Literature DB >> 11429173

Stability and reproductive fitness of Schistosoma mansoni isolates with decreased sensitivity to praziquantel.

S William1, A Sabra, F Ramzy, M Mousa, Z Demerdash, J L Bennett, T A Day, S Botros.   

Abstract

These studies are focused on schistosomes derived from human infections not cured by three successive doses of praziquantel that also produced infections in mice that were significantly more difficult to cure than infections with control worms. Half (three of six) of these isolates retained their decreased response to praziquantel after multiple passages through the life-cycle in the absence of therapeutic pressure. Two of the isolates, including the one initially least sensitive to praziquantel; reverted, to a sensitivity not significantly different from controls. For example, the EE6 isolate initially required 680 mg/kg praziquantel to affect a 50% reduction in worm load in murine infections, but after only six passages through the life cycle over 5 years this was reduced to 113 mg/kg, not different from control infections. The stability of some of the isolates and the reversion of others indicates that the biological or genetic factors conferring decreased praziquantel response varies among the isolates. The three isolates that retained decreased sensitivity to praziquantel all showed compromises in reproductive fitness in the laboratory, expressed most frequently as a decreased cercarial production from snails infected with those isolates compared to controls. For example, the total cercarial production of snails infected with the EE10 isolate was only 57% that of controls. The reversion of some of the isolates to a praziquantel sensitive state and the decreased reproductive fitness of those that did not revert suggest that there is some biological cost associated with the relative praziquantel insensitivity of these worms, which could help limit the impact of such isolates in the field. Infections with the less sensitive isolates also produced significantly less circulating schistosomal antigen in mice, suggesting that a decrease in the host immune response elicited by these worms could be one of the factors contributing to the diminished praziquantel efficacy.

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Year:  2001        PMID: 11429173     DOI: 10.1016/s0020-7519(01)00215-6

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  24 in total

1.  Effect of the in vivo activity of dihydroartemisinin against Schistosoma mansoni infection in mice.

Authors:  Hong-jun Li; Wei Wang; Guo-li Qu; You-zi Li; Yong-hui Tao; Yun-tian Xing; Xiao-ting Wang; Yang Dai; Jian-ying Wei; Jian-rong Dai; Gerald C Coles; You-sheng Liang
Journal:  Parasitol Res       Date:  2011-10-18       Impact factor: 2.289

2.  Bioavailability and in vivo efficacy of a praziquantel-polyvinylpyrrolidone solid dispersion in Schistosoma mansoni-infected mice.

Authors:  Naglaa El-Lakkany; Sayed Hassan Seif El-Din; Lamia Heikal
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2012-03-30       Impact factor: 2.441

3.  Antigenic profile and localization of Clonorchis sinensis proteins in the course of infection.

Authors:  S J Hong; T Y Kim; K Y Song; W M Sohn; S Y Kang
Journal:  Korean J Parasitol       Date:  2001-12       Impact factor: 1.341

4.  Schistosoma mansoni P-glycoprotein levels increase in response to praziquantel exposure and correlate with reduced praziquantel susceptibility.

Authors:  Shanta M Messerli; Ravi S Kasinathan; William Morgan; Stefani Spranger; Robert M Greenberg
Journal:  Mol Biochem Parasitol       Date:  2009-05-03       Impact factor: 1.759

Review 5.  Voltage-gated calcium channel subunits from platyhelminths: potential role in praziquantel action.

Authors:  Michael C Jeziorski; Robert M Greenberg
Journal:  Int J Parasitol       Date:  2006-03-07       Impact factor: 3.981

6.  Activity of 9-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]adenine against Schistosomiasis mansoni in mice.

Authors:  Sanaa Botros; Samia William; Olfat Hammam; Zdenĕk Zídek; Antonín Holý
Journal:  Antimicrob Agents Chemother       Date:  2003-12       Impact factor: 5.191

Review 7.  New approaches for understanding mechanisms of drug resistance in schistosomes.

Authors:  Robert M Greenberg
Journal:  Parasitology       Date:  2013-04-03       Impact factor: 3.234

8.  Dihydroartemisinin: a new story of an old drug against Schistosoma mansoni infection.

Authors:  Hong-Jun Li; Fu-Liang Xu; Yun-Hai Wang; Zheng-Jun Yi; Wei Wang
Journal:  Parasitol Res       Date:  2013-10-22       Impact factor: 2.289

9.  Genetic structure of Schstosoma mansoni in western Kenya: the effects of geography and host sharing.

Authors:  M L Steinauer; B Hanelt; L E Agola; G M Mkoji; E S Loker
Journal:  Int J Parasitol       Date:  2009-05-21       Impact factor: 3.981

10.  Role of the Pumilio gene in the reproductive system of Schistosoma japonicum.

Authors:  Yuanyuan Xia; Siyu He; Zian Sun; Xiunan Wang; Wei Shao; Cuiping Ren; Jijia Shen; Miao Liu
Journal:  Parasitol Res       Date:  2020-01-02       Impact factor: 2.289

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