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In This Article
 »  Abstract
 »  Introduction
 »  History
 »  Prerequisites of...
 »  Probiotics as th...
 »  Urogenital infec...
 »  Diarrhea
 »  Infectious diarrheas
 »  Prevention of CDD
 »  Treatment of CDD
 »  Lactose malabsor...
 »  Helicobacter ...
 »  Inflammatory bow...
 »  Allergy
 »  Hypertension
 »  Hypercholesterolemia
 »  Kidney stones
 »  Cancer
 »  Growth and well-...
 »  Safety and tolerance
 »  Conclusion
 »  References

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EDUCATIONAL FORUM
Year : 2005  |  Volume : 37  |  Issue : 6  |  Page : 358-365
 

Probiotics: Making a comeback


Department of Pharmacology, Armed Forces Medical College, Pune-411040., India

Correspondence Address:
A K Sharma
Department of Pharmacology, Armed Forces Medical College, Pune-411040.
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0253-7613.19071

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 » Abstract 

Probiotics are nonpathogenic microbes used to confer health benefits to the recipient. The derangement of normal body flora has been held responsible for causation of various disorders. Probiotics have been tried in a number of infective and noninfective disorders and found useful, primarily because of their ability to supplement the normal body flora. Their use offers various advantages over-existing antimicrobial agents in being relatively cheap and safe. However, there are few reports of systemic fungemia associated with their use especially, in immunocompromised and severely debilitated patients. They also carry a risk of transferring resistance to other microbes including pathogens. In conclusion, more studies are required to establish their definite place in therapeutics.


Keywords: Bifidobacterium, Lactobacilli, microflora, Saccharomyces


How to cite this article:
Sharma A K, Mohan P, Nayak B B. Probiotics: Making a comeback. Indian J Pharmacol 2005;37:358-65

How to cite this URL:
Sharma A K, Mohan P, Nayak B B. Probiotics: Making a comeback. Indian J Pharmacol [serial online] 2005 [cited 2017 May 24];37:358-65. Available from: http://www.ijp-online.com/text.asp?2005/37/6/358/19071



 » Introduction Top


Introduction of antibiotics brought revolution in the treatment of infectious diseases. The dramatic results of chemotherapy lead to an enhanced interest and funding in this field and its rapid development.

However, the use of antimicrobial therapy is associated with the risk of increased incidence of drug resistance and opportunistic infections,[1] which can be avoided if the use of the antimicrobial agents can be minimized. One of the contributory factors for acquiring the infections is the decrease in the normal microflora at various sites in the body.

The nonpathogenic, micro-organisms or microbial mixtures may be used to improve microbial balance and to confer health benefits to the recipient. The microbes used for this purpose are called probiotics. (The term 'probiotic' in Greek means 'for life'.)


 » History Top


Benefits of using fermented milk products and poultices of mould breads have been known since long. However, nobel laureate Elie Metchnikoff gave the first account of practice of probiotic therapy via fermented milk products in 1907.[2] Application of this therapy to urogenital infections dates back at least to 1915.[3]

However, due to increased interest in antibiotics, only few studies were done on probiotics in the intertwining period of 7-8 decades, and this field was labelled as 'alternative medicine'.

There is a recent resurgence of interest in probiotics due to consumer demand for better therapies and problems like drug resistance and opportunistic infections.


 » Prerequisites of probiotic Top


A microbe may be used as a probiotic if it has been scientifically demonstrated to be having beneficial physiological effects and safety. It should preferably be nonpathogenic, of human origin, stable in acid and bile and be able to adhere to human mucosa[4] also should retain viability during storage and use.[5]


 » Probiotics as therapeutic tools Top


Probiotics are under study for a variety of pathophysiological states. Their status in various conditions, where they have the potential to establish their place more firmly, are discussed below.


 » Urogenital infections Top


Incidence of nonsexually transmitted urogenital infections, including urinary tract infections (UTI), bacterial vaginosis (BV) and vaginal candidiasis, is estimated to be quite high (around 1 billion per year) around the world.[3]

The ready availability and efficacy of antimicrobials has limited the attention paid to probiotics for UTI and BV. However, probiotics have been found to have a definitive role in the management of these diseases especially in recurrent and chronic cases.

Prevention of UTI

A number of clinical studies with Lactobacilli have shown encouraging results in preventing the recurrence of UTI.

Intra-vaginal insertion and perineal implantation of Lactobacilli GR1 strain twice weekly in patients suffering from recurrent UTI have been shown to result in infection free periods ranging from 4 weeks to 6 months.[6]

In another randomized double blind study conducted in 55 women taking Lactobacillus GR-1 and B-54 strains weekly/twice weekly by vaginal insertion, the mean incidence of UTI was reduced by 79%.[7]

Reid and Bruce also demonstrated that the administration of Lactobacilli as vaginal suppositories after treatment with antimicrobial agents reduced the recurrence rate to 21% as compared to 47% seen in control group.[8]

The above reports confirm the usefulness of probiotics in UTI but the number of studies is limited and more work needs to be done to establish their role.

Prevention of bacterial vaginosis and candidal vaginal infections

Majority of women, especially in the first part of their menstrual cycle, have transient abnormal pattern of vaginal flora resembling in some cases to bacterial vaginosis. In most of these cases, vaginal flora reverts back to normal pattern,[9] but if a probiotic may also be a natural means of correcting this abnormality and maintaining urogenital health.

Reid G et al demonstrated that daily oral administration of L. rhamnosus GR-1 and L. fermentum RC-14 improved vaginal flora and lowered yeast and coliform count.[10] On oral ingestion, these microbes pass through the gut and ascend from rectum to vagina and colonize there.[11]

In another comparative study, prophylaxis of recurrent candidal vaginitis and recurrent BV was studied between groups taking yogurt enriched with H2O2 producing Lactobacilli and pasteurized yogurt. After one month of study, 25% women in enriched group had an episode of BV as compared to 50% in pasteurized yogurt group (p=0.04). However, reduction in percentage of women with candida positive cultures in both groups was same, indicating that perhaps nonviable yogurt cultures also have an anticandidal effect.[12]

Hilton et al administered Lactobacilli for a longer period and studied the incidence of candidal vaginal infections. One group of patients consumed H2O2 producing Lactobacilli and another group consumed no yogurt for 6 months and then both groups mutually crossed over. The number of candidal vaginal infections per patient was 0.38 in yogurt group and 2.54 during no yogurt period (p=0.001).[13]

Since only few strains of Lactobacilli have been shown to be effective in bacterial vaginosis and vaginal candidiasis, more studies are warranted before such an approach can be recommended for routine use.

Treatment of bacterial vaginosis


Bacterial vaginosis is effectively treated with metronidazole and clindamycin, but it is associated with adverse effects and frequent recurrences. A number of studies have shown that probiotics if taken with antimicrobials can reduce the risk of vulvo-vaginal perturbations.

Hillier et al . found that the incidence of vaginal infection in pregnant women was inversely related to the intravaginal presence of H2O2 producing Lactobacilli .[14]

Neri et al . (1993) also demonstrated higher success rate of 28/32 in pregnant bacterial vaginosis patients taking Lactobacilli acidophilus yogurt two doses for 7 days as compared to 12/32 in placebo group.[15]

In spite of probiotics being useful in treating and preventing urogenital infections,[16] the lack of knowledge about them amongst physicians limits their use in day-to-day practice and retards their growth.[17]


 » Diarrhea Top


Diarrhea is a common gastrointestinal problem, especially in the developing world. It can result from multiple aetiologies. Probiotics have been shown to prevent and assist the recovery from many types of diarrheas.


 » Infectious diarrheas Top


In developing countries, incidence of infectious diarrhoea is very high due to poor sanitation and nutrition. The problem is best addressed by improving sanitation and nutrition but an inexpensive and effective probiotic also has a value.

Probiotics have been shown to reduce the incidence of diarrheal episodes and facilitate the recovery when used as an adjunct to oral rehydration therapy for acute diarrheas.

Lactobacilli GG, Bifidobacterium and Streptococcus thermophilus have been shown to reduce the incidence of diarrhea as compared to control groups.[18],[19] The use of Bifidobacterium and Streptococcus thermophilus also reduced rotavirus shedding.[19]

The recovery (in terms of reduction in duration of diarrhea) from acute diarrheas has been shown to be facilitated by Lactobacilli GG, L. reuteri, L. casei and S. boulardii . [20],[21],[22],[23]In AIDS-associated diarrhea, S. boulardii has been found to help resolution in 10 of 18 patients as opposed to 1 of 11 in placebo when administered for 1 week.[24] In another study, patients with HIV-related chronic diarrhea, Elmer et al . found it to be useful in 7 of 11 patients but in 2-4 weeks.[25]

The role of E. faecium SF68 in acute diarrhea cannot be ignored. It has been found to be effective in reducing diarrhea in adults after 1 week of treatment (0.6% in treatment group and 8.7% in placebo group, P=0.01);[26] however, it was not found to be useful in patients infected with V. cholerae /ETEC after 3 days treatment.[27]

Antimicrobial agent associated diarrhea

Diarrhea is one of the most common adverse effects of antibiotic therapy. The precise mechanism is not known; however, perturbation of normal intestinal flora leading to the following events seems to be responsible.

1.Decrease in short chain fatty acid produced by normal flora. These fatty acids are important for the nutrition of the enterocyte and for the absorption of water and electrolytes. [28], [29]

2.Loss of carbohydrate digesting gut bacteria leading to osmotic diarrhea.[30]

3.Direct stimulation of gut motility: For instance, erythromycin acts as motilin agonist to produce diarrhea.[31]

The re-establishment of gut flora and cure of antimicrobial agent associated diarrhea (AMAAD) has been an area of interest since long. Anecdotal evidence indicates that consumption of commercial unpasteurized yogurt is helpful in AMAAD.

Saccharomyces boulardii has reduced the incidence of diarrhea in patients taking tetracyclines or b-lactam antibiotics to 4.5% as compared to 17.5% with placebo.[32]

L. rhamnosus GG taken as yogurt has been shown to have a beneficial effect in volunteers on erythromycin.

The group taking erythromycin and L. rhamnosus GG had diarrhea for 2 days instead of 8 days as seen in control group taking erythromycin and sterilized yogurt.[33]

Bifidobacterium longum in the form of fermented yogurt has also been found to be useful in reducing stool frequency and abdominal discomfort in a crossover study involving 10 volunteers receiving erythromycin.[34] However, in volunteers taking clindamycin, B. longum in combination with Lactobacilli acidophilus was more effective than when given alone and in comparison to placebo and produced least derangement of intestinal microflora and lower incidence of gastrointestinal discomfort.[35]

E. faecium is another strain having a beneficial role in AMAAD. Wunderlich et al . (1989) found E. faecium SF68 to reduce the incidence of antibiotic associated diarrhea from 27.2% in placebo group to 8.7% in treatment group.[26]

Cl. difficile associated diarrhea and colitis

Cl. difficile associated disease (CDD) is almost always initiated by antimicrobial therapy. It consists of simple diarrhea that may progress to colitis, pseudomembranous colitis and toxic megacolon.[36] Probiotics in various clinical studies have been found to have beneficial role in the management of CDD.


 » Prevention of CDD Top


In patients receiving antibiotic therapy, consumption of probiotic containing both Lactobacilli and Bifidobacterium has been associated with lower incidence of positivity for Cl. difficile associated toxins in stools. [37]


 » Treatment of CDD Top


Metronidazole (first choice) and vancomycin (second choice, for cases resistant or not tolerating metronidazole or in whom it is contraindicated) are adequate treatment for the first episode of CDD. However, antibiotic treatment has a recurrence rate of about 20% in whom multiple recurrences are the rule.[36] For prevention of recurrences, no simple treatment is uniformly effective, so probiotics are being tried to break the cycle of recurrence.

Saccharomyces boulardii when administered as 1 g/day for 4 weeks along with standard course of metronidazole or vancomycin in the treatment of CDD resulted in lower relative risk (RR) of recurrence than placebo group (RR 0.43; 95% confidence interval 0.20-0.97).[38] The efficacy of S. boulardii was significant (recurrence rate 34.6%, compared with 64.7% on placebo; p=0.04) in patients with recurrent CDD, but not in patients with initial CDD (recurrence rate 19.3% compared with 24.2% on placebo; p=0.86). [38]

In another study, to further refine a standard regimen of S. boulardii and vancomycin; a group of patients received vancomycin (2 g/day) for 10 days and then additional S. bourlardii (1 g/day) for 28 days or placebo. A decrease in recurrence rate was observed in patients treated with vancomycin and S. bourlardii (16.7%) compared with those who received vancomycin and placebo (50%; p=0.05).[39]

L. plantarum 299v has also been found to reduce the recurrence of CDD but the number of patients studied is small . [40]

Probiotics, at present, in spite of their documented beneficial effects in CDD, are not recommended for routine prophylactic use for want of larger studies.

Traveler's diarrhea

In contrast to AMAAD and CDD, traveler's diarrhea is caused by the introduction of pathogenic bacteria through food or water that overwhelm the protective effects of normal intestinal flora.

In a study conducted on 225 Americans, the group taking L. rhamnosus GG had a lower rate of diarrhea per day as compared to the placebo group (3.9% vs. 7.4%, respectively, p=0.05).[41]

Similar larger study conducted in travelers from Austria revealed that the group given lyophilized S. boulardii 1 g/day had diarrheal rate of 28.7% as compared to 39.1% in placebo group (p=0.02).[42]

Study conducted in travelers from Turkey also demonstrated that Lactobacilli GG use reduced the incidence of diarrhea to 41% as compared to 46.5% in placebo group with overall protection rate of 11.8%.[43]


 » Lactose malabsorption associated diarrhea Top


Enterocyte lactase activity declines throughout childhood, hence 90% of Africans, Asians and South American adults are totally lactase deficient. Consumption of dairy products in such individuals leads to signs and symptoms of lactose intolerance such as flatulence, bloating, loose motions and at times constipation.[44]

The use of S. thermophilus and Lactobacilli delbrueckii as starter culture in yogurt has shown improvement in lactose digestion.[45] The benefit is due to the presence of microbial β-galactosidase (lactose) in the bacteria.

In a number of studies, better lactose digestion and absorption and reduction in gastrointestinal symptoms have been demonstrated in subjects who consumed fresh yogurt (with live yogurt cultures) as compared to pasteurized product with heat killed bacteria.[46] - [48]

Mode of action in urogenital infections and diarrheas

The beneficial effects of probiotics in UG infections and diarrheas have been ascribed to the manipulation of local flora composition. These changes can be achieved by the following mechanisms.

Production of inhibitory substances : Inhibitory substances such as organic acids, H2O2 and bacteriocins are produced which are harmful to pathogens. L. rhamnosus GG and L. reuteri have been found to produce inhibitory substances like microcin and reutericin, respectively.[49], [50] Vaginal flora prevents vaginal infections by creating unfavourable vaginal conditions for pathogens by producing H2O2 and fermenting glycogen to produce lactic acid and an acidic pH.

Inhibition of pathogen attachment : Competitive inhibition of bacterial attachment sites on epithelial surfaces is another mechanism. L. acidophilus has been shown to inhibit the attachment of E. coli to mucosal cells in pig ileum. There is no effect if L. acidophilus if given after attachment has already taken place.[51]

Competition for nutrients : Probiotics also deplete nutrients, which are essential for the proliferation of pathogens. An example is the depletion of monosaccharides, which is essential for Cl. difficile .[52]

Stimulation of IgA : S. boulardii has been found to stimulate secretory IgA in small intestine in rats.[53] L. rhamnosus GG has been found to cause stimulation of local IgA secretion in human intestine in rotavirus infection. [54]

Trophic effects on intestinal mucosa : Bifidobacterium and other probiotics have been shown to produce substances like butyrate, which stimulate the proliferation of normal epithelium and play role in maintaining mucosal barrier defences.[5]

Inhibition of action of microbial toxin : S. boulardii destroys Cl. difficile toxin A receptor in isolated rat ileum.[55]


 » Helicobacter pylori infections Top


Helicobacter pylori, which colonizes the stomach, is implicated in the aetiology of gastric ulcers and gastric cancer. Various preclinical studies shown that antibacterial substances produced by some Lactobacilli inhibit the growth, colonization and survival of this pathogen.[56]

Preliminary results in humans shown that milk fermented with Lactobacilli johnsonii strain can help to control H. pylori gastric infections, but cannot eradicate H. pylori .[56]

In some studies conducted on subjects positive for H. pylori , the incidence of side effects associated with antipylori antibiotic therapy was less when administered with Lactobacilli GG[57] or Bacillus clausii [58] but one study failed to demonstrate any beneficial effect of probiotic use as a supplement to the classical triple therapy with antibiotics.[59] In lieu of above reports, more number of studies are required to clearly define the role of probiotics.


 » Inflammatory bowel disease Top


Inflammatory bowel disease (IBD) is a collective term used for ulcerative colitis (UC) and Crohn's disease (CD). Traditional medication used in IBD includes 5-aminosalicylic acid (5-ASA) and corticosteroids. Corticosteroids are very effective in inducing remission in both UC and CD, but have no role in maintaining remission and are fraught with many unwanted effects.[60]

There is enough evidence that IBD is caused by an abnormal immune response to a luminal antigen and it appears that the antigens are probably commensal bacteria. [61],[62],[63],[64] In experimental studies, it has been proved that different bacteria elicits different types of cytokine response. In Crohn's disease, commensal E. coli strain stimulate the release of tumour necrosis factor-a (TNF-a) and interleukin-8 (IL-8) by inflamed mucosa. However, some lactobacilli strains including L. casei down regulate the spontaneous release of TNF-a by the inflamed tissue and also the inflammatory response induced by E. coli . [65],[66] Therefore, it makes sense to either eliminate some bacteria with antibiotics or to alter the gut flora, in favour of more beneficial bacteria, by the use of probiotics and prebiotics. (Prebiotics are dietary substances usually nondigested carbohydrates that stimulate the growth and metabolism of protective commensal enteric bacteria.)

Clinical trials suggest that some probiotics can be beneficial in preventing the relapse of IBD. In ulcerative colitis, oral administration of viable E. coli strain Nissle 1917 has been found to be as effective as mesalazine (the standard therapy for the maintenance of remission) in maintaining remission.[67], [68] The same probiotic also lowered the relapse rate (33% in test group vs 63% in placebo group) in cases of Crohn's disease.[69]

Another probiotic, S. boulardii, when administered in patients with quiescent Crohn's disease as coadjuvant therapy with mesalazine, produced lower clinical relapse rate as compared to mesalazine alone.[70]

Although these initial studies show promising prospects in IBD patients, further research on mechanism of action is desired so as to optimize their use.


 » Allergy Top


Infants with atopic eczema or cow's milk allergy have shown that probiotics can be a useful tool in the treatment of food allergy. In infants receiving extensively hydrolyzed whey formula with Lactobacilli GG or Bb12, there is significant improvement in the clinical score of atopic dermatitis and reduction in the markers of inflammation compared with placebo groups.[71], [72]

Rosenfeldt et al . also confirmed that administration of L. rhamosus and L. reutri for 6 weeks in atopic children up to 13 years of age resulted in higher improvement rate of eczema (56% compared to 15% in placebo group).[73]

The antiallergic effects of probiotics are suggested to be mediated through the induction of regulatory T cells and counter regulation of Th1 cells, [74] reduced immunogenicity of potential allergens through modification of their structures [75] strengthening of mucus defenses (production of IgA ), stabilization of gut mucosal barrier and down regulation of inflammatory responses.[76]


 » Hypertension Top


A large population in the world is estimated to have hypertension. Evidence exists to suggest that some decrease in blood pressure (BP) may result from consumption of certain Lactobacilli , or milk fermented with Lactobacilli.

Studies with human subjects are limited. However, in one placebo controlled trial, milk fermented with Lactobacilli helveticus and Saccharomyces cerevisiae, reduced systolic BP by 9.4 mmHg and 14.1 mmHg after 4 and 8 weeks, respectively, and diastolic BP by 6.9 mmHg after 8 weeks of consumption in known hypertensives.[77]

Attempts to identify the antihypertensive mechanism suggest that it may be due to a bacterial cell wall component or angiotensin-converting enzyme inhibiting peptides generated by probiotics. [56]


 » Hypercholesterolemia Top


Cholesterol is a component of cell membranes and nerve cells. It also acts as a precursor to certain hormones and vitamins. However, elevated levels of total blood cholesterol or other blood lipids are considered risk factors for developing coronary heart disease.

Although humans synthesize cholesterol, diet also plays a role in determining serum cholesterol levels. Probiotic have been evaluated for their effect on serum cholesterol levels. Consumption of yogurt containing E. faecium is effective in lowering LDL and total cholesterol.[78], [79] In another study, probiotic consumption was also found to increase HDL and reduce the ratio of LDL to HDL from 3.24 to 2.48.[80]

Precise mechanism of this effect is not known. However, assimilation of cholesterol by bacterial cells, deconjugation of bile acids by bacterial acid hydrolases and inhibition of hepatic cholesterol synthesis are some of the proposed mechanisms.[81]


 » Kidney stones Top


High level of oxalate in the urine is a risk factor for the development of kidney stones. An intestinal microbe called Oxalobacter formigenes can degrade oxalate through the enzyme oxalyl-CoA decarboxylase and thus limits its absorption.

Patients with calcium oxalate stone have been shown to have lower rate of colonization with Oxalobacter formigenes . Among stone formers, absence of intestinal Oxalobacter correlates with higher oxalate concentration and increased risk of hyperoxaluria.[82]

In another study, Bifidobacterium breve was found to possess oxalate-degrading capabilities and hence has a potential to be used as a probiotic in oxalate stone diseases for prophylaxis against new stone formation.[83]


 » Cancer Top


Chemical exposure is a potential cause for high risk of cancer. Chemicals causing cancer (carcinogens) can be ingested or generated by the metabolic activity of microbes that harbor in the gastrointestinal system.

It has been hypothesized that probiotic might decrease the exposure to chemical carcinogens by (i) detoxifying ingested carcinogens, (ii) decreasing the population or metabolic activity of bacteria that may generate carcinogenic compounds, (iii) producing compounds that inhibit the growth of tumor cells, (iv) stimulating the immune system to defend better against cancer cell proliferation or (v) producing metabolic products (e.g. butyrate) which improve programmed cell death (apoptosis).[56]

It has been demonstrated in various animal studies that supplementation with specific strains of Lactobacilli can prevent establishment, growth and metastasis of transplantable and chemically induced tumours.[84]

In humans also, the consumption of fermented dairy products containing Lactobacilli or Bifidobacterium has been found to have inverse relationship with incidence of breast and colon cancer.[85], [86]

As direct evidence in humans, the consumption of L. casie fermented milk has been shown to significantly reduce the recurrence of superficial bladder cancer. [87]


 » Growth and well-being Top


In an Indian study, involving 100 malnourished children, the use of 50 ml of fermented curd for 6 months , produced higher weight gain (1.3 kg vs. 0.81 kg in controls), greater height (3.2 cm vs. 1.7 cm in placebo group), lower incidence of diarrhea (21 vs. 35 episodes in controls) and fever (30 vs. 44 episodes in placebo).[88]

In another study, administration of milk formulae supplemented with Bifidobacterium lactis and Streptococcus thermophilus reduced the incidence of colic and irritability in infants as compared to control group.[89]

These beneficial effects of probiotics may be attributed to their ability to prevent various pathological states common in children especially gastrointestinal infections and milk allergy.

Problems associated with probiotic use

Viability of probiotics

An important problem with the use of probiotics is the maintenance of their viability to produce beneficial effects to the consumer. The probiotics need to survive in several environments including processing treatments, storage conditions and human body conditions (especially gastric acidity and action of bile salts).

The ability to live through the stressful acidic conditions and bile solutions in human body vary among the strains of probiotic bacteria. Only those strains, which tolerate these adverse conditions better, should be preferred.

The viability of probiotics may also be improved by using a medium, nutrient and temperature, which supports their survival.

Viability of Lactobacilli has been enhanced by encapsulation in artificial sesame oil for storage and in simulated high gastric or bile salt condition as compared to free cells.[90]

Storage at 4o C temperature is reported to be a most important factor in keeping probiotic Bifidobacterium viable during 4-week storage time.[91]

The use of prebiotics like isomalto-oligosaccharides has been found to be associated with higher levels of probiotics like Lactobaillus and Bifidobacterium after 1 month storage.[92]

The issue of viability of probiotics from the stage of processing till it is used by the consumer to produce benefits still remains a fertile field for more research.[91]


 » Safety and tolerance Top


Fermented dairy products and cereals have been an integral part of food for centuries. The available probiotic micro-organisms are also considered nonpathogenic, but these can be infective in a severely debilitated or immunosuppressed patient. To date, there have been only isolated reports linking probiotics with adverse effects. Some cases of liver abscess,[93] Lactobacillemia[94], [95] and S. boulardii fungemia[96],[97],[98] have been reported in such patients. On the other hand, S. boulardii has been used without complications to treat chronic diarrhea in AIDS patients.[24], [25]

Another reason of concern is the risk of transfer of resistance via probiotic agents as these agents have to be resistant to the antibiotics because they are to be used alongside. In fact, a study has demonstrated transfer of plasmid pAMb1, from L. reuteri to E. faecium and from E. faecium to E. faecalis in mouse intestinal tract.[99]

In a long-term study, undertaken in children for 1 year, consumption of 106sub-109sub CFU of Lactobacilli and Bifidobacteria daily did not only result in any adverse effect but also showed that probiotics taken over a long time improve gastrointestinal function and reduce the incidence of diaper rash.[100]


 » Conclusion Top


Probiotics are likely to emerge as alternative to conventional antimicrobial therapy, as they are relatively cheap and may have lower risk of resistance due to multifaceted mechanisms of action.

Studies have shown their beneficial effects in urogenital infections, diarrheal diseases, hypertension, oxalate renal stones, allergic disorders, cancer and in children as growth promoters. However, further studies are required to establish their place in the management of these conditions.

Some major limitations in establishing their role in the therapeutics may be lack of adequate knowledge about them among prescribers, and probably the preparations available over the counter contain nonviable organisms or strains that possess no antipathogenic activity.

In general, the published reports suggest that the risk of therapy with the available probiotics is small. However, the risk of transmission of resistance and apprehension about their use in immunocompromised patients remain as some of the issues that need further clarification.

 
 » References Top

1.Henry FC. Antimicrobial agents: General considerations. In: Hardman JG, Limbird LE, Gilman AG, editors. Goodman and Gilman's The pharmacological basis of therapeutics. 10th ed: McGraw-Hill, Medical Publishing Division;2001. p.1143   Back to cited text no. 1    
2.Weese JS, Anderson EC. Preliminary evaluation of lactobacillus rhamnosus strain GG, a potential probiotic in dogs. Can Vet J 2002;43:771-4.  Back to cited text no. 2    
3.Gregor RG, Bruce AW. Could probiotics be an option for treating and preventing urogenital infections? Medscape General Medicine (MedGenMed on the internet). 2001 [cited 2004 Sep 20]. Available from: http://www.medscape.com/viewarticle/408951   Back to cited text no. 3    
4.Custom probiotics [home page on the internet]. California: Welcome to custom probiotics; c2002 [updated 2004 Mar 13; cited 2004 Oct 25]. Intestinal microflora and probiotics. Available from : http://www. customprobiotics.com  Back to cited text no. 4    
5.Anuradha S, Rajeshwari K. Probiotics in health and disease. JIACM 2005;6:67-72.  Back to cited text no. 5    
6.Bruce AW, Reid G. Intravaginal instillation of lactobacilli for prevention of recurrent urinary tract infections. Can J Microbiol 1988;34:339-43.  Back to cited text no. 6    
7.Reid G, Bruce AW, Taylor M. Instillation of Lactobacilli and stimulation of indigenous organisms to prevent recurrence of urinary tract infections. Microecol Ther 1995;23:32-45.  Back to cited text no. 7    
8.Reid G, Bruce AW, Taylor M. Influence of three-day antimicrobial therapy and Lacto-bacillus vaginal suppositories on recurrence of urinary tract infections. Clin Ther 1992;14:11-6.  Back to cited text no. 8  [PUBMED]  
9.Keane FE, Ison CA, Taylor-Robinson D. A longitudinal study of the vaginal flora over a menstrual cycle. Int J STD AIDS 1997;8:489-94.  Back to cited text no. 9  [PUBMED]  [FULLTEXT]
10.Reid G, Charbonneau D, Erb J, Kochanowski B, Beuerman D, Poehner R, et al . Oral use of Lactobacilli GR-1 and L. fermentum RC-14 significantly alters vaginal flora: randomized placebo controlled trial in 64 healthy women. FEMS Immunol Med Microbiol 2003;35:131-4.  Back to cited text no. 10    
11.Reid G, Bruce AW, Fraser N, Heininamm C, Owen J, Henning B. Oral probiotics can resolve urogenital infections. FEMS Immunol Med Microbiol 2001;30:49-52.   Back to cited text no. 11    
12.Shalev E, Battino S, Weiner E, Colodner R, Keness Y. Ingestion of yogurt containing Lactobacilli acidophilus compared with pasteurized yogurt as prophylaxis for recurrent candidal vaginitis and bacterial vaginosis. Arch Fam Med 1996;5:593-6.   Back to cited text no. 12  [PUBMED]  
13.Hilton E, Isenberg HD, Alperstein P, France K, Borenstein MT. Ingestion of yogurt containing Lactobacilli acidophilus as prophylaxis for candidal vaginitis. Ann Intern Med 1992;116:353-7.  Back to cited text no. 13    
14.Hillier SL, Krohn MA, Klebanoff SJ, Eschenbach DA. The relationship of hydrogen peroxide-producing lactobacilli to bacterial vaginosis and genital microflora in pregnant women. Obstet Gynecol 1992;79:369-73.  Back to cited text no. 14    
15.Neri A, Sabah G, Samra Z. Bacterial vaginosis in pregnancy treated with yogurt. Acta Obstet Gynecol Scand 1993;72:17-9.  Back to cited text no. 15    
16.Vanderhoof JA. Probiotics: Future directions. Am J Clin Nutr 2001;73:1152-5.  Back to cited text no. 16    
17.Edmunds L. The underuse of probiotics by family physicians. Can Med Assoc J 2001;164:1157.  Back to cited text no. 17    
18.Szajewska H, Kotowska M, Mrukowicz JZ, Armanaska M, Mikolajczyk W. Efficiency of lactobacillus GG in prevention of nosocomial diarrhea in infants. J Pediatr 2001;138:361-5.  Back to cited text no. 18    
19.Saavedra JM, Bauman NA, Oung I, Perman JA, Yolken RH. Feeding of Bifidobacterium bifidum and Streptococcus thermophilus to infants in hospital for prevention of diarrhoea and shedding of rotavirus. Lancet 1994;344:1046-9.  Back to cited text no. 19    
20.Szajewska H, Mrukawicz JZ. Probiotics in the treatment and prevention of acute infectious diarrhea in infants and children: a systematic review of published randomized, double blind, placebo controlled trials. J Pediatr gastroenterolol Nutr 2001;3:17-25.  Back to cited text no. 20    
21.Von Niel CW, Feudtner C, Garrison MM, Christakis DA. Lactobacilli therapy for acute infectious diarrhea in children: a meta analysis. Pediatrics 2002;109:678-84.  Back to cited text no. 21    
22.Hhuang JS, Bausvaros A, Lee JW, Diaz A, Davidson EJ. Efficacy of probiotic use in acute diarrhea in children: a meta analysis. Dig Dis Sci 2002;47:2625-34.  Back to cited text no. 22    
23.Kurugol Z, Koturoglu G. Effects of Saccharomyces boulardii in children with acute diarrhea. Acta Paediatr 2005;94:44-7.  Back to cited text no. 23    
24.Saint-Marc T, Rossello-Prats L, Touraine JL. Efficacitι de Saccharomyces boulardii dans le traitement des diarrhιes du SIDA. Ann Med Interne 1991;142:64-5.  Back to cited text no. 24    
25.Elmer GW, Moyer KA, Surawicz CM, Collier AC, Hooton TM, McFarland V. Evaluation of Saccharomyces boulardii for patients with HIV-related chronic diarrhoea and in healthy volunteers receiving anti-fungals. Microecol Ther 1995;25:23-31.  Back to cited text no. 25    
26.Wunderlich PF, Braun L, Fumagalli I, D'Appuzo V, Heim F, Karly M, et al . Double-blind report on the efficacy of lactic acid-producing Enterococcus SF68 in the prevention of antibiotic-associated diarrhoea and in the treatment of acute diarrhoea. J Int Med Res 1989;17:333-8.  Back to cited text no. 26    
27.Mitra AK, Rabbani GH. A double-blind, controlled trial of Bioflorin (Streptococcus faecium SF68) in adults with acute diarrhea due to Vibrio cholerae and enterotoxigenic Escherichia coli. Gastroenterol 1990;99:1149-52.  Back to cited text no. 27    
28.Ruppin H, Bar-Meir S, Soergel KH, Wood CM, Schmitt MG Jr. Absorption of short-chain fatty acids by colon. Gastroenterol 1980;78:1500-7.  Back to cited text no. 28    
29.Firmansyah A, Penn D, Lebenthal E. Isolated colonocyte metabolism of glucose, glutamine, n-butyrate, and beta-hydroxy-butyrate in malnutrition. Gastroenterol 1989;97:622-9.  Back to cited text no. 29    
30.Clausen MR, Bonnen H, Tvede M, Mortensen PB. Colonic fermentation to short-chain fatty acids is decreased in antibiotic-associated diarrhea. Gastroenterol 1991;101:1497-504.  Back to cited text no. 30    
31.Peeters T, Matthijs G, Depoortere I, Cachet T, Hoogmartens J, Vantrappen G. Erythromycin is a motilin receptor agonist. Am J Physiol 1989;257:470-4.  Back to cited text no. 31    
32.Adam J, Barret C, Barret-Bellet A. Essais cliniques contr τlιs en double insu de l'Ultra-Levure Lyophilisιe. Étude multicentrique par 25 mιdecins de 388 cas. Gaz Med Fr 1977;84:2072-8.  Back to cited text no. 32    
33.Siitonen S, Vapaatalo H, Salminen S, Gordin A, Saxelin M, Wikberg R, et al . Effect of Lactobacilli GG yoghurt in prevention of antibiotic associated diarrhoea. Ann Med 1990;22:57-9.  Back to cited text no. 33    
34.Colombel JF, Cortot A, Neut C, Romond C. Yoghurt with Bifidobacterium longum reduces erythromycin-induced gastrointestinal effects. Lancet 1987;2:43.  Back to cited text no. 34    
35.Orrhage K, Brismar B, Nord CE. Effects of supplements of Bifidobacterium longum and Lactobacilli acidophilus on the intestinal microbiota during administration of clindamycin. Microb Ecol Health Dis 1994;7:17-25.  Back to cited text no. 35    
36.McFarland LV. The epidemiology of Clostridium difficile infections. Gastroenterol Int Viewpoints on Dig Dis 1991;4:82-5.  Back to cited text no. 36    
37.Plummer S, Weaver MA, Harris JC, Dee P, Hunter J. Clostridium difficile pilot study: effects of probiotic supplementation on the incidence of C. difficile diarrhea. Int Microbiol 2004;7:59-62.  Back to cited text no. 37    
38.McFarland LV, Surawicz CM, Greenberg RN, Fekety R, Elmer GW, Moyer KA. A randomized placebo-controlled trial of Saccharomyces boulardii in combination with standard antibiotics for Clostridium difficile disease. JAMA 1994 Jun 22-29;271:1913-8. Erratum in: JAMA 1994;272:518.   Back to cited text no. 38    
39.Surawicz CM, McFarland LV, Greenberg RN, Rubin M, Fekety R, Mullingan ME. The search for a better treatment for recurrent Clostridium difficile disease: the use of high dose vancomycin combined with Saccharomyces boulardii. Clin Infect Dis 2000;31:1012-7.   Back to cited text no. 39    
40.Wullt M, Hagslatt ML, Odenholt I. Lactobacilli plantarum 299v for the treatment of recurrent Clostridium difficile-associated diarrhea: a double-blind, placebo-controlled trial. Scand J Infect Dis 2003;35:365-7.   Back to cited text no. 40    
41.Hilton E, Kolakowski P, Singer C, Smith M. Efficacy of Lactobacilli GG as a diarrheal preventive in travelers. J Travel Med 1997;4:41-3.  Back to cited text no. 41    
42.Kollaritsch H, Holst H, Grobara P, Wiedermann G. Prevention of traveler's diarrhea with Saccharomyces boulardii . Results of a placebo controlled double-blind study. Fortschr Med 1993;111:152-6.   Back to cited text no. 42    
43.Oksanen PJ, Salminen S, Saxelin M, Hamalainen P, Jhantola-Vormisto A, Muurasniemi-Isoviita L, et al . Prevention of traveler's diarrhea by Lactobacilli GG. Ann Med 1990;22:53-6.  Back to cited text no. 43    
44.Palmer KR, Penman ID. Diseases of alimentary tract and pancreas. In Haslett C, Edwin RC, John A A Hunter, Nicholas AB, Editors. Davidson's Principles and Practice of Medicine. 18th edition. London UK: Churchill Livingstone; 1999. p. 651.   Back to cited text no. 44    
45.Kolars JC, Levit MD, Aouji M, Savaiano DA. Yogurt - an autodigesting source of lactose. N Engl J Med 1984;310:1-3.  Back to cited text no. 45    
46.Rizkalla SW, Luo J, Kabir M, Chevalier A, Pacer N, Slasma G. Chronic consumption of fresh but not heated yogurt improves breath-hydrogen status and short chain fatty acid profiles: a controlled study in healthy men with or without lactose maldigestion. Am J Clin Nutr 2000;72:1474-9.   Back to cited text no. 46    
47.Labayen I, Forga L, Gonzalez A, Levoir-Wijnkoop I, Nutr R, Martinez JA. Relationship between lactose digestion, gastrointestinal transit time and symptoms in lactose malabsorbers after dairy consumption. Aliment Pharmacol Ther 2001;15:543-9.   Back to cited text no. 47    
48.Pelletier X, Laure-Boussuge S, Donazzolo Y. Hydrogen excretion upon ingestion of dairy products in lactose intolerant male subjects: importance of the live flora. Eur J Clin Nutr 2001;55:509-12.  Back to cited text no. 48    
49.Kabuki T, Saito T, Kawai Y, Uemura J, Itoh T. Production, purification and characterization of reutericin 6, a bacteriocin with lytic activity produced by Lactobacilli reuteri LA6. Int J Food Microbiol 1997;34:145-56.  Back to cited text no. 49    
50.Silva M, Jacobus NV, Deneke C, Gorbach SL. Antimicrobial substance from a human Lacto-bacillus strain. Antimicrob Agents Chemother 1987;31:1231-3.  Back to cited text no. 50    
51.Blomberg L, Henriiksson A, Conway PL. Inhibition of adhesion of Escherichia coli K88 to piglet ileal mucus by Lactobacilli spp. Appl environ Microbiol 1993;59:34-9.  Back to cited text no. 51    
52.Wilson KH, Perini F. Role of competition for nutrients in suppression of Clostridium difficile by the colonic microflora. Infect Immun 1988;56:2610-14.  Back to cited text no. 52    
53.Buts J-P, Bernasconi P, Vaerman J P, Dive C. Stimulation of secretory IgA and secretory component of immunoglobulins in small intestine of rats treated with Saccharomyces boulardii. Dig Dis Sci 1990;35:251-6.  Back to cited text no. 53    
54.Kaila M, Isolauri E, Saxelin M, Arvilommi H, Vesikari T. Viable versus inactivated Lactobacilli strain GG in acute rotavirus diarrhoea. Arch Dis Child 1995;72:51-3.  Back to cited text no. 54    
55.Pothoulakis C, Kelly CP, Joshi MA, Gao N, O'Keane CJ, Castagliuolo I, et al . Saccharomyces boulardii inhibits Clostridium difficile toxin A binding and enterotoxicity in rat ileum. Gastroenterol 1993;104:1108-15.  Back to cited text no. 55    
56.Usprobiotics [home page on the internet]. California: usprobiotics.org. c2004 [updated 2005 Jan 05; cited 2005 Jan 25]. Probiotics basics. Available from: http:// www.usprobiotics.org/index.htm   Back to cited text no. 56    
57.Armuzzi A, Cremonini F, Ojetti V, Bartolozzi F, Canducci F, Candelli M, et al . Effect of Lactobacilli GG supplementation on Antibiotic-Associated Gastrointestinal side effects during H. pylori eradication therapy: A pilot study. Digestion 2001;63:1-7.  Back to cited text no. 57    
58.Nista EC, Candelli M, Cremonini F, Cazzato IA, Zocco MA, Franceschi F, et al . Bacillus clausii therapy to reduce side effects of anti- Helicobacter pylori treatment: randomized, double-blind, placebo-controlled trial. Aliment Pharmacol Ther 2004;20:1181-8.  Back to cited text no. 58    
59.Sheu BS, Wu JJ, Lo CY, Wu HU, Chen JH, Lin YS, et al . Impact of supplement with Lactobacilli and Bifidobacterium containing yogurt on triple therapy for Helicobacter pylori eradication. Aliment Pharmacol Ther 2002;16:1669-75.  Back to cited text no. 59    
60.Irish medical news [home page on the internet]. Ireland:Irish medical news; [updated 2005 Mar 22; cited 2005 Mar 23]. Recent developments in inflammatory bowel disease. Available from: http://www.irishmedicalnews/articles.asp  Back to cited text no. 60    
61.Macpherson A, Khoo UY, Forgacs I, Philpott-Howard J, Bjarnason I. Mucosal antibodies in inflammatory bowel disease are directed against intestinal bacteria. Gut 1996;38:365-75.  Back to cited text no. 61    
62.Pirzer U, Schonhaar A, Fleischer B, Hermann E, Meyer Zum BKH, et al . Reactivity of infiltrating T lymphocytes with microbial antigens in Crohn's disease. Lancet 1991;338:1238-9.  Back to cited text no. 62    
63.D'Haens GR, Geboes K, Peeters M, Baert F, Penninckx F, Rutgeerts P. Early lesions of recurrant Crohn's disease caused by infusion of intestinal contents in excluded ileum. Gastroenterol 1998;114:262-7.  Back to cited text no. 63    
64.Casellas F, Barruel N, Papa M, Guarner F, Antolin M, Videla S, et al . Antiinflammatory effects of enterically coated amoxycillin-clavulanic acid in active ulcerative colitis. Inflamm Bowel Dis 1998;4:1-5.  Back to cited text no. 64    
65.Borruel N, Carol M, Casellas F, Antolin M, de Lara F, Espin E, et al . Increased mucosal TNF-α production in Crohn's disease can be downregulated ex vivo by probiotic bacteria. Gut 2002;51:659-64.   Back to cited text no. 65    
66.Borruel N, Casellas F, Antolin M, Llopis M, Carol M, Espiin E, et al . Effcets of nonpathogenic bacteria on cytokine secretion by human intestinal mucosa. Am J Gastroenterol 2003;98:865-70.   Back to cited text no. 66    
67.Kruis W, Schutz E, Fric P, Fixa B, Judmaier G, Stolte M. Double blind comparison of an oral Escherichia coli preparation and mesalazine in maintaining remission in ulcerative colitis. Aliment Pharmacol Ther 1997;11:853-8.  Back to cited text no. 67    
68.Rembacken BJ, Snelling AM, Hawkey PM, Chalmers DM, Axon AT. Non-pathogenic Escherichia coli versus mesalazine for the treatment of ulcerative colitis: a randomized trial. Lancet 1999;354:635-9.   Back to cited text no. 68    
69.Malchow HA. Crohn's disease and Escherichia coli. J Clin Gastroenterol 1997;25:653-8.  Back to cited text no. 69    
70.Guslandi M, Mezzi G, Sorghi M, Testoni PA. Saccharomyces boulardii in maintenance treatment of Crohn's disease. Dig Dis Sci 2000;45:1462-4.   Back to cited text no. 70    
71.Majamaa H, Isolauri E. Probiotics: a novel approach in the management of food allergy. J Allergy Clin Immunol 1997;99:179-86.  Back to cited text no. 71    
72.Isolauri E, Arvola T, Sutas Y, Moilanen E, Salminen S. Probiotics in the management of atopic eczema. Clin Exp Allergy 2000;30:1604-10.  Back to cited text no. 72    
73.Rosenfeldt V, Benfeldt E, Neilsen SD, Michaelsen KF, Jeppesen DL, Valerius NH, et al . Effects of probiotics Lactobacilli strains in children with atopic dematitis. J Allergy Clin Immunol 2003;111:390-5.  Back to cited text no. 73    
74.Von der Weid T, Billiard C, Schiffrin E. Induction by a Lactic acid bacterium of a population of CD4 T cells with low proliferative capacity that produce transforming growth factor and IL 10. Clin Diagnost Lab Immunol 2001;8:695-701.  Back to cited text no. 74    
75.Rokka T, Syvaoja EL, Tuomine J, Coronen H. Release of bioactive peptides by enzymatic proteolysis of Lactobaccilus GG fermented UHT milk. Milchwissenschaft 1997;52:675-8.  Back to cited text no. 75    
76.Kirjavainen PV. Probiotics and the management of food allergy. In: Mattila-Sandholm T, saarela M, editors. Functional dairy products. Cambridge, UK: Woodhill Publishing; 2003.   Back to cited text no. 76    
77. Hata Y, Yamamoto M, Ohni M, Nakajima K, Nakamura Y Takano T. A placebo-controlled study of the effect of sour milk on blood pressure in hypertensive subjects. Am J Clin Nutr 1996;64:767-71.  Back to cited text no. 77    
78.Agerholm-Larsen L , Bell ML, Grunwald GK, Astrup A. The effect of probiotic milk product on plasma cholesterol: a meta-analysis of short-term intervention studies. Eur J Clin Nutr 2000;54:856-60.  Back to cited text no. 78    
79.Hlivak P, Odraska J, Ferencik M, Ebringer L, Jahnova E, Mikes Z. One-year application of probiotic strain Enterococcus faecium M-74 decreases serum cholesterol levels. Bratisl Lek Listy. 2005;106:67-72.  Back to cited text no. 79    
80.Kiebling G , Schneider J, Jahreis G. Long-term consumption of fermented dairy products over 6 months increases HDL cholesterol. Eur J Clin Nutr 2002;56:843-9.   Back to cited text no. 80    
81.Lovegrove J,Jackson K. Coronary heart disease. In: Mattila Sandholm T, Saarela M, editors. Functional dairy products. Cambridge, UK: Woodhill Publishing; 2003.  Back to cited text no. 81    
82.Troxel SA, Sidhu H, Kaul P, Low RK. Intestinal Oxalobacter formigenes colonization in calcium oxalate stone formers and its relation to urinary oxalate. J Endourol 2003;17:173-6.  Back to cited text no. 82    
83.Kodama T, Mikami K, Akakura K, Takei K, Naya Y, Ueda T, et al . Detection of Oxalobacter formigenes in human feces and study of related genes in a new oxalate-degrading bacterium. Hinyokika Kiyo 2003;49:371-6.  Back to cited text no. 83    
84.Rafter J. Lactic acid bacteria and cancer. Br J Nutr 2002;88:89-94.  Back to cited text no. 84    
85.Von't Veer P, Von Leer EM, Rietdijk A, Kok FJ, Schouten EG, Hermus RJ, et al . Combination of dietary factors in relation to breast cancer occurance. Int J Cancer 1991;47:649-53.  Back to cited text no. 85    
86.Kampman E, Goldbohm RA, van-den Brandt PA, Van't Veer P. Fermented dairy products, calcium and colorectal cancer in the Netherland cohort study. Cancer Res 1994;54:363-5.  Back to cited text no. 86    
87.Aso Y, Akaza H, Kotake T, Tsukamoto T, Imai K, Naito S. Preventive effects of a Lactobacilli casei preparation on the recurrence of super-ficial bladder cancer in a double-blind trial. Eur Urol 1995;27:104-9.  Back to cited text no. 87    
88.Saran S, Gopalan S. and Krishna T.P. Use of fermented foods to combat stunting and failure to thrive. Nutrition 2002;18:393-6.  Back to cited text no. 88    
89.Jose M Saavedra, Adel Abi-Hanna, Nancy Moore, Robert H Yolken. Long-term consumption of infant formulas containing live probiotic bacteria: tolerance and safety. Am J Clin Nutr 2004;79:261-7.  Back to cited text no. 89    
90.RC Hou, MY Lin, MMC Wang, JTC Tzen. Increase of viability of entrapped cells of Lactobacilli delbrueckii ssp bulgaricus in Artificial Sesame oil Emulsions. J Dairy Sci 2003;86:424-8.   Back to cited text no. 90    
91.Jürgen Schrezenmeir, Michael de Vrese. Probiotics, prebiotics, and synbiotics-approaching a definition. Am J Clin Nutr 2001;73:361-4.  Back to cited text no. 91    
92.Ming-Ju Chen, Kun-Nan Chen, Chin-Wen Lin. Optimization of the Viability of Probiotics in a Fermented Milk Drink by the Response Surface Method. Asian-Aust J Anim Sci 2004;17:705-11.  Back to cited text no. 92    
93.Rautio M, Jousimies-Somer H, Kauma H, Pietarinen I, Saxelin M, Tynkkynen S, et al . Liver abscess due to a Lactobacilli rhamnosus strain indistinguishable from L. rhamnosus strain GG. Clin Infect Dis 1999;28:1159-60.   Back to cited text no. 93    
94.Horwitch CA, Furseth HA, Larson AM, Jones TL, Olliffe JF, Spach DH, et al . Lactobacillemia in three patients with AIDS. Clin Infect Dis 1995; 21:1460-2.   Back to cited text no. 94    
95.Saxelin M, Chuang NH, Chassy B, Rautelin M, Makela PH, Salminen S, et al . Lactobacilli and bacteremia in southern Finland, 1989-1992.Clin Infect Dis1996;22:564-6.   Back to cited text no. 95    
96.Pletincx M, Legein J, Vandenplas Y. Fungemia with Saccharomyces boulardii in a 1-year-old girl with protracted diarrhea. J Pediatr Gastroenterol Nutr 1995;21:113-5.   Back to cited text no. 96    
97.Piarroux R, Millon L, Bardonnet K, Vagner O, Koeing H. Are Saccharomyces yeasts harmful to patients? Lancet. 1999;353:1851-2.   Back to cited text no. 97    
98.Hennequin C, Kauffmann-Lacroix C, Jobert A, Viard JP, Ricour C, Jacquemin JL, et al . Possible role of catheters in Saccharomyces boulardii fungemia. Eur J Clin Microbiol Infect Dis 2000;19:16-20.   Back to cited text no. 98    
99.McConnell MA, Mercer AA, Tannock GW. Transfer of plasmid pAMb1 between members of the normal microflora inhabiting the murine digestive tract and modification of the plasmid in a Lactobacilli reuteri host. Microb Ecology Health Disease 1991;4:343-55.   Back to cited text no. 99    
100.Saavedra JM, Abi-Hanna A, Moore N, Yolken R. Effect of long term consumption of infant formulas with Bifidobacteria and S. thermophilus on stool pattern and diaper rash in infants. J Pediatr Gastroenterol Nutr 1998;27:82.  Back to cited text no. 100    



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