Gut microbiota in health and disease

The human intestinal microbiota refers to the total population of micro-organisms that colonise the human intestines. Most organisms in the gut are non-pathogenic and co-inhabit with the host enterocytes in a commensalic and mutualistic relationship. The gut commensals aid in nutrient metabolism, xe...

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Main Authors: Shreyashi Ganguly, P Chandrasekhara
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:APIK Journal of Internal Medicine
Online Access:http://www.ajim.in/article.asp?issn=2666-1802;year=2019;volume=7;issue=1;spage=19;epage=30;aulast=Ganguly;type=0
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spelling doaj-499a8d6b4b9d42e094be9514e086541f2021-01-08T02:51:32ZengWolters Kluwer Medknow PublicationsAPIK Journal of Internal Medicine2666-18022666-18102019-01-0171193010.4103/2666-1802.260257Gut microbiota in health and diseaseShreyashi GangulyP ChandrasekharaThe human intestinal microbiota refers to the total population of micro-organisms that colonise the human intestines. Most organisms in the gut are non-pathogenic and co-inhabit with the host enterocytes in a commensalic and mutualistic relationship. The gut commensals aid in nutrient metabolism, xenobiotic and drug metabolism, antimicrobial protection, immunomodulation and maintenance of the integrity of the gut barrier and structure of the gastro-intestinal tract. Dysbiosis of these organisms have been implicated in the pathogenesis of several diseases. The advent of culture independent techniques has enabled the identification and phylogenetic classification of these organisms. These study methods include gene sequencing by high-throughput amplicon pyrosequencing (16sRNA for bacteria, accuracy 99.9%). Microbiota composition is affected by the mode of delivery, antibiotics usage during pregnancy, preterm labour, diet in infancy, environment & lifestyle, geographical locations, individual host genetics, in adults ageing & diet. The dominant phyla (in a state of normal health) are Firmiculates (51%), Bacetroidetes (41%), Proteo bacteria (5%), Actinobacteria (1.8%) and Verrucomicrobia (1.2%). Most abundant fungi are Ascomycota and Microsporidia. The degree of archaeal diversity in the gut microbiota of healthy individuals appears to be low. The two genera Methanobrevibacter and Nitrososphaera appear to be mutually exclusive. Bacteriophages are the most predominant organism in the human gut microbiome. Role of gut microbiome is implicated in several diseases, which range from inflammatory bowel diseases to cancer, all the way to alzheimers. The understanding and recognition of various gut-microbiome axes has enabled elucidation of novel pathologic pathway that are ripe for therapeutic manipulation. Prebiotics and probiotics aid in the recolonization of the gut with normal "health-promoting-good" bacteria. Other therapeutic approaches are faecal microbial transplantation, which is being employed in clostridium difficile infection, and inflammatory bowel diseases. Their role and benefits in other diseases are emerging every day.http://www.ajim.in/article.asp?issn=2666-1802;year=2019;volume=7;issue=1;spage=19;epage=30;aulast=Ganguly;type=0
collection DOAJ
language English
format Article
sources DOAJ
author Shreyashi Ganguly
P Chandrasekhara
spellingShingle Shreyashi Ganguly
P Chandrasekhara
Gut microbiota in health and disease
APIK Journal of Internal Medicine
author_facet Shreyashi Ganguly
P Chandrasekhara
author_sort Shreyashi Ganguly
title Gut microbiota in health and disease
title_short Gut microbiota in health and disease
title_full Gut microbiota in health and disease
title_fullStr Gut microbiota in health and disease
title_full_unstemmed Gut microbiota in health and disease
title_sort gut microbiota in health and disease
publisher Wolters Kluwer Medknow Publications
series APIK Journal of Internal Medicine
issn 2666-1802
2666-1810
publishDate 2019-01-01
description The human intestinal microbiota refers to the total population of micro-organisms that colonise the human intestines. Most organisms in the gut are non-pathogenic and co-inhabit with the host enterocytes in a commensalic and mutualistic relationship. The gut commensals aid in nutrient metabolism, xenobiotic and drug metabolism, antimicrobial protection, immunomodulation and maintenance of the integrity of the gut barrier and structure of the gastro-intestinal tract. Dysbiosis of these organisms have been implicated in the pathogenesis of several diseases. The advent of culture independent techniques has enabled the identification and phylogenetic classification of these organisms. These study methods include gene sequencing by high-throughput amplicon pyrosequencing (16sRNA for bacteria, accuracy 99.9%). Microbiota composition is affected by the mode of delivery, antibiotics usage during pregnancy, preterm labour, diet in infancy, environment & lifestyle, geographical locations, individual host genetics, in adults ageing & diet. The dominant phyla (in a state of normal health) are Firmiculates (51%), Bacetroidetes (41%), Proteo bacteria (5%), Actinobacteria (1.8%) and Verrucomicrobia (1.2%). Most abundant fungi are Ascomycota and Microsporidia. The degree of archaeal diversity in the gut microbiota of healthy individuals appears to be low. The two genera Methanobrevibacter and Nitrososphaera appear to be mutually exclusive. Bacteriophages are the most predominant organism in the human gut microbiome. Role of gut microbiome is implicated in several diseases, which range from inflammatory bowel diseases to cancer, all the way to alzheimers. The understanding and recognition of various gut-microbiome axes has enabled elucidation of novel pathologic pathway that are ripe for therapeutic manipulation. Prebiotics and probiotics aid in the recolonization of the gut with normal "health-promoting-good" bacteria. Other therapeutic approaches are faecal microbial transplantation, which is being employed in clostridium difficile infection, and inflammatory bowel diseases. Their role and benefits in other diseases are emerging every day.
url http://www.ajim.in/article.asp?issn=2666-1802;year=2019;volume=7;issue=1;spage=19;epage=30;aulast=Ganguly;type=0
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