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Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni

BACKGROUND: The near exclusive use of praziquantel (PZQ) for treatment of human schistosomiasis has raised concerns about the possible emergence of drug-resistant schistosomes. METHODOLOGY/PRINCIPAL FINDINGS: We measured susceptibility to PZQ of isolates of Schistosoma mansoni obtained from patients...

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Autores principales: Melman, Sandra D., Steinauer, Michelle L., Cunningham, Charles, Kubatko, Laura S., Mwangi, Ibrahim N., Wynn, Nirvana Barker, Mutuku, Martin W., Karanja, Diana M. S., Colley, Daniel G., Black, Carla L., Secor, William Evan, Mkoji, Gerald M., Loker, Eric S.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721635/
https://www.ncbi.nlm.nih.gov/pubmed/19688043
http://dx.doi.org/10.1371/journal.pntd.0000504
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author Melman, Sandra D.
Steinauer, Michelle L.
Cunningham, Charles
Kubatko, Laura S.
Mwangi, Ibrahim N.
Wynn, Nirvana Barker
Mutuku, Martin W.
Karanja, Diana M. S.
Colley, Daniel G.
Black, Carla L.
Secor, William Evan
Mkoji, Gerald M.
Loker, Eric S.
author_facet Melman, Sandra D.
Steinauer, Michelle L.
Cunningham, Charles
Kubatko, Laura S.
Mwangi, Ibrahim N.
Wynn, Nirvana Barker
Mutuku, Martin W.
Karanja, Diana M. S.
Colley, Daniel G.
Black, Carla L.
Secor, William Evan
Mkoji, Gerald M.
Loker, Eric S.
author_sort Melman, Sandra D.
collection PubMed
description BACKGROUND: The near exclusive use of praziquantel (PZQ) for treatment of human schistosomiasis has raised concerns about the possible emergence of drug-resistant schistosomes. METHODOLOGY/PRINCIPAL FINDINGS: We measured susceptibility to PZQ of isolates of Schistosoma mansoni obtained from patients from Kisumu, Kenya continuously exposed to infection as a consequence of their occupations as car washers or sand harvesters. We used a) an in vitro assay with miracidia, b) an in vivo assay targeting adult worms in mice and c) an in vitro assay targeting adult schistosomes perfused from mice. In the miracidia assay, in which miracidia from human patients were exposed to PZQ in vitro, reduced susceptibility was associated with previous treatment of the patient with PZQ. One isolate (“KCW”) that was less susceptible to PZQ and had been derived from a patient who had never fully cured despite multiple treatments was studied further. In an in vivo assay of adult worms, the KCW isolate was significantly less susceptible to PZQ than two other isolates from natural infections in Kenya and two lab-reared strains of S. mansoni. The in vitro adult assay, based on measuring length changes of adults following exposure to and recovery from PZQ, confirmed that the KCW isolate was less susceptible to PZQ than the other isolates tested. A sub-isolate of KCW maintained separately and tested after three years was susceptible to PZQ, indicative that the trait of reduced sensitivity could be lost if selection was not maintained. CONCLUSIONS/SIGNIFICANCE: Isolates of S. mansoni from some patients in Kisumu have lower susceptibility to PZQ, including one from a patient who was never fully cured after repeated rounds of treatment administered over several years. As use of PZQ continues, continued selection for worms with diminished susceptibility is possible, and the probability of emergence of resistance will increase as large reservoirs of untreated worms diminish. The potential for rapid emergence of resistance should be an important consideration of treatment programs.
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spelling pubmed-27216352009-08-18 Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni Melman, Sandra D. Steinauer, Michelle L. Cunningham, Charles Kubatko, Laura S. Mwangi, Ibrahim N. Wynn, Nirvana Barker Mutuku, Martin W. Karanja, Diana M. S. Colley, Daniel G. Black, Carla L. Secor, William Evan Mkoji, Gerald M. Loker, Eric S. PLoS Negl Trop Dis Research Article BACKGROUND: The near exclusive use of praziquantel (PZQ) for treatment of human schistosomiasis has raised concerns about the possible emergence of drug-resistant schistosomes. METHODOLOGY/PRINCIPAL FINDINGS: We measured susceptibility to PZQ of isolates of Schistosoma mansoni obtained from patients from Kisumu, Kenya continuously exposed to infection as a consequence of their occupations as car washers or sand harvesters. We used a) an in vitro assay with miracidia, b) an in vivo assay targeting adult worms in mice and c) an in vitro assay targeting adult schistosomes perfused from mice. In the miracidia assay, in which miracidia from human patients were exposed to PZQ in vitro, reduced susceptibility was associated with previous treatment of the patient with PZQ. One isolate (“KCW”) that was less susceptible to PZQ and had been derived from a patient who had never fully cured despite multiple treatments was studied further. In an in vivo assay of adult worms, the KCW isolate was significantly less susceptible to PZQ than two other isolates from natural infections in Kenya and two lab-reared strains of S. mansoni. The in vitro adult assay, based on measuring length changes of adults following exposure to and recovery from PZQ, confirmed that the KCW isolate was less susceptible to PZQ than the other isolates tested. A sub-isolate of KCW maintained separately and tested after three years was susceptible to PZQ, indicative that the trait of reduced sensitivity could be lost if selection was not maintained. CONCLUSIONS/SIGNIFICANCE: Isolates of S. mansoni from some patients in Kisumu have lower susceptibility to PZQ, including one from a patient who was never fully cured after repeated rounds of treatment administered over several years. As use of PZQ continues, continued selection for worms with diminished susceptibility is possible, and the probability of emergence of resistance will increase as large reservoirs of untreated worms diminish. The potential for rapid emergence of resistance should be an important consideration of treatment programs. Public Library of Science 2009-08-18 /pmc/articles/PMC2721635/ /pubmed/19688043 http://dx.doi.org/10.1371/journal.pntd.0000504 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Melman, Sandra D.
Steinauer, Michelle L.
Cunningham, Charles
Kubatko, Laura S.
Mwangi, Ibrahim N.
Wynn, Nirvana Barker
Mutuku, Martin W.
Karanja, Diana M. S.
Colley, Daniel G.
Black, Carla L.
Secor, William Evan
Mkoji, Gerald M.
Loker, Eric S.
Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni
title Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni
title_full Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni
title_fullStr Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni
title_full_unstemmed Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni
title_short Reduced Susceptibility to Praziquantel among Naturally Occurring Kenyan Isolates of Schistosoma mansoni
title_sort reduced susceptibility to praziquantel among naturally occurring kenyan isolates of schistosoma mansoni
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721635/
https://www.ncbi.nlm.nih.gov/pubmed/19688043
http://dx.doi.org/10.1371/journal.pntd.0000504
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