Cargando…
Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae
Streptococcus pneumoniae is one of Gram-positive pathogen that causes invasive pneumococcal disease. Nowadays, many S. pneumoniae strains are resistant to commonly used antibiotics such as β-lactams and macrolides. 3-Acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivatives are known as novel...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691496/ https://www.ncbi.nlm.nih.gov/pubmed/33244098 http://dx.doi.org/10.1038/s41598-020-77694-8 |
_version_ | 1783614302859558912 |
---|---|
author | Lee, Sang-Yeop Lee, Hayoung Yun, Sung Ho Jun, Sangmi Lee, Yujeong Kim, Wooyoung Park, Edmond Changkyun Baek, Joonyoung Kwak, Yoonna Noh, Soojin Seo, Giwan Jang, Soojin Park, Chul Min Kim, Seung Il |
author_facet | Lee, Sang-Yeop Lee, Hayoung Yun, Sung Ho Jun, Sangmi Lee, Yujeong Kim, Wooyoung Park, Edmond Changkyun Baek, Joonyoung Kwak, Yoonna Noh, Soojin Seo, Giwan Jang, Soojin Park, Chul Min Kim, Seung Il |
author_sort | Lee, Sang-Yeop |
collection | PubMed |
description | Streptococcus pneumoniae is one of Gram-positive pathogen that causes invasive pneumococcal disease. Nowadays, many S. pneumoniae strains are resistant to commonly used antibiotics such as β-lactams and macrolides. 3-Acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivatives are known as novel chemicals having anti-pneumococcal activity against S. pneumoniae. The underlying mechanism of the anti-pneumococcal activity of this inhibitor remains unknown. Therefore, we tried to find the anti-pneumococcal mechanism of APDQ230122, one of the APDQ derivatives active against S. pneumoniae. We performed transcriptomic analysis (RNA-Seq) and proteomic analysis (LC–MS/MS analysis) to get differentially expressed genes (DEG) and differentially expressed proteins (DEP) of S. pneumoniae 521 treated with sub-inhibitory concentrations of APDQ230122 and elucidated the comprehensive expression changes of genes and proteins using multi-omics analysis. As a result, genes or proteins of peptidoglycan biosynthesis and DNA replication were significantly down-regulated. Electron microscopy analysis revealed that the structure of peptidoglycan was damaged by APDQ230122 in a chemical concentration-dependent manner. Therefore, we suggest peptidoglycan biosynthesis is a major target of APDQ230122. Multi-omics analysis can provide us useful information to elucidate anti-pneumococcal activity of APDQ230122. |
format | Online Article Text |
id | pubmed-7691496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76914962020-11-27 Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae Lee, Sang-Yeop Lee, Hayoung Yun, Sung Ho Jun, Sangmi Lee, Yujeong Kim, Wooyoung Park, Edmond Changkyun Baek, Joonyoung Kwak, Yoonna Noh, Soojin Seo, Giwan Jang, Soojin Park, Chul Min Kim, Seung Il Sci Rep Article Streptococcus pneumoniae is one of Gram-positive pathogen that causes invasive pneumococcal disease. Nowadays, many S. pneumoniae strains are resistant to commonly used antibiotics such as β-lactams and macrolides. 3-Acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivatives are known as novel chemicals having anti-pneumococcal activity against S. pneumoniae. The underlying mechanism of the anti-pneumococcal activity of this inhibitor remains unknown. Therefore, we tried to find the anti-pneumococcal mechanism of APDQ230122, one of the APDQ derivatives active against S. pneumoniae. We performed transcriptomic analysis (RNA-Seq) and proteomic analysis (LC–MS/MS analysis) to get differentially expressed genes (DEG) and differentially expressed proteins (DEP) of S. pneumoniae 521 treated with sub-inhibitory concentrations of APDQ230122 and elucidated the comprehensive expression changes of genes and proteins using multi-omics analysis. As a result, genes or proteins of peptidoglycan biosynthesis and DNA replication were significantly down-regulated. Electron microscopy analysis revealed that the structure of peptidoglycan was damaged by APDQ230122 in a chemical concentration-dependent manner. Therefore, we suggest peptidoglycan biosynthesis is a major target of APDQ230122. Multi-omics analysis can provide us useful information to elucidate anti-pneumococcal activity of APDQ230122. Nature Publishing Group UK 2020-11-26 /pmc/articles/PMC7691496/ /pubmed/33244098 http://dx.doi.org/10.1038/s41598-020-77694-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Sang-Yeop Lee, Hayoung Yun, Sung Ho Jun, Sangmi Lee, Yujeong Kim, Wooyoung Park, Edmond Changkyun Baek, Joonyoung Kwak, Yoonna Noh, Soojin Seo, Giwan Jang, Soojin Park, Chul Min Kim, Seung Il Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae |
title | Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae |
title_full | Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae |
title_fullStr | Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae |
title_full_unstemmed | Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae |
title_short | Application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (APDQ) derivative against Streptococcus pneumoniae |
title_sort | application of multi-omics technology for the elucidation of anti-pneumococcal activity of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one (apdq) derivative against streptococcus pneumoniae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691496/ https://www.ncbi.nlm.nih.gov/pubmed/33244098 http://dx.doi.org/10.1038/s41598-020-77694-8 |
work_keys_str_mv | AT leesangyeop applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT leehayoung applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT yunsungho applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT junsangmi applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT leeyujeong applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT kimwooyoung applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT parkedmondchangkyun applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT baekjoonyoung applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT kwakyoonna applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT nohsoojin applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT seogiwan applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT jangsoojin applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT parkchulmin applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae AT kimseungil applicationofmultiomicstechnologyfortheelucidationofantipneumococcalactivityof3acyl2phenylamino14dihydroquinolin4oneapdqderivativeagainststreptococcuspneumoniae |