Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 81

Warning: fopen(upload/ip_log/ip_log_2024-04.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 83

Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 84
Studies on the bladder worm, Cysticercus cellulosae: The ultrastructure of C. cellulosae
| Home | E-Submission | Sitemap | Contact us |  
top_img
Korean J Parasito Search

CLOSE

Korean J Parasito > Volume 21(1):1983 > Article

Original Article
Korean J Parasitol. 1983 Jun;21(1):75-82. English.
Published online Mar 20, 1994.  http://dx.doi.org/10.3347/kjp.1983.21.1.75
Copyright © 1983 by The Korean Society for Parasitology
Studies on the bladder worm, Cysticercus cellulosae: The ultrastructure of C. cellulosae
Soon-Hyung Lee
Department of Parasitology, College of Medicine, Seoul National University, Korea.
Abstract

An electron microscopic study was performed to know the basic tegumental structure of Cysticercus cellulosae. The scolex and bladder portions of cysticerci (human and porcine strains) were prepared for transmission and scanning electron microscopy by conventional procedures.

In general, the tegument of C. cellulosae showed the basic ultrastructure of cestode tegument on electron micrographs. The teguments of both scolex and bladder portions consisted of such components i.e., an outer vesicular layer with numerous microtriches and inner fibrous layer. Below the fibrous layer, there were layers of muscle bundles and tegumental cells.

The microtriches which covered the surface of cysticercus revealed two distinctly different shapes. The characteristic bladder-like, elongated pyramid shaped 'tetrahedral form' was observed on the surface of the scolex portion, whereas the elongated cylindrical 'filamentous form' was distributed on the surface of bladder portion.

In spite of the difference of isolated host and location, the cysticerci showed the same result. But dimensional variations of the tegument according to topography of the worm were observed. The possibility of application in making differential diagnosis from other larval cestodes and possible functions of this larval tegument were discussed.

Figures


Figs. 1-4
Fig. 1. An electron micrograph of cysticerous tegument (porcine strain) showing microtriches (m), vesicular layer (V), fibrous layer (F) and muscle layer (M). ×2,000.

Fig. 2. The microtriches (m) on the surface of scolex portion. Longitudinal section shows a characteristic elongated tetrahedral feature. ×8,000. The porcine strain.

Fig. 3. Detail of the characteristic microtriches (m) on the scolex of Cysticercus (human strain). Note the insertion of proximal part or base (b) into the vesicular layer of the tegument, and rigid, electrondense distal part or shaft (s). The proximal part also shows peripheral dense region (arrows) and inner lucid medullary region. ×20,000.

Fig. 4. Transverse sections through bases (b) and shafts(s) of microtriches on the scolex. note the characteristic triangular cut-surfaces which suggest their tetrahedral stereoscopic structures. Numerous vesicles & vacuoles, electron dense granules and mitochondria are also visible in vesicular layer(V). ×10,000.



Figs. 5-8
Fig. 5. Low power view of bladder portion of human strain showing straight filamentous microtriches(m). ×2,000.

Fig. 6. Cross section of filamentous microtriches of the bladder portion through bases (b) and shafts(s). Note circular cut-surfaces which support their cylindrical stereoscopic structure. ×8,000.

Fig. 7. Higher magnification of filamentous microtriches on the surface of bladder portion (porcine strain). Note the elongated filamentous shafts(s) and relatively short proximal bases (b). ×20,000.

Fig. 8. A scanning electron-micrograph of microtriches on the surface of bladder portion (porcine strain). Note the bundles of filamentous microtriches (m) which suggest their agitative function in the microhabitat to maintain a free flow of nutrients. ×20,000.


References
1. Andersen K. Comparison of surface topography of three species of Diphyllobothrium (Cestoda, Pseudophyllidea) by scanning electron microscopy. Int J Parasitol 1975;5(3):293–300.
  
2. Baron PJ. On the histology and ultrasturcture of Cysticercus longicollis, the cysticercus of Taenia crassiceps Zeder, 1800, (Cestoda, Cyclophyllidea). Parasitology 1968;58(3):497–513.
  
3. Berger J, Mettrick DF. Microtrichial polymorphism among hymenolepid tapeworms as seen by scanning electron microscopy. Trans Am Microsc Soc 1971;90(4):393–403.
  
4. Blitz NM, Smyth JD. Tegumental ultrastructure of Raillietina cesticillus during the larval-adult transformation, with emphasis on the rostellum. Int J Parasitol 1973;3(4):561–570.
  
5. Charles GH, Orr TS. Comparative fine structure of outer tegument of Ligula intestinalis and Schistocephalus solidus. Exp Parasitol 1968;22(2):137–149.
  
6. Chi HS, Chi JG. A Histopathological Study On Human Cysticercosis. Korean J Parasitol 1978;16(2):123–133.
 
7. Featherston DW. Taenia hydatigena. IV. Ultrastructure study of the tegument. Z Parasitenkd 1972;38(3):214–232.
  
8. Featherston DW. Taenia hydatigena--V. Surface structure of the adult worm and evaginated scolex. Int J Parasitol 1975;5(6):625–629.
  
9. Hayunga EG, Mackiewicz JS. An electron microscope study of the tegument of Hunterella nodulosa Mackiewicz and McCrae, 1962 (Cestoidea: Caryophyllidea). Int J Parasitol 1975;5(3):309–319.
  
10. Hess E, et al. Z Parasitenkd 1977;53:189–199.
 
11. Jha RK, Smyth JD. Ultrastructure of the rostellar tegument of Echinococcus granulosus with special reference to biogenesis of mitochondria. Int J Parasitol 1971;1(2):169–177.
  
12. Lee DL. The structure and composition of the helminth cuticle. Adv Parasitol 1966;4:187–254.
  
13. Lee DL. The structure of the helminth cuticle. Adv Parasitol 1972;10:347–379.
  
14. Lumsden RD. Cytological studies on the absorptive surfaces of cestodes. I. The fine structure of the strobilar integument. Z Parasitenkd 1966;27(4):355–382.
  
15. Lumsden RD. Cytological studies on the absorptive surfaces of cestodes. II. The synthesis and intracellular transport of protein in the strobilar integument of Hymenolepis diminuta. Z Parasitenkd 1966;28(1):1–13.
  
16. Lumsden RD. Surface ultrastructure and cytochemistry of parasitic helminths. Exp Parasitol 1975;37(2):267–339.
  
17. Lumsden RD. The tapeworm tegument: a model system for studies on membrane structure and function in host-parasite relationships. Trans Am Microsc Soc 1975;94(4):501–507.
  
18. Lumsden RD, Oaks JA, Alworth WL. Cytological studies on the absorptive surfaces of cestodes. IV. Localization and cytochemical properties of membrane-fixed cation binding sites. J Parasitol 1970;56(4):736–747.
  
19. Lumsden RD, Oaks JA, Mueller JF. Brush border development in the tegument of the tapeworm, Spirometra mansonoides. J Parasitol 1974;60(2):209–226.
  
20. Lumsden RD, Threadgold LT, Oaks JA, Arme C. On the permeability of cestodes to colloids: an evaluation of the transmembranosis hypothesis. Parasitology 1970;60(2):185–193.
  
21. McVicar AH. The ultrastructure of the parasite-host interface of three tetraphyllidean tapeworms of the elasmobranch Raja naevus. Parasitology 1972;65(1):77–88.
  
22. Mettrick DF, Podesta RB. Ecological and physiological aspects of helminth--host interactions in the mammalian gastrointestinal canal. Adv Parasitol 1974;12:183–278.
  
23. Mount PM. Histogenesis of the rostellar hooks of Taenia crassiceps (Zeder, 1800) (Cestoda). J Parasitol 1970;56(5):947–961.
  
24. Nieland ML, Weinbach EC. The bladder of Cysticercus fasciolaris: electron microscopy and carbohydrate content. Parasitology 1968;58(2):489–496.
  
25. Park WC, et al. ChungAng J Med 1981;6:29–38.
26. Rothman A. J Parasit 1959;45 suppl.:28.
27. Rothman A. J Parasit 1960;46 suppl.:10.
28. Rothman A. Trans Am Micro Soc 1963;82:22–30.
 
29. Slais J. Functional morphology of cestode larvae. Adv Parasitol 1973;11:395–480.
  
30. Slais J, Serbus C, Schramlová J. The microscopical anatomy of the bladder wall of Cysticercus bovis at the electron microscope level. Z Parasitenkd 1971;36(4):304–320.
  
31. Suk JS, Sim BS, Lee SH. Fine Structure Of Cysticercus Celluosae From Human Brain. Korean J Parasitol 1980;18(1):1–14.
 
32. Taylor EW, Thomas JN. Membrane (contact) digestion in the three species of tapeworm Hymenolepis diminuta, Hymenolepis microstoma and Moniezia expansa. Parasitology 1968;58(3):535–546.
  
33. Thompson RC, Hayton AR, Jue Sue LP. An ultrastructural study of the microtriches of adult Proteocephalus tidswelli (Cestoda: Proteocephalidea). Z Parasitenkd 1980;64(1):95–111.
  
34. Threadgold LT. Quarterly J Micro Sci 1962;103:135–140.
35. Threadgold LT. Parasitology 1965;55:467–472.
 
36. Trimble JJ 3rd, Lumsden RD. Cytochemical characterization of tegument membrane-associated carbohydrates in Taenia crassiceps larvae. J Parasitol 1975;61(4):665–676.
  
37. VOGE M. Observations on the structure of cysticerci of Taenia solium and Taenia saginata (Cestoda: Taeniidae). J Parasitol 1963;49:85–90.
  
38. Voge M, Brown WJ. Fine structure of a racemose cysticercus from human brain. J Parasitol 1979;65(2):262–266.
  
TOOLS
PDF Links  PDF Links
Full text via DOI  Full text via DOI
Download Citation  Download Citation
Share:      
METRICS
1
Crossref
2
Scopus
4,562
View
62
Download
Editorial Office
Department of Molecular Parasitology, Samsung Medical Center, School of Medicine, Sungkyunkwan University,
2066 Seobu-ro, Jangan-gu, Suwon 16419, Gyeonggi-do, Korea.
Tel: +82-31-299-6251   FAX: +82-1-299-6269   E-mail: kjp.editor@gmail.com
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © 2024 by The Korean Society for Parasitology and Tropical Medicine.     Developed in M2PI