Literature DB >> 23948341

Female biased sex-ratio in Schistosoma mansoni after exposure to an allopatric intermediate host strain of Biomphalaria glabrata.

Julie M J Lepesant1, Jérôme Boissier, Déborah Climent, Céline Cosseau, Christoph Grunau.   

Abstract

For parasites that require multiple hosts to complete their development, the interaction with the intermediate host may have an impact on parasite transmission and development in the definitive host. The human parasite Schistosoma mansoni needs two different hosts to complete its life cycle: the freshwater snail Biomphalaria glabrata (in South America) as intermediate host and a human or rodents as final host. To investigate the influence of the host environment on life history traits in the absence of selection, we performed experimental infections of two B. glabrata strains of different geographic origin with the same clonal population of S. mansoni. One B. glabrata strain is the sympatric host and the other one the allopatric host. We measured prevalence in the snail, the cercarial infectivity, sex-ratio, immunopathology in the final host and microsatellite frequencies of individual larvae in three successive generations. We show that, even if the parasite population is clonal based on neutral markers, S. mansoni keeps the capacity of generating phenotypic plasticity and/or variability for different life history traits when confront to an unusual environment, in this study the intermediate host. The most dramatic change was observed in sex-ratio: in average 1.7 times more female cercariae were produced when the parasite developed in an allopatric intermediate host.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Allopatric; Life history traits; Plasticity; Schistosoma mansoni; Sex-ratio; Sympatric

Mesh:

Year:  2013        PMID: 23948341     DOI: 10.1016/j.exppara.2013.07.023

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


  4 in total

1.  Compatibility of Schistosoma japonicum from the hilly region and Oncomelania hupensis hupensis from the marshland region within Anhui, China.

Authors:  Chen-Zhong Wang; Da-Bing Lu; Cheng-Xiang Guo; Ying Li; Yuan-Meng Gao; Chao-Rong Bian; Jing Su
Journal:  Parasitol Res       Date:  2014-09-09       Impact factor: 2.289

2.  Real-time PCR for sexing Schistosoma mansoni cercariae.

Authors:  Frédéric D Chevalier; Winka Le Clec'h; Ana Carolina Alves de Mattos; Philip T LoVerde; Timothy J C Anderson
Journal:  Mol Biochem Parasitol       Date:  2016-03-26       Impact factor: 1.759

3.  The Schistosoma mansoni genome encodes thousands of long non-coding RNAs predicted to be functional at different parasite life-cycle stages.

Authors:  Elton J R Vasconcelos; Lucas F daSilva; David S Pires; Guilherme M Lavezzo; Adriana S A Pereira; Murilo S Amaral; Sergio Verjovski-Almeida
Journal:  Sci Rep       Date:  2017-09-05       Impact factor: 4.379

4.  Epigenetic origin of adaptive phenotypic variants in the human blood fluke Schistosoma mansoni.

Authors:  Sara Fneich; André Théron; Céline Cosseau; Anne Rognon; Benoit Aliaga; Jérôme Buard; David Duval; Nathalie Arancibia; Jérôme Boissier; David Roquis; Guillaume Mitta; Christoph Grunau
Journal:  Epigenetics Chromatin       Date:  2016-07-04       Impact factor: 4.954

  4 in total

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