Ewch i’r prif gynnwys
Cedric Berger   PhD

Dr Cedric Berger

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PhD

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Timau a rolau for Cedric Berger

  • Uwch Ddarlithydd

    Ysgol y Biowyddorau

Trosolwg

Mae'r tîm yn gysylltiedig â'r grŵp Microbiomau, Microbau a Gwybodeg (MMI) yn Ysgol y Biowyddorau Caerdydd. Rydym yn astudio'r rhyngweithio rhwng pathogenau enterig a'u gwesteion gyda phwyslais penodol ar Enterohemorrhagig (EHEC), Enteropathogenig (EPEC), Escherichia coli (DAEC) ac Edwardsiella spp. Mae ein hymchwil yn cwmpasu bioleg, imiwnoleg ac atal clefydau enterig.

Mae gan fy nhîm bedwar maes thematig:
1- Deall epidemioleg clefyd dolur rhydd yn y DU ac mewn gwledydd ag incwm isel.
Gan fod y rhan fwyaf o'r bobl sy'n dioddef o ddolur rhydd yn hunan-feddyginiaethu ac nad ydynt yn adrodd eu symptomau i weithwyr iechyd proffesiynol, mae gwir achosion o glefydau dolur rhydd yn y DU yn dal i gael ei ddeall yn wael.

2- Archwilio'r berthynas â pathogen enterig a'r amgylchedd.
Mae clefyd dolur rhydd wedi bod yn gysylltiedig ers amser maith â dŵr halogedig gyda'r prif syniad, os ydym yn rhoi dŵr yfed glân, bydd effaith clefyd dolur rhydd yn gostwng mewn gwledydd ag incwm isel. Fodd bynnag, mae hyn wedi'i brofi'n anghywir. Yn ogystal, mae amlder clefyd dolur rhydd mewn gwledydd ag incwm uchel yn dal i fod yn uchel iawn gyda chyfartaledd o un episod bob blwyddyn ar gyfartaledd sy'n awgrymu bod elfennau eraill yn cael eu trosglwyddo'r pathogenau. Y nod yw deall o ble mae'r pathogenau yn dod yn yr amgylchedd a'u canfod.

3- Decrypther the molecular mechanism of the virulence factor:
Rydym yn gweithio ar sawl system pathogen gwesteiwr-bacteriol sy'n cyfuno ystod eang o dechnegau a dulliau o brofion celloedd in vitro i fodelau in vivo gyda'r nod o ddeall mecanwaith moleciwlaidd ffactorau virulence bacteriol a nodi eu targedau yn y gwesteiwr. Gan y gall haint arwain at ymatebion annormal sy'n gysylltiedig â llid cronig (clefydau llidiol y coluddyn) a chanserau colonig, rydym yn edrych ar y mecanwaith sy'n arwain at y ddau gyflwr.

4- Ymchwilio i ffyrdd newydd o driniaeth ac atal i leihau effaith haint enterig.
Nod y prosiect hwn yw datblygu brechlyn y gellid ei ddefnyddio mewn plant i atal datblygiad clefydau neu mewn anifeiliaid i newid gwladychu EPEC ac EHEC. Rydym hefyd yn ymchwilio i'r berthynas rhwng dolur rhydd ac atodiad sinc.

Mae fy ngrŵp yn gysylltiedig ag Ymchwil Caerdydd i Heintiau a Pharasitiaid mewn Systemau Ecolegol (CRIPES) a gyda 
Sefydliad Ymchwil Dŵr.

Gallwch hefyd ddod o hyd i'n gwybodaeth am gyhoeddiadau ar ResearchGate a chofnod wedi'i wirio o adolygiadau cyfnodolion ar Publons. 

Cyhoeddiad

2024

2021

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2005

2004

Adrannau llyfrau

Erthyglau

Ymchwil

Research

We are working on several host-bacterial pathogen systems combining a wide range of techniques and approaches from in-vitro cell assays to in vivo models. The aim of my group is to understand the molecular mechanism of bacterial virulence factors and identify their targets in the host.

Modulation of immune response

Escherichia coli is the major constitute of the aerobic gut microbiota. However, acquisition of virulence determinant by horizontal gene transfer led to the evolution of pathogenic E. coli clones. Pathogenic strains are divided into ExPEC (causing extra intestinal infection) and diarrhoeal E. coli, which are sub-divided into six categories: diffusely adherent (DAEC), entero-toxigenic (ETEC), -aggregative (EAEC), -invasive (EIEC), -pathogenic (EPEC) and -haemorrhagic (EHEC). Although EPEC and EHEC exhibit differences in their host specificity, epidemiology, virulence and disease symptoms, they colonise the gut mucosa of their respective hosts via attaching and effacing (A/E) lesions. A/E lesions are characterised by effacement of the brush border microvilli and intimate bacterial attachment to the enterocyte membrane (Figure 2). The ability to induce A/E lesions and colonize their hosts depend on a type III secretion system (T3SS) that injects effectors into colonic intestinal epithelial cells (IECs). Once injected, the effectors subvert processes involved in innate immune responses, cellular metabolism, and oxygenation of the mucosa. We recently reported that one of these effectors modulates the recruitment of neutrophils during mouse model of EPEC infection (Citrobacter rodentium). We are now focusing on other effectors that may target key signalling pathways that lead to the expression of cytokines.

Disease prevention

Different vaccinations, composed of virulence factors, DNA-based, attenuated bacteria or bacterial ghost against EPEC and EHEC, have been trialled in animals with mixed success. Vaccination against Intimin decreases EPEC colonization in the rabbit model. Vaccination targeting EspA, Tir and Intimin alters EHEC colonization in cattle but did not completely inhibit it. This vaccination was one of the two commercially available against EHEC, EconicheTM, but its production has stopped. The main problems of all these vaccinations is the diversity of the target among EPEC and EHEC suggesting that a single approach will not work.

The aim of this project is to develop a vaccine that could be used in children to prevent disease development or in animals to alter the colonization of EPEC and EHEC using C. rodentium, a mouse specific pathogen, used to study EPEC and EHEC infection in vivo as it shares the same virulence factors.

Current members of the Research Group

Technical staff:

Gareth Thomas working on plant contamination by Listeria

Master students:

Doyle Millard working on cell signalling induce by enteric pathogens

Undergraduate research students:

None

Addysgu

Rwy'n cynnal ystod o addysgu o flwyddyn 1 i flwyddyn olaf israddedig, a goruchwylio myfyrwyr prosiect MRes blwyddyn olaf ac ôl-raddedig.

Mae fy addysgu presennol yn cynnwys cyfraniadau i:

  • BI1001: Sgil ar gyfer Gwyddoniaeth - Datrys Problemau mewn Bioleg ac ymarfer ar dechnegau aseptig. 

  • BI1003: Organebau a'r Amgylchedd - Microbioleg feddygol

  • BI3155: Bioleg ac epidemioleg heintiau - Ymatebion gwesteiwr i haint (Arweinydd modiwl)

  • BI4001: Prosiect ymchwil meistr integredig (Arweinydd y modiwl)

Bywgraffiad

For almost 20 years I have been interested in bacterial infection and methods to prevent them. My PhD project at University Paris Sud at the faculty of Pharmacy in France focused on the interaction between Diffusely adherent Escherichia coli and the human epithelial cells. In 2006, I then moved to Imperial College London and developed my expertise on biomedical microbiology focusing on the human pathogens Enteropathogenic and Enterohemorrhagic E. coli and the mouse-restricted pathogen Citrobacter rodentium. In September 2018, I joined Cardiff School of Biosciences, Cardiff University, as a Senior Lecturer, to carry on my work on pathogenic bacteria.

Aelodaethau proffesiynol

Member of The Microbiology Society and American Society for Microbiology

Meysydd goruchwyliaeth

Profwr

Goruchwyliaeth gyfredol

Prosiectau'r gorffennol

  • Teresa Paradel Gil (pathogenau A/E)
  • Nicolaas Bruyniks (Listeria monocytogenes

Contact Details

Email [email protected]
Telephone +44 29208 74829
Campuses Adeilad Syr Martin Evans, Llawr 2, Ystafell Ystafell W/2.06, Rhodfa'r Amgueddfa, Caerdydd, CF10 3AX

Arbenigeddau

  • Afiechydon heintus
  • Genomeg pathogen
  • Rhyngweithio gwesteiwr-pathogenau
  • Microbioleg Bwyd
  • microbiome