Active Infection & Immunity Genetics & Molecular Biology

Functional Genetics Of Capsule Phase Variation In Antibiotic Resistant Bacterial Pathogens

In plain English

AI plain-English summary

Some of the most dangerous antibiotic-resistant bacteria, including *Klebsiella pneumoniae*, carry a sugar coat that they can switch on and off like a light, allowing them to evade the immune system in the bloodstream one moment and then colonise the gut or pick up new resistance genes the next. This genetic trick—called phase variation—has been a blind spot in our understanding of how superbugs cause disease. Researchers have long known that the capsule helps bacteria survive inside the body, but it also blocks them from sticking to surfaces or taking up foreign DNA. The discovery of a reversible ON/OFF switch explains how the same pathogen can do both. This project will map the genetic controls of that switch in over 1,000 clinical samples, then test how it affects immune evasion, bacterial fitness in live animals, and the evolution of new resistance. Later, the work will extend to *E. coli* and *Acinetobacter baumannii*. If successful, this fundamental science could reveal conserved weaknesses in how multiple superbugs regulate their defences. That knowledge might eventually lead to drugs that lock the capsule in the OFF position, preventing severe infections while leaving bacteria vulnerable to antibiotics and the immune system—slowing the spread of resistance without needing new antibiotics.

View original technical description
Capsular polysaccharides are major virulence factors and therapeutic targets in antibiotic-resistant (AMR) bacterial pathogens such as Klebsiella pneumoniae (Kp). While capsules are known to inhibit phagocytosis and complement-mediated lysis, they also impede epithelial colonisation and uptake of foreign DNA, raising the question: ‘how do encapsulated pathogens colonise the host, acquire AMR, and cause severe infections?’. I have identified an ON/OFF genetic switch of Kp capsule expression, driving a reversible ‘phase variation’ between systemic immune evasion, and colonisation/AMR acquisition. I show this mechanism is conserved in Kp and present in multiple additional AMR pathogens. Thus, I have established a prototype system to study the role of capsule phase variation in AMR pathogen biology. Here, we will characterise genetic determinants of capsule phase variation rate in Kp using comparative genomics of ~1000 clinical isolates, and in vitro assays with representative strains. We will define the role of capsule phase variation in immune evasion, bacterial population fitness in vivo, and the evolution of antibiotic resistance. In later years, we will extend this vision to the two additional AMR pathogens Escherichia coli and Acinetobacter baumannii, identifying conserved mechanisms of virulence regulation which will facilitate development of novel therapeutics and slow the spread of AMR.

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Researchers

Joseph Wanford (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Untangling gene regulatory networks controlling host-pathogen interactions of the antimicrobial-resistant human pathogen Klebsiella pneumoniae
Comparing the evolution and virulence of the carbapenem resistant Klebsiella pneumoniae (CRKP) clones and their plasmids in Europe and China
Investigating the epigenetic regulation of pneumococcal virulence
Klebsiella, phages and the capsule: what's going on?
Campylobacter phase variation and its impact on immunity and vaccine development.

Original classification

Career Development Award

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