Abstract
The regular or continuous use of antibiotics or chemotherapeutic agents to cure disease have led to problems of drug resistance towards various microorganism. The use of prebiotic and probiotic can solve this problem somehow due to their preventative and ecofriendly approaches, particularly in light of new trends toward organic production systems. Probiotics and Prebiotics deal with gastrointestinal lining and improve health benefits of human as well as animals. The components of these should be a part of our foods, or it may be including in our diet to increase health benefits at the nutritional and therapeutic levels. Prebiotics, being indigestible carbohydrates available in thousands of different plant foods, stimulate the beneficial probiotic microorganisms to grow and multiply and help to improve host intestinal probiotic balance. Probiotics are a diverse group of living organism having non-pathologic bacteria that are functionally beneficial for improving health due to their ability to prevent inflammation that takes place in intestine. Action mechanism of both these in relation to each other as well as their intestinal interactions has been discussed. The beneficial effects include disease treatment and prevention as well as improvement of digestion and absorption in the host. The alarming increase in inappropriate use of antibiotics and development of bacterial resistance makes prebiotic & probiotics a very interesting field for research. In the present scenario, both have shown a number of beneficial effects in a variety of disease related to gastrointestinal as well as non-gastrointestinal such as colon cancer, ulceration in intestine.
Introduction
People awakening and awareness of their diet and health has enhanced the demand for quality food products that increase health benefit beyond the level of providing basic nutrition from regular diet. The main reason behind this awareness is the fact that whenever body’s nearly perfect healthy micro-environment is disturbed and leads to path-physiological consequences, that may arise due to infection, weak immunity system, extra dose of medicine or poor development of the tissue etc. (De Simone et al., 1992; Link-Amster et al., 1994; Saavedra and Tschernia, 2002), there is always a need to attain normal status at the earliest possible. The latest concept of diet supplements with combinations of probiotics and prebiotics have also gained momentum as they help in keeping body fit by normalizing the healthy micro-environment. The micro-environment inside our body varies from place to place such as mouth, stomach, intestine, colon and this tract is ideally full of healthy microorganisms that not only thrive in a healthy ecosystem but are sometimes as beneficial to host as these are to them (Sihag and Sharma, 2012). Probiotics and prebiotics are quickly gaining popularity among scientific community being as a safe and effective agent that help to regulate the body's micro-environment. Selection of a suitable pre and probiotic is now-a-days a main concern as a wide range of these are available in market.
Probiotics and prebiotics do not simply stop doing an effective job of recolonizing the body's micro-environment but also monitor the colon. probiotics and prebiotics have observed to play an essential role in the treatment of metabolic disorders such as Type 2 diabetes (T2DM), Cardiovascular disease (CVD), and obesity etc (Yoo and kim, 2016). By using the supplements of these, the micro-environment of the host body can be enhanced and keep pathogenic bacteria away from attaining an unwelcome toehold on host body systems. The concept of symbiotic mechanism has been suggested to describe relation of colonic food with prebiotic and probiotic as health enhancing functional food. The advancement in Biotechnology with these as a health supplements need vaster detail about the function between enteric feeding and the microenvironment exist in it that play important role in host defense.
Prebiotic
Prebiotics are the component required for the growth of probiotic bacteria and help to colonize the bowels. These are the non-digestible food elements which trigger stimulate the activity of beneficial bacteria exist in the gastrointestinal tract of the host. The name prebiotic was given by Marcel Roberfroid in 1995 (Gibson and Roberfroid, 1995; Roberfroid, 2007). The exciting thing about prebiotics is that, while passing through our stomach and small intestines, these molecules clearly pass out from our digestive system due to unablity of digestive system to act upon its components and these are only accessible for probiotic bacteria to utilize as nutritional purpose for their own. Healthy bacteria with its Ideal nutrition build up a perfect environment inside the colon to colonize itself and swipe out the pathogenic bacteria. A small partion of prebiotics gets assimilated in the region of upper gastrointestinal tract. Prebiotic may perfom various function such as antimicrobial, anti-carcinogenic, anti-osteoporotic hypolipidemic, glucose-modulatory, mineral absorption and its balance.
A prebiotic is a basically fermented compound includes carbohydrates (such as oligosaccharides) as well as non-carbohydrates that permits specific changes in the microflora of gastrointestinal, both in its composition as well as its activity. The mostly used prebiotic include Fructooligosaccharide, Isomaltooligosaccharide (Grisdale-Helland et al., 2008), Xylooligosaccharide (Roberfroid, 1996; Ringø et al., 2010b; El-Dakar et al. ,2007; Burr et al., 2008, 2009; Hartung et al., 1997 and Lochmann et al. 2009), Inulin (Wang and Gibson, 1993; Ringø, 2004), Fibers (Eastwood and Kritchevsky, 2005), Oligomate, Palatinose, Pyrodextrin, Raftiline etc.
Prebiotics stimulate probiotic bacteria not only to grow but also to produce compounds advantageous to the host. Their colonic fermentation by bacterias like bifidobacterium, lactobacilli and some other certain bacteria in the colon that produce short chain fatty acids (SCFAs) like acetate, propionate and butyrate; the hydrogen gases, hydrogen sulphide, carbon dioxide, methane; acetate, pyruvate, succinate and formate which are the important factors to determine the pH of gastrointestinal tract (Campbell et al.,1997). The SCFA have strong influence on the metabolism of the host in order to colonic absorption of calcium and also magnesium ions. This can be useful in inhibiting osteoporosis and osteopenia. The increased concentration of calcium in the colon may assist to control the formation of insoluble bile or salts of fatty acids. As a result, the possible destructive influences of bile or fatty acids on colonocytes can be reduced. SCFA of non-digestible carbohydrates are fermented at much faster rate than long chain fatty acid (Macfarlane et al., 2006; Oufir et al., 1996 and Givson et al., 1996). Thus, the short chains are readily fermented in the proximal part of the colon whereas long chain fatty acid allow the stimulation of bacterial metabolism in a more distal part of the colon which is very much energetically depleted. Bacteria starve and the proteolysis of dead cells and the subsequent strictly anaerobic fermentation of the released amino acids result in production of cytotoxic putrefaction which release phenolic compounds like skatol, indole and resol. These compounds are very important for the prebiotic utilization.
Further, Prebiotics may encourage the growth of bifidobacteria and lactobacilli in the large intestines (Bertazzoni-Minelli et al., 1996). These bacteria are able to strengthen the barrier of the intestinal mucosa, assisting in suppressing the connection of pathogenic bacteria mainly by crowding them out (Bhuiyan et al., 2017; Thakur et al.,2018). Prebiotics can also increase antimicrobial materials and encourage antigen specific and non-specific immune responses. The prebiotics is believed to be able to reduce triglyceride extent due to the reduced hepatocyte De Novo synthesis of triglycerides. Further, they can reduce total cholesterol and LDL-cholesterol rates to some extent. The possible influence of the prebiotics on blood glucose can be explained in different ways; the oligosaccharides may postpone gastric emptying and /or decrease the transportation gap in small intestinal area. In vitro and animal-based studies indicated that these bacteria can be attach to and inactivate some carcinogens (Burns and Rowland, 2000). In addition, they are said to be capable of inhibiting the development of tumors and suppress the bacteria that are likely to convert precarcinogens into carcinogens. It is probably due to potential action of butyrate. Butyrate accompanied by other short-chain fatty acids are created by bacterial fermentation of different prebiotic oligosaccharides in the colon.
Probiotic and its selection criteria
Probiotic, the word originated from “pro” and “bios” (greek word) means life and this term was first described by Werner Kollath in 1953 (Gismondo et al., 1999; Hamilton-Miller et al. 2003). Further it is defined by Lilly and Stillwell (1965) as the substances produced by one bacterium that stimulated the growth of anothers. This definition was extended by Fuller (1989) in context of an agricultural perspective as a live microbial feed supplement which beneficially affects the host by improving its intestinal microbial balance and redefined by Gatesoupe (1999) on the perspective of aquaculture as microbial cells that are administered in such a way so as to enter the gastrointestinal tract and to be kept alive, with the aim of improving health. Irianto and Austin (2002) conclude the definition again as “a probiotic is an entire or components(s) of a microorganism that is beneficial to the health of the host”.
In present scenario, probiotics are quite well known as a health promoting efficient foods that can be used as therapeutic, prophylactic and growth supplements for humans and animals along with aquatic animals due to increase its demand for ecofriendly aquaculture. The microbial community present in the gastrointestinal tract of fish and shellfish depends upon the external environment through which the water flow passing into its the digestive tract. Most bacterial cells are temporary exist in the gut of aquatic animal that influences by the continuous interruption of microbes coming from water and food (Fuller, 1989 and Gibson, 1997).
Probiotics are different strains of living bacteria which may be in their natural state or in their spore form, has the capability to have long shelf life and survives through the journey of the stomach that ends upon the colon begins. The living bacteria further multiply here and develop itself into health colonies of its own and adhere to the wall of the colon. In general, a ‘probiotic' should be non-pathogenic and beneficially affect the host health; should withstand incorporation into a delivery vehicle at high cell counts, and should remain viable throughout the shelf-life of the product; should be accepted by the host, e.g. through ingestion and potential colonization and replication within the host. It should withstand transit through the gastrointestinal tract, that is, show acid and bile tolerance; should actually work in vivo as opposed to in vitro findings. Also should be able to adhere to cells of the intestinal epithelium and/or colonize the lumen of the tract (Guo et al., 2011; Bordoni et al., 2013). It should preferably not contain virulence resistance genes or antibiotic resistance genes and able to show antagonistic activity towards enteric pathogens and/or provide demonstrated health benefits (Spanggaard et al., 2001; Balcázar et al., 2006a; Vine et al., 2006; Farzanfar, 2006; Gómez and Balcázar, 2008; Singermann, 1990; Vijayan et al., 2006; Hai et al., 2007; Kesarcodi-Watson et al. 2008; Chythanya et al., 2002; Seddik et al., 2017). A list of probiotic bacteria (Irianto and Austin, 2002b; Panigrahi et al., 2004, 2005; Aubin et al., 2005a; Kim and Austin, 2006a; Balcázar et al., 2007a,b; Bagheri et al., 2008; Merrifield et al., 2010a,b,c,d) used commercially is given below:
Lactobacillus species: L. acidophilus, L. casei, L. fermentum, L. gasser,. L. Johnsonii, L. Lactis, L. Paracasei, L. Plantarum, L. reuteri, L. rhamnosus, L. salivarius,
Bifidobacterium species: B. Bifidum, B. Breve, B. Lactis, B. Longum
Streptococcus species: S. thermophilus
Saccharomyces cerevisiae (a yeast) which have probiotic features also has been usually studied to demonstrate immunostimulatory activity and production of inhibitory substances as observed in probiotic.
3.1 Action Mechanisms of Probiotics
3.1.1 Production of Incompatible Compounds
Antagonistic compounds are described as chemical substances produced by bacteria which are toxic or inhibitory towards other microorganisms or they have a bactericidal or bacteriostatic effect on other microbial populations. These substances may be produced as either primary or secondary metabolites and therefore have different modes of inhibitory action. The bacteria which produceinhibitory substances in the GI tract of the host (in vivo) or in its culture medium (in vitro) are thought to become a barricade against the propagation of opportunistic pathogens for example lactic acid bacteria which act as a probiotic produces bacteriocin and bacteriostatic substances which help to inhibit the growth of other microorganisms (Ghosh et al., 1996; de Valk and Marx, 1999; Kontoghiorghes, 2005; Dam, 2005).
3.1.2 Competition for Chemicals or Available Energy
Iron is the element which essentially required for the growth of all microorganisms but its solubility is very low, therefore its bioavailability is poor. To cope up the low availability of iron, Siderophores are used as an ion-specific chelating agents of ferric ions which can be dissolved precipitated iron and make it easy for microbial growth (Budzikiwwicz, 1997; Meyer and Stintzi, 1998; Meyer et al., 2002; Eberl and Collinson, 2009; Manual et al., 2008). The siderophores has the capability resides in their capacity to search an essential nutrient present in the environment and remove competitors to use of it. The bacterial pathogens are successful to compete for iron in the highly scarcity of iron in tissues and body fluids of the host. Those harmless bacteria which can produce siderophores can also be used as probiotics to compete with pathogens whose pathogenicity is known to be due to siderophore production and competition for iron or to outcompete all kind of organisms requiring ferric iron from solution ((Sugita, 2011; Hedia and Hermann, 2011).
3.1.3 Competition for Adhesion Sites
The pathogenic bacteria adhere to the gut wall or the surface of other tissue to harm these sites, to prevent colonization of these pathogenic bacteria is to compete with probiotic bacteria for adhesion. In order to that probiotics have more potential to attach the enteric mucus and wall surfaces for competition to pathogenic bacteria. Since bacterial adhesion to tissue surface is important at the primary stages of pathogenic infection, competition for adhesion receptors with pathogens might be the first probiotic effect. The intestinal bacteria isolates which compete efficiently with the pathogenic bacteria for the attachment to the mucosal intestinal surface are best observed in case of turbot fish. (Sugita et al., 1996, 1997; 1998; Vershuere et al., 2000; Olafsen, 2001; Vine, 2004; Gatesoupe 2008; Gòmez and Balcàzar, 2008; Ringø, 2008; Tinh et al., 2008).
3.1.4 Enhancement of the Immune Response
Immunostimulants are chemical compounds that stimulate the immune systems of human as well as animals and make them more resistant to infections by viruses, bacteria, fungi, and parasites. Probiotic (lactic acid) bacteria administeredorally may induce increased resistance to enteric infections has been observedin warm blooded animals (William et al., 2006; Macrthy et al.,2003; Zoumpopoulou et al., 2008; Lamine et al.,2004; Peran et al., 2007; Lee et al.,2008; Rachmilewitz et al.,2004; Di, 2005; Smits et al.,2005; Schultz et al., 2003; Schultz et al., 2000; Pronio et al., 2008; Gionchetti et al.,2000; Mimura et al., 2004; Spiller, 2007 and Martin et al., 2006; Matis et al., 2015).
3.1.5 Colonization and adhesion
It is stated above that a candidate probiotic which supplied on a regular basis is able to colonize and survive in the host or in it compatible environment. The ability of a probiotic strain to colonize into the gut of the host and quality of its to attach with the mucus layer of gut and the capacity to prevent the establishment of potentially pathogenic bacteria might be proved as good preselection criterion for appropriate potential probiotic among the putative probiotics (Wilson and Perini, 1988; Katayawa et al., 1997; Bernet et al., 1993; Katouli et al., 1997; Duffy et al., 1997; Conway et al. 1987; Goldin et al. 1992; Kleeman and Klaenhammer, 1982). Probiotics play an essential role in competitive prevention of bacterial attachment on the parts of GI tract of the host body. Therefore, certain probiotics strains have been considered according to their capability to adhere with the epithelial cells. (Conway et al. 1987, Goldin et al. 1992, Kleeman and Klaenhammer 1982). The first probiotic effect shows competition for adhesion receptors with pathogenic bacteria and Some bacteria have antiviral effects also for e.g. Bacillus foraminis and B. cereus biovartoyoi exhibited antagonism against Streptocoscus iniae and Photobacterium damselae (Montes & Pugh 1993; Wang et al., 2008; Guo et al. 2009; Sharma et al., 2017a,b).
3.1.6 Improvement of water quality
Research observed that the addition of the probiotics into the water, especially Bacillus strain of bacteria has been improved the water quality. The reason behind it that gram-positive Bacillus spp. is usually more effectual in transforming organic matter into CO2 than are gram-negative bacteria, which convert organic matter into bacterial biomass or slime (Stanier, 1993). The rationale is that by sustaining higher levels of these gram-positive bacteria, farmers can minimize the accumulation of dissolved and particulate organic carbon during the production of pond and these bacteria release inhibitory compound such as bacteriocines, lysozymes, proteases, and hydrogen-peroxide which make an antagonistic environment for pathogens (Nogami and Maeda, 1992; Jory, 1998; Moriarty, 1998; Verschuere et al., 1999; Ruiz-Ponte et al., 1999; Douillet, 2000b; Chythanya et al., 2002;Balaczar et al., 2007)
Probiotic research in other animals
While there has been a long standing interest in probiotics, increased concern that overexposure to antibiotics is resulting in the generation of treatment resistant strains of bacteria, compounded by the imminent ban on the use of antibiotics as feed additive. Thus, studies on the efficacy of different strains of direct fed microbials (DFM), alone or in conjunction with other bacteria, and also on the mode of action in production animals are becoming increasingly refined and important. Many different benefits have been attributed to the consumption of probiotics in both humans (Fuller, 1989; Saavedra et al., 2004; Connolly et al., 2005; Sartor, et al., 2005) and in animals, most notably production animals such as cattle and chickens. Benefits include increased lactose tolerance and improved immunity in human and increased feed efficiency and decreased pathogen shedding in animals (Marteau and Bputron- Ruault, 2002). A healthy balance of microflora of the gastrointestinal tract is crucial to the health of an animal as well human (Ryanet al., 2015). Current production methods lead to heavy stress which can have negative effects on the performance of animals, especially on young ones whose gut microflora is not yet established. DFM have been reported to moderate the negative effects which such practices have on the health of the animals. Beef cattle undergo severe stress in the process of weaning, transport, fasting, assembly, vaccination, castration, and dehorning. Such stress can lead to an imbalance in intestinal micro flora, leading to increased morbidity and even death. A number of studies have indicated that treatment with DFM can help to restabilize the gut microflora, thereby improving overall health and performance of animal. Feed supplemented with probiotic bacteria has been shown to reduce the numbers of pathogenic bacteria in cattle rumen and feces (Huber, 1997). DFM activity is limited to the gastro intestinal tract in most species while it includes the rumen in ruminants. In these animals, DFM use has been accredited with enhanced milk production in dairy cows, improved feed efficiency and daily gain in beef cattle (Nathanon and Chantelle, 2006). This study supports the others which suggest that DFM use is most effective in times of environmental or physical stress on the host and that effects are less noticeable on healthy hosts.
Probiotics in broilers
It has been found that Lactobacillus and Enterococcus are the most common intestinal bacteria present in poultry and Lactobacillus treatment in broilers resulted in improved immunity in bird that have deficiency of Vitamin A and were also able to demonstrate the effect of probiotic on local cell mediated immunity in chickens. This was evidenced by an apparent decrease in intestinal invasion by the pathogen Eimeria acervulina based on a higher serum level of Interlukin-2. Salmonella entérinais is a major food borne illness found in poultry and raw meat contamination has significant commercial implications Dalloul et al. (2003) Tellez et al. (2006) found that combining probiotics L. acidophilus and Streptococcus faecium with antibodies against Sal. entérinais, Sal. typhimurium and Sal. heidelberg successfully reduced the disease. Other studies have found that probiotics had a positive effect on chick weight gain (Zulkifli et al., 2000).
Probiotics in Horses
Horses are classified as herbivores, or roughage eaters and has its digestive system has a great potential to assimilate large quantities of high fiber forage on regular basis. The digestive system of the horse is considered as monogastric rather than ruminant not like most other herbivores. The stomach and small intestine are the part of the upper gut where most of the biomolecules like protein, fats, vitamins and minerals are digested and absorbed. The large intestine of the horse ends into an enlarged cecum where fermentation of food takes place. In the process of fermentation cellulose and hemi-cellulose fibers, (which are present in hay, especially stems and stalks) are broken down into its smaller sub unit that are utilize by the horse. There are so many beneficial micro-organisms like bacteria and protozoa which produce enzymes that break down plant fiber having cellulose. Cellulose is the chief constituent of the cell in the most plants. Bacteria lives in the large intestine of the horse act as probiotic which help the horse in digestion of cellulose. Combination of pre and probiotics are designed to support the natural microbial population of the gut that contains legal live yeasts which are proven to support the health of the horse's gut.
Horse is a powerful animal and requires a high energy diet for competition and modern management thus, it depend on the assistance of billions of beneficial micro-organisms which live in the gut (Shen et al., 2013). The enzymes produced by these bacteria convert their food into its basic constituents of their respective component which can be easily assimilated by the gut wall of horse. The essential minerals such as calcium and zinc can easily digest with the help pf probiotic and it also aids in the production and bioavailability of vitamin B. The antimicrobial property of the probiotics inhibits the production of harmful microbial community, its illness and also exclude harmful bacteria through competition for space and nutrients by colonization into the gut. Lactating mares have shown benefited to probiotics through the Improvement of quality and quantity of milk which can stimulate the initial growth of foals and also decrease the death in foals.
Thus, probiotic provides a healthy micro-flora in the horse gut that help them to improve general health, appearance, body structure and its performance along with its immunity power. Probiotic may prove an effective prophylactic measure when a horse Consume sand and dirt along with their food that can create obstruction in gastrointestinal tract that may lead into different illness like chronic diarrhea, weight loss, and colic (Allen et al., 2008). If a horse has an upset because of grain overload then adding more Lactobacillus in diet is the last thing to do, since it's the other species that are going to be adversely affected.
Conclusion
Microbiota of living organisms present in the gastrointestinal tract plays a vital role in terrestrial as well as aquatic animals along with humans to stimulate the digestive processes and also in improving the health of the host. Probiotics generates a useful effect on the host by administration of live micro-organisms such as those in traditional yoghurt and other fermented foods or in powders, tablets, liquid suspensions and lyophilized in capsules. They have considerable therapeutic advantages. They have the ability to prevent and treatment of a variety of intestinal disorders, aid in preventing intestinal bacterial enzymes involved in the production of colonic carcinogens. Probiotics are proving itself in modulation of immune function of the host, humoral, cellular and non-specific immunity in the host body. Some advantages of probiotics over conventional therapy include virtually low cost in addition to the fact that probiotics are not expected to increase the incidence of antibiotic resistance or the mechanisms in which probiotics may suppress pathogens (resulting in reduction the extent of resistance against the probiotic). Prebiotics may be more efficient than probiotics in obtaining colonic bacterial adaptation to provide beneficial effects on colonic disease and also affecting lactose intolerance. Basically prebiotic foods have certain absorption, fiber contribution, gut integrity, immune function, cholesterol control and also in the treatment of constipation and hepatic encephalopathy. They can protect against some intestinal pathogens and may be helpful in some inflammatory bowel disease. They can have some anticarcinogenic influences. Prebiotics are also able to facilitate mineral absorption into the bone of the host and aid to protect the bones against osteoporosis. In addition, certain prebiotics are believed to be effective on diabetes mellitus. Simultaneous taking of prebiotics and probiotics may develop the potential effectiveness of both the probiotics and the prebiotics. The growing demands of natural alternatives over conventional medicine are expected to improve the prebiotic market.
References
- Aubin J., F. J. Gatesoupe, L. Labbe and L. Lebrun L. (2005a). Trial of probiotics to prevent the vertebral column compression syndrome in rainbow trout (Oncorhynchus mykiss Walbaum). Aquacult. Res. 36: 758-767
View at Publisher |
View at Google Scholar
- Bagheri T., S. A. Hedayati, V. Yavari, M. Alizade and A. Farzanfar (2008). Growth, survival and gut microbial load of rainbow trout (Onchorhynchus mykiss) fry given diet supplemented with probiotic during the two months of first feeding. Turk. J. Fish. Aquat. Sci. 8: 43-48
View at Publisher |
View at Google Scholar
- Balcázar J. L., I. de Blas, I. Ruiz-Zazuela, A.C. Calvo, I. Márquez, O. Gironés and J.L. Muzquiz. (2007a). Changes in intestinal microbiota and humoral immune response following probiotic administration in brown trout (Salmo trutta). Brit. J. Nutr. 97: 522-552
View at Publisher |
View at Google Scholar
- Balcázar J. L., I. de Blas, I. Ruiz-Zazuela, A.C. Calvo, I. Márquez, O. Gironés and J.L. Muzquiz (2006a). The role of probiotics in aquaculture. Vet. Microbiol. 114: 173–=-186
View at Publisher |
View at Google Scholar
- Balcázar J. L., I. de Blas, I. Ruiz-Zazuela, A.C. Calvo, I. Márquez, O. Gironés and J.L. Muzquiz (2007b). Enhancement of the immune response and protection induced by probiotic lactic acid bacteria against furunculosis in rainbow trout (Oncorhynchus mykiss) FEMS.Immunol. Med. Microbiol. 51: 185-193
View at Publisher |
View at Google Scholar
- Bandyopadhyay P. and P.K. Das Mohapatra (2009). Effect of a probiotic bacterium Bacillus circulans PB7 in the formulated diets: on growth, nutritional quality and immunity of Catla catla (Ham.). Fish Physiol Biochem. 35(3): 467-78.
View at Publisher |
View at Google Scholar
- Bernet M. F., D. Brassart, J.R. Meeser and A. Servin (1993). Adhesion of human Bifidobacteria strains to cultured human intestinal epithelial cells and inhibition of enteropathogen-cell interactions. Appl. Environm. Microbiol. 59: 4121-4128.
View at Publisher |
View at Google Scholar
- Bertazzoni-Minelli E. A., L. Benini Vicentini, E. Andreoli, M. Oselladore and R. Cerutti (1996). Effect of Lactobacillus acidophilus and Bifidobacterium bifidum administration on colonic microbiota and its metabolic activity in premenstrual syndrome. Microb. Ecol. Health Dis. 9: 247-260
View at Publisher |
View at Google Scholar
- Bhuiyan, R., Shill, S., Islam, A and Chakrabortty, S., 2017. Screening of Lactobacillus spp. from raw goat milk showing probiotic activities against pathogenic bacteria. African J. Microbiol. Res. 11(15), 620-625.
View at Publisher |
View at Google Scholar
- Bordoni, A. Amaretti, A. Leonardi, E. Boschetti, F. Danesi, D. Matteuzzi, L. Roncaglia, S. Raimondi, M. Rossi, Cholesterol-lowering probiotics: in vitro selection and in vivo testing of bifidobacteria, Appl. Microbiol.Biotechnol. 97 (2013) 8273-8281.
View at Publisher |
View at Google Scholar
- Budzikiwwicz H. (1997). Siderophores of fluorescent pseudomonads. Z. Naturforsch 52: 713-720.
View at Publisher |
View at Google Scholar
- Burns A.J. and I.R. Rowland I. R. (2000). Anti-Carcinogenicity of Probiotics and Prebiotics Intest. Microbiol. 1(1), 13-24
View at Publisher |
View at Google Scholar
- Burr G., M. Hume, S. Ricke, D. Nisbet and D. Gatlin-III (2008) A preliminary in vitro assessment of GroBiotic®-A, brewer's yeast and fructooligosaccharide as Prebiotics for the red drum Sciaenops ocellatus. J. Environ. Sci. Health 43: 253-260.
View at Publisher |
View at Google Scholar
- Burr G., D. M. Gatlin-III and M. Hume (2009). Effects of the prebiotics GroBiotic®- and inulin on the intestinal microbiota of red drum, Sciaenops ocellatus. J. World Aquac. Soc. 40: 440-449.
View at Publisher |
View at Google Scholar
- Campbell J. M., G.C. Fahey and B.W. Wolf (1997) Selected indigestible oligosaccharides affect large bowel mass and fecal short-chain fatty acids, pH, and microflora in rats. J. Nutr. 127(1): 130–136
View at Publisher |
View at Google Scholar
- Chythanya R., I. Karunasagar and I. Karunasagar (2002) Inhibition of shrimp pathogenic vibrios by a marine Pseudomonas I-2 strain. Aquacult., 208: 1-10.
View at Publisher |
View at Google Scholar
- Chythanya, R. , Karunasagar, I. and Karunasagar, I. (2002) Inhibition of shrimp pathogenic vibrios by a marine I-2 strain. Aquacult. 208 , pp. 1-10.
View at Publisher |
View at Google Scholar
- Conway P. L., S.L. Gorbach and B.R. Goldin (1987) Survival of lactic acid bacteria in the human stomach and adhesion to intestinal cells. Journal of Dairy Science 70: 1-12.
View at Publisher |
View at Google Scholar
- Dam T. (2005). Siderophores-potential candidate in the therapy of neonatal meningitis. J. Med. Microbiol. 54: 613
View at Publisher |
View at Google Scholar
- Daniells S, 2010. Prebiotics may stop early stage colon cancer. (http://www.nutraingredients.com/Research/Prebioticsmay-stop-early-stage-colon-cancer-Study).
View at Publisher |
View at Google Scholar
- De Simone C., A. Ciardi, A. Grassi, G.S. Lambert, S. Tzantzoglou, V. Trinchieri, S. Moretti and E. Jirillo (1992) Effect of Bifidobacterium bifidum and Lactobacillus acidophilus on gut mucosa and peripheral blood B lymphocytes. Immunopharmacology Immunotoxicology 14: 331–340.
View at Publisher |
View at Google Scholar
- De Valk, B. and J.J.M. Marx (1999) Iron, atherosclerosis, and ischemic heart disease. Arch. Intern. Med. 159 (14), 1542–1548
View at Publisher |
View at Google Scholar
- Di G. C., M. Marinaro, M. Sanchez, W. Strober and M. Boirivant (2005) Probiotics ameliorate recurrent Th1-mediated murine colitis by inducing IL-10 and IL-10-dependent TGF-beta-bearing regulatory cells. J Immunol. 174: 3237-46.
View at Publisher |
View at Google Scholar
- Douillet P. A. (2000b) Bacterial additives that consistently enhance rotifer growth under synxenic culture conditions; 2. Use of single and multiple bacterial probiotics. Aquacult., 182: 241-248.
View at Publisher |
View at Google Scholar
- Duffy L.C., M.A. Zielezny, V. Carrion, E. Griffiths, D. Dryja, M. Hilty, M. Rook and F. Morin. (1997) Concordance of bacterial cultures with endotoxin and interleukin-6 in necrotizing enterocolitis. Dig. Dis. Sci. 42(2), 359–365.
View at Publisher |
View at Google Scholar
- Eastwood M. and D. Kritchevsky (2005)
View at Publisher |
View at Google Scholar
- Eberl H. J. and S. Collinson (2009) A modeling and simulation study of siderophore mediated antagonism in dual-species biofilms. Theor. Biol. Med. Model. 22: 6-30.
View at Publisher |
View at Google Scholar
- El-Dakar A.Y., S.M. Shalaby and I.P. Saoud (2007) Assessing the use of a dietary probiotic/prebiotic as an enhancer of spinefoot rabbitfish Siganus rivulatus survival and growth. Aqua. Nutr. 13: 407-412
View at Publisher |
View at Google Scholar
- Farzanfar A. (2006) The use of probiotics in shrimp aquaculture FEMS. Immunol. Med. Microbiol. 48: 149-158
View at Publisher |
View at Google Scholar
- Fotiadis CI, Stoidis CN, Spyropoulos BG, Zografos ED, 2008. Role of probiotics, prebiotics and synbiotics in chemoprevention for colorectal cancer. World Journal of Gastroenterology, 14(42): 6453-6457.
View at Publisher |
View at Google Scholar
- Friedenreich CM, Brant RF, Riboli E, 1994. Influence of methodologic factors in a pooled analysis of 13 case-control studies of colorectal cancer and dietary fiber. Epidemiology, 5: 66-79.
View at Publisher |
View at Google Scholar
- Fuller R. (1989) Probiotics in man and animals. Journal of Applied Bacteriology. 66: 365-378
View at Publisher |
View at Google Scholar
- Fuller R. and G.R. Gibson (1997) Modification of the intestinal microflora using probiotics and prebiotics. Scand. J. Gastroenterol. 32(suppl 222): 28-31
View at Publisher |
View at Google Scholar
- Gallaher D., W. Stallings, L. Blessing, F. Busta and L. Brady (1996) Probiotics, cecal microflora and aberrant crypts in the rat colon. J. Nutr. 126: 1362–137
View at Publisher |
View at Google Scholar
- Gatesoupe F. J. (1999) The use of probiotics in aquaculture. Aquaculture 180: 147-165
View at Publisher |
View at Google Scholar
- Gatesoupe F. J. (2008) Updating the importance of lactic acid bacteria in fish farming: natural occurrence and probiotic treatments. J. Mol. Microbiol. Biotechnol. 14: 107-114
View at Publisher |
View at Google Scholar
- Ghosh A., M. Ghosh, C. Niu, F. Malouin, U. Moellmann and M.J. Miller (1996) Iron transport-mediated drug delivery using mixed-ligand siderophore-beta-lactam conjugates. Chem. Biol. 3: 1011-1019
View at Publisher |
View at Google Scholar
- Gibson G. R. and M.B. Roberfroid (1995) Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics. J. Nutr. 125: 1401-1412.
View at Publisher |
View at Google Scholar
- Gibson G. R., A.L. McCartney and R.A. Rastall (2005). Prebiotics and resistance to gastrointestinal infections. Br J Nutr. 1: S31-4
View at Publisher |
View at Google Scholar
- Gibson G. R., H.M. Probert, J.V. Loo, R.A. Rastall and M.B. Roberfroid (2004) Dietary modulation of the human colonic microbiota: updating the concept of prebiotics. Nutr. Res. Rev. 17: 259-275
View at Publisher |
View at Google Scholar
- Gionchetti P., F. Rizzello, A. Venturi and et al. (2000). Oral bacteriotherapy as maintenance treatment in patients with chronic pouchitis: a double-blind, placebo-controlled trial. Gastroenterology 119: 305-9.
View at Publisher |
View at Google Scholar
- Gismondo M. R., L. Drago and A. Lombardi (1999) Review of probiotics available to modify gastrointestinal flora. International Journal of Antimicrobial Agents. 12: 287-292
View at Publisher |
View at Google Scholar
- Givson G. R., A. Willems, S. Reading and M.D. Collins (1996). Fermentation of non-digestible oligosaccharides by human colonic bacteria. Symposium 2. Proceedings of the Nutrition Society. 55: 899-912
View at Publisher |
View at Google Scholar
- Goldin B., S.L. Gorbach, M. Saxelin, S. Barakat, L. Gualtieri and S. Salminen (1992) Survival of Lactobacillus species (strain GG) in human gastrointestinal tract. Dig. Dis. Sci. 37: 121-128.
View at Publisher |
View at Google Scholar
- Gómez G. D. and J.L. Balcázar (2008) A review on the interactions between gut microbiota and innate immunity of fish FEMS. Immunol. Med. Microbiol. 52: 145–154
View at Publisher |
View at Google Scholar
- Gómez, G. D. and J.L. Balcázar (2008) A review on the interactions between gut microbiota and innate immunity of fish FEMS. Immunol. Med. Microbiol. 52: 145-154
View at Publisher |
View at Google Scholar
- Grisdale-Helland B., S.J. Helland, D.M. Gatlin III (2008) The effects of dietary supplementation with mannanoligosaccharide, fructooligosaccharide or galactooligosaccharide on the growth and feed utilization of Atlantic salmon (Salmo salar). Aquaculture 283: 163-167.
View at Publisher |
View at Google Scholar
- Hai N. V., Fotedar R. and Buller N. (2007) Selection of probiotics by various inhibition test methodsfor use in the culture of western king shrimps, (Kishinouye). Aquacult. 272, pp. 231-239.
View at Publisher |
View at Google Scholar
- Hamilton M., J.M.T. Professor , G.R. Gibson and W. Bruck (2003)
View at Publisher |
View at Google Scholar
- Hartung T., A. Sauer, C. Hermann, F. Brockhaus and A.Wendel (1997) Overactivation of the immune system by translocated bacteria and bacterial products. Scan. Jour. Gastroenterol. 222(suppl. B), 98-99.
View at Publisher |
View at Google Scholar
- Hedia F. and J. Hermann (2011). Antagonistic control of microbial pathogen sunderiron limitations by siderophore producing bacteria in a chemostat setup. Eberl Journal of Theoretical Biology 273: 103-114.
View at Publisher |
View at Google Scholar
- Hughes R, Rowland IR, 2001. Stimulation of apoptosis by two prebiotic chicory fructans in the rat colon. Carcinogenesis, 22: 43-47.
View at Publisher |
View at Google Scholar
- Irianto A. and B. Austin (2002) Probiotics in aquaculture. J Fish Dis. 25: 633-642
View at Publisher |
View at Google Scholar
- Irianto A. and B. Austin (2002b) Use of probiotics to control furunculosis in rainbow trout, Oncorhynchus mykiss (Walbaum). J. Fish Dis. 25: 333–342
View at Publisher |
View at Google Scholar
- Jory D. E. (1998) Use of probiotics in penaeid shrimp growout. Aquaculture Mag., 24: 62-67.
View at Publisher |
View at Google Scholar
- Katayawa M., X. Dazhong, R. Specian and E. Deitch (1997) Role of bacterial adherence and the mucus barrier on bacterial translocation. Ann. Surg. 225(3): 317–326
View at Publisher |
View at Google Scholar
- Katouli M., C.G. Nettebladt, V. Muratov, O. Ljungqvist, T. Bark, T. Svenberg and R. Mollby (1997) Selective translocation of coliform bacteria adhering to caecal epithelium of rats during catabolic stress. J Med. Microbiol. 46(7): 571-578
View at Publisher |
View at Google Scholar
- Kesarcodi-Watson A., Kaspar H., Lategan M. J. and Gibson L. (2008) Probiotics in aquaculture: The need, principles and mechanisms of action and screening processes. Aquacult. 274, pp. 1-14.
View at Publisher |
View at Google Scholar
- Kim D. H. and B. Austin (2006a). Innate immune responses in rainbow trout (Oncorhynchus mykiss, Walbaum) induced by probiotics. Fish Shellfish Immunol. 21: 513-524
View at Publisher |
View at Google Scholar
- Kleeman E. G. and T.R. Klaenhammer (1982) Adherence of Lactobacillus species to human fetal intestinal cells. J. Dairy Sci. 65: 2063-2069
View at Publisher |
View at Google Scholar
- Kontoghiorghes G. J. (2005) Regulatory Molecules and Chelators Used for the Control of Essential and Toxic Metals in Health and Disease: From Molecular Interac- tions to Clinical Effects and Applications. (Bentham Science Publishers Ltd).
View at Publisher |
View at Google Scholar
- Lamine F., H. Eutamene, J. Fioramonti, L. Bueno and V. Theodorou (2004) Colonic responses to Lactobacillus farciminis treatment in trinitrobenzene sulphonic acid-induced colitis in rats. Scand J Gastroenterol 39: 1250-8
View at Publisher |
View at Google Scholar
- Lee H. S., S.Y. Han, E.A. Bae and et al. (2008) Lactic acid bacteria inhibit proinflammatory cytokine expression and bacterial glycosaminoglycan degradation activity in dextran sulfate sodium-induced colitic mice. Int. Immunopharmacol. 8: 574-80.
View at Publisher |
View at Google Scholar
- Lilly D. M. and R.H. Stillwell (1965) Probiotics: growth promoting factors produced by microorganisms. Science. 147: 747-748
View at Publisher |
View at Google Scholar
- Link-Amster H., F. Rochat, K.Y. Saudan, O. Mignot and J.M. Aeschlimann (1994) Modulation of a specific humoral immune response and changes in intestinal flora mediated through fermented milk intake. FEMS Immunology & Medical Microbiology 10: 55-63.
View at Publisher |
View at Google Scholar
- Lochmann R. T., T.D. Sink and H. Phillips (2009) Effects of dietary lipid concentration, a dairy-yeast prebiotic, and fish and nonfish protein sources on growth, survival, and nonspecific immune response of golden shiners in indoor tanks and outdoor pools. North Am. J. Aquac. 71: 16-23.
View at Publisher |
View at Google Scholar
- Macfarlane S. (2006). Prebiotics in the gastrointestinal tract. Aliment Pharmacol Ther. 24(5):701-14
View at Publisher |
View at Google Scholar
- Manual S., C.S. Lucia, O.P. Maria and J.V. Maria (2008) Antagonismbetween Bacillus cereus and Pseudomonas fluorescens in planktonicsystemsinbiofilms. Biofouling 24 (5): 339–349.
View at Publisher |
View at Google Scholar
- Martin F. P., E.F. Verdu, Y. Wang and et al. (2006) Transgenomic metabolic interactions in a mouse disease model: interactions of Trichinella spiralis infection with dietary Lactobacillus paracasei supplementation. J Proteome Res 5: 2185-93.
View at Publisher |
View at Google Scholar
- Matis G., Kulcsar A., Turowski V., Febel H., Neogrady Z., Huber K. Effects of oral butyrate application on insulin signaling in various tissues of chickens. Domest. Anim. Endocrinol. 2015;50: 26-31.
View at Publisher |
View at Google Scholar
- Mccarthy J., L. O'mahony, L. O'callaghan and et al. (2003). Double blind, placebo controlled trial of two probiotic strains in interleukin 10 knockout mice and mechanistic link with cytokine balance. Gut 52: 975-80
View at Publisher |
View at Google Scholar
- Merrifield D. L, G. Bradley, R.T.M. Baker, A. Dimitroglou and S.J. Davies (2010a) Probiotic applications for rainbow trout (Oncorhynchus mykiss Walbaum) I. Effects on growth performance, feed utilisation, intestinal microbiota and related health criteria. Aqua. Nutr.
View at Publisher |
View at Google Scholar
- Merrifield D. L, G. Bradley, R.T.M. Baker, A. Dimitroglou and S.J. Davies (2010b). Probiotic applications for rainbow trout (Oncorhynchus mykiss Walbaum) II. Effects on growth performance,feed utilisation, intestinal microbiota and related health criteria post antibiotic treatment. Aqua. Nutr.
View at Publisher |
View at Google Scholar
- Merrifield D. L, G. Bradley, R.T.M. Baker, A. Dimitroglou and S.J. Davies (2010c). in press. Assessment of the effects of vegetative and lyophilised Pediococcus acidilactici on growth, feed utilisation, intestinal colonisation and health parameters of rainbow trout (Oncorhynchus mykiss Walbaum). Aqua. Nutr.
View at Publisher |
View at Google Scholar
- Merrifield D. L, G. Bradley, R.T.M. Baker, A. Dimitroglou and S.J. Davies (2010d). Possible influence of probiotic adhesion to intestinal mucosa on the activity and morphology of rainbow trout (Oncorhynchus mykiss) enterocytes. Aquacult. Res.
View at Publisher |
View at Google Scholar
- Meyer J. M. and A. Stintzi (1998). Iron metabolism and siderophores. In: Montie, T.C. (Eds.), Pseudomonas and Related Species, (New York: Plenum Press Ltd) pp., 201-243.
View at Publisher |
View at Google Scholar
- Meyer J. M., V.A. Geoffroy, N. Baida, L. Gardan, D. Izard, P. Lemancean, W. Achouak and N.J. Palleroni (2002). Siderophore typing, a powerful tool for the identifica- tion of fluorescent and nonfluorescent pseudomonad. Appl. Environ. Microbiol. 68: 2745-2753.
View at Publisher |
View at Google Scholar
- Mimura, T., F. Rizzello, U. Helwig, and et al. (2004) Once daily high dose probiotic therapy (VSL#3) for maintaining remission in recurrent or refractory pouchitis. Gut 53: 108-14.
View at Publisher |
View at Google Scholar
- Mitchell D, 2010. Prebiotics may help prevent colon cancer. http://www.emaxhealth.com/1275/100/33330/prebiotics-mayhelp-prevent-colon-cancer.html]
View at Publisher |
View at Google Scholar
- Montes A. J. and Pugh D. G. (1993) The use of probiotics in food-animal practice. Vet. Med. 88, pp. 282-288.
View at Publisher |
View at Google Scholar
- Moriarty D. J. W. (1998). Control of luminous Vibrio species in penaeid aquaculture ponds. Aquacult., 164: 351-358.
View at Publisher |
View at Google Scholar
- Nogami K. and M. Meada (1992). Bacteria as biocontrol agents for rearing larvae of the Crab Portunus trituber Culatus. Canadian. J. fish and aquatic sci., 4(9): 2373-2376.
View at Publisher |
View at Google Scholar
- Olafsen J. A. (2001) Interactions between fish larvae and bacteria in marine aquaculture. Aquacult. 200: 223-247
View at Publisher |
View at Google Scholar
- Oufir E. l., B.S. Flourié, B.D. Varannes, J.L. Barry, D. Cloarec, F. Bornet and J.P. Galmiche (1996) Relations between transit time, fermentation products, and hydrogen consuming flora in healthy humans. Gut. 38(6): 870-877
View at Publisher |
View at Google Scholar
- Panigrahi A., V. Kiron, J. Puangkaew, T. Kobayashi, S. Satoh and H. Sugita (2005) The viability of probiotic bacteria as a factor influencing the immune response in rainbow trout (Oncorhynchus mykiss). Aquacult. 243: 241-254
View at Publisher |
View at Google Scholar
- Panigrahi A., V. Kiron, T. Kobayashi, J. Puangkaew, S. Satoh and H. Sugita (2004) Immune responses in rainbow trout Oncorhynchus mykiss induced by a potential probiotic bacteria Lactobacillus rhamnosus JCM 1136. Vet. Immunol. Immunopathol. 102: 379-388
View at Publisher |
View at Google Scholar
- Peran L., S. Sierra, M. Comalada and et al. (2007) A comparative study of the preventative effects exerted by two probiotics, Lactobacillus reuteri and Lactobacillus fermentum, in the trinitrobenzenesulfonic acid model of rat colitis. Br J Nutr 97: 96-103.
View at Publisher |
View at Google Scholar
- Prebiotics,2010.[http://170.107.206.70/drug_info/nmdrugprofiles/nutsupdrugs/pre_0326.shtml]
View at Publisher |
View at Google Scholar
- Pronio A., C. Montesani and C. C. Butteroni (2008) Probiotic administration in patients with ileal pouch-anal anastomosis for ulcerative colitis is associated with expansion of mucosal regulatory cells. Inflamm. Bowel Dis. 14: 662-8
View at Publisher |
View at Google Scholar
- Rachmilewitz D., K. Katakura, F. Karmeli and et al. (2004) Toll-like receptor 9 signaling mediates the anti-inflammatory effects of probiotics in murine experimental colitis. Gastroenterology 126: 520-8
View at Publisher |
View at Google Scholar
- Ringø E. (2004) Lactic acid bacteria in fish and fish farming. In: S. Salminen, A. Ouwehand & A. and von Wrigth (Eds), Bacteria, Lactic Acid. (New York: Marcel Dekker publishers), pp. 581-610
View at Publisher |
View at Google Scholar
- Ringø E. and R.E. Olsen (2008) Gut health in aquatic species. In: Binder, E.M. and Schatzmayr, G. (Eds.), The Future of Animal Production (Nottingham University Press, Nottingham, UK) pp. 79-105
View at Publisher |
View at Google Scholar
- Roberfroid M. (2007) Prebiotics: the concept revised. Journal of Nutrition 137: 830S-837S
View at Publisher |
View at Google Scholar
- Roberfroid M. B. (1996). Functional effects of food components and the gastrointestinal system: Chicory fructooligosaccharides. Nutr. Rev. 54(11): S38-S42.
View at Publisher |
View at Google Scholar
- Ruiz-Ponte C., J.F. Samain, J.L. Sanchez and J.L.Nicolas (1999) The benefit of a Roseabacter species on the survival of scallop larvae. Mar. Biotechnol., 1: 52-59.
View at Publisher |
View at Google Scholar
- Ryan P.M., Ross R.P., Fitzgerald G.F., Caplice N.M., Stanton C. (2015). Functional food addressing heart health: Do we have to target the gut microbiota? Curr. Opin. Clin. Nutr. Metab. Care. 18:566-571.
View at Publisher |
View at Google Scholar
- Saavedra J.M. and A. Tschernia (2002) Human studies with probiotics and prebiotics: clinical implications. British Journal of Nutrition 87, Suppl. 2: S241-S246
View at Publisher |
View at Google Scholar
- Saveedra J. (1995) microbes to fight microbe: a not so novel approach to controlling diarrhoeal disease. J. paediatr. Gastroenterol nutr. 21: 125- 129
View at Publisher |
View at Google Scholar
- Schultz M., H.J. Linde and N. Lehn (2003) Immunomodulatory consequences of oral administration of Lactobacillus rhamnosus strain GG in healthy volunteers. J Dairy Res 70: 165-73.
View at Publisher |
View at Google Scholar
- Seddik, H.A., Bendali, F., Gancel, F., Fliss, I., Spano, G and Drider, D., 2017. Lactobacillus plantarum and its probiotic and food potentialities. Probiotics
View at Publisher |
View at Google Scholar
- Antimicro. Prot. DOI: 10.1007/s12602- 017-9264).
View at Publisher |
View at Google Scholar
- Sharma, C., Gulati, S., Thakur, N., Singh, B.P., Gupta, S., Kaur, S., Mishra, S.K., Puniya, A.K., Gill, J.P.S and Panwar, H., 2017a. Antibiotic sensitivity pattern of indigenous lactobacilli isolated from curd and human milk samples. 3 Biotech 7(1), 53.
View at Publisher |
View at Google Scholar
- Sharma, C., Singh, B.P., Thakur, N., Gulati, S., Gupta, S., Mishra, S.K., Panwar, H., 2017b. Antibacterial effects of Lactobacillus isolates of curd and human milk origin against food borne and human pathogens. 3 Biotech 7(31).
View at Publisher |
View at Google Scholar
- Shen J., Obin M.S., Zhao L.P. The gut microbiota, obesity and insulin resistance. Mol. Aspects. Med. 2013; 34:39–58. doi: 10.1016/j.mam.2012.11.001. [PubMed] [CrossRef]
View at Publisher |
View at Google Scholar
- Sihag R.C. and Sharma P. (2012). Probiotics: the new ecofriendly alternative measures of diseases control for sustainable aquaculture. Journal of Fisheries and Aquatic Science 7(2): 72-103.
View at Publisher |
View at Google Scholar
- Sihag R.C. and Sharma P. (2012). Relative Efficacy of Two Probiotics in Controlling the Epizootic Ulcerative Syndrome Disease in Mrigal (Cirrhinus mrigala Ham.). Journal of Fisheries and Aquatic Science. 8(2):305-322.
View at Publisher |
View at Google Scholar
- Singermann C. J. (1990) Principal diseases of marine fish and shellfish Academic Press , New York
View at Publisher |
View at Google Scholar
- Smits H. H., A. Engering, K.D. Van der and et al (2005) Selective probiotic bacteria induce IL-10-producing regulatory T cells in vitro by modulating dendritic cell function through dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin. J Allergy Clin Immunol. 115: 1260-7.
View at Publisher |
View at Google Scholar
- Spanggaard B., I. Huber, J. Nielsen, E.B. Sick, C.B. Pipper, T. Martinussen, W.J. Slierendrecht and L. Gram (2001) The probiotic potential against vibriosis of the indigenous microflora of rainbow trout. Environ. Microbiol. 3: 755–765
View at Publisher |
View at Google Scholar
- Spiller R.C. (2007) Irritable bowel syndrome: bacteria and inflammation - clinical relevance now. Curr Treat Options Gastroenterol 10: 312-21
View at Publisher |
View at Google Scholar
- Stanier R. Y., M. Doudoroff and E.A. Adelberg (2006) The microbial world. Prentice-Hall Inc., Englewood DOI: 10.1002/food.19710150539
View at Publisher |
View at Google Scholar
- Sugita H., Kawasaki J. and DeguchiY. (1997). Production of amylase by the intestinal microflora in cultured freshwater fish. FEMS Lett. Appl. Microbiol. 24: 105–108.
View at Publisher |
View at Google Scholar
- Sugita H., Mizuki H. and Itoi. S. (2011). Diversity of siderophore-producing bacteria isolated from the intestinal tracts of fish along the Japanese coast. DOI: 10.1111/j.1365-2109.2011.02851.x
View at Publisher |
View at Google Scholar
- Sugita H., Shibuya K., Shimooka H. and Deguchi Y. (1996). Antibacterial abilities of intestinal bacteria in freshwater cultured fish. Aquaculture 145: 195–203.
View at Publisher |
View at Google Scholar
- Sugita H., Y. Hirose, N. Matsuo and Y. Deguchi (1998) Production of the antibacterial substance by Bacillus sp. strain NM 12, an intestinal bacterium of Japanese coastal fish. Aquaculture 165: 269–280.
View at Publisher |
View at Google Scholar
- Thakur N, Sharma C, Rokana N, Singh B P, Gulhane R D, Mishra S K, Khatkar S K, Puniya A K and Panwar H (2018). In vitro Assessment of Antibiotic Resistance Pattern among Lactobacillus Strains Isolated from Goat Milk. International Journal of Current Microbiology and Applied Sciences 7(1): 2108-2116
View at Publisher |
View at Google Scholar
- The absolute importance of probiotics, 2009. [http://www.vitamintrader.com/articles/2006_12_probiotics.html] Gupta V, Garg R, 2009. Probiotics.
View at Publisher |
View at Google Scholar
- Tinh N. T. N., Dierckens K., Sorgeloos P. and Bossier P. (2008). A review of the functionality of probiotics in the larviculture food chain. Mar. Biotechnol. 10: 1–12
View at Publisher |
View at Google Scholar
- Verschuere L., Rombaut G., Huys G., Dhont J., Sorgeloos P. and Verstraete W. (1999). Microbial control of the culture of Artemia juveniles through preemptive colonization by selected bacterial strains. Appl. Environ. Microbiol., 65: 2527-2533.
View at Publisher |
View at Google Scholar
- Verschuere L., Rombaut G., Sorgeloos P. and Verstraete W. (2000). Probiotic bacteria as biological control agents in aquaculture. Microbiol Mol Biol R. 64: 655-671
View at Publisher |
View at Google Scholar
- Vijayan K. K., Bright Singh I.S., Jayaprakash N. S., Alavandi S.., Somnath Pai S., Preetha R., Rajan J. J. S. and Santiago T. C. (2006) A brackishwater isolate of PS-102, a potential antagonistic bacterium against pathogenic vibrios in penaeid and non-penaeid rearing systems. Aquacult. 251, pp. 192-200.
View at Publisher |
View at Google Scholar
- Vine N. G., Leukes W. D. and Kaiser H. (2006). Probiotics in marine larviculture. FEMS Microbiol. Rev. 30: 404–427
View at Publisher |
View at Google Scholar
- Vine N. G., Leukes W. D., Kaiser H., Daya S., Baxter J. and Hecht T. (2004). Competition for attachment of aquaculture candidate probiotic and pathogenic bacteria on fish intestinal mucus. J. Fish Dis. 27: 319–325
View at Publisher |
View at Google Scholar
- Wang X. and Gibson G. R. (1993). Effects of the in vitro fermentation of oligofructose and inulin by bacteria growing in the human large intestine. J. Appl. Bacteriol 75: 373–380.
View at Publisher |
View at Google Scholar
- Wang, Y. -B., Li, J. -R. and Lin, J. (2008) Probiotics in aquaculture: Challenges and outlook. Aquacult. 281, pp. 1-4. Patel KP, Patel VJ, 2010. Probiotics, prebiotics and synbiotics. [http://www.nhlmmcgym.com/indian-journal15.htm].
View at Publisher |
View at Google Scholar
- Williams A. M., Probert C. S., Stepankova R., Tlaskalova-Hogenova H., Phillips A. and Bland P. W. (2006). Effects of microflora on the neonatal development of gut mucosal T cells and myeloid cells in the mouse. Immunology 119: 470-8
View at Publisher |
View at Google Scholar
- Wilson K. H. and Perini F. (1988). Role of competition for nutrients in suppression of Clostridium difficile by the colonic microflora. Infect. Immun. 56: 2610–2614.
View at Publisher |
View at Google Scholar
- Yoo J.Yand Kim S.S (2016). Probiotics and Prebiotics: Present Status and Future Perspectives on Metabolic Disorders. Nutrients. 8(3):173.
View at Publisher |
View at Google Scholar
- Z. Guo, X. Liu, Q. Zhang, Z. Shen, F. Tian, H. Zhang, Z. Sun, H. Zhang, W. Chen, Influence of consumption of probiotics on the plasma lipid profile: a meta-analysis of randomised controlled trials, Nutrition, metabolism, and cardiovascular diseases: NMCD 21 (2011) 844-850.
View at Publisher |
View at Google Scholar
- Zoumpopoulou G., Foligne B., Christodoulou K., Grangette C., Pot B. and Tsakalidou E. (2008). Lactobacillus fermentum ACA-DC 179 displays probiotic potential in vitro and protects against trinitrobenzene sulfonic acid (TNBS)-induced colitis and Salmonella infection in murine models. Int J Food Microbiol 121: 18-26
View at Publisher |
View at Google Scholar