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Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets
Streptococcus sanguinis is a primary colonizer of teeth and is associated with oral health. When it enters the bloodstream, however, this bacterium may cause the serious illness infective endocarditis. The genes required for survival and proliferation in blood have not been identified. The products...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055731/ https://www.ncbi.nlm.nih.gov/pubmed/33084151 http://dx.doi.org/10.1111/mmi.14629 |
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author | Zhu, Bin Green, Shannon P. Ge, Xiuchun Puccio, Tanya Nadhem, Haider Ge, Henry Bao, Liang Kitten, Todd Xu, Ping |
author_facet | Zhu, Bin Green, Shannon P. Ge, Xiuchun Puccio, Tanya Nadhem, Haider Ge, Henry Bao, Liang Kitten, Todd Xu, Ping |
author_sort | Zhu, Bin |
collection | PubMed |
description | Streptococcus sanguinis is a primary colonizer of teeth and is associated with oral health. When it enters the bloodstream, however, this bacterium may cause the serious illness infective endocarditis. The genes required for survival and proliferation in blood have not been identified. The products of these genes could provide a rich source of targets for endocarditis‐specific antibiotics possessing greater efficacy for endocarditis, and also little or no activity against those bacteria that remain in the mouth. We previously created a comprehensive library of S. sanguinis mutants lacking every nonessential gene. We have now screened each member of this library for growth in human serum and discovered 178 mutants with significant abundance changes. The main biological functions disrupted in these mutants, including purine metabolism, were highlighted via network analysis. The components of an ECF‐family transporter were required for growth in serum and were shown for the first time in any bacterium to be essential for endocarditis virulence. We also identified two mutants whose growth was reduced in serum but not in saliva. This strategy promises to enable selective targeting of bacteria based on their location in the body, in this instance, treating or preventing endocarditis while leaving the oral microbiome intact. |
format | Online Article Text |
id | pubmed-8055731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80557312021-07-02 Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets Zhu, Bin Green, Shannon P. Ge, Xiuchun Puccio, Tanya Nadhem, Haider Ge, Henry Bao, Liang Kitten, Todd Xu, Ping Mol Microbiol Research Articles Streptococcus sanguinis is a primary colonizer of teeth and is associated with oral health. When it enters the bloodstream, however, this bacterium may cause the serious illness infective endocarditis. The genes required for survival and proliferation in blood have not been identified. The products of these genes could provide a rich source of targets for endocarditis‐specific antibiotics possessing greater efficacy for endocarditis, and also little or no activity against those bacteria that remain in the mouth. We previously created a comprehensive library of S. sanguinis mutants lacking every nonessential gene. We have now screened each member of this library for growth in human serum and discovered 178 mutants with significant abundance changes. The main biological functions disrupted in these mutants, including purine metabolism, were highlighted via network analysis. The components of an ECF‐family transporter were required for growth in serum and were shown for the first time in any bacterium to be essential for endocarditis virulence. We also identified two mutants whose growth was reduced in serum but not in saliva. This strategy promises to enable selective targeting of bacteria based on their location in the body, in this instance, treating or preventing endocarditis while leaving the oral microbiome intact. John Wiley and Sons Inc. 2020-11-30 2021-04 /pmc/articles/PMC8055731/ /pubmed/33084151 http://dx.doi.org/10.1111/mmi.14629 Text en © 2020 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Zhu, Bin Green, Shannon P. Ge, Xiuchun Puccio, Tanya Nadhem, Haider Ge, Henry Bao, Liang Kitten, Todd Xu, Ping Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets |
title | Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets |
title_full | Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets |
title_fullStr | Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets |
title_full_unstemmed | Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets |
title_short | Genome‐wide identification of Streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets |
title_sort | genome‐wide identification of streptococcus sanguinis fitness genes in human serum and discovery of potential selective drug targets |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055731/ https://www.ncbi.nlm.nih.gov/pubmed/33084151 http://dx.doi.org/10.1111/mmi.14629 |
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