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Details

Autor(en) / Beteiligte
Titel
Microbiota transplantation from younger to older mice could restore lost immunity to effectively clear salmonella infection in Th2-biased BALB/c mice
Ist Teil von
  • Life sciences (1973), 2022-01, Vol.288, p.120201-120201, Article 120201
Ort / Verlag
Netherlands: Elsevier Inc
Erscheinungsjahr
2022
Quelle
MEDLINE
Beschreibungen/Notizen
  • The composition, overtly abundance, and diversity of gut microbiota, play a significant role in maintaining physiological homeostasis with age. Reports revealed that the gut microbial profile might be correlated with immunity and metabolism. It is, therefore, tantamount to know if an older individual can achieve the immunity and metabolic profile of a younger individual by receiving the gut microbiome of a younger individual. In the current report, we have studied the effects of cecal microbiota transplantation (CMT) from younger to older mice. In this study, older BALB/c mice (23 weeks) received CMT from younger BALB/c mice (3 weeks). CMT recipient mice showed altered expressions of immune and tight junction protein genes in the colon of mice, while the non-CMT recipient mice did not. Older mice were treated with AVNM to make them compatible with CMT. Further data from metabolite studies revealed that AVNM treatment mainly affected the aromatic amino acid biosynthesis pathway while CMT mostly affected the metabolism of different carbohydrates. We repeated the analysis in C57BL/6 mice without any significant effects of CMT. Results revealed that mice who received CMT showed more efficient restoration of gut microbiota than non-CMT recipient mice. CMT caused the alleviation of Salmonella infection and efficient recovery of the cecal index in the mice following antibiotics treatment. [Display omitted] •Cecal matter Transplant (CMT) from younger to older mice•BALB/c mice (Th-2 biased) showed more promise than C57BL/6 (Th-1 biased).•CMT restored perturbed gut microbiota in older BALB/c mice.•CMT could reinstate protection against salmonella infection in older mice.

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