TY - JOUR
T1 - Transcriptome analysis of Escherichia coli K1 after therapy with hesperidin conjugated with silver nanoparticles
AU - Masri, Abdulkader
AU - Khan, Naveed Ahmed
AU - Zoqratt, Muhammad Zarul Hanifah Md
AU - Ayub, Qasim
AU - Anwar, Ayaz
AU - Rao, Komal
AU - Shah, Muhammad Raza
AU - Siddiqui, Ruqaiyyah
N1 - Funding Information:
This work was supported by the Sunway University, Malaysia, and the American University of Sharjah, United Arab Emirates.
Funding Information:
This work was supported by Sunway University GRTIN-RSF-SST-DBS-04-2020, and FRGS Malaysia FRGS/1/2018/SKK08/SYUC/01/2. FRGS helped in collection and interpretation of the data, whereas, GRTIN helped in the payment of APC.
Publisher Copyright:
© 2021, The Author(s).
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/2/17
Y1 - 2021/2/17
N2 - Backgrounds: Escherichia coli K1 causes neonatal meningitis. Transcriptome studies are indispensable to comprehend the pathology and biology of these bacteria. Recently, we showed that nanoparticles loaded with Hesperidin are potential novel antibacterial agents against E. coli K1. Here, bacteria were treated with and without Hesperidin conjugated with silver nanoparticles, and silver alone, and 50% minimum inhibitory concentration was determined. Differential gene expression analysis using RNA-seq, was performed using Degust software and a set of genes involved in cell stress response and metabolism were selected for the study. Results: 50% minimum inhibitory concentration with silver-conjugated Hesperidin was achieved with 0.5 μg/ml of Hesperidin conjugated with silver nanoparticles at 1 h. Differential genetic analysis revealed the expression of 122 genes (≥ 2-log FC, P< 0.01) in both E. coli K1 treated with Hesperidin conjugated silver nanoparticles and E. coli K1 treated with silver alone, compared to untreated E. coli K1. Of note, the expression levels of cation efflux genes (cusA and copA) and translocation of ions, across the membrane genes (rsxB) were found to increase 2.6, 3.1, and 3.3- log FC, respectively. Significant regulation was observed for metabolic genes and several genes involved in the coordination of flagella. Conclusions: The antibacterial mechanism of nanoparticles maybe due to disruption of the cell membrane, oxidative stress, and metabolism in E. coli K1. Further studies will lead to a better understanding of the genetic mechanisms underlying treatment with nanoparticles and identification of much needed novel antimicrobial drug candidates.
AB - Backgrounds: Escherichia coli K1 causes neonatal meningitis. Transcriptome studies are indispensable to comprehend the pathology and biology of these bacteria. Recently, we showed that nanoparticles loaded with Hesperidin are potential novel antibacterial agents against E. coli K1. Here, bacteria were treated with and without Hesperidin conjugated with silver nanoparticles, and silver alone, and 50% minimum inhibitory concentration was determined. Differential gene expression analysis using RNA-seq, was performed using Degust software and a set of genes involved in cell stress response and metabolism were selected for the study. Results: 50% minimum inhibitory concentration with silver-conjugated Hesperidin was achieved with 0.5 μg/ml of Hesperidin conjugated with silver nanoparticles at 1 h. Differential genetic analysis revealed the expression of 122 genes (≥ 2-log FC, P< 0.01) in both E. coli K1 treated with Hesperidin conjugated silver nanoparticles and E. coli K1 treated with silver alone, compared to untreated E. coli K1. Of note, the expression levels of cation efflux genes (cusA and copA) and translocation of ions, across the membrane genes (rsxB) were found to increase 2.6, 3.1, and 3.3- log FC, respectively. Significant regulation was observed for metabolic genes and several genes involved in the coordination of flagella. Conclusions: The antibacterial mechanism of nanoparticles maybe due to disruption of the cell membrane, oxidative stress, and metabolism in E. coli K1. Further studies will lead to a better understanding of the genetic mechanisms underlying treatment with nanoparticles and identification of much needed novel antimicrobial drug candidates.
KW - E. coli K1
KW - Gene expression
KW - Hesperidin
KW - Silver nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=85100999277&partnerID=8YFLogxK
U2 - 10.1186/s12866-021-02097-2
DO - 10.1186/s12866-021-02097-2
M3 - Article
C2 - 33596837
AN - SCOPUS:85100999277
SN - 1471-2180
VL - 21
JO - BMC Microbiology
JF - BMC Microbiology
IS - 1
M1 - 51
ER -