<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bing C</submitter><funding>the Fundamental Research Funds for the Central Universities</funding><funding>the Innovative Experiment Projects of Educational Ministry of China for Undergraduate</funding><pagination>771-782</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11290751</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(9)</volume><pubmed_abstract>&lt;b>Aim:&lt;/b> The response of &lt;i>E. coli&lt;/i> ATCC8739 to Brevinin-2CE (B2CE) was evaluated as a strategy to prevent the development of antimicrobial peptide (AMP)-resistant bacteria. &lt;b>Methods:&lt;/b> Gene expression levels were detected by transcriptome sequencing and RT-PCR. Target genes were knocked out using CRISPR-Cas9. MIC was measured to evaluate strain resistance. &lt;b>Results:&lt;/b> Expression of &lt;i>acrZ&lt;/i> and &lt;i>sugE&lt;/i> were increased with B2CE stimulation. ATCC8739Δ&lt;i>acrZ&lt;/i> and ATCC8739Δ&lt;i>sugE&lt;/i> showed twofold and fourfold increased sensitivity, respectively. The survival rate of ATCC8739 was reduced in the presence of B2CE/chlorpromazine (CPZ). Combinations of other AMPs with CPZ also showed antibacterial effects. &lt;b>Conclusion:&lt;/b> The results indicate that combinations of AMPs/efflux pump inhibitors (EPIs) may be a potential approach to combat resistant bacteria.</pubmed_abstract><journal>Future microbiology</journal><pubmed_title>Efflux pump inhibitor chlorpromazine effectively increases the susceptibility of &lt;i>Escherichia coli&lt;/i> to antimicrobial peptide Brevinin-2CE.</pubmed_title><pmcid>PMC11290751</pmcid><funding_grant_id>GK202302003</funding_grant_id><funding_grant_id>S202310718118</funding_grant_id><pubmed_authors>Mengjuan A</pubmed_authors><pubmed_authors>Zhi L</pubmed_authors><pubmed_authors>Chixin Z</pubmed_authors><pubmed_authors>Bing C</pubmed_authors><pubmed_authors>Yan S</pubmed_authors><pubmed_authors>Xinyu M</pubmed_authors><pubmed_authors>Xinyao T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efflux pump inhibitor chlorpromazine effectively increases the susceptibility of &lt;i>Escherichia coli&lt;/i> to antimicrobial peptide Brevinin-2CE.</name><description>&lt;b>Aim:&lt;/b> The response of &lt;i>E. coli&lt;/i> ATCC8739 to Brevinin-2CE (B2CE) was evaluated as a strategy to prevent the development of antimicrobial peptide (AMP)-resistant bacteria. &lt;b>Methods:&lt;/b> Gene expression levels were detected by transcriptome sequencing and RT-PCR. Target genes were knocked out using CRISPR-Cas9. MIC was measured to evaluate strain resistance. &lt;b>Results:&lt;/b> Expression of &lt;i>acrZ&lt;/i> and &lt;i>sugE&lt;/i> were increased with B2CE stimulation. ATCC8739Δ&lt;i>acrZ&lt;/i> and ATCC8739Δ&lt;i>sugE&lt;/i> showed twofold and fourfold increased sensitivity, respectively. The survival rate of ATCC8739 was reduced in the presence of B2CE/chlorpromazine (CPZ). Combinations of other AMPs with CPZ also showed antibacterial effects. &lt;b>Conclusion:&lt;/b> The results indicate that combinations of AMPs/efflux pump inhibitors (EPIs) may be a potential approach to combat resistant bacteria.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2025-06-27T03:05:33.239Z</modification><creation>2025-06-27T03:05:33.239Z</creation></dates><accession>S-EPMC11290751</accession><cross_references><pubmed>38683168</pubmed><doi>10.2217/fmb-2023-0272</doi></cross_references></HashMap>