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Nullscript inhibits Cryptosporidium and Toxoplasma growth
Cryptosporidium and Toxoplasma are parasites that have caused problems worldwide. Cryptosporidium causes severe watery diarrhoea and may be fatal in immunocompromised patients and in infants. Nitazoxanide is the only agent currently approved by the FDA, but its efficacy is limited. Toxoplasmosis is...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593347/ https://www.ncbi.nlm.nih.gov/pubmed/33120250 http://dx.doi.org/10.1016/j.ijpddr.2020.10.004 |
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author | Murakoshi, Fumi Bando, Hironori Sugi, Tatsuki Adeyemi, Oluyomi Stephen Nonaka, Motohiro Nakaya, Takaaki Kato, Kentaro |
author_facet | Murakoshi, Fumi Bando, Hironori Sugi, Tatsuki Adeyemi, Oluyomi Stephen Nonaka, Motohiro Nakaya, Takaaki Kato, Kentaro |
author_sort | Murakoshi, Fumi |
collection | PubMed |
description | Cryptosporidium and Toxoplasma are parasites that have caused problems worldwide. Cryptosporidium causes severe watery diarrhoea and may be fatal in immunocompromised patients and in infants. Nitazoxanide is the only agent currently approved by the FDA, but its efficacy is limited. Toxoplasmosis is also a problem in the immunocompromised, as currently available treatment options have limited efficacy and patient tolerance can be poor. In the present investigation, we screened libraries of epigenetic compounds to identify those that inhibited C. parvum growth. Nullscript was identified as a compound with an inhibitory effect on C. parvum and T. gondii growth, and was less toxic to host cells. Nullscript was also able to significantly decrease oocyst excretion in C. parvum-infected SCID mice. |
format | Online Article Text |
id | pubmed-7593347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75933472020-11-02 Nullscript inhibits Cryptosporidium and Toxoplasma growth Murakoshi, Fumi Bando, Hironori Sugi, Tatsuki Adeyemi, Oluyomi Stephen Nonaka, Motohiro Nakaya, Takaaki Kato, Kentaro Int J Parasitol Drugs Drug Resist Article Cryptosporidium and Toxoplasma are parasites that have caused problems worldwide. Cryptosporidium causes severe watery diarrhoea and may be fatal in immunocompromised patients and in infants. Nitazoxanide is the only agent currently approved by the FDA, but its efficacy is limited. Toxoplasmosis is also a problem in the immunocompromised, as currently available treatment options have limited efficacy and patient tolerance can be poor. In the present investigation, we screened libraries of epigenetic compounds to identify those that inhibited C. parvum growth. Nullscript was identified as a compound with an inhibitory effect on C. parvum and T. gondii growth, and was less toxic to host cells. Nullscript was also able to significantly decrease oocyst excretion in C. parvum-infected SCID mice. Elsevier 2020-10-15 /pmc/articles/PMC7593347/ /pubmed/33120250 http://dx.doi.org/10.1016/j.ijpddr.2020.10.004 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Murakoshi, Fumi Bando, Hironori Sugi, Tatsuki Adeyemi, Oluyomi Stephen Nonaka, Motohiro Nakaya, Takaaki Kato, Kentaro Nullscript inhibits Cryptosporidium and Toxoplasma growth |
title | Nullscript inhibits Cryptosporidium and Toxoplasma growth |
title_full | Nullscript inhibits Cryptosporidium and Toxoplasma growth |
title_fullStr | Nullscript inhibits Cryptosporidium and Toxoplasma growth |
title_full_unstemmed | Nullscript inhibits Cryptosporidium and Toxoplasma growth |
title_short | Nullscript inhibits Cryptosporidium and Toxoplasma growth |
title_sort | nullscript inhibits cryptosporidium and toxoplasma growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593347/ https://www.ncbi.nlm.nih.gov/pubmed/33120250 http://dx.doi.org/10.1016/j.ijpddr.2020.10.004 |
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