Related Experiment Video
Updated: Aug 19, 2026

Quantifying Yersinia pseudotuberculosis Type III Secretion System Activity Following Iron Starvation and Anaerobic Growth
Published on: May 31, 2024
Global gene expression profile of Yersinia pestis induced by streptomycin
Jingfu Qiu1, Dongsheng Zhou, Yanping Han
1Laboratory of Analytical Microbiology, National Center for Biomedical Analysis, Army Center for Microbial Detection and Research, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences (AMMS), Beijing 100071, China.
Abstract:
Plague, caused by Yersinia pestis, is one of the most dangerous diseases that impressed a horror onto human consciousness that persists to this day. Cases of plague can be normally controlled by timely antibiotic administration. Streptomycin is the first-line antibiotic for plague treatment. In this study, a DNA microarray was used to investigate the changes in the gene expression profile of Y. pestis upon exposure to streptomycin. A total of 345 genes were identified to be differentially regulated, 144 of which were up-regulated, and 201 down-regulated. Streptomycin-induced transcriptional changes occurred in genes responsible for heat shock response, drug/analogue sensitivity, biosynthesis of the branched-chain amino acids, chemotaxis and mobility and broad regulatory functions. A wide set of genes involved in energy metabolism, biosynthesis of small macromolecules, synthesis and modification of macromolecules and degradation of small and macro molecules were among those down-regulated. The results reveal general changes in gene expression that are consistent with known mechanisms of action of streptomycin and many new genes that are likely to play important roles in the response to streptomycin treatment, providing useful candidates for investigating the specific mechanisms of streptomycin action.
Insights
This study used DNA microarrays to analyze gene expression changes in Yersinia pestis when treated with streptomycin, revealing 345 differentially regulated genes. These findings offer new insights into streptomycin
Area of Science:
- Microbiology
- Genomics
- Pharmacology
Background:
- Plague, caused by Yersinia pestis, remains a significant threat.
- Timely antibiotic treatment, primarily streptomycin, is crucial for managing plague.
- Understanding Y. pestis's response to streptomycin is vital for effective treatment.
Purpose of the Study:
- To investigate gene expression profile changes in Y. pestis upon streptomycin exposure.
- To identify genes involved in the bacterium's response to streptomycin.
- To uncover potential mechanisms of streptomycin action.
Main Methods:
- Utilized DNA microarray technology to analyze Y. pestis gene expression.
- Quantified differential gene regulation following streptomycin treatment.
- Identified up-regulated and down-regulated genes.
Main Results:
- Identified 345 differentially regulated genes (144 up, 201 down).
- Observed streptomycin-induced changes in heat shock, drug sensitivity, amino acid biosynthesis, chemotaxis, and regulatory functions.
- Noted down-regulation in genes related to energy metabolism and macromolecule synthesis/degradation.
Conclusions:
- Results align with known streptomycin mechanisms and reveal novel responses.
- Identified new candidate genes for studying streptomycin's specific action.
- Provides a foundation for further research into Y. pestis streptomycin resistance and efficacy.
More Related Videos
10:18A Fast and Reliable Pipeline for Bacterial Transcriptome Analysis Case study: Serine-dependent Gene Regulation in Streptococcus pneumoniae
Published on: April 25, 2015
12:23Analysis of Yersinia enterocolitica Effector Translocation into Host Cells Using Beta-lactamase Effector Fusions
Published on: October 13, 2015
Related Concept Videos
Stringent Response in E. coli
Plague
Inhibitors of Bacterial Protein Synthesis
Coordination of Gene Expression Processes in Bacteria
Gene Regulation in Microbial Communities: Quorum Sensing
Gene Regulation During Sporulation