Community Research and Development Information Service - CORDIS


ELFBAD Report Summary

Project ID: 670980
Funded under: H2020-EU.1.1.

Periodic Reporting for period 1 - ELFBAD (L-form bacteria, biotechnology and disease)

Reporting period: 2015-10-01 to 2017-03-31

Summary of the context and overall objectives of the project

The peptidoglycan cell wall is a defining structure of the bacteria. It is the target for our best antibiotics and fragments of the wall trigger powerful innate immune responses against infection. The genes for peptidoglycan synthesis are present in most bacterial lineages, suggesting that the wall emerged early in cellular evolution. Surprisingly, many bacteria can switch almost effortlessly into a cell wall deficient “L-form” state in which they become completely resistant to many cell wall active antibiotics. Remarkably, L-form growth is completely independent of the complex FtsZ-based division machine that is essential for proliferation of most bacteria. Proliferation occurs instead by a seemingly haphazard process involving membrane blebbing or tubulation and scission, leading to progeny of highly irregular size. The switch to this mode of proliferation seems to require only the upregulation of membrane synthesis, leading to an increased surface area to volume ratio. L-forms may provide insights into how primitive cells proliferated before the evolution of the cell wall and the ancient bacterial radiation. L-forms have also been implicated in many recurrent or chronic diseases, although these claims have been controversial. The key aims of our project were first, to improve our understanding of key features of the L-forms of our best characterised model system, B. subtilis, including both basic science and possible biotechnological applications. Second to extend our analysis of basic L-from biology into several diverse bacterial systems, of relevance to both biotechnology and infectious disease. Finally, to explore in detail the possible clinical relevance of L-forms, aiming to identify specific clinical situations in which they are relevant or, at least, to establish model systems in which the interactions between L-form and mammalian systems can be studied.

Work performed from the beginning of the project to the end of the period covered by the report and main results achieved so far

The project is proceeding very nicely, with substantial progress against all of the original main objectives.
Our first publication involved completing a line of research initiated during our previous ERC grant. Mercier et al., 2016 (Nature Microbiology 1, 16091) describe how we were able to isolate, for the first time, an E. coli mutant deleted for the normally essential key cell division gene, ftsZ, by starting with L-form cells. We characterised the mutations need to enable bypassing of ftsZ and showed that the basis for mutant survival was through a highly aberrant form of growth which we called “coliflower”. The results show how remarkeably malleable bacterial cell morphology is and how simple in evolutionary terms the emergence of cells such as Mycoplasma, that can proliferate without FtsZ could have arisen.
Our first full research paper relating to work solely from the new grant, described the discovery of an unexpected gene in the cell wall synthesis pathway (Theme 1), and was also published in Nature Microbiology (Emami et al., 2016, Nature Microbiol. 2, 16253).
Our third paper describes a major breakthrough in understanding how antibiotics and lytic enzymes, such as lysozyme, interact during L-form switching. We found that penicillin unexpectedly prevents the L-form switch in B. subtilis and probably a range of other organisms, including important pathogens, such as S. aureus. We then found that this effect can be overcome by treating cells with exogenous lysozyme. Amazingly, the lysozyme can be supplied by mammalian cells, such as macrophages, and again that this applies to both B. subtilis and pathogens. This work impinges on key objectives from all three themes of the original proposal. We sent the paper to Nature and two of three reviewers were favourable but one reviewer and the editor required further experiments in animals or patients, which we are presently working on. We are confident that this paper will be published at a high level before the end of 2017.
A fourth major paper is in preparation relating to Theme 3 of the proposal and addresses the question of L-forms in patients. It is based on detailed analysis of samples from a large cohort of patients suffering from recurrent urinary tract infections, in which we describe detection of compelling evidence for involvement of L-forms. We anticipate sending this also to a high profile journal in the next quarter.
A fifth paper in preparation describes the growth of L-forms in microfluidic channels.
In addition to the research work we have three major reviews either published or in press. First, a major review on the general topic of L-forms (Errington et al., 2016, Phil. Trans. Royal Soc. B 371, 20150494). A second major review focuses on bacterial membranes, incorporating a substantial section on L-forms (Strahl & Errington, 2017, Ann Revs Microbiol., in press). The third review provides a personal perspective on the L-form story (Errington, 2017, Biochem. Soc. Transactions, in press).

Progress beyond the state of the art and expected potential impact (including the socio-economic impact and the wider societal implications of the project so far)

If we can succeed in publishing our latest work on the interaction of lysozyme and beta-lactam antibiotics on L-form biogenesis, and on the identification of L-forms in urinary tract infection patients, we could have a major impact on infectious disease research. We believe that many clinicians will go looking for L-forms in various chronic or recurrent infections, and may be able to find them using the methods we have developed.

We hope to be able to obtain proof of concept funding to develop L-forms for biotechnological applications. This again could have a very broad impact.
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