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Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae
Macrolide resistant Streptococcus pneumoniae infections have limited treatment options. While some resistance mechanisms are well established, ample understanding is limited by incomplete genome annotation (hypothetical genes). Some hypothetical genes encode a domain of unknown function (DUF), a con...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563660/ https://www.ncbi.nlm.nih.gov/pubmed/31223208 http://dx.doi.org/10.6026/97320630014488 |
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author | Goad, Blue Harris, Laura K |
author_facet | Goad, Blue Harris, Laura K |
author_sort | Goad, Blue |
collection | PubMed |
description | Macrolide resistant Streptococcus pneumoniae infections have limited treatment options. While some resistance mechanisms are well established, ample understanding is limited by incomplete genome annotation (hypothetical genes). Some hypothetical genes encode a domain of unknown function (DUF), a conserved protein domain with uncharacterized function. Here, we identify and confirm macrolide resistance genes. We further explore DUFs from macrolide resistance hypothetical genes to prioritize them for experimental characterization. We found gene similarities between two macrolide resistance gene signatures from untreated and either erythromycin- or spiramycin-treated resistant Streptococcus pneumoniae. We confirmed the association of these gene sets with macrolide resistance through comparison to gene signatures from (i) second erythromycin resistant Streptococcus pneumoniae strain, and (ii) erythromycin-treated sensitive Streptococcus pneumoniae strain, both from non-overlapping datasets. Examination into which cellular processes these macrolide resistance genes belong found connections to known resistance mechanisms such as increased amino acid biosynthesis and efflux genes, and decreased ribonucleotide biosynthesis genes, highlighting the predictive ability of the method used. 22 genes had hypothetical annotation with 10 DUFs associated with macrolide resistance. DUF characterization could uncover novel co-therapies that restore macrolide efficacy across multiple macrolide resistant species. Application of the methods to other antibiotic resistances could revolutionize treatment of resistant infections |
format | Online Article Text |
id | pubmed-6563660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-65636602019-06-20 Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae Goad, Blue Harris, Laura K Bioinformation Hypothesis Macrolide resistant Streptococcus pneumoniae infections have limited treatment options. While some resistance mechanisms are well established, ample understanding is limited by incomplete genome annotation (hypothetical genes). Some hypothetical genes encode a domain of unknown function (DUF), a conserved protein domain with uncharacterized function. Here, we identify and confirm macrolide resistance genes. We further explore DUFs from macrolide resistance hypothetical genes to prioritize them for experimental characterization. We found gene similarities between two macrolide resistance gene signatures from untreated and either erythromycin- or spiramycin-treated resistant Streptococcus pneumoniae. We confirmed the association of these gene sets with macrolide resistance through comparison to gene signatures from (i) second erythromycin resistant Streptococcus pneumoniae strain, and (ii) erythromycin-treated sensitive Streptococcus pneumoniae strain, both from non-overlapping datasets. Examination into which cellular processes these macrolide resistance genes belong found connections to known resistance mechanisms such as increased amino acid biosynthesis and efflux genes, and decreased ribonucleotide biosynthesis genes, highlighting the predictive ability of the method used. 22 genes had hypothetical annotation with 10 DUFs associated with macrolide resistance. DUF characterization could uncover novel co-therapies that restore macrolide efficacy across multiple macrolide resistant species. Application of the methods to other antibiotic resistances could revolutionize treatment of resistant infections Biomedical Informatics 2018-12-09 /pmc/articles/PMC6563660/ /pubmed/31223208 http://dx.doi.org/10.6026/97320630014488 Text en © 2018 Biomedical Informatics http://creativecommons.org/licenses/by/3.0/ This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License. |
spellingShingle | Hypothesis Goad, Blue Harris, Laura K Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae |
title | Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae |
title_full | Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae |
title_fullStr | Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae |
title_full_unstemmed | Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae |
title_short | Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae |
title_sort | identification and prioritization of macrolideresistance genes with hypothetical annotation instreptococcus pneumoniae |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563660/ https://www.ncbi.nlm.nih.gov/pubmed/31223208 http://dx.doi.org/10.6026/97320630014488 |
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