Primers used for RT-qPCR analysis.

<div><p>Background</p><p>Inflammatory bowel disease (IBD) increases the risk of colorectal cancer, and it has the potential to diminish the quality of life. Clinical and experimental evidence demonstrate protective aspects of parasitic helminth infection against IBD. However, studies on the inhibition of inflammation by helminth infection have overlooked a key determinant of health: the gut microbiota. Although infection with helminths induces alterations in the host microbiota composition, the potential influence and mechanism of helminth infections induced changes in the gut microbiota on the development of IBD has not yet been elucidated. In this study, we analyzed the intersection of helminth <i>Trichinella spiralis</i> and gut bacteria in the regulation of colitis and related mechanisms.</p><p>Methodology/Principal findings</p><p><i>T</i>. <i>spiralis</i> infected mice were treated with antibiotics or cohoused with wild type mice, then challenged with dextran sodium sulfate (DSS)-colitis and disease severity, immune responses and goblet cells assessed. Gut bacteria composition was assessed by 16S rRNA sequencing and short-chain fatty acids (SCFAs) were measured. We found that protection against disease by infection with <i>T</i>. <i>spiralis</i> was abrogated by antibiotic treatment, and cohousing with <i>T</i>. <i>spiralis</i>- infected mice suppressed DSS-colitis in wild type mice. Bacterial community profiling revealed an increase in the abundance of the bacterial genus <i>Muribaculum</i> and <i>unclassified_Muribaculaceae</i> in mice with <i>T</i>. <i>spiralis</i> infection or mice cohoused with <i>T</i>. <i>spiralis</i>- infected mice. Metabolomic analysis demonstrated significantly increased propionic acid in feces from <i>T</i>. <i>spiralis</i>- infected mice. Data also showed that the gut microbiome modulated by <i>T</i>. <i>spiralis</i> exhibited enhanced goblet cell differentiation and elevated IL-10 levels in mice.</p><p>Conclusions</p><p>These findings identify the gut microbiome as a critical component of the anti- colitic effect of <i>T</i>. <i>spiralis</i> and gives beneficial insights into the processes by which helminth alleviates colitis.</p></div>

Publication Details

Journal
Figshare
Published
2024-11-04
DOI
https://doi.org/10.1371/journal.pntd.0012645.s001
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
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article

Primers used for RT-qPCR analysis.

Figshare
Gut microbiota and health
article

Primers used for RT-qPCR analysis.

article en

Abstract

<div><p>Background</p><p>Inflammatory bowel disease (IBD) increases the risk of colorectal cancer, and it has the potential to diminish the quality of life. Clinical and experimental evidence demonstrate protective aspects of parasitic helminth infection against IBD. However, studies on the inhibition of inflammation by helminth infection have overlooked a key determinant of health: the gut microbiota. Although infection with helminths induces alterations in the host microbiota composition, the potential influence and mechanism of helminth infections induced changes in the gut microbiota on the development of IBD has not yet been elucidated. In this study, we analyzed the intersection of helminth <i>Trichinella spiralis</i> and gut bacteria in the regulation of colitis and related mechanisms.</p><p>Methodology/Principal findings</p><p><i>T</i>. <i>spiralis</i> infected mice were treated with antibiotics or cohoused with wild type mice, then challenged with dextran sodium sulfate (DSS)-colitis and disease severity, immune responses and goblet cells assessed. Gut bacteria composition was assessed by 16S rRNA sequencing and short-chain fatty acids (SCFAs) were measured. We found that protection against disease by infection with <i>T</i>. <i>spiralis</i> was abrogated by antibiotic treatment, and cohousing with <i>T</i>. <i>spiralis</i>- infected mice suppressed DSS-colitis in wild type mice. Bacterial community profiling revealed an increase in the abundance of the bacterial genus <i>Muribaculum</i> and <i>unclassified_Muribaculaceae</i> in mice with <i>T</i>. <i>spiralis</i> infection or mice cohoused with <i>T</i>. <i>spiralis</i>- infected mice. Metabolomic analysis demonstrated significantly increased propionic acid in feces from <i>T</i>. <i>spiralis</i>- infected mice. Data also showed that the gut microbiome modulated by <i>T</i>. <i>spiralis</i> exhibited enhanced goblet cell differentiation and elevated IL-10 levels in mice.</p><p>Conclusions</p><p>These findings identify the gut microbiome as a critical component of the anti- colitic effect of <i>T</i>. <i>spiralis</i> and gives beneficial insights into the processes by which helminth alleviates colitis.</p></div>

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Primers used for RT-qPCR analysis. · Figshare (2024) | TGRS Research Map | TGRS