In the modern world, there is a growing trend of exploring alternative feed ingredients for the dairy sector to enhance production efficiency (
Vlaicu and Untea, 2024). The term “effective microorganisms (EM)” is often used to introduce consortia of different genera of beneficial microorganisms, which could help the digestion process and nutrient absorption, as well as have probiotic effects
(Abraheem et al., 2024; Natt and Katyal, 2022;
Sugandhi et al., 2018). Effective microorganisms contain the strains of lactic acid bacteria (LAB), yeast, actinomycetes, photosynthetic bacteria and substrates such as molasses
(Ezeagu et al., 2023). In addition, EM could be contained with beneficial enzymes and some crude extracts. Malaysian company (
EMRO, 2024) has defined “EM as a feed additive that contains only naturally occurring three major genera of microorganisms, which are yeast, LAB and photosynthetic bacteria”. The fermentation process of these consortia of bacteria secretes additional beneficial substrates of bioavailable vitamins, chelated minerals and organic acids as well as antioxidants
(Sawant et al., 2025).
Effective microorganisms have been applied in the livestock industry for purposes such as reducing odour and manure management (
Tu-Kitaw et al., 2013). They have also been used as feed supplements to improve animal performance, including milk and egg production (
Yitbarek, 2023;
Kumar et al., 2017). Effective microorganisms can be supplied through feed, water and in some cases, via fermented products such as Bokashi.
Various interventions aimed at improving animal performance have been discussed in the literature, however, relatively few studies have focused specifically on dairy cows. Existing research has primarily focused on odour reduction, then it has expanded to one of the mitigation strategies of livestock greenhouse gas (GHG) emission
(Riaz et al., 2024). Moreover, with its beneficial probiotic activity, EM enhance the gut health and subsequently improves the animal performance as well (Fig 1).
However, limited studies have focused on the effects of EM on dairy cattle performance, focusing on the essential areas of nutrient digestibility, manure management and gut function (
Nalla et al., 2022). At present, the dairy sector faces different challenges, including high feed costs, seasonal forage scarcity, poor-quality feed and climate variability
(Damunupola et al., 2022; Vidanarachchi et al., 2019). Hence, it is worth reviewing the EM technology as a sustainable approach to improve nutrient utilisation, milk production and potentially reduce environmental impact. Therefore, this review summarises the current knowledge, study gaps and suggestions for future research to optimise the use of EM in dairy production.
Effective microorganisms on milk yield and quality in dairy farming
Milk production is the main purpose of dairy cattle farming and improvement in production over time is important for profitable dairy farming (
OECD, 2025). Today, the best nutritional regime and feeding management that influences milk production is of great importance
(Qin et al., 2025). Hence, the investigation for other sustainable alternatives for feeding is imperative
(Ngesi et al., 2025; Chanda et al., 2024). Therefore, this section centres around the effect of EM on milk production, with a particular focus on nutrient digestion, absorption and their overall influence on dairy performance.
The rumen is the largest of the anterior fore-stomach compartments of ruminant herbivores and together with the reticulum, it creates a spacious fermentation vessel (
Pokhrel and Jiang, 2024;
Liu et al., 2023; Gupta et al., 2016). In the rumen, there are a massive population of bacteria, fungi and protozoa, which is held at ~39°C under a continuous culture system (
Mayulu and Christiyanto, 2025;
Zahra et al., 2022). As already mentioned, dietary substrates passing to the rumen are fermented by the rumen microbes and the products of fermentation, which are volatile fatty acids (VFA), are the major source of energy in cows
(Dhakal et al., 2024; Fang et al., 2021) and microbial protein and gases such as methane (CH
4) and carbon dioxide (CO
2) (
Iddi-Mrutu et al., 2023;
Parchami et al., 2024). Addition of EM to the system improves the rumen ecosystem and microbial diversity
(Gao et al., 2022; Lv et al., 2020). With the process of fermentation, it is believed that EM can improve fermentation and subsequently milk synthesis
(Jiang et al., 2025; Marinho et al., 2025; Tadesse et al., 2024).
It was found that microbial solution supplementation enhanced the cellulolytic bacterial population and their activity in the rumen
(Nair et al., 2025). It causes more extensive degradation of complex fibrous feed ingredients and results in greater VFA production, especially in the form of acetate and propionate
(Jiang et al., 2025). Faster release of acetate and propionate and faster production by efficient fibre digestion subsequently increase milk fat and volume
(Yang et al., 2024; Shi et al., 2023; Mitchell et al., 2023). Alternatively, stimulating production or supplementation of butyrate enhances the rumen epithelial development and function by facilitating the required energy for better rumen wall function and performance
(Fukumori et al., 2022; Steele et al., 2016). Based on the above discussion, EM as the probiotic significantly helps to improve milk production and its quality by enhancing the availability of VFA for better cow performance
(Cappellozza et al., 2023; Nalla et al., 2022).
Supplementation of EM in small ruminants has been shown to improve ruminal degradability and improve the nitrogen utilisation and microbial protein synthesis
(Direkvandi et al., 2020). The EM affects the rumen microbial population and optimises the rumen microbial protein synthesis, which is achieved by optimising the conditions in the rumen. Produced microbial proteins are a great source of amino acids, which drives protein synthesis for milk production
(Tadesse et al., 2024; Zeeshan et al., 2023). Further, studies have shown that supplementation of microbial-based feeding enhances the body weight and milk yield in cows by efficient utilisation of available energy and microbial protein, especially increasing the synthesis of casein, which is the dominant protein found in milk
(Tadesse et al., 2024; Carresi et al., 2024).
Rumen fat digestion occurs only in minute quantities because dietary fat can be detrimental to the microbes. To alleviate this problem, microbes process fats by lipolysis and biohydrogenation
(Bionaz et al., 2020; Vasta et al., 2019). Lipolysis in the rumen secretes glycerol, which may be fermented by the microbes into propionates and other VFAs that may enhance milk yield and performance in cows
(Yang et al., 2025; Kupczyñski et al., 2020;
Torres et al., 2021). Such changes in energy production processes in the rumen are accomplished through intervention from efficient microorganisms that modify and change the microbial consortia within the rumen, with the end goal being to maximise milk yield
(Mohanty et al., 2023).
As shown in Fig 2, supplementation with microbial blends including EM supports quality milk production
(Polyorach et al., 2023) by producing beneficial enzymes, minerals and vitamins, such as B vitamins (thiamine, riboflavin, pyridoxine,
etc.), which are crucial for fibre, protein and fat digestion and absorption
(Shukla et al., 2024). By enhancing nutrient absorption, EM plays a crucial role in improving overall milk yield and composition.
Other than that, recent studies have shown that high-yielding and longer lifetime dairy cows reduce the ruminal bacterial diversity, due to a greater adaptation to lactation-specific diets. Thus, supplementation with direct-fed microbials such as
Lentilactobacillus buchneri, Bifidobacterium longum and
Pediococcus pentosaceus, improved digestibility of both crude protein and neutral detergent fibre while improving milk protein percentage through optimization of ruminal fermentation and microbial protein synthesis
(Yang et al., 2025; Mu et al., 2019; Tong et al., 2018). This may be literary evidence that the supplementation of EM could support and improve the longer lifetime of dairy rumen microbial diversity. Moreover, supplementation with EM results in an increase in milk yield together with improved quality parameters of milk, thereby supporting longevity of production through improved interactions between the microbiome and host
(Yang et al., 2025; Wu et al., 2024).
Effective microorganisms on nutrient utilisation and digestive efficiency in dairy cows
This section explores the effect of EM on nutrient digestibility, enzyme activities and the digestion of fibre, fat and protein, as well as its role in nutrient absorption. Many studies in dairy cows and other ruminants showed that beneficial microorganisms (
e.g., yeast,
Bacillus spp.) interact with native rumen microbes and promote the proliferation of cellulolytic and amylolytic bacteria (such as
Fibrobacter and
Ruminococcus) while suppressing pathogenic and competitive microbes
(Halfen et al., 2021; Lopreiato et al., 2020).
Usually, a cow’s diet consists of high-fibrous feed ingredients, which are particularly difficult to digest without fermentation
(Jardstedt et al., 2018). Supplementation with microbial additives (EM) has been shown in some studies to increase the fibrinolytic bacterial population (
e.g.,
Ruminococcus, Fibrobacter) in the rumen, which may enhance the digestion process by accelerating the fermentation process
(Wang et al., 2024; Wei et al., 2022; Mamuad et al., 2019). Ingested fibrous materials are fermented and broken down by the rumen native microbes (
Ruminococcus spp, Fibrobacter spp,
etc.) in a blend with EM by producing enzymes that break cellulose and hemicellulose and subsequently produce simple sugars such as glucose, which are the base substrates for VFA production
(Firrincieli et al., 2024; Weimer, 2022). In anaerobic conditions in the rumen, sugars (glucose) produced from fibrous feeds are converted into pyruvate through glycolysis and then converted into different VFS (
e.g., acetate, propionate, butyrate), which supply energy to the cows
(Zhu et al., 2025; Hassan and Karsl, 2022). Effective microorganisms influence the process of fiber digestion by altering the rumen environment
(Tadesse et al., 2024; Sheikh et al., 2018).
Focusing on N utilization and protein digestion, cows ingest N and protein sources from the legume forages, by-products, concentrates like soybean meal, cotton seed meal and supplemented non-protein nitrogen (NPN) compounds (
Castro-Montoya et al., 2021;
Wilson et al., 2020). These proteins basically can be divided into two groups; rumen degradable protein (RDP), which is crucial for producing microbial protein and rumen undegradable protein (RUP), which is bypassed through the rumen and absorbed in the small intestine
(Putri et al., 2021; Ahvenjärvi and Huhtanen, 2018). Both are crucial in fulfilling cows’ protein requirements.
By improving the rumen ecosystem and microbial population, microbial supplementation enhances the N and protein digestion process
(Jiang et al., 2025; Cappellozza et al., 2023; Hassanat and Benchaar, 2021). When RDP comes from the feed materials, they are broken down into peptides, amino acids and ammonia (NH
3) by the microbes through the process called proteolysis
(Putri et al., 2021; Cherif et al., 2018). Then the process of deamination separates the amine group (-NH‚ ) by the enzymes and subsequently produces NH
3 (Gervais et al., 2017). By utilizing these NH
3, microbes produce microbial proteins, which are digested and absorbed in the small intestine. Moreover, by a similar mechanism, NPNs are utilized to produce microbial protein in the rumen, which converts urea into NH
3 (Lima et al., 2023; Zurak et al., 2023). For the efficient production of microbial protein, EM contributes by stabilizing the rumen pH, enhancing the fermenting process by altering the whole rumen environment.
While focusing on fat digestion, it is unlike fiber and protein digestion in the rumen, excessive fats could be toxic to the rumen microbes
(Lee et al., 2019). Dietary fats are digested by lipolysis and biohydrogenation processes with minimal intervention of rumen microbes
(Huang et al., 2022). Through the lipolysis process, the rumen microbes break down the complex fats, such as triglycerides and glycolipids, into fatty acids and glycerol by the enzyme lipase
(Hao et al., 2021). Then the glycerol converts into VFA through microbial fermentation, which produces energy (
Cantalapiedra-Hijar et al., 2016). Apart from that, the microbes convert unsaturated fatty acids in feed material such as oleic acid and linoleic acids into saturated fatty acids by adding additional hydrogen (H
+) atoms
(Wei et al., 2018). This conversion reduces the harmful effect which can be caused by rumen microbes
(Karangiya et al., 2016). The small intestine is where the saturated fatty acids go next and then they get mixed with the bile and pancreatic enzymes of the pancreas, which digest them into free fatty acids and monoglycerides that can be absorbed into the blood
(Kand et al., 2018). Further, EM supplementation increases lipolysis and biohydrogenation by optimizing conditions for fat digestion and absorption (
Owens and Basalan, 2016).
As stated in Fig 3, EM supplementation increases the nutrients’ digestibility and absorption through optimum utilization of feed resources while enhancing FCE.
Furthermore, recent findings by
Liu et al., (2025) have highlighted that feed sorting behaviour may alter the rumen microbial ecosystem and certain metabolisms to a degree that negatively impacts the efficiency of fermentation and nutrient utilisation, underscoring the need to stabilize specific microbial populations to enhance digestive efficiency, even with balanced rations. Moreover, when comparing Sanhe with Holstein cows, differences in rumen microbiome composition were observed, indicating that relative to breed and parity, some microbiomes matured, resulting in increased binding of ATP transporters in lactating cows. This led to the enrichment of transport and bioconversion of certain monosaccharides and amino acids, which indirectly influenced digestion and nutrient metabolism
(Liu et al., 2025). Besides, the study conducted by
Alaa et al., (2025), which focuses on integrated metagenomic and single-cell RNA sequencing techniques deconstructing microbial consortia, exposed certain bacterial genomes linked to core cellulose, xylan and pectin polysaccharides with prominent fibre digestion efficiency, while identifying some epithelial cell subtypes that specifically absorb and metabolise VFA. Thus, improvements in microbial ecosystem functionality are able to maximise nutrient recovery within the digestive tract, reducing feeding costs and concomitant nutrient losses to the environment
(Alaa et al., 2025; Liu et al., 2025).
Effective microorganisms on blood plasma metabolites in dairy cows
Examination of blood plasma concentration is the key method for understanding how animals metabolize ingested feeds and concentrates, as well as their nutrient absorption efficiency. This section summarizes the impact of EM on important plasma parameters in dairy cows.
Blood plasma concentration can be assessed using haematological techniques, which are valuable for accurately predicting nutrition requirements, monitoring animal health and identifying metabolic disorders and other diseases. Table 1 shows the effect of EM on blood plasma concentrations, focusing on plasma nutrient levels, compositions, hormones and metabolic indicators.
As shown in Table 1, EM positively influences the important blood plasma parameters such as SUN, NEFA, Insulin-like hormones and immunoglobulins. These parameters are key indicators of efficient nutrient utilization and enhanced immunity, both of which may contribute to improved milk production when EM is supplemented.
Effective microorganisms on manure excretion and methane emission patterns in dairy cows
Effective microorganisms have shown insightful results in manure nutrient excretion and management
(Mohamed et al., 2018). This section focuses on the specific role of EM in manure composition and its effect on the environment.
As previously discussed, EM shows a promising intervention for digestion and nutrient absorption.
Oyebade et al., (2023) clearly showed that the supplementation of EM increases the N utilization and protein absorption and reduces the manure N retention, enteric CH
4 formation and NH
3 emission by modifying the rumen environment. In addition, when NH
3 volatilization is decreased, urinary N losses are decreased (
Kenney, 2013). Thus, EM application might be useful to the environment in terms of reducing malodor and the eutrophication of water bodies resulting from excessive nutrient inflow.
The EM aids the breakdown of fibrous constituents and enhances nutrient utilization toward faecal solids reduction, owing to augmented microbial activity
(Maylem et al., 2024; Williams et al., 2023; Seo et al., 2010). In addition, EM increases a number of enzymatic processes, which results in the lowering of Phosphorus (P) and organic matter excretion in the manure
(Ort et al., 2018). Decreased digestion and nutrient absorption efficiency would increase the volume and solid content of the manure, both of which EM could alleviate.
Further, it was reported that using EM reduces volatile compounds in manure such as NH
3 and hydrogen sulfide (H
2S), which causes malodour and sometimes even mortality of cows due to toxicity would be minimized. Further, it is concluded that effective microorganisms are beneficial in reducing the manure VFA content, which may cause instability and odour production
(Bastami et al., 2016). Those works claim that EM controls the emission of a broad range of volatile compounds and their effects.
Moreover, contemporary mitigation strategies have shown that probiotics and direct-fed microbials concurrently address enteric CH
4 production and manure-based greenhouse gas emissions and meta-analyses have shown that supplementation of probiotics decreases daily CH
4 emission by about 11%, while improving nitrogen utilisation efficiency that consequently reduces nitrogen excretion in manure
(Xie et al., 2025). Methanotroph-based probiotics resulted in significant CH
4 reductions in beef steers, with some results exceeding 40 to 50% during
in vitro trials, thus showing an opportunity for specialised microbial consortia to consume CH
4 produced during rumen fermentation directly
(Tseten et al., 2025). Further, comprehensive works showed that nitrous oxide and CH
4 emissions from dairy manure are greatly influenced by the storage period, along with management practices. Probiotics supplementation enhances nutrient retention in animals, thereby reducing the greenhouse gas emission potential from manure storage systems
(Cherif et al., 2018). Application of EM in manure management, therefore, results in a dual environmental benefit through a reduction of enteric CH
4 by 10 to 15% along with a further decrease in nitrogen excretion up to 15-20%, as well as reducing NH
3 volatilisation from manure by 25 to 30%, thus mitigating the atmospheric greenhouse gas contributions and nutrient pollution, further contributing toward sustainable dairy production systems
(Xie et al., 2025; Tseten et al., 2025; Zahra et al., 2024).
Fig 4 shows, EM minimizes the environmental effects by reducing nutrient excretion and the formation of GHG and odour-forming gases by efficient nutrient utilization.