Abstract:The presence of the toxic amino acid mimosine in Leucaena leucocephala restricts its use as a protein source for ruminants. Rumen bacteria degrade mimosine to 3,4- and 2,3-dihydroxypyridine (DHP), which remain toxic. Synergistes jonesii is believed to be the main bacterium responsible for degradation of these toxic compounds but other bacteria may also be involved. In this study, a commercial inoculum provided by the Queensland's Department of Agriculture, Fisheries, and Forestry was screened for isolation and… Show more
“…Non-protein amino acids can be incorporated into protein chains leading to the formation of non-functional products that cannot be metabolised [ 98 ]. The presence of non-protein amino acids in fodder poses risks to livestock due to their potential toxicity and anti-nutritional properties [ 25 , 64 , 99 ]. There are ca.…”
Section: Rumen Microbial Detoxification Of Plant Toxinsmentioning
confidence: 99%
“…Based on early studies, it was thought that mimosine detoxification would require synergism between a variety of rumen microorganisms, with Jones and Megarrity [ 15 ] demonstrating that there were a range of bacteria in the rumen able to degrade mimosine to 3,4-DHP. A number of bacteria have been isolated including Streptococcus lutetiensis , Clostridium butyricum , Lactobacillus vitulinus and Butyrivibrio fibrisolvens that are able to degrade mimosine to DHP [ 99 ]. Additional bacteria such as S. jonesii are required for the further breakdown of 3,4-DHP to 2,3-DHP which S. jonesii can further convert to unidentified non-toxic metabolites.…”
Section: Rumen Microbial Detoxification Of Plant Toxinsmentioning
Animal feeds may contain exogenous compounds that can induce toxicity when ruminants ingest them. These toxins are secondary metabolites originating from various sources including plants, bacteria, algae and fungi. Animal feed toxins are responsible for various animal poisonings which negatively impact the livestock industry. Poisoning is more frequently reported in newly exposed, naïve ruminants while ‘experienced’ ruminants are observed to better tolerate toxin-contaminated feed. Ruminants can possess detoxification ability through rumen microorganisms with the rumen microbiome able to adapt to utilise toxic secondary metabolites. The ability of rumen microorganisms to metabolise these toxins has been used as a basis for the development of preventative probiotics to confer resistance against the poisoning to naïve ruminants. In this review, detoxification of various toxins, which include plant toxins, cyanobacteria toxins and plant-associated fungal mycotoxins, by rumen microorganisms is discussed. The review will include clinical studies of the animal poisoning caused by these toxins, the toxin mechanism of action, toxin degradation by rumen microorganisms, reported and hypothesised detoxification mechanisms and identified toxin metabolites with their toxicity compared to their parent toxin. This review highlights the commercial potential of rumen inoculum derived probiotics as viable means of improving ruminant health and production.
“…Non-protein amino acids can be incorporated into protein chains leading to the formation of non-functional products that cannot be metabolised [ 98 ]. The presence of non-protein amino acids in fodder poses risks to livestock due to their potential toxicity and anti-nutritional properties [ 25 , 64 , 99 ]. There are ca.…”
Section: Rumen Microbial Detoxification Of Plant Toxinsmentioning
confidence: 99%
“…Based on early studies, it was thought that mimosine detoxification would require synergism between a variety of rumen microorganisms, with Jones and Megarrity [ 15 ] demonstrating that there were a range of bacteria in the rumen able to degrade mimosine to 3,4-DHP. A number of bacteria have been isolated including Streptococcus lutetiensis , Clostridium butyricum , Lactobacillus vitulinus and Butyrivibrio fibrisolvens that are able to degrade mimosine to DHP [ 99 ]. Additional bacteria such as S. jonesii are required for the further breakdown of 3,4-DHP to 2,3-DHP which S. jonesii can further convert to unidentified non-toxic metabolites.…”
Section: Rumen Microbial Detoxification Of Plant Toxinsmentioning
Animal feeds may contain exogenous compounds that can induce toxicity when ruminants ingest them. These toxins are secondary metabolites originating from various sources including plants, bacteria, algae and fungi. Animal feed toxins are responsible for various animal poisonings which negatively impact the livestock industry. Poisoning is more frequently reported in newly exposed, naïve ruminants while ‘experienced’ ruminants are observed to better tolerate toxin-contaminated feed. Ruminants can possess detoxification ability through rumen microorganisms with the rumen microbiome able to adapt to utilise toxic secondary metabolites. The ability of rumen microorganisms to metabolise these toxins has been used as a basis for the development of preventative probiotics to confer resistance against the poisoning to naïve ruminants. In this review, detoxification of various toxins, which include plant toxins, cyanobacteria toxins and plant-associated fungal mycotoxins, by rumen microorganisms is discussed. The review will include clinical studies of the animal poisoning caused by these toxins, the toxin mechanism of action, toxin degradation by rumen microorganisms, reported and hypothesised detoxification mechanisms and identified toxin metabolites with their toxicity compared to their parent toxin. This review highlights the commercial potential of rumen inoculum derived probiotics as viable means of improving ruminant health and production.
“… 23 – 25 and Eucalyptus extract has terpenes, acylphloroglucinols, euglobals, etc. 26 and mimosine presence in case of Leucaena 27 . The control MFC-C achieved a steady-state after 40 days of operation, depicting a stable OV value of 292 ± 5 mV.…”
Wastewater treatment coupled with electricity recovery in microbial fuel cell (MFC) prefer mixed anaerobic sludge as inoculum in anodic chamber than pure stain of electroactive bacteria (EAB), due to robustness and syntrophic association. Genetic modification is difficult to adopt for mixed sludge microbes for enhancing power production of MFC. Hence, we demonstrated use of eco-friendly plant secondary metabolites (PSM) with sub-lethal concentrations to enhance the rate of extracellular electron transfer between EAB and anode and validated it in both bench-scale as well as pilot-scale MFCs. The PSMs contain tannin, saponin and essential oils, which are having electron shuttling properties and their addition to microbes can cause alteration in cell morphology, electroactive behaviour and shifting in microbial population dynamics depending upon concentrations and types of PSM used. Improvement of 2.1-times and 3.8-times in power densities was observed in two different MFCs inoculated with Eucalyptus-extract pre-treated mixed anaerobic sludge and pure culture of Pseudomonas aeruginosa, respectively, as compared to respective control MFCs operated without adding Eucalyptus-extract to inoculum. When Eucalyptus-extract-dose was spiked to anodic chamber (125 l) of pilot-scale MFC, treating septage, the current production was dramatically improved. Thus, PSM-dosing to inoculum holds exciting promise for increasing electricity production of field-scale MFCs.
“…In other study systems, the GI microbiome has been directly shown to influence diet selection through a single identifiable secondary metabolite or toxin that can be broken down by known microbial species that inhabits an enlarged foregut. For instance, Australian cattle eat Leucaena leucocephala only when bacteria that degrade mimosine are introduced to the rumen [7,48]. Furthermore, when the foregut pouches of woodrats (Neotoma spp.)…”
Background: Differences between individuals in their gastrointestinal microbiomes can lead to variation in their ability to persist on particular diets. Koalas are dietary specialists, feeding almost exclusively on Eucalyptus foliage but many individuals will not feed on particular Eucalyptus species that are adequate food for other individuals, even when facing starvation. We undertook a faecal inoculation experiment to test whether a koala's gastrointestinal (GI) microbiome influences their diet. Wild-caught koalas that initially fed on the preferred manna gum (Eucalyptus viminalis) were brought into captivity and orally inoculated with encapsulated material derived from faeces from koalas feeding on either the less preferred messmate (E. obliqua; treatment) or manna gum (control). Results: The gastrointestinal microbiomes of wild koalas feeding primarily on manna gum were distinct from those feeding primarily on messmate. We found that the gastrointestinal microbiomes of koalas were unresponsive to dietary changes because the control koalas' GI microbiomes did not change even when the nocturnal koalas were fed exclusively on messmate overnight. We showed that faecal inoculations can assist the GI microbiomes of koalas to change as the treatment koalas' GI microbiomes became more similar to those of wild koalas feeding on messmate. There was no overall difference between the control and treatment koalas in the quantity of messmate they consumed. However, the greater the change in the koalas' GI microbiomes, the more messmate they consumed after the inoculations had established. Conclusions: The results suggest that dietary changes can only lead to changes in the GI microbiomes of koalas if the appropriate microbial species are present, and/or that the koala gastrointestinal microbiome influences diet selection.
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