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Guo, X.;  Okpara, E.S.;  Hu, W.;  Yan, C.;  Wang, Y.;  Liang, Q.;  Chiang, J.Y.L.;  Han, S. Architecture and Composition of the Intestinal Flora. Encyclopedia. Available online: https://encyclopedia.pub/entry/25888 (accessed on 31 July 2024).
Guo X,  Okpara ES,  Hu W,  Yan C,  Wang Y,  Liang Q, et al. Architecture and Composition of the Intestinal Flora. Encyclopedia. Available at: https://encyclopedia.pub/entry/25888. Accessed July 31, 2024.
Guo, Xiaohua, Edozie Samuel Okpara, Wanting Hu, Chuyun Yan, Yu Wang, Qionglin Liang, John Y. L. Chiang, Shuxin Han. "Architecture and Composition of the Intestinal Flora" Encyclopedia, https://encyclopedia.pub/entry/25888 (accessed July 31, 2024).
Guo, X.,  Okpara, E.S.,  Hu, W.,  Yan, C.,  Wang, Y.,  Liang, Q.,  Chiang, J.Y.L., & Han, S. (2022, August 05). Architecture and Composition of the Intestinal Flora. In Encyclopedia. https://encyclopedia.pub/entry/25888
Guo, Xiaohua, et al. "Architecture and Composition of the Intestinal Flora." Encyclopedia. Web. 05 August, 2022.
Architecture and Composition of the Intestinal Flora
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Intestinal microorganisms are composed of bacteria, archaea, eukaryotes, and viruses, and more than 99% of them are bacteria. Approximately 1014 bacteria are known to constitute the intestinal flora in the adult gut, and this number is 10 times the number of human somatic cells.

intestinal flora homeostatic imbalances diseases

1. Introduction

The intestinal flora co-exists harmoniously with the host, participate in the digestion and the absorption of nutrients, and also help to maintain the integrity of the host's immune system so as to prevent pathogen colonization [1]. Additionally, intestinal flora consists of various bacteria in low or high abundance, which co-evolve with the host. While the host provides nutrients and a suitable survival place for the intestinal flora, the intestinal flora assists the host in absorbing nutrients, such as vitamins and short-chain fatty acids, in a more efficient manner in order to drive growth processes and to support the functions of the intestinal system and the immune system [2]

2. Architecture and Composition of the Intestinal Flora

The gut microbiota exists throughout the life of the host. The diversity of bacteria in the intestines of infants is very low at first, and it gradually accelerates during the course of early development. The intestinal floras in newborn babes are mainly of the Enterobacteriaceae and Staphylococcus species, and the intestinal flora during lactation are mainly of the Bifidobacterium species. After the consumption of a solid diet, the bacteria colonizing the intestine are found to be mostly the anaerobic strains [3][4][5]. A low level of Bacteroidetes and a high level of Bifidobacterium are also found in adolescence, followed by the formation of intestinal microbial communities dominated by Bacteroidetes and Firmicutes, which are involved in carbohydrate and amino acid metabolism, fermentation, and oxidative phosphorylation [6][7]. Studies have shown that aging is associated with a number of important changes, including a decrease in the diversity of the intestinal flora; decreases in the proportions of Firmicutes and Bacteroidetes; decreases in the abundances of Ruminococcaceae, Lachnospiraceae, and Bacteroidaceae; increases in the abundances of opportunistic pathogens; and decreases in the populations of the bacteria crucial for producing short-chain fatty acids required for the maintenance of structural integrity and the prevention of inflammation in the intestine [8][9][10]
The composition of the intestinal microbiota varies throughout the digestive tract. Food is mixed with saliva before entering the stomach and intestine. The oral microbiota is complex and diverse: ~1000 species of bacteria have been identified to date [11][12]. Esophageal microbial communities mainly include Firmicutes, Bacteroidetes, Actinobacteria, Proteobacteria, and Fusobacteria [13][14]. Most of the bacteria in the host's body are localized in the gastrointestinal tract, and there are significant differences in bacterial diversity and quantity between the stomach and the intestine. There are 10 to 103 bacteria per gram of stomach content, mainly including Firmicutes, Bacteroidetes, Clostridium, Actinobacteria, along with Streptococcus and Haemophilus. Helicobacter pylori is the dominant bacterium in the stomach [15][16]. The small intestine consists of the duodenum, jejunum, and ileum. There are 103 bacteria per gram of duodenal content, and Firmicutes and Actinobacteria are the main bacteria [8]. The bacterial density in the jejunum is high; there are 104–107 bacteria per gram of content—mainly Gram-positive aerobic bacteria and facultative anaerobic bacteria, such as Lactobacillus, Enterococcus, and Streptococcus. The numbers of ileal anaerobic bacteria close to the ileocecal valve, gradually exceed those of aerobic bacteria, and Streptococcus is the dominant bacteria in this segment of the intestine [17]. The colon, located in the lower part of the large intestine, contains 1011–1012 bacteria per gram of content, which are mainly anaerobic bacteria, including Firmicutes and Bacteroidetes. There is a high population density and diversity. The ratio of Firmicutes to Bacteroidetes is related to the susceptibility to diseases. In the large intestine, Bacteroides, Bifidobacterium, Streptococcus, Enterobacteriaceae, Enterococcus, Clostridium, Lactobacillus, and Ruminococcus are the dominant bacteria. In addition, the colon also contains several pathogenic bacteria, such as Campylobacter jejuni, Salmonella enteritidis, Vibrio cholerae, Escherichia coli, and Bacteroides fragilis [15]. The distribution of bacteria in the digestive tract is shown in Figure 1.

Figure 1. Distribution of gastrointestinal bacteria: The distribution of intestinal bacteria in the digestive tract varies, and there are many types and quantities of bacteria in the oral cavity. Following their entry into the esophagus, the colonization of bacteria is reduced. Due to the secretion of gastric acid, most bacteria in the stomach cannot survive, allowing more acid-tolerant bacteria, such as Prevotella, Roche, and Streptococcus, to dominate. The number of bacteria increases from the duodenum to jejunum and ileum. These bacteria include Clostridium, Lactobacillus, and Enterococcus. A large number of bacteria exist in the colon, including Bifidobacterium, Clostridium, Ruminococcus, Bacteroides, Streptococcus, and Prevotella.

The intestinal flora is mainly classified according to natural attributes, including Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, Verrucomicrobia, Fusobacteria, and Cyanobacteria. Approximately 98% of the intestinal flora are composed of four main types of bacteria—Firmicutes, Bacteroidetes, Proteobacteria, and Actinomycetes—and the classification of the bacteria is shown below in Table 1. The most common bacterial genera are Bacteroides, Clostridium, Peptococcus, Bifidobacterium, Eubacterium, Ruminococcus, Enterococcus faecalis, and Peptostreptococcus [9]. Furthermore, most of the bacteria in Bacteroidetes belong to Bacteroidetes and Prevotella, and the Firmicutes are mainly Clostridium, Eubacteria, and Ruminococcus.

Table 1. Classification of bacterial species in the intestinal flora: According to classification by natural properties, intestinal bacteria can be divided into six categories for the most part: Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, Fusobacteria, and Verrucomicrobia. Each category includes bacterial species.

Phylum

Class

Order

Family

Genus

Species

Firmicutes

Clostridia

Clostridiales

Clostridiaceae

Faecalibacterium

Faecalibacterium prausnitzii

Clostridium

Clostridium spp.

Lachnospiraceae

Coprocococcus

Coprococcus eutactus

Peptostreptococcaceae

Peptostreptococcus

Peptostreptococcus anaerobius

Veillonellaceae

Veillonella

Veillonella parvula

Bacilli

Lactobacillales

Lactobacillaceae

Lactobacillus

Lactobacillus acidophilus

Enterococcaceae

Enterococcus

Enterococcus faecalis

Bacillales

Listeriaceae

Listeria

Listeria iuanuii

Bacteroidetes

Flavobacteria

Flavobacteriales

Flavobacteriaceae

Flavobacterium

 

Bacteroidetes

Bacteroidales

Bacteroidaceae

Bacteroides

Bacteroides fragilis

Bacteroides caccae

Bacteroides pyogenes

Porphyromonadaceae

Porphyromonas

 

Parabacteroides

Parabacteroides distasonis

Rikenellaceae

Alistipes

Alistipes finegoldii

Prevotellaceae

Prevotella

Prevotella spp.

Proteobacteria

Gamma proteobacteria

Enterobacteriales

Enterobacteriaceae

Escherichia

Escherichia coli

Enterobacter

Enterobacter areogenes

Delta proteobacteria

Desulfovibrionales

Desulfobacterales

Desulfovibrionaceae

Desulfobacteraceae

Desulfovibrio

Desulfovibrio intestinalis

Desulfobacter

 

Epsilon proteobacteria

Campylobacterales

Helicobacteraceae

Helicobacter

Helicobacter pylori

Actinobacteria

Actinobacteria

Actinomycetales

Actinomycetaceae

Actinobaculum

 

Corynebacteriaceae

Corynebacterium

Corynebacterium glutamicum

Bifidobacteriales

Bifidobacteriaceae

Bifidobacterium

Bifidobacterium adolescentis

Bifidobacterium longum

Fusobacteria

Fusobacteria

Fusobacteriales

Fusobacteriaceae

Fusobacterium

Fusobacterium nucleatum

Verrucomicrobia

Verrucomicrobiae

Verrucomicrobiales

Verrucomicrobiaceae

Akkermansia

Akkermansia muciniphila

References

  1. Albhaisi, S.A.M.; Bajaj, J.S.; Sanyal, A.J. Role of gut microbiota in liver disease. Am. J. Physiol. Gastrointest. Liver Physiol. 2020, 318, G84–G98.
  2. Shi, N.; Li, N.; Duan, X.; Niu, H. Interaction between the gut microbiome and mucosal immune system. Mil. Med. Res. 2017, 4, 14.
  3. Milani, C.; Ferrario, C.; Turroni, F.; Duranti, S.; Mangifesta, M.; van Sinderen, D.; Ventura, M. The human gut microbiota and its interactive connections to diet. J. Hum. Nutr. Diet. 2016, 29, 539–546.
  4. Tanaka, M.; Sanefuji, M.; Morokuma, S.; Yoden, M.; Momoda, R.; Sonomoto, K.; Ogawa, M.; Kato, K.; Nakayama, J. The association between gut microbiota development and maturation of intestinal bile acid metabolism in the first 3 y of healthy Japanese infants. Gut Microbes 2020, 11, 205–216.
  5. Adlerberth, I.; Wold, A.E. Establishment of the gut microbiota in Western infants. Acta Paediatr. 2009, 98, 229–238.
  6. Durack, J.; Lynch, S.V. The gut microbiome: Relationships with disease and opportunities for therapy. J. Exp. Med. 2019, 216, 20–40.
  7. Hollister, E.B.; Riehle, K.; Luna, R.A.; Weidler, E.M.; Rubio-Gonzales, M.; Mistretta, T.A.; Raza, S.; Doddapaneni, H.V.; Metcalf, G.A.; Muzny, D.M.; et al. Structure and function of the healthy pre-adolescent pediatric gut microbiome. Microbiome 2015, 3, 36.
  8. Adak, A.; Khan, M.R. An insight into gut microbiota and its functionalities. Cell Mol. Life Sci. 2019, 76, 473–493.
  9. Gomaa, E.Z. Human gut microbiota/microbiome in health and diseases: A review. Antonie Van Leeuwenhoek 2020, 113, 2019–2040.
  10. Gonzalez Olmo, B.M.; Butler, M.J.; Barrientos, R.M. Evolution of the Human Diet and Its Impact on Gut Microbiota, Immune Responses, and Brain Health. Nutrients 2021, 13, 196.
  11. Dewhirst, F.E.; Chen, T.; Izard, J.; Paster, B.J.; Tanner, A.C.; Yu, W.H.; Lakshmanan, A.; Wade, W.G. The human oral microbiome. J. Bacteriol. 2010, 192, 5002–5017.
  12. Wade, W.G. The oral microbiome in health and disease. Pharmacol. Res. 2013, 69, 137–143.
  13. Martinez-Guryn, K.; Leone, V.; Chang, E.B. Regional Diversity of the Gastrointestinal Microbiome. Cell Host Microbe 2019, 26, 314–324.
  14. Pei, Z.; Bini, E.J.; Yang, L.; Zhou, M.; Francois, F.; Blaser, M.J. Bacterial biota in the human distal esophagus. Proc. Natl. Acad. Sci. USA 2004, 101, 4250–4255.
  15. Jandhyala, S.M.; Talukdar, R.; Subramanyam, C.; Vuyyuru, H.; Sasikala, M.; Nageshwar Reddy, D. Role of the normal gut microbiota. World J. Gastroenterol. 2015, 21, 8787–8803.
  16. Nardone, G.; Compare, D. The human gastric microbiota: Is it time to rethink the pathogenesis of stomach diseases? United Eur. Gastroenterol. J. 2015, 3, 255–260.
  17. O’Hara, A.M.; Shanahan, F. The gut flora as a forgotten organ. EMBO Rep. 2006, 7, 688–693.
  18. Weaver, K.E. Enterococcal Genetics. Microbiol. Spectr. 2019, 7, 7.2.11.
  19. Ma, Q.; Li, Y.; Li, P.; Wang, M.; Wang, J.; Tang, Z.; Wang, T.; Luo, L.; Wang, C.; Wang, T.; et al. Research progress in the relationship between type 2 diabetes mellitus and intestinal flora. Biomed. Pharmacother. 2019, 117, 109138.
  20. Krawczyk, B.; Wityk, P.; Galecka, M.; Michalik, M. The Many Faces of Enterococcus spp.-Commensal, Probiotic and Opportunistic Pathogen. Microorganisms 2021, 9, 1900.
  21. Murphy, E.C.; Frick, I.M. Gram-positive anaerobic cocci—Commensals and opportunistic pathogens. FEMS Microbiol. Rev. 2013, 37, 520–553.
  22. Martin, R.M.; Bachman, M.A. Colonization, Infection, and the Accessory Genome of Klebsiella pneumoniae. Front. Cell Infect. Microbiol. 2018, 8, 4.
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