Cargando…
A diverse global fungal library for drug discovery
BACKGROUND: Secondary fungal metabolites are important sources for new drugs against infectious diseases and cancers. METHODS: To obtain a library with enough diversity, we collected about 2,395 soil samples and 2,324 plant samples from 36 regions in Africa, Asia, and North America. The collection a...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703384/ https://www.ncbi.nlm.nih.gov/pubmed/33312768 http://dx.doi.org/10.7717/peerj.10392 |
_version_ | 1783616626782896128 |
---|---|
author | Niu, Guodong Annamalai, Thirunavukkarasu Wang, Xiaohong Li, Sheng Munga, Stephen Niu, Guomin Tse-Dinh, Yuk-Ching Li, Jun |
author_facet | Niu, Guodong Annamalai, Thirunavukkarasu Wang, Xiaohong Li, Sheng Munga, Stephen Niu, Guomin Tse-Dinh, Yuk-Ching Li, Jun |
author_sort | Niu, Guodong |
collection | PubMed |
description | BACKGROUND: Secondary fungal metabolites are important sources for new drugs against infectious diseases and cancers. METHODS: To obtain a library with enough diversity, we collected about 2,395 soil samples and 2,324 plant samples from 36 regions in Africa, Asia, and North America. The collection areas covered various climate zones in the world. We examined the usability of the global fungal extract library (GFEL) against parasitic malaria transmission, Gram-positive and negative bacterial pathogens, and leukemia cells. RESULTS: Nearly ten thousand fungal strains were isolated. Sequences of nuclear ribosomal internal transcribed spacer (ITS) from 40 randomly selected strains showed that over 80% were unique. Screening GFEL, we found that the fungal extract from Penicillium thomii was able to block Plasmodium falciparum transmission to Anopheles gambiae, and the fungal extract from Tolypocladium album was able to kill myelogenous leukemia cell line K562. We also identified a set of candidate fungal extracts against bacterial pathogens. |
format | Online Article Text |
id | pubmed-7703384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77033842020-12-10 A diverse global fungal library for drug discovery Niu, Guodong Annamalai, Thirunavukkarasu Wang, Xiaohong Li, Sheng Munga, Stephen Niu, Guomin Tse-Dinh, Yuk-Ching Li, Jun PeerJ Molecular Biology BACKGROUND: Secondary fungal metabolites are important sources for new drugs against infectious diseases and cancers. METHODS: To obtain a library with enough diversity, we collected about 2,395 soil samples and 2,324 plant samples from 36 regions in Africa, Asia, and North America. The collection areas covered various climate zones in the world. We examined the usability of the global fungal extract library (GFEL) against parasitic malaria transmission, Gram-positive and negative bacterial pathogens, and leukemia cells. RESULTS: Nearly ten thousand fungal strains were isolated. Sequences of nuclear ribosomal internal transcribed spacer (ITS) from 40 randomly selected strains showed that over 80% were unique. Screening GFEL, we found that the fungal extract from Penicillium thomii was able to block Plasmodium falciparum transmission to Anopheles gambiae, and the fungal extract from Tolypocladium album was able to kill myelogenous leukemia cell line K562. We also identified a set of candidate fungal extracts against bacterial pathogens. PeerJ Inc. 2020-11-27 /pmc/articles/PMC7703384/ /pubmed/33312768 http://dx.doi.org/10.7717/peerj.10392 Text en ©2020 Niu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Molecular Biology Niu, Guodong Annamalai, Thirunavukkarasu Wang, Xiaohong Li, Sheng Munga, Stephen Niu, Guomin Tse-Dinh, Yuk-Ching Li, Jun A diverse global fungal library for drug discovery |
title | A diverse global fungal library for drug discovery |
title_full | A diverse global fungal library for drug discovery |
title_fullStr | A diverse global fungal library for drug discovery |
title_full_unstemmed | A diverse global fungal library for drug discovery |
title_short | A diverse global fungal library for drug discovery |
title_sort | diverse global fungal library for drug discovery |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703384/ https://www.ncbi.nlm.nih.gov/pubmed/33312768 http://dx.doi.org/10.7717/peerj.10392 |
work_keys_str_mv | AT niuguodong adiverseglobalfungallibraryfordrugdiscovery AT annamalaithirunavukkarasu adiverseglobalfungallibraryfordrugdiscovery AT wangxiaohong adiverseglobalfungallibraryfordrugdiscovery AT lisheng adiverseglobalfungallibraryfordrugdiscovery AT mungastephen adiverseglobalfungallibraryfordrugdiscovery AT niuguomin adiverseglobalfungallibraryfordrugdiscovery AT tsedinhyukching adiverseglobalfungallibraryfordrugdiscovery AT lijun adiverseglobalfungallibraryfordrugdiscovery AT niuguodong diverseglobalfungallibraryfordrugdiscovery AT annamalaithirunavukkarasu diverseglobalfungallibraryfordrugdiscovery AT wangxiaohong diverseglobalfungallibraryfordrugdiscovery AT lisheng diverseglobalfungallibraryfordrugdiscovery AT mungastephen diverseglobalfungallibraryfordrugdiscovery AT niuguomin diverseglobalfungallibraryfordrugdiscovery AT tsedinhyukching diverseglobalfungallibraryfordrugdiscovery AT lijun diverseglobalfungallibraryfordrugdiscovery |