  Immunochemical analysis of Cysticercus antigens is providing valuable information and may identify specific diagnostic components This approach has been applied with outstanding success to the diagnosis of T. solium cysticercosis in man . The immunoblotting technique used is not applicable to large-scale use for diagnosis of animal cysticercosis, but the information gained provides the basis for research towards the production of these particular diagnostic components using recombinant DNA techniques.
  • 9. Screening Of Drug  In Vitro culture of parasitic helminths provide an important tool to study cell regeneration and physiology as well as molecular biology and genetic engineering study.  We establish a cell line from the Echinococcus granulosus germinal layer and we propose it as important tool for practical purposes including the screening of new drugs and for obtaining parasite material.
  • 10. Cestode in cancer cells  Hydatid cyst is the larval stage of the tapeworm Echinococcus granulosus ,it is collected from sheep or cattle. When fluid of hydatid cyst protoscolices is added to Hella cell in the culture medium, its antigen inhibit the growth of cancer cell. This is one of the major development in cestode culture.
  • 11. Differentiation of cell  Kanan and Chain explored the effect of hydatid cyst fluid on differentiation of human monocyte to dendritic cell in the culture medium. Their results showed that hydatid cyst fluid modulated differentiation of dendritic cells.
  • 12. Eosinophil in cestode culturing  By continuous culturing of cestodes it was found that , eosinophils have been shown to be strong effectors killing cestode parasites in vitro, especially the larval stages. However, this function in vivo was established only for the very small number of parasites. The highly toxic basic proteins in eosinophil granules exert a range of biological effects against cestode parasites.
  • 13. Cultured cestodes showing phylogenitic relationship  Three hymenolepidid tapeworms, H. diminuta, H nana and H. microstoma, are commonly maintained laboratory rodents and used in experimental model systems of tapeworm infections. Authers examined partial sequences from the mitochondrial cytochrome c oxidase subunit 1 (CO1) gene and nuclear ribosomal internal transcribed spacer 2 sequences infer(conclude) phylogenetic relationships. Genes were amplied by PCR and sequenced directly. The CO1 gene sequence obtained was the same in length (391 bp) among specimens. (M. Okamoto et al.1997)
  • 14. Culture improve diagnosis by antigen preparation  Controlled study on lambs experimentally with E. granulosus have provide no doubt that sheep do respond to hydated infection by producing specific antibodies. This infected sheep shown a specific antibody response to E. granulosus does occur in sheep, even though of low titer ( antibody concentration) have encouraged attempts to improve the specificity of diagnosis by comparative analysis of result with different antigen preparation.
  • 15. Culture broadness  In addition to the economically and medically important culturing, other naturally occurring (taeniid) have been used extensively in experimental investigation of the immunobioogy of the host parasite relationship in cestode parasites..  Also cultured as a bioindecator for the purpose of identification.
  • 16. Culture aid in oncosphere gene cloning,sequencing and stored in cDNA library  Genes are cloned in vectors and stodred in data bank (cDNA library).  A cDNA library was constructed from oncosphere mRNA and screened with antibodies from vaccinated and immune sheep. One particular cloned antigen, designated EG95, induced high levels of protection (96% and 97%) in 2 independent vaccination trials (Heath et al. 1981)
  • 17.  Morphology , ultra structure, life cycle, mode of transmission, optimum temperature and all other information are mostly available by the blessing of culture biologist. This investigation aid in controlling of zoonotic infection.