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Secrets of Burkholderia thailandensis Revealed

Discover how a bacterium's genes help it thrive in changing environments.

Lillian C. Lowrey, Katlyn B. Mote, Peggy A. Cotter

― 6 min read


Bacterium's Genetic Bacterium's Genetic Tricks Uncovered Burkholderia thailandensis. Learn how genes drive biofilm growth in
Table of Contents

Burkholderia thailandensis is a type of bacterium that likes to live in warm, tropical places like Northern Australia and parts of Southeast Asia. It can thrive in wet environments like rice fields and needs to adapt to changing conditions while competing with other tiny organisms for resources.

Like many living beings, this bacterium has bits of DNA called insertion sequences and transposons scattered throughout its genetic material. These are basically genetic hitchhikers that can jump around and cause changes in the organism. One interesting version of this bacterium, known as strain E264, has two nearly identical jumping genes that affect a specific large piece of its DNA, which is 208.6 kilobases long.

The 208.6 kb Region

This special chunk of DNA is crucial for the bacterium’s ability to have different traits. It can create copies of itself, leading to variations in the bacterium’s ability to form slimy clumps known as Biofilms. So, some cells might have duplicates of this region, while others might not.

The presence of these duplicates can clearly change how the bacteria behave. For instance, bacteria with duplicate copies of this DNA can form biofilms faster than those without them. This means that in certain environments, the Dup+ bacteria thrive better, while Dup- bacteria might do well in other situations.

Biofilms: What Are They?

Biofilms are like a sticky party for bacteria. They attach to surfaces and form a protective layer, which helps them survive in tough conditions. Imagine a bunch of tiny people throwing a house party – they stick together, don’t leave, and can even fend off stuff that might try to harm them, like antibiotics.

For Burkholderia thailandensis, being able to quickly form these biofilms is super important because it allows them to grab onto surfaces and gather resources effectively. The Dup+ bacteria can make visible biofilms in just 24 hours, while the others take much longer to do the same. This ability gives the Dup+ cells a competitive edge in certain situations, while Dup- cells excel in open water where they don’t stick together as much.

Searching for the Secret Sauce

To figure out which genes in the 208.6 kb region are the real powerhouses behind this efficient biofilm formation, scientists divided this section of DNA into smaller parts. They wanted to see which of these sections helped the bacteria grow into robust biofilms. After a lot of trial and error, they found that duplicating a specific subregion, called subregion 4, allowed the bacteria to form these biofilms efficiently.

Subregion 4 contains 14 different protein-coding genes. Some of these are involved in creating structures called pili, which help bacteria stick to surfaces. Others are linked to regulatory systems that help the bacteria respond to their environment. By playing around with these genes, researchers could determine which ones were key to enhancing biofilm growth.

The Star Players

The team discovered that three genes from subregion 4 stood out: aplFABCDE, iou, and bubSR. Each had its role, but aplFABCDE and bubSR were especially important. When they deleted these genes, the bacteria struggled to form biofilms.

So, what does this mean? Well, with aplFABCDE and bubSR present in duplicate copies, the bacteria could grow efficient biofilms. But if they only had iou, the magic just wasn’t there.

Dynamic Biofilm Formation

To make sure the bacteria were really using their genes to form biofilms, the scientists used some clever techniques. They created “reporter strains” that shimmered under certain conditions, making it easier to see which bacteria had duplicated their DNA. These reporter strains helped in understanding how well each genetic combination worked for biofilm formation.

The researchers noticed that the Dup+ bacteria were better at sticking together in biofilms, while Dup- cells weren’t as great at it. This supports the idea that duplicating specific genes gives the bacteria some serious competitive advantages when it comes to living in a biofilm.

Bacteria's Secret Tactics

One of the fascinating ideas that emerged was the notion of “bet-hedging.” This is like a backup plan, where the bacteria create a mixed bag of cells to survive in environments that can change quickly. So, by producing some Dup+ and some Dup- cells, Burkholderia thailandensis can adapt to whatever comes its way!

If conditions shift rapidly, having both types in the population could mean that at least some bacteria survive. It’s like throwing a party with all sorts of snacks – if one kind goes bad, you still have other options to munch on.

BubSR: The Unsung Hero

The scientists went deeper into the mystery of the bubSR gene pair. It seems that this pair helps control how well the bacteria can form those sticky biofilms. BubSR is part of a two-component regulatory system which acts like a switch, turning on or off certain genes in response to environmental changes.

BubSR needs to work correctly for the efficient biofilm formation process. If it’s not functioning well, the bacteria will have a harder time getting their sticky biofilm game on. When another experiment showed that bacteria with disabled bubSR couldn’t form biofilms, it confirmed just how important this gene pair is.

The Role of Promoters

Another part of the story revolves around something called promoters, which help turn genes on. The research identified a promoter in the DNA sequence before the aplFABCDE gene. When this part was active, it caused the bacteria to produce the proteins needed to build biofilms.

With the promoter in full swing, the bacterium can ramp up production of the necessary materials for biofilm formation. The researchers found out that even when conditions were not perfect, if the bacteria had that promoter and the bubSR genes, they could still manage to form biofilms effectively.

Conclusion: The Takeaway

In summary, Burkholderia thailandensis uses an interesting mix of genetics to adapt to its environment. With the help of specific genes, it can change how it behaves, especially in forming biofilms. Thanks to the concept of duplication, bet-hedging, and the regulatory roles of specific genes, this bacterium shows how cleverly nature can work.

So, the next time you see a slimy spot on your kitchen counter, remember Burkholderia thailandensis and its clever ways of sticking around! It’s not just about survival; it’s about thriving in a world full of challenges. Just like us, these tiny organisms have their own strategies to tackle life’s ups and downs, proving yet again that nature is both smart and resourceful.

Original Source

Title: DNA duplication-mediated activation of a two-component regulatory system serves as a bet-hedging strategy for Burkholderia thailandensis

Abstract: Burkholderia thailandensis strain E264 (BtE264) and close relatives stochastically duplicate a 208.6 kb region of chromosome I via RecA-dependent recombination between two nearly identical insertion sequence elements. Because homologous recombination occurs at a constant, low level, populations of BtE264 are always heterogeneous, but cells containing two or more copies of the region (Dup+) have an advantage, and hence predominate, during biofilm growth, while those with a single copy (Dup-) are favored during planktonic growth. Moreover, only Dup+ bacteria form efficient biofilms within 24 hours in liquid medium. We determined that duplicate copies of a subregion containing genes encoding an archaic chaperone-usher pilus (aplFABCDE) and a two-component regulatory system (bubSR) are necessary and sufficient for generating efficient biofilms and for conferring a selective advantage during biofilm growth. BubSR functionality is required, as deletion of either bubS or bubR, or a mutation predicted to abrogate phosphorylation of BubR, abrogates biofilm formation. However, duplicate copies of the aplFABCDE genes are not required. Instead, we found that BubSR controls expression of aplFABCDE and bubSR by activating a promoter upstream of aplF during biofilm growth or when the 208.6 kb region, or just bubSR, are duplicated. Single cell analyses showed that duplication of the 208.6 kb region is sufficient to activate BubSR in 75% of bacteria during planktonic (BubSR OFF) growth conditions. Together, our data indicate that the combination of deterministic two-component signal transduction and stochastic, duplication-mediated activation of that TCS form a bet-hedging strategy that allows BtE264 to survive when conditions shift rapidly from those favoring planktonic growth to those requiring biofilm formation, such as may be encountered in the soils of Southeast Asia and Northern Australia. Our data highlight the positive impact that transposable elements can have on the evolution of bacterial populations. Author summaryTransposable elements naturally accumulate within genomes in all kingdoms of life. When present in the same orientation, a pair of homologous elements can act as substrates for DNA recombination reactions that can duplicate and delete intervening sequences - giving rise to genetically heterogenous populations. We showed here that Burkholderia thailandensis strain E264 uses this mechanism to amplify genes encoding a two-component regulatory system and an archaic chaperone usher pilus, priming the cells for rapid biofilm formation. The formation of a small subpopulation of biofilm-ready bacteria serves as a bet- hedging strategy, ensuring overall population survival should conditions change rapidly from those in which planktonic growth is optimal to those in which adherence and biofilm formation is required.

Authors: Lillian C. Lowrey, Katlyn B. Mote, Peggy A. Cotter

Last Update: 2024-12-09 00:00:00

Language: English

Source URL: https://www.biorxiv.org/content/10.1101/2024.12.09.627470

Source PDF: https://www.biorxiv.org/content/10.1101/2024.12.09.627470.full.pdf

Licence: https://creativecommons.org/licenses/by/4.0/

Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.

Thank you to biorxiv for use of its open access interoperability.

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