Effect OF M. koenigii on the expression of cell wall formation related genes (mecA and fmhb)

• Effects of the ethyl acetate leaf extract of murraya koenigii on the expression of cell wall formation related genes ( mecA and fmhb ) was determined. • The exposure of the bacterial cells to the plant extract caused upregulation of the selected genes ( mecA and fmhb ). • This indicates resistance of the bacteria to the treated extract against the selected cell wall formation genes. Generally, quantitative polymerase-chain-reaction technique (qPCR) has been recognized as the gold standard for gene expression analysis. It supersedes the original conventional PCR, due to its ability of measuring the amplification of cDNA in real time as the reaction progresses. The aim of this study was to determine the effects of the ethyl acetate leaf extract of Murraya koenigii ( M. koenigii ) on the expression of cell wall formation related genes ( mecA and fmhb ). Ribonucleic acid (RNA) of the bacterial cells ( Staphylococcus aureus ATCC 700,699) was extracted using Trizol reagent. The concentrations and purities of all RNA analysis were obtained from NanoDrop Spectrophotometer. cDNA Synthesis Kit was used for cDNA synthesis. The integrity of the cDNA was identified using ethidium bromide, through 1.5% agarose gel electrophoresis in 1 x TBE buffer. Finally, quantitative real-time PCR technique was employed to establish and validate the antibacterial activity of the plant extract on gene expression of the selected genes at the cellular level and the quantification of the gene's expression was determined using delta-delta Ct method. The result revealed that the exposure of the bacterial cells to the plant extract instigated upregulation of the selected genes. This indicates resistance of the bacteria to the treated extract against the selected cell wall formation genes These findings suggest that the ethyl acetate leaf extract of M. koenigii lacks potential antibacterial activity on the expression of cell wall formation related genes ( mecA and fmhb ) of S. aureus bacteria.

Authors

Institutions

Publication Details

Journal
Phytomedicine Plus
Published
2025-02-06
DOI
https://doi.org/10.1016/j.phyplu.2025.100757
Primary Topic
Molecular Biology Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Effect OF M. koenigii on the expression of cell wall formation related genes (mecA and fmhb)

Ibrahim Abuga, Mohammad Syaiful Bahari Abdull Rasad, Sulaimon Olayiwola Folam
Phytomedicine Plus
Molecular Biology Techniques and Applications
article

Effect OF M. koenigii on the expression of cell wall formation related genes (mecA and fmhb)

Ibrahim Abuga, Mohammad Syaiful Bahari Abdull Rasad, Sulaimon Olayiwola Folam
article en

Abstract

• Effects of the ethyl acetate leaf extract of murraya koenigii on the expression of cell wall formation related genes ( mecA and fmhb ) was determined. • The exposure of the bacterial cells to the plant extract caused upregulation of the selected genes ( mecA and fmhb ). • This indicates resistance of the bacteria to the treated extract against the selected cell wall formation genes. Generally, quantitative polymerase-chain-reaction technique (qPCR) has been recognized as the gold standard for gene expression analysis. It supersedes the original conventional PCR, due to its ability of measuring the amplification of cDNA in real time as the reaction progresses. The aim of this study was to determine the effects of the ethyl acetate leaf extract of Murraya koenigii ( M. koenigii ) on the expression of cell wall formation related genes ( mecA and fmhb ). Ribonucleic acid (RNA) of the bacterial cells ( Staphylococcus aureus ATCC 700,699) was extracted using Trizol reagent. The concentrations and purities of all RNA analysis were obtained from NanoDrop Spectrophotometer. cDNA Synthesis Kit was used for cDNA synthesis. The integrity of the cDNA was identified using ethidium bromide, through 1.5% agarose gel electrophoresis in 1 x TBE buffer. Finally, quantitative real-time PCR technique was employed to establish and validate the antibacterial activity of the plant extract on gene expression of the selected genes at the cellular level and the quantification of the gene's expression was determined using delta-delta Ct method. The result revealed that the exposure of the bacterial cells to the plant extract instigated upregulation of the selected genes. This indicates resistance of the bacteria to the treated extract against the selected cell wall formation genes These findings suggest that the ethyl acetate leaf extract of M. koenigii lacks potential antibacterial activity on the expression of cell wall formation related genes ( mecA and fmhb ) of S. aureus bacteria.

Phytomedicine PlusVol. 5(2)
International Islamic University Malaysia (MY), Abdullahi Fodio University of Science and Technology (NG), Kwara State University (NG)
Openalex Percentile: Top 98%
Molecular Biology Techniques and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.