Bio-informed synthesis of marine-sourced indole derivatives: suppressing gram-negative bacteria biofilm and virulence.

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Main Authors: Golberg, Karina, Elouarzaki, Kamal, Kagan, Bat-El, Shagan, Marilou, Shemesh, Netta, Kramarsky-Winter, Esti, Ben-Zvi, Anat, Nebenzahl, Yaffa Mizrachi, Marks, Robert S, Kushmaro, Ariel
Format: Artículo científico
Language:en
Published: BMC biology 2025
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author Golberg, Karina
Elouarzaki, Kamal
Kagan, Bat-El
Shagan, Marilou
Shemesh, Netta
Kramarsky-Winter, Esti
Ben-Zvi, Anat
Nebenzahl, Yaffa Mizrachi
Marks, Robert S
Kushmaro, Ariel
author_facet Golberg, Karina
Elouarzaki, Kamal
Kagan, Bat-El
Shagan, Marilou
Shemesh, Netta
Kramarsky-Winter, Esti
Ben-Zvi, Anat
Nebenzahl, Yaffa Mizrachi
Marks, Robert S
Kushmaro, Ariel
Golberg, Karina
Elouarzaki, Kamal
Kagan, Bat-El
Shagan, Marilou
Shemesh, Netta
Kramarsky-Winter, Esti
Ben-Zvi, Anat
Nebenzahl, Yaffa Mizrachi
Marks, Robert S
Kushmaro, Ariel
collection PubMed - marine biology
contents Bio-informed synthesis of marine-sourced indole derivatives: suppressing gram-negative bacteria biofilm and virulence. Golberg, Karina Elouarzaki, Kamal Kagan, Bat-El Shagan, Marilou Shemesh, Netta Kramarsky-Winter, Esti Ben-Zvi, Anat Nebenzahl, Yaffa Mizrachi Marks, Robert S Kushmaro, Ariel Biofilms Indoles Virulence Anti-Bacterial Agents Caenorhabditis elegans Pseudomonas aeruginosa Animals Acinetobacter baumannii Humans Gram-Negative Bacteria Biofilms cling to surfaces to form complex architectures allowing their bacterial creators to acquire multidrug resistance and claiming countless lives worldwide. Therefore, finding novel compounds that affect virulence and biofilm-forming capacity of resistant pathogenic bacteria is imperative. Recently, we identified indole-based compounds that possess anti-biofilm properties in coral-associated bacteria. We succeeded in efficiently synthesizing two of these compounds, 1,1'-bisindole (NN) and 2,3-dihydro-2,2'-bisindole (DIV). They were found to attenuate biofilms of gram-negative bacterial pathogens, including Pseudomonas aeruginosa and Acinetobacter baumannii. Combining these compounds with the antibiotic tobramycin resulted in significant biofilm inhibition, particularly in the eradication of mature P. aeruginosa biofilms. Both of the bisindole derivatives, suppressed a number of bacterial virulence factors, reduced bacterial adhesion, and improved survival rates in infected Caenorhabditis elegans and human lung epithelial cell models. Transcriptome analyses of the bacteria treated with these compounds revealed that NN repressed or upregulated 307 genes when compared to untreated P. aeruginosa. These bacteria-derived molecules act in resistance-quenching and are potentially important candidates for inclusion in treatment protocols. The use of compounds that prevent the biofilm from accumulating the high cell densities critical to its structural and functional maintenance represents significant progress in the management of bacterial persistence. Therefore, a possible clinical implementation of these innovative compounds holds a promising future.
format Artículo científico
id pubmed_40369603
institution PubMed
language en
publishDate 2025
publisher BMC biology
record_format pubmed
spellingShingle Bio-informed synthesis of marine-sourced indole derivatives: suppressing gram-negative bacteria biofilm and virulence.
Golberg, Karina
Elouarzaki, Kamal
Kagan, Bat-El
Shagan, Marilou
Shemesh, Netta
Kramarsky-Winter, Esti
Ben-Zvi, Anat
Nebenzahl, Yaffa Mizrachi
Marks, Robert S
Kushmaro, Ariel
Biofilms
Indoles
Virulence
Anti-Bacterial Agents
Caenorhabditis elegans
Pseudomonas aeruginosa
Animals
Acinetobacter baumannii
Humans
Gram-Negative Bacteria
Bio-informed synthesis of marine-sourced indole derivatives: suppressing gram-negative bacteria biofilm and virulence. Golberg, Karina Elouarzaki, Kamal Kagan, Bat-El Shagan, Marilou Shemesh, Netta Kramarsky-Winter, Esti Ben-Zvi, Anat Nebenzahl, Yaffa Mizrachi Marks, Robert S Kushmaro, Ariel Biofilms Indoles Virulence Anti-Bacterial Agents Caenorhabditis elegans Pseudomonas aeruginosa Animals Acinetobacter baumannii Humans Gram-Negative Bacteria Biofilms cling to surfaces to form complex architectures allowing their bacterial creators to acquire multidrug resistance and claiming countless lives worldwide. Therefore, finding novel compounds that affect virulence and biofilm-forming capacity of resistant pathogenic bacteria is imperative. Recently, we identified indole-based compounds that possess anti-biofilm properties in coral-associated bacteria. We succeeded in efficiently synthesizing two of these compounds, 1,1'-bisindole (NN) and 2,3-dihydro-2,2'-bisindole (DIV). They were found to attenuate biofilms of gram-negative bacterial pathogens, including Pseudomonas aeruginosa and Acinetobacter baumannii. Combining these compounds with the antibiotic tobramycin resulted in significant biofilm inhibition, particularly in the eradication of mature P. aeruginosa biofilms. Both of the bisindole derivatives, suppressed a number of bacterial virulence factors, reduced bacterial adhesion, and improved survival rates in infected Caenorhabditis elegans and human lung epithelial cell models. Transcriptome analyses of the bacteria treated with these compounds revealed that NN repressed or upregulated 307 genes when compared to untreated P. aeruginosa. These bacteria-derived molecules act in resistance-quenching and are potentially important candidates for inclusion in treatment protocols. The use of compounds that prevent the biofilm from accumulating the high cell densities critical to its structural and functional maintenance represents significant progress in the management of bacterial persistence. Therefore, a possible clinical implementation of these innovative compounds holds a promising future.
title Bio-informed synthesis of marine-sourced indole derivatives: suppressing gram-negative bacteria biofilm and virulence.
topic Biofilms
Indoles
Virulence
Anti-Bacterial Agents
Caenorhabditis elegans
Pseudomonas aeruginosa
Animals
Acinetobacter baumannii
Humans
Gram-Negative Bacteria
url https://pubmed.ncbi.nlm.nih.gov/40369603/