mja.com.au | The Medical Journal of Australia

Home | Issues | MJA shop | MJA Careers | Contact | Topics | Search | RSS  | Login | Buy full access

"Natural" therapy for infectious diseases

Clayton L Golledge and Thomas V Riley

Introduce the right kind of bacteria and several pathogens lose their niche in the human host -- that's the rationale behind probiotic therapy. These and some other "natural" therapies are popular with patients and increasingly supported by research results.

MJA 1996; 164: 94


Readers may print a single copy for personal use. No further reproduction or distribution of the articles should proceed without the permission of the publisher. For permission, contact the Australasian Medical Publishing Company
Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au/>".

Introduction - Useful bacteria - Other examples of "natural" therapies - References - Authors' details

Register to be notified of new articles by e-mail - Current contents list - ©MJA1997


 

Introduction

Antimicrobial therapy is at the crossroads. Drug development is palpably slowing and antimicrobial resistance is inexorably increasing. The early promise of exciting breakthroughs in the field of immunotherapy of infectious diseases has not been fulfilled, although progress continues to be made.

Patients too are changing and becoming better informed about their diseases and possible therapeutic strategies. More and more they are looking to providers of "alternative" therapies, either as adjunctive treatment or to replace conventional medical therapy.

There are several non-antibiotic approaches to the treatment and prevention of infection. Phytomedicines (plant-based remedies in the form of teas, extracts and oils) are a multimillion dollar industry worldwide,1 and many are targeted towards infectious diseases. Some of these remedies have been, or are being, studied in controlled clinical trials, although few good data currently exist. Nevertheless, it behoves the informed practitioner to be aware of some of the possibilities and the current status of research with these compounds.  

Useful bacteria

There is no doubt that the normal intestinal flora protects the host against many diseases.2 Our intestinal flora may be perturbed in disease and by diet and antibacterial substances, both prescribed and present in foodstuffs. "Probiotic" therapy uses a live microbial supplement to beneficially affect the host.2 Three genera that have been shown to be important components of the intestinal flora and probiotic therapies are lactobacilli, streptococci and bifidobacteria. Most work has been done with lactobacilli in the gut and in the urogenital tract of women.

Women suffering recurrences of urinary tract infection have a urogenital flora depleted of lactobacilli.2,3 Treatment with oestrogen supplementation can replace the lactobacillus biofilm and reduce the incidence of urinary tract infection.4 A lack of lactobacilli and overgrowth of anaerobes is a necessary precondition of bacterial vaginosis.5 Candida vaginitis is also associated with a lack of lactobacilli, usually induced by antimicrobial therapy. Lactobacilli are also susceptible to spermicidal preparations containing nonoxynol-9, which explains, at least in part, the increased incidence of urogenital infections seen in women who use such contraceptives.6

Lactobacilli have been used, with varying degrees of success, to prevent urinary tract infection in women,7 vulvovaginal candidosis8,9 and bacterial vaginosis.9 Unfortunately, all the studies, while showing at least some benefit, suffered from either a lack of adequate controls or low numbers of compliant patients.

Questions still to be answered are how best to deliver lactobacilli and which species is best to use. Lactobacilli taken orally do not persist in the gut, so continuous dosing is required.10 Commercial pasteurised yoghurts contain no useful viable bacteria. Direct high-concentration intravaginal delivery appears to be the most useful technique in the prevention of urogenital infections, as indicated by two recent publications employing vaginal pessaries containing 109 viable cells of Lactobacillus casei.11,12 Limited studies suggest that L. acidophilus or L. casei appear to be equally effective.9,11,12

Diarrhoea associated with Clostridium difficile (CDAD) may be difficult and expensive to treat, and relapse rates approximate 25% with a variety of different treatment regimens. Oral Lactobacillus GG has been used with success in the therapy of relapsing CDAD,13 and rectal administration of faecal enemas14 or pure cultures of a non-toxigenic strain of C.difficile15 has also been used in the treatment of difficult cases.

Lately the results of several clinical trials of the yeast Saccharomyces boulardii for the treatment of CDAD have been published. When swallowed, S. boulardii survives gastric acid, establishes itself in the intestinal tract and multiplies to high numbers. It is not inhibited by antibiotics and does not affect the normal flora significantly.16 S. boulardii is effective in preventing CDAD and in treating various types of infectious diarrhoea.17,18 It may be that S. boulardii therapy becomes an essential component of primary therapy for CDAD, particularly given concern about the use of oral vancomycin and the emergence of vancomycin-resistant enterococci.  

Other examples of "natural" therapies

Garlic was once used by millions to ward off vampires and was first prescribed in 3000 BC by the Sumerians.1 The antibacterial properties of garlic have been known for many years and can be attributed to the presence of allin which, when converted to allicin in vivo, is active against many bacteria.1 Traditional Chinese medicine has provided us with artesunate, a qinghaosu derivative, and a potentially useful agent for the treatment of malaria.19 Many traditional Australian Aboriginal remedies have yet to be investigated, but tea-tree oil is currently enjoying a renaissance in popularity as a topical antimicrobial agent. Recent studies have shown it to be effective in vitro against a variety of organisms, including methicillin-resistant Staphylococcus aureus,20 and several clinical trials are now under way. Cranberry juice has been a folk remedy for urinary tract infection since early this century and is widely used throughout the United States. Studies in vitro have shown that cranberry juice is able to diminish the binding of Escherichia coli to eukaryotic cells. A recent prospective, randomised, placebo-controlled trial21 among elderly women with asymptomatic bacteriuria showed a 50% reduction in the incidence of both asymptomatic and symptomatic bacteriuria. Cranberry juice is now being marketed in Australia and is also available in capsule form.

"Natural" therapies are viewed favourably by many patients, chiefly because they believe, often correctly, that they are associated with fewer detrimental effects than most antibiotics. Unfortunately, the medical profession has been slow to embrace natural therapies and good scientific data are lacking. For the few situations discussed here there may be an important role for these agents and, while the results of further trials are awaited, we think that judicious use of adjunctive or replacement natural therapy is easy to justify.  

References

  1. Sears C. The easy way to sell drugs. New Scientist 1995; 2002: 36-40.
  2. Fuller R. Probiotics in human medicine. Gut 1991; 32: 439-442.
  3. Marrie TJ, Swantee CA, Hartlen M. Aerobic and anaerobic urethral flora of healthy females in various age groups and of females with urinary tract infections. J Clin Microbiol 1980; 11: 654-657.
  4. Raz R, Stamm WE. A controlled trial of intravaginal estriol in postmenopausal women recurrent urinary tract infections. N Engl J Med 1993; 329: 753-803.
  5. Hillier SL, Krohn MA, Klebarolt SJ, Eschenbach DA. The relationship of hydrogen peroxide-producing lactobacilli to bacterial vaginosis and genital microflora in pregnant women. Obstet Gynecol 1992; 79: 369-373.
  6. Hooton TM, Fihn SD, Johnson C, et al. Association between bacterial vaginosis and acute cystitis in women using diaphragms. Arch Intern Med 1989; 149: 1932-1936.
  7. Bruce AW, Reid G, McGroanty JA. Preliminary study on the prevention of recurrent urinary tract infection in adult women using intravaginal lactobacilli. Int Urogynecol J 1992; 3: 22-25.
  8. Hilton E, Isenberg HD, Alperstein P. Ingestion of yogurt containing Lactobacilli acidophilus as prophylaxis for candidal vaginitis. Ann Intern Med 1992; 116: 353-357.
  9. Fredricsson B, Englund K, Weintraub L, et al. Ecological treatment of bacterial vaginosis [letter]. Lancet 1987; 1: 276.
  10. Goldin BR, Gorbach SL. The effect of milk and lactobacillus feeding on human intestinal bacterial enzyme activity. J Clin Nutr 1984; 39: 756-761.
  11. Reid G, Millsap K, Bruce AW. Implantation of Lactobacillus casei var rhamnosus into vagina [letter]. Lancet 1994; 344: 1229.
  12. Hilton E, Rindos P, Isenberg HD. Lactobacillus GG vaginal suppositories and vaginitis [letter]. J Clin Microbiol 1995; 33: 1433.
  13. Gorbach SL, Chang TW, Goldin B. Successful treatment of relapsing Clostridium difficile colitis with Lactobacillus GG [letter]. Lancet 1987; 2: 1519.
  14. Tvede M, Rask-Madsen J. Bacteriotherapy for chronic relapsing Clostridium difficile diarrhoea in six patients. Lancet 1989; 1: 1156-1160.
  15. Seal D, Borriello SP, Barclay F, et al. Treatment of relapsing Clostridium difficile diarrhoea by administration of a nontoxigenic strain. Eur J Clin Microbiol 1987; 6: 51-53.
  16. McFarland LV, Surawicz CM, Greenberg RN, et al. A randomized placebo-controlled trial of Saccharomyces boulardii in combination with standard antibiotics for Clostridium difficile disease. JAMA 1994; 271: 1913-1918.
  17. Surawicz CM, Elmer GW, Speelman P, et al. Prevention of antibiotic-associated diarrhea by Saccharomyces boulardii : a prospective study. Gastroenterology 1989; 96: 981-988.
  18. McFarland LV, Bernasconi P. A review of a novel biotherapeutic agent: Saccharomyces boulardii . Microb Ecology Health Dis 1993; 6: 157-171.
  19. Looareesuwan S, Viravan C, Vanijanonta S, et al. Randomised trial of artesunate and mefloquine alone and in sequence for uncomplicated falciparum malaria. Lancet 1992; 339: 821-824.
  20. Carson CF, Cookson BD, Farrelly HD, Riley TV. Susceptibility of methicillin-resistant Staphylococcus aureus to the essential oil of Melaleuca alternifolia . J Antimicrob Chemother 1995; 35: 421-424.
  21. Avorn J, Monane M, Gurwitz JH, et al . Reduction of bacteriuria and pyuria after ingestion of cranberry juice. JAMA 1994; 271: 751-754. o
 


Authors' details

Department of Microbiology and Infectious Diseases, Western Australian Centre for Pathology and Medical Research, Perth, WA.
Clayton L Golledge, FRCPA, FACTM, Consultant in Clinical Microbiology and Infectious Diseases.
Thomas V Riley, PhD, FASM, Associate Professor; also Principal Research Scientist, Department of Microbiology, The University of Western Australia.
No reprints will be available. Correspondence: Dr C L Golledge, Department of Microbiology and Infectious Diseases, The Western Australian Centre for Pathology and Medical Research, Queen Elizabeth II Medical Centre, Nedlands, WA 6009.
E-mail: triley AT cyllene.uwa.edu.au


Home | Issues | MJA shop | Terms of use | MJA Careers | More... | Contact | Topics | Search | RSS 

mja.com.au | The Medical Journal of Australia  

©MJA 1997

<URL: http://www.mja.com.au/> © 1997 Medical Journal of Australia.