- Open Access
Probiotic therapy - recruiting old friends to fight new foes
Gut Pathogensvolume 2, Article number: 5 (2010)
Against a backdrop of increasing antibiotic resistance, and the emergence of new and evolving pathogens, clinicians are increasingly forced to consider alternative therapies - probiotics are one such alternative.
With life-cycles measured in minutes as opposed to years, bacteria have an extraordinary ability to evolve and adapt rapidly to changes in their environment . Thus, in a world where only the fittest survive, those bacteria which have developed resistance to antibiotics will predominate. This is particularly apparent in hospital environments where bacteria are in constant contact with many different antibiotics; such repeated exposure has facilitated the development of multiple antibiotic resistance and the emergence of ever more virulent nosocomial infections.
Probiotic Therapy - a possible solution?
Faced with an emerging pandemic of antibiotic resistance, clinicians and scientists alike are now struggling to find viable therapeutic alternatives to our failing antibiotic wonder drugs . One such alternative may be bacteria themselves - the application of probiotics; so called "good bugs" (Fig. 1), for therapeutic effect [3, 4]. While the exact mechanisms by which probiotic bacteria inhibit pathogens are as yet poorly understood, some advances have nevertheless been made in our understanding of probiotic function . In addition to competing with pathogens for niches and nutrients, "competitively excluding" disease causing microbes from the host , certain probiotic bacteria have also been shown to produce potent antimicrobial peptides (bacteriocins) which specifically target the invading pathogen  (Fig. 2A). While traditional antibiotics usually exert their activities via a specific mode of action; for example, penicillin interferes with the cross-linking of two linear polymers by inhibiting the transpeptidase reaction, bacteriocins on the other hand have quite diverse activities. Nisin and many other structurally related lantibiotics for example, use the cell wall precursor lipid II bound to the membrane as a docking molecule for pore formation and combine at least two modes of action, i.e., pore formation and inhibition of cell wall biosynthesis, for antibacterial activity at nanomolar concentrations . These multiple modes of action significantly reduce (but do no eliminate) the risk of resistance development .
However, despite their potent anti-pathogenic effect, a significant limitation of this approach is that probiotic bacteria tend to be physiologically fragile; often not surviving to sufficiently high numbers during prolonged storage in delivery matrices such as foods (yogurt and probiotic drinks) or tablet formulations . Furthermore, following ingestion, the already depleted probiotics must face the considerable physiological defences of the host (gastric acidity, bile, low iron, elevated osmolarity and temperature) in order to colonize the gastrointestinal tract in sufficient numbers to exert a therapeutic effect [11, 12].
Patho-biotechnology - making good bugs better
One approach to improving the physiological robustness and stress tolerance of probiotic strains is patho-biotechnology [13, 14]. Essentially, this novel approach involves the generation of "improved" probiotic strains, using stress survival systems mined from more physiologically robust pathogenic microbes . The physiological versatility of pathogenic genera, oscillating between the external environment and the host, makes them a veritable treasure trove of genes that could potentially be used to improve the technological robustness of less well adapted probiotic strains . Indeed, recent work in our laboratory has shown that cloning and heterologous expression of a single bile resistance gene, from the food borne pathogen Listeria monocytogenes in the probiotic strain Bifidobacterium breve, not only improves gastrointestinal colonisation and persistence, but also significantly bolsters the clinical efficacy of the probiotic strain .
In addition to improving their physiological stress tolerance, resulting in improved delivery and persistence within the gut, recent studies have led to the development of 'designer probiotics' which specifically target enteric infections by blocking crucial ligand-receptor interactions between the pathogen and its target host cell [10, 18, 19]. Many disease causing bacteria exploit oligosaccharides displayed on the surface of host cells as receptors for toxins and/or adhesions, enabling colonization of the mucosa and entry of the pathogen or secreted toxins into the host cell. Blocking this adherence prevents infection (Fig. 2B), while toxin neutralization ameliorates symptoms until the pathogen is eventually overcome by the host immune system (Fig. 2C). 'Designer probiotics' have been engineered to express receptor-mimic structures on their surface . When administered orally these probiotics bind to and neutralize toxins in the gut lumen and interfere with pathogen adherence to the intestinal epithelium - thus essentially "mopping up" the infection. A particularly attractive feature of this toxin neutralisation strategy is that, unlike antibiotic therapy, it applies no selective pressure for evolution of resistance by the pathogen. Blocking toxin mediated host injury by the receptor mimic would negatively affect the capacity of the pathogen to survive and reproduce. Furthermore, mutations in a toxin sequence that prevents binding to a receptor mimic would logically also prevent the toxin from interacting with its natural target, thereby attenuating virulence. Therefore, widespread use of such agents in a therapeutic setting should have negligible long-term adverse consequences. As well as treating enteric infections, 'designer probiotics' are among the most recent conscripts in the war against AIDS, expressing HIV receptors which compete with host cell receptors for the virus, thus providing a natural innate barrier to HIV attachment and infection .
In addition to infection control (Fig. 3), probiotics can also be engineered to function as novel vaccine delivery vehicles which can stimulate both innate and acquired immunity, but lack the possibility of toxicity which exists with more conventional vaccines that rely on live attenuated pathogens . Probiotic vaccine carriers administered by the mucosal route (i.e. orally or by nasal spray) mimic the immune response elicited by natural infection and can lead to long lasting protection. Mucosal vaccine delivery also offers significant technological and commercial advantages over traditional formulations including: reduced pain and the possibility of cross contamination associated with intramuscular injection, as well as the lack of necessity for medically trained personnel to administer the vaccine - important considerations for large scale vaccination protocols in less well developed countries. Furthermore, not only do probiotics circumvent in vivo sensitivity to gastric acidity associated with oral application of therapeutic or prophylactic compounds, they can also be produced cheaply; grown to high levels, dried and stored for years at ambient temperatures.
Beyond conventional antibiotic therapies
In conclusion then, "designer probiotics" can be engineered to kill pathogens, neutralise toxins, and facilitate re-colonisation of the resident beneficial microflora while at the same time priming both the innate and adaptive immune system; strengthening the host against subsequent infection - an approach far beyond the reach of conventional antibiotic therapies. Thus, the war against the antibiotic resistant "super bugs" may eventually be won by recruiting engineered "good bugs" as our allies.
Sleator is Editor-in-Chief of the peer reviewed scientific journal Bioengineered Bugs http://www.landesbioscience.com/journals/biobugs.
MacLean RC, Hall AR, Perron GG, Buckling A: The population genetics of antibiotic resistance: integrating molecular mechanisms and treatment contexts. Nat Rev Genet. 2010, 11: 405-414. 10.1038/nrg2778.
Joerger RD: Alternatives to antibiotics: bacteriocins, antimicrobial peptides and bacteriophages. Poult Sci. 2003, 82: 640-647.
Sleator RD, Hill C: Battle of the bugs. Science. 2008, 321: 1294-1295. 10.1126/science.321.5894.1294b.
Ohashi Y, Ushida K: Health-beneficial effects of probiotics: Its mode of action. Anim Sci J. 2009, 80: 361-371. 10.1111/j.1740-0929.2009.00645.x.
Sleator RD, Hill C: New frontiers in probiotic research. Lett Appl Microbiol. 2008, 46: 143-147. 10.1111/j.1472-765X.2007.02293.x.
Callaway TR, Edrington TS, Anderson RC, Harvey RB, Genovese KJ, Kennedy CN, Venn DW, Nisbet DJ: Probiotics, prebiotics and competitive exclusion for prophylaxis against bacterial disease. Anim Health Res Rev. 2008, 9: 217-225. 10.1017/S1466252308001540.
Asaduzzaman SM, Sonomoto K: Lantibiotics: diverse activities and unique modes of action. J Biosci Bioeng. 2009, 107: 475-487. 10.1016/j.jbiosc.2009.01.003.
Wiedemann I, Breukink E, van Kraaij C, Kuipers OP, Bierbaum G, de Kruijff B, Sahl HG: Specific binding of nisin to the peptidoglycan precursor lipid II combines pore formation and inhibition of cell wall biosynthesis for potent antibiotic activity. J Biol Chem. 2001, 276: 1772-1779.
Sang Y, Blecha F: Antimicrobial peptides and bacteriocins: alternatives to traditional antibiotics. Anim Health Res Rev. 2008, 9: 227-235. 10.1017/S1466252308001497.
Culligan EP, Hill C, Sleator RD: Probiotics and gastrointestinal disease: successes, problems and future prospects. Gut Pathog. 2009, 1: 19-10.1186/1757-4749-1-19.
Sleator RD, Watson D, Hill C, Gahan CG: The interaction between Listeria monocytogenes and the host gastrointestinal tract. Microbiology. 2009, 155: 2463-2475. 10.1099/mic.0.030205-0.
Bezkorovainy A: Probiotics: determinants of survival and growth in the gut. Am J Clin Nutr. 2001, 73: 399S-405S.
Sleator RD, Hill C: Patho-biotechnology: using bad bugs to do good things. Curr Opin Biotechnol. 2006, 17: 211-216.
Sleator RD, Hill C: 'Bioengineered Bugs' - a patho-biotechnology approach to probiotic research and applications. Med Hypotheses. 2008, 70: 167-169. 10.1016/j.mehy.2007.03.008.
Sleator RD, Hill C: Rational design of improved pharmabiotics. J Biomed Biotechnol. 2009, 2009: 87-2752.
Sheehan VM, Sleator RD, Hill C, Fitzgerald GF: Improving gastric transit, gastrointestinal persistence and therapeutic efficacy of the probiotic strain Bifidobacterium breve UCC2003. Microbiology. 2007, 153: 3563-3571. 10.1099/mic.0.2007/006510-0.
Watson D, Sleator RD, Hill C, Gahan CG: Enhancing bile tolerance improves survival and persistence of Bifidobacterium and Lactococcus in the murine gastrointestinal tract. BMC Microbiol. 2008, 8: 176-10.1186/1471-2180-8-176.
Sleator RD, Hill C: Designer probiotics: a potential therapeutic for Clostridium difficile?. J Med Microbiol. 2008, 57: 793-794. 10.1099/jmm.0.47697-0.
Elson CO: From cheese to pharma: a designer probiotic for IBD. Clin Gastroenterol Hepatol. 2006, 4: 836-837. 10.1016/j.cgh.2006.05.034.
Paton AW, Morona R, Paton JC: Receptor-mimic probiotics: potential therapeutics for bacterial toxin-mediated enteric diseases. Expert Rev Gastroenterol Hepatol. 2010, 4: 253-255. 10.1586/egh.10.30.
Liu JJ, Reid G, Jiang Y, Turner MS, Tsai CC: Activity of HIV entry and fusion inhibitors expressed by the human vaginal colonizing probiotic Lactobacillus reuteri RC-14. Cell Microbiol. 2007, 9: 120-130. 10.1111/j.1462-5822.2006.00772.x.
Amdekar S, Dwivedi D, Roy P, Kushwah S, Singh V: Probiotics: multifarious oral vaccine against infectious traumas. FEMS Immunol Med Microbiol. 2010, 58: 299-306.
The author wishes to acknowledge the continued financial assistance of the Alimentary Pharmabiotic Centre, through funding by Science Foundation Ireland (SFI), the Health Research Board (HRB) and The Department of Agriculture, through the Food Institutional Research Measure (FIRM).