There is not a definition of what can be considered a healthy microbiota, and consequently a correct intestinal health, although a series of mechanisms involved in the loss of the intestinal function can be considered, among them the appearance of dysbiosis, the loss of the intestinal barrier integrity and inflammation.

Product Manager – Intestinal Health
Adiveter
The gut is a complex system in which several factors act in order to achieve its optimal function. These factors that we could consider key are the immune system – based on the local action of certain immunoglobulins -, the intestinal morphology – based on the enterocytes integrity and the unions between them -, the diet, and the whole of the microorganisms present – the microbiota-.
A good intestinal health relies on the balance between the saprophytic and pathogenic floras found in the gut. The breakdown of this balance is what is known as dysbiosis and can lead to disease when the saprophyte flora decreases or disappears and the pathogenic one increases. There are authors who consider dysbiosis as a breakdown of the balance between the microbiota and the host, considering the whole factors involved in the functioning of the digestive system. This perspective is given by the introduction of the concept of holobiont, in which the association of a macroorganism and the microorganisms that make up its microbiota is considered as a single entity (Van de Guchte et al., 2018).
There is not a clear definition of what can be considered a healthy microbiota, even so, a high microbial diversity in the animal can be associated with a healthy situation (Ocejo et al., 2018).
The advances made in molecular biology allow carrying out studies on the set of the genomes present in a given medium, the metagenome, without having to make the isolation and the culture of the different microorganisms, field that is dealt with by metagenomics. Thus, the set of genes of the microorganisms present in an animal (the microbiota) is called microbioma.
Although there are few studies on this subject, there is evidence that the gut microbiota composition may partly explain differences in feed efficiency in pigs and consequently have an obvious impact on the productive performance. Although microbial diversity doesn’t vary between animals, feed efficiency can be related to some specific intestinal microorganisms, so they could potentially be used as biomarkers of this feed efficiency and even consider the use of these microorganisms as a probiotic.
MICROBIOTA
The distribution of microorganisms throughout the animal intestinal tract is not uniform. This microbial configuration varies according to the gut section considered. For example, in the case of birds, a greater number and diversity of microorganisms is observed in the cecum in relation to sections of the small intestine (Ocejo et al., 2018), and in the case of pigs, diversity and composition vary between the small intestine and the large intestine (Crespo et al., 2017).
This high microbial diversity in the bird caecum is due to greater intake retention and to the fermentations that occur in this gut section (Ocejo et al., 2018). In the case of pigs, reasons are similar (Donaldson et al., 2016).
Diversity measures of the microbial population:
Alpha Diversity: This diversity measure describes the number of different species in a given population and its structure. The main indices used are:
• Observed Species: Expresses the number of species present in a given environment.
• Chao 1: Basically reflects the number of species present in a specific population based on the determination of presence-absence data, so they are an expression of richness.
• Shannon and Simpson: These estimators describe the structure of a population with respect to the proportional abundance of each species. These indices consider the number of species present (richness) and the relative quantity of individuals of each one (abundance).
Beta Diversity: This measurement of diversity describes the variation in the structure of a given community, in a given environment, over time, or the difference between populations of different environments in a given time. The estimator used is the Bray-Curtis index that quantifies the dissimilarity between two environments. It expresses whether two populations have the same composition or they don’t share any species.
Phylogenetic Diversity Measurements: The indices described above describe diversity considering all species in the same way without taking into account the evolutionary differences between them. There are other indices that also express diversity between populations based on the genealogic relationships between them.
Taxonomy
There are three predominant phyla in the animal gut;
• Firmicutes: Formed by Gram+ bacteria. It includes the families Lachnospiraceae, formed by butyric acid producing bacteria, Clostridiaceae and Lactobaciliaceae.
• Bacteroidetes: Formed by Gram– bacteria. It includes the families Prevotellaceae and Rikenellaceae (Alistepes)
• Proteobacteria: It includes a wide variety of pathogenic microorganisms, such as Enterobacteriaceae; E. coli, Samonella, Vibrio, Neisseria…
Other bacterial families of interest and belonging to other phyla are the Bifidobateriaceae, belonging to the phylum Actinobacteria, and the Akkermansia genus (phylum Verrucomicrobia).
The intestinal flora varies with the age of the animal. The microbiota evolution throughout the whole live of the animal is influenced initially by the population provided by the parents and the environment and later by the feed source used.
Variations in the microbiota have also been observed depending on the breed of the animals, so the genetic profile can be considered a predisposing factor of intestinal infection due to these changes in the microbiota (Guevarra et al., 2019). Other factors can affect the microbiota evolution such as environmental factors.
INTESTINAL HEALTH
There is not a definition of what can be considered a healthy microbiota, and consequently a correct intestinal health, although a series of mechanisms involved in the loss of the intestinal function can be considered, among them the appearance of dysbiosis, the loss of the intestinal barrier integrity and inflammation (Van de Guchte et al., 2018).
The challenge is presented when trying to predict the appearance of this loss of intestinal health in a predictive way, before the start of the problem, and not in a diagnostic way, once it appears. Hence there is need to define which could be the useful biomarkers for this purpose.
Two groups of markers could be considered: microorganisms, that indicate a change in the microbiota and the host own molecules that reflect cellular inflammation, intestinal integrity breakdown or the epithelial cells condition. In human medicine, for example, faecal levels of calprotectin are assessed as a biomarker of intestinal inflammation.
Considered as indicators of good intestinal health, at the hindgut level, are the presence of butyrate producing bacteria, such as those belonging to the Lachnospiraceae and Ruminococcaceae families. In animals with intestinal challenge, a decrease of these families and an increase of Proteobacteria is observed.

It has been observed that piglets with diarrhoea, on day 38, showed a lower Simpson Index at day 7 than healthy piglets (Dou et al. 2017). The same study showed, when comparing the microbiota of these piglets, that healthy piglets had a higher abundance of Prevotellaceae, Lachnospiraceae, Ruminococcaceae and Lactobacillaceae.
These remarks suggest that the intestinal microbiota affects the development of post weaning diarrhoea, and not only specific pathogens, and that it’s possible to differentiate diarrhoea susceptible piglets based on early life bacterial composition (Dou et al. 2017).
MICROBIOTA EVOLUTION
The intestinal flora doesn’t remain constant throughout the animal life. This evolution that occurs over time can be influenced by many factors.

POULTRY
Broiler
The intestine of chickens that come from the hatchery is not colonized by microorganisms from the hen, but by those from the environment. Initially, chicken microbiota is made up of facultative anaerobic bacteria. These bacteria consume oxygen and decrease its levels in the intestine, thus increasing the strict anaerobic bacteria population.
In one-day-old chicks, coming directly from the hatchery, the dominance of the phylum Proteobacteria is observed at caecal level, with a significant proportion of enterobacteria. As the chick grows a decrease of this phylum is observed and the presence of Firmicutes and Bacteroides increases (Adiveter 2020).
In a study carried out by Adiveter in a commercial farm, the values of the Shannon Index were determined at days 0, 10, 22 and 42; and an increase of this estimator was observed as the animals grew.

Regarding Beta Diversity, two different bacterial communities were observed according to age groups, showing that the bacteria of the one-day-old chicks are different from those of the rest of the animal life.
Chicken rearing could be divided in three different stages. First days of chicken life in which Proteobacteria is the predominant phylum; a second stage, around 22 days of life, in which a clear decrease of proteobacteria and a significant increase in firmicutes is observed; and a third one, around 42 days of life, in which Bacteroidetes replaces part of the firmicutes.

Within Firmicutes, the predominant families are Lachnospiraceae and Ruminococcaceae that are butyrate producing bacteria. In the case of Bacteroidetes, the main genus are Bacteroides and Alistipes, mainly propionate producers (Qi et al, 2019; Polansky et al., 2015). Several authors explain this variation of the bacterial populations regarding the type of Volatile Fatty Acids produced. The production of butyrate could probably be associated to the high nutritional requirements of this early stage of the animal development. In the case of propionate production it could be related to a balance between energy acquisition from available nutrients and a more sustained growth (Ocejo et al., 2018).
Even so, it must be taken into account that the microbiota profile of these chickens corresponds to animals that have never had contact with hens because they come from hatcheries. When chickens are reared in contact with adult hens, it has been observed that about 40% of its caecal microbiota was made up of Bacteroidetes, compared to animals without contact with hens whose microbiota was dominated by Firmicutes (Kubasova et al., 2019).

Laying Hens
In studies in which the caecal microbiota of laying hens was determined, it was observed that the microbiota, until 24 weeks of age, was practically similar to that observed in chickens.
The study stretched on until 7 months of age, observing that Firmicutes and Bacteroidetes were still predominant and each one of them represented half of the total (Videnska et al., 2014).
PIGS
The pig microbiota colonization and evolution over time is hardly influenced by diet. The greatest change occurs in the weaning period with the shift from a breast milk based diet to another one based on solid feed (Nowland et al., 2019).
Studies have shown an increase in Alpha Diversity after weaning, and regarding Beta Diversity, significant differences between suckling and weaned piglets were also observed (Guevarra et al. 2019).
After weaning, an increase of Bacteroidetes phylum was observed. At the family level it goes from a population in which Ruminococcaceae and Prevotellaceae prevails in the case of suckling piglets, to another one with a higher proportion of Prevotellaceae and Lactobacillaceae.
In the same way, in the case of the weaned piglets, Prevotella and Lactobacillus were the predominant genus and in the case of the suckling piglets, Prevotella and Bacteroides (Guevarra et al. 2018).
These variations in the microbiota are mainly due to the type of diet the piglet receives. Bacteroides are microorganisms that use milk oligosaccharides as a source of energy and Prevotella is related to the fermentation of fibrous polysaccharides present in plants, as well as Lactobacillus that also metabolizes carbohydrates from plants, including starch (Guevarra et al. 2019).
MICROBIOTA MANIPULATION
Among the different elements that take part in the microbiota modulation, the following should be highlighted:
Environment
The environment in which the animal develops itself affects the colonization of the intestinal tract and factors such as the hygienic state affects this development. Piglets reared together with their mother have greater flora diversity compared to their siblings weaned at 24 hours of age and reared in isolators (Inman et al., 2010).
Antibiotic use
When a group of piglets was subjected to a combination of antibiotics, an increase in Proteobacteria was observed (from 1% to 11%), mostly E. coli which represented 62% of these microorganisms (Looft et al., 2012).
Feed processing
The distribution of the microbial species in the gastrointestinal tract is also determined by the chemical composition and the structure of the digesta, since bacterial species differ in their substrate preferences and growth requirements.
It is known that particle size affects the digestibility of the diet and consequently their productive parameters. Likewise studies made at gastrointestinal microbiology level also demonstrated such an influence.
In the case of pigs, it is known that coarse particle size decrease gastric pH, thus maximizing the effectiveness of the “gastric barrier” against the transmission of faecal-oral pathogenic bacteria. Likewise, the low pH of the digesta ensures a higher proportion of Volatile Fatty Acids in its undissociated form, thus increasing its antimicrobial capacity. In addition to the gastric level effect, particle size also affects at cecum and colon levels, since it is possible that coarse particle size promote an increase of the population of Short Chain Fatty Acids-producing bacteria and consequently preventing the proliferation of pathogenic bacteria (Kiarie et al., 2019).
In the case of poultry, it has been observed that the gizzard pH decreases when providing a coarse diet compared to a fine one due to an increase of the HCl secretion. Branton et al observed that birds fed with a coarse diet showed a lower mortality due to Necrotic Enteritis. This can be associated to the gastric function stimulation, including both HCl secretion and better utilization of nutrients in the small intestine that is related to coarse diets and influences the proliferation of C. perfringens (Engberg et al., 2002).
Hydrothermal treatments affect the chemical structure of feed nutrients. In pelleted feed, part of the starch is retrograded and becomes resistant starch that can only be degraded by its fermentation by the large intestine microorganisms with the consequent production of short chain fatty acids. Even so, there are few studies on the effect of hydrothermal feed treatment on the microbial composition of the gastrointestinal tract (Kiarie et al. 2019).
Additives (prebiotics-probiotics)
Prebiotics and probiotics are additives often used in animal nutrition.
A prebiotic is a substance that without being hydrolysed or absorbed at gastrointestinal level selectively stimulates beneficial bacteria growth.
Probiotics are cultures of potentially beneficial bacteria for the intestinal flora and are administrated in order to colonize the large intestine and modify its microbiota.
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