Literature DB >> 2458958

Schistosoma mansoni: analysis of cercarial transformation methods.

B Salafsky1, A C Fusco, K Whitley, D Nowicki, B Ellenberger.   

Abstract

Four methods of transforming cercariae to schistosomulae in vitro in ELAC buffer (pH 7.2, 37 C, 0-6 hr incubation) were compared in relation to biochemical and ultrastructural characteristics. The transformation methods used were chemical (3 mM linoleate), mechanical (centrifuge/vortex), mechanical/chemical, and heat (incubation at 37 C). Ultrastructural characteristics examined were based on the presence or absence of glycocalyx, heptalaminate membrane, cyton granules, and nuclear condition. Two EM fixation methods were used. Biochemical parameters assayed were loss of water tolerance (uptake of trypan blue dye), eicosanoid biosynthesis (PGE, LTB4, and 5-HETE), protein synthesis (leucine uptake), RNA synthesis (uracil and orotic acid uptake), and DNA synthesis (thymidine uptake). EM characteristics were remarkably similar for all transformation methods except heat incubation, with transformed cercariae evidencing the characteristics of schistosomulae (cyton granule migration, absence of glycocalyx and heptalaminate membrane); however, euchromatic nuclei could not be demonstrated using in vivo or in vitro transformation methods. Despite the ultrastructural similarities between transformation methods, biochemical data demonstrated that the resultant organisms were quite different. The chemical transformation method gave the highest rate of loss of water tolerance and eicosanoid production. RNA and protein synthesis were not correlated to ultrastructural changes and were highest in those organisms undergoing mechanical transformation methods, significantly higher than in those cercariae transformed by the chemical method. DNA synthesis was not demonstrated using any transformation method, although thymidine uptake did occur. Our data indicate substantial biochemical differences exist between morphologically similar organisms. Thus, experiments using any type of artificially transformed schistosomule must be interpreted with caution until additional biochemical and physiological studies on cercarial transformation are undertaken.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2458958     DOI: 10.1016/0014-4894(88)90014-8

Source DB:  PubMed          Journal:  Exp Parasitol        ISSN: 0014-4894            Impact factor:   2.011


  13 in total

Review 1.  Biology of the schistosome lung-stage schistosomulum.

Authors:  G N Gobert; M Chai; D P McManus
Journal:  Parasitology       Date:  2006-11-17       Impact factor: 3.234

2.  In vitro cercariae transformation: comparison of mechanical and nonmechanical methods and observation of morphological changes of detached cercariae tails.

Authors:  Kristen A Coultas; Si-Ming Zhang
Journal:  J Parasitol       Date:  2012-04-20       Impact factor: 1.276

3.  Suppression of mRNAs encoding tegument tetraspanins from Schistosoma mansoni results in impaired tegument turnover.

Authors:  Mai H Tran; Tori C Freitas; Leanne Cooper; Soraya Gaze; Michelle L Gatton; Malcolm K Jones; Erica Lovas; Edward J Pearce; Alex Loukas
Journal:  PLoS Pathog       Date:  2010-04-15       Impact factor: 6.823

4.  Schistosoma japonicum and S. mansoni cercariae: different effects of protein in medium, of mechanical stress, and of an intact complement system on in vitro transformation to schistosomula.

Authors:  Wenshi Wang; Michael Kirschfink; Andreas Ruppel
Journal:  Parasitol Res       Date:  2006-03-18       Impact factor: 2.289

5.  Development of an in vitro drug screening assay using Schistosoma haematobium schistosomula.

Authors:  Monika Marxer; Katrin Ingram; Jennifer Keiser
Journal:  Parasit Vectors       Date:  2012-08-09       Impact factor: 3.876

6.  Comparative study of transcriptome profiles of mechanical- and skin-transformed Schistosoma mansoni schistosomula.

Authors:  Anna V Protasio; David W Dunne; Matthew Berriman
Journal:  PLoS Negl Trop Dis       Date:  2013-03-14

7.  Functional expression of a novel Kunitz type protease inhibitor from the human blood fluke Schistosoma mansoni.

Authors:  Shiwanthi L Ranasinghe; Katja Fischer; Geoffrey N Gobert; Donald P McManus
Journal:  Parasit Vectors       Date:  2015-08-04       Impact factor: 3.876

8.  A Microtus fortis protein, serum albumin, is a novel inhibitor of Schistosoma japonicum schistosomula.

Authors:  Rong Li; Guo-Jun Wu; De-Hui Xiong; Qiang Gong; Ruan-Jing Yu; Wei-Xin Hu
Journal:  Mem Inst Oswaldo Cruz       Date:  2013-11       Impact factor: 2.743

9.  Functional characterisation of Schistosoma japonicum acetylcholinesterase.

Authors:  Hong You; Geoffrey N Gobert; Xiaofeng Du; Gabor Pali; Pengfei Cai; Malcolm K Jones; Donald P McManus
Journal:  Parasit Vectors       Date:  2016-06-10       Impact factor: 3.876

10.  Hsp70 May Be a Molecular Regulator of Schistosome Host Invasion.

Authors:  Kenji Ishida; Emmitt R Jolly
Journal:  PLoS Negl Trop Dis       Date:  2016-09-09
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.