H2020Индивидуална стипендия2019–2021

PolyBact · Identifying Chemical Cues in the Polymer-Mediated Engineering of Microorganisms

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период
2019-02-01 → 2021-08-01
Финансиране от ЕС
195 455 €
Участници
1
Схема
MSCA-IF-EF-ST

Линиите свързват координатора с партньорите.

Накратко на български

Взаимодействието между полимери и бактерии, като например Vibrio cholerae, се анализира, за да се разбере как химичните сигнали променят поведението на микрооргамите. Това помага при предотвратяването на инфекции и повреди в индустрията, както и при създаването на полезни химикали.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Identifying Chemical Cues in the Polymer-Mediated Engineering of Microorganisms

Understanding and controlling the interaction of polymers and microorganisms such as bacteria is of critical importance because the binding of microorganisms to polymers and surfaces has major consequences in healthcare, biotechnology and industry. On one hand, we need to understand how to inhibit adhesion and thus prevent unwanted fouling of surfaces, which results in infection, or in damage to industrial equipment. On the other hand, biofilms provide a unique platform for biocatalysis, where bacteria make chemicals for a variety of purposes. This way the toughness and resistance of biofilms to external damage is exploited to prepare high end value products. An underlying limitation that is compromising the development of polymers for these applications, is our lack of understanding of how these materials are affecting microbial physiology. Whilst we have a basic understanding of what chemistries need to be used for each application, for example to induce cell death, or inhibit the adhesion to host or surfaces, little is known about how bacteria respond and adapt to the presence of these polymers: we do not know how complex chemical and physical cues affect downstream cellular signalling following interaction with these materials, to affect phenotypical changes such as biofilm production or virulence factor expression. As a consequence, many candidate polymers are not translated to application because eventually they do not induce the expected effect. Therefore, the overall objectives of the project was to identify the roles of different types of polymer-bacteria interactions in bacterial behaviour. To this end, we synthesized a series of polymers bearing different functionalities and, using Vibrio cholerae as a model organism, explored the responses of bacteria to these nanomaterials. We discovered that cationic and hydrophobic functionalities were able to induce formation of cell clusters whereas polymers containing sugars demonstrated only short-lived interaction with cells and did not form stable clusters. Then we found that cationic polymers with high charge density and hydrophobic polymers induced biofilm formation, this effect was dependent on pH and polymer concentration. A decrease in biofilm production was observed only for polymers showing high cytotoxicity. At the same time, none of the tested polymers had significant effect on cholera toxin production.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Here, we will identify how polymer chemistry and composition affects the microbiology of a model pathogen, Vibrio cholerae. To this end, we will explore the chemical space that mediates bacterial adhesion because this bacteria activates complex signaling networks that regulate its physiology following binding to surfaces and hosts.Three main research objectives are:a) To identify what is the role of charge: Electrostatic interactions are critical in the initial attachment of bacteria to hosts and surfaces. Here we will explore how cationic polymers with different degrees of protonation under model conditions affect the behaviour of V. choleraeb) To identify what is the role of hydrophobicity: Early stages of adhesion to hosts and surfaces are also mediated by hydrophobic interactions. Here, we will evaluate a series of cationic polymers carrying similar degrees of protonation but different hydrophobicities.c) To identify the role of selective binding: We will prepare polymers carrying mannose and N-acetylglucosamine, carbohydrates that are involved in the selective binding of V. cholerae to hosts.To achieve these research objectives, we will use a modular strategy that relies on the controlled synthesis of a poly(acryloyl hydrazide) scaffold, its post-polymerisation functionalisation under aqueous conditions, and the in-situ evaluation of activity using phenotypic and transcriptional assays (Part B, Section 1.1.1). We will focus on identifying how non-toxic polymers affect three critical responses in V. cholerae. 1) Clustering and motility; 2) Biofilm formation and maturation, and 3) Virulence and toxicity against a model of the human gut.The main scientific challenge lies in developing new knowledge of how polymer chemistry affects microbial physiology and behaviour, and this knowledge should underpin the future development of new polymers for antimicrobial therapy and microbial biotechnology, research priorities of the European Commission

Оригинален текст от CORDIS (на английски).

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Данни: CORDIS, © Европейски съюз