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Bacteriocin biosynthesis contributes to the anti-inflammatory capacities of probiotic Lactobacillus plantarum
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Plantaricin EF (PlnEF) is a class IIb bacteriocin produced by
Lactobacillus plantarum
. We compared
L. plantarum
NCIMB8826 and LM0419, a
plnEFI
deletion mutant of that strain lacking
plnEF
and the gene for the cognate immunity protein
plnI
, in a 2,4,6-trinitrobenzenesulfonic acid (TNBS) induced mouse model of acute inflammatory bowel disease. Mice fed either
L. plantarum
NCIMB8826 or LM0419 were not protected against TNBS according to either disease activity or histology (Ameho) scores. Mice consuming NCIMB8826 exhibited intermediate (non-significant) levels of colonic tumour necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) that ranged between the TNBS-treated animals and healthy controls. By comparison, TNF-α and IL-6 quantities were elevated in mice given
L. plantarum
LM0419 and equivalent to mice given TNBS alone. Both strains survived digestive tract transit in equal numbers and did not result in global changes to the bacterial composition in the intestine according to 16S rRNA gene sequencing either prior to or after TNBS administration. Examination of intestinal taxa showed that mice consuming wild-type
L. plantarum
, but not LM0419 contained lower proportions of
Mucispirillum
(
Deferribacteres
phylum) in the faeces prior to TNBS administration and
Parabacteroides
(
Bacteroidetes
phylum) in the caecum after disease induction.
Parabacteroides
also positively correlated with disease activity and histology scores. These findings suggest a role for PlnEFI production by
L. plantarum
in benefiting digestive tract health.
Walter de Gruyter GmbH
Title: Bacteriocin biosynthesis contributes to the anti-inflammatory capacities of probiotic Lactobacillus plantarum
Description:
Plantaricin EF (PlnEF) is a class IIb bacteriocin produced by
Lactobacillus plantarum
.
We compared
L.
plantarum
NCIMB8826 and LM0419, a
plnEFI
deletion mutant of that strain lacking
plnEF
and the gene for the cognate immunity protein
plnI
, in a 2,4,6-trinitrobenzenesulfonic acid (TNBS) induced mouse model of acute inflammatory bowel disease.
Mice fed either
L.
plantarum
NCIMB8826 or LM0419 were not protected against TNBS according to either disease activity or histology (Ameho) scores.
Mice consuming NCIMB8826 exhibited intermediate (non-significant) levels of colonic tumour necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) that ranged between the TNBS-treated animals and healthy controls.
By comparison, TNF-α and IL-6 quantities were elevated in mice given
L.
plantarum
LM0419 and equivalent to mice given TNBS alone.
Both strains survived digestive tract transit in equal numbers and did not result in global changes to the bacterial composition in the intestine according to 16S rRNA gene sequencing either prior to or after TNBS administration.
Examination of intestinal taxa showed that mice consuming wild-type
L.
plantarum
, but not LM0419 contained lower proportions of
Mucispirillum
(
Deferribacteres
phylum) in the faeces prior to TNBS administration and
Parabacteroides
(
Bacteroidetes
phylum) in the caecum after disease induction.
Parabacteroides
also positively correlated with disease activity and histology scores.
These findings suggest a role for PlnEFI production by
L.
plantarum
in benefiting digestive tract health.
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