Gene Regulation in Biofilms

A special issue of Pathogens (ISSN 2076-0817).

Deadline for manuscript submissions: closed (31 March 2021) | Viewed by 16226

Special Issue Editor


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Guest Editor
Illinois State University School of Biological Sciences PO Box 4120 Normal, IL 61790
Interests: Biofilm formation; Redox Biology; Oxidative Stress; Thiols; Sulfur; Iron-sulfur cluster; Polyphosphate; Pseudomonas aeruginosa; uropathogenic E. coli; Gram-negative Bacteria; Reactive Oxygen Species; Virulence factors; Antibiotic Resistance; Bacterial Pathogenicity; Bacterial Stress Response

Special Issue Information

Dear Colleagues,

For a long time, bacteria have only been considered to live a planktonic lifestyle as floating or actively swimming single organisms. Over the past five decades, however, it has become increasingly clear that many bacteria can live in multicellular communities, e.g., through the formation of stress-resistant biofilms. Biofilm formation is a tightly regulated process found both in Gram-negative and Gram-positive bacteria that involves several steps: (i) attachment of planktonic bacteria to biotic or abiotic surfaces; (ii) microcolony formation through replication and cell-to-cell adhesion; (iii) development into highly organized mature biofilms embedded in an extracellular polymeric matrix; and (iv) dispersal of biofilm cells by switching to the planktonic state. In comparison with their planktonic counterparts, biofilm cells have been shown to have significantly better protection from the host immune response and up to 1000-fold less susceptibility to various antimicrobial agents due to their reduced metabolic rates, differential expression of efflux pumps, the presence of a self-produced extracellular polymeric matrix, and reduced uptake/increased sequestration of antimicrobial compounds. Hence, the ability of bacteria to form stress-resistant biofilms represents an exceptional adaption strategy for their survival in hostile environments, including human hosts. The biofilm lifestyle of many pathogens is currently recognized as the underlying cause for many difficult-to-treat persistent infections and represents a major challenge in hospital settings. To accomplish the exceptionally complex differentiation of planktonic bacteria into biofilm communities in a highly concerted fashion, bacteria employ numerous sophisticated regulatory mechanisms involving finely altered gene expression. A near-ubiquitous second messenger that coordinates diverse aspects of bacterial growth and behavior, including motility, virulence, and the transition of planktonic to biofilm lifestyle, is c-di-GMP. Elevated levels of c-di-GMP result in increased production of extracellular matrix components, adhesive pili, non-fimbrial adhesins, extracellular DNA, and other biofilm-associated characteristics such as impaired motility. Quorum sensing regulates cell density and induces changes in gene expression depending on the availability of signaling molecules and small non-coding RNAs. RNA-binding proteins, toxin-antitoxin systems, and riboswitches represent additional regulatory mechanisms that are known to be involved in biofilm regulation.

This Special Issue in Pathogens on “Gene Regulation in Biofilms” will focus on the latest state-of-art developments and current knowledge in the field of gene regulation in bacterial biofilms, both in vitro and in vivo. We invite authors to submit research or review manuscripts covering these important molecular aspects of biofilm regulation.

Prof. Dr. Jan-Ulrik Dahl
Guest Editor

Manuscript Submission Information

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Keywords

  • bacterial biofilms
  • antimicrobial resistance
  • quorum sensing
  • c-di-GMP
  • sigma factor
  • two-component regulatory systems
  • bacterial stress response
  • pathogen

Published Papers (3 papers)

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Research

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22 pages, 3889 KiB  
Article
Transposon Insertion in the purL Gene Induces Biofilm Depletion in Escherichia coli ATCC 25922
by Virginio Cepas, Victoria Ballén, Yaiza Gabasa, Miriam Ramírez, Yuly López and Sara Mª Soto
Pathogens 2020, 9(9), 774; https://doi.org/10.3390/pathogens9090774 - 22 Sep 2020
Cited by 8 | Viewed by 3148
Abstract
Current Escherichia coli antibiofilm treatments comprise a combination of antibiotics commonly used against planktonic cells, leading to treatment failure. A better understanding of the genes involved in biofilm formation could facilitate the development of efficient and specific new antibiofilm treatments. A total of [...] Read more.
Current Escherichia coli antibiofilm treatments comprise a combination of antibiotics commonly used against planktonic cells, leading to treatment failure. A better understanding of the genes involved in biofilm formation could facilitate the development of efficient and specific new antibiofilm treatments. A total of 2578 E. coli mutants were generated by transposon insertion, of which 536 were analysed in this study. After sequencing, Tn263 mutant, classified as low biofilm-former (LF) compared to the wild-type (wt) strain (ATCC 25922), showed an interruption in the purL gene, involved in the de novo purine biosynthesis pathway. To elucidate the role of purL in biofilm formation, a knockout was generated showing reduced production of curli fibres, leading to an impaired biofilm formation. These conditions were restored by complementation of the strain or addition of exogenous inosine. Proteomic and transcriptional analyses were performed to characterise the differences caused by purL alterations. Thirteen proteins were altered compared to wt. The corresponding genes were analysed by qRT-PCR not only in the Tn263 and wt, but also in clinical strains with different biofilm activity. Overall, this study suggests that purL is essential for biofilm formation in E. coli and can be considered as a potential antibiofilm target. Full article
(This article belongs to the Special Issue Gene Regulation in Biofilms)
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20 pages, 2461 KiB  
Article
CRISPR-cas3 of Salmonella Upregulates Bacterial Biofilm Formation and Virulence to Host Cells by Targeting Quorum-Sensing Systems
by Luqing Cui, Xiangru Wang, Deyu Huang, Yue Zhao, Jiawei Feng, Qirong Lu, Qinqin Pu, Yulian Wang, Guyue Cheng, Min Wu and Menghong Dai
Pathogens 2020, 9(1), 53; https://doi.org/10.3390/pathogens9010053 - 10 Jan 2020
Cited by 47 | Viewed by 7694
Abstract
Salmonella is recognized as one of the most common microbial pathogens worldwide. The bacterium contains the clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated (Cas) systems, providing adaptive immunity against invading foreign nucleic acids. Previous studies suggested that certain bacteria employ the Cas proteins [...] Read more.
Salmonella is recognized as one of the most common microbial pathogens worldwide. The bacterium contains the clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated (Cas) systems, providing adaptive immunity against invading foreign nucleic acids. Previous studies suggested that certain bacteria employ the Cas proteins of CRISPR-Cas systems to target their own genes, which also alters the virulence during invasion of mammals. However, whether CRISPR-Cas systems in Salmonella have similar functions during bacterial invasion of host cells remains unknown. Here, we systematically analyzed the genes that are regulated by Cas3 in a type I-E CRISPR-Cas system and the virulence changes due to the deletion of cas3 in Salmonella enterica serovar Enteritidis. Compared to the cas3 gene wild-type (cas3 WT) Salmonella strain, cas3 deletion upregulated the lsrFGBE genes in lsr (luxS regulated) operon related to quorum sensing (QS) and downregulated biofilm-forming-related genes and Salmonella pathogenicity island 1 (SPI-1) genes related to the type three secretion system (T3SS). Consistently, the biofilm formation ability was downregulated in the cas3 deletion mutant (Δcas3). The bacterial invasive and intracellular capacity of Δcas3 to host cells was also reduced, thereby increasing the survival of infected host cells and live chickens. By the transcriptome-wide screen (RNA-Seq), we found that the cas3 gene impacts a series of genes related to QS, the flagellum, and SPI-1-T3SS system, thereby altering the virulence phenotypes. As QS SPI-1-T3SS and CRISPR-Cas systems are widely distributed in the bacteria kingdom, our findings extend our understanding of virulence regulation and pathogenicity in mammalian hosts for Salmonella and potentially other bacteria. Full article
(This article belongs to the Special Issue Gene Regulation in Biofilms)
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17 pages, 3429 KiB  
Review
Gene Regulation of Biofilm-Associated Functional Amyloids
by Khushal Khambhati, Jaykumar Patel, Vijaylaxmi Saxena, Parvathy A and Neha Jain
Pathogens 2021, 10(4), 490; https://doi.org/10.3390/pathogens10040490 - 19 Apr 2021
Cited by 11 | Viewed by 4739
Abstract
Biofilms are bacterial communities encased in a rigid yet dynamic extracellular matrix. The sociobiology of bacterial communities within a biofilm is astonishing, with environmental factors playing a crucial role in determining the switch from planktonic to a sessile form of life. The mechanism [...] Read more.
Biofilms are bacterial communities encased in a rigid yet dynamic extracellular matrix. The sociobiology of bacterial communities within a biofilm is astonishing, with environmental factors playing a crucial role in determining the switch from planktonic to a sessile form of life. The mechanism of biofilm biogenesis is an intriguingly complex phenomenon governed by the tight regulation of expression of various biofilm-matrix components. One of the major constituents of the biofilm matrix is proteinaceous polymers called amyloids. Since the discovery, the significance of biofilm-associated amyloids in adhesion, aggregation, protection, and infection development has been much appreciated. The amyloid expression and assembly is regulated spatio-temporarily within the bacterial cells to perform a diverse function. This review provides a comprehensive account of the genetic regulation associated with the expression of amyloids in bacteria. The stringent control ensures optimal utilization of amyloid scaffold during biofilm biogenesis. We conclude the review by summarizing environmental factors influencing the expression and regulation of amyloids. Full article
(This article belongs to the Special Issue Gene Regulation in Biofilms)
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