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Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response

Immunoglobulin A (IgA) is one of the important and most abundant immunoglobulins which neutralize invading pathogens at mucosal sites. Gut microbial community and their metabolites which are responsible for higher IgA are poorly known. The current study was carried out to determine those microbial c...

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Autores principales: Rajput, Mrigendra, Momin, Tooba, Singh, Amit, Banerjee, Surya, Villasenor, Andrew, Sheldon, Jessica, Paudel, Pratikshya, Rajput, Ravindra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9755367/
https://www.ncbi.nlm.nih.gov/pubmed/36533218
http://dx.doi.org/10.1016/j.vas.2022.100279
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author Rajput, Mrigendra
Momin, Tooba
Singh, Amit
Banerjee, Surya
Villasenor, Andrew
Sheldon, Jessica
Paudel, Pratikshya
Rajput, Ravindra
author_facet Rajput, Mrigendra
Momin, Tooba
Singh, Amit
Banerjee, Surya
Villasenor, Andrew
Sheldon, Jessica
Paudel, Pratikshya
Rajput, Ravindra
author_sort Rajput, Mrigendra
collection PubMed
description Immunoglobulin A (IgA) is one of the important and most abundant immunoglobulins which neutralize invading pathogens at mucosal sites. Gut microbial community and their metabolites which are responsible for higher IgA are poorly known. The current study was carried out to determine those microbial community and their metabolites. Twenty-two healthy, 26 days wean piglets were used in the study. After 10 days of weaning, piglets were divided into two groups. Group 1 with significantly higher fecal IgA while group 2 with significantly lower IgA concentrations from each other. Both groups were analyzed for the fecal inflammatory cytokine, fecal microbial community using 16S ribosomal sequencing, and microbial metabolites using GC–MS. Results showed that Firmicutes and Bacteroidetes constituted 90.56% of the microbiome population in the fecal matter of pigs with higher IgA concentration while pigs with lower fecal IgA had Firmicutes and Bacteroidetes abundance as of 95.56%. Pigs with higher IgA had significantly higher Bacteroidota and Desulfobacterota populations, while significantly lower Firmicutes and Firmicutes/ Bacteroidota ratio (p <0.05). Roughly at the species level, animals with higher fecal IgA concentration had significantly higher bacteria which are associated with gut inflammation and infectious such Prevotella spp and Lachnospiraceae AC2044. Pigs with higher IgA had comparatively lower short-chain fatty acid (SCFA) such as acetic acid, butyric, formic acid, isovaleric acid, and propionic acid which has been associated with gut immune tolerance and immune homeostasis.
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spelling pubmed-97553672022-12-17 Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response Rajput, Mrigendra Momin, Tooba Singh, Amit Banerjee, Surya Villasenor, Andrew Sheldon, Jessica Paudel, Pratikshya Rajput, Ravindra Vet Anim Sci Article Immunoglobulin A (IgA) is one of the important and most abundant immunoglobulins which neutralize invading pathogens at mucosal sites. Gut microbial community and their metabolites which are responsible for higher IgA are poorly known. The current study was carried out to determine those microbial community and their metabolites. Twenty-two healthy, 26 days wean piglets were used in the study. After 10 days of weaning, piglets were divided into two groups. Group 1 with significantly higher fecal IgA while group 2 with significantly lower IgA concentrations from each other. Both groups were analyzed for the fecal inflammatory cytokine, fecal microbial community using 16S ribosomal sequencing, and microbial metabolites using GC–MS. Results showed that Firmicutes and Bacteroidetes constituted 90.56% of the microbiome population in the fecal matter of pigs with higher IgA concentration while pigs with lower fecal IgA had Firmicutes and Bacteroidetes abundance as of 95.56%. Pigs with higher IgA had significantly higher Bacteroidota and Desulfobacterota populations, while significantly lower Firmicutes and Firmicutes/ Bacteroidota ratio (p <0.05). Roughly at the species level, animals with higher fecal IgA concentration had significantly higher bacteria which are associated with gut inflammation and infectious such Prevotella spp and Lachnospiraceae AC2044. Pigs with higher IgA had comparatively lower short-chain fatty acid (SCFA) such as acetic acid, butyric, formic acid, isovaleric acid, and propionic acid which has been associated with gut immune tolerance and immune homeostasis. Elsevier 2022-12-06 /pmc/articles/PMC9755367/ /pubmed/36533218 http://dx.doi.org/10.1016/j.vas.2022.100279 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Rajput, Mrigendra
Momin, Tooba
Singh, Amit
Banerjee, Surya
Villasenor, Andrew
Sheldon, Jessica
Paudel, Pratikshya
Rajput, Ravindra
Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response
title Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response
title_full Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response
title_fullStr Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response
title_full_unstemmed Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response
title_short Determining the association between gut microbiota and its metabolites with higher intestinal Immunoglobulin A response
title_sort determining the association between gut microbiota and its metabolites with higher intestinal immunoglobulin a response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9755367/
https://www.ncbi.nlm.nih.gov/pubmed/36533218
http://dx.doi.org/10.1016/j.vas.2022.100279
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