Microbiota Intervention Strategies Limiting Selection and Transmission of Antibiotic Resistance burden in the One Health domain
Lead Research Organisation:
UNIVERSITY OF EXETER
Department Name: Biosciences
Abstract
Antimicrobial resistance (AMR) is a major threat to human health, often described as a slow spreading global pandemic. A key factor in driving AMR is the extensive use of antimicrobial drugs in humans, animals and environment, which leads to selection for resistant bacteria and genes, and facilitates spread of resistant bacteria and AMR genes between the different One Health domains (human, animals and the environment). The MISTAR project aims to reduce AMR levels in environments where AMR infections thrive - hospitals and farms, with the ultimate goal to block the selection and transmission of AMR within different One Health settings. To do so we will develop, test and implement intervention strategies that promote microbiota preservation using a range of different approaches.
Firstly, we will develop gut microbiota-based interventions (fecal microbiota transplantation (FMT) and microbiota-based index at point-of-care) and test their effect in hospitalized patients to reduce AMR. Specifically, we will analyze how FMT modulates the abundance, diversity, and dynamics of AMR genes. In addition, tools for monitoring the AMR carriage at admission to hospital high-risk areas, and for characterizing FMT associated changes as indicators of selection and/or transmission will be developed and validated. This will allow patients to receive tailored interventions including FMT, substantially shorten the time-to-result, preventing inadvertent antibiotic prescription/FMT, and allowing a timely switch to the required targeted antibacterial therapy. Research in this objective will also help us to identify bacterial species in a microbial community that are inversely correlated with the abundance of AMR genes, which can then be tested for their use as potential biotherapeutics to be tested in Objective 3.
Second, we will develop and test the effects of interventions aimed at reducing airborne dust-bound pollution and transmission of AMR, in three different One Health settings (community, farm and hospital) and in three different countries (Brazil, Netherlands, and Spain). Specifically, we will implement the following interventions (i) household air purifiers, (ii) feeding practices in farmed pigs, and (iii) hospital air filtration systems, and test their effect on AMR transmission via air and dust particles. To do so, we will analyze the bioaerosols from hospital air, farm wind-borne dust, gut and nasal microbiota and resistomes of humans, dogs and pigs.
Thirdly, we will develop and test novel experimental intervention strategies to modulate the microbiota to eradicate AMR in gut microbial communities. These approaches are based on the idea that microbial community composition can be altered through competition between different community members. The first intervention uses bacterial antagonists that can outcompete resistant bacteria in a community context, while the second one uses the naturally occurring endonuclease CRISPR-Cas9 as a mobile tool to remove AMR genes from the microbial community. After in vitro validation we will test the efficacy of both interventions in vivo using the insect model Galleria melonella and by a final proof-of-concept experiment using a mouse gut colonization model.
MISTAR delivers key scientific insights, new technical skills and new interventions to help stop the spread of AMR, that can be applied in both high- and low income countries.
Firstly, we will develop gut microbiota-based interventions (fecal microbiota transplantation (FMT) and microbiota-based index at point-of-care) and test their effect in hospitalized patients to reduce AMR. Specifically, we will analyze how FMT modulates the abundance, diversity, and dynamics of AMR genes. In addition, tools for monitoring the AMR carriage at admission to hospital high-risk areas, and for characterizing FMT associated changes as indicators of selection and/or transmission will be developed and validated. This will allow patients to receive tailored interventions including FMT, substantially shorten the time-to-result, preventing inadvertent antibiotic prescription/FMT, and allowing a timely switch to the required targeted antibacterial therapy. Research in this objective will also help us to identify bacterial species in a microbial community that are inversely correlated with the abundance of AMR genes, which can then be tested for their use as potential biotherapeutics to be tested in Objective 3.
Second, we will develop and test the effects of interventions aimed at reducing airborne dust-bound pollution and transmission of AMR, in three different One Health settings (community, farm and hospital) and in three different countries (Brazil, Netherlands, and Spain). Specifically, we will implement the following interventions (i) household air purifiers, (ii) feeding practices in farmed pigs, and (iii) hospital air filtration systems, and test their effect on AMR transmission via air and dust particles. To do so, we will analyze the bioaerosols from hospital air, farm wind-borne dust, gut and nasal microbiota and resistomes of humans, dogs and pigs.
Thirdly, we will develop and test novel experimental intervention strategies to modulate the microbiota to eradicate AMR in gut microbial communities. These approaches are based on the idea that microbial community composition can be altered through competition between different community members. The first intervention uses bacterial antagonists that can outcompete resistant bacteria in a community context, while the second one uses the naturally occurring endonuclease CRISPR-Cas9 as a mobile tool to remove AMR genes from the microbial community. After in vitro validation we will test the efficacy of both interventions in vivo using the insect model Galleria melonella and by a final proof-of-concept experiment using a mouse gut colonization model.
MISTAR delivers key scientific insights, new technical skills and new interventions to help stop the spread of AMR, that can be applied in both high- and low income countries.
Technical Summary
Antimicrobial resistance (AMR) has become an endemic and increasing problem, partially under the radar and depriving future generations of effective therapies. A main AMR driver is antimicrobial overuse in humans, animals and environment, facilitating selection and spread of resistant bacteria and genes between the different One Health domains. The goal of MISTAR is to ameliorate the AMR pollution in "hothouses" (hospitals and farms) and thus, to curtail the selection and transmission of AMR within different One Health settings. We will develop and implement intervention strategies to promote microbiota preservation using cutting-edge omics technologies. To reach this goal we will design, implement and quantify (i) the effect of gut microbiota-based interventions (fecal microbiota transplantation and microbiota-based index at point-of care) in hospitalized patients to reduce AMR, (ii) the effects of interventions aimed at reducing airborne dustbound pollution and transmission of AMR and (iii) design and develop novel experimental intervention strategies to modulate the microbiota to eradicate AMR. MISTAR delivers important scientific knowledge, technical skills and new interventions to curtail AMR emergence that can be applied in both high- and low income countries. A targeted communication plan (scientific, high-quality grey literature and social media) will make the findings of MISTAR accessible to a wide range of stakeholders. Ultimately, the deliverables of this project will guide policymakers to implement novel strategies to control this Global Health challenge.
Publications
McCallum GE
(2023)
Noise reduction strategies in metagenomic chromosome confirmation capture to link antibiotic resistance genes to microbial hosts.
in Microbial genomics
McInnes R
(2024)
Integration of vanHAX downstream of a ribosomal RNA operon restores vancomycin resistance in a susceptible Enterococcus faecium strain
in npj Antimicrobials and Resistance
Sünderhauf D
(2023)
Interspecific competition can drive plasmid loss from a focal species in a microbial community.
in The ISME journal
Walker-Sünderhauf D
(2023)
Removal of AMR plasmids using a mobile, broad host-range CRISPR-Cas9 delivery tool.
in Microbiology (Reading, England)
Description | MUSIC: MGE Uptake and Spread In microbial Communities |
Amount | £2,146,382 (GBP) |
Funding ID | EP/X026507/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 01/2023 |
End | 12/2027 |
Title | Genome sequence data Enterococcus faecium strains |
Description | This dataset contains both short- (Illumina) and long-read data of Enterococcus faecium genomes, which were collected during an outbreak of vancomycin-resistant Enterococcus faecium infection and colonisation events in a hospital in Birmingham (UK). |
Type Of Material | Database/Collection of data |
Year Produced | 2022 |
Provided To Others? | Yes |
Impact | This dataset has underpinned a publication (doi: 10.1038/s44259-023-00017-0) |
URL | https://www.ebi.ac.uk/ena/browser/view/PRJEB57409 |
Description | Topical or oral antibiotics for children with acute otitis media: impact on the gut microbiota |
Organisation | University Medical Center Utrecht (UMC) |
Country | Netherlands |
Sector | Academic/University |
PI Contribution | In this project, we will contribute bioinformatics skills to analyse the impact of oral vs topical antibiotic therapy for otitis media on the gut microbiota and its reservoir of antibiotic resistance genes ('the resistome'). |
Collaborator Contribution | Partners have contributed samples, DNA isolation and sequencing. |
Impact | No outputs yet. |
Start Year | 2022 |