dc.contributor.author
Mousavi, Soraya
dc.contributor.author
Foote, Minnja S.
dc.contributor.author
Du, Ke
dc.contributor.author
Bandick, Rasmus
dc.contributor.author
Bereswill, Stefan
dc.contributor.author
Heimesaat, Markus M.
dc.date.accessioned
2025-07-04T10:59:48Z
dc.date.available
2025-07-04T10:59:48Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/48127
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-47849
dc.description.abstract
Food-borne Campylobacter jejuni infections constitute serious threats to human health worldwide. Since antibiotic treatment is usually not indicated in infected immune-competent patients, antibiotic-independent treatment approaches are needed to tackle campylobacteriosis. To address this, we orally applied carvacrol, deferoxamine, deoxycholate, and 2-fucosyl-lactose either alone or all in combination to human microbiota-associated IL-10(-/-) mice from day 2 until day 6 following oral C. jejuni infection. Neither treatment regimen affected C. jejuni loads in the colon, whereas carvacrol lowered the pathogen numbers in the ileum on day 6 post-infection (p.i.). The carvacrol and combination treatment regimens resulted in alleviated diarrheal symptoms, less distinct histopathological and apoptotic epithelial cell responses in the colon, as well as diminished numbers of colonic neutrophils and T lymphocytes on day 6 p.i., whereas the latter cells were also decreased upon deferoxamine, deoxycholate, or 2-fucosyl-lactose application. Remarkably, the carvacrol, deferoxamine, and combination treatment regimens dampened ex-vivo IFN-gamma secretion in the colon, the kidneys, and even in the serum to basal concentrations on day 6 p.i. In conclusion, carvacrol alone and its combination with deferoxamine, deoxycholate, and 2-fucosyl-lactose constitute promising antibiotics-independent treatment options to fight acute campylobacteriosis.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
natural compounds
en
dc.subject
Campylobacter jejuni
en
dc.subject
immune-modulatory effects
en
dc.subject
secondary abiotic IL-10(-/-) mice
en
dc.subject
human gut microbiota associated mice
en
dc.subject
campylobacteriosis model
en
dc.subject
host-pathogen interaction
en
dc.subject
placebo-controlled preclinical intervention study
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Oral treatment of human gut microbiota associated IL-10−/− mice suffering from acute campylobacteriosis with carvacrol, deferoxamine, deoxycholic acid, and 2-fucosyl-lactose
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
1290490
dcterms.bibliographicCitation.doi
10.3389/fmicb.2024.1290490
dcterms.bibliographicCitation.journaltitle
Frontiers in Microbiology
dcterms.bibliographicCitation.originalpublishername
Frontiers Media SA
dcterms.bibliographicCitation.volume
15
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
38343716
dcterms.isPartOf.eissn
1664-302X